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Evaluation of Polymeric Gene Delivery Nanoparticles by Nanoparticle Tracking Analysis and High-throughput Flow Cytometry
Published on: March 1, 2013
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Polymeric nanocarriers for therapeutic gene delivery
Jiayuan Zhang1,2, Xinyu Yang1, Zhichao Chang1
1Key Laboratory of Smart Drug Delivery of Ministry of Education, School of Pharmacy, Fudan University, Shanghai 201203, China.
Asian Journal of Pharmaceutical Sciences
|February 11, 2025
Summary
Polymeric nanocarriers offer a promising alternative for gene therapy, enhancing stability and targeted delivery of nucleic acid drugs. This review explores their potential for efficient therapeutic gene delivery.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Gene Therapy
Background:
- Gene therapy advancements are driving demand for effective gene delivery vectors.
- Viral and lipid-based nanocarriers are currently dominant but have limitations.
- Polymeric nanocarriers present versatile functionalities for improved nucleic acid drug delivery.
Purpose of the Study:
- To provide an overview of polymeric nanocarriers for therapeutic gene delivery.
- To highlight key cationic polymers, nanocarrier types, and preparation methods.
- To discuss targeted diseases, strategies for enhancing delivery efficiency, and future research directions.
Main Methods:
- Literature review focusing on polymeric nanocarriers in gene therapy.
- Analysis of existing research on cationic polymers and nanocarrier systems.
- Examination of strategies for improving stability, cellular uptake, and endosomal escape.
Main Results:
- Polymeric nanocarriers demonstrate potential for enhanced stability, cellular uptake, and endosomal escape.
- Versatile functionalities enable precise delivery to targeted tissues.
- Various preparation methods and cationic polymers are suitable for gene delivery applications.
Conclusions:
- Polymeric nanocarriers are emerging as a promising platform for therapeutic gene delivery.
- Further development and optimization are needed for clinical translation.
- This field holds significant potential for advancing gene therapy applications.

