Simultaneous quantification of four benzodiazepines from whole blood by highperformance liquid chromatography in forensic toxicological analysis

Author:

Miresan Horatiu1,Rosca Cosmin1,Matei Nicoleta2,Roncea Florentina1,Cazacincu Radu1,Iancu Irina1,Stefanescu Emil3,Enache Daniel4,Bratu Mihaela1,Popescu Antoanela1

Affiliation:

1. Ovidius University, Faculty of Pharmacy, University Street No.1, Constanta, Romania

2. Ovidius University, Faculty of Applied Science and Engineering, 124 Mamaia Blvd., Constanta, Romania

3. UMF ”Carol Davila”, Faculty of Pharmacy, Traian Vuia Street No.6, Bucharest, Romania

4. Daimara Style Co SRL, Constanta

Abstract

Abstract A rapid high performance liquid chromatography method, using a monolithic column, was developed for quantitative determinations of benzodiazepines (diazepam, clonazepam, lorazepam, midazolam) in whole blood. A liquid-liquid extraction step with n-chlorobutane isolates the drugs from alkalinized blood. The separation was carried out in reversed phase conditions using a Chromolith Performance (RP-18 100x4.6 mm) column. For the mobile phase, a mixture of a phosphate buffer (pH= 2.5)/acetonitrile (65/35 v/v), in isocratic mode at 2 mL/min. An ultraviolet spectrophotometer was used as the detector at the wavelength of 220 nm. The total run time of the analytical method is less than 4-6 minutes. The calibration curves showed linearity and the correlation coefficient of each individual curve was greater than 0.995. The method was linear over a concentration range of 0.03-0.6 μg/mL for clonazepam, lorazepam and midazolam. For diazepam of linearity was over the range 0.04-5.0μg/mL. Quantification limits ranged from 0.03-0.04μg/mL and the accuracy were from 80% to 105% for the recovery test. The results indicate that this analytical method is simple, specific, accuracy, sensitive, demonstrating from the validation data and a higher robustness. The proposed method is applied routinely in forensic toxicological analysis involving blood.

Publisher

Walter de Gruyter GmbH

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