17 results on '"Patel, Paritosh"'
Search Results
2. Magnetic nanoparticles: fabrication, characterization, properties, and application for environment sustainability
- Author
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Patel, Paritosh, primary, Nandi, Aditya, additional, Jha, Ealisha, additional, Sinha, Adrija, additional, Mohanty, Swabhiman, additional, Panda, Pritam Kumar, additional, Mishra, Suman, additional, Verma, Suresh K., additional, and Suar, Mrutyunjay, additional
- Published
- 2021
- Full Text
- View/download PDF
3. List of contributors
- Author
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Abdollahinia, Elaheh Dalir, primary, Abou-Hassan, Ali, additional, Aghanejad, Ayuob, additional, Ahmadi, Nahid, additional, Ahmed, Isteaque, additional, Álvarez de Cienfuegos, Luis, additional, Amiryaghoubi, Nazanin, additional, Anik, Muzahidul I., additional, Attia, Mohammed, additional, Bagheri, Babak, additional, Bahrani, Sonia, additional, Baryeh, Kwaku, additional, Bertuit, Enzo, additional, Blidar, Adrian, additional, Chandra, Amrish, additional, Chawla, Harshita, additional, Cova, Tânia, additional, Cristea, Cecilia, additional, Doha, Rashed M., additional, Durán, Juan D.G., additional, Farahbakhsh, Javad, additional, Fathi, Marziyeh, additional, Feier, Bogdan, additional, Ferreira, Maria Inês, additional, Filice, Marco, additional, Florea, Anca, additional, Ganjali, Mohammad Reza, additional, Garg, Seema, additional, Gila-Vilchez, Cristina, additional, Guzmán Bernardo, Francisco Javier, additional, Habibzadeh, Sajjad, additional, Hashemi, Seyyed Alireza, additional, Hossain, Imran, additional, Hossain, M. Khalid, additional, Hosu, Oana, additional, Jafaryar, M., additional, Jha, Ealisha, additional, Khodadadi, Ali, additional, Kim, Ilgook, additional, Lopez-Lopez, Modesto T., additional, Lozano Chamizo, Laura, additional, Luengo Morato, Yurena, additional, Maiorov, Mikhail, additional, Maleki, Ali, additional, Mañas-Torres, Mari C., additional, Marciello, Marzia, additional, Mishra, Suman, additional, Mohanty, Swabhiman, additional, Mousavi, Seyyed Mojtaba, additional, Mozafari, Masoud, additional, Nandi, Aditya, additional, Nguyen, Tuan Anh, additional, Nosike, Elvis Ikechukwu, additional, Omidi, Yadollah, additional, Omidian, Hossein, additional, Ovejero Paredes, Karina, additional, Pais, Alberto, additional, Paixão, José A., additional, Panda, Pritam Kumar, additional, Park, Chan Woo, additional, Patel, Paritosh, additional, Ramazani, Ali, additional, Rashidi, Ladan, additional, Ríos, Ángel, additional, Rodríguez Martín-Doimeadios, Rosa Carmen, additional, Saeb, Mohammad Reza, additional, Salem, Samaa, additional, Sanchez, Laura M., additional, Segal, Izolda, additional, Shafee, Ahmad, additional, Sheikholeslami, M., additional, Sheremet, Mikhail A., additional, Sihn, Youngho, additional, Singh, Swati, additional, Sinha, Adrija, additional, Suar, Mrutyunjay, additional, Taheri-Ledari, Reza, additional, Tertis, Mihaela, additional, Ulloa, Joshua Chaj, additional, Vatanpour, Vahid, additional, Verma, Suresh K., additional, Vilela, Diana, additional, Villalonga, Anabel, additional, Villalonga, Reynaldo, additional, Vitorino, Carla, additional, Wu, Aiguo, additional, Yang, Hee-Man, additional, Yazdi, Mohsen Khodadadi, additional, Ye, Jing Yong, additional, Yilmaz, Erkan, additional, Yoon, In-Ho, additional, Yousefi, Khadije, additional, Zablotskaya, Alla, additional, Zablotsky, Dmitry, additional, Zarrintaj, Payam, additional, Zhang, Yujie, additional, and Zougagh, Mohammed, additional
- Published
- 2021
- Full Text
- View/download PDF
4. Contributors
- Author
