IP Library Patent Application 11684968
Patent Application
App. No. 11/684,968

COMPOSITIONS AND METHODS OF ENHANCING SURVIVABILITY AND REDUCING INJURY OF CELLS, TISSUES, ORGANS, AND ORGANISMS UNDER HYPOXIC OR ISCHEMIC CONDITIONS

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
11/684,968
Abstract

The present invention provides methods, compositions, and articles of manufacture comprising adenosine, an adenosine derivative or analog, an adenosine receptor agonist, a chemical entity that is taken up by a nucleoside transporter, or a chemical entity that binds to and/or modulates a nucleoside transporter, which protect biological material from cellular or tissue damage resulting from ischemia or hypoxia, including ischemia and hypoxia due to injury, disease, or hemorrhaging. These methods, compositions, and articles of manufacture also enhance the survivability of biological material subjected to ischemia due to injury, disease, or hemorrhage.

Claims (58)

1 . A method for enhancing the survivability of a biological material exposed to ischemic or hypoxic conditions comprising contacting the biological material with an effective amount of a chemical entity selected from the group consisting of:

(a) adenosine or a derivative, analog, or salt thereof;

(b) an adenosine receptor agonist;

(c) a chemical entity that is transported into a cell by a nucleoside transporter; and

(d) a chemical entity that binds to and/or modulates the action of a nucleoside transporter.

2 . The method of claim 1 , wherein the chemical entity is adenosine.

3 . The method of claim 2 , wherein the adenosine is 5′-AMP.

4 . (canceled)

5 . The method of claim 1 , wherein the ischemic or hypoxic condition result from an injury to the material, the onset or progression of a disease that adversely affects the material, or hemorrhaging of the material.

6 - 10 . (canceled)

11 . The method of claim 1 , wherein the biological material is selected from the group consisting of: cells, tissues, organs, organisms, and animals.

12 . (canceled)

13 . The method of claim 11 , wherein the animal is a mammal.

14 - 15 . (canceled)

16 . The method of claim 11 , wherein the biological material is to be transplanted.

17 . The method of claim 1 , wherein the biological material is at risk for reperfusion injury or hemorrhagic shock.

18 - 19 . (canceled)

20 . The method of claim 1 , wherein the chemical entity is adenosine, which is provided to the biological material by infusion at a dosage in the range of 10 μg/kg/min to 350 μg/kg/min.

21 - 24 . (canceled)

25 . The method of claim 1 , further comprising contacting the biological material with an effective amount of an active compound.

26 - 37 . (canceled)

38 . The method of claim 1 , wherein the chemical entity is provided to the biological material as a pharmaceutical composition.

39 . A method for preventing or reducing damage to a biological material exposed to ischemic or hypoxic conditions comprising contacting the biological material with an effective amount of a chemical entity selected from the group consisting of:

(a) adenosine or a derivative, analog, or salt thereof;

(b) an adenosine receptor agonist;

(c) a chemical entity that is transported into a cell by a nucleoside transporter; and

(d) a chemical entity that binds to and/or modulates the action of a nucleoside transporter.

40 . A method for reversibly inhibiting metabolism in a biological material comprising contacting the biological material with an effective amount of a chemical entity selected from the group consisting of:

(a) adenosine or a derivative, analog, or salt thereof;

(b) an adenosine receptor agonist;

(c) a chemical entity that is transported into a cell by a nucleoside transporter; and

(d) a chemical entity that binds to and/or modulates the action of a nucleoside transporter.

41 . (canceled)

42 . A method of enhancing survivability of a mammal suffering from hemorrhagic shock or at risk of hemorrhagic shock, comprising contacting the mammal with an effective amount of a chemical entity selected from the group consisting of:

(a) adenosine or a derivative, analog, or salt thereof;

(b) an adenosine receptor agonist;

(c) a chemical entity that is transported into a cell by a nucleoside transporter; and

(d) a chemical entity that binds to and/or modulates the action of a nucleoside transporter.

43 . (canceled)

44 . A method of enhancing survivability of a mammal undergoing a surgery, comprising contacting the mammal with an effective amount of a chemical entity selected from the group consisting of:

(a) adenosine or a derivative, analog, or salt thereof;

(b) an adenosine receptor agonist;

(c) a chemical entity that is transported into a cell by a nucleoside transporter; and

(d) a chemical entity that binds to and/or modulates the action of a nucleoside transporter.

45 . (canceled)

46 . A method of preserving biological material ex vivo comprising contacting the biological material with a chemical entity selected from the group consisting of:

(a) adenosine or a derivative, analog, or salt thereof;

(b) an adenosine receptor agonist;

(c) a chemical entity that is transported into a cell by a nucleoside transporter; and

(d) a chemical entity that binds to and/or modulates the action of a nucleoside transporter.

47 - 59 . (canceled)

60 . A pharmaceutical composition comprising an active compound, a pharmaceutically acceptable diluent or carrier, and a chemical entity selected from the group consisting of:

(a) adenosine or a derivative, analog, or salt thereof;

(b) an adenosine receptor agonist;

(c) a chemical entity that is transported into a cell by a nucleoside transporter; and

(d) a chemical entity that binds to and/or modulates the action of a nucleoside transporter,

wherein said composition is formulated for administration to a mammal.

61 - 66 . (canceled)

Assignments (7)
RELEASE OF SECURITY INTEREST Recorded Feb 14, 2014
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
To: IKARIA INC.; INO THERAPEUTICS LLC
Reel/Frame 032264/0517 →
CHANGE OF NAME Recorded Dec 14, 2012
From: IKARIA, INC.
To: IKARIA RESEARCH, INC.
Reel/Frame 029475/0615 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2012
From: IKARIA RESEARCH, INC.
To: FRED HUTCHINSON CANCER RESEARCH CENTER
Reel/Frame 028981/0130 →
SECURITY AGREEMENT Recorded Jul 31, 2011
From: IKARIA, INC.; INO THERAPEUTICS LLC
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
Reel/Frame 026676/0954 →
RELEASE OF SECURITY INTEREST Recorded Jul 29, 2011
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
To: IKARIA ACQUISITION INC.; IKARIA, INC.; IKARIA INTERNATIONAL, INC.; IKARIA THERAPEUTICS LLC; IKARIA DEVELOPMENT SUBSIDIARY ONE LLC; IKARIA DEVELOPMENT SUBSIDIARY TWO LLC; IKARIA RESEARCH, INC.; INO THERAPEUTICS LLC
Reel/Frame 026676/0277 →
SECURITY AGREEMENT Recorded Jun 25, 2010
From: IKARIA ACQUISITION INC.; IKARIA, INC.; IKARIA RESEARCH, INC.; INO THERAPEUTICS, LLC; IKARIA INTERNATIONAL, INC.; IKARIA THERAPEUTICS LLC; IKARIA DEVELOPMENT SUBSIDIARY ONE LLC; IKARIA DEVELOPMENT SUBSIDIARY TWO LLC
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
Reel/Frame 024588/0619 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2007
From: TOMASELLI, KEVIN J.; DECKWERTH, THOMAS L.
To: IKARIA, INC.
Reel/Frame 019618/0302 →