# US 2025/0083142 A1 · Multiplexed nucleic acid amplification test on semiconductor substrate > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 2025/0083142 A1 - Document ID: US20250083142A1 - Status: Published application - Kind: A1 - Application number: 18/428,825 - Filed: 2024-01-31 - Published: 2025-03-13 - Earliest claimed: 2023-09-08 - Assignees: Texas Instruments Incorporated - Applicants: Texas Instruments Incorporated - Inventors: Sebastian MEIER; Ernst MUELLNER - Web page: https://patentgrep.com/patent/US20250083142A1 ## CPC - B01L 3/502715: {characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces} - B01L 3/502707: {characterised by the manufacture of the container or its components} - B01L 7/52: {with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples} - G01N 27/227: {Sensors changing capacitance upon adsorption or absorption of fluid components, e.g. electrolyte-insulator-semiconductor sensors, MOS capacitors (G01N27/225 takes precedence)} - G01N 27/4145: {specially adapted for biomolecules, e.g. gate electrode with immobilised receptors} - B01L 2200/10: Integrating sample preparation and analysis in single entity, e.g. lab-on-a-chip concept - B01L 2200/16: Reagents, handling or storing thereof - B01L 2300/0636: Integrated biosensor, microarrays - B01L 2300/0645: Electrodes - B01L 2300/0663: Whole sensors - B01L 2300/0816: Cards, e.g. flat sample carriers usually with flow in two horizontal directions - B01L 2300/0867: Multiple inlets and one sample wells, e.g. mixing, dilution - B01L 2300/0877: Flow chambers - B01L 2300/0887: Laminated structure - B01L 2300/1805: Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks - B01L 2300/1822: using Peltier elements - B01L 2300/1827: using resistive heater - B01L: CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE - G01N: INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES (measuring or testing apparatus or processes other than immunoassay, involving enzymes or microorganisms C12M, C12Q) ## Abstract Example packaged integrated circuit (IC) sensors comprise a semiconductor substrate; a back end of line (BEOL) structure on the semiconductor substrate, the BEOL structure including multiple microfluidic channels, each microfluidic channel including a flow control device configured to selectively permit and restrict flow of fluids; multiple fluid sensors including first and second fluid sensors in the BEOL structure; a main reaction reservoir on the BEOL structure configured to store a reagent, in which the reagent is operable to replicate a nucleic strand in a biological sample to cause a pH change, and the first fluid sensor is exposed in the main reaction reservoir; an auxiliary reservoir on the BEOL structure and coupled to the main reaction reservoir via a microfluid channel of the multiple microfluidic channels, in which the second fluid sensor is exposed in the auxiliary reaction reservoir; and a controller coupled to the first and second fluid sensors. ## Claims ### Claim 1 A packaged integrated circuit (IC) sensor comprising: a semiconductor substrate; a back end of line (BEOL) structure on the semiconductor substrate, the BEOL structure including multiple microfluidic channels, each microfluidic channel including a flow control device configured to selectively permit and restrict flow of fluids; multiple fluid sensors including first and second fluid sensors in the BEOL structure; a main reaction reservoir on the BEOL structure configured to store a reagent, in which the reagent is operable to replicate a nucleic strand in a biological sample to cause a pH change, and the first fluid sensor is exposed in the main reaction reservoir; an auxiliary reservoir on the BEOL structure and coupled to the main reaction reservoir via a microfluid channel of the multiple microfluidic channels, in which the second fluid sensor is exposed in the auxiliary reaction reservoir; and a controller coupled to the first and second fluid sensors. ### Claim 2 (depends on 1) The packaged IC sensor of claim 1, wherein the reagent is a first reagent, the multiple fluid sensors include a third fluid sensor, the auxiliary reaction reservoir is a first auxiliary reaction reservoir, and the packaged fluid sensor further comprises a second auxiliary reservoir on the BEOL structure coupled to the main reaction reservoir via a second microfluidic channel of the multiple microfluid channels, the second auxiliary reservoir is configured as a detection reservoir, the detection reservoir configured to store a second reagent operable to replicate genetic material of a detection target, and the third fluid sensor is exposed in the second auxiliary reservoir. ### Claim 3 (depends on 2) The packaged IC sensor of claim 2, wherein the detection reservoir is a first detection reservoir, the detection target is a first detection target, the multiple fluid sensors include a fourth fluid sensor, and the packaged