IP Library Granted Patent US 9,644,019
Granted Patent B2
US 9,644,019 · App. 14/110,805 · Granted May 9, 2017

Compounds for treating cardiac damage after ischaemia/reperfusion

Inventors: Carlos Zaragoza Sánchez (Madrid, ES); Mónica Gómez Parrizas (Madrid, ES); Begoña Lavín Plaza (Madrid, ES); Carlos Tarín Cerezo (Madrid, ES)
Assignees: Carlos Zaragoza Sánchez; Carlos Tarín Cerezo
C07K14/70503A61K47/48861C07K16/2803G01N33/54346A61K38/00A61K2039/505B82Y5/00C07K2317/76
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Quick Facts
Patent No.
US 9,644,019
App. No.
14/110,805
Granted
May 9, 2017
Kind
B2
Abstract

The present invention relates to the use of an Extracellular Matrix Metalloproteinase Inducer (EMMPRIN) inhibitor for preventing and/or treating cardiac damage arising after an ischemic process followed by reperfusion. The authors of the present invention have observed that EMMPRIN expression increases in subjects who have suffered ischemia/reperfusion, ascertaining that an EMMPRIN inhibitor is capable of reducing the cardiac damage caused after ischemia followed by reperfusion, both in vitro and in vivo.

Claims (11)

1. A nanoparticle comprising on its surface a molecule with Extracellular Matrix Metalloproteinase Inducer (EMMPRIN) binding capacity, wherein the molecule with EMMPRIN binding capacity is the inhibitory AP-9 peptide, the sequence of which is SEQ ID NO: 3.

2. The nanoparticle according to claim 1 comprising an outer phospholipid shell.

3. The nanoparticle according to claim 2 , wherein the phospholipid shell is modified with polyethylene glycol.

4. The nanoparticle according to claim 2 , wherein the phospholipid shell is modified with a fluorophore.

5. The nanoparticle according to claim 1 , wherein the core of the nanoparticle comprises iron oxide.

6. A method for preventing and/or treating cardiac damage arising after ischemia followed by reperfusion comprising administering to a patient in need of such treatment an inhibitory AP-9 peptide, the sequence of which is SEQ ID NO: 3.

7. A method for diagnosing a pathology in which Extracellular Matrix Metalloproteinase Inducer (EMMPRIN) is overexpressed in a subject comprising contacting a sample from said subject with the nanoparticle according to claim 1 and detecting binding of the nanoparticle to said sample, wherein the pathology in which EMMPRIN is overexpressed is myocardial damage.

8. A nanoparticle comprising on its surface an Extracellular Matrix Metalloproteinase Inducer (EMMPRIN) binding molecule and internally an inhibitory AP-9 peptide, the sequence of which is SEQ ID NO: 3, wherein the EMMPRIN binding molecule is an anti-EMMPRIN antibody or the AP-9 peptide, the sequence of which is SEQ ID NO:3.

9. The nanoparticle according to claim 8 comprising an outer phospholipid shell.

10. The nanoparticle according to claim 9 wherein the phospholipid shell is modified with polyethylene glycol.

11. A method for preventing and/or treating cardiac damage arising after ischemia followed by reperfusion comprising administering to a patient in need of such treatment the nanoparticle according to claim 8 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2014
From: ZARAGOZA SANCHEZ, CARLOS; GOMEZ PARRIZAS, MONICA; LAVIN PLAZA, BEGONA; TARIN CEREZO, CARLOS
To: ZARAGOZA SANCHEZ, CARLOS; TARIN CEREZO, CARLOS
Reel/Frame 032179/0308 →
Priority Claims (1)
ES 201031794 · Dec 2, 2010 · national
Continuity (1)
Related Publication 20140148396A1 · May 29, 2014