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1.
Phys Rev Lett ; 106(25): 256103, 2011 Jun 24.
Article in English | MEDLINE | ID: mdl-21770657

ABSTRACT

Surface self-diffusion has been measured for an organic glass for the first time. The flattening of 1000 nm surface gratings of liquid indomethacin occurs by viscous flow at 12 K or more above the glass transition temperature and by surface diffusion at lower temperatures. Surface diffusion is at least 10(6) times faster than bulk diffusion, indicating a highly mobile surface. Our data suggest that surface diffusion is the leading mechanism of surface evolution for organic glasses at micrometer to nanometer length scales.


Subject(s)
Glass/chemistry , Indomethacin/chemistry , Organic Chemicals/chemistry , Diffusion , Kinetics , Surface Properties
2.
Anal Chem ; 71(9): 1767-72, 1999 May 01.
Article in English | MEDLINE | ID: mdl-10330907

ABSTRACT

Ratiometric and lifetime-based sensors have been designed for cellular detection of nitric oxide. These sensors incorporate cytochrome c', a hemoprotein known to bind nitric oxide selectively. The cytochrome c' is labeled with a fluorescent reporter dye, and changes in this dye's intensity or fluorescence lifetime are observed as the protein binds nitric oxide. The ratiometric sensors are composed of dye-labeled cytochrome c' attached to the optical fiber via colloidal gold, along with fluorescent microspheres as intensity standards. These ratiometric sensors exhibit linear response, have fast response times (< or = 0.25 s), and are completely reversible. The sensors are selective over numerous common interferents such as nitrite, nitrate, and oxygen species, and the limit of detection is 8 microM nitric oxide. The lifetime-based measurements are made using free, dye-labeled cytochrome c' in solution and have a limit of detection of 30 microM nitric oxide. The use of these two techniques has allowed measurement of intra- and extracellular macrophage nitric oxide. Employing the ratiometric fiber sensors gave a multicell culture average extracellular nitric oxide concentration of 210 +/- 90 microM for activated macrophages, while an average intracellular concentration of 160 +/- 10 microM was determined from the lifetime-based measurements of dye-labeled cytochrome c' in the macrophage cytosol. Microscopic adaptation of the lifetime-based methods described here would allow direct correlation of intracellular nitric oxide levels with specific cellular activities, such as phagocytosis.


Subject(s)
Biosensing Techniques , Cytochrome c Group/metabolism , Macrophages/metabolism , Nitric Oxide/analysis , Nitric Oxide/metabolism , Animals , Arginine/analogs & derivatives , Arginine/pharmacology , Cytochrome c Group/chemistry , Cytosol/metabolism , Enzyme Inhibitors/pharmacology , Extracellular Matrix/metabolism , Fluorescence , Fluorescent Dyes/chemistry , Hydrogen Peroxide/pharmacology , Hydrogen-Ion Concentration , Interferon-gamma/pharmacology , Lipopolysaccharides/pharmacology , Macrophages/drug effects , Mice , Mice, Inbred BALB C , Microspheres , Spectrometry, Fluorescence/methods , Superoxides/metabolism , Tetradecanoylphorbol Acetate/pharmacology
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