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通过超高效液相色谱-串联质谱联用技术同时测定苹果汁中常见的九种生物活性酚类成分。

Determination of nine bioactive phenolic components usually found in apple juice by simultaneous UPLC-MS/MS.

作者信息

Li Qiu-Lin, Chen Fu-Xin, Luo Zi-Teng, Wang Meng-Rang, Han Xiang, Zhu Jun-Feng, Li Juan E, Liu Jing, Li Kan-She, Gong Pin

机构信息

School of Chemistry and Chemical Engineering Xi'an University of Science and Technology Xi'an China.

School of Food Science and Engineering Shaanxi University of Science and Technology Xi'an China.

出版信息

Food Sci Nutr. 2023 May 4;11(7):4093-4099. doi: 10.1002/fsn3.3399. eCollection 2023 Jul.

Abstract

The functional food ingredients of apple juice can significantly change during processing, transportation, and storage, thus affecting the quality of the product. A simple and derivation-free analytical method based on ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was developed and optimized for the simultaneous determination of functional food ingredients in apple juice bought in the market. Cleanup steps and chromatographic conditions were optimized to remove interference and decrease the matrix effect. The nine target analytes were separated on an Acquity UPLC system equipped with a BEH C18 column and detected by electrospray ionization source (ESI) operating in positive subsection acquisition mode under multiple reaction monitoring (MRM) conditions. The results showed that p-hydroxybenzoic acid, protocatechuate, caffeic acid, chlorogenic acid, epicatechin, phloridzin, hyperoside, procyanidin B, and rutin could be sufficiently separated for content determination within 6 min. In the concentration range of 20 μg/L-50 mg/L, nine standard samples exhibited a good linear fit with correlation coefficients above .985.

摘要

苹果汁中的功能性食品成分在加工、运输和储存过程中会发生显著变化,从而影响产品质量。本文建立并优化了一种基于超高效液相色谱-串联质谱(UPLC-MS/MS)的简单且无需衍生化的分析方法,用于同时测定市售苹果汁中的功能性食品成分。对净化步骤和色谱条件进行了优化以去除干扰并降低基质效应。在配备BEH C18柱的Acquity UPLC系统上分离9种目标分析物,并采用电喷雾电离源(ESI)在多反应监测(MRM)条件下的正离子模式进行检测。结果表明,对羟基苯甲酸、原儿茶酸、咖啡酸、绿原酸、表儿茶素、根皮苷、金丝桃苷、原花青素B和芦丁在6分钟内可实现充分分离以进行含量测定。在20μg/L - 50mg/L浓度范围内,9种标准品呈现良好的线性关系,相关系数均大于0.985。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f562/10345717/16c04d571aa9/FSN3-11-4093-g001.jpg

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