TY - JOUR
T1 - All-near-infrared multiphoton microscopy interrogates intact tissues at deeper imaging depths than conventional single-and two-photon near-infrared excitation microscopes
AU - Sarder, Pinaki
AU - Yazdanfar, Siavash
AU - Akers, Walter J.
AU - Tang, Rui
AU - Sudlow, Gail P.
AU - Egbulefu, Christopher
AU - Achilefu, Samuel
N1 - Funding Information:
This study was supported by National Institutes of Health grants R21/R33 CA12353701, R01 CA171651, and R01 EB008111. We acknowledge the Bakewell NeuroImaging Laboratory, Washington University School of Medicine (WUSM), for use of their state-of-the-art multiphoton microscopy system. We thank Professor Deborah Novack (Medicine and Pathology & Immunology, WUSM) for examining the H&E images presented in this study. We appreciate Professor James Ballard’s (director, Engineering Communication Center, Washington University in St. Louis) close reading of the manuscript.
PY - 2013/10
Y1 - 2013/10
N2 - The era of molecular medicine has ushered in the development of microscopic methods that can report molecular processes in thick tissues with high spatial resolution. A commonality in deep-tissue microscopy is the use of near-infrared (NIR) lasers with single-or multiphoton excitations. However, the relationship between different NIR excitation microscopic techniques and the imaging depths in tissue has not been established. We compared such depth limits for three NIR excitation techniques: NIR single-photon confocal microscopy (NIR SPCM), NIR multiphoton excitation with visible detection (NIR/VIS MPM), and all-NIR multiphoton excitation with NIR detection (NIR/NIR MPM). Homologous cyanine dyes provided the fluorescence. Intact kidneys were harvested after administration of kidney-clearing cyanine dyes in mice. NIR SPCM and NIR/VIS MPM achieved similar maximum imaging depth of ~100 μ m. The NIR/NIR MPM enabled greater than fivefold imaging depth (500 μ m) using the harvested kidneys. Although the NIR/NIR MPM used 1550-nm excitation where water absorption is relatively high, cell viability and histology studies demonstrate that the laser did not induce photothermal damage at the low laser powers used for the kidney imaging. This study provides guidance on the imaging depth capabilities of NIR excitation-based microscopic techniques and reveals the potential to multiplex information using these platforms.
AB - The era of molecular medicine has ushered in the development of microscopic methods that can report molecular processes in thick tissues with high spatial resolution. A commonality in deep-tissue microscopy is the use of near-infrared (NIR) lasers with single-or multiphoton excitations. However, the relationship between different NIR excitation microscopic techniques and the imaging depths in tissue has not been established. We compared such depth limits for three NIR excitation techniques: NIR single-photon confocal microscopy (NIR SPCM), NIR multiphoton excitation with visible detection (NIR/VIS MPM), and all-NIR multiphoton excitation with NIR detection (NIR/NIR MPM). Homologous cyanine dyes provided the fluorescence. Intact kidneys were harvested after administration of kidney-clearing cyanine dyes in mice. NIR SPCM and NIR/VIS MPM achieved similar maximum imaging depth of ~100 μ m. The NIR/NIR MPM enabled greater than fivefold imaging depth (500 μ m) using the harvested kidneys. Although the NIR/NIR MPM used 1550-nm excitation where water absorption is relatively high, cell viability and histology studies demonstrate that the laser did not induce photothermal damage at the low laser powers used for the kidney imaging. This study provides guidance on the imaging depth capabilities of NIR excitation-based microscopic techniques and reveals the potential to multiplex information using these platforms.
KW - all-near-infrared multiphoton microscopy
KW - cyanine dyes
KW - laser-induced photodamage
KW - multiphoton microscopy
KW - near-infrared fluorescent molecular probes
KW - near-infrared single-photon confocal microscopy
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U2 - 10.1117/1.JBO.18.10.106012
DO - 10.1117/1.JBO.18.10.106012
M3 - Article
C2 - 24150231
AN - SCOPUS:84892641795
SN - 1083-3668
VL - 18
JO - Journal of biomedical optics
JF - Journal of biomedical optics
IS - 10
M1 - 106012
ER -