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一种用于宫颈内应用前列腺素E2的新型凝胶。

A new gel for intracervical application of prostaglandin E2.

作者信息

Ulmsten U, Kirstein-Pedersen A, Stenberg P, Wingerup L

出版信息

Acta Obstet Gynecol Scand Suppl. 1979;84:19-21. doi: 10.3109/00016347909156817.

Abstract

A new gel-formulation for intracervical application of prostaglandin E2 (PGE2) has been prepared. As a vehicle for the gel a cross-link starch polymer is used. PGE2 substance is added to the starch polymer and after homogenization and lyophilization a PGE2 powder is obtained. The powder can be stored at room temperature for more than four months without inactivation of the prostaglandin. Before clinical application a few ml of saline is added to the powder giving, within 30 seconds, an easily-handled ready to use PGE2-gel. Chemical analysis by spectrophotometric technique reveals that the amount of unchanged PGE2 is the same in the new gel-formulation as in a conventional cellulose gel. In a randomized double-blind study the new PGE2-gel was intracervically applied to twenty nulliparae before abortion by dilatation and evacuation (D & E). Ten women were given a gel containing 0.25 mg PGE2 (PGE2-gel) and ten a gel without PGE2 (placebo gel). It was found that the PGE2-gel, in contrast to the placebo gel, produced a rapid ripening of the cervix facilitating the subsequent D & E. No adverse systemic or local reactions were found during or after the treatment.

摘要

已制备出一种用于宫颈内应用前列腺素E2(PGE2)的新型凝胶制剂。作为凝胶的载体,使用了一种交联淀粉聚合物。将PGE2物质添加到淀粉聚合物中,经过均质化和冻干后得到PGE2粉末。该粉末可在室温下储存四个多月而前列腺素不会失活。在临床应用前,向粉末中加入几毫升生理盐水,在30秒内即可得到易于处理的即用型PGE2凝胶。通过分光光度技术进行的化学分析表明,新型凝胶制剂中未改变的PGE2含量与传统纤维素凝胶中的相同。在一项随机双盲研究中,在通过扩张和刮宫术(D&E)进行流产前,将新型PGE2凝胶宫颈内应用于20名未生育过的女性。10名女性使用含有0.25 mg PGE2的凝胶(PGE2凝胶),10名女性使用不含PGE2的凝胶(安慰剂凝胶)。结果发现,与安慰剂凝胶相比,PGE2凝胶可使宫颈迅速成熟,便于随后的D&E操作。治疗期间及治疗后未发现不良的全身或局部反应。

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