Author: "Sub General Pharmaceutics" / Publication Year Range: Last 50 years - Searchworks@Jio Institute Digital Library Search Results

Your search keyword '"Sub General Pharmaceutics"' showing total 612 results

Start Over Author "Sub General Pharmaceutics" Publication Year Range Last 50 years

612 results on '"Sub General Pharmaceutics"'

1. Non-Standard Errors

Author: Leerstoel Stigchel, Helmholtz Institute, Experimental Psychology (onderzoeksprogramma PF), Finance, UU LEG Research UUSE Multidisciplinary Economics, Sub General Pharmaceutics, Menkveld, Albert J., Abudy, Menachem (Meni), Grammig, Joachim, Gregoire, Vincent, Hagströmer, Björn, Hambuckers, Julien, Hapnes, Erik, Harris, Jeffrey H., Harris, Lawrence, Hartmann, Simon, Hasse, Jean-Baptiste, Hautsch, Nikolaus, Adrian, Tobias, He, Xue-Zhong 'Tony', Heath, Davidson, Hediger, Simon, Hendershott, Terrence J., Hibbert, Ann Marie, Hjalmarsson, Erik, Hoelscher, Seth, Hoffmann, Peter, Holden, Craig W., Horenstein, Alex R., Ait-Sahalia, Yacine, Huang, Wenqian, Huang, Da, Hurlin, Christophe, Ivashchenko, Alexey, Iyer, Subramanian R., Jahanshahloo, Hossein, Jalkh, Naji, Jones, Charles M., Jurkatis, Simon, Jylha, Petri, Akmansoy, Olivier, Kaeck, Andreas, Kaiser, Gabriel, Karam, Arzé, Karmaziene, Egle, Kassner, Bernhard, Kaustia, Markku, Kazak, Ekaterina, Kearney, Fearghal, van Kervel, Vincent, Khan, Saad, Alcock, Jamie, Khomyn, Marta, Klein, Tony, Klein, Olga, Klos, Alexander, Koetter, Michael, Krahnen, Jan Pieter, Kolokolov, Aleksey, Korajczyk, Robert A., Kozhan, Roman, Kwan, Amy, Alexeev, Vitali, Lajaunie, Quentin, Lam, Full Yet Eric Campbell, Lambert, Marie, Langlois, Hugues, Lausen, Jens, Lauter, Tobias, Leippold, Markus, Levin, Vladimir, Li, Yijie, Li, (Michael) Hui, Aloosh, Arash, Liew, Chee Yoong, Lindner, Thomas, Linton, Oliver B., Liu, Jiacheng, Liu, Anqi, Llorente-Alvarez, Jesus-Guillermo, Lof, Matthijs, Lohr, Ariel, Longstaff, Francis A., Lopez-Lira, Alejandro, Amato, Livia, Mankad, Shawn, Mano, Nicola, Marchal, Alexis, Martineau, Charles, Mazzola, Francesco, Meloso, Debrah C, Mihet, Roxana, Mohan, Vijay, Moinas, Sophie, Moore, David, Amaya, Diego, Mu, Liangyi, Muravyev, Dmitriy, Murphy, Dermot, Neszveda, Gabor, Neumeier, Christian, Nielsson, Ulf, Nimalendran, Mahendrarajah, Nolte, Sven, Nordén, Lars L., O'Neill, Peter, Angel, James J., Obaid, Khaled, Ødegaard, Bernt Arne, Östberg, Per, Painter, Marcus, Palan, Stefan, Palit, Imon, Park, Andreas, Pascual Gascó, Roberto, Pasquariello, Paolo, Pastor, Lubos, Dreber, Anna, Bach, Amadeus, Patel, Vinay, Patton, Andrew J., Pearson, Neil D., Pelizzon, Loriana, Pelster, Matthias, Pérignon, Christophe, Pfiffer, Cameron, Philip, Richard, Plíhal, Tomáš, Prakash, Puneet, Baidoo, Edwin, Press, Oliver-Alexander, Prodromou, Tina, Putnins, Talis J., Raizada, Gaurav, Rakowski, David A., Ranaldo, Angelo, Regis, Luca, Reitz, Stefan, Renault, Thomas, Wang, Renjie, Bakalli, Gaetan, Renò, Roberto, Riddiough, Steven, Rinne, Kalle, Rintamäki, Paul, Riordan, Ryan, Rittmannsberger, Thomas, Rodríguez Longarela, Iñaki, Rösch, Dominik, Rognone, Lavinia, Roseman, Brian, Barbon, Andrea, Rosu, Ioanid, Roy, Saurabh, Rudolf, Nicolas, Rush, Stephen, Rzayev, Khaladdin, Rzeźnik, Aleksandra, Sanford, Anthony, Sankaran, Harikumar, Sarkar, Asani, Sarno, Lucio, Bashchenko, Oksana, Scaillet, Olivier, Scharnowski, Stefan, Schenk-Hoppé, Klaus Reiner, Schertler, Andrea, Schneider, Michael, Schroeder, Florian, Schürhoff, Norman, Schuster, Philipp, Schwarz, Marco A., Seasholes, Mark S., Bindra, Parampreet Christopher, Seeger, Norman, Shachar, Or, Shkilko, Andriy, Shui, Jessica, Sikic, Mario, Simion, Giorgia, Smales, Lee A., Söderlind, Paul, Sojli, Elvira, Sokolov, Konstantin, Bjonnes, Geir Hoidal, Spokeviciute, Laima, Stefanova, Denitsa, Subrahmanyam, Marti G., Neusüss, Sebastian, Szaszi, Barnabas, Talavera, Oleksandr, Tang, Yuehua, Taylor, Nicholas, Tham, Wing Wah, Theissen, Erik, Black, Jeffrey R., Thimme, Julian, Tonks, Ian, Tran, Hai, Trapin, Luca, Trolle, Anders B., Valente, Giorgio, Van Ness, Robert A., Vasquez, Aurelio, Verousis, Thanos, Verwijmeren, Patrick, Black, Bernard S., Vilhelmsson, Anders, Vilkov, Grigory, Vladimirov, Vladimir, Vogel, Sebastian, Voigt, Stefan, Wagner, Wolf, Walther, Thomas, Weiss, Patrick, van der Wel, Michel, Werner, Ingrid M., Bohorquez, Santiago, Westerholm, P. Joakim, Westheide, Christian, Wipplinger, Evert, Wolf, Michael, Wolff, Christian C. P., Wolk, Leonard, Wong, Wing-Keung, Wrampelmeyer, Jan, Xia, Shuo, Xiu, Dacheng, Holzmeister, Felix, Bondarenko, Oleg, Xu, Ke, Xu, Caihong, Yadav, Pradeep K., Yagüe, José, Yan, Cheng, Yang, Antti, Yoo, Woongsun, Yu, Wenjia, Yu, Shihao, Yueshen, Bart Zhou, Bos, Charles S., Yuferova, Darya, Zamojski, Marcin, Zareei, Abalfazl, Zeisberger, Stefan, Zhang, Lu, Zhang, Xiaoyu, Zhong, Zhuo, Zhou, Z. Ivy, Zhou, Chen, Zhu, Xingyu, Bosch-Rosa, Ciril, Zoican, Marius, Zwinkels, Remco C.J., Chen, Jian, Duevski, Teodor, Gao, Ge, Gemayel, Roland, Gilder, Dudley, Kuhle, Paul, Pagnotta, Emiliano, Pelli, Michele, Bouri, Elie, Sönksen, Jantje, Ilczuk, Konrad, Bogoev, Dimitar, Qian, Ya, Wika, Hans C., Yu, Yihe, Zhao, Lu, Mi, Michael, Bao, Li, Brownlees, Christian T., Vaduva, Andreea, Prokopczuk, Marcel, Avetikian, Alejandro, Wu, Zhen-Xing, Calamia, Anna, Cao, Viet Nga, Capelle-Blancard, Gunther, Capera, Laura, Caporin, Massimiliano, Huber, Juergen, Carrion, Allen, Caskurlu, Tolga, Chakrabarty, Bidisha, Chernov, Mikhail, Cheung, William Ming Yan, Chincarini, Ludwig B., Chordia, Tarun, Chow, Sheung Chi, Clapham, Benjamin, Colliard, Jean-Edouard, Johanneson, Magnus, Comerton-Forde, Carole, Curran, Edward, Dao, Thong, Dare, Wale, Davies, Ryan J., De Blasis, Riccardo, De Nard, Gianluca, Declerck, Fany, Deev, Oleg, Degryse, Hans, Kirchler, Michael, Deku, Solomon, Desagre, Christophe, Dim, Chukwuma, Dimpfl, Thomas, Dong, Yun Jiang, Drummond, Philip, Dudda, Tom, Dumitrescu, Ariadna, Dyakov, Teodor, Razen, Michael, Dyhrberg, Anne Haubo, Dzieliński, Michał, Eksi, Asli, El Kalak, Izidin, ter Ellen, Saskia, Eugster, Nicolas, Evans, Martin D.D., Farrell, Michael, Félez-Viñas, Ester, Ferrara, Gerardo, Weitzel, Utz, FERROUHI, El Mehdi, Flori, Andrea, Fluharty-Jaidee, Jonathan, Foley, Sean, Fong, Kingsley Y. L., Foucault, Thierry, Franus, Tatiana, Franzoni, Francesco A., Frijns, Bart, Frömmel, Michael, Abad, David, Fu, Servanna Mianjun, Füllbrunn, Sascha, Gan, Baoqing, Gehrig, Thomas, Gerritsen, Dirk, Gil-Bazo, Javier, Glosten, Lawrence R., Gomez, Thomas, Gorbenko, Arseny, Güçbilmez, Ufuk, Van Dijk, Matthijs A., Leerstoel Stigchel, Helmholtz Institute, Experimental Psychology (onderzoeksprogramma PF), Finance, UU LEG Research UUSE Multidisciplinary Economics, Sub General Pharmaceutics, Menkveld, Albert J., Abudy, Menachem (Meni), Grammig, Joachim, Gregoire, Vincent, Hagströmer, Björn, Hambuckers, Julien, Hapnes, Erik, Harris, Jeffrey H., Harris, Lawrence, Hartmann, Simon, Hasse, Jean-Baptiste, Hautsch, Nikolaus, Adrian, Tobias, He, Xue-Zhong 'Tony', Heath, Davidson, Hediger, Simon, Hendershott, Terrence J., Hibbert, Ann Marie, Hjalmarsson, Erik, Hoelscher, Seth, Hoffmann, Peter, Holden, Craig W., Horenstein, Alex R., Ait-Sahalia, Yacine, Huang, Wenqian, Huang, Da, Hurlin, Christophe, Ivashchenko, Alexey, Iyer, Subramanian R., Jahanshahloo, Hossein, Jalkh, Naji, Jones, Charles M., Jurkatis, Simon, Jylha, Petri, Akmansoy, Olivier, Kaeck, Andreas, Kaiser, Gabriel, Karam, Arzé, Karmaziene, Egle, Kassner, Bernhard, Kaustia, Markku, Kazak, Ekaterina, Kearney, Fearghal, van Kervel, Vincent, Khan, Saad, Alcock, Jamie, Khomyn, Marta, Klein, Tony, Klein, Olga, Klos, Alexander, Koetter, Michael, Krahnen, Jan Pieter, Kolokolov, Aleksey, Korajczyk, Robert A., Kozhan, Roman, Kwan, Amy, Alexeev, Vitali, Lajaunie, Quentin, Lam, Full Yet Eric Campbell, Lambert, Marie, Langlois, Hugues, Lausen, Jens, Lauter, Tobias, Leippold, Markus, Levin, Vladimir, Li, Yijie, Li, (Michael) Hui, Aloosh, Arash, Liew, Chee Yoong, Lindner, Thomas, Linton, Oliver B., Liu, Jiacheng, Liu, Anqi, Llorente-Alvarez, Jesus-Guillermo, Lof, Matthijs, Lohr, Ariel, Longstaff, Francis A., Lopez-Lira, Alejandro, Amato, Livia, Mankad, Shawn, Mano, Nicola, Marchal, Alexis, Martineau, Charles, Mazzola, Francesco, Meloso, Debrah C, Mihet, Roxana, Mohan, Vijay, Moinas, Sophie, Moore, David, Amaya, Diego, Mu, Liangyi, Muravyev, Dmitriy, Murphy, Dermot, Neszveda, Gabor, Neumeier, Christian, Nielsson, Ulf, Nimalendran, Mahendrarajah, Nolte, Sven, Nordén, Lars L., O'Neill, Peter, Angel, James J., Obaid, Khaled, Ødegaard, Bernt Arne, Östberg, Per, Painter, Marcus, Palan, Stefan, Palit, Imon, Park, Andreas, Pascual Gascó, Roberto, Pasquariello, Paolo, Pastor, Lubos, Dreber, Anna, Bach, Amadeus, Patel, Vinay, Patton, Andrew J., Pearson, Neil D., Pelizzon, Loriana, Pelster, Matthias, Pérignon, Christophe, Pfiffer, Cameron, Philip, Richard, Plíhal, Tomáš, Prakash, Puneet, Baidoo, Edwin, Press, Oliver-Alexander, Prodromou, Tina, Putnins, Talis J., Raizada, Gaurav, Rakowski, David A., Ranaldo, Angelo, Regis, Luca, Reitz, Stefan, Renault, Thomas, Wang, Renjie, Bakalli, Gaetan, Renò, Roberto, Riddiough, Steven, Rinne, Kalle, Rintamäki, Paul, Riordan, Ryan, Rittmannsberger, Thomas, Rodríguez Longarela, Iñaki, Rösch, Dominik, Rognone, Lavinia, Roseman, Brian, Barbon, Andrea, Rosu, Ioanid, Roy, Saurabh, Rudolf, Nicolas, Rush, Stephen, Rzayev, Khaladdin, Rzeźnik, Aleksandra, Sanford, Anthony, Sankaran, Harikumar, Sarkar, Asani, Sarno, Lucio, Bashchenko, Oksana, Scaillet, Olivier, Scharnowski, Stefan, Schenk-Hoppé, Klaus Reiner, Schertler, Andrea, Schneider, Michael, Schroeder, Florian, Schürhoff, Norman, Schuster, Philipp, Schwarz, Marco A., Seasholes, Mark S., Bindra, Parampreet Christopher, Seeger, Norman, Shachar, Or, Shkilko, Andriy, Shui, Jessica, Sikic, Mario, Simion, Giorgia, Smales, Lee A., Söderlind, Paul, Sojli, Elvira, Sokolov, Konstantin, Bjonnes, Geir Hoidal, Spokeviciute, Laima, Stefanova, Denitsa, Subrahmanyam, Marti G., Neusüss, Sebastian, Szaszi, Barnabas, Talavera, Oleksandr, Tang, Yuehua, Taylor, Nicholas, Tham, Wing Wah, Theissen, Erik, Black, Jeffrey R., Thimme, Julian, Tonks, Ian, Tran, Hai, Trapin, Luca, Trolle, Anders B., Valente, Giorgio, Van Ness, Robert A., Vasquez, Aurelio, Verousis, Thanos, Verwijmeren, Patrick, Black, Bernard S., Vilhelmsson, Anders, Vilkov, Grigory, Vladimirov, Vladimir, Vogel, Sebastian, Voigt, Stefan, Wagner, Wolf, Walther, Thomas, Weiss, Patrick, van der Wel, Michel, Werner, Ingrid M., Bohorquez, Santiago, Westerholm, P. Joakim, Westheide, Christian, Wipplinger, Evert, Wolf, Michael, Wolff, Christian C. P., Wolk, Leonard, Wong, Wing-Keung, Wrampelmeyer, Jan, Xia, Shuo, Xiu, Dacheng, Holzmeister, Felix, Bondarenko, Oleg, Xu, Ke, Xu, Caihong, Yadav, Pradeep K., Yagüe, José, Yan, Cheng, Yang, Antti, Yoo, Woongsun, Yu, Wenjia, Yu, Shihao, Yueshen, Bart Zhou, Bos, Charles S., Yuferova, Darya, Zamojski, Marcin, Zareei, Abalfazl, Zeisberger, Stefan, Zhang, Lu, Zhang, Xiaoyu, Zhong, Zhuo, Zhou, Z. Ivy, Zhou, Chen, Zhu, Xingyu, Bosch-Rosa, Ciril, Zoican, Marius, Zwinkels, Remco C.J., Chen, Jian, Duevski, Teodor, Gao, Ge, Gemayel, Roland, Gilder, Dudley, Kuhle, Paul, Pagnotta, Emiliano, Pelli, Michele, Bouri, Elie, Sönksen, Jantje, Ilczuk, Konrad, Bogoev, Dimitar, Qian, Ya, Wika, Hans C., Yu, Yihe, Zhao, Lu, Mi, Michael, Bao, Li, Brownlees, Christian T., Vaduva, Andreea, Prokopczuk, Marcel, Avetikian, Alejandro, Wu, Zhen-Xing, Calamia, Anna, Cao, Viet Nga, Capelle-Blancard, Gunther, Capera, Laura, Caporin, Massimiliano, Huber, Juergen, Carrion, Allen, Caskurlu, Tolga, Chakrabarty, Bidisha, Chernov, Mikhail, Cheung, William Ming Yan, Chincarini, Ludwig B., Chordia, Tarun, Chow, Sheung Chi, Clapham, Benjamin, Colliard, Jean-Edouard, Johanneson, Magnus, Comerton-Forde, Carole, Curran, Edward, Dao, Thong, Dare, Wale, Davies, Ryan J., De Blasis, Riccardo, De Nard, Gianluca, Declerck, Fany, Deev, Oleg, Degryse, Hans, Kirchler, Michael, Deku, Solomon, Desagre, Christophe, Dim, Chukwuma, Dimpfl, Thomas, Dong, Yun Jiang, Drummond, Philip, Dudda, Tom, Dumitrescu, Ariadna, Dyakov, Teodor, Razen, Michael, Dyhrberg, Anne Haubo, Dzieliński, Michał, Eksi, Asli, El Kalak, Izidin, ter Ellen, Saskia, Eugster, Nicolas, Evans, Martin D.D., Farrell, Michael, Félez-Viñas, Ester, Ferrara, Gerardo, Weitzel, Utz, FERROUHI, El Mehdi, Flori, Andrea, Fluharty-Jaidee, Jonathan, Foley, Sean, Fong, Kingsley Y. L., Foucault, Thierry, Franus, Tatiana, Franzoni, Francesco A., Frijns, Bart, Frömmel, Michael, Abad, David, Fu, Servanna Mianjun, Füllbrunn, Sascha, Gan, Baoqing, Gehrig, Thomas, Gerritsen, Dirk, Gil-Bazo, Javier, Glosten, Lawrence R., Gomez, Thomas, Gorbenko, Arseny, Güçbilmez, Ufuk, and Van Dijk, Matthijs A.
Published: 2024

2. Size matters: Functional differences of small extracellular vesicle subpopulations in cardiac repair responses

Author: Afd Biomol.Mass Spect. and Proteomics, Sub Biomol.Mass Spectrometry & Proteom., Afd Pharmaceutics, Sub General Pharmaceutics, van de Wakker, Simonides Immanuel, Bauzá-Martinez, Julia, Ríos Arceo, Carla, Manjikian, Herak, Snijders Blok, Christian Jamie Bernard, Roefs, Marieke Theodora, Willms, Eduard, Maas, Renee Goverdina Catharina, Pronker, Matti Feije, de Jong, Olivier Gerrit, Wu, Wei, Görgens, André, El Andaloussi, Samir, Sluijter, Joost Petrus Gerardus, Vader, Pieter, Afd Biomol.Mass Spect. and Proteomics, Sub Biomol.Mass Spectrometry & Proteom., Afd Pharmaceutics, Sub General Pharmaceutics, van de Wakker, Simonides Immanuel, Bauzá-Martinez, Julia, Ríos Arceo, Carla, Manjikian, Herak, Snijders Blok, Christian Jamie Bernard, Roefs, Marieke Theodora, Willms, Eduard, Maas, Renee Goverdina Catharina, Pronker, Matti Feije, de Jong, Olivier Gerrit, Wu, Wei, Görgens, André, El Andaloussi, Samir, Sluijter, Joost Petrus Gerardus, and Vader, Pieter
Published: 2024

3. Extracellular vesicle-mediated delivery of CRISPR/Cas9 ribonucleoprotein complex targeting proprotein convertase subtilisin-kexin type 9 (Pcsk9) in primary mouse hepatocytes

Author: Afd Pharmaceutics, Sub General Pharmaceutics, Pharmaceutics, Ilahibaks, Nazma F., Kluiver, Thomas A., de Jong, Olivier G., de Jager, Saskia C.A., Schiffelers, Raymond M., Vader, Pieter, Peng, Weng Chuan, Lei, Zhiyong, Sluijter, Joost P.G., Afd Pharmaceutics, Sub General Pharmaceutics, Pharmaceutics, Ilahibaks, Nazma F., Kluiver, Thomas A., de Jong, Olivier G., de Jager, Saskia C.A., Schiffelers, Raymond M., Vader, Pieter, Peng, Weng Chuan, Lei, Zhiyong, and Sluijter, Joost P.G.
Published: 2024

4. The potential of PARP as a therapeutic target across pediatric solid malignancies

Author: Sub General Pharmaceutics, Afd Pharmaceutics, Pharmaceutics, Keller, Kaylee M., Koetsier, Joost, Schild, Linda, Amo-Addae, Vicky, Eising, Selma, van den Handel, Kim, Ober, Kimberley, Koopmans, Bianca, Essing, Anke, van den Boogaard, Marlinde L., Langenberg, Karin P.S., Jäger, Natalie, Kool, Marcel, Pfister, Stefan, Dolman, M. Emmy M., Molenaar, Jan J., van Hooff, Sander R., Sub General Pharmaceutics, Afd Pharmaceutics, Pharmaceutics, Keller, Kaylee M., Koetsier, Joost, Schild, Linda, Amo-Addae, Vicky, Eising, Selma, van den Handel, Kim, Ober, Kimberley, Koopmans, Bianca, Essing, Anke, van den Boogaard, Marlinde L., Langenberg, Karin P.S., Jäger, Natalie, Kool, Marcel, Pfister, Stefan, Dolman, M. Emmy M., Molenaar, Jan J., and van Hooff, Sander R.
Published: 2023

5. Cardiac progenitor cell-derived extracellular vesicles promote angiogenesis through both associated- and co-isolated proteins

