Evaluation of new cellulose-based chiral stationary phases Sepapak-2 and Sepapak-4 for the enantiomeric separation of pesticides by nano liquid chromatography and capillary electrochromatography

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• 作者：Virginia Pé ; rez-Ferná ; ndez^a ; ^{virginia.perezf@uah.es} ; Elena Dominguez-Vega^a ; ^{elena.dominguezv@uah.es} ; Bezhan Chankvetadze^b ; ^{bezhan_chankvetadze@yahoo.com} ; Antonio L. Crego^a ; ^{antonio.crego@uah.es} ; Maria Á ; ngeles Garc&#237 ; a^a ; ^{angeles.garcia@uah.es} ; Maria Luisa Marina^a ; ^{mluisa.marina@uah.es}
• 关键词：Pesticides ; Metalaxyl ; Capillary electrochromatography ; Nano-liquid chromatography ; Polysaccharide-based chiral stationary phase
• 刊名：Journal of Chromatography A
• 出版年：2012
• 期刊代码：47_00219673
• 类别：ch
• 出版时间：20 April, 2012
• 卷：1234
• 期：Complete
• 页码：22-31
• 文件大小：1015 K

摘要

Two novel polysaccharide-based chiral stationary phases (CSPs), known as Sepapak-2 (cellulose tris(3-chloro-4-methylphenylcarbamate)) and Sepapak-4 (cellulose tris(4-chloro-3-methylphenylcarbamate)), have been evaluated in this work for the chiral separation of a group of 16 pesticides including herbicides, insecticides and fungicides. The optimization of the mobile phase employed in nano-liquid chromatography (nano-LC) enabled the chiral separation of seven pesticides on Sepapak-2 and of nine pesticides on Sepapak-4. Due to the fact that Sepapak-4 gave better results, this column was selected to compare nano-LC and capillary electrochromatography (CEC) under the same conditions that consisted in the use of a 90/9/1 (v/v/v) ACN/H₂O/ammonium formate (pH 2.5) background electrolyte (BGE). As expected, both the efficiency and the chiral resolution obtained in CEC experiments were higher than in nano-LC for all the analyzed compounds. The analytical characteristics of the CEC developed methodology were evaluated in terms of linearity, LODs, LOQs, precision, selectivity, and accuracy allowing its application to the quantitation of metalaxyl and its enantiomeric impurity in a commercial fungicide product marketed as enantiomerically pure (metalaxyl-M) and in soil and tap water samples after solid phase extraction (SPE). The determined amount of metalaxyl-M was found to be a 26%above the labeled content and it contained an enantiomeric impurity of a 3.7%of S-metalaxyl was determined.