Multimodal SPION-CREKA peptide based agents for molecular imaging of microthrombus in a rat myocardial ischemia-reperfusion model

被引:76
作者
Song, Yanan [1 ]
Huang, Zheyong [1 ]
Xu, Jianfeng [1 ]
Ren, Daoyuan [1 ]
Wang, Yu [2 ]
Zheng, Xinde [3 ]
Shen, Yunli [4 ]
Wang, Lili [3 ]
Gao, Hongxiang [5 ]
Hou, Jiayun [6 ]
Pang, Zhiqing [2 ]
Qian, Juying [1 ]
Ge, Junbo [1 ,7 ]
机构
[1] Fudan Univ, Shanghai Inst Cardiovasc Dis, Zhongshan Hosp, Shanghai 200032, Peoples R China
[2] Fudan Univ, Key Lab Smart Drug Delivery, Minist Educ, Sch Pharm, Shanghai 201203, Peoples R China
[3] Fudan Univ, Zhongshan Hosp, Dept Radiol, Shanghai 200032, Peoples R China
[4] Tongji Univ, Shanghai East Hosp, Dept Cardiol, Shanghai 200120, Peoples R China
[5] Fudan Univ, Zhongshan Hosp, Dept Lab, Shanghai 200032, Peoples R China
[6] Fudan Univ, Zhongshan Hosp, Biomed Res Ctr, Shanghai 200032, Peoples R China
[7] Fudan Univ, Inst Biomed Sci, Shanghai 200032, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
Microthrombosis; Fibrin; Multimodal nanoagents; Magnetic resonance imaging; Optical imaging; SUPERPARAMAGNETIC IRON-OXIDE; MR CONTRAST AGENTS; IN-VIVO; MICROVASCULAR OBSTRUCTION; THROMBUS DETECTION; FIBRIN; PATHOPHYSIOLOGY; NANOPARTICLES; FERUMOXIDES; FERUMOXTRAN;
D O I
10.1016/j.biomaterials.2013.12.038
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Microthrombosis plays a key role in many cardiovascular diseases. Although it is not difficult to localize thrombus within large or middle-sized vessels, the noninvasive diagnostic regimen for the detection of microthrombus remains scarce. Here we developed a nanoagent by conjucting superparamagnetic iron-oxide nanoparticle with fluorophore and a targeting element, CREKA, a peptide with special affinity for fibrin. In a rat model of myocardial ischemia-reperfusion (MI/R), the multimodal nanoagents were readily and selectively accumulated within microthrombosis, which was detectable by both magnetic resonance and optical imaging modalities. The fibrin-targeted nanoagent could be expected to have utility not only in molecular imaging of fibrin, understanding the mechanisms of microcirculation disorders, but also in targeted therapy with fibrinolytic agents. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2961 / 2970
页数:10
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