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微波辅助深共熔溶剂从[具体来源]中提取花青素及大孔树脂纯化:工艺优化、结构表征与定量分析

Microwave-assisted deep eutectic solvent extraction and macroporous resin purification of anthocyanins from : Process optimization, structural characterization and quantitative analysis.

作者信息

Jin Peiyi, Wang Liping, Pi Jiaju, Yuan Tiefeng, Zhong Jinjian, Chen Linzhou, Huang Jilong, Gan Lin, Lin Chen, Fan Huajun

机构信息

Guangdong Provincial Key Laboratory of Chemical Measurement and Emergency Test Technology, Institute of Analysis, Guangdong Academy of Sciences (China national Analytical Center), Guangzhou 510070, China.

School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China.

出版信息

Food Chem X. 2025 Jul 4;29:102736. doi: 10.1016/j.fochx.2025.102736. eCollection 2025 Jul.

Abstract

A novel approach for extraction and purification of the anthocyanins from was developed by microwave-assisted deep eutectic solvent extraction (MAE-DES) coupled to macroporous resin separation (MRS). Citric acid-based DES as the extractant was screened and characterized from 13 synthesized deep eutectic solvents due to the excellent performance. Through RSM optimization of MAE-DES process, the anthocyanin yield reached 6.442 ± 0.135 mg/g, demonstrating that MAE-DES significantly superior to that of conventional methods. With AB-8 MRS purification, the anthocyanin purity was increased by 63-fold. By UHPLC-Q-TOF-MS/MS, the anthocyanins obtained from were dominantly composed of pelargonins. Based on composition analysis, pH differential method was first modified by introducing weighting factors, avoiding serious underestimation of the anthocyanins content in . MAE-DES and the modified spectrophotometry were successfully applied for assessment of anthocyanin extraction and sample drying methods, providing an efficient alternative to development and application of the anthocyanins from .

摘要

通过微波辅助深共熔溶剂萃取(MAE-DES)与大孔树脂分离(MRS)相结合的方法,开发了一种从[具体来源未给出]中提取和纯化花青素的新方法。由于性能优异,从13种合成的深共熔溶剂中筛选并表征了基于柠檬酸的深共熔溶剂作为萃取剂。通过响应面法(RSM)对MAE-DES工艺进行优化,花青素产量达到6.442±0.135mg/g,表明MAE-DES明显优于传统方法。通过AB-8大孔树脂分离纯化,花青素纯度提高了63倍。通过超高效液相色谱-四极杆飞行时间串联质谱(UHPLC-Q-TOF-MS/MS)分析,从[具体来源未给出]中获得的花青素主要由天竺葵色素组成。基于成分分析,首次通过引入加权因子对pH差值法进行了改进,避免了严重低估[具体来源未给出]中的花青素含量。MAE-DES和改进的分光光度法成功应用于评估花青素提取和样品干燥方法,为[具体来源未给出]中花青素的开发和应用提供了一种有效的替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cc4/12275140/36dd749a707c/gr1.jpg

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