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Browsing Department of Biomedical Engineering by Author "Anderson, Gregory G."
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Item An improved dental composite with potent antibacterial function(Elsevier, 2019-07) Almousa, Rashed; Wen, Xin; Anderson, Gregory G.; Xie, Dong; Biomedical Engineering, School of Engineering and TechnologyA new BisGMA-based antibacterial dental composite has been formulated and evaluated. Compressive strength and bacterial viability were utilized to evaluate the formed composites. It was found that the new composite exhibited a significantly enhanced antibacterial function along with improved mechanical and physical properties. The bromine-containing derivative-modified composite was more potent in antibacterial activity than the chlorine-containing composite. The modified composites also exhibited an increase of 30–53% in compressive yield strength, 15–30% in compressive modulus, 15–33% in diametral tensile strength and 6–20% in flexural strength, and a decrease of 57–76% in bacterial viability, 23–37% in water sorption, 8–15% in shrinkage, 8–13% in compressive strength, and similar degree of conversion, than unmodified composite. It appears that this experimental composite may possibly be introduced to dental clinics as an attractive dental restorative due to its improved properties as well as enhanced antibacterial function.Item Polyurethane coated with polyvinylpyrrolidones via triazole links for enhanced surface fouling resistance(Wiley, 2021-12) Wen, Xin; Almousa, Rashed; Na, Sungsoo; Anderson, Gregory G.; Xie, Dong; Biomedical Engineering, School of Engineering and TechnologySurfaces with hydrophilic and antimicrobial properties are very attractive for cardiovascular device-associated applications. The aim of this study was to prepare and coat a hydrophilic polymer containing a functional group capable of forming triazole functionality onto the surface of polyurethane (PU). The modified surfaces were assessed with cell adhesion, bacterial adhesion and bacterial viability. Mouse fibroblast cells (NIH-3T3) and three bacterial species were used for assessment. The results showed that the modified surface not only exhibited a significant reduction in cell adhesion with a 25%–59% decrease to mouse fibroblast but also showed a significant reduction in bacterial attachment with 26%–67%, 24%–61% and 23%–57% decrease to Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa, respectively, as compared with original PU. Furthermore, the polymer-modified surface exhibited a significant antibacterial function by inhibiting bacterial growth with reduction of 49%–84%, 44%–79% and 53%–79% to S. aureus, E. coli and P. aeruginosa, respectively, as compared with original PU. These results indicate that covalent polymer attachment enhanced the antibacterial and antifouling properties of the PU surface.