Hyperuniform-structured profiling system
A a hyperuniform-structured microchip is configured for providing viable resolution of CTC subpopulations supporting the ability to determine whether there is a correlation between CTC heterogeneity and tumor progression, the microchip including a substrate, a microfluidic enclosure around the substrate, and a plurality of microposts configured on the substrate in a hyperuniform pattern.
1 . A system comprising:
a substrate comprising:
a nanostructured layer comprising a silicon dioxide nanoparticle layer with a size of 5-200 nm; and
positively-charged polymers;
a microfluidic enclosure around the substrate; and
a plurality of microposts configured on the substrate in a hyperuniform pattern.
2 . The system of claim 1 wherein the plurality of microposts comprises at least one of:
columns;
squares; and
triangles.
3 . The system of claim 1 wherein the hyperuniform pattern further comprises multiple zones with different hyperuniform patterns.
4 . The system of claim 1 further comprising:
a fluidic input to the microfluidic enclosure configured to accept cells; and
a fluidic output from the microfluidic enclosure configured to accept cells.
5 . The system of claim 1 wherein the substrate and the microfluidic enclosure are configured of at least one of:
Polydimethylsiloxane;
Polyethylene;
Polycarbonate;
Cyclo-olefin copolymer; and
Polylactic acid.
6 . The system of claim 1 wherein the positively-charged polymers comprise at least one of:
a poly-L-arginine layer;
a poly(allylamine hydrochloride) layer;
a Poly-L-lysine layer;
a low molecular weight chitosan layer; and
a Diethylaminoethyl Dextran.
7 . The system of claim 1 further comprising:
a surface coating applied to the substrate and the plurality of microposts comprising:
negatively-charged polymers; and
positively-charged polymers.
8 . The system of claim 7 wherein the negatively-charged polymers comprises at least one of:
biotinylated alginate;
Alginate; and
Hyaluronic acid.
9 . The system of claim 7 wherein the positively-charged polymers comprise at least one of:
poly-L-arginine;
a poly(allylamine hydrochloride) layer;
a Poly-L-lysine layer;
a low molecular weight chitosan layer; and
a Diethylaminoethyl Dextran.
10 . The system of claim 7 wherein the surface coating further comprise:
at least one antibody that targets an antigen overexpressed on cancer cells.
11 . The system of claim 10 wherein the antibody comprises at least one of:
an Anti-EpCAM;
an Anti-HER2;
an Anti-EGFR; and
a surface antigen on a cell surface, comprising one of:
Anti-CD4; and
Anti-CD8.
12 . The system of claim 1 further comprising:
an imaging device, the imaging device configured to capture image data of flow patterns of fluid and cell movement in the microfluidic enclosure.
13 . The system of claim 12 wherein the imaging device comprises at least one of:
a camera;
a video camera; and
a microscope.
14 . The system of claim 13 further comprising:
a computer system, said computer system comprising:
at least one processor; and
a computer-usable medium embodying computer program code, the computer-usable medium capable of communicating with the at least one processor, the computer program code comprising instructions executable by the at least one processor and configured for:
accepting input of the image data from the image device;
determining flow rate data associated with cell flow through the microfluidic enclosure; and
identifying at least one cell type according to the flow rate data.
15 . A method for cell identification comprising:
introducing a cell sample to a microchip comprising a hyperuniform configuration of microposts;
capturing flow rates of the cell sample at least one location on the microchip;
integrating images of the microchip to identify a flow field in the microchip;
determining an adhesion force of at least one cell in the cell sample according to the captured flow rate;
identifying locations on the microchip for capture certain types of cells based on cell-surface interaction; and
identifying the at least one cell in the cell sample according to the determined adhesion force.
16 . The method of claim 15 wherein the microchip further comprises:
a substrate;
a microfluidic enclosure around the substrate;
a fluidic input to the microfluidic enclosure configured to accept cells; and
a fluidic output from the microfluidic enclosure configured to accept cells.
17 . The method of claim 16 further comprising:
applying a surface coating to the substrate and the plurality of microposts comprising:
biotinylated alginate;
Alginate;
Hyaluronic acid;
a poly-L-arginine layer;
a poly(allylamine hydrochloride) layer;
a Poly-L-lysine layer;
a low molecular weight chitosan layer; and
a Diethylaminoethyl Dextran.
18 . A microchip test system comprising:
a substrate;
a microfluidic enclosure around the substrate;
a plurality of microposts configured on the substrate in a hyperuniform pattern;
an imaging device, the imaging device configured to capture image data of flow patterns of fluid and cell movement in the microfluidic enclosure; and
a computer system, said computer system comprising:
at least one processor; and
a computer-usable medium embodying computer program code, the computer-usable medium capable of communicating with the at least one processor, the computer program code comprising instructions executable by the at least one processor and configured for:
accepting input of the image data from the imaging device;
determining flow rate data associated with cell flow through the microfluidic device; and
identifying at least one cell type according to the flow rate data.