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US5858238A Expired / Lapsed US ⏱️ 0.0 years remaining

Salvage of autologous blood via selective membrane/sorption technologies

Assignee: Jostra Bentley Inc
•
Filing: 1997-03-07
•
Granted: 1999-01-12
•
Expires: 2017-03-07
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Abstract

Abstract Methods and apparatuses for salvaging blood from a patient are disclosed. A blood salvaging and/or blood processing circuit coupled to a cardiopulmonary bypass circuit, cardiotomy circuit, or directly to the patient comprises a hemocentrator for removing water, fluids, and low molecular weight solutes by ultrafiltration and a sorbent-containing plasma separator for removing a selected solute, such as heparin. A combination device for salvaging blood comprises a closed plasma chamber containing a plasma chamber solution, a hollow fiber plasma-separating membrane for receiving blood and permitting plasma to be transported therethrough into the plasma chamber solution and for refiltering the treated plasma back into the blood circuit, a selective sorbent for contacting the selected solute in the plasma and binding the selected solute, and an ultrafiltration membrane for removing water, fluids, and low molecular weight components from the plasma.

Inventors

  • 👤 James C. McRea
  • 👤 Stephanie Poulsen
  • 👤 Yong Nian Xia
  • 👤 Kirk Fowers

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 04:10
CPC Classifications
B; B01; B01D; B01D61/00; B01D61/14; B01D61/145; A; A61; A61M; A61M1/00; A61M1/34; A61M1/342; A61M1/3424; A61M1/3427; A61M1/3472; A61M1/3475; A61M1/3482; A61M1/3493; A61M1/36; A61M1/3601; A61M1/3603; A61M1/3621; B01D61/146; B01D61/24; B01D61/243; B01D63/00; B01D63/02; B01D63/04; B01D63/046; A61M1/3672; A61M1/3675; B01D2313/00; B01D2313/40; B01D2315/00; B01D2315/06

Claims Analysis

Total Claims: 46
Claim 1
Independent Claim 346 words
A system for salvaging blood from a patient for the selective removal of a targeted solute in the blood and the removal of water, fluids, and low molecular weight solutes comprising: (a) a hemoconcentrator comprising an inlet port, and outlet port, and a porous ultrafiltration membrane having a selected molecular weight cut-off for retaining components selected from the group consisting of cells and solutes with a molecular weight greater than the cut-off and for allowing water, fluids, and solutes with a molecular weight less than the cut-off to be removed from blood or plasma; and (b) a first solute removal device for selectively removing the targeted solute from blood by means of convective and diffusive transport of plasma from said blood across a hollow fiber plasma-separating membrane into a closed plasma chamber where the selective removal of the targeted solute from non-targeted solutes using a sorbent is accomplished followed by the subsequent transport of the non-targeted solutes across the hollow fiber plasma-separating membrane back into the blood, comprising (i) the closed plasma chamber configured for being filled with a plasma chamber solution and to freely circulate, equilibrate, and interact plasma in said plasma chamber solution under relatively uniform pressure; (ii) the hollow fiber plasma-separating membrane, wherein said hollow fiber plasma-separating membrane has an inlet arm and an outlet arm and is configured for being immersed in said plasma chamber solution in said closed plasma chamber; (iii) at least one sorbent having an affinity for binding said targeted solute, wherein said sorbent is contained in said closed plasma chamber; (iv) means for securing said inlet arm and outlet arm of said hollow fiber plasma-separating membrane in said closed plasma chamber; and (v) means for circulating said blood into said inlet arm, through said hollow fiber plasma-separating membrane, and out through said outlet arm; and (c) means for coupling said hemoconcentrator to said first solute removal device to permit liquid communication therebetween and for coupling said hemoconcentrator and said first solute removal device to said patient to permit blood to be received from and returned to said patient.
