Suppr超能文献

含淀粉多颗粒片剂在阴道内的分布与滞留情况:通过阴道镜进行评估

Vaginal distribution and retention of tablets comprising starch-based multiparticulates: evaluation by colposcopy.

作者信息

Mehta Samata, Verstraelen Hans, Vandaele Leen, Mehuys Els, Remon Jean Paul, Vervaet Chris

机构信息

Laboratory of Pharmaceutical Technology, Ghent University , Ghent , Belgium.

出版信息

Drug Dev Ind Pharm. 2013 Dec;39(12):1944-50. doi: 10.3109/03639045.2012.723217. Epub 2012 Sep 26.

Abstract

We have developed fast-disintegrating tablets comprising starch-based pellets and excipient granules for intravaginal drug delivery. The purpose of this study was to evaluate the intravaginal disintegration, distribution and retention behavior of these tablets in sheep and women using colposcopy as visualization technique. One tablet was administered to each study subject (n = 6) and repeated colposcopy examination was performed over a 48 h and 24 h period in sheep and women, respectively. Colposcopy in sheep indicated that in vivo tablet disintegration was initiated within 30 min of vaginal administration and that due to disintegration of the pellets themselves, the formulation was transformed into a gel-like mass which distributed throughout the entire vaginal cavity within 2-4 h. In vivo tablet disintegration after intravaginal administration to women was complete within 4 h, whereby the formulation gradually spread throughout the vaginal cavity as complete covering was observed after 12 and 24 h. The persistent retention (up to 24 and 48 h in women and sheep, respectively) confirmed the long retention time of this vaginal formulation.

摘要

我们研发了包含淀粉基微丸和辅料颗粒的速崩片,用于阴道给药。本研究的目的是使用阴道镜作为可视化技术,评估这些片剂在绵羊和女性体内的阴道崩解、分布和滞留行为。给每个研究对象(n = 6)服用一片片剂,并分别在绵羊和女性中于48小时和24小时内进行重复阴道镜检查。绵羊的阴道镜检查表明,体内片剂在阴道给药后30分钟内开始崩解,并且由于微丸本身的崩解,制剂转变为凝胶状物质,在2-4小时内分布于整个阴道腔。给女性阴道给药后的体内片剂崩解在4小时内完成,制剂逐渐扩散至整个阴道腔,在12小时和24小时后观察到完全覆盖。持续滞留(分别在女性和绵羊中长达24小时和48小时)证实了这种阴道制剂的长滞留时间。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验