TY - JOUR
T1 - Finite-difference time-domain-based optical microscopy simulation of dispersive media facilitates the development of optical imaging techniques
AU - Zhang, Di
AU - Capoglu, Ilker
AU - Li, Yue
AU - Cherkezyan, Lusik
AU - Chandler, John
AU - Spicer, Graham
AU - Subramanian, Hariharan
AU - Taflove, Allen
AU - Backman, Vadim
N1 - Funding Information:
This study was supported by the National Institutes of Health (NIH) (R01CA155284, R01CA165309, and R01EB016983) and the National Science Foundation (NSF) (EFRI-1240416). The FDTD simulations were made possible by a computational allocation from the Quest high-performance computing facility at Northwestern University.
Publisher Copyright:
© 2016 Society of Photo-Optical Instrumentation Engineers (SPIE).
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Combining finite-difference time-domain (FDTD) methods and modeling of optical microscopy modalities, we previously developed an open-source software package called Angora, which is essentially a "microscope in a computer." However, the samples being simulated were limited to nondispersive media. Since media dispersions are common in biological samples (such as cells with staining and metallic biomarkers), we have further developed a module in Angora to simulate samples having complicated dispersion properties, thereby allowing the synthesis of microscope images of most biological samples. We first describe a method to integrate media dispersion into FDTD, and we validate the corresponding Angora dispersion module by applying Mie theory, as well as by experimentally imaging gold microspheres. Then, we demonstrate how Angora can facilitate the development of optical imaging techniques with a case study.
AB - Combining finite-difference time-domain (FDTD) methods and modeling of optical microscopy modalities, we previously developed an open-source software package called Angora, which is essentially a "microscope in a computer." However, the samples being simulated were limited to nondispersive media. Since media dispersions are common in biological samples (such as cells with staining and metallic biomarkers), we have further developed a module in Angora to simulate samples having complicated dispersion properties, thereby allowing the synthesis of microscope images of most biological samples. We first describe a method to integrate media dispersion into FDTD, and we validate the corresponding Angora dispersion module by applying Mie theory, as well as by experimentally imaging gold microspheres. Then, we demonstrate how Angora can facilitate the development of optical imaging techniques with a case study.
KW - imaging
KW - microscopy
KW - simulations
KW - spectroscopy
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U2 - 10.1117/1.JBO.21.6.065004
DO - 10.1117/1.JBO.21.6.065004
M3 - Article
C2 - 27283256
AN - SCOPUS:84974603467
SN - 1083-3668
VL - 21
JO - Journal of Biomedical Optics
JF - Journal of Biomedical Optics
IS - 6
M1 - 065004
ER -