Polymer particles

US9546236B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9546236-B2
Application numberUS-201414491776-A
CountryUS
Kind codeB2
Filing dateSep 19, 2014
Priority dateSep 19, 2013
Publication dateJan 17, 2017
Grant dateJan 17, 2017

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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.

Biodegradable, cross-linked polymer particle embolics and methods of making the same are described. The particle embolics can be used as embolization agents.

First claim

Opening claim text (preview).

We claim: 1. A polymer particle comprising: at least one monomer including at least one functional group; and at least one crosslinker; wherein the polymer particle has a diameter between about 40 μm and about 1,200 μm and is susceptible to degradation through hydrolysis or enzymatic action. 2. The polymer particle of claim 1 , wherein the polymer particle has a diameter between about 75 μm and about 1,200 μm. 3. The polymer particle of claim 1 , wherein the at least one functional group is acrylate, acrylamide, methacrylate, or methacrylamide. 4. The polymer particle of claim 1 , wherein the at least one monomer includes an ionizable functional group. 5. The polymer particle of claim 4 , wherein the ionizable functional group is basic. 6. The polymer particle of claim 4 , wherein the ionizable functional group is acidic. 7. The polymer particle of claim 1 , wherein the at least one crosslinker includes at least two functional groups. 8. The polymer particle of claim 1 , wherein the crosslinker includes at least one linkage susceptible to degradation through hydrolysis or enzymatic action. 9. The polymer particle of claim 8 , wherein the crosslinker is bis-glycidyl amino alcohol. 10. The polymer particle of claim 8 , wherein the crosslinker is wherein a, b, c, d, e, and f are each independently 1-20. 11. The polymer particle of claim 8 , wherein the at least one linkage is an ester, a thioester, a carbonate, a peptide cleavable by matrix metalloproteinases, a peptide cleavable by matrix collagenases, a peptide cleavable by matrix elastases, a peptide cleavable by matrix cathepsins, or a combination thereof. 12. The polymer particle of claim 11 , including a second crosslinker including a second linkage selected from an ester, a thioester, a carbonate, a peptide cleavable by matrix metalloproteinases, a peptide cleavable by matrix collagenases, a peptide cleavable by matrix elastases, and a peptide cleavable by matrix cathepsins. 13. The polymer particle of claim 1 , wherein the polymer particle is biodegradable. 14. The polymer particle of claim 1 , wherein the polymer particle is substantially degraded within about 1 months of implantation. 15. The polymer particle of claim 11 , wherein the at least one monomer is dimethylacrylamide and the at least one crosslinker is bis-glycidyl amino alcohol. 16. The polymer particle of claim 11 , wherein the at least one monomer is acrylamide and the at least one crosslinker is bi-functionalized methacryloyl-Ala-Pro-Gly-Leu-AEE-methacrylate. 17. A method of making a polymer particle comprising: reacting a prepolymer solution including at least one monomer including at least one functional group, at least one crosslinker susceptible to degradation through hydrolysis or enzymatic action, and an initiator in an oil; and forming the polymer particle, wherein the polymer particle has a diameter between about 40 μm and about 1,200 μm. 18. The method of claim 17 , wherein the oil is mineral oil. 19. The method of claim 17 , wherein the initiator is N,N,N′,N′-tetramethylethylenediamine. 20. The method of claim 17 , wherein the polymer particle has a circularity of at least about 0.90. 21. The method of claim 17 , wherein the at least one functional group is acrylate, acrylamide, methacrylate, or methacrylamide. 22. The method of claim 17 , wherein the at least one crosslinker is bis-glycidyl amino alcohol. 23. The method of claim 17 , wherein the at least one crosslinker is wherein a, b, c, d, e, and f are each independently 1-20. 24. The method of claim 17 , wherein the polymer particle is biodegradable. 25. The method of claim 24 , wherein the polymer particle is substantially degraded within about 6 months of implantation. 26. The method of claim 24 , wherein the at least one monomer is acrylamide and the at least one crosslinker is bis-glycidyl amino alcohol. 27. The method of claim 24 , wherein the at least one monomer is acrylamide and the at least one crosslinker is bi-functionalized methacryloyl-Ala-Pro-Gly-Leu-AEE-methacrylate.

Assignees

Inventors

Classifications

  • substituted imides comprising other heteroatoms · CPC title

  • Nitrogen-containing compounds {(C08K5/0091 takes precedence)} · CPC title

  • C08F220/56Primary

    Acrylamide; Methacrylamide · CPC title

  • obtained by reactions only involving carbon-to-carbon unsaturated bonds {(A61L24/043, A61L24/046 take precedence)} · CPC title

  • for embolization or occlusion, e.g. vaso-occlusive compositions or devices · CPC title

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Frequently asked questions

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What does patent US9546236B2 cover?
Biodegradable, cross-linked polymer particle embolics and methods of making the same are described. The particle embolics can be used as embolization agents.
Who is the assignee on this patent?
Microvention Inc, Terumo Corp
What technology area does this patent fall under?
Primary CPC classification C08F220/56. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 17 2017 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 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).