Author: Afd Biomol.Mass Spect. and Proteomics, Sub General Pharmaceutics, Biomolecular Mass Spectrometry and Proteomics, Roefs, Marieke Theodora, Bauzá-Martinez, Julia, van de Wakker, Simonides Immanuel, Qin, Jiabin, Olijve, Willem Theodoor, Tuinte, Robin, Rozeboom, Marjolein, Snijders Blok, Christian, Mol, Emma Alise, Wu, Wei, Vader, Pieter, Sluijter, Joost Petrus Gerardus, Afd Biomol.Mass Spect. and Proteomics, Sub General Pharmaceutics, Biomolecular Mass Spectrometry and Proteomics, Roefs, Marieke Theodora, Bauzá-Martinez, Julia, van de Wakker, Simonides Immanuel, Qin, Jiabin, Olijve, Willem Theodoor, Tuinte, Robin, Rozeboom, Marjolein, Snijders Blok, Christian, Mol, Emma Alise, Wu, Wei, Vader, Pieter, and Sluijter, Joost Petrus Gerardus
Published: 2023

6. MEK inhibition causes BIM stabilization and increased sensitivity to BCL-2 family member inhibitors in RAS-MAPK-mutated neuroblastoma

Author: Sub General Pharmaceutics, Afd Pharmaceutics, Pharmaceutics, Eleveld, Thomas F., Vernooij, Lindy, Schild, Linda, Koopmans, Bianca, Alles, Lindy K., Ebus, Marli E., Dandis, Rana, van Tinteren, Harm, Caron, Huib N., Koster, Jan, van Noesel, Max M., Tytgat, Godelieve A.M., Eising, Selma, Versteeg, Rogier, Dolman, M. Emmy M., Molenaar, Jan J., Sub General Pharmaceutics, Afd Pharmaceutics, Pharmaceutics, Eleveld, Thomas F., Vernooij, Lindy, Schild, Linda, Koopmans, Bianca, Alles, Lindy K., Ebus, Marli E., Dandis, Rana, van Tinteren, Harm, Caron, Huib N., Koster, Jan, van Noesel, Max M., Tytgat, Godelieve A.M., Eising, Selma, Versteeg, Rogier, Dolman, M. Emmy M., and Molenaar, Jan J.
Published: 2023

7. Methods for the identification and characterization of extracellular vesicles in cardiovascular studies - from exosomes to microvesicles

Author: Sub General Pharmaceutics, Celbiologie, dB&C I&I, Cell Biology, Metabolism & Cancer - Cellbiology, Davidson, Sean M, Boulanger, Chantal M, Aikawa, Elena, Badimon, Lina, Barile, Lucio, Binder, Christoph J, Brisson, Alain, Buzas, Edit, Emanueli, Costanza, Jansen, Felix, Katsur, Miroslava, Lacroix, Romaric, Lim, Sai Kiang, Mackman, Nigel, Mayr, Manuel, Menasché, Philippe, Nieuwland, Rienk, Sahoo, Susmita, Takov, Kaloyan, Thum, Thomas, Vader, Pieter, Wauben, Marca H M, Witwer, Kenneth, Sluijter, Joost P G, Sub General Pharmaceutics, Celbiologie, dB&C I&I, Cell Biology, Metabolism & Cancer - Cellbiology, Davidson, Sean M, Boulanger, Chantal M, Aikawa, Elena, Badimon, Lina, Barile, Lucio, Binder, Christoph J, Brisson, Alain, Buzas, Edit, Emanueli, Costanza, Jansen, Felix, Katsur, Miroslava, Lacroix, Romaric, Lim, Sai Kiang, Mackman, Nigel, Mayr, Manuel, Menasché, Philippe, Nieuwland, Rienk, Sahoo, Susmita, Takov, Kaloyan, Thum, Thomas, Vader, Pieter, Wauben, Marca H M, Witwer, Kenneth, and Sluijter, Joost P G
Published: 2023

8. Mesenchymal tumor organoid models recapitulate rhabdomyosarcoma subtypes

Author: Meister, Michael T., Groot Koerkamp, Marian J.A., de Souza, Terezinha, Breunis, Willemijn B., Frazer-Mendelewska, Ewa, Brok, Mariël, DeMartino, Jeff, Manders, Freek, Calandrini, Camilla, Kerstens, Hinri H.D., Janse, Alex, Dolman, M. Emmy M., Eising, Selma, Langenberg, Karin P.S., van Tuil, Marc, Knops, Rutger R.G., van Scheltinga, Sheila Terwisscha, Hiemcke-Jiwa, Laura S., Flucke, Uta, Merks, Johannes H.M., van Noesel, Max M., Tops, Bastiaan B.J., Hehir-Kwa, Jayne Y., Kemmeren, Patrick, Molenaar, Jan J., van de Wetering, Marc, van Boxtel, Ruben, Drost, Jarno, Holstege, Frank C.P., Sub General Pharmaceutics, Afd Pharmaceutics, Pharmaceutics, University of Zurich, Drost, Jarno, Holstege, Frank C P, Sub General Pharmaceutics, Afd Pharmaceutics, and Pharmaceutics
Subjects: Organoids, tumoroid, 10036 Medical Clinic, 1313 Molecular Medicine, Humans, Molecular Medicine, 610 Medicine & health, drug screening, rhabdomyosarcoma, mesenchymal, Child, CRISPR/Cas9
Abstract: SummaryRhabdomyosarcomas (RMS) are mesenchyme-derived tumors and the most common childhood soft tissue sarcomas. Treatment is intense, with a nevertheless poor prognosis for high-risk patients. Discovery of new therapies would benefit from additional preclinical models. Here we describe the generation of a collection of pediatric RMS tumor organoid (tumoroid) models comprising all major subtypes. For aggressive tumors, tumoroid models can often be established within four to eight weeks, indicating the feasibility of personalized drug screening. Molecular, genetic and histological characterization show that the models closely resemble the original tumors, with genetic stability over extended culture periods of up to six months. Importantly, drug screening reflects established sensitivities and the models can be modified by CRISPR/Cas9 with TP53 knockout in an embryonal RMS model resulting in replicative stress drug sensitivity. Tumors of mesenchymal origin can therefore be used to generate organoid models, relevant for a variety of preclinical and clinical research questions.
Published: 2022

9. Preparation, Characterization, and Biological Evaluation of a Hydrophilic Peptide Loaded on PEG-PLGA Nanoparticles

Author: Marinelli, Lisa, Ciulla, Michele, Ritsema, Jeffrey A S, van Nostrum, Cornelus F, Cacciatore, Ivana, Dimmito, Marilisa Pia, Palmerio, Ferdinando, Orlando, Giustino, Robuffo, Iole, Grande, Rossella, Puca, Valentina, Di Stefano, Antonio, Sub Drug delivery, Sub General Pharmaceutics, Afd Pharmaceutics, Pharmaceutics, Sub Drug delivery, Sub General Pharmaceutics, Afd Pharmaceutics, and Pharmaceutics
Subjects: nanoprecipitation, polymeric nanoparticles, double emulsion, PEG-PLGA, quorum sensing inhibitors, RNAIII inhibiting peptide, S. aureus biofilm, Pharmaceutical Science
Abstract: The encapsulation of peptides and proteins in nanosystems has been extensively investigated for masking unfavorable biopharmaceutical properties, including short half-life and poor permeation through biological membranes. Therefore, the aim of this work was to encapsulate a small antimicrobial hydrophilic peptide (H-Ser-Pro-Trp-Thr-NH2, FS10) in PEG-PLGA (polyethylene glycol-poly lactic acid-co-glycolic acid) nanoparticles (Nps) and thereby overcome the common limitations of hydrophilic drugs, which because they facilitate water absorption suffer from rapid degradation. FS10 is structurally related to the well-known RNAIII inhibiting peptide (RIP) and inhibits S. aureus biofilm formation. Various parameters, including different method (double emulsion and nanoprecipitation), pH of the aqueous phase and polymeric composition, were investigated to load FS10 into PEG-PLGA nanoparticles. The combination of different strategies resulted in an encapsulation efficiency of around 25% for both the double emulsion and the nanoprecipitation method. It was found that the most influential parameters were the pH—which tailors the peptides charge—and the polymeric composition. FS10-PEG-PLGA nanoparticles, obtained under optimized parameters, showed size lower than 180 nm with zeta potential values ranging from −11 to −21 mV. In vitro release studies showed that the Nps had an initial burst release of 48–63%, followed by a continuous drug release up to 21 h, probably caused by the porous character of the Nps. Furthermore, transmission electron microscopy (TEM) analysis revealed particles with a spherical morphology and size of around 100 nm. Antimicrobial assay showed that the minimum inhibitory concentration (MIC) of the FS10-loaded Nps, against S. aureus strains, was lower (>128 µg/mL) than that of the free FS10 (>256 µg/mL). The main goal of this work was to develop polymeric drug delivery systems aiming at protecting the peptide from a fast degradation, thus improving its accumulation in the target site and increasing the drug-bacterial membrane interactions.
Published: 2022

10. Questionable micelle formation of the double hydrophilic block copolymer PEG-pHPMA

Author: van Nostrum, Cornelus F, Lammers, Twan, Hennink, Wim E, Afd Pharmaceutics, Sub General Pharmaceutics, and Pharmaceutics
Subjects: Paclitaxel, Taverne, Polymeric micelles, Pharmaceutical Science
Published: 2022

11. Magnetic beads for the evaluation of drug release from biotinylated polymeric micelles in biological media

Author: Wang, Yan, Fens, Marcel H, van Kronenburg, Nicky C H, Shi, Yang, Lammers, Twan, Heger, Michal, van Nostrum, Cornelus F, Hennink, Wim E, Afd Pharmaceutics, Sub General Pharmaceutics, Sub Membrane Biochemistry & Biophysics, Pharmaceutics, Afd Pharmaceutics, Sub General Pharmaceutics, Sub Membrane Biochemistry & Biophysics, and Pharmaceutics
Subjects: Drug Carriers, Curcumin, Paclitaxel, Polymers, Magnetic Phenomena, Polysorbates, Reproducibility of Results, Biotin, Pharmaceutical Science, Serum Albumin, Bovine, Drug release, Cytostatic Agents, Polyethylene Glycols, Drug Liberation, Mice, Drug Delivery Systems, Solvents, Animals, Polymeric micelles, Streptavidin, Particle Size, Streptavidin-coated magnetic beads, Micelles
Abstract: Journal of controlled release 349, 954-962 (2022). doi:10.1016/j.jconrel.2022.07.044 special issue: "Journal of Controlled Release Editorial Board Special Issue / Edited by Devika Manickam, Daishun Ling, Ana Beloqui García", Published by Elsevier, New York, NY [u.a.]
Published: 2022
Full Text: View/download PDF

12. Magnetic beads for the evaluation of drug release from biotinylated polymeric micelles in biological media

Author: Afd Pharmaceutics, Sub General Pharmaceutics, Sub Membrane Biochemistry & Biophysics, Pharmaceutics, Wang, Yan, Fens, Marcel H, van Kronenburg, Nicky C H, Shi, Yang, Lammers, Twan, Heger, Michal, van Nostrum, Cornelus F, Hennink, Wim E, Afd Pharmaceutics, Sub General Pharmaceutics, Sub Membrane Biochemistry & Biophysics, Pharmaceutics, Wang, Yan, Fens, Marcel H, van Kronenburg, Nicky C H, Shi, Yang, Lammers, Twan, Heger, Michal, van Nostrum, Cornelus F, and Hennink, Wim E
Published: 2022

13. Mesenchymal tumor organoid models recapitulate rhabdomyosarcoma subtypes

Author: Sub General Pharmaceutics, Afd Pharmaceutics, Pharmaceutics, Meister, Michael T., Groot Koerkamp, Marian J.A., de Souza, Terezinha, Breunis, Willemijn B., Frazer-Mendelewska, Ewa, Brok, Mariël, DeMartino, Jeff, Manders, Freek, Calandrini, Camilla, Kerstens, Hinri H.D., Janse, Alex, Dolman, M. Emmy M., Eising, Selma, Langenberg, Karin P.S., van Tuil, Marc, Knops, Rutger R.G., van Scheltinga, Sheila Terwisscha, Hiemcke-Jiwa, Laura S., Flucke, Uta, Merks, Johannes H.M., van Noesel, Max M., Tops, Bastiaan B.J., Hehir-Kwa, Jayne Y., Kemmeren, Patrick, Molenaar, Jan J., van de Wetering, Marc, van Boxtel, Ruben, Drost, Jarno, Holstege, Frank C.P., Sub General Pharmaceutics, Afd Pharmaceutics, Pharmaceutics, Meister, Michael T., Groot Koerkamp, Marian J.A., de Souza, Terezinha, Breunis, Willemijn B., Frazer-Mendelewska, Ewa, Brok, Mariël, DeMartino, Jeff, Manders, Freek, Calandrini, Camilla, Kerstens, Hinri H.D., Janse, Alex, Dolman, M. Emmy M., Eising, Selma, Langenberg, Karin P.S., van Tuil, Marc, Knops, Rutger R.G., van Scheltinga, Sheila Terwisscha, Hiemcke-Jiwa, Laura S., Flucke, Uta, Merks, Johannes H.M., van Noesel, Max M., Tops, Bastiaan B.J., Hehir-Kwa, Jayne Y., Kemmeren, Patrick, Molenaar, Jan J., van de Wetering, Marc, van Boxtel, Ruben, Drost, Jarno, and Holstege, Frank C.P.
Published: 2022

14. Preparation, Characterization, and Biological Evaluation of a Hydrophilic Peptide Loaded on PEG-PLGA Nanoparticles

Author: Sub Drug delivery, Sub General Pharmaceutics, Afd Pharmaceutics, Pharmaceutics, Marinelli, Lisa, Ciulla, Michele, Ritsema, Jeffrey A S, van Nostrum, Cornelus F, Cacciatore, Ivana, Dimmito, Marilisa Pia, Palmerio, Ferdinando, Orlando, Giustino, Robuffo, Iole, Grande, Rossella, Puca, Valentina, Di Stefano, Antonio, Sub Drug delivery, Sub General Pharmaceutics, Afd Pharmaceutics, Pharmaceutics, Marinelli, Lisa, Ciulla, Michele, Ritsema, Jeffrey A S, van Nostrum, Cornelus F, Cacciatore, Ivana, Dimmito, Marilisa Pia, Palmerio, Ferdinando, Orlando, Giustino, Robuffo, Iole, Grande, Rossella, Puca, Valentina, and Di Stefano, Antonio
Published: 2022

15. Questionable micelle formation of the double hydrophilic block copolymer PEG-pHPMA

Author: Afd Pharmaceutics, Sub General Pharmaceutics, Pharmaceutics, van Nostrum, Cornelus F, Lammers, Twan, Hennink, Wim E, Afd Pharmaceutics, Sub General Pharmaceutics, Pharmaceutics, van Nostrum, Cornelus F, Lammers, Twan, and Hennink, Wim E
Published: 2022

16. Dual-contrast computed tomography enables detection of equine posttraumatic osteoarthritis in vitro

Author: Equine Musculoskeletal Biology, dES RMSC, Sub General Pharmaceutics, Heelkunde, dES AVR, Dep Clinical Sciences, Saukko, Annina E.A., Sarin, Jaakko K., Nykänen, Olli, Nissi, Mikko J., te Moller, Nikae C.R., Weinans, Harrie, Mancini, Irina A.D., Visser, Jetze, Brommer, Harold, van Weeren, P. Réné, Malda, Jos, Grinstaff, Mark W., Töyräs, Juha, Equine Musculoskeletal Biology, dES RMSC, Sub General Pharmaceutics, Heelkunde, dES AVR, Dep Clinical Sciences, Saukko, Annina E.A., Sarin, Jaakko K., Nykänen, Olli, Nissi, Mikko J., te Moller, Nikae C.R., Weinans, Harrie, Mancini, Irina A.D., Visser, Jetze, Brommer, Harold, van Weeren, P. Réné, Malda, Jos, Grinstaff, Mark W., and Töyräs, Juha
Published: 2022

17. Standardization of extracellular vesicle measurements by flow cytometry through vesicle diameter approximation

Author: van der Pol, E., Sturk, A., van Leeuwen, T., Nieuwland, R., Coumans, F., Mobarrez, F., Arkesteijn, G., Wauben, M., Siljander, P. R.M., Sánchez-López, V., Otero-Candelera, R., Ramón, L. A., Dolz, S., Vila, V., Mackman, N., Geddings, J., Mullier, F., Bailly, N., Han, J. Y., Kwaan, H. C., Weiss, I. M., Buzás, E. I., Pállinger, E., Harrison, P., Kraan, J., Hedley, B. D., LazoLangner, A., Enjeti, A., Norris, P. J., Paris, C., Susen, S., Bonnefoy, A., Delorme, I., Chandler, W. L., Hau, C., Aass, H. C.D., Connor, D., Wu, X., Dragovic, R., Uotila, L. M., Lacroix, R., Robert, S., Dep Infectieziekten Immunologie, LS Celbiologie-Algemeen, Sub General Pharmaceutics, Sub Algebra,Geometry&Mathem. Logic begr., LS Pharma, dB&C I&I, Hematology, Erasmus School of Economics, Medical Oncology, General Practice, Business Economics, ACS - Atherosclerosis & ischemic syndromes, CCA - Imaging and biomarkers, Biomedical Engineering and Physics, ACS - Microcirculation, Laboratory for General Clinical Chemistry, Laboratory Specialized Diagnostics & Research, Dep Infectieziekten Immunologie, LS Celbiologie-Algemeen, Sub General Pharmaceutics, Sub Algebra,Geometry&Mathem. Logic begr., LS Pharma, and dB&C I&I
Subjects: 0301 basic medicine, Materials science, Light, Platelet Function Tests, cell-derived microparticles, blood platelets, exosomes, 030204 cardiovascular system & hematology, Bead, Light scattering, Flow cytometry, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, medicine, Calibration, Humans, Scattering, Radiation, Particle Size, Cell Size, Observer Variation, standardization, medicine.diagnostic_test, Vesicle, flow cytometry, Integrin beta3, Reproducibility of Results, Phycoerythrin, Hematology, Extracellular vesicle, Volumetric flow rate, 030104 developmental biology, chemistry, visual_art, visual_art.visual_art_medium, Polystyrene, extracellular vesicles, Biomarkers, Biomedical engineering
Abstract: Essentials Platelet extracellular vesicles (EVs) concentrations measured by flow cytometers are incomparable. A model is applied to convert ambiguous scatter units to EV diameter in nanometer. Most included flow cytometers lack the sensitivity to detect EVs of 600 nm and smaller. The model outperforms polystyrene beads for comparability of platelet EV concentrations. Summary: Background Detection of extracellular vesicles (EVs) by flow cytometry has poor interlaboratory comparability, owing to differences in flow cytometer (FCM) sensitivity. Previous workshops distributed polystyrene beads to set a scatter-based diameter gate in order to improve the comparability of EV concentration measurements. However, polystyrene beads provide limited insights into the diameter of detected EVs. Objectives To evaluate gates based on the estimated diameter of EVs instead of beads. Methods A calibration bead mixture and platelet EV samples were distributed to 33 participants. Beads and a light scattering model were used to set EV diameter gates in order to measure the concentration of CD61–phycoerythrin-positive platelet EVs. Results Of the 46 evaluated FCMs, 21 FCMs detected the 600–1200-nm EV diameter gate. The 1200–3000-nm EV diameter gate was detected by 31 FCMs, with a measured EV concentration interlaboratory variability of 81% as compared with 139% with the bead diameter gate. Part of the variation in both approaches is caused by precipitation in some of the provided platelet EV samples. Flow rate calibration proved essential because systems configured to 60 μL min−1 differed six-fold in measured flow rates between instruments. Conclusions EV diameter gates improve the interlaboratory variability as compared with previous approaches. Of the evaluated FCMs, 24% could not detect 400-nm polystyrene beads, and such instruments have limited utility for EV research. Finally, considerable differences were observed in sensitivity between optically similar instruments, indicating that maintenance and training affect the sensitivity.
Published: 2018

18. Focal adhesion signaling affects regeneration by human nucleus pulposus cells in collagen- but not carbohydrate-based hydrogels

Author: Krouwels, Anita, Melchels, Ferry P W, van Rijen, Mattie H P, Ten Brink, Corlinda B M, Dhert, Wouter J A, Cumhur Öner, F, Tryfonidou, Marianna A, Creemers, Laura B, Faculteit Diergeneeskunde, Orthopedie en neurochirurgie, dCSCA RMSC-1, Sub General Pharmaceutics, Faculteit Diergeneeskunde, Orthopedie en neurochirurgie, dCSCA RMSC-1, and Sub General Pharmaceutics
Subjects: 0301 basic medicine, Compressive Strength, Nucleus pulposus, Intervertebral Disc Degeneration, 02 engineering and technology, Matrix (biology), Biochemistry, Stiffness, Extracellular matrix, chemistry.chemical_compound, Hyaluronic acid, Glycosaminoglycans, Focal adhesion kinase, Hydrogels, General Medicine, Middle Aged, 021001 nanoscience & nanotechnology, Cell biology, Self-healing hydrogels, Collagen, 0210 nano-technology, Signal Transduction, Biotechnology, Adult, Nucleus Pulposus, Materials science, Carbohydrates, Biomedical Engineering, Biomaterials, Focal adhesion, 03 medical and health sciences, Humans, Regeneration, Protein Kinase Inhibitors, Molecular Biology, Aged, Integrin binding, Focal Adhesions, Staining and Labeling, Regeneration (biology), DNA, Chondrogenesis, Actins, Vinculin, Hydrogel, 030104 developmental biology, Gene Expression Regulation, chemistry, Focal Adhesion Protein-Tyrosine Kinases
Abstract: Hydrogel-based 3D cell cultures are an emerging strategy for the regeneration of cartilage. In an attempt to regenerate dysfunctional intervertebral discs, nucleus pulposus (NP) cells can be cultured in hydrogels of various kinds and physical properties. Stiffness sensing through focal adhesions is believed to direct chondrogenesis, but the mechanisms by which this works are largely unknown. In this study we compared focal adhesion formation and glycosaminoglycan (GAG) deposition by NP cells in a range of hydrogels. Using a focal adhesion kinase (FAK) inhibitor, we demonstrated that focal adhesion signaling is involved in the response of NP cells in hydrogels that contain integrin binding sites (i.e. methacrylated gelatin (gelMA) and type II collagen), but not in hydrogels deplete from integrin binding sites such as alginate and agarose, or CD44-binding hydrogels based on hyaluronic acid. As a result of FAK inhibition we observed enhanced proteoglycan production in gelMA, but decreased production in type II collagen hydrogels, which could be explained by alteration in cell fate as supported by the increase in the adipogenic marker peroxisome proliferator-activated receptor gamma (PPARy). Furthermore, GAG deposition was inversely proportional to polymer concentration in integrin-binding gelMA, while no direct relationship was found for the non-integrin binding gels alginate and agarose. This corroborates our finding that focal adhesion formation plays an important role in NP cell response to its surrounding matrix. Statement of Significance Biomaterials are increasingly being investigated for regenerative medicine applications, including regeneration of the nucleus pulposus. Cells interact with their environment and are influenced by extracellular matrix or polymer properties. Insight in these interactions can improve regeneration and helps to understand degeneration processes. The role of focal adhesion formation in the regenerative response of nucleus pulposus cells is largely unknown. Therefore, the relation between materials, stiffness and focal adhesion formation is studied here.
Published: 2018
Full Text: View/download PDF

