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Comparative maxillary bone‐defect healing by calcium‐sulphate or deproteinized bovine bone particles and extra cellular matrix membranes in a guided bone regeneration setting: an experimental study in rabbits
Author(s) -
Turri Alberto,
Dahlin Christer
Publication year - 2015
Publication title -
clinical oral implants research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.407
H-Index - 161
eISSN - 1600-0501
pISSN - 0905-7161
DOI - 10.1111/clr.12425
Subject(s) - resorption , bone healing , extracellular matrix , chemistry , regeneration (biology) , dentistry , matrix (chemical analysis) , bone resorption , wound healing , calcium , biomedical engineering , pathology , anatomy , medicine , surgery , microbiology and biotechnology , biology , biochemistry , chromatography , organic chemistry
Objectives The aim of this study was to histologically compare the dynamics of bone healing response between calcium sulphate (CaS) and deproteinized bovine bone mineral ( DBBM ) particles in guided bone regeneration utilizing an extracellular matrix membrane ( ECM ) as barrier. Materials and methods Eighteen rabbits were used in thisstudy. 5 × 5 mm defects were created in the edentulous space between the incisors and molars in the maxilla. The CaS and DBBM particles were placed in the defects, with or without the placement of a membrane by means of random selection. Healing was evaluated at 2, 4 and 8 weeks by histology. Results A total resorption of the CaS material was seen already at 2 weeks. Only minor resorption could be seen of the DBBM particles. The CaS group showed significantly more bone regeneration at all three healing periods compared to the DBBM group. The addition of an ECM membrane demonstrated significant additional effect on bone regeneration. The CaS group showed significant increased amounts of blood vessels compared to the DBBM group. Conclusions Thisstudy showed that CaS in combination with an ECM membrane provided synergistic effects on bone regeneration, seemingly due to stimulating angiogenesis in the early healing process.