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基于深共晶溶剂作为接受相的三相中空纤维液相微萃取用于中药配方中主要活性化合物的萃取和预浓缩。

Three-phase hollow-fiber liquid-phase microextraction based on deep eutectic solvent as acceptor phase for extraction and preconcentration of main active compounds in a traditional Chinese medicinal formula.

机构信息

School of Pharmacy, Shanxi Medical University, Taiyuan, P. R. China.

出版信息

J Sep Sci. 2019 Jul;42(13):2239-2246. doi: 10.1002/jssc.201900184. Epub 2019 May 15.

Abstract

A three-phase hollow-fiber liquid-phase microextraction based on deep eutectic solvent as acceptor phase was developed and coupled with high-performance capillary electrophoresis for the simultaneous extraction, enrichment, and determination of main active compounds (hesperidin, honokiol, shikonin, magnolol, emodin, and β,β'-dimethylacrylshikonin) in a traditional Chinese medicinal formula. In this procedure, two hollow fibers, impregnated with n-heptanol/n-nonanol (7:3, v/v) mixture in wall pores as the extraction phase and a combination (9:1, v/v) of methyltrioctylammonium chloride/glycerol (1:3, n/n) and methanol in lumen as the acceptor phase, were immersed in the aqueous sample phase. The target analytes in the sample solution were first extracted through the organic phase, and further back-extracted to the acceptor phase during the stirring process. Important extraction parameters such as types and composition of extraction solvent and deep eutectic solvent, sample phase pH, stirring rate, and extraction time were investigated and optimized. Under the optimal conditions, detection limits were 0.3-0.8 ng/mL with enrichment factors of 6-114 for the analytes and linearities of 0.001-13 μg/mL (r ≥ 0.9901). The developed method was successfully applied to the simultaneous extraction and concentration of the main active compounds in a formula of Zi-Cao-Cheng-Qi decoction with the major advantages of convenience, effectiveness, and environmentally friendliness.

摘要

建立了一种基于深共晶溶剂作为接受相的三相中空纤维液相微萃取方法,并将其与高效毛细管电泳联用,用于同时提取、富集和测定中药配方中主要活性化合物(橙皮苷、和厚朴酚、紫草素、厚朴酚、大黄素和β,β'-二甲基丙烯酰紫草素)。在该方法中,将浸渍有正庚醇/正壬醇(7:3,v/v)混合物的两根中空纤维(壁孔中的萃取相)和甲基三辛基氯化铵/甘油(1:3,n/n)与甲醇的混合物(内腔中的接受相)浸入水相样品中。目标分析物首先从样品溶液中通过有机相萃取,然后在搅拌过程中进一步反萃取到接受相。考察并优化了萃取溶剂和深共晶溶剂的类型和组成、样品相 pH 值、搅拌速度和萃取时间等重要萃取参数。在最佳条件下,检测限为 0.3-0.8ng/mL,分析物的富集因子为 6-114,线性范围为 0.001-13μg/mL(r≥0.9901)。该方法成功应用于自拟复方紫草酸成气汤中主要活性化合物的同时提取和浓缩,具有方便、有效和环境友好的优点。

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