US20050135655A1 - Ultra high throughput microfluidic analytical systems and methods - Google Patents

Abstract

Analytical systems and methods that use a modular interface structure for providing an interface between a sample substrate and an analytical unit, where the analytical unit typically has a particular interface arrangement for implementing various analytical and control functions. Using a number of variants for each module of the modular interface structure advantageously provides cost effective and efficient ways to perform numerous tests using a particular substrate or class of substrates with a particular analytical and control systems interface arrangement. Improved optical illumination and detection system for simultaneously analyzing reactions or conditions in multiple parallel microchannels are also provided. Increased throughput and improved emissions detection is provided by the present invention by simultaneously illuminating multiple parallel microchannels at a non-normal incidence using an excitation beam including multiple excitation frequencies, and simultaneously detecting emissions from the substances in the microchannels in a direction normal to the substrate using a detection module with multiple detectors.

Description

BACKGROUND OF THE INVENTION
• The present invention relates generally to systems and methods for performing chemical and biological analyses. More particularly, the present invention relates to the design and use of an analyzer system which employs analytical substrates evaluated in a modular interface structure having one or more interchangeable modules with varying functionality for interfacing with an arrangement of analytical and control systems instruments.
• Numerous systems and instruments are available for performing chemical, clinical, and environmental analyses of chemical and biological specimens. Conventional systems may employ a variety of detection devices for monitoring a chemical or physical change which is related to the composition or other characteristic of the specimen being tested. Such instruments includes spectrophotometers, fluorometers, light detectors, radioactive counters, magnetometers galvanometers, reflectometers, ultrasonic detectors, temperature detectors, pressure detectors, mephlometers, electrophoretic detectors, PCR systems, LCR systems, and the like. Such instruments are often combined with electronic support systems, such as microprocessors, timers, video displays, LCD displays, input devices, output devices, and the like, in a stand-alone analyzer. Such analyzers may be adapted to receive a sample directly but will more usually be designed to receive a sample placed on a sample-receiving substrate such as a dipstick, cuvette, analytical rotor or the like. Usually, the sample-receiving substrate will be made for a single use (i.e., will be disposable), and the analyzer will include the circuitry, optics, sample manipulation, and other structure necessary for performing the assay on the substrate. As a result, most analyzers are intended to work only with a single type of sample-receiving substrate and are not readily adaptable to be used with other substrates.
• Recently, a new class of sample-receiving substrate has been developed, referred to as “microfluidic” systems. Microfluidic substrates have networks of chambers connected by channels which have mesoscale dimensions, where at least one dimension is usually between 0.1 μm and 500 μm. Such microfluidic substrates may be fabricated using photolithographic techniques similar to those used in the semi-conductor industry, and the resulting devices can be used to perform a variety of sophisticated chemical and biological analytical techniques. Microfluidic analytical technology has a number of advantages, including the ability to use very small sample sizes, typically on the order of nanoliters. The substrates may be produced at a relatively low cost, and can be formatted to perform numerous specific analytical operations, including mixing, dispensing, valving, reactions, and detections.
• Another recently developed class of sample-receiving microfluidic substrates includes substrates having a capillary interface that allows compounds to be brought onto the test substrate from an external source, and which can be advantageously used in a number of assay formats for high-throughput screening applications. These assay formats include fluorogenic assays, fluorescence polarization assays, non-fluorogenic mobility shift assays, dose response assays, and calcium flux cell-based assays.
• Because of the variety of analytical techniques and potentially complex sample flow patterns that may be incorporated into particular microfluidic test substrates, significant demands may be placed on the analytical units which support the test substrates. The analytical units not only have to manage the direction and timing of flow through the network of channels and reservoirs on the substrate, they may also have to provide one or more physical interactions with the samples at locations distributed around the substrate, including heating, cooling, exposure to light or other radiation, detection of light or other radiation or other emissions, measuring electrical/electrochemical signals, pH, and the like. The flow control management may also comprise a variety of interactions, including the patterned application of voltage, current, or power to the substrate (for electrokinetic flow control), or the application of pressure, vacuum, acoustic energy or other mechanical interventions for otherwise inducing flow.
• It can thus be seen that a virtually infinite number of specific test formats may be incorporated into microfluidic test substrates. Because of such variety and complexity, many if not most of the test substrates will require specifically configured analyzers in order to perform a particular test. It is indeed possible that particular test substrates use more than one analyzer for performing different tests. The need to provide one dedicated analyzer for every substrate and test, however, will significantly reduce the flexibility and cost advantages of the microfluidic systems. Additionally, for a specifically configured analyzer, test substrates are generally only useful for performing a limited number of assay formats and functions. As the complexity and costs of test substrates increase, it becomes more desirable to increase the number of useful assay formats and functions for a particular test substrate-analyzer combination, or for a particular class of substrates in combination with a specifically configured analyzer.
• It would therefore be desirable to provide improved analytical systems and methods that overcome or substantially mitigate at least some of the problems set forth above. In particular, it would be desirable to provide analytical systems including a modular interface structure which can support a number of different microfluidic or other test substrates having substantially different flow patterns, chemistries, and other analytical characteristics. It would also be particularly desirable to provide analytical systems including a modular substrate-to-instrument interface structure comprised of interchangeable modules to accommodate various combinations of assay formats and functions, such as different flow patterns, for a particular test substrate or a particular class of test substrates having similar design layouts and/or properties. The costs for modifying the analytical and control systems interface as well as the costs required for obtaining test substrates for desired assays would be significantly reduced.
SUMMARY OF THE INVENTION
• The present invention overcomes at least some of the deficiencies described above by providing analytical systems and methods that use a modular interface structure for providing an interface between a sample substrate and an analytical unit, where the analytical unit typically has a particular interface arrangement for implementing various analytical and control functions. Using a number of variants for each module of the modular interface structure advantageously provides cost effective and efficient ways to perform numerous tests using a particular substrate or class of substrates with a particular analytical and control systems interface arrangement.
• The present invention also provides an improved optical illumination and detection system for simultaneously analyzing reactions or conditions in multiple parallel microchannels. Increased throughput and improved emissions detection is provided by the present invention by simultaneously illuminating multiple parallel microchannels at a non-normal incidence using an excitation beam including multiple excitation wavelengths, and simultaneously detecting emissions from the substances in the microchannels in a direction normal to the substrate using a detection module with multiple detectors.
• According to one aspect of the invention, an illumination and detection system is provided for use in illuminating a plurality of samples in a plurality of microchannels located in a detection region on a microfluidic device, and for detecting radiation emitted from the detection region, wherein the microchannels are substantially parallel along a first direction within the detection region. The system typically comprises an illumination source for providing an excitation beam having two or more excitation wavelengths, and focussing optics for focussing the excitation beam onto a first plane defined by the plurality of microchannels in the detection region such that the focussed excitation beam is elongated, having a major axis substantially perpendicular to the first direction, wherein the excitation beam impinges upon the detection region at a non-normal angle of incidence relative to the first plane, and wherein the excitation beam simultaneously excites the samples in at least two of the microchannels so as to cause the excited samples to emit radiation. The system also typically includes two or more detectors, wherein each detector detects a specific range of radiation wavelengths, and detection optics for directing radiation from the samples toward the detectors such that the wavelengths of the emitted radiation within each specific radiation wavelength range are directed toward the corresponding detector.
