IP Library Granted Patent US 10,952,964
Granted Patent B2
US 10,952,964 · App. 16/435,061 · Granted Mar 23, 2021

Targeted delivery of drugs to the myometrium via polypeptides that bind to the oxytocin receptor

Inventors: Susan Hua (Charlestown, AU); Jonathan Paul (Cardiff, AU); Roger Smith (Newcastle, AU)
Assignee: The University of Newcastle
A61K9/1271A61K31/137A61K31/18A61K31/4015A61K31/4422
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Quick Facts
Patent No.
US 10,952,964
App. No.
16/435,061
Granted
Mar 23, 2021
Kind
B2
Abstract

Provided herein are methods and compositions for the targeted delivery to myometrial tissue of one or more agents capable of regulating contractility of myometrial tissue, wherein the one or more agents are contained or encapsulated within a polymeric delivery vehicle conjugated with one or more molecules that recognizes and/or is capable of binding, directly or indirectly, to the oxytocin receptor.

Claims (10)

1. A method for targeted delivery to myometrial tissue of one or more agents capable of inhibiting or reducing contractility of said myometrial tissue, comprising exposing myometrial tissue to an effective amount of the one or more agents, wherein the one or more agents are contained or encapsulated within a polymeric delivery vehicle conjugated with anti-oxytocin receptor antibodies or a peptide that binds to the oxytocin receptor,

wherein the polymeric delivery vehicles containing the agent(s) are administered to a pregnant female mammal, and

wherein the administration is to slow down labour or prevent premature labour.

2. A method according to claim 1 , wherein the polymeric delivery vehicle is a liposome.

3. A method according to claim 1 , wherein the polymeric delivery vehicle is coated with anti-oxytocin receptor antibodies or a peptide that binds to the oxytocin receptor.

4. A method according to claim 1 , wherein the anti-oxytocin receptor antibodies bind to an extracellular domain of the oxytocin receptor.

5. A method according to claim 1 , wherein the one or more agents are selected from calcium channel inhibitors, β 2 -adrenergic receptor agonists and phosphodiesterase inhibitors.

6. A method according to claim 5 , wherein the calcium channel inhibitor is nifedipine.

7. A method according to claim 5 , wherein the β 2 -adrenergic receptor agonist is salbutamol or ritodrine.

8. A method according to claim 5 , wherein the phosphodiesterase inhibitor is rolipram.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2019
From: HUA, SUSAN; PAUL, JONATHAN; SMITH, ROGER
To: NEWCASTLE INNOVATION LIMITED
Reel/Frame 051296/0653 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2019
From: NEWCASTLE INNOVATION LIMITED
To: THE UNIVERSITY OF NEWCASTLE
Reel/Frame 051297/0027 →
Priority Claims (1)
AU 2013901842 · May 23, 2013 · national
Continuity (2)
Continuation 14892927
Related Publication 20190290584A1 · Sep 26, 2019