A chondroitin sulfate based injectable hydrogel for delivery of stem cells in cartilage regeneration.


Journal

Biomaterials science
ISSN: 2047-4849
Titre abrégé: Biomater Sci
Pays: England
ID NLM: 101593571

Informations de publication

Date de publication:
04 Jun 2021
Historique:
pubmed: 7 5 2021
medline: 8 6 2021
entrez: 6 5 2021
Statut: ppublish

Résumé

Chondroitin sulfate (CS), as a popular material for cartilage tissue engineering scaffolds, has been extensively studied and reported for its safety and excellent biocompatibility. However, the rapid degradation of pure CS scaffolds has brought a challenge to regenerate neo-tissue similar to natural articular cartilage effectively. Meanwhile, the poly(ethene glycol) (PEG) -based biopolymer is frequently applied as a structural constituent material because of its remarkable mechanical properties, long-lasting in vivo stability, and hypo-immunity. Here, we report that the combination of CS and hyperbranched multifunctional PEG copolymer (HB-PEG) could synergistically promote cartilage repair. The thiol functionalised CS (CS-SH)/HB-PEG hydrogel scaffolds were fabricated via thiol-ene reaction, which exhibits rapid gelation, excellent mechanical properties and prolonged degradation properties. We found that rat adipose-derived mesenchymal stem cells presented great cell viability and improved chondrogenesis in CS-SH/HB-PEG hydrogels. Moreover, the injectable hydrogel scaffolds reduced stem cell inflammatory response, consistent with the well-documented anti-inflammatory activities of CS.

Identifiants

pubmed: 33955435
doi: 10.1039/d1bm00482d
doi:

Substances chimiques

Hydrogels 0
Chondroitin Sulfates 9007-28-7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4139-4148

Auteurs

Xiaolin Li (X)

Charles Institute of Dermatology, School of Medicine, University College Dublin, Dublin 4, Ireland. sigen.a@ucd.ie wenxin.wang@ucd.ie.

Qian Xu (Q)

Charles Institute of Dermatology, School of Medicine, University College Dublin, Dublin 4, Ireland. sigen.a@ucd.ie wenxin.wang@ucd.ie.

Melissa Johnson (M)

Charles Institute of Dermatology, School of Medicine, University College Dublin, Dublin 4, Ireland. sigen.a@ucd.ie wenxin.wang@ucd.ie.

Xi Wang (X)

Charles Institute of Dermatology, School of Medicine, University College Dublin, Dublin 4, Ireland. sigen.a@ucd.ie wenxin.wang@ucd.ie and Ashland Specialties Ireland Ltd, National Science Park, Building V, Dublin Road, Petitswood, Mullingar, Co. Westmeath, Ireland.

Jing Lyu (J)

Charles Institute of Dermatology, School of Medicine, University College Dublin, Dublin 4, Ireland. sigen.a@ucd.ie wenxin.wang@ucd.ie.

Yinghao Li (Y)

Charles Institute of Dermatology, School of Medicine, University College Dublin, Dublin 4, Ireland. sigen.a@ucd.ie wenxin.wang@ucd.ie.

Sean McMahon (S)

Ashland Specialties Ireland Ltd, National Science Park, Building V, Dublin Road, Petitswood, Mullingar, Co. Westmeath, Ireland.

Udo Greiser (U)

Ashland Specialties Ireland Ltd, National Science Park, Building V, Dublin Road, Petitswood, Mullingar, Co. Westmeath, Ireland.

Sigen A (S)

Charles Institute of Dermatology, School of Medicine, University College Dublin, Dublin 4, Ireland. sigen.a@ucd.ie wenxin.wang@ucd.ie.

Wenxin Wang (W)

Charles Institute of Dermatology, School of Medicine, University College Dublin, Dublin 4, Ireland. sigen.a@ucd.ie wenxin.wang@ucd.ie.

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Classifications MeSH