3D-printing-assisted fabrication of chitosan scaffolds from different sources and cross-linkers for dental tissue engineering.
Adolescent
Adult
Biocompatible Materials
/ administration & dosage
Cells, Cultured
Chitosan
/ chemistry
Compressive Strength
/ drug effects
Dental Pulp
/ drug effects
Female
Humans
Iridoids
/ administration & dosage
Male
Materials Testing
/ methods
Porosity
Printing, Three-Dimensional
Silanes
/ administration & dosage
Stem Cells
/ drug effects
Tissue Engineering
/ methods
Tissue Scaffolds
/ chemistry
Young Adult
Journal
European cells & materials
ISSN: 1473-2262
Titre abrégé: Eur Cell Mater
Pays: Switzerland
ID NLM: 100973416
Informations de publication
Date de publication:
05 05 2021
05 05 2021
Historique:
entrez:
5
5
2021
pubmed:
6
5
2021
medline:
11
1
2022
Statut:
epublish
Résumé
The aim of the present study was to fabricate and characterise chitosan scaffolds from animal and fungal sources, with or without gelatine as a co-polymer, and cross-linked to 3-glycidyloxyproply trimethoxysilane (GPTMS) or genipin for application in dental root tissue engineering.
Chitosan-based scaffolds were prepared by the emulsion freeze-drying technique. Scanning electron microscopy (SEM) and nano-focus computed tomography (nano-CT) were used to characterise scaffold microstructure. Chemical composition and cross-linking were evaluated by Fourier transform infrared-attenuated total reflectance spectroscopy. Compression tests were performed to evaluate scaffold mechanical properties. Scaffold degradation was evaluated by gravimetric method and SEM. Scaffold bioactivity immersed in simulated body fluid was evaluated by SEM, with associated electron dispersive X-ray spectroscopy, and apatite formation was examined by X-ray diffraction. Finally, human dental pulp stem cells (hDPSCs) viability was evaluated.
The fabrication method used was successful in producing scaffolds with organised porosity. Chitosan source (animal vs. fungal), co-polymerisation with gelatine and cross-linking using GPTMS or genipin had a significant effect on scaffold properties and hDPSCs response. Chitosan-genipin (CS-GEN) scaffolds had the largest pore diameter, while the chitosan-gelatine-GPTMS (CS-GEL-GPTMS) scaffolds had the smallest. Animal chitosan-gelatine co-polymerisation increased scaffold compressive strength, while fungal chitosan scaffolds (fCS-GEL-GPTMS) had the fastest degradation rate, losing 80 % of their weight by day 21. Gelatine co-polymerisation and GPTMS cross-linking enhanced chitosan scaffolds bioactivity through the formation of an apatite layer as well as improved hDPSCs attachment and viability.
Tailored chitosan scaffolds with tuned properties and favourable hDPSCs response can be obtained for regenerative dentistry applications.
Identifiants
pubmed: 33948929
doi: 10.22203/eCM.v041a31
pii: vol041a31
doi:
Substances chimiques
Biocompatible Materials
0
Iridoids
0
Silanes
0
Chitosan
9012-76-4
genipin
A3V2NE52YG
trimethoxysilane
V1J39XPF91
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM