IP Library Granted Patent US 8,551,450
Granted Patent B2
US 8,551,450 · App. 12/782,783 · Granted Oct 8, 2013

Targeting vector-phospholipid conjugates

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Quick Facts
Patent No.
US 8,551,450
App. No.
12/782,783
Granted
Oct 8, 2013
Kind
B2
Abstract

Peptide vectors having high KDR binding affinity and processes for making such vectors are provided. The peptide vectors may be conjugated to phospholipids and included in ultrasound contrast agent compositions. Such ultrasound contrast agents are particularly useful in therapeutic and diagnostic methods, such as in imaging KDR-containing tissue and in the evaluation and treatment of angiogenic processes associated with neoplastic conditions. The present invention also provides processes for the large scale production of highly pure dimeric and monomeric peptide phospholipid conjugates as well as precursor materials used to form the conjugates. The present invention further provides processes for the large scale production of highly pure peptide phospholipid conjugates which contain very low levels of TFA.

Claims (16)

1. An ultrasound contrast agent composition comprising a gas-filled microbubble comprising a peptide-phospholipid conjugate:

which comprises SEQ ID NO: 4.

2. The ultrasound contrast agent of claim 1 comprising two or more components selected from the group consisting of DSPC, DPPG, DPPA, DSPA, DPPE, DSPE-PEG1000, DSPE-PEG2000, palmitic acid and stearic acid.

3. The composition of claim 2 wherein the contrast agent comprises DSPC and DPPG.

4. The composition of claim 2 wherein the contrast agent comprises DSPE-PEG1000, DPPE and DPPG.

5. An ultrasound contrast agent composition comprising a gas-filled microbubble comprising a peptide-phospholipid conjugate:

which comprises SEQ ID NO: 1.

6. The ultrasound contrast agent of claim 5 comprising two or more components selected from the group consisting of DSPC, DPPG, DPPA, DSPA, DPPE, DSPE-PEG1000, DSPE-PEG2000, palmitic acid and stearic acid.

7. The composition of claim 6 wherein the contrast agent comprises DSPE-PEG2000, DSPC and DSPA.

8. The composition of claim 6 wherein the contrast agent comprises DSPC and DSPA.

9. The composition of claim 6 wherein the contrast agent comprises DSPE-PEG2000, DSPC and stearate.

10. The composition of claim 6 wherein the contrast agent comprises DSPE-PEG1000, DSPC and stearate.

11. A peptide monomer comprising Ac-Arg-Ala-Gln-Asp-Trp-Tyr-Tyr-Asp-Glu-Ile-Leu-Ser-Met-Ala-Asp-Gln-Leu-Arg-His-Ala-Phe-Leu-Ser-Gly-Gly-Gly-Gly-Gly-Lys-NH2.

12. A peptide-phospholipid conjugate comprising one or more peptide monomers of claim 11 .

13. The peptide-phospholipid conjugate of claim 12 , wherein the phospholipid is selected from the group consisting of: phosphatidylethanolamines and modified phospatidylethanolamines.

14. The peptide-phospholipid conjugate of claim 13 wherein the phospholipid is DSPE-PEG2000.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2010
From: BRACCO INTERNATIONAL B.V.
To: BRACCO SUISSE SA
Reel/Frame 024990/0087 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 21, 2010
From: BUSSAT, PHILIPPE; CHERKAOUI, SAMIR; FAN, HONG (HELEN); LAMY, BERNARD; NANJAPPAN, PALANIAPPA; PILLAI, RADHAKRISHNA; POCHON, SIBYLLE; SONG, BO; SWENSON, ROLF E.
To: BRACCO INTERNATIONAL B.V.
Reel/Frame 024422/0826 →