Peng Youyuan, Chu Qingcui, Liu Fanghua, Ye Jiannong
Department of Chemistry, East China Normal University, North Zhongshan Road, Shanghai 200062, People's Republic of China.
J Agric Food Chem. 2004 Jan 28;52(2):153-6. doi: 10.1021/jf030280c.
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.
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。