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Updated: May 19, 2026

Delivery of Therapeutic siRNA to the CNS Using Cationic and Anionic Liposomes
Published on: July 23, 2016
Translational siRNA therapeutics using liposomal carriers: prospects & challenges
Dhiraj Bhavsar1, Krishnakumar Subramanian, Swaminathan Sethuraman
1Centre for Nanotechnology & Advanced Biomaterials, School of Chemical & Biotechnology, SASTRA University, Thanjavur, India.
Lipid-based nanoparticles, particularly liposomes, are crucial for advancing gene silencing therapies. This review details challenges and innovations in liposomal delivery systems for small interfering RNA (siRNA) to improve molecular therapies.
Area of Science:
- Biotechnology and Molecular Medicine
- Drug Delivery Systems
- Gene Therapy
Background:
- Gene silencing offers therapeutic potential for various diseases but faces significant delivery challenges.
- Developing effective delivery systems is critical for translating gene silencing from research to clinical applications.
- Small interfering RNA (siRNA) requires robust delivery vehicles for targeted and efficient gene silencing.
Purpose of the Study:
- To review the challenges and advancements in liposomal delivery systems for gene silencing.
- To explore modifications in siRNA and liposomal formulations for improved therapeutic efficacy.
- To provide an overview of current clinical trials involving liposomal gene silencing tools.
Main Methods:
- Literature review of gene silencing strategies and liposomal delivery systems.
- Analysis of chemical modifications in siRNA and synthesis of cationic lipids.
- Examination of hybrid liposomal systems and their performance.
- Assessment of clinical trial data for liposomal gene silencing formulations.
Main Results:
- Liposomes offer versatile properties for siRNA delivery, including tunable size and surface functionality.
- Chemical modifications of siRNA and development of designer cationic lipids enhance delivery efficiency and reduce toxicity.
- Hybrid liposomal systems represent an evolution towards improved target specificity and cellular uptake.
- Clinical trials indicate the potential of liposomal formulations as therapeutic tools, though challenges remain.
Conclusions:
- Liposomal systems are pivotal in overcoming barriers to effective siRNA-mediated gene silencing.
- Innovations in siRNA modification and liposome design are crucial for advancing gene therapy.
- Further research and clinical validation are necessary to fully realize the therapeutic potential of liposomal gene silencing.
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