科研之友
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摘要
Opioids and cocaine are widely used at present, both for recreational purposes and as drugs of abuse. This raises the need to develop new analytical methods specifically designed for the simultaneous detection of several drugs of abuse in biological samples. In this work, dispersive liquid-liquid microextraction (DLLME) was assessed as a new sample treatment for the simultaneous extraction of morphine (MOR), 6-acetylmorphine (6AM), cocaine (COC), benzoylecgonine (BZE) and methadone (MET) from human plasma. Preliminary assays were done before developing an experimental design based on a Uniform Network Doehlert which allowed the optimum extraction conditions to be identified, namely: a volume of extractant solvent (chloroform) and dispersant solvent (acetonitrile) of 220 mu l and 3.2 ml, respectively; 0.2 g of NaCl as a salting-out additive; pH 10.6 and ultrasound stirring for 3.5 min. The resulting extracts were analyzed by high-performance liquid chromatography with photodiode array detection (HPLC-PDA), using an XBridge (R) RP18 column (250 x 4.6 mm i.d., 5 mu m particle size). Calibration graphs were linear over the concentration range 0.1-10 mu g ml(-1), and detection limits ranged from 13.9 to 28.5 ng ml(-1). Precision calculated at three different concentration levels in plasma was included in the range 0.1-6.8% RSD. Recoveries of the five drugs were all higher than 84% on average. Finally the proposed method was successfully applied to 22 plasma samples from heroin, cocaine and/or methadone users, and the most frequently detected drug was benzoylecgonine, followed by methadone, cocaine and morphine. Copyright (c) 2014 John Wiley & Sons, Ltd. A method consisting of dispersive liquid-liquid microextraction and high-performance liquid chromatography with photodiode array detection (DLLME/HPLC-PDA) was used to determine morphine, 6-acetylmorphine, cocaine, benzoylecgonine and methadone in human plasma. An experimental design based on a Uniform Network Doehlert allowed the optimization of the extraction conditions. The chromatographic method was validated assessing linearity, limits of detection and quantitation, selectivity, precision and accuracy. Finally, the proposed method was successfully applied to 22 plasma samples from drug users.
- 出版日期2015-4
