Advanced search
Start date

Monomer selectivity by dentin collagen in different mobile phases and strategies to preserve the hybrid layer

Grant number: 16/10544-6
Support type:Regular Research Grants
Duration: October 01, 2016 - March 31, 2019
Field of knowledge:Health Sciences - Dentistry - Dental Materials
Principal researcher:Josimeri Hebling Costa
Grantee:Josimeri Hebling Costa
Home Institution: Faculdade de Odontologia (FOAr). Universidade Estadual Paulista (UNESP). Campus de Araraquara. Araraquara , SP, Brazil
Assoc. researchers:Carlos Alberto de Souza Costa


Two main challenges to establish more efficient and stable resin-dentin bonds are: (1) infiltrating the etched dentin with more hydrophobic monomers and (2) making the collagen resistant to degradation. Current researches on adhesion are designed to better understanding how to overcome these challenges. By developing the experiments included in the present project, we aim to investigate the selectivity imposed by both mineralized and demineralized dentin (collagen matrix) on monomers found in adhesive systems and to contribute to the understanding of how different mobile phases could influence such selectivity and could allow the infiltration of hydrophobic monomers. Also, it will be an objective of this project to determine the minimum amount of water necessary to allow dentin proteolytic enzymes (MMPs) to break down collagen. In order to accomplish that, we will first have to demonstrate if the rate of collagen degradation is comparable between human and bovine dentin matrices. That is important because bovine teeth will be used in one of the experiments of this project. Finally, we want to investigate if the dentin collagen biomodification using a cross-linker (proanthocyanidin, PA) can improve the mechanical properties of collagen to withstand air drying (physical dehydration) without shrinking. Additionally, in the last experiment, it will be evaluated the effect of this collagen biomodification on the immediate and long-term bond strength to dentin. In order to respond to these objectives, several methodologies will be used such as total MMPs activity, dry mass determination, ICTP and CTX fragments release, hydroxyproline release, exclusion chromatography (collagen column), immediate and 12-month microtensile and nanoleakage. All collected data will be analyzed as to distribution and homoscedasticity of the groups to be compared. Based on the results of these initial tests, parametric or non-parametric tests will be selected considering the number of groups and type of the response variable. All statistical inferences will be taken considering the 5% level of significance. (AU)