Dimethylaminododecyl Methacrylate-Incorporated Dental Materials Could Be the First Line of Defense against Helicobacter pylori.

Oral cavity is an essential reservoir for H. pylori. We aimed to investigate the antibacterial effects of dimethylaminododecyl methacrylate (DMADDM) against H. pylori. Modified giomers were prepared by introducing 0%, 1.25% and 2.5% DMADDM monomers. Broth microdilution assay, spot assay, Alamer Blue assay, PMA-qPCR, crystal violet staining, scanning electron microscopy observation and live/dead bacterial staining were performed to evaluate the antibacterial and antibiofilm effects of DMADDM and modified giomers in vitro. Urease assay, qPCR, hematoxylin-eosin staining and ELISA were performed to evaluate the inflammation levels and colonization of H. pylori in vivo. In vitro experiments indicated that the minimum inhibitory concentration and minimum bactericidal concentration of DMADDM were 6.25 µg/mL and 25 µg/mL, respectively. It inhibited H. pylori in a dose- and time-dependent manner, and significantly reduced the expression of cagA, vacA, flaA and ureB. DMADDM-modified giomers inhibited the formation of H. pylori biofilm and reduced live cells within it. In vivo experiments confirmed that the pretreatment with DMADDM-modified dental resin effectively reduced the gastric colonization of oral-derived H. pylori, suppressed systemic and local gastric inflammation. DMADDM monomers and DMADDM-modified giomers possessed excellent antibacterial and antibiofilm effects on H. pylori. Pretreatment with DMADDM-modified giomers significantly inhibited the gastric infection by H. pylori.

Cone beam computed tomography analysis of accessory canals of the canalis sinuosus: A prevalent but often overlooked anatomical variation in the anterior maxilla.

STATEMENT OF PROBLEM: Accessory canals of the canalis sinuosus, a bony canal carrying the anterior superior alveolar nerve and vessels, can often be present but overlooked in the anterior maxilla. Dental implant placement in this area may damage neurovascular branches if this anatomic variation is not carefully identified, resulting in unexpected complications. PURPOSE: The purpose of this retrospective study was to identify accessory canals of the canalis sinuosus and analyze their relationship to the terminal canalis sinuosus and anterior maxilla in Chinese patients to provide a warning for surgeons operating in the anterior maxilla. MATERIAL AND METHODS: Cone beam computed tomography (CBCT) scans of 1007 Chinese patients were examined to identify the prevalence and size of accessory canals with at least 1.0-mm diameter. Axial position of this canal was classified referring to the nasal cavity and adjacent teeth. Its sagittal position was determined by the distance from the bifurcation site of canalis sinuosus to the buccal alveolar crest and the distance from the canal opening to the palatal alveolar crest. Diameter of the terminal canalis sinuosus, distance from the terminal canalis sinuosus to the buccal alveolar crest, and anterior maxillary volume were measured on all scans. Binary logistic regression and the Spearman rank correlation coefficient were used for prevalence and diameter analysis. RESULTS: The prevalence of the accessory canal was 36.9%, positively correlated the anterior maxillary volume (OR 1.408) and negatively correlated with the distance from the terminal canalis sinuosus to the buccal alveolar crest (OR 0.921). Average diameter of such canal was 1.1 ±0.1 mm, significantly higher in men, positively correlated with the diameter of terminal canalis sinuosus (rs=0.163) and the distance from the canal opening to the palatal alveolar crest (rs=0.192). All accessory canals started below the buccal cortical bone, 19.3 ±2.7 mm away from the buccal alveolar crest. There were 61.9% accessory canals opened between the central and the lateral incisors. Openings here and in the central incisor region were closer to the alveolar crest than that between the lateral incisor and the canine (P<.05). CONCLUSIONS: Accessory canals of the canalis sinuosus have high prevalence in the anterior maxilla in a Chinese population. Large anterior maxillary volume has been demonstrated as a risk factor associated with the presence of such canals. The region between the central and the lateral incisors was a predominant location. Openings in this region were closer to the alveolar crest than those between the lateral incisor and the canine.

Dodecylmethylaminoethyl methacrylate inhibits Enterococcus faecalis in a pH-dependent manner.

