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采用液相色谱-串联质谱法同时测定人血浆中的对乙酰氨基酚、伪麻黄碱、右美沙芬和氯苯那敏。

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

机构信息

Division of Clinical Pharmacology, the 2nd Affiliated Hospital, College of Medicine, Zhejiang University, 88 Jiefang Road, Hangzhou 310009, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Mar 1;878(7-8):682-8. doi: 10.1016/j.jchromb.2010.01.005. Epub 2010 Jan 18.

Abstract

For the first time, a highly sensitive and simple LC-MS/MS method after one-step precipitation was developed and validated for the simultaneous determination of paracetamol (PA), pseudoephedrine (PE), dextrophan (DT) and chlorpheniramine (CP) in human plasma using diphenhydramine as internal standard (IS). The analytes and IS were separated on a YMC-ODS-AQ C(18) Column (100 mm x 2.0 mm, 3 microm) by a gradient program with mobile phase consisting of 0.3% (v/v) acetic acid and methanol at a flow rate of 0.30 mL/min. Detection was performed on a triple quadrupole tandem mass spectrometer via electrospray ionization in the positive ion mode. The method was validated and linear over the concentration range of 10-5000 ng/mL for PA, 2-1000 ng/mL for PE, 0.05-25 ng/mL for DT and 0.1-50 ng/mL for CP. The accuracies as determined from quality control samples were in range of -8.37% to 3.13% for all analytes. Intra-day and inter-day precision for all analytes were less than 11.54% and 14.35%, respectively. This validated method was successfully applied to a randomized, two-period cross-over bioequivalence study in 20 healthy Chinese volunteers receiving multicomponent formulations containing 325 mg of paracetamol, 30 mg of pseudoephedrine hydrochloride, 15 mg of dextromethorphan hydrobromide and 2 mg of chlorphenamine maleate.

摘要

首次建立并验证了一种在一步沉淀后,通过 LC-MS/MS 测定人血浆中扑热息痛(PA)、伪麻黄碱(PE)、右美沙芬(DT)和氯苯那敏(CP)的高灵敏度、简单方法,内标为苯海拉明。采用梯度洗脱程序,以 0.3%(v/v)乙酸和甲醇为流动相,流速为 0.30 mL/min,在 YMC-ODS-AQ C(18)柱(100mm×2.0mm,3μm)上分离分析物和内标。采用电喷雾电离正离子模式的三重四极杆串联质谱仪进行检测。该方法在 10-5000ng/mL 范围内对 PA、2-1000ng/mL 范围内对 PE、0.05-25ng/mL 范围内对 DT 和 0.1-50ng/mL 范围内对 CP 进行了验证和线性。从质控样品中确定的准确度范围为所有分析物的-8.37%至 3.13%。所有分析物的日内和日间精密度均小于 11.54%和 14.35%。该验证方法成功应用于 20 名健康中国志愿者的随机、两周期交叉生物等效性研究,志愿者接受含有 325mg 扑热息痛、30mg 盐酸伪麻黄碱、15mg 氢溴酸右美沙芬和 2mg 马来酸氯苯那敏的复方制剂。

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