IC sensor includes a third auxiliary reaction reservoir configured as a second detection reservoir on the BEOL structure coupled to the main reaction reservoir via a third microfluidic channel of the multiple microfluid channels, and the second detection reservoir is configured to store a third reagent operable to replicate genetic material of a second detection target, and the fourth fluid sensor is exposed in the second detection reservoir. ### Claim 4 (depends on 3) The packaged IC sensor of claim 3, wherein the first reagent includes the second and third reagents. ### Claim 5 (depends on 2) The packaged IC sensor of claim 2, wherein the main reaction reservoir is configured to receive the biological sample directly or via a cartridge, and the controller is configured to open a valve of the flow control device of the first microfluidic channel to transfer the biological sample to the detection reservoir after a reaction time has elapsed. ### Claim 6 (depends on 1) The packaged IC sensor of claim 1, wherein the controller is configured to close a valve of the flow control devices of the second microfluidic channel to prevent the biological sample from moving into the auxiliary reaction reservoir configured as a reference reservoir. ### Claim 7 (depends on 1) The packaged sensor of claim 1, wherein the controller is configured to provide an output based on a difference in a first signal provided by the first fluid sensor and a second signal provided by the second fluid sensor, the difference representing a pH difference. ### Claim 8 (depends on 1) The packaged sensor of claim 1, further comprising a heat exchanger thermally coupled to each of the main and first detection reservoirs. ### Claim 9 (depends on 8) The packaged sensor of claim 8, wherein the heat exchanger includes a metal member covered with an inert coating. ### Claim 10 (depends on 1) The packaged IC sensor of claim 1, wherein each of the multiple fluid sensors includes an ion-sensitive field-effect transistor (ISFET). ### Claim 11 (depends on 1) The packaged IC sensor of claim 1, wherein the flow control device includes at least one of a pump or a valve. ### Claim 12 (depends on 1) The packaged IC sensor of claim 1, further comprising a heating element configured to maintain the main reaction reservoir at a particular temperature. ### Claim 13 (depends on 1) The packaged IC sensor of claim 1, further comprising a cavity configured to carry fluids of differing temperatures, the fluids of differing temperatures to adjust a temperature of the biological sample stored in the main reaction reservoir. ### Claim 14 (depends on 1) The packaged IC sensor of claim 1, wherein the BEOL structure includes a heating element to apply heat to at least one of the main and reference reservoirs. ### Claim 15 (depends on 14) The packaged IC sensor of claim 14, wherein the heating element is configured to heat the at least one of the main and reference reservoirs by radiant heating. ### Claim 16 (depends on 1) The packaged IC sensor of claim 1, further comprising a cartridge to which the second reagent is coupled. ### Claim 17 (depends on 1) The packaged IC sensor of claim 1, further comprising a heating element configured to dynamically adjust a temperature of the biological sample. ### Claim 18 (depends on 17) The packaged IC sensor of claim 17, wherein the heating element includes a first conductive member inside the main reaction reservoir that is configured to be wirelessly energized by a second conductive member outside the main reaction reservoir. ### Claim 19 (depends on 2) The packaged IC sensor of claim 2, further comprising an electrode in the main reaction reservoir and in the detection reservoir, the electrode configured to provide electrical currents into the main reservoir and the detection reservoir to control pH levels of contents of the main reservoir and of the detection reservoir respectively. ### Claim 20 (depends on 19) The packaged IC sensor of claim 19, wherein the fluid sensor includes a pH sensor, and the electrode is configured to provide the electrical current into the main reaction reservoir responsive to a signal from the pH sensor. ### Claim 21 (depends on 1) The packaged IC sensor of claim 1, wherein the main and auxiliary reaction reservoir each includes a metal or a dielectric wall covered with an inert metal. ### Claim 22 A method, comprising: providing a fluid containing a biological sample to a main reaction reservoir of a packaged integrated circuit (IC) sensor, the biological sample including a nucleic strand, and the main reaction reservoir stores a first reagent; allowing the fluid to flow from the main reaction reservoir to a first detection reservoir and a second detection reservoir of the packaged IC sensor, in which the first detection reservoir stores a second reagent to replicate nucleic strands of a first detection target, and the second detection reservoir