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A novel versatile flow-donor chamber as biorelevant ex-vivo test assessing oral mucoadhesive formulations
Malmö Univ, Fac Hlth & Soc, Biomed Sci, SE-20506 Malmö, Sweden.;Malmö Univ, Biofilms Res Ctr Biointerfaces BRCB, SE-20506 Malmö, Sweden..
Malmö Univ, Fac Hlth & Soc, Biomed Sci, SE-20506 Malmö, Sweden.;Malmö Univ, Biofilms Res Ctr Biointerfaces BRCB, SE-20506 Malmö, Sweden..
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Surface and Corrosion Science. Nanologica AB, SE-15136 Södertälje, Sweden.ORCID iD: 0000-0003-3004-9190
CTC Clin Trial Consultants AB, S-75237 Uppsala, Sweden..
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2021 (English)In: European Journal of Pharmaceutical Sciences, ISSN 0928-0987, E-ISSN 1879-0720, Vol. 166, article id 105983Article in journal (Refereed) Published
Abstract [en]

Oral transmucosal drug delivery is a non-invasive administration route for rapid therapeutic onset and greater bioavailability avoiding the first-pass metabolism. Mucoadhesive formulations are advantageous as they may retain the drug at the administration site. Proper equipment to assess mucoadhesive properties and corresponding drug absorption is fundamental for the development of novel drug delivery systems. Here we developed a new flow-through donor chamber for well-established diffusion cells, and we tested the effects on drug and formulation retention in situ of adding mucoadhesive polymers or mesoporous silica particles to a reference formulation. Mesoporous silica particles are of particular interest as they may be used to encapsulate and retain drug molecules. Compared to other ex-vivo methods described in literature for assessing mucoadhesive performance and transmucosal drug delivery, this new donor chamber provides several advantages: i) it reflects physiological conditions better as a realistic saliva flow can be provided over the administration site, ii) it is versatile since it can be mounted on any kind of vertical diffusion cell allowing simultaneous detection of drug retention at the administration site and drug permeation through the tissue, and iii) it enables optical quantification of formulations residence time aided by image processing. This new flow-through donor diffusion cell set-up proved sensitive to differentiate a reference formulation from one where 20 %(w/w) Carbomer was added (to further improve the mucoadhesive properties), with respect to both drug and formulation residence times. We also found that mesoporous silica particles, investigated as particles only and mixed together with the reference formulation, gave very similar drug and formulation retention to what we observed with the mucoadhesive Carbomer. However, after some time (>30 min) it became obvious that the tablet excipients in the reference formulation promote particle retention on the mucosa. This work provides a new simple and versatile biorelevant test for the evaluation of oral mucoadhesive formulations and paves the way for further studies on mesoporous silica particles as valuable excipients for enhancing oral mucoadhesion.

Place, publisher, year, edition, pages
Elsevier BV , 2021. Vol. 166, article id 105983
Keywords [en]
Oral transmucosal delivery, Mucoadhesion, Mesoporous silica particles, Ex-vivo release-permeation systems, Flow through diffusion cells, Intraoral drug delivery
National Category
Pharmaceutical Sciences
Identifiers
URN: urn:nbn:se:kth:diva-303954DOI: 10.1016/j.ejps.2021.105983ISI: 000704269600004PubMedID: 34461276Scopus ID: 2-s2.0-85114373054OAI: oai:DiVA.org:kth-303954DiVA, id: diva2:1605529
Note

QC 20211025

Available from: 2021-10-25 Created: 2021-10-25 Last updated: 2022-06-25Bibliographically approved

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Feiler, Adam

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