Immunoassay diagnostic probe and a method for use thereof

• US 20030119030A1
• Filed: 12/31/2002
• Published: 06/26/2003
• Est. Priority Date: 03/15/2000
• Status: Abandoned Application

• Current Assignee: Segen Technologies Limited
• Original Assignee: Segen Technologies Limited
• Inventors: Zilber, Gil
• Application Number:
  US10/221,665
• Publication Number:
  US 20030119030A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/001 Enzyme electrodes
• CPC Class Codes: C12Q 1/6825 Nucleic acid detection involving sensors
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings

Abstract

A disposable probe, an immunoassay diagnostic device and a method for the quantitative detection of specific biomolecules, being the analyte, in a fluid sample, by any immunoassay procedure based on spectroscopic detection, the disposable probe comprises at least one photodiode having a layer of first immunoreactant molecules attached permanently to its surface, wherein the first immunoreactant binds specifically to the analyte, and the photodiode has electronic connectors for transferring the electronic signal generated in the photodiode, upon exposure to light, to a signal processing unit.

The immunoassay diagnostic device comprises a disposable probe, a non-disposable probe-base and means for electronically connecting the probe to the probe-base, and the probe-base comprises means for reading the signal generated by the disposable probe, a signal processing unit and a display unit. The method for the detection of specific biomolecules in a fluid sample, in particular a serum, by using a disposable probe, comprises the steps of any known immunoassay procedure suitable for the detection of the specific biomolecules, the layer attached to the photodiode surface consists of the first immunoreactant of the immunoassay.

Claims

1. ) A disposable probe for the quantitative detection of specific biomolecules, being the analyte, in a fluid sample, by any immunoassay procedure based on spectroscopic detection, comprising;

at least one photodiode having a layer of first immunoreactant molecules attached permanently to its surface, wherein said first immunoreactant binds specifically to said analyte,

and said photodiode has electronic connectors for transferring the electronic signal generated in the photodiode, upon exposure to light, to a signal processing unit.

2. ) A disposable immunoassay diagnostic probe according to claim 1 wherein said analyte is one component of an antigen-antibody or antibody-antibody specific reaction and said first immunoassay reactant is the complementary component.

3. ) A disposable immunoassay diagnostic probe according to claim 1 wherein said analyte and said first immunoreactant are the two components of the binding pair selected from enzyme-substrate, enzyme-inhibitor, complementary nucleic acid strands, binding protein-nucleic acid, or any other biospecific binding pair.

4. ) A disposable immunoassay diagnostic probe according to claim 1 for use in chemiluminescence assay.

5. ) A disposable immunoassay diagnostic probe according to claim 1 for use in fluorescence assay.

6. ) A disposable immunoassay diagnostic probe according to claim 1 for use in enzyme-linked immunosorbent assay wherein the enzyme catalyses a color producing reaction.

7. ) A disposable immunoassay diagnostic probe according to claim 1 wherein part or all of the signal processing components are packaged together with said photodiode in a single semiconductor chip.

8. ) A disposable immunoassay diagnostic probe according to claim 1 wherein the surface of the photodiode is coated by an optical filter capable of passing only a specific range of wavelengths.

9. ) A disposable immunoassay diagnostic probe according to claim 1 wherein the surface of the photodiode is coated by a thin layer of any material suitable for increasing the bonding affinity of said first immunoreactant to the surface of the photodiode and/or to protect the photodiode form the environment.

10. ) A disposable immunoassay diagnostic probe according to claim 9 wherein said thin layer is a removable membrane covered by a layer of the immunoreactant molecules and said membrane can be removed from the surface of the photodiode after use and replaced by a fresh membrane.

11. ) A disposable immunoassay diagnostic probe according to claim 1 for the detection of more than one analyte wherein the layer of molecules bound to the photodiode surface comprises more than one reactant, wherein each reactant is bound to a specific defined area of said surface and each react is a first immunoreactant specific to said analyte.

12. ) A disposable immunoassay diagnostic probe according to claim 1 for the detection of more than one analyte wherein said probe comprises an array of photodiodes, each photodiode covered by a first immunoreactant specific to said analyte.

16. ) A method for the detection of specific biomolecules in a fluid sample, in particular a serum, by using a disposable probe as defined in claim 1, comprising the steps of any known immunoassay procedure suitable for the detection of said specific biomolecules, wherein the layer attached to the photodiode surface consists of the first immunoreactant of said immunoassay.

17. ) A method for the detection of specific biomolecules in a fluid sample, in particular a serum, by using an immunoassay diagnostic probe as defined in claim 1 comprising the following steps;

a) immersing said disposable probe in said sample for a predetermined period of time, allowing said tested specific biomolecules, if present in sample, to bind to the probe through binding to the layer of specific first immunoreactant molecules;

b) rinsing said disposable probe to remove unbound molecules;

c) soaking the probe in a solution containing a predetermined concentration of a conjugate that selectively binds to the tested biomolecules, wherein said component is either already labeled by a marker that can be detected by optical means or upon reacting with additional components will produce an optical signal;

d) rinsing said disposable probe to remove unbound molecules;

e) adding, if needed, an appropriate substrate or initiator to produce an optically detectable reaction.

f) exposing the probe to light radiation if needed in order to produce an optically detectable signal.

g) reading the electrical signal generated by said probe in response to said optical signal and interpreting said signal in terms of concentration of the analyte.

18. ) A method for the detection of specific molecules in a serum according to claim 17 wherein said conjugate of step (c) contains a chemiluminescent molecule that emits light radiation upon addition of a chemiluminescent initiator in step (d).

19. ) A method for the detection of specific molecules in a serum according to claim 17 wherein said conjugate of step (c) contains a fluorescent molecule that emits light radiation upon exposure to light of a specified wavelength range in step (f).

20. ) A method for the detection of specific molecules in a serum according to claim 17 wherein said conjugate of step (c) contains an enzyme that catalyzes a reaction that produces a detectable color change upon the addition of an appropriate substrate in step (d) and wherein the detected optical signal is the optical density of the sample measured by exposing the probe to light of a specified wavelength range in step (f).

13. ) An immunoassay diagnostic device comprising a disposable probe as defined in preceding claims, a non-disposable probe-base and means for electronically connecting said probe to said probe-base, and wherein said probe-base comprises means for reading the signal generated by the disposable probe, a signal processing unit and a display unit.

14. ) An immunoassay diagnostic device according to claim 13 in the form of a pipette, wherein the pipette body is the probe-base containing the signal processing unit and the display unit, and wherein said disposable probe is attached to, or being an integral part of, a disposable pipette tip and wherein upon fitting said pipette tip to said pipette body, electronic connection is established between the two, allowing the reading and processing of a signal generated in the probe and displaying the result.

15. ) An immunoassay diagnostic device according to claim 13 further comprising a light source for use in immunoassays based on fluorescence or optical-density measurements.