中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Chitosan N-betainates/DNA self-assembly nanoparticles for gene delivery: In vitro uptake and transfection efficiency

文献类型:期刊论文

作者Gao, Yu; Zhang, Zhiwen; Chen, Lingli; Gu, Wangwen; Li, Yaping
刊名INTERNATIONAL JOURNAL OF PHARMACEUTICS
出版日期2009-04-17
卷号371期号:1-2页码:156-162
关键词Chitosan N-betainates Gene vector DNA Chitosan Nanoparticles
ISSN号0378-5173
DOI10.1016/j.ijpharm.2008.12.012
文献子类Article
英文摘要The aim of this work is to investigate the effect of betaine substitution degree of chitosan N-betainates (CsB) on cellular uptake, cytotoxicity and transfection efficiency of CsB/DNA complex nanoparticles (CsBNs) against COS-7 and MDA-MB-468 cells. The polymers with three substitution degrees (CsB12, CsB47 and CsB85) complexed with pDNA formed CsBN12s, CsBN47s and CsBN85s. The CsBNs showed less pH dependency with smaller particle size and higher zeta potential than that of chitosan/pDNA complex nanoparticles (CsNs) at neutral pH. CsBN85s showed stronger cellular uptake than that of CsBN47s or CsBN12s. CsBNs showed higher cytotoxicity than CsNs, and a trend increasing toxicity with substitution degree increasing. In COS-7 cells, the transfection efficiency increased with the substitution degree increasing, while the opposite result was observed in MDA-MB-468 cells. Chitosan modified with betaine could increase its ability to facilitate DNA uptake and its cytotoxicity, both of which showed the influence on transfection efficiency. It was able to increase cellular uptake and transfection efficiency of complex nanoparticles in COS-7 cells to increase betaine substitution of CsB, however, the higher sensitivity of MDA-MB-468 cells to CsBs led to decreased transfection efficiency due to the increased cytotoxicity with betaine substitution increasing. The predominant role of cellular uptake or toxicity in affecting transfection efficiency was different in two cell lines. These results provided an important guidepost for further development of chitosan derivatives/pDNA complexes as non-viral gene vectors. (C) 2009 Published by Elsevier B.V.
WOS关键词TRIMETHYL CHITOSAN ; BLOCK-COPOLYMERS ; CHLORIDE ; CYTOTOXICITY ; VECTORS ; VIABILITY ; THERAPY ; CELLS ; MICE
资助项目National Basic Research Program of China[2009CB930300] ; National Basic Research Program of China[2007CB935804] ; National Natural Science Foundation of China[30873169] ; Important Direction Program of CAS[KJCX2.YW.M02]
WOS研究方向Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000265361300021
出版者ELSEVIER SCIENCE BV
源URL[http://119.78.100.183/handle/2S10ELR8/279263]  
专题药物制剂研究中心
上海中药现代化研究中心
通讯作者Li, Yaping
作者单位Chinese Acad Sci, Ctr Drug Delivery Syst, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
推荐引用方式
GB/T 7714
Gao, Yu,Zhang, Zhiwen,Chen, Lingli,et al. Chitosan N-betainates/DNA self-assembly nanoparticles for gene delivery: In vitro uptake and transfection efficiency[J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS,2009,371(1-2):156-162.
APA Gao, Yu,Zhang, Zhiwen,Chen, Lingli,Gu, Wangwen,&Li, Yaping.(2009).Chitosan N-betainates/DNA self-assembly nanoparticles for gene delivery: In vitro uptake and transfection efficiency.INTERNATIONAL JOURNAL OF PHARMACEUTICS,371(1-2),156-162.
MLA Gao, Yu,et al."Chitosan N-betainates/DNA self-assembly nanoparticles for gene delivery: In vitro uptake and transfection efficiency".INTERNATIONAL JOURNAL OF PHARMACEUTICS 371.1-2(2009):156-162.

入库方式: OAI收割

来源:上海药物研究所

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