Drug release from PLGA microparticles can be slowed down by a surrounding hydrogel.

Agarose gel Drug release mechanism Experimental setup Microparticles PLGA Swelling

Journal

International journal of pharmaceutics: X
ISSN: 2590-1567
Titre abrégé: Int J Pharm X
Pays: Netherlands
ID NLM: 101753452

Informations de publication

Date de publication:
15 Dec 2023
Historique:
received: 24 07 2023
revised: 23 11 2023
accepted: 25 11 2023
medline: 26 12 2023
pubmed: 26 12 2023
entrez: 26 12 2023
Statut: epublish

Résumé

This study aimed to evaluate and better understand the potential impact that a layer of surrounding hydrogel (mimicking living tissue) can have on the drug release from PLGA microparticles. Ibuprofen-loaded microparticles were prepared with an emulsion solvent extraction/evaporation method. The drug loading was about 48%. The surface of the microparticles appeared initially smooth and non-porous. In contrast, the internal microstructure of the particles exhibited a continuous network of tiny pores. Ibuprofen release from

Identifiants

pubmed: 38146325
doi: 10.1016/j.ijpx.2023.100220
pii: S2590-1567(23)00064-6
pmc: PMC10749250
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100220

Informations de copyright

© 2023 The Authors. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

The authors declare the following financial interests/personal relationships which may be considered as potential competing interests. Juergen Siepmann reports financial support was provided by Interreg 2 Seas programme. Juergen Siepmann reports financial support was provided by 10.13039/501100008530European Regional Development Fund. Axel Zeitler reports financial support was provided by Interreg 2 Seas programme. Axel Zeitler reports financial support was provided by 10.13039/501100008530European Regional Development Fund. The Editor-in-Chief of the journal (Juergen Siepmann) is one of the co-authors of this article. Also, one of the guest editors of this special issue (Axel Zeitler) is one of the co-authors of this article. The manuscript has been subject to all of the journal's usual procedures, including peer review, which has been handled independently of the Editor-in-Chief and of the guest editor Axel Zeitler.

Auteurs

L A Lefol (LA)

Univ. Lille, Inserm, CHU Lille, U1008, Lille F-59000, France.

P Bawuah (P)

Univ. Cambridge, Department of Chemical Engineering and Biotechnology, Cambridge CB3 0AS, UK.

J A Zeitler (JA)

Univ. Cambridge, Department of Chemical Engineering and Biotechnology, Cambridge CB3 0AS, UK.

J Verin (J)

Univ. Lille, Inserm, CHU Lille, U1008, Lille F-59000, France.

F Danede (F)

Univ. Lille, USTL UMET UMR CNRS 8207, Villeneuve d'Ascq F-59650, France.

J F Willart (JF)

Univ. Lille, USTL UMET UMR CNRS 8207, Villeneuve d'Ascq F-59650, France.

F Siepmann (F)

Univ. Lille, Inserm, CHU Lille, U1008, Lille F-59000, France.

J Siepmann (J)

Univ. Lille, Inserm, CHU Lille, U1008, Lille F-59000, France.

Classifications MeSH