کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1198432 1493468 2016 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Comprehensive two-dimensional liquid chromatography–tandem mass spectrometry for the simultaneous determination of wine polyphenols and target contaminants
ترجمه فارسی عنوان
جامع اسپکترومتری جرمی کروماتوگرافی مایع جامع دوگانه برای تعیین همزمان پلی فنل های شراب و آلودگی های هدف
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• An LC × LC method was developed for the analysis of wine constituents and contaminants.
• Triple quadrupole MS was employed for sensitive targeted pesticide determination.
• Orthogonality metrics were calculated for the full and shift gradient approaches.

A novel system for comprehensive two-dimensional liquid chromatography coupled to a triple quadrupole mass spectrometer is described for the analysis of wine components. The first dimension consisted of a 250-mm microbore cyano column utilizing 5 μm diameter particles, interfaced to a 50-mm superficially-porous particle C18 column with 2.7 μm diameter particles. Both columns were operated under reversed-phase conditions. Correlation between the two chromatographic separation modes was decreased by designing a 60-s shift gradient program in the second dimension, and the increase in orthogonality was evaluated quantitatively utilizing a number of orthogonality metrics. The system was employed for the analysis of a red wine sample, without preliminary clean-up procedures, and a total of 43 polyphenols were separated and identified. Comparison with a one-dimensional LC system showed a large increase in the number of identified components with the two-dimensional system. Optimized multiple reaction monitoring experiments allowed for the determination of trans-resveratrol, which is one of the most active antioxidant component of wine, and for monuron, a plant protection product (herbicide) of interest to regulatory agencies. The estimated limits of detection and of quantification were 0.3 μg L−1 and 1 μg L−1, respectively, well below the minimum detection limit (10 μg L−1) set by current regulation.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography A - Volume 1458, 5 August 2016, Pages 54–62
نویسندگان
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