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Antiretroviral Drugs-Loaded Nanoparticles Fabricated by Dispersion Polymerization with Potential for HIV/AIDS Treatment
Highly active antiretroviral (ARV) therapy (HAART) for chronic suppression of HIV replication has revolutionized the treatment of HIV/AIDS. HAART is no panacea; treatments must be maintained for life. Although great progress has been made in ARV therapy, HIV continues to replicate in anatomical and...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4803317/ https://www.ncbi.nlm.nih.gov/pubmed/27013886 http://dx.doi.org/10.4137/IDRT.S38108 |
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author | Ogunwuyi, Oluwaseun Kumari, Namita Smith, Kahli A. Bolshakov, Oleg Adesina, Simeon Gugssa, Ayele Anderson, Winston A. Nekhai, Sergei Akala, Emmanuel O. |
author_facet | Ogunwuyi, Oluwaseun Kumari, Namita Smith, Kahli A. Bolshakov, Oleg Adesina, Simeon Gugssa, Ayele Anderson, Winston A. Nekhai, Sergei Akala, Emmanuel O. |
author_sort | Ogunwuyi, Oluwaseun |
collection | PubMed |
description | Highly active antiretroviral (ARV) therapy (HAART) for chronic suppression of HIV replication has revolutionized the treatment of HIV/AIDS. HAART is no panacea; treatments must be maintained for life. Although great progress has been made in ARV therapy, HIV continues to replicate in anatomical and intracellular sites where ARV drugs have restricted access. Nanotechnology has been considered a platform to circumvent some of the challenges in HIV/AIDS treatment. Dispersion polymerization was used to fabricate two types (PMM and ECA) of polymeric nanoparticles, and each was successfully loaded with four ARV drugs (zidovudine, lamivudine, nevirapine, and raltegravir), followed by physicochemical characterization: scanning electron microscope, particle size, zeta potential, drug loading, and in vitro availability. These nanoparticles efficiently inhibited HIV-1 infection in CEM T cells and peripheral blood mononuclear cells; they hold promise for the treatment of HIV/AIDS. The ARV-loaded nanoparticles with polyethylene glycol on the corona may facilitate tethering ligands for targeting specific receptors expressed on the cells of HIV reservoirs. |
format | Online Article Text |
id | pubmed-4803317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-48033172016-03-24 Antiretroviral Drugs-Loaded Nanoparticles Fabricated by Dispersion Polymerization with Potential for HIV/AIDS Treatment Ogunwuyi, Oluwaseun Kumari, Namita Smith, Kahli A. Bolshakov, Oleg Adesina, Simeon Gugssa, Ayele Anderson, Winston A. Nekhai, Sergei Akala, Emmanuel O. Infect Dis (Auckl) Original Research Highly active antiretroviral (ARV) therapy (HAART) for chronic suppression of HIV replication has revolutionized the treatment of HIV/AIDS. HAART is no panacea; treatments must be maintained for life. Although great progress has been made in ARV therapy, HIV continues to replicate in anatomical and intracellular sites where ARV drugs have restricted access. Nanotechnology has been considered a platform to circumvent some of the challenges in HIV/AIDS treatment. Dispersion polymerization was used to fabricate two types (PMM and ECA) of polymeric nanoparticles, and each was successfully loaded with four ARV drugs (zidovudine, lamivudine, nevirapine, and raltegravir), followed by physicochemical characterization: scanning electron microscope, particle size, zeta potential, drug loading, and in vitro availability. These nanoparticles efficiently inhibited HIV-1 infection in CEM T cells and peripheral blood mononuclear cells; they hold promise for the treatment of HIV/AIDS. The ARV-loaded nanoparticles with polyethylene glycol on the corona may facilitate tethering ligands for targeting specific receptors expressed on the cells of HIV reservoirs. Libertas Academica 2016-03-20 /pmc/articles/PMC4803317/ /pubmed/27013886 http://dx.doi.org/10.4137/IDRT.S38108 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License. |
spellingShingle | Original Research Ogunwuyi, Oluwaseun Kumari, Namita Smith, Kahli A. Bolshakov, Oleg Adesina, Simeon Gugssa, Ayele Anderson, Winston A. Nekhai, Sergei Akala, Emmanuel O. Antiretroviral Drugs-Loaded Nanoparticles Fabricated by Dispersion Polymerization with Potential for HIV/AIDS Treatment |
title | Antiretroviral Drugs-Loaded Nanoparticles Fabricated by Dispersion Polymerization with Potential for HIV/AIDS Treatment |
title_full | Antiretroviral Drugs-Loaded Nanoparticles Fabricated by Dispersion Polymerization with Potential for HIV/AIDS Treatment |
title_fullStr | Antiretroviral Drugs-Loaded Nanoparticles Fabricated by Dispersion Polymerization with Potential for HIV/AIDS Treatment |
title_full_unstemmed | Antiretroviral Drugs-Loaded Nanoparticles Fabricated by Dispersion Polymerization with Potential for HIV/AIDS Treatment |
title_short | Antiretroviral Drugs-Loaded Nanoparticles Fabricated by Dispersion Polymerization with Potential for HIV/AIDS Treatment |
title_sort | antiretroviral drugs-loaded nanoparticles fabricated by dispersion polymerization with potential for hiv/aids treatment |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4803317/ https://www.ncbi.nlm.nih.gov/pubmed/27013886 http://dx.doi.org/10.4137/IDRT.S38108 |
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