4.7 Article

Controlled release of 5-fluorouracil to melanoma cells using a hydrogel/micelle composites based on deoxycholic acid and carboxymethyl chitosan

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 206, Issue -, Pages 159-166

Publisher

ELSEVIER
DOI: 10.1016/j.ijbiomac.2022.02.096

Keywords

Micelle; 5-Fluorouracil; Deoxycholic acid; Anticancer; Controlled release

Funding

  1. Research Council of Ker-manshah University of Medical Sciences [4000211]

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The study introduces a pH-responsive micellar hydrogel system to enhance the efficacy of 5-FU against skin cancer and reduce systemic side effects by improving its delivery into the skin. The results demonstrate that the system has enhanced anticancer activity against melanoma cells, suggesting it as a promising delivery platform.
5-Fluorouracil (5-FU) is an antimetabolite drug widely used for the treatment of skin cancer. Despite its proven efficacy in treating malignancies, its systemic administration is limited due to severe side effects. To address this issue, topical delivery of 5-FU has been proposed as an alternative approach for the treatment of skin cancer, however, the poor permeability of 5-FU through the skin is still a challenge. Here, we introduced a pH-responsive micellar hydrogel system based on deoxycholic acid micelle (DCA Mic) and carboxymethyl chitosan hydrogel (CMC Hyd) to enhance 5-FU efficacy against skin cancer and reduce its systemic side effects by improving its delivery into the skin. The properties of the Mic/Hyd system were determined by Fourier-transform infrared spectroscopy (FT-IR), dynamic light scattering (DLS), zeta sizer, atomic force microscopy (AFM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Drug release studies showed pH dependent properties of the Hyd. The final formulation was demonstrated to have enhanced anticancer activity than 5-FU against the growth of melanoma cells. The 5-FU@Mic-Hyd could be a promising delivery platform with enhanced efficacy in the management of skin cancer without systemic toxicity.

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