Plant sources of pelargonidin derivatives for anthocyanin identification

Authors

  • Irina P. Blinova Belgorod State National Research University, Belgorod
  • Victor I. Deineka Belgorod State National Research University, Belgorod
  • Vladimir F. Selemenev Voronezh State University, Voronezh
  • Dmitry N. Blinov Belgorod State National Research University, Belgorod
  • Lyudmila A. Deineka Belgorod State National Research University, Belgorod
  • Yan Van Nguyen Food Industry University of Ho Chi Minh, Ho Chi Minh City

DOI:

https://doi.org/10.17308/sorpchrom.2025.25/13575

Keywords:

standard samples, qualitative analysis, pelargonidin derivatives, strawberry fruits, scarlet tulip flowers, scarlet rose flowers

Abstract

The problem of standard substances for qualitative and quantitative analysis, which has recently arisen in connection with sanctions, can be partially solved (for qualitative determination) by using extracts of plant materials, the composition of which has little or no dependence on the cultivar and growing conditions. It has been shown that for the reliable determination of some pelargonidin derivatives in plant extracts, extracts of fruits or flowers of specially selected plants can be prepared in laboratories. In this case, to identify the corresponding pelargonidin glycosides, it is sufficient to compare the retention times and electronic absorption spectra of the anthocyanins of the test compound with the extract of the selected plant material. Thus, based on many years of research carried out at the Belgorod National Research University, to identify cyanidin-3-glucoside, you can use an extract of the fruits of ordinary strawberries sold on the market, the composition of which is discussed in this work and contains cyanidin-3-glucoside as the main component (more than 80% in terms of peak areas). An alternative option is the scarlet fruits of barberry, containing more than 50% of this anthocyanin with the addition of 3-glucosides cyanidin and delphinidin. Control of plant material can be carried out by electronic absorption spectra that differ from anthocyanins based on the other five common aglycones (cyanidin and peonidin, delphinidin, petunidin and malvidin). For the identification of pelargonidin-3-rutinoside, a convenient source of this anthocyanin is the petals of scarlet tulips (not dark red, brown or purple). An alternative is the fruits of downy cherries, which are quite popular among gardeners. To identify pelargonidin-3,5-diglucoside, a scarlet rose or pelargonium flowers of the same color can be used. The work presents the necessary electronic absorption spectra. The work presents the necessary electronic absorption spectra. It has been shown that during internal normalization it is desirable to record peaks at the wavelength corresponding to the maximum absorption. But you can use special correction factors calculated based on the individual spectrum of anthocyanins. The retention of pelargonidin derivatives on several brands of stationary phases was compared.

Downloads

Download data is not yet available.

Author Biographies

  • Irina P. Blinova, Belgorod State National Research University, Belgorod

    Docent of General Chemistry Department. Dr. Ph.(Chemistry), Belgorod State University, Belgorod, Russian Federation, e-mail: blinova@bsuedu.ru

  • Victor I. Deineka, Belgorod State National Research University, Belgorod

    Professor of General Chemistry Department. Dr. Sci.(Chemistry), Belgorod State University, Belgorod, Russian Federation, e-mail: deineka@bsuedu.ru

  • Vladimir F. Selemenev, Voronezh State University, Voronezh

    Professor of Analytical Chemistry Department, Dr. Sci.(Chemistry), Voronezh State University, Voronezh, Russian Federation

  • Dmitry N. Blinov, Belgorod State National Research University, Belgorod

    PhD student, Department of General Chemistry, Belgorod State National Research University, Belgorod, Russian Federation, e-mail: 1466805@bsuedu.ru

  • Lyudmila A. Deineka, Belgorod State National Research University, Belgorod

    Docent of General Chemistry Department. Dr. Ph.(Chemistry), Belgorod State University, Belgorod, Russian Federation, e-mail: deyneka@bsuedu.ru

  • Yan Van Nguyen, Food Industry University of Ho Chi Minh, Ho Chi Minh City

    a lecturer at the Faculty of Food Technology, PhD in Chemistry, Ho Chi Minh City Food Industry University, Russian Federation,  anhnv@hufi.edu.vn

References

Lee J., Rennaker C., Wrolstad R.E. Food Chem. 2008; 110: 782-786. https://doi.org/10.1016/j.foodchem.2008.03.010

