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采用毛细管电泳-电化学检测法测定红酒中具有生物学意义的酚类成分。

Determination of phenolic constituents of biological interest in red wine by capillary electrophoresis with electrochemical detection.

作者信息

Peng Youyuan, Chu Qingcui, Liu Fanghua, Ye Jiannong

机构信息

Department of Chemistry, East China Normal University, North Zhongshan Road, Shanghai 200062, People's Republic of China.

出版信息

J Agric Food Chem. 2004 Jan 28;52(2):153-6. doi: 10.1021/jf030280c.

Abstract

A simultaneous determination of trans-resveratrol, (-)-epicatechin, and (+)-catechin in red wine by capillary electrophoresis with electrochemical detection (CE-ED) is reported. The effects of the potential of the working electrode, pH and concentration of running buffer, separation voltage, and injection time on CE-ED were investigated. Under the optimum conditions, the analytes could be separated in a 100 mmol/L borate buffer (pH 9.2) within 20 min. A 300 microm diameter carbon disk electrode has a good response at +0.85 V (vs SCE) for all analytes. The response was linear over 3 orders of magnitude with detection limit (S/N = 3) ranging from 2 x 10(-7) to 5 x 10(-7) g/mL for all analytes. This method has been used for the determination of these analytes in red wine without enrichment, and the assay result was satisfactory.

摘要

报道了一种采用毛细管电泳 - 电化学检测(CE - ED)同时测定红酒中反式白藜芦醇、( - ) - 表儿茶素和( + ) - 儿茶素的方法。研究了工作电极电位、运行缓冲液的pH值和浓度、分离电压以及进样时间对CE - ED的影响。在最佳条件下,分析物可在100 mmol/L硼酸盐缓冲液(pH 9.2)中于20分钟内分离。直径为300微米的碳盘电极对所有分析物在 +0.85 V(相对于SCE)时具有良好的响应。响应在3个数量级范围内呈线性,所有分析物的检测限(S/N = 3)为2×10^(-7)至5×10^(-7) g/mL。该方法已用于未经富集的红酒中这些分析物的测定,测定结果令人满意。

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