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UPLC-MS/MS同时测定结核患者体内异烟肼、利福平的浓度 被引量:2

Simultaneous Determination of Isoniazid and Rifampin in Tuberculosis Patients by UPLC-MS/MS
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摘要 目的建立超高效液相色谱-串联质谱法(UPLC-MS/MS)检测结核患者体内异烟肼、利福平的浓度。方法血液经过蛋白沉淀,以对乙酰氨基酚为内标采用Thermo Syncronis C_(18)柱(2.1 mm×100 mm,1.7μm)色谱分离,以甲醇和醋酸水溶液(0.1%)梯度洗脱进行UPLC-MS/MS检测。结果异烟肼在0.05~5μg·mL^(-1)内,利福平在0.01~10μg·mL^(-1)内响应值与质量浓度呈良好线性关系,相关系数均大于0.999 0,加标回收率分别为100.5%~102.5%和92.0%~96.4%,检出限分别为0.05和0.01μg·mL^(-1),相对标准偏差(RSD)分别为0.5%~4.3%和1.1%~3.9%。结论采用内标法建立了可同时定量检测INH和RFP的检测方法,该方法特异性好、灵敏度高、重现性和准确度可靠,可用于检测结核患者血液中INH和RFP的浓度。 OBJECTIVE To establish an UPLC-MS/MS method for the determination of isoniazid and rifampin in tuberculosis patients. METHODS The blood protein was precipitated by methanol after adding acetaminophen as internal standard, chromatography separation was performed on Thermo Syncronis C18 column (2.1 mm×100 mm,1.7 μm), gradient elution was conducted using methanol and acetic acid aqueous solution(0.1%) as mobile phase, and MS/MS was used for detection. RESULTS The correlation coefficients were greater than 0.999 0 for isoniazid in the range of 0.05-5 μg·mL^-1 and rifampin in the range of 0.01-10 μg·mL^-1, the recoveries were 100.5%-102.5% and 92.0%-96.4%, the limits of detection were 0.05 and 0.01 μg·mL^-1, and the relative standard deviations (RSDs) were 0.5%-4.3% and 1.1%-3.9%, respectively. CONCLUSION The established internal standard method can simultaneously detect rifampin and isoniazid with good specificity, high sensitivity, reproducibility and accuracy, which can be used to determine the blood concentrations of rifampin and isoniazid in tuberculosis patients.
作者 张瑞雨 师真 李文廷 农蕊瑜 李明武 ZHANG Rui-yu;SHI Zhen;LI Wen-ting;NONG Rui-yu;LI Ming-wu(Kunming Center for Disease Control and Prevention, Kunming 650228, China;Third People′s Hospital of Kunming, Kunming 650041, China)
出处 《中国药学杂志》 CAS CSCD 北大核心 2019年第5期407-410,共4页 Chinese Pharmaceutical Journal
基金 昆明市科技计划重点项目"异烟肼 利福平不同剂型在肺结核治疗中的差异性研究资助(2015-2-S-01429)"
关键词 异烟肼 利福平 结核患者 超高效液相色谱-串联质谱法 isoniazid rifampin tuberculosis patient UPLC/MS/MS
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