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Biophysical characterization of small molecule antiviral-loaded nanolipogels for HIV-1 chemoprophylaxis and topical mucosal application

机译:用于HIV-1化学预防和局部黏膜应用的小分子抗病毒纳米脂质凝胶的生物物理表征

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摘要

Nanocarriers are versatile vehicles for drug delivery, and emerging as platforms to formulate and deliver multiple classes of antiretroviral (ARV) drugs in a single system. Here we describe the fabrication of hydrogel-core and lipid-shell nanoparticles (nanolipogels) for the controlled loading and topical, vaginal delivery of maraviroc (MVC) and tenofovir disoproxil fumarate (TDF), two ARV drugs with different mechanisms of action that are used in the treatment of HIV. The nanolipogel platform was used to successfully formulate MVC and TDF, which produced ARV drug-loaded nanolipogels that were characterized for their physical properties and antiviral activity against HIV-1 BaL in cell culture. We also show that administration of these drug carriers topically to the vaginal mucosa in a murine model leads to antiviral activity against HIV-1 BaL in cervicovaginal lavages. Our results suggest that nanolipogel carriers are promising for the encapsulation and delivery of hydrophilic small molecule ARV drugs, and may expand the nanocarrier systems being investigated for HIV prevention or treatment.
机译:纳米载体是用于药物输送的多功能载体,并且正在成为在单个系统中配制和输送多种类型的抗逆转录病毒(ARV)药物的平台。在这里,我们描述了水凝胶核心和脂质壳纳米粒子(nanolipogels)的制备,用于控制装载和局部递送maraviroc(MVC)和替诺福韦富马酸替诺福韦酯(TDF),这两种具有不同作用机制的ARV药物治疗艾滋病毒。纳米脂质凝胶平台用于成功配制MVC和TDF,从而生产出载有抗逆转录病毒药物的纳米脂质凝胶,其特征在于其物理特性和在细胞培养物中针对HIV-1 BaL的抗病毒活性。我们还显示,在鼠模型中将这些药物载体局部给药至阴道粘膜可导致宫颈阴道灌洗液中抗HIV-1 BaL的抗病毒活性。我们的结果表明,纳米脂质凝胶载体有望用于亲水性小分子ARV药物的包封和递送,并且可能会扩展正在研究的用于HIV预防或治疗的纳米载体系统。

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