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通过超高效液相色谱-串联质谱法对血浆中耐多药结核病药物JBD0131及其代谢物进行定量分析:在人体首次研究中的应用

Quantification of MDR-TB drug JBD0131 and its metabolite in plasma via UPLC-MS/MS: application in first-in-human study.

作者信息

Gao Tiantao, Ou Xiaoxue, Miao Jia, Qin Yongping

机构信息

Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, 610041, China.

NMPA Key Laboratory for Clinical Research and Evaluation of Innovative Drug, Clinical Trial Center, West China Hospital, Sichuan University, Chengdu, 610041, China.

出版信息

Bioanalysis. 2024 Dec-Dec;16(23-24):1229-1240. doi: 10.1080/17576180.2024.2404311. Epub 2024 Oct 7.

Abstract

JBD0131, a novel anti-multidrug-resistant tuberculosis (MDR-TB) drug, can target and inhibit the synthesis of mycolic acids, which are crucial components of the cell wall of the complex. To support the results of this clinical trial in healthy subjects, development of a specific and accurate quantification method for detecting JBD0131 and its metabolite DM131 in human plasma is needed. Samples with prior added stabilizer were pretreated by protein precipitation method and the extracts were subjected to ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). The m/z transitions for the precursor/product ion pairs were 402.1/273 for JBD0131, 333.1/273 for DM131 and 386.1/257 for the internal standard (IS). This method showed good linearity from 1 to 2000 ng/ml for JBD0131 and 0.25 to 500 ng/ml for DM131 and was validated in terms of selectivity, linearity, accuracy, precision, matrix effect, recovery of pretreament and stability. This method was sensitive and specific for measuring the plasma concentrations of JBD0131 and its metabolites. And it was applied for the investigation of the pharmacokinetics of JBD0131 and DM131 in a clinical trial.

摘要

JBD0131是一种新型抗耐多药结核病(MDR-TB)药物,可靶向并抑制分枝菌酸的合成,而分枝菌酸是该菌细胞壁的关键成分。为了支持这项在健康受试者中进行的临床试验结果,需要开发一种特异性强且准确的定量方法,用于检测人血浆中的JBD0131及其代谢物DM131。对预先添加了稳定剂的样品采用蛋白沉淀法进行预处理,提取物采用超高效液相色谱-串联质谱法(UPLC-MS/MS)分析。JBD0131的前体离子/产物离子对的m/z转换为402.1/273,DM131为333.1/273,内标(IS)为386.1/257。该方法在1至2000 ng/ml范围内对JBD0131呈现良好的线性,在0.25至500 ng/ml范围内对DM131呈现良好的线性,并在选择性、线性、准确性、精密度、基质效应、预处理回收率和稳定性方面得到了验证。该方法对测定JBD0131及其代谢物的血浆浓度具有灵敏性和特异性。并且它被应用于一项临床试验中JBD0131和DM131的药代动力学研究。

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