Hydroxytyrosol encapsulated in biocompatible water-in-oil microemulsions: How the structure affects in vitro absorption.
Antioxidants
/ chemistry
Biocompatible Materials
/ chemistry
Caco-2 Cells
Cell Survival
/ drug effects
Drug Compounding
/ methods
Dynamic Light Scattering
Electron Spin Resonance Spectroscopy
Emulsions
/ chemistry
HT29 Cells
Humans
Intestinal Absorption
Oils
/ chemistry
Phenylethyl Alcohol
/ analogs & derivatives
Water
/ chemistry
Coculture model
Dynamic light scattering (DLS)
Electron paramagnetic resonance (EPR)
Encapsulation
LC–MS/MS
Transepithelial electrical resistance (TEER)
Journal
Colloids and surfaces. B, Biointerfaces
ISSN: 1873-4367
Titre abrégé: Colloids Surf B Biointerfaces
Pays: Netherlands
ID NLM: 9315133
Informations de publication
Date de publication:
01 Dec 2019
01 Dec 2019
Historique:
received:
07
07
2019
revised:
30
08
2019
accepted:
31
08
2019
pubmed:
21
9
2019
medline:
21
4
2020
entrez:
21
9
2019
Statut:
ppublish
Résumé
Over the last years, the incorporation of natural antioxidants in food and pharmaceutical formulations has gained attention, delaying or preventing oxidation phenomena in the final products. In order to take full advantage of their properties, protection in special microenvironments is of great importance. The unique features of the natural phenolic compound hydroxytyrosol (HT) - including antioxidant, anti-inflammatory, antiproliferative and cardioprotective properties - have been studied to clarify its mechanism of action. In the present study novel biocompatible water-in-oil (W/O) microemulsions were developed as hosts for HT and subsequently examined for their absorption profile following their oral uptake. The absorption of HT in solution was compared with the encapsulated one in vitro, using a coculture model (Caco-2/TC7 and HT29-MTX cell lines). The systems were structurally characterized by means of Dynamic Light Scattering (DLS) and Electron Paramagnetic Resonance (EPR) techniques. The diameter of the micelles remained unaltered after the incorporation of 678 ppm of HT but the interfacial properties were slightly affected, indicating the involvement of the HT molecules in the surfactant monolayer. EPR was used towards a lipophilic stable free radial, namely galvinoxyl, indicating a high scavenging activity of the systems and encapsulated HT. Finally, after the biocompatibility study of the microemulsions the intestinal absorption of the encapsulated HT was compared with its aqueous solution in vitro. The higher the surfactants' concentration in the system the lower the HT concentration that penetrated the constructed epithelium, indicating the involvement of the amphiphiles in the antioxidant's absorption and its entrapment in the mucus layer.
Identifiants
pubmed: 31539752
pii: S0927-7765(19)30626-5
doi: 10.1016/j.colsurfb.2019.110482
pii:
doi:
Substances chimiques
Antioxidants
0
Biocompatible Materials
0
Emulsions
0
Oils
0
Water
059QF0KO0R
3,4-dihydroxyphenylethanol
10597-60-1
Phenylethyl Alcohol
ML9LGA7468
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
110482Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.