The antifungal agent of silver nanoparticles activated by diode laser as light source to reduce C. albicans biofilms: An in vitro study
Candida albicans is a normal flora caused fungal infections and has the ability to form biofilms. The aim of this study was to improve the antifungal effect of silver nanoparticles (AgNPs) and the light source for reducing the biofilm survival of C. albicans. AgNPs were prepared by silver nitrate (A...
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my.utm.873952020-11-08T03:56:02Z http://eprints.utm.my/id/eprint/87395/ The antifungal agent of silver nanoparticles activated by diode laser as light source to reduce C. albicans biofilms: An in vitro study Astuti, S. Puspita, P. S. Putra, A. P. Zaidan, A. H. Fahmi, M. Z. Syahrom, A. Suhariningsih, Suhariningsih TJ Mechanical engineering and machinery Candida albicans is a normal flora caused fungal infections and has the ability to form biofilms. The aim of this study was to improve the antifungal effect of silver nanoparticles (AgNPs) and the light source for reducing the biofilm survival of C. albicans. AgNPs were prepared by silver nitrate (AgNO3) and trisodium citrate (Na3C6H5O7). To determine the antifungal effect of treatments on C. albicans biofilm, samples were distributed into four groups; L + P+ was treatment with laser irradiation and AgNPs; L + P− was treatment with laser irradiation only; L − P+ was treatment with AgNPs only (control positive); L − P− was no treatment with laser irradiation or AgNPs (control negative). The growth of fungi had been monitored by measuring the optical density at 405 nm with ELISA reader. The particle size of AgNPs was measured by using (particle size analyzer) and the zeta potential of AgNPs was measured by using Malvern zetasizer. The PSA test showed that the particle size of AgNPs was distributed between 7.531–5559.644 nm. The zeta potentials were found lower than − 30 mV with pH of 7, 9 or 11. The reduction percentage was analyzed by ANOVA test. The highest reduction difference was given at a lower level irradiation because irradiation with a density energy of 6.13 ± 0.002 J/cm2 resulted in the biofilm reduction of 7.07 ± 0.23% for the sample without AgNPs compared to the sample with AgNPs that increased the biofilm reduction of 64.48 ± 0.07%. The irradiation with a 450-nm light source had a significant fungicidal effect on C. albicans biofilm. The combination of light source and AgNPs provides an increase of biofilm reduction compared to the light source itself. Springer London 2019-07 Article PeerReviewed Astuti, S. and Puspita, P. S. and Putra, A. P. and Zaidan, A. H. and Fahmi, M. Z. and Syahrom, A. and Suhariningsih, Suhariningsih (2019) The antifungal agent of silver nanoparticles activated by diode laser as light source to reduce C. albicans biofilms: An in vitro study. Lasers in Medical Science, 34 (5). pp. 929-937. ISSN 0268-8921 http://dx.doi.org/10.1007/s10103-018-2677-4 |
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TJ Mechanical engineering and machinery Astuti, S. Puspita, P. S. Putra, A. P. Zaidan, A. H. Fahmi, M. Z. Syahrom, A. Suhariningsih, Suhariningsih The antifungal agent of silver nanoparticles activated by diode laser as light source to reduce C. albicans biofilms: An in vitro study |
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Candida albicans is a normal flora caused fungal infections and has the ability to form biofilms. The aim of this study was to improve the antifungal effect of silver nanoparticles (AgNPs) and the light source for reducing the biofilm survival of C. albicans. AgNPs were prepared by silver nitrate (AgNO3) and trisodium citrate (Na3C6H5O7). To determine the antifungal effect of treatments on C. albicans biofilm, samples were distributed into four groups; L + P+ was treatment with laser irradiation and AgNPs; L + P− was treatment with laser irradiation only; L − P+ was treatment with AgNPs only (control positive); L − P− was no treatment with laser irradiation or AgNPs (control negative). The growth of fungi had been monitored by measuring the optical density at 405 nm with ELISA reader. The particle size of AgNPs was measured by using (particle size analyzer) and the zeta potential of AgNPs was measured by using Malvern zetasizer. The PSA test showed that the particle size of AgNPs was distributed between 7.531–5559.644 nm. The zeta potentials were found lower than − 30 mV with pH of 7, 9 or 11. The reduction percentage was analyzed by ANOVA test. The highest reduction difference was given at a lower level irradiation because irradiation with a density energy of 6.13 ± 0.002 J/cm2 resulted in the biofilm reduction of 7.07 ± 0.23% for the sample without AgNPs compared to the sample with AgNPs that increased the biofilm reduction of 64.48 ± 0.07%. The irradiation with a 450-nm light source had a significant fungicidal effect on C. albicans biofilm. The combination of light source and AgNPs provides an increase of biofilm reduction compared to the light source itself. |
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Article |
author |
Astuti, S. Puspita, P. S. Putra, A. P. Zaidan, A. H. Fahmi, M. Z. Syahrom, A. Suhariningsih, Suhariningsih |
author_facet |
Astuti, S. Puspita, P. S. Putra, A. P. Zaidan, A. H. Fahmi, M. Z. Syahrom, A. Suhariningsih, Suhariningsih |
author_sort |
Astuti, S. |
title |
The antifungal agent of silver nanoparticles activated by diode laser as light source to reduce C. albicans biofilms: An in vitro study |
title_short |
The antifungal agent of silver nanoparticles activated by diode laser as light source to reduce C. albicans biofilms: An in vitro study |
title_full |
The antifungal agent of silver nanoparticles activated by diode laser as light source to reduce C. albicans biofilms: An in vitro study |
title_fullStr |
The antifungal agent of silver nanoparticles activated by diode laser as light source to reduce C. albicans biofilms: An in vitro study |
title_full_unstemmed |
The antifungal agent of silver nanoparticles activated by diode laser as light source to reduce C. albicans biofilms: An in vitro study |
title_sort |
antifungal agent of silver nanoparticles activated by diode laser as light source to reduce c. albicans biofilms: an in vitro study |
publisher |
Springer London |
publishDate |
2019 |
url |
http://eprints.utm.my/id/eprint/87395/ http://dx.doi.org/10.1007/s10103-018-2677-4 |
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1683230761653633024 |
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13.214268 |