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Lentiviral Vector-mediated Gene Therapy of Hepatocytes Ex Vivo for Autologous Transplantation in Swine
Published on: November 4, 2018
Recent Advances in Non-Viral Gene Delivery Systems for Hepatic Gene Therapy
Roshanak Yadegarazari1, Shima Lotfollahzadeh2, Zahra Shabaninejad3
1Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Non-viral nanocarriers offer a safer, more effective method for gene therapy targeting liver diseases. This review explores advancements in polymeric nanoparticles, lipid-based nanocarriers, and MOFs for improved hepatic gene delivery.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Hepatology
Background:
- Gene therapy aims to treat diseases by modifying genetic material.
- Hepatic disorders represent a significant area for gene therapy intervention.
- Traditional viral vectors for gene delivery face safety and immunogenicity challenges.
Purpose of the Study:
- To review recent advancements in non-viral nanocarrier systems for liver-targeted gene delivery.
- To highlight the advantages of nanocarriers over viral vectors in hepatic gene therapy.
- To discuss the design, mechanisms, and challenges of nanocarrier-based hepatic gene delivery.
Main Methods:
- Review of current literature on non-viral nanocarriers for gene delivery.
- Analysis of polymeric nanoparticles, lipid-based nanocarriers, and metal-organic frameworks.
- Examination of studies focusing on gene delivery to the liver using these nanocarriers.
Main Results:
- Non-viral nanocarriers show promise as alternatives to viral vectors for hepatic gene delivery.
- These systems offer improved safety, payload capacity, specificity, and reduced immunogenicity.
- Various nanocarrier platforms have been designed and studied for liver-targeted gene delivery.
Conclusions:
- Non-viral nanocarriers are a rapidly developing field with significant potential for treating liver diseases.
- Further research is needed to optimize nanocarrier design and overcome delivery challenges.
- Nanotechnology offers a promising avenue for advancing gene therapy in hepatology.
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