IP Library Granted Patent US 8,257,723
Granted Patent B2
US 8,257,723 · App. 12/651,502 · Granted Sep 4, 2012

Fillers and methods for displacing tissues to improve radiological outcomes

Assignee: Incept LLC
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Quick Facts
Patent No.
US 8,257,723
App. No.
12/651,502
Granted
Sep 4, 2012
Kind
B2
Abstract

Certain embodiments include a method of improvising radiological outcomes by introducing a filler to between a first tissue location and a second tissue location to increase a distance between the first tissue location and the second tissue location, and administering a dose of radioactivity to at least the first tissue location or the second tissue location. Collagen and hyaluronic acid are examples of fillers. Certain embodiments include a medical device having a biocompatible, biodegradable filler material, wherein the device comprises at least a portion that has a shape that substantially conforms to Denovillier's space between the rectum and prostate. Certain embodiments include a kit, the kit comprising a filler and instructions for placing the filler between a first tissue location and a second tissue location to increase a distance between the first tissue location and the second tissue location.

Claims (24)

1. A method of delivering a therapeutic dose of radiation to a patient comprising introducing a biocompatible, biodegradable filler between an organ and a nearby tissue to increase a distance between the organ and the tissue, and treating the tissue with the therapeutic dose of radiation so that the presence of the filler causes the organ to receive less of the dose of radiation compared to the amount of the dose of radiation the organ would receive in the absence of the filler, wherein the filler is introduced as an injectable material and is a gel in the patient, and wherein the filler is removable by biodegradation in the patient.

2. The method of claim 1 wherein the organ comprises an ovary.

3. The method of claim 1 wherein the organ is at least part of a nerve.

4. The method of claim 1 wherein the organ comprises a bone.

5. The method of claim 1 wherein the organ is located in a brain.

6. The method of claim 1 wherein the filler comprises a member of the group consisting of polylactide, polyglycolide, polycaprolactone, and poly(alpha-hydroxy acid).

7. The method of claim 1 wherein the filler comprises alginate.

8. The method of claim 1 wherein the filler comprises gelatin.

9. The method of claim 1 wherein the filler comprises fibrin or fibrinogen.

10. The method of claim 1 wherein the filler comprises albumin.

11. The method of claim 1 wherein the filler comprises polyethylene glycol.

12. The method of claim 1 wherein the filler comprises a thixotropic polymer.

13. The method of claim 1 wherein the filler comprises a thermoreversible polymer.

14. The method of claim 1 wherein the filler comprises at least one therapeutic agent.

15. The method of claim 1 wherein the at least one therapeutic agent is a member of the group consisting of an anti-inflammatory drug, an antibiotic, an antimycotic, a hemostat, a steroid, and an analgesic.

16. The method of claim 1 wherein the filler is biodegradable in vivo in between three months and twelve months.

17. The method of claim 1 wherein the biocompatible, biodegradable material consists essentially of collagen.

18. The method of claim 1 wherein the filler comprises at least one polysaccharide.

19. The method of claim 1 wherein the at least one polysaccharide comprises hyaluronic acid.

20. The method of claim 1 wherein the filler material comprises a synthetic polymer.

21. The method of claim 1 wherein the filler further comprises a member of the group consisting of a degradation inhibitor, a radio opaque marker, and an osmotic agent that causes water to become associated with the filler material by osmosis.

22. The method of claim 1 wherein the filler further comprises a pH buffering agent.

23. The method of claim 1 wherein the filler occupies a volume in the range of about 10 to about 200 cubic centimeters in the patient.

24. The method of claim 1 wherein the therapeutic dose of radiation is between 70 to 300 Gy, and wherein that the filler causes organ to receive less than 50% of the dose of radiation compared to the amount of the dose of radiation that the organ would have received in the absence of the filler device.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Oct 17, 2018
From: MIDCAP FINANCIAL TRUST, AS AGENT
To: AUGMENIX, INC.
Reel/Frame 047191/0471 →
RELEASE OF SECURITY INTEREST Recorded Oct 17, 2018
From: MIDCAP FINANCIAL TRUST, AS AGENT
To: AUGMENIX, INC.
Reel/Frame 047197/0559 →
SECURITY INTEREST (TERM) Recorded Jul 19, 2017
From: AUGMENIX, INC.
To: MIDCAP FINANCIAL TRUST, AS AGENT
Reel/Frame 043251/0853 →
SECURITY INTEREST (REVOLVER) Recorded Jul 19, 2017
From: AUGMENIX, INC.
To: MIDCAP FINANCIAL TRUST, AS AGENT
Reel/Frame 043251/0878 →
Continuity (5)
Continuation 10602526 · Jun 24, 2003
Provisional Application 60427662 · Nov 19, 2002
Provisional Application 60391027 · Jun 24, 2002
Provisional Application 60444143 · Jan 31, 2003
Related Publication 20100160711A1 · Jun 24, 2010