IP Library Granted Patent US 7,931,916
Granted Patent B2
US 7,931,916 · App. 12/634,203 · Granted Apr 26, 2011

Composition of biocompatible microparticles of alginic acid for the controlled release of active ingredients by intravenous administration

Assignee: Grifols, S.A.
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Quick Facts
Patent No.
US 7,931,916
App. No.
12/634,203
Granted
Apr 26, 2011
Kind
B2
Abstract

Composition of biocompatible microparticles of alginic acid for the controlled release of active ingredients by intravenous administration. The invention relates to a biocompatible composition which comprises microparticles of alginic acid or its salts and an active ingredient. More particularly, the invention relates to microparticles for the encapsulation of an active ingredient to be administered intravenously to a patient who needs it. These microparticles are of a combination of size sufficient to increase the half-life or survival of the active ingredient in blood, with a low uptake in the liver and a fast cell clearance when administered intravenously.

Claims (12)

1. A biocompatible composition for intravenous administration comprising microparticles of alginic acid or salt thereof less than or equal to 5 μm in size and having a negative Z potential, and wherein the alginic acid or salt thereof is complexed with a therapeutic active ingredient.

2. A composition according to claim 1 , wherein the size of the microparticles is between 1 and 4.5 μm.

3. A composition according to claim 1 , wherein the Z potential is between −70 and 0, not including 0.

4. A composition according to claim 1 , wherein the active ingredient is a peptide, a protein or a hormone.

5. A composition according to claim 4 , wherein the active ingredient is of human, animal, recombinant or transgenic origin.

6. A composition according to claim 4 , wherein the active ingredient exhibits labile biological activity.

7. A composition according to claim 4 , wherein the active ingredient is a blood clotting factor.

8. A composition according to claim 4 , wherein the active ingredient is factor VIII.

9. A composition according to claim 4 , wherein the active ingredient is VWF.

10. A composition according to claim 4 , wherein the active ingredient is the complex formed by FVIII and VWF.

11. A composition according to claim 4 , wherein the active ingredient is factor IX.

12. A composition according to claim 4 , wherein the active ingredient is factor VIIa.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Feb 6, 2017
From: DEUTSCHE BANK AG NEW YORK BRANK
To: GRIFOLS THERAPEUTICS INC.; GRIFOLS SHARED SERVICES NORTH AMERICA INC.; GRIFOLS DIAGNOSTIC SOLUTIONS INC.
Reel/Frame 041638/0527 →
RELEASE OF SECURITY INTEREST RECORDED AT REEL/FRAME 26390/0193 Recorded Jan 25, 2017
From: DEUTSCHE BANK AG NEW YORK BRANCH
To: GRIFOLS, S.A.; GRIFOLS INC.; TALECRIS BIOTHERAPEUTICS, INC.
Reel/Frame 041494/0017 →
SECURITY AGREEMENT Recorded Feb 27, 2014
From: GRIFOLS INC.; GRIFOLS THERAPEUTICS INC.; GRIFOLS-CHIRON DIAGNOSTICS CORP.
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENT
Reel/Frame 032367/0001 →
SECURITY AGREEMENT Recorded Jun 3, 2011
From: GRIFOLS, S.A.; GRIFOLS INC.; TALECRIS BIOTHERAPEUTICS, INC.
To: DEUTSCHE BANK AG NEW YORK BRANCH
Reel/Frame 026390/0193 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 1, 2010
From: GRANCHA GAMON, SALVADOR; NARDI RICART, ANNA; SUNE NEGRE, JOSEPH MARIA; TICO GRAU, JOSEF RAMON; MINARRO CARMONA, MONTSERRAT
To: GRIFOLS, S.A.
Reel/Frame 024007/0888 →
Priority Claims (1)
ES 200803671 · Dec 23, 2008 · national
Continuity (1)
Related Publication 20100159017A1 · Jun 24, 2010