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Development of a dual test procedure for DNA typing and methamphetamine detection using a trace amount of stimulant-containing blood

机译:开发了使用微量含兴奋剂的血液进行DNA分型和甲基苯丙胺检测的双重测试程序

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Investigation of drug-related crimes, such as violation of the Stimulant Drug Control Law, requires identifying the used drug (mainly stimulant drugs, methamphetamine hydrochloride) from a drug solution and the DNA type of the drug user from a trace of blood left in the syringe used to inject the drug. In current standard test procedures, DNA typing and methamphetamine detection are performed as independent tests that use two separate portions of a precious sample. The sample can be entirely used up by either analysis. Therefore, we developed a new procedure involving partial lysis of a stimulant-containing blood sample followed by separation of the lysate into a precipitate for DNA typing and a liquid-phase fraction for methamphetamine detection. The method enables these two tests to be run in parallel using a single portion of sample. Samples were prepared by adding methamphetamine hydrochloride water solution to blood. Samples were lysed with Proteinase K in PBS at 56 degrees C for 20 min, cooled at -20 degrees C after adding methanol, and then centrifuged at 15,000 rpm. Based on the biopolymer-precipitating ability of alcohol, the precipitate was used for DNA typing and the liquid-phase fraction for methamphetamine detection. For DNA typing, the precipitate was dissolved and DNA was extracted, quantified, and subjected to STR analysis using the AmpFlSTR (R) Identifier (R) Plus PCR Amplification Kit. For methamphetamine detection, the liquid-phase fraction was evaporated with N-2 gas after adding 20 mu L acetic acid and passed through an extraction column; the substances captured in the column were eluted with a solvent, derivatized, and quantitatively detected using gas chromatograph/mass spectrometry. This method was simple and could be completed in approximately 2 h. Both DNA typing and methamphetamine detection were possible, which suggests that this method may be valuable for use in criminal investigations. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
机译:要调查与毒品有关的犯罪,例如违反《兴奋剂药物管制法》,需要从药液中识别使用过的药物(主要是兴奋剂,盐酸甲基苯丙胺),并从残留在血液中的微量血液中识别出吸毒者的DNA类型。用于注射药物的注射器。在当前的标准测试程序中,DNA分型和甲基苯丙胺检测是作为独立测试进行的,使用贵重样品的两个独立部分。任一分析均可完全耗尽样品。因此,我们开发了一种新方法,包括部分裂解含兴奋剂的血样,然后将裂解物分离成沉淀物以进行DNA分型,并分离出液相部分用于甲基苯丙胺检测。该方法使这两个测试可以使用单个样本并行进行。通过向血液中添加盐酸甲基苯丙胺水溶液制备样品。将样品用蛋白酶K在PBS中的蛋白酶K在56摄氏度下裂解20分钟,添加甲醇后冷却至-20摄氏度,然后以15,000 rpm离心。基于醇的生物聚合物沉淀能力,沉淀物用于DNA分型,液相部分用于甲基苯丙胺检测。为了进行DNA分型,将沉淀物溶解并提取DNA,定量,并使用AmpFlSTR Identifier Plus PCR扩增试剂盒进行STR分析。为了进行甲基苯丙胺的检测,在加入20μL乙酸后,将液相部分用N-2气体蒸发,并通过萃取柱。柱中捕获的物质用溶剂洗脱,衍生化并使用气相色谱/质谱法进行定量检测。该方法很简单,可以在大约2小时内完成。 DNA分型和甲基苯丙胺检测都是可能的,这表明该方法对于刑事调查可能是有价值的。 (C)2016 Elsevier Ireland Ltd.保留所有权利。

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