TY - JOUR
T1 - Deep tissue fluorescence imaging and in vivo biological applications
AU - Crosignani, Viera
AU - Dvornikov, Alexander
AU - Aguilar, Jose S.
AU - Stringari, Chiara
AU - Edwards, Robert
AU - Mantulin, William W.
AU - Gratton, Enrico
PY - 2012/11/1
Y1 - 2012/11/1
N2 - We describe a novel technical approach with enhanced fluorescence detection capabilities in twophoton microscopy that achieves deep tissue imaging, while maintaining micron resolution. Compared to conventional two-photon microscopy, greater imaging depth is achieved by more efficient harvesting of fluorescence photons propagating in multiple-scattering media. The system maintains the conventional two-photon microscopy scheme for excitation. However, for fluorescence collection the detection system harvests fluorescence photons directly from a wide area of the turbid sample. The detection scheme relies on a wide area detector, minimal optical components and an emission path bathed in a refractive-index-matching fluid that minimizes emission photon losses. This detection scheme proved to be very efficient, allowing us to obtain high resolution images at depths up to 3 mm. This technique was applied to in vivo imaging of the murine small intestine (SI) and colon. The challenge is to image normal and diseased tissue in the whole live animal, while maintaining high resolution imaging at millimeter depth. In Lgr5-GFP mice, we have been successful in imaging Lgr5-eGFP positive stem cells, present in SI and colon crypt bases.
AB - We describe a novel technical approach with enhanced fluorescence detection capabilities in twophoton microscopy that achieves deep tissue imaging, while maintaining micron resolution. Compared to conventional two-photon microscopy, greater imaging depth is achieved by more efficient harvesting of fluorescence photons propagating in multiple-scattering media. The system maintains the conventional two-photon microscopy scheme for excitation. However, for fluorescence collection the detection system harvests fluorescence photons directly from a wide area of the turbid sample. The detection scheme relies on a wide area detector, minimal optical components and an emission path bathed in a refractive-index-matching fluid that minimizes emission photon losses. This detection scheme proved to be very efficient, allowing us to obtain high resolution images at depths up to 3 mm. This technique was applied to in vivo imaging of the murine small intestine (SI) and colon. The challenge is to image normal and diseased tissue in the whole live animal, while maintaining high resolution imaging at millimeter depth. In Lgr5-GFP mice, we have been successful in imaging Lgr5-eGFP positive stem cells, present in SI and colon crypt bases.
KW - colon
KW - deep-tissue imaging
KW - fluorescence
KW - multiple scattering
KW - small intestine
KW - two-photon microscopy
U2 - 10.1117/1.JBO.17.11.116023
DO - 10.1117/1.JBO.17.11.116023
M3 - Article
C2 - 23214184
AN - SCOPUS:84870596266
SN - 1083-3668
VL - 17
JO - Journal of Biomedical Optics
JF - Journal of Biomedical Optics
IS - 11
M1 - 116023
ER -