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US4963468A Expired / Lapsed US ⏱️ 0.0 years remaining

Immunoseparating strip

Assignee: Abbott Laboratories
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Filing: 1987-02-12
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Granted: 1990-10-16
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Expires: 2007-02-12
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Abstract

Abstract A method and device for determining the presence of an analyte in a sample suspected of containing the analyte is disclosed. The method involves contacting a test solution containing the sample, an antibody for the analyte, and a conjugate of the analyte and a label with a contact portion of a piece of bibulous material capable of being traversed in at least one direction by the test solution through capillary action. The bibulous material contains a first receptor capable of binding to said conjugate. The first receptor is non-diffusively bound to a situs on the bibulous material separate from the contact portion. The bibulous material further contains a second receptor capable of binding the antibody to the analyte between the situs and the contact portion. The second receptor is non-diffusively bound to the bibulous material. At least a portion of the test solution is allowed to traverse the bibulous material by capillary action and thereby contact the situs. The situs is examined for the presence of the conjugate. To this end, the situs can be exposed to a signal producing means capable of interacting with the label to produce a signal in relation to the amount of analyte in the test solution. The signal produced at the situs is then detected.

Inventors

  • 👤 John D. Olson

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 22:12
CPC Classifications
G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/53; G01N33/543; G01N33/54366; G01N33/54386; G01N33/54387; G01N33/54388; Y; Y10; Y10S; Y10S435/00; Y10S435/805; Y10S435/973; Y10S436/00; Y10S436/807; Y10S436/81; Y10S436/815; Y10S436/816

