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一种热熔挤出阴道内环,用于持续释放抗逆转录病毒微物 UC781。

A hot-melt extruded intravaginal ring for the sustained delivery of the antiretroviral microbicide UC781.

机构信息

CONRAD, Department of Obstetrics and Gynecology, Eastern Virginia Medical School, Arlington, Virginia 22209, USA.

出版信息

J Pharm Sci. 2012 Feb;101(2):576-87. doi: 10.1002/jps.22781. Epub 2011 Oct 4.

DOI:10.1002/jps.22781
PMID:21976110
Abstract

Microbicide intravaginal rings (IVRs) are a promising woman-controlled strategy for preventing sexual transmission of human immunodeficiency virus (HIV). An IVR was prepared and developed from polyether urethane (PU) elastomers for the sustained delivery of UC781, a highly potent nonnucleoside reverse transcriptase inhibitor of HIV-1. PU IVRs containing UC781 were fabricated using a hot-melt extrusion process. In vitro release studies of UC781 demonstrated that UC781 release profiles are loading dependent and resemble matrix-type, diffusion-limited kinetics. The in vitro release methods employed over predicted the in vivo release rates of UC781 in rabbits. Accelerated stability studies showed good chemical stability of UC781 in prototype formulations, but surface crystallization of UC781 was observed following long-term storage at higher UC781 loadings, unless formulated with a polyvinylpyrrolidone/glycerol surface coating. Mechanical stability testing of prototype rings showed moderate stiffening upon storage. The PU and UC781 had minimal to no impact on viability, tissue integrity, barrier function, or cytokine expression in the tissue irritation model, and UC781 was shown to be delivered to and permeate through this tissue construct in vitro. Overall, UC781 was formulated in a stable PU IVR and provided controlled release of UC781 both in vitro and in vivo.

摘要

杀微生物剂阴道环(IVR)是一种有前途的女性控制策略,可用于预防人类免疫缺陷病毒(HIV)的性传播。一种 IVR 是由聚醚型聚氨酯(PU)弹性体制备和开发的,用于持续输送 UC781,这是一种高效的 HIV-1 非核苷类逆转录酶抑制剂。含有 UC781 的 PU IVR 是使用热熔挤出工艺制造的。UC781 的体外释放研究表明,UC781 的释放曲线是负载依赖性的,类似于基质型、扩散限制动力学。所采用的体外释放方法可以预测 UC781 在兔体内的释放率。加速稳定性研究表明,原型配方中 UC781 的化学稳定性良好,但在较高 UC781 负载下长期储存时会观察到 UC781 的表面结晶,除非与聚乙烯吡咯烷酮/甘油表面涂层一起配制。原型环的机械稳定性测试表明,储存时会适度变硬。PU 和 UC781 对组织刺激模型中的细胞活力、组织完整性、屏障功能或细胞因子表达的影响最小或没有影响,并且在体外研究中 UC781 已被证明可输送到并渗透到该组织构建体中。总体而言,UC781 被稳定地配制在 PU IVR 中,并且在体外和体内都提供了 UC781 的控制释放。

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