Plateforme Polyphénols, SPO, INRA, Montpellier SupAgro, Université de Montpellier, 2 place Viala, 34060, Montpellier, France.
Departamento de Ciência e Tecnologia de Alimentos CAL/CCA, Universidade Federal de Santa Catarina, Rod. Admar Gonzaga, 1346, Itacorubi, Florianópolis, SC, 88034-001, Brazil.
Anal Bioanal Chem. 2018 Jun;410(15):3483-3490. doi: 10.1007/s00216-017-0759-y. Epub 2017 Dec 18.
A UHPLC-MS/MS method was developed for the quantification of the main compounds involved in oxidation reactions occurring in white musts and wines such as hydroxycinnamic acids, their glutathione and cysteinylglycine adducts (GRP, GRP2, 5-(S-glutathionyl)-trans-caftaric acid, 2-(S-cysteinylglycyl)-trans-caftaric acid, and 2-(S-glutathionyl)-trans-caffeic acid), and reduced and oxidized glutathione (GSH, GSSG) in wine. Since oxidation is the main concern in white wine-making, directly affecting its quality, the developed method was then applied in a series of white wines made with different pre-fermentation treatments to limit oxidation at must stage. The glucose esters and/or glucosides of hydroxycinnamic acids were quantified as glucogallin equivalent. The developed method led to an overall improvement in the limits of detection (LODs) and quantification (LOQs) for all the compounds studied in comparison to other methods such as high-performance liquid chromatography with fluorescence detection (HPLC-FLD) or diode array UV detection (HPLC-DAD). LOD values ranged from 0.0002 to 0.0140 mg/L and LOQs from 0.0005 to 0.0470 mg/L. The recoveries ranged between 80 and 110% in wines, and the relative standard deviation (RSD) for precision intra- and inter-day was below 15%. The accuracy and intra- and inter-day precision met the acceptance criteria of the AOAC international norms. As far as we know, this study is the first report of quantification of GRP, 2-(S-cysteinylglycyl)-trans-caftaric acid, and 2-(S-glutathionyl)-trans-caffeic acid using these non-commercially available compounds as external standards. Those compounds represent a significant proportion of hydroxycinnamic acid derivatives in wines. The methodology described is suitable for the analysis of hydroxycinnamic derivatives in wines.
建立了一种 UHPLC-MS/MS 方法,用于定量测定白葡萄酒和葡萄酒中发生氧化反应的主要化合物,如羟基肉桂酸、它们的谷胱甘肽和半胱氨酸甘氨酸加合物(GRP、GRP2、5-(S-谷胱甘肽)-反式咖啡酰酸、2-(S-半胱氨酸甘氨酰)-反式咖啡酰酸和 2-(S-谷胱甘肽)-反式咖啡酸)以及还原型和氧化型谷胱甘肽(GSH、GSSG)。由于氧化是白葡萄酒酿造过程中的主要关注点,直接影响其质量,因此该方法随后应用于一系列采用不同预发酵处理的白葡萄酒中,以限制发酵前阶段的氧化。羟基肉桂酸的葡萄糖酯和/或糖苷被定量为没食子酰葡萄糖苷当量。与高效液相色谱-荧光检测(HPLC-FLD)或二极管阵列紫外检测(HPLC-DAD)等其他方法相比,该方法提高了所有研究化合物的检测限(LOD)和定量限(LOQ)。LOD 值范围为 0.0002 至 0.0140mg/L,LOQ 值范围为 0.0005 至 0.0470mg/L。葡萄酒中的回收率在 80%至 110%之间,日内和日间精密度的相对标准偏差(RSD)低于 15%。准确性和日内、日间精密度符合 AOAC 国际标准的验收标准。据我们所知,这是首次使用这些非商业可得的化合物作为外标物来定量测定 GRP、2-(S-半胱氨酸甘氨酰)-反式咖啡酰酸和 2-(S-谷胱甘肽)-反式咖啡酸。这些化合物在葡萄酒中代表了羟基肉桂酸衍生物的重要比例。所描述的方法适用于葡萄酒中羟基肉桂酸衍生物的分析。