IP Library Granted Patent US 9,050,331
Granted Patent B2
US 9,050,331 · App. 10/588,513 · Granted Jun 9, 2015

Pharmaceutical formulations comprising paraoxonase

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Quick Facts
Patent No.
US 9,050,331
App. No.
10/588,513
Granted
Jun 9, 2015
Kind
B2
Abstract

The present invention provides a pharmaceutical formulation comprising paraoxonase (PON), a purification and stabilization method of PON, and an agent for prophylactic and/or therapeutic treatment of a disease resulting from ischemia reperfusion and/or cerebral infarction containing PON as an active ingredient.

Claims (22)

1. A method for improving prognosis, neurological symptoms, or motor dysfunction of a disease resulting from cerebral infarction, comprising:

intravenously administering an effective amount of paraoxonase in combination with an effective amount of 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate to improve one of prognosis, neurological symptoms and motor dysfunction of a disease resulting from cerebral infarction to a patient in need thereof,

wherein the paraoxonase is a purified paraoxonase having a specific activity of not less than 500 U/A 280 .

2. The method of claim 1 , wherein the intravenously administering of the effective amount of paraoxonase comprises intravenously administering the effective amount of paraoxonase in the presence of a polyol.

3. The method of claim 1 , wherein the intravenously administering of the effective amount of paraoxonase comprises intravenously administering the effective amount of paraoxonase in the presence of a glycerol.

4. The method of claim 1 , wherein the paraoxonase is a purified paraoxonase having a specific activity in a range of 500 to 2000 U/A 280 .

5. The method of claim 1 , wherein the paraoxonase is a purified paraoxonase having a specific activity in a range of 500 to 1800 U/A 280 .

6. The method of claim 1 , wherein the intravenously administering of the effective amount of paraoxonase comprises intravenously administering an effective amount of a detergent to stabilize an activity of the paraoxonase in combination.

7. The method of claim 1 , wherein the intravenously administering of the effective amount of paraoxonase comprises intravenously administering 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate in an amount of about 0.01 w/v % to about 1 w/v % in combination with paraoxonase.

8. The method of claim 1 , wherein the intravenously administering of the effective amount of paraoxonase comprises intravenously administering 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate in an amount of 0.05 w/v % to 0.5 w/v % in combination with paraoxonase.

9. The method of claim 1 , wherein the intravenously administering of the effective amount of paraoxonase comprises intravenously administering 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate in an amount of 0.05 w/v % in combination with paraoxonase.

10. The method of claim 9 , wherein paraoxonase is administered at a concentration of 10 mg/mL.

11. A method for improving prognosis, neurological symptoms, or motor dysfunction of a disease resulting from cerebral infarction, comprising:

intravenously administering an effective amount of paraoxonase in combination with 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate in an amount of about 0.01 w/v % to 1 w/v % once daily for 1 to 14 days to improve one of prognosis, neurological symptoms and motor dysfunction of a disease resulting from cerebral infarction to a patient in need thereof,

wherein the intravenously administering of the combination is started within 48 hours after onset of a disease resulting from cerebral infarction, and the paraoxonase is a purified paraoxonase having a specific activity of not less than 500 U/A 280 .

12. The method of claim 11 , wherein the combination is administered intravenously once daily for 1 to 7 days.

13. The method of claim 12 , wherein the combination is administered intravenously within 24 hours after onset of a disease resulting from cerebral infarction.

14. The method of claim 12 , wherein the combination is administered intravenously within 12 hours after onset of a disease resulting from cerebral infarction.

15. The method of claim 12 , wherein the combination is administered intravenously within 3 hours after onset of a disease resulting from cerebral infarction.

16. The method of claim 11 , wherein the intravenously administering of the effective amount of paraoxonase comprises intravenously administering 3[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate in an amount of 0.05 w/v % to 0.5 w/v % in combination with paraoxonase.

17. The method of claim 11 , wherein the intravenously administering of the effective amount of paraoxonase comprises intravenously administering 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate in an amount of 0.05 w/v % in combination with paraoxonase.

18. The method of claim 17 , wherein paraoxonase is administered at a concentration of 10 mg/mL.

Assignments (2)
CHANGE OF NAME Recorded Apr 17, 2008
From: MITSUBISHI PHARMA CORPORATION
To: MITSUBISHI TANABE PHARMA CORPORATION
Reel/Frame 020838/0701 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 1, 2007
From: ASAHARA, NAOMI; HASHIMOTO, MOTONORI; YUKI, SATOSHI
To: MITSUBISHI PHARMA CORPORATION
Reel/Frame 019367/0198 →