Ligand-modified Biopolymeric Nanoparticles as Efficient Tools for Targeted Cancer Therapy
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Updated: Mar 1, 2026

Polymalic Acid-based Nano Biopolymers for Targeting of Multiple Tumor Markers: An Opportunity for Personalized Medicine?
Published on: June 13, 2014
Hasan Kouchakzadeh1, Tooba Soudi2, Niloofar Heshmati Aghda2
1Protein Research Center, Shahid Beheshti University, G.C., Velenjak, Tehran, Iran.
Abstract:
Non-specific distribution of chemotherapeutic agents in the body where they affect both cancer as well as normal cells resulting in serious side effects is the major reason for the high mortality rate of cancer. Thus, there is a need for developing targeted delivery strategies specially employing nanoplatform-based cancer therapies that provide specific targeting to tumor cells. In this regard, biopolymeric nanoplatforms such as liposomes, protein- and polysaccharide- based nanoparticles have gained more attention due to their biocompatibility, biodegradability and less toxicity. In terms of targeting, monoclonal antibodies (mAbs), folic acid (FA) and transferrin (Tf) can be considered as the moieties to be attached to the nanoplatforms to deliver their payload to its site of action. This review article focuses on the recent progress in the field of targeted drug and gene delivery systems with emphasizes on liposomes, protein (specially human and bovine serum albumin)-based nanoparticles and polysaccharide (specially chitosan and dextran)-based nanoparticles as the biopolymeric nanoplatforms, which are decorated with mAbs, FA and Tf as the targeting ligands.
Insights
Targeted cancer therapies using nanoplatforms improve drug delivery. Biopolymeric nanoparticles decorated with targeting ligands like monoclonal antibodies (mAbs) offer a promising strategy to reduce side effects and enhance treatment efficacy.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Pharmacology
Background:
- Chemotherapy's non-specific distribution causes severe side effects, contributing to high cancer mortality.
- Targeted delivery strategies are crucial for improving cancer treatment outcomes.
- Nanoplatform-based therapies offer a promising approach for specific tumor cell targeting.
Purpose of the Study:
- To review recent advancements in targeted drug and gene delivery systems for cancer therapy.
- To highlight the role of biopolymeric nanoplatforms in enhancing therapeutic efficacy.
- To discuss the application of specific targeting ligands for improved drug localization.
Main Methods:
- Focus on biopolymeric nanoplatforms including liposomes, protein-based nanoparticles (e.g., albumin), and polysaccharide-based nanoparticles (e.g., chitosan, dextran).
- Exploration of targeting moieties such as monoclonal antibodies (mAbs), folic acid (FA), and transferrin (Tf) for ligand decoration.
- Review of recent literature on the design and application of these targeted nanocarriers.
Main Results:
- Biopolymeric nanoplatforms demonstrate biocompatibility, biodegradability, and reduced toxicity.
- Decoration with targeting ligands (mAbs, FA, Tf) enables specific delivery to tumor cells.
- Targeted delivery systems show potential for improved drug and gene delivery efficiency.
Conclusions:
- Biopolymeric nanoplatforms decorated with targeting ligands represent a significant advancement in targeted cancer therapy.
- These strategies offer a viable approach to minimize systemic toxicity and maximize therapeutic impact.
- Further research in this area holds promise for developing more effective and safer cancer treatments.
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