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

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          Abstract

          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.

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          Author and article information

          Journal
          8309336
          1076
          J Pharm Biomed Anal
          J Pharm Biomed Anal
          Journal of pharmaceutical and biomedical analysis
          0731-7085
          1873-264X
          15 December 2016
          11 November 2016
          05 February 2017
          05 February 2018
          : 134
          : 243-251
          Affiliations
          Molecular Modeling and Biopharmaceutical Center and Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 789 South Limestone Street, Lexington, KY 40536
          Author notes
          Correspondence to: Chang-Guo Zhan, Ph.D. Director, Molecular Modeling and Biopharmaceutical Center (MMBC) Director, Chemoinformatics and Drug Design Core of CPRI Endowed College of Pharmacy Professor in Pharmaceutical Sciences Professor, Department of Pharmaceutical Sciences College of Pharmacy University of Kentucky 789 South Limestone Street Lexington, KY 40536 Tel.: 859-323-3943 FAX: 859-257-7585
          Article
          PMC5196007 PMC5196007 5196007 nihpa834480
          10.1016/j.jpba.2016.11.024
          5196007
          27923200
          02dc268d-421a-4d0a-b017-ffc306971347
          History
          Categories
          Article

          SPE,Cocaine,alcohol,drug metabolism,LC-MS/MS
          SPE, Cocaine, alcohol, drug metabolism, LC-MS/MS

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