紫杉醇
化学
PLGA公司
细胞毒性
聚赖氨酸
阳离子聚合
单克隆抗体
纳米颗粒
体外
抗体
生物物理学
分子生物学
生物化学
纳米技术
癌症
材料科学
高分子化学
生物
免疫学
遗传学
作者
Geng Kou,Jie Gao,Hao Wang,Huaiwen Chen,Bohua Li,Dapeng Zhang,Shuhui Wang,Sheng Hou,Weizhu Qian,Jianxin Dai,Yanqiang Zhong,Yajun Guo
标识
DOI:10.5483/bmbrep.2007.40.5.731
摘要
The purpose of this study was to develop paclitaxel-loaded poly(lactide-co-glycolide) (PLGA) nanoparticles coated with cationic SM5-1 single-chain antibody (scFv) containing a polylysine (SMFv-polylys). SM5-1 scFv (SMFv) is derived from SM5-1 monoclonal antibody, which binds to a 230 kDa membrane protein specifically expressed on melanoma, hepatocellular carcinoma and breast cancer cells. SMFv-polylys was expressed in Escherichia coli and purified by cation-exchange chromatography. Purified SMFv-polylys was fixed to paclitaxel-loaded PLGA nanoparticles to form paclitaxel-loaded PLGA nanoparticles coated with SMFv-polylys (Ptx-NP-S). Ptx-NP-S was shown to retain the specific antigen-binding affinity of SMFv-polylys to SM5-1 binding protein-positive Ch-hep-3 cells. Finally, the cytotoxicity of Ptx-NP-S was evaluated by a non-radioactive cell proliferation assay. It was demonstrated that Ptx-NP-S had significantly enhanced in vitro cytotoxicity against Ch-hep-3 cells as compared with non-targeted paclitaxel-loaded PLGA nanoparticles. In conclusion, our results suggest that cationic SMFv-polylys has been successfully generated and may be used as targeted ligand for preparing cancer-targeted nanoparticles.
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