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Open AccessJournal ArticleDOI

In vivo two-photon microscopy to 1.6-mm depth in mouse cortex

Demirhan Kobat, +2 more
- 01 Oct 2011 - 
- Vol. 16, Iss: 10, pp 106014-106014
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TLDR
Deep tissue in vivo two-photon fluorescence imaging of cortical vasculature in a mouse brain using 1280-nm excitation is presented, approximately reaching the fundamental depth limit in scattering tissue.
Abstract
Deep tissue in vivo two-photon fluorescence imaging of cortical vasculature in a mouse brain using 1280-nm excitation is presented. A record imaging depth of 1.6 mm in mouse cortex is achieved in vivo, approximately reaching the fundamental depth limit in scattering tissue.

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Citations
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In vivo three-photon microscopy of subcortical structures within an intact mouse brain

TL;DR: Non-invasive, high-resolution, in vivo imaging of subcortical structures (the external capsule and hippocampus) within an intact mouse brain is demonstrated using three-photon fluorescence microscopy at the new spectral window of 1700 nm.
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Through-skull fluorescence imaging of the brain in a new near-infrared window

TL;DR: Through-scalp and through-skull fluorescence imaging of mouse cerebral vasculature without craniotomy is reported utilizing the intrinsic photoluminescence of single-walled carbon nanotubes in the 1.3–1.4 micrometre near-infrared window, providing real-time assessment of blood flow anomaly in a mouse middle cerebral artery occlusion stroke model.
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Development of organic semiconducting materials for deep-tissue optical imaging, phototherapy and photoactivation

TL;DR: This review summarizes the recent progress in the development of OSMs based on small-molecule fluorophores, aggregation-induced emission (AIE) dyes and semiconducting oligomer/polymer nanoparticles (SONs/SPNs) for advanced biophotonic applications and highlights OSMs as a multifunctional platform for a wide range of biomedical applications.
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Advances in multiphoton microscopy technology

TL;DR: The basic architecture of a multiphoton microscope capable of real-time analysis of cellular structure and function is discussed and the state-of-the-art technologies for the quantitative imaging of biological phenomena are summarized.
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Brain Tissue Responses to Neural Implants Impact Signal Sensitivity and Intervention Strategies

TL;DR: This review summarizes the magnitude, variability, and time course of the dynamic molecular and cellular level neural tissue responses induced by state-of-the-art implantable devices.
References
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Book

The Mouse Brain in Stereotaxic Coordinates

TL;DR: The 3rd edition of this atlas is now in more practical 14"x11" format for convenient lab use and includes a CD of all plates and diagrams, as well as Adobe Illustrator files of the diagrams, and a variety of additional useful material.
Journal ArticleDOI

Deep tissue two-photon microscopy

TL;DR: Fundamental concepts of nonlinear microscopy are reviewed and conditions relevant for achieving large imaging depths in intact tissue are discussed.
Journal ArticleDOI

Imaging Large-Scale Neural Activity with Cellular Resolution in Awake, Mobile Mice

TL;DR: A technique for two-photon fluorescence imaging with cellular resolution in awake, behaving mice with minimal motion artifact is reported, demonstrating that running-associated brain motion is limited to approximately 2-5 microm.
Journal ArticleDOI

Two-photon imaging to a depth of 1000 µm microm in living brains by use of a Ti:Al2O3 regenerative amplifier

TL;DR: It is shown that two-photon fluorescence images can be obtained throughout almost the entire gray matter of the mouse neocortex by using optically amplified femtosecond pulses.
Journal ArticleDOI

Deep tissue multiphoton microscopy using longer wavelength excitation.

TL;DR: The maximal two-photon fluorescence microscopy (TPM) imaging depth achieved with 775-nm excitation is compared to that achieved with 1280- nm excitation through in vivo and ex vivo TPM of fluorescently-labeled blood vessels in mouse brain.
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