• Journal of Innovative Optical Health Sciences
  • Vol. 7, Issue 5, 1440001 (2014)
Nanguang Chen1、2, Shakil Rehman1、2, and Colin J. R. Sheppard3、*
Author Affiliations
  • 1Department of Biomedical Engineering National University of Singapore, Singapore 117576
  • 2Singapore-MIT Alliance for Research and Technology (SMART) Centre, Singapore 138602
  • 3Department of Nanophysics, Istituto Italiano di Tecnologia via Morego 30, 16163 Genova, Italy
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    DOI: 10.1142/s179354581440001x Cite this Article
    Nanguang Chen, Shakil Rehman, Colin J. R. Sheppard. Advanced optical microscopy methods for in vivo imaging of sub-cellular structures in thick biological tissues[J]. Journal of Innovative Optical Health Sciences, 2014, 7(5): 1440001 Copy Citation Text show less

    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.
    Nanguang Chen, Shakil Rehman, Colin J. R. Sheppard. Advanced optical microscopy methods for in vivo imaging of sub-cellular structures in thick biological tissues[J]. Journal of Innovative Optical Health Sciences, 2014, 7(5): 1440001
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