IADR Abstract Archives

Formulate and Characterization of New Experimental Antibacterial Dental Bonding Agents

Objectives: To formulate and characterize new experimental antibacterial dental bonding agents.
Methods: The synthesized self-etching methacrylamide monomer MAUAEP containing phosphonic acid and the antibacterial dimethacrylate monomer C2DC12DMA containing DABCO dications have been previously reported. The adhesive dimethacrylate monomer 4,4-Bis[(4-(2-methacryloyloxy)ethoxy)phenyl]-pentanoic acid (BMEPPA) has been synthesized. A two-bottle bonding agent (Control) was formulated as follows: Bottle-A (primer): 7.5% MAUAEP, 7.5% DEGDA, 24%HEMA, 30% EtOH, 30% H2O, 1% Photo Initiator; and Bottle-B (adhesive): 15%BisGMA, 30%TEGDMA, 20%UEDMA, 24%HEMA and 10%BMEPPA, 1% photo initiator. Three experimental antibacterial adhesives were formulated by adding 5%, 7.5%, and 10% of C2DC12DMA to the control adhesive. Experimental primer is the same as control primer. Antibacterial activity of light-cured adhesive discs (6 mm diameter, 2 mm thick, n=5) against S. mutans biofilm were tested using modified direct-contact biofilm assay and drop plating. Microtensile bonding strength (MTBS) of experimental bonding agents was tested on the dentin of extracted human teeth (n=12) after 24h storage in de-ionized water. The data were analyzed using ANOVA and Tukey test (α=0.05).
Results: Results: See Table 1.
The adhesives of experimental antibacterial dental bonding agents have significantly higher inhibitory effects against S. mutans biofilm than the control adhesive (P<0.05), and their biofilm-inhibitory effect increases with increase of the content of antibacterial monomer. The experimental antibacterial dental bonding agents have similar MTBS to the control (P>0.05).
Conclusions: The new experimental antibacterial dental bonding agents containing 7.5% or higher amount of antibacterial dimethacrylate monomer C2DC12DMA has significant antibacterial effect and good bonding strength.

Division: IADR/AADR/CADR General Session
Meeting: 2020 IADR/AADR/CADR General Session (Washington, D.C., USA)
Location: Washington, D.C., USA
Year: 2020
Final Presentation ID: 3356
Abstract Category|Abstract Category(s): Dental Materials 2:Polymer-based Materials
Authors
  • Wang, Yapin  ( Louisiana State University Health-New Olreans School of Dentistry , New Orleans , Louisiana , United States )
  • Mon, Htwe  ( Louisiana State University Health-New Olreans School of Dentistry , New Orleans , Louisiana , United States )
  • Wen, Zezhang  ( Louisiana State University Health-New Olreans School of Dentistry , New Orleans , Louisiana , United States )
  • Xu, Xiaoming  ( Louisiana State University Health-New Olreans School of Dentistry , New Orleans , Louisiana , United States )
  • Support Funding Agency/Grant Number: NIH/NIDCR R01DE026782
    Financial Interest Disclosure: None
    SESSION INFORMATION
    Poster Session
    Polymer-based Materials: Antimicrobial Materials
    TABLES
    Table 1. Properties of experimental antibacterial bonding agents (mean ± SD).
    MaterialsS. mutans biofilm CFU on cured adhesives
    (n=5)
    MTBS (MPa)
    (n=12)
    Control(2.94 ± 0.18)x107,A32.07±4.07
    5%C2DC12DMA (1.87 ± 0.52)x106, B31.24±6.23
    7.5%C2DC12DMA(4.51 ± 1.82)x104,C 34.16±3.97
    10%C2DC12DMA(1.37 ± 0.35)x104,C34.83±4.53
    The groups with the different superscript letters have significant difference (P<0.05).