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Determination of polyphenols in spanish wines by capillary zone electrophoresis. Application to wine characterization by using chemometrics

机译:毛细管区带电泳法测定西班牙葡萄酒中的多酚。化学计量学在葡萄酒表征中的应用

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摘要

A capillary zone electrophoresis method for the simultaneous determination of twenty polyphenols in wine was developed. The separation was performed using fused-silica capillaries of 75 µm I.D. and a 30 mM sodium tretraborate buffer solution at pH 9.2 with 5% isopropanol as a background electrolyte. A capillary voltage of +25 kV with pressure-assisted (3.5 kPa) separation from min 18 was applied, thus, achieving a total analysis time lower than 20 min. Instrumental quality parameters such as limits of detection (LOD values between 0.3 and 2.6 mg/L), linearity (r2>0.990), and run-to-run and day-to-day precisions (RSD values lower than 6.5% and 15.7%, respectively) were established. Three different calibration procedures were evaluated for polyphenol quantitation in wines: external calibration using standards prepared in Milli-Q water, standard addition, and pseudo-matrix matched calibration using wine as a matrix. For a 95% confidence level, no statistical differences were observed, in general, between the three calibration methods (p-values between 0.11 and 0.84), while for some specific polyphenols, such as cinnamic acid, syringic acid and gallic acid, results were not comparablewhen external calibration used. CZE method using pseudo-matrix matched calibration was then proposed and applied to the analysis of polyphenols in 49 Spanish wines, showing satisfactory results and a wide compositional variation between wines. Electrophoretic profiles and other compositional data (e.g., peak areas of selected peaks) were considered as fingerprints of wines to be used for characterization and classification purposes. The corresponding data were analyzed by PCA in order to extract information on the most significant features contributing to wine discrimination according to their origins. Results showed that a reasonable distribution of wines depending on the elaboration areas was found, being tirosol, gallic, protocatechuic, p-coumaric and caffeic acids some representative discriminant compounds.
机译:建立了同时测定葡萄酒中二十种多酚的毛细管区带电泳方法。使用内径为75 µm的熔融石英毛细管进行分离。以及pH 9.2的30 mM四硼酸钠缓冲溶液,其中5%异丙醇作为背景电解质。从分钟18开始施加+25 kV的毛细管电压,并从压力18分钟分离出压力(3.5 kPa),因此,总分析时间少于20分钟。仪器质量参数,例如检出限(LOD值在0.3和2.6 mg / L之间),线性(r2> 0.990)以及逐次运行和日常精度(RSD值分别低于6.5%和15.7%) )。针对葡萄酒中的多酚定量,评估了三种不同的校准程序:使用Milli-Q水制备的标准品进行外部校准,添加标准品以及使用葡萄酒作为基质的伪矩阵匹配校准。对于95%的置信度,通常在三种校准方法之间没有观察到统计学差异(p值在0.11和0.84之间),而对于某些特定的多酚,例如肉桂酸,丁香酸和没食子酸,结果是使用外部校准时无法比较。然后提出了使用伪矩阵匹配校准的CZE方法,并将其用于49种西班牙葡萄酒中的多酚分析,结果令人满意,葡萄酒之间的成分差异很大。电泳图谱和其他组成数据(例如,选定峰的峰面积)被视为葡萄酒的指纹,可用于表征和分类。 PCA对相应的数据进行了分析,以提取有关根据其来源对葡萄酒进行区分的最重要特征的信息。结果表明,根据精制区域的不同,发现葡萄酒的合理分配是:浓香酚,没食子酸,原儿茶酸,对香豆酸和咖啡酸,这是一些代表性的鉴别化合物。

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