Literature DB >> 15468110

Calibration and validation of confocal spectral imaging systems.

Jeremy M Lerner1, Robert M Zucker.   

Abstract

BACKGROUND: Confocal spectral imaging (CSI) microscopic systems currently on the market delineate multiple fluorescent proteins, labels, or dyes within biological specimens by performing spectral characterizations. However, some CSI systems have been found to present inconsistent spectral profiles of reference spectra within a particular system and between related and unrelated instruments. This variability confirms that there is a need for a standardized, objective calibration and validation protocol.
METHODS: Our protocol uses an inexpensive multi-ion discharge lamp (MIDL) that contains Hg(+), Ar(+), and inorganic fluorophores that emit distinct, stable, spectral features in place of a sample. We derived reference spectra from the MIDL data to accurately predict the spectral resolution, ratio of wavelength to wavelength, contrast, and aliasing parameters of any CSI system. We were also able to predict and confirm the influence of pinhole diameter on spectral profiles.
RESULTS: Using this simulation, we determined that there was good agreement between observed and theoretical expectations, thus enabling us to identify malfunctioning subsystems. We examined eight CSI systems and one nonconfocal spectral system, all of which displayed spectral inconsistencies. No instrument met its optimal performance expectations. In two systems, we established the need for factory realignment that had not been otherwise recognized.
CONCLUSIONS: We found that using a primary light source that emits an absolute standard "reference spectrum" enabled us to diagnose instrumental errors and measure accuracy and reproducibility under normalized conditions. With this information, a CSI operator can determine whether a CSI system is working optimally and make objective comparisons with the performance of other CSI systems. We determined that, if CSI systems were standardized to produce the same spectral profile of a MIDL lamp, researchers could be confident that the same experimental findings would be obtained on any CSI system. Copyright 2004 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2004        PMID: 15468110     DOI: 10.1002/cyto.a.20087

Source DB:  PubMed          Journal:  Cytometry A        ISSN: 1552-4922            Impact factor:   4.355


  7 in total

1.  How to improve quality assurance in fluorometry: fluorescence-inherent sources of error and suited fluorescence standards.

Authors:  U Resch-Genger; K Hoffmann; W Nietfeld; A Engel; J Neukammer; R Nitschke; B Ebert; R Macdonald
Journal:  J Fluoresc       Date:  2005-05       Impact factor: 2.217

2.  Cytomics emerging from cytometry.

Authors:  A Tárnok; G Brockhoff
Journal:  Cell Prolif       Date:  2006-10       Impact factor: 6.831

3.  Hyperspectral imaging microscopy for identification and quantitative analysis of fluorescently-labeled cells in highly autofluorescent tissue.

Authors:  Silas J Leavesley; Naga Annamdevula; John Boni; Samantha Stocker; Kristin Grant; Boris Troyanovsky; Thomas C Rich; Diego F Alvarez
Journal:  J Biophotonics       Date:  2011-10-11       Impact factor: 3.207

Review 4.  Cytomics - importance of multimodal analysis of cell function and proliferation in oncology.

Authors:  A Tárnok; J Bocsi; G Brockhoff
Journal:  Cell Prolif       Date:  2006-12       Impact factor: 6.831

5.  An integrated imaging approach to the study of oxidative stress generation by mitochondrial dysfunction in living cells.

Authors:  Wan-Yun Cheng; Haiyan Tong; Evan W Miller; Christopher J Chang; James Remington; Robert M Zucker; Philip A Bromberg; James M Samet; Thomas P J Hofer
Journal:  Environ Health Perspect       Date:  2010-04-22       Impact factor: 9.031

6.  Retromer terminates the generation of cAMP by internalized PTH receptors.

Authors:  Timothy N Feinstein; Vanessa L Wehbi; Juan A Ardura; David S Wheeler; Sebastien Ferrandon; Thomas J Gardella; Jean-Pierre Vilardaga
Journal:  Nat Chem Biol       Date:  2011-03-27       Impact factor: 15.040

7.  ConfocalCheck--a software tool for the automated monitoring of confocal microscope performance.

Authors:  Keng Imm Hng; Dirk Dormann
Journal:  PLoS One       Date:  2013-11-05       Impact factor: 3.240

  7 in total

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