Claim 2
Independent Claim 346 words
A system for salvaging blood from a patient for the selective removal of a targeted solute in the blood and the removal of water, fluids, and low molecular weight solutes comprising: (a) a hemoconcentrator comprising an inlet port, and outlet port, and a porous ultrafiltration membrane having a selected molecular weight cut-off for retaining components selected from the group consisting of cells and solutes with a molecular weight greater than the cut-off and for allowing water, fluids, and solutes with a molecular weight less than the cut-off to be removed from blood or plasma; and (b) a first solute removal device for selectively removing the targeted solute from blood by means of convective and diffusive transport of plasma from said blood across a hollow fiber plasma-separating membrane into a closed plasma chamber where the selective removal of the targeted solute from non-targeted solutes using a sorbent is accomplished followed by the subsequent transport of the non-targeted solutes across the hollow fiber plasma-separating membrane back into the blood, comprising (i) the closed plasma chamber configured for being filled with a plasma chamber solution and to freely circulate, equilibrate, and interact plasma in said plasma chamber solution under relatively uniform pressure; (ii) the hollow fiber plasma-separating membrane, wherein said hollow fiber plasma-separating membrane has an inlet arm and an outlet arm and is configured for being immersed in said plasma chamber solution in said closed plasma chamber; (iii) at least one sorbent having an affinity for binding said targeted solute, wherein said sorbent is contained in said closed plasma chamber; (iv) means for securing said inlet arm and outlet arm of said hollow fiber plasma-separating membrane in said closed plasma chamber; and (v) means for circulating said blood into said inlet arm, through said hollow fiber plasma-separating membrane, and out through said outlet arm; and (c) means for coupling said hemoconcentrator to said first solute removal device to permit liquid communication therebetween and for coupling said hemoconcentrator and said first solute removal device to said patient to permit blood to be received from and returned to said patient.
Claim 3
Dependent Claim 19 words
The system of claim 1 wherein said porous ultrafiltration membrane of said hemoconcentrator comprises a plurality of hollow fibers.
Claim 4
Dependent Claim 24 words
The system of claim 2 wherein the molecular weight cut-off of said porous ultrafiltration membrane is in the range of about 10,000 to 100,000.
Claim 5
Dependent Claim 31 words
The system of claim 3 wherein said porous ultrafiltration membrane is made from a material selected from the group consisting of polyacrylonitrile, polysulfone, polynethylmethacrylate, cellulose acetate, cellulose diacetate, and cellulose triacetate.
Claim 6
Dependent Claim 18 words
The system of claim 1 wherein said hollow fiber plasma-separating membrane comprises a bundle of parallel hollow fibers.
Claim 7
Dependent Claim 27 words
The system of claim 5 wherein said sorbent is of a size and configuration such that said sorbent is not permeable to the hollow fiber plasma-separating membrane.
Claim 8
Dependent Claim 50 words
The system of claim 6 wherein said hollow fibers making up said hollow fiber plasma-separating membrane are constructed of a blood-compatible material having a suitable pore size to allow passage of plasma into the plasma chamber solution while retaining blood cells and platelets from the blood within the hollow fibers.
Claim 9
Dependent Claim 27 words
The system of claim 7 wherein the pore sizes in said hollow fibers of said hollow fiber plasma-separating membrane range between about 0.01 μm to 1.0 μm.
Claim 10
Dependent Claim 37 words
The system of claim 8 wherein said hollow fibers of said hollow fiber plasma-separating membrane are made from a material selected from the group consisting of polypropylene, cellulose diacetate, polycarbonate, polyvinylchloride, polyvinylalcohol, polymethylmethacrylate, polyethylene, polysulfone, and polyethylenevinylalcohol.
Claim 11
Dependent Claim 45 words
The system according to claim 9 wherein the sorbent comprises a ligand immobilized on a substrate and said ligand is a member selected from the group consisting of enzymes, living tissue, fragments of tissue, cells, antibodies, peptides, macromolecules, nucleic acids, lectins, carbohydrates, and chelating agents.
Claim 12
Dependent Claim 12 words
The system of claim 10 wherein said sorbent has affinity for heparin.
Claim 13
Dependent Claim 10 words
The system of claim 11 wherein the substrate is agarose.
Claim 14
Dependent Claim 11 words
The system of claim 12 wherein the sorbent is poly-L-lysine-coupled agarose.
Claim 15
Dependent Claim 40 words
The system of claim 1 wherein said hemoconcentrator is disposed within said closed plasma chamber of said first solute removal device in fluid communication with said plasma chamber solution to thereby effect simultaneous hemoconcentration and removal of the targeted solute.
Claim 16
Dependent Claim 59 words
The system of claim 1 wherein said hemoconcentrator is disposed in fluid communication with said first solute removal device such that said blood is permitted to pass from said hemoconcentrator to said first solute removal device, or vice-versa, to thereby effect sequential hemoconcentration and removal of the targeted solute or sequential removal of the targeted solute and hemoconcentration, respectively.
