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Preparation and characterization of chitosan/β-cyclodextrin nanoparticles containing plasmid DNA encoding
M Nahaei1, H Valizadeh, B Baradaran
1Hematology and Oncology Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
Low Molecular Weight chitosan/β-cyclodextrin nanoparticles effectively deliver Interleukin-12 (IL-12) DNA for cancer therapy. These non-viral nanoparticles show high encapsulation and enhanced transfection without toxicity, offering a promising gene delivery system.
Area of Science:
- Biotechnology
- Nanomedicine
- Gene Therapy
Background:
- Interleukin-12 (IL-12) is a cytokine with demonstrated antitumor effects through immune system stimulation.
- Non-viral gene delivery systems offer advantages like safety, low cost, and high genetic material capacity.
Purpose of the Study:
- To prepare and characterize Interleukin-12 (IL-12) encoding plasmid DNA (pUMVC3-hIL12) loaded Low Molecular Weight chitosan/β-cyclodextrin (LMW CS/CD) nanoparticles.
- To evaluate the efficacy and safety of these nanoparticles as a gene delivery system for potential cancer therapy.
Main Methods:
- pUMVC3-hIL12 loaded LMW CS/CD nanoparticles were synthesized using the ionotropic gelation method.
- Characterization included size, zeta potential, polydispersity index, morphology, DNA loading efficiency, and cytotoxicity assays against CT-26 colon carcinoma cells.
Main Results:
- The nanoparticles were spherical, nano-sized (171.3±2.165 nm) with a positive zeta potential (34.3±1.55) and good encapsulation efficiency (83.315%±2.067).
- No significant cytotoxicity was observed in CT-26 cells.
- Transfection ability of nanoparticles was superior to naked DNA at 0.1 µg/ml concentration.
Conclusions:
- LMW CS/CD nanoparticles loaded with IL-12 plasmid DNA are a safe and effective non-viral gene delivery system.
- These nanoparticles show potential for enhanced IL-12 expression in future in vitro and in vivo gene therapy studies for cancer treatment.
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