聚乙烯亚胺
转染
基因传递
脂质体
遗传增强
化学
报告基因
体内
小RNA
分子生物学
生物物理学
组合化学
基因
载体(分子生物学)
基因表达
生物
生物化学
重组DNA
生物技术
作者
Yingying Wang,Baiyan Wang,Yong Xiao,Qingchun Cai,Jiadi Xing,Jing Tang,LI Rui-qin,Hongtao Zhang
标识
DOI:10.3389/fbioe.2023.1290413
摘要
The security and efficiency of gene delivery vectors are inseparable for the successful construction of a gene delivery vector. This work provides a practical method to construct a charge-regulated, hydrophobic-modified, and functionally modified polyethylenimine (PEI) with effective gene delivery and perfect transfection performance through a condensation reaction, named BA-PEI. The carrier was shown to possess a favorable compaction of miRNAs into positively charged nanoparticles with a hydrodynamic size of approximately 100 nm. Additionally, BA-PEI possesses perfect degradability, which benefits the release of miR-34a from the complexes. In A549 cells, the expression level of the miR-34a gene was checked by Western blotting, which reflects the transfection efficiency of BA-PEI/miR-34a. When miR-34a is delivered to the cell, the perfect anti-tumor ability of the BA-PEI/miR-34a complex was systematically evaluated with the suppressor tumor gene miR-34a system in vitro and in vivo . BA-PEI-mediated miR-34a gene transfection is more secure and effective than the commercial transfection reagent, thus providing a novel approach for miR-34a-based gene therapy.
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