Polymer particles
US-9938367-B2 · Apr 10, 2018 · US
US10632226B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10632226-B2 |
| Application number | US-201816237298-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 31, 2018 |
| Priority date | Sep 28, 2016 |
| Publication date | Apr 28, 2020 |
| Grant date | Apr 28, 2020 |
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Biodegradable, cross-linked polymer particle embolics and methods of making the same are described. The particle embolics can be used as embolization agents.
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We claim: 1. An embolic system including: a syringe, a vial, or a combination thereof; and polymer particles comprising at least one monomer including at least one functional group and at least one crosslinker having a structure 2. The embolic system of claim 1 , wherein the polymer particles have a diameter between about 40 μm and about 1,200 μm. 3. The embolic system of claim 1 , wherein the polymer particles have a diameter between about 75 μm and about 1,200 μm. 4. The embolic system of claim 1 , wherein the at least one functional group is acrylate, acrylamide, methacrylate, or methacrylamide. 5. The embolic system of claim 1 , wherein the at least one monomer includes an ionizable functional group. 6. The embolic system of claim 5 , wherein the ionizable functional group is basic. 7. The embolic system of claim 5 , wherein the ionizable functional group is acidic. 8. The embolic system of claim 1 , wherein the polymer particles include 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. 9. The embolic system of claim 1 , wherein the polymer particles are biodegradable. 10. The embolic system of claim 1 , wherein the polymer particles are substantially degraded within about 1 months of implantation. 11. The embolic system of claim 1 , wherein the at least one monomer is dimethylacrylamide. 12. The embolic system of claim 1 , wherein the at least one monomer is acrylamide. 13. A method of treatment, the method comprising: delivering a solution including polymer particles through a delivery device to a treatment site, wherein the polymer particles include at least one monomer including at least one functional group and at least one crosslinker having a structure 14. The method of claim 13 , wherein the polymer particles have a diameter between about 40 μm and about 1,200 μm. 15. The method of claim 13 , further comprising: mixing a radiopaque contrast agent with the polymer particles. 16. The method of claim 13 , wherein the delivering is through a catheter, a microcatheter, or a needle. 17. The method of claim 13 , further comprising: occluding blood flow using the polymer particles. 18. The method of claim 13 , wherein the polymer particles include 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. 19. The method of claim 13 , wherein the polymer particles are biodegradable. 20. The method of claim 19 , wherein the polymer particles are substantially degraded within about 6 months of implantation.
Use of materials characterised by their function or physical properties · CPC title
obtained by reactions only involving carbon-to-carbon unsaturated bonds · CPC title
condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines (yohimbine derivatives, vinblastine A61K31/475; ergoline derivatives A61K31/48) · CPC title
obtained by reactions only involving carbon-to-carbon unsaturated bonds (A61L31/041 takes precedence) · CPC title
with nitrogen-containing functional groups, e.g. aminoxides, nitriles, guanidines · CPC title
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