首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simultaneous quantitation of paracetamol, caffeine, pseudoephedrine, chlorpheniramine and cloperastine in human plasma by liquid chromatography-tandem mass spectrometry.
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Simultaneous quantitation of paracetamol, caffeine, pseudoephedrine, chlorpheniramine and cloperastine in human plasma by liquid chromatography-tandem mass spectrometry.

机译:液相色谱-串联质谱法同时定量测定人血浆中对乙酰氨基酚,咖啡因,伪麻黄碱,扑尔敏和氯吡汀。

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摘要

A rapid and sensitive method based on liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the simultaneous quantitation of paracetamol, caffeine, pseudoephedrine, chlorpheniramine and cloperastine in human plasma has been developed and validated. After sample preparation by liquid-liquid extraction, the analytes and internal standard (diphenhydramine) were analyzed by reversed-phase HPLC on a Venusil Mp-C(18) column (50mmx4.6mm, 5microm) using formic acid:10mM ammonium acetate:methanol (1:40:60, v/v/v) as mobile phase in a run time of 2.6min. Detection was carried out by electrospray positive ionization mass spectrometry in the multiple-reaction monitoring mode. The method was linear for all analytes over the following concentration (ng/ml) ranges: paracetamol 5.0-2000; caffeine 10-4000; pseudoephedrine 0.25-100; chlorpheniramine 0.05-20; cloperastine 0.10-40. Intra- and inter-day precisions (as relative standard deviation) were all < or =11.3% with accuracy (as relative error) of +/-5.0%. The method was successfully applied to a study of the pharmacokinetics of the five analytes after administration of a combination oral dose to healthy Chinese volunteers.
机译:建立并验证了一种基于液相色谱-串联质谱(LC-MS / MS)的快速灵敏的方法,用于同时定量测定人血浆中对乙酰氨基酚,咖啡因,伪麻黄碱,扑尔敏和氯吡汀。通过液-液萃取制备样品后,使用甲酸:10mM乙酸铵:甲醇,在Venusil Mp-C(18)色谱柱(50mmx4.6mm,5μm)上通过反相HPLC分析分析物和内标(苯海拉明) (1:40:60,v / v / v)作为流动相,运行时间为2.6分钟。通过电喷雾正电离质谱法以多重反应监测模式进行检测。对于以下浓度(ng / ml)范围内的所有分析物,该方法均为线性:扑热息痛5.0-2000;对乙酰氨基酚5.0-2000。咖啡因10-4000;伪麻黄碱0.25-100;氯苯那敏0.05-20;氯吡斯汀0.10-40。日内和日间精度(作为相对标准偏差)均为<或= 11.3%,精度(作为相对误差)为+/- 5.0%。该方法已成功应用于对健康的中国志愿者口服联合剂量后对五种分析物的药代动力学研究。

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