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Spherical PEG/SiO(2) promising agents for Lamivudine antiviral drug delivery, a molecular dynamics simulation study
Spherical nanocarriers can lead to a bright future to lessen problems of virus infected people. Spherical polyethylene glycol (PEG) and spherical silica (SiO(2)) are novel attractive nanocarriers as drug delivery agents, especially they are recently noticed to be reliable for antiviral drugs like an...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969043/ https://www.ncbi.nlm.nih.gov/pubmed/36849795 http://dx.doi.org/10.1038/s41598-023-30493-3 |
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author | Razzaghi, Sahar Vafaee, Mohsen Kharazian, Bahar Nasrollahpour, Mokhtar |
author_facet | Razzaghi, Sahar Vafaee, Mohsen Kharazian, Bahar Nasrollahpour, Mokhtar |
author_sort | Razzaghi, Sahar |
collection | PubMed |
description | Spherical nanocarriers can lead to a bright future to lessen problems of virus infected people. Spherical polyethylene glycol (PEG) and spherical silica (SiO(2)) are novel attractive nanocarriers as drug delivery agents, especially they are recently noticed to be reliable for antiviral drugs like anti-HIV, anti-covid-19, etc. Lamivudine (3TC) is used as a first line drug for antiviral therapy and the atomic view of 3TC-PEG/SiO(2) complexes enable scientist to help improve treatment of patients with viral diseases. This study investigates the interactions of 3TC with Spherical PEG/SiO(2), using molecular dynamics simulations. The mechanism of adsorption, the stability of systems and the drug concentration effect are evaluated by analyzing the root mean square deviation, the solvent accessible surface area, the radius of gyration, the number of hydrogen bonds, the radial distribution function, and Van der Waals energy. Analyzed data show that the compression of 3TC is less on PEG and so the stability is higher than SiO(2); the position and intensity of the RDF peaks approve this stronger binding of 3TC to PEG as well. Our studies show that PEG and also SiO(2) are suitable for loading high drug concentrations and maintaining their stability; therefore, spherical PEG/SiO(2) can reduce drug dosage efficiently. |
format | Online Article Text |
id | pubmed-9969043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99690432023-02-28 Spherical PEG/SiO(2) promising agents for Lamivudine antiviral drug delivery, a molecular dynamics simulation study Razzaghi, Sahar Vafaee, Mohsen Kharazian, Bahar Nasrollahpour, Mokhtar Sci Rep Article Spherical nanocarriers can lead to a bright future to lessen problems of virus infected people. Spherical polyethylene glycol (PEG) and spherical silica (SiO(2)) are novel attractive nanocarriers as drug delivery agents, especially they are recently noticed to be reliable for antiviral drugs like anti-HIV, anti-covid-19, etc. Lamivudine (3TC) is used as a first line drug for antiviral therapy and the atomic view of 3TC-PEG/SiO(2) complexes enable scientist to help improve treatment of patients with viral diseases. This study investigates the interactions of 3TC with Spherical PEG/SiO(2), using molecular dynamics simulations. The mechanism of adsorption, the stability of systems and the drug concentration effect are evaluated by analyzing the root mean square deviation, the solvent accessible surface area, the radius of gyration, the number of hydrogen bonds, the radial distribution function, and Van der Waals energy. Analyzed data show that the compression of 3TC is less on PEG and so the stability is higher than SiO(2); the position and intensity of the RDF peaks approve this stronger binding of 3TC to PEG as well. Our studies show that PEG and also SiO(2) are suitable for loading high drug concentrations and maintaining their stability; therefore, spherical PEG/SiO(2) can reduce drug dosage efficiently. Nature Publishing Group UK 2023-02-27 /pmc/articles/PMC9969043/ /pubmed/36849795 http://dx.doi.org/10.1038/s41598-023-30493-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Razzaghi, Sahar Vafaee, Mohsen Kharazian, Bahar Nasrollahpour, Mokhtar Spherical PEG/SiO(2) promising agents for Lamivudine antiviral drug delivery, a molecular dynamics simulation study |
title | Spherical PEG/SiO(2) promising agents for Lamivudine antiviral drug delivery, a molecular dynamics simulation study |
title_full | Spherical PEG/SiO(2) promising agents for Lamivudine antiviral drug delivery, a molecular dynamics simulation study |
title_fullStr | Spherical PEG/SiO(2) promising agents for Lamivudine antiviral drug delivery, a molecular dynamics simulation study |
title_full_unstemmed | Spherical PEG/SiO(2) promising agents for Lamivudine antiviral drug delivery, a molecular dynamics simulation study |
title_short | Spherical PEG/SiO(2) promising agents for Lamivudine antiviral drug delivery, a molecular dynamics simulation study |
title_sort | spherical peg/sio(2) promising agents for lamivudine antiviral drug delivery, a molecular dynamics simulation study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969043/ https://www.ncbi.nlm.nih.gov/pubmed/36849795 http://dx.doi.org/10.1038/s41598-023-30493-3 |
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