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

被引:48
作者
Clark, Meredith R. [1 ,2 ]
Johnson, Todd J. [1 ]
Mccabe, R. Tyler [1 ]
Clark, Justin T. [1 ]
Tuitupou, Anthony [1 ]
Elgendy, Hoda [2 ]
Friend, David R. [2 ]
Kiser, Patrick F. [1 ,3 ]
机构
[1] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
[2] Eastern Virginia Med Sch, CONRAD, Dept Obstet & Gynecol, Arlington, VA 22209 USA
[3] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
关键词
UC781; polyurethane; intravaginal ring; microbicides; controlled release; polymeric drug delivery system; extrusion; stability; mucosal drug delivery; in vitro; in vivo release; REVERSE-TRANSCRIPTASE INHIBITOR; NONNUCLEOSIDE INHIBITOR; HIV; SAFETY; DAPIVIRINE; PHARMACOKINETICS; CRYSTALLIZATION; TOLERABILITY; GUAIFENESIN; PREVENTION;
D O I
10.1002/jps.22781
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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. (C) 2011 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 101:576587, 2012
引用
收藏
页码:576 / 587
页数:12
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