Biomarker detection from fluid samples

Patent metadata

Field	Value
Publication number	US-11732293-B2
Application number	US-201816649894-A
Country	US
Kind code	B2
Filing date	Oct 5, 2018
Priority date	Oct 6, 2017
Publication date	Aug 22, 2023
Grant date	Aug 22, 2023

Abstract

Described herein are systems and methods which utilize an array of wells to isolate pathogens and nucleic acid detection techniques to accurately and rapidly detect pathogens in fluid samples, even in very low concentrations, including from solid or semi-solid samples that have been fluidized. The provided systems and methods dry the fluid sample to deposit a fraction of the total volume in a number of wells and perform nucleic acid detection on individual wells to detect even individual pathogens and provide a quantitative analysis of the amount of pathogen within the sample. Also provided are methods and systems for precise delivery of dried materials, including biomolecules that are enzymes of use in the process, to microwells.

First claim

We claim:

1. A method of detecting one or more target analytes from a liquid sample, the method comprising the steps of:
applying a liquid sample to a substrate, wherein the substrate has an array of wells;
drying the liquid sample to generate a plurality of dried sample islands, with each sample island confined to a unique well;
applying a liquid having a reagent suspended in a liquid buffer to each well, wherein the reagent is used for nucleic acid detection;
eluting a nucleic acid from the dried sample islands with a liquid phase having the applied reagent;
detecting a target nucleic acid if present in a dried sample island by a bi-phasic reaction, that occurs in both the dried sample islands and in the liquid having the reagent suspended in the liquid buffer, wherein the detecting is by electrical or optical detection;

thereby detecting the one or more target analytes from the liquid biological sample.

2. The method of claim 1 , wherein the eluting comprises:
forming microchannels and/or nanochannels in the dried sample islands to facilitate introduction of reagent-containing liquid into an interior portion of the dried sample islands;
wherein eluted nucleic acid remains in the microchannels and/or nanochannels; diffuses from the microchannels and/or nanochannels to the liquid phase that is a supernatant to the dried sample islands; or both.

3. The method of claim 1 , wherein the eluting step comprises one or more of thermally, chemically and enzymatically eluting the nucleic acid of the dried sample islands.

4. The method of claim 1 , wherein the liquid sample is a biological sample.

5. The method of claim 4 , wherein the liquid sample is minimally processed, including an unprocessed raw sample, without any purification steps.

6. The method of claim 1 , wherein the applying the liquid having the reagent step is before or after the applying the liquid sample step.

7. The method of claim 1 , wherein the detecting step comprises amplifying a target nucleic acid in the liquid phase.

8. The method of claim 1 , wherein the bi-phasic reaction comprises the dried sample island and the reagent suspended in the liquid buffer, wherein the liquid buffer is positioned over the dried sample island in the well.

9. The method of claim 1 , further comprising a step of forming high surface area structures in the plurality of dried sample islands and/or the liquid having the reagent positioned over the dried sample islands.

10. The method of claim 9 , wherein the high surface area structures are formed by mixing gas with the liquid sample before or during the drying step.

11. The method of claim 9 , wherein the high surface area structures comprise a reagent-connected bead suspended in the liquid having the reagent.

12. The method of claim 1 , comprising a bead-based molecule delivery system, wherein the molecule is used in an amplifying or detecting step.

13. The method of claim 12 , wherein said molecule is an enzyme.

14. The method of claim 12 , wherein said bead-based molecule delivery system comprises a liquid bi-layer application, wherein:
the liquid having the reagent suspended in the liquid buffer covers the dried sample islands;
a carrier fluid having said bead-molecule suspended therein is disposed over said liquid having the reagent suspended in the liquid buffer; and
the method further comprising a step of forcing said bead-molecule into the liquid having the reagent suspended in the liquid buffer.

15. The method of claim 12 , wherein said bead-based molecule delivery system comprises a liquid tri-layer application, wherein:
a buffer mixture covers the dried sample islands;
an immiscible separating fluid that covers said buffer mixture;
a carrier fluid having said bead-molecule suspended therein is disposed over said immiscible separating fluid, wherein the carrier fluid further comprises a surfactant that forms micelles around the bead-molecule to protect the molecule from denaturing; and
the method further comprising a step of forcing said bead-molecule into the buffer mixture.

16. The method of claim 12 , wherein said bead-based molecule delivery system comprises a liquid layer and frozen liquid layer application, wherein:
the liquid having the reagent suspended in the liquid buffer covers the dried sample islands;
a carrier fluid having said bead-molecule suspended therein, wherein said carrier fluid has a freezing point less than a freezing point of said liquid having the reagent suspended in the liquid buffer; and
the method further comprising the steps of:
freezing the liquid having the reagent suspended in the liquid buffer mixture by cooling the liquid having the reagent suspended in the liquid buffer mixture to a temperature that is below the liquid having the reagent suspended in the liquid buffer mixture freezing point and that is above the carrier fluid freezing point;
applying the carrier fluid on top of the frozen liquid having the reagent suspended in the liquid buffer mixture;
forcing the bead-molecule to the frozen liquid having the reagent suspended in the liquid buffer liquid carrier fluid interface;
thawing the frozen liquid having the reagent suspended in the liquid buffer; and
forcing said bead-molecule into the liquid having the reagent suspended in the liquid buffer.

17. The method of claim 9 , wherein the high surface area structures comprise a microrelief structure having a molecule connected thereto, the method further comprising the steps of:
aligning the microrelief structure with the array of wells;
inserting the microrelief structure into liquid having the reagent suspended in the liquid buffer that occupies the wells and covers the dried sample islands; and
wherein the inserted microrelief structure introduces a reagent molecule to the liquid having the reagent suspended in the liquid buffer and prevents evaporation from the wells.

18. The method claim 1 , having a sensitivity as high as 1 copy of a target nucleic acid per reaction well in a total liquid sample volume of between 1 mL and 10 mL.

19. The method of claim 1 , used in an application selected from the group consisting of:
cancer molecular screening;
pathogen detection from body fluids, including for diagnosis of sepsis;
treatment efficacy assessment;
detection of pathogens from food and water samples;
detection of rare cells in biological sample, including circulating tumor cells; and
detection of cell-free DNA from a body fluid sample.

20. The method of claim 1 , wherein the liquid sample is selected from the group consisting of: whole blood; saliva; urine; sweat; throat swab; vaginal swab; sputum; drinkable fluid; environmental sample and edible food.

21. The method of claim 1 , wherein the nucleic acid amplification comprises PCR or isothermal processes.

22. The method of claim 1 , wherein the one or more target analytes comprise a nucleic acid sequence indicative of a pathogen or a disease state.

23. The method of claim 1 , wherein the liquid buffer comprises:
an amplification enzyme and primers for nucleic acid amplification of a target analyte; and
the amplification occurs in both the solid phase dried sample and in the liquid having the reagent suspended in the liquid buffer through simultaneous diffusion of enzymes and buffer components into the dried fluid sample and target nucleic acid into the liquid buffer.

24. The method of claim 1 , wherein each well has a well volume select

Assignees

• Univ Illinois

Inventors

• Bashir Rashid
• Ganguli Anurup

Classifications

• C12Q1/6848 Primary

  characterised by the means for preventing contamination or increasing the specificity or sensitivity of an amplification reaction · CPC title

• B01L3/5027

  by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip · CPC title

• C12Q1/6806

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title

• C12Q1/689

  for bacteria · CPC title

• C12Q1/6851

  Quantitative amplification · CPC title