IP Library Granted Patent US 7,319,035
Granted Patent B2
US 7,319,035 · App. 10/688,305 · Granted Jan 15, 2008

Biological scaffolding material

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Quick Facts
Patent No.
US 7,319,035
App. No.
10/688,305
Granted
Jan 15, 2008
Kind
B2
Abstract

The invention provides methods of generating a natural, living biological matrix that can serve as, or form a part of, a natural biological scaffold. The matrix is generated by incubating together biological cells and cellular debris. Any naturally occurring cell can be a biological cell included in the matrix. The invention also provides methods of treating a patient by implanting the matrix or scaffolding into a tissue of the patient, thereby augmenting the existing tissue.

Claims (37)

1. A method of generating a living biological matrix in vitro, the method consisting essentially of: (a) obtaining a cell sample; (b) disrupting the cell sample to create a mixture containing cells and cellular debris; (c) culturing the mixture, retaining the cellular debris, in culture medium for a time and under conditions sufficient to form a living biological matrix in vitro; and (d) separating the biological matrix from the culturing medium, wherein the cells include spore-like cells.

2. The method of claim 1 , wherein the cell sample of step (a) is obtained from a subject who will be a recipient of the biological matrix.

3. The method of claim 1 , wherein the cell sample of step (a) is obtained from a human.

4. The method of claim 1 , wherein the cell sample comprises a bodily fluid.

5. The method of claim 4 , wherein the bodily fluid is blood.

6. The method of claim 4 , wherein the bodily fluid is cerebrospinal fluid.

7. The method of claim 1 , wherein the cell sample comprises a portion of an organ.

8. The method of claim 1 , wherein the cell sample comprises aurticular cartilage.

9. The method of claim 8 , wherein before disrupting the cell sample, the perichondrium is removed from the cartilage.

10. The method of claim 1 , further adding to the separated mixture a component that adds shape, structure, or support to the matrix.

11. The method of claim 10 , wherein the component is a hydrogel or an adhesive.

12. The method of claim 1 , further adding to the matrix an antibiotic.

13. A method of augmenting a tissue defect in a subject, the method comprising: (a) preparing a living biological matrix according to the method of claim 1 ; and (b) administering the living biological matrix to the subject in the region of the tissue defect, wherein the matrix develops a characteristic of the endogenous tissue and thereby augments the tissue defect.

14. The method of claim 13 , wherein the tissue defect is in a muscle.

15. The method of claim 14 , wherein the muscle is the heart.

16. The method of claim 13 , wherein the tissue defect is in a portion of a lung, pancreas, spinal cord, joint, head, neck, skin, kidney, or liver of the subject.

17. The method of claim 13 , wherein the subject is a human.

18. A living biological matrix comprising cells, cell fragments, lipids, and polysaccharides,

wherein the matrix is made by a method consisting essentially of

(a) obtaining a cell sample;

(b) disrupting the cell sample to create a mixture containing cells and cellular debris;

(c) culturing the mixture, retaining the cellular debris, in culture medium for a time and under conditions sufficient to form a living biological matrix in vitro; and

(d) separating the biological matrix from the culturing medium, wherein the cells include spore-like cells.

19. The matrix of claim 18 , further comprising a component that adds shape, structure, or support to the matrix.

20. The matrix of claim 18 , further comprising a hydrogel or adhesive.

21. The matrix of claim 18 , further comprising an antibiotic.

22. The matrix of claim 18 , further comprising a cellular component selected from the group consisting of a fibronectin, laminin, collagen, glycoprotein, thrombospondin, elastin, fibrillin, mucopolysaccharide, glycolipid, heparin sulfate, chondroitin sulfate, keratin sulfate, glycosaminoglycan, and hyaluronic acid.

23. The matrix of claim 18 , wherein the cell sample of step (a) is obtained from a subject who will be a recipient of the biological matrix.

24. The matrix of claim 18 , wherein the cell sample is obtained from a human.

25. The matrix of claim 18 , wherein the cell sample comprises a bodily fluid.

26. The matrix of claim 25 , wherein the bodily fluid is blood.

27. The matrix of claim 25 , wherein the bodily fluid is cerebrospinal fluid.

28. The matrix of claim 18 , wherein the cell sample comprises a part of an organ.

29. The matrix of claim 18 , wherein the cell sample comprises auricular cartilage.

30. The matrix of claim 29 , wherein, before disrupting the cell sample, the perichondrium is removed from the cartilage.

31. The matrix of claim 18 , wherein the biological matrix is added to shape, structure, or support material.

32. A method of augmenting a tissue defect in a subject, the method comprising: (a) obtaining a living biological matrix of claim 18 ; and (b) administering the living biological matrix to the subject in the region of the tissue defect, wherein the matrix develops a characteristic of the endogenous tissue and thereby augments the tissue defect.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 21, 2018
From: VBI TECHNOLOGIES, L.L.C.
To: VCELL THERAPEUTICS, INC.
Reel/Frame 046644/0537 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2007
From: VACANTI, MARTIN P.; VACANTI, CHARLES A.
To: UNIVERSITY OF MASSACHUSETTS
Reel/Frame 019301/0273 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 22, 2005
From: VACANTI, JOSEPH P.; VACANTI, CHARLES A.; VACANTI, MARTIN P.
To: VBI TECHNOLOGIES, L.L.C.
Reel/Frame 016800/0511 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2004
From: UNIVERSITY OF MASSACHUSETTS
To: VACANTI, MARTIN P.; VACANTI, JOSEPH P.; VACANTI, CHARLES A.
Reel/Frame 015334/0359 →