首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >A sensitive combined assay for the quantification of paclitaxel, docetaxel and ritonavir in human plasma using liquid chromatography coupled with tandem mass spectrometry
【24h】

A sensitive combined assay for the quantification of paclitaxel, docetaxel and ritonavir in human plasma using liquid chromatography coupled with tandem mass spectrometry

机译:液相色谱-串联质谱联用法定量测定人血浆中紫杉醇,多西紫杉醇和利托那韦的灵敏组合测定法

获取原文
获取原文并翻译 | 示例
       

摘要

A combined assay for the determination of paclitaxel, docetaxel and ritonavir in human plasma is described. The drugs were extracted from 200μL human plasma using liquid-liquid extraction with tertiar-butylmethylether, followed by high performance liquid chromatography analysis using 10mM ammonium hydroxide pH 10:methanol (3:7, v/v) as mobile phase. Chromatographic separation was obtained using a Zorbax Extend C_(18) column. Labelled analogues of the analytes are used as internal standards. For detection, positive ionization electrospray tandem mass spectrometry was used. Method development including optimisation of the mass transitions and response, mobile phase optimisation and column selection are discussed. The method was validated according to FDA guidelines and the principles of Good Laboratory Practice (GLP). The validated range was 0.5-500ng/mL for paclitaxel and docetaxel and 2-2000ng/mL for ritonavir. For quantification, quadratic calibration curves were used (r~2>0.99). The total runtime of the method is 9min and the assay combines analytes with differences in ionisation and desired concentration range. Inter-assay accuracy and precision were tested at four concentration levels and were within 10% and less than 10%, respectively, for all analytes. Carry-over was less than 6% and endogenous interferences or interferences between analytes and internal standards were less than 20% of the response at the lower limit of quantification level. The matrix factor and recovery were determined at low, mid and high concentration levels. The matrix factor was around 1 for all analytes and total recovery between 77.5 and 104%. Stability was investigated in stock solutions, human plasma, dry extracts, final extracts and during 3 freeze/thaw cycles. The described method was successfully applied in clinical studies with oral administration of docetaxel or paclitaxel in combination with ritonavir.
机译:描述了用于测定人血浆中紫杉醇,多西紫杉醇和利托那韦的组合测定法。使用叔丁基甲基醚进行液-液萃取,从200μL人血浆中提取药物,然后使用10mM pH 10:甲醇的氢氧化铵(3:7,v / v)作为流动相进行高效液相色谱分析。使用Zorbax Extend C_(18)色谱柱进行色谱分离。被分析物的标记类似物用作内标。为了进行检测,使用了正电离电喷雾串联质谱。讨论了方法开发,包括质量转移和响应的优化,流动相优化和色谱柱选择。该方法已根据FDA指南和良好实验室规范(GLP)的原则进行了验证。紫杉醇和多西他赛的验证范围为0.5-500ng / mL,利托那韦的验证范围为2-2000ng / mL。为了量化,使用二次校准曲线(r〜2> 0.99)。该方法的总运行时间为9分钟,该测定法结合了电离度和所需浓度范围不同的分析物。在四种浓度水平下测试的批间准确性和精密度均对所有分析物均在10%以内和小于10%。在定量水平的下限,残留量小于6%,内源干扰物或分析物与内标之间的干扰小于响应的20%。在低,中和高浓度水平下确定基质因子和回收率。所有分析物的基质系数约为1,总回收率在77.5%至104%之间。在原液,人血浆,干提取物,最终提取物中以及3个冷冻/融化循环中研究了稳定性。所描述的方法通过口服多西他赛或紫杉醇联合利托那韦成功用于临床研究。

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