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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Therapeutic drug monitoring of albendazole: Determination of albendazole, albendazole sulfoxide, and albendazole sulfone in human plasma using nonaqueous capillary electrophoresis
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Therapeutic drug monitoring of albendazole: Determination of albendazole, albendazole sulfoxide, and albendazole sulfone in human plasma using nonaqueous capillary electrophoresis

机译:阿苯达唑的治疗药物监测:使用非水毛细管电泳法测定人血浆中的阿苯达唑,阿苯达唑亚砜和阿苯达唑砜

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摘要

A nonaqueous capillary electrophoretic method (NACE) for the fast determination of plasma levels of albendazole (ABZ), albendazole sulfoxide (ABZSO), and albendazole sulfone (ABZSO(2)) is described. TI-le assay is based upon liquid/liquid extraction of these compounds using dichloromethane at pH 10.2 (recovery between 63 and 98%), followed by a NACE separation performed within 8 min employing a 0.036 M berate buffer (apparent pH 9.9) in a mixture of methanol and N-methylfermamide (1:3) and on-column absorbance detection at 280 nm. Using 0.5 mt of plasma and extract reconstitution in 200 mu L N-methylformamide, drug levels between 1.0-10 mu M were found to provide linear calibration graphs. Intraday and interday imprecisions evaluated from peak area ratios (n = 5) were < 10% and < 12%, respectively. Corresponding imprecisions of detection times (n = 5) were < 1% and < 6%, respectively. The limit of detection (LOD) for ABZ, ABZSO and ABZSO(2) was 8 x 10(-7) M. The reliability of the method developed was verified via analysis of 45 plasma samples obtained from patients treated with ABZ. Good agreement was obtained between the levels of ABZSO and those determined by routine HPLC. ABZ was found to be undetectable in all patient samples, whereas the levels of ABZSO(2) were below or close to LOD. [References: 23]
机译:描述了一种用于快速测定血浆阿苯达唑(ABZ),阿苯达唑亚砜(ABZSO)和阿苯达唑砜(ABZSO(2))的非水毛细管电泳方法(NACE)。 TI-le分析是基于使用pH 10.2的二氯甲烷(回收率在63%和98%之间)进行液/液萃取这些化合物的方法,然后在8分钟内使用0.036 M的berate缓冲液(表观pH值为9.9)进行NACE分离。甲醇和N-甲基亚铁酰胺(1:3)的混合物,并在280 nm处进行柱上吸光度检测。使用0.5 mt血浆和提取物在200μL N-甲基甲酰胺中的重构,发现1.0-10μM之间的药物水平可提供线性校准图。根据峰面积比(n = 5)评估的日内和日间不精确度分别为<10%和<12%。相应的检测时间误差(n = 5)分别为<1%和<6%。 ABZ,ABZSO和ABZSO(2)的检出限(LOD)为8 x 10(-7)M。通过分析从ABZ治疗的患者获得的45个血浆样品,验证了所开发方法的可靠性。 ABZSO的水平与常规HPLC测定的水平之间取得了良好的一致性。发现在所有患者样品中均检测不到ABZ,而ABZSO(2)的水平低于或接近LOD。 [参考:23]

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