Biocompatible Naringin loaded low molecular peptide Nanogels are effective against human melanoma cells
Jülide Secerli1, Burcu Karayavuz2, Rahime Aksoy3
1Gülhane Faculty of Pharmacy Department of Pharmaceutical Toxicology, University of Health Sciences Turkey, 06018 Ankara, Türkiye.
Abstract:
Melanoma, a type of cancer, has the ability to metastasize and can be fatal. The lack of success in the treatment of melanoma with chemotherapeutic agents and the side effects have led to the search for new agents. Moreover, developing systems that will provide reduce side effects by using biocompatible carriers, may be beneficial. Naringin (NAR), from Citrus plants, has anticancer and anti-inflammatory properties. NAR is useful in formulations where it is used with a carrier due to its low water solubility and bioavailability with few toxicity. This study aimed to evaluate the effects of NAR-loaded peptide based Fmoc-FF nanogels on human melanoma (SK-MEL-30) cells. Characterization of NAR-loaded Fmoc-FF nanogels was carried out. The biocompatibility properties of Fmoc-FF and NAR-loaded nanogels were evaluated in mouse fibroblast (L929) cells, and their cytotoxic effects were evaluated in human melanoma (SK-MEL-30) cells by the MTT method. While the DCF-DA method was used to measure the effects on reactive oxygen species (ROS) release, the changes in oxidative stress biomarkers were examined by spectrophotometric analysis, tyrosinase enzyme activity and inflammation biomarkers were investigated by ELISA method. Comet method was used to evaluate antigenotoxic effects. It has been observed that loading NAR into Fmoc peptide gels may be effective in causing cytotoxic, genotoxic, anti-inflammatory and anti-tyrosinase effects and an increase in ROS release in melanoma cells. These results indicate that NAR-loaded Fmoc-FF gels, which have the feature of easy application to the skin, may be effective in the treatment of melanoma without causing toxic effects.
Insights
Naringin (NAR)-loaded Fmoc-FF nanogels show potential for melanoma treatment. These nanogels demonstrated cytotoxic, genotoxic, anti-inflammatory, and anti-tyrosinase effects, increasing reactive oxygen species (ROS) in melanoma cells with minimal toxicity.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Dermatology
Background:
- Melanoma is a fatal cancer with limited treatment options.
- Chemotherapy for melanoma has side effects and limited efficacy.
- Biocompatible carriers can reduce side effects of cancer treatments.
Purpose of the Study:
- To evaluate Naringin (NAR)-loaded Fmoc-FF nanogels against human melanoma cells.
- To assess the biocompatibility and cytotoxic effects of these nanogels.
- To investigate the impact on reactive oxygen species (ROS), oxidative stress, and inflammation.
Main Methods:
- Characterization of NAR-loaded Fmoc-FF nanogels.
- Biocompatibility testing on mouse fibroblast (L929) cells.
- Cytotoxicity assessment using MTT assay on SK-MEL-30 melanoma cells.
- ROS measurement via DCF-DA assay.
- Oxidative stress, tyrosinase activity, and inflammation biomarkers analyzed by spectrophotometry and ELISA.
- Antigenotoxic effects evaluated using the Comet assay.
Main Results:
- NAR-loaded Fmoc-FF nanogels exhibited cytotoxic and genotoxic effects on melanoma cells.
- Increased ROS release was observed in melanoma cells.
- Anti-inflammatory and anti-tyrosinase activities were demonstrated.
- Nanogels showed good biocompatibility with L929 cells.
Conclusions:
- NAR-loaded Fmoc-FF nanogels are effective against melanoma cells.
- These nanogels possess cytotoxic, genotoxic, anti-inflammatory, and anti-tyrosinase properties.
- The formulation shows promise for topical melanoma treatment with reduced toxicity.


