首页> 外文期刊>Journal of Chromatography, Biomedical Applications >Sensitive liquid chromatographic technique to measure isoniazid in alveolar cells, bronchoalveolar lavage and plasma in HIV-infected patients
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Sensitive liquid chromatographic technique to measure isoniazid in alveolar cells, bronchoalveolar lavage and plasma in HIV-infected patients

机译:灵敏液相色谱技术检测HIV感染患者肺泡细胞,支气管肺泡灌洗液和血浆中的异烟肼

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The need to monitor the effectiveness of antimicrobial drugs in treating opportunistic infections such as tuberculosis in HIV-infected patients requires the development of sensitive assays. A suitable HPLC method was developed to measure the concentration of isoniazid (INH) in plasma 1 h after a standard 300 mg dose and to detect the low levels typically found in alveolar cells obtained by bronchoalveolar lavage of subjects maintained on a standard regimen of the drug, Following extraction with a chloroform-butanol mixture, the INH was back-extracted into dilute acid which was subsequently analyzed by HPLC using a CN reversed-phase column and an acetonitrile-isopropanol based mobile phase. Another HPLC method was developed using direct injection and a polymer based column to measure minute concentrations of INH in the cell-free lavage. In both systems, detection of the drug was accomplished with a sealed coulometric detector (+0.6 V) capable of giving a consistent daily response without adjustment. When saline, cellular extracts and plasma from untreated subjects were spiked with various amounts of INH and analyzed, the lowest level of quantitation was 10, 25 and 100 ng/ml, respectively. Calibration curves showed good linearity when spiked concentrations were compared to peak areas (r=0.991, 0.993 and 0.998, respectively). Alveolar cell extracts and cell-free bronchoalveolar fluid from HIV-positive patients maintained on a standard INH regimen had detectable levels of INH 4 h after a 300 mg oral dose. The plasma INH at 1 h had a range of 0.3-7.1 mu g/ml (n=50). Precision studies with plasma spiked at 0.1, 0.5, 1.0 and 5.0 mu g/ml revealed within-run coefficients of variation (C.V.s) of 8.9, 7.2, 4.2 and 4.9%, respectively and analytical recoveries of 97, 108, 108 and 98%, respectively. The day-to-day C.V.s for the plasma method were 7.6, 4.9 and 3.8% at concentrations of 0.5, 1.0 and 3.0 mu g/ml, respectively. The results suggest that this rugged HPLC technique can quantitate INH in 1 h plasma with good precision and can be used to estimate the very low INH concentrations found in alveolar cells and cell-free lavage recovered from patients undergoing anti-tuberculosis therapy. (C) 1998 Elsevier Science B.V. [References: 13]
机译:需要监测抗微生物药物在治疗机会性感染(如HIV感染的患者的结核病)中的有效性的需求,因此需要开发灵敏的检测方法。开发了一种合适的HPLC方法,以在标准300 mg剂量后1小时测量血浆中的异烟肼(INH)浓度,并检测通过标准方法维持受试者的支气管肺泡灌洗获得的肺泡细胞中通常存在的低水平用氯仿-丁醇混合物萃取后,将INH反萃取至稀酸中,然后使用反相色谱柱和乙腈-异丙醇基流动相通过HPLC分析。使用直接进样和基于聚合物的色谱柱开发了另一种HPLC方法,以测量无细胞灌洗液中INH的微量浓度。在这两个系统中,药物的检测都是通过密封库仑检测器(+0.6 V)完成的,该检测器无需调整即可提供一致的每日响应。当将未经处理的受试者的盐水,细胞提取物和血浆掺入各种量的INH并进行分析时,最低定量水平分别为10、25和100 ng / ml。当将加标浓度与峰面积进行比较时,校准曲线显示出良好的线性(分别为r = 0.991、0.993和0.998)。维持标准INH方案的HIV阳性患者的肺泡细胞提取物和无细胞支气管肺泡液在300 mg口服剂量后4小时具有可检测的INH水平。 1 h时血浆INH的范围为0.3-7.1μg / ml(n = 50)。血浆浓度分别为0.1、0.5、1.0和5.0μg / ml的精密度研究表明,运行中变异系数(CV)分别为8.9、7.2、4.2和4.9%,分析回收率分别为97、108、108和98% , 分别。血浆方法的每日C.V.s在浓度分别为0.5、1.0和3.0μg / ml时分别为7.6、4.9和3.8%。结果表明,这种坚固耐用的HPLC技术可以在1 h血浆中对INH进行高精度定量,可用于估计从接受抗结核治疗的患者的肺泡细胞和无细胞灌洗液中发现的非常低的INH浓度。 (C)1998 Elsevier Science B.V. [参考:13]

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