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反相高效液相色谱法有效分离和同时测定人体尿液中7种喹诺酮

Effective separation and simultaneous determination of seven quinolones by reversed phase high performance

中文摘要英文摘要

目 的 建立一种同时检测人体尿液中吡哌酸与6种氟喹诺酮类药物的反相高效液相色谱法。 方 法 色谱柱为ZY1104型C18色谱柱(250 mm×4.6 mm,5 μm),柱温30 ℃,流动相为乙腈–0.02 mol/L四丁基溴化铵–三氟乙酸缓冲液(体积比为9:91, pH 2.87), 流速1.0 ml/min, 检测波长282 nm,进样量20 μl。结 果 7种药物的校准曲线在0.5~100 μg/ml浓度范围内呈良好的线性,相关系数r≥0.9996,检出限为0.036~0.088 μg/ml,样品的平均加标回收率在91.6%~99.5%之间,RSD<7%(n=5)。结 论 所提出的方法简便,快速,可靠,能有效分离和同时测定人体尿液中的多种喹诺酮。

Objective To establish a new method for effective separation and simultaneous determination of pipemidic acid and six fluoroquinolones in human urine by reversed phase high performance liquid chromatography with diode array detector. Methods The chromatographic separation was performed on ZY1104 C18 column (250 mm×4.6 mm, 5μm) at column temperature of 30 ℃. The mobile phase, a mixture of acetonitrile-0.02 mol/L tetrabuty lammonium bromide(v/v=9:91)– trifluoracetic acid buffer (pH 2.87), was delivered at a flow rate of 1.0 ml/min. The detection wavelength was 282 nm and the injection volume was 20 μl. Results The calibration curves for the seven quinolones were good linearity in the range from 0.5 μg/ml to 100 μg/ml with correlation coefficients of ≥ 0.9996. The detection limits were 0.036~0.088 μg/ml.The mean recoveries of the seven drugs ranged from 91.6% to 99.5% with relative standard deviations below 7% (n=5). Conclusion The method was convenient, rapid and accurate for effective separation and simultaneous determination of seven quinolones studied in human urine.

刘广宇、孙汉文、乔凤霞

药学制药化学工业

反相高效液相色谱法吡哌酸氟喹诺酮人体尿液

Reversed phase high performance liquid chromatographyPipemidic acidFluoroquinolonesHuman urine

刘广宇,孙汉文,乔凤霞.反相高效液相色谱法有效分离和同时测定人体尿液中7种喹诺酮[EB/OL].(2008-01-28)[2025-08-02].http://www.paper.edu.cn/releasepaper/content/200801-782.点此复制

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