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2000
Volume 23, Issue 1
  • ISSN: 1567-2018
  • E-ISSN: 1875-5704

Abstract

Introduction

Metastatic melanoma poses a significant threat globally, with a distressingly low ten-year survival rate of only 10%. While FDA-approved treatments such as dacarbazine and high-dose IL-2 have been employed in clinical settings, their limitations underscore the urgent need for more effective therapies.

Aim

This study aimed to develop a potential anticancer local treatment through the extraction of various amounts of ginger extract loaded into Poly(vinyl alcohol) (PVA) nanofibers.

Methods

The anticancer activity of the produced membranes was studied on human skin melanoma B16F10 cells. Other experiments such as cell migration assay, cell proliferation assay, cell viability assay, scanning electron microscopy assay, real-time PCR assay, and ant-inflammatory assay were performed for the characterization of the delivery system. Tissue toxicity of the developed patches was studied in a rat model.

Results

The study showed that scaffolds loaded with 2%, 4%, 6%, 8%, and 0% of ginger extract had around 784.98 ± 202.31 nm, 771.86 ± 219.07 nm, 820.65 ± 242.43 nm, 785.19 ± 203.99 nm, and 671.29 ± 184.09 nm of mean fiber size, respectively. The ginger extract-loaded membranes suppressed the growth and migration activity of human skin melanoma B16F10 cells in a dose and time-dependent manner. Real-time PCR assay showed that the developed membranes modulated the expression levels of Ras/ERK and PI3K/AKT signaling pathways. Animal study results showed that our developed patches were not toxic against liver or skin tissues.

Conclusion

Ginger extract-loaded PVA nanofibers exhibited promising anticancer potential against melanoma cells, suggesting a viable localized treatment option.

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  • Article Type:
    Research Article
Keyword(s): drug delivery, anti-cancer, local treatment, melanoma; Ginger; nanofibers
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