Method and apparatus for pulsed electrochemical detection using polymer electroactive electrodes

• US 5,403,451 A
• Filed: 03/04/1994
• Issued: 04/04/1995
• Est. Priority Date: 03/05/1993
• Status: Expired due to Term

• Current Assignee: Gordon Wallace, John M. Riviello, Omowunmi A. Sadik
• Original Assignee: Gordon Wallace, John M. Riviello, Omowunmi A. Sadik
• Inventors: Riviello, John M., Sadik, Omowunmi A., Wallace, Gordon
• Primary Examiner(s): Niebling, John
• Assistant Examiner(s): Bell, Bruce F.
• Application Number:
  US08/206,136
• Time in Patent Office: 396 Days
• Field of Search: 204/163.1, 204/153.12, 204/403, 204/409, 204/412, 204/434, 435/7.1, 435/7.8, 435/7.93
• US Class Current: 205/777.5
• CPC Class Codes: G01N 27/3277 being a redox reaction, e.g. detection by cyclic voltammetry voltammetry per se G01N27/42, G01N27/48

Abstract

In a first embodiment, a target analyte in solution is detected by exposing the solution to an electrode that includes a conducting electroactive polymer to which a periodic alternating voltage is coupled. Upon exposure to the analyte, an electrode characteristic is varied, which variation is detected by measuring electrode current as a function of time and as a function of the periodic alternating voltage. The alternating voltage waveform has an oxidizing time period and a reduction time period, which periods and waveform duty cycle may be controlled to enhance electrode sensitivity, selectivity, and to substantially eliminate electrode fouling and data hysteresis. In a second embodiment, a receptor is bound to the electrode, to which is coupled an alternating voltage waveform that permits a mating target substance to reversibly bind to the receptor such that measurement of electrode current provides a measure of such reversible binding. The second embodiment is especially useful for detecting antibodies, antigens, haptens, DNA, RNA, and enzymes. Either embodiment may be used for detection in flow-through electrochemical cells, flow injection analysis, liquid, and ion chromatography, as well as in capillary electrophoresis.

Claims

1. A method for detecting a target analyte within a solution, the method comprising the following steps:

(a) exposing said solution to an electrode that includes a conducting electroactive polymer;

(b) coupling a periodic alternating voltage to said electrode; and

(c) measuring current flow through said electrode as a function of time and as a function of said alternating voltage to detect said target analyte within said solution;

wherein a characteristic of said electrode is varied upon exposure to said target analyte, causing current flow through said electrode to vary.

2. The method of claim 1, wherein at step (b), said alternating voltage has a period that includes at least an oxidizing time interval during which said voltage causes said electrode to be oxidized, and a reduction time interval during which said voltage causes less oxidation or reduction or both to said electrode reduced.

3. The method of claim 2, wherein said alternating voltage has a duty cycle and period set to meet at least one criterion selected from the group consisting of (i) minimization of electrode fouling by an analyte, (ii) enhancement of electrode detection sensitivity to an analyte, (iii) enhancement of selectivity to a chosen target analyte group, (iv) enhancement of selectivity to a chosen target analyte, (v) reduction of hysteresis effect in detected data, and (vi) said periodic alternating voltage is asymmetrical.

4. The method of claim 2, wherein:

said target analyte is an anion; and

said target analyte reversibly attaches to said electrode during at least a portion of said oxidizing time interval.

5. The method of claim 2, wherein:

said target analyte is a cation; and

said target analyte reversibly attaches to said electrode during at least a portion of said reduction time interval.

6. The method of claim 1, wherein at step (c), said current flow includes at least one component selected from the group consisting of (i) a Faradaic current associated with application of said voltage, (ii) a current associated with a migration of said analyte to said electrode, and (iii) a counter current associated with migration to said electrode of an ion of charge opposite to said target analyte.

7. The method of claim 1, wherein at step (c), said voltage has at least one characteristic selected from the group consisting of (i) a voltage magnitude that varies from about +2 VDC to about -2 VDC in a single period;

(ii) a period of about 50 ms to about 250 ms, (iii) a period that includes a first time interval ranging from about 10 ms to about 50 ms during which interval said voltage causes said electrode to oxidize, and (iv) a period that includes a second interval ranging from about 10 ms to about 50 ms during which interval said voltage causes said electrode to re-oxidize.

8. The method of claim 1, wherein said voltage has a waveform which reduces hysteresis in repetitive measurements of said current as a function of said voltage.

9. The method of claim 1, wherein said solution is selected from the group consisting of (i) a stream associated with an output from a flow injection analysis system, (ii) a stream associated with output from liquid chromatography, (iii) a stream associated with output from ion chromatography, and (iv) a stream associated with output from a capillary electrophoresis system.

10. A method for detecting a bindable target substance having an attachment affinity for an immobilized receptor, the method comprising the following steps:

(i) (a) forming an electrode having an conducting electroactive polymer layer that includes an immobilized receptor will bind to a bindable target substance;

(b) contacting said electrode with an aqueous solution including a bindable target substance;

(c) coupling a periodic alternating voltage to said electrode; and

(d) measuring current flow through said electrode as a function of time and as a function of said alternating voltage to determine whether attachment of said bindable target substance to said immobilized receptor has occurred;

wherein at least one characteristic of said electrode is varied upon an attachment between said immobilized receptor and bindable target substance, causing current flow through said electrode to vary.

11. The method of claim 10, wherein said immobilized receptor is selected from the group consisting of (i) antibody, (ii) antigen, (iii) hapten, (iv) DNA, (v) RNA, and (vi) enzymes.

12. The method of claim 10, wherein at step (c), said alternating voltage has a period that includes at least an oxidizing time interval during which said voltage causes said electrode to be oxidized, and a reduction time interval during which said voltage causes less oxidation or reduction or both to said electrode reduced.

13. The method of claim 10, wherein said alternating voltage has a duty cycle and period set to meet at least one criterion selected from the group consisting of (i) minimization of electrode fouling, (ii) enhancement of electrode detection sensitivity, (iii) enhancement of selectivity, (iv) promote reversibility of attachment between said immobilized receptor and said bindable target substance, (v) reduction of hysteresis in repetitive measurements of said current as a function of said voltage, and (vi) said alternating voltage is asymmetrical.

14. The method of claim 10, wherein at step (d), said alternating voltage has at least one characteristic selected from the group consisting of (i) a voltage magnitude that varies from about +2 V to about -2 V in a single period;

(ii) a period of about 50 ms to about 250 ms, (iii) a period that includes a oxidizing time interval ranging from about 10 ms to about 50 ms during which interval said voltage causes said electrode to oxidize, and (iv) a period that includes a reduction time interval ranging from about 10 ms to about 50 ms during which interval said voltage causes said electrode to re-oxidize.

15. The method of claim 10, wherein at step (b) said solution is selected from the group consisting of (i) a stream associated with an output from a flow injection analysis system, (ii) a stream associated with output from liquid chromatography, (iii) a stream associated with output from ion chromatography, and (iv) a stream associated with output from a capillary electrophoresis system.