Promoted Transfection Efficiency of pDNA Polyplexes-Loaded Biodegradable Microparticles Containing Acid-Labile Segments and Galactose Grafts

被引:11
作者
Chen, Zhu [1 ,2 ]
Cai, Xiaojun [1 ]
Yang, Ye [1 ]
Wu, Guannan [1 ]
Liu, Yaowen [1 ]
Chen, Fang [1 ]
Li, Xiaohong [1 ]
机构
[1] SW Jiaotong Univ, Key Lab Adv Technol Mat, Minist Educ China, Sch Mat Sci & Engn, Chengdu 610031, Peoples R China
[2] N Sichuan Med Coll, Clin Hosp 2, Res Inst Tissue Engn & Stem Cells, Nanchong 637000, Peoples R China
基金
中国国家自然科学基金;
关键词
acid-labile biodegradable polymers; endosomal escape; pDNA polyplexes; targeting effect; transfection efficiency; GENE DELIVERY; DNA VACCINE; INTRACELLULAR DELIVERY; KUPFFER CELLS; IN-VITRO; MICROSPHERES; RELEASE; CARRIER; DEGRADATION; MACROPHAGES;
D O I
10.1007/s11095-011-0577-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Targeting to antigen-presenting cells and efficient intracellular delivery of pDNA are essential for development of microsphere formulations of DNA vaccine. Biodegradable polymers containing acid-labile segments and galactose grafts were developed to entrap pDNA polyplexes into microspheres, which were proposed to promote transfection efficiency of pDNA. Acid-labile characteristics were approved by the hemolysis capabilities of red blood cells and degradation behaviors of matrix polymers; release of pDNA polyplexes from microspheres was significantly accelerated after incubation in acid buffers. Presence of galactose moieties enhanced cellular uptake of microspheres and increased acid-lability due to hydrophilic grafts on acid-labile segments. There was no apparent cytotoxicity of blank microspheres; cytotoxicity of pDNA polyplexes was significantly decreased after encapsulation into and sustained release from microspheres. High transfection efficiency and a dose-dependent transfection were indicated for pDNA polyplex-loaded acid-labile microspheres when balancing with cytotoxicity. Integration of acid-lability, targeting effect into full biodegradable backbone represents an exciting approach to promote transfection efficiency through modulating release of pDNA polyplexes, targeting to antigen-presenting cells and intracellular delivery of pDNA.
引用
收藏
页码:471 / 482
页数:12
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