非索非那定
瑞舒伐他汀
怀孕
药代动力学
有机阴离子转运多肽
有机阴离子转运蛋白1
医学
内科学
内分泌学
药理学
妊娠期
化学
运输机
生物化学
生物
遗传学
基因
作者
Álef Machado Gomes Pego,Maria Paula Marques,Fernanda de Lima Moreira,Tiago Antunes Paz,Maria Martha de Barros Tarozzo,Rogério Pereira Mattos,Patrícia Pereira dos Santos Melli,Geraldo Duarte,Ricardo de Carvalho Cavalli,Vera Lúcia Lanchote
摘要
This study investigates the influence of pregnancy on the in vivo activity of the intestinal P-glycoprotein (P-gp) and hepatic organic anion transporters polypeptide (OATP/BCRP) using, respectively, fexofenadine and rosuvastatin as probe drugs. Eleven healthy participants were investigated during the third trimester of pregnancy (Phase 1, 28 to 38 weeks of gestation) and in the postpartum period (Phase 2, 8 to 12 weeks postpartum). In both phases, after administration of a single oral dose of fexofenadine (60 mg) and rosuvastatin (5 mg), serial blood samples were collected for up to 24 h. Rosuvastatin and fexofenadine in plasma were analyzed by LC-MS/MS using previously validated methods. The pharmacokinetic parameters of fexofenadine and rosuvastatin (Phoenix WinNonLin software) with normal distribution (Shapiro-Wilk test) are presented as geometric mean and 90% confidence interval. Phases 1 and 2 were compared using the t test (P < .05). Fexofexadine AUC
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