Lee J., Durst R.W., Wrolstad R.E. J. AOAC Intern. 2005; 88: 1269-1278. https://doi.org/10.1093/jaoac/88.5.1269

Rivas-Gonzalo J.C., Gutierrez Y., Hebrero E., Santos-Buelga C. Am. J. Enol. Vitic. 1992; 43: 210-214. https://doi.org/10.5344/ajev.1992.43.2.210

Deineka L.A., Sidorov A.N., Deineka V.I. Kul’chenko Ya.Yu., Blinova I.P., J. Anal. Chem. 2020; 75: 754-758. https://doi.org/10.1134/S1061934820060064

Deineka V.I., Oleinits E.Yu., Kul’chenko Ya.Yu., Blinova I.P., Deineka L.A. J. Anal. Chem. 2020; 75: 1443-1450. https://doi.org/10.1134/S1061934820090087

Deineka V.I., Oleinits E.Yu., Kulchenko Y.Yu., Blinova I.P., Deineka L.A. Russ. J. Phys. Chem. A. 2021; 95: 1729-1734. https://doi.org/10.1134/S0036024421080094

Dejneka L.A., Blinova I.P., Kul'chenko YA.I., Ozer P.S., Saenko I.I., Dejneka V.I. Uspekhi sovremennogo estestvoznaniya. 2016; 2: 16-20 (In Russ.)

ZHbanova E.V., Luk"yanchuk I.V., Pak N.A. Sovremennye nauchnye issledovaniya i innovacii. 2016; 3: 241-253 (in Russ.)

Karaaslan N.M., Yaman M. Intern. J. Food Prop. 2017; 20: S2313-S2322. https://doi.org/10.1080/10942912.2017.1368548

Bridle P., Garcia-Viguera C. Food Chem. 1997; 59: 299-304. https://doi.org/10.1016/S0308-8146(96)00176-8

Aaby K., Mazur S., Nes A., Skrede G. Food Chem. 2012; 132: 86-97. https://doi.org/10.1016/j.foodchem.2011.10.037

Comandini P., Blanda G., Cardinali A., Cerretani L., Bendini A., Caboni M. J. Sep. Sci. 2008; 31: 3257-3264. https://doi.org/10.1002/jssc.200800199

da Silva F.L., Escribano-Bailón M.T., Alonso J.P., Rivas-Gonzalo J.C., Santos-Buelga C. LWT - Food Sci. Technol. 2007; 40: 374-382. https://doi.org/10.1016/j.lwt.2005.09.018

Tamura H., Takada M., Yoshida Y. Nyoho. Biosci. Biotechnol. Biochem. 1995; 59(6): 1157-1158. https://doi.org/10.1271/bbb.59.1157

Sorokopudov V.N., Hlebnikov V.A., Dejneka V.I. Himiya rastitel'nogo syr'ya. 2005; 4: 57-60. (IN Russ.)

Deineka, V.I., Deineka, L.A., Sele-menev, V.F., Chulkov, A.N., Kulchenko, Y.Y. VEZHKH. Sorbcionnye i hromatograficheskie processy. 2016.; 16: 464-471. (In Russ.)

Cao J., Jiang Q., Lin J., Li X., Sun C., Chen K. Food Chem. 2015; 173: 855-863. https://doi.org/10.1016/j.foodchem.2014.10.094

Deineka V.I., Deineka L.A., Saenko I.I. J. Anal. Methods Chem. 2015; 2015: ID 732918. https://doi.org/10.1155/2015/732918

Gardeli C., Varela K., Krokida E., Mallouchos A. Medicines. 2019; 6: 90. https://doi.org/10.3390/medicines6030090

Siriwoharn T., Wrolstad R.E., Finn C.E., Pereira C.BJ. Agric. Food Chem. 2004; 52: 8021-8030. https://doi.org/10.1021/jf048619y

Downloads

Published

2026-02-10

How to Cite

Plant sources of pelargonidin derivatives for anthocyanin identification. (2026). Sorbtsionnye I Khromatograficheskie Protsessy, 25(6), 911-919. https://doi.org/10.17308/sorpchrom.2025.25/13575

Most read articles by the same author(s)

<< < 1 2 3 4