MICROCHANNEL PLASMON RESONANCE BIOSENSOR

• US 20150247797A1
• Filed: 09/24/2013
• Published: 09/03/2015
• Est. Priority Date: 09/25/2012
• Status: Abandoned Application

• Current Assignee: Alfred E. Mann Foundation For Scientific Research
• Original Assignee: Alfred E. Mann Foundation For Scientific Research
• Inventors: Oberg, Keith
• Application Number:
  US14/430,196
• Publication Number:
  US 20150247797A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: A61B 2560/0219 of externally powered implanted units
• CPC Class Codes: A61B 2562/0233 Special features of optical sensors or probes classified in A61B5/00
• CPC Class Codes: A61B 5/076 Permanent implantations telemetry using implanted circuitry A61B5/0031; implanted stimulators for therapy A61N1/3605, A61N1/362, A61N1/372
• CPC Class Codes: A61B 5/1451 for interstitial fluid
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1459 invasive, e.g. introduced into the body by a catheter A61B5/1464 takes precedence
• CPC Class Codes: A61B 5/14735 comprising an immobilised reagent
• CPC Class Codes: A61B 5/6833 Adhesive patches
• CPC Class Codes: G01N 21/554 detecting the surface plasmon resonance of nanostructured metals, e.g. localised surface plasmon resonance

Abstract

Methods and systems for biosensing are disclosed, based on microchannel surface plasmon resonance. A surface plasmon resonance (SPR) sensor (100) for detecting the presence of a target analyte in a fluid, comprising: a light source (105); a light transmissive substrate (112); a metal coating (114) of gold, silver or copper disposed on the substrate; a test SPR element formed in the metal coating, the test SPR element comprising: at least one test microchannel (122) in the metal coating, the at least one test microchannel having at least one aperture (124) for the passage of light from the light source through the substrate, the at least one test microchannel configured to sustain a test plasmon resonance wave, wherein the test plasmon resonance wave emits a test surface plasmon emission (SPE); and a first coating (126) in the test microchannel, the first coating comprising capture molecules selected to interact with the target analyte; a test detector (130) configured to detect the intensity of the light of the test channel (120) SPE in a predetermined wavelength band; and a reference SPR element formed in the substrate, the reference SPR element comprising: at least one reference microchannel (142) in the metal coating, the at least one reference microchannel having at least one aperture (144) for the passage of light from the light source through the substrate, the at least one reference microchannel configured to sustain a reference plasmon resonance wave, wherein the reference plasmon resonance wave emits a reference SPE, a reference detector (150) configured to detect the intensity of the light of the reference SPE in the predetermined wavelength band; and a controller (160) coupled to the test detector and the reference detector. The sensor can be implanted in a human body and can communicate and be powered wirelessly with an external coil placed in proximity to the implanted sensor or with a coil in an adhesive, external patch.

Claims

1. A surface plasmon resonance (SPR) sensor for detecting the presence of a target analyte in a fluid, the sensor comprising:

a light source;

a light transmissive substrate;

a metal coating of gold, silver or copper disposed on the substrate;

a test SPR element formed in the metal coating, the test SPR element comprising;

at least one test microchannel in the metal coating, the at least one test microchannel having at least one aperture for the passage of light from the light source through the substrate, the at least one test microchannel configured to sustain a test plasmon resonance wave, wherein the test plasmon resonance wave emits a test surface plasmon emission (SPE); and

a first coating in the test microchannel, the first coating comprising capture molecules selected to interact with the target analyte;

a test detector configured to detect the intensity of the light of the test channel SPE in a predetermined wavelength band; and

a reference SPR element formed in the substrate, the reference SPR element comprising;

at least one reference microchannel in the metal coating, the at least one reference microchannel having at least one aperture for the passage of light from the light source through the substrate, the at least one reference microchannel configured to sustain a reference plasmon resonance wave, wherein the reference plasmon resonance wave emits a reference surface plasmon emission (SPE),

a reference detector configured to detect the intensity of the light of the reference SPE in the predetermined wavelength band; and

a controller coupled to the test detector and the reference detector.

2. The sensor of claim 1, wherein the controller determines the ratio of:

the intensity of the light detected by the test detector and

the intensity of the light detected by the reference detector.

3. The sensor of claim 2, wherein the controller is configured to determine a concentration of the target analyte in the fluid.

4. The sensor of claim 1, wherein the first coating in the test microchannel further comprises a crosslinker for immobilizing the capture molecules to the at least one test microchannel.

5. The sensor of claim 1 further comprising a first coating in the reference microchannel, the first coating comprising inert molecules selected not to interact with the target analyte.

6. The sensor of claim 5, wherein the first coating in the reference microchannel further comprises a crosslinker for immobilizing the inert molecules to the at least one reference microchannel.

