The antifungal activity and cytotoxicity of silver containing denture base material


KURT A., Erkose-Genc G., UZUN M., EMRENCE Z., Ustek D., Isik-Ozkol G.

Nigerian Journal of Clinical Practice, cilt.20, sa.3, ss.290-295, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 20 Sayı: 3
  • Basım Tarihi: 2017
  • Doi Numarası: 10.4103/1119-3077.181362
  • Dergi Adı: Nigerian Journal of Clinical Practice
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.290-295
  • Anahtar Kelimeler: Candida albicans, cytotoxicity, denture base, silver microparticles
  • Trakya Üniversitesi Adresli: Evet

Özet

Objective: Denture base materials are susceptible to fungal adhesion, which is an important etiological issue in the pathogenesis of denture stomatitis. The purpose of this in vitro study was to evaluate the antifungal activity and cytotoxicity of denture base material containing silver microparticles. Materials and Methods: The polymethyl methacrylate (PMMA) denture base material was used, and silver microparticles were added to the polymer powder in different concentrations by volume (0%, 0.25%, 0.5%, and 1%). Their antifungal activity against Candida albicans was assessed in terms of colony-forming units. PMMA disc specimens containing silver microparticles were eluted with culture medium for 1, 2, and 5 days. The cytotoxicity of the eluates to cultured L929 mouse fibroblast cells was evaluated using a real-time cell analysis (RTCA) system and the 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) assay. Results: The antifungal effect against C. albicans increased with the percentage of silver microparticles (P < 0.05). For both tests, both RTCA and the MTT assay, no time-or silver-dependent cytotoxicity of PMMA denture base material containing silver microparticles was observed. Conclusions: PMMA denture base material containing silver microparticles have antifungal activity and no cytotoxic effect.