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采用液相色谱-串联质谱法对人血浆中贝达喹啉进行生物分析:在药代动力学研究中的应用。

Bioanalysis of bedaquiline in human plasma by liquid chromatography-tandem mass spectrometry: Application to pharmacokinetic study.

作者信息

Bezawada Viritha, Mogili Padma, Rao Polagani Srinivasa, Dodda Sireesha

机构信息

Aurora Degree and PG College, Hyderabad, Telangana, India.

Department of Engineering Chemistry, College of Engineering, Andhra University, Visakhapatnam, Andhra Pradesh, India.

出版信息

J Mass Spectrom Adv Clin Lab. 2024 Jan 13;31:27-32. doi: 10.1016/j.jmsacl.2024.01.001. eCollection 2024 Jan.

Abstract

INTRODUCTION

A sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed for estimation of bedaquiline (BDQ) in human plasma using the deuterated analogue of the analyte, bedaquiline-d6 (BDQ-d6) as the internal standard.

METHODS

The plasma sample of 50 µL was extracted by liquid-liquid extraction using methyl tertiary butyl ether (MTBE). The separation was achieved on Zodiac C (50 x 4.6 mm, 5 µm) column with a mobile phase consisting of methanol and 5 mM ammonium formate in 0.1 % formic acid (w/v) (90:10, v/v) at a flow rate of 1.0 mL/min. Protonated analyte and internal standard were detected on a triple quadrupole mass spectrometer using multiple reaction monitoring (MRM) mode.

RESULTS

The linearity of the method was established in the concentration range of 5---1800 ng/mL with correlation coefficient, r ≥ 0.99. All the validated parameters were found well within the limits.

DISCUSSION

The method was applied for the first time to evaluate the pharmacokinetic parameters after single oral dose of BDQ 100 mg under fed conditions in healthy human volunteers, and the results were further authenticated by incurred sample reanalysis.

摘要

引言

建立了一种灵敏的液相色谱 - 串联质谱(LC-MS/MS)方法,以氘代分析物苯达喹啉 - d6(BDQ-d6)作为内标,用于测定人血浆中的苯达喹啉(BDQ)。

方法

50 μL血浆样品采用甲基叔丁基醚(MTBE)进行液 - 液萃取。在Zodiac C(50×4.6 mm,5 µm)柱上进行分离,流动相由甲醇和0.1%甲酸(w/v)中的5 mM甲酸铵(90:10,v/v)组成,流速为1.0 mL/min。在三重四极杆质谱仪上使用多反应监测(MRM)模式检测质子化分析物和内标。

结果

该方法在5---1800 ng/mL浓度范围内建立了线性关系,相关系数r≥0.99。所有验证参数均在规定范围内。

讨论

该方法首次应用于评估健康人类志愿者在进食条件下单次口服100 mg BDQ后的药代动力学参数,结果通过实际样品再分析得到进一步验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d131/10874975/2bfc90cd2149/gr1.jpg

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