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Harnessing nd: YAG laser technology to combat antifungal resistance in yeast-driven onychomycosis
Taraneh Razaviyoun1, Parvin Mansouri2, Seyed Jamal Hashemi3
1Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran. Taraneh.Razaviyoun@gmail.com.
Abstract:
Onychomycosis is a persistent nail infection often caused by dermatophytes or yeasts, with conventional treatments limited by long durations, poor compliance, and resistance. The long-pulsed Nd: YAG 1064 nm laser (NDYL) has emerged as a potential adjunct; however, its effects in combination with antifungals against yeast-related cases are unclear. This study examined the in vitro synergistic effect of NDYL with four antifungal agents-Ketoconazole (KET), Itraconazole (ITK), Voriconazole (VRC), and Terbinafine(TRB)-on clinical yeasts isolates from patients with onychomycosis. Yeast isolates were identified through ITS PCR sequencing. Susceptibility testing was conducted using the CLSI disk diffusion method (document M44-A2). Two experimental series-vital nail scrapings and cultured colonies-were exposed to standardized NDYL laser parameters. Antifungal activity was assessed by measuring inhibition zone diameters, and statistical comparisons were performed using paired t-tests. NDYL significantly enhanced antifungal activity, with the most pronounced effects observed for KET and ITC (p < 0.05). KET achieved up to 100% sensitivity improvement in nail scraping samples. VRC and TRB demonstrated moderate but consistent enhancements. Recorded irradiation temperatures remained below 42 °C, suggesting primarily non-thermal mechanisms. The relative frequencies of increased inhibition zone diameters in nail scrapings, yeast colonies, and combined datasets were: ITC (83.3%, 50.0%, 66.7%), VRC (66.7%, 50.0%, 58.3%), TRB (33.3%, 16.7%, 25.0%), and KET (100%, 66.7%, 83.3%). These findings support NDYL as a potential adjunctive tool for enhancing antifungal efficacy in yeast-associated onychomycosis. Further in vivo research is warranted to confirm clinical applicability and refine treatment protocols.
Insights
The long-pulsed Nd: YAG laser (NDYL) combined with antifungals significantly boosted efficacy against yeast onychomycosis in vitro. Ketoconazole and Itraconazole showed the most pronounced synergistic effects, enhancing antifungal activity.
Area of Science:
- Medical Mycology
- Dermatology
- Laser Medicine
Background:
- Onychomycosis is a common nail infection with challenging treatment outcomes.
- Conventional antifungal therapies face limitations including resistance and poor patient compliance.
- The efficacy of long-pulsed Nd: YAG 1064 nm laser (NDYL) as an adjunct to antifungals for yeast-related onychomycosis remains under investigation.
Purpose of the Study:
- To evaluate the in vitro synergistic effects of NDYL combined with four antifungal agents (Ketoconazole, Itraconazole, Voriconazole, Terbinafine) against clinical yeast isolates from onychomycosis patients.
- To assess the impact of NDYL on antifungal susceptibility in both vital nail scrapings and cultured yeast colonies.
Main Methods:
- Clinical yeast isolates from onychomycosis were identified using ITS PCR sequencing.
- Antifungal susceptibility testing was performed using the CLSI disk diffusion method (M44-A2).
- Nail scrapings and cultured yeast colonies were exposed to standardized NDYL parameters, and antifungal activity was measured by inhibition zone diameters.
Main Results:
- NDYL significantly enhanced the antifungal activity of Ketoconazole (KET) and Itraconazole (ITC), with KET achieving 100% sensitivity improvement in nail scrapings.
- Voriconazole (VRC) and Terbinafine (TRB) also showed moderate, consistent enhancements in antifungal efficacy.
- Irradiation temperatures remained below 42°C, indicating predominantly non-thermal mechanisms of action.
Conclusions:
- NDYL shows promise as an adjunctive therapy to improve antifungal treatment outcomes for yeast-associated onychomycosis.
- The synergistic effects observed in vitro warrant further in vivo investigation to establish clinical applicability and optimize treatment protocols.
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