Portraiture and Double Bond Conversion of a Monomethacrylate-based Oral Prosthetic Resin Substituted with a Novel Tri(azine-acrylate) Cross-linker

Abstract

To formulate, design, and chemically characterize a novel denture base resin (DBR) copolymer containing triazine-based antimicrobial comonomer and also to evaluate the double bond conversion (DC) in the copolymer with various concentrations of the comonomer by fourier transform infrared (FTIR) spectroscopy. The study groups comprise a control group G0 in which the specimens (n = 10) were polymerized without the triazine comonomer and trial groups G10 and G20 where the polymerized specimens (n = 10 each) contained 10 and 20% triazine comonomer, respectively. FTIR was employed to ascertain and evaluate copolymerization (CP) and DC. The obtained DC values were subjected to statistical analysis. A new denture base copolymer containing antimicrobial triazine comonomer was formed with ascertained copolymerization and higher DC than the control group. Twenty percent triazine comonomer in the copolymer exhibited the maximum DC. Incorporation of the antimicrobial comonomer copolymerized with DBR to form a novel denture base copolymer exhibiting high DC. The novel denture base copolymer may prevent the microbial adhesion on the denture surface thereby preventing denture-induced stomatitis in the edentulous patients. Nonetheless, this novel copolymer may enhance the other necessary properties of the DBR and would ameliorate the living quality of the senile geriatric population with good in vivo serviceability.