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Detection and quantitation of additions of soybean proteins in cured-meat products by perfusion reversed-phase high-performance liquid chromatography

机译:灌注反相高效液相色谱法检测和定量肉制品中大豆蛋白的添加

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摘要

Perfusion liquid chromatography has been applied in this work to the determination of soybean proteins in commercially available cured meat products, enabling the detection of additions of soybean proteins in cured meat products to which the addition of these vegetable proteins is forbidden and the quantitation of soybean proteins in cured meat products to which the addition of these proteins is allowed up to a certain limit. The analytical methodology is based on a sample treatment (fat extraction and soybean protein solubilization) prior to chromatographic analysis. Fat extraction with acetone and soybean protein solubilization with a buffer solution at basic pH (pH 10 or 9) were necessary to obtain selective and sensitive conditions. Use of water-acetonitrile-trifluoroacetic acid or water-tetrahydrofuran-trifluoroacetic acid linear binary gradients at a flow rate of 3 mL/min, a temperature of 50 degrees C, and UV detection at 280 nm enabled chromatographic analysis of soybean proteins in cured meat products in less than 3 min.
机译:灌注液相色谱已用于这项工作中,以确定可商购的腌制肉制品中的大豆蛋白,从而能够检测禁止添加这些植物蛋白的腌制肉制品中添加的大豆蛋白,并对大豆蛋白进行定量在允许添加这些蛋白质的腌制肉制品中达到一定限度。分析方法基于色谱分析之前的样品处理(脂肪提取和大豆蛋白溶解)。为了获得选择性和敏感的条件,必须用丙酮进行脂肪提取,并用碱性pH(pH 10或9)的缓冲溶液溶解大豆蛋白。使用水-乙腈-三氟乙酸或水-四氢呋喃-三氟乙酸线性二元梯度以3 mL / min的流速,50摄氏度的温度和280 nm的紫外线检测能够对腌制肉中的大豆蛋白进行色谱分析不到3分钟的产品。

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