| Literature DB >> 33536904 |
Manjula Gunawardana1, Mariana Remedios-Chan1, Debbie Sanchez1, Simon Webster1, Patricia Galvan1, Rob Fanter1, Amalia E Castonguay1, Paul Webster1, John A Moss1, Joseph Kuo2, Philippe A Gallay2, Kathleen L Vincent3, Massoud Motamedi3, Dana Weinberger4, Mark A Marzinke5,6, Craig W Hendrix5, Marc M Baum1.
Abstract
New HIV-1 infection rates far outpace the targets set by global health organizations, despite important progress in curbing the progression of the epidemic. Long-acting (LA) formulations delivering antiretroviral (ARV) agents for HIV-1 pre-exposure prophylaxis (PrEP) hold significant promise, potentially facilitating adherence due to reduced dosing frequency compared to oral regimens. We have developed a subdermal implant delivering the potent ARV drug tenofovir alafenamide that could provide protection from HIV-1 infection for 6 months, or longer. Implants from the same lot were investigated in mice and sheep for local safety and pharmacokinetics (PKs). Ours is the first report using these animal models to evaluate subdermal implants for HIV-1 PrEP. The devices appeared safe, and the plasma PKs as well as the drug and metabolite concentrations in dermal tissue adjacent to the implants were studied and contrasted in two models spanning the extremes of the body weight spectrum. Drug and drug metabolite concentrations in dermal tissue are key in assessing local exposure and any toxicity related to the active agent. Based on our analysis, both animal models were shown to hold significant promise in LA product development.Entities:
Keywords: HIV prevention; long-acting; pre-exposure prophylaxis; subdermal implant; sustained release; tenofovir alafenamide
Year: 2020 PMID: 33536904 PMCID: PMC7849190 DOI: 10.3389/fphar.2020.569373
Source DB: PubMed Journal: Front Pharmacol ISSN: 1663-9812 Impact factor: 5.810