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妊娠晚期Sprague-Dawley大鼠中喷他脒的药代动力学

Pharmacokinetics of pentamidine in Sprague-Dawley rats in late pregnancy.

作者信息

Little B B, Harstad T H, Bawdon R E, Sobhi S, Roe D A, Knoll K A, Ghali F E

机构信息

Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas 75235-9032.

出版信息

Am J Obstet Gynecol. 1991 Mar;164(3):927-30. doi: 10.1016/0002-9378(91)90541-x.

Abstract

To our knowledge, placental transfer of pentamidine has not been previously studied in vivo. In the present study, the pharmacokinetics of pentamidine were analyzed in late gestation (18 days) among Sprague-Dawley rats. Pentamidine's kinetics were assessed in the following maternal compartments over a 12-hour period in 16 timed-pregnant rats: serum, liver, and kidney. Placentas were also analyzed for pentamidine concentration as were fetal brain, liver, and kidney tissues. Significant placental transfer of the drug was found, with pentamidine reaching all fetal compartments studied. Notably, by the twelfth hour fetal brain tissue achieved pentamidine concentrations that were not significantly different from those of maternal serum at the second hour of the experiment. This is an interesting observation because adult mouse and rat brains were found to be unexposed to the drug.

摘要

据我们所知,喷他脒的胎盘转运此前尚未在体内进行过研究。在本研究中,对妊娠晚期(18天)的斯普拉格-道利大鼠的喷他脒药代动力学进行了分析。在16只定时怀孕的大鼠中,在12小时内对以下母体隔室中的喷他脒动力学进行了评估:血清、肝脏和肾脏。还分析了胎盘以及胎儿脑、肝和肾组织中的喷他脒浓度。发现该药物有显著的胎盘转运,喷他脒到达了所有研究的胎儿隔室。值得注意的是,到第12小时,胎儿脑组织中的喷他脒浓度与实验第2小时母体血清中的浓度无显著差异。这是一个有趣的观察结果,因为发现成年小鼠和大鼠的大脑未接触该药物。

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