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Abdollahi, Mohammad, primary, Advani, Dia, additional, Ahlawat, Jyoti, additional, Albino, Melissa, additional, Allen, Josh, additional, Ambasta, Rashmi K., additional, Antal, Diana Simona, additional, Apostolova, Nadezda, additional, Ardelean, Florina, additional, Bagshaw, Olivia R.M., additional, Balardo, Christopher J., additional, Birch-Machin, Mark A., additional, Bland, Nicholas A., additional, Callahan, Leigh Ann, additional, Caruncho, Hector J., additional, Ckless, Karina, additional, Das, Biswadeep, additional, Diego, Castanares-Zapatero, additional, Farzaei, Mohammad Hosein, additional, Ferreira, Bruna K., additional, Ferreira, Gustavo C., additional, García-Rivas, Gerardo, additional, Garg, Priyanka, additional, Gaspar, Maria Manuela, additional, Geary, Sean M., additional, Gupta, Rohan, additional, Hernández-Fontes, Paulina, additional, Idowu, Olusola, additional, Intra, Janjira, additional, Jaiswal, Asmita, additional, Kalynchuk, Lisa E., additional, Kulkarni, Aditya, additional, Kumar, Pravir, additional, Lopes, Joana, additional, Lozano, Omar, additional, Matias, Mariana, additional, Misra, Manju, additional, Nandi, Aditya, additional, Narayan, Mahesh, additional, Padh, Harish, additional, Pandey, Abhay K., additional, Pandey, Akanksha, additional, Pardiwalla, Niyati, additional, Patel, Paritosh, additional, Philippe, Hantson, additional, Pinho, Jacinta Oliveira, additional, Reis, Catarina, additional, Ren, Jun, additional, Rocha, Milagros, additional, Rodrigues, Melissa T., additional, Ruddy, Elizabeth, additional, Ruktanonchai, Uracha, additional, Salem, Aliasger K., additional, Samuel, Irene A.J., additional, Sandhir, Rajat, additional, Sawangchan, Phawanan, additional, Schroder, Elizabeth A., additional, Schuck, Patricia F., additional, Sharma, Amit Kumar, additional, Sharma, Sudhanshu, additional, Shenoy, Snehal, additional, Singh, Amit Kumar, additional, Singhal, Nitin, additional, Stuart, Jeffrey A., additional, Suksiriworapong, Jiraphong, additional, Sunasee, Rajesh, additional, Supinski, Gerald, additional, Taghipour, Yasamin Davatgaran, additional, Thakkar, Shreya, additional, Tripathi, Rahul, additional, Verma, Suresh K., additional, Vezza, Teressa, additional, Victor, Victor M., additional, Wang, Lin, additional, Wongrakpanich, Amaraporn, additional, Wu, Lin, additional, Zhang, Yingmei, additional, Zhu, Gewei, additional, and Zoso, Sean L.S., additional
- Published
- 2021
- Full Text
- View/download PDF
5. Aurora Borealis in dentistry : The applications of cold plasma in biomedicine
- Author
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Lata, S., Chakravorty, Shibani, Mitra, Tamoghni, Pradhan, Prasanti Kumari, Mohanty, Soumyakanta, Patel, Paritosh, Jha, Ealisha, Panda, Pritam Kumar, Verma, Suresh K., Suar, Mrutyunjay, Lata, S., Chakravorty, Shibani, Mitra, Tamoghni, Pradhan, Prasanti Kumari, Mohanty, Soumyakanta, Patel, Paritosh, Jha, Ealisha, Panda, Pritam Kumar, Verma, Suresh K., and Suar, Mrutyunjay
- Abstract
Plasma is regularly alluded to as the fourth form of matter. Its bounty presence in nature along with its potential antibacterial properties has made it a widely utilized disinfectant in clinical sciences. Thermal plasma and nonthermal (or cold atmospheric) plasma (NTP) are two types of plasma. Atoms and heavy particles are both available at the same temperature in thermal plasma. Cold atmospheric plasma (CAP) is intended to be nonthermal since its electrons are hotter than the heavier particles at ambient temperature. Direct barrier discharge (DBD), atmospheric plasma pressure jet (APPJ), etc. methods can be used to produce plasma, however, all follow a basic concept in their generation. This review focuses on the anticipated uses of cold atmospheric plasma in dentistry, such as its effectiveness in sterilizing dental instruments by eradicating bacteria, its advantage in dental cavity decontamination over conventional methods, root canal disinfection, its effects on tooth whitening, the benefits of plasma treatment on the success of dental implant placement, and so forth. Moreover, the limitations and probable solutions has also been anticipated. These conceivable outcomes thus have proclaimed the improvement of more up-to-date gadgets, for example, the plasma needle and plasma pen, which are efficient in treating the small areas like root canal bleaching, biofilm disruption, requiring treatment in dentistry.
