Flavonoids in Horse Chestnut (Aesculus hippocastanum) Seeds and Powdered Waste Water Byproducts

Ireneusz Kapusta, Bogdan Janda, Barbara Szajwaj, Anna Stochmal, Sonia Piacente, Cosimo Pizza, Federico Franceschi§, Chlodwig Franz and Wieslaw Oleszek*
Department of Biochemistry, Institute of Soil Science and Plant Cultivation, State Research Institute, ul. Czartoryskich 8, 24-100 Pulawy, Poland, Dipartimento di Scienze Farmaceutiche, Università degli Studi di Salerno, Via Ponte Don Melillo, 84084 Fisciano, Salerno, Italy, Indena S.p.A., Viale Ortles, 12, 20139 Milan, Italy, Leiter des Instituts für Angewandte Botanik und Pharmakognosie, Veterinärmedizinische Universität Wien, Veterinärplatz 1, A-1210 Wien, Austria
J. Agric. Food Chem., 2007, 55 (21), pp 8485–8490
DOI: 10.1021/jf071709t
Publication Date (Web): September 15, 2007
Copyright © 2007 American Chemical Society

Department of Biochemistry, Institute of Soil Science and Plant Cultivation.

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Dipartimento di Scienze Farmaceutiche, Università degli Studi di Salerno.

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§

Indena S.p.A.

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Leiter des Instituts für Angewandte Botanik und Pharmakognosie, Veterinärmedizinische Universität Wien.

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* Corresponding author. Tel. 48-81-8863421 ; Fax 48-81-8864547; E-mail: wo@iung.pulawy.pl

Abstract

Horse chestnut extracts are widely used in pharmacy and cosmetic industries. The main active constituents are saponins of oleane type, but seeds of horse chestnut also contain flavonoids, being glycosides of quercetin and kaempferol. Their contribution to the overall activity of the extracts was not clear. In the present work, the main flavonoids from horse chestnut seeds were isolated and their structures established with spectral methods. Seven glycosides were isolated, out of which six (2, 3, 4, 7, 11, 13) were previously reported and one (9) was identified as a new tamarixetin 3-O- [β-d-glucopyranosyl(1→3)]-O-β-d-xylopyranosyl-(1→2)-O-β-d-glucopyranoside. The structures of three additional compounds 1, 10, and 12, not previously reported, were deduced on the basis of their LC-ESI/MS/MS fragmentation characteristics. A new ultraperformance liquid chromatographic (UPLC) method has been developed for profiling and quantitation of horse chestnut flavonoids. The method allowed good separation over 4.5 min. Thirteen compounds could be identified in the profile, out of which di- and triglycoisdes of quercetin and kaempferol were the dominant forms and their acylated forms occurred in just trace amounts. The total concentration of flavonoids in the powdered horse chestnut seed was 0.88% of dry matter. The alcohol extract contained 3.46%, and after purification on C18 solid phase, this concentration increased to 9.40% of dry matter. The flavonoid profile and their content were also measured in the horse chestnut wastewater obtained as byproduct in industrial processing of horse chestnut seeds. The total flavonoid concentration in the powder obtained after evaporation of water was 2.58%, while after purification on solid phase, this increased to 11.23% dry matter. It was concluded that flavonoids are present in a horse chestnut extract in a relatively high amount and have the potential to contribute to the overall activity of these extracts. Industrial horse chestnut wastewater can be used to obtain quercetine and kaempferol glycosides for cosmetic, nutraceutical, and food supplement industries.

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History

  • Published In Issue October 17, 2007
  • Article ASAPSeptember 15, 2007
  • Received: June 11, 2007
    Accepted: July 31, 2007
    Revised: July 30, 2007

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