Systems and methods for on-chip analysis of nucleic acids and for multiplexed analysis of cells

Patent metadata

Field	Value
Publication number	US-12303899-B2
Application number	US-201917298507-A
Country	US
Kind code	B2
Filing date	Nov 29, 2019
Priority date	Nov 28, 2018
Publication date	May 20, 2025
Grant date	May 20, 2025

Abstract

A microfluidic chip for on-chip detection of the presence or absence of a target nucleic acid region in an isolated nucleic acid sample is disclosed. The microfluidic chip includes a nucleic acid entanglement array, an isolated nucleic acid sample immobilized in the nucleic acid entanglement array, and at least one probe specific to a target nucleic acid region. Systems and methods of using the microfluidic chip are disclosed. An integrated microfluidic cell processing system is disclosed, which includes: a multiplexed microfluidic flow directing system having a plurality of reconfigurable microfluidic layers that form a plurality of reconfigurable microfluidic channels, where the multiplexed microfluidic flow directing system function to assist in directing flow of materials into, through, and out of the integrated cell processing system; and at least one microfluidic chip functionally integrated into at least one layer of the multiplexed microfluidic flow directing system, and operates under continuous flow conditions.

First claim

What is claimed is:

1. An integrated microfluidic cell processing system comprising:
a flow directing system comprising a plurality of reconfigurable microfluidic layers that include:
an affinity microcolumn layer comprising a plurality of substantially vertical microcolumns passing therethrough and containing an affinity chromatography agent; and
at least one microfluidic chip functionally integrated into a layer below the affinity microcolumn layer, wherein said at least one microfluidic chip comprises a cell capture component and a nucleic acid entanglement component,

wherein the system operates under continuous flow conditions to process one or more cell.

2. The integrated microfluidic cell processing system according to claim 1 , wherein said cell capture component comprises a cell capture array comprising a plurality of cell capture micropillars, and wherein said nucleic acid entanglement component comprises a nucleic acid entanglement array comprising a plurality of nucleic acid entanglement micropillars.

3. The integrated microfluidic cell processing system according to claim 1 , wherein the at least one microfluidic chip is integrated with the flow directing system in a manner so that flow of materials into the flow directing system is directed into and through the at least one microfluidic chip before being exported from the flow directing system, and wherein the flow directing system is configured to: receive and export one or more sample in manual and/or automated fashion; and/or assist in sorting materials for export from the microfluidic system for further collection, purification, and/or analysis.

4. The integrated microfluidic cell processing system according to claim 1 , further comprising:
a top capping layer proximately disposed at a top surface of the affinity microcolumn layer and comprising a patterned grid having at least one opening in fluid alignment with at least one microcolumn so as to allow a sample liquid to pass through the top capping layer and into the at least one microcolumn;
a bottom capping layer beneath a bottom surface of the affinity microcolumn layer and comprising a parallel patterned grid of openings in fluid alignment with the microcolumns; and
a bottom frit gasket layer deposited between the bottom surface of the affinity microcolumn layer and the bottom capping layer for aiding the containment of the affinity chromatography agent.

5. The integrated microfluidic cell processing system according to claim 4 further comprising:
a top channel layer disposed between the top capping layer and the top surface of the microcolumn layer, wherein the top channel layer comprises a plurality of substantially horizontal channel portions each forming a flow channel fluidly connecting adjacent microcolumns of the microcolumns through which a single liquid sample is desired to pass in a serial manner, and wherein the top channel layer is optionally patterned to work in fluid and serial connection with the bottom capping layer so as to pass the single liquid sample through the microcolumns in a serial manner.

6. The integrated microfluidic cell processing system according to claim 4 further comprising:
a top port layer proximately disposed on the top capping layer, said top port layer comprising one or more input port each in fluidic alignment with a corresponding microcolumn so as to effectuate introduction of a sample liquid into a desired microcolumn.

