Bianchi Federica, Careri Maria, Corradini Claudio
Dipartimento di Chimica Generale ed Inorganica, Chimica Analitica, Chimica Fisica, Università degli Studi di Parma, Parco Area delle Scienze 17/A, 1-43100 Parma, Italy.
J Sep Sci. 2005 Jun;28(9-10):898-904. doi: 10.1002/jssc.200500046.
An innovative protocol for the fast analysis of some organic acids in red wine by co-electroosmotic capillary zone electrophoresis and indirect UV detection using hexadimethrine bromide (HDB) as coating agent was proposed. The adsorption of HDB onto the capillary wall provided a stable electroosmotic flow and separation of small anions was carried out using background electrolytes containing no polymer additive. Low RSD% values (<3.6%) in terms of migration times and effective mobilities were obtained from the analysis of a mixture of nitrate and nitrite and of a mixture of organic acids. An experimental design approach was used to investigate the effects of temperature, separation voltage, and percentage of methanol added to the running buffer solution on the separation of the analytes. A faster method allowing the separation of the organic acids involved in the malolactic fermentation of wine was developed. Using a running electrolyte consisting of 35% (v/v) methanol in a solution of 22 mM benzoic acid at pH 6.10 adjusted with 1.0 M TRIS-base buffer, the separation of tartaric, malic, succinic, acetic, and lactic acids was feasible in less than 210 s. Application of the method to the quantification of the above-mentioned organic acids in Italian red wine samples is reported.
提出了一种创新方案,通过共电渗毛细管区带电泳和以溴化己二甲铵(HDB)为涂层剂的间接紫外检测快速分析红葡萄酒中的某些有机酸。HDB在毛细管壁上的吸附提供了稳定的电渗流,并且使用不含聚合物添加剂的背景电解质对小阴离子进行分离。通过分析硝酸盐和亚硝酸盐混合物以及有机酸混合物,在迁移时间和有效迁移率方面获得了低相对标准偏差值(<3.6%)。采用实验设计方法研究了温度、分离电压和运行缓冲溶液中甲醇添加百分比对分析物分离的影响。开发了一种更快的方法,可用于分离葡萄酒苹果酸-乳酸发酵中涉及的有机酸。使用由22 mM苯甲酸在pH 6.10的溶液中含35%(v/v)甲醇且用1.0 M三羟甲基氨基甲烷碱缓冲液调节而成的运行电解质,酒石酸、苹果酸、琥珀酸、乙酸和乳酸在不到210 s内即可实现分离。报道了该方法在意大利红葡萄酒样品中上述有机酸定量分析中的应用。