Department of Physical Chemistry and Technology of Polymers, Faculty of Chemistry, Silesian University of Technology, Strzody 9 Str., 44-100 Gliwice, Poland.
Department of Inorganic Chemistry, Analytical Chemistry and Electrochemistry, Faculty of Chemistry, Silesian University of Technology, Krzywoustego 6 Str., 44-100 Gliwice, Poland; Biotechnology Centre, Silesian University of Technology, Krzywoustego 8 Str., 44-100 Gliwice, Poland.
Dent Mater. 2023 Jul;39(7):659-664. doi: 10.1016/j.dental.2023.05.008. Epub 2023 May 20.
This study assumed that the quaternary ammonium urethane-dimethacrylate derivative (QAUDMA-m, where m was 8, 10, 12, 14, 16, 18, and corresponded to the number of carbon atoms in the N-alkyl substituent) can be used to achieve copolymers with high mechanical performance and antibacterial activity.
Photocured copolymers of bisphenol A glycerolate dimethacrylate (Bis-GMA) 40 wt%, QAUDMA-m 40 wt%, and triethylene glycol dimethacrylate (TEGDMA) 20 wt% (BG:QAm:TEG) were characterized by the degree of conversion (DC), flexural strength (FS), flexural modulus (E), hardness (HB), and antibacterial properties (the number of bacteria colonies adhered to copolymer surfaces and inhibition zone diameter (IZD)) against Staphylococcus aureus and Escherichia coli. Reference copolymers of Bis-GMA, urethane-dimethacrylate monomer (UDMA), and TEGDMA (BG:TEG and BG:UD:TEG) were also characterized.
The DC of BG:QAm:TEGs ranged from 0.59 to 0.68, HB from 83.84 to 153.91 MPa, FS from 50.81 to 74.47 MPa, and E from 1986.74 to 3716.68 MPa. The number of S. aureus and E. coli bacteria adhered to BG:QAm:TEG surfaces was from 0 (no bacteria observed) to 6.47 and 4.99 log(CFU/mL), respectively. IZD was from 10 and 5 mm (no inhibition zone) to 23 and 21 mm, respectively. Three copolymers: BG:QA8:TEG, BG:QA10:TEG, and BG:QA12:TEG had similar or better mechanical properties than the reference copolymers, but unlike them, they showed high antibacterial activity against both bacteria strains.
The obtained copolymers can offer a good, mechanically efficient, bioactive alternative to BG:TEG and BG:UD:TEG copolymers. The use of such materials can help to make progress in dental health care.
本研究假设季铵基氨甲酸酯-二甲基丙烯酸酯衍生物(QAUDMA-m,其中 m 为 8、10、12、14、16、18,分别对应于 N-烷基取代基中的碳原子数)可用于合成具有高机械性能和抗菌活性的共聚物。
用光固化 Bis-GMA(40wt%)、QAUDMA-m(40wt%)和三甘醇二甲基丙烯酸酯(TEGDMA)(20wt%)(BG:QAm:TEG)制备的共聚物的转化率(DC)、弯曲强度(FS)、弯曲模量(E)、硬度(HB)和抗菌性能(粘附在共聚物表面的细菌菌落数量和抑菌圈直径(IZD))进行了评估,测试的细菌包括金黄色葡萄球菌和大肠杆菌。同时还对参考共聚物 Bis-GMA、氨甲酸酯二甲基丙烯酸酯单体(UDMA)和 TEGDMA(BG:TEG 和 BG:UD:TEG)进行了特征描述。
BG:QAm:TEG 的 DC 范围为 0.59 至 0.68,HB 为 83.84 至 153.91MPa,FS 为 50.81 至 74.47MPa,E 为 1986.74 至 3716.68MPa。粘附在 BG:QAm:TEG 表面的金黄色葡萄球菌和大肠杆菌的数量分别为 0(未观察到细菌)至 6.47 和 4.99log(CFU/mL)。IZD 分别为 10 和 5mm(无抑制区)至 23 和 21mm。三种共聚物:BG:QA8:TEG、BG:QA10:TEG 和 BG:QA12:TEG 的机械性能与参考共聚物相似或更好,但与参考共聚物不同的是,它们对两种细菌都表现出了高抗菌活性。
所获得的共聚物可为具有良好机械性能的生物活性材料提供一种替代 BG:TEG 和 BG:UD:TEG 共聚物的选择,这类材料的使用有助于在牙科保健方面取得进展。