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Fluoroquinolone compositions

a technology of fluoroquinolone and composition, applied in the field of pharmaceutical compositions, can solve the problems of preventing the use of nalidixic acid in other types of infections, unable to meet the needs of patients, and difficult to swallow solid oral pharmaceutical compositions, etc., and achieve the effect of convenient administration

Inactive Publication Date: 2007-08-23
IDEXX LABORATORIES
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Nalidixic acid, however, has several limitations that prevents its use in other types of infections.
Solid oral pharmaceutical compositions, such as tablets and capsules, can be difficult for some individuals to swallow.
For example, pediatric patients often find it difficult to swallow solid oral pharmaceutical compositions.
Furthermore, solid oral pharmaceutical compositions can be difficult to administer to animals, such as cats.
Fluoroquinolones, however, are difficult to dissolve in liquids.

Method used

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Examples

Experimental program
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Effect test

example 1

Oral Liquid Enrofloxacin Composition—Zinc Cation and Strawberry Flavored

[0294] 2.3 gr of enrofloxacin and 0.7024 gr of zinc acetate were mixed well with 15 mL of de-ionized water in a 100 ml volumetric flask. To the resulting composition was added 60 mL of glycerol with mixing to provide a homogeneous solution. To this solution was added 5 mL of strawberry flavor and the resulting solution mixed well. The volume of the solution was made up to 100 mL with glycerol and mixed well to provide a liquid oral enrofloxacin formulation. The concentration of enrofloxacin in the formulation is 23 mg / mL.

[0295] A pharmaceutical composition similar to that described above can be prepared except that the flavoring is not included in the composition and the pharmaceutical composition is sterile filtered to provide an injectable pharmaceutical composition.

example 2

Oral Liquid Enrofloxacin Composition—Magnesium Cation and Strawberry Flavored

[0296] 575 mg of enrofloxacin and 114 mg of magnesium acetate (0.8 mL of 1 M aqueous solution, commercially available from Sigma-Aldrich of Milwaukee, Wis.) were mixed well with 3.75 mL of de-ionized water in a 25 mL volumetric flask. To the resulting composition was added 15 mL of glycerol with mixing to provide a homogeneous solution. To the resulting solution was added 1.25 mL of strawberry flavor with mixing. The volume of the solution was made up to 25 mL with glycerol and mixed well to provide a liquid oral enrofloxacin formulation. The concentration of enrofloxacin in the formulation is 23 mg / mL.

[0297] A pharmaceutical composition similar to that described above can be prepared except that the flavoring is not included in the composition and the pharmaceutical composition is sterile filtered to provide an injectable pharmaceutical composition.

example 3

Oral Liquid Enrofloxacin Composition—Magnesium Cation and Mint Flavored

[0298] 575 mg of enrofloxacin and 114 mg of magnesium acetate (0.8 mL of 1 M aqueous solution, commercially available from Sigma-Aldrich of Milwaukee, Wis.) were mixed well with 3.75 mL of de-ionized water in a 25 ml volumetric flask. To the resulting composition was added 15 mL of glycerol with mixing to provide a homogeneous solution. To the resulting solution was added 1.25 mL of mint oil with mixing. The volume of the solution was made up to 25 mL with glycerol and mixed well to provide a liquid oral enrofloxacin formulation. The concentration of enrofloxacin in the formulation is 23 mg / mL.

[0299] A pharmaceutical composition similar to that described above can be prepared except that the flavoring is not included in the composition and the pharmaceutical composition is sterile filtered to provide an injectable pharmaceutical composition.

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PUM

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Abstract

The invention relates to pharmaceutical compositions comprising (i) a fluoroquinolone, (ii) a salt formed between a carboxylate anion and a divalent metal cation, (iii) a liquid comprising an organic solvent selected from the group consisting of glycerol, propylene glycol, glycerol formal, and (iv) optionally water. The invention further relates to methods of treating or preventing a condition in an animal comprising administering to the animal in need thereof a pharmaceutical composition of the invention.

Description

CROSS REFERENCE TO RELATED APPLICATIONS [0001] Not Applicable. STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT [0002] Not Applicable. INCORPORATION BY REFERENCE OF MATERIAL SUBMITTED ON A COMPACT DISC [0003] Not Applicable. FIELD OF THE INVENTION [0004] The present invention relates to pharmaceutical compositions comprising (i) a fluoroquinolone, (ii) a salt formed between a carboxylate anion and a divalent metal cation, and (iii) a liquid comprising (a) an organic solvent selected from the group consisting of glycerol, propylene glycol, glycerol formal, and mixtures thereof and (b) optionally water. The invention further relates to methods of treating or preventing a condition in an animal comprising administering to the animal in need thereof a pharmaceutical composition of the invention. BACKGROUND OF THE INVENTION [0005] The following discussion of the background of the invention is merely provided to aid the reader in understanding the invention and is not admit...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/496A61K31/4709
CPCA61K9/0019A61K9/0095A61K9/08A61K31/4709A61K47/40A61K47/02A61K47/10A61K47/12A61K31/496A61P31/04
Inventor MURTHY, YERRAMILLI V. S. N.
Owner IDEXX LABORATORIES
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