• According to another aspect of the invention, a method is provided for simultaneously analyzing a plurality of samples in a plurality of microchannels on a microfluidic device, wherein the plurality of microchannels are substantially parallel along a first direction within a detection region on the microfluidic device. The method typically comprises the step of simultaneously exciting the samples in at least two of the microchannels in the detection region by focussing an excitation beam having two or more excitation wavelengths onto a first plane defined by the plurality of microchannels in the detection region such that the focussed excitation beam is elongated, having a major axis substantially perpendicular to the first direction, wherein the excitation beam impinges upon the detection region at a non-normal angle of incidence relative to the first plane, and wherein the excited samples emit radiation. The method also typically includes the step of simultaneously detecting the radiation emitted by the two or more excited samples using two or more detectors, wherein each of the detectors detects a specific range of radiation wavelengths. Illuminating the detection region at a non-normal incidence generally rids the detection system of any zero order reflections.
• According to yet another aspect of the invention, a microfluidic device is provided, which typically comprises a fluid reservoir for holding a conducting fluid, a conducting capillary for supplying the fluid to the reservoir, wherein one end of the capillary is positioned at a first location in the reservoir, a voltage source having a first terminal and a second terminal, a first lead connecting the first terminal to the conducting capillary, and a second lead connecting the second terminal to a second location in the reservoir. In a typical operation of the microfluidic device, when the level of the fluid within the reservoir is at least at the first location, an electric current is present between the first and second terminals, and wherein when the fluid level is below the first location such that there is no contact between the fluid and the capillary, no electric current between the first and second terminals is present. The microfluidic device may also include a fluid monitoring element, such as a syringe pump, in fluid communication with the capillary. In operation, the fluid monitoring element provides fluid to the reservoir through the capillary when no electric current between the first and second terminals is present.
• According to a further aspect of the invention, a method is provided for automatically refilling a fluid reservoir in a microfluidic device, wherein the device typically includes a conducting capillary and a voltage supply, wherein a first end of the capillary is typically positioned at a first level within the reservoir, wherein a first terminal of the voltage supply is typically connected to the capillary and wherein a second terminal of the voltage supply is typically connected to a location at a second level within the reservoir, the second level being below the first level. The method typically comprises the steps of detecting an absence of electric current between the first and second terminals through the capillary, wherein no electric current flows between the first and second terminals when the fluid level is below the first level in the reservoir, and automatically supplying fluid to the reservoir through the capillary using a fluid monitoring device in response to the absence of current so as to raise the fluid level within the reservoir.
• According to yet a further aspect of the invention, an analytical system is provided which typically comprises a sample substrate having a plurality of substrate reservoirs and a plurality of microchannels disposed thereon, wherein the plurality of microchannels connects the plurality of substrate reservoirs, and wherein two or more of the microchannels are substantially parallel in a detection region on the substrate, and a modular interface, having two or more removably attachable interface modules, for interfacing with a plurality of instrument connectors. The modular interface typically includes a substrate interface module having at least one fluid reservoir disposed therein, wherein the substrate interface module is removably attached to the substrate, and wherein the at least one fluid reservoir is positioned so as to provide increased capacity to one of the substrate reservoirs, and an instrument interface module having a plurality of first connectors for connecting to one or more of the plurality of instrument connectors, and a plurality of second connectors for providing a connection between the instrument connectors and the substrate interface module when the substrate interface module is removably attached to the instrument interface module. The modular interface may also include other modules, such as a fluid supply module removably attached between the instrument and substrate interface modules, wherein the fluid supply module typically includes at least one fluid supply reservoir, wherein the fluid supply module also provides a connection between the substrate interface module and the second connectors of the instrument interface module.
• According to still a further aspect of the invention, a microfluidic device arranged on a sample substrate is provided, which typically comprises a plurality of substrate reservoirs disposed on the substrate, and a plurality of microchannels disposed on the substrate, wherein the plurality of microchannels connects the plurality of substrate reservoirs, and wherein two or more of the microchannels are substantially parallel in a detection region on the substrate. The device also typically includes a non-linear arrangement of a plurality of sampling capillary connection regions disposed on the substrate for interfacing with one or more sampling capillaries, wherein the sampling capillary connection regions are connected to the plurality of microchannels.
• Reference to the remaining portions of the specification, including the drawings and claims, will realize other features and advantages of the present invention. Further features and advantages of the present invention, as well as the structure and operation of various embodiments of the present invention, are described in detail below with respect to the accompanying drawings. In the drawings, like reference numbers indicate identical or functionally similar elements.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 illustrates an example of a microfluidic device according to an embodiment of the present invention;
• FIG. 2 illustrates an example of a wafer mask for use in fabricating four microfluidic devices similar to the microfluidic device shown inFIG. 1 using photolithographic techniques;
• FIG. 3 is a block diagram that illustrates a modular substrate-to-instrument interface structure according to an embodiment of the present invention;
• FIGS. 4a-dillustrate various isometric and side views of an exemplary modular interface structure according to an embodiment of the present invention;
• FIGS. 5a-billustrate isometric views (top and sides) of the exemplary modular interface structure ofFIGS. 4a-daccording to an embodiment of the present invention
• FIG. 6 illustrates a mask design with a spacing pattern for a linear array of four capillary connection regions that is compatible with typical microtiter plate format spacings according to one embodiment of the invention;
• FIG. 7aillustrates a capillary spacing pattern according to one embodiment which is compatible with both 96-well microtiter plate formats having up to 6 sampling capillaries and with 384-well microtiter plate formats having any number of sampling capillaries;
• FIG. 7billustrates various capillary placement patterns associated with the spacing pattern ofFIG. 7a;
• FIGS. 8a-billustrate various capillary placement patterns according to an embodiment of the present invention;
• FIGS. 9 and 10 illustrate sampling capillary patterns for a 16-well format for 4 capillaries and a 30-well format for 12 capillaries, respectively, according to one embodiment;
• FIG. 11 illustrates a thermoelectric temperature control unit and a heater block for controlling temperatures according to one embodiment of the present invention;
• FIGS. 12a-cillustrate a simple circuit used to control the replenishment of fluid within the reservoir according to an embodiment of the present invention;
• FIG. 13 illustrates an illumination and detection system according to an embodiment of the present invention;
• FIG. 14 illustrates details of an excitation source for providing an excitation beam for exciting samples in a plurality of microchannels according to an embodiment of the present invention; and
• FIG. 15 illustrates various optical elements of an illumination and detection system in more detail according to an embodiment of the present invention; and
• FIG. 16 is a block diagram illustrating the control system electronics according to an embodiment of the present invention.
DESCRIPTION OF THE SPECIFIC EMBODIMENTS
• Chip Design and Manufacture
• FIG. 1 illustrates an example of amicrofluidic device10 according to an embodiment of the present invention. As shown,device10 includes abody structure20 which has an integrated network of microfluidic channels25 disposed therein. In a preferred embodiment,device10 includes at least two intersecting microfluidic channels to provide for various reactions, material combinations, etc. as desired. Thebody structure20 also includes a plurality ofreservoirs30 disposed therein for holding reagents, sample materials and the like. The network25 of microfluidic channels is used to connect any combination, or all, of thereservoirs30 in any fashion as is desired by the substrate designer for the specific class of assays to be performed. Also included arewaste reservoirs35 and samplingcapillary connection regions40. Samplingcapillary connection regions40 each provide an interface with a sampling capillary that brings compounds ontodevice10 from an external reservoir or reservoirs. For example, in a preferred embodiment including fourcapillary connection regions40 as shown, one to four capillaries can be used to bring compounds ontodevice10 from one or more external sources, such as one or more wells on a multi-well microtiter plate as is standard in the industry. In this embodiment, thecapillary connection regions40, and therefore the associated capillaries, are preferably spaced so as to be compatible with industry standard microtiter plate format spacings. A samplingcapillary connection region40 can include a reservoir interconnected with one or more of the microfluidic channels of network25, or it can include a direct connection between the sampling capillary and one or more microfluidic channels. Examples of microfluidic devices incorporating sampling capillary elements are described in U.S. Pat. No. 5,779,868, which is incorporated herein by reference in its entirety for all purposes.