19. Non-Standard Errors

Author: Leerstoel Stigchel, Helmholtz Institute, Experimental Psychology (onderzoeksprogramma PF), Finance, UU LEG Research UUSE Multidisciplinary Economics, LS Algemene Literatuurwetenschap, Hydrogeology, Sub General Pharmaceutics, Finance and Financial Markets, Menkveld, Albert J., Abudy, Menachem (Meni), Grammig, Joachim, Gregoire, Vincent, Hagströmer, Björn, Hambuckers, Julien, Hapnes, Erik, Harris, Jeffrey H., Harris, Lawrence, Hartmann, Simon, Hasse, Jean-Baptiste, Hautsch, Nikolaus, Adrian, Tobias, He, Xue-Zhong 'Tony', Heath, Davidson, Hediger, Simon, Hendershott, Terrence J., Hibbert, Ann Marie, Hjalmarsson, Erik, Hoelscher, Seth, Hoffmann, Peter, Holden, Craig W., Horenstein, Alex R., Ait-Sahalia, Yacine, Huang, Wenqian, Huang, Da, Hurlin, Christophe, Ivashchenko, Alexey, Iyer, Subramanian R., Jahanshahloo, Hossein, Jalkh, Naji, Jones, Charles M., Jurkatis, Simon, Jylha, Petri, Akmansoy, Olivier, Kaeck, Andreas, Kaiser, Gabriel, Karam, Arzé, Karmaziene, Egle, Kassner, Bernhard, Kaustia, Markku, Kazak, Ekaterina, Kearney, Fearghal, van Kervel, Vincent, Khan, Saad, Alcock, Jamie, Khomyn, Marta, Klein, Tony, Klein, Olga, Klos, Alexander, Koetter, Michael, Krahnen, Jan Pieter, Kolokolov, Aleksey, Korajczyk, Robert A., Kozhan, Roman, Kwan, Amy, Alexeev, Vitali, Lajaunie, Quentin, Lam, Full Yet Eric Campbell, Lambert, Marie, Langlois, Hugues, Lausen, Jens, Lauter, Tobias, Leippold, Markus, Levin, Vladimir, Li, Yijie, Li, (Michael) Hui, Aloosh, Arash, Liew, Chee Yoong, Lindner, Thomas, Linton, Oliver B., Liu, Jiacheng, Liu, Anqi, Llorente-Alvarez, Jesus-Guillermo, Lof, Matthijs, Lohr, Ariel, Longstaff, Francis A., Lopez-Lira, Alejandro, Amato, Livia, Mankad, Shawn, Mano, Nicola, Marchal, Alexis, Martineau, Charles, Mazzola, Francesco, Meloso, Debrah C, Mihet, Roxana, Mohan, Vijay, Moinas, Sophie, Moore, David, Amaya, Diego, Mu, Liangyi, Muravyev, Dmitriy, Murphy, Dermot, Neszveda, Gabor, Neumeier, Christian, Nielsson, Ulf, Nimalendran, Mahendrarajah, Nolte, Sven, Nordén, Lars L., O'Neill, Peter, Angel, James J., Obaid, Khaled, Ødegaard, Bernt Arne, Östberg, Per, Painter, Marcus, Palan, Stefan, Palit, Imon, Park, Andreas, Pascual Gascó, Roberto, Pasquariello, Paolo, Pastor, Lubos, Dreber, Anna, Bach, Amadeus, Patel, Vinay, Patton, Andrew J., Pearson, Neil D., Pelizzon, Loriana, Pelster, Matthias, Pérignon, Christophe, Pfiffer, Cameron, Philip, Richard, Plíhal, Tomáš, Prakash, Puneet, Baidoo, Edwin, Press, Oliver-Alexander, Prodromou, Tina, Putnins, Talis J., Raizada, Gaurav, Rakowski, David A., Ranaldo, Angelo, Regis, Luca, Reitz, Stefan, Renault, Thomas, Wang, Renjie, Bakalli, Gaetan, Renò, Roberto, Riddiough, Steven, Rinne, Kalle, Rintamäki, Paul, Riordan, Ryan, Rittmannsberger, Thomas, Rodríguez Longarela, Iñaki, Rösch, Dominik, Rognone, Lavinia, Roseman, Brian, Barbon, Andrea, Rosu, Ioanid, Roy, Saurabh, Rudolf, Nicolas, Rush, Stephen, Rzayev, Khaladdin, Rzeźnik, Aleksandra, Sanford, Anthony, Sankaran, Harikumar, Sarkar, Asani, Sarno, Lucio, Bashchenko, Oksana, Scaillet, Olivier, Scharnowski, Stefan, Schenk-Hoppé, Klaus Reiner, Schertler, Andrea, Schneider, Michael, Schroeder, Florian, Schürhoff, Norman, Schuster, Philipp, Schwarz, Marco A., Seasholes, Mark S., Bindra, Parampreet Christopher, Seeger, Norman, Shachar, Or, Shkilko, Andriy, Shui, Jessica, Sikic, Mario, Simion, Giorgia, Smales, Lee A., Söderlind, Paul, Sojli, Elvira, Sokolov, Konstantin, Bjonnes, Geir Hoidal, Spokeviciute, Laima, Stefanova, Denitsa, Subrahmanyam, Marti G., Neusüss, Sebastian, Szaszi, Barnabas, Talavera, Oleksandr, Tang, Yuehua, Taylor, Nicholas, Tham, Wing Wah, Theissen, Erik, Black, Jeffrey R., Thimme, Julian, Tonks, Ian, Tran, Hai, Trapin, Luca, Trolle, Anders B., Valente, Giorgio, Van Ness, Robert A., Vasquez, Aurelio, Verousis, Thanos, Verwijmeren, Patrick, Black, Bernard S., Vilhelmsson, Anders, Vilkov, Grigory, Vladimirov, Vladimir, Vogel, Sebastian, Voigt, Stefan, Wagner, Wolf, Walther, Thomas, Weiss, Patrick, van der Wel, Michel, Werner, Ingrid M., Bohorquez, Santiago, Westerholm, P. Joakim, Westheide, Christian, Wipplinger, Evert, Wolf, Michael, Wolff, Christian C. P., Wolk, Leonard, Wong, Wing-Keung, Wrampelmeyer, Jan, Xia, Shuo, Xiu, Dacheng, Holzmeister, Felix, Bondarenko, Oleg, Xu, Ke, Xu, Caihong, Yadav, Pradeep K., Yagüe, José, Yan, Cheng, Yang, Antti, Yoo, Woongsun, Yu, Wenjia, Yu, Shihao, Yueshen, Bart Zhou, Bos, Charles S., Yuferova, Darya, Zamojski, Marcin, Zareei, Abalfazl, Zeisberger, Stefan, Zhang, Sarah, Zhang, Xiaoyu, Zhong, Zhuo, Zhou, Z. Ivy, Zhou, Chen, Zhu, Xingyu, Bosch-Rosa, Ciril, Zoican, Marius, Zwinkels, Remco C.J., Chen, Jian, Duevski, Teodor, Gao, Ge, Gemayel, Roland, Gilder, Dudley, Kuhle, Paul, Pagnotta, Emiliano, Pelli, Michele, Bouri, Elie, Sönksen, Jantje, Zhang, Lu, Ilczuk, Konrad, Bogoev, Dimitar, Qian, Ya, Wika, Hans C., Yu, Yihe, Zhao, Lu, Mi, Michael, Bao, Li, Brownlees, Christian T., Vaduva, Andreea, Prokopczuk, Marcel, Avetikian, Alejandro, Wu, Zhen-Xing, Calamia, Anna, Cao, Viet Nga, Capelle-Blancard, Gunther, Capera, Laura, Caporin, Massimiliano, Huber, Juergen, Carrion, Allen, Caskurlu, Tolga, Chakrabarty, Bidisha, Chernov, Mikhail, Cheung, William Ming Yan, Chincarini, Ludwig B., Chordia, Tarun, Chow, Sheung Chi, Clapham, Benjamin, Colliard, Jean-Edouard, Johanneson, Magnus, Comerton-Forde, Carole, Curran, Edward, Dao, Thong, Dare, Wale, Davies, Ryan J., De Blasis, Riccardo, De Nard, Gianluca, Declerck, Fany, Deev, Oleg, Degryse, Hans, Kirchler, Michael, Deku, Solomon, Desagre, Christophe, Dim, Chukwuma, Dimpfl, Thomas, Dong, Yun Jiang, Drummond, Philip, Dudda, Tom, Dumitrescu, Ariadna, Dyakov, Teodor, Razen, Michael, Dyhrberg, Anne Haubo, Dzieliński, Michał, Eksi, Asli, El Kalak, Izidin, ter Ellen, Saskia, Eugster, Nicolas, Evans, Martin D.D., Farrell, Michael, Félez-Viñas, Ester, Ferrara, Gerardo, Weitzel, Utz, FERROUHI, El Mehdi, Flori, Andrea, Fluharty-Jaidee, Jonathan, Foley, Sean, Fong, Kingsley Y. L., Foucault, Thierry, Franus, Tatiana, Franzoni, Francesco A., Frijns, Bart, Frömmel, Michael, Abad, David, Fu, Servanna Mianjun, Füllbrunn, Sascha, Gan, Baoqing, Gehrig, Thomas, Gerritsen, Dirk, Gil-Bazo, Javier, Glosten, Lawrence R., Gomez, Thomas, Gorbenko, Arseny, Güçbilmez, Ufuk, Van Dijk, Matthijs A., Leerstoel Stigchel, Helmholtz Institute, Experimental Psychology (onderzoeksprogramma PF), Finance, UU LEG Research UUSE Multidisciplinary Economics, LS Algemene Literatuurwetenschap, Hydrogeology, Sub General Pharmaceutics, Finance and Financial Markets, Menkveld, Albert J., Abudy, Menachem (Meni), Grammig, Joachim, Gregoire, Vincent, Hagströmer, Björn, Hambuckers, Julien, Hapnes, Erik, Harris, Jeffrey H., Harris, Lawrence, Hartmann, Simon, Hasse, Jean-Baptiste, Hautsch, Nikolaus, Adrian, Tobias, He, Xue-Zhong 'Tony', Heath, Davidson, Hediger, Simon, Hendershott, Terrence J., Hibbert, Ann Marie, Hjalmarsson, Erik, Hoelscher, Seth, Hoffmann, Peter, Holden, Craig W., Horenstein, Alex R., Ait-Sahalia, Yacine, Huang, Wenqian, Huang, Da, Hurlin, Christophe, Ivashchenko, Alexey, Iyer, Subramanian R., Jahanshahloo, Hossein, Jalkh, Naji, Jones, Charles M., Jurkatis, Simon, Jylha, Petri, Akmansoy, Olivier, Kaeck, Andreas, Kaiser, Gabriel, Karam, Arzé, Karmaziene, Egle, Kassner, Bernhard, Kaustia, Markku, Kazak, Ekaterina, Kearney, Fearghal, van Kervel, Vincent, Khan, Saad, Alcock, Jamie, Khomyn, Marta, Klein, Tony, Klein, Olga, Klos, Alexander, Koetter, Michael, Krahnen, Jan Pieter, Kolokolov, Aleksey, Korajczyk, Robert A., Kozhan, Roman, Kwan, Amy, Alexeev, Vitali, Lajaunie, Quentin, Lam, Full Yet Eric Campbell, Lambert, Marie, Langlois, Hugues, Lausen, Jens, Lauter, Tobias, Leippold, Markus, Levin, Vladimir, Li, Yijie, Li, (Michael) Hui, Aloosh, Arash, Liew, Chee Yoong, Lindner, Thomas, Linton, Oliver B., Liu, Jiacheng, Liu, Anqi, Llorente-Alvarez, Jesus-Guillermo, Lof, Matthijs, Lohr, Ariel, Longstaff, Francis A., Lopez-Lira, Alejandro, Amato, Livia, Mankad, Shawn, Mano, Nicola, Marchal, Alexis, Martineau, Charles, Mazzola, Francesco, Meloso, Debrah C, Mihet, Roxana, Mohan, Vijay, Moinas, Sophie, Moore, David, Amaya, Diego, Mu, Liangyi, Muravyev, Dmitriy, Murphy, Dermot, Neszveda, Gabor, Neumeier, Christian, Nielsson, Ulf, Nimalendran, Mahendrarajah, Nolte, Sven, Nordén, Lars L., O'Neill, Peter, Angel, James J., Obaid, Khaled, Ødegaard, Bernt Arne, Östberg, Per, Painter, Marcus, Palan, Stefan, Palit, Imon, Park, Andreas, Pascual Gascó, Roberto, Pasquariello, Paolo, Pastor, Lubos, Dreber, Anna, Bach, Amadeus, Patel, Vinay, Patton, Andrew J., Pearson, Neil D., Pelizzon, Loriana, Pelster, Matthias, Pérignon, Christophe, Pfiffer, Cameron, Philip, Richard, Plíhal, Tomáš, Prakash, Puneet, Baidoo, Edwin, Press, Oliver-Alexander, Prodromou, Tina, Putnins, Talis J., Raizada, Gaurav, Rakowski, David A., Ranaldo, Angelo, Regis, Luca, Reitz, Stefan, Renault, Thomas, Wang, Renjie, Bakalli, Gaetan, Renò, Roberto, Riddiough, Steven, Rinne, Kalle, Rintamäki, Paul, Riordan, Ryan, Rittmannsberger, Thomas, Rodríguez Longarela, Iñaki, Rösch, Dominik, Rognone, Lavinia, Roseman, Brian, Barbon, Andrea, Rosu, Ioanid, Roy, Saurabh, Rudolf, Nicolas, Rush, Stephen, Rzayev, Khaladdin, Rzeźnik, Aleksandra, Sanford, Anthony, Sankaran, Harikumar, Sarkar, Asani, Sarno, Lucio, Bashchenko, Oksana, Scaillet, Olivier, Scharnowski, Stefan, Schenk-Hoppé, Klaus Reiner, Schertler, Andrea, Schneider, Michael, Schroeder, Florian, Schürhoff, Norman, Schuster, Philipp, Schwarz, Marco A., Seasholes, Mark S., Bindra, Parampreet Christopher, Seeger, Norman, Shachar, Or, Shkilko, Andriy, Shui, Jessica, Sikic, Mario, Simion, Giorgia, Smales, Lee A., Söderlind, Paul, Sojli, Elvira, Sokolov, Konstantin, Bjonnes, Geir Hoidal, Spokeviciute, Laima, Stefanova, Denitsa, Subrahmanyam, Marti G., Neusüss, Sebastian, Szaszi, Barnabas, Talavera, Oleksandr, Tang, Yuehua, Taylor, Nicholas, Tham, Wing Wah, Theissen, Erik, Black, Jeffrey R., Thimme, Julian, Tonks, Ian, Tran, Hai, Trapin, Luca, Trolle, Anders B., Valente, Giorgio, Van Ness, Robert A., Vasquez, Aurelio, Verousis, Thanos, Verwijmeren, Patrick, Black, Bernard S., Vilhelmsson, Anders, Vilkov, Grigory, Vladimirov, Vladimir, Vogel, Sebastian, Voigt, Stefan, Wagner, Wolf, Walther, Thomas, Weiss, Patrick, van der Wel, Michel, Werner, Ingrid M., Bohorquez, Santiago, Westerholm, P. Joakim, Westheide, Christian, Wipplinger, Evert, Wolf, Michael, Wolff, Christian C. P., Wolk, Leonard, Wong, Wing-Keung, Wrampelmeyer, Jan, Xia, Shuo, Xiu, Dacheng, Holzmeister, Felix, Bondarenko, Oleg, Xu, Ke, Xu, Caihong, Yadav, Pradeep K., Yagüe, José, Yan, Cheng, Yang, Antti, Yoo, Woongsun, Yu, Wenjia, Yu, Shihao, Yueshen, Bart Zhou, Bos, Charles S., Yuferova, Darya, Zamojski, Marcin, Zareei, Abalfazl, Zeisberger, Stefan, Zhang, Sarah, Zhang, Xiaoyu, Zhong, Zhuo, Zhou, Z. Ivy, Zhou, Chen, Zhu, Xingyu, Bosch-Rosa, Ciril, Zoican, Marius, Zwinkels, Remco C.J., Chen, Jian, Duevski, Teodor, Gao, Ge, Gemayel, Roland, Gilder, Dudley, Kuhle, Paul, Pagnotta, Emiliano, Pelli, Michele, Bouri, Elie, Sönksen, Jantje, Zhang, Lu, Ilczuk, Konrad, Bogoev, Dimitar, Qian, Ya, Wika, Hans C., Yu, Yihe, Zhao, Lu, Mi, Michael, Bao, Li, Brownlees, Christian T., Vaduva, Andreea, Prokopczuk, Marcel, Avetikian, Alejandro, Wu, Zhen-Xing, Calamia, Anna, Cao, Viet Nga, Capelle-Blancard, Gunther, Capera, Laura, Caporin, Massimiliano, Huber, Juergen, Carrion, Allen, Caskurlu, Tolga, Chakrabarty, Bidisha, Chernov, Mikhail, Cheung, William Ming Yan, Chincarini, Ludwig B., Chordia, Tarun, Chow, Sheung Chi, Clapham, Benjamin, Colliard, Jean-Edouard, Johanneson, Magnus, Comerton-Forde, Carole, Curran, Edward, Dao, Thong, Dare, Wale, Davies, Ryan J., De Blasis, Riccardo, De Nard, Gianluca, Declerck, Fany, Deev, Oleg, Degryse, Hans, Kirchler, Michael, Deku, Solomon, Desagre, Christophe, Dim, Chukwuma, Dimpfl, Thomas, Dong, Yun Jiang, Drummond, Philip, Dudda, Tom, Dumitrescu, Ariadna, Dyakov, Teodor, Razen, Michael, Dyhrberg, Anne Haubo, Dzieliński, Michał, Eksi, Asli, El Kalak, Izidin, ter Ellen, Saskia, Eugster, Nicolas, Evans, Martin D.D., Farrell, Michael, Félez-Viñas, Ester, Ferrara, Gerardo, Weitzel, Utz, FERROUHI, El Mehdi, Flori, Andrea, Fluharty-Jaidee, Jonathan, Foley, Sean, Fong, Kingsley Y. L., Foucault, Thierry, Franus, Tatiana, Franzoni, Francesco A., Frijns, Bart, Frömmel, Michael, Abad, David, Fu, Servanna Mianjun, Füllbrunn, Sascha, Gan, Baoqing, Gehrig, Thomas, Gerritsen, Dirk, Gil-Bazo, Javier, Glosten, Lawrence R., Gomez, Thomas, Gorbenko, Arseny, Güçbilmez, Ufuk, and Van Dijk, Matthijs A.
Published: 2021

20. Evaluation of articular cartilage with quantitative MRI in an equine model of post-traumatic osteoarthritis

Author: Equine Musculoskeletal Biology, dES RMSC, Sub General Pharmaceutics, Heelkunde, dES AVR, Kajabi, Abdul Wahed, Casula, Victor, Sarin, Jaakko K, Ketola, Juuso H, Nykänen, Olli, Te Moller, Nikae C R, Mancini, Irina A D, Visser, Jetze, Brommer, Harold, René van Weeren, P, Malda, Jos, Töyräs, Juha, Nieminen, Miika T, Nissi, Mikko J, Equine Musculoskeletal Biology, dES RMSC, Sub General Pharmaceutics, Heelkunde, dES AVR, Kajabi, Abdul Wahed, Casula, Victor, Sarin, Jaakko K, Ketola, Juuso H, Nykänen, Olli, Te Moller, Nikae C R, Mancini, Irina A D, Visser, Jetze, Brommer, Harold, René van Weeren, P, Malda, Jos, Töyräs, Juha, Nieminen, Miika T, and Nissi, Mikko J
Published: 2021

21. Phenylglyoxaldehyde-Functionalized Polymeric Sorbents for Urea Removal from Aqueous Solutions

Author: Jong, Jacobus A W, Guo, Yong, Veenhoven, Cas, Moret, Marc-Etienne, van der Zwan, Johan, Lucini Paioni, Alessandra, Baldus, Marc, Scheiner, Karina C, Dalebout, Remco, van Steenbergen, Mies J, Verhaar, Marianne C, Smakman, Robert, Hennink, Wim E, Gerritsen, Karin G F, van Nostrum, Cornelus F, Afd Pharmaceutics, Sub Organic Chemistry and Catalysis, Sub NMR Spectroscopy, Sub Inorganic Chemistry and Catalysis, Sub General Pharmaceutics, Pharmaceutics, Pharmaceutics, Afd Pharmaceutics, Sub Organic Chemistry and Catalysis, Sub NMR Spectroscopy, Sub Inorganic Chemistry and Catalysis, and Sub General Pharmaceutics
Subjects: Sorbent, Polymers and Plastics, 02 engineering and technology, urea, chemisorption, 010402 general chemistry, Artificial kidney, 01 natural sciences, Article, Styrene, chemistry.chemical_compound, phenylglyoxaldehyde, Aqueous solution, Urea binding, Chromatography, Chemistry, Process Chemistry and Technology, Organic Chemistry, sorbent, 021001 nanoscience & nanotechnology, 0104 chemical sciences, kinetics, Urea, dialysis, Suspension polymerization, 0210 nano-technology, Dialysis (biochemistry)
Abstract: For realization of a wearable artificial kidney based on regeneration of a small volume of dialysate, efficient urea removal from dialysate is a major challenge. Here a potentially suitable polymeric sorbent based on phenylglyoxaldehyde (PGA), able to covalently bind urea under physiological conditions, is described. Sorbent beads containing PGA groups were obtained by suspension polymerization of either styrene or vinylphenylethan-1-one (VPE), followed by modification of the aromatic groups of poly(styrene) and poly(VPE) into PGA. It was found that PGA-functionalized sorbent beads had maximum urea binding capacities of 1.4–2.2 mmol/g and removed ∼0.6 mmol urea/g in 8 h at 37 °C under static conditions from urea-enriched phosphate-buffered saline, conditions representative of dialysate regeneration. This means that the daily urea production of a dialysis patient can be removed with a few hundred grams of this sorbent which, is an important step forward in the development of a wearable artificial kidney.
Published: 2019

22. Visible Light Cross-Linking of Gelatin Hydrogels Offers an Enhanced Cell Microenvironment with Improved Light Penetration Depth

Author: Lim, Khoon S, Klotz, Barbara J, Lindberg, Gabriella C J, Melchels, Ferry P W, Hooper, Gary J, Malda, Jos, Gawlitta, Debby, Woodfield, Tim B F, Afd Pharmaceutics, Sub General Pharmaceutics, LS Equine Muscoskeletal Biology, dES RMSC, Afd Pharmaceutics, Sub General Pharmaceutics, LS Equine Muscoskeletal Biology, and dES RMSC
Subjects: Materials science, food.ingredient, Light, Polymers and Plastics, Cell Survival, Polymers, chemistry.chemical_element, Bioengineering, 02 engineering and technology, 010402 general chemistry, 01 natural sciences, Gelatin, cell encapsulation, transdermal crosslinking, Polymerization, Sodium persulfate, Biomaterials, chemistry.chemical_compound, Chondrocytes, food, Materials Chemistry, Journal Article, Humans, light penetration depth, Cell encapsulation, Cells, Cultured, hydrogels, visible light, Tissue Engineering, Cell Differentiation, 021001 nanoscience & nanotechnology, 0104 chemical sciences, Ruthenium, Cross-Linking Reagents, Cellular Microenvironment, chemistry, Chemical engineering, gelatin-methacryloyl (Gel-MA), Self-healing hydrogels, 0210 nano-technology, Biofabrication, Visible spectrum, Biotechnology
Abstract: In this study, the cyto-compatibility and cellular functionality of cell-laden gelatin-methacryloyl (Gel-MA) hydrogels fabricated using a set of photo-initiators which absorb in 400-450 nm of the visible light range are investigated. Gel-MA hydrogels cross-linked using ruthenium (Ru) and sodium persulfate (SPS), are characterized to have comparable physico-mechanical properties as Gel-MA gels photo-polymerized using more conventionally adopted photo-initiators, such as 1-[4-(2-hydroxyethoxy)-phenyl]-2-hydroxy-2-methyl-1-propan-1-one (Irgacure 2959) and lithium phenyl(2,4,6-trimethylbenzoyl) phosphinate (LAP). It is demonstrated that the Ru/SPS system has a less adverse effect on the viability and metabolic activity of human articular chondrocytes encapsulated in Gel-MA hydrogels for up to 35 days. Furthermore, cell-laden constructs cross-linked using the Ru/SPS system have significantly higher glycosaminoglycan content and re-differentiation capacity as compared to cells encapsulated using I2959 and LAP. Moreover, the Ru/SPS system offers significantly greater light penetration depth as compared to the I2959 system, allowing thick (10 mm) Gel-MA hydrogels to be fabricated with homogenous cross-linking density throughout the construct. These results demonstrate the considerable advantages of the Ru/SPS system over traditional UV polymerizing systems in terms of clinical relevance and practicability for applications such as cell encapsulation, biofabrication, and in situ cross-linking of injectable hydrogels.
Published: 2019

23. Microwave control of thermal-magnon spin transport

Author: Liu, J., Feringa, F., Flebus, B., Cornelissen, L. J., Leutenantsmeyer, J. C., Duine, R. A., van Wees, B. J., Sub General Pharmaceutics, Sub Cond-Matter Theory, Stat & Comp Phys, Sub General Pharmaceutics, Sub Cond-Matter Theory, Stat & Comp Phys, Physics of Nanodevices, and Physics of Nanostructures
Subjects: Field (physics), INSTABILITY, Yttrium iron garnet, FOS: Physical sciences, 02 engineering and technology, FERROMAGNETIC-RESONANCE, FILMS, 01 natural sciences, chemistry.chemical_compound, Condensed Matter::Materials Science, Mesoscale and Nanoscale Physics (cond-mat.mes-hall), 0103 physical sciences, Electronic, Optical and Magnetic Materials, 010306 general physics, Spin-½, IRREVERSIBLE-PROCESSES, Physics, Condensed Matter - Mesoscale and Nanoscale Physics, Condensed matter physics, Magnon, Resonance, 021001 nanoscience & nanotechnology, Magnetostatics, Condensed Matter Physics, Ferromagnetic resonance, Electronic, Optical and Magnetic Materials, RECIPROCAL RELATIONS, ROOM-TEMPERATURE, chemistry, WAVE SPECTRUM, Condensed Matter::Strongly Correlated Electrons, Radio frequency, 0210 nano-technology
Abstract: We observe that an rf microwave field strongly influences the transport of incoherent thermal magnons in yttrium iron garnet. Ferromagnetic resonance in the nonlinear regime suppresses thermal magnon transport by 95%. The transport is also modulated at nonresonant conditions in two cases, both related to the magnon band minimum. Firstly, a strong enhancement of the nonlocal signal appears at a static magnetic field below the resonance condition. This increase only occurs at one field polarity and can be as large as 800%. We attribute this effect to magnon kinetic processes, which give rise to band-minimum magnons and high-energy chiral surface modes. Secondly, the signal increases at a static field above the resonance condition, where the rf frequency coincides with the magnon band minimum. Our study gives insight into the interplay between coherent and incoherent spin dynamics: the rf field modifies the occupation of relevant magnon states and, via kinetic processes, the magnon spin transport.
Published: 2019

24. Biological membranes in EV biogenesis, stability, uptake, and cargo transfer: an ISEV position paper arising from the ISEV membranes and EVs workshop

Author: Russell, Ashley E, Sneider, Alexandra, Witwer, Kenneth W, Bergese, Paolo, Bhattacharyya, Suvendra N, Cocks, Alexander, Cocucci, Emanuele, Erdbrügger, Uta, Falcon-Perez, Juan M, Freeman, David W, Gallagher, Thomas M, Hu, Shuaishuai, Huang, Yiyao, Jay, Steven M, Kano, Shin-Ichi, Lavieu, Gregory, Leszczynska, Aleksandra, Llorente, Alicia M, Lu, Quan, Mahairaki, Vasiliki, Muth, Dillon C, Noren Hooten, Nicole, Ostrowski, Matias, Prada, Ilaria, Sahoo, Susmita, Schøyen, Tine Hiorth, Sheng, Lifu, Tesch, Deanna, Van Niel, Guillaume, Vandenbroucke, Roosmarijn E, Verweij, Frederik J, Villar, Ana V, Wauben, Marca, Wehman, Ann M, Yin, Hang, Carter, David Raul Francisco, Vader, Pieter, LS Celbiologie-Algemeen, dB&C I&I, Sub General Pharmaceutics, Universidad de Cantabria, LS Celbiologie-Algemeen, dB&C I&I, and Sub General Pharmaceutics
Subjects: 0301 basic medicine, fusion, Biogenesis, Exosomes, Extracellular vesicles, Fusion, Membranes, Uptake, Nanoparticles, purl.org/becyt/ford/1 [https], 0302 clinical medicine, IMMERSION DEPTH, Medicine and Health Sciences, MEDIATED ENDOCYTOSIS, GENE-EXPRESSION, lcsh:Cytology, 3. Good health, ISEV workshop, Membrane, membranes, 030220 oncology & carcinogenesis, uptake, technology, Position Paper, position paper, Histology, Membrane biology, Nanotechnology, DENDRITIC CELLS, 03 medical and health sciences, VDP::Medisinske Fag: 700, lcsh:QH573-671, purl.org/becyt/ford/1.6 [https], Biology, paper, MULTIVESICULAR BODIES, Biology and Life Sciences, Biological membrane, Cell Biology, biogenesis, EMERGING ROLE, biogenesisfusion, EXOSOME SECRETION, FAS LIGAND, position, 030104 developmental biology, PLASMA-MEMBRANE, Position paper, Business
Abstract: Paracrine and endocrine roles have increasingly been ascribed to extracellular vesicles (EVs) generated by multicellular organisms. Central to the biogenesis, content, and function of EVs are their delimiting lipid bilayer membranes. To evaluate research progress on membranes and EVs, the International Society for Extracellular Vesicles (ISEV) conducted a workshop in March 2018 in Baltimore, Maryland, USA, bringing together key opinion leaders and hands-on researchers who were selected on the basis of submitted applications. The workshop was accompanied by two scientific surveys and covered four broad topics: EV biogenesis and release; EV uptake and fusion; technologies and strategies used to study EV membranes; and EV transfer and functional assays. In this ISEV position paper, we synthesize the results of the workshop and the related surveys to outline important outstanding questions about EV membranes and describe areas of consensus. The workshop discussions and survey responses reveal that while much progress has been made in the field, there are still several concepts that divide opinion. Good consensus exists in some areas, including particular aspects of EV biogenesis, uptake and downstream signalling. Areas with little to no consensus include EV storage and stability, as well as whether and how EVs fuse with target cells. Further research is needed in these key areas, as a better understanding of membrane biology will contribute substantially towards advancing the field of extracellular vesicles. Fil: Russell, Ashley E.. University Johns Hopkins; Estados Unidos Fil: Sneider, Alexandra. University Johns Hopkins; Estados Unidos Fil: Witwer, Kenneth W.. University Johns Hopkins; Estados Unidos Fil: Bergese, Paolo. Università Degli Studi Di Brescia; Italia Fil: Bhattacharyya, Suvendra N.. Indian Institute of Chemical Biology; India Fil: Cocks, Alexander. Cardiff University; Reino Unido Fil: Cocucci, Emanuele. Ohio State University; Estados Unidos Fil: Erdbrügger, Uta. University of Virginia; Estados Unidos Fil: Falcon Perez, Juan M.. Ikerbasque Basque Foundation for Science; España Fil: Freeman, David W.. National Institute On Aging National Institute for Helth ; Estados Unidos Fil: Gallagher, Thomas M.. Loyola University Of Chicago; Estados Unidos Fil: Hu, Shuaishuai. Technological University Dublin; Irlanda Fil: Huang, Yiyao. University Johns Hopkins; Estados Unidos. Southern Medical University; China Fil: Jay, Steven M.. University of Maryland; Estados Unidos Fil: Kano, Shin-ichi. The University of Alabama at Birmingham School of Medicine; Estados Unidos Fil: Lavieu, Gregory. Institut Curie; Francia Fil: Leszczynska, Aleksandra. University of California at San Diego; Estados Unidos Fil: Llorente, Alicia M.. Oslo University Hospital; Noruega Fil: Lu, Quan. Harvard University. Harvard School of Public Health; Estados Unidos Fil: Mahairaki, Vasiliki. University Johns Hopkins; Estados Unidos Fil: Muth, Dillon C.. University Johns Hopkins; Estados Unidos Fil: Noren Hooten, Nicole. National Institute On Aging National Institute for Helth ; Estados Unidos Fil: Ostrowski, Matias. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas en Retrovirus y Sida. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Biomédicas en Retrovirus y Sida; Argentina Fil: Prada, Ilaria. Consiglio Nazionale delle Ricerche; Italia Fil: Sahoo, Susmita. Icahn School of Medicine at Mount Sinai ; Estados Unidos Fil: Schøyen, Tine Hiorth. Uit The Arctic University Of Norway; Noruega. University Johns Hopkins; Estados Unidos Fil: Sheng, Lifuy. University of Washington. School of Medicine; Estados Unidos Fil: Tesch, Deanna. Shaw University; Estados Unidos Fil: Van Niel, Guillaume. No especifíca; Fil: Vandenbroucke, Roosmarijn E.. University of Ghent; Bélgica Fil: Verweij, Frederik J.. No especifíca; Fil: Villar, Ana V.. Universidad de Cantabria; España Fil: Wauben, Marca. University of Utrecht; Países Bajos Fil: Wehman, Ann M.. Universität Würzburg; Alemania Fil: Ardavan, Arzhang. Peking University; ; China Fil: Carter, David Raul Francisco. Oxford Brookes University; Reino Unido Fil: Vader, Pieter. University Medical Center Utrecht; Países Bajos
Published: 2019
Full Text: View/download PDF

25. Prospects for fundamental physics with LISA

Author: Theoretical Physics, Sub NMR Spectroscopy, LS Immunologie, Afd Subatomic Physics (SAP), Afd OT Educatie en pedagogiek, Sub General Pharmaceutics, Sub RvdM overig, Sub String Theory Cosmology and ElemPart, Dep Natuurkunde, Sub Inorganic Chemistry and Catalysis, LS Wijsgerige Ethiek, Section Geography and Education, Barausse, Enrico, Berti, Emanuele, Hertog, Thomas, Hughes, Scott A., Jetzer, Philippe, Pani, Paolo, Sotiriou, Thomas P., Tamanini, Nicola, Witek, Helvi, Yagi, Kent, Yunes, Nicolas, Abdelsalhin, T., Achucarro, A., van Aelst, K., Afshordi, N., Akcay, S., Annulli, L., Arun, K. G., Ayuso, I., Baibhav, V., Baker, T., Bantilan, H., Barreiro, T., Barrera-Hinojosa, C., Bartolo, N., Baumann, D., Belgacem, E., Bellini, E., Bellomo, N., Ben-Dayan, I., Bena, I., Benkel, R., Bergshoefs, E., Bernard, L., Bernuzzi, S., Bertacca, D., Besancon, M., Beutler, F., Beyer, F., Bhagwat, S., Bicak, J., Biondini, S., Bize, S., Blas, D., Boehmer, C., Boller, K., Bonga, B., Bonvin, C., Bosso, P., Bozzola, G., Brax, P., Breitbach, M., Brito, R., Bruni, M., Bruegmann, B., Bulten, H., Buonanno, A., Burko, L. M., Burrage, C., Cabral, F., Calcagni, G., Caprini, C., Cardenas-Avendano, A., Celoria, M., Chatziioannou, K., Chernoff, D., Clough, K., Coates, A., Comelli, D., Compere, G., Croon, D., Cruces, D., Cusin, G., Dalang, C., Danielsson, U., Das, S., Datta, S., de Boer, J., De Luca, V., De Rham, C., Desjacques, V., Destounis, K., Filippo, F. Di, Dima, A., Dimastrogiovanni, E., Dolan, S., Doneva, D., Duque, F., Durrer, R., East, W., Easther, R., Elley, M., Ellis, J. R., Emparan, R., Ezquiaga, J. M., Fairbairn, M., Fairhurst, S., Farmer, H. F., Fasiello, M. R., Ferrari, V., Ferreira, P. G., Ficarra, G., Figueras, P., Fisenko, S., Foffa, S., Franchini, N., Franciolini, G., Fransen, K., Frauendiener, J., Frusciante, N., Fujita, R., Gair, J., Ganz, A., Garcia, P., Garcia-Bellido, J., Garriga, J., Geiger, R., Geng, C., Gergely, L. a., Germani, C., Gerosa, D., Giddings, S. B., Gourgoulhon, E., Grandclement, P., Graziani, L., Gualtieri, L., Haggard, D., Haino, S., Halburd, R., Han, W. -B., Hawken, A. J., Hees, A., Heng, I. S., Hennig, J., Herdeiro, C., Hervik, S., Holten, J. v., Hoyle, C. D., Hu, Y., Hull, M., Ikeda, T., Isi, M., Jenkins, A., Julie, F., Kajfasz, E., Kalaghatgi, C., Kaloper, N., Kamionkowski, M., Karas, V., Kastha, S., Keresztes, Z., Kidder, L., Kimpson, T., Klein, A., Klioner, S., Kokkotas, K., Kolesova, H., Kolkowitz, S., Kopp, J., Koyama, K., Krishnendu, N. V., Kroon, J. A. V., Kunz, M., Lahav, O., Landragin, A., Lang, R. N., Poncin-Lafitte, C. Le, Lemos, J., Li, B., Liberati, S., Liguori, M., Lin, F., Liu, G., Lobo, F. S. N., Loll, R., Lombriser, L., Lovelace, G., Macedo, R. P., Madge, E., Maggio, E., Maggiore, M., Marassi, S., Marcoccia, P., Markakis, C., Martens, W., Martinovic, K., Martins, C. J. A. P., Maselli, A., Mastrogiovanni, S., Matarrese, S., Matas, A., Mavromatos, N. E., Mazumdar, A., Meerburg, P. D., Megias, E., Miller, J., Mimoso, J. P., Mittnacht, L., Montero, M. M., Moore, B., Martin-Moruno, P., Musco, I., Nakano, H., Nampalliwar, S., Nardini, G., Nielsen, A., Novak, J., Nunes, N. J., Okounkova, M., Oliveri, R., Oppizzi, F., Orlando, G., Oshita, N., Pappas, G., Paschalidis, V., Peiris, H., Peloso, M., Perkins, S., Pettorino, V., Pikovski, I., Pilo, L., Podolsky, J., Pontzen, A., Prabhat, S., Pratten, G., Prokopec, T., Prouza, M., Qi, H., Raccanelli, A., Rajantie, A., Randall, L., Raposo, G., Raymond, V., Renaux-Petel, S., Ricciardone, A., Riotto, A., Robson, T., Roest, D., Rollo, R., Rosofsky, S., Ruan, J. J., Rubiera-Garcia, D., Ruiz, M., Rusu, M., Sabatie, F., Sago, N., Sakellariadou, M., Saltas, I. D., Sberna, L., Sathyaprakash, B., Scheel, M., Schmidt, P., Schutz, B., Schwaller, P., Shao, L., Shapiro, S. L., Shoemaker, D., Silva, A. d., Simpson, C., Sopuerta, C. F., Spallicci, A., Stefanek, B. A., Stein, L., Stergioulas, N., Stott, M., Sutton, P., Svarc, R., Tagoshi, H., Tahamtan, T., Takeda, H., Tanaka, T., Tantilian, G., Tasinato, G., Tattersall, O., Teukolsky, S., Tiec, A. L., Theureau, G., Trodden, M., Tolley, A., Toubiana, A., Traykova, D., Tsokaros, A., Unal, C., Unnikrishnan, C. S., Vagenas, E. C., Valageas, P., Vallisneri, M., Brand, J. Van den, Broeck, C. Van den, de Meent, M. van, Vanhove, P., Varma, V., Veitch, J., Vercnocke, B., Verde, L., Vernieri, D., Vernizzi, F., Vicente, R., Vidotto, F., Visser, M., Vlah, Z., Vretinaris, S., Voelkel, S., Wang, Q., Wang, Yu-Tong, Werner, M. C., Westernacher, J., Weygaert, R. v. d., Wiltshire, D., Wiseman, T., Wolf, P., Wu, K., Yamada, K., Yang, H., Yi, L., Yue, X., Yvon, D., Zilhao, M., Zimmerman, A., Zumalacarregui, M., Theoretical Physics, Sub NMR Spectroscopy, LS Immunologie, Afd Subatomic Physics (SAP), Afd OT Educatie en pedagogiek, Sub General Pharmaceutics, Sub RvdM overig, Sub String Theory Cosmology and ElemPart, Dep Natuurkunde, Sub Inorganic Chemistry and Catalysis, LS Wijsgerige Ethiek, Section Geography and Education, Barausse, Enrico, Berti, Emanuele, Hertog, Thomas, Hughes, Scott A., Jetzer, Philippe, Pani, Paolo, Sotiriou, Thomas P., Tamanini, Nicola, Witek, Helvi, Yagi, Kent, Yunes, Nicolas, Abdelsalhin, T., Achucarro, A., van Aelst, K., Afshordi, N., Akcay, S., Annulli, L., Arun, K. G., Ayuso, I., Baibhav, V., Baker, T., Bantilan, H., Barreiro, T., Barrera-Hinojosa, C., Bartolo, N., Baumann, D., Belgacem, E., Bellini, E., Bellomo, N., Ben-Dayan, I., Bena, I., Benkel, R., Bergshoefs, E., Bernard, L., Bernuzzi, S., Bertacca, D., Besancon, M., Beutler, F., Beyer, F., Bhagwat, S., Bicak, J., Biondini, S., Bize, S., Blas, D., Boehmer, C., Boller, K., Bonga, B., Bonvin, C., Bosso, P., Bozzola, G., Brax, P., Breitbach, M., Brito, R., Bruni, M., Bruegmann, B., Bulten, H., Buonanno, A., Burko, L. M., Burrage, C., Cabral, F., Calcagni, G., Caprini, C., Cardenas-Avendano, A., Celoria, M., Chatziioannou, K., Chernoff, D., Clough, K., Coates, A., Comelli, D., Compere, G., Croon, D., Cruces, D., Cusin, G., Dalang, C., Danielsson, U., Das, S., Datta, S., de Boer, J., De Luca, V., De Rham, C., Desjacques, V., Destounis, K., Filippo, F. Di, Dima, A., Dimastrogiovanni, E., Dolan, S., Doneva, D., Duque, F., Durrer, R., East, W., Easther, R., Elley, M., Ellis, J. R., Emparan, R., Ezquiaga, J. M., Fairbairn, M., Fairhurst, S., Farmer, H. F., Fasiello, M. R., Ferrari, V., Ferreira, P. G., Ficarra, G., Figueras, P., Fisenko, S., Foffa, S., Franchini, N., Franciolini, G., Fransen, K., Frauendiener, J., Frusciante, N., Fujita, R., Gair, J., Ganz, A., Garcia, P., Garcia-Bellido, J., Garriga, J., Geiger, R., Geng, C., Gergely, L. a., Germani, C., Gerosa, D., Giddings, S. B., Gourgoulhon, E., Grandclement, P., Graziani, L., Gualtieri, L., Haggard, D., Haino, S., Halburd, R., Han, W. -B., Hawken, A. J., Hees, A., Heng, I. S., Hennig, J., Herdeiro, C., Hervik, S., Holten, J. v., Hoyle, C. D., Hu, Y., Hull, M., Ikeda, T., Isi, M., Jenkins, A., Julie, F., Kajfasz, E., Kalaghatgi, C., Kaloper, N., Kamionkowski, M., Karas, V., Kastha, S., Keresztes, Z., Kidder, L., Kimpson, T., Klein, A., Klioner, S., Kokkotas, K., Kolesova, H., Kolkowitz, S., Kopp, J., Koyama, K., Krishnendu, N. V., Kroon, J. A. V., Kunz, M., Lahav, O., Landragin, A., Lang, R. N., Poncin-Lafitte, C. Le, Lemos, J., Li, B., Liberati, S., Liguori, M., Lin, F., Liu, G., Lobo, F. S. N., Loll, R., Lombriser, L., Lovelace, G., Macedo, R. P., Madge, E., Maggio, E., Maggiore, M., Marassi, S., Marcoccia, P., Markakis, C., Martens, W., Martinovic, K., Martins, C. J. A. P., Maselli, A., Mastrogiovanni, S., Matarrese, S., Matas, A., Mavromatos, N. E., Mazumdar, A., Meerburg, P. D., Megias, E., Miller, J., Mimoso, J. P., Mittnacht, L., Montero, M. M., Moore, B., Martin-Moruno, P., Musco, I., Nakano, H., Nampalliwar, S., Nardini, G., Nielsen, A., Novak, J., Nunes, N. J., Okounkova, M., Oliveri, R., Oppizzi, F., Orlando, G., Oshita, N., Pappas, G., Paschalidis, V., Peiris, H., Peloso, M., Perkins, S., Pettorino, V., Pikovski, I., Pilo, L., Podolsky, J., Pontzen, A., Prabhat, S., Pratten, G., Prokopec, T., Prouza, M., Qi, H., Raccanelli, A., Rajantie, A., Randall, L., Raposo, G., Raymond, V., Renaux-Petel, S., Ricciardone, A., Riotto, A., Robson, T., Roest, D., Rollo, R., Rosofsky, S., Ruan, J. J., Rubiera-Garcia, D., Ruiz, M., Rusu, M., Sabatie, F., Sago, N., Sakellariadou, M., Saltas, I. D., Sberna, L., Sathyaprakash, B., Scheel, M., Schmidt, P., Schutz, B., Schwaller, P., Shao, L., Shapiro, S. L., Shoemaker, D., Silva, A. d., Simpson, C., Sopuerta, C. F., Spallicci, A., Stefanek, B. A., Stein, L., Stergioulas, N., Stott, M., Sutton, P., Svarc, R., Tagoshi, H., Tahamtan, T., Takeda, H., Tanaka, T., Tantilian, G., Tasinato, G., Tattersall, O., Teukolsky, S., Tiec, A. L., Theureau, G., Trodden, M., Tolley, A., Toubiana, A., Traykova, D., Tsokaros, A., Unal, C., Unnikrishnan, C. S., Vagenas, E. C., Valageas, P., Vallisneri, M., Brand, J. Van den, Broeck, C. Van den, de Meent, M. van, Vanhove, P., Varma, V., Veitch, J., Vercnocke, B., Verde, L., Vernieri, D., Vernizzi, F., Vicente, R., Vidotto, F., Visser, M., Vlah, Z., Vretinaris, S., Voelkel, S., Wang, Q., Wang, Yu-Tong, Werner, M. C., Westernacher, J., Weygaert, R. v. d., Wiltshire, D., Wiseman, T., Wolf, P., Wu, K., Yamada, K., Yang, H., Yi, L., Yue, X., Yvon, D., Zilhao, M., Zimmerman, A., and Zumalacarregui, M.
Published: 2020

