Targeted gold-coated iron oxide nanoparticles for CD163 detection in atherosclerosis by MRI

被引:64
作者
Tarin, Carlos [1 ]
Carril, Monica [2 ,3 ]
Luis Martin-Ventura, Jose [1 ]
Markuerkiaga, Irati [4 ]
Padro, Daniel [4 ]
Llamas-Granda, Patricia [1 ]
Moreno, Juan Antonio [1 ]
Garcia, Isabel [2 ,5 ]
Genicio, Nuria [2 ]
Plaza-Garcia, Sandra [4 ]
Miguel Blanco-Colio, Luis [1 ]
Penades, Soledad [2 ,5 ]
Egido, Jesus [1 ]
机构
[1] Univ Autonoma Madrid, IIS Fdn Jimenez Diaz, Lab Patol Vasc & Renal, Madrid 28040, Spain
[2] CIC biomaGUNE, Lab Gliconanotecnol, Biofunct Nanomat Unit, San Sebastian 20009, Spain
[3] Ikerbasque, Basque Fdn Sci, Bilbao 48011, Spain
[4] CIC biomaGUNE, Mol Imaging Unit, San Sebastian 20009, Spain
[5] Biomed Res Networking Ctr Bioengn Biomat & Nanome, San Sebastian 20009, Spain
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
关键词
ULTRASMALL SUPERPARAMAGNETIC PARTICLES; MAGNETIC-RESONANCE DETECTION; IN-VIVO; PLAQUE; MACROPHAGES; GLYCONANOPARTICLES; ANTIBODIES; LESIONS; PROBES;
D O I
10.1038/srep17135
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CD163 is a membrane receptor expressed by macrophage lineage. Studies performed in atherosclerosis have shown that CD163 expression is increased at inflammatory sites, pointing at the presence of intraplaque hemorrhagic sites or asymptomatic plaques. Hence, imaging of CD163 expressing macrophages is an interesting strategy in order to detect atherosclerotic plaques. We have prepared a targeted probe based on gold-coated iron oxide nanoparticles vectorized with an anti-CD163 antibody for the specific detection of CD163 by MRI. Firstly, the specificity of the targeted probe was validated in vitro by incubation of the probe with CD163(+) or (-) macrophages. The probe was able to selectively detect CD163(+) macrophages both in human and murine cells. Subsequently, the targeted probe was injected in 16 weeks old apoE deficient mice developing atherosclerotic lesions and the pararenal abdominal aorta was imaged by MRI. The accumulation of probe in the site of interest increased over time and the signal intensity decreased significantly 48 hours after the injection. Hence, we have developed a highly sensitive targeted probe capable of detecting CD163-expressing macrophages that could provide useful information about the state of the atheromatous lesions.
引用
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页数:9
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