Optimization of the Enzymatic Extraction of Naringenin from Pink Grapefruit Pulp (<i>Citrus</i> × <i>paradisi</i> Macfad.)
Curro Polo-Castellano,
Rosa María Mateos,
Francisco Visiedo,
Miguel Palma,
Gerardo Fernández Barbero,
Marta Ferreiro-González
Affiliations
Curro Polo-Castellano
Department of Analytical Chemistry, Faculty of Sciences, Agrifood Campus of International Excellence (ceiA3), Institute for Viticulture and Agrifood Research (IVAGRO), University of Cadiz, 11510 Puerto Real, Spain
Rosa María Mateos
Research Unit, Biomedical Research and Innovation Institute of Cadiz (INiBICA), Puerta del Mar University Hospital, 11009 Cadiz, Spain
Francisco Visiedo
Research Unit, Biomedical Research and Innovation Institute of Cadiz (INiBICA), Puerta del Mar University Hospital, 11009 Cadiz, Spain
Miguel Palma
Department of Analytical Chemistry, Faculty of Sciences, Agrifood Campus of International Excellence (ceiA3), Institute for Viticulture and Agrifood Research (IVAGRO), University of Cadiz, 11510 Puerto Real, Spain
Gerardo Fernández Barbero
Department of Analytical Chemistry, Faculty of Sciences, Agrifood Campus of International Excellence (ceiA3), Institute for Viticulture and Agrifood Research (IVAGRO), University of Cadiz, 11510 Puerto Real, Spain
Marta Ferreiro-González
Department of Analytical Chemistry, Faculty of Sciences, Agrifood Campus of International Excellence (ceiA3), Institute for Viticulture and Agrifood Research (IVAGRO), University of Cadiz, 11510 Puerto Real, Spain
Naringenin is one of the main phenolic compounds found in grapefruit (Citrus × paradisi Macfad.). This compound is known for its therapeutical properties as an antioxidant, antidiabetic, antihyperlipidemic and antineoplastic agent. In order to enable the development of drugs based on this compound, an appropriate extraction method needs to be developed. For this study, enzymatic extraction was chosen, as it is a cheap and green extraction method. Optimal extraction conditions (pH, temperature, agitation, solvent composition, sample-to-solvent ratio and enzyme-to-sample ratio) were determined through a Plackett–Burman and a Box–Behnken design, resulting in pH 6.0, 40 °C, 50 rpm, 20% EtOH, 0.2 g sample per 15 mL solvent and 1000 U/g. Once extraction conditions were determined, a single-factor experiment was performed under optimal conditions to determine extraction time, which resulted in 10 min per extraction. Finally, repeatability and intermediate precision were evaluated through naringenin quantification. Good values were obtained for both parameters (1.80% and 2.05%, respectively). Furthermore, extracts presented significant amount of naringenin (0.18 ± 0.02 mg/g).