Fluorescent microspheres of diameter 10μm embedded in a turbid medium consisting of polystyrene beads suspended in water are imaged under two-photon and single-photon excitation. A comparison of two-photon and single-photon fluorescence images shows that multiple scattering leads to a dominant limiting factor of the signal-to-noise ratio in the former case, while it results in a dominant limiting factor of resolution in the latter case. These results are qualitatively consistent with the predication by the Monte-Carlo simulation based on Mie scattering theory
There is a growing effort to image single neurons in vivo, and observe their individual contribution...
We have analyzed how the maximal imaging depth of two-photon microscopy in scattering samples depend...
Penetration depth is investigated in terms of the performance of transverse image resolution and sig...
A numerical model was developed to simulate the effects of tissue optical properties, objective nume...
In this article, effective point spread functions for fluorescence microscopic imaging are introduce...
The effect of multiple scattering in a turbid medium on single-photon and two-photon fluorescence mi...
Image resolution and signal level in fluorescence microscopy through inhomogeneous turbid media cons...
Image formation in multiphoton fluorescence microscopy through double-layer turbid tissue media is i...
In this paper, image formation under single-photon (1-p), two-photon (2-p) and three-photon (3-p) fl...
International audienceWe report on measurements and Monte Carlo analysis of the spatial distribution...
International audienceImaging depth in two-photon microscopy is ultimately limited by the out-of-foc...
We show, both theoretically and experimentally, that for a turbid tissue medium where Mie scattering...
The depth of two-photon fluorescence imaging in turbid media can be significantly enhanced by the us...
Summary. Two-photon absorption induced fluorescence microscopy was used as a tool for the examinatio...
Two-photon fluorescence microscopy allows three-dimensional imaging of biological specimens in vivo....
There is a growing effort to image single neurons in vivo, and observe their individual contribution...
We have analyzed how the maximal imaging depth of two-photon microscopy in scattering samples depend...
Penetration depth is investigated in terms of the performance of transverse image resolution and sig...
A numerical model was developed to simulate the effects of tissue optical properties, objective nume...
In this article, effective point spread functions for fluorescence microscopic imaging are introduce...
The effect of multiple scattering in a turbid medium on single-photon and two-photon fluorescence mi...
Image resolution and signal level in fluorescence microscopy through inhomogeneous turbid media cons...
Image formation in multiphoton fluorescence microscopy through double-layer turbid tissue media is i...
In this paper, image formation under single-photon (1-p), two-photon (2-p) and three-photon (3-p) fl...
International audienceWe report on measurements and Monte Carlo analysis of the spatial distribution...
International audienceImaging depth in two-photon microscopy is ultimately limited by the out-of-foc...
We show, both theoretically and experimentally, that for a turbid tissue medium where Mie scattering...
The depth of two-photon fluorescence imaging in turbid media can be significantly enhanced by the us...
Summary. Two-photon absorption induced fluorescence microscopy was used as a tool for the examinatio...
Two-photon fluorescence microscopy allows three-dimensional imaging of biological specimens in vivo....
There is a growing effort to image single neurons in vivo, and observe their individual contribution...
We have analyzed how the maximal imaging depth of two-photon microscopy in scattering samples depend...
Penetration depth is investigated in terms of the performance of transverse image resolution and sig...