Antifungal Activity of Essential Oils against Candida albicans Strains Isolated from Users of Dental Prostheses

• Published in: Evidence-based complementary and alternative medicine Vol. 2017; no. 2017; pp. 1 - 9
• Main Authors: Guerra, Felipe Queiroga Sarmento, Sousa, Janiere Pereira de, Silva, Daniele de Figueredo, Júnior, José Klidenberg de Oliveira, Freire, Julliana Cariry Palhano, Lima, Edeltrudes Oliveira
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Publishing Corporation 01.01.2017; Hindawi; John Wiley & Sons, Inc
• Subjects: Antifungal activity; Antifungal agents; Antimicrobial agents; Aromatherapy; Bioassays; Candida; Candida albicans; Chemotherapy; Citral; Dental prosthetics; Dentistry; Essential oils; Fungicidal activity; Herbal medicine; Implants, Artificial; Laboratories; Limonene; Microorganisms; Minimum inhibitory concentration; Natural products; Nystatin; Oils & fats; Pharmaceutical sciences; Physiology; Prostheses; Prosthesis
• ISSN: 1741-427X; 1741-4288
• DOI: 10.1155/2017/7158756

Objective. The objective of this study was to analyze the antifungal activity of citral, selected by screening natural products, against Candida albicans isolates from subjects who use dental prostheses. Methodology. Screening of essential oils, including those from Mentha piperita L. (Briq), Origanum vulgare, and Zingiber officinale L., and the phytoconstituents citral and limonene, to select an appropriate natural product. Citral, which mediated the best antifungal response, was selected for biological assays. The minimum inhibitory concentrations (MICs) and minimum fungicidal concentrations (MFCs) for citral and nystatin were determined by the microdilution method. Micromorphological analyses, time-kill curve, and modulation tests were performed. Results. The MIC and MFC of citral were established as 32 μg/mL, consistent with fungicidal activity. The clinical strains were resistant to nystatin. Citral caused micromorphological alteration in the strains. In the time-kill curve, the growth of the clinical strain was reduction in growth equal to 3 log10 colony-forming units per milliliter after exposure to the MIC and MIC×2 of citral for 2 h. Citral did not modulate the resistance of the studied strains to nystatin. Conclusion. This study revealed the potential of citral as a fungicidal agent and highlighted the resistance of clinical strains of C. albicans to nystatin.