Mucoadhesive buccal films based on a graft co-polymer - A mucin-retentive hydrogel scaffold.
Adhesiveness
Administration, Buccal
Animals
Cell Line, Tumor
Chemistry, Pharmaceutical
/ methods
Drug Delivery Systems
/ methods
Drug Liberation
/ drug effects
HT29 Cells
Humans
Hydrogels
/ chemistry
Hypromellose Derivatives
/ chemistry
Micelles
Mouth Mucosa
/ drug effects
Mucins
/ chemistry
Permeability
/ drug effects
Polyethylene Glycols
/ chemistry
Polymers
/ chemistry
Polyvinyls
/ chemistry
Swine
Buccal permeability
Furosemide
HPMC
Lycoat®
Mucoadhesion
Soluplus®
Solvent casting
TR146 cells
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:
15 Jan 2020
15 Jan 2020
Historique:
received:
03
07
2019
revised:
04
11
2019
accepted:
06
11
2019
pubmed:
11
11
2019
medline:
2
6
2020
entrez:
11
11
2019
Statut:
ppublish
Résumé
From a patient-centric perspective, oromucosal drug delivery is highly attractive due to the ease of administration without the need of swallowing, and improved patient safety. The aim of the presented work was to prepare a buccal film using a self-forming micellar drug solubiliser as the film matrix, combining it with a mucoadhesive polymer for an enhanced retention on the buccal mucosa. Specifically, we propose the use of a graft co-polymer (Soluplus®), as a solubiliser and film former, supplemented with polymers with more hydrophilic properties and known mucoadhesive properties; hydroxypropyl methylcellulose (HPMC) or modified hydroxypropyl pea starch (Lycoat®). The film was manufactured by the solvent casting method. The resulting dual polymer film containing HPMC exhibited resistance to erosion and mucoadhesive properties superior to the control films of single polymers. In an in vitro oral cavity model, these properties were shown to correlate with increased residence time on simulated oral mucosa. Furthermore, all films containing the graft co-polymer showed similar permeability characteristics of furosemide towards buccal TR146 epithelial cells. This work illustrated that it is possible to manufacture dry, solid, dual polymer films containing an advanced drug delivery system with a cheap and simple method. The combination of a graft co-polymer with a mucoadhesive polymer transform into drug solubilising micelles in a mucin-retentive hydrogel scaffold with longer retention time on buccal mucosa for safe and enhanced advanced formulation.
Identifiants
pubmed: 31707042
pii: S0928-0987(19)30415-4
doi: 10.1016/j.ejps.2019.105142
pii:
doi:
Substances chimiques
Hydrogels
0
Micelles
0
Mucins
0
Polymers
0
Polyvinyls
0
polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer
0
Hypromellose Derivatives
3NXW29V3WO
Polyethylene Glycols
3WJQ0SDW1A
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
105142Informations de copyright
Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.