QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE

UDC 547.9:582.284.5

  • Tat'yana Petrovna Kukina Novosibirsk Institute of Organic Chemistry, SB RAS N.N. Vorozhtsova Email: kukina@nioch.nsc.ru
  • Dmitriy Nikolayevich Shcherbakov Altai State University; FBUN SSC VB "Vector"; Ltd IPK Zetgen Email: dnshcherbakov@gmail.com
  • Nina Vital'yevna Panteleyeva FBUN SSC VB "Vector" Email: nino4ka_panteleeva@mail.ru
  • Ol'ga Iosifovna Sal'nikova Novosibirsk Institute of Organic Chemistry, SB RAS N.N. Vorozhtsova Email: olga@nioch.nsc.ru
  • Petr Vladimirovich Kolosov Altai State University Email: petro.kolosov@gmail.com
Keywords: sunflower oil, lipid composition, aliphatic acids, distillation, GLC-MS, HPLC

Abstract

The composition of the sunflower oil deodorization distillate has been investigated. 18 acidic components have been identified, more than 40% of the composition of the studied sample falls on linoleic acid with F-vitamin activity. More than 30 components of neutral nature have been found that are of interest as bioactive compounds. Of these, 10 are phytosterols, 14 are triterpene alcohols, 5 are tocopherols. The diterpene hydrocarbons, alcohols and acids of the kauran structure found in the composition of deodorization distillate indicate that the original sunflower oil was native, since it is known that kauran derivatives are a chemotaxonomic marker of many plants of the compositae family, including sunflower. In addition to the above compounds, hydrocarbons (more than a quarter of the unsaponifiable matter), both aliphatic and diterpenic, in the studied sample, was found. Aliphatic components are predominantly unsaturated, which may indicate their artifact origin, i.e. they are the products of the dehydration of aliphatic alcohols. Phytadiene isomers, products of phytol dehydration and isomerization, have been found. The data obtained indicate the prospects for the use of oil deodorization distillate as a source of bioactive substances, cosmetic ingredients and pharmaceutical components.

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Author Biographies

Tat'yana Petrovna Kukina, Novosibirsk Institute of Organic Chemistry, SB RAS N.N. Vorozhtsova

старший научный сотрудник, доцент

Dmitriy Nikolayevich Shcherbakov, Altai State University; FBUN SSC VB "Vector"; Ltd IPK Zetgen

кандидат биологических наук, доцент кафедры органической химии

Nina Vital'yevna Panteleyeva, FBUN SSC VB "Vector"

cтажер-исследователь отдела биоинженерии

Ol'ga Iosifovna Sal'nikova, Novosibirsk Institute of Organic Chemistry, SB RAS N.N. Vorozhtsova

ведущий инженер

Petr Vladimirovich Kolosov, Altai State University

кандидат химических наук, доцент кафедры органической химии

References

Shcherbakov V.G.Tekhnologiya polucheniya rastitel'nykh masel. [The technology of obtaining vegetable oils].Leningrad, 1982, 168 p. (inRuss.).

Ghosh S., Bhattacharyya D.K. J. Am. Oil Chem. Soc., 1996, vol. 73, no. 10, pp. 1271–1274. DOI: 10.1007/BF02525456.

Moreira E.A., Baltanás M.A. J. Am. Oil Chem. Soc., 2004, vol. 81, no. 2, pp. 161–167. DOI: 10.1007/s11746-004-0875-x.

Verleyen T., Verhe R., Garcia L., Dewettinck K., Huyghebaert A., De Greyt W. J. Chromatogr. A, 2001, vol. 921, no. 2, pp. 277–285. DOI: 10.1016/S0021-9673(01)00881-0.

Kukina T.P., Shcherbakov D.N., Gen'sh K.V., Panteleyeva N.V., Tulysheva Ye.A., Sal'nikova O.I., Grazhdanni-kov A.Ye. Khimiya rastitel'nogo syr'ya, 2019, no. 1, pp. 157–164. DOI: 10.14258/jcprm.2019014340(inRuss.).

Kukina T.P., Shcherbakov D.N., Gen'sh K.V., Tulysheva Ye.A., Sal'nikova O.I., Grazhdannikov A.Ye., Koloso-va Ye.A.Khimiya rastitel'nogo syr'ya, 2016, no. 1, pp. 37–42. DOI: 10.14258/jcprm.2016011100(inRuss.).

Villa-Ruano N., Lozoya-Gloria E., Pacheco-Hernández Y.Studies in Natural Products Chemistry, 2016, vol. 51, pp. 151–174. DOI: 10.1016/B978-0-444-63932-5.00003-6.

Carmona M.A., Jiménez C., Jiménez-Sanchidrián C., Peña F., Ruiz J.R. J. Food Eng., 2010, vol. 101, no. 2, pp. 210–213. DOI: 10.1016/j.jfoodeng.2010.07.004.

Martins P.F., Ito V.M., Batistella C.B., MacIel M.R.W. Sep. Purif. Technol., 2006, vol. 48, no. 1, pp. 78–84. DOI: 10.1016/j.seppur.2005.07.028.

Naz S., Hussain Sherazi S.T., Talpur F.N., Kara H., Uddin S., Khaskheli A.R. Polish J. Food Nutr. Sci, 2014, vol. 64, no. 2, pp. 115–120. DOI: 10.2478/pjfns-2013-0008.

Schwartz H., Ollilainen V., Piironen V., Lampi A.M. J. Food Compos. Anal., 2008, vol. 21, no. 2, pp. 152–161. DOI: 10.1016/j.jfca.2007.07.012.

Bonvehi J.S., Coll F.V., Rius I.A. J. AOAC Int., 2000, vol. 83, no. 3, pp. 627–634.

Fedeli E., Lanzani A., Capella P., Jacini G. J. Am. Oil Chem. Soc., 1966, vol. 43, no. 4, pp. 254–256. DOI: 10.1007/BF02641098.

Akihisa T., Yasukawa K., Oinuma H., Kasahara Y., Yamanouchi S., Takido M. et al. Phytochemistry, 1996, vol. 43, no. 6, pp. 1255–1260. DOI: 10.1016/S0031-9422(96)00343-3.

Tasan M., Demirci M. Eur. Food Res. Technol., 2005, vol. 220, no. 3–4, pp. 251–254. DOI: 10.1007/s00217-004-1045-8.

Fambrini M., Mariotti L., Parlanti S., Picciarelli P., Salvini M., Ceccarelli N., Pugliesi C. Plant Molecular Biology, 2011, vol. 75, no. 4, pp. 431–450. DOI: 10.1007/s11103-011-9740-x.

Boller S., Soldi C., Marques M.C.A., Santos E.P., Cabrini D.A., Pizzolatti M.G., Zampronio A.R., Otuki M.F. Journal of Ethnopharmacology, 2010, vol. 130, no. 2, pp. 262–266. DOI: 10.1016/j.jep.2010.05.001.

Published
2020-03-05
How to Cite
1. Kukina T. P., Shcherbakov D. N., Panteleyeva N. V., Sal’nikova O. I., Kolosov P. V. QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE // Chemistry of plant raw material, 2020. № 1. P. 199-206. URL: https://journal.asu.ru/cw/article/view/5909.
Section
Low-molecular weight compounds