Methods and apparatuses for electronic determination of analytes

• US 20050037407A1
• Filed: 07/22/2004
• Published: 02/17/2005
• Est. Priority Date: 04/27/2001
• Status: Abandoned Application

• Current Assignee: Febit AG (FEBIT)
• Original Assignee: Febit AG (FEBIT)
• Inventors: Beier, Markus, Stahler, Cord F.
• Application Number:
  US10/895,981
• Publication Number:
  US 20050037407A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/5438 Electrodes

Abstract

The invention relates to a method and an apparatus for determining analytes by electronic detection using a microfluidic support.

Claims

1. A method for determining analytes, which comprises the following steps:

(a) providing an apparatus comprising

(i) a light source matrix,

(ii) a microfluidic support having channels which contain a plurality of predetermined areas at which in each case different receptors are immobilized on the support,

(iii) means for supplying fluids to the support and for discharging fluids from the support and

(iv) an electronic detection matrix having a plurality of electrodes assigned to the predetermined areas containing immobilized receptors on the support,

(b) contacting the support with a sample containing analytes and

(c) determining the analytes by electronic detection via binding thereof to the receptors immobilized on the support.

2. The method as claimed in claim 1, wherein a programmable light source matrix selected from the group consisting of a light valve matrix, a mirror array and a UV-laser array is used.

4. The method as claimed in claim 1, wherein an apparatus is used which contains at least the components (ii), (iii) and (iv) in an integrated form.

5. The method as claimed in claim 1, wherein electrodes are used which contain a conductive material such as, for example, a metal, a conductive polymer or a conductive glass.

6. The method as claimed in claim 1, wherein electrodes having an area in the range from 15-250,000 μ

m² are used.

7. The method as claimed in claim 1, wherein the electronic detection comprises measuring the conductivity, impedance, voltage and/or current via said electrodes.

8. The method as claimed in claim 7, wherein the measurement comprises a potentiometric measurement, a cyclovoltametric measurement, an amperometric measurement or a chronopotentiometric measurement.

9. The method as claimed in claim 1, wherein the detection comprises a light source matrix-initiated redox process which correlates with the binding of analytes to the receptors immobilized on the support.

10. The method as claimed in claim 1, wherein the receptors are selected from biopolymers such as, for example, nucleic acids, nucleic acid analogs, proteins, peptides and carbohydrates.

11. The method as claimed in claim 10, wherein the receptors are selected from the group consisting of nucleic acids and nucleic acid analogs and binding of the analytes is a hybridization.

12. The method as claimed in claim 1, wherein a plurality of analytes are determined in parallel in the sample.

13. The method as claimed in claim 12, wherein at least 50, preferably at least 100, analytes are determined in parallel.

14. The method as claimed in claim 1, wherein the receptors are immobilized to the support via covalent binding, noncovalent self assembly, charge interaction or combinations thereof.

15. The method as claimed in claim 1, wherein the receptors are synthesized in situ on the support.

16. The method as claimed in claim 15, wherein the receptor synthesis comprises:

directing fluid containing receptor synthesis building blocks over the support, immobilizing said building blocks time-and/or location-specifically at in each case predetermined positions on the support and repeating said steps until the desired receptors have been synthesized at the in each case predetermined positions.

17. The method as claimed in claim 15, wherein the receptor synthesis comprises at least one illumination step initiated by the light source matrix or/and a process step mediated by the electronic detection matrix.

18. The method as claimed in claim 15, wherein receptor synthesis comprises on-line process monitoring.

19. The method as claimed in claim 18, wherein the on-line process monitoring is carried out by the electronic detection matrix.

20. The method as claimed in claim 15, wherein electronically removable protective groups such as, for example, p-nitrobenzyloxycarbonyl or 2,4-dinitrobenzyloxycarbonyl are used for receptor synthesis.

3. The method as claimed in 1, wherein as microfluidic support with closed channels is used.

21. An apparatus for determining analytes, which comprises

(i) a light source matrix,

(ii) a support containing a plurality of predetermined positions at which in each case different receptors are immobilized on the support,

(iii) means for supplying fluids to the support and for discharging fluids from the support and

(iv) an electronic detection matrix having a plurality of electrodes assigned to the predetermined positions containing immobilized receptors on the support.

22. The apparatus as claimed in claim 21, wherein at least the components (ii), (iii) and (iv) are present in an integrated form.

23. The apparatus as claimed in claim 21, wherein the support is arranged between light source matrix and electronic detection matrix.

24. The use of an apparatus as claimed in claim 21 in a method for parallel determination of a multiplicity of analytes.