Literature DB >> 18204458

High-speed, low-photodamage nonlinear imaging using passive pulse splitters.

Na Ji1, Jeffrey C Magee, Eric Betzig.   

Abstract

Pulsed lasers are key elements in nonlinear bioimaging techniques such as two-photon fluorescence excitation (TPE) microscopy. Typically, however, only a percent or less of the laser power available can be delivered to the sample before photoinduced damage becomes excessive. Here we describe a passive pulse splitter that converts each laser pulse into a fixed number of sub-pulses of equal energy. We applied the splitter to TPE imaging of fixed mouse brain slices labeled with GFP and show that, in different power regimes, the splitter can be used either to increase the signal rate more than 100-fold or to reduce the rate of photobleaching by over fourfold. In living specimens, the gains were even greater: a ninefold reduction in photobleaching during in vivo imaging of Caenorhabditis elegans larvae, and a six- to 20-fold decrease in the rate of photodamage during calcium imaging of rat hippocampal brain slices.

Entities:  

Mesh:

Year:  2008        PMID: 18204458     DOI: 10.1038/nmeth.1175

Source DB:  PubMed          Journal:  Nat Methods        ISSN: 1548-7091            Impact factor:   28.547


  68 in total

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7.  Improved two-photon imaging of living neurons in brain tissue through temporal gating.

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8.  The smart and gentle microscope.

Authors:  Nico Scherf; Jan Huisken
Journal:  Nat Biotechnol       Date:  2015-08       Impact factor: 54.908

9.  Longitudinal in vivo two-photon fluorescence imaging.

Authors:  Sarah E Crowe; Graham C R Ellis-Davies
Journal:  J Comp Neurol       Date:  2014-06-01       Impact factor: 3.215

10.  Pulse splitter-based nonlinear microscopy for live-cardiomyocyte imaging.

Authors:  Zhonghai Wang; Wan Qin; Yonghong Shao; Siyu Ma; Thomas K Borg; Bruce Z Gao
Journal:  Proc SPIE Int Soc Opt Eng       Date:  2014-02-28
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