Literature DB >> 24251437

Compact non-contact total emission detection for in vivo multiphoton excitation microscopy.

Christian A Combs1, Aleksandr Smirnov2, Brian Glancy3, Nader S Karamzadeh4, Amir H Gandjbakhche4, Glen Redford5, Karl Kilborn5, Jay R Knutson2, Robert S Balaban3.   

Abstract

We describe a compact, non-contact design for a total emission detection (c-TED) system for intra-vital multiphoton imaging. To conform to a standard upright two-photon microscope design, this system uses a parabolic mirror surrounding a standard microscope objective in concert with an optical path that does not interfere with normal microscope operation. The non-contact design of this device allows for maximal light collection without disrupting the physiology of the specimen being examined. Tests were conducted on exposed tissues in live animals to examine the emission collection enhancement of the c-TED device compared to heavily optimized objective-based emission collection. The best light collection enhancement was seen from murine fat (5×-2× gains as a function of depth), whereas murine skeletal muscle and rat kidney showed gains of over two and just under twofold near the surface, respectively. Gains decreased with imaging depth (particularly in the kidney). Zebrafish imaging on a reflective substrate showed close to a twofold gain throughout the entire volume of an intact embryo (approximately 150 μm deep). Direct measurement of bleaching rates confirmed that the lower laser powers, enabled by greater light collection efficiency, yielded reduced photobleaching in vivo. The potential benefits of increased light collection in terms of speed of imaging and reduced photo-damage, as well as the applicability of this device to other multiphoton imaging methods is discussed. Published 2013. This article is a U.S. Government work and is in the public domain in the USA.

Entities:  

Keywords:  Imaging; light collection; two-photon microscopy

Mesh:

Substances:

Year:  2013        PMID: 24251437      PMCID: PMC4132828          DOI: 10.1111/jmi.12099

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  17 in total

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Authors:  Markus Rehberg; Fritz Krombach; Ulrich Pohl; Steffen Dietzel
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2.  Optimization of multiphoton excitation microscopy by total emission detection using a parabolic light reflector.

Authors:  Christian A Combs; Aleksandr V Smirnov; Jason D Riley; Amir H Gandjbakhche; Jay R Knutson; Robert S Balaban
Journal:  J Microsc       Date:  2007-12       Impact factor: 1.758

3.  Enhanced fluorescence signal in nonlinear microscopy through supplementary fiber-optic light collection.

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4.  Efficient large core fiber-based detection for multi-channel two-photon fluorescence microscopy and spectral unmixing.

Authors:  Mathieu Ducros; Marcel van 't Hoff; Marcel van't Hoff; Alexis Evrard; Christian Seebacher; Elke M Schmidt; Serge Charpak; Martin Oheim
Journal:  J Neurosci Methods       Date:  2011-03-30       Impact factor: 2.390

5.  Two-photon laser scanning fluorescence microscopy.

Authors:  W Denk; J H Strickler; W W Webb
Journal:  Science       Date:  1990-04-06       Impact factor: 47.728

6.  Optimizing multiphoton fluorescence microscopy light collection from living tissue by noncontact total emission detection (epiTED).

Authors:  C A Combs; A Smirnov; D Chess; D B McGavern; J L Schroeder; J Riley; S S Kang; M Lugar-Hammer; A Gandjbakhche; J R Knutson; R S Balaban
Journal:  J Microsc       Date:  2010-06-21       Impact factor: 1.758

7.  Short communication: Subcellular motion compensation for minimally invasive microscopy, in vivo: evidence for oxygen gradients in resting muscle.

Authors:  James L Schroeder; Merav Luger-Hamer; Randall Pursley; Tom Pohida; Chris Chefd'hotel; Peter Kellman; Robert S Balaban
Journal:  Circ Res       Date:  2010-02-18       Impact factor: 17.367

8.  Deep tissue fluorescence imaging and in vivo biological applications.

Authors:  Viera Crosignani; Alexander Dvornikov; Jose S Aguilar; Chiara Stringari; Robert Edwards; William W Mantulin; Enrico Gratton
Journal:  J Biomed Opt       Date:  2012-11       Impact factor: 3.170

9.  Three-dimensional motion tracking for high-resolution optical microscopy, in vivo.

Authors:  Matthew Bakalar; James L Schroeder; Randall Pursley; Thomas J Pohida; Brian Glancy; Joni Taylor; David Chess; Peter Kellman; Hui Xue; Robert S Balaban
Journal:  J Microsc       Date:  2012-06       Impact factor: 1.758

10.  Maximizing fluorescence collection efficiency in multiphoton microscopy.

Authors:  Joseph P Zinter; Michael J Levene
Journal:  Opt Express       Date:  2011-08-01       Impact factor: 3.894

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  4 in total

1.  Imaging in turbid media: a transmission detector gives 2-3 order of magnitude enhanced sensitivity compared to epi-detection schemes.

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Journal:  Biomed Opt Express       Date:  2016-08-30       Impact factor: 3.732

2.  A pragmatic guide to multiphoton microscope design.

Authors:  Michael D Young; Jeffrey J Field; Kraig E Sheetz; Randy A Bartels; Jeff Squier
Journal:  Adv Opt Photonics       Date:  2015-06-30       Impact factor: 20.107

Review 3.  Motion compensation for in vivo subcellular optical microscopy.

Authors:  B Lucotte; R S Balaban
Journal:  J Microsc       Date:  2014-04       Impact factor: 1.758

Review 4.  Modeling cardiac complexity: Advancements in myocardial models and analytical techniques for physiological investigation and therapeutic development in vitro.

Authors:  Neal I Callaghan; Sina Hadipour-Lakmehsari; Shin-Haw Lee; Anthony O Gramolini; Craig A Simmons
Journal:  APL Bioeng       Date:  2019-02-05
  4 in total

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