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dc.title | Edible flowers - antioxidant activity and impact on cell viability | en |
dc.contributor.author | Kuceková, Zdenka | |
dc.contributor.author | Mlček, Jiří | |
dc.contributor.author | Humpolíček, Petr | |
dc.contributor.author | Rop, Otakar | |
dc.relation.ispartof | Central European Journal of Biology | |
dc.identifier.issn | 1895-104X Scopus Sources, Sherpa/RoMEO, JCR | |
dc.date.issued | 2013 | |
utb.relation.volume | 8 | |
utb.relation.issue | 10 | |
dc.citation.spage | 1023 | |
dc.citation.epage | 1031 | |
dc.type | article | |
dc.language.iso | en | |
dc.publisher | Versita | en |
dc.identifier.doi | 10.2478/s11535-013-0212-y | |
dc.relation.uri | https://link.springer.com/article/10.2478/s11535-013-0212-y | |
dc.subject | Antioxidants | en |
dc.subject | Cancer cells | en |
dc.subject | Herbs | en |
dc.subject | Polyphenols | en |
dc.description.abstract | The phenolic compound composition, antioxidant activity and impact on cell viability of edible flower extracts of Allium schoenoprasum; Bellis perennis; Cichorium intybus; Rumex acetosa; Salvia pratensis; Sambucus nigra; Taraxacum officinale; Tragopogon pratensis; Trifolium repens and Viola arvensis was examined for the first time. Total phenolic content of the flowers of these plants fell between 11.72 and 42.74 mg of tannin equivalents/kg of dry matter. Antioxidant activity ranged from 35.56 to 71.62 g of ascorbic acid equivalents/kg of dry matter. Using the Human Hepatocellular Carcinoma cell-line (HepG2) and the Human Immortalized Non-tumorigenic Keratinocyte cell line (HaCaT), we assessed cell viability following a 3 day incubation period in media containing 25, 50, 75 and 100 μg/ml of total phenolic compounds using a colorimetric MTT assay. These three properties could make the herbs useful in treatment of various diseases like cancer. The tested extracts had significant effects on cell viability, but the effects were dependent not only on the phenolic compound concentration and the edible flowers species, but also on the phenolic compound and antioxidant profiles. In addition, responses differed between cell lines. © 2013 Versita Warsaw and Springer-Verlag Wien. | en |
utb.faculty | Faculty of Technology | |
dc.identifier.uri | http://hdl.handle.net/10563/1003440 | |
utb.identifier.obdid | 43869925 | |
utb.identifier.scopus | 2-s2.0-84881082319 | |
utb.identifier.wok | 000322674300010 | |
utb.source | j-scopus | |
dc.date.accessioned | 2013-08-21T10:17:33Z | |
dc.date.available | 2013-08-21T10:17:33Z | |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Unported | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/3.0/ | |
dc.rights.access | openAccess | |
utb.contributor.internalauthor | Kuceková, Zdenka | |
utb.contributor.internalauthor | Mlček, Jiří | |
utb.contributor.internalauthor | Humpolíček, Petr |