# US 7,744,762 B2 · Microfluidic devices and methods facilitating high-throughput, on-chip detection and separation techniques > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 7,744,762 B2 - Document ID: US7744762B2 - Status: Granted - Kind: B2 - Application number: 11/466,818 - Filed: 2006-08-24 - Published: 2008-03-27 - Granted: 2010-06-29 - Earliest claimed: 2006-08-24 - Assignees: Virginia Tech Intellectual Properties, Inc. - Inventors: Iuliana M. Lazar - Web page: https://patentgrep.com/patent/US7744762B2 ## CPC - H01J 49/04: Arrangements for introducing or extracting samples to be analysed, e.g. vacuum locks; Arrangements for external adjustment of electron- or ion-optical components - G01N 2001/4038: {electric methods, e.g. electromigration, electrophoresis, ionisation} - G01N 2035/00237: {Handling microquantities of analyte, e.g. microvalves, capillary networks} - H01J: ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS (spark-gaps H01T; electric arc lamps H05B31/00; particle accelerators H05H) - 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 The present invention provides a microfluidic device and method for facilitating on-chip complex sample processing and detection. In general, the device comprises at least a separation channel of a separation system, an interface, and an array of microreservoirs disposed within the same chip. The interface is configured to orthogonally transfer separated components from the separation channel into the array of microreservoirs, enabling direct analyte detection from the chip and high-throughput analysis. ## Claims ### Claim 1 A microfluidic device for on-chip complex sample processing, comprising: a separation system including at least one pump and a separation channel for separating a complex liquid sample, wherein the separation channel includes a liquid chromatography medium; an interface fluidly coupled to the separation channel and configured to transfer separated sample components from the separation channel into an array of microreservoirs; wherein the interface comprises multiple microchannels having cross-sectional diameters or depths small enough to act as valves by way of hydraulic resistance, which substantially precludes leakage of the sample out of the separation channel and into the microchannels, wherein different microreservoirs in said array of microreservoirs are connected by different microchannels positioned at different points along a length of said separation channel, wherein the microchannels in the interface are adapted to translate separated components by an electroosmotic mechanism, such that when separation in the separation channel is completed, and the pump is turned off, a potential differential applied across the separation channel via the interface transfers the contents of the separation channel to the microreservoirs by said electroosmotic mechanism; and wherein at least the separation channel, interface, and microreservoirs are disposed within the same chip, facilitating analyte detection directly on the chip. ### Claim 2 (depends on 1) The microfluidic device of claim 1, wherein the separation system comprises a high performance liquid chromatography (HPLC) system. ### Claim 3 (depends on 1) The microfluidic device of claim 1, wherein the interface comprises a pumping and/or valving interface. ### Claim 4 (depends on 1) The microfluidic device of claim 1, wherein the depth of the interface microchannels is less than 5 micrometers. ### Claim 5 (depends on 1) The microfluidic device of claim 1, wherein the length of the interface microchannels is less than 20 millimeters. ### Claim 6 (depends on 1) The microfluidic device of claim 1, wherein the lengths of the microchannels vary along the separation channel. ### Claim 7 (depends on 1) The microfluidic device of claim 1, wherein the interface includes a plurality of eluting microchannels coupled to the microreservoirs on one side of the separation channel and a plurality of rinsing microchannels coupled to a rinse channel on an opposite side of the separation channel. ### Claim 8 (depends on 1) The microfluidic device of claim 1, interfaced with a matrix assisted laser desorption ionization (MALDI), an atmospheric pressure (AP)-MALDI, subatmospheric MALDI, surface enhanced laser desorption ionization (SELDI), desorption/ionization on silicon (DIOS), laser desorption, or other mass spectrometry (MS) source. ### Claim 9 (depends on 1) The microfluidic device of claim 1, further comprising a means to interface with a sample component detection system for detection of analytes directly from the microreservoirs. ### Claim 10 (depends on 1) The microfluidic device of claim 1, wherein the microreservoirs are at least partially exposed to air. ### Claim 11 (depends on 1) The microfluidic device of claim 1, interfaced with a removal device operable to remove samples from the microreservoirs. ### Claim 12 (depends on 1) The microfluidic device of claim 1, comprising a multiplexed configuration of at least two or more separation channels and interfaces on the same chip, facilitating high-throughput analysis. ### Claim 13 A method for microfluidic on-chip complex sample processing, said method comprising: providing a microchip including: a pump and a separation channel of a complex sample separation system, and an array of microreservoirs, and an interface fluidly coupling the separation channel and array of microreservoirs; wherein the interface comprises a plurality of microchannels having cross-sectional diameters or depths small enough to act as valves by way of hydraulic resistance, which substantially precludes leakage of the sample and/or sample components out of the separation channel and into the microchannels; turning on the pump; separating the sample components in