Matar Kamal M, Marafie Najlaa A
Department of Applied Therapeutics, Faculty of Pharmacy, Kuwait University, Kuwait.
Xenobiotica. 2011 May;41(5):416-21. doi: 10.3109/00498254.2010.549969. Epub 2011 Jan 27.
Pregnancy is associated with various physiological changes that may lead to significant alterations in the pharmacokinetic profiles of many drugs. The present study was designed to investigate the potential effects of pregnancy on the pharmacokinetics of topiramate (TPM) in the rabbit model. Nineteen female New Zealand white rabbits (nine pregnant and 10 non-pregnant) were used in this study. Blood samples were collected from the animals just before receiving TPM orally at a dose of 20 mg/kg and then serially for up to 24 h. TPM plasma samples were analysed using a validated tandem mass spectrometric (LC-MS/MS) method. The mean values of TPM pharmacokinetic parameters (t(1/2), T(max), AUC(0-∞), and CL/F) were significantly modified in pregnant rabbits as compared with non-pregnant group. Pregnancy significantly (P < 0.05) increased TPM half-life (t(1/2)), time to attain the maximum plasma concentration (T(max)), and the area under TPM plasma concentration-time curve (AUC(0-∞)) and decreased the drug's oral clearance (CL/F) compared with non-pregnancy state in rabbits. The present study demonstrates that pregnancy alters the pharmacokinetics of TPM in rabbits in late gestational period and considerable inter-animal variability was observed. The findings of the present study indicate that TPM CL/F is decreased during late pregnancy in the rabbit model.
妊娠与多种生理变化相关,这些变化可能导致许多药物的药代动力学特征发生显著改变。本研究旨在探讨妊娠对兔模型中托吡酯(TPM)药代动力学的潜在影响。本研究使用了19只雌性新西兰白兔(9只怀孕,10只未怀孕)。在动物口服20mg/kg剂量的TPM之前采集血样,然后连续采集长达24小时。使用经过验证的串联质谱(LC-MS/MS)方法分析TPM血浆样本。与未怀孕组相比,怀孕兔的TPM药代动力学参数(t(1/2)、T(max)、AUC(0-∞)和CL/F)的平均值有显著改变。与兔的非妊娠状态相比,妊娠显著(P<0.05)延长了TPM半衰期(t(1/2))、达到最大血浆浓度的时间(T(max))以及TPM血浆浓度-时间曲线下面积(AUC(0-∞)),并降低了药物的口服清除率(CL/F)。本研究表明,妊娠会改变兔妊娠晚期TPM的药代动力学,并且观察到动物间存在相当大的变异性。本研究结果表明,在兔模型中,妊娠晚期TPM的CL/F降低。