Journal of Capital Medical University ›› 2026, Vol. 47 ›› Issue (3): 457-469.doi: 10.3969/j.issn.1006-7795.2026.03.007

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Establishment and performance evaluation of a candidate reference method for 4 anti-tuberculosis drugs in human plasma

Miao Wenxuan1,2 ,  Chen Qi3 ,  Mei Shenghui1*   

  1. 1. Department of Pharmacy, Beijing Tiantan Hospital, Capital Medical University, Beijing 100070,  China; 2. Department of Laboratory Medicine, Yanjing Medical College, Capital Medical University, Beijing 101300,   China; 3. Shulan International Medical College of Zhejiang Shuren University, Hangzhou 310000, China
  • Received:2026-02-02 Revised:2026-04-15 Online:2026-06-21 Published:2026-06-26
  • Supported by:
    This study was supported by Beijing Municipal Hospital Administration Cultivation Program (PX2024020) and National Key Research and Development Program (2020YFC2008306).

Abstract: Objective  To establish a candidate reference method for the simultaneous, accurate and sensitive determination of four first-line anti-tuberculosis drugs (rifampicin, isoniazid, pyrazinamide and ethambutol) in human plasma, and to provide technical support for individualized and precise clinical diagnosis and treatment. Methods  An ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed. Rifampicin-d8, isoniazid-d4, ethambutol-d4 and pyrazinamide-d3 were used as internal standards, and acetonitrile was selected as the extraction solvent for the quantitative determination of the four drugs in human plasma. The blood samples were centrifuged, and the supernatant was directly injected for analysis. The mobile phase was composed of 0.1% formic acid aqueous solution (v/v) (A) and methanol (B). The flow rate was set as 0.3 mL/min, the column temperature was set at 40℃ and the injection volume was 1 μL. Methodological validation was performed according to General Chapter 9012 of the Chinese Pharmacopoeia, including specificity, linearity, precision, accuracy, matrix effect and stability. Results  All four drugs showed good linearity in their respective concentration ranges, with all the correlation coefficients (r2) of the calibration curves greater than 0.995. The intra-batch recoveries were in the range of 94.4% to 108.2% with the relative standard deviations (RSD) less than 6.34%, and the inter-batch recoveries were 92.4% to 104.8% with the RSD less than 4.44%. All the validation parameters met the requirements of methodological verification. Conclusion  The established UPLC-MS/MS method for the determination of four first-line anti-tuberculosis drugs in human plasma is accurate, rapid, simple, and highly sensitive, with a wide linear range. It provides a reliable technical basis for therapeutic drug monitoring (TDM) and individualized dosing regimens for anti-tuberculosis treatment.

Key words: anti-tuberculosis drugs, therapeutic drug monitoring, rifampicin, isoniazid, pyrazinamide, ethambutol, ultra performance liquid chromatography-tandem mass spectrometry

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