• A “microfluidic” channel, or “microchannel” is a channel (sealed enclosed groove, depression, tube, capillary, etc.) which is adapted to handle small volumes of fluid. In a typical embodiment, the channel is a tube, channel or conduit having at least one subsection with at least one cross-sectional dimension of between about 0.1 μm and 500 μm, and typically less than 100 μm. Ports or reservoirs are provided in fluid communication with the channels, in order to provide fluid or other access to the interior of the channel. In operation, materials that are being analyzed, e.g., subjected to optical analysis for fluorescence emission signals, in these microscale fluidic systems, are transported along the microscale fluid channels, past a detection point, where a detectable fluorescence emission signal is measured. The signals within these channels typically result from the presence of fluorescent substances therein, e.g., fluorophores that inherently fluoresce, or are made to fluoresce, and which are used as indicators of the presence or absence of some material or condition.
• Referring toFIG. 1, samples, reagents, compounds, etc. are transported from theirrespective reservoirs30 and samplingcapillary connection regions40, either separately or together with other reagents, samples, compounds, etc. from other reservoirs and sampling capillary connection regions through the network25 of microchannels into a plurality ofanalysis channels45, andpast detection region50 towardwaste reservoirs35. Although four microfluidic channels are shown indetection region50, as few as one microfluidic channel, and preferably two or more, four or more, six or more, eight or more, and even twelve or more microfluidic channels can be present indetection region50.Detection region50 is typically transparent to allow radiation to reach the materials in the microchannels within the region and/or to allow emitted or detected radiation to leave the region.Detection region50, in one embodiment is comprised of a transparent region ofbody structure20, but may be a separate transparent window fabricated intobody structure20. Typically, thebody structure20 is itself fabricated from a transparent material, such as glass or transparent polymers, thereby obviating the need for a separate transparent region to define the detection window.
• In an exemplary application, themicrofluidic device10 shown inFIG. 1 is used to perform high throughput assay operations, screening multiple samples or compounds against one to more different reagent systems, e.g., biochemical system components. Examples of microfluidic high throughput screening assays and systems are described in commonly owned U.S. Pat. No. 5,942,443, which is incorporated herein by reference.
• Briefly, reagents that are used in the particular screening assay, e.g., an enzyme and substrate, specific binding reagents, e.g., receptor ligand pairs, complementary pairs of nucleic acids, etc., cells which encompass more complex biochemical systems, are placed into the appropriate reservoirs of thedevice10. For example, in the case of paired reagents, e.g., and enzyme and its substrate, the enzyme solution is placed into, e.g.,reservoir30₁, while the substrate is placed intoreservoir30₂. By applying a constant vacuum atreservoir35₁, the enzyme and substrate begin flowing from the reservoir through channels25₁and25₂, respectively, and intoanalysis channel45₁. Concurrently, the applied pressure differential draws plugs of sample materials into the analysis channel through thecapillary connection region40₁. Specifically, a capillary element having a capillary channel disposed therethrough (not shown) is provided attached to the device and in fluid communication with thecapillary connection region40₁of the device. The open end of the capillary channel is then contacted with sources of sample material, drawing in a small aliquot of the material and transporting that aliquot as a plug into the analysis channel.
• Withinanalysis channel45₁, the enzyme and substrate mix together to form a reaction mixture which flows alonganalysis channel45₁past detection region50. There, the results of the reaction between the enzyme and substrate are measured. Barring any outside influence, e.g., change in environment, flow rate, etc., the signal detected at thedetection region50 is at a constant level, reflecting the enzymatic reaction that takes place while the reaction mixture flows alonganalysis channel45₁. Periodically, the sample material plugs are introduced into theanalysis channel45₁via thecapillary connection region40₁. Where the sample material has an effect on the reaction that is occurring, it will result in a change in the steady state signal observed at thedetection zone50.
• As can be seen inFIG. 1, thereagent reservoirs30₁and30₂, which contained the enzyme and substrate in the present example, are also fluidly connected to anotheranalysis channel45₂via channels25₃and25₄, respectively. Thus, while a screening assay is being carried out inanalysis channel45₁, a parallel screening assay can be carried out inanalysis channel45₂. Becauseanalysis channel45₂is coupled to a different capillary element viacapillary connection region40₂, it can sample from different sources of sample material than the other capillary elements. As shown, the capillary elements are positioned to sample from different wells on a multiwell plate, e.g., 96 well, 384 well or 1536 well. The channels, reservoirs and capillary elements on the opposite side of thedevice10 perform similar functions, while sampling from still different sources of sample material.
• In the device shown, the reagents from each of the various reservoirs and the capillary elements are transported at equivalent rates among the various different analytical modules. This is generally accomplished by providing channel layouts for each module that are equivalent to the other modules in terms of flow resistance. Accordingly, when a constant vacuum is applied atreservoirs35₁and35₂, the flow rates of reagents into and through each of the fouranalysis channels45_1-4is equivalent, allowing direct comparison of results from one channel versus another channel.
• In one embodiment, microfluidic devices such asdevice10 are fabricated using photolithographic techniques similar to those used in the semiconductor industry.FIG. 2 illustrates an example of a wafer mask for use in fabricating four microfluidic devices1014 similar tomicrofluidic device10 ofFIG. 1 using such techniques. A four chip mask pattern such as that shown inFIG. 2 is optimal for use with a standard 5″ square wafer (e.g., glass or quartz) with chips having 57×57 mm dimensions.
• Modular Interface
• The present invention is particularly useful for a number of assay formats for high-throughput screening applications, including, for example, fluorogenic assays, fluorescence polarization assays, non-fluorogenic mobility shift assays, dose response assays, and a variety of cell-based assays including, e.g., calcium flux based assays, viability assays, etc. For increased throughput, these assay formats and compound accession modes can be operated in multiple sampling capillary formats, using anywhere from one to twelve or more parallel channels within the device, and one, two, four, six, eight, or twelve or more discrete sampling capillary elements. Many of the designs for these formats will generally require different numbers of reagent wells and a different interface with vacuum, electrode, and temperature controls from the instrument array. To avoid needing a different interface for each chip design, a modular substrate-to-instrument, or chip-to-instrument, interface in discrete layers is provided to accommodate various combinations of assay formats and functions using a number of variants for each layer. One embodiment of a modular interface structure according to the present invention is illustrated schematically inFIG. 3. According to the embodiment, a modular chip-to-instrument interface structure for interfacing an array of instruments with a substrate is provided in two or more discrete layers. For example, according to the embodiment shown inFIG. 3, a chip-to-instrument interface structure is provided in four discrete layers: theadapter layer110, thefluid supply layer130, theholder layer120 and theheater block layer160.
• In a preferred embodiment, each modular interface layer is embodied in a separate module, each having an array of one or more interface connectors, or components, for interfacing with connectors of other modules, the substrate and/or the analytical and control instrument array. As used herein, the phrase “interface component,” or “interface connector,” refers to any one of a variety of discrete components or regions present in the interface arrays of the various interface modules, theinstrument array150 and thesample substrate140. Interface components, or connectors, will generally provide for electrical or other energy transfer, analog or digital signal transfer, fluid transfer, heat transfer, pressure and vacuum transfer, energy transmission such as the transmission of light or other radiation, energy emission detection and the like.
• Adapter layer110 generally provides an interface to the array of analytical and control instrument connectors (the “instrument array”) of theinstrument layer150.Adapter layer110 also provides an interface to the next interface layer with any desired configuration of interface connectors (e.g., any specific configuration of electrodes, pressure and vacuum ports, and temperature control regions) as are needed for the desired assay format and/or selected substrate layout.Holder layer120 provides an interface to the array of connectors present on the sample substrate with any desired configuration of interface connectors as are needed for the desired assay format and/or selected substrate layout.Holder layer120, in one embodiment, is comprised of a plastic material, or other composite material.Holder layer120, in one embodiment also provides capacity for reagent and buffer reservoirs, orwells125, and provides electrical insulation to prevent surface conduction between wells.Holder layer120 in some embodiments may serve as a three dimensional fluid distribution system for reagents and buffers.
