首页> 美国卫生研究院文献>other >A quantitative LC-MS/MS method for simultaneous determination of cocaine and its metabolites in whole blood
【2h】

A quantitative LC-MS/MS method for simultaneous determination of cocaine and its metabolites in whole blood

机译:同时测定全血中可卡因及其代谢物的定量LC-MS / MS方法

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

As new metabolic pathways of cocaine were recently identified, a high performance liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed to simultaneously determine cocaine and nine cocaine-related metabolites in whole blood samples. One-step solid phase extraction was used to extract all of the ten compounds and corresponding internal standards from blood samples. All compounds and internal standards extracted were separated on an Atlantis T3 (100Å, 3 µm, 2.1 mm × 150 mm I.D) column and detected in positive ion and high sensitivity mode with multiple reaction monitoring. This method was validated for its sensitivity, linearity, specificity, accuracy, precision, recovery, and stability. All of the ten compounds were quantifiable ranging from the lower limit of quantification (LLOQs) of ~10 nM (1.9–3.2 ng/ml) to ~1000 nM (190–320 ng/ml) without any interfering substance. Accuracy and precision were determined, and both of them were within the acceptance criteria of the United States (US) Food and Drug Administration (FDA) and European Medicines Agency (EMA) guidelines. The recovery was above 66.7% for all compounds. Stability tests demonstrated the stability of compounds under different storage conditions in whole blood samples. The method was successfully applied to a pharmacokinetic study with co-administration of cocaine and alcohol in rats.
机译:由于最近发现了可卡因的新的代谢途径,因此开发了一种高效液相色谱串联质谱(LC-MS / MS)方法来同时测定全血样品中的可卡因和9种可卡因相关的代谢物。一步固相萃取用于从血样中萃取所有十种化合物和相应的内标。提取的所有化合物和内标物均在Atlantis T3(100Å,3 µm,2.1 mm×150 mm I.D)色谱柱上分离,并在阳离子和高灵敏度模式下通过多反应监测进行检测。该方法的灵敏度,线性,特异性,准确性,精密度,回收率和稳定性均得到验证。十种化合物中的所有化合物都是可定量的,范围从〜10 nM(1.9–3.2 ng / ml)的下限(LLOQ)到〜1000 nM(190-320 ng / ml),无任何干扰物质。确定了准确性和精密度,并且它们均在美国(US)食品和药物管理局(FDA)和欧洲药品管理局(EMA)准则的接受标准之内。所有化合物的回收率均高于66.7%。稳定性测试表明化合物在全血样品中不同储存条件下的稳定性。该方法已成功应用于可卡因和酒精共同给药在大鼠体内的药代动力学研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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