IP Library Granted Patent US 6,998,140
Granted Patent B2
US 6,998,140 · App. 09/926,484 · Granted Feb 14, 2006

Dispersion comprising a non-ionic emulsifier

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Quick Facts
Patent No.
US 6,998,140
App. No.
09/926,484
Granted
Feb 14, 2006
Kind
B2
Abstract

The invention relates to a dispersion suitable for use as coating agent and binder for pharmaceutical forms, having a solids content of 10–70% by weight consisting of a) from 90 to 99% by weight of a methacrylate copolymer consisting of at least 90% by weight of (meth)acrylate monomers containing neutral radicals and having a glass transition temperature Tg of from −20° C. to +20° C. as determined by the DSC method, and b) 1–10% by weight of a nonionic emulsifier having an HLB of from 15.2 to 17.3.

Claims (26)

1. A dispersion, comprising:

a solids content of 10–70% by weight comprising

a) from 90 to 99% by weight of a methacrylate copolymer comprising at least 90% by weight of a (meth)acrylate monomer containing at least one neutral radical and having a glass transition temperature Tg of from −20° C. to +20 C. as determined by the DSC method, and

b) 1–10% by weight of a nonionic emulsifier having an HLB of from 15.2 to 17.3.

2. The dispersion according to claim 1 , wherein the methacrylate copolymer comprises from 20 to 50% by weight of methyl methacrylate, and from 80 to 50% by weight of ethyl acrylate.

3. The dispersion according to claim 1 , wherein the nonionic emulsifier is selected from the group consisting of ethoxylated fatty acid ester, ethoxylated fatty acid ethers, ethoxylated sorbitan ethers, ethoxylated alkyl-phenols, glycerol esters, glycerol sugar esters, wax derivatives and mixtures thereof.

4. The dispersion according to claim 1 , wherein the nonionic emulsifier is selected from the group consisting of polyoxyethyleneglycerol monolaurate, polyoxyethyleneglycerol monostearate, polyoxyethylene-20-cetyl stearate, polyoxyethylene-25-cetyl stearate, polyoxyethylene (25)-oxypropylene monostearate, polyoxyethylene-20-sorbitan monopalmitate, poly-oxyethylene-16-tert-octylphenol, polyoxyethylene-20-cetyl ether, polyethylene glycol(1000) monocetyl ether, ethoxylated castor oil, polyoxyethylene sorbitol-lanolin derivatives, polyoxyethylene(25)propylene glycol stearate, polyoxyethylenesorbitol esters, polyoxyethylene-20-sorbitan monopalmitate, polyoxyethylene-16-tert-octylphenol, polyoxyethylene-20-cetyl ether and mixtures thereof.

5. A process for preparing the dispersion claimed in claim 1 , comprising: emulsion polymerizing said (meth)acrylate monomer.

6. A pharmaceutical composition, comprising:

the dispersion as claimed in claim 1 , and a pharmaceutically active substance.

7. The pharmaceutical composition as claimed in claim 6 , wherein said pharmaceutically active substance comprises an active substance selected from the group consisting of morphine, morphine derivatives, tramadol, acetylsalicylic acid, diclofenac, indomethacin, lonazolac, ibuprofen, ketoprofen, propyphenazone, naproxen, paracetamol, flurbiprofen, dimetindene, quinidine, metoprolol, propanolol, oxprenolol, pindolol, atenolol, metoprolol, disopyramide, verapamil, diltiazem, gallopamil, nifedipine, nicardipine, nisoldipine, nimodipine, amlodipine, theophylline, salbutamol, terbutaline, ambroxol, aminophylline, choline theophyllinate, pyridostigmine, piretanide, furosemide, pentoxifylline, naftidrofuryl, buflomedil, xanthinol nicotinate, bencyclane, allopurinol, norephedrine, chlorphenamine, isosorbide mononitrate, isosorbide dinitrate, glycerol trinitrate, molsidomine, bezafibrate, fenofibrate, gemfibrozil, cerivastatin, prava-statin, fluvastatin, lovastatin, atorvastatin, simvastatin, xanthinol, methoclopramide, amitriptyline, dibenzepine, venlafaxine, thioridazine, oxazepam, lithium, nitrofurantoin, dry plant extract, diprophylline, ascorbic acid, potassium, pharmaceutical salts thereof and mixtures thereof.

8. A pharmaceutical composition, comprising:

an active pharmaceutical substance and the dispersion as claimed in claim 1 , wherein said active pharmaceutical substance is bound or coated with said dispersion.

9. A method for coating a pharmaceutical composition, comprising:

encapsulating the pharmaceutical composition with the dispersion claimed in claim 1 .

10. The dispersion according to claim 1 , wherein the methacrylate copolymer comprises from 20 to 50% by weight of methyl methacrylate and from 80 to 50% by weight of ethyl acrylate and from 0 to 10% by weight of methacrylic acid.

11. The dispersion according to claim 1 , wherein the nonionic emulsifier is polyoxyethylene-25-cetyl stearate.

12. The pharmaceutical composition claimed in claim 7 , wherein said pharmaceutical salts are potassium salts.

13. The dispersion as claimed in claim 1 , wherein said (meth)acrylate monomer contains C 1 to C 4 alkyl radicals.

14. The dispersion as claimed in claim 1 , wherein said (meth)acrylate monomer is methyl methacrylate, ethyl acrylate, methyl acrylate or mixtures thereof.

15. The dispersion as claimed in claim 1 , wherein not more than 10% by weight of said (meth)acrylate monomers contains an anionic radical.

16. The dispersion as claimed in claim 1 , wherein said copolymer comprises methacrylic acid.

17. The dispersion as claimed in claim 1 , wherein said emulsifier is polyoxyethylene-25-cetyl stearate, polyoxyethylene-20-sorbitan monopalmitate, polyoxyethylene-16-tert-octylphenol, polyoxyethylene-20-cetyl ether or mixtures thereof.

18. A coating agent, comprising:

the dispersion as claimed in claim 1 .

19. The dispersion according to claim 1 , wherein said emulsifier does not crystallize after drying said dispersion.

Assignments (3)
CHANGE OF NAME Recorded Feb 11, 2020
From: EVONIK ROEHM GMBH
To: ROEHM GMBH
Reel/Frame 051893/0671 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 11, 2020
From: ROEHM GMBH
To: EVONIK DEGUSSA GMBH
Reel/Frame 051893/0727 →
CHANGE OF NAME Recorded Feb 11, 2020
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 051894/0001 →