Claim 17
Dependent Claim 63 words
The system of claim 1 wherein said outlet port of said hemoconcentrator is coupled to the inlet arm of said first solute removal device such that blood passes through said hemoconcentrator for removal of water, fluids, and low molecular weight solutes to result in concentrated blood, which concentrated blood then passes through said first solute removal device for removal of the targeted solute.
Claim 18
Dependent Claim 62 words
The system of claim 1 wherein the outlet arm of said first solute removal device is coupled to the inlet port of said hemoconcentrator such that blood passes through said first solute removal device for removal of the targeted solute resulting in targeted-solute-depleted blood, which targeted-solute-depleted blood then passes through said hemoconcentrator for removal of water, fluids, and low molecular weight solutes.
Claim 19
Dependent Claim 13 words
The system of claim 1 wherein said plasma chamber solution is an electrolyte.
Claim 20
Dependent Claim 34 words
The system of claim 1 wherein said porous ultrafiltration membrane is contained in said closed plasma chamber such that water, fluids, and low molecular weight solutes can be removed from said plasma by ultrafiltration.
Claim 21
Dependent Claim 253 words
The system of claim 1 further comprising a second solute removal device, which comprises (i) A closed plasma chamber configured for being filled with a plasma chamber solution and to freely circulate, equilibrate, and interact plasma in said plasma chamber solution under relatively uniform pressure; (ii) a hollow fiber plasma-separating membrane, wherein said hollow fiber plasma-separating membrane has an inlet arm and an outlet arm and is configured for being immersed in said plasma chamber solution in said closed plasma chamber; (iii) at least one sorbent having an affinity for binding said targeted solute, wherein said sorbent is contained in said closed plasma chamber; (iv) means for securing said inlet arm and outlet arm of said hollow fiber plasma-separating membrane in said closed plasma chamber; and (v) means for circulating blood into said inlet arm, through said hollow fiber plasma-separating membrane, and out through said outlet arm; wherein the closed plasma chamber of said first solute removal device is coupled to the inlet port of said hemoconcentrator and the outlet port of said hemoconcentrator is coupled to the closed plasma chamber of said second solute removal device such that plasma can flow from said first solute removal device through said hemoconcentrator to said second solute removal device such that water, fluids, and low molecular weight solutes can be removed from said plasma by ultrafiltration, and wherein said outlet arm of said first solute removal device is coupled to the inlet arm of said second solute removal device such that blood can flow therebetween.
Claim 22
Independent Claim 281 words
An apparatus for selectively removing a targeted solute from blood by binding said targeted solute to an affinity sorbent and removing water, fluids, and low molecular weight solutes by ultrafiltration, comprising: (a) a closed plasma chamber configured for being filled with a plasma chamber solution and to freely circulate, equilibrate, and interact plasma in said plasma chamber solution under relatively uniform pressure; (b) a hollow fiber plasma-separating membrane having an inlet arm and an outlet arm and configured for being immersed in said plasma chamber solution in said closed plasma chamber; (c) at least one sorbent having an affinity for binding said targeted solute, wherein said sorbent is contained in said closed plasma chamber; (d) means for securing said inlet arm and outlet arm of said hollow fiber plasma-separating membrane in said close plasma chamber; and (e) a porous ultrafiltration membrane disposed in said closed plasma chamber and configured for being immersed in said plasma chamber solution, said ultrafiltration membrane having a selected molecular weight cut-off for allowing water, fluids, and solutes with a molecular weight lower than the cut-off and means for withdrawing said water, fluids, and solutes that pass through said ultrafiltration membrane; and (f) means for circulating said blood into said inlet arm such that plasma, including water, fluids, and low molecular weight solutes therein, is transported from said blood across said hollow fiber plasma-separating membrane by convective and diffusive transport into the plasma chamber solution where the selective removal of the targeted solute from non-targeted solutes using said affinity sorbent is accomplished followed by the subsequent transport of the non-targeted solutes across the hollow fiber plasma-separating membrane back into the blood and out through said outlet arm.
Claim 23
Independent Claim 281 words
An apparatus for selectively removing a targeted solute from blood by binding said targeted solute to an affinity sorbent and removing water, fluids, and low molecular weight solutes by ultrafiltration, comprising: (a) a closed plasma chamber configured for being filled with a plasma chamber solution and to freely circulate, equilibrate, and interact plasma in said plasma chamber solution under relatively uniform pressure; (b) a hollow fiber plasma-separating membrane having an inlet arm and an outlet arm and configured for being immersed in said plasma chamber solution in said closed plasma chamber; (c) at least one sorbent having an affinity for binding said targeted solute, wherein said sorbent is contained in said closed plasma chamber; (d) means for securing said inlet arm and outlet arm of said hollow fiber plasma-separating membrane in said close plasma chamber; and (e) a porous ultrafiltration membrane disposed in said closed plasma chamber and configured for being immersed in said plasma chamber solution, said ultrafiltration membrane having a selected molecular weight cut-off for allowing water, fluids, and solutes with a molecular weight lower than the cut-off and means for withdrawing said water, fluids, and solutes that pass through said ultrafiltration membrane; and (f) means for circulating said blood into said inlet arm such that plasma, including water, fluids, and low molecular weight solutes therein, is transported from said blood across said hollow fiber plasma-separating membrane by convective and diffusive transport into the plasma chamber solution where the selective removal of the targeted solute from non-targeted solutes using said affinity sorbent is accomplished followed by the subsequent transport of the non-targeted solutes across the hollow fiber plasma-separating membrane back into the blood and out through said outlet arm.
Claim 24
Independent Claim 446 words
A system for salvaging blood from a patient for the selective removal of a targeted solute in the blood and the removal of water, fluids, and low molecular weight solutes comprising: (a) a hemoconcentrator comprising an inlet port, an outlet port, and a porous ultrafiltration membrane having a selected molecular weight cut-off for retaining components selected from the group consisting of cells and solutes with a molecular weight greater than the cut-off and for allowing water, fluids, and solutes with a molecular weight less than the cut-off to be removed from blood or plasma; and (b) first and second solute removal devices for selectively removing the targeted solute from blood by means of convective and diffusive transport of plasma from said blood across a hollow fiber plasma-separating membrane into a closed plasma chamber where the selective removal of the targeted solute from non-targeted solutes using a sorbent is accomplished followed by the subsequent transport of the non-targeted solutes across the hollow fiber plasma-separating membrane back into the blood, each said first and second solute removal device comprising (i) the closed plasma chamber configured for being filled with a plasma chamber solution and to freely circulate, equilibrate, and interact plasma in said plasma chamber solution under relatively uniform pressure; (ii) the hollow fiber plasma-separating membrane, wherein said hollow fiber plasma-separating membrane has an inlet aim and an outlet arm and is configured for being immersed in said plasma chamber solution in said closed plasma chamber; (iii) at least one sorbent having an affinity for binding said targeted solute, wherein said sorbent is contained in said closed plasma chamber; (iv) means for securing said inlet arm and outlet arm of said hollow fiber plasma-separating membrane in said closed plasma chamber; and (v) means for circulating said blood into said inlet arm, through said hollow fiber plasma-separating membrane, and out through said outlet arm; (c) means for coupling the closed plasma chamber of said first solute removal device to the inlet port of said hemoconcentrator and means for coupling the outlet port of said hemoconcentrator to the closed plasma chamber of said second solute removal device such that plasma can flow from said first solute removal device through said hemoconcentrator to said second solute removal device such that water, fluids, and low molecular weight solutes can be removed from said plasma by ultrafiltration, and means for coupling the outlet arm of said first solute removal device to the inlet arm of said second solute removal device such that blood can flow therebetween; and (d) means for coupling said first and second solute removal devices to said patient to permit blood to be received from and returned to said patient.