• Fluid supply layer130 is optionally provided for those chips where the volume of buffer required is larger than that defined byholder layer120. For example, the use offluid supply layer130 is advantageous for chips having the DMSO sipping/dilution function when the volume of buffer required is larger than that defined byholder layer120 under extended operating times. In one embodiment, the buffer feed rate fromfluid supply layer130 to the wells onholder layer120 can be controlled using electrical conductivity detection techniques as described in more detail below.Fluid supply layer130 also provides any desired configuration of interface connectors for interfacing with adjacent layers (e.g.,adapter layer110 andholder layer120 as shown inFIG. 3) as are needed for the desired assay format and/or selected substrate layout.
• Heater block layer160 is optionally provided for heating and cooling fluid wells and reservoirs and reaction channels as will be described in more detail later.
• A particular advantage of the present invention is that each layer, or module, of the interface structure can be configured to interface with any one of a variety of connector configurations provided by each adjacent interface array (e.g., the interface array of an adjacent module, the substrate, or the instrument array) as is desired to perform the desired assay. For example, for a specific array of instrument connectors,adapter layer110 can be configured to interface with any or all connectors of theinstrument array150, and likewise can be configured to provide an array of connectors to the next layer, e.g.,fluid layer130, when used, orholder layer120. The array of connectors provided byadapter layer110 may include all, or a subset, or a superset, of the functionality provided by theinstrument array150. For example,adapter layer110 may interface with one electrode connector and one vacuum connector of theinstrument interface array150, but it may be configured to provide only one electrode connector and no vacuum connector to the next layer (i.e., subset), or it may be configured to supply two electrode connectors and two vacuum connectors to the next layer (i.e., superset). Likewise, when used,fluid supply layer130 can be configured to interface with any or all connectors provided byadapter layer110, and likewise can be configured to provide an array of connectors to the next layer, e.g.,holder layer120. The array of connectors provided byfluid layer130 may include all or a subset of the functionality provided tofluid layer130 byadapter layer110. Similarly,holder layer120 can be configured to interface with any or all connectors provided by it's adjacent layer, e.g.,fluid layer130 oradapter layer110, and likewise can be configured to provide an array of connectors to thesample substrate140. The array of connectors provided byholder layer120 may include all, or a subset, or a superset, of the functionality provided toholder layer120.
• In this manner, the designer of the sample substrate is free to optimize the size, flow paths, and other features of the sample substrate without undue regard to the nature of the instrument array or the interface structure. Likewise, the designer of the analytical and control instruments is free to optimize the connectivity and functionality, and other features of the instruments without undue regard to the nature of the sample substrate or the interface structure. Within a wide latitude, most specific design features of a sample substrate and a specific instrument array may be accommodated by appropriately designing the various layers of the modular interface structure. It will therefore be appreciated that the system architecture using the modular interface structure as an interface between the sample substrate and an instrument array provides for significant design flexibility.
• Electrical connections, both for power and signal transfer, will generally include conventional connectors in the form of electrodes, pins, plugs, zero insertion force (ZIF) connectors, and the like. Such electrical connections will usually require mating connectors in the interface modules which are brought together when the system is put together. The electrical connectors will often be present on a surface or edge of an interface module so that corresponding components will be engaged against each other when the modules are removably attached to each other and to the substrate. Similarly, surface or edge electrodes in the substrate interface module, e.g.,holder module120, may be provided to mate with corresponding surface or edge electrodes on the sample substrate. The electrodes on the sample substrate may then be connected internally in the substrate to the desired reservoirs or fluid flow channels in order to effect electrokinetic flow control. In other cases, however, it will be desirable to provide interface components in the sample substrate interface module, e.g.,holder module120, which directly contact the fluid to be electrokinetically controlled. For example, probes or pins may be provided which will penetrate into open wells or through septums on the sample substrate in order to permit direct contact and application of electrical potential when modules are removably attached. In an embodiment where wells onholder module120 are in fluid communication with wells on the sample substrate for the purpose of providing extra capacity to the substrate wells, it may be desirable to provide interface components in theadapter module110, or influid module130 when used, which directly contact the fluid in the wells ofholder module120. For example, capillaries or other connectors that provide fluid communication, may be provided which will penetrate into open wells or through septums on the sample substrate and/or the holder module in order to permit direct contact and application of electrical potential when modules are removably attached.
• A particular class of interface components employed by the analytical systems of the present invention are referred to as “flow biasing connectors.” Flow biasing connectors are intended to identify those interface components which can effect fluid flow in sample substrates, particularly on microfluidic substrates having a network of flow channels and reservoirs. For microfluidic substrates employing electrokinetic flow management, the flow biasing connectors on the interface modules will typically include electrodes, probes, pins, or the like distributed within, or on, each module to mate with any reservoirs on the modules and with the network of flow channels and reservoirs in the sample substrate as generally described above. The electrodes will usually have corresponding electrode terminals present on the sample substrate so that the electrode terminals may be interconnected to corresponding electrical connectors on the sample substrate interface. In other cases, as described above, the flow biasing connectors may be probes or pins which are positioned to directly engage fluids present on or in the sample substrate or the holder module. For example, an array of pins may be provided on theadapter module110, or thefluid module130 when used, such that when removably attached toholder module120, the pins penetrate intoopen sample wells125 on theholder module120. The wells on thesample substrate140 and thewells125 on theholder module120, of course, need not be open and could be covered with any penetrable membrane or septum which is pierced by the pins or fluid connectors, such as capillaries, when the cover is closed. Other flow biasing connectors include acoustic energy sources (e.g., piezoelectric transducers) positioned within the sample substrate interface module so that they engage thesample substrate140 and/orholder module120 at positions intended to induce fluid flow through the flow channels. In preferred aspects, however, material movement through the channel networks is governed by applied pressure differentials. Typically this involves application of a negative and/or positive pressure to one or more of the reservoirs of the device to draw or force material through channels connected to those reservoirs. Thus, in such cases, the flow biasing connectors represent pressure or vacuum sources coupled to one or more reservoirs of the device. As noted previously, negative pressure applied at a common waste reservoir (e.g.,reservoir35₁ofFIG. 1) is used to draw material into and through the channels of the device. Further, by appropriately configuring the interconnected channels coupled to the particular waste reservoir, one can accurately regulate the relative flow rates of materials in the various interconnected channels, e.g., by varying the channel resistances. In alternative aspects, multiple positive pressure sources are coupled to the various reagent supply reservoirs (e.g.,reservoirs30₁and30₂) to drive material flow through the channels of the device, which may be used alone or in combination with an applied vacuum at the waste reservoir, e.g., to ensure the drawing of sample materials into the capillary element.
• FIG. 4aillustrates an isometric view of an exemplarymodular interface structure200 according to an embodiment of the present invention. As shown in an “unattached” state inFIG. 4a,interface structure200 according to this embodiment includesholder module220,adapter module210 andsample substrate240.Holder module220 is provided as a structure for holding the modular interface structure. For example, one or more of the interface modules can be provided with locating pins or holes for mating with locating holes or pins250 ofholder220. Alternately,adapter module210, or any other module, may act as a holding or support structure. In such an embodiment, the module(s) providing structural support is provided with one or more locating pins and/or holes to mate with one or more pins and/or locating holes on the other modules.
• As shown inFIG. 4a,adapter module210 includes anarray215 ofelectrical connectors222 for mating with an array of instrument connectors (not shown).Array215 provides connectivity to analytical and control instruments through the array of instrument connectors (not shown).Electrical connectors222 onarray215 includes any of a variety of electrodes, pins, plugs, zero insertion force connectors, or other types of connectors capable of effecting power and signal transfer. Also included inarray215 is apneumatic port connector225, such as a vacuum or pressure port, for interfacing with a vacuum or pressure source (not shown) and which connects to one or more of the parts on the substrate. Although only a specific number of connectors in a specific arrangement are illustrated inFIG. 4a, it will be apparent that any number of connectors in any configuration can be used. Additionally,adapter module210 includes a window or opening217 defined therein to allow radiation to pass therethrough.Sample substrate240 as shown inFIG. 4ais a chip including fluid wells andreservoirs30,capillary connection regions40 and a detection region50 (reaction channels are not shown). In one embodiment,optional heater block260 is included for providing temperature control as will be described later. Also in one embodiment, a spring mechanism (not shown), coupled toholder220, is provided for biasing thechip240 towardadapter module210 and against datum pins of the adapter plate (e.g.,datum pin248 as shown inFIG. 5a). The datum pins are provided for maintaining and controlling the z-axis position of the modules in thestructure200.