- Published
- 2022
- Full Text
- View/download PDF
6. Molecular toxicity of Benzo(a)pyrene mediated by elicited oxidative stress infer skeletal deformities and apoptosis in embryonic zebrafish
- Author
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Elfawy, Hasnaa A., Anupriya, S., Mohanty, Swabhiman, Patel, Paritosh, Ghosal, Sayam, Panda, Pritam Kumar, Das, Biswadeep, Verma, Suresh K., Patnaik, Srinivas, Elfawy, Hasnaa A., Anupriya, S., Mohanty, Swabhiman, Patel, Paritosh, Ghosal, Sayam, Panda, Pritam Kumar, Das, Biswadeep, Verma, Suresh K., and Patnaik, Srinivas
- Abstract
Benzo(a)pyrene (BaP) has become an integral component of disposed of plastic waste, organic pollutants, and remnants of combustible materials in the aquatic environment due to their persistent nature. The accumulation and integration of these polycyclic aromatic hydrocarbons (PAHs) have raised concern to human health and ecological safety. This study assessed the BaP-induced in vivo molecular toxicity with embryonic zebrafish inferred by oxidative stress and apoptosis. BaP was found to induce morphological and physiological abnormalities like delayed hatching (p < 0.05). Computational analysis demonstrated the high-affinity interaction of BaP with the zebrafish hatching enzyme (ZHE1) with Arg, Cys, Ala, Tyr, and Phe located at the active site revealing the influence of BaP on delayed hatching due to alteration of the enzyme structure. RT-PCR analysis revealed significant down-regulation of the skeletal genes Sox9a, SPP1/OPN, and Col1a1 (p < 0.05) genes. The cellular investigations unraveled that the toxicity of BaP extends to the skeletal regions of zebrafish (head, backbone, and tail) because of the elicited oxidative stress leading to apoptosis. The study extended the horizon of understanding of BaP toxicity at the molecular level which will enhance the indulgent and designing of techniques for better ecological sustainability., De två första författarna delar förstaförfattarskapet.