the separation channel; when the sample components are separated in the separation channel, turning off the pump; and applying a potential differential across the separation channel and the interface to orthogonally transfer the separated sample components from the separation channel into the array of microreservoirs through an electroosmotic mechanism, facilitating analyte detection directly from the chip and further comprising performing HPLC in the separation channel. ### Claim 14 (depends on 13) The method of claim 13, further comprising using the interface as a pump or a valve to controllably translate the separated components. ### Claim 15 (depends on 13) The method of claim 13, wherein the step of using the interface includes transferring the separated sample components from the separation channel into the microreservoirs via the plurality of microchannels exhibiting hydraulic resistance. ### Claim 16 (depends on 13) The method of claim 13, further comprising evaporating eluent from the microreservoirs such that the sample components are deposited in the reservoirs and correspond to a plurality of spots. ### Claim 17 (depends on 13) The method of claim 13, further comprising performing matrix assisted laser desorption ionization (MALDI) mass spectrometry (MS) of the separated sample components directly from the microreservoirs. ### Claim 18 (depends on 13) The method of claim 13, further comprising interfacing the chip with an atmospheric pressure (AP)-MALDI, subatmospheric MALDI, surface enhanced laser desorption ionization (SELDI), desorption/ionization on silicon (DIOS), laser desorption, or other mass spectrometry (MS) source. ### Claim 19 (depends on 13) The method of claim 13, further comprising removing sample components from the chip for electrospraying, deposition onto another chip, or into another detection device. ### Claim 20 A device for on-chip complex sample processing, said device comprising: a separation means including a pump and a separation channel for receiving a complex sample and separating it into components wherein the separation channel includes a liquid chromatography medium; an interface means coupled to the separation channel for transferring the separated sample components into a plurality of microreservoirs; wherein the interface means comprises multiple microchannels having cross-sectional diameters or depths small enough to act as valves by way of hydraulic resistance, which substantially precludes leakage of the sample and/or separated components out of the separation channel and into the microchannels, wherein different microreservoirs in said plurality of microreservoirs are connected by different microchannels in said interface means that are positioned at different points along a length of said separation channel, wherein the microchannels in the interface means are adapted to translate separated components by an electroosmotic mechanism, such that when separation in the separation channel is completed, and the pump is turned off, a potential differential applied across the separation channel via the interface means transfers the contents of the separation channel to the microreservoirs by said electroosmotic mechanism, and wherein at least the separation channel, interface means, and the plurality of microreservoirs are fabricated within a single chip, facilitating analyte detection on the chip. ### Claim 21 (depends on 20) An apparatus comprising the device of claim 20 interfaced with a removal means for removing separated components from the chip. ### Claim 22 (depends on 20) The device of claim 20, further comprising a multiplexed configuration of at least two or more separation channels and interface means on the same chip, facilitating high-throughput analysis. ### Claim 23 A mass spectrometry (MS) interface disposed within a microfluidic device enabling high-throughput, on-chip complex sample processing, said interface in fluid connection with a separation channel of separation means which includes a pump communicating a sample to the sample channel, the interface and comprising a plurality of microchannels, the microchannels having cross-sectional diameters or depths small enough to act as valves by way of hydraulic resistance, which substantially precludes leakage of the sample and/or sample component out of the separation channel and into the microchannels, the interface, separation means, microchannels and microreservoirs all being fabricated on a single chip; and the microchannels configured to orthogonally transfer separated components from a complex sample separation channel to an array of microreservoirs using Electroosmotic Flow (EOF) after separation of sample components in the separation channel is complete, facilitating analyte detection directly on the chip wherein the separation channel includes a liquid chromatography medium; and wherein the different microreservoirs in said array of microreservoirs are connected by different microchannels positioned at different points along a length of said separation channel. ### Claim 24 (depends on 23) The interface of claim 23, wherein the interface is a pumping/valving interface. ### Claim 25 (depends on 1) The microfluidic device of claim 1, wherein the separation channel is 2-4 centimeters in length and 50 micrometers in depth, and the microchannels are 5-20 millimeters in length and 0.1-2 micrometers in depth. ### Claim 26 A microchip integrated complex sample processing system comprising: a separation system comprising: one or more pumps, including an eluent inlet reservoir, an eluent outlet reservoir, the eluent inlet and outlet reservoirs being fluidly connected by hundreds/thousands of micro/nanochannels, a mixer receiving outputs for said one or more pumps, a separation channel, a sample inlet