US2023233419A1PendingUtilityA1

Pharmaceutical formulation

Assignee: CUTTING EDGE TECH LLCPriority: Nov 18, 2016Filed: Apr 3, 2023Published: Jul 27, 2023
Est. expiryNov 18, 2036(~10.3 yrs left)· nominal 20-yr term from priority
Inventors:Larry P. Bleier
A61K 6/69A61C 3/00A61K 31/65A61C 5/40A61K 31/327A61K 6/15A61K 6/52A61K 6/58A61K 9/06A61K 33/40A61K 47/02A61K 9/006A61K 9/0063
78
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Claims

Abstract

A pharmaceutical formulation for topical dental administration or medical (e.g., implant) treatment, including effective amounts of: at least one antimicrobial compound; at least one peroxide source compound; and at least one gel agent. Also disclosed are methods of oral anatomy treatment. The pharmaceutical formulation and treatment methods provide the patient with oral anatomy benefits including, for example, decreased or arrested gum recession; decreased or arrested bone recession; decreased or arrested bone mass loss; decreased or eliminated pain; decreased or eliminated bleeding; decreased or eliminated swelling; enhanced regeneration of bone; enhanced soft tissue repair; or a combination thereof.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of oral anatomy treatment, comprising:
 administering to a patient in need of such administration an effective amount of a topical dental pharmaceutical formulation comprising:
 at least one antimicrobial compound in an effective amount from 5 to 90 weight % of the total weight of the formulation; 
 at least one peroxide source compound in an effective amount from 1.5 to 44 weight % of the total weight of the formulation; and 
 at least one gel agent in an effective amount from 1.0 to 90 weight % of the total weight of the formulation, 
   
       wherein at least one condition is minimized or eliminated and the condition is selected from:
 bleeding of the patient's gums; 
 swelling of the patient's gums; 
 experiencing a pain sensation in the patient's gums or teeth; 
 receding of the patient's gums; 
 receding of the patient's tooth-support bone; 
 loss of the patient's tooth-support bone mass; or a combination thereof, compared to the patient without the administration of the topical dental pharmaceutical formulation. 
 
     
     
         2 . The method of  claim 1 , further comprising applying an anesthetic to at least one root of the patient's teeth before, during, after, or a combination thereof, the administration of the topical dental pharmaceutical formulation. 
     
     
         3 . The method of  claim 1 , further comprising topically administering to the patient in an effective amount of at least one growth-factor enhanced matrix material comprising a human growth factor and an osteoconductive matrix, wherein the topical administration of the matrix material is accomplished before, during, after, or a combination thereof, the administration of the topical dental pharmaceutical formulation. 
     
     
         4 . The method of  claim 1 , further comprising systemically administering to the patient an effective amount of at least one antimicrobial compound in an effective amount, wherein the systemic administration of at least one antimicrobial compound is accomplished before, during, after, or a combination thereof, the administration of the topical dental pharmaceutical formulation. 
     
     
         5 . The method of  claim 1 , wherein the receding of the patient's gums, the receding of the patient's tooth-support bone, loss of the patient's tooth-support bone mass, or a combination thereof are eliminated. 
     
     
         6 . The method of  claim 1 , wherein the administering to a patient an effective amount of the topical dental pharmaceutical formulation comprises at least one of:
 the amount of the formulation administered to the patient in a treatment session;   the duration of contact of the formulation with the patient's oral anatomy having at least one condition;   the frequency the formulation is administered to the patient's affected oral areas, or combinations thereof.   
     
     
         7 . The method of  claim 1 , wherein administering to a patient an effective amount of a topical dental pharmaceutical formulation is accomplished free of one or more of: general anesthesia; local anesthetics; or analgesics. 
     
     
         8 . The method of  claim 1 , further comprising flushing the patient's mouth with one or more washes to accomplish at least one of: remove excess or residual topical dental pharmaceutical formulation; avoid patient swallowing the topical dental pharmaceutical formulation, or both. 
     
     
         9 . The method of  claim 1 , wherein administering to a patient an effective amount of the topical dental pharmaceutical formulation provides superior wound healing to the patient who has had oral surgery compared to the patient without the administration of the topical dental pharmaceutical formulation. 
     
     
         10 . The method of  claim 1 , wherein administering the topical dental pharmaceutical formulation to a patient in need of such administration provides synergistic results, including:
 decreased or arrested gum recession;   decreased or arrested tooth support bone recession;   decreased or arrested tooth support bone mass loss;   decreased or eliminated bleeding of the oral anatomy;   decreased or eliminated swelling of the oral anatomy;   decreased or eliminated pain sensation of the oral anatomy;   enhanced regeneration of bone;   enhanced soft tissue repair; or a combination thereof.   
     
     
         11 . The method of  claim 1 , wherein administering to a patient an effective amount of the topical dental pharmaceutical formulation provides oral prophylaxis to the patient.

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