A novel sodium caseinate lipid-based auto-emulsifying delivery system to increase resveratrol intestinal permeation: characterization and in vitro assessment.

Caco-2 bioavailability lipid-based formulations sodium caseinate t-resveratrol

Journal

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
ISSN: 1879-0720
Titre abrégé: Eur J Pharm Sci
Pays: Netherlands
ID NLM: 9317982

Informations de publication

Date de publication:
18 Sep 2024
Historique:
received: 01 08 2024
revised: 11 09 2024
accepted: 14 09 2024
medline: 21 9 2024
pubmed: 21 9 2024
entrez: 20 9 2024
Statut: aheadofprint

Résumé

In recent years, nutraceuticals have emerged as a promising strategy for maintaining health and represent a high-growth market in Italy and across Europe. However, the lack of strict regulations regarding formulation requirements and proof of efficacy raises serious concerns about their poor bioavailability and, consequently, their uncertain health benefits. An emblematic example is t-resveratrol (RES), a cardioprotective stilbene polyphenol that undergoes extensive metabolism in the intestine and liver, resulting in a bioavailability of less than 1%. This manuscript describes a novel technological matrix developed with the primary goal of improving RES oral bioavailability. This technology can be classified as a lipid-based autoemulsifying drug delivery system (LIBADDS), in which RES is thoroughly solubilized in a hot liquid phase composed of lipids and surfactants, and the mixture is further adsorbed onto a powder composed of polysaccharides and sodium caseinate (NaC), along with inert excipients, and then compressed. In this study, NaC was used for the first time to trigger pancreatin-mediated hydrolysis of an enteric-coated tablet, allowing micellar delivery of RES to the small intestine. The RES-containing tablets were characterized via differential scanning calorimetry (DSC) and X-ray diffraction (PXRD). The digested formulation, with simulated gastric and enteric fluids, was dimensionally assessed via dynamic light scattering (DLS). Finally, calculations of the bioaccessible fraction, dissolution tests, and in vitro permeability experiments using Caco-2 cell monolayers were carried out to preliminarily define the overall efficiency and applicability of this new technology in improving RES intestinal permeability.

Identifiants

pubmed: 39303769
pii: S0928-0987(24)00225-2
doi: 10.1016/j.ejps.2024.106912
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106912

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors have no conflicts of interest to declare.

Auteurs

Andrea Fratter (A)

Department of Pharmaceutical and Pharmacological Sciences (DSFarm), University of Padova, Italy; Italian Society of Nutraceutical Formulators (SIFNut), Italy. Electronic address: andrea.fratter@phd.unipd.it.

Andrea Cignarella (A)

Department of Medicine, University of Padova, Italy; Italian Society of Nutraceutical Formulators (SIFNut), Italy.

Giovanni Eugenio Ramaschi (GE)

Department of Pharmaceutical and Pharmacological Sciences (DSFarm), University of Padova, Italy.

Adele Papetti (A)

Department of Drug Sciences, University of Pavia, Italy; Italian Society of Nutraceutical Formulators (SIFNut), Italy.

Vanessa Pellicorio (V)

Department of Drug Sciences, University of Pavia, Italy.

Chiara Milanese (C)

Department of Chemistry, Physical Chemistry Section, University of Pavia and C.S.G.I., Italy.

Luca Casettari (L)

Department of Biomolecular Sciences (DISB), School of Pharmacy, University of Urbino, Italy; Italian Society of Nutraceutical Formulators (SIFNut), Italy.

Chiara Bolego (C)

Department of Pharmaceutical and Pharmacological Sciences (DSFarm), University of Padova, Italy.

Classifications MeSH