Theranostic Unimolecular Micelles Based on Brush-Shaped Amphiphilic Block Copolymers for Tumor-Targeted Drug Delivery and Positron Emission Tomography Imaging

被引:72
|
作者
Guo, Jintang [1 ,2 ,3 ]
Hong, Hao [4 ,5 ]
Chen, Guojun [3 ,6 ]
Shi, Sixiang [6 ]
Nayak, Tapas R. [4 ,5 ]
Theuer, Charles P. [7 ]
Barnhart, Todd E. [4 ,5 ]
Cai, Weibo [4 ,5 ,6 ]
Gong, Shaoqin [2 ,3 ,6 ]
机构
[1] Tianjin Univ, Sch Chem Engn, Tianjin 300072, Peoples R China
[2] Univ Wisconsin, Dept Biomed Engn, Madison, WI 53706 USA
[3] Univ Wisconsin, Wisconsin Inst Discovery, Madison, WI 53715 USA
[4] Univ Wisconsin, Dept Radiol, Madison, WI 53705 USA
[5] Univ Wisconsin, Dept Med Phys, Madison, WI 53705 USA
[6] Univ Wisconsin, Mat Sci Program, Madison, WI 53706 USA
[7] TRACON Pharmaceut Inc, San Diego, CA USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
brush polymer; unimolecular micelles; nanocarriers; brush-shaped amphiphilic block copolymer; cancer; theranostics; CD105; angiogenesis; positron emission tomography (PET); Cu-64; CD105; EXPRESSION; VASCULATURE; ANTIBODY; CORE; METHACRYLATE); NANOPARTICLES; POLYMERS; CARRIER; ATRP; PCL;
D O I
10.1021/am5002585
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Brush-shaped amphiphilic block copolymers were conjugated with a monoclonal antibody against CD105 (i.e., TRC105) and a macrocyclic chelator for Cu-64-labeling to generate multifunctional theranostic unimolecular micelles. The backbone of the brush-shaped amphiphilic block copolymer was poly(2-hydroxyethyl methacrylate) (PHEMA) and the side chains were poly(l-lactide)-poly(ethylene glycol) (PLLA-PEG). The doxorubicin (DOX)-loaded unimolecular micelles showed a pH-dependent drug release profile and a uniform size distribution. A significantly higher cellular uptake of TRC105-conjugated micelles was observed in CD105-positive human umbilical vein endothelial cells (HUVEC) than nontargeted micelles due to CD105-mediated endocytosis. In contrast, similar and extremely low cellular uptake of both targeted and nontargeted micelles was observed in MCF-7 human breast cancer cells (CD105-negative). The difference between the in vivo tumor accumulation of Cu-64-labeled TRC105-conjugated micelles and that of nontargeted micelles was studied in 4T1 murine breast tumor-bearing mice, by serial positron emission tomography (PET) imaging and validated by biodistribution studies. These multifunctional unimolecular micelles offer pH-responsive drug release, noninvasive PET imaging capability, together with both passive and active tumor-targeting abilities, thus making them a desirable nanoplatform for cancer theranostics.
引用
收藏
页码:21769 / 21779
页数:11
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