Lee Maw-Rong, Chang Li-Yo, Dou Jianpeng
Department of Chemistry, National Chung Hsing University, Taichung 40227, Taiwan, ROC.
Anal Chim Acta. 2007 Jan 16;582(1):19-23. doi: 10.1016/j.aca.2006.08.042. Epub 2006 Aug 26.
A method has been developed to determine acrylamide in aqueous matrices by using direct immersion solid-phase microextraction (SPME) coupled to gas chromatography-positive chemical ionization tandem mass spectrometry (GC-PCI-MS-MS) in the selected reaction monitoring (SRM) mode. The optimized SPME experimental procedures to extract acrylamide in water solutions were: use of a carbowax/divinylbenzene (CW/DVB)-coated fiber at pH 7, extraction time of 20 min and analyte desorption at 210 degrees C for 3 min. A detection limit of 0.1 microg L(-1) was obtained. The linear range was 1-1000 microg L(-1). The relative standard deviation was 10.64% (n=7). The proposed analytical method was successfully used for the quantification of trace acrylamide in foodstuffs such as French fries (1.2 microg g(-1)) and potato crisps (2.2 microg g(-1)).
已开发出一种方法,通过在选定反应监测(SRM)模式下使用直接浸入式固相微萃取(SPME)与气相色谱-正化学电离串联质谱(GC-PCI-MS-MS)联用,来测定水性基质中的丙烯酰胺。用于萃取水溶液中丙烯酰胺的优化SPME实验程序如下:在pH 7条件下使用涂有聚乙二醇/二乙烯基苯(CW/DVB)的纤维,萃取时间为20分钟,在210℃下进行分析物解吸3分钟。获得的检测限为0.1微克/升。线性范围为1-1000微克/升。相对标准偏差为10.64%(n = 7)。所提出的分析方法已成功用于测定食品(如炸薯条(1.2微克/克)和薯片(2.2微克/克))中的痕量丙烯酰胺。