Targeted nanotechnology for cancer imaging

被引:135
|
作者
Toy, Randall [1 ,2 ]
Bauer, Lisa [2 ,3 ]
Hoimes, Christopher [4 ,5 ]
Ghaghada, Ketan B. [6 ,7 ]
Karathanasis, Efstathios [1 ,2 ,4 ,8 ]
机构
[1] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Case Ctr Imaging Res, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Phys, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Case Comprehens Canc Ctr, Cleveland, OH 44106 USA
[5] Univ Hosp Case Med Ctr, Cleveland, OH 44106 USA
[6] Texas Childrens Hosp, Edward B Singleton Dept Pediat Radiol, Houston, TX 77030 USA
[7] Baylor Coll Med, Dept Radiol, Houston, TX 77030 USA
[8] Case Western Reserve Univ, Dept Radiol, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
Targeted nanoparticles; Cancer imaging; MRI; CT; Ultrasound; PET; SPECT; Optical imaging; RAY COMPUTED-TOMOGRAPHY; UP-CONVERSION NANOPARTICLES; IRON-OXIDE NANOPARTICLES; GROWTH-FACTOR RECEPTOR; MESOPOROUS SILICA NANOPARTICLES; TUMOR VASCULAR-PERMEABILITY; QUANTUM DOT BINDING; CELLS IN-VIVO; MAGNETIC-RESONANCE; GOLD-NANOPARTICLES;
D O I
10.1016/j.addr.2014.08.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Targeted nanoparticle imaging agents provide many benefits and new opportunities to facilitate accurate diagnosis of cancer and significantly impact patient outcome. Due to the highly engineerable nature of nanotechnology, targeted nanoparticles exhibit significant advantages including increased contrast sensitivity, binding avidity and targeting specificity. Considering the various nanoparticle designs and their adjustable ability to target a specific site and generate detectable signals, nanoparticles can be optimally designed in terms of biophysical interactions (i.e., intravascular and interstitial transport) and biochemical interactions (i.e., targeting avidity towards cancer-related biomarkers) for site-specific detection of very distinct microenvironments. This review seeks to illustrate that the design of a nanoparticle dictates its in vivo journey and targeting of hard-to-reach cancer sites, facilitating early and accurate diagnosis and interrogation of the most aggressive forms of cancer. We will report various targeted nanoparticles for cancer imaging using X-ray computed tomography, ultrasound, magnetic resonance imaging, nuclear imaging and optical imaging. Finally, to realize the full potential of targeted nanotechnology for cancer imaging, we will describe the challenges and opportunities for the clinical translation and widespread adaptation of targeted nanoparticles imaging agents. (C) 2014 Elsevier B.V. All rights reserved
引用
收藏
页码:79 / 97
页数:19
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