Optimization of a cationic liposomal gene delivery system and study of its endocytic pathway

被引:0
作者
Yu, Ting [1 ,3 ]
Song, Xiaowei [2 ,4 ]
Jin, Guangyu [2 ]
Sun, Jingxin [1 ]
Jin, Zhehao [2 ]
Quan, Jishan [1 ,5 ]
机构
[1] Yanbian Univ, Coll Pharm, Dept pharmaceut, Jilin, Peoples R China
[2] Yanbian Univ Hosp, Dept Radiol, Jilin, Peoples R China
[3] Hansoh pharmaceut Grp Co Ltd, Jiangsu, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 2, Sch Med, Dept Radiol, Hangzhou, Peoples R China
[5] Yanbian Univ, Coll Pharm, Dept pharmaceut, No 977 Gongyuan Rd, Yanji 133002, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Cationic liposomes; Gene delivery; Lyophilization; Uptake mechanism; SIRNA DELIVERY; TRANSFECTION; LIPIDS; NANOPARTICLES; FORMULATION; STABILITY; COMPLEXES;
D O I
10.1590/s2175-97902022e20225
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A cationic liposomal gene delivery system comprising DOTAP, DOPE, and cholesterol was prepared and optimized. The results showed that the liposome/DNA (LP/DNA) system had spherical morphology, with a particle size of around 150 nm and zeta potential of approximately 30 mV. Cytotoxicity experiments showed that cells treated with all of the liposome carriers- with the exception of LP1-had more than 80% viability even at a weight ratio of 30. The in vitro transfection efficiency was measured using a PromegaTM Luciferase Assay System. Of the tested lipoplexes, LP2/DNA showed the highest cell transfection efficiency (at a weight ratio of 10)-which was similar to or slightly lower than that of Lipofectamine (R) 2000 in HeLa, A549, and SPC-A1 cell lines. After freeze-drying, the cell transfection efficiency decreased slightly (P>0.05). The cell uptake mechanism study showed that LP/DNA lipoplexes mainly entered cells via clathrin-mediated and caveolin-mediated endocytic pathways. The results confirmed that LP2 has potential for use as an effective gene carrier, and provides experimental evidence to support its further development as a safe and effective gene delivery system.
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页数:13
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