Mucoadhesive buccal films based on a graft co-polymer - A mucin-retentive hydrogel scaffold.


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
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

105142

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Julia F Alopaeus (JF)

Department of Pharmacy, University of Oslo, Norway.

Marie Hellfritzsch (M)

Department of Pharmaceutics and Biopharmaceutics, Kiel University, Germany.

Tobias Gutowski (T)

Department of Pharmaceutics and Biopharmaceutics, Kiel University, Germany.

Regina Scherließ (R)

Department of Pharmaceutics and Biopharmaceutics, Kiel University, Germany.

Andreia Almeida (A)

I3S - Institute for Research and Innovation in Health, University of Porto, Portugal; INEB - Institute of Biomedical Engineering, University of Porto, Portugal; ICBAS - Institute of Biomedical Sciences Abel Salazar, University of Porto, Portugal.

Bruno Sarmento (B)

I3S - Institute for Research and Innovation in Health, University of Porto, Portugal; INEB - Institute of Biomedical Engineering, University of Porto, Portugal; CESPU, IINFACTS - Institute for Research and Advanced Training in Health Sciences and Technologies, Portugal.

Nataša Škalko-Basnet (N)

Department of Pharmacy, University of Tromsø The Arctic University of Norway, Norway.

Ingunn Tho (I)

Department of Pharmacy, University of Oslo, Norway. Electronic address: ingunn.tho@farmasi.uio.no.

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Classifications MeSH