IP Library Granted Patent US 8,092,837
Granted Patent B2
US 8,092,837 · App. 11/741,333 · Granted Jan 10, 2012

Fibrin based glue with functionalized hydrophilic polymer protein binding agent

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Quick Facts
Patent No.
US 8,092,837
App. No.
11/741,333
Granted
Jan 10, 2012
Kind
B2
Abstract

The present invention provides a non-liquid biomaterial that may be used as a surgical sealant, a suture support, a blood flow controller, an adhesion reducing agent, an adhesion preventing agent, a tissue support, a tissue filler, a wound dressing or a combination thereof. The non-liquid biomaterial may comprise a blood derived material such as plasma, platelet poor plasma, platelet rich plasma or a material derived from blood containing tissue aspirate, such as bone marrow aspirate, a protein binding agent and a polymerizing agent. Methods for making and using the non-liquid biomaterial are also provided.

Claims (20)

1. A biomaterial comprising: a blood product mixture and a hemostatic agent comprising thrombin, the biomaterial being formed by initially mixing together a blood derived material and a hydrophilic polymer to form a blood product mixture, and

then subsequently mixing the blood product mixture with the hemostatic agent comprising thrombin to form a non-liquid biomaterial;

wherein the hydrophilic polymer has a protein binding functionality of at least two and is selected from at least one of poly(ethylene glycol), poly(ethylene oxide), poly(vinyl alcohol), poly(vinylpyrrolidine), poly(ethyloxazoline, poly(ethylene glycol-co-poly(propylene glycol) block polymer, and copolymers or combinations thereof; and

wherein the blood derived material is plasma, platelet rich plasma or platelet poor plasma.

2. The biomaterial of claim 1 wherein the thrombin is selected from at least one of autologous thrombin, xenogenic thrombin and recombinant thrombin and is present in an amount of from about 10 U/ml to about 1000 U/ml with respect to the blood product solution.

3. The biomaterial of claim 1 wherein the plasma, platelet rich plasma or platelet poor plasma is concentrated.

4. The biomaterial of claim 1 wherein the plasma, platelet rich plasma or platelet poor plasma is concentrated from about 1-fold to about 8-fold.

5. The biomaterial of claim 1 wherein the hydrophilic polymer has a molecular weight of from about 1,000 to about 30,000.

6. The biomaterial of claim 1 wherein the hydrophilic polymer comprises at least three arms.

7. The biomaterial of claim 1 wherein the hydrophilic polymer has a protein binding functionality from 2 to about 8.

8. The biomaterial of claim 1 , wherein the protein binding functionality of the hydrophilic polymer comprises an ester or an aldehyde.

9. The biomaterial of claim 1 , wherein the protein binding functionality of the hydrophilic polymer comprises an active ester of N-hydroxy succinimide.

10. The biomaterial of claim 1 , wherein the hydrophilic polymer has a concentration of from about 0.25 mg/ml to about 10 tm/ml with respect to the blood derived material.

11. The biomaterial of claim 1 wherein the hemostatic agent converts fibrinogen in the blood derived material to fibrin.

12. The biomaterial of claim 1 wherein the hemostatic agent activates platelets.

13. The biomaterial of claim 1 , wherein the blood derived material further comprises an anticoagulant; and wherein at least one of the blood product mixture or the hemostatic agent further comprises Ca 2+ .

14. The biomaterial of claim 1 wherein the non-liquid biomaterial is formed within one minute after mixing the blood product solution and the hemostatic agent.

15. The biomaterial of claim 1 wherein the non-liquid biomaterial is a surgical sealant, a suture support, a blood flow controller, an adhesion reducing agent, an adhesion preventing agent, a tissue support, a tissue filler, a tissue or cell scaffold, a wound dressing or a combination thereof.

16. The biomaterial of claim 1 wherein the non-liquid biomaterial further comprises tissue regenerative cells.

17. The biomaterial of claim 1 wherein the non-liquid biomaterial comprises cells derived from tissue aspirate, stem cells, osteoblasts, fibroblasts, erythrocytes, leukocytes, adipocytes or combinations thereof.

Assignments (4)
RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT REEL 023505/ FRAME 0241 Recorded Nov 23, 2015
From: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
To: LVB ACQUISITION, INC.; BIOMET, INC.; BIOMET 3I, LLC; BIOMET BIOLOGICS, LLC.; BIOMET EUROPE LTD.; BIOMET FAIR LAWN LLC; BIOMET HOLDINGS LTD.; BIOMET INTERNATIONAL LTD.; BIOMET LEASING, INC.; BIOMET MANUFACTURING CORPORATION; BIOMET MICROFIXATION, LLC; BIOMET ORTHOPEDICS, LLC; BIOMET SPORTS MEDICINE, LLC; BIOMET TRAVEL, INC.; BIOLECTRON, INC.; CROSS MEDICAL PRODUCTS, LLC; ELECTR-OBIOLOGY, LLC; EBI HOLDINGS, LLC; EBI, LLC; EBI MEDICAL SYSTEMS, LLC; BIOMET FLORIDA SERVICES, LLC; INTERPORE CROSS INTERNATIONAL, LLC; INTERPORE SPINE, LTD.; KIRSCHNER MEDICAL CORPORATION; IMPLANT INNOVATIONS HOLDINGS, LLC
Reel/Frame 037155/0082 →
CHANGE OF NAME Recorded Jul 19, 2013
From: BIOMET MANUFACTURING CORPORATION
To: BIOMET MANUFACTURING, LLC
Reel/Frame 030837/0737 →
SECURITY AGREEMENT Recorded Nov 12, 2009
From: LVB ACQUISITION, INC.; BIOMET, INC.; BIOMET 3I, LLC; BIOMET BIOLOGICS, LLC; BIOMET EUROPE LTD.; BIOMET FAIR LAWN LLC; BIOMET HOLDINGS LTD.; BIOMET INTERNATIONAL LTD.; BIOMET LEASING, INC.; BIOMET MANUFACTURING CORPORATION; BIOMET MICROFIXATION, LLC; BIOMET ORTHOPEDICS, LLC; BIOMET SPORTS MEDICINE, LLC; BIOMET TRAVEL, INC.; BIOLECTRON, INC.; CROSS MEDICAL PRODUCTS, LLC; ELECTRO-BIOLOGY, LLC; EBI HOLDINGS, LLC; EBI, LLC; EBI MEDICAL SYSTEMS, LLC; BIOMET FLORIDA SERVICES, LLC; INTERPORE CROSS INTERNATIONAL, LLC; INTERPORE SPINE, LTD.; KIRSCHNER MEDICAL CORPORATION; IMPLANT INNOVATIONS HOLDINGS, LLC
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT FOR THE SECURED PARTIES
Reel/Frame 023505/0241 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2007
From: ENYART, HILARY; HOEPPNER, JACY; LEACH, MICHAEL D.; STEGER, SHON; SUNDARAMURTHY, SONA
To: BIOMET MANUFACTURING CORP.
Reel/Frame 019238/0564 →