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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Multicriteria optimization methodology in development of HPLC separation of mycophenolic acid and mycophenolic acid glucuronide in human urine and plasma.
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Multicriteria optimization methodology in development of HPLC separation of mycophenolic acid and mycophenolic acid glucuronide in human urine and plasma.

机译:开发用于人尿和血浆中麦考酚酸和麦考酚酸葡糖醛酸苷HPLC分离的多标准优化方法。

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摘要

Multicriteria optimization methodology was applied for development of isocratic reversed-phased HPLC method for simultaneous determination of mycophenolic acid (MPA) and mycophenolic acid glucuronide (MPAG) in human urine and plasma. In the first stage of method development, pH value of the water phase, percentage of acetonitrile, temperature of the column and flow rate of the mobile phase were investigated using fractional factorial design. Afterwards, the optimal conditions were found employing central composite design and Derringer's desirability function. Two goals were considered, the retention factor of the MPAG to be in the range, between 0.8 and 1.118 which allowed well separation of MPAG from the urine and plasma peaks, and the shortest possible total analysis run time. Then, the obtained sigmoid functions were used to transform the optimization criteria into the desirability values. The satisfactory chromatographic conditions were obtained with mobile phase consisted of acetonitrile-phosphate buffer (pH 2.4; 0.04 M KH(2)PO(4)) (28:72, v/v). The separation was performed on C(18) Chromolith column (100 mm x 4.6 mm) with flow rate of 5 mL/min, the temperature of the column was 25 degrees C and the chosen wavelength for simultaneous determination of MPA and MPAG was 215 nm. The MPAG eluted at 0.552 min and the duration of run was 3.092 min. Afterwards, the method was subjected to validation. Linearity was observed over the concentration range of 1-50 microg/mL for MPA and 1-500 microg/mL for MPAG in urine and 1-60 microg/mL for MPA and 1-70 microg/mL for MPAG in plasma matrix. The method showed intra-day and inter-day precision with relative standard deviation lower then 5% and accuracy as recovery (%) between 100+/-5%.
机译:应用多标准优化方法开发了等度反相HPLC方法,用于同时测定人尿和血浆中的麦考酚酸(MPA)和麦考酚酸葡糖醛酸(MPAG)。在方法开发的第一阶段,使用分数阶乘设计研究了水相的pH值,乙腈的百分比,色谱柱的温度以及流动相的流速。之后,使用中央复合设计和Derringer的合意函数找到了最佳条件。考虑了两个目标,MPAG的保留因子在0.8到1.118之间,可以使MPAG与尿液和血浆峰良好分离,并且总分析时间最短。然后,使用获得的S形函数将优化标准转换为期望值。流动相由乙腈-磷酸盐缓冲液(pH 2.4; 0.04 M KH(2)PO(4))(28:72,v / v)组成,获得令人满意的色谱条件。分离是在C(18)色谱柱(100 mm x 4.6 mm)上以5 mL / min的流速进行的,色谱柱的温度为25摄氏度,同时测定MPA和MPAG的选定波长为215 nm 。 MPAG在0.552分钟洗脱,运行时间为3.092分钟。之后,对该方法进行验证。在血浆基质中,MPA的浓度范围为1-50微克/毫升,MPAG的浓度为1-500微克/毫升,MPA的浓度范围为1-60微克/毫升,MPAG的浓度范围为1-70微克/毫升,呈线性。该方法显示出日内和日间精度,相对标准偏差低于5%,准确度为100 +/- 5%之间的回收率(%)。

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