Assembly of Interfacial Polyelectrolyte Complexation Fibers with Mineralization Gradient for Physiologically-inspired Ligament Regeneration.
bone‐ligament interface
hierarchical structure
interfacial polyelectrolyte complexation
ligament tissue engineering
mineralization gradient
Journal
Advanced materials (Deerfield Beach, Fla.)
ISSN: 1521-4095
Titre abrégé: Adv Mater
Pays: Germany
ID NLM: 9885358
Informations de publication
Date de publication:
04 Apr 2024
04 Apr 2024
Historique:
revised:
29
03
2024
received:
28
12
2023
medline:
4
4
2024
pubmed:
4
4
2024
entrez:
4
4
2024
Statut:
aheadofprint
Résumé
Current synthetic grafts for ligament rupture repair often fail to integrate well with the surrounding biological tissue, leading to complications such as graft wear, fatigue, and subsequent re-rupture. To address this medical challenge, this study aims at advancing the development of a biological ligament through the integration of physiologically-inspired principles and tissue engineering strategies. In this study, we utilize interfacial polyelectrolyte complexation spinning technique, along with a custom-designed collection system, to fabricate a hierarchical scaffold mimicking native ligament structure. To emulate the bone-ligament interface and alleviate stress concentration, a hydroxyapatite mineral gradient is strategically introduced near both ends of the scaffold to enhance interface integration and diminish the risk of avulsion rupture. Biomimetic viscoelasticity is successfully displayed to provide similar mechanical support to native ligamentous tissue under physiological conditions. By introducing the connective tissue growth factor and conducting mesenchymal stem cells transplantation, we significantly amplify the regenerative potential of the synthetic ligament. This pioneering study offers a multifaceted solution combining biomimetic materials, regenerative therapies, and advanced techniques to potentially transform ligament rupture treatment. This article is protected by copyright. All rights reserved.
Identifiants
pubmed: 38572797
doi: 10.1002/adma.202314294
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2314294Informations de copyright
This article is protected by copyright. All rights reserved.