IP Library Patent Application 12028361
Patent Application
App. No. 12/028,361

TREATMENT OF TISSUE DEFECTS WITH A THERAPEUTIC COMPOSITION

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Patent No.
US None
App. No.
12/028,361
Abstract

Methods for treating a tissue defect include applying therapeutic compositions to the tissue defect. Treatment of a tissue defect, including wound healing can be enhanced by a process including obtaining blood compatible with the subject, fractionating the blood from the subject to produce a blood component, obtaining stromal cells from the subject, combining the stromal cells and the blood component to form a therapeutic composition, and delivering the therapeutic composition to the tissue defect. Therapeutic compositions for promoting wound healing include isolated stromal cells and a blood component.

Claims (43)

1 . A method for treating a tissue defect in a human subject comprising:

obtaining blood compatible with the subject;

fractionating said blood to produce a blood component, said blood component selected from the group consisting of platelet-poor plasma, concentrated platelet-poor plasma, platelet-rich plasma, and combinations thereof;

obtaining stromal cells compatible with the subject;

combining said stromal cells and said blood component to form a therapeutic composition; and

administering said therapeutic composition to the tissue defect.

2 . The method for treating a tissue defect in a human subject according to claim 1 , wherein fractionating said blood to produce a blood component comprises centrifugation of said blood to form said blood component.

3 . The method for treating a tissue defect in a human subject according to claim 2 , wherein centrifugation of said blood to form said blood component comprises centrifuging said blood in a container including at least one buoy that is able to separate said blood into three or more fractions having different densities.

4 . The method for treating a tissue defect in a human subject according to claim 3 , wherein centrifuging blood in a container comprises displacing a buoy during centrifugation so as to separate said blood into platelet-poor plasma, platelet-rich plasma, and red blood cells.

5 . The method for treating a tissue defect in a human subject according to claim 1 , wherein said stromal cells are isolated from tissue obtained from said subject.

6 . The method for treating a tissue defect in a human subject according to claim 1 , wherein said stromal cells are washed at least once with a fluid selected from the group consisting of platelet-rich plasma, platelet-poor plasma, concentrated platelet-poor plasma, whole blood, and combinations thereof.

7 . The method for treating a tissue defect in a human subject according to claim 1 , wherein the isolated stromal cells are able to differentiate into cells selected from the group consisting of chondrocytes, endothelial cells, osteoblasts, myocytes, neural cells, glial cells, adipocytes, pericytes, cardiomyocytes, epithelial cells, fibroblasts, and combinations thereof.

8 . The method for treating a tissue defect in a human subject according to claim 1 , further comprising administering to the tissue defect an additive selected from the group consisting of a cytokine, bioactive material, scaffold, buffer, or combinations thereof.

9 . The method for treating a tissue defect in a human subject according to claim 1 , further comprising administering to the tissue defect a platelet activator selected from the group consisting of thrombin, autologous thrombin, CaCl 2 , a coagulation factor, or combinations thereof.

10 . The method for treating a tissue defect in a human subject according to claim 1 , wherein the defect is a diabetic ulcer, a defect associated with peripheral vascular disease, cardiac muscle damage associated with myocardial infarct, tendinosis, a defect at a site of chemotherapy and/or radiotherapy, or a cartilage defect.

11 . A method for treating a tissue defect in a human subject comprising:

obtaining blood and stromal cells compatible with the subject;

combining said blood and said stromal cells;

centrifuging said blood and said stromal cells so that said stromal cells sediment with a blood component comprising platelet-rich plasma;

isolating said stromal cells and said blood component to form a therapeutic composition; and

administering said therapeutic composition to said tissue defect.

12 . The method for treating a tissue defect in a human subject according to claim 11 , further comprising washing said stromal cells with platelet-poor plasma or concentrated platelet-poor plasma prior to combining said blood and said stromal cells.

13 . The method for treating a tissue defect in a human subject according to claim 11 , wherein obtaining blood and stromal cells compatible with the subject comprises:

drawing blood from the subject; and

isolating stromal cells from adipose tissue harvested from the subject.

14 . A method for treating a tissue defect in a human subject according to claim 13 , wherein isolating stromal cells from adipose tissue harvested from the subject comprises:

enzymatically digesting said adipose tissue;

separating stromal cells from adipocytes; and

washing said stromal cells with platelet-poor plasma, concentrated platelet-poor plasma, platelet-rich plasma, or whole blood.

15 . The method for treating a tissue defect in a human subject according to claim 11 , wherein obtaining blood and stromal cells compatible with the subject comprises:

drawing blood from the subject; and

isolating stromal cells from bone marrow aspirate harvested from the subject.

16 . A method for treating a tissue defect in a human subject according to claim 11 , wherein administering said therapeutic composition to the tissue defect further comprises administering an additive selected from the group consisting of a cytokine, bioactive material, scaffold, platelet activator, and combinations thereof.

17 . The method for treating a tissue defect in a human subject according to claim 11 , further comprising administering to the tissue defect a platelet activator selected from the group consisting of thrombin, CaCl 2 , a coagulation factor, or combinations thereof.

18 . The method for treating a tissue defect in a human subject according to claim 11 , further comprising washing said stromal cells with platelet-poor plasma or concentrated platelet-poor plasma prior to combining said blood and said stromal cells.

19 . A therapeutic composition for treating a tissue defect, comprising:

isolated stromal cells; and

a blood component, wherein said blood component is selected from the group consisting of platelet-poor plasma, concentrated platelet-poor plasma, platelet-rich plasma, whole blood, and combinations thereof.

20 . The therapeutic composition for treating a tissue defect according to claim 19 , wherein said isolated stromal cells are cultured cells.

21 . The therapeutic composition for treating a tissue defect according to claim 19 , wherein said isolated stromal cells and said blood component are derived from the same subject.

22 . The therapeutic composition for treating a tissue defect according to claim 19 , wherein the stromal cells are selected from the group consisting of adipose stromal cells, bone marrow derived stromal cells, and combinations thereof.

23 . The therapeutic composition for treating a tissue defect according to claim 19 , wherein said isolated stromal cells are able to differentiate into cells selected from the group consisting of chondrocytes, endothelial cells, osteoblasts, myocytes, neural cells, glial cells, adipocytes, pericytes, cardiomyocytes, epithelial cells, fibroblasts, and combinations thereof.

24 . The therapeutic composition for treating a tissue defect according to claim 19 , further comprising an additive selected from the group consisting of a cytokine, bioactive material, scaffold, buffer, 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 Feb 10, 2011
From: BIOMET BIOLOGICS, INC.
To: BIOMET BIOLOGICS, LLC
Reel/Frame 025787/0954 →
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 Sep 2, 2009
From: MCKALE, JAMES M.; HIGGINS, JOEL C.; SWIFT, MATTHEW
To: BIOMET BIOLOGICS, INC.
Reel/Frame 023185/0540 →