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采用柱耦合芯片上的等速电泳样品预处理进行区带电泳法测定葡萄酒中的游离亚硫酸盐。

Determination of free sulfite in wine by zone electrophoresis with isotachophoresis sample pretreatment on a column-coupling chip.

作者信息

Masár Marián, Danková Mariana, Olvecká Eva, Stachurová Adela, Kaniansky Dusan, Stanislawski Bernd

机构信息

Department of Analytical Chemistry, Faculty of Natural Sciences, Comenius University, Mlynská Dolina CH-2, SK-84215 Bratislava, Slovak Republic.

出版信息

J Chromatogr A. 2004 Feb 13;1026(1-2):31-9. doi: 10.1016/j.chroma.2003.11.038.

Abstract

This work deals with the determination of free sulfite in wine by zone electrophoresis (ZE) with on-line isotachophoresis (ITP) sample pretreatment on a column-coupling (CC) chip with conductivity detection. A rapid pre-column conversion of sulfite to hydroxymethanesulfonate (HMS), to minimize oxidation losses of the analyte, was included into the developed analytical procedure, while ITP and ZE were responsible for specific analytical tasks in the separations performed on the CC chip. ITP, for example, eliminated the sample matrix from the separation compartment and, at the same time, provided a selective concentration of HMS before its transfer to the ZE stage of the separation. On the other hand, ZE served as a final separation (destacking) method and it was used under the separating conditions favoring a sensitive conductivity detection of HMS. In this way, ITP and ZE cooperatively contributed to a 900 microg/l concentration detectability for sulfite as attained for a 60 nl load of wine (a 15-fold wine dilution and the use of a 0.9 microl sample injection channel of the chip) and, consequently, to the determination of free sulfite when this was present in wine at the concentrations as low as 3 mg/l. The separations were carried out in a closed separation compartment of the chip with suppressed hydrodynamic and electroosmotic flows. Such transport conditions, minimizing fluctuations of the migration velocities of the separated constituents, made a frame for precise migration and quantitation data as achieved for HMS in both the model and wine samples. Ninety percent recoveries, as typically obtained for free sulfite in wine samples, indicate promising potentialities of the present method as far as the accuracies of the provided analytical results are concerned.

摘要

本研究通过柱耦合(CC)芯片上的在线等速电泳(ITP)样品预处理结合区带电泳(ZE)和电导检测来测定葡萄酒中的游离亚硫酸盐。所开发的分析方法包括将亚硫酸盐快速预柱转化为羟甲基磺酸盐(HMS),以尽量减少分析物的氧化损失,而ITP和ZE则负责在CC芯片上进行的分离中的特定分析任务。例如,ITP从分离室中去除样品基质,同时在将HMS转移到分离的ZE阶段之前对其进行选择性浓缩。另一方面,ZE用作最终分离(去堆积)方法,并在有利于对HMS进行灵敏电导检测的分离条件下使用。通过这种方式,ITP和ZE协同作用,对于60 nl进样量的葡萄酒(葡萄酒稀释15倍并使用芯片上0.9 μl的样品进样通道),实现了900 μg/l的亚硫酸盐浓度检测限,从而能够测定葡萄酒中低至3 mg/l浓度的游离亚硫酸盐。分离在芯片的封闭分离室中进行,抑制了流体动力流和电渗流。这种传输条件使分离成分的迁移速度波动最小化,为模型样品和葡萄酒样品中的HMS获得精确的迁移和定量数据提供了框架。葡萄酒样品中游离亚硫酸盐通常获得的90%回收率表明,就所提供分析结果的准确性而言,本方法具有良好的潜力。

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