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US5773587A Expired / Lapsed US ⏱️ 0.0 years remaining

Hydrophlic polymer coated perflurocarbon polymer matrices for bioaffinity separations

Assignee: Arkion Life Sciences LLC
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Filing: 1996-08-06
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Granted: 1998-06-30
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Expires: 2016-08-06
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Abstract

Abstract Perfluorocarbon polymer-based matrices are coated with a hydrophilic polymer for use in bioaffinity separations. Coating is carried out by dispersing porous particles of inert perfluorocarbon polymer in a water-miscible organic solvent such as acetone or tetrafydrofuran to wet surfaces of the particles, forming a dispersion of the wetted particles in an aqueous solution of hydrophilic polymer such as poly(vinyl alcohol) containing a plurality of hydroxyl groups, at least one being at an end of a polymer chain, to adsorb the hydrophilic polymer onto the wetted surfaces of the particles, admixing a homobifunctional cross-linking agent such as glutaraldehyde with the particles to cross-link the hydrophilic polymer, activating hydroxyl groups on the surface of the cross-linked hydrophilic polymer and covalently bonding a ligand or ligand binder to the activated hydroxyl groups.

Inventors

  • 👤 Christopher Robin Lowe
  • 👤 Norman A Parris
  • 👤 Ian Pitfield
  • 👤 Duncan Ross Purvis

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 17:12
CPC Classifications
B; B01; B01J; B01J20/00; B01J20/22; B01J20/26; B01J20/261; B01J20/265; B01J20/267; B01J20/281; B01J20/286; B01J20/30; B01J20/32; B01J20/3231; B01J20/3242; B01J20/3268; B01J20/327; B01J20/3272; B01J20/3274; B01J20/328; B01J20/3282; B01J2220/00; B01J2220/40; B01J2220/49; B01J2220/50; B01J2220/54; Y; Y10; Y10S; Y10S435/00; Y10S435/814; Y10S435/815; Y10S530/00; Y10S530/81; Y10S530/812; Y10S530/815; Y10S530/816

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 223 words
A method for making adsorbent particles comprising the sequential steps: (1) dispersing porous particles of inert perfluorocarbon polymer in water-miscible organic solvent to wet the surfaces of the porous particles; (2) separating the porous perfluorocarbon polymer particles, the surfaces of which are wetted with the water-miscible solvent, from the water-miscible solvent in the dispersion from step (1); (3) forming a dispersion of the miscible solvent-wetted perfluorocarbon polymer particles from step (2) in an aqueous solution of hydrophilic polymer having a molecular weight of at least 1,000 up to the point of insolubility of the polymer in water, the chains of the polymer containing a plurality of hydroxyl groups at least one of which is located at an end of a polymer chain, by which the hydrophilic polymer is adsorbed onto the wetted surfaces of the perfluorocarbon polymer; (4) admixing a homobifunctional cross-linking agent with the dispersion from step (3) to effect cross-linking of the adsorbed hydrophilic polymer adsorbed on the surfaces of the fluorocarbon polymer; (5) separating the cross-linked hydrophilic polymer-coated particles from the dispersion from step (4); (6) activating hydroxyl groups on the surface of the cross-linked hydrophilic polymer to provide for covalent bonding thereto of a ligand or ligand binder; and (7) covalently bonding a ligand or ligand binder to the activated hydroxyl groups on the surface of the hydrophilic polymer.
Claim 2
Independent Claim 223 words
A method for making adsorbent particles comprising the sequential steps: (1) dispersing porous particles of inert perfluorocarbon polymer in water-miscible organic solvent to wet the surfaces of the porous particles; (2) separating the porous perfluorocarbon polymer particles, the surfaces of which are wetted with the water-miscible solvent, from the water-miscible solvent in the dispersion from step (1); (3) forming a dispersion of the miscible solvent-wetted perfluorocarbon polymer particles from step (2) in an aqueous solution of hydrophilic polymer having a molecular weight of at least 1,000 up to the point of insolubility of the polymer in water, the chains of the polymer containing a plurality of hydroxyl groups at least one of which is located at an end of a polymer chain, by which the hydrophilic polymer is adsorbed onto the wetted surfaces of the perfluorocarbon polymer; (4) admixing a homobifunctional cross-linking agent with the dispersion from step (3) to effect cross-linking of the adsorbed hydrophilic polymer adsorbed on the surfaces of the fluorocarbon polymer; (5) separating the cross-linked hydrophilic polymer-coated particles from the dispersion from step (4); (6) activating hydroxyl groups on the surface of the cross-linked hydrophilic polymer to provide for covalent bonding thereto of a ligand or ligand binder; and (7) covalently bonding a ligand or ligand binder to the activated hydroxyl groups on the surface of the hydrophilic polymer.
Claim 3
Dependent Claim 13 words
The method of claim 1 in which the hydrophilic polymer is poly(vinyl alcohol).
Claim 4
Dependent Claim 21 words
The method of claim 1 in which the water-miscible organic solvent is selected from the group consisting of acetone and tetrahydrofuran.
Claim 5
Dependent Claim 24 words
The method of claim 1 in which the homobifunctional crosslinking agent contains groups capable of covalent bonding selected from --COCl, --COBr, --NCO and --CHO.
Claim 6
Dependent Claim 30 words
A bioaffinity separation process comprising capturing a binder or ligand binder complementary to the binder or ligand binder attached to an adsorbent particle made by the method of claim 1.
Claim 7
Dependent Claim 12 words
An adsorbent matrix made by the method of any of claims 1-4.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 2001-06-29 2001-12-29 2002-06-30 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2005-06-29 2005-12-29 2006-06-30 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2009-06-29 2009-12-29 2010-06-30 $7700.00 Window Closed / Lapsed

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