Durable photopolymerizable cross-linked anti-fouling coatings
US-2020308440-A1 · Oct 1, 2020 · US
US12116498B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12116498-B2 |
| Application number | US-202318507969-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 13, 2023 |
| Priority date | Jun 24, 2016 |
| Publication date | Oct 15, 2024 |
| Grant date | Oct 15, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Durable, anti-fouling, crosslinked zwitterionic coatings that are grafted to the surface of a substrate through covalent bonding are disclosed. When exposed to a light source, zwitterionic monomers react with a crosslinker and with activated radicals at the surface of the substrate, simultaneously forming the crosslinked zwitterionic coating and anchoring it to the surface of the substrate. Photomasking techniques can be used to micropattern the zwitterionic coatings. The zwitterionic coatings can be applied to a variety of substrates, including medical devices and systems.
Opening claim text (preview).
The invention claimed is: 1. An implantable system, comprising: a substrate having at least one outer surface; a photopolymerized zwitterionic hydrogel coating covalently bonded to at least a portion of the outer surface, wherein the photopolymerized zwitterionic hydrogel coating comprises zwitterionic monomer units and a crosslinker selected from the group consisting of ethylene glycol dimethacrylate (EGDMA), poly(ethylene glycol) di(meth)acrylate (PEGD(M)A), propylene glycol diacrylate, bisphenol A ethoxylate diacrylate, N,N′-methylenebis acrylamide, pentaerythritol tetraacrylate, 1,3-butylene glycol dimethacrylate (BGDMA), 1,4-butane diol diacrylate (BDDA), 1,6-hexane diol diacrylate (HDDA), hexanediol dimethacrylate (HDDMA), 1-carboxy-N-methyl-N-di(2-methacryloyloxy-ethyl) methanaminium inner salt (CBMX), neopentylglycol diacrylate (NPGDA), and trimethylolpropane triacrylate (TMPTA), and wherein the photopolymerized zwitterionic hydrogel coating is configured to resist adhesion by biomolecules, cells, tissue or bacteria. 2. The implantable system of claim 1 , wherein the substrate is a component of a cochlear implant. 3. The implantable system of claim 1 , wherein the zwitterionic monomer unit contains a phosphoryl choline moiety, a sulfobetaine moiety, a carboxybetaine moiety, or combinations thereof. 4. The implantable system of claim 3 , wherein the zwitterionic monomer unit is carboxybetaine (meth)acrylate, phosphoryl choline (meth)acrylate, sulfobetaine (meth)acrylate, carboxybetaine (meth)acrylamide, or sulfobetaine (meth)acrylamide. 5. The implantable system of claim 1 , wherein at least a portion of the outer surface of the substrate is formed from a polymeric material, and the photopolymerized zwitterionic hydrogel coating is covalently bonded to the polymeric material. 6. The implantable system of claim 5 , wherein the polymeric material is polydimethyl siloxane. 7. The implantable system of claim 1 , wherein the at least one outer surface of the substrate has uncoated regions, and the uncoated regions and the photopolymerized zwitterionic hydrogel coating form a micropattern on the outer surface of the substrate. 8. The implantable system of claim 7 , wherein the micropattern is configured to direct cell growth of one or more of neurite cells, fibroblast cells, or glial cells on the uncoated regions. 9. The implantable system of claim 1 , wherein the photopolymerized zwitterionic hydrogel coating has a thickness of at least about 100 nm. 10. The implantable system of claim 1 , wherein the zwitterionic monomer unit comprises carboxybetaine methacrylate (CBMA) or sulfobetaine methacrylate (SBMA). 11. The implantable system of claim 1 , wherein the photopolymerized zwitterionic hydrogel coating is covalently bonded to the at least one portion of the surface with a first photo initiator and is cross-linked by a second photo initiator. 12. The implantable system of claim 11 , wherein the first photo initiator and the second photoinitiator are simultaneously photoactivated by a light source. 13. A cochlear implant comprising: a substrate having at least one outer surface; a photopolymerized zwitterionic hydrogel coating covalently bonded to at least a portion of the outer surface, wherein the photopolymerized zwitterionic hydrogel coating comprises zwitterionic monomer units and a crosslinker selected from the group consisting of ethylene glycol dimethacrylate (EGDMA), poly(ethylene glycol) di(meth)acrylate (PEGD(M)A), propylene glycol diacrylate, bisphenol A ethoxylate diacrylate, N,N′-methylenebis acrylamide, pentaerythritol tetraacrylate, 1,3-butylene glycol dimethacrylate (BGDMA), 1,4-butane diol diacrylate (BDDA), 1,6-hexane diol diacrylate (HDDA), hexanediol dimethacrylate (HDDMA), 1-carboxy-N-methyl-N-di(2-methacryloyloxy-ethyl) methanaminium inner salt (CBMX), neopentylglycol diacrylate (NPGDA), and trimethylolpropane triacrylate (TMPTA), and wherein the photopolymerized zwitterionic hydrogel coating is configured to resist adhesion by biomolecules, cells, tissue or bacteria. 14. The cochlear implant of claim 13 , wherein the at least one outer surface of the substrate has uncoated regions, and the uncoated regions and the photopolymerized zwitterionic hydrogel coating form a micropattern on the outer surface of the substrate. 15. The cochlear implant of claim 14 , wherein the uncoated regions on the outer surface enable patterned regions of fibrosis.
on to polysiloxanes · CPC title
Homopolymers or copolymers of acrylamide or methacrylamide · CPC title
Polyorganosiloxane-containing compositions · CPC title
of acyclic polycarboxylic acids · CPC title
Coatings comprising two or more layers · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.