Title:  Method for treatment and prevention of mastitis

United States Patent:  6,562,820

Issued:  May 13, 2003

Inventors:  Watts; Jeffrey L. (Portage, MI); Sanchez; Margaret S. (Kalamazoo, MI)

Assignee:  Pharmacia & Upjohn Company (Kalamazoo, MI)

Appl. No.:  888634

Filed:  June 23, 2001

The invention is directed to a method of treatment or prevention of mastitis in mammals with known oxazolidinone anti-bacterial agents, either alone or in combination with exogenous lactoferrins.

SUMMARY OF INVENTION

It has been surprisingly found that oxazolidinone is effective in treating and preventing mastitis caused by Gram-negative, as well as by Gram-positive, pathogens in mammals. It has also been surprisingly found that the anti-mastitis effect of oxazolidinone is enhanced by lactoferrins. The oxazolidinones in the present invention are disclosed in, e.g., U.S. Pat. Nos. 5,688,792 and 6,040,306 and International Publication WO 98/54161, none of which discloses the use of oxazolidinones for treating or preventing mastitis. The disclosure of each of U.S. Pat. Nos. 5,688,792 and 6,040,306 and International Publication WO 98/54161 is incorporated here by reference.

Disclosed is a method of treating or preventing mastitis in a mammal, comprising administration to said mammal during dry period of an therapeutically effective amount of an oxazolidinone selected from the group consisting of (S)-N-[[3-[3-fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]a cetamide and N[[(5S)-3-[3-fluoro-4-(4-thiomorpholinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl ]methyl]acetamide and pharmaceutically acceptable salts thereof.

Also disclosed is a method of treating or preventing mastitis in a mammal, comprising administration to said mammal of an therapeutically effective amount of an oxazolidinone selected from the group consisting of (S)-N-[[3-[3-fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]a cetamide and N-[[(5S)-3-[3-fluoro-4-(4-thiomorpholinyl)phenyl]-2-oxo-1,3-oxazolidin-5-y l]methyl]acetamide and pharmaceutically acceptable salts thereof, in combination with intramammary administration of a lactoferrin in an amount effective to enhance the therapeutic effect of the oxazolidinone.

Further disclosed is a composition for use in the treatment or prevention of mastitis in a mammal, comprising

(a) an oxazolidinone selected from (S)-N-[[3-[3-fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]a cetamide and N-[[(5S)-3-[3-fluoro-4-(4-thiomorpholinyl)phenyl]-2-oxo-1,3-oxazolidin-5-y l]methyl]acetamide or pharmaceutically acceptable salts thereof, and

(b) a lactoferrin at an amount effective to enhance the therapeutic effect of said oxazolidinone.

DETAILED DESCRIPTION OF THE INVENTION

In one embodiment the invention is directed to a method of treating or preventing mastitis in a mammal comprising administering to said mammal a therapeutically effective amount of an oxazolidinone. In another embodiment the invention is directed to a method of treating or preventing mastitis in a mammal comprising administering to said mammal a therapeutically effective amount of an oxazolidinone in combination with administration of an exogenous lactoferrin at amount effective to enhance the therapeutic effect of the oxazolidinone. In a preferred embodiment the present invention is directed to a method of treating or preventing coliform mastitis in a cow by intramammary infusion of an oxazolidinone during the dry period. These and other embodiments of the present invention will readily occur to those of ordinary skill in the art in view of the disclosure therein.

The following description of the invention concerns mainly with dairy cows; however, it is to be understood that the invention is contemplated with the treatment and prevention of mastitis in all types of mammals.

The oxazolidinones in the present invention are disclosed in, e.g., U.S. Pat. Nos. 5,688,792 and 6,040,306 and International Publication WO 98/54161. Examples of suitable oxazolidinones include (S)-N-[[3-[3-fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]a cetamide and N-[[(5S)-3-[3-fluoro-4-(4-thiomorpholinyl)phenyl]-2-oxo-1,3-oxazolidin-5-y l]methyl]acetamide, and pharmaceutically acceptable salts thereof.

The active agents of the subject invention can be given to a mammal either after the onset of mastitis, thus serving as a treatment, or prior to the onset of mastitis, thus serving as a preventive measure. The preventive use of the subject invention is particularly important, for instance, in case mastitis has been detected in some animals in the same herd. It is often desirable to treat all animals in same herd affected in order to eliminate the infection from the whole herd.

