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Interference-free determination of acrylamide in potato and cereal-based foods by a laboratory validated liquid chromatography-mass spectrometry method

机译:实验室验证的液相色谱-质谱法无干扰测定马铃薯和谷类食品中的丙烯酰胺

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摘要

A simple and rapid method was developed and validated for the determination of acrylamide in potato and cereal-based foods by using a single quadrupole liquid chromatography-mass spectrometry (LC-MS) interfaced with positive atmospheric pressure chemical ionization (APCI+). Acrylamide was simply extracted with 0.01 mM acetic acid in a vortex mixer prior to LC-MS analysis. The applicability of validated method was shown for a wide range of processed foods including chips, fries, crisps, breads, biscuits and cookies. The mean recovery was found to be 99.7 with a repeatability of 1.8% in the range 100-1000 ng/g. During LC-MS analyses, the major interfering co-extractive was identified as valine which yields characteristic [M + H]~+ and compound specific product ions having m/z of 118 and 72, respectively. Valine increased the baseline signal preventing accurate and precise quantitation, and resulted in poorer sensitivity in selected ion monitoring mode. The adverse effect of valine could be limited by instrumentally adjusted delay time or by solid-phase extraction with strong cation-exchanger sorbent.
机译:开发了一种简单而快速的方法,并通过使用正四极杆液相色谱-质谱联用(LC-MS)和正大气压化学电离(APCI +)接口,用于测定马铃薯和谷类食品中的丙烯酰胺。在LC-MS分析之前,只需在涡旋混合器中用0.01 mM乙酸萃取丙烯酰胺。验证的方法适用于各种加工食品,包括薯片,薯条,薯片,面包,饼干和饼干。发现平均回收率为99.7,重复性为1.8%,范围为100-1000 ng / g。在LC-MS分析过程中,主要干扰共提取物被鉴定为缬氨酸,可产生特征性[M + H]〜+和化合物特定产物离子,其m / z分别为118和72。缬氨酸会增加基线信号,从而无法进行准确准确的定量,并导致所选离子监测模式下的灵敏度较差。缬氨酸的不利影响可通过仪器调整延迟时间或使用强阳离子交换吸附剂进行固相萃取来限制。

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