IP Library Granted Patent US 6,841,146
Granted Patent B2
US 6,841,146 · App. 10/391,712 · Granted Jan 11, 2005

Spray composition

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 6,841,146
App. No.
10/391,712
Granted
Jan 11, 2005
Kind
B2
Abstract

An aqueous-based sprayable composition comprises a therapeutic or palliative agent, water and a mixture of microcrystalline cellulose and alkali metal carboxyalkylcellulose. In one embodiment, the composition is a non-Newtonian nasal spray exhibiting a very rapid viscosity recovery upon removal of shear forces.

Claims (26)

1. A spray composition comprising water, a soluble therapeutic or palliative agent and a mixture of microcrystalline cellulose and an alkali metal carboxyalkylcellulose, wherein complex viscosity of the composition increases to at least about 10 times a minimum complex viscosity of the composition as measured under high shear conditions, within about 20 seconds after the high shear conditions terminate.

2. The spray composition of claim 1 , wherein the microcrystalline cellulose comprises about 85 to about 95 weight percent of the mixture with alkali metal carboxyalkylcellulose.

3. The spray composition of claim 1 , wherein the alkali metal carboxyalkylcellulose comprises carboxymethylcellulose sodium.

4. The spray composition of claim 1 , wherein the mixture of microcrystalline cellulose and an alkali metal carboxyalkylcellulose comprises about 2.5 to about 5 weight percent.

5. The spray composition of claim 1 , further comprising up to about 10 weight percent of a rheology-modifying polymer.

6. The spray composition of claim 1 , further comprising up to about 10 weight percent of a polymer selected from the group consisting of algin, carageenans, carbomers, galactomannans, hydroxypropyl methylcellulose, hydroxypropyl cellulose, polyethylene glycols, polyvinyl alcohol, polyvinylpyrrolidone, sodium carboxymethyl chitin, sodium carboxymethyl dextran, sodium carboxymethyl starch, xanthan gum and mixtures of any two or more thereof.

7. The spray composition of claim 1 , wherein the therapeutic agent comprises a nasal decongestant.

8. The spray composition of claim 1 , wherein the therapeutic agent comprises a nasal decongestant selected from the group consisting of levmetamfetamine, ephedrine, ephedrine hydrochloride, ephedrine sulfate, naphazoline hydrochloride, oxymetazoline hydrochloride, phenylephrine hydrochloride, propylhexedrine and xylometazoline hydrochloride.

9. The spray composition of claim 1 , wherein the therapeutic agent comprises a topical anesthetic.

10. The spray composition of claim 9 , which is intended for application to oropharyngeal tissue.

11. The spray composition of claim 9 , which is intended for application to the skin.

12. The spray composition of claim 1 , wherein the therapeutic agent comprises a topical anesthetic selected from the group consisting of phenol, hexylresorcinol, salicyl alcohol, benzyl alcohol, dyclonine, dibucaine, benzocaine, buticaine, cetylpyridinium chloride, diperidon, clove oil, menthol, camphor, eugenol, lidocaine, tetracaine, pramoxine and mixtures of any two or more thereof.

13. A nasal spray composition comprising water, a soluble nasal decongestant and a mixture of microcrystalline cellulose and an alkali metal carboxyalkylcellulose, wherein complex viscosity of the composition increases to at least about 10 times a minimum complex viscosity of the composition as measured under high shear conditions, within about 20 seconds after the high shear conditions terminate.

14. The spray composition of claim 13 , wherein the nasal decongestant is selected from the group consisting of levmetamfetamine, ephedrine, ephedrine hydrochloride, ephedrine sulfate, naphazoline hydrochloride, oxymetazoline hydrochloride, phenylephrine hydrochloride, propylhexedrine and xylometazoline hydrochloride.

15. The spray composition of claim 13 , wherein the nasal decongestant comprises oxymetazoline.

16. The spray composition of claim 13 , wherein the microcrystalline cellulose comprises about 85 to about 95 weight percent of the mixture with alkali metal carboxyalkylcellulose.

17. The spray composition of claim 13 , wherein the alkali metal carboxyalkylcellulose comprises carboxymethylcellulose sodium.

18. The spray composition of claim 13 , wherein the mixture of microcrystalline cellulose and an alkali metal carboxyalkylcellulose comprises about 2.5 to about 5 weight percent.

19. The spray composition of claim 13 , wherein the mixture of microcrystalline cellulose and an alkali metal carboxyalkylcellulose comprises about 2.5 to about 3.5 weight percent.

20. The spray composition of claim 13 , wherein the mixture of microcrystalline cellulose and an alkali metal carboxyalkylcellulose comprises about 3 weight percent.

21. The spray composition of claim 13 , further comprising up to about 10 weight percent of a rheology-modifying polymer.

22. The spray composition of claim 13 , further comprising up to about 10 weight percent of a polymer selected from the group consisting of algin, carageenans, carbomers, galactomannans, hydroxypropyl methylcellulose, hydroxypropyl cellulose, polyethylene glycols, polyvinyl alcohol, polyvinylpyrrolidone, sodium carboxymethyl chitin, sodium carboxymethyl dextran, sodium carboxymethyl starch, xanthan gum and mixtures of any two or more thereof.

23. The spray composition of claim 13 , further comprising about 0.5 to about 5 weight percent of polyvinylpyrrolidine.

24. The spray composition of claim 1 , wherein the mixture of microcrystalline cellulose and an alkali metal carboxyalkylcellulose comprises about 2.5 to about 3.5 weight percent.

25. The spray composition of claim 1 , wherein the mixture of microcrystalline cellulose and an alkali metal carboxyalkylcellulose comprises about 3 weight percent.

26. The spray composition of claim 13 , further comprising mometasone furoate monohydrate.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2019
From: BAYER CONSUMER CARE HOLDINGS LLC
To: BAYER HEALTHCARE LLC
Reel/Frame 048698/0224 →
CHANGE OF NAME Recorded Mar 19, 2019
From: MSD CONSUMER CARE HOLDINGS LLC
To: BAYER CONSUMER CARE HOLDINGS LLC
Reel/Frame 048638/0753 →
CHANGE OF NAME Recorded Jul 14, 2011
From: SCHERING-PLOUGH HEALTHCARE PRODUCTS, INC.
To: MSD CONSUMER CARE, INC.
Reel/Frame 026594/0364 →