Cartridges for immunoassay tests and methods of using the same
US-11879901-B2 · Jan 23, 2024 · US
US10197568B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10197568-B2 |
| Application number | US-201214130047-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 16, 2012 |
| Priority date | Jun 28, 2011 |
| Publication date | Feb 5, 2019 |
| Grant date | Feb 5, 2019 |
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This invention provides a base material comprising a plastic-containing support and, on its surface, a hydrophilic layer comprising an ethylene glycol chain (an EG chain) composed of one or more ethylene glycol units, as well as a method for producing such base material. A polysiloxane-containing primer layer is provided on the support comprising a plastic material on its surface, and the EG chain is covalently bound to a polysiloxane side chain of the primer layer. Thus, a hydrophilic layer comprising the EG chain can be provided on the surface of the plastic-containing support.
Opening claim text (preview).
We claim: 1. A base material comprising at least: a support containing polystyrene on its surface; a polysiloxane-containing primer layer on the surface of the support, wherein the polysiloxane-containing primer layer comprises a hydrolyzed form of 3-glycidoxypropyltrimethoxysilane or 3-glycidoxypropyltriethoxysilane and wherein the primer layer is bound to the surface of the support by Van der Waals force or hydrophobic interaction between the polystyrene and 3-glycidoxypropyl groups of the primer layer; and on the primer layer, a hydrophilic layer containing an ethylene glycol chain with a number average molecular weight from 2,700 to 12,500, wherein one end of the ethylene glycol chain is covalently bound to other 3-glycidoxypropyl groups of the primer layer and the other end of the ethylene glycol chain is bound to a functional group selected from a (1H-imidazol-1-yl)carbonyl group or a succinimidyloxycarbonyl group, wherein the nitrogen concentration in the hydrophilic layer is from 0.010 to 0.050 when the functional group is a succinimidyloxycarbonyl group relative to a carbon concentration resulting from the C—O bonds in the hydrophilic layer being 1 and the nitrogen concentration in the hydrophilic layer is from 0.020 to 0.100 when the functional group is a (1H-imidazol-1-yl)carbonyl group relative to a carbon concentration resulting from the C—O bonds in the hydrophilic layer being 1. 2. A method for producing the base material according to claim 1 .
with ligand attached to the carrier via a chemical coupling agent (coatings G01N33/54393) · CPC title
Improving reaction conditions or stability, e.g. by coating or irradiation of surface, by reduction of non-specific binding, by promotion of specific binding · CPC title
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