Polymeric surface having reduced biomolecule adhesion to thermoplastic articles of such substrate
A substrate is described having a treated contact surface comprising a carbon or silicon compound comprising from 1 to 30 atomic percent oxygen, from 0.1 to 30 atomic percent nitrogen, or both, each as measured by XPS. The treated contact surface has a biomolecule recovery percentage greater than the biomolecule recovery percentage of the surface before treatment according to the method.
1 . A method for providing a non-specific biomolecule adsorption and/or non-specific biomolecule binding resistant coated surface, the method comprising the steps:
(a) providing a substrate with a prepared surface;
(b) reacting the prepared surface with at least one zwitterionic copolymer, thus forming a non-specific biomolecule adsorption and/or biomolecule binding resistant coated surface;
wherein reacting the prepared surface with at least one zwitterionic copolymer comprises:
reacting the prepared surface with a vapor comprising at least one silyl amine coupling agent to provide an amine modified surface;
contacting the amine modified surface with a copolymer solution comprising a solvent, wherein the copolymer comprises at least one copolymerizable zwitterionic monomer and at least one copolymerizable epoxy monomer, optionally in the presence of a polymerization initiator; and
wherein the at least one copolymerizable epoxy monomer is selected from the group consisting of (E)-(oxiran-2-yl)methyl but-2-enoate, (3,3-dimethyloxiran-2-yl)methyl methacrylate, (E)-(oxiran-2-yl)methyl cinnamate, (oxiran-2-yl)methyl 2-methylenebutanoate, 1-(oxiran-2-yl) propyl acrylate, 1-(oxiran-2-yl)ethyl methacrylate, (oxiran-2-yl)methyl 3-methyl-2-methylenebutanoate, (oxiran-2-yl)methyl 2-methylenepentanoate, (3-methyloxiran-2-yl)methyl acrylate, 2-(oxiran-2-yl) propan-2-yl acrylate, (oxiran-2-yl)methyl 2-methylenehexanoate, (3-methyloxiran-2-yl)methyl methacrylate, (3,3-dimethyloxiran-2-yl)methyl acrylate, and combinations thereof.
2 . The method of claim 1 , wherein providing the substrate with the prepared surface comprises:
(i) providing a substrate in a reaction chamber;
(ii) drawing a vacuum in the reaction chamber;
(iii) providing a gas comprising O 2 or an organosilicon precursor and optionally O 2 in the vicinity of the substrate surface; and
(iv) generating a plasma from the gas, thus forming the prepared substrate surface.
3 . The method of claim 1 , wherein the at least one silyl amine coupling agent is selected from the group consisting of 3-aminopropyltriethoxysilane, 3-aminopropyltrimethoxysilane, 4-aminobutyltriethoxysilane, m-aminophenyltrimethoxysilane, p-aminophenyltrimethoxysilane, o-aminophenyltrimethoxysilane, 3-aminopropyltris(methoxyethoxyethoxy) silane, 11-aminoundecyltriethoxysilane, 3-(m-aminophenoxy) propyltrimethoxysilane, aminopropylsilanetriol, 3-aminopropylmethyldiethoxysilane, 3-aminopropyl-diisopropylethoxysilane, 3-aminopropyldimethylethoxysilane, N-(2-aminoethyl)-3-aminopropyltrimethoxysilane, N-[3-(trimethoxysilyl) propyl]ethylenediamine, N-(2-aminoethyl)-3-aminopropyltriethoxysilane, N-(6-aminohexyl)aminomethyltriethoxysilane, N-(6-aminohexyl)aminopropyltrimethoxysilane, N-(2-aminoethyl)-11-aminoundecyltrimethoxysilane, (aminoethylaminomethyl) phenethyltrimethoxysilane, N-3-[(amino (polypropylenoxy)]aminopropyltrimethoxysilane, N-(2-aminoethyl)-3-aminopropylsilanetriol, N-(2-aminoethyl)-3-aminopropylmethyldimethoxysilane, N-(2-aminoethyl)-3-aminoisobutylmethyldimethoxysilane, (aminoethylamino)-3-isobutyldimethylmethoxysilane, (3-trimethoxysilylpropyl) diethylenetriamine, N-butylaminopropyltrimethoxysilane, N-ethylaminoisobutyltrimethoxysilane, N-methylaminopropyltrimethoxysilane, N-phenylaminopropyltrimethoxysilane, 