• FIG. 4billustrates an isometric view of the interface structure ofFIG. 4ain an “attached” state, i.e., the modules are removably attached to each other, and theholder module220 is removably attached to thesample substrate240.
• FIG. 4cillustrates the underside of anexemplary adapter module210 according to an embodiment of the present invention. As shown, adapter module includes various connectors, such as multipleelectrode pin connectors234 and pressure seal connectors232 (e.g., for vacuum and/or positive pressure), for interfacing withwells30 onchip240. Also shown are datum registration holes251.
• FIG. 4dillustrates side views of an exemplarymodular interface structure200 according to an embodiment of the present invention. As shown inFIG. 4d,interface structure200 is in an “attached” state, i.e., each module is removably attached to the next, and theholder module220 is removably attached to thesample substrate240. Aframe245 is optionally provided as a structure for holding the modular interface structure. For example, one or more of the interface modules can be provided with locating pins or holes for mating with locating holes or pins250 offrame245. Alternately,adapter module210, or any other module, may act as a frame structure.Sample substrate240 as shown is a chip including a connection to four sampling capillaries6514 (each side view only shows two of the capillaries). As will be described later, optionalheater block module260 is provided for heating and cooling fluid wells and reservoirs and reaction channels.
• FIG. 5aillustrates an isometric view of the exemplarymodular interface structure200 ofFIG. 4 including aframe structure245 according to an embodiment of the present invention. As illustrated,optional frame245 includes a window or opening247 defined therein to allow radiation to pass therethrough, such that when attached to structure200, window or opening217 ofadapter210 is adjacent to the window or opening247 offrame245. Any additional modules in theinterface structure200 positioned betweenadapter module210 and substrate240 (e.g., a fluid supply module) include a window or opening defined therein to allow radiation to pass to and from the detection region on thesubstrate240. Aseparate connection bracket265 is optionally provided to add connectivity functionality for the overall interface structure.Connection bracket265 includes locating pins and/or holes for mating with locating holes and/or pins offrame245 and/or the various modules. Also included areguide portions252 for mating with correspondingportions252′ on holdingmodule220. For example, as shown,guide portion252 is a ledge for slidably receiving a corresponding ledge onholder module220. Also shown isrelease lever249 in the “open” position.FIG. 5billustrates an isometric view of the exemplary modular structure ofFIG. 5ain an “attached” state according to an embodiment of the present invention.Release lever249, as shown, is in the “closed” position.
• Locations and Patterns of Sampling Capillaries
• As discussed above, sampling capillaries bring compounds onto chips from an external source. In current practices used by the pharmaceutical industry, desired compounds are primarily stored in microtiter plate formats, typically having 96 wells, 384 wells, or 1536 wells, and having well center spacings of 9 mm, 4.5 mm and 2.25 mm. Thus, in one embodiment, the spacing pattern of sampling capillary connection regions on chips, and therefore the spacing of any attached sampling capillaries, is preferably compatible with the microtiter plate spacing of 9 mm, 4.5 mm and/or 2.25 mm, although other spacings may be used as desired.
• FIG. 6 illustrates a linear array of fourcapillary connection regions310 on amicrofluidic device300 that is compatible with typical microtiter plate format spacings according to one embodiment of the invention. As shown, thecapillary connection regions310 are aligned linearly with an equal spacing between each. In one embodiment, the spacing between eachconnection region310 is approximately 9 mm. When such a linear array is extended to 12 capillary connection regions, the dimension of the device becomes very large, and the outer channels became very long when channels are necked down into the middle for detection. Such qualities are generally undesirable in such microfluidic devices. In general, therefore, an optimal spacing arrangement of an array of capillary connection regions on a microfluidic device should satisfy some or all of the following criteria:
• • 1. Maintain spacing compatible with microtiter plate formats;
  • 2. Sample all compounds on the microtiter plate with only a single visit from the capillaries for each well;
  • 3. Minimize the need for very long channels connecting to some of the capillaries;
  • 4. Minimize substrate (wafer) usage per chip;
  • 5. Allow adequate spacing for on-chip reagent wells to provide easy reagent delivery to all channels;
  • 6. Provide a common spacing format to allow for scaling up the number of capillaries with minimal or no redesign; and
  • 7. Design spacing patterns so that patterns of a smaller number of sampling capillaries are perfect subsets of a pattern of a larger number of capillaries so that channel redesign is minimal in scaling, e.g., from 12 capillaries to 4 capillaries to 1 capillary.
• FIG. 7aillustrates a capillary spacing pattern according to one embodiment which satisfies all of the above design criteria. The pattern shown is compatible with both 96-well microtiter plates for chips having up to 6 sampling capillaries and with 384-well microtiter plates for chips having any number of sampling capillaries as shown inFIG. 7b. In a preferred embodiment, a non-linear array ofcapillary connection regions320 is provided as shown, where the spacing betweencapillary connection regions320 along a first direction defined by the plurality ofmicrochannels325 entering thedetection region330 are equally spaced so as to be compatible with microtiter plate format spacings. For example, in one embodiment as shown, two parallel linear arrays (altogether a non-linear array) ofcapillary connection regions320 are provided with the spacing along the first direction being approximately 4.5 mm apart and the spacing of the two linear arrays being approximately 18 mm apart. This spacing pattern shown also fits into a 57×57 mm diced quartz or glass chip, which maximizes the use of 5″ square wafers with 4 chips per wafer as shown inFIG. 2.FIG. 7billustrates various capillary placement patterns associated with the spacing pattern ofFIG. 7awhere the number of attached sampling capillaries is displayed to the left of each pattern.
• In some embodiments, it may be necessary to rotate the orientation of the chip relative to the microtiter plate by 90 degrees to provide proper accession (i.e., visiting all wells with each well only visited once). For example, for the six capillary spacing pattern ofFIG. 7b, it may be necessary to rotate by 90 degrees the orientation of the chip relative to the microtiter plate to provide proper accession for a 96 well microtiter format. It will be apparent that either the plate or the chip can be rotated while keeping the other fixed, although rotating both the chip and the plate to provide the 90 degree rotation is also possible.
• FIGS. 8a-billustrate various capillary placement patterns according to another embodiment of the present invention. In the placement patterns shown, the spacing of the capillary connection regions are preferably compatible with microtiter plate format spacings as described above.
• Although sampling capillaries are often comprised of capillaries attached to the body structure, in some cases the sampling capillaries will comprise mere extensions of the body structure, e.g., from a side or surface of the body structure. Such an extension would include a channel to the exterior of the device for sampling materials.
• Number, Locations and Sizes of Reagent and Buffer Wells
• Due to topological constraints of the two-dimensional micromachined channel networks, on-chip reagent wells can usually only be shared between two parallel channel networks. Consequently, the minimum number of reagent wells required increases with the number of sampling capillary connection regions provided on a chip. It is therefore desirable to provide a common reagent well format inholder module120 to allow flexibility in the selection of assay formats and in the selection of the number of attached sampling capillaries such that it is easy to scale up multiple sampling capillary compatible microchips. One consideration of a common format is that for most assays it is advantageous that the entry points for on-chip reagents and buffers into a reaction channel be located near a capillary-to-channel junction, i.e., samplingcapillary connection region40, to minimize compound dispersion due to flow and thermal diffusion. Another consideration is the volume requirement for extended operations, such as 8 continuous hours of operation per day. For example, the buffer flow rate for DMSO dilution is generally much higher than the enzyme and substrate flow rates in an enzymatic assay. With these considerations in mind, many different well formats with different sampling capillary connection region locations can be designed for use with any number of sampling capillaries. For example,FIG. 9 illustrates a format including 16wells335 and a non-linear array of 4 samplingcapillary connection regions320 for use with up to 4 sampling capillaries according to one embodiment of the present invention.FIG. 10 illustrates a format including 30wells335 and a non-linear array of 12 samplingcapillary connection regions320 for use with up to 12 sampling capillaries according to one embodiment of the present invention.
• Heating and Cooling of Reagents and Channels
