Label-Free Biosensor Imaging on Photonic Crystal Surfaces

被引:51
作者
Zhuo, Yue [1 ]
Cunningham, Brian T. [1 ,2 ]
机构
[1] Univ Illinois, Dept Bioengn, Champaign, IL 61822 USA
[2] Univ Illinois, Dept Elect & Comp Engn, Champaign, IL 61822 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
photonic crystal; photonic crystal surface; photonic crystal biosensor; photonic crystal enhanced microscopy (PCEM); photonic crystal enhanced fluorescence (PCEF); label-free bioimaging; nanophotonics; biomaterial detection; live cell imaging; nanoparticle detection; protein-protein binding detection; WAVE-GUIDE; ENHANCED-FLUORESCENCE; SPONTANEOUS EMISSION; CELL ATTACHMENT; BAND-STRUCTURE; CYTOTOXICITY; SENSITIVITY; EXTRACTION; MICROPLATE; ANOMALIES;
D O I
10.3390/s150921613
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We review the development and application of nanostructured photonic crystal surfaces and a hyperspectral reflectance imaging detection instrument which, when used together, represent a new form of optical microscopy that enables label-free, quantitative, and kinetic monitoring of biomaterial interaction with substrate surfaces. Photonic Crystal Enhanced Microscopy (PCEM) has been used to detect broad classes of materials which include dielectric nanoparticles, metal plasmonic nanoparticles, biomolecular layers, and live cells. Because PCEM does not require cytotoxic stains or photobleachable fluorescent dyes, it is especially useful for monitoring the long-term interactions of cells with extracellular matrix surfaces. PCEM is only sensitive to the attachment of cell components within similar to 200 nm of the photonic crystal surface, which may correspond to the region of most interest for adhesion processes that involve stem cell differentiation, chemotaxis, and metastasis. PCEM has also demonstrated sufficient sensitivity for sensing nanoparticle contrast agents that are roughly the same size as protein molecules, which may enable applications in digital diagnostics with single molecule sensing resolution. We will review PCEM's development history, operating principles, nanostructure design, and imaging modalities that enable tracking of optical scatterers, emitters, absorbers, and centers of dielectric permittivity.
引用
收藏
页码:21613 / 21635
页数:23
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