IP Library Granted Patent US 7,019,113
Granted Patent B2
US 7,019,113 · App. 10/444,662 · Granted Mar 28, 2006

Reversible modification of membrane interaction

View Patent ↗
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 7,019,113
App. No.
10/444,662
Granted
Mar 28, 2006
Kind
B2
Abstract

An process for the reversible modification of membrane interaction of a compound is described. Modification of membrane interaction can be used to facilitate delivery of molecules to cells in vitro and in vivo. The described modifiers, which are used to reversibly inactivate the membrane active compounds, can also be utilized as cross-linkers or to reverse the charge of a molecule.

Claims (18)

1. A process for reversibly modifying an amine-containing compound to inhibit interaction of the compound with membrane lipids comprising covalently attaching to the amine on the compound a substituted maleic anhydride.

2. The process of claim 1 wherein modification of the compound consists of reducing positive charge on the compound.

3. A process for reversibly modifying a cell penetrating compound to inhibit interaction of the compound with membrane lipids comprising: covalently attaching a substituted maleic anhydride to the cell penetrating compound.

4. The process of claim 3 wherein the cell penetrating compound is selected from the group consisting of: arginine-rich peptide, VP22 peptide, ANTp peptide and short guanidinium-rich polymer.

5. The process of claim 3 wherein the cell penetrating compound consists of a TAT peptide.

6. A process fur modifying a membrane permeable drug to reversibly inhibit membrane permeability of the drug comprising: covalently attaching a substituted maleic anhydride to the drug.

7. The process of claim 1 wherein the substituted maleic anhydride consists of a disubstituted maleic anhydride.

8. The process of claim 7 wherein the disubstituted maleic anhydride consists of a negatively charged disubstituted maleic anhydride.

9. The process of claim 8 wherein the negatively charged disubstituted maleic anhydride consists of 2-propionic-3-methylmaleic anhydride.

10. The process of claim 1 wherein the substituted maleic anhydride consists of a bifunctional maleic anhydride.

11. The process of claim 10 wherein the substituted maleic anhydride consists of a thioester substituted maleic anhydride.

12. The process of claim 11 wherein the thioester substituted maleic anhydride consists of CDM-thioester.

13. The process of claim 1 wherein the substituted maleic anhydride consists of a PEG substituted maleic anhydride.

14. The process of claim 1 wherein the compound consists of a membrane active compound.

15. The process of claim 14 wherein modification of the membrane active compound inactivates the membrane activity of the compound.

16. The process of claim 14 wherein the membrane active compound consists of melittin.

17. The process of claim 1 wherein modification of the compound consists of reversing the charge of the compound.

18. The process of claim 1 wherein modification reduces toxicity of the compound.

Assignments (3)
CHANGE OF NAME Recorded Feb 26, 2014
From: ROCHE MADISON INC.
To: ARROWHEAD MADISON INC.
Reel/Frame 032302/0843 →
CHANGE OF NAME Recorded Apr 6, 2009
From: MIRUS BIO CORPORATION
To: ROCHE MADISON INC.
Reel/Frame 022629/0791 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2006
From: ROZEMA, DAVID B.; WAKEFIELD, DARREN; WOLFF, JON A.; EKENA, KIRK; HAGSTROM, JAMES E.
To: MIRUS BIO CORPORATION
Reel/Frame 017232/0537 →