7. The integrated microfluidic cell processing system according to claim 4 further comprising:
a bottom port layer proximately disposed on the bottom capping layer, said bottom port layer comprising one or more outlet port each in fluidic alignment with a corresponding microcolumn so as to effectuate expulsion of a liquid sample from a desired microcolumn.

8. The integrated microfluidic cell processing system according to claim 4 further comprising:
a top frit gasket layer for aiding the containment of the affinity chromatography agent, wherein said top frit gasket layer is deposited between the top surface of the microcolumn layer and the top capping layer.

9. The integrated microfluidic cell processing system according to claim 4 further comprising:
a top port layer proximately disposed on the top capping layer, said top port layer comprising one or more input port each in fluidic alignment with a corresponding microcolumn so as to effectuate introduction of a sample liquid into a desired microcolumn;
an optional bottom port layer proximately disposed on the bottom capping layer, said bottom port layer comprising one or more outlet port each in fluidic alignment with a corresponding microcolumn so as to effectuate expulsion of a liquid sample from a desired microcolumn; and
a top washer layer and/or a bottom washer layer for securing the ports of the top port layer and the optional bottom port layer in alignment with their corresponding microcolumns,
wherein said top washer layer is proximately deposited at the top capping layer and comprises a plurality of openings through which the ports of the top port layer protrude, and
wherein said bottom washer layer is proximately deposited at the bottom capping layer and comprises a plurality of openings through which the ports of the optional bottom port layer protrude.

10. The integrated microfluidic cell processing system according to claim 4 , wherein the affinity chromatography agent comprises an immobilized target molecule selected from the group consisting of a whole cell, a virus, a virus particle, a protein, a modified protein, a polypeptide, a modified polypeptide, an RNA molecule, a DNA molecule, a modified DNA molecule, a polysaccharide, an amino acid, an antibiotic, a pharmaceutical agent, an organic non-pharmaceutical agent, a macromolecular complex, a carbohydrate, a lipid, a small molecule, a chemical compound, a mixture of lysed cells, and a mixture of purified, partially purified, or non-purified protein, and optionally the immobilized target molecule is labeled and/or provided from a mixture of lysed cells, a mixture of purified, partially purified, or non-purified protein.

11. The integrated microfluidic cell processing system according to claim 1 , wherein said at least one microfluidic chip is configured for on-chip detection of a presence or absence of a target nucleic acid region in an isolated nucleic acid sample, wherein the nucleic acid entanglement component comprises a plurality of nucleic acid entanglement micropillars configured and arranged in a manner effective to physically entangle and maintain thereon an isolated nucleic acid sample; the at least one microfluidic chip further comprising:
the isolated nucleic acid sample immobilized in the nucleic acid entanglement array; and
at least one probe specific to a target nucleic acid region, said at least one probe being specifically bound to the target nucleic acid region and detectable when said isolated nucleic acid sample includes the target nucleic acid region,
thereby enabling on-chip analysis of the presence or absence of the target nucleic acid region in the isolated nucleic acid sample.

12. The integrated microfluidic cell processing system according to claim 11 , wherein the isolated nucleic acid sample comprises genomic DNA (gDNA), extrachromosomal DNA, chromatin, plasmid DNA, a nucleic acid aptamer, an oligonucleotide, or a nucleic acid biomarker and/or wherein the target nucleic acid region comprises a gene, mutation, or nucleotide sequence from a eukaryotic cell, a human or a non-human animal.

13. The integrated microfluidic cell processing system according to claim 11 , wherein the target nucleic acid region comprises a ge

Assignees

• Univ Cornell

Inventors

• Craighead Harold G
• Tian Harvey C
• Lin David M
• Bisogni Adam J

Classifications

• C12Q1/6837

  using probe arrays or probe chips (C12Q1/6874 takes precedence) · CPC title

• B01L2400/086

  using baffles or other fixed flow obstructions · CPC title

• B01L2300/123

  Flexible; Elastomeric · CPC title

• B01L2300/0887

  Laminated structure · CPC title

• B01L2300/0819

  Microarrays; Biochips · CPC title