The influence of light‐curing time on fluoride release, surface topography, and bacterial adhesion in resin‐modified glass ionomer cements: AFM and SEM in vitro study
| Autor: | Maykel González-Torres, Bernardo Teutle-Coyotecatl, Rosalía Contreras-Bulnes, Cristian D Román-Mendez, Gabriela Olmos-Olmos, María de los Angeles Moyaho-Bernal, Laura Emma Rodríguez-Vilchis, Rosendo Carrasco-Gutiérrez |
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| Rok vydání: | 2021 |
| Předmět: |
Curing Lights
Dental Histology medicine.medical_treatment Glass ionomer cement 02 engineering and technology Dental Caries Microscopy Atomic Force Composite Resins Bacterial Adhesion Fluorides 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Materials Testing medicine Humans MTT assay Viability assay Instrumentation Saline Light-Curing of Dental Adhesives biology Biomaterial 030206 dentistry Adhesion 021001 nanoscience & nanotechnology biology.organism_classification Streptococcus mutans Resin Cements Medical Laboratory Technology chemistry Glass Ionomer Cements Brain heart infusion Anatomy 0210 nano-technology Nuclear chemistry |
| Zdroj: | Microscopy Research and Technique. 84:1628-1637 |
| ISSN: | 1097-0029 1059-910X |
| DOI: | 10.1002/jemt.23723 |
| Popis: | Reinforced glass ionomer cements have been widely used in pediatric dentistry to prevent dental caries. However, the influence of biomaterial light-curing and its anti-cariogenic effects remain unclear. This study evaluates the influence of the light-curing time on fluoride release, surface topography, and bacterial adhesion in two types of resin-modified glass ionomer cements (RMGICs). One hundred disks were made, and samples were divided into two groups (n = 50 per group), according to each dental material (Vitremer™ and Ketac™ N100), and also divided into different light-cured times (10, 20, 30, 40, and 60 s). They were placed in phosphate-buffered saline solution (PBS) to measure the fluoride release. Subsequently, an independent sample of RMGICs per group was examined using atomic force microscopy (AFM). Four disks per group were incubated in a brain heart infusion (BHI) medium that was inoculated with Streptococcus mutans GS5 to evaluate the bacterial adhesion by 3-4, [5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide cell viability assay (MTT assay). The fluoride release was related to the light-curing time and gradually decreased as the light-curing time increased in both materials. Surface topography in Vitremer™ presents more irregular surfaces than Ketac™ N100. For S. mutans adhesion, the smallest number of cells per milliliter (cell/ml) was found at 40 s for Vitremer™ and at 30 s for Ketac™ N100. Thus, the shorter light-curing times allowed for major fluoride release in both materials. However, the RMGICs showed different patterns of bacterial adhesion according to the brand and light-curing time. |
| Databáze: | OpenAIRE |
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