Partially erodable systems for treatment of obstructive sleep apnea

• US 8,167,787 B2
• Filed: 01/03/2008
• Issued: 05/01/2012
• Est. Priority Date: 01/03/2008
• Status: Expired due to Fees

• Current Assignee: ReVENT Medical, Inc.
• Original Assignee: ReVENT Medical, Inc.
• Inventors: Gillis, Edward M.
• Primary Examiner(s): Lacyk, John
• Assistant Examiner(s): Dorna, Carrie R
• Application Number:
  US11/969,201
• Publication Number:
  US 20090177027A1
• Time in Patent Office: 1,580 Days
• Field of Search: 600/37, 128/848, 128897-898
• US Class Current: 600/37
• CPC Class Codes: A61F 5/56 Devices for preventing snoring by influencing the respiratory system by gas treatment A61M16/00
• CPC Class Codes: A61F 5/566 Intra-oral devices

Abstract

The invention relates to devices and methods for reforming tissue surrounding the airway of a subject suffering from obstructive sleep apnea so as to open the airway and alleviate the occurrence of apneic events. Devices comprise a combination of resiliently deformable material and bioerodible material. The deformable portion of the device has a preferred shape that corresponds to the desired final shape of the device once placed in an airway. In making a transplant-ready device, however, the deformable portion is placed into a deformed shape and constrained in that shape by the bioerodible material. After implantation, the device gradually assumes the preferred shape as the constraining bioerodible material erodes. As the device gradually reforms toward the preferred shape, it reforms the tissue into the therapeutically desirable configuration. The gradual nature of the shape change generally stabilizes the device in the tissue, and supports tissue reforming into a stable configuration.

Claims

1. A device for alleviating tissue obstruction of an airway in a human subject comprising:

a plurality of resiliently expandable inner portions each having an axially expanded configuration in which the inner portion is stretched into axial tension and an axially unexpanded configuration in which the inner portion is not stretched in axial tension; and

a plurality of discrete bioerodible outer portions maintaining the expandable inner portions in the axially expanded configuration,

the expandable inner portions being configured to return toward the axially unexpanded configuration upon erosion of the bioerodible outer portions,

the device being sized and shaped to be implanted in an airway-forming tissue site in a manner compatible with normal physiological function of the site.

2. The device of claim 1 wherein the unexpanded configuration is adapted to remodel the shape of the airway so as to provide a more open airway during sleep.

3. The device of claim 1 wherein the bioerodible portions may include any one or more of polycaprolactone, polylactic acid, polyglycolic acid, polylactide coglycolide, polyglactin, poly-L-lactide, polyhydroxalkanoates, starch, cellulose, chitosan, or structural protein.

4. The device of claim 1 further comprising a hook or a barb.

5. The device of claim 1 wherein the device is configured with sufficient elasticity to allow normal physiological movement around the airway-forming tissue implant site when the device is implanted in the implant site.

6. The device of claim 1 wherein the bioerodible portions include an elutable bioactive agent incorporated therein.

7. The device of claim 1 wherein the airway-forming tissue site for which the device is sized and shaped to conform includes pharyngeal wall tissue.

8. The device of claim 1 wherein the airway-forming tissue site for which the device is sized and shaped to conform includes soft palate tissue.

9. The device of claim 1 wherein the airway-forming tissue site for which the device is sized and shaped to conform includes tongue tissue.

10. The device of claim 9 wherein the device has a substantially linear shape, is configured to reside in an anterior-posterior orientation, and has a length that ranges between about 4 to about 8 cm.

11. The device of claim 1 wherein the expandable portions are linearly and resiliently stretched in the expanded configuration.

12. The device of claim 1 wherein the expandable portions comprise silicone rubber.

13. The device of claim 1 wherein the expandable portions each comprise a narrow cross-sectional portion, the device further comprising a plurality of wide cross-sectional portions, the narrow cross-sectional portions each extending between first and second wide cross-sectional portions.

14. The device of claim 13 wherein the wide cross-sectional portions and the narrow cross-sectional portions comprise a stretchable material.

15. The device of claim 14 wherein the narrow cross-sectional portions are configured to stretch more easily than the wide cross-sectional portions.

16. The device of claim 14 wherein the stretchable material comprises silicone rubber.

17. The device of claim 1 further comprising a base disposed at an end of the device.

18. The device of claim 17 wherein the base is broad and flat.

19. The device of claim 17 wherein the base is triangular.

20. The device of claim 1 further comprising an opening across which tissue can grow when the device is implanted in the tissue site.

21. The device of claim 1 wherein at least one of the bioerodible portions comprises a plurality of separate pieces.

22. The device of claim 1 wherein the bioerodible portions comprise at least two different materials that bioerode at different rates.