Suppr超能文献

一种同时测定人血浆中氯氮卓和克利溴铵的新型液相色谱-串联质谱法及其在药代动力学评估中的应用。

A novel LC-MS/MS method for simultaneous estimation of chlordiazepoxide and clidinium in human plasma and its application to pharmacokinetic assessment.

作者信息

Dubey Naveen Kumar, Jain Peeyush, Raj Ankit, Tiwari Sandeep

机构信息

Department Clinical Research, Jubilant Generics Limited, Noida, India.

出版信息

Bioanalysis. 2025 May;17(9):621-628. doi: 10.1080/17576180.2025.2501921. Epub 2025 May 14.

Abstract

A highly sensitive and selective LC-MS/MS assay was developed and validated for the simultaneous quantification of Chlordiazepoxide and Clidinium in human plasma for the first time, employing solid-phase extraction. Chromatographic separation of the analytes and their deuterated internal standards was performed on a reversed-phase Kinetex XB-C18 (150 × 4.6 mm, 5 μm) column with a gradient mobile phase. Mass spectrometric detection was achieved using electrospray ionization in positive ion mode, employing the ion transitions: m/z 300.0 → 227.1 for Chlordiazepoxide, m/z 352.1 → 142.1 for Clidinium, m/z 305.1 → 232.1 for Chlordiazepoxide D5, and m/z 357.2 → 142.2 for Clidinium D5. The assay demonstrated a linear calibration range of 504.0-500,198.3 pg/mL for Chlordiazepoxide and 5.0-3,004.7 pg/mL for Clidinium, ensuring precise pharmacokinetic evaluation. The method was validated with a lower limit of quantification (LLOQ) of 504.0 pg/mL for Chlordiazepoxide and 5.0 pg/mL for Clidinium, precision within 15% RSD, and accuracy within 85-115% of the nominal values. No matrix interference from haemolysed or lipemic plasma was observed, and recovery exceeded 90%. This study presents a novel LC-MS/MS method with significant improvements in sensitivity and specificity, facilitating its direct application in pharmacokinetic and bioequivalence studies.

摘要

首次开发并验证了一种高灵敏度和高选择性的液相色谱-串联质谱(LC-MS/MS)分析法,用于同时定量测定人血浆中的氯氮卓和克利溴铵,采用固相萃取法。在反相Kinetex XB-C18(150×4.6mm,5μm)柱上,使用梯度流动相进行分析物及其氘代内标的色谱分离。采用电喷雾电离正离子模式进行质谱检测,离子跃迁如下:氯氮卓的m/z 300.0→227.1,克利溴铵的m/z 352.1→142.1,氯氮卓D5的m/z 305.1→232.1,克利溴铵D5的m/z 357.2→142.2。该分析法显示氯氮卓的线性校准范围为504.0-500,198.3 pg/mL,克利溴铵的线性校准范围为5.0-3,004.7 pg/mL,确保了精确的药代动力学评估。该方法经验证,氯氮卓的定量下限(LLOQ)为504.0 pg/mL,克利溴铵的定量下限为5.0 pg/mL,精密度在RSD的15%以内,准确度在标称值的85-115%以内。未观察到溶血或高脂血浆的基质干扰,回收率超过90%。本研究提出了一种新颖的LC-MS/MS方法,在灵敏度和特异性方面有显著提高,便于其直接应用于药代动力学和生物等效性研究。

相似文献

本文引用的文献

5
Benzodiazepine metabolism: an analytical perspective.苯二氮䓬类药物的代谢:分析视角
Curr Drug Metab. 2008 Oct;9(8):827-44. doi: 10.2174/138920008786049258.
6
Esophageal rings, webs, and diverticula.食管环、食管蹼和食管憩室。
J Clin Gastroenterol. 1998 Dec;27(4):285-95. doi: 10.1097/00004836-199812000-00003.
7
Clinical pharmacokinetics of chlordiazepoxide.氯氮䓬的临床药代动力学
Clin Pharmacokinet. 1978 Sep-Oct;3(5):381-94. doi: 10.2165/00003088-197803050-00004.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验