• In a multiple sampling capillary format (i.e., including more than one sampling capillary connected to the substrate), it is generally desirable to provide reagent cooling in some or all wells to slow down degradation during an extended period of operation. It is also desirable to provide reaction mixture heating in some channels, and particularly in the two or more channels entering the detection region of the substrate, to speed up the rates of reactions. According to one embodiment, a thermoelectric temperature control interface is optionally provided to control temperatures in the wells, and a heater module (e.g.,heater module160 ofFIG. 3) is optionally positioned below the chip along the reaction channels for heating the reaction channels, which in one embodiment generally run parallel withinheating zone350 as shown inFIG. 11. In one embodiment, the thermoelectric temperature control interface includes “cold fingers,” e.g. pins or electrodes or any other type of connector that provides for heat transfer, that dip into one or more reagent wells to reduce the temperature of reagents in the wells as desired. The transition zones between the cooled and heated regions will generally assume a temperature gradient depending on the thermal properties of the materials being used for the holder layer and the substrate. Examples of desired materials include plastics and polymers such as polymethylmethacrylate (PMMA), polycarbonate, polytetrafluoroethylene (TEFLON™), polyvinylchloride (PVC), polydimethysiloxane (PDMS), polysulfone, polystyrene, polymethylpentene, polypropylene, polyethylene, polyvinylidine fluoride, ABS (acrylonitrile-butadiene-styrene copolymer), and the like for the holder layer and glass or quartz for the substrate. In general, the temperature range of the extreme using these desired materials will be relatively small (for example, from 4° C. to 30° C.) so that local thermal expansion should not cause problems such as delamination of a holder from a quartz chip.
• Automatic Refilling of Fluid Reservoirs
• According to one embodiment, the electrical conductivity of the fluid within a reservoir is used to control the replenishment of fluid within the reservoir.FIG. 12aillustrates a simple circuit constructed from a conductingcapillary510, a conductingfluid520 within afluid reservoir530, avoltage source540, and twoelectrical leads542 and544. Examples of fluids having conducting properties include aqueous buffers with dissolved ionic species, such as salt solutions, assay buffers, and water. Examples of such assay buffers include CAPS (3 cyclohexylamino-1-propane sulfonic acid), TRIS (tris hydroxymethyl amino methane), PBS and HEPES. In general, any fluids with ionic species will have conducting properties, depending on the concentration of the ionic species. As shown, lead542 originating from the positive terminal ofvoltage source540 is connected tocapillary510, one end of which is initially immersed in conductingfluid520. Lead544, connected to the negative terminal ofvoltage source540, is also placed inreservoir530, but to a level slightly below that ofcapillary510. It will be apparent to one skilled in the art that the polarity ofvoltage supply540 as shown can be reversed without affecting the operation of the circuit. In operation, application of a voltage allows current to pass from the positive terminal, throughcapillary510, through conductingfluid520 and back to the negative terminal ofvoltage source540. As the fluid520 is consumed by the microfluidic device, the liquid level insidereservoir530 drops untilcapillary510 is no longer in contact with conductingfluid520. This situation is illustrated inFIG. 12b. The resulting open circuit triggers a dispense of fluid throughcapillary510 toreservoir530 using an appropriatefluid metering device550, such as a syringe pump or other device capable of providing fluid from a reservoir of fluid. For example, in one embodiment, the open circuit triggers a fixed volume dispense of fluid from a second reservoir usingfluid metering device550.FIG. 12cillustrates an example of the level offluid520 inreservoir530 after fluid has been dispensed from a second reservoir using metering device550 (as shown inFIGS. 12a-c, the second reservoir is integrated with metering device550). This process is repeated each time the fluid level falls below the capillary, and may be operated continuously without user intervention. In an alternate embodiment, any low (e.g., non-zero) voltage level can be used to trigger the fluid refill dispense.
• For example, in one embodiment, referring toFIG. 3, this technique is used to refill one or more reservoirs inholder layer120 with fluid from one or more separate fluid reservoirs influid layer130. In this embodiment, leads542 and544 can be implemented as electrodes or other electrical connectors in the interface modules, capillary510 can be implemented as a capillary or any other type of fluid connector, andvoltage source540 can be provided in any of the modules or as an external voltage source.
• In an alternate embodiment, a non-conducting capillary can be used for fluid refill. In this embodiment, automatic refill is triggered using two electrodes (each coupled to different terminals of voltage supply540) positioned at different locations within the reservoir. In yet another embodiment, one of the electrodes can be positioned in a second reservoir in fluid communication with the first reservoir, which is refilled by the non-conducting capillary.
• Illumination and Detection System
• According to one embodiment of the present invention, an illumination and detection system is provided for simultaneously exciting multiple samples with multiple wavelengths and for simultaneously detecting emissions of multiple wavelengths. For example, the illumination and detection system of the present invention is useful for a variety of optical analytic assays and applications using the various microfluidic devices and systems (e.g.,device10 ofFIG. 1) described herein. Such analytical assays and applications include fluorescence detection assays, fluorogenic assay enzyme inhibition applications, fluorescence polarization assays, genetic screening assays, DNA sequencing by measuring the lifetime of fluorescent labels, etc.
• FIG. 13 illustrates an illumination anddetection system600 according to an embodiment of the present invention. Illumination anddetection system600 includes anexcitation source610 and adetector array620 including one or more optical detectors such as CCD arrays.Excitation source610 provides anexcitation beam612, which is optically focussed and controlled by one or more optical elements614 (only one optical element is shown). In a preferred embodiment,optical elements614 include one or more lenses, such as piano-convex lenses and plano-cylindrical lenses, that focusexcitation beam612 into a large aspect ratioelliptical illumination beam616 as shown.Optical elements614 are positioned and arranged such thatelliptical spot616 is focused to thedetection region625 on thesample substrate630. Preferably,source610 and/oroptical elements614 are positioned such thatelliptical excitation beam616 impinges onsubstrate630 at a non-normal angle of incidence, φ. In a preferred embodiment, φ is approximately 45 degrees relative to the plane defined bysubstrate630, although other non-normal angles of incidence may be used, e.g., from about 30 degrees to about 60 degrees. In one embodiment,source610 andoptical elements614 are arranged such thatelliptical excitation beam616 is polarized with a polarization direction/vector618 that is substantially parallel to the major axis ofelliptical excitation beam616.Optical elements614 are also preferably arranged such that the major axis of the resultingelliptical excitation beam616 is substantially perpendicular to the direction of themicrochannels622 indetection region625 as shown. Alternatively, the major axis of the elliptical excitation beam spot is oriented along the length of one or more of themicrochannels622 indetection region625, in order to excite and detect a longer region of each of the channels, e.g., where a time dependent reaction is being monitored, or where detection sensitivity requires extended detection. In this manner, substances in each of themicrofluidic channels622 may be simultaneously excited byelliptical excitation beam616. Emissions emanating from the samples in each of the plurality ofmicrochannels622 indetection region625 are focussed and/or directed by one or more optical elements634 (two element shown) ontodetector array620. At least one optical element, e.g., element6341, such as an objective lens, is preferably positioned to direct emissions received fromdetection region625 in a direction normal to the plane defined by thechip630 as shown. One or more band-pass filter elements636 are provided to help prevent undesired wavelengths from reachingdetector array620. A more detailed description of the various elements of illumination anddetection system600 will be presented with reference toFIGS. 14 and 15 below.
• FIG. 14 illustrates details of anexcitation source610 according to an embodiment of the present invention. In a preferred embodiment,excitation source610 includes two or more optical radiation sources, each of which emits a radiation beam at a specific wavelength. For example, as shown inFIG. 14,excitation source610 includes fourlaser sources640_1-4, each outputting aradiation beam642 having at least one defined wavelength. Output beams642_1-4fromlasers640_1-4are combined through the use of various beamsplitter elements and other optical elements to createexcitation beam612. In one embodiment,telescopes644 of various magnifications are used to expand some or all ofbeams642_1-4so as to equalize the geometries of output beams642_1-4.Filters646, such as neutral density filter wheels, are also provided to equalize the powers of output beams642_1-4.Beam samplers648 andreference detectors650 are optionally provided to monitor power levels and to permit subsequent signal normalization, e.g., fluorescence signal normalization. In the embodiment as shown inFIG. 14, only twooutput beams642₁and642₂require the use of telescopes and filters. However, it will be apparent that none, some or allbeams642 may require expansion and filtering to equalize powers and geometries depending on the particular radiation source used.Shutters652 are optionally provided to allow the capability to cut off therespective beam642, as well asbeam612, when not required for the specific application or assay. A half wave retarder, or other polarization altering element, is optionally provided for eachoutput beam642 to provide polarization adjustment capability as needed.
