期刊
JOURNAL OF BIOPHOTONICS
卷 2, 期 8-9, 页码 505-520出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/jbio.200910039
关键词
finite-difference time-domain (FDTD) method; light scattering; cytometry; gold nanoparticle; optical phase contrast microscopy; refractive index matching; image contrast enhancement; nanoscale cell imaging
资金
- RF President's Supporting of Leading Scientific Schools [NSHA-208.2008.2 (2008-2009)]
- PF Program on the Development of High School Potential [2.1.1/4989, 2.2.1.1/2950]
- National Institute of Health [EB000873, EB009239, CA131164, CA139373]
- National Science Foundation [IDBR 0852737]
- [22401.4 PHOTONICS4LIFE-FP7-ICT-2007-2]
- NATIONAL CANCER INSTITUTE [R21CA139373, R01CA131164] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [R21EB005123, R01EB000873] Funding Source: NIH RePORTER
The formulation of the finite-difference time-domain (FDTD) approach is presented in the framework of its potential applications to in-vivo flow cytometry based on light scattering. The consideration is focused on comparison of light scattering by a single biological cell alone in controlled refractive-index matching conditions and by cells labeled by gold-nanoparticles. The optical schematics including phase contrast (OPCM) microscopy as a prospective modality for in-vivo flow cytometry is also analyzed. The validation of the FDTD approach for the simulation of flow cytometry may open up a new avenue in the development of advanced. cytometric techniques based on scattering effects from nanoscale targets. [GRAPHICS] A group of 42-gold NPs randomly distributed on the surface of the cell nucleus: (a) cell model; (h) nucleus and cluster model, The NP size on the right-hand graph is slightly exaggerated. (C) 2009 by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
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