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一种经过验证的液相色谱-串联质谱分析法,用于分析尿液中的异烟肼及其代谢产物乙酰异烟肼。

A validated liquid chromatography-tandem mass spectrometry assay for the analysis of isoniazid and its metabolite acetyl-isoniazid in urine.

作者信息

Maputla Sydwell Poulo, Van Dalen Willem, Joubert Anton, Norman Jennifer, Castel Sandra, van der Merwe Marthinus, Wiesner Lubbe

机构信息

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

出版信息

J Mass Spectrom Adv Clin Lab. 2024 Feb 6;32:11-17. doi: 10.1016/j.jmsacl.2024.02.001. eCollection 2024 Apr.

Abstract

INTRODUCTION

Isoniazid (INH) is one of the most effective and potent first-line anti-tubercular drug. INH is also effectively administered as a preventative monotherapy and has been shown to significantly reduce TB incidence. INH is primarily metabolised to acetyl-isoniazid (AcINH) in the liver. AcINH is mainly excreted in urine presenting as a target for monitoring adherence to INH therapy.

OBJECTIVE

The study aimed to develop and fully validate a bioanalytical method using liquid chromatography-tandem mass spectrometry for the quantification of INH and AcINH in human urine.

METHODS

The samples were prepared using solid phase extraction, with the internal standards isoniazid-d4 and acetyl-isoniazid-d4 being used. The extracts were chromatographed on an Atlantis T3 analytical column with an isocratic mobile phase. For detection, a AB Sciex™ API 5500 triple quadrupole mass spectrometer was used at unit resolution in the multiple reaction monitoring mode, following positive electrospray ionization.

RESULTS

The analytical method demonstrated sufficient sensitivity, as indicated by average signal-to-noise ratios of 7.07 and 6.23 at the lower limit of quantification for INH and AcINH, respectively. Validation was performed over three consecutive batches, demonstrating accuracy, precision, and overall robustness based on peak area ratios within the analytical range of 0.234-30.0 µg/mL for both INH and AcINH. All required validation experiments were assessed and met the acceptance criteria guidelines of the US Food and Drug Administration and European Medicines Agency. The validated method was utilized to measure concentrations of AcINH in urine as a means of assessing adherence to the intake of isoniazid in order to prevent TB infection during a phase III open-label multicenter trial.

CONCLUSION

A bioanalytical method was developed and fully validated for quantifying isoniazid (INH) and acetyl-isoniazid (AcINH) in 100 µL of human urine.

摘要

引言

异烟肼(INH)是最有效且强效的一线抗结核药物之一。异烟肼作为预防性单一疗法给药也很有效,并且已被证明能显著降低结核病发病率。异烟肼主要在肝脏中代谢为乙酰异烟肼(AcINH)。乙酰异烟肼主要经尿液排泄,可作为监测异烟肼治疗依从性的一个指标。

目的

本研究旨在开发并全面验证一种采用液相色谱 - 串联质谱法测定人尿液中异烟肼和乙酰异烟肼含量的生物分析方法。

方法

样品采用固相萃取法制备,使用内标物异烟肼 - d4和乙酰异烟肼 - d4。提取物在Atlantis T3分析柱上进行色谱分离,采用等度流动相。检测时,使用AB Sciex™ API 5500三重四极杆质谱仪,在正电喷雾电离后,于多反应监测模式下以单位分辨率运行。

结果

该分析方法显示出足够的灵敏度,异烟肼和乙酰异烟肼在定量下限处的平均信噪比分别为7.07和6.23。连续三个批次进行了验证,基于异烟肼和乙酰异烟肼在0.234 - 30.0 μg/mL分析范围内的峰面积比,证明了该方法的准确性、精密度和整体稳健性。所有必需的验证实验均经评估并符合美国食品药品监督管理局和欧洲药品管理局的验收标准指南。在一项III期开放标签多中心试验中,该经过验证的方法被用于测量尿液中乙酰异烟肼的浓度,以此作为评估异烟肼摄入依从性的一种手段,以预防结核感染。

结论

开发并全面验证了一种生物分析方法,用于定量100 μL人尿液中的异烟肼(INH)和乙酰异烟肼(AcINH)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e05c/10865391/ff9594277892/gr1.jpg

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