Please use this identifier to cite or link to this item: https://doi.org/10.1142/S179354581440001X
Title: Advanced optical microscopy methods for in vivo imaging of sub-cellular structures in thick biological tissues
Authors: Chen N. 
Rehman S. 
Sheppard C.J.R.
Keywords: Confocal microscopy
Histology
Image acquisition
Mobile security
Optical data storage
Optical microscopy
Optical tomography
Tissue
Biological process
Diffraction limited
Focal modulation microscopy (FMM)
High resolution image
Indispensable tools
Multiphoton microscopy
Optical coherence microscopy
Optical gatings
Modulation
Issue Date: 2014
Citation: Chen N., Rehman S., Sheppard C.J.R. (2014). Advanced optical microscopy methods for in vivo imaging of sub-cellular structures in thick biological tissues. Journal of Innovative Optical Health Sciences 7 (5) : 1440001. ScholarBank@NUS Repository. https://doi.org/10.1142/S179354581440001X
Abstract: Optical microscopy has become an indispensable tool for visualizing sub-cellular structures and biological processes. However, scattering in biological tissues is a major obstacle that prevents high-resolution images from being obtained from deep regions of tissue. We review common techniques, such as multiphoton microscopy (MPM) and optical coherence microscopy (OCM), for diffraction limited imaging beyond an imaging depth of 0.5 mm. Novel implementations have been emerging in recent years giving higher imaging speed, deeper penetration, and better image quality. Focal modulation microscopy (FMM) is a novel method that combines confocal spatial filtering with focal modulation to reject out-of-focus background. FMM has demonstrated an imaging depth comparable to those of MPM and OCM, near-real-time image acquisition, and the capability for multiple contrast mechanisms. © 2014 The Authors.
Source Title: Journal of Innovative Optical Health Sciences
URI: https://scholarbank.nus.edu.sg/handle/10635/174157
ISSN: 17935458
DOI: 10.1142/S179354581440001X
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