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1.
Turk J Med Sci ; 48(4): 873-879, 2018 Aug 16.
Article in English | MEDLINE | ID: mdl-30119595

ABSTRACT

Background/aim: This study was designed to evaluate the effect of antimicrobial photodynamic treatment (APDT) in a biofilm model using combinations of various dyes (rose bengal, riboflavin, and methylene blue) as photosensitizers and light sources (LED and UVA) against staphylococcal and candidal biofilms. Materials and methods: Sterile microtiter plates were used for the development and quantification of the biofilms. APDT was carried out using combinations of the light sources and dyes. The percentage of the growth inhibition was then calculated using a spectrophotometer. The broth media in the wells were aspirated, wells were stained with crystal violet, and optical density values were measured spectrophotometrically. SEM analysis of the impact of APDT on bacterial and fungal biofilms was also performed. Results: The experiments showed that the most efficacious combination was red LED + methylene blue against both staphylococcal and candidal biofilms. A marked inhibition (45.4%) was detected on both C. albicans and C. parapsilosis biofilms. Red LED + methylene blue was also effective on S. aureus and S. epidermidis biofilms. SEM images suggested that the number of adherent cells and biofilm mass were markedly reduced after APDT treatment. Conclusion: Although the results of this study indicated the in vitro efficacy of APDT, it might also be a promising technique for the control of biofilm growth within intravenous catheters.


Subject(s)
Anti-Bacterial Agents/pharmacology , Biofilms/drug effects , Candida/drug effects , Coloring Agents , Photochemotherapy , Photosensitizing Agents/pharmacology , Staphylococcus/drug effects , Candida/growth & development , Candida albicans/drug effects , Candida albicans/growth & development , Humans , Light , Methylene Blue , Riboflavin , Rose Bengal , Staphylococcus/growth & development , Staphylococcus aureus/drug effects , Staphylococcus aureus/growth & development
2.
Cornea ; 37(11): 1463-1467, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30161054

ABSTRACT

PURPOSE: To investigate voriconazole (VRZ) penetration and fungal load in the cornea after applying VRZ therapy with various treatment combinations in a fungal keratitis model. METHODS: Fifty-four eyes of 27 young albino rabbits were provided for this experimental study. Twelve corneas were inoculated with Candida albicans, 12 corneas were inoculated with Fusarium solani, and 6 eyes were selected as controls. Infected corneas received various treatment combinations including VRZ 1% drop therapy alone, VRZ 1% plus amphotericin B 1% drop combination therapy, iontophoretic VRZ therapy, and VRZ 1% drop therapy after corneal cross-linking. Fungal load was measured by log reduction, and VRZ levels were quantified by liquid chromatography-tandem mass spectrometry. RESULTS: Iontophoresis-assisted VRZ application showed the highest antifungal activity against F. solani keratitis (4-log reduction) and C. albicans keratitis (5-log reduction) compared with other treatment applications. VRZ levels were also found to be the highest in corneas that received iontophoretic VRZ treatment (3.6313 ± 0.0990 ppb for F.solani keratitis and 1.7001 ± 0.0065 ppb for C. albicans keratitis) compared with other treatment applications. CONCLUSIONS: Iontophoresis seems to provide the highest VRZ concentration and highest antifungal activity in the cornea compared with other treatment applications for C. albicans and F. solani keratitis.


Subject(s)
Antifungal Agents/therapeutic use , Cornea/metabolism , Cross-Linking Reagents/therapeutic use , Eye Infections, Fungal/drug therapy , Iontophoresis , Photochemotherapy/methods , Voriconazole/therapeutic use , Animals , Antifungal Agents/pharmacokinetics , Candida albicans/isolation & purification , Candidiasis/drug therapy , Collagen/metabolism , Cornea/microbiology , Disease Models, Animal , Fusariosis/drug therapy , Fusarium/isolation & purification , Keratitis/drug therapy , Rabbits , Ultraviolet Rays , Voriconazole/pharmacokinetics
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