Lunell N O, Bondesson U, Grunewald C, Ingemarsson I, Nisell H, Wide-Swensson D
Department of Obstetrics and Gynecology, Karolinska Institute, Hudding University Hospital, Sweden.
Am J Hypertens. 1993 Mar;6(3 Pt 2):110S-111S. doi: 10.1093/ajh/6.3.110s.
The aim of this study was to assess the concentration of isradipine in maternal and fetal plasma, and in amniotic fluid under steady-state conditions. Eight women were treated with 5-mg isradipine tablets twice daily and eight women were given slow-release isradipine capsules (SRO) twice daily for hypertension in pregnancy. Blood and amniotic fluid sampling for analysis of drug concentration was performed at delivery. In the isradipine tablet group, maternal and fetal plasma levels were 788 +/- 701 pg/mL (mean +/- SD) and 270 +/- 90 pg/mL, respectively. The corresponding levels in the SRO-treated group were 463 +/- 217 pg/mL and 185 +/- 95 pg/mL, respectively. In the amniotic fluid, the concentration was 74 +/- 42 pg/mL in the tablet group and 45 +/- 14 pg/mL in the SRO group. Therefore, isradipine passes the placental barrier, but its concentration is considerably lower in the fetal compartments.
本研究的目的是评估稳态条件下孕妇和胎儿血浆以及羊水中伊拉地平的浓度。八名女性每日两次服用5毫克伊拉地平片,八名女性每日两次服用伊拉地平缓释胶囊(SRO)以治疗妊娠期高血压。分娩时采集血液和羊水样本用于分析药物浓度。在伊拉地平片组中,母体和胎儿血浆水平分别为788±701皮克/毫升(平均值±标准差)和270±90皮克/毫升。SRO治疗组的相应水平分别为463±217皮克/毫升和185±95皮克/毫升。在羊水中,片剂组的浓度为74±42皮克/毫升,SRO组为45±14皮克/毫升。因此,伊拉地平可通过胎盘屏障,但其在胎儿各部位的浓度显著较低。