详细信息

Magainin II modified polydiacetylene micelles for cancer therapy  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Magainin II modified polydiacetylene micelles for cancer therapy

作者:Yang, Danling;Zou, Rongfeng;Zhu, Yu;Liu, Ben;Yao, Defan;Jiang, Juanjuan[1];Wu, Junchen;Tian, He

机构:[1]E China Univ Sci & Technol, Key Labs Adv Mat, Shanghai 200237, Peoples R China; E China Univ Sci & Technol, Inst Fine Chem, Shanghai 200237, Peoples R China

年份:2014

卷号:6

期号:24

起止页码:14772

外文期刊名:NANOSCALE

收录:;EI(收录号:20144800258031);WOS:【SCI-EXPANDED(收录号:WOS:000345458200026)】;

基金:This work was supported by grants from the National Basic Research 973 Program (2013CB733700) and the Fundamental Research Funds for the Central Universities (WJ1213007), the Program of Shanghai Pujiang (K100-2-1275) and the Innovation Program of Shanghai Municipal Education Commission (J100-2-13104) for financial support.

语种:英文

外文关键词:Cancer cells - Tumors - Drug delivery - Diseases - Energy transfer - Fluorescence - Liposomes - Acetylene - Cell culture - Cells

摘要:Polydiacetylene (PDA) micelles have been widely used to deliver anticancer drugs in the treatment of a variety of tumours and for imaging living cells. In this study, we developed an effective strategy to directly conjugate magainin II (MGN-II) to the surface of PDA micelles using a fluorescent dye. These stable and well-defined PDA micelles had high cytotoxicity in cancer cell lines, and were able to reduce the tumour size in mice. The modified PDA micelles improved the anticancer effects of MGN-II in the A549 cell line only at a concentration of 16.0 mu g mL(-1) (IC50). In addition, following irradiation with UV light at 254 nm, the PDA micelles gave rise to an energy transfer from the fluorescent dye to the backbone of PDA micelles to enhance the imaging of living cells. Our results demonstrate that modified PDA micelles can not only be used in the treatment of tumors in vitro and in vivo in a simple and directed way, but also offer a new platform for designing functional liposomes to act as anticancer agents.

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