Paper
17 March 2014 Enhancing the depth of tissue microscope imaging using two-photon excitation of the second singlet state of fluorescent agents
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Proceedings Volume 8940, Optical Biopsy XII; 894017 (2014) https://doi.org/10.1117/12.2035334
Event: SPIE BiOS, 2014, San Francisco, California, United States
Abstract
Increasing the depth to image inside tissue is critical in biomedicine. Two-photon (2P) excitation of the second singlet (S2) state of a group of fluorescent agents with near infrared emission, Chlorophyll a (Chl a) and Indocyanine green (ICG), is used to extend the optical imaging regime of 2PM into “tissue optical window” for deep tissue penetration. The fast nonradiative from S2 to S1 yields both emission and absorption wavelengths in the therapeutic window. The salient feature is to place both the 2P excitation and emission wavelengths of the imaging agents falling into the “tissue optical window”. As a first step to achieve deeper optical imaging, Chl a and ICG are investigated and demonstrated as imaging agents for 2P S2 excitation microscope image.
© (2014) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Yang Pu, Lingyan Shi, Sebastião Pratavieira, and R. R. Alfano "Enhancing the depth of tissue microscope imaging using two-photon excitation of the second singlet state of fluorescent agents", Proc. SPIE 8940, Optical Biopsy XII, 894017 (17 March 2014); https://doi.org/10.1117/12.2035334
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KEYWORDS
Tissue optics

Microscopes

Near infrared

Biomedical optics

Absorption

Luminescence

Tissues

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