OBJECTIVES: Considering the correlation between survival microenvironment of E. faecalis and acidic pH value, this study aimed to investigate the potential of utilizing pH-responsive DMAEM monomers and their copolymers with resin-based root canal sealers to inhibit E. faecalis. METHODS: Broth microdilution assay, crystal violet staining and qPCR were performed to evaluate antibacterial effects of DMAEM monomers against E. faecalis at different pH. Methacrylate-resin based root canal sealers were prepared and copolymerized with DMAEM. The flow, solubility, water sorption, apical sealing ability and cytotoxicity of sealers were investigated to optimize formulation. The anti-E. faecalis effects of DMAEM copolymers with sealers were evaluated by direct contact test, colony-forming unit counting and live/dead staining. RESULTS: DMAEM monomers inhibited the growth, biofilm formation and virulence factors expression of E. faecalis in a concentration- and pH-dependent manner. Incorporation of 1.25 % and 2.5 % DMAEM into experimental sealers would not affect the flowability, solubility and periapical sealing ability (P > 0.05), but increased the water sorption of sealers (P < 0.01). Cells viability was higher than 90 % in both 1.25 % and 2.5 % DMAEM groups at pH 7.0. DMAEM copolymers with sealers reduced E. faecalis counts, inhibited biofilm formation and decreased live cells within the biofilm in response to pH values. SIGNIFICANCE: DMAEM monomers and their copolymers with resin-based sealers possessed antibacterial and antibiofilm effects on E. faecalis in response to pH values. DMAEM is promising to inhibit intraradicular E. faecalis in response to its acidic survival environment and maintain low cytotoxicity under neutral conditions, ensuring their biosafety in case of inadvertent entry into periapical tissues.

The Antibacterial Effect of Graphene Oxide on Streptococcus mutans.

To select the optimal graphene oxide (GO) for anticaries dental applications, aqueous dispersions containing GO nanosheets with various oxygen-containing functional groups were prepared and characterized using atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. The antibacterial effect towards Streptococcus mutans (S. mutans) in both planktonic and biofilm forms was studied by colony forming units (CFU) counting, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) reduction assay, live/dead fluorescent staining, and confocal laser scanning microscopy (CLSM) observation. The oxidation capacity of different GO nanosheets was examined by 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) assay and in vitro glutathione (GSH) oxidation assay. The results indicated that GO exerted strong antibacterial activities in a concentration-dependent manner towards S. mutans in both planktonic and biofilm forms. The minimum bactericidal concentration (MBC) was 40 µg/mL for planktonic S. mutans. When the concentration was higher than 80 µg/mL, 80% of the bacteria in the biofilms were devitalized. GO nanosheets with more oxygen-containing functional groups exerted higher toxicity at low concentrations. The functional groups of GO played a crucial role in its antibacterial outcome.

The inhibitory effect of carboxyl-terminated polyamidoamine dendrimers on dentine host-derived matrix metalloproteinases in vitro in an etch-and-rinse adhesive system.

The biomimetic remineralization of collagen fibrils has increased interest in restoring the demineralized dentine generated by dental caries. Carboxyl-terminated polyamidoamine dendrimers (PAMAM-COOH), hyperbranched polymeric macromolecules, can act as non-collagenous proteins to induce biomimetic remineralization on a dentine organic matrix. However, in vivo remineralization is an extremely time-consuming process; before complete remineralization, demineralized dentine collagen fibrils are susceptible to degradation by host-derived matrix metalloproteinases (MMPs). Therefore, we examined the effect of fourth-generation PAMAM-COOH (G4-PAMAM-COOH) on the collagenolytic activities of endogenous MMPs, the interaction between G4-PAMAM-COOH and demineralized dentine collagen and the influence of G4-PAMAM-COOH pre-treatment on resin-dentine bonding. G4-PAMAN-COOH not only inhibited exogenous soluble rhMMP9 but also hampered the proteolytic activities of dentine collagen-bound MMPs. Cooperated with the results of G4-PAMAM-COOH absorption and desorption, FTIR spectroscopy provided evidence for the exclusive electrostatic interaction rather than hydrogen or covalent bonding between G4-PAMAM-COOH and dentine collagen. Furthermore, G4-PAMAM-COOH pre-treatment showed no damage to resin-dentine bonding because it did not significantly decrease the elastic modulus of the demineralized dentine, degree of conversion, penetration of the adhesive into the dentinal tubules or ultimate tensile strength. Thus, G4-PAMAM-COOH can effectively inactivate MMPs, retard the enzymolysis of collagen by MMPs and scarcely influence the application of resin-dentine bonding.

Novel Biomedical Applications of Crosslinked Collagen.

Collagen is one of the most useful biopolymers because of its low immunogenicity and biocompatibility. The biomedical potential of natural collagen is limited by its poor mechanical strength, thermal stability, and enzyme resistance, but exogenous chemical, physical, or biological crosslinks have been used to modify the molecular structure of collagen to minimize degradation and enhance mechanical stability. Although crosslinked collagen-based materials have been widely used in biomedicine, there is no standard crosslinking protocol that can achieve a perfect balance between stability and functional remodeling of collagen. Understanding the role of crosslinking agents in the modification of collagen performance and their potential biomedical applications are crucial for developing novel collagen-based biopolymers for therapeutic gain.