In Vivo Targeting and Imaging of Tumor Vasculature with Radiolabeled, Antibody-Conjugated Nanographene

被引:268
作者
Hong, Hao [2 ]
Yang, Kai [1 ]
Zhang, Yin [3 ]
Engle, Jonathan W. [3 ]
Feng, Liangzhu [1 ]
Yang, Yunan [2 ]
Nayak, Tapas R. [2 ]
Goel, Shreya [4 ]
Bean, Jero [2 ]
Theuer, Charles P. [5 ]
Barnhart, Todd E. [3 ]
Liu, Zhuang [1 ]
Cai, Weibo [2 ,3 ,6 ]
机构
[1] Soochow Univ, Inst Funct Nano & Soft Mat Lab FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou, Jiangsu, Peoples R China
[2] Univ Wisconsin Madison, Dept Radiol, Madison, WI 53706 USA
[3] Univ Wisconsin Madison, Dept Med Phys, Madison, WI 53706 USA
[4] Indian Inst Technol, Ctr Nanotechnol, Roorkee, Uttar Pradesh, India
[5] TRACON Pharmaceut Inc, San Diego, CA USA
[6] Univ Wisconsin, Carbone Canc Ctr, Madison, WI 53792 USA
基金
中国国家自然科学基金;
关键词
nanographene; tumor angiogenesis; positron emission tomography (PET); CD105 (endoglin); molecular imaging; Cu-64; cancer; POSITRON-EMISSION-TOMOGRAPHY; ENDOTHELIAL GROWTH-FACTOR; GRAPHENE OXIDE; FACTOR RECEPTOR; CANCER; PET; SENSOR; BIOCOMPATIBILITY; CD105; MICE;
D O I
10.1021/nn204625e
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Herein we demonstrate that nanographene can be specifically directed to the tumor neovasculature in vivo through targeting of CD105 (i.e., endoglin), a vascular marker for tumor angiogenesis. The covalently functionalized nanographene oxide (GO) exhibited excellent stability and target specificity. Pharmacokinetics and tumor targeting efficacy of the GO conjugates were investigated with serial noninvasive positron emission tomography imaging and biodistribution studies, which were validated by in vitro, in vivo, and ex vivo experiments. The incorporation of an active targeting ligand (THC105, a monoclonal antibody that binds to CD105) led to significantly improved tumor uptake of functionalized GO, which was specific for the neovasculature with little extravasation, warranting future investigation of these GO conjugates for cancer-targeted drug delivery and/or photothermal therapy to enhance therapeutic efficacy. Since poor extravasation is a major hurdle for nanomaterial-based tumor targeting in vivo, this study also establishes CD105 as a promising vascular target for future cancer nanomedicine.
引用
收藏
页码:2361 / 2370
页数:10
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