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HPLC-DAD 法同时测定人血浆中阿莫西林和舒巴坦浓度及其生物等效性评价

Simultaneous analysis of amoxicillin and sulbactam in human plasma by HPLC-DAD for assessment of bioequivalence.

机构信息

Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University Xiangya School of Medicine, Changsha, Hunan 410078, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Jul 1;879(21):2000-4. doi: 10.1016/j.jchromb.2011.05.021. Epub 2011 May 23.

Abstract

A simple and accurate high-performance liquid chromatography with diode array detection-based (HPLC-DAD) method has been developed and validated for simultaneous determination of amoxicillin and sulbactam in human plasma. Sample preparation was involved in protein precipitation with acetonitrile followed by one-step extraction procedure. Chromatographic separation was achieved on a C18 column with an isocratic mobile phase consisting of water (containing 30 mM potassium dihydrogen phosphate, pH 2.8) and acetonitrile. The detection wavelengths of a diode array detector were set at 210 nm for amoxicillin and sulbactam, and 263 nm for the internal standard (cefadroxil). The method was validated for linearity, accuracy, precision, and stability. The calibration curve was linear from 0.163 to 14.7 μg/mL with correlation coefficient squared of 0.9991 for amoxicillin and 0.250-15.0 μg/mL with correlation coefficient squared of 0.9988 for sulbactam using 500 μL plasma samples. The lower limit of quantification was 0.163 and 0.250 μg/mL for amoxicillin and sulbactam, respectively. The imprecisions of intra- and inter-day validations for amoxicillin and sulbactam were <11% and their accuracies (%) were within the range of 95.4-105.7%. Mean recoveries were 75.9, 72.8, and 70.0% for amoxicillin, sulbactam, and cefadroxil, respectively. The established method was successfully applied to a bioequivalence study of two combination formulations of amoxicillin and sulbactam pivoxil in healthy male volunteers.

摘要

建立并验证了一种简单、准确的高效液相色谱二极管阵列检测法(HPLC-DAD),用于同时测定人血浆中的阿莫西林和舒巴坦。样品制备包括用乙腈进行蛋白沉淀,然后进行一步提取。色谱分离在 C18 柱上进行,采用水(含 30mM 磷酸二氢钾,pH2.8)和乙腈的等度流动相。二极管阵列检测器的检测波长分别设定为 210nm 用于阿莫西林和舒巴坦,263nm 用于内标(头孢羟氨苄)。该方法经过线性、准确度、精密度和稳定性验证。阿莫西林的校准曲线线性范围为 0.163-14.7μg/mL,相关系数平方为 0.9991;舒巴坦的校准曲线线性范围为 0.250-15.0μg/mL,相关系数平方为 0.9988,均采用 500μL 血浆样品。阿莫西林和舒巴坦的定量下限分别为 0.163 和 0.250μg/mL。阿莫西林和舒巴坦日内和日间验证的精密度均<11%,准确度(%)均在 95.4-105.7%范围内。阿莫西林、舒巴坦和头孢羟氨苄的平均回收率分别为 75.9%、72.8%和 70.0%。所建立的方法成功应用于两种阿莫西林和舒巴坦匹伏酯复方制剂在健康男性志愿者中的生物等效性研究。

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