Abstract:The minimal invasiveness and high selectivity of 5-aminolevulinic acid (5-ALA)-based photodynamic therapy (PDT; 5-ALA-PDT) renders it a viable therapeutic option for the treatment of various types of cancer. Compared with conventional lasers, light-emitting diodes (LEDs) are an inexpensive and convenient low-energy light source option. Nevertheless, the scope of LEDs in the 5-ALA-PDT of colorectal cancer (CRC) has yet to be fully determined. Thus, the aim of the present study was to assess the efficacy of LEDs… Show more
“…Et when comparing the two types of treatments, PDT and dark. This low reduction in cell viability is not related to exposure to LED, considering that cell viability is higher when cells were exposed to PDT (Figure 5A), which was also observed in studies by Shah et al [31], in which they evaluated the photodynamic activity of four types of LEDs when cancer cells were exposed to them. Furthermore, it was observed that LEDs at wavelengths of 630 nm (red), 515 nm (green), and 410-456 nm (blue) did not influence the reduction in cell viability.…”
Melanoma, a severe form of skin cancer intricately linked to genetic and environmental factors, is predicted to reach 100,000 new cases worldwide by 2040, underscoring the need for effective and safe treatment options. In this study, we assessed the efficacy of a photosensitizer called Chlorophyll A (Chl-A) incorporated into hydrogels (HGs) made of chitosan (CS) and poloxamer 407 (P407) for Photodynamic Therapy (PDT) against the murine melanoma cell line B16-F10. The HG was evaluated through various tests, including rheological studies, SEM, and ATR-FTIR, along with cell viability assays. The CS- and P407-based HGs effectively released Chl-A and possessed the necessary properties for topical application. The photodynamic activity of the HG containing Chl-A was evaluated in vitro, demonstrating high therapeutic potential, with an IC50 of 25.99 µM—an appealing result when compared to studies in the literature reporting an IC50 of 173.8 µM for cisplatin, used as a positive control drug. The developed formulation of CS and P407-based HG, serving as a thermosensitive system for topical applications, successfully controlled the release of Chl-A. In vitro cell studies associated with PDT exhibited potential against the melanoma cell line.
“…Et when comparing the two types of treatments, PDT and dark. This low reduction in cell viability is not related to exposure to LED, considering that cell viability is higher when cells were exposed to PDT (Figure 5A), which was also observed in studies by Shah et al [31], in which they evaluated the photodynamic activity of four types of LEDs when cancer cells were exposed to them. Furthermore, it was observed that LEDs at wavelengths of 630 nm (red), 515 nm (green), and 410-456 nm (blue) did not influence the reduction in cell viability.…”
Melanoma, a severe form of skin cancer intricately linked to genetic and environmental factors, is predicted to reach 100,000 new cases worldwide by 2040, underscoring the need for effective and safe treatment options. In this study, we assessed the efficacy of a photosensitizer called Chlorophyll A (Chl-A) incorporated into hydrogels (HGs) made of chitosan (CS) and poloxamer 407 (P407) for Photodynamic Therapy (PDT) against the murine melanoma cell line B16-F10. The HG was evaluated through various tests, including rheological studies, SEM, and ATR-FTIR, along with cell viability assays. The CS- and P407-based HGs effectively released Chl-A and possessed the necessary properties for topical application. The photodynamic activity of the HG containing Chl-A was evaluated in vitro, demonstrating high therapeutic potential, with an IC50 of 25.99 µM—an appealing result when compared to studies in the literature reporting an IC50 of 173.8 µM for cisplatin, used as a positive control drug. The developed formulation of CS and P407-based HG, serving as a thermosensitive system for topical applications, successfully controlled the release of Chl-A. In vitro cell studies associated with PDT exhibited potential against the melanoma cell line.
“…Thus, there is an unmet need for new therapeutic approaches to augment and improve the current standard of care for ES. Although 5-ALA-mediated PDT has been shown to be a viable therapeutic option for the treatment of various types of cancer [ 18 , 30 , 36 ], its use with soft tissue sarcomas such as ES is not well documented. The goal of this study was to investigate the therapeutic effects of 5-ALA PDT and DOX on ES cell lines, both individually and in combination.…”
Ewing sarcomas (ES) are aggressive primary bone tumors that require radical therapy. Promising low toxicity, 5-aminolevulinic acid (5-ALA)-mediated photodynamic therapy (PDT) could enhance the effectiveness of conventional treatment modalities (e.g., doxorubicin (DOX)), improving, thus, the anti-tumorigenic effects. In this study, we investigated the effects of DOX and 5-ALA PDT alone or in combination on three different human ES cell lines. Cell viability, reactive oxygen species (ROS) production, and cellular stiffness were measured 24 h after PDT (blue light-wavelength 436 nm with 5-ALA) with or without DOX. ES cell lines have a different sensitivity to the same doses and exposure of 5-ALA PDT. DOX in combination with 5-ALA PDT was found to be effective in impairing the viability of all ES cells while also increasing cytotoxic activity by high ROS production. The stiffness of the ES cells increased significantly (p < 0.05) post treatment. Overall, our results showed that across multiple ES cell lines, 5-ALA PDT can successfully and safely be combined with DOX to potentiate the therapeutic effect. The 5-ALA PDT has the potential to be a highly effective treatment when used alone or in conjunction with other treatments. More research is needed to assess the effectiveness of 5-ALA PDT in in vivo settings.
“…As 5-ALA and thus PPIX are specifically enriched in brain tumors, their application in PDT was expected to be a promising approach. Several studies were performed to investigate the potential of 5-ALA-PDT for PDT applications (17)(18)(19). Eskiler et al demonstrated the effectiveness of 5-ALA-PDT in the treatment of breast cancer (20), whereas its photodamaging capabilities on rhabdomyosarcoma were shown by Atif et al (21).…”
Malignant primary brain tumors are a group of highly aggressive and often infiltrating tumors that lack adequate therapeutic treatments to achieve long time survival. Complete tumor removal is one precondition to reach this goal. A promising approach to optimize resection margins and eliminate remaining infiltrative so-called guerilla cells is photodynamic therapy (PDT) using organic photosensitizers that can pass the disrupted blood-brain-barrier and selectively accumulate in tumor tissue. Hypericin fulfills these conditions and additionally offers outstanding photophysical properties, making it an excellent choice as a photosensitizing molecule for PDT. However, the actual hypericin-induced PDT cell death mechanism is still under debate. In this work, hypericin-induced PDT was investigated by employing the three distinct fluorescent probes hypericin, resorufin and propidium iodide (PI) in fluorescence-lifetime imaging microscopy (FLIM). This approach enables visualizing the PDT-induced photodamaging and dying of single, living glioma cells, as an in vitro tumor model for glioblastoma. Hypericin PDT and FLIM image acquisition were simultaneously induced by 405 nm laser irradiation and sequences of FLIM images and fluorescence spectra were recorded to analyze the PDT progression. The reproducibly observed cellular changes provide insight into the mechanism of cell death during PDT and suggest that apoptosis is the initial mechanism followed by necrosis after continued irradiation. These new insights into the mechanism of hypericin PDT of single glioma cells may help to adjust irradiation doses and improve the implementation as a therapy for primary brain tumors.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.