Contribution of Phenolic Compounds to the Antioxidant Activity of Leaf and Flower Extracts of Sinapis pubescens L. subsp. pubescens (Brassicaceae)

Author:

Taviano Maria Fernanda1ORCID,Arena Paola12ORCID,Davì Federica12,Cavò Emilia1,Spadaro Vivienne3ORCID,Raimondo Francesco Maria4ORCID,Cacciola Francesco5ORCID,Laganà Vinci Roberto6,Mondello Luigi67ORCID,Miceli Natalizia1ORCID

Affiliation:

1. Department of Chemical Biological Pharmaceutical and Environmental Sciences University of Messina Viale F. Stagno d'Alcontres 31 98166 Messina Italy

2. Foundation “Prof. Antonio Imbesi” University of Messina Piazza Pugliatti 1 98122 Messina Italy

3. Department of Biological Chemical and Pharmaceutical Sciences and Technologies Section of Botany Anthropology and Zoology University of Palermo Via Archirafi 38 90123 Palermo Italy

4. PLANTA/Research, Documentation and Training Center Via Serraglio Vecchio 28 90123 Palermo Italy

5. Department of Biomedical Dental Morphological and Functional Imaging Sciences University of Messina Via Consolare Valeria 98125 Messina Italy

6. Messina Institute of Technology c/o Department of Chemical Biological Pharmaceutical and Environmental Sciences former Veterinary School University of Messina Viale G. Palatucci snc 98168 – Messina Italy

7. Chromaleont s.r.l. c/o Department of Chemical Biological Pharmaceutical and Environmental Sciences former Veterinary School University of Messina Viale G. Palatucci snc 98168 – Messina Italy

Abstract

AbstractWithin a study focused on Sinapis pubescens subsp. pubescens wild from Sicily (Italy), an edible species still unexplored, our earlier published work has demonstrated good in vitro antioxidant properties for the flower and leaf hydroalcoholic extracts, exhibiting quite different qualitative‐quantitative phenolic profiles. Herein, further research was designed to elucidate the role played by phenolic compounds in the different antioxidant mechanisms highlighted for the extracts. To achieve this goal, the crude extracts were subjected to liquid‐liquid partitioning with solvents of increasing polarity; then, the fractions were investigated for their antioxidant properties using different in vitro assays. For both flowers and leaves, the ethyl acetate fractions exhibited the best activity in DPPH and reducing power assays, followed by n‐butanol. The total phenolic content determination indicated these fractions as the phenolic‐rich ones, which were characterized by HPLC‐PDA/ESI‐MS analysis. Conversely, the phenolic‐rich fractions did not show any chelating activity, which was highlighted for the more hydrophobic ones.

Publisher

Wiley

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