Claim 25
Independent Claim 446 words
A system for salvaging blood from a patient for the selective removal of a targeted solute in the blood and the removal of water, fluids, and low molecular weight solutes comprising: (a) a hemoconcentrator comprising an inlet port, an outlet port, and a porous ultrafiltration membrane having a selected molecular weight cut-off for retaining components selected from the group consisting of cells and solutes with a molecular weight greater than the cut-off and for allowing water, fluids, and solutes with a molecular weight less than the cut-off to be removed from blood or plasma; and (b) first and second solute removal devices for selectively removing the targeted solute from blood by means of convective and diffusive transport of plasma from said blood across a hollow fiber plasma-separating membrane into a closed plasma chamber where the selective removal of the targeted solute from non-targeted solutes using a sorbent is accomplished followed by the subsequent transport of the non-targeted solutes across the hollow fiber plasma-separating membrane back into the blood, each said first and second solute removal device comprising (i) the closed plasma chamber configured for being filled with a plasma chamber solution and to freely circulate, equilibrate, and interact plasma in said plasma chamber solution under relatively uniform pressure; (ii) the hollow fiber plasma-separating membrane, wherein said hollow fiber plasma-separating membrane has an inlet aim and an outlet arm and is configured for being immersed in said plasma chamber solution in said closed plasma chamber; (iii) at least one sorbent having an affinity for binding said targeted solute, wherein said sorbent is contained in said closed plasma chamber; (iv) means for securing said inlet arm and outlet arm of said hollow fiber plasma-separating membrane in said closed plasma chamber; and (v) means for circulating said blood into said inlet arm, through said hollow fiber plasma-separating membrane, and out through said outlet arm; (c) means for coupling the closed plasma chamber of said first solute removal device to the inlet port of said hemoconcentrator and means for coupling the outlet port of said hemoconcentrator to the closed plasma chamber of said second solute removal device such that plasma can flow from said first solute removal device through said hemoconcentrator to said second solute removal device such that water, fluids, and low molecular weight solutes can be removed from said plasma by ultrafiltration, and means for coupling the outlet arm of said first solute removal device to the inlet arm of said second solute removal device such that blood can flow therebetween; and (d) means for coupling said first and second solute removal devices to said patient to permit blood to be received from and returned to said patient.
Claim 26
Independent Claim 538 words
A method of selectively removing a targeted solute and water, fluids, and low molecular weight solutes from blood comprising: (a) providing a system comprising: (1) a hemoconcentrator comprising an inlet port, an outlet port, and a porous ultrafiltration membrane having a selected molecular weight cut-off for retaining components selected from the group consisting of cells and solutes with a molecular weight greater than the cut-off and for allowing water, fluids, and solutes with a molecular weight less than the cut-off to be removed from blood or plasma; and (2) a first solute removal device for selectively removing the targeted solute from blood by means of convective and diffusive transport of plasma from said blood across a hollow fiber plasma-separating membrane into a closed plasma chamber where the selective removal of the targeted solute from non-targeted solutes using a sorbent is accomplished followed by the subsequent transport of the non-targeted solutes across the hollow fiber plasma-separating membrane back into the blood, comprising (i) the closed plasma chamber configured for being filled with a plasma chamber solution and to freely circulate, equilibrate, and interact plasma in said plasma chamber solution under relatively uniform pressure; (ii) the hollow fiber plasma-separating membrane, wherein said hollow fiber plasma-separating membrane has an inlet arm and an outlet arm and is configured for being immersed in said plasma chamber solution in said closed plasma chamber; (iii) at least one sorbent having an affinity for binding said targeted solute, wherein said sorbent is contained in said closed plasma chamber; (iv) means for securing said inlet arm and outlet arm of said hollow fiber plasma-separating membrane in said closed plasma chamber; and (v) means for circulating said blood into said inlet arm, through said hollow fiber plasma-separating membrane, and out through said outlet arm; and (3) means for coupling said hemoconcentrator to said first solute removal device to permit liquid communication therebetween and for coupling said hemoconcentrator and said first solute removal device to a blood source to permit blood to be received from and returned to said blood source; (b) directing said blood from said blood source into said inlet arm by said means for circulating said blood, through said hollow fiber plasma-separating membrane and out said outlet arm at a volume and a velocity that permits convective and convective and diffusive transport of plasma from said blood across said hollow fiber plasma-separating membrane along the inlet arm of said hollow fiber plasma-separating membrane into said plasma chamber solution; (c) causing said plasma in said plasma chamber solution to come into contact with said sorbent such that said targeted solute is selectively bound to said sorbent; (d) causing said non-targeted solutes to pass by diffusive and convective transport from said plasma chamber solution across the hollow fiber plasma-separating membrane into the blood retained by said hollow fiber plasma-separating membrane and out of said first solute removal device; (e) causing said blood or plasma to pass through said hemoconcentrator such that water, fluids, and solutes with a molecular weight less than said cut-off pass through said porous ultrafiltration membrane and are withdrawn from said blood or plasma, and said ultrafiltration retains cells and solutes with a molecular weight greater than said cut-off in said blood or plasma.
