Issue 1, 2026

Polymeric β-cyclodextrin/alginate/Colocasia esculenta mucilage (β-CD/Alg/CEM) nanocomposites for the controlled delivery of 5-fluorouracil

Abstract

5-Fluorouracil (5-FU) is a widely used cytotoxic chemotherapy drug in cancer management; its effectiveness in therapy is reduced due to a short half-life and toxic effects on healthy cells. This study aimed to overcome these limitations by preparing β-cyclodextrin/alginate/Colocasia esculenta mucilage (β-CD/Alg/CEM) nanocomposites containing 5-FU, designed for controlled release in various pH environments. Stable nanocomposites were successfully synthesized through the ionotropic gelation technique, achieving a drug content of 87.33 ± 1.75%, while the %age yield was found to be 79.06 ± 0.53%. Particle size analysis revealed a range of 80–100 nm with a polydispersity index (PDI) of 0.611. The zeta potential analysis showed that the nanocomposites possessed a surface charge of −27.1 mV. The nanocomposites displayed a porous and irregular morphology with a notably rough surface. In the acidic conditions of simulated gastric fluid (pH 1.2), the 5-FU release was markedly less than in the neutral conditions of simulated colorectal fluid (pH 7.4), indicating effective pH-sensitive release properties. The cytotoxic assay confirmed significant tumor–suppressive activity against MCF-7 and minimal effect on normal cells.

Graphical abstract: Polymeric β-cyclodextrin/alginate/Colocasia esculenta mucilage (β-CD/Alg/CEM) nanocomposites for the controlled delivery of 5-fluorouracil

Article information

Article type
Paper
Submitted
17 Oct 2025
Accepted
17 Dec 2025
First published
02 Jan 2026
This article is Open Access
Creative Commons BY license

RSC Adv., 2026,16, 642-656

Polymeric β-cyclodextrin/alginate/Colocasia esculenta mucilage (β-CD/Alg/CEM) nanocomposites for the controlled delivery of 5-fluorouracil

M. Anoosh, S. A. Ghumman, H. Hameed, S. Noureen, R. Kausar, A. Irfan, M. A. A. Alrobesh, M. Arshad, P. A. Shah, M. Rana and Y. A. Bin Jardan, RSC Adv., 2026, 16, 642 DOI: 10.1039/D5RA07963B

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