A highly effective gene delivery vector – hyperbranched poly(2-(dimethylamino)ethyl methacrylate) from in situ deactivation enhanced ATRP

2010 ◽  
Vol 46 (26) ◽  
pp. 4698 ◽  
Author(s):  
Ben Newland ◽  
Hongyun Tai ◽  
Yu Zheng ◽  
Diego Velasco ◽  
Andrea Di Luca ◽  
...  
Keyword(s):  
Gene Delivery ◽  
Gene Delivery Vector ◽  
Ethyl Methacrylate ◽  
Delivery Vector ◽  
Hyperbranched Poly ◽  
Highly Effective

Photoluminescent Hyperbranched Poly(amido amine) Containing β-Cyclodextrin as a Nonviral Gene Delivery Vector

2011 ◽  
Vol 22 (6) ◽  
pp. 1162-1170 ◽  
Author(s):  
Yan Chen ◽  
Linzhu Zhou ◽  
Yan Pang ◽  
Wei Huang ◽  
Feng Qiu ◽  
...  
Keyword(s):  
Gene Delivery ◽  
Nonviral Gene Delivery ◽  
Gene Delivery Vector ◽  
Delivery Vector ◽  
Hyperbranched Poly

Exosome as a Natural Gene Delivery Vector for Cancer Treatment

2020 ◽  
Vol 20 (11) ◽  
pp. 821-830
Author(s):  
Prasad Pofali ◽  
Adrita Mondal ◽  
Vaishali Londhe
Keyword(s):  
Gene Therapy ◽  
Gene Delivery ◽  
Nucleic Acids ◽  
Cancer Treatment ◽  
Intestinal Barrier ◽  
Gene Carrier ◽  
Gene Delivery Vector ◽  
Delivery Vector

Background: Current gene therapy vectors such as viral, non-viral, and bacterial vectors, which are used for cancer treatment, but there are certain safety concerns and stability issues of these conventional vectors. Exosomes are the vesicles of size 40-100 nm secreted from multivesicular bodies into the extracellular environment by most of the cell types in-vivo and in-vitro. As a natural nanocarrier, exosomes are immunologically inert, biocompatible, and can cross biological barriers like the blood-brain barrier, intestinal barrier, and placental barrier. Objective: This review focusses on the role of exosome as a carrier to efficiently deliver a gene for cancer treatment and diagnosis. The methods for loading of nucleic acids onto the exosomes, advantages of exosomes as a smart intercellular shuttle for gene delivery and therapeutic applications as a gene delivery vector for siRNA, miRNA and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) and also the limitations of exosomes as a gene carrier are all reviewed in this article. Methods: Mostly, electroporation and chemical transfection are used to prepare gene loaded exosomes. Results: Exosome-mediated delivery is highly promising and advantageous in comparison to the current delivery methods for systemic gene therapy. Targeted exosomes, loaded with therapeutic nucleic acids, can efficiently promote the reduction of tumor proliferation without any adverse effects. Conclusion: In the near future, exosomes can become an efficient gene carrier for delivery and a biomarker for the diagnosis and treatment of cancer.

Polyethylenimine-poly(amidoamine) dendrimer modified with l-arginines as an efficient gene delivery vector

2015 ◽  
Vol 23 (8) ◽  
pp. 726-733 ◽  
Author(s):  
Nan Young Ahn ◽  
Tae-Hun Kim ◽  
Su Jeong Song ◽  
Jeong-Mi Moon ◽  
Tai Hwan Ha ◽  
...  
Keyword(s):  
Gene Delivery ◽  
Gene Delivery Vector ◽  
Delivery Vector ◽  
Efficient Gene

scholarly journals An efficient nonviral gene-delivery vector based on hyperbranched cationic glycogen derivatives

2014 ◽  
pp. 419 ◽  
Author(s):  
Liqun Yang ◽  
Xuan Liang ◽  
Xianyue Ren ◽  
Zhenzhen Liu ◽  
Yingliang Liu ◽  
...  
Keyword(s):  
Gene Delivery ◽  
Nonviral Gene Delivery ◽  
Gene Delivery Vector ◽  
Delivery Vector

Polyamidoamine-Decorated Nanodiamonds as a Hybrid Gene Delivery Vector and siRNA Structural Characterization at the Charged Interfaces

2017 ◽  
Vol 9 (37) ◽  
pp. 31543-31556 ◽  
Author(s):  
Dae Gon Lim ◽  
Nirmal Rajasekaran ◽  
Dukhee Lee ◽  
Nam Ah Kim ◽  
Hun Soon Jung ◽  
...  
Keyword(s):  
Gene Delivery ◽  
Structural Characterization ◽  
Hybrid Gene ◽  
Gene Delivery Vector ◽  
Delivery Vector
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