Anthocyanins of grape fruits: the determination of types by gradient RP HPLC and the separation into two parts by flash chromatography
Abstract
In the paper the method of reversed-phase HPLC with diode-array and mass spectroscopic detection was used for investigated of the grape anthocyanin species composition of the popular local grape variety unknown breeding. The appearance of derivatives of 3,5-diglucosides indicates the hybrid nature of this grape variety. The anthocyanins specie composition has some specific fixture – the prevalence of delphinidine derivatives compared to that of petunidin and malvidin, as well as relatively high degree of acylation with acetic and p-coumaric acids. In this case only a gradient reversed-phase HPLC is an effective method for solute separation. But it has been shown that the solvatochromic effect impairs uncertainty to quantitative assessment of species composition by the areas of the peaks on the chromatogram. Though comparison of the grape anthocyanin spectra for various acetonitrile concentrations revealed a specific point on the spectra with absorption not dependent upon solvent composition. The wave length of the point was proposed to register the chromatogram for quantitative calculation of anthocyanins species composition. To make it possible to perform the anthocyanins separation by isocratic HPLC the flash chromatography was used to separate anthocyanin components into two parts, non-acylated and acylated compounds by the usage of syringe cartridges for the solid phase extraction
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References
2. Prior R.L., Wu X., Free Radical Res., 2006, Vol. 40, pp. 1014-1028. http://dx.doi.org/
10.1080/10715760600758522
3. Ferrières J., Heart, 2004, Vol. 90, pp. 107-111, https://www.ncbi.nlm.nih.gov/pmc
/articles/PMC1768013/pdf/hrt09000107.pdf
4. Flamini R., Tomasi D., Vitis. 2000. Vol. 39, pp. 79-81, http://www.vitis-vea.de/admin/
volltext/e043505.pdf
5. Berente B., Reichenbächer M., Danzer K., Fresenius J. Anal. Chem., 2001, Vol. 371, pp. 68-72, Available at https://link.springer.
com/article/10.1007/s002160100940
6. Lee J., Rennaker C., Wrolstad R.E., Food Chem., 2008, Vol. 110, pp. 782–786. http://doi.org/10.1016/j.foodchem.2008.03.010 Available at: http://www.sciencedirect.com/
science/article/pii/S030881460800304X
7. Makarevitch S.L., Chulkov A.N., Deineka V.I., Kostenko М.О. et al., Sorbtsionnye i khromatograficheskie protsessy, 2014, Vol. 14, No 6, pp. 1024-1031.
8. Giusti M.M., Wrolstad, R.E. / Current Protocols in Food Analytical Chemistry / Ed. Wrolstad R.E., New York, NY: John Wiley & Sons, 2001. UNIT F1.2. DOI: 10.1002/0471142913.faf0102s00. Available at: http://onlinelibrary.wiley.com/
doi/10.1002/0471142913.faf0102s00/abstract
9. Reichardt C., Chem. Rev., 1994, Vol. 94, pp. 2319-2358. DOI: 10.1021/cr00032a005. Available at: http://pubs.acs.org/doi/abs
/10.1021/cr00032a005
10. Deineka L.A., Livin Yu.Yu., Deineka V.I., Nauchnye vedomosti BelGU. Seriya: Estestvennye nauki, 2008, Vol. 7(47), No 7, pp. 71-78.
11. Deineka V.I., Deineka L.A., Sidorov A.N., Saenko I.I. et al., Sorbtsionnye i khromatograficheskie protsessy, 2016, Vol. 16, No 5, pp. 624-630.