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用于宫颈成熟的控释水凝胶聚合物阴道栓剂中PGE2的体外和体内同步释放。

The concurrent in vitro and in vivo release of PGE2 from a controlled-release hydrogel polymer pessary for cervical ripening.

作者信息

Taylor A V, Boland J, MacKenzie I Z

机构信息

Nuffield Department of Obstetrics & Gynaecology, John Radcliffe Hospital, Headington, Oxford, U.K.

出版信息

Prostaglandins. 1990 Jul;40(1):89-98. doi: 10.1016/0090-6980(90)90059-5.

Abstract

Twenty five patients booked for induction of labour, at 38 weeks or more gestation, were administered a controlled release vaginal polymer pessary containing 10 mg prostaglandin E2 (PGE2), designed to release 0.6 mg per hour in vivo. The release profile from the polymer was linear throughout the eight hour observation period with a correlation coefficient of 0.81, and regression slope of 0.93 mg/hr. with 95% confidence intervals of 0.63 mg/hr. to 1.23 mg/hr. This compared with a concomitant release profile in vitro which was uniform with time for the first five hours, but then continued at a decreasing rate with a correlation coefficient of 0.98. The relationship between PGE2 release and cervical score change was linear, with a correlation coefficient of 0.65. The results show that PGE2 release from the pessary in vivo is predictable, and suggest that the controlled release pessary offers the advantages of greater control of cervical ripening than alternative vehicles currently available.

摘要

25名计划在妊娠38周及以上进行引产的患者使用了一种含有10毫克前列腺素E2(PGE2)的控释阴道聚合物 pessary,该 pessary设计为在体内每小时释放0.6毫克。在整个8小时的观察期内,聚合物的释放曲线呈线性,相关系数为0.81,回归斜率为0.93毫克/小时,95%置信区间为0.63毫克/小时至1.23毫克/小时。相比之下,体外的伴随释放曲线在前5小时随时间均匀,但随后以递减速率持续,相关系数为0.98。PGE2释放与宫颈评分变化之间的关系呈线性,相关系数为0.65。结果表明,体内 pessary中PGE2的释放是可预测的,这表明控释 pessary比目前可用的其他载体具有更好地控制宫颈成熟的优势。

相似文献

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Prostaglandin E2 for cervical ripening: a randomized comparison of Cervidil versus Prepidil.
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