脂质体
细胞毒性
化学
PLGA公司
重组DNA
体外
抗体
体内
癌细胞
药物输送
癌症研究
癌症
分子生物学
药理学
医学
免疫学
生物化学
生物
内科学
有机化学
生物技术
基因
作者
Xin Lin,Jiaqing Cao,Chuan Liu,Fei Zeng,Hua Cheng,Xiao Hu,Jianghua Shao
标识
DOI:10.1166/jbn.2015.2062
摘要
Stealth PLGA/Liposome nanoparticles (NPs) modified with tumor-targeting single-chain antibody fragment (scFV-P/L) for systemic delivery of recombinant methioninase (rMETase) for gastric cancer were prepared. The morphologies and therapeutic effects of rMETase-loaded scFV-P/L (scFV-rMETase-P/L) in vitro were analyzed. Functional scFV-P/L NPs composed of PLGA, DOPC and DSPE-PEG display low cell cytoxicity in SGC-7901 cells, and has more cell uptake ability than P/L NPs. scFV-rMETase-P/L was more effective in inhibiting tumor growth in the subcutaneous gastric carcinoma tumor model than free rMETase in solution (p < 0.05) and rMETase-loaded P/L (rMETase-P/L) (p < 0.05). Our findings collectively support the utility of scFV-targeted P/L NPs as a potentially effective drug delivery system.
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