Fontana Ariel, Rodríguez Isaac, Cela Rafael
Laboratorio de Bioquímica Vegetal, Instituto de Biología Agrícola de Mendoza, Consejo Nacional de Investigaciones Científicas y Técnicas-Universidad Nacional de Cuyo, Almirante Brown 500, M5528AHB Chacras de Coria, Argentina.
Departamento de Química Analítica, Nutrición y Bromatología, Instituto de Investigación y Análisis Alimentario (IIAA), Universidad de Santiago de Compostela, Santiago de Compostela 15782, Spain.
J Chromatogr A. 2017 Sep 15;1515:30-36. doi: 10.1016/j.chroma.2017.07.085. Epub 2017 Jul 29.
A new reliable method for the determination 3-alkyl-2-methoxypyrazines (MPs) in wine samples based on the sequential combination of solid-phase extraction (SPE), dispersive liquid-liquid microextraction (DLLME) and gas chromatography (GC) quadrupole time-of-flight accurate tandem mass spectrometry (QTOF-MS/MS) is presented. Primary extraction of target analytes was carried out by using a reversed-phase Oasis HLB (200mg) SPE cartridge combined with acetonitrile as elution solvent. Afterwards, the SPE extract was submitted to DLLME concentration using 0.06mL carbon tetrachloride (CCl) as extractant. Under final working conditions, sample concentration factors above 379 times and limits of quantification (LOQs) between 0.3 and 2.1ngL were achieved. Moreover, the overall extraction efficiency of the method was unaffected by the particular characteristics of each wine; thus, accurate results (relative recoveries from 84 to 108% for samples spiked at concentrations from 5 to 25ngL) were obtained using matrix-matched standards, without using standard additions over every sample. Highly selective chromatographic records were achieved considering a mass window of 5mDa, centered in the quantification product ion corresponding to each compound. Twelve commercial wines, elaborated with grapes from different varieties and geographical origins, were processed with the optimized method. The 2-isobutyl-3-methoxypyrazine (IBMP) was determined at levels above the LOQs of the method in half of the samples.
本文提出了一种基于固相萃取(SPE)、分散液液微萃取(DLLME)和气相色谱(GC)四极杆飞行时间精确串联质谱(QTOF-MS/MS)顺序联用的测定葡萄酒样品中3-烷基-2-甲氧基吡嗪(MPs)的可靠新方法。采用反相Oasis HLB(200mg)固相萃取柱结合乙腈作为洗脱溶剂对目标分析物进行初步萃取。之后,使用0.06mL四氯化碳(CCl)作为萃取剂对固相萃取提取物进行分散液液微萃取浓缩。在最终工作条件下,实现了高于379倍的样品浓缩因子和0.3至2.1ng/L的定量限(LOQs)。此外,该方法的整体萃取效率不受每种葡萄酒特定特性的影响;因此,使用基质匹配标准品获得了准确的结果(对于添加浓度为5至25ng/L的样品,相对回收率为84%至108%),而无需对每个样品使用标准加入法。考虑到以每种化合物对应的定量产物离子为中心的5mDa质量窗口,实现了高选择性的色谱记录。使用优化后的方法对12种由不同品种和地理来源的葡萄酿造的市售葡萄酒进行了处理。在一半的样品中检测到2-异丁基-3-甲氧基吡嗪(IBMP)的含量高于该方法的定量限。