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高效液相色谱法测定马来酸桂哌齐特及其在大鼠体内药代动力学研究中的应用。

High performance liquid chromatographic method for the determination of cinepazide maleate and its application to a pharmacokinetic study in rats.

机构信息

Department of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, PR China.

Department of Clinical Pharmacology, General Hospital of Beijing Military Command of PLA, Beijing 100700, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Apr 15;957:105-9. doi: 10.1016/j.jchromb.2014.02.038. Epub 2014 Mar 4.

Abstract

A simple and reliable high performance liquid chromatographic (HPLC) method has been developed and validated to quantify cinepazide maleate, a calcium blocker, in rat plasma. Cinepazide maleate and Tinidazole (internal standard) have been extracted by a simple liquid-liquid extraction before injection into chromatographic system. Chromatographic separation was achieved on a reversed phase C18 column with a mobile phase consisted of a water mixture of 10mM potassium dihydrogen phosphate (pH=4.5):methanol (40:60, v/v), pumped at flow rate of 1.0mL/min, and detected at 303nm. The method exhibited a linear range of 0.12-120μg/mL in blank rat plasma, with the lower detection limit of 0.06μg/mL. The method was statistically validated for linearity, accuracy, precision, selectivity and stability following FDA guidelines. The intra- and inter-assay coefficients of variation did not exceed ±15% from the nominal concentration. The accuracy of cinepazide maleate was within ±15% of the theoretical value. The assay has been applied successfully in a pharmacokinetic study of cinepazide maleate after a single intravenous at three doses in rat. And cinepazide maleate injection can improve the bioavailability of cinepazide maleate greatly, and has a dose-dependence profile in rats.

摘要

已经建立并验证了一种简单可靠的高效液相色谱(HPLC)方法,用于定量测定马来酸桂哌齐特(一种钙通道阻滞剂)在大鼠血浆中的浓度。在进样到色谱系统之前,马来酸桂哌齐特和替硝唑(内标)通过简单的液-液萃取进行提取。在反相 C18 柱上,以水相为 10mM 磷酸二氢钾(pH=4.5):甲醇(40:60,v/v)的混合物作为流动相,以 1.0mL/min 的流速泵入,在 303nm 处检测,实现了色谱分离。该方法在空白大鼠血浆中的线性范围为 0.12-120μg/mL,检测下限为 0.06μg/mL。该方法根据 FDA 指南进行了线性、准确性、精密度、选择性和稳定性的统计验证。内标和日间变异系数均不超过标称浓度的±15%。马来酸桂哌齐特的准确度在理论值的±15%范围内。该方法已成功应用于大鼠三种剂量单次静脉注射后马来酸桂哌齐特的药代动力学研究。马来酸桂哌齐特注射液可显著提高马来酸桂哌齐特的生物利用度,并在大鼠体内呈剂量依赖性。

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