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Research Article Open access CC BY 4.0

Histological Response and Bone Neoformation of Bioceramic Cements in Rat Calvaria

Ravel Bezerra Brasileiro, Edgar Pereira Carreiro Junior, Zildenilson da Silva Sousa, Eduardo Diogo Gurgel-Filho, Fábio de Almeida-Gomes, Roberta Barroso Cavalcante

Journal of Advances in Medicine and Medical Research · pp. 1–13 · Published 12 Mar 2025

10.9734/jammr/2025/v37i45775

Abstract

Aims: This study evaluated the level of inflammatory infiltrate, vasodilation, granulation tissue, and bone regeneration of two repair materials: White MTA (Angelus, Londrina, Brazil) and Bio-C Repair (Angelus, Londrina, Brazil) in rat calvaria. Study Design:  This is an in vivo study with a sample of adult Wistar rats, approximately three months old and weighing between 250 and 300 grams. Place and Duration of Study: The selected analysis periods were 7, 30, and 60 days, corresponding to the following divisions: Group 1 (7 days): 5 rats; Group 2 (30 days): 5 rats; Group 3 (60 days): 5 rats. Methodology: A total of 15 Wistar rats were divided into three groups (n=5) based on the euthanasia period (G7, G30, and G60 days). After sedation, two bone defects, approximately 1.5 mm in depth and 5 mm in diameter, were created in the calvaria of each animal. After euthanasia, the calvaria were removed, histologically prepared in 6 µm sections, and stained with hematoxylin-eosin (H/E). The material was quantitatively analyzed using the Statistical Package for the Social Sciences (SPSS), adopting a significance level of 5% (p < 0.05). Results: At 7 days, both materials showed an acute inflammatory response. After 30 days, there was a reduction in the inflammatory process in both bioceramics cements. At 60 days, both White MTA and Bio C Repair did not induce severe inflammation. During this period, Bio C Repair showed greater bone tissue formation, with inflammatory infiltrate levels at 60 days being equivalent between the two materials. Conclusion: Both bioceramics cements preserved the integrity of the bone tissue and stimulated bone neoformation.

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