reservoir, a sample outlet reservoir, and injector means for coupling the output of the mixer and a sample in the sample reservoir to the separation channel; a waste reservoir and side packing channel located at a far end of the separation channel, wherein the separation channel is a Liquid Chromatography (LC) separation system; an interface, and an array of microreservoirs, wherein the array of microreservoirs flanks the separation channel to one side, and the interface fluidly couples sections of the separation channel to the microreservoirs, the interface including a plurality of eluting microchannels between the separation channel and the microreservoirs, wherein different microreservoirs in said array of microreservoirs are connected by different microchannels positioned at different points along a length of said separation channel, wherein when separation in the main channel is completed, the pumps are turned off, and a potential differential is applied across the separation channel via the interface, transferring the contents of channel to reservoirs through an electroosmotic mechanism, facilitating analyte detection directly on the chip. ### Claim 27 (depends on 26) The microchip integrated complex sample processing system according to claim 26, wherein the interface is a Matrix Assisted Laser Desorption Ionization (MALDI) interface. ### Claim 28 (depends on 26) The microchip integrated complex sample processing system according to claim 26, wherein the injector means for coupling the output of the mixer and a sample in the sample reservoir to the separation channel is a double-T injector receiving the output of the mixer, one side of the double-T injector being coupled to the sample reservoir and the opposite side of the double-T injector being coupled to the sample waste reservoir via sample inlet and outlet channels, respectively, wherein the double-T injector outputs to the separation channel for separating the sample components. ### Claim 29 (depends on 26) The microchip integrated complex sample processing system according to claim 26, further comprising a rinsing channel longitudinally disposed along the opposite side of the separation channel and is fluidly coupled to the separation channel via a plurality of rinsing microchannels which help to flush the separation channel contents out of the separation channel, wherein the potential differential is applied between rinsing channel and each microreservoir and transfer of the contents of channel is further promoted with the aid of eluent coining from the rinsing channel. ### Claim 30 (depends on 26) The microchip integrated complex sample processing system according to claim 26, wherein the pumps are Electroosmotic Flow (EOF) pumps. ### Claim 31 A method for microfluidic on-chip complex sample processing, comprising the steps of: providing a separation system comprising: one or more pumps, including an eluent inlet reservoir, and an eluent outlet reservoir, the eluent inlet and outlet reservoirs being fluidly connected by hundreds/thousands of micro/nanochannels a mixer receiving outputs from said one or more pumps, a separation channel, a sample inlet reservoir, a sample outlet reservoir, and injector means for coupling the output of the mixer and a sample in the sample reservoir to the separation channel; a waste reservoir and side packing channel located at a far end of the separation channel; wherein the separation channel is a Liquid Chromatography (LC) separation system, providing an interface, and providing an array of microreservoirs, wherein the array of microreservoirs flanks the separation channel to one side, and the interface fluidly couples sections of the separation channel to the microreservoirs, the interface including a plurality of eluting microchannels between the separation channel and the microreservoirs; turning on said one or more pumps; separating the sample components in the separation channel; and when separation in the separation channel is completed, turning pumps off; applying a potential differential across the separation channel via the interface; orthogonally transferring separated sample components from the separation channel to reservoirs through an electroosmotic mechanism, facilitating analyte detection directly on the chip. ### Claim 32 (depends on 31) The method for microfluidic on-chip sample processing according to claim 31, wherein the step of providing an interface comprises the step of providing a Matrix Assisted Laser Desorption Ionization (MALDI) interface. ### Claim 33 (depends on 31) The method for microfluidic on-chip processing according to claim 31, wherein the step of providing a separation system provides a double-T injector for said injector means, said double-T injector receiving the output of the mixer, one side of the double-T injector being coupled to the sample reservoir and the opposite side of the double-T injector being coupled to the sample waste reservoir via sample inlet and outlet channels, respectively, wherein the double-T injector outputs to the separation channel for separating the sample components. ### Claim 34 (depends on 31) The method for microfluidic on-chip complex sample processing according to claim 31, wherein the separation system further comprises a rinsing channel longitudinally disposed along the opposite side of the separation channel and is fluidly coupled to the separation channel via a plurality of rinsing microchannels, and wherein the potential differential is applied between rinsing channel and each microreservoir, further comprising the steps of: promoting transfer of the contents of channel with the aid of eluent coming from the rinsing channel; and flushing the separation channel contents out of the separation channel with eluent from the rinsing channel.