Protein-Polymer Hybrid Nanoparticles for Drug Delivery

被引:80
作者
Ge, Jun [1 ,3 ]
Neofytou, Evgenios [2 ]
Lei, Jiandu [1 ,4 ]
Beygui, Ramin E. [2 ]
Zare, Richard N. [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Cardiothorac Surg, Falk Cardiovasc Res Ctr, Stanford, CA 94305 USA
[3] Tsinghua Univ, Dept Chem Engn, Beijing 100084, Peoples R China
[4] Chinese Acad Sci, Inst Proc Engn, Natl Key Lab Biochem Engn, Beijing 100190, Peoples R China
基金
美国国家科学基金会;
关键词
nanoparticles; protein-polymer conjugates; albumin; poly(methyl methacrylate); drug delivery; CORE-SHELL NANOPARTICLES; POLY(METHYL METHACRYLATE); TARGETED NANOPARTICLES; INTRACELLULAR UPTAKE; OXIDE NANOPARTICLES; RAFT POLYMERIZATION; CELLULAR UPTAKE; IN-VITRO; RELEASE; CAMPTOTHECIN;
D O I
10.1002/smll.201200889
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amphiphilic bovine serum albumin-poly(methyl methacrylate) conjugate forms nanoparticles with the uniform size of ∼100 nm by self-assembling. Loaded with the hydrophobic anti-tumor drug camptothecin, the nanoparticle efficiently delivers drugs into cancer cells, and thus inhibits ∼79% of tumor growth in animals compared with free drug. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:3573 / 3578
页数:6
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