IP Library Granted Patent US 10,456,377
Granted Patent B2
US 10,456,377 · App. 15/490,011 · Granted Oct 29, 2019

Anesthetic comprising tetracaine and a vasoconstrictor for administration to a subject

Inventor: Mark D. Kollar (Fort Collins, CO)
Assignee: St. Renatus, LLC
A61K31/4164A61K9/0043A61K9/14A61K31/245A61K31/4174A61M19/00A61K2300/00
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Quick Facts
Patent No.
US 10,456,377
App. No.
15/490,011
Granted
Oct 29, 2019
Kind
B2
Abstract

The present invention relates to tetracaine based anesthetic formulations and methods of use thereof. The invention further relates to topical formulations of tetracaine and methods of topically anesthetizing body tissues. The present invention also relates to tetracaine based dental anesthetic formulations and methods for anesthetizing the maxillary dental arch using these formulations.

Claims (41)

1. A pharmaceutical composition comprising:

about 3% (w/v) tetracaine HCl;

about 0.05% oxymetazoline HCl; and

a pharmaceutically acceptable carrier, wherein said pharmaceutical composition has a pH of about 4.0-7.5.

2. The pharmaceutical composition according to claim 1 , wherein said composition further comprises benzyl alcohol.

3. The pharmaceutical composition according to claim 2 , wherein said composition comprises about 0.5-2.0% (w/v) benzyl alcohol.

4. The pharmaceutical composition according to claim 3 , wherein said composition comprises about 0.9% (w/v) benzyl alcohol.

5. The pharmaceutical composition according to claim 1 , wherein said composition further comprises hydroxyethylcellulose.

6. The pharmaceutical composition according to claim 5 , wherein said composition comprises about 0.01-1.0% (w/v) hydroxyethylcellulose.

7. The pharmaceutical composition according to claim 6 , wherein said composition comprises about 0.05% (w/v) hydroxyethylcellulose.

8. The pharmaceutical composition according to claim 1 , wherein said pharmaceutically acceptable carrier is water, sugar alcohol, or alcohol.

9. The pharmaceutical composition according to claim 8 , wherein said pharmaceutically acceptable carrier is water.

10. The pharmaceutical composition according to claim 1 , wherein said composition has a pH of 4.0-6.5.

11. The pharmaceutical composition according to claim 1 , wherein said composition has a pH of 5.5-6.5.

12. The pharmaceutical composition according to claim 1 , wherein said composition further comprises a preservative and a viscosity enhancing agent.

13. The pharmaceutical composition according to claim 1 , wherein said composition comprises:

Ingredient

Formulation (% w/v)

Tetracaine hydrochloride, USP

3.00

Oxymetazoline hydrochloride, USP

0.05

Citric acid anhydrous, USP

1.00

Sodium hydroxide, NF

q.s.

Benzyl alcohol, NT

0.90

Hydrochloric acid, NF

q.s.

Hydroxyethylcellulose, NF (5000 cps)

0.05

Purified water, USP

q.s. to 100%.

14. The pharmaceutical composition according to claim 1 , wherein said wherein said composition is in the form of a gel.

15. The pharmaceutical composition according to claim 14 , wherein said gel formulation further comprises: modified celluloses, carbopol homopolymers and copolymers, solvents such as diglycol monoethyl ether, alkylene glycols, dimethyl isosorbide, alcohols, isopropyl myristate, ethyl acetate, C12-C15 alkyl benzoates, mineral oil, squalane, cyclomethicone, capric/caprylic triglycerides, or combinations thereof.

16. The pharmaceutical composition according to claim 1 , wherein said formulation is a foam further comprising an emulsion and a gaseous propellant.

17. The pharmaceutical composition according to claim 16 , wherein said emulsion and a gaseous propellant of said foam formulation further comprises a hydrofluoroalkane (HFA) is selected from the group consisting of: 1,1,1,2-tetrafluoroethane (HFA 134a), and 1,1,1,2,3,3,3-heptafluoropropane (HFA 227).

18. The pharmaceutical composition according to claim 1 , wherein said wherein said composition is in the form of a powder.

19. The pharmaceutical composition according to claim 1 , wherein the particle size of said pharmaceutical composition that is delivered to a subject is about 5-50 microns.

20. The pharmaceutical composition according to claim 1 , wherein the particle size of said pharmaceutical composition that is delivered to a subject is about 10-20 microns.

Assignments (2)
SECURITY INTEREST Recorded Sep 28, 2022
From: ST. RENATUS, LLC
To: TEBO, STEPHEN D
Reel/Frame 061247/0092 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2017
From: KOLLAR, MARK DAVID
To: ST. RENATUS, LLC
Reel/Frame 042042/0123 →
Continuity (5)
Continuation 15058324 · Mar 2, 2016
Continuation 14027033 · Sep 13, 2013
Continuation 13262704
Provisional Application 61166680 · Apr 3, 2009
Related Publication 20170319547A1 · Nov 9, 2017