- Published
- 2021
- Full Text
- View/download PDF
7. Green synthesized MgO nanoparticles infer biocompatibility by reducing in vivo molecular nanotoxicity in embryonic zebrafish through arginine interaction elicited apoptosis
- Author
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Verma, Suresh K., Nisha, Kumari, Panda, Pritam Kumar, Patel, Paritosh, Kumari, Puja, Mallick, M. A., Sarkar, Biplab, Das, Biswadeep, Verma, Suresh K., Nisha, Kumari, Panda, Pritam Kumar, Patel, Paritosh, Kumari, Puja, Mallick, M. A., Sarkar, Biplab, and Das, Biswadeep
- Abstract
Increasing demand for magnesium oxide (MgO) nanoparticles (NP) due to their extensive use in different physical and biological applications has raised concern on their biocompatibility and toxicity to human health and ecological safety. This has instigated guest for detailed information on their toxicity mechanism, along with ecofriendly synthesis as a potential solution. This study explores the toxicity of MgO NP at the molecular level using embryonic zebrafish (Danio rerio) and depicts the green synthesis of MgO (G-MgO) NP using the extract from a medicinal plant Calotropis gigantea. Synthesized G-MgO NP were characterized using microscopy, spectroscopy. and dynamic light scattering. Stable 55 +/- 10 nm sized MgO NP were generated with a zeta potential of 45 +/- 15 mV and hydrodynamic size 110 +/- 20 nm. UV-Vis spectrum showed a standard peak at 357 nm. Comparative cellular toxicity analysis showed higher biocompatibility of G-MgO NP compared to MgO NP with reference to the morphological changes. notochord development, and heartbeat rate in embryonic zebrafish LC50 of G-MgO NP was 520 mu g/mL compared to 410 mu g/mL of MgO NP. Molecular toxicity investigation revealed that the toxic effects of MgO NP was mainly due to the influential dysregulation in oxidative stress leading to apoptosis because of the accumulation and internalization of nanoparticles and their interaction with cellular proteins like Sod1 and p53, thereby affecting structural integrity and functionality. The study delineated the nanotoxicity of MgO NP and suggests the adoption and use of new green methodology for future production.
- Published
- 2020
- Full Text
- View/download PDF
8. Biocompatible plasma-treated liquids: A sustainable approach for decontaminating gastrointestinal-infection causing pathogens.
- Author
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Negi M, Kaushik N, Lamichhane P, Jaiswal A, Borkar SB, Patel P, Singh P, Choi EH, and Kaushik NK
- Subjects
- Decontamination methods, Biocompatible Materials chemistry, Biocompatible Materials pharmacology, Humans, Hydrogen Peroxide chemistry, Plasma Gases pharmacology, Anti-Bacterial Agents pharmacology, Anti-Bacterial Agents chemistry
- Abstract
Nosocomial infections are a serious threat and difficult to cure due to rising antibiotic resistance in pathogens and biofilms. Direct exposure to cold atmospheric plasma (CAP) has been widely employed in numerous biological research endeavors. Nonetheless, plasma-treated liquids (PTLs) formulated with physiological solutions may offer additional benefits such as enhanced portability, and biocompatibility. Additionally, CAP-infused long-lived reactive oxygen and nitrogen species (RONS) such as nitrite (NO
2 - ), nitrate (NO3 - ), and hydrogen peroxide (H2 O2 ) can synergistically induce their antibacterial activity. Herein, we investigated those argon-plasma jet-treated liquids, including Ringer's lactate (RL), phosphate-buffered saline (PBS), and physiological saline, have significant antibacterial activity against nosocomial/gastrointestinal-causing pathogens, which might be due to ROS-mediated lipid peroxidation. Combining the conventional culture-based method with propidium iodide monoazide quantitative PCR (PMAxx™-qPCR) indicated that PTLs induce a minimal viable but non-culturable (VBNC) state and moderately affect culturable counts. Specifically, the PTL exposure resulted in pathogenicity dysfunction via controlling T3SS-related effector genes of S. enterica. Overall, this study provides insights into the effectiveness of PTLs for inducing ROS-mediated damage, controlling the virulence of diarrheagenic bacteria, and modulating homeostatic genes., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)- Published
- 2024
- Full Text
- View/download PDF
9. Synergistic degradation of Chlorpyrifos by modified solar Photo-Fenton process with bacterial metabolism reduces in vivo biotoxicity in zebrafish (Danio rerio).
