Combined Extraction and PCR Systems
US-2019309346-A1 · Oct 10, 2019 · US
US12590340B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12590340-B2 |
| Application number | US-202217662732-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 10, 2022 |
| Priority date | May 10, 2021 |
| Publication date | Mar 31, 2026 |
| Grant date | Mar 31, 2026 |
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There is provided a microfluidic chip for sensing an analyte in a sample by colorimetry. The microfluidic chip comprises: an inlet adapted to receive the sample; an incubation chamber having an incubation chamber inlet fluidly connected to the inlet downstream thereof, to incubate the analyte in the sample; a filter barrier fluidly connected to the incubation chamber, downstream of the incubation chamber inlet; a sensing chamber fluidly connected to the incubation chamber, downstream of the filter barrier, the sensing chamber having a plasmonic nanosurface, the plasmonic nanosurface including nanostructures protruding from the plasmonic nanosurface, the nanostructures having a size that is smaller than that of the diffraction limit of light, the nanostructures having a metallic layer that is plasmon-supported on top of a back reflector layer; and an outlet fluidly connected to the sensing chamber downstream thereof.
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What is claimed is: 1 . A microfluidic chip for sensing an analyte in a sample by colorimetry, the microfluidic chip comprising: an inlet adapted to receive the sample, an incubation chamber having an incubation chamber inlet fluidly connected to the inlet downstream thereof, to incubate the analyte in the sample; a filter barrier fluidly connected to the incubation chamber, downstream of the incubation chamber inlet; a sensing chamber fluidly connected to the incubation chamber, downstream of the filter barrier, the sensing chamber having a plasmonic nanosurface, the plasmonic nanosurface including nanostructures protruding from the plasmonic nanosurface, the nanostructures having a size that is smaller than that of the diffraction limit of light, the nanostructures having a metallic layer that is plasmon-supported on top of a back reflector layer; and an outlet fluidly connected to the sensing chamber downstream thereof. 2 . The microfluidic chip of claim 1 , wherein the nanostructures have a diameter between 200 nm and 1000 nm. 3 . The microfluidic chip of claim 1 , wherein nanocavities are defined in between the nanostructures, the nanocavities define an interparticle gap of between 20 nm and 500 nm between the nanostructures. 4 . The microfluidic chip of claim 1 , wherein the plasmonic nanosurface is free of color pigments. 5 . The microfluidic chip of claim 1 , wherein the filter barrier comprises at least two rows of micropillars. 6 . The microfluidic chip of claim 1 , wherein the filter barrier is enclosed in the incubation chamber and occupies a portion of a total volume thereof. 7 . The microfluidic chip of claim 1 , wherein the nanostructures comprise a monolayer of polystyrene nanoparticles coated by the back reflector layer and further coated by the metallic layer. 8 . The microfluidic chip of claim 1 , wherein the microfluidic chip further comprises a heating element. 9 . The microfluidic chip of claim 1 , wherein the back reflector layer is selected from the group consisting of ZnO, TiO 2 , hydrogen silsesquioxane (HSQ), AZ MiR™, and polymethyl methacrylate (PMMA). 10 . The microfluidic chip of claim 1 , wherein the metallic surface comprises at least one of Al, Ag and Au. 11 . The microfluidic chip of claim 7 , wherein the polystyrene nanoparticles have a diameter of between 200 nm to 1000 nm. 12 . The microfluidic chip of claim 1 , wherein the back reflector has a thickness of 10 to 500 nm. 13 . The microfluidic chip of claim 1 , wherein the metallic surface has a thickness of 5 to 100 nm. 14 . The microfluidic chip of claim 1 , wherein the inlet, the incubation chamber, the sensing chamber and the outlet are defined in a layer of negative photoresist forming part of the microfluidic chip. 15 . The microfluidic chip of claim 1 , wherein the microfluidic chip includes a silicon base layer, an epoxy-based negative photoresist layer onto the silicon base layer, and a curable transparent polymer layer, the incubation chamber and the sensing chamber defined in the epoxy-based negative photoresist layer. 16 . A method of sensing an analyte in a sample comprising: providing a microfluidic chip as defined in claim 1 ; providing the sample at the inlet; incubating the sample in the incubation chamber for a predetermined period of time; flowing the sample across the filter barrier to the sensing chamber; and analyzing a plasmonic color change of the sample. 17 . The method according to claim 16 , wherein further comprising providing a colorimetric sensor at a second inlet of the microfluidic chip. 18 . The method according to claim 17 , further comprising mixing the colorimetric sensor and the sample in microchannels of the microfluidic device. 19 . The method according to claim 16 , further comprising, before providing the sample at the inlet, mixing the sample with a colorimetric sensor. 20 . The method according to claim 16 , wherein the incubating of the sample in the incubation chamber comprises heating the microfluidic chip to induce a nucleic acid amplification of the analyte being a nucleic acid sequence.
Filter · CPC title
Serpentine channels · CPC title
Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks · CPC title
Reagents, handling or storing thereof · CPC title
Nucleic acid amplification reactions · CPC title
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