Extracellular vesicle-embedded materials.

biomaterial extracellular vesicle formulation scaffold stability

Journal

Journal of controlled release : official journal of the Controlled Release Society
ISSN: 1873-4995
Titre abrégé: J Control Release
Pays: Netherlands
ID NLM: 8607908

Informations de publication

Date de publication:
09 2023
Historique:
received: 27 06 2023
revised: 27 07 2023
accepted: 31 07 2023
medline: 11 9 2023
pubmed: 4 8 2023
entrez: 3 8 2023
Statut: ppublish

Résumé

Extracellular vesicles (EVs) are small membrane-bound vesicles released by cells. EVs are emerging as a promising class of therapeutic entity that could be adapted in formulation due to their lack of immunogenicity and targeting capabilities. EVs have been shown to have similar regenerative and therapeutic effects to their parental cells and also have potential in disease diagnosis. To improve the therapeutic potential of EVs, researchers have developed various strategies for modifying them, including genetic engineering and chemical modifications which have been examined to confer target specificity and prevent rapid clearance after systematic injection. Formulation efforts have focused on utilising hydrogel and nano-formulation strategies to increase the persistence of EV localisation in a specific tissue or organ. Researchers have also used biomaterials or bioscaffolds to deliver EVs directly to disease sites and prolong EV release and exposure. This review provides an in-depth examination of the material design of EV delivery systems, highlighting the impact of the material properties on the molecular interactions and the maintenance of EV stability and function. The various characteristics of materials designed to regulate the stability, release rate and biodistribution of EVs are described. Other aspects of material design, including modification methods to improve the targeting of EVs, are also discussed. This review aims to offer an understanding of the strategies for designing EV delivery systems, and how they can be formulated to make the transition from laboratory research to clinical use.

Identifiants

pubmed: 37536545
pii: S0168-3659(23)00483-2
doi: 10.1016/j.jconrel.2023.07.059
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

280-296

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

Auteurs

Yingchang Ma (Y)

UCL School of Pharmacy, University College London, 29 - 39 Brunswick Square, London WC1N 1AX, UK.

Steve Brocchini (S)

UCL School of Pharmacy, University College London, 29 - 39 Brunswick Square, London WC1N 1AX, UK.

Gareth R Williams (GR)

UCL School of Pharmacy, University College London, 29 - 39 Brunswick Square, London WC1N 1AX, UK. Electronic address: g.williams@ucl.ac.uk.

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Classifications MeSH