Nanomaterials for In Vivo Imaging

被引:897
作者
Smith, Bryan Ronain [1 ]
Gambhir, Sanjiv Sam [2 ]
机构
[1] Stanford Univ, 3155 Porter Dr,1214, Palo Alto, CA 94304 USA
[2] James H Clark Ctr, 318 Campus Dr,First Floor,E-150A, Stanford, CA 94305 USA
关键词
IRON-OXIDE NANOPARTICLES; OPTICAL COHERENCE TOMOGRAPHY; UP-CONVERSION NANOPARTICLES; POSITRON-EMISSION-TOMOGRAPHY; ELECTRICAL-IMPEDANCE TOMOGRAPHY; NANOSTRUCTURED LIPID CARRIERS; RAY COMPUTED-TOMOGRAPHY; CARBON QUANTUM DOTS; PERSISTENT LUMINESCENT NANOPARTICLES; HYPERPOLARIZED MAGNETIC-RESONANCE;
D O I
10.1021/acs.chemrev.6b00073
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In vivo imaging, which enables us to peer deeply within living subjects, is producing tremendous opportunities both for clinical diagnostics and as a research tool. Contrast material is often required to clearly visualize the functional architecture of physiological structures. Recent advances in nanomaterials are becoming pivotal to generate the high-resolution, high-contrast images needed for accurate, precision diagnostics. Nanomaterials are playing major roles in imaging by delivering large imaging payloads, yielding improved sensitivity, multiplexing capacity, and modularity of design. Indeed, for several imaging modalities, nanomaterials are now not simply ancillary contrast entities, but are instead the original and sole source of image signal that make possible the modality's existence. We address the physicochemical makeup/ design of nanomaterials through the lens of the physical properties that produce contrast signal for the cognate imaging modality we stratify nanomaterials on the basis of their (i) magnetic, (ii) optical, (iii) acoustic, and/or (iv) nuclear properties. We evaluate them for their ability to provide relevant information under preclinical and clinical circumstances, their in vivo safety profiles (which are being incorporated into their chemical design), their modularity in being fused to create multimodal nanomaterials (spanning multiple different physical imaging modalities and therapeutic/theranostic capabilities), their key properties, and critically their likelihood to be clinically translated.
引用
收藏
页码:901 / 986
页数:86
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