Claim 27
Independent Claim 538 words
A method of selectively removing a targeted solute and water, fluids, and low molecular weight solutes from blood comprising: (a) providing a system comprising: (1) a hemoconcentrator comprising an inlet port, an outlet port, and a porous ultrafiltration membrane having a selected molecular weight cut-off for retaining components selected from the group consisting of cells and solutes with a molecular weight greater than the cut-off and for allowing water, fluids, and solutes with a molecular weight less than the cut-off to be removed from blood or plasma; and (2) a first solute removal device for selectively removing the targeted solute from blood by means of convective and diffusive transport of plasma from said blood across a hollow fiber plasma-separating membrane into a closed plasma chamber where the selective removal of the targeted solute from non-targeted solutes using a sorbent is accomplished followed by the subsequent transport of the non-targeted solutes across the hollow fiber plasma-separating membrane back into the blood, comprising (i) the closed plasma chamber configured for being filled with a plasma chamber solution and to freely circulate, equilibrate, and interact plasma in said plasma chamber solution under relatively uniform pressure; (ii) the hollow fiber plasma-separating membrane, wherein said hollow fiber plasma-separating membrane has an inlet arm and an outlet arm and is configured for being immersed in said plasma chamber solution in said closed plasma chamber; (iii) at least one sorbent having an affinity for binding said targeted solute, wherein said sorbent is contained in said closed plasma chamber; (iv) means for securing said inlet arm and outlet arm of said hollow fiber plasma-separating membrane in said closed plasma chamber; and (v) means for circulating said blood into said inlet arm, through said hollow fiber plasma-separating membrane, and out through said outlet arm; and (3) means for coupling said hemoconcentrator to said first solute removal device to permit liquid communication therebetween and for coupling said hemoconcentrator and said first solute removal device to a blood source to permit blood to be received from and returned to said blood source; (b) directing said blood from said blood source into said inlet arm by said means for circulating said blood, through said hollow fiber plasma-separating membrane and out said outlet arm at a volume and a velocity that permits convective and convective and diffusive transport of plasma from said blood across said hollow fiber plasma-separating membrane along the inlet arm of said hollow fiber plasma-separating membrane into said plasma chamber solution; (c) causing said plasma in said plasma chamber solution to come into contact with said sorbent such that said targeted solute is selectively bound to said sorbent; (d) causing said non-targeted solutes to pass by diffusive and convective transport from said plasma chamber solution across the hollow fiber plasma-separating membrane into the blood retained by said hollow fiber plasma-separating membrane and out of said first solute removal device; (e) causing said blood or plasma to pass through said hemoconcentrator such that water, fluids, and solutes with a molecular weight less than said cut-off pass through said porous ultrafiltration membrane and are withdrawn from said blood or plasma, and said ultrafiltration retains cells and solutes with a molecular weight greater than said cut-off in said blood or plasma.
Claim 28
Dependent Claim 19 words
The method of claim 23 wherein said porous ultrafiltration membrane of said hemoconcentrator comprises a plurality of hollow fibers.
Claim 29
Dependent Claim 24 words
The method of claim 24 wherein the molecular weight cut-off of said porous ultrafiltration membrane is in the range of about 10,000 to 100,000.
Claim 30
Dependent Claim 31 words
The method of claim 25 wherein said porous ultrafiltration membrane is made from a material selected from the group consisting of polyacrylonitrile, polysulfone, polynethylmethacrylate, cellulose acetate, cellulose diacetate, and cellulose triacetate.
Claim 31
Dependent Claim 18 words
The method of claim 23 wherein said hollow fiber plasma-separating membrane comprises a bundle of parallel hollow fibers.
Claim 32
Dependent Claim 27 words
The method of claim 27 wherein said sorbent is of a size and configuration such that said sorbent is not permeable to the hollow fiber plasma-separating membrane.
Claim 33
Dependent Claim 50 words
The method of claim 28 wherein said hollow fibers making up said hollow fiber plasma-separating membrane are constructed of a blood-compatible material having a suitable pore size to allow passage of plasma into the plasma chamber solution while retaining blood cells and platelets from the blood within the hollow fibers.
Claim 34
Dependent Claim 27 words
The method of claim 29 wherein the pore sizes in said hollow fibers of said hollow fiber plasma-separating membrane range between about 0.01 μm to 1.0 μm.
