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Updated: Feb 3, 2026

Quantifying the Antifungal Activity of Peptides Against Candida albicans
Published on: January 13, 2023
Antifungal activity of magnoflorine against Candida strains
Jaegoo Kim1, Thinh Ha Quang Bao1, Yu-Kyong Shin2
1Graduate School of Biotechnology, Kyung Hee University, Yongin-si, Gyeonggi-do, Republic of Korea.
Abstract:
Candida albicans is a major invasive pathogen, and the development of strains resistant to conventional antifungal agents has been reported in recent years. We evaluated the antifungal activity of 44 compounds against Candida strains. Magnoflorine showed the highest growth inhibitory activity of the tested Candida strains, with a minimum inhibitory concentration (MIC) of 50 μg/mL based on microdilution antifungal susceptibility testing. Disk diffusion assay confirmed the antifungal activity of magnoflorine and revealed that this activity was stable over 3 days compared to those of berberine and cinnamaldehyde. Cytotoxicity testing showed that magnoflorine could potentially be used in a clinical setting because it didn't have any toxicity to HaCaT cells even in 200 μg/mL of treatment. Magnoflorine at 50 μg/mL inhibited 55.91 ± 7.17% of alpha-glucosidase activity which is required for normal cell wall composition and virulence of Candida albicans. Magnoflorine also reduced the formation of C. albicans' biofilm. Combined treatment with magnoflorine and miconazole decreased the amount of miconazole required to kill various Candida albicans. Therefore, magnoflorine is a good candidate lead compound for novel antifungal agents.
Insights
Magnoflorine effectively inhibits Candida albicans growth and biofilm formation, showing potential as a novel antifungal agent. It demonstrates low toxicity and enhances conventional antifungal drug efficacy.
Area of Science:
- Microbiology
- Pharmacology
- Natural Products Chemistry
Background:
- Candida albicans is a significant invasive fungal pathogen.
- Antifungal resistance in Candida strains is a growing clinical concern.
- There is a need for novel antifungal agents with improved efficacy and safety profiles.
Purpose of the Study:
- To evaluate the antifungal activity of 44 compounds against Candida strains.
- To identify potential lead compounds for new antifungal drug development.
- To investigate the mechanism of action and safety of promising compounds.
Main Methods:
- Microdilution antifungal susceptibility testing to determine minimum inhibitory concentration (MIC).
- Disk diffusion assays to assess antifungal activity and stability.
- Cytotoxicity testing on HaCaT cells to evaluate safety.
- Enzyme inhibition assays to determine alpha-glucosidase activity.
- Biofilm formation assays.
- Combination treatment studies with miconazole.
Main Results:
- Magnoflorine exhibited the highest growth inhibitory activity against Candida strains, with an MIC of 50 μg/mL.
- Antifungal activity of magnoflorine was stable over 3 days.
- Magnoflorine showed no toxicity to HaCaT cells at concentrations up to 200 μg/mL.
- Magnoflorine inhibited 55.91 ± 7.17% of alpha-glucosidase activity at 50 μg/mL.
- Magnoflorine reduced Candida albicans biofilm formation.
- Combined treatment with magnoflorine and miconazole enhanced the efficacy of miconazole.
Conclusions:
- Magnoflorine is a potent inhibitor of Candida albicans growth and virulence factors.
- Magnoflorine possesses a favorable safety profile for potential clinical applications.
- Magnoflorine demonstrates synergistic effects when combined with conventional antifungals.
- Magnoflorine represents a promising candidate lead compound for the development of novel antifungal therapies.
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