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优化碱性水解RP-HPLC预处理以提高大豆异黄酮测定的准确性。

Optimizing pre-treatment of alkaline hydrolysis RP-HPLC for enhancing accuracy of soy isoflavone determination.

作者信息

Yang Hong, Li Tong, Cao Wenming

机构信息

Wilmar (Shanghai) Biotechnology Research & Development Center Co., Ltd. Shanghai 200137, China.

Wilmar (Shanghai) Biotechnology Research & Development Center Co., Ltd. Shanghai 200137, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2022 Sep 1;1207:123382. doi: 10.1016/j.jchromb.2022.123382. Epub 2022 Jul 19.

Abstract

Isoflavones (IFs) are important bioactive compounds which offers several benefits to human health. Despite the importance of IFs content, there are still some deficiencies in the existing methods. The objective of this study is to optimize key parameters of alkaline hydrolysis method for enhancing both reliability and accuracy of quantitative analysis of IFs contents in soybeans and soy protein products. Solvent type, extraction temperature, heating mode, alkaline concentration, hydrolysis temperature, hydrolysis time and some details are key points to target analytes which yield determining parameters. The biggest IFs content was obtained by extraction using methanol (MeOH)/water (80:20, v/v) in a 75 ℃ oven for 2 h, and hydrolyzation with 3 M NaOH solution at a room temperature for 10 mins. The total IFs content obtained by the improved method has increased by 16.4% compared with AOAC Official Method 2001.10. The accuracy of the method was evaluated using the relative standard deviation (RSD). Intraday accuracies in the total amount of isoflavones of four samples were 0.03%-0.63% (n = 3). Interday accuracy in the total amount of isoflavones was 2.71% (n = 6). LOD of IFs ranged from 0.1μg/mL for aglycones to 0.2μg/mL for glucosides. LOQ of IFs ranged from 0.3μg/mL for aglycones to 0.5μg/mL for glucosides. The improved method was proven to be a more accurate way to determine IFs contents in soybeans and soy protein products and thus making it useful for quality control and systematic in-depth study of soybeans and soy products; even to further assess the dietary soy exposure and the soy-health association.

摘要

异黄酮(IFs)是重要的生物活性化合物,对人体健康有诸多益处。尽管IFs含量很重要,但现有方法仍存在一些不足。本研究的目的是优化碱性水解法的关键参数,以提高大豆和大豆蛋白产品中IFs含量定量分析的可靠性和准确性。溶剂类型、提取温度、加热方式、碱浓度、水解温度、水解时间以及一些细节是针对目标分析物的关键点,这些因素会产生决定性参数。通过在75℃烘箱中用甲醇(MeOH)/水(80:20,v/v)提取2小时,并在室温下用3M NaOH溶液水解10分钟,可获得最大的IFs含量。与AOAC官方方法2001.10相比,改进后的方法获得的总IFs含量增加了16.4%。使用相对标准偏差(RSD)评估该方法的准确性。四个样品中异黄酮总量的日内准确度为0.03%-0.63%(n = 3)。异黄酮总量的日间准确度为2.71%(n = 6)。IFs的检测限范围为苷元0.1μg/mL至糖苷0.2μg/mL。IFs的定量限范围为苷元0.3μg/mL至糖苷0.5μg/mL。事实证明,改进后的方法是测定大豆和大豆蛋白产品中IFs含量更准确的方法,因此可用于大豆和大豆制品的质量控制和系统深入研究;甚至可进一步评估膳食中大豆的摄入量以及大豆与健康的关系。

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