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首页> 外文期刊>Forensic science international >Comparison and classification of methamphetamine seized in Japan and Thailand using gas chromatography with liquid-liquid extraction and solid-phase microextraction.
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Comparison and classification of methamphetamine seized in Japan and Thailand using gas chromatography with liquid-liquid extraction and solid-phase microextraction.

机译:使用液相色谱-液相萃取和固相微萃取技术在日本和泰国缉获的甲基苯丙胺的比较和分类。

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摘要

Methamphetamine (MA) is one of the most frequently abused drugs worldwide. The aim of this study is to improve the analytical method for profiling MA impurity in order to compare and classify MA crystals seized in different countries and to investigate the relationships between seizures. To compare MA samples seized in Japan and Thailand, the following analytical method was adopted. A 50mg sample of MA.HCl was dissolved in 1ml of buffer solution (four parts 0.1M phosphate buffer, pH 7.0, and one part 10% Na(2)CO(3)), impurities were extracted with 0.5ml of ethyl acetate containing four internal standards (n-decane, n-pentadecane, n-eicosane and n-octacosane) and analyzed by gas chromatography with a flame ionization detector on a DB-5 capillary column (0.32mm i.d.x30m, film thickness 1.0mum). Fourteen characteristic peaks on chromatograms were selected for the comparison and classification of samples, and the data were evaluated by the Euclidean distance of the relative peak areas after logarithmic transformation. Sixty-nine samples seized in Japan and 42 seized in Thailand were analyzed. The samples were classified into four groups roughly by cluster analysis. In addition, when it was difficult to compare samples that had fewer impurities on chromatograms obtained from liquid-liquid extraction (LLE), solid-phase microextraction (SPME) was effective. Because many characteristic peaks were detected using SPME, SPME made it easy to compare samples of high purity. The combination of LLE and SPME was useful for impurity profiling of MA samples seized in different countries.
机译:甲基苯丙胺(MA)是世界上最常滥用的药物之一。这项研究的目的是改进分析MA杂质的分析方法,以便比较和分类在不同国家缉获的MA晶体,并研究癫痫发作之间的关系。为了比较在日本和泰国缉获的MA样品,采用了以下分析方法。将50mg MA.HCl样品溶解在1ml缓冲溶液(四份0.1M磷酸盐缓冲液,pH 7.0和一份10%Na(2)CO(3))中,用0.5ml乙酸乙酯萃取杂质四个内标(正癸烷,正十五烷,正二十烷和正十八烷),并在DB-5毛细管柱(0.32mm idx30m,膜厚1.0mum)上用火焰离子化检测器进行气相色谱分析。选择色谱图上的14个特征峰进行样品的比较和分类,并通过对数转换后相对峰面积的欧式距离估算数据。分析了在日本缉获的69个样品和在泰国缉获的42个样品。通过聚类分析将样品大致分为四类。另外,当难以比较从液-液萃取(LLE)获得的色谱图中杂质较少的样品时,固相微萃取(SPME)是有效的。由于使用SPME检测到许多特征峰,因此SPME使得比较高纯度样品变得容易。 LLE和SPME的组合可用于在不同国家/地区缉获的MA样品进行杂质分析。

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