Improving the Phloroglucinolysis Protocol and Characterization of Sagrantino Wines Proanthocyanidins

Molecules. 2021 Feb 19;26(4):1087. doi: 10.3390/molecules26041087.

Abstract

Proanthocyanidins are key metabolites that explain wine sensorial character (bitterness and astringency) and red wine color changes during aging. Therefore, a fast and accurate method to evaluate the degree of polymerization and the structural composition of the polymeric proanthocyanidins is a crucial analytical tool. Phloroglucinolysis is the most used method for this analysis but, unfortunately, the phloroglucinol adducts of the monomeric flavan-3-ols are not commercially available, making the results less accurate. The aim of this work was the isolation by semi-preparative high performance liquid chromatography (HPLC) of these non-commercial compounds and their use for the development of an accurate UHPLC-MS/MS protocol. The purity of each adduct was established via quantitative 1H-nuclear magnetic resonance (NMR) measurements with 3-trimethylsilyl-propionic-d4 acid sodium salt as the calibration standard. The developed method was applied to evaluate the proanthocyanidins profile of Sagrantino di Montefalco wines in comparison to other well-known tannic wines. Commercial, 6-8 years old Sagrantino wines were demonstrated to be very rich in epicatechin type B procyanidins, to have low galloylation %, and to have a high mean degree of polymerization of the proanthocyanidins with respect to the other analyzed wines.

Keywords: Cabernet Sauvignon; Merlot; Nebbiolo; Sangiovese; Tannat; condensed tannins; epicatechin; phloroglucinol; polyphenols; quantitative NMR; tannins.

MeSH terms

  • Calibration
  • Chromatography, High Pressure Liquid
  • Flavonoids / chemistry
  • Phloroglucinol / chemistry*
  • Polymerization
  • Proanthocyanidins / analysis*
  • Tandem Mass Spectrometry
  • Wine / analysis*

Substances

  • Flavonoids
  • Proanthocyanidins
  • flavan-3-ol
  • Phloroglucinol