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液相色谱串联质谱法测定人血浆中巴洛沙韦酸浓度

何文娟 崔文彦 安雪松 张心慧 李梦豪 李德强 刘秀菊

中国药业2026,Vol.35Issue(3):76-80,5.
中国药业2026,Vol.35Issue(3):76-80,5.DOI:10.3969/j.issn.1006-4931.2026.03.014

液相色谱串联质谱法测定人血浆中巴洛沙韦酸浓度

Concentration Determination of Baloxavir Acid in Human Plasma by LC-MS/MS Method

何文娟 1崔文彦 2安雪松 2张心慧 2李梦豪 2李德强 1刘秀菊1

作者信息

  • 1. 河北医科大学第二医院,河北 石家庄 050000
  • 2. 河北医科大学,河北 石家庄 050017
  • 折叠

摘要

Abstract

Objective To establish a liquid chromatography-tandem mass spectrometry(LC-MS/MS)method for determining the concentration of baloxavir acid in human plasma.Methods After protein precipitation with methanol,plasma samples were analyzed with dolutegravir as the internal standard.The chromatographic column was Phenomenex Luna®-C8 column(50 mm×2.1 mm,3 μm),the mobile phase was methanol-0.1%aqueous formic acid solution(gradient elution),the flow rate was 0.35 mL/min,the column temperature was 25℃,and the injection volume was 10 μL.Electrospray ionization was used with a positive ion mode for multiple reaction monitoring.The ion pairs for analysis with mass-to-charge ratios(m/z)of 484.20 → 247.20(baloxavir acid)and 420.00 → 277.10(dolutegravir)were adopted.Results The linear range of baloxavir acid was 0.50-80.00 ng/mL(r=0.999 3,n=8).The lower limit of quantification was 0.50 ng/mL.The RSDs of the intra-day and inter-day precision tests were in the ranges of 3.27%-5.87%(n=3)and 0.62%-9.12%(n=3),respectively.The RSD of the stability test was lower than 5%.The extraction recovery rate was in the range of 89.90%-96.94%,and the matrix effect was in the range of 100.76%-115.00%.Conclusion This method is simple,highly specific,accurate,and stable,which can be used to determine the concentration of baloxavir acid in human plasma.

关键词

液相色谱串联质谱法/巴洛沙韦酸/血药浓度

Key words

LC-MS/MS/baloxavir acid/blood drug concentration

分类

医药卫生

引用本文复制引用

何文娟,崔文彦,安雪松,张心慧,李梦豪,李德强,刘秀菊..液相色谱串联质谱法测定人血浆中巴洛沙韦酸浓度[J].中国药业,2026,35(3):76-80,5.

基金项目

河北省卫生健康委员会医学科学研究课题计划项目[20211192]. ()

中国药业

1006-4931

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