26. Phenylglyoxaldehyde-Functionalized Polymeric Sorbents for Urea Removal from Aqueous Solutions

Author: Afd Pharmaceutics, Sub Organic Chemistry and Catalysis, Sub NMR Spectroscopy, Sub Inorganic Chemistry and Catalysis, Sub General Pharmaceutics, Pharmaceutics, Jong, Jacobus A W, Guo, Yong, Veenhoven, Cas, Moret, Marc-Etienne, van der Zwan, Johan, Lucini Paioni, Alessandra, Baldus, Marc, Scheiner, Karina C, Dalebout, Remco, van Steenbergen, Mies J, Verhaar, Marianne C, Smakman, Robert, Hennink, Wim E, Gerritsen, Karin G F, van Nostrum, Cornelus F, Afd Pharmaceutics, Sub Organic Chemistry and Catalysis, Sub NMR Spectroscopy, Sub Inorganic Chemistry and Catalysis, Sub General Pharmaceutics, Pharmaceutics, Jong, Jacobus A W, Guo, Yong, Veenhoven, Cas, Moret, Marc-Etienne, van der Zwan, Johan, Lucini Paioni, Alessandra, Baldus, Marc, Scheiner, Karina C, Dalebout, Remco, van Steenbergen, Mies J, Verhaar, Marianne C, Smakman, Robert, Hennink, Wim E, Gerritsen, Karin G F, and van Nostrum, Cornelus F
Published: 2020

27. Phenylglyoxaldehyde-Functionalized Polymeric Sorbents for Urea Removal from Aqueous Solutions

Author: Pharmaceutics, Afd Pharmaceutics, Sub Organic Chemistry and Catalysis, Sub NMR Spectroscopy, Sub Inorganic Chemistry and Catalysis, Sub General Pharmaceutics, Jong, Jacobus A W, Guo, Yong, Veenhoven, Cas, Moret, Marc-Etienne, van der Zwan, Johan, Lucini Paioni, Alessandra, Baldus, Marc, Scheiner, Karina C, Dalebout, Remco, van Steenbergen, Mies J, Verhaar, Marianne C, Smakman, Robert, Hennink, Wim E, Gerritsen, Karin G F, van Nostrum, Cornelus F, Pharmaceutics, Afd Pharmaceutics, Sub Organic Chemistry and Catalysis, Sub NMR Spectroscopy, Sub Inorganic Chemistry and Catalysis, Sub General Pharmaceutics, Jong, Jacobus A W, Guo, Yong, Veenhoven, Cas, Moret, Marc-Etienne, van der Zwan, Johan, Lucini Paioni, Alessandra, Baldus, Marc, Scheiner, Karina C, Dalebout, Remco, van Steenbergen, Mies J, Verhaar, Marianne C, Smakman, Robert, Hennink, Wim E, Gerritsen, Karin G F, and van Nostrum, Cornelus F
Published: 2020

28. Evolution and domestication of the Bovini species

Author: LS Psycholinguistiek, One Health Toxicologie, Energy, Resources & Technological Change, Sustainable Energy Supply Systems, Sub General Pharmaceutics, Zhang, K, Lenstra, J A, Zhang, S, Liu, W, Liu, J, LS Psycholinguistiek, One Health Toxicologie, Energy, Resources & Technological Change, Sustainable Energy Supply Systems, Sub General Pharmaceutics, Zhang, K, Lenstra, J A, Zhang, S, Liu, W, and Liu, J
Published: 2020

29. Engineering of a complex bone tissue model with endothelialised channels and capillary-like networks

Author: Klotz, B J, Lim, Khoon S, Chang, Y X, Soliman, B J, Pennings, I, Melchels, F P, Rosenberg, Antoine J W P, Malda, J, Gawlittal, D, Afd Pharmaceutics, Sub General Pharmaceutics, LS Equine Muscoskeletal Biology, and dES RMSC
Subjects: 0301 basic medicine, Materials science, culture medium, lcsh:Diseases of the musculoskeletal system, Endothelium, endothelium, Capillary action, Sus scrofa, lcsh:Surgery, Neovascularization, Physiologic, 02 engineering and technology, Bone tissue, Bone and Bones, Hydrogel, Polyethylene Glycol Dimethacrylate, osteogenesis, vasculogenesis, endothelial colony-forming cells, 03 medical and health sciences, Vasculogenesis, medicine, Animals, Humans, endothelial-colony-forming cells, capillaries, Oxygen supply, Tissue Engineering, Tissue Scaffolds, Mesenchymal stem cell, Endothelial Cells, Biomaterial, lcsh:RD1-811, 021001 nanoscience & nanotechnology, Culture Media, gelatine-methacryloyl, 030104 developmental biology, medicine.anatomical_structure, Self-healing hydrogels, Gelatin, Methacrylates, hydrogel, Co-culture, lcsh:RC925-935, Pericytes, 0210 nano-technology, mesenchymal stromal cells, Biomedical engineering
Abstract: In engineering of tissue analogues, upscaling to clinically-relevant sized constructs remains a significant challenge. The successful integration of a vascular network throughout the engineered tissue is anticipated to overcome the lack of nutrient and oxygen supply to residing cells. This work aimed at developing a multiscale bone-tissue-specific vascularisation strategy. Engineering pre-vascularised bone leads to biological and fabrication dilemmas. To fabricate channels endowed with an endothelium and suitable for osteogenesis, rather stiff materials are preferable, while capillarisation requires soft matrices. To overcome this challenge, gelatine-methacryloyl hydrogels were tailored by changing the degree of functionalisation to allow for cell spreading within the hydrogel, while still enabling endothelialisation on the hydrogel surface. An additional challenge was the combination of the multiple required cell-types within one biomaterial, sharing the same culture medium. Consequently, a new medium composition was investigated that simultaneously allowed for endothelialisation, capillarisation and osteogenesis. Integrated multipotent mesenchymal stromal cells, which give rise to pericyte-like and osteogenic cells, and endothelial-colony-forming cells (ECFCs) which form capillaries and endothelium, were used. Based on the aforementioned optimisation, a construct of 8 × 8 × 3 mm, with a central channel of 600 µm in diameter, was engineered. In this construct, ECFCs covered the channel with endothelium and osteogenic cells resided in the hydrogel, adjacent to self-assembled capillary-like networks. This study showed the promise of engineering complex tissue constructs by means of human primary cells, paving the way for scaling-up and finally overcoming the challenge of engineering vascularised tissues.
Published: 2018

30. A Synthetic Thermosensitive Hydrogel for Cartilage Bioprinting and Its Biofunctionalization with Polysaccharides

Author: Abbadessa, Anna, Mouser, Vivian H M, Blokzijl, Maarten M, Gawlitta, Debby, Dhert, Wouter J A, Hennink, Wim E, Malda, Jos, Vermonden, Tina, Sub Drug delivery, Sub General Pharmaceutics, Faculteit Diergeneeskunde, Dep Farmaceutische wetenschappen, dES RMSC, Pharmaceutics, dCSCA RMSC-1, Sub Drug delivery, Sub General Pharmaceutics, Faculteit Diergeneeskunde, Dep Farmaceutische wetenschappen, dES RMSC, Pharmaceutics, and dCSCA RMSC-1
Subjects: Polymers and Plastics, Cell Survival, Polymers, Bioengineering, 02 engineering and technology, Polyethylene glycol, 010402 general chemistry, complex mixtures, 01 natural sciences, Article, Hydrogel, Polyethylene Glycol Dimethacrylate, Biomaterials, chemistry.chemical_compound, Chondrocytes, Tissue engineering, Polysaccharides, Taverne, Materials Testing, Hyaluronic acid, Polymer chemistry, Journal Article, Materials Chemistry, Animals, Methacrylamide, Horses, Chondroitin sulfate, Cells, Cultured, chemistry.chemical_classification, Tissue Engineering, Tissue Scaffolds, Chemistry, Bioprinting, Temperature, technology, industry, and agriculture, Polymer, 021001 nanoscience & nanotechnology, Chondrogenesis, 0104 chemical sciences, Cartilage, Self-healing hydrogels, 0210 nano-technology, Biomedical engineering
Abstract: Hydrogels based on triblock copolymers of polyethylene glycol and partially methacrylated poly[N-(2-hydroxypropyl) methacrylamide mono/dilactate] make up an attractive class of biomaterials because of their biodegradability, cytocompatibility, and tunable thermoresponsive and mechanical properties. If these properties are fine-tuned, the hydrogels can be three-dimensionally bioprinted, to generate, for instance, constructs for cartilage repair. This study investigated whether hydrogels based on the polymer mentioned above with a 10% degree of methacrylation (M10P10) support cartilage formation by chondrocytes and whether the incorporation of methacrylated chondroitin sulfate (CSMA) or methacrylated hyaluronic acid (HAMA) can improve the mechanical properties, long-term stability, and printability. Chondrocyte-laden M10P10 hydrogels were cultured for 42 days to evaluate chondrogenesis. M10P10 hydrogels with or without polysaccharides were evaluated for their mechanical properties (before and after UV photo-cross-linking), degradation kinetics, and printability. Extensive cartilage matrix production occurred in M10P10 hydrogels, highlighting their potential for cartilage repair strategies. The incorporation of polysaccharides increased the storage modulus of polymer mixtures and decreased the degradation kinetics in cross-linked hydrogels. Addition of HAMA to M10P10 hydrogels improved printability and resulted in three-dimensional constructs with excellent cell viability. Hence, this novel combination of M10P10 with HAMA forms an interesting class of hydrogels for cartilage bioprinting.
Published: 2016
Full Text: View/download PDF

31. A Kinetic Degradation Study of Curcumin in Its Free Form and Loaded in Polymeric Micelles

Author: Naksuriya, Ornchuma, van Steenbergen, Mies J., Sastre Torano, Javier, Okonogi, Siriporn, Hennink, Wim E., Biomolecular Analysis, Pharmaceutics, Sub General Pharmaceutics, Sub Drug delivery, Afd Chemical Biology and Drug Discovery, Sub Biomolecular analysis, Dep Farmaceutische wetenschappen, Biomolecular Analysis, Pharmaceutics, Sub General Pharmaceutics, Sub Drug delivery, Afd Chemical Biology and Drug Discovery, Sub Biomolecular analysis, and Dep Farmaceutische wetenschappen
Subjects: 0301 basic medicine, Polymers, Pharmaceutical Science, 02 engineering and technology, Micelle, Antioxidants, Polyethylene Glycols, chemistry.chemical_compound, Drug Stability, curcumin, Chromatography, High Pressure Liquid, Micelles, autooxidation, degradation, Drug Carriers, Aqueous solution, Autoxidation, tyloxapol, Chemistry, clinical trial, Hydrogen-Ion Concentration, 021001 nanoscience & nanotechnology, degradation kinetics, polymerization, chemical reaction kinetics, 0210 nano-technology, Drug carrier, Research Article, Half-Life, Curcumin, Buffers, precipitation, rate constant, Article, 03 medical and health sciences, Reaction rate constant, half life time, micelle, Humans, human, Curcuminoid, methanol, Chromatography, stability, Culture Media, Kinetics, 030104 developmental biology, kinetics, dielectric constant, macrogol, aqueous solution, Ethylene glycol, Nuclear chemistry
Abstract: Curcumin, a phenolic compound, possesses many pharmacological activities and is under clinical evaluation to treat different diseases. However, conflicting data about its stability have been reported. In this study, the kinetic degradation of curcumin from a natural curcuminoid mixture under various conditions (pH, temperature, and dielectric constant of the medium) was investigated. Moreover, the degradation of pure curcumin at some selected conditions was also determined. To fully solubilize curcumin and to prevent precipitation of curcumin that occurs when low concentrations of co-solvent are present, a 50:50 (v/v) aqueous buffer/methanol mixture was used as standard medium to study its degradation kinetics. The results showed that degradation of curcumin both as pure compound and present in the curcuminoid mixture followed first order kinetic reaction. It was further shown that an increasing pH, temperature, and dielectric constant of the medium resulted in an increase in the degradation rate. Curcumin showed rapid degradation due to autoxidation in aqueous buffer pH = 8.0 with a rate constant of 280 × 10(-3) h(-1), corresponding with a half-life (t1/2) of 2.5 h. Dioxygenated bicyclopentadione was identified as the final degradation product. Importantly, curcumin loaded as curcuminoid mixture in ω-methoxy poly (ethylene glycol)-b-(N-(2-benzoyloxypropyl) methacrylamide) (mPEG-HPMA-Bz) polymeric micelles and in Triton X-100 micelles was about 300-500 times more stable than in aqueous buffer. Therefore, loading of curcumin into polymeric micelles is a promising approach to stabilize this compound and develop formulations suitable for further pharmaceutical and clinical studies.
Published: 2016
Full Text: View/download PDF

32. Acylation of arginine in goserelin-loaded PLGA microspheres

Author: Shirangi, Mehrnoosh, Hennink, Wim E., Somsen, Govert W., Van Nostrum, Cornelus F., Pharmaceutics, Sub General Pharmaceutics, Sub Drug delivery, Dep Farmaceutische wetenschappen, Pharmaceutics, Sub General Pharmaceutics, Sub Drug delivery, Dep Farmaceutische wetenschappen, AIMMS, and BioAnalytical Chemistry
Subjects: Arginine, Acylation, Lysine, Pharmaceutical Science, Peptide, 02 engineering and technology, 030226 pharmacology & pharmacy, Mass Spectrometry, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Polylactic Acid-Polyglycolic Acid Copolymer, Taverne, Controlled release, Lactic Acid, Guanidine, Glycolic acid, chemistry.chemical_classification, Chromatography, PLGA, General Medicine, 021001 nanoscience & nanotechnology, Microspheres, LC-MS, chemistry, Goserelin, 0210 nano-technology, Peptides, SDG 6 - Clean Water and Sanitation, Polyglycolic Acid, Chromatography, Liquid, Biotechnology
Abstract: Acylation of peptides is a well-known but unwanted phenomenon in polyester matrices such as poly(d,l-lactic-co-glycolic acid) (PLGA) microspheres used as controlled release formulations. Acylation normally occurs on lysine residues and the N-terminus of the peptide. The purpose of the present work was to assess other possible acylation sites on peptides. Goserelin was used as a model peptide that lacks lysine and a free N-terminus, but contains other nucleophilic residues, i.e. serine, tyrosine and arginine, which potentially can be acylated. Goserelin loaded PLGA microspheres were prepared by a double emulsion solvent evaporation technique. Liquid chromatography ion-trap mass spectrometry (LC-ITMS) was used for determining and monitoring acylation of released goserelin. It is demonstrated that arginine is subjected to acylation with glycolic acid and lactic acid units of PLGA, which was followed by loss of NH3 from the guanidine group to obtain 2-oxazolin-4-one and 5-methyl-2-oxazolin-4-one residues with masses that are 41 and 55 Da higher, respectively, than the native goserelin. There was no evidence for acylation of serine and tyrosine in goserelin. Our results demonstrate that beside lysine also acylation of arginine can occur in peptides and proteins that are loaded and released from PLGA matrixes.
Published: 2016
Full Text: View/download PDF

33. Ultrasound-mediated drug delivery to the brain: principles, progress and prospects

Author: Dasgupta, Anshuman, Liu, Mengjiao, Ojha, Tarun, Storm, G, Kiessling, Fabian, Lammers, Twan, Sub Drug targeting, Sub General Pharmaceutics, Pharmaceutics, Sub Drug targeting, Sub General Pharmaceutics, Pharmaceutics, Biomaterials Science and Technology, and Faculty of Science and Technology
Subjects: Central nervous system, Drug delivery to the brain, 02 engineering and technology, Pharmacology, Permeability, Article, 03 medical and health sciences, Drug Delivery Systems, 0302 clinical medicine, Drug Discovery, Animals, Humans, Medicine, METIS-320801, business.industry, Drug discovery, Ultrasound, Brain, 021001 nanoscience & nanotechnology, 3. Good health, IR-103530, medicine.anatomical_structure, Ultrasonic Waves, nervous system, Drug delivery, Microbubbles, cardiovascular system, Nanomedicine, Molecular Medicine, 0210 nano-technology, business, Sonoporation, 030217 neurology & neurosurgery, Biotechnology
Abstract: The blood–brain barrier (BBB) limits drug delivery to the central nervous system. When combined with microbubbles, ultrasound can transiently permeate blood vessels in the brain. This approach, which can be referred to as sonoporation or sonopermeabilization, holds significant promise for shuttling large therapeutic molecules, such as antibodies, growth factors and nanomedicine formulations, across the BBB. We here describe the basic principles of BBB permeation using ultrasound and microbubbles, and we summarize several (pre-) clinical studies showing the potential of BBB opening for improving the treatment of cancer and neurodegenerative disorders.
Published: 2016
Full Text: View/download PDF

34. Radionuclide imaging of liposomal drug delivery

Author: van der Geest, Tessa, Laverman, Peter, Metselaar, Josbert M., Storm, G, Boerman, Otto C., Sub General Pharmaceutics, Sub Drug targeting, Pharmaceutics, Biomaterials Science and Technology, Faculty of Science and Technology, Sub General Pharmaceutics, Sub Drug targeting, and Pharmaceutics
Subjects: liposomes, theranostics, Chemistry, Pharmaceutical, Pharmaceutical Science, 02 engineering and technology, Pharmacology, digestive system, 03 medical and health sciences, Drug Delivery Systems, 0302 clinical medicine, Pharmacokinetics, In vivo, Animals, Humans, Medicine, In patient, Radionuclide imaging, Pharmaceutical sciences, radionuclide imaging, Radioisotopes, Tomography, Emission-Computed, Single-Photon, Liposome, medicine.diagnostic_test, business.industry, METIS-320762, 021001 nanoscience & nanotechnology, PET, Positron emission tomography, Positron-Emission Tomography, 030220 oncology & carcinogenesis, SPECT, Drug delivery, IR-103634, Nanomedicine Radboud Institute for Health Sciences [Radboudumc 19], 0210 nano-technology, business, Nanomedicine Radboud Institute for Molecular Life Sciences [Radboudumc 19]
Abstract: Expert opinion on drug delivery 13(9), 1231-1242 (2016). doi:10.1080/17425247.2016.1205584, Published by Taylor & Francis Group, Abingdon
Published: 2016
Full Text: View/download PDF