- Author
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Nayak T, Patel P, Ghosh A, Simnani FZ, Kumari K, Das S, Nandi A, Ghosh A, Panda PK, Kaushik NK, Raina V, and Verma SK
- Subjects
- Animals, Humans, Zebrafish, Waste Disposal, Fluid methods, Iron, Acetylcholinesterase, Ecosystem, Hydrogen Peroxide, Bacteria, Oxidation-Reduction, Chlorpyrifos toxicity, Water Pollutants, Chemical toxicity
- Abstract
The extensive use of Chlorpyrifos (CP) as insecticide has raised concern to their hazardous impact on human health and ecosystems. Bioremediation has been proved as one of the key eco-compatible method for reducing these environmental toxicants. This study explores and evaluate the effectiveness of a combined process including solar Photo-Fenton process followed by bacterial degradation using Ochrobactrum sp. CPD-03 for effective CP degradation in wastewater. Moreover, the in vivo molecular biotoxicity of CP and degraded CP has been evaluated with embryonic zebrafish. The solar Photo-Fenton treatment showed CP degradation efficiency of ∼42 % in 4 h and ∼92 % in 96 h with combined bacterial degradation process. In vivo biotoxicity analysis showed increased survivability of embryonic zebrafish exposed to CP with CPD-03 in water with lesser morphological abnormalities. The mechanistic molecular analysis showed decreased acetylcholinesterase inhibition and GST activity in embryos exposed to CP with CPD-03 for a lesser apoptosis due to influential intrinsic interaction with metabolic proteins. The study advocated to the use of solar Photo-Fenton process followed by bacterial degradation for an efficient ecological degradation of CP for effective reduction of in vivo biotoxicity., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)
- Published
- 2023
- Full Text
- View/download PDF
10. Glycolytic stress deteriorates 229E virulence to improve host defense response.
- Author
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Kaushik N, Patel P, Bhartiya P, Shin Y, Kim JH, Choi EH, and Kaushik NK
- Subjects
- Humans, Virulence, Glycolysis, Glucose metabolism, Antiviral Agents pharmacology, Deoxyglucose pharmacology, Coronavirus
- Abstract
Viral infection treatment is a difficult task due to its complex structure and metabolism. Additionally, viruses can alter the metabolism of host cells, mutate, and readily adjust to harsh environments. Coronavirus stimulates glycolysis, weakens mitochondrial activity, and impairs infected cells. In this study, we investigated the efficacy of 2-DG in inhibiting coronavirus-induced metabolic processes and antiviral host defense systems, which have not been explored so far. 2-Deoxy-d-glucose (2-DG), a molecule restricting substrate availability, has recently gained attention as a potential antiviral drug. The results revealed that 229E human coronavirus promoted glycolysis, producing a significant increase in the concentration of fluorescent 2-NBDG, a glucose analog, particularly in the infected host cells. The addition of 2-DG decreased its viral replication and suppressed infection-induced cell death and cytopathic effects, thereby improving the antiviral host defense response. It was also observed that administration of low doses of 2-DG inhibited glucose uptake, indicating that 2-DG consumption in virus-infected host cells was mediated by high-affinity glucose transporters, whose levels were amplified upon coronavirus infection. Our findings indicated that 2-DG could be a potential drug to improve the host defense system in coronavirus-infected cells., Competing Interests: Declaration of competing interest The authors have declared no conflict of interest., (Copyright © 2023 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2023
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- View/download PDF
11. Atmospheric microplastic and nanoplastic: The toxicological paradigm on the cellular system.
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Choudhury A, Simnani FZ, Singh D, Patel P, Sinha A, Nandi A, Ghosh A, Saha U, Kumari K, Jaganathan SK, Kaushik NK, Panda PK, Suar M, and Verma SK
- Subjects
- Humans, Plastics toxicity, Environmental Pollution, Lung chemistry, Microplastics toxicity, Water Pollutants, Chemical toxicity
- Abstract
The increasing demand for plastic in our daily lives has led to global plastic pollution. The improper disposal of plastic has resulted in a massive amount of atmospheric microplastics (MPs), which has further resulted in the production of atmospheric nanoplastics (NPs). Because of its intimate relationship with the environment and human health, microplastic and nanoplastic contamination is becoming a problem. Because microplastics and nanoplastics are microscopic and light, they may penetrate deep into the human lungs. Despite several studies demonstrating the abundance of microplastics and nanoplastics in the air, the potential risks of atmospheric microplastics and nanoplastics remain unknown. Because of its small size, atmospheric nanoplastic characterization has presented significant challenges. This paper describes sampling and characterization procedures for atmospheric microplastics and nanoplastics. This study also examines the numerous harmful effects of plastic particles on human health and other species. There is a significant void in research on the toxicity of airborne microplastics and nanoplastics upon inhalation, which has significant toxicological potential in the future. Further study is needed to determine the influence of microplastic and nanoplastic on pulmonary diseases., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2023
