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Effect of Antimicrobial Denture Base Resin on Multi-Species Biofilm Formation

机译:抗菌义齿基料树脂对多种生物膜形成的影响

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Our aims of the research were to study the antimicrobial effect of dimethylaminododecyl methacrylate (DMADDM) modified denture base resin on multi-species biofilms and the biocompatibility of this modified dental material. Candida albicans ( C. albicans ), Streptococcus mutans ( S. mutans ), Streptococcus sanguinis ( S. sanguinis ), as well as Actinomyces naeslundii ( A. naeslundii ) were used for biofilm formation on denture base resin. Colony forming unit (CFU) counts, microbial viability staining, and 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) array were used to evaluate the antimicrobial effect of DMADDM. C. albicans staining and Real-time PCR were used to analyze the morphology and expression of virulence genes of C. albicans in biofilm. Lactate dehydrogenase (LDH) array and Real-time PCR were conducted to examine the results after biofilm co-cultured with epithelial cell. Hematoxylin and eosin (HE) staining followed by histological evaluation were used to study the biocompatibility of this modified material. We found that DMADDM containing groups reduced both biomass and metabolic activity of the biofilm significantly. DMADDM can also inhibit the virulence of C. albicans by means of inhibiting the hyphal development and downregulation of two virulence related genes. DMADDM significantly reduced the cell damage caused by multi-species biofilm according to the LDH activity and reduced the expression of IL-18 gene of the cells simultaneously. The in vivo histological evaluation proved that the addition of DMADDM less than 6.6% in denture material did not increase the inflammatory response ( p > 0.05). Therefore, we proposed that the novel denture base resin containing DMADDM may be considered as a new promising therapeutic system against problems caused by microbes on denture base such as denture stomatitis.
机译:我们的研究目标是研究甲基丙烯酸二甲基氨基十二烷基酯(DMADDM)改性的义齿基料树脂对多种生物膜的抗菌作用以及该改性牙科材料的生物相容性。白色假丝酵母(C. albicans),变形链球菌(S. mutans),血链球菌(S. sanguinis)以及纳氏放线菌(A. naeslundii)用于在义齿基料树脂上形成生物膜。使用菌落形成单位(CFU)计数,微生物生存力染色和2,3-双(2-甲氧基-4-硝基-5-硝基苯基)-2H-四唑-5-甲酰苯胺(XTT)阵列评估抗菌效果DMADDM。使用白色念珠菌染色和实时荧光定量PCR分析生物膜中白色念珠菌的毒力基因的形态和表达。生物膜与上皮细胞共培养后,进行乳酸脱氢酶(LDH)阵列和实时荧光定量PCR检测结果。苏木精和曙红(HE)染色,然后进行组织学评估,以研究这种改性材料的生物相容性。我们发现含DMADDM的基团显着降低了生物膜的生物量和代谢活性。 DMADDM还可以通过抑制两个毒力相关基因的菌丝发育和下调来抑制白色念珠菌的毒力。 DMADDM可根据LDH活性显着降低多种生物膜对细胞的损害,并同时降低细胞中IL-18基因的表达。体内组织学评估证明,在义齿材料中添加少于6.6%的DMADDM不会增加炎症反应(p> 0.05)。因此,我们提出,含有DMADDM的新型义齿基体树脂可以被认为是针对由义齿基体上的微生物例如义齿口炎引起的问题的有希望的新治疗系统。

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