7. The sensor of claim 5 further comprising a second coating in the test microchannel;

and a second coating in the reference microchannel.

8. The sensor of claim 7, wherein the second coating in the test microchannel immobilizes the molecules of the first coating in the test microchannel;

and the second coating in the reference microchannel immobilizes the molecules of the first coating in the reference microchannel.

9. The sensor of claim 5, wherein the second coating in the test microchannel comprises a hydrogel and the second coating in the reference microchannel comprises a hydrogel.

10. The sensor of claim 5 wherein the first and second coating in the test microchannel are mixed to form a porous matrix to fill the test microchannel;

and the first and second coating in the reference microchannel are mixed to form a porous matrix to fill the reference microchannel.

11. The sensor of claim 1, wherein the at least one test microchannel and the at least one reference microchannel each comprise at least one microchannel with a width of about 1 micron, a length of at least 2 microns and a depth of about 100 nanometers.

12. The sensor of claim 1, wherein the target analyte is a biomarker in a fluid comprising human or animal blood, interstitial fluid, urine, sputum or mucus.

13. The sensor of claim 1, wherein the target analyte is glucose in a fluid comprising human or animal blood or interstitial fluid.

14. The sensor of claim 12, wherein the first coating in the at least one test microchannel is selected from the group consisting of:

an antibody, cellular receptor molecules, restriction endonuclease, lectin, DNA, DNA analog or component of a multiprotein complex, a natural or synthetic enzyme, a catalytically inactivated enzyme, glucose oxidase, catalytically inactivated glucose oxidase, phenylboronic acid derivative and non-fluorescent phenylboronic acid derivative.

15. The sensor of claim 1 further comprising a communications system coupled to the controller for wireless communications to an external controller or implantable infusion pump.

16. The sensor of claim 1 further comprising a wireless power transfer system for powering the sensor from an external power source.

17. The sensor of claim 1, wherein the sensor is implantable in a human or animal body.

18. The sensor of claim 1, wherein the sensor is hermetically sealed.

19. A system comprising:

the sensor of claim 1;

a wireless communication and power transfer device;

wherein the wireless communication and power transfer device is coupled to the sensor.

20. The system of claim 19, wherein the communication and power transfer device comprises an adhesive patch configured to adhere to a biological surface.

21. The system of claim 20, wherein the biological surface is human skin.

22. The system of claim 19, wherein the communication and power transfer device is coupled to a computer and configured to receive software instructions, thereby allowing providing instructions to the controller.

23. The sensor of claim 1, further comprising a coil configured for telemetry and charging, a high-efficiency capacitor configured for power storage, and a control circuitry, and wherein the light source is an LED light source, and the detectors are photodiodes.

24. The system of claim 19, wherein the communication and power transfer device comprises a control chip, a memory chip, a telemetry module, a battery, and an RF coil configured to communicate and power the sensor.

25. The sensor of claim 13, wherein the at least one aperture in the at least one test microchannel and the at least one aperture in the at least one reference microchannel each have a maximum width less than a set wavelength.

26. The sensor of claim 25, wherein the at least one aperture in the at least one test microchannel and the at least one aperture in the at least one reference microchannel each have a maximum width of 10-500 nanometers.

27. The sensor of claim 25, wherein the at least one aperture in the at least one test microchannel and the at least one aperture in the at least one reference microchannel each have a maximum width of 100-300 nanometers.

28. The sensor of claim 1, wherein the target analyte is selected from the group consisting of:

an antigen, a protein, a DNA sequence, a RNA sequence, small molecules, sugar molecules, biomolecules, biomarkers and a nutrient.

29. The sensor of claim 1, wherein a binding constant of the capture molecules is a function of an expected target analyte concentration.

30. The sensor of claim 29, wherein the binding constant is less than ten times and more than one tenth of the expected target analyte concentration.

31. The sensor of claim 29, wherein the binding constant is less than a hundred times and more than one hundredth of the expected target analyte concentration.

32. A method comprising:

providing the sensor of claim 1;

providing a solution to be analyzed by the sensor;

activating the light source;

detecting, by the sensor, the intensity of the light of the test and reference channel SPE in the predetermined wavelength band, thereby detecting the presence of the target analyte.

33. The method of claim 32, further comprising choosing a binding constant of the capture molecules as a function of an expected target analyte concentration.

34. The method of claim 33, wherein the binding constant is less than ten times and more than one tenth of the expected target analyte concentration.

35. The method of claim 33, wherein the binding constant is less than a hundred times and more than one hundredth of the expected target analyte concentration.

36. The method of claim 32, where a concentration of the target analyte is calculated from the intensity of the light of the test and reference channel SPE in the predetermined wavelength band.