Laboratory of Drug Informatics, Gifu Pharmaceutical University, Gifu, Japan.
J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Apr 15;879(13-14):1029-32. doi: 10.1016/j.jchromb.2011.03.008. Epub 2011 Mar 10.
A direct-injection HPLC-based method has been developed for determining amounts of micafungin in human plasma using a novel hydrophobic/hydrophilic hybrid ODS column. The method is easy to perform and requires only 10 μL of a filtered plasma sample. The chromatographic separations were carried out with a gradient mode. The fluorescence detection wavelengths of excitation and emission were set at 273 nm and 464 nm, respectively. Retention times for micafungin and IS were 22.4 and 23.7 min, respectively. Micafungin and FR195743 (IS) peaks were completely separated with little tailing, and no interference was observed. The calibration curve of micafungin showed good linearity in the range of 0.5-20.0 μg/mL (r(2)=1.00). The intra-day accuracy ranged from -4.5 to 5.3%. The inter-day accuracy ranged from -9.8 to 1.5%. The precisions were less than 10%. This method is useful for the determination of micafungin in human plasma.
已开发出一种基于高效液相色谱直接进样法,用于使用新型疏水/亲水混合 ODS 柱测定人血浆中米卡芬净的含量。该方法易于操作,仅需过滤后的 10μL 血浆样品。采用梯度模式进行色谱分离。荧光检测的激发和发射波长分别设定为 273nm 和 464nm。米卡芬净和内标(IS)的保留时间分别为 22.4 和 23.7min。米卡芬净和 FR195743(IS)峰完全分离,拖尾小,无干扰。米卡芬净的校准曲线在 0.5-20.0μg/mL 范围内呈良好线性(r(2)=1.00)。日内准确度范围为-4.5%至 5.3%。日间准确度范围为-9.8%至 1.5%。精密度小于 10%。该方法可用于测定人血浆中的米卡芬净。