Flavonoids in horse chestnut (Aesculus hippocastanum) seeds and powdered waste water byproducts
- PMID: 17867637
- DOI: 10.1021/jf071709t
Flavonoids in horse chestnut (Aesculus hippocastanum) seeds and powdered waste water byproducts
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- [beta- d-glucopyranosyl(1-->3)]- O-beta- d-xylopyranosyl-(1-->2)- O-beta- 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.
Similar articles
-
Kaempferol and its glycosides in the seeds hair of Asclepias syriaca L.Acta Pol Pharm. 2001 May-Jun;58(3):211-5. Acta Pol Pharm. 2001. PMID: 11712739
-
Fractionation and structural characterization of polyphenolic antioxidants from seed shells of Japanese horse chestnut (Aesculus turbinata BLUME).J Agric Food Chem. 2008 Dec 24;56(24):12046-51. doi: 10.1021/jf802506r. J Agric Food Chem. 2008. PMID: 19053354
-
Antioxidant activities and structural characterization of flavonol O-glycosides from seeds of Japanese horse chestnut (Aesculus turbinata BLUME).Food Chem. 2017 Aug 1;228:348-355. doi: 10.1016/j.foodchem.2017.01.084. Epub 2017 Jan 19. Food Chem. 2017. PMID: 28317733
-
Phytochemical, ethanomedicinal and pharmacological applications of escin from Aesculus hippocastanum L. towards future medicine.J Basic Clin Physiol Pharmacol. 2020 Jul 10;31(5):/j/jbcpp.2020.31.issue-5/jbcpp-2019-0115/jbcpp-2019-0115.xml. doi: 10.1515/jbcpp-2019-0115. J Basic Clin Physiol Pharmacol. 2020. PMID: 32649293 Review.
-
Chemical analysis and quality control of Ginkgo biloba leaves, extracts, and phytopharmaceuticals.J Chromatogr A. 2009 Mar 13;1216(11):2002-32. doi: 10.1016/j.chroma.2009.01.013. Epub 2009 Jan 15. J Chromatogr A. 2009. PMID: 19195661 Review.
Cited by
-
Unraveling the Glucosylation of Astringency Compounds of Horse Chestnut via Integrative Sensory Evaluation, Flavonoid Metabolism, Differential Transcriptome, and Phylogenetic Analysis.Front Plant Sci. 2022 Feb 3;12:830343. doi: 10.3389/fpls.2021.830343. eCollection 2021. Front Plant Sci. 2022. PMID: 35185970 Free PMC article.
-
Corynanthean-Epicatechin Flavoalkaloids from Corynanthe pachyceras.Molecules. 2020 Jun 7;25(11):2654. doi: 10.3390/molecules25112654. Molecules. 2020. PMID: 32517373 Free PMC article.
-
New Indole Glycosides from Aesculus chinensis var. chekiangensis and Their Neuroprotective Activities.Molecules. 2019 Nov 9;24(22):4063. doi: 10.3390/molecules24224063. Molecules. 2019. PMID: 31717579 Free PMC article.
-
The content of phenolic compounds in leaf tissues of Aesculus glabra and Aesculus parviflora walt.Molecules. 2015 Jan 28;20(2):2176-89. doi: 10.3390/molecules20022176. Molecules. 2015. PMID: 25635381 Free PMC article.
-
Research Progress of Tamarixetin and its Glycosides.Mini Rev Med Chem. 2024;24(7):689-703. doi: 10.2174/1389557523666230828123425. Mini Rev Med Chem. 2024. PMID: 37642001 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources