Reisenberger K, Egarter C, Sternberger B, Eckenberger P, Eberle E, Weissenbacher E R
Department of Obstetrics and Gynecology, University of Vienna, Austria.
Am J Obstet Gynecol. 1996 May;174(5):1450-5. doi: 10.1016/s0002-9378(96)70587-2.
Placental passage of the angiotensin-converting enzyme inhibitors temocapril and enalapril was investigated in a placental perfusion model.
In an open system a placental lobe was perfused on both the maternal and the fetal side with a blood-free medium containing the test substances plus a reference substance on the maternal side. Six placentas were perfused with temocapril and five with enalapril. The drugs were measured by gas chromatography-mass spectrometry.
Both angiotensin-converting enzyme inhibitors crossed the human placenta in the maternal-fetal direction in similar quantities. Temocapril showed the same pharmacokinetic characteristics as enalapril.
This was the first study to quantify the placental transfer of angiotensin-converting enzyme inhibitors. These antihypertensive agents should not be taken during pregnancy, to avoid any potential hazards to the fetus.
在胎盘灌注模型中研究血管紧张素转换酶抑制剂替莫卡普利和依那普利的胎盘转运情况。
在开放系统中,胎盘叶的母体侧和胎儿侧均用不含血液的介质灌注,母体侧介质中含有受试物质加一种参考物质。六个胎盘用替莫卡普利灌注,五个胎盘用依那普利灌注。通过气相色谱 - 质谱法测定药物。
两种血管紧张素转换酶抑制剂均以相似的量沿母胎方向穿过人胎盘。替莫卡普利表现出与依那普利相同的药代动力学特征。
这是首次对血管紧张素转换酶抑制剂的胎盘转运进行定量的研究。孕期不应服用这些降压药,以避免对胎儿造成任何潜在危害。