{"title":"液相色谱-串联质谱法对人血浆中的贝达喹啉进行生物分析:在药代动力学研究中的应用","authors":"Viritha Bezawada , Padma Mogili , Srinivasa Rao Polagani , Sireesha Dodda","doi":"10.1016/j.jmsacl.2024.01.001","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>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.</p></div><div><h3>Methods</h3><p>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<sub>18</sub> (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.</p></div><div><h3>Results</h3><p>The linearity of the method was established in the concentration range of 5–––1800 ng/mL with correlation coefficient, r<sup>2</sup> ≥ 0.99. All the validated parameters were found well within the limits.</p></div><div><h3>Discussion</h3><p>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.</p></div>","PeriodicalId":52406,"journal":{"name":"Journal of Mass Spectrometry and Advances in the Clinical Lab","volume":"31 ","pages":"Pages 27-32"},"PeriodicalIF":3.1000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667145X24000014/pdfft?md5=ff1b006fbe489d9590a4699210ba7696&pid=1-s2.0-S2667145X24000014-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Bioanalysis of bedaquiline in human plasma by liquid chromatography-tandem mass spectrometry: Application to pharmacokinetic study\",\"authors\":\"Viritha Bezawada , Padma Mogili , Srinivasa Rao Polagani , Sireesha Dodda\",\"doi\":\"10.1016/j.jmsacl.2024.01.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>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.</p></div><div><h3>Methods</h3><p>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<sub>18</sub> (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.</p></div><div><h3>Results</h3><p>The linearity of the method was established in the concentration range of 5–––1800 ng/mL with correlation coefficient, r<sup>2</sup> ≥ 0.99. All the validated parameters were found well within the limits.</p></div><div><h3>Discussion</h3><p>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.</p></div>\",\"PeriodicalId\":52406,\"journal\":{\"name\":\"Journal of Mass Spectrometry and Advances in the Clinical Lab\",\"volume\":\"31 \",\"pages\":\"Pages 27-32\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2667145X24000014/pdfft?md5=ff1b006fbe489d9590a4699210ba7696&pid=1-s2.0-S2667145X24000014-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Mass Spectrometry and Advances in the Clinical Lab\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667145X24000014\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICAL LABORATORY TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Mass Spectrometry and Advances in the Clinical Lab","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667145X24000014","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
方法 采用甲基叔丁基醚(MTBE)进行液-液萃取,以甲醇和5 mM甲酸铵(0.1%甲酸(体积分数))为流动相,在Zodiac C18 (50 x 4.6 mm, 5 µm)色谱柱上分离,以甲醇和5 mM甲酸铵(0.1%甲酸(体积分数))为内标物,建立了人血浆中贝达喹啉(BDQ)的液相色谱-串联质谱(LC-MS/MS)检测方法。采用 Zodiac C18(50 x 4.6 mm,5 µm)色谱柱,以甲醇和 5 mM 甲酸铵溶于 0.1 % 甲酸(w/v)(90:10, v/v)为流动相,流速为 1.0 mL/min。结果该方法在5--1800 ng/mL浓度范围内线性关系良好,相关系数r2≥0.99。该方法首次应用于健康人志愿者在进食条件下单次口服BDQ 100 mg后的药代动力学参数评价,并对结果进行了再分析。
Bioanalysis of bedaquiline in human plasma by liquid chromatography-tandem mass spectrometry: Application to pharmacokinetic study
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 C18 (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, r2 ≥ 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.