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Syzygium aromaticum essential oil and its major constituents: Assessment of activity against Candida spp. and toxicity.
Vasconcelos, Priscilla Guimarães Silva; Abuna, Gabriel Flores; Raimundo E Silva, Joanda Paolla; Tavares, Josean Fechine; Costa, Edja Maria Melo de Brito; Murata, Ramiro Mendonça.
Affiliation
  • Vasconcelos PGS; Department of Dentistry, Postgraduate Program in Dentistry, State University of Paraiba, Campina Grande, Paraíba, Brazil.
  • Abuna GF; Department of Foundational Sciences, School of Dental Medicine, East Carolina University, Greenville, North Carolina, United States of America.
  • Raimundo E Silva JP; Multi-User Laboratory for Characterization and Analysis, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
  • Tavares JF; Multi-User Laboratory for Characterization and Analysis, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
  • Costa EMMB; Department of Dentistry, Postgraduate Program in Dentistry, State University of Paraiba, Campina Grande, Paraíba, Brazil.
  • Murata RM; Department of Foundational Sciences, School of Dental Medicine, East Carolina University, Greenville, North Carolina, United States of America.
PLoS One ; 19(6): e0305405, 2024.
Article in En | MEDLINE | ID: mdl-38889118
ABSTRACT
Syzigium aromaticum essential oil (EO), eugenol, and ß-caryophyllene were evaluated regarding antifungal, antibiofilm, and in vitro toxicity. Additionally, in vivo toxicity of EO was observed. Anti-Candida activity was assessed through broth microdilution assay for all compounds. Time-kill assay (0, 1, 10, 30 min, 1, 2, and 4 h) was used to determine the influence of EO and eugenol on Candida Growth kinetics. Thereafter, both compounds were evaluated regarding their capacity to act on a biofilm formation and on mature biofilm, based on CFU/ml/g of dry weight. Cell Titer Blue Viability Assay was used for in vitro cytotoxicity, using oral epithelial cells (TR146) and human monocytes (THP-1). Lastly, Galleria mellonella model defined the EO in vivo acute toxicity. All compounds, except ß-cariofilene (MIC > 8000 µg/ml), presented antifungal activity against Candida strains (MIC 500-1000 µg/ml). The growth kinetics of Candida was affected by the EO (5xMIC 30 min onward; 10xMIC 10 min onward) and eugenol (5xMIC 10 min onward; 10xMIC 1 min onward). Fungal viability was also affected by 5xMIC and 10xMIC of both compounds during biofilm formation and upon mature biofilms. LD50 was defined for TR146 and THP1 cells at, respectively, 59.37 and 79.54 µg/ml for the EO and 55.35 and 84.16 µg/ml for eugenol. No sign of toxicity was seen in vivo up to 10mg/ml (20 x MIC) for the EO. S. aromaticum and eugenol presented antifungal and antibiofilm activity, with action on cell growth kinetics. In vivo acute toxicity showed a safe parameter for the EO up to 10 mg/ml.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Candida / Eugenol / Oils, Volatile / Microbial Sensitivity Tests / Biofilms / Syzygium / Antifungal Agents Limits: Animals / Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2024 Document type: Article Affiliation country: Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Candida / Eugenol / Oils, Volatile / Microbial Sensitivity Tests / Biofilms / Syzygium / Antifungal Agents Limits: Animals / Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2024 Document type: Article Affiliation country: Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA