4.5 Article

Effect of white mineral trioxide aggregate compared with biomimetic carbonated apatite on dentine bridge formation and inflammatory response in a dental pulp model

Journal

INTERNATIONAL ENDODONTIC JOURNAL
Volume 45, Issue 1, Pages 26-34

Publisher

WILEY
DOI: 10.1111/j.1365-2591.2011.01943.x

Keywords

biocompatibility; carbonated apatite; mineral trioxide aggregate; pulp capping

Funding

  1. Dental Research Center, Tehran University of Medical Sciences [5522-70-02-86]

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Danesh F, Vahid A, Jahanbani J, Mashhadiabbas F, Arman E. Effect of white mineral trioxide aggregate compared with biomimetic carbonated apatite on dentine bridge formation and inflammatory response in a dental pulp model. International Endodontic Journal, 45, 26-34, 2012. Aim To evaluate the effects of apatite precipitation on the biocompatibility and hard tissue induction properties of white mineral trioxide aggregate (WMTA) in a dental pulp model. Methodology Pulp exposures were created on the axial walls of 32 sound canine teeth of eight dogs. Four additional sound teeth served as controls. The pulps were capped either with WMTA or apatite derivatives [biomimetic carbonated apatite (BCAp)] in the interaction of WMTA with a synthetic tissue fluid and restored with zinc oxideeugenol cement. After 7 and 70 days, the animals were killed, and the histological specimens taken from the teeth were stained with haematoxylin and eosin for histomorphological evaluation. The Brown and Brenn technique was employed to stain bacteria. The data were subjected to nonparametric KruskallWallis analysis and MannWhitney U_tests. Results Biomimetic carbonated apatite did not induce hard tissue bridge formation. WMTA performed significantly better than BCAp in this respect at both periods (P < 0.05). BCAp was associated with a significantly greater inflammatory response as compared with WMTA after 7 days (P < 0.05). Both materials were associated with similar reactions after 70 days (P > 0.05). Conclusions White mineral trioxide aggregate induced hard tissue formation via a mechanism other than that postulated via apatite formation.

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