PROTEIN BASED MATERIALS, PLASTIC ALBUMIN DEVICES AND RELATED METHODS

• US 20130325121A1
• Filed: 05/30/2013
• Published: 12/05/2013
• Est. Priority Date: 05/31/2012
• Status: Abandoned Application

• Current Assignee: Clemson University
• Original Assignee: Clemson University
• Inventors: Luzinov, Igor, Whatley, Benjamin R., Wen, Xuejun, Sharma, Suraj
• Application Number:
  US13/905,726
• Publication Number:
  US 20130325121A1
• Time in Patent Office: Days
• US Class Current: 623/10
• CPC Class Codes: A61F 2/18 Internal ear or nose parts, e.g. ear-drums implants for middle ear ventilation or drainage A61F11/202
• CPC Class Codes: A61F 2002/183 Ear parts
• CPC Class Codes: A61L 2300/404 Biocides, antimicrobial agents, antiseptic agents
• CPC Class Codes: A61L 29/085 Macromolecular materials
• CPC Class Codes: A61L 29/16 Biologically active materials, e.g. therapeutic substances A61L29/048 takes precedence
• CPC Class Codes: C08L 89/00 Compositions of proteins; Compositions of derivatives thereof foodstuff preparations A23J3/00

Abstract

Medical devices with a plastic albumin body with a defined three dimensional shape that are particularly suitable for pressure equalization tubes. The plastic albumin body can be a unitary substantially monolithic body of albumin. The plastic albumin body has an antibacterial property such that it is resistant to bacterial adhesions and/or bacterial biofilm formation thereon. Methods and processes are described for forming a consolidated protein-based coating on an implant, and coated implants produced therefrom, with improved biocompatibility, nonthrombogenity and antimicrobiality that are suitable for various medical implants and drug delivery devices, such as bone implants, catheters, cannuale, guide wires, stents, shunts, vascular grafts, heart valves, heart and ventricular assist devices, oxygenators, dialyzers, medical devices, and other substrates, such as furniture, keyboards, etc.

Claims

1. A medical device comprising:

a plastic albumin body having a defined three dimensional shape.

2. The medical device of claim 1, wherein the plastic albumin body is a unitary substantially monolithic body.

3. The medical device of claim 1, wherein the plastic albumin body has an antibacterial property such that it is resistant to bacterial adhesions and/or bacterial biofilm formation thereon.

4. The medical device of claim 1, wherein the plastic albumin body comprises at least one therapeutic agent.

5. The medical device of claim 1, wherein the plastic albumin body is sized and configured as a pressure equalization tube for an ear.

6. The medical device of claim 1, wherein the plastic albumin body is substantially rigid and has a substantially medial extending through channel.

7. The medical device of claim 1, wherein the plastic albumin body comprises cooperating discrete components.

8. The medical device of claim 1, wherein the plastic albumin body is an overmold or coating on a substrate.

9. The medical device of claim 1, wherein the medical device is a biodegradeable pressure equalization (PE) tube for an ear.

10. The medical device of claim 9, wherein the plastic albumin resides on a pre-molded PE tube substrate formed of a different material.

11. The medical device of claim 10, wherein the PE tube substrate comprises TEFLON.

12. The medical device of claim 1, wherein the medical device is an implantable device.

13. A method of fabricating a device, comprising;

introducing a liquid solution of albumin into a mold having a mold cavity with a defined shape;

heating the liquid solution in the mold for a defined time and temperature; and

forming a device having a solid plastic albumin shape in response to the heating step.

14. The method of claim 13, wherein the introducing step is carried out using a liquid solution having a concentration of albumin between about 5% to about 90%.

15. The method of claim 13, wherein the heating step is carried out by placing the mold in an autoclave at between about 80 degrees Celsius and 200 degrees Celsius for between about 10 minutes to 4 hours.

16. The method of claim 13, wherein the introducing step is carried out by providing powder albumin that is dissolved in a liquid and mixed with at least one therapeutic agent.

17. The method of claim 13, wherein the device is a medical device, the method further comprising applying at least one therapeutic agent onto the albumin before, during or after the forming step.

18. The method of claim 13, further comprising placing a rod in the mold before the introducing step to be in communication with a respective mold cavity, wherein the introducing step introduces the liquid under pressure into the mold about the rod, and wherein the forming step is carried out to forms a through channel in the solid albumin body with a diameter corresponding to a diameter of the rod.

19. The method of claim 13, further comprising placing a substrate in the mold before the introducing step to be in communication with a respective mold cavity, wherein the introducing step introduces the liquid under pressure into the mold about the substrate, and wherein the forming step is carried out to overmold the plastic albumin onto a surface or surfaces of the substrate.

20. A method of treating a patient, comprising;

providing a tube with an open channel, the tube comprising a substrate with a plastic albumin coating or overmold or a tube having a plastic albumin substrate defining the tube;

placing the tube in a target location of a patient; and

providing at least one of a (i) drainage channel (ii) access path or (ii) vent or air path;

or (iii) tissue support using the tube.

21. The method of claim 20, wherein the placing step comprises placing the tube as a pressure equalization tube in an ear of the patient.

22. A method of treating substrates to provide anti-bacterial properties, comprising:

providing a target substrate;

applying liquid albumin to the target substrate; and

heating the substrate with the applied liquid albumin to transform the albumin into plastic albumin on the target substrate.

23. The method of claim 22, wherein the target substrate is a pressure equalization (PE) tube.

24. The method of claim 22, wherein the target substrate is a device used in a patient or baby care facility.