Validation of a fast UPLC–MS/MS method for quantitative analysis of opioids, cocaine, amphetamines (and their derivatives) in human whole blood

Author:

Feliu Catherine1,Millart Hervé1,Guillemin Hélène1,Vautier Damien1,Binet Laurent1,Fouley Aurelie1,Djerada Zoubir1

Affiliation:

1. Department of Pharmacology, EA3801, SFR CAP-santé, Reims University Hospital, 51, rue Cognacq-Jay, 51095 Reims Cedex, France

Abstract

Background: Conventional methods for analysis of drugs of abuse require multiple assays which can be both expensive and time-consuming. This work describes a novel, rapid, simple and sensitive method for the quantification of 14 illicit drugs and their metabolites in whole blood. Results/methodology: This method employed a rapid liquid–liquid sample extraction of whole blood followed by UPLC–MS/MS analysis. Calibration curves were validated for analysis of appropriate concentrations. Inter- and intra-assay variations were <14.8%. Deviation of accuracy was <14.9% from target concentration for each quality control level. Conclusion: This work described the development and the full validation of a precise, sensitive and accurate assay. After validation, this new assay was successfully applied to routine toxicological analysis.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

Reference47 articles.

1. EMCDDA. Annual report on the state of the drugs problem in Europe. www.emcdda.europa.eu/publications/annual-report/2012.

2. Rapport 2011 de l'OEDT sur l'état du phénomène de la drogue en Europe. www.ofdt.fr/ofdtdev/live/donneeseuro.html.

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