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非水相硅酮弹性体凝胶作为 HIV-1 进入抑制剂马拉维若的阴道杀微生物剂递送系统。

Non-aqueous silicone elastomer gels as a vaginal microbicide delivery system for the HIV-1 entry inhibitor maraviroc.

机构信息

School of Pharmacy, Queen's University Belfast, Belfast BT9 7BL, UK.

出版信息

J Control Release. 2011 Dec 10;156(2):161-9. doi: 10.1016/j.jconrel.2011.08.006. Epub 2011 Aug 12.

Abstract

Aqueous semi-solid polymeric gels, such as those based on hydroxyethylcellulose (HEC) and polyacrylic acid (e.g. Carbopol®), have a long history of use in vaginal drug delivery. However, despite their ubiquity, they often provide sub-optimal clinical performance, due to poor mucosal retention and limited solubility for poorly water-soluble actives. These issues are particularly pertinent for vaginal HIV microbicides, since many lead candidates are poorly water-soluble and where a major goal is the development of a coitally independent, once daily gel product. In this study, we report the use of a non-aqueous silicone elastomer gel for vaginal delivery of the HIV-1 entry inhibitor maraviroc. In vitro rheological, syringeability and retention studies demonstrated enhanced performance for silicone gels compared with a conventional aqueous HEC gel, while testing of the gels in the slug model confirmed a lack of mucosal irritancy. Pharmacokinetic studies following single dose vaginal administration of a maraviroc silicone gel in rhesus macaques showed higher and sustained MVC levels in vaginal fluid, vaginal tissue and plasma compared with a HEC gel containing the same maraviroc loading. The results demonstrate that non-aqueous silicone gels have potential as a formulation platform for coitally independent vaginal HIV microbicides.

摘要

水凝胶和半固体聚合物凝胶,如羟乙基纤维素(HEC)和聚丙烯酸(如 Carbopol®)凝胶,在阴道给药中有着悠久的应用历史。然而,尽管它们广泛应用,但由于较差的黏膜保留性和有限的对低水溶性活性成分的溶解度,它们通常提供的临床效果并不理想。这些问题在阴道用 HIV 微凝胶中尤为突出,因为许多候选药物的水溶性较差,而主要目标是开发一种无需性交、每日一次的凝胶产品。在这项研究中,我们报告了使用非水性硅酮弹性体凝胶来传递 HIV-1 进入抑制剂马拉维若。体外流变学、可推注性和保留性研究表明,与传统的水性 HEC 凝胶相比,硅酮凝胶具有更好的性能,而在弹丸模型中的凝胶测试证实了其对黏膜没有刺激性。在恒河猴中进行单次阴道给予马拉维若硅酮凝胶的药代动力学研究表明,与含有相同马拉维若载药量的 HEC 凝胶相比,阴道液、阴道组织和血浆中的 MVC 水平更高且更持久。这些结果表明,非水性硅酮凝胶有可能成为一种无需性交的阴道用 HIV 微凝胶的制剂平台。

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