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
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
111701Informations de copyright
Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.