Optimization of hyaluronic acid-tyramine/silk-fibroin composite hydrogels for cartilage tissue engineering and delivery of anti-inflammatory and anabolic drugs.

Cartilage Chondrocytes Drug delivery Enzymatic cross-linking Hyaluronic acid-tyramine Hydrogel Mechanical testing Silk-fibroin Tissue engineering

Journal

Materials science & engineering. C, Materials for biological applications
ISSN: 1873-0191
Titre abrégé: Mater Sci Eng C Mater Biol Appl
Pays: Netherlands
ID NLM: 101484109

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 19 06 2020
revised: 21 10 2020
accepted: 02 11 2020
entrez: 6 2 2021
pubmed: 7 2 2021
medline: 15 5 2021
Statut: ppublish

Résumé

Injury of articular cartilage leads to an imbalance in tissue homeostasis, and due to the poor self-healing capacity of cartilage the affected tissue often exhibits osteoarthritic changes. In recent years, injectable and highly tunable composite hydrogels for cartilage tissue engineering and drug delivery have been introduced as a desirable alternative to invasive treatments. In this study, we aimed to formulate injectable hydrogels for drug delivery and cartilage tissue engineering by combining different concentrations of hyaluronic acid-tyramine (HA-Tyr) with regenerated silk-fibroin (SF) solutions. Upon enzymatic crosslinking, the gelation and mechanical properties were characterized over time. To evaluate the effect of the hydrogel compositions and properties on extracellular matrix (ECM) deposition, bovine chondrocytes were embedded in enzymatically crosslinked HA-Tyr/SF composites (in further work abbreviated as HA/SF) or HA-Tyr hydrogels. We demonstrated that all hydrogel formulations were cytocompatible and could promote the expression of cartilage matrix proteins allowing chondrocytes to produce ECM, while the most prominent chondrogenic effects were observed in hydrogels with HA20/SF80 polymeric ratios. Unconfined mechanical testing showed that the compressive modulus for HA20/SF80 chondrocyte-laden constructs was increased almost 10-fold over 28 days of culture in chondrogenic medium which confirmed the superior production of ECM in this hydrogel compared to other hydrogels in this study. Furthermore, in hydrogels loaded with anabolic and anti-inflammatory drugs, HA20/SF80 hydrogel showed the longest and the most sustained release profile over time which is desirable for the long treatment duration typically necessary for osteoarthritic joints. In conclusion, HA20/SF80 hydrogel was successfully established as a suitable injectable biomaterial for cartilage tissue engineering and drug delivery applications.

Identifiants

pubmed: 33545860
pii: S0928-4931(20)33620-1
doi: 10.1016/j.msec.2020.111701
pii:
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Hydrogels 0
Hyaluronic Acid 9004-61-9
Fibroins 9007-76-5
Tyramine X8ZC7V0OX3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111701

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Reihane Ziadlou (R)

AO Research Institute Davos, Davos Platz 7270, Switzerland; Department of Biomedical Engineering, University of Basel, Allschwil 4123, Switzerland.

Stijn Rotman (S)

AO Research Institute Davos, Davos Platz 7270, Switzerland.

Andreas Teuschl (A)

Department of Biochemical Engineering, University of Applied Sciences Technikum Wien, 1200 Vienna, Austria.

Elias Salzer (E)

Department of Biochemical Engineering, University of Applied Sciences Technikum Wien, 1200 Vienna, Austria; Orthopaedic Biomechanics, Department of Biomedical Engineering, Eindhoven University of Technology, 5600 MB Eindhoven, The Netherlands.

Andrea Barbero (A)

Department of Biomedical Engineering, University of Basel, Allschwil 4123, Switzerland.

Ivan Martin (I)

Department of Biomedical Engineering, University of Basel, Allschwil 4123, Switzerland; Department of Biomedicine, University Hospital Basel, University of Basel, Basel 4001, Switzerland.

Mauro Alini (M)

AO Research Institute Davos, Davos Platz 7270, Switzerland.

David Eglin (D)

AO Research Institute Davos, Davos Platz 7270, Switzerland.

Sibylle Grad (S)

AO Research Institute Davos, Davos Platz 7270, Switzerland; Department of Health Sciences and Technology, ETH Zürich, Zürich 8092, Switzerland. Electronic address: sibylle.grad@aofoundation.org.

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