Shape changing drug delivery devices and methods

US10420724B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10420724-B2
Application numberUS-201615360430-A
CountryUS
Kind codeB2
Filing dateNov 23, 2016
Priority dateNov 25, 2015
Publication dateSep 24, 2019
Grant dateSep 24, 2019

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Drug delivery using bio-affecting drugs, particularly with shape changing drug delivery devices. Embodiments are included for depots for delivery of a therapeutic agent that change from an elongated state ex vivo to a coil in vivo where the agent is released.

First claim

Opening claim text (preview).

The invention claimed is: 1. A device for drug delivery comprising a therapeutic agent disposed in a solid vehicle that comprises a first xerogel and a second xerogel, wherein the first xerogel is a rod and the second xerogel is a layer on the first xerogel, wherein the first xerogel and the second xerogel differentially swell and/or elongate in physiological solution to change the rod into a curve shape in response to a phosphate buffered saline (PBS) at 37° C., pH 7.4, wherein the solid vehicle provides a controlled release of the therapeutic agent. 2. The device of claim 1 wherein the solid vehicle has an aspect ratio of at least 1:10. 3. The device of claim 1 wherein the first xerogel has a first coefficient of elongation and/or a first coefficient of swelling in aqueous solution and the second xerogel has a second coefficient of elongation and/or a second coefficient of swelling in aqueous solution, with the first and the second coefficients being different. 4. The device of claim 3 wherein the curve shape comprises a coil. 5. The device of claim 4 with the solid vehicle forming the coil within 30 seconds of introduction to PBS at 37° C., pH 7.4. 6. The device of claim 1 wherein, in a cross-section taken perpendicular to a central axis of the rod, the second material xerogel has a larger cross-sectional area than a cross-sectional area of the first xerogel, as measured in PBS at 37° C., pH 7.4. 7. The device of claim 6 wherein a ratio of the cross-sectional area of the second xerogel to the cross-sectional area of the first xerogel is at least 1:1 and is no more than 5:1. 8. The device of claim 6 wherein the first xerogel is eccentrically coaxial within the second xerogel. 9. The device of claim 1 wherein the first xerogel has a first coefficient of elongation in aqueous solution and the second xerogel has a second coefficient of elongation in aqueous solution, wherein the first coefficient of elongation is less than 1 and the second coefficient of elongation is at least 1. 10. The device of claim 9 wherein the first coefficient of elongation is from 0.1 to 0.5 and the second coefficient of elongation is from 1 to 10. 11. The device of claim 1 wherein the first xerogel has a first coefficient of swelling in aqueous solution and the second xerogel has a second coefficient of swelling in aqueous solution, wherein the first coefficient of swelling is less than the second coefficient of swelling. 12. The device of claim 11 wherein the first coefficient of swelling is from 1.0 to 2.0 and the second coefficient of swelling is from 2.0 to 10. 13. The device of claim 1 wherein the first xerogel and the second material degrade in PBS at 37° C., pH 7.4, at a rate independently selected from 2 days to 5 years. 14. The device of claim 1 wherein the first xerogel comprises at least a first crosslinked polymer and the second xerogel comprises at least a second crosslinked polymer. 15. The device of claim 1 wherein the first xerogel and the second xerogel are independently selected from the group consisting of natural, synthetic, and biosynthetic polymers. 16. The device of claim 1 wherein the xerogel and the second xerogel are joined by covalent bonds. 17. The device of claim 1 wherein the therapeutic agent has a solubility in aqueous solution of no more than 10 micrograms per milliliter, is a protein with MW greater than 1000 Da, or is encapsulated in a microparticle. 18. The device of claim 1 wherein the therapeutic agent comprises an anti-angiogenic agent, a tyrosine kinase inhibitor, anti-VEGF agent, an anti-PDGF agent, anti-Ang2 agent, steroid, antibiotic, or NSAID. 19. The device of claim 1 wherein the vehicle is a first vehicle, the rod is a first rod, the therapeutic agent is a first therapeutic agent, further comprising a second vehicle that comprises a third xerogel and a fourth xerogel, wherein the third xerogel is a second rod and the fourth xerogel is a layer on the third xerogel, wherein the third xerogel and the fourth xerogel differentially swell and/or elongate to curl the second rod into a curved shape in response to a physiological solution. 20. The device of claim 19 wherein the first therapeutic agent and the second therapeutic agent are an identity with each other. 21. The device of claim 19 wherein the first rod and the second rod are identical in length before placement into physiological solution. 22. The device of claim 19 wherein the first rod and the second rod are different in length before placement into physiological solution. 23. The device of claim 19 further comprising an applicator wherein the first vehicle and the second vehicle are disposed end to end relative to each other in the applicator. 24. The device of claim 23 wherein the first vehicle and/or the second vehicle comprise an end that is cut at an angle of 30-60 degrees relative to a perpendicular cross-section. 25. The device of claim 19 further comprising a third vehicle that comprises a fifth xerogel and a sixth xerogel, wherein the fifth xerogel is a third rod and the sixth xerogel is a layer on the fifth xerogel, wherein the fifth xerogel and the sixth xerogel differentially swell and/or elongate to curl the third rod into a curved shape in response to a physiological solution.

Assignees

Inventors

Classifications

  • Ophthalmic agents · CPC title

  • A61K47/10Primary

    Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers · CPC title

  • containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole (nicotine A61K31/465) · CPC title

  • A61K9/2072Primary

    characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms (A61K9/0004, A61K9/0056, A61K9/0065 take precedence) · CPC title

  • A61K9/0051Primary

    Ocular inserts or implants · CPC title

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What does patent US10420724B2 cover?
Drug delivery using bio-affecting drugs, particularly with shape changing drug delivery devices. Embodiments are included for depots for delivery of a therapeutic agent that change from an elongated state ex vivo to a coil in vivo where the agent is released.
Who is the assignee on this patent?
Incept Llc
What technology area does this patent fall under?
Primary CPC classification A61K47/10. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Sep 24 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 6 related publications on this page (citations in our corpus or others sharing the same primary CPC).