Determination of Putrescine and Tyramine in Fish by Micellar Liquid Chromatography with UV Detection Using Direct Injection

Mei-Liang Chin-Chen, D. Bose, J. Esteve-Romero, J. Peris-Vicente, M. Rambla-Alegre, S. Carda‐Broch
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引用次数: 22

Abstract

This paper shows how fish samples could be directly injected into a chromatograph, without any previous extraction, using micellar liquid chromatography, taking as an example the determination of two biogenic amines: putrescine and tyramine, derivatized with 3,5-dinitrobenzoyl chloride. First, the method has been optimized, using an interpretive model, and the best conditions for analysis were: mobile phase containing 0.15 M SDS-6% (v/v) butanol-pH 7, C18 column (125 � 0.46 mm, 5 μm particle size), UV detection of derivatives set at 260 nm. Second, the method has been validated using spiked samples following the guidelines proposed by the US Food and Drug Administration: linear in the range from 0.5 to 1000 ppm (r 2 >0.999), detection limits of 30 and 40 ppb for putrescine and tyramine, respectively, a 500 ppb limit of quantification in both cases, intra- and inter-day precision (RSD) below 2%, and accuracy between 99.5% and 102.7%. The method is adequate for routine analysis in the determination of these compounds in fish sauces.
直接进样胶束液相色谱-紫外检测法测定鱼中的腐胺和酪胺
本文以3,5-二硝基苯甲酰氯衍生的腐胺和酪胺两种生物胺的测定为例,介绍了如何将鱼类样品直接注入色谱仪,而无需事先提取。首先,利用解释模型对方法进行了优化,确定了最佳分析条件为:流动相为0.15 M SDS-6% (v/v)丁醇- ph 7, C18色谱柱(125 μ 0.46 mm, 5 μm粒径),紫外检测波长为260 nm。其次,根据美国食品和药物管理局提出的指导方针,使用加标样品对该方法进行了验证:在0.5至1000 ppm范围内呈线性(r 2 >0.999),腐胺和酪胺的检出限分别为30和40 ppb,两种情况下的定量限均为500 ppb,日内和日间精密度(RSD)低于2%,准确度在99.5%至102.7%之间。本方法适用于鱼酱中这些化合物的常规分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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