- Full Text
- View/download PDF
12. Zebrafish-based platform for emerging bio-contaminants and virus inactivation research.
- Author
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Patel P, Nandi A, Verma SK, Kaushik N, Suar M, Choi EH, and Kaushik NK
- Subjects
- Humans, Animals, Mice, Rats, Rabbits, Zebrafish, Virus Inactivation, SARS-CoV-2, COVID-19, Viruses, Influenza in Birds
- Abstract
Emerging bio-contaminants such as viruses have affected health and environment settings of every country. Viruses are the minuscule entities resulting in severe contagious diseases like SARS, MERS, Ebola, and avian influenza. Recent epidemic like the SARS-CoV-2, the virus has undergone mutations strengthen them and allowing to escape from the remedies. Comprehensive knowledge of viruses is essential for the development of targeted therapeutic and vaccination treatments. Animal models mimicking human biology like non-human primates, rats, mice, and rabbits offer competitive advantage to assess risk of viral infections, chemical toxins, nanoparticles, and microbes. However, their economic maintenance has always been an issue. Furthermore, the redundancy of experimental results due to aforementioned aspects is also in examine. Hence, exploration for the alternative animal models is crucial for risk assessments. The current review examines zebrafish traits and explores the possibilities to monitor emerging bio-contaminants. Additionally, a comprehensive picture of the bio contaminant and virus particle invasion and abatement mechanisms in zebrafish and human cells is presented. Moreover, a zebrafish model to investigate the emerging viruses such as coronaviridae and poxviridae has been suggested., Competing Interests: Declaration of competing interest The authors declare that they have no competing interests., (Copyright © 2023. Published by Elsevier B.V.)
- Published
- 2023
- Full Text
- View/download PDF
13. Hydoxylated β- and δ-Hexacholorocyclohexane metabolites infer influential intrinsic atomic pathways interaction to elicit oxidative stress-induced apoptosis for bio-toxicity.
- Author
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Singh K, Verma SK, Patel P, Panda PK, Sinha A, Das B, Raina V, Suar M, and Ray L
- Subjects
- Animals, Apoptosis, Biodegradation, Environmental, Humans, Oxidative Stress, Soil, Hexachlorocyclohexane toxicity, Zebrafish metabolism
- Abstract
Hexachlorocyclohexane (HCH) has been recognized as an effective insecticide to protect crops against grasshoppers, cohort insects, rice insects, wireworms, and other agricultural pests and; for the control of vector-borne diseases such as malaria. It is a cyclic, saturated hydrocarbon, which primarily exists as five different stable isomers in the environment. Though the use of HCH is banned in most countries owing to its adverse effects on the environment, its metabolites still exist in soil and groundwater, because of its indiscriminate applications. In this study, a dose-dependent toxicity assay of the HCH isomers isolated from soil and water samples of different regions of Odisha, India was performed to assess the in vivo developmental effects and oxidative stress in zebrafish embryos. Toxicity analysis revealed a significant reduction in hatching and survivability rate along with morphological deformities (edema, tail malformations, spinal curvature) upon an increase in the concentration of HCH isomers; beta isomer exhibiting maximum toxicity (p < 0.05). Oxidative stress assay showed that ROS and apoptosis were highest in the fish exposed to β-2 and δ-2 isomers of HCH in comparison to the untreated one. Zebrafish proved to be a useful biological model to assess the biological effects of HCH isomers. In addition, the results suggest the implementation of precautionary measures to control the use of organochlorine compounds that can lead to a decrease in the HCH isomers in the field for a healthier environment., (Copyright © 2022 Elsevier Inc. All rights reserved.)
