Multispectral fluorescence imaging to assess pH in biological specimens

Simple, quantitative assays to measure pH in tissue could improve the study of complicated biological processes and diseases such as cancer. We evaluated multispectral fluorescence imaging (MSFI) to quantify extracellular pH (pH ) in dye-perfused, surgically-resected tumor specimens with commerciall...

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Published inJournal of Biomedical Optics Vol. 16; no. 1; p. 016007
Main Authors Hight, Matthew R, Nolting, Donald D, McKinley, Eliot T, Lander, Adam D, Wyatt, Shelby K, Gonyea, Mark, Zhao, Ping, Manning, H. Charles
Format Journal Article
LanguageEnglish
Published United States Society of Photo-Optical Instrumentation Engineers (SPIE) 01.01.2011
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Summary:Simple, quantitative assays to measure pH in tissue could improve the study of complicated biological processes and diseases such as cancer. We evaluated multispectral fluorescence imaging (MSFI) to quantify extracellular pH (pH ) in dye-perfused, surgically-resected tumor specimens with commercially available instrumentation. Utilizing a water-soluble organic dye with pH-dependent fluorescence emission (SNARF-4F), we used standard fluorimetry to quantitatively assess the emission properties of the dye as a function of pH. By conducting these studies within the spectroscopic constraints imposed by the appropriate imaging filter set supplied with the imaging system, we determined that correction of the fluorescence emission of deprotonated dye was necessary for accurate determination of pH due to suboptimal excitation. Subsequently, employing a fluorimetry-derived correction factor (C ), MSFI data sets of aqueous dye solutions and tissuelike phantoms could be spectrally unmixed to accurately quantify equilibrium concentrations of protonated (HA) and deprotonated (A ;) dye and thus determine solution pH. Finally, we explored the feasibility of MSFI for high-resolution pH mapping of human colorectal cancer cell-line xenografts. Data presented suggest that MSFI is suitable for quantitative determination of pH in dye-perfused tissue, potentially enabling measurement of pH across a variety of preclinical models of disease.
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Address all correspondence to: H. Charles Manning, Vanderbilt University Institute of Imaging Science, Vanderbilt University Medical Center, AA-1105 Medical Center North, 1161 21st Avenue South, Nashville, Tennessee 37232-2310. Tel: 615-322-3793; Fax: 615-322-0734; E-mail: henry.c.manning@vanderbilt.edu.
These authors contributed equally to this paper.
ISSN:1083-3668
1560-2281
DOI:10.1117/1.3533264