Scaffold and method for implanting cells
An organ implant, such as a heart implant, including a support structure having a plurality of pores and defining passages configured for the growth of blood vessels; and stem cells from at least one soft tissue source of a patient deposited into the pores of the support structure is described. The implant is configured to repair a portion of an organ of the patient.
1. A heart implant comprising:
a support structure comprising:
an interior vascular scaffold defining a plurality of passages configured to facilitate growth of blood vessels within the support structure,
wherein the passages are configured to facilitate the growth of capillaries, arterioles, and venules within the support structure, and
a tissue scaffold defining a plurality of pores, wherein the pores are configured to receive and facilitate growth of a plurality of cells and/or stem cells therein to grow at least one tissue,
wherein the implant is configured to repair a portion of a heart of a patient.
2. The heart implant of claim 1 , further comprising fibroblast and endothelial cells harvested from at least one soft tissue source of the patient, deposited into the pores of the support structure, and cultured and exposed to environmental conditions.
3. The heart implant of claim 1 , wherein the implant is at least one of a biologic implant and a graft.
4. The heart implant of claim 1 , wherein the support structure further comprises at least one of a hydrophilic material and collagen.
5. The heart implant of claim 1 , wherein the stem cells are harvested from the patient by at least one of a robotic and haptic system.
6. The heart implant of claim 1 , wherein implant is configured to be positioned on the heart of the patient with a robotic mechanism.
7. The heart implant of claim 1 , further comprising at least one of therapeutic agents and additives incorporated into the support structure.
8. The heart implant of claim 1 , wherein the at least one environmental condition includes at least one of static mechanical forces, dynamic mechanical forces, chemical stimuli, and electromagnetic stimuli.
9. The heart implant of claim 1 , wherein the implant is configured to be stitched or adhered to the heart of the patient.
10. The heart implant of claim 1 , wherein the cells and/or stem cells are harvested from at least one soft tissue source of a patient and deposited into the pores of the support structure.
11. The heart implant of claim 1 , wherein the stem cells are cultured and exposed to at least one environmental condition.
12. The heart implant of claim 1 , wherein the implant is configured to connect a first side of the support structure to one or more arterioles of the patient and to connect a second side of the support structure to one or more venules of the patient to provide a flow of blood through the support structure.
13. The heart implant of claim 1 , wherein the interior vascular scaffold is configured for flow of blood in one direction.
14. An organ implant comprising:
a support structure comprising:
an interior vascular scaffold defining a plurality of passages configured to facilitate growth of blood vessels within the support structure,
wherein the passages are configured to facilitate the growth of capillaries, arterioles, and venules within the support structure, and
a tissue scaffold defining a plurality of pores, wherein the pores are configured to receive and facilitate growth of a plurality of cells and/or stem cells therein to grow at least one tissue,
wherein the implant is configured to repair a portion of an organ of a patient.
15. The organ implant of claim 14 , wherein the implant is at least one of a biologic implant and a graft.
16. The organ implant of claim 14 , wherein the support structure further comprises at least one of a hydrophilic material and collagen.
17. The organ implant of claim 14 , wherein the stem cells are harvested from the patient by at least one of a robotic and haptic system.
18. The organ implant of claim 14 , wherein implant is configured to be positioned in the patient with a robotic mechanism.
19. The organ implant of claim 14 , further comprising at least one of therapeutic agents and additives incorporated into the support structure.
20. The organ implant of claim 14 , wherein the at least one environmental condition includes at least one of static mechanical forces, dynamic mechanical forces, chemical stimuli, and electromagnetic stimuli.
21. The organ implant of claim 14 , wherein the implant is configured to be stitched or adhered to the organ of the patient.
22. The organ implant of claim 14 , wherein the organ is a heart.
23. The organ implant of claim 14 , wherein the organ is at least one of a blood vessel, brain, intestine, stomach, adrenal gland, liver, pancreas, skeleton, spinal cord, kidney, cartilage, and bone.
24. The organ implant of claim 14 , wherein the cells and/or stem cells are harvested from at least one soft tissue source of a patient and deposited into the pores of the support structure.
25. The organ implant of claim 14 , wherein the stem cells are cultured and exposed to at least one environmental condition.
26. The organ implant of claim 14 , wherein the implant is configured to connect a first side of the support structure to one or more arterioles of the patient and to connect a second side of the support structure to one or more venules of the patient to provide a flow of blood through the support structure.
27. The organ implant of claim 14 , wherein the interior vascular scaffold is configured for flow of blood in one direction.
28. An organ implant comprising:
a support structure comprising:
an interior vascular scaffold defining a plurality of passages configured to facilitate growth of blood vessels within the support structure,
wherein passages are configured to facilitate the growth of capillaries, arterioles, and venules within the support structure, and
a tissue scaffold defining a plurality of pores, wherein the pores are configured to receive and facilitate growth of a plurality of stem cells therein to grow at least one tissue,
wherein the stem cells are harvested from at least one soft tissue source of a patient and deposited into the pores of the support structure, wherein the stem cells are cultured and exposed to at least one environmental condition,
wherein the implant is configured to connect a first side of the support structure to one or more arterioles of the patient and to connect a second side of the support structure to one or more venules of the patient to provide a flow of blood through the support structure,
wherein the support structure further comprises a hydrophilic material that absorbs body fluid, and
wherein the implant is configured to repair a portion of an organ of the patient.