stores a third reagent to replicate nucleic strands of a second detection target; replicating the nucleic strand in the main reaction reservoir using the first reagent; providing first and second portions of the replicated nucleic strands to the first and second detection reservoirs, respectively, by pumping; replicating the first portion of the replicated nucleic strands in the first detection reservoir using the second reagent; comparing pH levels of the first and second portions of the biological sample in the first and second detection reservoirs to a pH level of a reference reservoir of the packaged IC sensor; and based on the comparisons, determining whether the biological sample contains the first detection target. ### Claim 23 (depends on 22) The method of claim 22, further comprising, after replicating the nucleic strand in the main reaction reservoir and before providing the first and second portions of the multiple nucleic strands to the first test and second detection reservoirs: comparing pH levels of contents of the main and reference reservoirs and determining, based on the comparison, that the biological sample provided to the main reaction reservoir contains the first and second detection targets. ### Claim 24 (depends on 22) The method of claim 22, wherein replicating the nucleic strand in the main reaction reservoir comprises applying and removing heat from the nucleic strand. ### Claim 25 (depends on 22) The method of claim 22, wherein replicating the nucleic strand in the main reaction reservoir comprises passing a current through the main reaction reservoir using an electrode in the main reaction reservoir to increase a pH of the biological sample in the main reaction reservoir. ### Claim 26 (depends on 25) The method of claim 25, further comprising determining an amount of the current and, based on the amount of current, determining that the nucleic strand belongs to one of a group of targets. ### Claim 27 A method comprising: providing a fluid containing a biological sample to a main reaction reservoir of a packaged integrated circuit (IC) sensor, the biological sample including a nucleic strand, and the main reaction reservoir stores a first reagent; allowing the fluid to flow from the main reaction reservoir to a reference reservoir; replicating the nucleic strand in the main reaction reservoir using the first reagent; determining a pH change in the main reaction reservoir; responsive to the pH change exceeding a threshold, providing first and second portions of the replicated nucleic strands to the first and second detection reservoirs, respectively, by opening valves, in which the first detection reservoir stores a second reagent to replicate nucleic strands of a first detection target, and the second detection reservoir stores a third reagent to replicate nucleic strands of a second detection target; replicating the first portion of the replicated nucleic strands in the first detection reservoir using the second reagent; comparing pH levels of the first and second portions of the biological sample in the first and second detection reservoirs to a pH level of the reference reservoir; and based on the comparisons, determining whether the biological sample contains the first detection target. ### Claim 28 A method, comprising: forming a semiconductor substrate; forming a back end of line (BEOL) on the semiconductor substrate, the BEOL including a microfluidic channel, the microfluidic channel having first and second openings that extend through the BEOL and away from the semiconductor substrate; and forming a fluidic structure on the BEOL having a first cavity and a second cavity, the first cavity being directly over the first opening, and the second cavity being directly over the second opening, wherein the first and second cavities are configured to replicate nucleic strands using the first and second reagents, respectively. ### Claim 29 (depends on 28) The method of claim 28, wherein forming the fluidic structure includes: forming first and second walls on the BEOL, the first and second walls defining the first and second cavities, respectively; and positioning an insulative material on the BEOL and contacting the first and second walls. ### Claim 30 (depends on 29) The method of claim 29, wherein the first and second walls are made of a metal or a dielectric material. ### Claim 31 (depends on 29) The method of claim 29, further comprising: coupling a cartridge to the first and second walls and the insulative material, the cartridge including a third cavity in vertical alignment with the first cavity and a fourth cavity in vertical alignment with the second cavity, the cartridge further including a channel in fluidic communication with the fourth cavity. ### Claim 32 (depends on 28) The method of claim 28, wherein forming the fluidic structure includes coupling a cartridge having the first and second cavities to the BEOL.