3-(N-allylamino) propyltrimethoxysilane, (cyclohexylaminomethyl)triethoxysilane, N-cyclohexylaminopropyltrimethoxysilane, N-ethylaminoisobutylmethyldiethoxysilane, (phenylaminomethyl)methyldimethoxysilane, N-phenylaminomethyltriethoxysilane, N-methylaminopropylmethyldimethoxysilane, bis(2-hydroxyethyl)-3-aminopropyltriethoxysilane, 3-(N-styrylmethyl-2-aminoethylamino)-propyltrimethoxysilane hydrochloride, (2-N-benzylaminoethyl)-3-aminopropyl-trimethoxysilane, bis(triethoxysilylpropyl)amine, bis(trimethoxysilylpropyl)amine, bis[(3-trimethoxysilyl) propyl]-ethylenediamine, bis[(3-trimethoxysilyl) propyl]-ethylenediamine, bis(methyldiethoxysilylpropyl)amine, N-allyl-aza-2,2-dimethoxysilacyclopentane, N-aminoethyl-aza-2,2,4-trimethyl-silacyclopentane, N-(3-aminopropyldimethylsila) aza-2,2-dimethyl-2-silacyclopentane, N—N-butyl-aza-2,2-dimethoxysilacyclopentane, 2,2-dimethoxy-1,6-diaza-2-silacyclooctane, N-methyl-aza-2,2,4-trimethylsilacylcopentane, 1-(N—(N′,N′-dimethylaminoethyl))-1-aza-2,2,4-trimethyl-2-silacyclopentane, and combinations thereof.
4 . The method of claim 1 , wherein the at least one copolymerizable zwitterionic monomer is selected from the group consisting of 2-(meth)acryloyloxyethyl-2′-(trimethylammonio)ethyl phosphate; 2-(methacryloxy)ethyl 2-(diimethylammonio)ethyl phosphate; 2-(methacryloxy)ethyl-2-(dimethylammonio)ethylcarboxylate; 2-(methacryloxy)ethyl-2-(dimethylammonio) propylsulfonate; 2-(methyacrylamido)ethyl-2-(dimethylammonio)-propylsulfonate; phosphoric acid 2-(methacryloyloxy)ethyl 2-(trimethylammonio)ethyl ester); 3-(meth)acryloyloxypropyl-2′-(trimethylammonio)ethyl phosphate, 4-(meth)acryloyloxybutyl-2′-(trimethylammonio)ethyl phosphate, 5-(meth)acryloyloxypentyl-2′-(trimethylammonio)ethyl phosphate, 6-(meth)acryloyloxyhexyl-2′-(trimethylammonio)ethyl phosphate, 2-(meth)acryloyloxyethyl-2′-(trimethylammonio)ethyl phosphate, 2-(meth)acryloyloxyethyl-2′-(tripropylammonio)ethyl phosphate, 2-(meth)acryloyloxyethyl-2′-(tributylammonio)ethyl phosphate, 2-(meth)acryloyloxypropyl-2′-(trimethylammonio)ethyl phosphate, 2-(meth)acryloyloxybutyl-2′-(trimethylammonio)ethyl phosphate, 2-(meth)acryloyloxypentyl-2′-(trimethylammonio)ethyl phosphate, 2-(meth)acryloyloxyhexyl-2′-(trimethylammonio)ethyl phosphate, 2-(meth)acryloyloxyethyl-3′-(trimethylammonio) propyl phosphate, 3-(meth)acryloyloxypropyl-3′-(trimethylammonio) propyl phosphate, 4-(meth)acryloyloxybutyl-3′-(trimethylammonio) propyl phosphate, 5-(meth)acryloyloxypentyl-3′-(trimethylammonio)-propyl phosphate, 6-(meth)acryloyloxyhexyl-3′-(trimethylammonio) propyl phosphate, 2-(meth)acryloyloxyethyl-4′-(trimethylammonio)butyl phosphate, 3-(meth)acryloyloxypropyl-4′-(trimethylammonio)butyl phosphate, 4-(meth)acryloyloxybutyl-4′-(trimethylammonio)butyl phosphate, 5-(meth)acryloyloxypentyl-4′-(trimethylammonio)butyl phosphate, 6-(meth)acryloyloxyhexyl-4′-(trimethylammonio)butyl phosphate, 2-(vinyloxy)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(allyloxy)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(p-vinylbenzyloxy)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(p-vinylbenzoyloxy)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(styryloxy)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(p-vinylbenzyl)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(vinyloxycarbonyl)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(allyloxycarbonyl)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(acryloylamino)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(vinylcarbonylamino)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(allyloxycarbonylamino)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(butyroyloxy)ethyl-2′-(trimethylammonio)ethyl phosphate, 2-(crotonoyloxy)ethyl-2′-(trimethylammonio)ethyl phosphate, ethyl-(2′-trimethylammonioethylphosphorylethyl) fumarate, butyl-(2′-trimethylammonio-ethylphosphorylethyl) fumarate, hydroxyethyl-(2′-trimethylammonioethyl-phosphorylethyl) fumarate, β-carboxyethyl-3,3-dimethyammoniumethylmethacrylate, sulfopropyl-3,3-dimethylammoniumethylmethacrylate, and combinations thereof.