- Published
- 2022
- Full Text
- View/download PDF
14. In vivo intrinsic atomic interaction infer molecular eco-toxicity of industrial TiO 2 nanoparticles via oxidative stress channelized steatosis and apoptosis in Paramecium caudatum.
- Author
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Mohanty S, Patel P, Jha E, Panda PK, Kumari P, Singh S, Sinha A, Saha AK, Kaushik NK, Raina V, Verma SK, and Suar M
- Subjects
- Apoptosis, Oxidative Stress, Titanium toxicity, Nanoparticles chemistry, Nanoparticles toxicity, Paramecium caudatum
- Abstract
The ecotoxicological effect of after-usage released TiO
2 nanoparticles in aquatic resources has been a major concern owing to their production and utilization in different applications. Addressing the issue, this study investigates the detailed in vivo molecular toxicity of TiO2 nanoparticles with Paramecium caudatum. TiO2 nanoparticles were synthesized at a lab scale using high energy ball milling technique; characterized for their physicochemical properties and investigated for their ecotoxicological impact on oxidative stress, steatosis, and apoptosis of cells through different biochemical analysis, flow cytometry, and fluorescent microscopy. TiO2 nanoparticles; TiO2 (N15); of size 36 ± 12 nm were synthesized with a zeta potential of - 20.2 ± 8.8 mV and bandgap of 4.6 ± 0.3 eV and exhibited a blue shift in UV-spectrum. Compared to the Bulk TiO2 , the TiO2 (N15) exhibited higher cytotoxicity with a 24 h LC50 of 202.4 µg/ml with P. Caudatum. The mechanism was elucidated as the size and charge-dependent internalization of nanoparticles leading to abnormal physiological metabolism in oxidative stress, steatosis, and apoptosis because of their influential effect on the activity of metabolic proteins like SOD, GSH, MDA, and catalase. The study emphasized the controlled usage TiO2 nanoparticles in daily activity with a concern for ecological and biomedical aspects., (Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.)- Published
- 2022
- Full Text
- View/download PDF
15. Molecular toxicity of Benzo(a)pyrene mediated by elicited oxidative stress infer skeletal deformities and apoptosis in embryonic zebrafish.
- Author
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Elfawy HA, Anupriya S, Mohanty S, Patel P, Ghosal S, Panda PK, Das B, Verma SK, and Patnaik S
- Abstract
Benzo(a)pyrene (BaP) has become an integral component of disposed of plastic waste, organic pollutants, and remnants of combustible materials in the aquatic environment due to their persistent nature. The accumulation and integration of these polycyclic aromatic hydrocarbons (PAHs) have raised concern to human health and ecological safety. This study assessed the BaP-induced in vivo molecular toxicity with embryonic zebrafish inferred by oxidative stress and apoptosis. BaP was found to induce morphological and physiological abnormalities like delayed hatching (p < 0.05). Computational analysis demonstrated the high-affinity interaction of BaP with the zebrafish hatching enzyme (ZHE1) with Arg, Cys, Ala, Tyr, and Phe located at the active site revealing the influence of BaP on delayed hatching due to alteration of the enzyme structure. RT-PCR analysis revealed significant down-regulation of the skeletal genes Sox9a, SPP1/OPN, and Col1a1 (p < 0.05) genes. The cellular investigations unraveled that the toxicity of BaP extends to the skeletal regions of zebrafish (head, backbone, and tail) because of the elicited oxidative stress leading to apoptosis. The study extended the horizon of understanding of BaP toxicity at the molecular level which will enhance the indulgent and designing of techniques for better ecological sustainability., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)
- Published
- 2021
- Full Text
- View/download PDF
16. Green synthesized MgO nanoparticles infer biocompatibility by reducing in vivo molecular nanotoxicity in embryonic zebrafish through arginine interaction elicited apoptosis.
