Purpose: This study was designed to investigate the in vitro effects of geraniol (GE) and thymoquinone (TQ) on Candida biofilms on denture acrylic and any accompanying changes in acrylic surface roughness or color. Methods: The susceptibility of Candida species to GE and TQ was determined using the broth microdilution method and time-kill assay. A minimum biofilm eradication concentration (MBEC) assay was performed using 7-day Candida biofilms grown on denture acrylic. Results: The minimum inhibitory concentration (MIC) of GE and TQ for Candida spp. was 256 and 32 µg/mL, respectively. The Candida strain complete kill rates for GE and TQ at 5-fold MIC were determined after 1 h of incubation. At 5-fold MIC, GE and TQ inhibited the preformed biofilm activity (MBEC80) of all Candida strains on denture acrylic by more than 80% after treatment for 3 h. At sub-MIC levels, GE and TQ prevented the development of C. albicans and C. tropicalis hyphae. SEM images demonstrated that GE and TQ damaged the fungal cell membrane and induced cell lysis. On the other hand, GE and TQ at 10-fold MIC did not alter the surface roughness or color of the denture acrylic. Conclusion: GE and TQ are interesting natural substances that could be developed as promising disinfectants for removable dentures.
Fungal infection is one of the main clinical problems due to the extensive uses of broad-spectrum antibiotics and immunosuppressive therapy. Among all, candida species are the most prevalent. Piper betle Linn., a tropical plant intimately associated with pepper, has been widely used as a traditional herb in many Asian countries. The purpose of this study was to evaluate the antimicrobial effect of essential oil extracted from fresh leaves of P. betle against four strains of candida species, C. albicans, C. glabrata, C. krusei, C. parapsilosis, C. tropicalis, C. pseudotropicalis and C. stellatoidia. Inhibitory activity was primarily screened by Kirby-Bauer disc diffusion technique and subsequently the minimum inhibitory concentration (MIC) was determined by agar dilution technique. Betel oil exhibited a high potential of antifungal property against all strains of yeast with inhibition zones ranged from 32 to 33 mm. in diameter and MIC values of 0.039-0.078 % v/v. Data from this study demonstrates a potential application of betel oil in drug preparations and development for the treatment of candida infection. Further investigations are required to define the antifungal mechanism of this oil as well as clinical trial in the patients.
Cratoxylumformosumis a plant widely distributed in mountainous area of various Asian countries. The extract prepared from the burnt bark has been used among the local people as a varnish to prevent tooth decay and other oral diseases. The aim of this study was to examine antifungal activity ofC. formosumgum againstCandidaalbicansand to evaluate its cytotoxicity. The gum prepared from the extract ofC.formosumwas investigated for antimicrobial activity against 3 strains ofC.albicans. Inhibition of microbial growth was primarily tested by agar diffusion method. A two-fold broth dilution method was then used to determine the minimum inhibitory concentration (MIC) of the gum. Based on the MIC value, cytotoxicity test was performed on mouse fibroblasts (ATCC clone 929) using agar overlay technique. Inhibitory effect of the gum was seen againstC. albicanswith zones of inhibition ranging from 8.0 to 9.3 mm. MIC values were between 0.50 and 1.25 mg/mL. In term of cytotoxicity,C. formosumgum at the concentration of 20 MIC (25 mg/mL) was classified as grade 3 (moderate cytotoxicity) whereas those of 10 MIC and 1 MIC were grade 1 (slight cytotoxicity). In conclusion, the gum prepared fromC. formosumextract exhibited antimicrobial activities against all the test strains ofC. albicans. From the present study, it can be suggested that this plant can be used as a novel antifungal agent, effective againstC.albicansinfections, due to its inhibitory effects onC. albicansand acceptable biocompatibility. Furtherin vitro/in vivostudies should be conducted to understand the mechanisms of action and to establish the safe profile of this gum for clinical usage.
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