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毛细管电泳-电化学检测法测定牡丹皮中的糖苷和糖类成分

Determination of glycosides and sugars in Moutan Cortex by capillary electrophoresis with electrochemical detection.

作者信息

Chen Gang, Zhang Luyan, Zhu Yizhun

机构信息

Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433, China.

出版信息

J Pharm Biomed Anal. 2006 Apr 11;41(1):129-34. doi: 10.1016/j.jpba.2005.11.001. Epub 2005 Dec 15.

Abstract

A method based on capillary electrophoresis with electrochemical detection has been developed for the separation and determination of paeoniflorin, sucrose, paeonoside, glucose, and fructose in Moutan Cortex for the first time. Effects of several important factors such as the concentration of NaOH, separation voltage, injection time, and detection potential were investigated to acquire the optimum conditions. The detection electrode was a 300 microm diameter copper disc electrode at a working potential of +0.60 V (versus saturated calomel electrode (SCE)). The five analytes can be well-separated within 12 min in a 40 cm length fused silica capillary at a separation voltage of 12 kV in a 75 mM NaOH aqueous solution. The relation between peak current and analyte concentration was linear over about 3 orders of magnitude with detection limits (S/N = 3) ranging from 0.9 to 1.3 microM for all analytes. The proposed method has been successfully applied to monitor glycoside and sugar contents in the real plant samples with satisfactory assay results.

摘要

首次开发了一种基于毛细管电泳-电化学检测的方法,用于分离和测定牡丹皮中的芍药苷、蔗糖、芍药苷、葡萄糖和果糖。研究了氢氧化钠浓度、分离电压、进样时间和检测电位等几个重要因素的影响,以获得最佳条件。检测电极是直径为300微米的铜盘电极,工作电位为+0.60 V(相对于饱和甘汞电极(SCE))。在75 mM氢氧化钠水溶液中,在12 kV的分离电压下,五个分析物可在40 cm长的熔融石英毛细管中于12分钟内良好分离。峰电流与分析物浓度之间的关系在约3个数量级内呈线性,所有分析物的检测限(S/N = 3)为0.9至1.3 microM。该方法已成功应用于监测实际植物样品中的糖苷和糖含量,测定结果令人满意。

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