Metabolite detection apparatus and method of detecting metabolites

Patent metadata

Field	Value
Publication number	US-2023118814-A1
Application number	US-202218067673-A
Country	US
Kind code	A1
Filing date	Dec 16, 2022
Priority date	May 24, 2017
Publication date	Apr 20, 2023
Grant date	—

Abstract

A CMOS-based chip having one or more sensing modalities that are able independently to detect multiple metabolites present in a biological sample. The multiple sensing modalities may be provided at different locations with respect to the chip, whereby the chip can simultaneously detect a plurality of metabolites by measuring behaviour of a test material in the different locations. The chip may utilise paper as a transport mechanism for the sample. The paper either conveys the sample to the different locations or itself provides discrete testing zones in which different metabolites can be independently detected. With this technique, multiple metabolites may be measured in real time using a small scale point-of-care device.

First claim

What is claimed:

1 . An apparatus for detecting metabolites in a biological sample, the apparatus comprising:
a sample receiving module arranged to receive the biological sample, the sample receiving module comprising a capillary transport structure configured to transport the biological sample to a reaction zone for testing, wherein the reaction zone comprises a first testing region and a second testing region spatially separated from the first testing region; a CMOS-based sensor unit disposed adjacent to the reaction zone; and a controller in communication with the CMOS-based sensor unit, wherein the first testing region and the second testing region each comprise a microfluidic channel formed on the capillary transport structure, wherein the microfluidic channel of the first testing region comprises an assay region comprising a first test material arranged to support a first metabolite-activated reaction with a first metabolite, the first test material having an observable property that is associated with the amount of first metabolite in the biological sample, wherein the microfluidic channel of the second testing region comprises an assay region having a second test material arranged to support a second metabolite-activated reaction with a second metabolite that is different from the first metabolite, the second test material having an observable property that is associated with the amount of second metabolite in the biological sample, wherein the CMOS-based sensor unit is configured to detect the observable property of the first test material and the observable property of the second test material, and generate therefrom separate electrical signals for each of the first testing region and the second testing region, wherein the controller is configured to determine an amount of the first metabolite and second metabolite in the biological sample based on a change over time in amplitude of the separate electrical signals generated by the CMOS-based sensor unit, wherein the capillary transport structure is configured not to contact the surface of the CMOS-based sensor unit.

2 . The apparatus according to claim 1 , wherein the capillary transport structure is a paper strip is disposed over the CMOS-based sensor unit.

3 . The apparatus according to claim 1 , further comprising a fluid flow barrier separating the first testing region from the second testing region, wherein the fluid flow barrier comprises a hydrophobic polymer or a photoresist layer disposed between the microfluidic channels.

4 . An apparatus for detecting metabolites in a biological sample, the apparatus comprising:
a reaction zone arranged to receive the biological sample for testing, wherein the reaction zone comprises a first testing region and a second testing region spatially separated from the first testing region, and wherein properties of the first testing region and the second testing region are affected by the presence of metabolites to be detected; and a CMOS-based sensor unit disposed in relation to the reaction zone to detect independently the properties of the first testing region and the second testing region thereby to obtain separate signals indicative of the presence of metabolites in each of the first testing region and the second testing region, wherein the reaction zone comprises a separation wall that defines separate reaction chambers within the reaction zone, each of the separate reaction chambers being configured to receive a respective portion of the biological sample, wherein each of the separate reaction chambers further comprises a base layer disposed between the CMOS-based sensor unit and the reaction zone except at a respective micro-well, wherein the first testing region and the second testing region each comprise the respective micro-well formed in a respective reaction chamber by an absence of the base layer, wherein the respective micro-wells are separated from each other by a barrier portion that is defined by a portion of the separation wall that contacts a surface of the CMOS-based sensor unit.

5 . The apparatus according to claim 4 , wherein the base layer and separation wall are formed from epoxy.

6 . The apparatus according to claim 4 , wherein the reaction zone includes a control region that is not sensitive to the presence of metabolites to be detected.

7 . The apparatus according to claim 4 , wherein at least one of the first testing region and the second testing region comprises a test material arranged to support a metabolite-activated reaction upon receiving the biological sample.

8 . The apparatus according to claim 4 , wherein the CMOS-based sensor unit comprises an optical sensor.

9 . The apparatus according to claim 8 including an optical source for illuminating the reaction zone with optical radiation.

10 . The apparatus according to claim 8 , wherein the optical sensor is at least one of a photodiode an a single photon avalanche diode.

11 . The apparatus according to claim 4 , wherein the CMOS-based sensor unit has multiple sensing modalities, and comprises a substrate having a first sensing element and a second sensing element fabricated thereon.

12 . The apparatus according to claim 11 , wherein the first sensing element comprises an optical sensor that incorporates at least one of a photodiode and single photon avalanche diode.

13 . The apparatus according to claim 11 , wherein the second sensing element is a chemical sensor.

14 . The apparatus according claim 11 , wherein the second sensing element is a pH sensor.

15 . The apparatus according to claim 11 , wherein the second sensing element comprises an ion sensitive field effect transistor (ISFET) having a gate electrode in contact with the reaction zone.

16 . The apparatus according to claim 15 including a reference electrode arranged to apply a voltage to the reaction zone.

17 . The apparatus according to claim 4 comprising an array of CMOS-based sensor units, wherein each CMOS-based sensor unit in the array is independently addressable.

18 . An apparatus for detecting metabolites in a biological sample, the apparatus comprising:
a sample receiving module arranged to receive the biological sample, the sample receiving module comprising a capillary transport structure configured to transport the biological sample to a reaction zone for testing, wherein the reaction zone comprises a first testing region and a second testing region spatially separated from the first testing region; a CMOS-based sensor unit; and a controller in communication with the CMOS-based sensor unit, wherein the first testing region and the second testing region each comprise a microfluidic channel formed on a surface of the CMOS-based sensor unit and the capillary transport structure includes corresponding microfluidic channels configured to contact the surface of the CMOS-based sensor unit, wherein the microfluidic channel of the first testing region comprises an assay region comprising a first test material arranged to support a first metabolite-activated reaction with a first metabolite, the first test material having an observable property that is associated with the amount of first metabolite in the biological sample, wherein the microfluidic channel of the second testing region comprises an assay region having a second test material arranged to support a second metabolite-activated reaction with a second metabolite that is different from the first metabolite, the second test material having an observable property that is associated with the amount of second

Assignees

• Univ Glasgow Court

Inventors

• Cumming David Robert Sime
• Patil Samadahn
• Al-Rawhani Mohammed
• Barrett Michael
• Dheeman Dharmendra
• Xu Chunxiao

Classifications

• G01N27/4145

  specially adapted for biomolecules, e.g. gate electrode with immobilised receptors · CPC title

• G01N33/492 Primary

  Determining multiple analytes · CPC title

• G01N21/76 Primary

  Chemiluminescence; Bioluminescence · CPC title

• G01N21/255

  Details, e.g. use of specially adapted sources, lighting or optical systems · CPC title

• G01N21/8483

  Investigating reagent band (test-element handling not specific to a test method G01N33/4875; analytical elements specific to chemical analysis of biological material G01N33/52; autometer with reagent band G01N35/04) · CPC title