Deep two-photon microscopic imaging through brain tissue using the second singlet state from fluorescent agent chlorophyll α in spinach leaf
Related Experiment Video
Updated: Apr 27, 2026

Two-photon Imaging of Cellular Dynamics in the Mouse Spinal Cord
Published on: February 22, 2015
Lingyan Shi1, Adrián Rodríguez-Contreras2, Yury Budansky3
1The City College of the City University of New York, Department of Biomedical Engineering, 160 Convent Avenue, New York 10031bThe City College of the City University of New York, Institute for Ultrafast Spectroscopy and Lasers, Departments of Electrical E.
Abstract:
Two-photon (2P) excitation of the second singlet (S₂) state was studied to achieve deep optical microscopic imaging in brain tissue when both the excitation (800 nm) and emission (685 nm) wavelengths lie in the "tissue optical window" (650 to 950 nm). S₂ state technique was used to investigate chlorophyll α (Chl α) fluorescence inside a spinach leaf under a thick layer of freshly sliced rat brain tissue in combination with 2P microscopic imaging. Strong emission at the peak wavelength of 685 nm under the 2P S₂ state of Chl α enabled the imaging depth up to 450 μm through rat brain tissue.

