Wang Li, Zhang Zhujun, Yang Weiping
Department of Chemistry, Shaanxi Normal University, Xi'an 710062, China.
J Pharm Biomed Anal. 2005 Sep 15;39(3-4):399-403. doi: 10.1016/j.jpba.2005.02.046.
In vivo microdialysis was used together with capillary electrophoresis (CE) to monitor the concentration of trimebutine maleate (TM) in rabbit blood. Dialysis probe was perfused at 3 microl/min resulting in relative recovery of 26.6+/-3.1% (n=3). After a one step sample preparation the samples were injected directly into the capillary. TM was detected on-column using UV detector at 214 nm. Separation of TM from other components in the dialysate was achieved within 15 min. Evaluation was based on the relative collected peak height (TM/IS). The response for TM in the blood dialysate was linear over the range of 0.5-100 microg/ml. The detection limit of TM in the blood dialysate was 0.1 microg/ml (S/N=3). This method has been successfully applied to the pharmacokinetic study of trimebutine maleate in rabbit blood following oral administration of 200 mg/kg. It provides a fast and simple technique for the pharmacokinetic study of TM in vivo.
采用体内微透析技术结合毛细管电泳(CE)监测家兔血液中马来酸曲美布汀(TM)的浓度。透析探针以3微升/分钟的速度灌注,相对回收率为26.6±3.1%(n = 3)。经过一步样品制备后,将样品直接注入毛细管。使用紫外检测器在214nm波长处对柱上的TM进行检测。在15分钟内实现了TM与透析液中其他成分的分离。评估基于相对收集峰高(TM/内标)。血液透析液中TM的响应在0.5 - 100微克/毫升范围内呈线性。血液透析液中TM的检测限为0.1微克/毫升(信噪比 = 3)。该方法已成功应用于家兔口服200毫克/千克后马来酸曲美布汀的药代动力学研究。它为体内TM的药代动力学研究提供了一种快速简便的技术。