Coulometric assay system

• US 5,149,629 A
• Filed: 04/04/1988
• Issued: 09/22/1992
• Est. Priority Date: 04/07/1987
• Status: Expired due to Fees

• Current Assignee: Ramot University Authority For Applied Research and Industrial Development Limited
• Original Assignee: Ramot University Authority For Applied Research and Industrial Development Limited
• Inventors: Rishpon, Judith, Rosen, Ilara
• Primary Examiner(s): Kepplinger, Esther L.
• Assistant Examiner(s): Scheiner, Toni R.
• Application Number:
  US07/177,463
• Time in Patent Office: 1,632 Days
• Field of Search: 204/1 T, 204/403, 436/525, 436/527, 436/806, 435/7, 435/18, 435/21, 435/25, 435/26, 435/288, 435/291, 435/817, 435/7.9, 435/7.5
• US Class Current: 435/7.9
• CPC Class Codes: G01N 27/423 Coulometry
• CPC Class Codes: G01N 33/5438 Electrodes
• CPC Class Codes: Y10S 435/817 Enzyme or microbe electrode
• CPC Class Codes: Y10S 436/806 Electrical property or magnetic property

Abstract

The invention relates to a novel assay for the determination of entities having biological activity and to a device for carrying out such determinations. The assay is a very sensitive one and quantities in the picogram per milliliter range can be determined. The assay is based on chrono-coulometric measurements with sequential measurements of a plurality of samples being carried out with the aid of a multiplexer, in combination with a potentiostat, there being provided suitable electrodes and means for applying a predetermined voltage. One of the electrodes is advantageously a glassy carbon electrode, carbon felt or cloth or carbon paper. Amongst biologically active entities there are antibodies/antigens; hormones/receptors; nuclotides/nucleotide probes, one of the members of such a pair being immobilized on an electrode surface, being tagged with an enzyme providing a signal in coulometric measurements.

Claims

1. Apparatus for the sequential rapid qualitative or quantitative assay of a plurality of samples of members of biospecific binding pairs by coulometric measurement, comprising:

a plurality of working electrodes corresponding to the number of samples to be assayed, said electrodes immersed in a common solution in a vessel,

a multiplexer for effecting sequential coulometric measurements,

a potentiostat;

there being provided in said vessel a reference electrode and a counter electrode, means for applying a predetermined voltage during each such measurement;

which measurements are that of the electric charge passing between each working electrode and the evaluation thereof indicating the quantity of one of the members of the biospecific binding pairs, or its presence, said working electrodes comprising an electrically inert support which supports a member selected from the group consisting of carbon felt, carbon paper or carbon cloth to which there is firmly bonded one of the biospecific pair members which specifically binds the second complementary member, which second member is tagged by an enzyme or which second member is coupled to at least one further biospecific member, the last of which further biospecific members is tagged with an enzyme;

whereby when the electrodes are introduced into a substrate of the enzyme, a coulometric signal is formed, thereby sequentially measuring said samples.

2. Apparatus according to claim 1 wherein each working electrode comprises a carbon felt attached to an electrically non-conducting inert support, said felt being electrically connected to the multiplexer.

3. Apparatus according to claim 1 wherein one of the members of the biospecific binding pairs is bonded to the carbon felt, paper or cloth of the working electrode by a carbodiimide linkage.

4. An apparatus according to claim 1 further comprising means for rotating the working electrodes during the incubation of the two members of the binding pair or during the time of measurement.

5. An apparatus according to claim 1 wherein means are provided for connecting and disconnecting at will the potential applied to the working electrodes between measurements.

6. An assay for the qualitative or quantitative sequential determination of a plurality of samples of members of specific binding pairs selected from the group consisting of antibodies/antigens, hormones, receptors, and nucleotides/nucleotide probes, wherein a first member of a pair is immobilized in an apparatus as claimed in claim 1, wherein the method comprises:

(a) contacting the working electrode with a sample containing the second member of the pair, said second member being labelled with an enzyme, so as to bind said second member to the first member immobilized on the electrode,

(b) immersing the electrode into a solution containing a substrate of the enzyme,

(c) generating a coulometric signal,

(d) measuring and evaluating said signal, and

(e) repeating said assay sequentially for each sample.

7. A sequential assay according to claim 6 wherein a known amount of biotin-tagged antigen is present together with an unknown amount of the same antigen in an aqueous system, wherein an antibody is bound to the working electrode, and where the antibody bound to the electrode reacts with a biotin-labelled antigen and an unlabeled antigen followed by incubation with an avidin-conjugated enzyme, wherein one of the members of the biotin-tagged antigen and the avidin-conjugated enzyme is bonded to a carbon felt, carbon paper or carbon cloth by a carbodiimide linkage.

8. An assay according to claim 6 wherein the linkage of the one member of the biospecific binding pair to the carbon felt of the working electrode is via a linkage selected from the group consisting of carbodiimide or biotin-avidin linkage.

9. An assay according to claim 6 wherein the working electrodes are rotated during the period of incubation of the binding pair and during the time of the actual coulometric measurement.

10. An assay according to claim 6 wherein the working electrodes are rotated during the period of incubation and during the period of time of actual coulometric measurement.

11. An assay according to claim 6 wherein means are provided for disconnecting any of the working electrodes during the period between actual measurement, and reconnecting said electrodes to the source of electric potential during the measurement.