[Determination of anaprazole in human plasma by LC-MS/MS in pharmacokinetic study].

药学学报 Pub Date : 2016-12-01
Dong-xia Cheng, Xiao-jian Dai, Yi-fan Zhang, Yong-qian Wu, Chong-tie Shi, Xi-feng Ma, Jin Li, Xiao-yan Chen, Da-fang Zhong
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引用次数: 0

Abstract

Anaprazole is a proton pump inhibitor clinically used for curing peptic ulcer. A rapid, sensitive and convenient LC-MS/MS method was first established for the determination of anaprazole in human plasma. d(3), (13)C-anaprazole was used as internal standard (IS). After extraction from human plasma by protein precipitation with acetonitrile, all components were separated on an Extend C(18) column (100 mm × 4.6 mm, 3.5 μm). The assay was linear over the concentration range of 5.00-3 000 ng·m L(-1) (r(2) > 0.995). The method was successfully applied to a pharmacokinetic study of 40 mg anaprazole enteric-coated tablets in 14 Chinese healthy volunteers under fasting or high fat diet conditions. C(max) was (1 020 ± 435) ng·m L(-1) and AUC(0-t) was (2 370 ±754) h·ng·m L(-1) under fasting condition. And C(max) was (538 ± 395) ng·m L(-1) and AUC(0-t) was (1 610 ± 650) h·ng·m L(-1) under high fat diet condition. The plasma results suggest that the exposure of anaprazole is reduced by the high fat diet.

[LC-MS/MS法测定人血浆中阿纳拉唑的药代动力学研究]。
阿那普拉唑是一种质子泵抑制剂,临床上用于治疗消化性溃疡。首次建立了一种快速、灵敏、方便的LC-MS/MS测定人血浆中阿那帕唑的方法。d(3),(13)用c -阿那拉唑作为内标(IS)。用乙腈沉淀蛋白从人血浆中提取后,所有成分在Extend C(18)色谱柱(100 mm × 4.6 mm, 3.5 μm)上分离。在5.00 ~ 3 000 ng·m L(-1)范围内呈线性关系(r(2) > 0.995)。该方法成功应用于14名健康志愿者在空腹和高脂饮食条件下服用40mg阿那帕唑肠溶片的药代动力学研究。禁食条件下C(max)为(1 020±435)ng·m L(-1), AUC(0-t)为(2 370±754)h·ng·m L(-1)。高脂饲粮条件下,C(max)为(538±395)ng·m L(-1), AUC(0-t)为(1 610±650)h·ng·m L(-1)。血浆结果表明,高脂肪饮食减少了阿那普拉唑的暴露。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
药学学报
药学学报 Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.20
自引率
0.00%
发文量
0
期刊介绍: Acta Pharmaceutica Sinica B (APSB) is a bimonthly English peer-reviewed online journal in ScienceDirect, which publishes significant original research articles, communications and high quality reviews of recent advances. APSB encourages submissions from all areas of pharmaceutical sciences, including pharmacology, pharmaceutics, medicinal chemistry, natural products, pharmacognosy, pharmaceutical analysis and pharmacokinetics. APSB is a part of the series Acta Pharmaceutica Sinica, which was founded in 1953. The journal is co-published by Elsevier B.V., in association with the Institute of MateriaMedica, Chinese Academy of Medical Sciences and Chinese Pharmaceutical Association.
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