35. Liposomal prednisolone promotes macrophage lipotoxicity in experimental atherosclerosis

Author: van der Valk, Fleur M, Schulte, Dominik M, Meiler, Svenja, Tang, Jun, Zheng, Kang He, Van den Bossche, Jan, Seijkens, Tom, Laudes, Matthias, de Winther, Menno, Lutgens, Esther, Alaarg, Amr, Metselaar, Josbert M, Dallinga-Thie, Geesje M, Mulder, Willem J M, Stroes, Erik S G, Hamers, Anouk A J, Sub General Pharmaceutics, Sub Condensed Matter and Interfaces, Pharmaceutics, Vascular Medicine, Other departments, Graduate School, ACS - Amsterdam Cardiovascular Sciences, AII - Amsterdam institute for Infection and Immunity, Medical Biochemistry, Sub General Pharmaceutics, Sub Condensed Matter and Interfaces, Pharmaceutics, Biomaterials Science and Technology, and Faculty of Science and Technology
Subjects: 0301 basic medicine, Prednisolone, Biomedical Engineering, Pharmaceutical Science, Medicine (miscellaneous), Bioengineering, Inflammation, Pharmacology, Mice, 03 medical and health sciences, Animals, Humans, Medicine, Macrophage, General Materials Science, business.industry, Macrophages, Monocyte, Atherosclerosis, Plaque, Atherosclerotic, 030104 developmental biology, medicine.anatomical_structure, Lipotoxicity, Apoptosis, Liposomes, Immunology, LDL receptor, Liposomal nanoparticles, Molecular Medicine, lipids (amino acids, peptides, and proteins), medicine.symptom, business, Lipoprotein, medicine.drug
Abstract: Atherosclerosis is a lipid-driven inflammatory disease, for which nanomedicinal interventions are under evaluation. Previously, we showed that liposomal nanoparticles loaded with prednisolone (LN-PLP) accumulated in plaque macrophages, however, induced proatherogenic effects in patients. Here, we confirmed in low-density lipoprotein receptor knockout (LDLr−/−) mice that LN-PLP accumulates in plaque macrophages. Next, we found that LN-PLP infusions at 10 mg/kg for 2 weeks enhanced monocyte recruitment to plaques. In follow up, after 6 weeks of LN-PLP exposure we observed (i) increased macrophage content, (ii) more advanced plaque stages, and (iii) larger necrotic core sizes. Finally, in vitro studies showed that macrophages become lipotoxic after LN-PLP exposure, exemplified by enhanced lipid loading, ER stress and apoptosis. These findings indicate that liposomal prednisolone may paradoxically accelerate atherosclerosis by promoting macrophage lipotoxicity. Hence, future (nanomedicinal) drug development studies are challenged by the multifactorial nature of atherosclerotic inflammation.
Published: 2016
Full Text: View/download PDF

36. Minimal information for studies of extracellular vesicles 2018 (MISEV2018):a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines

Author: Théry, Clotilde, Witwer, Kenneth W, Aikawa, Elena, Alcaraz, Maria Jose, Anderson, Johnathon D, Andriantsitohaina, Ramaroson, Antoniou, Anna, Arab, Tanina, Archer, Fabienne, Atkin-Smith, Georgia K, Ayre, D Craig, Bach, Jean-Marie, Bachurski, Daniel, Baharvand, Hossein, Balaj, Leonora, Baldacchino, Shawn, Bauer, Natalie N, Baxter, Amy A, Bebawy, Mary, Beckham, Carla, Bedina Zavec, Apolonija, Benmoussa, Abderrahim, Berardi, Anna C, Bergese, Paolo, Bielska, Ewa, Blenkiron, Cherie, Bobis-Wozowicz, Sylwia, Boilard, Eric, Boireau, Wilfrid, Bongiovanni, Antonella, Borràs, Francesc E, Bosch, Steffi, Boulanger, Chantal M, Breakefield, Xandra, Breglio, Andrew M, Brennan, Meadhbh Á, Brigstock, David R, Brisson, Alain, Broekman, Marike Ld, Bromberg, Jacqueline F, Bryl-Górecka, Paulina, Buch, Shilpa, Buck, Amy H, Burger, Dylan, Busatto, Sara, Buschmann, Dominik, Bussolati, Benedetta, Buzás, Edit I, Byrd, James Bryan, Camussi, Giovanni, Carter, David Rf, Caruso, Sarah, Chamley, Lawrence W, Chang, Yu-Ting, Chen, Chihchen, Chen, Shuai, Cheng, Lesley, Chin, Andrew R, Clayton, Aled, Clerici, Stefano P, Cocks, Alex, Cocucci, Emanuele, Coffey, Robert J, Cordeiro-da-Silva, Anabela, Couch, Yvonne, Coumans, Frank Aw, Coyle, Beth, Crescitelli, Rossella, Criado, Miria Ferreira, D'Souza-Schorey, Crislyn, Das, Saumya, Datta Chaudhuri, Amrita, de Candia, Paola, De Santana, Eliezer F, De Wever, Olivier, Del Portillo, Hernando A, Demaret, Tanguy, Deville, Sarah, Devitt, Andrew, Dhondt, Bert, Di Vizio, Dolores, Dieterich, Lothar C, Dolo, Vincenza, Dominguez Rubio, Ana Paula, Dominici, Massimo, Dourado, Mauricio R, Driedonks, Tom Ap, Duarte, Filipe V, Duncan, Heather M, Eichenberger, Ramon M, Ekström, Karin, El Andaloussi, Samir, Elie-Caille, Celine, Erdbrügger, Uta, Falcón-Pérez, Juan M, Fatima, Farah, Fish, Jason E, Flores-Bellver, Miguel, Försönits, András, Frelet-Barrand, Annie, Fricke, Fabia, Fuhrmann, Gregor, Gabrielsson, Susanne, Gámez-Valero, Ana, Gardiner, Chris, Gärtner, Kathrin, Gaudin, Raphael, Gho, Yong Song, Giebel, Bernd, Gilbert, Caroline, Gimona, Mario, Giusti, Ilaria, Goberdhan, Deborah Ci, Görgens, André, Gorski, Sharon M, Greening, David W, Gross, Julia Christina, Gualerzi, Alice, Gupta, Gopal N, Gustafson, Dakota, Handberg, Aase, Haraszti, Reka A, Harrison, Paul, Hegyesi, Hargita, Hendrix, An, Hill, Andrew F, Hochberg, Fred H, Hoffmann, Karl F, Holder, Beth, Holthofer, Harry, Hosseinkhani, Baharak, Hu, Guoku, Huang, Yiyao, Huber, Veronica, Hunt, Stuart, Ibrahim, Ahmed Gamal-Eldin, Ikezu, Tsuneya, Inal, Jameel M, Isin, Mustafa, Ivanova, Alena, Jackson, Hannah K, Jacobsen, Soren, Jay, Steven M, Jayachandran, Muthuvel, Jenster, Guido, Jiang, Lanzhou, Johnson, Suzanne M, Jones, Jennifer C, Jong, Ambrose, Jovanovic-Talisman, Tijana, Jung, Stephanie, Kalluri, Raghu, Kano, Shin-Ichi, Kaur, Sukhbir, Kawamura, Yumi, Keller, Evan T, Khamari, Delaram, Khomyakova, Elena, Khvorova, Anastasia, Kierulf, Peter, Kim, Kwang Pyo, Kislinger, Thomas, Klingeborn, Mikael, Klinke, David J, Kornek, Miroslaw, Kosanović, Maja M, Kovács, Árpád Ferenc, Krämer-Albers, Eva-Maria, Krasemann, Susanne, Krause, Mirja, Kurochkin, Igor V, Kusuma, Gina D, Kuypers, Sören, Laitinen, Saara, Langevin, Scott M, Languino, Lucia R, Lannigan, Joanne, Lässer, Cecilia, Laurent, Louise C, Lavieu, Gregory, Lázaro-Ibáñez, Elisa, Le Lay, Soazig, Lee, Myung-Shin, Lee, Yi Xin Fiona, Lemos, Debora S, Lenassi, Metka, Leszczynska, Aleksandra, Li, Isaac Ts, Liao, Ke, Libregts, Sten F, Ligeti, Erzsebet, Lim, Rebecca, Lim, Sai Kiang, Linē, Aija, Linnemannstöns, Karen, Llorente, Alicia, Lombard, Catherine A, Lorenowicz, Magdalena J, Lörincz, Ákos M, Lötvall, Jan, Lovett, Jason, Lowry, Michelle C, Loyer, Xavier, Lu, Quan, Lukomska, Barbara, Lunavat, Taral R, Maas, Sybren Ln, Malhi, Harmeet, Marcilla, Antonio, Mariani, Jacopo, Mariscal, Javier, Martens-Uzunova, Elena S, Martin-Jaular, Lorena, Martinez, M Carmen, Martins, Vilma Regina, Mathieu, Mathilde, Mathivanan, Suresh, Maugeri, Marco, McGinnis, Lynda K, McVey, Mark J, Meckes, David G, Meehan, Katie L, Mertens, Inge, Minciacchi, Valentina R, Möller, Andreas, Møller Jørgensen, Malene, Morales-Kastresana, Aizea, Morhayim, Jess, Mullier, François, Muraca, Maurizio, Musante, Luca, Mussack, Veronika, Muth, Dillon C, Myburgh, Kathryn H, Najrana, Tanbir, Nawaz, Muhammad, Nazarenko, Irina, Nejsum, Peter, Neri, Christian, Neri, Tommaso, Nieuwland, Rienk, Nimrichter, Leonardo, Nolan, John P, Nolte-'t Hoen, Esther NM, Noren Hooten, Nicole, O'Driscoll, Lorraine, O'Grady, Tina, O'Loghlen, Ana, Ochiya, Takahiro, Olivier, Martin, Ortiz, Alberto, Ortiz, Luis A, Osteikoetxea, Xabier, Østergaard, Ole, Ostrowski, Matias, Park, Jaesung, Pegtel, D Michiel, Peinado, Hector, Perut, Francesca, Pfaffl, Michael W, Phinney, Donald G, Pieters, Bartijn Ch, Pink, Ryan C, Pisetsky, David S, Pogge von Strandmann, Elke, Polakovicova, Iva, Poon, Ivan Kh, Powell, Bonita H, Prada, Ilaria, Pulliam, Lynn, Quesenberry, Peter, Radeghieri, Annalisa, Raffai, Robert L, Raimondo, Stefania, Rak, Janusz, Ramirez, Marcel I, Raposo, Graça, Rayyan, Morsi S, Regev-Rudzki, Neta, Ricklefs, Franz L, Robbins, Paul D, Roberts, David D, Rodrigues, Silvia C, Rohde, Eva, Rome, Sophie, Rouschop, Kasper Ma, Rughetti, Aurelia, Russell, Ashley E, Saá, Paula, Sahoo, Susmita, Salas-Huenuleo, Edison, Sánchez, Catherine, Saugstad, Julie A, Saul, Meike J, Schiffelers, Raymond M, Schneider, Raphael, Schøyen, Tine Hiorth, Scott, Aaron, Shahaj, Eriomina, Sharma, Shivani, Shatnyeva, Olga, Shekari, Faezeh, Shelke, Ganesh Vilas, Shetty, Ashok K, Shiba, Kiyotaka, Siljander, Pia R-M, Silva, Andreia M, Skowronek, Agata, Snyder, Orman L, Soares, Rodrigo Pedro, Sódar, Barbara W, Soekmadji, Carolina, Sotillo, Javier, Stahl, Philip D, Stoorvogel, Willem, Stott, Shannon L, Strasser, Erwin F, Swift, Simon, Tahara, Hidetoshi, Tewari, Muneesh, Timms, Kate, Tiwari, Swasti, Tixeira, Rochelle, Tkach, Mercedes, Toh, Wei Seong, Tomasini, Richard, Torrecilhas, Ana Claudia, Tosar, Juan Pablo, Toxavidis, Vasilis, Urbanelli, Lorena, Vader, Pieter, van Balkom, Bas Wm, van der Grein, Susanne G, Van Deun, Jan, van Herwijnen, Martijn Jc, Van Keuren-Jensen, Kendall, van Niel, Guillaume, van Royen, Martin E, van Wijnen, Andre J, Vasconcelos, M Helena, Vechetti, Ivan J, Veit, Tiago D, Vella, Laura J, Velot, Émilie, Verweij, Frederik J, Vestad, Beate, Viñas, Jose L, Visnovitz, Tamás, Vukman, Krisztina V, Wahlgren, Jessica, Watson, Dionysios C, Wauben, Marca Hm, Weaver, Alissa, Webber, Jason P, Weber, Viktoria, Wehman, Ann M, Weiss, Daniel J, Welsh, Joshua A, Wendt, Sebastian, Wheelock, Asa M, Wiener, Zoltán, Witte, Leonie, Wolfram, Joy, Xagorari, Angeliki, Xander, Patricia, Xu, Jing, Yan, Xiaomei, Yáñez-Mó, María, Yin, Hang, Yuana, Yuana, Zappulli, Valentina, Zarubova, Jana, Žėkas, Vytautas, Zhang, Jian-Ye, Zhao, Zezhou, Zheng, Lei, Zheutlin, Alexander R, Zickler, Antje M, Zimmermann, Pascale, Zivkovic, Angela M, Zocco, Davide, Zuba-Surma, Ewa K, dB&C I&I, LS Celbiologie-Algemeen, Celbiologie, Afd Pharmaceutics, Sub General Pharmaceutics, Sub Biomol.Mass Spect. and Proteomics, Afd Pharmacology, Urology, Pathology, Medical Oncology, Immunité et cancer, Institut Curie [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM), Johns Hopkins University School of Medicine [Baltimore], Stress Oxydant et Pathologies Métaboliques (SOPAM), Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM), Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U 1192 (PRISM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Infections Virales et Pathologie Comparée - UMR 754 (IVPC), Institut National de la Recherche Agronomique (INRA)-École pratique des hautes études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon, Immuno-Endocrinologie Cellulaire et Moléculaire [Nantes] (IECM), Institut National de la Recherche Agronomique (INRA)-Université de Nantes (UN)-École nationale vétérinaire, agroalimentaire et de l'alimentation Nantes-Atlantique (ONIRIS), Department for Molecular Biology and Nanobiotechnology, National Institute of chemitry, Slovenia, Biologie, génétique et thérapies ostéoarticulaires et respiratoires (BIOTARGEN), Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU), Institut de pharmacologie moléculaire et cellulaire (IPMC), Université Nice Sophia Antipolis (1965 - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS), Franche-Comté Électronique Mécanique, Thermique et Optique - Sciences et Technologies (UMR 6174) (FEMTO-ST), Université de Technologie de Belfort-Montbeliard (UTBM)-Ecole Nationale Supérieure de Mécanique et des Microtechniques (ENSMM)-Centre National de la Recherche Scientifique (CNRS)-Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC), Immuno-Endocrinologie Cellulaire et Moléculaire (IECM), Institut National de la Recherche Agronomique (INRA)-Université de Nantes (UN)-Ecole Nationale Vétérinaire de Nantes, Paris-Centre de Recherche Cardiovasculaire (PARCC - UMR-S U970), Hôpital Européen Georges Pompidou [APHP] (HEGP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Physiopathologie des Adaptations Nutritionnelles (PhAN), Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Imagerie Moléculaire et Nanobiotechnologies - Institut Européen de Chimie et Biologie (IECB), Université Sciences et Technologies - Bordeaux 1-Centre National de la Recherche Scientifique (CNRS), Molecular Biotechnology Center, Università degli studi di Torino = University of Turin (UNITO), Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science, La Trobe University, Centre for Sustainable Tropical Fisheries and Aquaculture, James Cook University (JCU), Department of Oncology - Pathology, Cancer Center Karolinska [Karolinska Institutet] (CCK), Karolinska Institutet [Stockholm]-Karolinska Institutet [Stockholm], Departamento de Ciências Biológicas, Universidade do Porto = University of Porto, Laboratory of Experimental Cancer Research, Department of Radiation Oncology and Experimental Cancer Research, Cancer Research Institute Ghent (CRIG), Universiteit Gent = Ghent University [Belgium] (UGENT), Department of Medical and Surgical Sciences for Children and Adults [Modena, Italy] (Laboratory of Cellular Therapy), Università degli Studi di Modena e Reggio Emilia (UNIMORE), Clinical Research Center, Department of Laboratory Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Huddinge, Sweden, Karolinska Institutet [Stockholm]-Karolinska University Hospital [Stockholm], Center for Cooperative Research in Biosciences (CIC bioGUNE), Partner site Munich, German Centre for Infection Research (DZIF), Institute for Transfusion Medicine, University Hospital Essen, Universität Duisburg-Essen [Essen], Mécanismes Adaptatifs et Evolution (MECADEV), Muséum national d'Histoire naturelle (MNHN)-Centre National de la Recherche Scientifique (CNRS), Psychiatry, Institute of Biological, Environmental and Rural Sciences (IBERS), Aberystwyth University, Department of Bacteriology and Immunology [Helsinki], Haartman Institute [Helsinki], Faculty of Medecine [Helsinki], Helsingin yliopisto = Helsingfors universitet = University of Helsinki-Helsingin yliopisto = Helsingfors universitet = University of Helsinki-Faculty of Medecine [Helsinki], Helsingin yliopisto = Helsingfors universitet = University of Helsinki-Helsingin yliopisto = Helsingfors universitet = University of Helsinki, Rigshospitalet [Copenhagen], Copenhagen University Hospital, Dalhousie University [Halifax], Department of Biology, Molecular Cell Biology, University of Mainz, Johannes Gutenberg - Universität Mainz = Johannes Gutenberg University (JGU), Glycobiologie et signalisation cellulaire, Université Paris-Sud - Paris 11 (UP11)-Institut National de la Santé et de la Recherche Médicale (INSERM), Krefting Research Centre, Department of Internal Medicine and Clinical Nutrition, University of Gothenburg (GU), Universidad de Alicante, École supérieure du professorat et de l'éducation - Académie de Créteil (UPEC ESPE Créteil), Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), University of Antwerp (UA), Université Catholique de Louvain = Catholic University of Louvain (UCL), Research Institute, IRCCS Ospedale Pediatrico Bambino Gesù [Roma], Department of Veterinary Disease Biology [Copenhagen], Faculty of Health and Medical Sciences, University of Copenhagen = Københavns Universitet (KU)-University of Copenhagen = Københavns Universitet (KU), Biologie et Pathologie du Neurone (Brain-C), Adaptation Biologique et Vieillissement = Biological Adaptation and Ageing (B2A), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Department of Mathematics and Statistics, American University, University of Pretoria [South Africa], Ecole des Ingénieurs de la Ville de Paris (EIVP), Universitat Pompeu Fabra [Barcelona] (UPF), Instituto de Investigaciones Biomedicas, Universidad Nacional Autónoma de México (UNAM), Istituto Ortopedico Rizzoli, Department of Molecular Therapeutics, The Scripps Research Institute, Laboratoire d'Informatique de Grenoble (LIG ), Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019]), Montreal Children's Hospital, McGill University Health Center [Montreal] (MUHC), Compartimentation et dynamique cellulaires (CDC), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut Curie [Paris]-Centre National de la Recherche Scientifique (CNRS), National Cancer Institute [Bethesda] (NCI-NIH), National Institutes of Health [Bethesda] (NIH), Cardiovasculaire, métabolisme, diabétologie et nutrition (CarMeN), Institut National de la Recherche Agronomique (INRA)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Hospices Civils de Lyon (HCL)-Institut National de la Santé et de la Recherche Médicale (INSERM), Cardiovascular Research Center, Massachusetts General Hospital [Boston], University Medical Center [Utrecht], University of Toronto, Fiocruz Minas - René Rachou Research Center / Instituto René Rachou [Belo Horizonte, Brésil], Fundação Oswaldo Cruz (FIOCRUZ), Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Centre de Recherche en Cancérologie de Marseille (CRCM), Aix Marseille Université (AMU)-Institut Paoli-Calmettes, Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Federal University of Sao Paulo (Unifesp), Functional Genomics / Genómica Funcional [Montevideo], Institut Pasteur de Montevideo, Dipartimento di Medicina Sperimentale e Scienze Biochimiche, Università degli Studi di Perugia (UNIPG), Hospital Santa Cristina Instituto de Investigación Sanitaria Princesa C, Unidad de Investigación, Institut Curie [Paris]-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS), Department of Physiology, University of California [San Francisco] (UCSF), University of California-University of California, University of Vermont [Burlington], Peking University [Beijing], Shandong Agricultural University (SDAU), State Key Laboratory of Quality Research in Chinese Medicine Taipa, Macau SAR, (Institute of Chinese Medical Sciences), Human Genetics, Universität Ulm - Ulm University [Ulm, Allemagne], INSERM, Institut Curie, INCa [INCA-11548], French National Research Agency [ANR-10-IDEX-0001-02 PSL*, ANR-11-LABX-0043], SIDACTION [17-1-AAE-1138], Fondation ARC [PGA1 RF20180206962, PJA 20171206453], NIDA [DA040385, DA047807], Ministry of Education, NIA [AG057430], NIMH [MH118164], Institut National de la Recherche Agronomique (INRA)-École Pratique des Hautes Études (EPHE), Institut National de la Recherche Agronomique (INRA)-Université de Nantes (UN)-Ecole Nationale Vétérinaire de Nantes-École nationale vétérinaire, agroalimentaire et de l'alimentation Nantes-Atlantique (ONIRIS), Institut National de la Recherche Agronomique (INRA)-Université de Nantes (UN), Université Sciences et Technologies - Bordeaux 1 (UB)-Centre National de la Recherche Scientifique (CNRS), Universiteit Gent = Ghent University (UGENT), Università degli Studi di Modena e Reggio Emilia = University of Modena and Reggio Emilia (UNIMORE), Universität Duisburg-Essen = University of Duisburg-Essen [Essen], Biotechnology and Biological Sciences Research Council (BBSRC)-Aberystwyth University, University of Copenhagen = Københavns Universitet (UCPH)-University of Copenhagen = Københavns Universitet (UCPH), Universidad Nacional Autónoma de México = National Autonomous University of Mexico (UNAM), The Scripps Research Institute [La Jolla, San Diego], Fundação Oswaldo Cruz / Oswaldo Cruz Foundation (FIOCRUZ), Università degli Studi di Perugia = University of Perugia (UNIPG), Instituto de Investigacion Sanitaria del Hospital de la Princesa, Hospital Universitario de La Princesa, University of California [San Francisco] (UC San Francisco), University of California (UC)-University of California (UC), ANR-17-CE09-0025,MADNESS,Une approche microfluidique générique pour la qualification des nanoparticules biologiques(2017), Institut National de la Recherche Agronomique (INRA)-École pratique des hautes études (EPHE)-Université Claude Bernard Lyon 1 (UCBL), Biomedical Engineering and Physics, ACS - Atherosclerosis & ischemic syndromes, ACS - Microcirculation, Laboratory Specialized Diagnostics & Research, Radiotherapie, RS: GROW - R2 - Basic and Translational Cancer Biology, Université de Lille-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Institut National de la Recherche Agronomique (INRA)-Université de Nantes (UN)-Ecole Nationale Vétérinaire, Agroalimentaire et de l'alimentation Nantes-Atlantique (ONIRIS), Université Nice Sophia Antipolis (... - 2019) (UNS), Université de Technologie de Belfort-Montbeliard (UTBM)-Ecole Nationale Supérieure de Mécanique et des Microtechniques (ENSMM)-Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC)-Centre National de la Recherche Scientifique (CNRS), Ecole Nationale Vétérinaire de Nantes-Université de Nantes (UN)-Institut National de la Recherche Agronomique (INRA), Università degli studi di Torino (UNITO), Universidade do Porto, University of Helsinki-University of Helsinki-Faculty of Medecine [Helsinki], University of Helsinki-University of Helsinki, Johannes Gutenberg - Universität Mainz (JGU), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Institut Curie [Paris]-Université Pierre et Marie Curie - Paris 6 (UPMC), Hospices Civils de Lyon (HCL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Institut National de la Recherche Agronomique (INRA), Université de Toronto [Canada], Institut Curie-Institut National de la Santé et de la Recherche Médicale (INSERM), Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192 (PRISM), Université de Lille-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Côte d'Azur (UCA)-Université Côte d'Azur (UCA)-Centre National de la Recherche Scientifique (CNRS), Université de Franche-Comté (UFC)-Centre National de la Recherche Scientifique (CNRS)-Ecole Nationale Supérieure de Mécanique et des Microtechniques (ENSMM)-Université de Technologie de Belfort-Montbeliard (UTBM), Assistance publique - Hôpitaux de Paris (AP-HP) (APHP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Assistance publique - Hôpitaux de Paris (AP-HP) (APHP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Physiopathologie de la Résorption Osseuse et Thérapie des Tumeurs Osseuses Primitives, Université de Nantes (UN)-Institut National de la Santé et de la Recherche Médicale (INSERM), Universidade do Porto [Porto], Ghent University [Belgium] (UGENT), FEMTO-ST Institute, Université de Technologie de Belfort-Montbeliard (UTBM)-Université de Franche-Comté (UFC)-CNRS : UMR6174, Mécanismes adaptatifs : des organismes aux communautés (MECADEV), Centre National de la Recherche Scientifique (CNRS)-Muséum national d'Histoire naturelle (MNHN), Johannes Gutenberg - University of Mainz (JGU), Université Catholique de Louvain (UCL), Universitat Pompeu Fabra [Barcelona], Laboratoire d'Informatique de Grenoble (LIG), Université Pierre Mendès France - Grenoble 2 (UPMF)-Université Joseph Fourier - Grenoble 1 (UJF)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP)-Institut National Polytechnique de Grenoble (INPG)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA), Centre National de la Recherche Scientifique (CNRS)-Institut Curie-Université Pierre et Marie Curie - Paris 6 (UPMC), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Hospices Civils de Lyon (HCL), Laboratoire Réactions et Génie des Procédés (LRGP), Fiocruz Minas - René Rachou Research Center / Instituto René Rachou, Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Paoli-Calmettes, Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Aix Marseille Université (AMU), Functional Genomics Unit, Institut Curie-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), University of Vermont College of Medicine [Burlington, VT, USA], Extracellular Vesicles, Molecular and Integrative Biosciences Research Programme, Thery, C., Witwer, K. W., Aikawa, E., Alcaraz, M. J., Anderson, J. D., Andriantsitohaina, R., Antoniou, A., Arab, T., Archer, F., Atkin-Smith, G. K., Ayre, D. C., Bach, J. -M., Bachurski, D., Baharvand, H., Balaj, L., Baldacchino, S., Bauer, N. N., Baxter, A. A., Bebawy, M., Beckham, C., Bedina Zavec, A., Benmoussa, A., Berardi, A. C., Bergese, P., Bielska, E., Blenkiron, C., Bobis-Wozowicz, S., Boilard, E., Boireau, W., Bongiovanni, A., Borras, F. E., Bosch, S., Boulanger, C. M., Breakefield, X., Breglio, A. M., Brennan, M. A., Brigstock, D. R., Brisson, A., Broekman, M. L. D., Bromberg, J. F., Bryl-Gorecka, P., Buch, S., Buck, A. H., Burger, D., Busatto, S., Buschmann, D., Bussolati, B., Buzas, E. I., Byrd, J. B., Camussi, G., Carter, D. R. F., Caruso, S., Chamley, L. W., Chang, Y. -T., Chaudhuri, A. D., Chen, C., Chen, S., Cheng, L., Chin, A. R., Clayton, A., Clerici, S. P., Cocks, A., Cocucci, E., Coffey, R. J., Cordeiro-da-Silva, A., Couch, Y., Coumans, F. A. W., Coyle, B., Crescitelli, R., Criado, M. F., D'Souza-Schorey, C., Das, S., de Candia, P., De Santana, E. F., De Wever, O., del Portillo, H. A., Demaret, T., Deville, S., Devitt, A., Dhondt, B., Di Vizio, D., Dieterich, L. C., Dolo, V., Dominguez Rubio, A. P., Dominici, M., Dourado, M. R., Driedonks, T. A. P., Duarte, F. V., Duncan, H. M., Eichenberger, R. M., Ekstrom, K., EL Andaloussi, S., Elie-Caille, C., Erdbrugger, U., Falcon-Perez, J. M., Fatima, F., Fish, J. E., Flores-Bellver, M., Forsonits, A., Frelet-Barrand, A., Fricke, F., Fuhrmann, G., Gabrielsson, S., Gamez-Valero, A., Gardiner, C., Gartner, K., Gaudin, R., Gho, Y. S., Giebel, B., Gilbert, C., Gimona, M., Giusti, I., Goberdhan, D. C. I., Gorgens, A., Gorski, S. M., Greening, D. W., Gross, J. C., Gualerzi, A., Gupta, G. N., Gustafson, D., Handberg, A., Haraszti, R. A., Harrison, P., Hegyesi, H., Hendrix, A., Hill, A. F., Hochberg, F. H., Hoffmann, K. F., Holder, B., Holthofer, H., Hosseinkhani, B., Hu, G., Huang, Y., Huber, V., Hunt, S., Ibrahim, A. G. -E., Ikezu, T., Inal, J. M., Isin, M., Ivanova, A., Jackson, H. K., Jacobsen, S., Jay, S. M., Jayachandran, M., Jenster, G., Jiang, L., Johnson, S. M., Jones, J. C., Jong, A., Jovanovic-Talisman, T., Jung, S., Kalluri, R., Kano, S. -I., Kaur, S., Kawamura, Y., Keller, E. T., Khamari, D., Khomyakova, E., Khvorova, A., Kierulf, P., Kim, K. P., Kislinger, T., Klingeborn, M., Klinke, D. J., Kornek, M., Kosanovic, M. M., Kovacs, A. F., Kramer-Albers, E. -M., Krasemann, S., Krause, M., Kurochkin, I. V., Kusuma, G. D., Kuypers, S., Laitinen, S., Langevin, S. M., Languino, L. R., Lannigan, J., Lasser, C., Laurent, L. C., Lavieu, G., Lazaro-Ibanez, E., Le Lay, S., Lee, M. -S., Lee, Y. X. F., Lemos, D. S., Lenassi, M., Leszczynska, A., Li, I. T. S., Liao, K., Libregts, S. F., Ligeti, E., Lim, R., Lim, S. K., Line, A., Linnemannstons, K., Llorente, A., Lombard, C. A., Lorenowicz, M. J., Lorincz, A. M., Lotvall, J., Lovett, J., Lowry, M. C., Loyer, X., Lu, Q., Lukomska, B., Lunavat, T. R., Maas, S. L. N., Malhi, H., Marcilla, A., Mariani, J., Mariscal, J., Martens-Uzunova, E. S., Martin-Jaular, L., Martinez, M. C., Martins, V. R., Mathieu, M., Mathivanan, S., Maugeri, M., Mcginnis, L. K., Mcvey, M. J., Meckes, D. G., Meehan, K. L., Mertens, I., Minciacchi, V. R., Moller, A., Moller Jorgensen, M., Morales-Kastresana, A., Morhayim, J., Mullier, F., Muraca, M., Musante, L., Mussack, V., Muth, D. C., Myburgh, K. H., Najrana, T., Nawaz, M., Nazarenko, I., Nejsum, P., Neri, C., Neri, T., Nieuwland, R., Nimrichter, L., Nolan, J. P., Nolte-'t Hoen, E. N. M., Noren Hooten, N., O'Driscoll, L., O'Grady, T., O'Loghlen, A., Ochiya, T., Olivier, M., Ortiz, A., Ortiz, L. A., Osteikoetxea, X., Ostegaard, O., Ostrowski, M., Park, J., Pegtel, D. M., Peinado, H., Perut, F., Pfaffl, M. W., Phinney, D. G., Pieters, B. C. H., Pink, R. C., Pisetsky, D. S., Pogge von Strandmann, E., Polakovicova, I., Poon, I. K. H., Powell, B. H., Prada, I., Pulliam, L., Quesenberry, P., Radeghieri, A., Raffai, R. L., Raimondo, S., Rak, J., Ramirez, M. I., Raposo, G., Rayyan, M. S., Regev-Rudzki, N., Ricklefs, F. L., Robbins, P. D., Roberts, D. D., Rodrigues, S. C., Rohde, E., Rome, S., Rouschop, K. M. A., Rughetti, A., Russell, A. E., Saa, P., Sahoo, S., Salas-Huenuleo, E., Sanchez, C., Saugstad, J. A., Saul, M. J., Schiffelers, R. M., Schneider, R., Schoyen, T. H., Scott, A., Shahaj, E., Sharma, S., Shatnyeva, O., Shekari, F., Shelke, G. V., Shetty, A. K., Shiba, K., Siljander, P. R. -M., Silva, A. M., Skowronek, A., Snyder, O. L., Soares, R. P., Sodar, B. W., Soekmadji, C., Sotillo, J., Stahl, P. D., Stoorvogel, W., Stott, S. L., Strasser, E. F., Swift, S., Tahara, H., Tewari, M., Timms, K., Tiwari, S., Tixeira, R., Tkach, M., Toh, W. S., Tomasini, R., Torrecilhas, A. C., Tosar, J. P., Toxavidis, V., Urbanelli, L., Vader, P., van Balkom, B. W. M., van der Grein, S. G., Van Deun, J., van Herwijnen, M. J. C., Van Keuren-Jensen, K., van Niel, G., van Royen, M. E., van Wijnen, A. J., Vasconcelos, M. H., Vechetti, I. J., Veit, T. D., Vella, L. J., Velot, E., Verweij, F. J., Vestad, B., Vinas, J. L., Visnovitz, T., Vukman, K. V., Wahlgren, J., Watson, D. C., Wauben, M. H. M., Weaver, A., Webber, J. P., Weber, V., Wehman, A. M., Weiss, D. J., Welsh, J. A., Wendt, S., Wheelock, A. M., Wiener, Z., Witte, L., Wolfram, J., Xagorari, A., Xander, P., Xu, J., Yan, X., Yanez-Mo, M., Yin, H., Yuana, Y., Zappulli, V., Zarubova, J., Zekas, V., Zhang, J. -Y., Zhao, Z., Zheng, L., Zheutlin, A. R., Zickler, A. M., Zimmermann, P., Zivkovic, A. M., Zocco, D., Zuba-Surma, E. K., dB&C I&I, LS Celbiologie-Algemeen, Celbiologie, Afd Pharmaceutics, Sub General Pharmaceutics, Sub Biomol.Mass Spect. and Proteomics, Afd Pharmacology, CCA - Imaging and biomarkers, Amsterdam Neuroscience - Neuroinfection & -inflammation, and Amsterdam Neuroscience - Cellular & Molecular Mechanisms
Subjects: ectosome, ectosomes, exosomes, extracellular vesicles, guidelines, microparticles, microvesicles, minimal information requirements, reproducibility, rigor, standardization, Histology, Cell Biology, [SDV]Life Sciences [q-bio], size-exclusion, Medicine and Health Sciences, CELL-DERIVED MICROPARTICLES, FIELD-FLOW FRACTIONATION, requirements, circulating, ComputingMilieux_MISCELLANEOUS, Manchester Cancer Research Centre, lcsh:Cytology, PROSTATE-CANCER, microparticle, Cell interaction, microvesicle, chromatography, Position Paper, guideline, Life Sciences & Biomedicine, ectosomes, exosomes, extracellular vesicles, guidelines, microparticles, microvesicles, minimal information requirements, reproducibility, rigor, standardization, MEMBRANE-VESICLES, FETAL BOVINE, Ectosomes, Exosomes, Extracellular Vesicles, Guidelines, Microparticles, Microvesicles, Minimal Information Requirements, Reproducibility, Rigor, Standardization, CIRCULATING MICROPARTICLES, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, ddc:570, exosome, SURFACE-PLASMON RESONANCE, ddc:610, lcsh:QH573-671, Biology, Interacció cel·lular, Science & Technology, ResearchInstitutes_Networks_Beacons/mcrc, Cell membranes, HUMAN URINARY EXOSOMES, PREANALYTICAL PARAMETERS, minimal information requirement, SIZE-EXCLUSION CHROMATOGRAPHY, 1182 Biochemistry, cell and molecular biology, extracellular vesicle, Human medicine, Membranes cel·lulars
Abstract: The last decade has seen a sharp increase in the number of scientific publications describing physiological and pathological functions of extracellular vesicles (EVs), a collective term covering various subtypes of cell-released, membranous structures, called exosomes, microvesicles, microparticles, ectosomes, oncosomes, apoptotic bodies, and many other names. However, specific issues arise when working with these entities, whose size and amount often make them difficult to obtain as relatively pure preparations, and to characterize properly. The International Society for Extracellular Vesicles (ISEV) proposed Minimal Information for Studies of Extracellular Vesicles ("MISEV") guidelines for the field in 2014. We now update these "MISEV2014" guidelines based on evolution of the collective knowledge in the last four years. An important point to consider is that ascribing a specific function to EVs in general, or to subtypes of EVs, requires reporting of specific information beyond mere description of function in a crude, potentially contaminated, and heterogeneous preparation. For example, claims that exosomes are endowed with exquisite and specific activities remain difficult to support experimentally, given our still limited knowledge of their specific molecular machineries of biogenesis and release, as compared with other biophysically similar EVs. The MISEV2018 guidelines include tables and outlines of suggested protocols and steps to follow to document specific EV-associated functional activities. Finally, a checklist is provided with summaries of key points.
Published: 2018
Full Text: View/download PDF

37. Arthroscopic near infrared spectroscopy enables simultaneous quantitative evaluation of articular cartilage and subchondral bone in vivo

Author: Sarin, Jaakko K, Te Moller, Nikae C R, Mancini, Irina A D, Brommer, Harold, Visser, Jetze, Malda, Jos, van Weeren, P René, Afara, Isaac O, Töyräs, Juha, LS Equine Muscoskeletal Biology, dES RMSC, dES AVR, LS Heelkunde, Sub General Pharmaceutics, Dep Gezondheidszorg Paard, Geneeskunde van gezelschapsdieren, LS Equine Muscoskeletal Biology, dES RMSC, dES AVR, LS Heelkunde, Sub General Pharmaceutics, Dep Gezondheidszorg Paard, and Geneeskunde van gezelschapsdieren
Subjects: Cartilage, Articular, 0301 basic medicine, Bone density, 0206 medical engineering, lcsh:Medicine, 02 engineering and technology, Osteoarthritis, Article, Arthroscopy, 03 medical and health sciences, Bone Density, In vivo, Animals, Osteochondrosis, Medicine, Clinical significance, Horses, lcsh:Science, General, Bone mineral, Spectroscopy, Near-Infrared, Multidisciplinary, medicine.diagnostic_test, business.industry, Cartilage, lcsh:R, medicine.disease, 020601 biomedical engineering, 030104 developmental biology, medicine.anatomical_structure, Subchondral bone, Cancellous Bone, lcsh:Q, Neural Networks, Computer, business, Biomedical engineering
Abstract: Arthroscopic assessment of articular tissues is highly subjective and poorly reproducible. To ensure optimal patient care, quantitative techniques (e.g., near infrared spectroscopy (NIRS)) could substantially enhance arthroscopic diagnosis of initial signs of post-traumatic osteoarthritis (PTOA). Here, we demonstrate, for the first time, the potential of arthroscopic NIRS to simultaneously monitor progressive degeneration of cartilage and subchondral bone in vivo in Shetland ponies undergoing different experimental cartilage repair procedures. Osteochondral tissues adjacent to the repair sites were evaluated using an arthroscopic NIRS probe and significant (p ρ = 0.63–0.87, NMRSE = 8.5–17.2%, RPIQ = 1.93–3.03) estimation of articular cartilage biomechanical properties, subchondral bone plate thickness and bone mineral density (BMD), and subchondral trabecular bone thickness, bone volume fraction (BV), BMD, and structure model index (SMI) from in vitro spectral data. The trained ANNs also reliably predicted the properties of an independent in vitro test group (ρ = 0.54–0.91, NMRSE = 5.9–17.6%, RPIQ = 1.68–3.36). However, predictions based on arthroscopic NIR spectra were less reliable (ρ = 0.27–0.74, NMRSE = 14.5–24.0%, RPIQ = 1.35–1.70), possibly due to errors introduced during arthroscopic spectral acquisition. Adaptation of NIRS could address the limitations of conventional arthroscopy through quantitative assessment of lesion severity and extent, thereby enhancing detection of initial signs of PTOA. This would be of high clinical significance, for example, when conducting orthopaedic repair surgeries.
Published: 2018
Full Text: View/download PDF

38. Bio-resin for high resolution lithography-based biofabrication of complex cell-laden constructs

Author: Lim, Khoon S, Levato, Riccardo, Ferreira da Costa, Pedro, Castilho, Miguel D, Alcala-Orozco, Cesar R, van Dorenmalen, Kim M A, Melchels, Ferry P W, Gawlitta, Debby, Hooper, Gary J, Malda, Jos, Woodfield, Tim B F, LS Equine Muscoskeletal Biology, Sub General Pharmaceutics, dES RMSC, LS Equine Muscoskeletal Biology, Sub General Pharmaceutics, and dES RMSC
Subjects: Fabrication, Materials science, bio-resin, digital light processing, Light, Cell Survival, Biomedical Engineering, Acrylic Resins, Cell Culture Techniques, 3D printing, Bioengineering, Nanotechnology, 02 engineering and technology, 010402 general chemistry, 01 natural sciences, Biochemistry, Biomaterials, Tissue engineering, medicine, Humans, Lithography, Cells, Cultured, visible light, Tissue Engineering, Tissue Scaffolds, business.industry, biofabrication, Bioprinting, Cell Differentiation, Hydrogels, General Medicine, Complex cell, 021001 nanoscience & nanotechnology, 0104 chemical sciences, medicine.anatomical_structure, Polyvinyl Alcohol, Self-healing hydrogels, Gelatin, Methacrylates, lithography, Digital Light Processing, hydrogel, 0210 nano-technology, business, Biotechnology, Biofabrication
Abstract: Lithography-based three-dimensional (3D) printing technologies allow high spatial resolution that exceeds that of typical extrusion-based bioprinting approaches, allowing to better mimic the complex architecture of biological tissues. Additionally, lithographic printing via digital light processing (DLP) enables fabrication of free-form lattice and patterned structures which cannot be easily produced with other 3D printing approaches. While significant progress has been dedicated to the development of cell-laden bioinks for extrusion-based bioprinting, less attention has been directed towards the development of cyto-compatible bio-resins and their application in lithography-based biofabrication, limiting the advancement of this promising technology. In this study, we developed a new bio-resin based on methacrylated poly(vinyl alcohol) (PVA-MA), gelatin-methacryloyl (Gel-MA) and a transition metal-based visible light photoinitiator. The utilization of a visible light photo-initiating system displaying high molar absorptivity allowed the bioprinting of constructs with high resolution features, in the range of 25-50 μm. Biofunctionalization of the resin with 1 wt% Gel-MA allowed long term survival (>90%) of encapsulated cells up to 21 d, and enabled attachment and spreading of endothelial cells seeded on the printed hydrogels. Cell-laden hydrogel constructs of high resolution with complex and ordered architecture were successfully bioprinted, where the encapsulated cells remained viable, homogenously distributed and functional. Bone and cartilage tissue synthesis was confirmed by encapsulated stem cells, underlining the potential of these DLP-bioprinted hydrogels for tissue engineering and biofabrication. Overall, the PVA-MA/Gel-MA bio-resin is a promising material for biofabrication and provides important cues for the further development of lithography-based bioprinting of complex, free-form living tissue analogues.
Published: 2018

39. Spin-Current-Controlled Modulation of the Magnon Spin Conductance in a Three-Terminal Magnon Transistor

Author: Cornelissen, L. J., Liu, J., van Wees, B. J., Duine, R. A., Sub General Pharmaceutics, Sub Cond-Matter Theory, Stat & Comp Phys, Sub General Pharmaceutics, Sub Cond-Matter Theory, Stat & Comp Phys, Physics of Nanostructures, and Physics of Nanodevices
Subjects: Yttrium iron garnet, General Physics and Astronomy, MAGNETIC INSULATOR, 02 engineering and technology, Physics and Astronomy(all), 01 natural sciences, law.invention, chemistry.chemical_compound, Condensed Matter::Materials Science, law, 0103 physical sciences, 010306 general physics, Spin-½, Physics, Condensed matter physics, Spintronics, Condensed Matter::Other, Magnon, Transistor, Conductance, 021001 nanoscience & nanotechnology, chemistry, Modulation, Logic gate, Condensed Matter::Strongly Correlated Electrons, 0210 nano-technology
Abstract: Efficient manipulation of magnon spin transport is crucial for developing magnon-based spintronic devices. In this Letter, we provide proof of principle of a method for modulating the diffusive transport of thermal magnons in an yttrium iron garnet channel between injector and detector contacts. The magnon spin conductance of the channel is altered by increasing or decreasing the magnon chemical potential via spin Hall injection of magnons by a third modulator electrode. We obtain a modulation efficiency of 1.6%/ mA at T = 250 K. Finite element modeling shows that this could be increased to well above 10%/ mA by reducing the thickness of the channel, providing interesting prospects for the development of thermal-magnon-based logic circuits.
Published: 2018

