Root maturation and dentin–pulp response to enamel matrix derivative in pulpotomized permanent teeth

Author:

Darwish Sherif S1,Abd El Meguid Shadia H23,Wahba Nadia A4,Mohamed Ahmed A-R4,Chrzanowski Wojciech5,Abou Neel Ensanya A678

Affiliation:

1. Pediatric Dentistry and Dental Public Health Department, Faculty of Dentistry, Pharos University, Egypt

2. Oral Biology Department, King Abdulaziz University, Jeddah, Saudi Arabia

3. Oral Biology Department, Faculty of Dentistry, Alexandria University, Egypt

4. Pediatric Dentistry and Dental Public Health Department, Faculty of Dentistry, Alexandria University, Egypt

5. The Faculty of Pharmacy, The University of Sydney, NSW 2006 Australia

6. Division of Biomaterials, Conservative Dental Sciences Department, King Abdulaziz University, Jeddah, Saudi Arabia

7. Biomaterials Department, Faculty of Dentistry, Tanta University, Tanta, Egypt

8. UCL Eastman Dental Institute, Biomaterials and Tissue Engineering Division, 256 Gray’s Inn Road, London, WC1X 8LD

Abstract

The success of pulpotomy of young permanent teeth depends on the proper selection of dressing materials. This study aimed to evaluate the histological and histomorphometric response of dentin–pulp complex to the enamel matrix derivative (Emdogain® gel) compared to that of calcium hydroxide when used as a pulp dressing in immature young permanent dogs’ teeth. Dentin-like tissues bridging the full width of the coronal pulp at the interface between the injured and healthy pulp tissues were seen after 1 month in both groups. With time, the dentin bridge increased in thickness for calcium hydroxide but disintegrated and fully disappeared for Emdogain-treated group. Progressive inflammation and total pulp degeneration were only evident with Emdogain-treated group. The root apices of Emdogain-treated teeth became matured and closed by cementum that attached to new alveolar bone by a well-oriented periodontal ligament. In young permanent dentition, Emdogain could be a good candidate for periodontium but not dentino–pulpal complex regeneration.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials,Medicine (miscellaneous)

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