Aerosol formulation for the inhalation of beta-agonists

• US 20050256115A1
• Filed: 05/10/2005
• Published: 11/17/2005
• Est. Priority Date: 05/14/2004
• Status: Abandoned Application

• Current Assignee: Boehringer Ingelheim International GmbH (C.H. Boehringer Sohn AG & Co. KG)
• Original Assignee: Boehringer Ingelheim International GmbH (C.H. Boehringer Sohn AG & Co. KG)
• Inventors: Aven, Michael
• Application Number:
  US11/125,756
• Publication Number:
  US 20050256115A1
• Time in Patent Office: Days
• US Class Current: 514/230.500
• CPC Class Codes: A61K 31/538 ortho- or peri-condensed with carbocyclic ring systems
• CPC Class Codes: A61P 11/00 Drugs for disorders of the respiratory system

Abstract

The present invention relates to a propellant-free aerosol formulation which [contains] one or more compounds of general formula 1
wherein the groups R¹, R², R³ and X⁻ may have the meanings given in the claims and specification, for inhalation.

Claims

1. ) A pharmaceutical formulation comprising as sole active substance one or more compounds of formula 1

wherein

R¹ denotes hydrogen, C₁-C₄-alkyl, C₁-C₄-alkoxy or halogen;

R² denotes hydrogen, C₁-C₄-alkyl, C₁-C₄-alkoxy or halogen;

R³ denotes hydrogen, c₁-C₄-alkyl, c₁-C₄-alkoxy, halogen, oh, —

O-C₁-C₄-alkylene-COOH or —

O-C₁-C₄-alkylene-COO-C₁-C₄-alkyl,

X⁻

denotes an anion with a single negative charge, preferably an anion with a single negative charge selected from the group consisting of chloride, bromide, iodide, sulphate, phosphate, methanesulphonate, nitrate, maleate, acetate, benzoate, citrate, salicylate, trifluoroacetate, fumarate, tartrate, oxalate, succinate, benzoate and p-toluenesulphonate,

optionally in the form of their tautomers, enantiomers, mixtures of enantiomers, racemates or solvates,

at least one pharmacologically acceptable acid, optionally other pharmacologically acceptable excipients and/or complexing agents and, as solvent, water, ethanol or a mixture of water and ethanol.

2. ) The pharmaceutical formulation according to claim 1, characterised in that it contains one or more compounds of formula 1, wherein

R¹ denotes hydrogen, methyl, ethyl, fluorine or chlorine;

R² denotes hydrogen, methyl, ethyl, fluorine or chlorine;

R³ denotes hydrogen, methyl, ethyl, propyl, OH, methoxy, ethoxy, fluorine, chlorine, bromine, —

O—

CH₂—

COOH, —

O—

CH₂—

COOmethyl or —

O—

CH₂—

COOethyl, —

O—

CH₂—

CH₂COOH, —

O—

CH₂—

CH₂COOmethyl or —

O—

CH₂—

CH₂COOethyl, —

O—

CH₂—

CH₂—

CH₂COOH, —

O—

CH₂—

CH₂—

CH₂COOmethyl or —

O—

CH₂—

CH₂—

CH₂COOethyl;

X⁻

denotes an anion with a single negative charge wherein the anion with a single negative charge is selected from the group consisting of chloride, bromide, iodide, sulphate, phosphate, methanesulphonate, nitrate, maleate, acetate, benzoate, citrate, salicylate, trifluoroacetate, fumarate, tartrate, oxalate, succinate, benzoate and p-toluenesulphonate,

optionally in the form of their tautomers, enantiomers, mixtures of enantiomers, racemates or solvates.

3. ) The pharmaceutical formulation according to claim 1, characterised in that it contains one or more compounds of formula 1, wherein

R¹ denotes hydrogen or methyl;

R² denotes hydrogen or methyl;

R³ denotes methyl, OH, methoxy, fluorine, chlorine, bromine, —

O—

CH₂—

COOH or —

O—

CH₂—

COOethyl;

X⁻

denotes an anion with a single negative charge selected from the group consisting of chloride, bromide, sulphate, methanesulphonate, maleate, acetate, benzoate, citrate, salicylate, trifluoroacetate, fumarate, tartrate and succinate;

optionally in the form of their tautomers, enantiomers, mixtures of enantiomers, racemates or solvates.

4. ) The pharmaceutical formulation according to claim 1, wherein the pharmacologically acceptable acid is selected from inorganic acids hydrochloric acid, hydrobromic acid, nitric acid, sulphuric acid and phosphoric acid or from the organic acids ascorbic acid, citric acid, malic acid, tartaric acid, maleic acid, succinic acid, fumaric acid, acetic acid, formic acid and propionic acid.

5. ) The pharmaceutical formulation according to claim 1, characterised by a pH of 2.5 to 6.5.

6. ) The pharmaceutical formulation according to claim 1, characterised in that it contains benzalkonium chloride as excipient.

7. ) The pharmaceutical formulation according to claim 6, characterised in that the content of benzalkonium chloride is 1 to 50 mg per 100 ml solution.

8. ) The pharmaceutical formulation according to claim 1, characterised in that the content of formula 1′

is about 0.1 to 1600 mg per 100 ml solution.

9. ) The pharmaceutical formulation according to claim 1, characterised in that it contains a complexing agent as a further ingredient.

10. ) The pharmaceutical formulation according to claim 9, characterised in that the content of complexing agent is 1 to 50 mg per 100 ml solution.

11. ) The pharmaceutical formulation according to claim 1, characterised in that it contains pure water as solvent.

12. ) The pharmaceutical formulation according to claim 1, characterised in that it contains pure ethanol as solvent.

13. ) The pharmaceutical formulation according to claim 1, characterised in that it contains a mixture of water and ethanol as solvent.

14. ) The pharmaceutical formulation according to claim 13, characterised in that it contains as solvent a mixture of water and ethanol, wherein the percentage proportion of ethanol by mass is in the range from 5 to 99% ethanol.

15. ) A pharmaceutical formulation containing as sole active substance a free base of formula 1′

wherein the groups R¹, R² and R³ may have the meanings given in claim 1, optionally in the form of their tautomers, enantiomers, mixtures of enantiomers, racemates or solvates, at least one pharmacologically acceptable acid, optionally other pharmacologically acceptable excipients and/or complexing agents

and, as solvent, water, ethanol or a mixture of water and ethanol.

16. ) A pharmaceutical composition comprising a compound according to claim 1 or claim 15 and a pharmaceutically acceptable carrier or excipient thereof.

17. ) An inhalation kit comprising a pharmaceutical formulation according to claim 1 or claim 15 and an inhaler suitable for nebulising said pharmaceutical formulation.

18. ) The inhalation kit according to claim 17, wherein the inhaler is a Respimat®

.