Anthony Booth - Chester NJ William T. Sherman - Hendersonville NC Peter Raven - Forth Worth TX James L. Caffrey - Burelson TX Thomas Yorio - Burelson TX Michael Forster - Fort Worth TX Patricia Gwirtz - Forth Worth TX
Assignee:
Warner-Lambert Company - Morris Plains NJ
International Classification:
A61K 31135
US Classification:
514 55, 514648, 514649, 514912
Abstract:
The present invention provides pharmaceutical compositions which include (-)-pseudoephedrine and a pharmaceutically acceptable carrier, wherein the (-)-pseudoephedrine is substantially-free of (+)-pseudoephedrine. In another embodiment, the present invention provides methods of relieving nasal and bronchial congestion and of inducing pupil dilation which include administering a pharmaceutically effective amount of (-)-pseudoephedrine to a mammal. The (-)-pseudoephedrine used in the present methods is substantially free of (+)-pseudoephedrine and also substantially free of side effects caused by administration of (+)-pseudoephedrine.
Isotope Labeled Dinitrophenylhydrazines And Methods Of Use
The subject invention provides novel isotope-labeled dinitrophenylhydrazines (DNPHs) and methods for their use in detecting and/or quantifying carbonyl groups in proteins and other analytes. In particular, the present invention provides novel methods for identifying biomarkers of oxidative stress, which can be used to either forecast or detect diseases and/or conditions associated with oxidative stress. In one embodiment of the invention, isotope-labeled DNPHs are derived from [C]chlorobenzene.
Anthony Booth - Chester NJ, US William T. Sherman - Hendersonville NC, US Peter Raven - Fort Worth TX, US James L. Caffrey - Burelson TX, US Thomas Yorio - Burelson TX, US Michael Forster - Fort Worth TX, US Patricia Gwirtz - Fort Worth TX, US
International Classification:
A61K 31/137 A61P 11/00
US Classification:
514653
Abstract:
The present invention provides pharmaceutical compositions which include (−)-pseudoephedrine and a pharmaceutically acceptable carrier, wherein the (−)-pseudoephedrine is substantially-free of (+)-pseudoephedrine. In another embodiment, the present invention provides methods of relieving nasal and bronchial congestion and of inducing pupil dilation which include administering a pharmaceutically effective amount of (−)-pseudoephedrine to a mammal. The (−)-pseudoephedrine used in the present methods is substantially free of (+)-pseudoephedrine and also substantially free of side effects caused by administration of (+)-pseudoephedrine.