首页> 外文期刊>Journal of separation science. >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
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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

机译:基于深凝胶溶剂的三相空心纤维液相微萃取,作为中药式主要活性化合物的萃取和前浓度的受体相

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摘要

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 beta, beta'-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 mu g/mL (r(2) >= 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.
机译:基于深度共晶溶剂作为受体相的三相空心纤维液相微萃取并与高性能毛细管电泳同时提取,富集和测定主要活性化合物(Husperidin,Honokiol,Shikonin,Magnolol ,在中药配方中,大黄素和β - 二甲基丙烯酸胆管素)。在该方法中,两种中空纤维浸渍在壁孔中浸渍的正庚醇/ N-壬醇(7:3,v / v)混合物作为萃取相和甲基三烷基氯化铵的组合(9:1,v / v)/将甘油(1:3,N / N)和甲醇的腔内作为受体相浸入水性样品相中。首先通过有机相提取样品溶液中的靶分析物,并在搅拌过程中进一步回到受体相。研究和优化提取溶剂和深对共晶溶剂,样品相pH,搅拌速率和提取时间等重要提取参数。在最佳条件下,检测限为0.3-0.8ng / ml,富集因子为6-114,用于分析物和0.001-13μg/ ml(R(2)> = 0.9901)的分析物和线性。成功地应用于Zi-Cao-Cheng-QI汤中的主要活性化合物的同时提取和浓缩,其具有方便,有效性和环境友好的主要优点。

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