2017
DOI: 10.1016/j.jphotobiol.2017.06.034
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Incorporation of triclosan and acridine orange into liposomes for evaluating the susceptibility of Candida albicans

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Cited by 8 publications
(3 citation statements)
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“…The obtained IC 50 value was 0.4 µM. These results are in agreement with the AO spectrum, which exhibits characteristic peaks in the UV region around 230 nm, 270 nm and 290 nm [ 50 ]; in the visible region at 490 nm (maximum absorbance) due to the AO molecule (monomer); and a shoulder at 470 nm that can turn into a peak with an increase in concentration, possibly due to AO dimers [ 51 ]. Like AO, several molecules with intense absorption peaks in the blue wavelength region (Soret peak) are described in the literature as very efficient PS [ 7 ].…”
Section: Resultssupporting
confidence: 77%
“…The obtained IC 50 value was 0.4 µM. These results are in agreement with the AO spectrum, which exhibits characteristic peaks in the UV region around 230 nm, 270 nm and 290 nm [ 50 ]; in the visible region at 490 nm (maximum absorbance) due to the AO molecule (monomer); and a shoulder at 470 nm that can turn into a peak with an increase in concentration, possibly due to AO dimers [ 51 ]. Like AO, several molecules with intense absorption peaks in the blue wavelength region (Soret peak) are described in the literature as very efficient PS [ 7 ].…”
Section: Resultssupporting
confidence: 77%
“…4b) associated with appropriate markers can be used to evaluate cell viability. The vital dye, acridine orange, enters cells, mixes with intact DNA, and fluoresces green; if damaged, the cells appear orange-red [24]. The images confirm the susceptibility results presented in Fig.…”
Section: Antifungal Susceptibilitysupporting
confidence: 86%
“…This work used a viability assay based on the exclusion of the methylene blue dye [18][19][20][21][22], which acts as an indicator of cell viability. The counting in the Neubauer chamber was done with the help of the optical microscope, which considered the cells that were stained blue to be dead and the transparent ones to be viable [23].For morphological analysis, films with the dispersion of fungi were prepared by the casting technique [24], which involves the spreading of the material on a substrate. The entire procedure was performed in a laminar flow hood.…”
Section: Methodsmentioning
confidence: 99%