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Molecular Pharmacology, Vol 13, 113-121, Copyright © 1977 by the American Society for Pharmacology and Experimental Therapeutics
1 Departments of Anesthesiology, Pathology, and Biochemistry, Division of Health Affairs, University of North
Carolina, Chapel Hill, North Carolina 27514
This study of solvent effects on halothane 19F nuclear magnetic resonance chemical
shifts was undertaken in order to elucidate environmental factors contributing to
observed halothane 19F NMR shifts in the presence of phospholipid suspensions in
aqueous media. Halothane 19F NMR chemical shifts are correlated by Hildebrands
function or refractive index for non-hydrogen-bonding solvents. No significant correlation was observed for other solvent properties, such as dielectric constant. Water and
alcohols show positive deviations from the correlation with
. Halothane molecules
associated with both synthetic and natural phospholipid multilayer vesicles show significant line broadening of the fluorine signal and appear to be in an environment which
may be characterized by a
value of 9.3 ± 0.3 (cal/cm3)1/2 by comparison with the
observed correlation of chemical shift with
in isotropic solvent systems.
Note:
ACKNOWLEDGMENTS
The authors express their appreciation to Drs. P.
D. Ellis, E. T. Fossel, W. Freeman, M. K. Jain, C.
N. Reilley, A. K. Solomon, and K. Sugioka for simultaneously discouraging, helpful, and stimulating conversations, and to Dr. D. Harris for obtaining
spectra on the XL-100 spectrometer.
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