Review highlights improved drug delivery and chemosensitivity in cancer treatment with konjac glucomannan.
Abstract: 5-Fluorouracil (5-FU) has been a prominent chemotherapeutic agent for several solid tumors, but its application is hindered by rapid systemic clearance, dose-limiting toxicity, and suboptimal tumor response. Konjac glucomannan (KGM) is a natural, biocompatible polysaccharide that has proved to be a promising carrier in the development of controlled-release drug delivery systems. This review addresses recent developments in KGM-based systems, particularly designed to deliver 5-FU. It focuses on myriad aspects of KGM, such as its molecular weight, acetylation, crosslinking density, degradation behaviour, control drug loading, and release kinetics. Mechanistic evidence of increased chemosensitivity, as observed in various carcinoma models, has been succinctly elucidated. Moreover, this review outlines the potential of KGM-engineered systems to enhance 5-FU therapy by highlighting the concepts of formulation design along with innovative release- control strategies that translate its therapeutic potential into improved clinical outcomes.
No takes yet. Share an insight, caveat, or question.
Fatima et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: