US2004198816A1PendingUtilityA1

Local anesthetic methods and kits

Assignee: NOVALAR PHARMACEUTICALS INCPriority: May 12, 2000Filed: Apr 5, 2004Published: Oct 7, 2004
Est. expiryMay 12, 2020(expired)· nominal 20-yr term from priority
A61P 43/00A61P 37/06A61P 25/02A61P 25/00A61K 31/44A61P 23/02A61K 31/24A61K 31/445A61K 31/165A61K 31/135Y10S435/81A61K 31/415A61K 31/505
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Claims

Abstract

Methods of reversing local anesthesia are disclosed. The methods comprise administering a local anesthetic and alpha adrenergic receptor agonist to induce local anesthesia followed by reversing anesthesia with a low dose of an alpha adrenergic receptor antagonist. Also disclosed are kits comprising a local anesthetic, an alpha adrenergic receptor agonist and a low dose of an alpha adrenergic receptor antagonist.

Claims

exact text as granted — not AI-modified
1 - 32 . (canceled)  
     
     
         33 . A unit dose of a composition, said unit dose comprising between about 0.0018 mg and about 0.45 mg phentolamine mesylate or a molar equivalent of another alpha adrenergic receptor antagonist and a pharmaceutically acceptable carrier for administration to a mammal.  
     
     
         34 . The unit dose of  claim 33 , comprising between about 0.09 mg and about 0.45 mg phentolamine mesylate or a molar equivalent of another alpha adrenergic receptor antagonist.  
     
     
         35 . The unit dose of  claim 33 , wherein said composition is a solution formulated for administration to a mammal by injection, infiltration, or topical application.  
     
     
         36 . The unit dose of  claim 35 , wherein said solution is formulated for topical application to mucosal tissue.  
     
     
         37 . The unit dose of  claim 36 , wherein said solution is used to impregnate a wafer, pellet, or cotton ball, for application to mucosal tissue.  
     
     
         38 . The unit dose of  claim 33 , wherein said composition is a gel or a paste formulated for topical administration to a mammal.  
     
     
         39 . The unit dose of  claim 38 , wherein said composition is formulated for topical application to mucosal tissue.  
     
     
         40 . The unit dose of  claim 33 , wherein said alpha adrenergic receptor antagonist is selected from the group consisting of phentolamine, phentolamine hydrochloride, phentolamine mesylate, tolazoline, yohimbine, rauwolscine, doxazosine, labetalol, prazosine, tetrazosine and trimazosine.  
     
     
         41 . The unit dose of  claim 40 , wherein said alpha adrenergic receptor antagonist is phentolamine mesylate.  
     
     
         42 . The unit dose of  claim 33 , wherein said unit dose is present in a container that fits into a standard dental local anesthetic syringe.  
     
     
         43 . The unit dose of  claim 42 , wherein said container has a volume of between 1.6 ml and 1.8 ml.  
     
     
         44 . The unit dose of  claim 33 , wherein the unit dose comprises phentolamine mesylate, said unit dose being present in a container that fits into a standard dental local anesthetic syringe.

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