Method of treating premature uterine contractions using the optically active R(-)-isomer of albuterol
OwnerE. Charles Pesterfield, Jr.inventor
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Abstract
The optically pure R-isomer of the adrenergic beta-2 agonist albuterol, substantially free of its corresponding S-isomer, has been found to potently inhibit premature uterine contractions in female subjects, suffering from said condition, while avoiding side effects associated with the corresponding S-isomer. A new method is disclosed utilizing the optically pure R(-)-isomer of albuterol for treating premature uterine contractions while minimizing the side effects associated with administration of racemic albuterol.
Claims10
A method of preventing or treating premature uterine contractions in an individual with the R-isomer of albuterol or a pharmaceutically acceptable salt thereof, while reducing side effects associated with administration of the corresponding racemic drug or with the corresponding S-isomer, comprising acutely or chronically administering to an individual, a quantity of said R-isomer or of a pharmaceutically acceptable salt thereof sufficient to result in the reduction or the elimination of premature uterine contractions while simultaneously eliminating or reducing undesirable side effects residing in the corresponding S-isomer, said R-isomer of albuterol or salt thereof being substantially free of its S-isomer.
A method of preventing or treating premature uterine contractions in an individual with R-albuterol or its pharmaceutically acceptable salt, while reducing side effects associated with administration of racemic albuterol, comprising administering to the individual a quantity of R-albuterol or its pharmaceutically acceptable salt, substantially free of its S-isomer, sufficient to result in the relaxation of the uterus while simultaneously reducing undesirable side effects, in combination with at least one additional drug selected from the group consisting of smooth muscle relaxants, antihistamines, antiserotonergics, anticholinergics, leucotriene antagonists, lipoxygenase inhibitors, PAF-antagonists, thromboxane antagonists and metabolic inhibitors.
Dependencies are inferred from the claim text.