Claims Analysis

Total Claims: 27
Claim 1
Independent Claim 206 words
A method for determining the presence of an analyte, that is capable of binding specifically to an antibody, in a sample suspected of containing said analyte, which comprises (a) contacting, with a test solution containing said sample, antibodies to said analyte and a conjugate of said analyte and a label, a contact portion of a piece of bibulous material capable of being traversed in at least one direction by said test solution by capillary migration, said bibulous material containing non-diffusively bound to a situs on said bibulous material separated from said contact portion a first receptor capable of binding to said conjugate, the surface area of said situs being less than that of said bibulous material, said bibulous material further containing a second receptor capable of binding said antibodies to said analyte wherein said second receptor is non-diffusively bound to said bibulous material at a portion thereof between said situs and said contact portion, (b) allowing at least a portion of said test solution to traverse said bibulous material by capillary migration and thereby contact said situs, and (c) examining said situs for the presence of said conjugate, and relating the presence of said conjugate at said situs to the presence of analyte in the sample.
Claim 2
Independent Claim 206 words
A method for determining the presence of an analyte, that is capable of binding specifically to an antibody, in a sample suspected of containing said analyte, which comprises (a) contacting, with a test solution containing said sample, antibodies to said analyte and a conjugate of said analyte and a label, a contact portion of a piece of bibulous material capable of being traversed in at least one direction by said test solution by capillary migration, said bibulous material containing non-diffusively bound to a situs on said bibulous material separated from said contact portion a first receptor capable of binding to said conjugate, the surface area of said situs being less than that of said bibulous material, said bibulous material further containing a second receptor capable of binding said antibodies to said analyte wherein said second receptor is non-diffusively bound to said bibulous material at a portion thereof between said situs and said contact portion, (b) allowing at least a portion of said test solution to traverse said bibulous material by capillary migration and thereby contact said situs, and (c) examining said situs for the presence of said conjugate, and relating the presence of said conjugate at said situs to the presence of analyte in the sample.
Claim 3
Dependent Claim 13 words
The method of claim 1 wherein said bibulous material is a cellulosic material.
Claim 4
Dependent Claim 20 words
The method of claim 1 wherein said situs is examined directly for the presence of a signal from the label.
Claim 5
Dependent Claim 36 words
The method of claim 1 wherein said situs is exposed to a signal producing means capable of interacting with said label to produce a signal in relation to the amount of analyte in the test solution.
Claim 6
Dependent Claim 41 words
The method of claim 4 wherein the signal produced at said situs has a sharp-edged distinctive pattern that provides a sharp contrast to a signal produced at adjacent sites on said bibulous material when analyte is present in said test solution.
Claim 7
Dependent Claim 25 words
The method of claim 4 wherein said signal at said situs is compared with signal at a portion of the strip other than said situs.
Claim 8
Dependent Claim 19 words
The method of claim 4 wherein said signal producing means comprises a substrate and said label is a catalyst.
Claim 9
Dependent Claim 25 words
The method of claim 7 wherein at least the portion of said bibulous material containing said situs is immersed in a solution of said substrate.
Claim 10
Dependent Claim 37 words
The method of claim 7 wherein the contact portion of said bibulous material is contacted with a solution of said substrate which is allowed to traverse said bibulous material past said situs by means of capillary migration.
Claim 11
Dependent Claim 12 words
The method of claim 1 wherein said first receptor is an antibody.
Claim 12
Dependent Claim 28 words
The method of claim 1 wherein said antibodies for said analyte are selected from the group consisting of antibodies for theopylline, antibodies for phenobarbital, and antibodies for quinidine.
Claim 13
Dependent Claim 14 words
The method of claim 1 wherein said second receptor is antibody for said antibodies.
Claim 14
Dependent Claim 11 words
The method of claim 1 wherein said label is an enzyme.
Claim 15
Dependent Claim 35 words
The method of claim 13 wherein a second enzyme is bound at said situs to said bibulous material, the enzymes being related in that the product of one enzyme is the substrate of the other.
Claim 16
Dependent Claim 85 words
The method of claim 1 for determining a plurality of analytes in said sample, wherein (i) a plurality of conjugates, each comprising one of said analytes and a label, and (ii) a plurality of antibodies, each specific to one or more of said analytes, are combined with said sample, and a plurality of situses, non-contiguous to each other and to said contact portion of said bibulous material, are employed each having non-diffusively bound thereto a different first receptor capable of binding to a different conjugate.
Claim 17
Dependent Claim 24 words
The method of claim 1 wherein said situs is a band transverse to the direction of traversal of said sample along said bibulous material.
Claim 18
Dependent Claim 11 words
The method of claim 1 wherein said analyte is a drug.
Claim 19
Independent Claim 259 words
A method for determining the presence of one or more of a plurality of analytes, each capable of binding specifically to an antibody, in a sample suspected of containing one or more of said analytes, which comprises (a) contacting, with a test solution containing said sample, one or more of a plurality of antibodies each respectively complementary to one of said analytes, and one or more of a plurality of conjugates of one of said analytes and a label, a contact portion of a piece of bibulous material capable of being traversed by said test solution by capillary migration, said bibulous material containing non-diffusively bound to one or more situses on said bibulous material separate from said contact portion, one or more of a plurality of first receptors each respectively capable of binding to one of said conjugates, the surface area of each of said situses being less than that of said bibulous material, said bibulous material further containing one or more second receptors, capable of binding all of said antibodies to said analytes, non-diffusively bound to said bibulous material at least at a portion thereof between said situses and said contact portion, (b) allowing at least a portion of said test solution to traverse said bibulous material by capillary migration and thereby contact said situses, and (c) examining each of said situses for the presence of one or more of said conjugates, and relating the presence of said one or more conjugates at each of said, situses to the presence of one or more analytes in the sample.
Claim 20
Independent Claim 259 words
A method for determining the presence of one or more of a plurality of analytes, each capable of binding specifically to an antibody, in a sample suspected of containing one or more of said analytes, which comprises (a) contacting, with a test solution containing said sample, one or more of a plurality of antibodies each respectively complementary to one of said analytes, and one or more of a plurality of conjugates of one of said analytes and a label, a contact portion of a piece of bibulous material capable of being traversed by said test solution by capillary migration, said bibulous material containing non-diffusively bound to one or more situses on said bibulous material separate from said contact portion, one or more of a plurality of first receptors each respectively capable of binding to one of said conjugates, the surface area of each of said situses being less than that of said bibulous material, said bibulous material further containing one or more second receptors, capable of binding all of said antibodies to said analytes, non-diffusively bound to said bibulous material at least at a portion thereof between said situses and said contact portion, (b) allowing at least a portion of said test solution to traverse said bibulous material by capillary migration and thereby contact said situses, and (c) examining each of said situses for the presence of one or more of said conjugates, and relating the presence of said one or more conjugates at each of said, situses to the presence of one or more analytes in the sample.
Claim 21
Dependent Claim 15 words
The method of claim 18 wherein said piece of bibulous material is a cellulosic material.
Claim 22
Dependent Claim 22 words
The method of claim 18 wherein each of said situses is examined directly for the presence of a signal from the label.
Claim 23
Dependent Claim 38 words
The method of claim 18 wherein each of said situses is exposed to a signal producing means capable of interacting with said label to produce a signal in relation to the amount of analyte in the test solution.
Claim 24
Dependent Claim 27 words
The method of claim 21 wherein said signal at each of said situses is compared with signal at a portion of the strip other than said situses.
Claim 25
Dependent Claim 14 words
The method of claim 18 wherein said second receptor is antibody for said antibodies.
Claim 26
Dependent Claim 11 words
The method of claim 18 wherein said label is an enzyme.
Claim 27
Dependent Claim 11 words
The method of claim 18 wherein said analyte is a drug.

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Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1993-10-15 1994-04-16 1994-10-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1997-10-15 1998-04-16 1998-10-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2001-10-15 2002-04-16 2002-10-16 $7700.00 Window Closed / Lapsed

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