Analysis of the Uptake of Hypericin by Candida albicans Yeast Cells Using Fluorescence Methods and Comparison of the Dynamics of This Process over Time
Radosław Turski, Jakub Fiegler-Rudol, Hanna Hüpsch-Marzec, Dariusz Skaba, Rafał Wiench

TL;DR
This study uses fluorescence methods to track how Candida albicans yeast cells take up hypericin over time, revealing a dynamic and light-dependent process.
Contribution
The study provides a detailed time-dependent characterization of hypericin uptake in Candida albicans using fluorescence and image analysis.
Findings
Fluorescence increased rapidly and showed a nonlinear, biphasic uptake profile under light.
Local maxima in fluorescence were observed around 5–7 and 15–30 minutes.
Dark-only samples showed lower fluorescence and lacked a biphasic pattern.
Abstract
Background: Hypericin is a natural photosensitizer with promising antifungal potential, but its uptake kinetics in Candida (C.) albicans are not well defined. Objective: To characterize the time-dependent uptake of hypericin by C. albicans in vitro using fluorescence microscopy and quantitative image analysis. Methods: C. albicans ATCC 90028 was standardized to 0.5 McFarland and incubated with hypericin dissolved in DMSO. Samples were illuminated with an LED system tuned near 550 nm and imaged using a CCD fluorescence microscope with emission recorded above ≈600 nm. Images were analyzed in ImageJ, using a control-based threshold and percentage area (the percentage of pixels above the threshold in the whole field) as a fluorescence measure. Time points were 1, 3, 5, 7, 10, 15, 20, 25, 30, 35, 40, and 45 min, plus a separate dark-only series at 35–45 min. Data from three experiments were…
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Taxonomy
TopicsPhotodynamic Therapy Research Studies · Nanoplatforms for cancer theranostics · Antifungal resistance and susceptibility
