An improved high performance liquid chromatography (HPLC) method for the analysis of the main organic compounds in musts and wines is presented. A column packed with hydrogen sulfonated divinyl benzene-styrene copolymer and two detectors connected in series were used (UV at 210 nm and RI, respectively). The addition of acetonitrile (6%) to the mobile phase (0.045N H2SO4) allowed the simultaneous separation and quantification of several organic acids, glucose, fructose, glycerol, and ethanol. Direct injection and sample clean-up with a SAX cartridge was tested and compared. The SAX fractionation gave satisfactory results, however the direct injection of diluted wine (1:20) provided the best precision (CV ≤ 2.1%) and accuracy of analysis. Statistical analysis (paired t- test) disclosed significant differences only for glucose, fructose, α-ketoglutaric, and pyruvic acid. The role of column temperature for the analysis of vitamin C (ascorbic acid) was also investigated. Vitamin C underwent thermal degradation during analysis with column temperature ≥30°C.
Castellari M., Versari A., Spinabelli U., Galassi S., Amati A. (2000). An improved HPLC method for the analysis of organic acids, carbohydrates, and alcohols in grape musts and wines. JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 23(13), 2047-2056 [10.1081/JLC-100100472].
An improved HPLC method for the analysis of organic acids, carbohydrates, and alcohols in grape musts and wines
Versari A.
Membro del Collaboration Group
;Spinabelli U.Membro del Collaboration Group
;Galassi S.Membro del Collaboration Group
;Amati A.Membro del Collaboration Group
2000
Abstract
An improved high performance liquid chromatography (HPLC) method for the analysis of the main organic compounds in musts and wines is presented. A column packed with hydrogen sulfonated divinyl benzene-styrene copolymer and two detectors connected in series were used (UV at 210 nm and RI, respectively). The addition of acetonitrile (6%) to the mobile phase (0.045N H2SO4) allowed the simultaneous separation and quantification of several organic acids, glucose, fructose, glycerol, and ethanol. Direct injection and sample clean-up with a SAX cartridge was tested and compared. The SAX fractionation gave satisfactory results, however the direct injection of diluted wine (1:20) provided the best precision (CV ≤ 2.1%) and accuracy of analysis. Statistical analysis (paired t- test) disclosed significant differences only for glucose, fructose, α-ketoglutaric, and pyruvic acid. The role of column temperature for the analysis of vitamin C (ascorbic acid) was also investigated. Vitamin C underwent thermal degradation during analysis with column temperature ≥30°C.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
