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采用混合模式柱上的液相色谱-紫外检测法同时分析甜菊醇和甜菊糖苷:应用于甜叶菊植物材料和含甜叶菊的膳食补充剂

Simultaneous analysis of steviol and steviol glycosides by liquid chromatography with ultraviolet detection on a mixed-mode column: application to Stevia plant material and Stevia-containing dietary supplements.

作者信息

Jaworska Karolina, Krynitsky Alexander J, Rader Jeanne I

机构信息

U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition, Office of Regulatory Science, 5100 Paint Branch Pkwy, College Park, MD 20740, USA.

出版信息

J AOAC Int. 2012 Nov-Dec;95(6):1588-96. doi: 10.5740/jaoacint.11-435.

Abstract

Simultaneous separation of steviol and steviol glycosides is challenging because of differences in their polarity and chemical structure. In this study, simultaneous analysis of steviol and steviol glycosides was achieved by LC with UV detection using a mixed-mode RP weak anion exchange chromatography column. Steviol and seven steviol glycosides were analyzed on an Acclaim Mixed-Mode Wax-1 (Dionex) column with a linear gradient of deionized water adjusted to pH 3.00 with phosphoric acid and acetonitrile. The extraction was performed by sonicating dry plant material at 40 degreesC in acetonitrile-water (30 + 70, v/v). LOQ values (mg/g dry weight of plant material) were rebaudioside B, 0.50; steviol, 0.70, dulcoside A, 1.0; steviolbioside, 1.2; stevioside and rebaudioside C, 2.0; rebaudioside D, 3.3; and rebaudioside A, 5.0. The method demonstrated suitable performance for all analytes tested with respect to accuracy (mean recoveries 95-99%), intraday and interday precision for retention times (0.070-0.28% and 0.33-1.0% RSD, respectively), and linearity. The method was used to authenticate steviol glycosides in several samples of Stevia plant material as well as to quantitate steviol glycosides in dietary supplements containing Stevia.

摘要

由于甜菊醇和甜菊糖苷的极性和化学结构存在差异,同时分离它们具有挑战性。在本研究中,使用混合模式反相弱阴离子交换色谱柱,通过配有紫外检测的液相色谱法实现了甜菊醇和甜菊糖苷的同时分析。在Acclaim混合模式Wax - 1(戴安公司)色谱柱上,用磷酸将去离子水调至pH 3.00,并与乙腈形成线性梯度,对甜菊醇和七种甜菊糖苷进行分析。通过在40℃下将干燥的植物材料在乙腈 - 水(30 + 70,v/v)中超声处理来进行提取。定量限(mg/g植物材料干重)分别为:莱鲍迪苷B,0.50;甜菊醇,0.70;杜克苷A,1.0;甜菊苷,1.2;甜菊糖苷和莱鲍迪苷C,2.0;莱鲍迪苷D,3.3;莱鲍迪苷A,5.0。该方法在准确性(平均回收率95 - 99%)、保留时间的日内和日间精密度(分别为0.070 - 0.28%和0.33 - 1.0% RSD)以及线性方面,对所有测试分析物均表现出合适的性能。该方法用于鉴定几种甜叶菊植物材料样品中的甜菊糖苷,以及定量含有甜叶菊的膳食补充剂中的甜菊糖苷。

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