• Mirror element658, which in one embodiment is a dielectric mirror, is optionally provided and positioned to reflectbeam642₄toward beamsplitter elements656.Laser source640₄may be positioned such thatoutput beam642₄is directed toward beamsplitter elements656. Beamsplitter elements656 are provided and positioned to combine output beams642. For example, as shown, beamsplitter element656₃combinesbeam642₄withbeam642₃. Beam element656₃reflects at least a substantial portion ofbeam642₃toward beamsplitter elements656₂and656₁, and allows at least a substantial portion of reflectedbeam642₄to pass through toward beamsplitter elements656₂and656₁, such that the two beams are combined. In the same manner, beamsplitter elements656₂and656₁each reflect at least a substantial portion ofbeams642₂and642₁, respectively, and each allows at least a substantial portion of the combined upstream beams to pass so as to ultimately produceexcitation beam612. In one embodiment, beamsplitter elements656 are dichroic beamsplitters that are capable of reflecting the defined wavelength of therespective laser source640 and that are capable of allowing the other defined wavelengths to pass, as are well known in the art. It will, of course, be apparent that other elements that provide such capabilities may be used, e.g., dichroic “cold” mirrors.Mirror elements680 are optionally provided todirect excitation beam612 toward focussing optics614 (seeFIGS. 13 and 15).
• According to one embodiment, eachlaser source640 is capable of outputting radiation having at least one primary wavelength. Examples of useful laser sources include HeNe lasers, Argon Ion lasers, tunable dye lasers, semiconductor lasers, free electron lasers, excimer lasers, etc. Different laser sources can be selected depending on the desired output wavelengths and power requirements. In general, it is desirable to provide at least two laser sources, each outputting a beam having a different wavelength in a range from about 300 nm (UV) to about 700 nm (red). For example, in a preferred embodiment, depending on the desired application,laser sources640 are selected so thatexcitation beam612 includes at least two or more of the following approximate wavelengths: 355 nm, 457 nm, 488 nm, 532 nm and 633 nm. For fluorescein excitation applications, or fluorescence polarization detection applications, for example, an Argon ion laser outputting a beam with a wavelength of approximately 488 nm is desirable.
• FIG. 15 illustrates various optical elements of illumination anddetection system600 in more detail according to an embodiment of the present invention. In one embodiment, one ormore mirror elements680 are optionally provided and positioned to directexcitation beam612 towardoptical elements614 in a desired direction. In a preferred embodiment,excitation source610, ormirror elements680, andoptical elements614 are positioned such thatexcitation beam612 illuminates the excitation and detection region onchip630 at an angle of incidence of approximately 45°, although other non-normal angles may be used. This illumination is also preferably s-polarized.Optical elements614, in one embodiment, include atelescope682 for magnifying, or expanding,excitation beam612, and an arrangement of a plano-convex lens684 and a plano-cylindrical lens686 as shown. Plano-convex lens684 and plano-cylindrical lens686 act in concert to create and focuselliptical excitation beam616 from expandedexcitation beam612.Elliptical excitation beam616 is focused onto the detection region ofchip630 with an elliptical spot having the desired dimensions and orientation so as to excite samples in two ormore microchannels622 indetection region625 simultaneously. For example, in one embodiment, wheremicrochannels622 indetection region625 have a width of approximately 100 micrometers and are spaced approximately 100 micrometers apart (relative to the center of each adjacent channel), the 1/e²dimensions of the elliptical excitation spot are approximately 50×1000 micrometers formed with numerical apertures (NA's) of 0.010 and 0.017, respectively. In the present embodiment, plano-convex lens684 in conjunction with plano-cylindrical lens686 form an anamorphic focusing doublet which is responsible for formingelliptical excitation beam616. However, plano-convex lens684 may be replaced by a custom broadband triplet for significant chromatic aberration correction, where this triplet is optimized for this application where the specific wavelength range, plano-cylindrical lens686,chip630 cover glass thickness, and non-normal angle of incidence are taken into account (e.g., modified version of U.S. Pat. No. 3,486,805, by K. Kobayashi), which will enhance the performance of the optics.
• Chip630 is preferably aligned such that, withindetection region625,microchannels622 run parallel to the elliptical excitation spot's minor axis, and such that the chemistry flows in the same direction as the illumination flux. One advantage of illuminating the chip at a non-normal angle of incidence is that doing so effectively prevents zero order reflections at a normal incidence relative to the chip, i.e., zeroorder reflections612′ will typically reflect offchip630 at the same relative angle, φ, at whichexcitation beam612 impinges onchip630. In one embodiment, as shown, a zeroorder stop688 is provided to prevent any zeroorder reflections612′ from interfering with other parts of the system. Additionally, one advantage of exciting samples in two or more microchannels simultaneously is that multi-channel detection can be performed without scanning a beam across the microchannels.
• The emission, or collection, optics will be described with reference to one embodiment wherein emissions fromdetection region625 include fluorescence emissions from two or more ofmicrochannels622. The collections optics includes a focussingelement670, which in one embodiment is an objective lens, such as a large working distance, modest NA, fluorescence microscope objective lens (OL). A large working distance is helpful in accommodating complex chip designs. In the present embodiment,objective lens670 may be used in an afocal mode in combination with focusinglenses664, e.g., plano-convex lenses, to image the fluorescing chip channels ontodetector arrays620, which in one embodiment are CCD arrays.Objective lens670 in this embodiment may be manually focussed, or may be focussed by a computer system as will be described later. The various fluorescence wavelengths, in one embodiment, are separated through the use ofdichroic beamsplitters660 in combination with band-pass filters662. These beamsplitters operate in a similar fashion as beamsplitter elements656 as described with reference toFIG. 14. For example, eachbeamsplitter element660 directs fluorescence emissions within a specific wavelength range toward itrespective detector620, and allows wavelengths outside that range to pass. As shown, four detector arrays are included, each of which is provided for detecting a specific wavelength range. It will be apparent, however, that fewer or more detector arrays, and associated beamsplitter and focussing elements, may be used depending on the number of different wavelengths to be detected. Additionally, in one embodiment, some or all offilters662 are polarizing specific filters to allow detection of specific polarization.
• According to one embodiment, there are at least asmany detector arrays620 as laser sources640. For example, in an embodiment using a first laser source emitting radiation having a wavelength of approximately 355 nm, and a second laser source emitting radiation having a wavelength of approximately 457 nm, at least two detectors (and at least one beamsplitter element) are provided for detecting fluorescence emissions from excited samples in the detection region of a substrate of approximately 440 nm and 530 nm, respectively.
• Control System
• FIG. 16 presents a block diagram of acontrol system700 for configuring and operating the various systems, instrument interface array components, and modules referred to above.Control system700 includes ahost computer710 that is preferably implemented as an industry standard Pentium-based personal computer executing the Microsoft Windows NT operating system, although any other processor and any other operating system may be used as desired. As part of its function,computer710 coordinates the operation of all analytical systems, control systems and related components.
• A local area network (LAN), based in one embodiment on Ethernet, is used to interface the various electronic modules that comprise the instrument, such as theCCD array modules620,pump module720,high voltage module730, and a three-axes robot740. Threeaxis robot740 provides the capability to automatically place or replace microtiter plates, e.g., from a tray of microtiter plates, and interconnect them with the appropriate instrument interface array.Twister robot760 is provided to place desired microtiter plates, e.g., from a tray of microtiter plates, to a specific area for access and placement by three-axis robot740.Bar code reader770 is provided to allowtwister robot760 to identify microtiter plates having bar code identifiers thereon. One or more Ethernet hubs or switches are provided to direct Ethernet protocol control signals to the desired modules to allow the various modules to be controlled. For example, in one embodiment, an Ethernet/RS232 converter712 is configured to interface withhigh voltage module730,pump module720 andexcitation module610. In this embodiment,Ethernet switch714 is configured to interface withdetection module750, which includesdetector arrays620 and theirs associated driver(s)755.Host PC710 in one embodiment is also connected to a main network. The host PC can configure and operate the entire instrument interface array through the use of custom control and data acquisition computer code/software. Such code is preferably stored on a hard disk coupled tocomputer710, but may be stored on a server accessible byPC710 over the main network. The entire program code, or portions thereof, may also be stored in any other memory device such as a ROM or RAM, or provided on any media capable of storing program code, such as a compact disk medium, a floppy disk, or the like.
• While the invention has been described by way of example and in terms of the specific embodiments, it is to be understood that the invention is not limited to the disclosed embodiments. To the contrary, it is intended to cover various modifications and similar arrangements as would be apparent to those skilled in the art. Therefore, the scope of the appended claims should be accorded the broadest interpretation so as to encompass all such modifications and similar arrangements.

