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Accessing the Cytotoxicity and Cell Response to Biomaterials
Published on: July 8, 2021
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In vitro cytotoxicity evaluation of different pulp capping materials: a comparative study.
Arhiv Za Higijenu Rada I Toksikologiju
|October 8, 2015
Summary
Biodentine® and mineral trioxide aggregate (MTA) showed lower cytotoxicity compared to calcium hydroxide materials in direct pulp capping. This in vitro study suggests Biodentine® as a viable alternative due to its biocompatibility.
Area of Science:
- Biomaterials Science
- Dental Materials
- Regenerative Dentistry
Background:
- Direct pulp capping aims to preserve pulp vitality and function after exposure.
- Evaluating the biocompatibility of various pulp-capping agents is crucial for clinical success.
- Calcium hydroxide-based materials have been traditionally used but can exhibit cytotoxicity.
Purpose of the Study:
- To compare the in vitro biocompatibility of seven different direct pulp-capping materials.
- To assess the cytocompatibility of Dycal®, Calcicur®, Calcimol LC®, TheraCal LC®, ProRoot MTA®, MTA-Angelus®, and Biodentine®.
- To evaluate the potential of newer materials like Biodentine® as alternatives to traditional agents.
Main Methods:
- In vitro study using murine odontoblast cells (MDPC-23).
- Transwell insert methodology with Alamar blue assay to assess cytocompatibility at 24, 48, and 72 hours.
- MTT assay and Confocal Laser Scanning Microscopy for cell viability and morphological analysis.
Main Results:
- Significant differences in biocompatibility were observed among the tested materials.
- Biodentine® and mineral trioxide aggregate (MTA)-based materials demonstrated lower cytotoxicity.
- Calcium hydroxide-based materials exhibited higher cytotoxicity compared to MTA and Biodentine®.
Conclusions:
- Biodentine® and MTA-based materials show promising biocompatibility for direct pulp capping.
- Calcium hydroxide-based materials present higher cytotoxic effects in vitro.
- Biodentine® may be a suitable alternative to calcium hydroxide materials in pulp-capping treatments.
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