40. Biosimilar monoclonal antibodies: the scientific basis for extrapolation

Author: Schellekens, Huub, Lietzan, Erika, Faccin, Freddy, Venema, Jaap, Pharmaceutics, Sub Biotechnological drugs, Sub General Pharmaceutics, Pharmaceutics, Sub Biotechnological drugs, and Sub General Pharmaceutics
Subjects: medicine.medical_specialty, medicine.drug_class, Clinical Biochemistry, extrapolation, Pharmacology, Regulatory Application, Monoclonal antibody, TNF inhibitors, Arthritis, Rheumatoid, Biologic Products, Biosimilar Pharmaceuticals, Crohn Disease, Drug Discovery, medicine, Humans, media_common.cataloged_instance, biosimilars, Spondylitis, Ankylosing, European union, Intensive care medicine, media_common, Tumor Necrosis Factor-alpha, business.industry, Antibodies, Monoclonal, Biosimilar, Infliximab, Clinical trial, monoclonal antibodies, infliximab, business, medicine.drug
Abstract: Introduction: Biosimilars are biologic products that receive authorization based on an abbreviated regulatory application containing comparative quality and nonclinical and clinical data that demonstrate similarity to a licensed biologic product. Extrapolation of safety and efficacy has emerged as an important way to simplify biosimilar development. Regulatory authorities have generally reached the consensus that extrapolation of similarity from one indication to other approved indications of the reference product can be permitted if it is scientifically justified. Areas covered: Recently, the first biosimilar, biosimilar infliximab (Remsima/Inflectra) to the innovator monoclonal antibody infliximab (Remicade), was approved in the European Union, Canada and South Korea; the USA subsequently approved its first biosimilar, a less complex molecule (filgrastim-sndz). Based on two clinical trials of biosimilar infliximab in patients with rheumatoid arthritis and ankylosing spondylitis, the European Medicines Agency allowed extrapolation to all eight approved indications for innovator infliximab, whereas Health Canada did not permit extrapolation to the indications for ulcerative colitis and Crohn's disease. These differing decisions on extrapolation of indications for biosimilar infliximab highlight important unanswered regulatory and scientific questions. Here, we propose substantive scientific considerations for indication extrapolation. Expert opinion: The preclinical and clinical criteria that are currently required to merit indication extrapolation have not been rigorously evaluated.
Published: 2015
Full Text: View/download PDF

41. Pharmaceutical development and preclinical evaluation of a GMP-grade anti-inflammatory nanotherapy

Author: Lobatto, Mark E., Calcagno, Claudia, Otten, Maarten J., Millon, Antoine, Ramachandran, Sarayu, Paridaans, Maarten P M, van der Valk, Fleur M., Storm, G, Stroes, Erik S G, Fayad, Zahi A., Mulder, Willem J M, Metselaar, Josbert M., Pharmaceutics, Sub Drug targeting, Sub General Pharmaceutics, Hospices Civils de Lyon (HCL), Cardiovasculaire, métabolisme, diabétologie et nutrition (CarMeN), Hospices Civils de Lyon (HCL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Institut National de la Recherche Agronomique (INRA), Radiology and Nuclear Medicine, Other departments, Amsterdam Cardiovascular Sciences, Vascular Medicine, Experimental Vascular Medicine, Institut National de la Recherche Agronomique (INRA)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Hospices Civils de Lyon (HCL), Biomaterials Science and Technology, Faculty of Science and Technology, Pharmaceutics, Sub Drug targeting, and Sub General Pharmaceutics
Subjects: Male, Chemistry, Pharmaceutical, [SDV]Life Sciences [q-bio], Anti-Inflammatory Agents, Wistar, Pharmaceutical Science, Medicine (miscellaneous), use/toxicity, Pharmacology, GMP-grade, Rats, Sprague-Dawley, General Materials Science, Clinical imaging, Pharmaceutical sciences, Prednisolone/administration & dosage/*analogs &, Aorta, Liposome, Prednisolone phosphate, Anti-Inflammatory Agents/*administration & dosage/pharmacokinetics/therapeutic, METIS-315196, Pharmaceutical/*methods, IR-99924, 3. Good health, Chemistry, Nanomedicine, Aorta/drug effects/pathology, Molecular Medicine, Rabbits, Half-Life, medicine.drug_class, Prednisolone, Biomedical Engineering, Bioengineering, Article, Anti-inflammatory, derivatives/pharmacokinetics/therapeutic use/toxicity, Materials Science(all), Pharmacokinetics, medicine, Humans, Animals, Toxicokinetics, Glucocorticoids/*administration & dosage/pharmacokinetics/therapeutic, Rats, Wistar, Glucocorticoids, business.industry, Atherosclerosis, Rats, Clinical trial, Formulation design, Liposomes, Sprague-Dawley, Atherosclerosis/*drug therapy/pathology, business
Abstract: International audience; The present study describes the development of a good manufacturing practice (GMP)-grade liposomal nanotherapy containing prednisolone phosphate for the treatment of inflammatory diseases. After formulation design, GMP production was commenced which yielded consistent, stable liposomes sized 100nm+/-10nm, with a prednisolone phosphate (PLP) incorporation efficiency of 3%-5%. Pharmacokinetics and toxicokinetics of GMP-grade liposomal nanoparticles were evaluated in healthy rats, which were compared to daily and weekly administration of free prednisolone phosphate, revealing a long circulatory half-life with minimal side effects. Subsequently, non-invasive multimodal clinical imaging after liposomal nanotherapy's intravenous administration revealed anti-inflammatory effects on the vessel wall of atherosclerotic rabbits. The present program led to institutional review board approval for two clinical trials with patients with atherosclerosis. FROM THE CLINICAL EDITOR: In drug discovery, bringing production to industrial scale is an essential process. In this article the authors describe the development of an anti-inflammatory nanoparticle according to good manufacturing practice. As a result, this paves the way for translating laboratory studies to clinical trials in humans.
Published: 2015
Full Text: View/download PDF

42. A novel approach for the intravenous delivery of leuprolide using core-cross-linked polymeric micelles

Author: Hu, Qizhi, Van Gaal, Ethlinn V B, Brundel, Paul, Ippel, Hans, Hackeng, Tilman, Rijcken, Cristianne J F, Storm, Gert, Hennink, Wim E., Prakash, Jai, Sub Drug delivery, UIPS - Utrecht Institute for Pharmaceutical Sciences, Sub General Pharmaceutics, Biochemie, RS: CARIM - R1 - Thrombosis and haemostasis, RS: CARIM - R3 - Vascular biology, Sub Drug delivery, UIPS - Utrecht Institute for Pharmaceutical Sciences, Sub General Pharmaceutics, and Biomaterials Science and Technology
Subjects: Male, Metabolic Clearance Rate, Polymers, Chemistry, Pharmaceutical, Kinetics, Pharmaceutical Science, Peptide, Pharmacology, Micelle, Rats, Sprague-Dawley, Pharmacokinetics, In vivo, Therapeutic peptide, Animals, Technology, Pharmaceutical, Testosterone, Micelles, chemistry.chemical_classification, Drug Carriers, Chemistry, Hydrolysis, METIS-308682, Esters, Biological activity, IR-95553, Cross-Linking Reagents, Solubility, Covalent bond, Area Under Curve, Delayed-Action Preparations, Injections, Intravenous, Polymeric micelles, Leuprolide, Drug carrier, Half-Life, Sustained release
Abstract: Therapeutic peptides are highly attractive drugs for the treatment of various diseases. However, their poor pharmacokinetics due to rapid renal elimination limits their clinical applications. In this study, a model hormone peptide, leuprolide, was covalently linked to core-cross-linked polymeric micelles (CCL-PMs) via two different hydrolysable ester linkages, thereby yielding a nanoparticulate system with tuneable drug release kinetics. The ester linkage that provided the slowest peptide release kinetics was selected for in vivo evaluation. Compared to the soluble peptide, the leuprolide-entrapped CCL-PMs showed a prolonged circulation half-life (14.4 h) following a single intravenous injection in healthy rats and the released leuprolide was detected in blood for 3 days. In addition, the area under the plasma concentration-time curve (AUC) value was >100-fold higher for leuprolide-entrapped CCL-PMs than for soluble leuprolide. Importantly, the released peptide remained biologically active as demonstrated by increased and long-lasting plasma testosterone levels. This study shows that covalent linkage of peptides to CCL-PMs via hydrolytically sensitive ester bonds is a promising approach to achieving sustained systemic levels of peptides after intravenous administration.
Published: 2015
Full Text: View/download PDF

43. Local therapeutic efficacy with reduced systemic side effects by rapamycin-loaded subcapsular microspheres

Author: Falke, Lucas L, van Vuuren, Stefan H, Kazazi-Hyseni, Filis, Ramazani, Farshad, Nguyen, Tri Q, Veldhuis, Gert J, Maarseveen, Erik M, Zandstra, Jurjen, Zuidema, Johan, Duque, Luisa F, Steendam, Rob, Popa, Eliane R, Kok, Robbert Jan, Goldschmeding, Roel, Sub Drug delivery, Sub General Pharmaceutics, Pharmaceutics, Restoring Organ Function by Means of Regenerative Medicine (REGENERATE), Nanotechnology and Biophysics in Medicine (NANOBIOMED), Sub Drug delivery, Sub General Pharmaceutics, and Pharmaceutics
Subjects: Microsphere, Subcapsular delivery, Pathology, T-Lymphocytes, Anti-Inflammatory Agents, PROGRESSION, Pharmacology, Fibrosis, Chronic kidney disease, Tissue Distribution, Myofibroblasts, Non-U.S. Gov't, Kidney, IMMUNOSUPPRESSION, Research Support, Non-U.S. Gov't, TOR Serine-Threonine Kinases, IN-VIVO CHARACTERIZATION, Microspheres, Treatment Outcome, medicine.anatomical_structure, Mechanics of Materials, mTOR, Female, Myofibroblast, Infiltration (medical), Ureteral Obstruction, medicine.medical_specialty, Biophysics, Capsules, Bioengineering, Research Support, Biomaterials, KIDNEY, medicine, Renal fibrosis, Journal Article, INJURY, Animals, RENAL FIBROSIS, Rapamycin, MTOR INHIBITION, PI3K/AKT/mTOR pathway, Sirolimus, business.industry, TRANSPLANTATION, medicine.disease, Rats, Inbred F344, Transplantation, Gene Expression Regulation, DELIVERY-SYSTEM, CELLS, Microscopy, Electron, Scanning, Ceramics and Composites, business, Kidney disease
Abstract: Kidney injury triggers fibrosis, the final common pathway of chronic kidney disease (CKD). The increase of CKD prevalence worldwide urgently calls for new therapies. Available systemic treatment such as rapamycin are associated with serious side effects. To study the potential of local antifibrotic therapy, we administered rapamycin-loaded microspheres under the kidney capsule of ureter-obstructed rats and assessed the local antifibrotic effects and systemic side effects of rapamycin. After 7 days, microsphere depots were easily identifiable under the kidney capsule. Both systemic and local rapamycin treatment reduced intrarenal mTOR activity, myofibroblast accumulation, expression of fibrotic genes, and T-lymphocyte infiltration. Upon local treatment, inhibition of mTOR activity and reduction of myofibroblast accumulation were limited to the immediate vicinity of the subcapsular pocket, while reduction of T-cell infiltration was widespread. In contrast to systemically administered rapamycin, local treatment did not induce off target effects such as weight loss. Thus subcapsular delivery of rapamycin-loaded microspheres successfully inhibited local fibrotic response in UUO with less systemic effects. Therapeutic effect of released rapamycin was most prominent in close vicinity to the implanted microspheres. (C) 2014 Elsevier Ltd. All rights reserved.
Published: 2015
Full Text: View/download PDF

44. Formulation and characterization of microspheres loaded with imatinib for sustained delivery

Author: Ramazani, F., Chen, W., Van Nostrum, C. F., Storm, G., Kiessling, F., Lammers, T., Hennink, W. E., Kok, R. J., Sub Drug delivery, Sub General Pharmaceutics, Sub Drug targeting, Pharmaceutics, Biomaterials Science and Technology, Faculty of Science and Technology, Sub Drug delivery, Sub General Pharmaceutics, Sub Drug targeting, and Pharmaceutics
Subjects: Time Factors, METIS-315202, Pharmaceutical Science, Matrix (chemical analysis), chemistry.chemical_compound, Differential scanning calorimetry, Polylactic Acid-Polyglycolic Acid Copolymer, hemic and lymphatic diseases, Taverne, medicine, Double emulsion (W/O/W), Lactic Acid, Particle Size, neoplasms, drug release, chemistry.chemical_classification, Drug Carriers, Chromatography, Mesylate, PLGA microspheres, Imatinib, Polymer, log D, IR-99929, Microspheres, Solvent, PLGA, Drug Liberation, Imatinib mesylate, chemistry, Solubility, Delayed-Action Preparations, Loading efficiency, Polyglycolic Acid, medicine.drug
Abstract: The aim of this study was the development of imatinib-loaded poly(d,l-lactide-co-glycolide) (PLGA) microspheres with high loading efficiency which can afford continuous release of imatinib over a prolonged period of time. Imatinib mesylate loaded PLGA microspheres with a size of 6-20 μm were prepared by a double emulsion (W1/O/W2) method using dichloromethane as volatile solvent. It was found that the microspheres were spherical with a non-porous surface; imatinib loading efficiency (LE) was highly dependent on the pH of the external water phase (W2). By increasing the pH of W2 phase above the highest pKa of imatinib (pKa 8.1), at which imatinib is mainly uncharged, the LE increased from 10% to 90% (pH 5.0 versus pH 9.0). Conversely, only 4% of its counter ion, mesylate, was retained in the microspheres at the same condition (pH 9.0). Since mesylate is highly water soluble, it is unlikely that it partitions into the organic phase. We demonstrated, using differential scanning calorimetry (DSC), that imatinib was molecularly dispersed in the polymeric matrix at loadings up to 8.0%. At higher drug loading, imatinib partially crystallized in the matrix. Imatinib microspheres released their cargo during three months by a combination of diffusion through the polymer matrix and polymer erosion. In conclusion, we have formulated imatinib microspheres with high LE and LC. Although we started with a double emulsion of imatinib mesylate, the obtained microspheres contained imatinib base which was mainly molecularly dispersed in the polymer matrix. These microspheres release imatinib over a 3-month period which is of interest for local treatment of cancer.
Published: 2015
Full Text: View/download PDF

45. Intercalating quaternary nicotinamide-based poly(amido amine)s for gene delivery

Author: van der Aa, L J, Vader, P, Storm, G, Schiffelers, R M, Engbersen, J F J, Sub General Pharmaceutics, Sub Drug targeting, Pharmaceutics, Sub General Pharmaceutics, Sub Drug targeting, Pharmaceutics, Faculty of Science and Technology, and Biomaterials Science and Technology
Subjects: Niacinamide, Erythrocytes, Quaternary nicotinamide, Cell Survival, Polymers, Stereochemistry, Green Fluorescent Proteins, Gene Expression, Pharmaceutical Science, Gene delivery, Transfection, Hemolysis, chemistry.chemical_compound, Genes, Reporter, Cell Line, Tumor, Chlorocebus aethiops, Polymer chemistry, Intercalation, Side chain, Animals, Humans, Moiety, chemistry.chemical_classification, Nicotinamide, Gene Transfer Techniques, Cationic polymerization, DNA, Polymer, Poly(amido amine), Intercalating Agents, Polyplex, chemistry, COS Cells, Nicotinamide cation, Amine gas treating, NAD+ kinase, Plasmids
Abstract: In the development of potent polymeric gene carriers for gene therapy, a good interaction between the polymer and the nucleotide is indispensable to form small and stable polyplexes. Polymers with relatively high cationic charge density are frequently used to provide these interactions, but high cationic charge is usually associated with severe cytotoxicity. In this study an alternative, nucleotide specific binding interaction based on intercalation was investigated to improve polymer/pDNA complex formation. For this purpose bioreducible poly(amido amine) copolymers (p(CBA-ABOL/Nic)) were synthesized with different degrees of intercalating quaternary nicotinamide (Nic) groups and amide-substituted derivatives in their side chains. The quaternary nicotinamide group was chosen as intercalating moiety because this group is part of the naturally occurring NAD+ coenzyme and is therefore expected to be non-toxic and non-carcinogenic. The presence of the quaternary nicotinamide moieties in the poly(amido amine) copolymers showed to effectively promote self-assembled polyplex formation already at low polymer/DNA ratios and results in decreased polyplex size and increased stability of the polyplexes. Furthermore, in contrast to the primary amine functionalized analogs the quaternary nicotinamide polymers showed to be non-hemolytic, indicating their compatibility with cell membranes. Polymers with 25% of Nic in the side chains induced GFP expressions of about 4-5 times that of linear PEI, which is comparable with p(CBA-ABOL), the parent PAA without Nic, but at a two- to fourfold lower required polymer dose. N-phenylation of the nicotinamide functionality even further reduces the required polymer dose to form stable polyplexes, which is a major improvement for these kinds of cationic polymers.
Published: 2014
Full Text: View/download PDF

46. Arthroscopic Determination of Cartilage Proteoglycan Content and Collagen Network Structure with Near-Infrared Spectroscopy

Author: LS Equine Muscoskeletal Biology, dES RMSC, LS Heelkunde, Sub General Pharmaceutics, Geneeskunde van gezelschapsdieren, Dep Gezondheidszorg Paard, Sarin, Jaakko K., Nykänen, Olli, Tiitu, Virpi, Mancini, Irina A.D., Brommer, Harold, Visser, Jetze, Malda, Jos, van Weeren, P. René, Afara, Isaac O., Töyräs, Juha, LS Equine Muscoskeletal Biology, dES RMSC, LS Heelkunde, Sub General Pharmaceutics, Geneeskunde van gezelschapsdieren, Dep Gezondheidszorg Paard, Sarin, Jaakko K., Nykänen, Olli, Tiitu, Virpi, Mancini, Irina A.D., Brommer, Harold, Visser, Jetze, Malda, Jos, van Weeren, P. René, Afara, Isaac O., and Töyräs, Juha
Published: 2019

47. Microwave control of thermal-magnon spin transport

Author: Sub General Pharmaceutics, Sub Cond-Matter Theory, Stat & Comp Phys, Liu, J., Feringa, F., Flebus, B., Cornelissen, L. J., Leutenantsmeyer, J. C., Duine, R. A., van Wees, B. J., Sub General Pharmaceutics, Sub Cond-Matter Theory, Stat & Comp Phys, Liu, J., Feringa, F., Flebus, B., Cornelissen, L. J., Leutenantsmeyer, J. C., Duine, R. A., and van Wees, B. J.
Published: 2019

48. Biological membranes in EV biogenesis, stability, uptake, and cargo transfer: an ISEV position paper arising from the ISEV membranes and EVs workshop

Author: LS Celbiologie-Algemeen, dB&C I&I, Sub General Pharmaceutics, Russell, Ashley E, Sneider, Alexandra, Witwer, Kenneth W, Bergese, Paolo, Bhattacharyya, Suvendra N, Cocks, Alexander, Cocucci, Emanuele, Erdbrügger, Uta, Falcon-Perez, Juan M, Freeman, David W, Gallagher, Thomas M, Hu, Shuaishuai, Huang, Yiyao, Jay, Steven M, Kano, Shin-Ichi, Lavieu, Gregory, Leszczynska, Aleksandra, Llorente, Alicia M, Lu, Quan, Mahairaki, Vasiliki, Muth, Dillon C, Noren Hooten, Nicole, Ostrowski, Matias, Prada, Ilaria, Sahoo, Susmita, Schøyen, Tine Hiorth, Sheng, Lifu, Tesch, Deanna, Van Niel, Guillaume, Vandenbroucke, Roosmarijn E, Verweij, Frederik J, Villar, Ana V, Wauben, Marca, Wehman, Ann M, Yin, Hang, Carter, David Raul Francisco, Vader, Pieter, LS Celbiologie-Algemeen, dB&C I&I, Sub General Pharmaceutics, Russell, Ashley E, Sneider, Alexandra, Witwer, Kenneth W, Bergese, Paolo, Bhattacharyya, Suvendra N, Cocks, Alexander, Cocucci, Emanuele, Erdbrügger, Uta, Falcon-Perez, Juan M, Freeman, David W, Gallagher, Thomas M, Hu, Shuaishuai, Huang, Yiyao, Jay, Steven M, Kano, Shin-Ichi, Lavieu, Gregory, Leszczynska, Aleksandra, Llorente, Alicia M, Lu, Quan, Mahairaki, Vasiliki, Muth, Dillon C, Noren Hooten, Nicole, Ostrowski, Matias, Prada, Ilaria, Sahoo, Susmita, Schøyen, Tine Hiorth, Sheng, Lifu, Tesch, Deanna, Van Niel, Guillaume, Vandenbroucke, Roosmarijn E, Verweij, Frederik J, Villar, Ana V, Wauben, Marca, Wehman, Ann M, Yin, Hang, Carter, David Raul Francisco, and Vader, Pieter
Published: 2019

49. Mogelijkheden van 3D-printen in de geneeskunde: 5 jaar later

Author: Sub General Pharmaceutics, LS Equine Muscoskeletal Biology, dES RMSC, Visser, Jetze, Melchels, Ferry P.W., Weinans, Harrie, Kruyt, Moyo C., Malda, Jos, Sub General Pharmaceutics, LS Equine Muscoskeletal Biology, dES RMSC, Visser, Jetze, Melchels, Ferry P.W., Weinans, Harrie, Kruyt, Moyo C., and Malda, Jos
Published: 2019

50. Visible Light Cross-Linking of Gelatin Hydrogels Offers an Enhanced Cell Microenvironment with Improved Light Penetration Depth

Author: Afd Pharmaceutics, Sub General Pharmaceutics, LS Equine Muscoskeletal Biology, dES RMSC, Lim, Khoon S, Klotz, Barbara J, Lindberg, Gabriella C J, Melchels, Ferry P W, Hooper, Gary J, Malda, Jos, Gawlitta, Debby, Woodfield, Tim B F, Afd Pharmaceutics, Sub General Pharmaceutics, LS Equine Muscoskeletal Biology, dES RMSC, Lim, Khoon S, Klotz, Barbara J, Lindberg, Gabriella C J, Melchels, Ferry P W, Hooper, Gary J, Malda, Jos, Gawlitta, Debby, and Woodfield, Tim B F
Published: 2019

Catalog

Books, media, physical & digital resources

See catalog results

Searchworks

Select search scope, currently: Articles Catalog books, media & more in Jio Institute collections Articles journal articles & other e-resources

Search

Search Constraints

Refine your results

Search Limiters

Topic

Publication Year Range

Language

Publication Type

Journal

Database

Publisher

612 results on '"Sub General Pharmaceutics"'

Search Results

Catalog

Select search scope, currently: Articles

Catalog

books, media & more in Jio Institute collections

Articles

journal articles & other e-resources