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Updated: Nov 21, 2025

Accessing the Cytotoxicity and Cell Response to Biomaterials
Published on: July 8, 2021
A novel bio-active adhesive monomer induces odontoblast differentiation: a comparative study
1Division of Clinical Cariology and Endodontology, Department of Oral Rehabilitation, Health Sciences University of Hokkaido, Hokkaido, Japan.
The novel adhesive monomer CMET demonstrated the lowest cytotoxicity and effectively promoted odontoblast-like cell proliferation, differentiation, and mineralization, showing great potential for dentine regeneration.
Area of Science:
- Biomaterials Science
- Dental Materials
- Regenerative Dentistry
Background:
- Odontoblast-like cells are crucial for dentine formation and repair.
- Novel adhesive monomers are being developed to improve dental restorative materials.
- Evaluating the biocompatibility and bioactivity of new monomers is essential for their clinical application.
Purpose of the Study:
- To assess the in vitro effects of the novel adhesive monomer CMET on odontoblast-like cell proliferation, mineralization, and differentiation.
- To compare CMET's performance with 4-methacryloxyethyl trimellitate (4-MET), calcium hydroxide (CH), and mineral trioxide aggregate (MTA).
Main Methods:
- Rat odontoblast-like MDPC-23 cells were treated with CMET, 4-MET, CH, and MTA at various concentrations.
- Cell viability was measured using CCK-8 assay.
- Gene expression of odontogenic markers, cytokines, and integrins was analyzed via real-time RT-PCR.
- Alkaline phosphatase (ALPase) activity and alizarin red S staining assessed mineralization capacity.
Main Results:
- CMET exhibited the lowest cytotoxicity and significantly enhanced cell viability at appropriate concentrations compared to controls.
- CMET treatment upregulated odontogenic markers and integrin expression more than CH and MTA.
- CMET dose-dependently increased mineralization and maintained this effect after 8 weeks of storage.
- CH and MTA treatments induced higher levels of pro-inflammatory cytokines and mineralization.
Conclusions:
- CMET demonstrates excellent biocompatibility and low cytotoxicity.
- This novel monomer effectively stimulates odontoblast-like cell proliferation, differentiation, and mineralization.
- CMET shows significant potential for application in dentine regeneration therapies.
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