Zhou Zhifeng, Chen Lingyun, Liu Peng, Shen Mei, Zou Fei
Hygiene Detection Center, School of Public Health and Tropical Medicine, Southern Medical University, 1838 North Guangzhou Avenue, Guangzhou 510515, PR China.
Anal Sci. 2010;26(11):1133-8. doi: 10.2116/analsci.26.1133.
A sensitive and accurate high-performance liquid-chromatography method was developed and validated for the simultaneous determination of pyrazinamide (PZA), isoniazid (INH), rifampicin (RFP) and acetylisoniazid (AcINH) in human plasma. Separation was performed on a Max-RP C(12) column using gradient elution and a flow-rate program. The mobile phase was methanol-acetonitrile-buffer (20 mM of heptanesulfonic acid sodium, pH 2.5) with a ratio of 10:8:82 (v/v/v) at the initial phase. All calibration curves had good linearity (r(2) > 0.99) between the test ranges. The intra- and inter-day precision was less than 8.8% in good accuracy (<15%). The limit of detection with a signal-to-noise (S/N) of 3 was 0.014, 0.009, 0.023 and 0.054 µg mL(-1) for PZA, AcINH, INH and RFP, respectively. The method was selective, sensitive and reliable, and is a good alternative for routine therapeutic drug monitoring of the four compounds during the treatment of tuberculosis patients.
建立并验证了一种灵敏、准确的高效液相色谱法,用于同时测定人血浆中的吡嗪酰胺(PZA)、异烟肼(INH)、利福平(RFP)和乙酰异烟肼(AcINH)。采用梯度洗脱和流速程序,在Max-RP C(12)柱上进行分离。流动相为甲醇-乙腈-缓冲液(20 mM庚烷磺酸钠,pH 2.5),初始阶段比例为10:8:82(v/v/v)。所有校准曲线在测试范围内均具有良好的线性(r(2) > 0.99)。日内和日间精密度在良好的准确度(<15%)下小于8.8%。信噪比(S/N)为3时,PZA、AcINH、INH和RFP的检测限分别为0.014、0.009,、0.023和0.054 µg mL(-1)。该方法具有选择性、灵敏性和可靠性,是结核病患者治疗期间对这四种化合物进行常规治疗药物监测的良好替代方法。