Assessment of Efficiency of Bioactive Glass, Self-Assembling Peptide, and Ozone Remineralising Agents on Artificial Carious Lesion

ABSTRACT Objective: To assess the efficacy of bioactive glass, self-assembling peptide, and ozone-remineralizing agents on the artificial carious lesion. Material and Methods: On the extracted 60 premolar teeth, an artificial carious lesion/demineralization was created. Later, the remineralization of demineralized teeth was done with respective remineralizing agents (Group A: Calcium sodium phosphosilicate (bioactive glass), Group B: Self-assembling peptide, Group C: Ozone remineralizing agents and Group D (Control): De ionized water. The degree of demineralization and remineralization were evaluated using the Vickers Hardness Number. Results: There was a decrease in microhardness from baseline to demineralization in all the groups, and this reduction was found to be statistically considerable. After the remineralization of demineralized samples with respective remineralizing agents, there was an increase in microhardness of 312.38, 276.67, and 254.42 in groups A, B, and C, respectively. In contrast, in Group D, there were no changes. Conclusion: Bioactive glass and self-assembling peptides had higher remineralizing capacities, which can be used to treat early carious lesions.

Clinical and CBCT Assessment of Crestal Bone Changes in Immediate and Delayed Placement of Implant.

Objectives: The present research was done to assess the crestal bone changes in immediate and delayed dental implant placement. Materials and Method: Twenty four implant sites in participants within the age group of 25-60 years in both genders were done with immediate (Group I) and delayed implant (Group II) placement method. Clinical parameters such as pain, mobility, and radiographic assessment for crestal bone alterations were recorded at baseline, 3 months, and 6 months. Results and Conclusion: On intergroup assessment, the mean variation of the pain, mobility, and crestal bone loss was insignificant.

Assessment of Static and Dynamic Load Tolerance of the Implant Mounts on its Particular Implant.

Objectives: We compared the loads at which the implant holders from Astra Tech (AST) (AstraOsseoSpeed) and Osseotite Certain failed under static compression after experiencing fatigue, as well as the gap that resulted from dynamic loading between the implant-holder complexes. Materials and Method: The ISO 14801 recommendation served as the foundation for the test protocol. Each brand's five implant-implant holder assemblies underwent dynamic loading. A load of 200 N was applied at a stress frequency of 12 Hz and a cycle rate of 5105. (Eden Prairie, MN, USA). Using scanning electron microscopy (S3700N, HITACHI, Japan), the gap (m) at the interface was measured post-fatigue. Static loading was then used to determine the highest load (N) after the point of failure. Controls included definitive abutment-implant complexes. Statistics were used to analyze the data. Result: The Osseotite Certain group showed a slight trend toward greater resistance, but there was no diversity among the two implant holder groups (P 0.05). AST (AstraOsseoSpeed) implants had a larger interface gap, but the difference was not statistically significant. Conclusion: With respect to greatest compression load or the interface gap following dynamic loading, there were no discernible differences between the two experimental groups.