Journal of controlled release : official journal of the Controlled Release Society · 2025
Ultra-long-acting injectable, biodegradable, and removable in-situ forming implant with cabotegravir for HIV prevention.
СтатьяПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
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Le Thy, Young Isabella C, King Jasmine L, Cottrell Mackenzie L, Kumbhar Amar Shankar, Sykes Craig, Schauer Amanda, De la Cruz Gabriela, Kozuszek Caleb T, Kalathil Nanditha Chundayil, Abel Alexandra, Sellers Rani S, Kashuba Angela D M, Benhabbour S Rahima
Аннотация
HIV is a global health issue affecting approximately 40 million people worldwide, with low patient adherence being the primary challenge for maintaining effective pre-exposure prophylaxis (PrEP). Limitations of oral PrEP are mainly attributed to lack of adherence due to pill fatigue or stigma [1, 2]. Recently introduced long-acting injectables offer several advantages over daily PrEP, namely by improving adherence and improving efficacy [3-5]. The approved long-acting injectable Apretude® is administered every two months and elicits a long pharmacokinetic tail of >15 months that can lead to potential drug-resistant virus [6]. To address these limitations, we report on an ultra-long-acting injectable cabotegravir/barium sulfate (CAB/BaSO₄) in-situ forming implant (ISFI) capable of maintaining therapeutic CAB concentrations (> 4× PA-IC90) for up to 390 days. In this work, we optimized the ISFI formulation to include a contrast agent, BaSO4, to assess in vivo depot visualization and migration using X-ray imaging. CAB/BaSO4 ISFIs were investigated in vitro to determine CAB release kinetics, and in vivo to assess safety and pharmacokinetics in BALB/c mice. The CAB/BaSO₄ ISFI was well-tolerated and showed minimal to moderate signs of local inflammation and none to minimal systemic inflammation. At 24 hours post removal of the CAB/BaSO₄ ISFI, CAB plasma concentrations reached below the 1×PA-IC90 benchmark and below the limit of quantification within 14 days for 5 out of 6 mice. A full biodistribution study showed that CAB was mainly localized at the injection site subcutaneous tissue and plasma, with no detectable concentrations in other organs. Whole-body X-ray imaging showed that implants were visible for up to 268 days post administration with no noticeable migration. This is the first report of a CAB/BaSO₄ ISFI that is imageable, ultra-long-acting (>180 days), biodegradable, and removable, that can potentially revolutionize current HIV PrEP and help curb the global HIV epidemic.