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Analysis of sweet diterpene glycosides from Stevia rebaudiana: ImprovedHPLC method

机译:甜叶菊甜二萜糖苷的分析:改进的HPLC方法

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An improved analytical method was developed which may be applied to quality control of stevioside and rebaudioside A contents in dried leaves of Stevia rebaudiana before processing; in a selective sampling program searching for plants of higher yield in diterpene glycosides content; or when a large number of samples are sent to the laboratory for analysis. The procedure developed involves two steps: solvent extraction followed by an isocratic HPLC analysis. The sample, 1 g of dried leaves of S. rebaudiana, is ground and solvent-extracted with EtOH 70% (w/w) in Erlenmeyer flasks by shaking for 30 min in a 70 degreesC water bath. After the extract was cooled, it was filtered and analyzed by HPLC using an NH2 column (250 x 4.6 mm) and a mixture of acetonitrile/water (80:20, v/v) as mobile phase, pH 5 adjusted with acetic acid. The detection was in the UV range at 210 nm (0.04 AUFS). Quantitation was performed by means of an external standard calibration curve for each analyte which had been obtained from standard solutions of pure stevioside and rebaudioside A. Working under these conditions there were no observed interference effects. The method saves time in sample preparation, and reduces sample handling and chromatographic analysis time, while having little loss of precision [coefficient of variation (CV%) between 1.8% and 3.0%] and recovery [between 98.5% and 100.5%]. The method was applied to 30 samples of S. rebaudiana from Misiones (Northeastern Argentina), and the stevioside content found ranged between 3.78 and 9.75% (weight) whereas Rebaudioside A content ranged between 1.62 and 7.27% (weight).
机译:开发了一种改进的分析方法,可用于加工前甜叶菊干叶中甜菊苷和莱鲍迪甙A含量的质量控制。在选择性抽样计划中,寻找具有更高产量的二萜糖苷含量的植物;或将大量样品发送到实验室进行分析时。开发的程序包括两个步骤:溶剂萃取,然后进行等度HPLC分析。将样品(1 g葡萄干沙门氏干叶)磨碎,并在70℃水浴中振摇30分钟,然后在锥形瓶中用70%(w / w)的EtOH萃取溶剂。将提取物冷却后,将其过滤并使用NH 2柱(250×4.6mm)和作为流动相的乙腈/水的混合物(80:20,v / v)通过HPLC进行分析,用乙酸调节pH 5。检测在210 nm(0.04 AUFS)的UV范围内。借助于外标校准曲线对从纯甜菊糖苷和莱鲍迪苷A的标准溶液中获得的每种分析物进行定量。在这些条件下工作,未观察到干扰效应。该方法节省了样品制备时间,并减少了样品处理和色谱分析时间,同时几乎没有精度损失[1.8%至3.0%之间的变异系数(CV%)]和回收率[98.5%至100.5%之间]。该方法应用于Misiones(阿根廷东北部)的30个雷氏链球菌样品,甜菊糖苷含量范围为3.78至9.75%(重量),而莱鲍迪苷A含量范围为1.62至7.27%(重量)。

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