5 . The method of claim 1 , wherein the solvent is selected from the group consisting of water, methanol, ethanol, isopropanol, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, N,N-dimethylformamide, dimethylsulfoxide, methylene chloride, 1,2-dicholorethane, and combinations thereof.
6 . The method of claim 1 , wherein the substrate is a polymer.
7 . The method of claim 6 , wherein the polymer is selected from the group consisting of an olefin polymer; polypropylene (PP); polyethylene (PE); cyclic olefin copolymer (COC); cyclic olefin polymer (COP); polymethylpentene; polyester; polyethylene terephthalate; polyethylene naphthalate; polybutylene terephthalate (PBT); PVdC (polyvinylidene chloride); polyvinyl chloride (PVC); polycarbonate; polymethylmethacrylate; polylactic acid; polylactic acid; polystyrene; hydrogenated polystyrene; poly(cyclohexylethylene) (PCHE); epoxy resin; nylon; polyurethane polyacrylonitrile; polyacrylonitrile (PAN); and an ionomeric resin.
8 . The method of claim 1 , wherein the non-specific biomolecule adsorption and/or non-specific binding resistant coated surface has decreased binding of biomolecules compared to a non-treated substrate.
9 . The method of claim 8 , wherein the biomolecules are selected from the group consisting of nucleotides, amino acids, sugars, fatty acids, nucleic acid molecules, polypeptides, polynucleotides, polysaccharides, lipids, steroids, glycoproteins, lipoproteins, glycolipids, DNA, DNA-protein conjugates, RNA, RNA-conjugates, antibodies, and receptors, receptor fusion constructs, receptor fusion proteins, chimeric proteins, antibody fusion constructs, and antibody fusion proteins.
10 . The method of claim 1 , wherein the substrate is a surface of a vessel.
11 . The method of claim 10 , wherein the vessel is selected from the group consisting of a microplate; a centrifuge tube; a pipette tip; a cuvette, a microwell plate; an ELISA plate; a microtiter plate; a 96-well plate; a 384-well plate; a 1536-well plate; a round bottom flask; and an Erlenmeyer flask.
12 . The method of claim 10 , wherein the substrate is the interior surface of a vessel.
13 . The method of claim 12 , wherein the vessel is a vial, a syringe, or a cartridge.
14 . The method of claim 13 , wherein the interior surface comprises a coating or layer of PECVD deposited SiOxCyHz or SiNxCyHz, in which x is from about 0.5 to about 2.4 as measured by x-ray photoelectron spectroscopy (XPS), y is from about 0.6 to about 3 as measured by XPS, and z is from about 2 to about 9 as measured by Rutherford backscattering spectrometry (RBS).
15 . The method of claim 13 , wherein the interior surface comprises a barrier coating or layer of SiOx, in which x is from about 1.5 to about 2.9 as measured by x-ray photoelectron spectroscopy (XPS).
16 . A product comprising a non-specific biomolecule adsorption and/or non-specific biomolecule binding resistant coated surface prepared by the method according to claim 1 .
17 . The product of claim 16 , wherein the product is a vessel, and wherein at least a portion of an interior surface of the vessel comprises the non-specific biomolecule adsorption and/or non-specific biomolecule binding resistant coated surface.