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通过顶空衍生化固相微萃取-气相色谱-质谱法测定血清中的苯丙胺和甲基苯丙胺。

Determination of amphetamine and methamphetamine in serum via headspace derivatization solid-phase microextraction-gas chromatography-mass spectrometry.

作者信息

Lee M R, Song Y S, Hwang B H, Chou C C

机构信息

Department of Chemistry, National Chung-Hsing University, Taichung, Taiwan.

出版信息

J Chromatogr A. 2000 Oct 27;896(1-2):265-73. doi: 10.1016/s0021-9673(00)00596-3.

Abstract

This study evaluates solid-phase microextraction (SPME) coupled with gas chromatography-mass spectrometry (GC-MS) to determine trace levels of amphetamine and methamphetamine in serum. Headspace post-derivatization in a laboratory-made design with heptafluorobutyric anhydride vapor following SPME was compared with that without derivatization SPME. The SPME experimental procedures to extract amphetamine and methamphetamine in serum were optimized with a relatively non-polar poly(dimethylsiloxane) coated fiber at pH 9.5, extraction time for 40 min and desorption at 260 degrees C for 2 min. Experimental results indicate that the concentration of the serum matrix diluted to a quarter of original (1:3) ratio by using one volume of buffer solution of boric acid mixed with sodium hydroxide and two volumes of water improves the extraction efficiency. Headspace derivatization following SPME was performed by using 6 microl 20% (v/v) heptafluorobutyric anhydride ethyl acetate solution at an oil bath temperature of 270 degrees C for 10 s. The precision was below 7% for analysis for without derivatization and below 17% for headspace derivatization. Detection limits were obtained at the ng/l level, one order better obtained in headspace derivatization than those achieved without derivatization. The feasibility of applying the methods to determine amphetamine and methamphetamine in real samples was examined by analyzing serum samples from methamphetamine abused suspects. Concentrations of the amphetamine and methamphetamine ranged from 6.0 microg/l (amphetamine) to 77 microg/l (methamphetamine) in serum.

摘要

本研究评估了固相微萃取(SPME)与气相色谱-质谱联用(GC-MS)技术用于测定血清中痕量苯丙胺和甲基苯丙胺的情况。将固相微萃取后在自制装置中用七氟丁酸酐蒸汽进行顶空衍生化的方法与未衍生化的固相微萃取方法进行了比较。采用pH值为9.5的相对非极性聚二甲基硅氧烷涂层纤维、萃取时间40分钟以及在260℃解吸2分钟等条件,对血清中苯丙胺和甲基苯丙胺的固相微萃取实验程序进行了优化。实验结果表明,用一份硼酸与氢氧化钠混合的缓冲溶液和两份水将血清基质稀释至原体积的四分之一(1:3比例)可提高萃取效率。固相微萃取后的顶空衍生化是通过使用6微升20%(v/v)七氟丁酸酐乙酸乙酯溶液,在270℃油浴温度下进行10秒。未衍生化分析的精密度低于7%,顶空衍生化的精密度低于17%。检测限达到纳克/升水平,顶空衍生化获得的检测限比未衍生化的情况好一个数量级。通过分析甲基苯丙胺滥用嫌疑人的血清样本,检验了该方法用于测定实际样本中苯丙胺和甲基苯丙胺的可行性。血清中苯丙胺和甲基苯丙胺的浓度范围为6.0微克/升(苯丙胺)至77微克/升(甲基苯丙胺)。

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