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首页> 外文期刊>Analytica chimica acta >Determination of acrylamide in Chinese traditional carbohydrate-rich foods using gas chromatography with micro-electron capture detector and isotope dilution liquid chromatography combined with electrospray ionization tandem mass spectrometry
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Determination of acrylamide in Chinese traditional carbohydrate-rich foods using gas chromatography with micro-electron capture detector and isotope dilution liquid chromatography combined with electrospray ionization tandem mass spectrometry

机译:气相色谱-微电子捕获检测器-同位素稀释液相色谱-电喷雾电离串联质谱法测定中国传统富含碳水化合物的食品中的丙烯酰胺

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摘要

The present study developed two analytical methods for quantification of acrylamide in complex food matrixes, such as Chinese traditional carbohydrate-rich foods. One is based on derivatization with potassium bromate and potassium bromide without clean-up prior to gas chromatography with micro-electron capture detector (GC-MECD). Alternatively, the underivatized acrylamide was detected by high-performance liquid chromatography coupled to quadrupole tandem mass spectrometry (HPLC-MS/MS) in the positive electrospray ionization mode. For both methods, the Chinese carbohydrate-rich samples were homogenized, defatted with petroleum ether and extracted with aqueous solution of sodium chloride. Recovery rates for acrylamide from spiked Chinese style foods with the spiking level of 50, 500 and 1000 mu g kg(-1) were in the range of 79-93% for the GC-MECD including derivatization and 84-97% for the HPLC-MS/MS method. Typical quantification limits of the HPLC-MSMS method were 4 mu g kg(-1) for acrylamide. The GC-MECD method achieved quantification limits of 10 mu g kg(-1) in Chinese style foods. Thirty-eight Chinese traditional foods purchased from different manufacturers were analyzed and compared with four Western style foods. Acrylamide contaminant was found in all of samples at the concentration up to 771.1 and 734.5 mu g kg(-1) detected by the GC and HPLC method, respectively. The concentrations determined with the two different quantitative methods corresponded well with each other. A convenient and fast pretreatment procedure will be optimized in order to satisfy further investigation of hundreds of samples. (c) 2006 Elsevier B.V. All rights reserved.
机译:本研究开发了两种分析方法,用于定量分析复杂食物基质中的丙烯酰胺,例如中国传统的富含碳水化合物的食物。一种基于溴酸钾和溴化钾的衍生化,而无需在使用微电子捕获检测器(GC-MECD)进行气相色谱分析之前进行纯化。或者,通过高效液相色谱-四极串联质谱法(HPLC-MS / MS),以正电喷雾电离模式检测未衍生的丙烯酰胺。对于这两种方法,均将富含中国碳水化合物的样品均化,用石油醚脱脂,然后用氯化钠水溶液萃取。加标浓度为50、500和1000μgkg(-1)的加标中式食品中丙烯酰胺的回收率在GC-MECD包括衍生化中为79-93%,在HPLC中为84-97% -MS / MS方法。 HPLC-MSMS方法的典型定量限为丙烯酰胺为4μg kg(-1)。 GC-MECD方法在中式食品中的定量限为10μg kg(-1)。分析了从不同制造商处购买的38种中国传统食品,并将其与四种西式食品进行了比较。通过GC和HPLC方法检测到的所有样品中的丙烯酰胺污染物浓度分别高达771.1和734.5μg kg(-1)。用两种不同的定量方法测定的浓度相互对应。为了满足对数百个样品的进一步研究,将优化便捷,快速的预处理程序。 (c)2006 Elsevier B.V.保留所有权利。

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