We present a strategy to preserve contrast over a deeper range of imaging depths in the context of confocal microscopy using low-power (0.5 mW) diode laser illumination. While the dual-axis confocal microscope architecture's intersecting illumination and collection beams significantly improves the spatial-filtering and optical-sectioning performance of confocal microscopy, we propose that modulating the spatial alignment of the dual-axis beams at a frequency f will generate a focal volume signal modulated at 2f, which further provides nearly an order-of-magnitude improvement in optical-sectioning contrast. Lock-in detection is used to remove the unmodulated background light, thereby enhancing our ability to image deeply within highly scattering tissues.
Modulated Alignment Dual-Axis (MAD) Confocal Microscopy for Deep Optical Sectioining in Tissues
S. Y. Leigh,Ye Chen,Jonathan T. C. Liu
Published 2014 in International Symposium on Optomechatronic Technologies
ABSTRACT
PUBLICATION RECORD
- Publication year
2014
- Venue
International Symposium on Optomechatronic Technologies
- Publication date
2014-05-19
- Fields of study
Medicine, Materials Science, Engineering
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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