- Author
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Verma SK, Nisha K, Panda PK, Patel P, Kumari P, Mallick MA, Sarkar B, and Das B
- Subjects
- Animals, Apoptosis, Arginine, Magnesium Oxide, Zebrafish, Metal Nanoparticles
- Abstract
Increasing demand for magnesium oxide (MgO) nanoparticles (NP) due to their extensive use in different physical and biological applications has raised concern on their biocompatibility and toxicity to human health and ecological safety. This has instigated quest for detailed information on their toxicity mechanism, along with ecofriendly synthesis as a potential solution. This study explores the toxicity of MgO NP at the molecular level using embryonic zebrafish (Danio rerio) and depicts the green synthesis of MgO (G-MgO) NP using the extract from a medicinal plant Calotropis gigantea. Synthesized G-MgO NP were characterized using microscopy, spectroscopy, and dynamic light scattering. Stable 55 ± 10 nm sized MgO NP were generated with a zeta potential of 45 ± 15 mV and hydrodynamic size 110 ± 20 nm. UV-Vis spectrum showed a standard peak at 357 nm. Comparative cellular toxicity analysis showed higher biocompatibility of G-MgO NP compared to MgO NP with reference to the morphological changes, notochord development, and heartbeat rate in embryonic zebrafish LC50 of G-MgO NP was 520 μg/mL compared to 410 μg/mL of MgO NP. Molecular toxicity investigation revealed that the toxic effects of MgO NP was mainly due to the influential dysregulation in oxidative stress leading to apoptosis because of the accumulation and internalization of nanoparticles and their interaction with cellular proteins like Sod1 and p53, thereby affecting structural integrity and functionality. The study delineated the nanotoxicity of MgO NP and suggests the adoption and use of new green methodology for future production., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
17. Selective in vivo molecular and cellular biocompatibility of black peppercorns by piperine-protein intrinsic atomic interaction with elicited oxidative stress and apoptosis in zebrafish eleuthero embryos.
- Author
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Patel P, Panda PK, Kumari P, Singh PK, Nandi A, Mallick MA, Das B, Suar M, and Verma SK
- Subjects
- Alkaloids analysis, Animals, Benzodioxoles analysis, Piper nigrum chemistry, Piper nigrum embryology, Piperidines analysis, Plant Extracts chemistry, Plant Extracts toxicity, Polyunsaturated Alkamides analysis, Seeds chemistry, Seeds toxicity, Superoxide Dismutase metabolism, Tumor Suppressor Protein p53 metabolism, Zebrafish embryology, Zebrafish physiology, Zebrafish Proteins chemistry, Zebrafish Proteins metabolism, Alkaloids chemistry, Apoptosis drug effects, Benzodioxoles chemistry, Oxidative Stress drug effects, Piper nigrum toxicity, Piperidines chemistry, Polyunsaturated Alkamides chemistry
- Abstract
Day to day consumption of black pepper raise concern about the detailed information about their medicinal, pharmaceutical values and knowledge about the biocompatibility with respect to ecosystem. This study investigates the in vivo selective molecular biocompatibility of its seed cover (SC) and seed core (SP) powder extract using embryonic zebrafish model. Gas chromatography mass spectrometry (GCMS) analysis of the extract prepared by grinding showed presence of different components with "piperine" as principle component. Biocompatibility analysis showed dose and time dependent selective effect of SC and SP with LC50 of 30.4 μg/ml and 35.6 μg/ml, respectively on survivability, hatching and heartbeat rate in embryonic zebrafish. Mechanistic investigation elucidated it as effect of accumulation and internalization of black pepper leading to their influence on structure and function of cellular proteins hatching enzyme (he1a), superoxide dismutase (sod1) and tumor protein (tp53) responsible for delayed hatching, oxidative stress induction and apoptosis. The study provided insight to selective biocompatibility of black pepper expedient to produce higher quality spices with respect to pharmaceutical, clinical and environmental aspects., (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
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