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    Optical artefacts in transflection mode FTIR microspectroscopic images of single cells on a biological support: the effect of back-scattering into collection optics

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    Authors
    Lee, Joe
    Gazi, Ehsan
    Dwyer, John
    Brown, Michael D
    Clarke, Noel W
    Nicholson, James M
    Gardner, Peter
    Affiliation
    School of Chemistry, University of Manchester, P.O. Box 88, Manchester, UK M60 1QD.
    Issue Date
    2007-08
    
    Metadata
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    Abstract
    Infrared microspectroscopic imaging data of single human prostate cancer cells, on an artificial extracellular matrix (Matrigel) thin-film surface, are presented. The spectral intensity maps, obtained in reflection mode, appear to show that the protein intensity distribution observed at the location of a cell changes dramatically depending on the concentration and/or thickness of the underlying Matrigel layer. Specifically, cells adhered to a low protein concentration or thin surface exhibit a higher protein intensity signal than the surrounding layer whereas those on a high protein concentration or thick surface exhibit a lower protein intensity signal. These results are qualitatively explained by a simple model that takes into account the fact that radiation scattered from cells can enter the collection optics of the microscope without passing through the Matrigel layer. This leads to an apparent reduction in absorption at the cell.
    Citation
    Optical artefacts in transflection mode FTIR microspectroscopic images of single cells on a biological support: the effect of back-scattering into collection optics. 2007, 132 (8):750-5 Analyst
    Journal
    The Analyst
    URI
    http://hdl.handle.net/10541/71275
    DOI
    10.1039/b702064c
    PubMed ID
    17646874
    Type
    Article
    Language
    en
    ISSN
    0003-2654
    ae974a485f413a2113503eed53cd6c53
    10.1039/b702064c
    Scopus Count
    Collections
    All Paterson Institute for Cancer Research

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