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LC-MS/MS 中有限同位素标记内标同时定量分析 11 种抗癫痫药物:准确度评估。

Simultaneous quantification of 11 antiepileptic drugs using limited isotope-labeled internal standards in LC-MS/MS: An accuracy assessment.

机构信息

Organic Metrology Group, Korea Research Institute of Standards and Science, Yuseong-gu, Daejeon 34113, Republic of Korea; Department of Bio-Analytical Science, University of Science and Technology, 217 Gajeong-ro, Yuseong-gu, Daejeon 34113, Republic of Korea; Department of Nutrition and Food Science, National Research Centre, Dokki, Cairo 12622, Egypt.

Organic Metrology Group, Korea Research Institute of Standards and Science, Yuseong-gu, Daejeon 34113, Republic of Korea; Department of Bio-Analytical Science, University of Science and Technology, 217 Gajeong-ro, Yuseong-gu, Daejeon 34113, Republic of Korea.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2024 Jun 1;1240:124143. doi: 10.1016/j.jchromb.2024.124143. Epub 2024 May 10.

DOI:10.1016/j.jchromb.2024.124143
PMID:38761469
Abstract

This study aims to establish an LC-MS/MS method to simultaneously analyze 11 antiepileptic drugs with a particular focus on maintaining accuracy while reducing the number of isotope-labeled internal standards employed for cost-effectiveness. By applying a water/acetonitrile gradient elution containing 0.1 % formic acid and 2 mM ammonium formate as the mobile phase, optimal sensitivity for the target drugs could be obtained in positive ESI mode in LC-MS/MS. After optimizing various extraction techniques, extraction with 70 % acetonitrile was selected as it provided good recoveries (>93 %) for all targets without matrix effects. Accuracies within 3 % were achieved from the combination of six internal standards, while accuracies of 5 % and 10 % were obtained by reducing the number of internal standards to four and two, respectively, for more economical analysis. The accuracy of the established method was maintained in hyperglycemia, hyperlipidemia, and hyperalbuminemia sera, suggesting that it can be successfully applied to individual serum samples with various properties.

摘要

本研究旨在建立一种 LC-MS/MS 方法,同时分析 11 种抗癫痫药物,特别关注在降低成本效益的同时保持准确性,减少使用的同位素标记内标数量。通过应用含有 0.1%甲酸和 2mM 甲酸铵的水/乙腈梯度洗脱作为流动相,在 LC-MS/MS 的正电喷雾模式下,可以获得目标药物的最佳灵敏度。在优化了各种提取技术后,选择 70%乙腈进行提取,因为它对所有目标都提供了良好的回收率(>93%),且无基质效应。通过使用六个内标组合,可以达到 3%以内的准确度,而通过将内标数量减少到四个和两个,分别可以获得 5%和 10%的准确度,从而实现更经济的分析。该方法在高血糖、高血脂和高白蛋白血症血清中的准确度得以保持,表明它可以成功应用于具有各种性质的个体血清样本。

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