Injectable preformed macroscopic 3-dimensional scaffolds for minimally invasive administration

US10045947B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10045947-B2
Application numberUS-201214112096-A
CountryUS
Kind codeB2
Filing dateApr 27, 2012
Priority dateApr 28, 2011
Publication dateAug 14, 2018
Grant dateAug 14, 2018

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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.

The invention provides polymer compositions for cell and drug delivery.

First claim

Opening claim text (preview).

What is claimed is: 1. An injectable cell-compatible highly crosslinked cryogel composition comprising open interconnected pores, wherein said cryogel composition comprises at least 75% pores, and wherein said cryogel composition is characterized by shape memory following deformation by compression through a needle, such that said cryogel composition returns to its original undeformed three-dimensional shape less than one second after compression through the needle, and wherein said cryogel composition comprises a cryo-crosslinked alginate polymer, wherein said alginate is methacrylated. 2. The cryogel composition of claim 1 , comprising at least 90% pores. 3. The cryogel composition of claim 1 , comprising at least 90% water when water is within said pores such that said cryogel is in a fully hydrated state. 4. The cryogel composition of claim 1 , comprising less than 25% water when compressed. 5. The cryogel composition of claim 1 , comprising a cell adhesion composition covalently attached to said polymer. 6. The cryogel composition of claim 5 , wherein said cell adhesion composition comprises a peptide comprising an RGD amino acid sequence. 7. The cryogel composition of claim 1 , comprising a eukaryotic cell in one or more of said open interconnected pores. 8. The cryogel composition of claim 7 , wherein said eukaryotic cell comprises a live attenuated cancer cell. 9. The cryogel composition of claim 1 , comprising a biomolecule in one or more of said open interconnected pores. 10. The cryogel composition of claim 9 , wherein said biomolecule comprises a small molecule, nucleic acid, or protein. 11. The cryogel composition of claim 10 , wherein said protein comprises granulocyte macrophage-colony stimulating factor (GM-CSF). 12. The cryogel composition of claim 10 , wherein said nucleic acid comprises a CpG nucleic acid oligonucleotide. 13. The cryogel composition of claim 1 , which is injectable through a hollow needle. 14. The cryogel composition of claim 1 , wherein upon compression, said cryogel composition maintains structural integrity and shape memory properties. 15. The cryogel composition of claim 1 , further comprising gelatin, heparin, dextran, carob gum, PEG, a PEG derivative, collagen, chitosan, carboxymethylcellulose, pullulan, PVA, PHEMA, PNIPAAm, or PAAc. 16. The cryogel composition of claim 1 , comprising the shape of a disc, cylinder, square, rectangle, or string. 17. The cryogel composition of claim 1 , which is between 100 μm 3 to 100 mm 3 in size. 18. A method for delivering genetic material to a tissue, comprising administering the cryogel composition of claim 1 , wherein said cryogel composition further comprises a nucleic acid. 19. The method of claim 18 , wherein said nucleic acid comprises plasmid DNA. 20. A method for eliciting an immune response, comprising administering to a subject the cryogel composition of claim 8 . 21. The method of claim 20 , wherein said cryogel composition is administered prophylactically or therapeutically. 22. The cryogel composition of claim 1 , wherein the highly crosslinked cryogel composition comprises a crosslinking density of at least 50% polymer crosslinking. 23. The cryogel composition of claim 1 , wherein the highly crosslinked cryogel composition comprises a crosslinking density of at least 50-100% polymer crosslinking. 24. The cryogel composition of claim 8 , wherein said live attenuated cancer cell is a live attenuated melanoma cancer cell. 25. The cryogel composition of claim 4 , which returns to its original undeformed three-dimensional shape after it is compressed by up to 90% of its volume. 26. The cryogel composition of claim 1 , further comprising a tumor antigen. 27. A syringe comprising (i) a needle, (ii) a reservoir that comprises the cryogel composition of claim 1 , and (iii) a plunger. 28. The syringe of claim 27 , comprising a 16-gauge, an 18-gauge, a 22-gauge, a 24-gauge, a 26-gauge, a 28-gauge, a 30-gauge, a 32-gauge, or a 34-gauge needle. 29. The syringe of claim 27 , comprising an 18 to 30-gauge needle. 30. The syringe of claim 28 , wherein the device is between 1 mm 3 to 50 mm 3 in size. 31. The syringe of claim 28 , therein the cryogel composition further comprises live attenuated cancer cells, wherein 90% or more of the cancer cells survive passage of the cryogel composition through the bore of the needle. 32. The syringe of claim 27 , wherein the cryogel composition is filled with a physiologically-compatible solution, wherein said cryogel composition is characterized by shape memory following deformation by compression from the reservoir through the needle, such that said cryogel composition returns to its original undeformed three-dimensional shape less than one second after compression from the reservoir through the needle. 33. The cryogel composition of claim 1 , wherein said cryogel composition comprises macropores having a diameter of 10 μm to 600 μm. 34. The syringe of claim 27 , wherein said cryogel composition comprises macropores having a diameter of 10 μm to 600 μm. 35. The cryogel composition of claim 9 , wherein said biomolecule comprises a pathogen-associated molecular pattern (PAMP). 36. The cryogel composition of claim 1 , wherein said cryogel composition is characterized by shape memory following deformation by compression from a reservoir of a syringe, in which the cryogel composition is filled with a physiologically-compatible solution, through a needle of the syringe, such that said cryogel composition returns to its original undeformed three-dimensional shape less than one second after compression from the reservoir through the needle. 37. The cryogel composition of claim 1 , wherein said cryogel composition comprises a Young's modulus of 4±2 kPa. 38. The syringe of claim 27 , wherein the reservoir holds a liquid. 39. The syringe of claim 38 , wherein the liquid is a physiologically-compatible solution.

Assignees

Inventors

Classifications

  • Drugs used in surgical methods, e.g. surgery adjuvants for preventing adhesion or for vitreum substitution · CPC title

  • Immunomodulators · CPC title

  • Antineoplastic agents · CPC title

  • for soft tissue reconstruction · CPC title

  • Materials with shape-memory or superelastic properties · CPC title

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Frequently asked questions

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What does patent US10045947B2 cover?
The invention provides polymer compositions for cell and drug delivery.
Who is the assignee on this patent?
Bencherif Sidi A, Mooney David J, Edwards David, and 2 more
What technology area does this patent fall under?
Primary CPC classification A61K9/7007. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Aug 14 2018 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 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).