You’re using a public version of DrugPatentWatch with 5 free searches available | Register to unlock more free searches. CREATE FREE ACCOUNT

Last Updated: April 26, 2024

Claims for Patent: 5,855,616


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 5,855,616
Title: Bioartificial pancreas
Abstract:An implantable bioartificial pancreas device having an islet chamber containing glucose responsive and insulin-secreting islets of Langerhans or similar hormone secreting cells, one or more vascularizing chambers open to surrounding tissue, a semi-permeable membrane between the islet and vascularizing chambers that allows passage of small molecules including insulin, oxygen and glucose and does not allow passage of agents of the immune system such as white cells and antibodies, the vascularizing chambers containing a growth factor soaked fibrous or foam matrix having a porosity of about 40 to 95%, the matrix providing small capillary growth and preventing the blood from clotting in the lower chamber.
Inventor(s): Fournier; Ronald L. (Sylvania, OH), Goldblatt; Peter J. (Toledo, OH), Horner; James M. (Sylvania, OH), Sarver; Jeffrey G. (Rossford, OH)
Assignee: The University of Toledo (Toledo, OH)
Application Number:08/711,364
Patent Claims:1. A bioartificial device for implantation into an animal comprising:

a housing having an enclosed chamber containing metabolically active cells,

at least one vascularizing compartment having an opening that provides access to surrounding tissue,

inlet means for supplying cells to the chamber,

outlet means for removing cells from the chamber, and

a semi-permeable membrane separating and in communication with the chamber and vascularizing compartment, the membrane providing immunoprotection of the active cells from the vascularizing compartment and around the implanted device, the membrane allowing passage of small molecules including nutrients and waste products between the chamber and vascularizing compartment and not allowing passage of agents of an immune system to the chamber, and

a biocompatible matrix in the vascularizing compartment to provide a neovascular formation region for enhancing growth of small capillaries for providing efficient mass transfer of substances between the chamber and the capillaries in the vascularizing compartment, the matrix having a porosity of about 40 to 95 percent and interconnecting passageways of about 10 to 120 microns.

2. An organ as defined in claim 1 in which the metabolically active cells are islets of Langerhans.

3. An organ as defined in claim 1 in which the porosity is about 80 to 85 percent.

4. An organ as defined in claim 1 wherein the vascularizing compartment contains at least one growth factor for promoting ingrowth of capillaries into the vascularizing compartment.

5. An organ as defined in claim 1 in which a layer of islets is formed adjacent the membrane, the layer having a thickness and having a diameter that is greater than its thickness.

6. An organ as defined in claim 1 wherein the metabolically active cells produce at least one substance of therapeutic benefit to the animal.

7. An organ as defined in claim 5 wherein the cells produce at least one of parathyroid hormone, dopamine, insulin, glucagon, calcitonin.

8. An organ as defined in claim 1 in which a disc-like layer of active cells is formed in the chamber adjacent the membrane, the layer having a thickness and a diameter, wherein the diameter of the layer is at least as great as the thickness of the layer.

9. An organ as defined in claim 1 wherein metabolically active cells metabolize at least one toxic substance that diffuses from capillaries contained in the vascularizing compartment into the chamber.

10. An organ as defined in claim 1 wherein metabolically active cells secrete insulin in response to glucose which has diffused from capillaries contained in the vascularizing compartment into the chamber.

11. An organ as defined in claim 10 wherein metabolically active cells also secrete at least one of somatostatin, pancreatic polypeptide and glucagon.

12. An organ as defined in claim 1 wherein the membrane has an average number molecular weight cut-off of less than 100,000.

13. An organ as defined in claim 1 wherein the metabolically active cells are genetically engineered.

14. A bioartificial device for implantation into an animal comprising:

a housing having an enclosed chamber containing metabolically active cells that produce at least one substance of therapeutic benefit to the animal,

at least on e vascularizing compartment having an opening that provides access to surrounding tissue, the at least one vascularizing compartment containing at least one growth factor for promoting ingrowth of capillaries into the vascularizing compartment,

inlet means for supplying cells to the chamber, outlet means for removing cells from the chamber, and

a semi-permeable membrane separating and in communication with the chamber and vascularizing compartment, the membrane providing immunoprotection of the active cells from the vascularizing compartment and around the implanted device, the membrane allowing passage of small molecules including nutrients and waste products between the chamber and vascularizing compartment and not allowing passage of agents of an immune system to the chamber, and

a biocompatible matrix in the vascularizing compartment to provide a neovascular formation region for enhancing growth of small capillaries for providing efficient mass transfer of substances between the chamber and the capillaries in the vascularizing compartment, the matrix having a porosity of about 40 to 95 percent and interconnecting passageways of about 10 to 120 microns.

15. An organ as defined in claim 14 in which the metabolically active cells are islets of Langerhans.

16. An organ as defined in claim 15 in which a layer of islets is formed adjacent the membrane, the layer having a thickness and having a diameter, wherein the diameter of the layer is at least as great as the thickness of the layer.

17. An organ as defined in claim 14 wherein the cells produce at least one of parathyroid hormone, dopamine, insulin, glucagon, calcitonin.

18. An organ as defined in claim 14 wherein metabolically active cells metabolize at least one toxic substance that diffuses from capillaries contained in the vascularizing compartment into the chamber.

19. An organ as defined in claim 14 wherein metabolically active cells secrete insulin in response to glucose which has diffused from capillaries contained in the vascularizing compartment into the chamber.

20. An organ as defined in claim 14 wherein metabolically active cells also secrete at least one of somatostatin, pancreatic polypeptide and glucagon.

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.