Colloidal chitosan-integrated functional nanoparticles for combination cancer therapy: Synergistic strategies in oncology via step-delivery of genes/proteins and small drugs

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Authors: Mohammad Ali Khorasani, Seyed Morteza Naghib, Ghasem Takdehghan, Taha Jafari
Cited by: 3
References: 195

Abstract

Colloidal chitosan-integrated functional nanoparticles (CCIFN)-based multi-delivery carriers have considered as effective materials and biostructures for targeted drug delivery that offer improved therapeutic outcomes, controlled release mechanisms and reduced systemic toxicity. These nano-based carriers exhibit remarkable properties like biocompatibility, biodegradability, mucoadhesion ability and tunable surface chemistry that make them highly adjustable for various biomedical applications. By applying functional nanoparticles, micelles, hydrogels and composite structures, multimodal CCIFNs assist the step-delivery of multiple therapeutic agents that enhance drug bioavailability and site-specific targeting while they can minimize off-target effects. In spite of the advantages these nanoplatforms, several challenges hinder the clinical translation of multimodal CCIFN-based drug delivery systems including solubility limitations, molecular weight (MW) variability and large-scale production difficulties. More research works is required to refine their physicochemical properties, to optimize manufacturing processes and to address regulatory concerns for broader clinical adoption. Affirmation of these systems in precision medicine is being boosted by developments in stimuli-responsive formulations, chemical alterations and nanotechnology-based methodologies. Effectiveness and selectivity of CCIFN-based carriers are further enriched by the incorporation of functionalized bioactive compounds, ligands and externally driven release mechanisms.

Fields of Study & Subjects

RNA Interference and Gene Delivery Advanced Drug Delivery Systems Nanoparticle-Based Drug Delivery

Publication details

Journal / source
Colloids and Interface Science Communications
Publisher
Elsevier BV
Volume
73
Pages
100882–100882
Publication date
20 April 2026
Language
EN