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 >Development and validation of an ultrafast chromatographic method for quantification of the immunosuppressant mycophenolic acid in canine, feline and human plasma
【24h】

Development and validation of an ultrafast chromatographic method for quantification of the immunosuppressant mycophenolic acid in canine, feline and human plasma

机译:犬,猫素和人血浆中免疫抑制剂霉菌酸定量超快色谱法的发展与验证

获取原文
获取原文并翻译 | 示例
       

摘要

Mycophenolic acid (MPA) is the active metabolite of the prodrug mycophenolate mofetiL In this study, we developed and validated a novel ultra-high performance liquid chromatography (UHPLC) method for the rapid quantification of MPA in plasma from dogs, cats and humans. Following the protein precipitation, calibration standards and quality controls were separated by UHPLC reversed-phase on a 1.5 mu m 2.1 x 100 mm C-18 column and quantified using UV detection at 215 nm. The procedure produced a linear curve (r(2) > 0.997) over the concentration range 0.4-50 mu g/mL and exhibited a high degree of repeatability (CV% <11%). The limit of detection (LOD) and lower limit of quantitation (LLOQ) were 0.1 and <= 0.4 mu g/mL, respectively and the overall recovery was >= 87%. By combining isocratic conditions with a UHPLC column containing solid core particles, we were able to elute MPA and the internal standard (mycophenolic acid carboxybutoxy ether) within 3.0 min. The short total run time makes this method ideal to study the disposition of MPA in large batches of plasma samples and/or monitor plasma drug concentrations, as recommended for patients that require optimized immunosuppression. (C) 2016 Elsevier B.V. All rights reserved.
机译:霉酚酸(MPA)是本研究中的前药霉酚酸酯的活性代谢物,我们开发并验证了一种新型超高效液相色谱(UHPLC)方法,用于从狗,猫和人类的血浆中快速定量MPa。在蛋白质沉淀后,通过UHPLC反相分离校准标准和质量控制在1.5μm2.1×100mm C-18柱上,并在215nm处使用紫外检测量化。该方法在浓度范围内产生线性曲线(R(2)> 0.997)0.4-50μmg/ ml,并且表现出高度的重复性(CV%<11%)。检测极限(LOD)和定量下限(LLOQ)分别为0.1和<=0.4μg/ mL,总回收率> = 87%。通过将具有含有固体核颗粒的UHPLC柱组合的等级条件,我们能够在3.0分钟内洗脱MPa和内标(霉酚酸羧丁糖醚)。短的总运行时间使得该方法是研究MPa在大批等离子体样品和/或监测血浆药物浓度的情况下研究MPa,这适用于需要优化免疫抑制的患者。 (c)2016 Elsevier B.v.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号