Claim 35
Dependent Claim 37 words
The method of claim 30 wherein said hollow fibers of said hollow fiber plasma-separating membrane are made from a material selected from the group consisting of polypropylene, cellulose diacetate, polycarbonate, polyvinylchloride, polyvinylalcohol, polymethylmethacrylate, polyethylene, polysulfone, and polyethylenevinylalcohol.
Claim 36
Dependent Claim 45 words
The method according to claim 31 wherein the sorbent comprises a ligand immobilized on a substrate and said ligand is a member selected from the group consisting of enzymes, living tissue, fragments of tissue, cells, antibodies, peptides, macromolecules, nucleic acids, lectins, carbohydrates, and chelating agents.
Claim 37
Dependent Claim 12 words
The method of claim 32 wherein said sorbent has affinity for heparin.
Claim 38
Dependent Claim 10 words
The method of claim 33 wherein the substrate is agarose.
Claim 39
Dependent Claim 11 words
The method of claim 34 wherein the sorbent is poly-L-lysine-coupled agarose.
Claim 40
Dependent Claim 40 words
The method of claim 23 wherein said hemoconcentrator is disposed within said closed plasma chamber of said first solute removal device in fluid communication with said plasma chamber solution to thereby effect simultaneous hemoconcentration and removal of the targeted solute.
Claim 41
Dependent Claim 60 words
The method of claim 23 wherein said hemoconcentrator is disposed in fluid communication with said first solute removal device such that said blood is permitted to pass from said hemoconcentrator to said first solute removal device, or vice versa, to thereby effect sequential hemoconcentration and removal of the targeted solute or sequential removal of the targeted solute and hemoconcentration, respectively.
Claim 42
Dependent Claim 63 words
The method of claim 23 wherein said outlet port of said hemoconcentrator is coupled to the inlet arm of said first solute removal device such that blood passes through said hemoconcentrator for removal of water, fluids, and low molecular weight solutes to result in concentrated blood, which concentrated blood then passes through said first solute removal device for removal of the targeted solute.
Claim 43
Dependent Claim 62 words
The method of claim 23 wherein said outlet arm of said first solute removal device is coupled to the inlet port of said hemoconcentrator such that blood passed through said first solute removal device for removal of the targeted solute resulting in targeted-solute-depleted blood, which targeted-solute-depleted blood then passes through said hemoconcentrator for removal of water, fluids, and low molecular weight solutes.
Claim 44
Dependent Claim 13 words
The method of claim 23 wherein said plasma chamber solution is an electrolyte.
Claim 45
Dependent Claim 34 words
The method of claim 23 wherein said porous ultrafiltration membrane is contained in said closed plasma chamber such that water, fluids, and low molecular weight solutes can be removed from said plasma by ultrafiltration.
Claim 46
Dependent Claim 253 words
The method of claim 23 further comprises a second solute removal device, which comprises (i) a closed plasma chamber configured for being filled with a plasma chamber solution and to freely circulate, equilibrate, and interact plasma in said plasma chamber solution under relatively uniform pressure; (ii) a hollow fiber plasma-separating membrane, herein said hollow fiber plasma-separating membrane has an inlet arm and an outlet arm and is configured for being immersed in said plasma chamber solution in said closed plasma chamber; (iii) at least one sorbent having an affinity for binding said targeted solute, wherein said sorbent is contained in said closed plasma chamber; (iv) means for securing said inlet arm and outlet arm of said hollow fiber plasma-separating membrane in said closed plasma chamber; and (v) means for circulating blood into said inlet arm, through said hollow fiber plasma-separating membrane, and out through said outlet arm; wherein the closed plasma chamber of said first solute removal device is coupled to the inlet port of said hemoconcentrator and the outlet port of said hemoconcentrator is coupled to the closed plasma chamber of said second solute removal device such that plasma can flow from said first solute removal device through said hemoconcentrator to said second solute removal device such that water, fluids, and low molecular weight solutes can be removed from said plasma by ultrafiltration, and wherein said outlet arm of said first solute removal device is coupled to the inlet arm of said second solute removal device such that blood can flow therebetween.

References Cited (Backward Citations)

US4071444A Cited
US4581141A Cited
US4348283A Cited
US4661246A Cited
US4995268A Cited
US5211850A Cited
US5277820A Cited
US5536412A Cited

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