Introduction Fruit and vegetable-derived foods have become a very significant source of nutraceutical phytochemicals. Diets rich of these compounds are associated to a lower risk of cancer and cardiovascular diseases [1]. Some vegetables have gained attention due Brassica oleracea L. to their phenolic content, in particular anthocyanins, natural colorants with health-promoting properties [2]. The aim of this study was to evaluate total polyphenols content and antioxidant activity among different extracts from three common vegetables: cabbage, red cabbage and red chicory. Method Dried samples of two varieties of (cabbage and red cabbage) and Chicorium intybus L. (red chicory) were extracted by sequential maceration by using n-hexane, chloroform and acidified methanol. Methanol was acidified by 1% HCl to extract anthocyanins, phenolic compounds abundant in selected vegetables. Methanol extracts were partitioned by H2O/buthanol. All extracts and fractions were tested to evaluate radical-scavenging activity, reducing power and inhibition of lipid peroxidation by three different assays: DPPH (2,2-diphenyl-1-picrylhydrazyl), FRAP (ferric reducing ability power) and BCB (beta-carotene bleaching), respectively [1]. Total polyphenols content was also investigated by Folin-Ciocalteu test [3], and anthocyanin content was also measured. Results / Discussion / Conclusion Results showed that buthanol fractions had the highest content of polyphenols and radical-scavenging and reducing power. Among investigated vegetables, Cichorium inthybus demonstrated the highest antioxidant activity related to the highest polyphenols content. The present work demonstrated that C. Intybus is a most promising source of bioactive compounds with wide range of potential applications. Further investigations may be focused on characterization and isolation of secondary metabolites, responsible of antioxidant activity.
Biological activities and phenolic content in extracts of Brassica and Chicorium species
RUSSO, DANIELAMethodology
;SCRANO, LauraMethodology
;CANDIDO, VincenzoWriting – Original Draft Preparation
;MILELLA, LUIGIWriting – Original Draft Preparation
2014-01-01
Abstract
Introduction Fruit and vegetable-derived foods have become a very significant source of nutraceutical phytochemicals. Diets rich of these compounds are associated to a lower risk of cancer and cardiovascular diseases [1]. Some vegetables have gained attention due Brassica oleracea L. to their phenolic content, in particular anthocyanins, natural colorants with health-promoting properties [2]. The aim of this study was to evaluate total polyphenols content and antioxidant activity among different extracts from three common vegetables: cabbage, red cabbage and red chicory. Method Dried samples of two varieties of (cabbage and red cabbage) and Chicorium intybus L. (red chicory) were extracted by sequential maceration by using n-hexane, chloroform and acidified methanol. Methanol was acidified by 1% HCl to extract anthocyanins, phenolic compounds abundant in selected vegetables. Methanol extracts were partitioned by H2O/buthanol. All extracts and fractions were tested to evaluate radical-scavenging activity, reducing power and inhibition of lipid peroxidation by three different assays: DPPH (2,2-diphenyl-1-picrylhydrazyl), FRAP (ferric reducing ability power) and BCB (beta-carotene bleaching), respectively [1]. Total polyphenols content was also investigated by Folin-Ciocalteu test [3], and anthocyanin content was also measured. Results / Discussion / Conclusion Results showed that buthanol fractions had the highest content of polyphenols and radical-scavenging and reducing power. Among investigated vegetables, Cichorium inthybus demonstrated the highest antioxidant activity related to the highest polyphenols content. The present work demonstrated that C. Intybus is a most promising source of bioactive compounds with wide range of potential applications. Further investigations may be focused on characterization and isolation of secondary metabolites, responsible of antioxidant activity.File | Dimensione | Formato | |
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