Controllable fabrication of hydroxybutyl chitosan/oxidized chondroitin sulfate hydrogels by 3D bioprinting technique for cartilage tissue engineering.
Animals
Biocompatible Materials
/ chemistry
Biopolymers
/ chemistry
Bioprinting
/ methods
Cartilage
/ physiology
Cartilage, Articular
/ drug effects
Cell Survival
Chitosan
/ analogs & derivatives
Chondroitin Sulfates
/ chemistry
Cross-Linking Reagents
/ chemistry
Humans
Hydrogels
/ chemistry
Immune System
Inflammation
Macrophages
/ metabolism
Mesenchymal Stem Cells
/ cytology
Mice
Oxygen
/ chemistry
Porosity
Printing, Three-Dimensional
Regeneration
Regenerative Medicine
/ methods
Rheology
Spectroscopy, Fourier Transform Infrared
Tissue Engineering
/ methods
Tissue Scaffolds
Journal
Biomedical materials (Bristol, England)
ISSN: 1748-605X
Titre abrégé: Biomed Mater
Pays: England
ID NLM: 101285195
Informations de publication
Date de publication:
10 01 2019
10 01 2019
Historique:
pubmed:
18
12
2018
medline:
9
8
2019
entrez:
18
12
2018
Statut:
epublish
Résumé
Biological regeneration of articular cartilage continues to be a challenge at present. Functional engineered implants with patient-specific sizes are difficult to achieve. The aim of this study is to fabricate a biocompatible cell-laden hydrogel with a designable structure. Covalent hydrogels were prepared with water soluble hydroxybutyl chitosan (HBC) and oxidized chondroitin sulfate (OCS) via a Schiff-base reaction. With the aid of three-dimensional (3D) bioprinted sacrificial molds, HBC/OCS hydrogel with various structures were obtained. After the material constituent optimization process, an injectable hydrogel with a uniform porous structure of 100 μm average pore size was developed to form macroporous hydrogel. In vitro and in vivo biocompatibility of optimized HBC/OCS hydrogel were also carefully assessed. The results indicated that human adipose-derived mesenchymal stem cells could be 3D cultured in HBC/OCS hydrogel maintaining good viability. Moreover, the hydrogels were found to trigger the least amount of pro-inflammatory gene expression of macrophage and to inhibit acute immune responses in 7 d. These results demonstrate the potential of HBC/OCS hydrogels as a cell delivery system for cartilage tissue engineering.
Identifiants
pubmed: 30557856
doi: 10.1088/1748-605X/aaf8ed
doi:
Substances chimiques
Biocompatible Materials
0
Biopolymers
0
Cross-Linking Reagents
0
Hydrogels
0
hydroxybutyl chitosan
0
Chondroitin Sulfates
9007-28-7
Chitosan
9012-76-4
Oxygen
S88TT14065
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng