# Analysis of the Uptake of Hypericin by Candida albicans Yeast Cells Using Fluorescence Methods and Comparison of the Dynamics of This Process over Time

**Authors:** Radosław Turski, Jakub Fiegler-Rudol, Hanna Hüpsch-Marzec, Dariusz Skaba, Rafał Wiench

PMC · DOI: 10.3390/pharmaceutics18020189 · 2026-01-31

## 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.

## Key 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 evaluated by ANOVA. Results: Fluorescence increased rapidly and showed a nonlinear, biphasic profile under light, with local maxima around 5–7 and 15–30 min. Dark-only samples at 35–45 min had a lower %Area and lacked a clear biphasic pattern. Conclusions: Hypericin uptake by C. albicans is dynamic, nonlinear, and light-dependent. These kinetics should be considered when designing hypericin-based antifungal photodynamic therapy protocols.

## Linked entities

- **Chemicals:** hypericin (PubChem CID 3663), DMSO (PubChem CID 679)
- **Species:** Candida albicans (taxon 5476)

## Full-text entities

- **Diseases:** oral cancers (MESH:D009062), bleeding (MESH:D006470), phototoxicity (MESH:D017484), denture stomatitis (MESH:D013282), cancer (MESH:D009369), injury to (MESH:D014947), pocket (MESH:D005888), fungal infections (MESH:D009181), Candida infections (MESH:D002177), cytotoxic (MESH:D064420), chronic periodontitis (MESH:D055113), oral precancerous lesions (MESH:D011230), dental caries (MESH:D003731)
- **Chemicals:** toluidine blue (MESH:D014048), ethanol (MESH:D000431), DCFH DA (MESH:C029569), MB (MESH:D008751), agar (MESH:D000362), azoles (MESH:D001393), polymers (MESH:D011108), NaCl (MESH:D012965), DMSO (MESH:D004121), anthraquinone (MESH:D000880), glucose (MESH:D005947), Berberine (MESH:D001599), ROS (MESH:D017382), verapamil (MESH:D014700), KI (MESH:C066186), lipids (MESH:D008055), nystatin (MESH:D009761), lignin (MESH:D008031), riboflavin (MESH:D012256), Hypericin (MESH:C004965), MTT (MESH:C070243), C30H16O8 (-), porphyrins (MESH:D011166), curcumin (MESH:D003474)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Candida albicans (species) [taxon 5476], Hypericum perforatum (species) [taxon 65561], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** ATCC 90028 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_C6PI)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12944341/full.md

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Source: https://tomesphere.com/paper/PMC12944341