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Antiretroviral Drugs-Loaded Nanoparticles Fabricated by Dispersion Polymerization with Potential for HIV/AIDS Treatment
Author(s) -
Oluwaseun Ogunwuyi,
Namita Kumari,
Kahli Smith,
Oleg Bol’shakov,
Simeon K. Adesina,
Ayele Gugssa,
Winston A. Anderson,
Sergeï Nekhai,
Emmanuel O. Akala
Publication year - 2016
Publication title -
infectious diseases research and treatment
Language(s) - English
Resource type - Journals
ISSN - 1178-6337
DOI - 10.4137/idrt.s38108
Subject(s) - zidovudine , lamivudine , raltegravir , polyethylene glycol , medicine , peripheral blood mononuclear cell , nevirapine , nanoparticle , zeta potential , virology , pharmacology , nanotechnology , human immunodeficiency virus (hiv) , in vitro , materials science , chemistry , antiretroviral therapy , virus , viral load , viral disease , hepatitis b virus , organic chemistry , biochemistry
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.

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