In vitro evaluation of surface properties of Pro Seal® and Opal® SealTM in preventing white spot lesions.

OBJECTIVES: To evaluate the surface properties of two commercially available sealants (Pro Seal® (PS) and Opal® SealTM (OS)) in terms of fluoride(F) release, biofilm formation of Streptococcus mutans and Lactobacillus and the ability to resist acid penetration. SETTING: University of Nebraska Medical Center. MATERIAL & METHODS: Discs of similar diameter and thickness were made from OS and PS. Discs were soaked in double-distilled water, and F released was measured with fluoride meter daily for 14 consecutive days, then at 21 and 28 days. Biofilm formation was evaluated with Streptococcus mutans and Lactobacilli grown on sealant discs using confocal microscopy. Extracted human teeth (n=8) with sealant-coated buccal surfaces and untreated lingual surfaces were exposed to 0.1M lactic acid(pH=4.5) to test the acid penetration. After 1-4 weeks of exposure, teeth were subjected to microhardness testing and SEM microscopy. RESULTS: PS released significantly higher levels of F than OS. PS showed more S. mutans adherence than OS, whereas Lactobacillus did not show any differences in adherence. Both sealants protected enamel surfaces, showing statistically significant difference in the depth of acid penetration compared to their unsealed control sides. CONCLUSION: F release was adequate to aid in remineralization, although clinically it would not likely aid in preventing demineralization as there was no prolonged release of F by both sealants tested. S. mutans adherence to OS surface was less compared to PS surface, which could be of relevance in biofilm formation and white spot lesions. Both sealants protected enamel surfaces from acid penetration.

Collagen gel delivery of Tgf-beta3 non-viral plasmid DNA in rat osteoblast and calvarial culture.

Different forms of collagen as a carrier for naked plasmid DNA have shown potential as vehicles for therapeutic gene delivery and tissue engineering. The objective of this study was to determine the suitability of a dense collagen gel as a vehicle for sustained delivery of plasmid DNA in cell and organ culture. Plasmid DNA encoding Tgf-beta(3) was combined with collagen gel. DNA released into the media was measured by Pico-Green spectrophotometry. Results showed that DNA was released from the collagen gel at a gradual rate for up to 14 days. To evaluate collagen-mediated transfection in tissue, calvariae were exposed to collagen containing plasmid encoding GFP or DsRed. Transfection was visualized by fluorescence localized to tissue adjacent to the vehicle. To evaluate protein production, fetal rat calvarial osteoblasts were cultured with a collagen/Tgf-beta(3) plasmid mixture or in media containing plasmid alone. Media was collected at various time points to measure Tgf-beta(3) protein production. ELISA assays showed that collagen-transfected osteoblasts demonstrated an elevated Tgf-beta(3) protein production for up to 14 days. Therefore, collagen delivery of viable plasmid DNA created a sustained transient transfection of calvarial osteoblasts resulting in prolonged and elevated growth factor production. Together, these results suggest that use of collagen gel as a vehicle may provide a strategy to achieve localized and controlled, non-viral gene delivery in vivo.