Polymeric surface having reduced biomolecule adhesion to thermoplastic articles and methods of plasma treatment
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. A method is also provided for treating a surface of a substrate. The method includes treating the surface with plasma comprising one or more non-polymerizing compounds. The treated contact surface has a biomolecule recovery percentage greater than the biomolecule recovery percentage of the surface prior to treatment according to the method.
1. A method for treating a surface comprising:
employing a first conditioning treatment of the surface with a conditioning plasma of one or more non-polymerizing compounds at a remote point, where the ratio of the radiant energy density at the remote point to the radiant energy density at the brightest point of the conditioning plasma is less than 0.5; and
employing a second conversion treatment of the surface with a conversion plasma of water vapor at a remote point to form a converted surface, where the ratio of the radiant energy density at the remote point of conversion treatment to the radiant energy density at the brightest point of the conversion plasma is less than 0.5;
wherein the converted surface has a biomolecule recovery percentage greater than the biomolecule recovery percentage of the surface prior to treatment according to the method.
2. The method of claim 1 , wherein the converted surface has a biomolecule recovery percentage after 24 hours of at least 40%.
3. The method of claim 1 , wherein the biomolecule recovery percentage of the converted surface after 24 hours is at least 80%.
4. The method of claim 1 , wherein the biomolecule recovery percentage of the converted surface after 24 hours is from 82% to 90%.
5. The method of claim 1 , wherein the surface is a vessel lumen surface.
6. The method of claim 1 , wherein the converted surface has a biomolecule recovery percentage greater than the biomolecule recovery percentage of the untreated surface for at least one of: mammal serum albumin; Bovine Serum Albumin (BSA); Fibrinogen (FBG); Transferrin (TFN); egg white ovotransferrin (conalbumin); membrane-associated melanotransferrin; Protein A (PrA); Protein G (PrG); Protein A/G; Protein L; Insulin; Pharmaceutical protein; blood or blood component proteins; and any recombinant form, modification, full length precursor, signal peptide, propeptide, or mature variant of these proteins.
7. The method of claim 1 , wherein the surface comprises a thermoplastic material.
8. The method of claim 1 , wherein the thermoplastic material comprises olefin polymer, polypropylene (PP), polyethylene (PE), cyclic olefin copolymer (COC), cyclic olefin polymer (COP), polymethylpentene, polyester, polyethylene terephthalate, polyethylene naphthalate, polybutylene terephthalate (PBT), polyvinylidene chloride (PVdC), polyvinyl chloride (PVC), polycarbonate, polylactic acid, polystyrene, hydrogenated polystyrene, polycyclohexylethylene (PCHE), epoxy resin, nylon, polyurethane polyacrylonitrile, polyacrylonitrile (PAN), an ionomeric resin, or any combination, composite or blend of any two or more of the above materials.
9. The method of claim 1 wherein the first treatment step and/or second treatment step are carried out using plasma excited by extremely low frequency (ELF) of 3 to 30 Hz, super low frequency (SLF) of 30 to 300 Hz, voice or ultra-low frequency (VF or ULF) of 300 Hz to 3 kHz, very low frequency (VLF) of 3 to 30 kHz, low frequency (LF) of 30 to 300 kHz, medium frequency (MF) of 300 kHz to 3 MHz, high frequency (HF) of 3 to 30 MHz, very high frequency (VHF) of 30 to 300 MHZ, ultra-high frequency (UHF) of 300 MHz to 3 GHZ, or any combination of two or more of these.
10. The method of claim 1 , in which the surface is a coating or layer of PECVD deposited SiO x C y H z or SiN x C y H z , 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); or a barrier coating or layer of SiOx, in which x is from about 1.5 to about 2.9 as measured by XPS.
11. The method of claim 1 , wherein the surface is a fluid contact surface of an article of labware.
12. The method of claim 1 , wherein the surface is a fluid contact surface of a microplate, a centrifuge tube, a pipette tip, a well plate, a microwell plate, an ELISA plate, a microtiter plate, a 96-well plate, a 384-well plate, a vial, a bottle, a jar, a syringe, a cartridge, a blister package, an ampoule, an evacuated blood collection tube, a specimen tube, a centrifuge tube, or a chromatography vial.
13. The method of claim 1 , wherein the method is carried out in a plasma chamber having a treatment volume of 100 mL to 50 liters a tubular fluid inlet projects into the treatment volume, through which one or more feed gases are fed into the plasma chamber; and the plasma chamber further comprises a vacuum source for at least partially evacuating the treatment volume.
14. The method of claim 1 , further comprising the steps, prior to treating the surface with the conditioning plasma, of:
applying a solvent, also known as a polar liquid treatment agent, to the surface, and
applying ionized gas to the surface.
15. The method of claim 14 where the ionized gas is air.
16. The method of claim 14 wherein the conditioning plasma; is comprised of nitrogen.
17. The method of claim 1 , further comprising the steps of:
applying a solvent, also known as a polar liquid treatment agent, to the surface prior to treating the surface with the conditioning plasma.
18. The method of claim 17 where the solvent, also known as a polar liquid treatment agent, is water.
19. The method of claim 17 where the conditioning plasma, is comprised of nitrogen.
20. An article treated according to a method as described in claim 1 .