Abstract
Both point-scanning and line-scanning confocal microscopes provide resolution and optical sectioning to observe nuclear and cellular detail in human tissues, and are being translated for clinical applications. While traditional point-scanning is truly confocal and offers the best possible optical sectioning and resolution, line-scanning is partially confocal but may offer a relatively simpler and lower-cost alternative for more widespread dissemination into clinical settings. The loss of sectioning and loss of contrast due to scattering in tissue is more rapid and more severe with a line-scan than with a point-scan. However, the sectioning and contrast may be recovered with the use of a divided-pupil. Thus, as part of our efforts to translate confocal microscopy for detection of skin cancer, and to determine the best possible approach for clinical applications, we are now developing a quantitative understanding of imaging performance for a set of scanning and pupil conditions. We report a Fourier-analysis-based computational model of confocal microscopy for six configurations. The six configurations are point-scanning and line-scanning, with full-pupil, half-pupil and divided-pupils. The performance, in terms of on-axis irradiance (signal), resolution and sectioning capabilities, is quantified and compared among these six configurations.
Highlights
Both point-scanning and line-scanning confocal microscopes have proven successful for imaging of human tissues, providing resolution and optical sectioning to observe nuclear and cellular detail
We report a Fourier-analysis-based computational model of confocal microscopy for six configurations
We have presented a Fourier-analysis computational model for optimal pupil design of confocal microscopy
Summary
Both point-scanning and line-scanning confocal microscopes have proven successful for imaging of human tissues, providing resolution and optical sectioning to observe nuclear and cellular detail. Both technologies are being translated for diverse clinical applications [1,2,3]. The optical sectioning and contrast with line-scanning confocal microscopy may be recovered with the use of a divided-pupil, as was experimentally discovered in human skin [8,9,10]. The results to date indicate that the divided-pupil approach may offer improved imaging performance in scattering tissues, compared to the full-pupil, with either point-scanning or line-scanning. We present results of integrated intensity in the coherent-transmission path and incoherent-receive path, which can be used to understand background speckle from scattered light
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