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Updated: Aug 24, 2026

Nanoparticle Delivery of an Oligonucleotide Payload in a Glioblastoma Multiforme Animal Model
Published on: September 27, 2024
Oligonucleotide delivery to tumours using macromolecular carriers
1RareCellect, Genetic Technologies Research Laboratories, 60-66 Hanover Street, Fitzroy 3065, Melbourne, Victoria 3073, Australia. cris_dass@yahoo.com.au
Abstract:
Microparticles have been used for delivery of chemo- and radio-therapeutic agents to tumours in patients for more than a decade, whereas cationic liposomes have been used for introducing nucleic acids into mammalian cells for the same period of time. This minireview discusses the potential of delivering therapeutic ONs (oligonucleotides) to tumours using cationic liposomes and the major obstacles to such delivery. It also proposes how microparticles can be utilized for delivery of ONs to solid tumours. Prospects for improved ON delivery using these carriers and ways to achieve this are discussed.
Insights
This review explores using microparticles and cationic liposomes for delivering therapeutic oligonucleotides (ONs) to tumors. It highlights challenges and strategies for effective ON delivery to solid tumors.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Drug Delivery Systems
Background:
- Microparticles are established carriers for chemo- and radio-therapeutic agents in cancer treatment.
- Cationic liposomes have a decade-long history in delivering nucleic acids into mammalian cells.
Purpose of the Study:
- To review the potential and obstacles of using cationic liposomes for delivering therapeutic oligonucleotides (ONs) to tumors.
- To propose microparticle-based strategies for ON delivery to solid tumors.
- To discuss prospects and methods for enhancing ON delivery using these carriers.
Main Methods:
- Literature review and synthesis of existing research on microparticle and cationic liposome drug delivery.
- Analysis of challenges associated with oligonucleotide delivery to tumor sites.
- Exploration of potential applications and improvements for nanoparticle-based therapeutic delivery.
Main Results:
- Cationic liposomes show potential for therapeutic ON delivery but face significant obstacles.
- Microparticles offer a viable alternative for delivering ONs to solid tumors.
- Various strategies can be employed to improve the efficacy of ON delivery systems.
Conclusions:
- Both microparticles and cationic liposomes hold promise for oligonucleotide-based cancer therapy.
- Overcoming delivery barriers is crucial for successful clinical translation.
- Further research into carrier design and optimization is needed to enhance therapeutic outcomes.
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