The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Antimicrobial efficacy of eucalyptus oil and 1,8-cineole alone and in combination with chlorhexidine digluconate against microorganisms grown in planktonic and biofilm cultures
Abstract
OBJECTIVES: Effective disinfection and antisepsis is pivotal in preventing infections within the healthcare setting. Chlorhexidine digluconate (CHG) is a widely used disinfectant/antiseptic possessing broad-spectrum antimicrobial activity; however, its penetration into bacterial biofilms and human skin is poor. The aim of this study was to investigate the antimicrobial efficacy of crude eucalyptus oil (EO) and its main component 1,8-cineole (a recognized permeation enhancer), alone and in combination with CHG, against a panel of clinically relevant microorganisms grown in planktonic and biofilm cultures. METHODS: MICs and minimum bactericidal/fungicidal concentrations were determined for each microorganism grown in suspension and biofilm using microbroth dilution and ATP bioluminescence, respectively. Chequerboard assays were used to determine synergistic, indifferent or antagonistic interactions between CHG and EO or 1,8-cineole. RESULTS: Antimicrobial activity was demonstrated by CHG, EO and 1,8-cineole; however, CHG was significantly more active against microorganisms in both planktonic and biofilm modes of growth (P < 0.05). Crude EO was significantly more efficacious against microorganisms grown in suspension compared with 1,8-cineole (P < 0.05). Synergistic activity was demonstrated between CHG and both EO and 1,8-cineole against suspensions of Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), Escherichia coli and Candida albicans, and biofilm cultures of MRSA and Pseudomonas aeruginosa. CONCLUSIONS: In conclusion, CHG may be combined with either crude EO or its major component 1,8-cineole for enhanced, synergistic antimicrobial activity against a wide range of microorganisms in planktonic and biofilm modes of growth; however, the superior antimicrobial efficacy associated with crude EO alone, compared with 1,8-cineole, favours its combination with CHG.
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Cites
Plant Products as Antimicrobial Agents
Cowan, M. M. (1999) · Clinical Microbiology Reviews · doi:10.1128/cmr.12.4.564 · Cited by 9,043
Antimicrobial activity of essential oils and other plant extracts
Hammer, K. A., Carson, C. F., & Riley, T. V. (1999) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.1999.00780.x · Cited by 2,560
Cited by
Why do plants produce so many terpenoid compounds?
Pichersky, E., & Raguso, R. A. (2018) · New Phytologist · doi:10.1111/nph.14178 · Cited by 709
van Vuuren, S., & Viljoen, A. (2011) · Planta Medica · doi:10.1055/s-0030-1250736 · Cited by 367
1,8-Cineole: a review of source, biological activities, and application
Cai, Z.-M., Peng, J.-Q., Chen, Y., Tao, L., Zhang, Y.-Y., Fu, L.-Y., Long, Q.-D., & Shen, X.-C. (2021) · Journal of Asian Natural Products Research · doi:10.1080/10286020.2020.1839432 · Cited by 308
Kouidhi, B., Al Qurashi, Y. M. A., & Chaieb, K. (2015) · Microbial Pathogenesis · doi:10.1016/j.micpath.2015.02.007 · Cited by 180
Ameur, E., Sarra, M., Yosra, D., Mariem, K., Nabil, A., Lynen, F., & Larbi, K. M. (2021) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-021-03379-y · Cited by 36
Metadata
- Authors
- Hendry, E. R., Worthington, T., Conway, B. R., & Lambert, P. A.
- Venue
- Journal of Antimicrobial Chemotherapy
- Publisher
- Oxford University Press (OUP)
- Published
- 2009-10-16
- Volume
- 64
- Issue
- 6
- Pages
- 1219-1225
- ISSN
- 0305-7453 (ISSN-L)
- 1460-2091
- OpenAlex
- W2160861478
- Cited by
- 291
- References
- 2
- FWCI
- 12.18
- Type
- journal article
- Language
- en
- Open access
- closed
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- Hendry, E. R., Worthington, T., Conway, B. R., & Lambert, P. A. (2009). Antimicrobial efficacy of eucalyptus oil and 1,8-cineole alone and in combination with chlorhexidine digluconate against microorganisms grown in planktonic and biofilm cultures. Journal of Antimicrobial Chemotherapy. https://doi.org/10.1093/jac/dkp362
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