6 results on '"SIGEA SRL"'
Search Results
2. MIXED BUTYRIC-FORMIC ESTERS OF ACID POLYSACCHARIDES, AND THEIR PREPARATION AND USE AS SKIN COSMETICS
- Author
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SIGEA SRL, BOSCO MARCO, STUCCHI LUCA, GIANNI RITA, and TREVISAN ANTONIA
- Abstract
Disclosed are acid polysaccharides characterised by the concomitant presence of alcohol groups esterified with butyric and formic acids.
3. Approaching tumour therapy beyond platinum drugs. Status of the art and perspectives of ruthenium drug candidates
- Author
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Bergamo, A., Gaiddon, C., Schellens, J.H.M., Beijnen, J.H., Sava, G., Bergamo, Alberta, Gaiddon, C., Schellens, J. H. M., Beijnen, J. H., Sava, Gianni, Gaiddon, Christian, Callerio Foundation Onlus [Trieste, Italy], Laboratoire de signalisation moléculaire et neurodégénerescence, Université Louis Pasteur - Strasbourg I-IFR37-Institut National de la Santé et de la Recherche Médicale (INSERM), Netherlands Cancer Institute (NKI), Antoni van Leeuwenhoek Hospital, Department of Pharmaceutical Sciences [Utrecht, The Netherlands], Utrecht University [Utrecht], Department of Life Sciences [Trieste, Italy], Università degli studi di Trieste = University of Trieste, Work done within the frame of COST D39 WG3 and with the financial support of SIGEA srl., and Università degli studi di Trieste
- Subjects
Clinical Trials as Topic ,Molecular Structure ,Cell Survival ,[SDV]Life Sciences [q-bio] ,farmaci ,rutenio ,Antineoplastic Agents ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,Tumori ,metastasi ,attività clinica ,Ruthenium ,[SDV] Life Sciences [q-bio] ,[SDV.CAN] Life Sciences [q-bio]/Cancer ,Neoplasms ,Organometallic Compounds ,Animals ,Humans ,Drug Screening Assays, Antitumor - Abstract
International audience; The study of metal complexes for the treatment of cancer diseases has resulted in the identification of some unique properties of ruthenium-based compounds. Among these inorganic-based agents, two of them, namely the ruthenium(III) drugs NAMI-A and KP1019 have undertaken with some success the clinical evaluations of phase I and preliminary phase II trials in patients. Here we highlight the strategies that have led to the discovery of metal-based (NAMI-A and KP1019) and of organometallic (RM175, RAPTA-T, RDC11 and DW1/2) ruthenium-based complexes, and we report their main biological/pharmacological characteristics and expectations for further development.
- Published
- 2012
- Full Text
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4. Comparison of three different application routes of butyrate to improve colonic anastomotic strength in rats.
- Author
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Bosmans JW, Jongen AC, Boonen BT, van Rijn S, Scognamiglio F, Stucchi L, Gijbels MJ, Marsich E, and Bouvy ND
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- Anastomosis, Surgical, Anastomotic Leak pathology, Animals, Collagen metabolism, Drug Administration Routes, Gene Expression Regulation drug effects, Inflammation pathology, Matrix Metalloproteinases metabolism, Pressure, Rats, Wistar, Real-Time Polymerase Chain Reaction, Butyric Acid administration & dosage, Butyric Acid pharmacology, Colon drug effects, Colon surgery
- Abstract
Introduction: Despite extensive research, anastomotic leakage (AL) remains one of the most dreaded complications after colorectal surgery. Since butyrate enemas are known to enhance anastomotic healing, several administration routes have been explored in this study., Methods: Three intraluminal approaches involving butyrate were investigated: (1) butyrin-elucidating patch, (2) a single injection of hyaluronan-butyrate (HA-But) prior to construction of the proximal anastomosis and (3) rectal hyaluronan-butyrate (HA-But) enemas designed for distal anastomoses. The main outcome was AL and secondary outcomes were bursting pressure, histological analysis of the anastomosis, zymography to detect MMP activity and qPCR for gene expression of MMP2, MMP9, MUC2 and TFF3., Results: Neither the patches nor the injections led to a reduction of AL in experiments 1 and 2. In experiment 3, a significant reduction of AL was accomplished with the (HA-But) enema compared to the control group together with a higher bursting pressure. Histological analysis detected only an increased inflammation in experiment 2 in the hyaluronan injection group compared to the control group. No other differences were found regarding wound healing. Zymography identified a decreased proenzyme of MMP9 when HA-But was administered as a rectal enema. qPCR did not show any significant differences between groups in any experiment., Conclusion: Butyrate enemas are effective in the enhancement of colonic anastomosis. Enhanced butyrate-based approaches designed to reduce AL in animal models for both proximal and distal anastomoses were not more effective than were butyrate enemas alone. Further research should focus on how exogenous butyrate can improve anastomotic healing after gastrointestinal surgery.
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- 2017
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5. A silver complex of hyaluronan-lipoate (SHLS12): Synthesis, characterization and biological properties.
- Author
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Sacco P, Sechi A, Trevisan A, Picotti F, Gianni R, Stucchi L, Fabbian M, Bosco M, Paoletti S, and Marsich E
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- 3T3 Cells, Animals, Anti-Bacterial Agents chemistry, Anti-Bacterial Agents pharmacology, Biocompatible Materials chemistry, Biocompatible Materials pharmacology, Biofilms drug effects, Gels chemical synthesis, Gels chemistry, Gels pharmacology, Humans, Hyaluronic Acid chemical synthesis, Mice, Silver chemistry, Thioctic Acid chemical synthesis, Anti-Bacterial Agents chemical synthesis, Biocompatible Materials chemical synthesis, Hyaluronic Acid analogs & derivatives, Hyaluronic Acid chemistry, Thioctic Acid analogs & derivatives, Thioctic Acid chemistry
- Abstract
In this study we present a novel silver complex of hyaluronan-lipoate (SHLS12) in a gel-state form. NMR analysis, conductometry and elemental analysis demonstrated stable non-covalent interactions between silver ions and the polysaccharide-lipoate backbone, whereas rheological investigations confirmed its gel-like physical-chemical behavior. Biological studies showed the ability of SHLS12 to exert a straightforward activity against different bacterial strains grown in sessile/planktonic state. The biocompatibility was also proved toward two eukaryotic cell lines. By considering both its ability to preserve antibacterial properties when exposed to the serum protein BSA and its low susceptibility to be degraded by hyaluronidase enzyme, this novel complex may be considered as a promising biomaterial for future in vivo applications., (Copyright © 2015 Elsevier Ltd. All rights reserved.)
- Published
- 2016
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6. Hyaluronic acid lipoate: synthesis and physicochemical properties.
- Author
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Picotti F, Fabbian M, Gianni R, Sechi A, Stucchi L, and Bosco M
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- Animals, Biocatalysis, Cross-Linking Reagents, Formamides chemistry, Free Radical Scavengers chemistry, Hyaluronic Acid chemistry, Hyaluronic Acid physiology, Hyaluronoglucosaminidase chemistry, Hydrogel, Polyethylene Glycol Dimethacrylate chemistry, Imidazoles chemistry, Spectroscopy, Fourier Transform Infrared, Thioctic Acid analogs & derivatives, Ultraviolet Rays, Viscosity, Chemical Phenomena, Hyaluronic Acid analogs & derivatives, Thioctic Acid chemistry
- Abstract
The synthesis and physicochemical characterisation of mixed lipoic and formic esters of hyaluronan (Lipohyal) are presented in this paper. The synthesis was conducted by activating lipoic acid with 1,1'-carbonyldiimidazole to obtain lipoyl imidazolide, which reacted with hyaluronan (HA) in formamide under basic conditions. This procedure allows researchers to modulate easily the degree of substitution over a range of 0.05-1.8. Radical scavenger properties were analysed by UV-vis spectroscopy, where improved performance was demonstrated for Lipohyal with respect to the HA row material and lipoic acid. The chemical modification also causes HA to show an improved resistance to hyaluronidase digestion. These findings show that Lipohyal is a highly interesting derivative for applications in the tricological and dermo-cosmetic field and as an anti-aging ingredient. Moreover, Lipohyal can be easily crosslinked by UV irradiation, resulting in an innovative hydrogel with distinctive viscoelastic properties that is suitable as both a dermal-filler and as an intra-articular medical device., (Copyright © 2012 Elsevier Ltd. All rights reserved.)
- Published
- 2013
- Full Text
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