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采用液相色谱-串联质谱法对人血浆中的泮托拉唑进行定量分析,用于药代动力学和生物等效性研究。

Quantification of pantoprazole in human plasma using LC-MS/MS for pharmacokinetics and bioequivalence study.

作者信息

Li Yun, Ding Mei-Juan, Ma Jing, Wang Shu, Wu Xiao-Li, Xu Hui-Juan, Lu Zheng-Yu, Zou Jian-Jun, Fan Hong-Wei, Zhou Xue-Min

机构信息

School of Pharmacy, Nanjing Medical University, and Nanjing First Hospital, Nanjing, 210029, People's Republic of China.

出版信息

Eur J Drug Metab Pharmacokinet. 2011 Jan;35(3-4):147-55. doi: 10.1007/s13318-010-0018-5. Epub 2010 Dec 25.

Abstract

A highly sensitive and rapid method for the analysis of pantoprazole in human plasma using liquid chromatography coupled to tandem electrospray ionization mass spectrometry was developed. The procedure involves a simple protein precipitation method with methyl alcohol and separation by RP-HPLC. Detection was performed by positive ion electrospray ionization in multiple reaction monitoring mode, monitoring the transitions m/z 384.1→200.0 and m/z 346.1→198.0, for quantification of pantoprazole and IS, respectively. The standard calibration curves showed good linearity within the range of 5-5,000 ng mL(-1). The lower limit of quantitation (LLOQ) was about 5 ng mL(-1). The extractive recovery of pantoprazole from the biological matrix was more than 77.58% and the matrix effect was complied with relevant provision. The intra-day accuracy of the drug containing serum samples was more than 92.19% with a precision of 0.79-5.36%. The inter-day accuracy was 85.49% or more, with a precision of 0.91-12.67%. Intra and inter-day accuracy of the assay at four concentrations were 97.9-98.2% with a precision of 4.2-13.9%. This method offered good precision and accuracy and was successfully applied to the pharmacokinetic and bioequivalence studies of 40 mg of enteric-coated pantoprazole in 20 healthy Chinese volunteers.

摘要

建立了一种使用液相色谱-串联电喷雾电离质谱法分析人血浆中泮托拉唑的高灵敏度快速方法。该方法采用甲醇进行简单的蛋白沉淀法,并通过反相高效液相色谱法进行分离。在多反应监测模式下通过正离子电喷雾电离进行检测,分别监测m/z 384.1→200.0和m/z 346.1→198.0的跃迁,用于定量泮托拉唑和内标物。标准校准曲线在5-5000 ng mL(-1)范围内显示出良好的线性。定量下限(LLOQ)约为5 ng mL(-1)。从生物基质中提取泮托拉唑的回收率超过77.58%,基质效应符合相关规定。含药血清样品的日内准确度超过92.19%,精密度为0.79-5.36%。日间准确度为85.49%或更高,精密度为0.91-12.67%。该方法在四个浓度下的日内和日间准确度为97.9-98.2%,精密度为4.2-13.9%。该方法具有良好的精密度和准确度,并成功应用于20名健康中国志愿者中40 mg肠溶泮托拉唑的药代动力学和生物等效性研究。

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