Regardless of whether the oxazolidinones are used to treat or prevent mastitis, the oxazolidinones can either be used individually, in combination with each other, or in combination with exogenous lactoferrins. When used during the dry period, the oxazolidinones are preferred to be administered without exogenous lactoferrins. When used during lactation period, the oxazolidinones are preferred to be administered in combination with the administration of exogenous lactoferrins.

Regardless of whether or not lactoferrins are administered, the oxazolidinones are administered either intramammarily or systemically. Intramammary administration, however, is the preferred route when the oxazolidinones are administered in combination with lactoferrins.

When administered intramammarily, the oxazolidinones are administered by injection into the mammary gland, typically by infusion into the teat through the milk canal. The dosage of the oxazolidinones by intramammary injection is from about 25 mg to about 1000 mg, and preferably from about 125 mg to about 500 mg. The oxazolidinones are typically given once.

When administered systemically, the oxazolidinones are administered parenterally or orally, and typically once per day for three or more consecutive days.

When administered orally, the oxazolidinones can be administered in tablet, capsule or liquid (suspension or solution) dosage form in a pharmaceutically acceptable vehicle. The oxazolidinones can also be administered in feed or drinking water. Oral administration in any of these dosage forms is well known in the art and may be carried out in ways common in the animal veterinary medical art. Regardless of the dosage form, the anti-mastitis effective amount of the oxazolidinones is from about 1 mg/kg/day to about 10 mg/kg/day, and preferably from about 2.5 mg/kg/day to about 5 mg/kg/day.

When administered parenterally, the oxazolidinones are administered by subcutaneous, intradermal, intramuscular, or intravenous injection. Parenteral administration is well known in the art and may be carried out in ways common in the animal veterinary or human medical art. When prepared as injectables, the oxazolidinones are usually prepared as liquid formulations in a pharmaceutically acceptable vehicle as is known to those skilled in the art. Regardless of the route, the daily dosage of the oxazolidinones by patrenteral administration is from about 1 mg/kg/day to about 10 mg/kg/day, and preferably from about 2.5 mg/kg/day to about 5 mg/kg/day.

The exact dosage and frequency duration of administration of the oxazolidinones may be changed in response to numerous variables such as the particular oxazolidinone used, the severity of the condition being treated, the general physical condition of the animal, the response of the animal to the treatment, the size of the animal, and whether lactoferrin is used and the dosage thereof.

When lactoferrin is used in combination with the oxazolidinones, the lactoferrin should be administered via intramammary injection, typically by infusion into the teat through the milk canal, and in the same frequency and duration as the oxazolidinones.

Lactoferrin is formulated as a liquid dosage form (solution or suspension) in a pharmaceutically acceptable vehicle as is known to those skilled in the art, and is preferably formulated together with the oxazolidinone as a liquid dosage form (solution or suspension) in a composite formulation.

In another embodiment, the invention is directed to a composition for use in the treatment or prevention of mastitis in a mammal, comprising (a) an oxazolidinone and (b) a lactoferrin at an amount effective to enhance the therapeutic effect of said oxazolidinone. The composition should be prepared in liquid dosage forms in any pharmaceutically acceptable carriers as are known in the art. The composition is preferably administered by intramammary injection.

When formulated together with the oxazolidinone in a composite formulation, the lactoferrin is administered simultaneously with the oxazolidinones. When formulated separately from the oxazolidinones, the lactoferrin is typically administered within 1 hour of the oxazolidinone administration. The amount of lactoferrin effective to enhance the anti-mastitis effect of the oxazolidinones is from about 0.5 g to about 5 gram, and preferably from about 2 g to about 3 g, regardless of the size and species of the animal being treated. The exact dosage and frequency and duration of administration of the lactoferrin may be changed in response to numerous variables, such as the particular oxazolidinone used and the dosage thereof, the severity of the condition being treated, the general physical condition of the animal, the response of the animal to the treatment, and levels of endogenous lactoferrins.

Claim 1 of 31 Claims

What is claimed is:

1. A method of treating or preventing mastitis caused by Escherichia coli in a mammal, comprising administration to said mammal during dry period of an therapeutically effective amount of an oxazolidinone selected from the group consisting of (S)-N-[[3-[3-fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]a cetamide and N-[[(5S)-3-[3-fluoro-4-(4-thiomorpholinyl)phenyl]-2oxo-1,3-oxazolidin-5-yl ]methyl]acetamide and pharmaceutically acceptable salts thereof.
 

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