首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >SCREENING AND IDENTIFICATION OF DRUGS IN HUMAN HAIR BY HIGHPERFORMANCE LIQUID CHROMATOGRAPHY PHOTODIODE-ARRAY UV DETECTION AND GAS CHROMATOGRAPHY MASS SPECTROMETRY AFTER SOLID-PHASE EXTRACTION - A POWERFUL TOOL IN FORENSIC MEDICINE
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SCREENING AND IDENTIFICATION OF DRUGS IN HUMAN HAIR BY HIGHPERFORMANCE LIQUID CHROMATOGRAPHY PHOTODIODE-ARRAY UV DETECTION AND GAS CHROMATOGRAPHY MASS SPECTROMETRY AFTER SOLID-PHASE EXTRACTION - A POWERFUL TOOL IN FORENSIC MEDICINE

机译:固相萃取后高效液相色谱-光电二极管-紫外检测和气相色谱-质谱联用对人发中的药物进行筛分和鉴定

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A method is described to screen for a wide rang of pharmaceuticals in human hair. 75 mg of powdered hair are incubated oe (12 h at 56 degrees C) in 2 ml of distilled water (acidic compounds) or 0.1 M hydrochloric acid (neutral and basic compounds). A twin solid-phase extraction on C-18 cartridges is used for the sample clean-up procedure. Acidic drugs are fixed at pH 2 and eluted with 1% ammoniacal methanol while neutral and basic drugs are retained on the column at pH 8.6 and eluted with methanol containing 0.5% acetic acid. The internal standard (I.S.) for the acidic extraction was bupivacaine while the I.S. for the basic extraction was prazepam. The separation of the drugs was performed using both the liquid and the gas chromatographic techniques whereas identification was achieved using photodiode array and mass spectrometric detection, respectively. The liquid chromatographic system gives an elution of the drugs following a multi step gradient from a Symmetry C, (Waters) 5 mu m column (250x4.6 mm I.D.) at +30 degrees C with acetonitrile-phosphate buffer (pH 3.8). Identification is achieved using the reference data (retention times and spectra) of 675 pharmaceuticals, toxicants and drugs of abuse stored in a personal library. The present method has been applied during 6 months in our laboratory. By establishing a victim's drug use history, it is a very powerful tool in forensic medicine. We illustrate the method with some real cases of police crime investigation.
机译:描述了一种筛选人发中多种药物的方法。将75 mg粉末状头发在2 ml蒸馏水(酸性化合物)或0.1 M盐酸(中性和碱性化合物)中孵育(56摄氏度下12小时)。 C-18小柱上的双固相萃取用于样品净化程序。将酸性药物固定在pH 2并用1%氨甲醇洗脱,而中性和碱性药物则保留在pH 8.6的色谱柱上并用含0.5%乙酸的甲醇洗脱。酸性萃取的内标(I.S.)是布比卡因,而I.S.基本提取为巴西raz。药物的分离使用液相色谱和气相色谱技术进行,而鉴定则分别使用光电二极管阵列和质谱检测进行。液相色谱系统在+30摄氏度下用乙腈-磷酸盐缓冲液(pH 3.8)从Symmetry C(Waters)5μm色谱柱(250x4.6 mm I.D.)进行多步梯度洗脱后,洗脱出药物。使用个人图书馆中存储的675种药物,有毒物质和滥用药物的参考数据(保留时间和光谱)可以进行识别。本方法已在我们的实验室中使用了6个月。通过建立受害者的药物使用历史,它是法医中非常强大的工具。我们以一些实际的警察犯罪调查案例来说明该方法。

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