IP Library Granted Patent US 9,603,801
Granted Patent B2
US 9,603,801 · App. 14/211,170 · Granted Mar 28, 2017

Bioerodible silicon-based compositions for delivery of therapeutic agents

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Quick Facts
Patent No.
US 9,603,801
App. No.
14/211,170
Granted
Mar 28, 2017
Kind
B2
Abstract

The invention comprises a composition comprising a bioerodible porous silicon-based carrier material wherein the carrier material carries at least one large molecule therapeutic agent and at least one amorphous sugar, optionally further comprising a crystallization inhibitor. The composition may be used in vitro or in vivo to deliver the therapeutic agent, preferably in a controlled fashion over an intended period of time such as over multiple days, weeks or months. The composition may be used for treating or preventing conditions of a patient such as chronic diseases.

Claims (26)

1. A composition comprising a bioerodible porous silicon-based carrier material wherein at least one large-molecule therapeutic agent and an amorphous sugar are disposed in pores of the carrier material.

2. The composition of claim 1 , wherein the carrier material is resorbable.

3. The composition of claim 1 , wherein the therapeutic agent is selected from proteins, peptides, antibodies, carbohydrates, polymers and polynucleotides.

4. The composition of claim 3 , wherein the therapeutic agent is an antibody.

5. The composition of claim 1 , wherein the amorphous sugar is selected from trehalose, trehalose dihydrate, sucrose, mannitol, sorbitol, xylitol or glycerol, or a combination thereof.

6. The composition of claim 1 , wherein the carrier material has a porosity in the range of about 40% to about 80%.

7. The composition of claim 1 , wherein the average pore size is in the range 2-50 nm.

8. The composition of claim 7 , wherein the average pore size is in the range of 10-50 nm.

9. The composition of claim 1 , wherein the average width of the walls in the carrier material which separate the pores is less than 5 nm.

10. The composition of claim 9 , wherein the average width of the walls is less than 3 nm.

11. The composition of claim 1 , wherein a length of the carrier material measured at its longest point is between 1 and 500 microns.

12. The composition of claim 11 , wherein the length of the carrier material as its longest point is between 5 and 100 microns.

13. The composition of claim 1 , wherein the load level of the carrier material is less than 80% by weight based on the combined weight of the carrier material and therapeutic agent.

14. The composition of claim 1 , wherein the load level of the carrier material is from about 1% to about 70% by weight based on the combined weight of the carrier material and therapeutic agent.

15. The composition of claim 1 , wherein the load level of the carrier material is from about 3% to about 50% by weight based on the combined weight of the carrier material and therapeutic agent.

16. The composition of claim 1 , wherein the load level of the carrier material is from about 5% to about 40% by weight based on the combined weight of the carrier material and therapeutic agent.

17. The composition of claim 1 , wherein the load level of the carrier material is less than about 40% by weight based on the weight of the composition.

18. The composition of claim 1 , wherein the load level of the carrier material is from about 1% to about 40% by weight based on the weight of the composition.

19. The composition of claim 1 , wherein the carrier material is coated with a polymer.

20. The composition of claim 19 , wherein the polymer is a controlled release polymer.

21. A method of preparing the composition of claim 1 , comprising contacting the porous silicon-based carrier material with the therapeutic agent and the amorphous sugar.

22. The method of claim 21 , wherein the average pore size of the carrier material is selected to allow for entry of the therapeutic agent and controlled release of the therapeutic agent into a biological medium over at least about three days.

23. The method of claim 22 , wherein the average pore size is from about 15 nm to about 40 nm and the therapeutic agent has a molecular weight from about 100,000 to about 200,000amu.

24. The method of claim 22 , wherein the average pore size is from about 25 nm to about 40 nm and the therapeutic agent has a molecular radius from about 6 nm to about 8 nm.

25. The method of claim 22 , wherein the average pore size is from about 2 nm to about 10 nm and the therapeutic agent has a molecular weight from about 5,000 to about 50,000 amu.

26. A method of treating a condition in a patient, comprising administering a therapeutically effective amount of the composition of claim 1 to a patient in need thereof.

Assignments (7)
RELEASE OF SECURITY INTEREST Recorded Mar 14, 2022
From: CRG SERVICING LLC, AS ADMINISTRATIVE AGENT
To: EYEPOINT PHARMACEUTICALS, INC.; EYEPOINT PHARMACEUTICALS US, INC.; ICON BIOSCIENCE, INC.
Reel/Frame 059365/0112 →
CHANGE OF NAME Recorded Apr 2, 2019
From: PSIVIDA US, INC.
To: EYEPOINT PHARMACEUTICALS, INC.
Reel/Frame 049108/0700 →
RELEASE OF SECURITY INTEREST Recorded Feb 13, 2019
From: SWK FUNDING LLC, AS AGENT
To: PSIVIDA CORP.; PSIVIDA US, INC.; ICON BIOSCIENCE, INC.
Reel/Frame 048329/0136 →
SECURITY INTEREST Recorded Feb 13, 2019
From: EYEPOINT PHARMACEUTICALS, INC.; EYEPOINT PHARMACEUTICALS US, INC.; ICON BIOSCIENCE, INC.
To: CRG SERVICING LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 048329/0045 →
SECURITY INTEREST Recorded Apr 5, 2018
From: PSIVIDA CORP.
To: SWK FUNDING LLC, AS AGENT
Reel/Frame 045848/0670 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2014
From: ASHTON, PAUL
To: PSIVIDA US, INC.
Reel/Frame 033437/0123 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2014
From: BARNETT, CHRISTIAN; CANHAM, LEIGH T.
To: PSIMEDICA LIMITED
Reel/Frame 033437/0133 →