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液相色谱-串联质谱法同时测定人血浆中的氯苯那敏和伪麻黄碱

Simultaneous determination of chlorpheniramine and pseudoephedrine in human plasma by liquid chromatography-tandem mass spectrometry.

作者信息

Chen Xiaoyan, Zhang Yong, Zhong Dafang

机构信息

Laboratory of Drug Metabolism and Pharmacokinetics, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, People's Republic of China.

出版信息

Biomed Chromatogr. 2004 May;18(4):248-53. doi: 10.1002/bmc.311.

Abstract

A sensitive and specific procedure for simultaneous quantitation of chlorpheniramine and pseudoephedrine in human plasma has been developed and validated. Analytes were extracted from plasma samples by liquid-liquid extraction, separated on a Diamonsil C18 column (250 x 4.6 mm i.d.) and detected by tandem mass spectrometry with an atmospheric pressure chemical ionization interface. Diphenhydramine was used as the internal standard. The method has a lower limit of quantitation of 0.2 and 2.0 ng/mL for chlorpheniramine and pseudoephedrine, respectively. The intra- and inter-day relative standard deviation, calculated from quality control (QC) samples were below 4.3% for chlorpheniramine and below 9.5% for pseudoephedrine. The inter-day relative error as determined from QC samples was within 4.7% for each analyte. The overall extraction recoveries of chlorpheniramine and pseudoephedrine were 77 and 61% on average, respectively. The method was successfully applied to pharmaockinetic study of chlorpheniramine and pseudoephedrine in volunteers receiving formulations containing 4 mg of chlorpheniramine maleate and 60 mg of pseudoephedrine hydrochloride.

摘要

已开发并验证了一种同时定量测定人血浆中氯苯那敏和伪麻黄碱的灵敏且特异的方法。通过液-液萃取从血浆样品中提取分析物,在Diamonsil C18柱(内径250×4.6 mm)上进行分离,并采用大气压化学电离接口的串联质谱进行检测。苯海拉明用作内标。该方法对氯苯那敏和伪麻黄碱的定量下限分别为0.2和2.0 ng/mL。根据质量控制(QC)样品计算的日内和日间相对标准偏差,氯苯那敏低于4.3%,伪麻黄碱低于9.5%。由QC样品确定的日间相对误差,每种分析物均在4.7%以内。氯苯那敏和伪麻黄碱的总体萃取回收率平均分别为77%和61%。该方法成功应用于接受含4 mg马来酸氯苯那敏和60 mg盐酸伪麻黄碱制剂的志愿者中氯苯那敏和伪麻黄碱的药代动力学研究。

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