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Chlorin e6-Based Photodynamic Therapy for Metastatic Melanoma: An In Vitro Efficacy Study
Aishat Adejoke Obalola1, Heidi Abrahamse1, Sathish Sundar Dhilip Kumar1
1Laser Research Centre, University of Johannesburg-Doornfontein Campus, Johannesburg 2028, Gauteng South Africa.
ACS Omega
|May 11, 2026
Summary
Chlorin e6 (Ce6)-mediated photodynamic therapy (PDT) effectively reduced metastatic melanoma cell viability and induced apoptosis. This study highlights Ce6 as a promising photosensitizer for melanoma treatment.
Area of Science:
- Oncology
- Biochemistry
- Photomedicine
Background:
- Melanoma is an aggressive skin cancer with limited treatment options.
- Photodynamic therapy (PDT) offers a localized, noninvasive treatment approach.
- Photosensitizers are key to PDT, generating reactive oxygen species (ROS) to kill cancer cells.
Purpose of the Study:
- To investigate the in vitro efficacy of Chlorin e6 (Ce6)-mediated PDT on metastatic melanoma (A375) cells.
- To evaluate the impact of different laser fluence levels (5 and 15 J/cm²) and time points (24 and 48 hours) on Ce6-PDT effectiveness.
Main Methods:
- Utilized ATP viability testing, microscopy, oxidative stress assessment, and apoptosis assays.
- Applied Ce6-mediated photodynamic therapy with a 660 nm laser at 5 J/cm² and 15 J/cm².
- Examined cellular alterations in A375 melanoma cells at 24 and 48 hours post-treatment.
Main Results:
- Ce6-PDT significantly decreased metastatic melanoma cell viability at both tested fluence levels.
- Increased ROS generation and induction of apoptosis were observed in A375 cells following Ce6-PDT.
- Cellular damage and death were evident at 5 J/cm² and 15 J/cm² PDT doses.
Conclusions:
- Ce6-mediated PDT demonstrates significant in vitro efficacy against metastatic melanoma cells.
- Ce6 shows potential as a photosensitizer for melanoma treatment, particularly within nanobioconjugate platforms.

