Method of forming a tissue structure by introducing cells into an implanted matrix
View Patent ↗Polymeric materials are used to make a pliable, non-toxic, injectable porous template for vascular ingrowth. The pore size, usually between approximately 100 and 300 microns, allows vascular and connective tissue ingrowth throughout approximately 10 to 90% of the matrix following implantation, and the injection of cells uniformly throughout the implanted matrix without damage to the cells or patient. The introduced cells attach to the connective tissue within the matrix and are fed by the blood vessels. The preferred material for forming the matrix or support structure is a biocompatible synthetic polymer which degrades in a controlled manner by hydrolysis into harmless metabolites, for example, polyglycolic acid, polylactic acid, polyorthoester, polyanhydride, or copolymers thereof. The rate of tissue ingrowth increases as the porosity and/or the pore size of the implanted devices increases. The time required for the tissue to fill the device depends on the polymer crystallinity and is less for amorphous polymers versus semicrystalline polymers. The vascularity of the advancing tissue is consistent with time and independent of the biomaterial composition and morphology.
1. A method of forming a tissue structure comprising the steps of:
(a) implanting into a patient a polymeric matrix lacking cells, wherein said matrix is formed of a biodegradable, biocompatible, synthetic polymer having a porosity between 50% to 95% and a median pore size between 100 and 300 microns; and
(b) introducing dissociated cells into the implanted matrix of step (a),
wherein the implanted matrix in step (b) is vascularized, thereby forming a tissue structure in said patient.
2. The method of claim 1 , wherein the matrix has a pore size between approximately 150 and 250 microns and porosity between 75% and 95% and allows for the introduction of dissociated cells into the implanted matrix without damage to the cells or the patient.
3. The method of claim 1 , wherein the biodegradable polymer is selected from the group consisting of polyanhydrides, polyorthoesters, polyglycolic acid, polylactic acid, copolymers, and blends thereof.
4. The method of claim 1 , wherein said matrix further comprises a wetting agent.
5. The method of claim 1 , wherein the polymer is an amorphous polymer.
6. The method of claim 1 , wherein the polymer is semicystalline polymer.
7. The method of claim 1 , wherein the polymer is amorphous polylactic acid having 90% porosity and 200 micron median pore diameter.
8. The method of claim 1 , wherein said dissociated cells are selected from the group consisting of hepatocytes, pancreatic islet cells, fibroblasts, chondrocytes, osteoblasts, exocrine cells, cells of intestinal origin, bile duct cells, parathyroid cells, thyroid cells, cells of the adrenal-hypothalamic-pituitary axis, heart muscle cells, kidney epithelial cells, kidney tubular cells, kidney basement cells, kidney tubular cells, kidney basement membrane cells, nerve cells, blood vessel cells, cells forming bone and cartilage, and smooth and skeletal muscle cells.
9. The method of claim 1 , wherein the matrix further comprises a material enhancing cell attachment to the polymer, wherein the material overlays the polymer.