Claims (19)

1. An illumination and detection system for use in illuminating a plurality of samples in a plurality of microchannels located in a detection region on a microfluidic device, and for detecting radiation emitted from the detection region, wherein the microchannels are substantially parallel along a first direction within the detection region, the system comprising:

an illumination source for providing an excitation beam having two or more excitation wavelengths;

focussing optics for focussing the excitation beam onto a first plane defined by the plurality of microchannels in the detection region such that the focussed excitation beam is elongated, having a major axis substantially perpendicular to the first direction, wherein the excitation beam impinges upon the detection region at a non-normal angle of incidence relative to the first plane, and wherein the excitation beam simultaneously excites the samples in at least two of the microchannels so as to cause the excited samples to emit radiation;

two or more detectors, wherein each detector detects a specific range of radiation wavelengths; and

detection optics for directing radiation from the samples toward the detectors such that the wavelengths of the emitted radiation within each specific radiation wavelength range are directed toward the corresponding detector.

2. The system ofclaim 1, wherein the illumination source includes:

two or more laser sources, wherein each laser source emits a radiation beam having one of the excitation wavelengths; and

illumination optics for combining each of the radiation beams into the excitation beam.

3. The system ofclaim 1, wherein the excitation beam is polarized in a direction parallel to the major axis.

4. The system ofclaim 1, wherein the illumination source includes:

a first laser that emits a radiation beam having a first primary wavelength;

a second laser that emits a radiation beam having a second primary wavelength;

a third laser that emits a radiation beam having a third primary wavelength; and

wherein the illumination optics includes optical elements for combining the first, second and third radiation beams so as to form the excitation beam.

5. The system ofclaim 4, wherein the illumination source further includes a fourth laser that emits a radiation beam having a fourth primary wavelength, and wherein the optical elements combine the fourth radiation beam into the excitation beam.

6. The system ofclaim 4, wherein the optical elements include:

a first beamsplitter element for combining the radiation beam of the first laser with the radiation beam of the second laser so as to form a first combined radiation beam;

a second beamsplitter element for combining the first combined radiation beam with the radiation beam of the third laser so as to form the excitation beam.

7. The system ofclaim 4, wherein the first, second and third primary wavelengths are different, and wherein each of the first, second and third primary wavelengths are one of approximately 633 nm, approximately 457 nm, approximately 532 nm, and approximately 355 nm.

8. The system ofclaim 1, wherein the detection optics includes:

one or more beamsplitter elements, wherein each beamsplitter element is associated with one of the detectors, and wherein each beamsplitter element directs radiation having the specific range of wavelengths associated with one of the detectors toward that detector; and

a focusing element that focuses and directs the emitted radiation from the excited samples to the beamsplitter elements.

9. The system ofclaim 8, wherein the focusing element is positioned between the detection region and the beamsplitter elements, and wherein the beamsplitter elements are linearly positioned relative to the focussing element and the detection region so as to form a linear arrangement.

10. The system ofclaim 8, wherein the focusing element and the beamsplitter elements are positioned such that the linear arrangement is normal to the first plane.

11. The system ofclaim 1, wherein each of the detectors includes a CCD array.

12. The system ofclaim 1, wherein each of the detectors provides an output signal proportional to the radiation received from the detection region within its specific range of wavelengths, and wherein the system further includes a processor coupled to each of the detectors for analyzing the output signals of the detectors.

13. The system ofclaim 1, wherein the microfluidic device includes at least two intersecting microchannels.

14. The system ofclaim 1, wherein each of the plurality of microchannels has at least one cross-sectional dimension between about 0.1 and about 500 micrometers.

15. The system ofclaim 1, wherein the detection optics includes:

one or more beamsplitter elements, wherein each beamsplitter element is associated with one of the detectors, and wherein each beamsplitter element directs radiation having a specific polarization toward the associated detector; and

a focusing element that focuses and directs the emitted radiation from the excited samples to the beamsplitter elements.

16. An analytical system comprising:

an analysis chip having a plurality of microchannels disposed thereon, wherein at least two of the plurality of microchannels are located in a detection region;

an optical illumination and detection subsystem including:

an illumination source for illuminating the at least two microchannels in the detection region with an excitation beam at a non-normal angle of incidence, said excitation beam having at least two excitation wavelengths, wherein the excitation beam simultaneously excites samples in the at least two microchannels in the detection region; and

at least two detectors, wherein each detector detects a specific range of wavelengths;

an instrument array including a plurality of interface components for providing control of analyses performed on the chip; an

a modular interface structure, including at least one module, for holding the chip and for interfacing the chip with the instrument array, wherein the at least one module is configured to interface with at least one of the interface components.

17. An illumination and detection system for use in illuminating a plurality of samples in a plurality of microchannels located in a detection region on a microfluidic device, and for detecting radiation emitted from the detection region, wherein the microchannels are substantially parallel along a first direction within the detection region, the system comprising:

an illumination source for providing an excitation beam, wherein the illumination source is configured so that excitation beam impinges at a non-normal angle of incidence onto a first plane defined by the plurality of microchannels in the detection region, wherein on the first plane the excitation beam is elongated, having a major axis substantially perpendicular to the first direction, and wherein the excitation beam simultaneously excites the samples in at least two of the microchannels so as to cause the excited samples to emit radiation;

one or more detectors, wherein each detector detects a specific range of radiation wavelengths; and

detection optics for directing radiation from the samples toward the one or more detectors such that the wavelengths of the emitted radiation within each specific radiation wavelength range are directed toward the corresponding detector.

18. An illumination and detection system for use in illuminating a plurality of samples in a plurality of microchannels located in a detection region on a microfluidic device, and for detecting radiation emitted from the detection region, wherein the microchannels are substantially parallel along a first direction within the detection region, the system comprising:

an illumination source for providing an excitation beam having two or more excitation wavelengths;

focussing optics for focussing the excitation beam onto a first plane defined by the plurality of microchannels in the detection region such that the focussed excitation beam is elongated, having a major axis substantially perpendicular to the first direction, wherein the excitation beam impinges upon the detection region at a non-normal angle of incidence relative to the first plane, and wherein the excitation beam simultaneously excites the samples in at least two of the microchannels so as to cause the excited samples to emit radiation;

two or more detectors, wherein each detector detects a specific range of radiation wavelengths and a specific polarization; and

detection optics for directing radiation from the samples toward the detectors such that the emitted radiation having both the specific polarization and wavelengths within the specific radiation wavelength range are directed toward the corresponding detector.

19. The system ofclaim 18, wherein each specific polarization is one of a linear polarization and a circular polarization.

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