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1.
Molecules ; 26(15)2021 Jul 24.
Article in English | MEDLINE | ID: mdl-34361616

ABSTRACT

The extraction of phenolic compounds from olive mill wastes is important, not only to avoid environmental damages, but also because of the intrinsic value of those biophenols, well-known for their high antioxidant potential and health benefits. This study focuses on tyrosol (Tyr) and hydroxytyrosol (HT), two of the main phenolic compounds found in olive mill wastes. A new, simple, and eco-friendly extraction process for the removal of phenolic compounds from aqueous solutions using native ß-cyclodextrin (ß-CD) in the solid state has been developed. Several ß-CD/biophenol molar ratios and biophenol concentrations were investigated, in order to maintain ß-CD mostly in the solid state while optimizing the extraction yield and the loading capacity of the sorbent. The extraction efficiencies of Tyr and HT were up to 61%, with a total solid recovery higher than 90% using an initial concentration of 100 mM biophenol and 10 molar equivalents of ß-CD. The photochemical stability of the complexes thus obtained was estimated from ∆E*ab curve vs. illumination time. The results obtained showed that the phenols encapsulated into solid ß-CD are protected against photodegradation. The powder obtained could be directly developed as a safe-grade food supplement. This simple eco-friendly process could be used for extracting valuable biophenols from olive mill wastewater.


Subject(s)
Antioxidants , Olea/chemistry , Olive Oil/chemistry , Phenylethyl Alcohol/analogs & derivatives , Plant Extracts/chemistry , Antioxidants/chemistry , Antioxidants/isolation & purification , Dietary Supplements , Phenylethyl Alcohol/chemistry , Phenylethyl Alcohol/isolation & purification , Wastewater/chemistry , beta-Cyclodextrins/chemistry
2.
J Agric Food Chem ; 66(18): 4614-4620, 2018 May 09.
Article in English | MEDLINE | ID: mdl-29663812

ABSTRACT

Hydroxytyrosol bioaccessibility and absorption by the intestinal cells were studied using an in vitro digestion model and Caco-2 TC7 monolayers cells in culture in the presence and absence of ß-cyclodextrin and foods. Hydroxytyrosol was either provided as a pure standard or in an alperujo powder. The presence of foods significantly decreased hydroxytyrosol bioaccessibility and absorption (-20 and -10%, respectively), while ß-cyclodextrin had no effect. Moreover, the presence of other compounds from alperujo in the intestinal compartment reduced hydroxytyrosol absorption by Caco-2 cells compared to pure standard (-60%). The final bioavailability of hydroxytyrosol, defined as its quantity at the basolateral side of cultured cell monolayers compared to the initial amount in the test meal, was 6.9 ± 0.4, 31.1 ± 1.1, and 40.9 ± 1.5% when hydroxytyrosol was from alperujo or a standard administered with or without food, respectively. Our results show that conversely to foods, ß-cyclodextrin does not alter hydroxytyrosol bioavailability.


Subject(s)
Olea/chemistry , Phenylethyl Alcohol/analogs & derivatives , Plant Extracts/metabolism , Waste Products/analysis , beta-Cyclodextrins/chemistry , Biological Availability , Caco-2 Cells , Digestion , Drug Carriers/chemistry , Drug Delivery Systems , Humans , Intestinal Absorption , Models, Biological , Phenylethyl Alcohol/chemistry , Phenylethyl Alcohol/metabolism , Plant Extracts/chemistry
3.
Nutrients ; 10(11)2018 Nov 03.
Article in English | MEDLINE | ID: mdl-30400310

ABSTRACT

Alperujo-a two-phase olive mill waste that is composed of olive vegetation water and solid skin, pulp, and seed fragments - is a highly valuable olive by-product due to its high content in phenolic compounds. In this study, we assessed whether ß-cyclodextrin (ß-CD), which is used to extract and protect alpejuro phenolic compounds (hydroxytyrosol-O-glucoside, tyrosol, caffeic, and p-coumaric acids) could impact on their bioaccessibility (i.e., the percentage of molecule found in the aqueous phase of the digesta) and uptake by intestinal cells, by using an in vitro digestion model and Caco-2 TC7 cells in culture, respectively. Our results showed that ß-CD did not change the bioaccessibility of the selected phenols. Hydroxytyrosol-O-glucoside and caffeic did not cross Caco-2 cell monolayers. Conversely ferulic acid, identified as the main caffeic acid intestinal metabolite, was absorbed through intestinal cell monolayers (~20%). Interestingly, ß-CD moderately but significantly improved the local absorption of tyrosol and p-coumaric acid (2.3 + 1.4% and 8.5 ± 4.2%, respectively, p < 0.05), even if their final bioavailability (expressed as bioaccessibility × absorption by Caco-2 cells) was not modified (16.2 ± 0.6% vs. 16.8 ± 0.5% for tyrosol and 32.0 ± 3.2% vs. 37.2 ± 3.2% for p-coumaric acid, from pure alperujo and alperujo complexed with ß-CD, respectively). Overall, our results show that ß-CD is an interesting extraction and storage agent for phenolic compounds that does not alter their in vitro bioavailability.


Subject(s)
Olea/chemistry , Phenols/pharmacokinetics , beta-Cyclodextrins/pharmacology , Antioxidants/pharmacokinetics , Biological Availability , Caco-2 Cells , Caffeic Acids/pharmacokinetics , Coumaric Acids , Glucosides/pharmacokinetics , Humans , Phenylethyl Alcohol/analogs & derivatives , Phenylethyl Alcohol/pharmacokinetics , Plant Extracts/pharmacology , Propionates/pharmacokinetics
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