Granted Patent B2

US 7,871,608 · App. 12/197,617 · Granted Jan 18, 2011

Abstract

Claims (23)

1. A method of treating a subject suffering from a disorder susceptible to improvement with plasmin comprising administering to the subject a therapeutically effective amount of a composition comprising:

a reversibly inactivated, acidified plasmin, the plasmin being substantially free of a plasminogen activator; and

a low buffering capacity buffer;

wherein the composition is a solution suitable for pharmaceutical use that can be raised to physiological pH by adding no more than about 5 volumes of serum to the solution relative to a volume of the solution.

2. The method of claim 1 , wherein the plasmin is Glu-plasmin, Lys-plasmin, midi-plasmin, mini-plasmin, or micro-plasmin.

3. The method of claim 1 , wherein the composition further comprises an aqueous carrier.

4. The method of claim 1 , wherein the composition further comprises an anticoagulant.

5. The method of claim 1 , wherein the composition has a pH of about 2.5 to about 4.

6. The method of claim 1 , wherein the composition is a sterile solution suitable for parenteral administration to humans.

7. The method of claim 1 , wherein the buffer comprises at least one acid.

8. The method of claim 7 , wherein the acid is in the concentration range of about 1 mM to about 100 mM.

9. The method of claim 1 , wherein the buffer comprises a carboxylic acid, at least one amino acid, a dipeptide, an oligopeptide which includes the at least one amino acid, or a combination thereof.

10. The method of claim 1 , wherein the buffer is formic acid, acetic acid, citric acid, hydrochloric acid, lactic acid, malic acid, tartaric acid, benzoic acid, serine, threonine, methionine, glutamine, alanine, glycine, isoleucine, valine, aspartic acid, or combinations thereof.

11. The method of claim 1 , wherein the plasmin is in the concentration range of about 0.01 mg/ml to about 50 mg/ml.

12. The method of claim 1 , wherein the composition further comprises a stabilizing agent.

13. The method of claim 12 , wherein the stabilizing agent is a polyhydric alcohol, a salt, citrulline, or combinations thereof.

14. The method of claim 12 , wherein the stabilizing agent is a pharmaceutically acceptable carbohydrate, salt, glucosamine, thiamine, niacinamide, citrulline, or combinations thereof.

15. The method of claim 12 , wherein the stabilizing agent is a sugar or sugar alcohol selected from the group consisting of glucose, maltose, mannitol, sorbitol, sucrose, lactose, trehalose, and combinations thereof.

16. The method of claim 12 , wherein the stabilizing agent is selected from the group consisting of monosacchrides, disaccharides, polysaccharides, polyhydric alcohols, and combinations thereof.

17. The method of claim 12 , wherein the stablizing agent is a carbohydrate having a concentration in the range of about 0.2% w/v to about 20% w/v.

18. The method of claim 12 , wherein the stabilizing agent is selected from the group consisting of sodium chloride, potassium chloride, magnesium chloride, calcium chloride, manganese chloride, and combinations thereof.

19. The method of claim 12 , wherein the stabilizing agent is selected from the group consisting of a salt, glucosamine, thiamine, niacinamide, and combinations thereof, and the concentration of the stabilizing agent is in the range of about 0.01M to about 1M.

20. The method of claim 1 , wherein the composition can be raised to physiological pH by adding no more than about one volume of serum to the solution relative to a volume of the solution.

Assignments (29)