Microfluidic devices and methods including porous polymer monoliths
US-9201069-B2 · Dec 1, 2015 · US
US9535062B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9535062-B2 |
| Application number | US-201414470775-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 27, 2014 |
| Priority date | Dec 29, 2006 |
| Publication date | Jan 3, 2017 |
| Grant date | Jan 3, 2017 |
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Dual-functional nonfouling surfaces and materials, methods for making dual-functional nonfouling surfaces and materials, and devices that include dual-functional nonfouling surfaces and materials. The dual-functional surfaces are nonfouling surfaces that resist non-specific protein adsorption and cell adhesion. The dual-functional surfaces and materials include covalently coupled biomolecules (e.g., target binding partners) that impart specific biological activity thereto. The surfaces and materials are useful in medical diagnostics, biomaterials and bioprocessing, tissue engineering, and drug delivery.
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The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows: 1. A block copolymer having a plurality of covalently coupled target binding partners having affinity toward a target molecule, the block copolymer having a first hydrophilic block and a second hydrophobic block, wherein the hydrophilic block comprises a plurality of carboxylic acid groups and a plurality of positive charged groups, wherein the hydrophilic block is substantially electronically neutral, and wherein the target binding partners are selected from the group consisting of enzymes, antibodies, protein-based antigens, receptors, polysaccharide ligands, and oligosaccharides ligands. 2. The block copolymer of claim 1 , wherein the hydrophilic block is a poly(carboxybetaine). 3. The block copolymer of claim 2 , wherein the poly(carboxybetaine) is prepared from one or more monomers selected from the group consisting of carboxybetaine acrylates, carboxybetaine acrylamides, carboxybetaine vinyl compounds, carboxybetaine epoxides, and mixture thereof. 4. The block copolymer of claim 1 , wherein the block copolymer is in the form of a microparticle or a nanoparticle. 5. The block copolymer of claim 1 , wherein the hydrophobic block is selected from the group consisting of poly(propylene oxide), polymethacrylates, polyacrylates, polyacrylamides, polyesters, polyethers, polyurethanes, and polyamides. 6. The block copolymer of claim 1 , wherein the hydrophobic block is a polyester. 7. The block copolymer of claim 1 , wherein the hydrophilic block is a zwitterionic polymer block. 8. The block copolymer of claim 1 , wherein the poly (carboxybetaine) is prepared from 2-carboxy-N,N-dimethyl-N-(2′-methacryloyloxyethyl) ethanaminium inner salt.
with ligand attached to the carrier via a chemical coupling agent (coatings G01N33/54393) · CPC title
Esters containing nitrogen · CPC title
Synthetic resin · CPC title
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