All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference.
The subject matter relates generally to systems and devices for processing biological materials and more particularly to a microfluidics device including ganged reservoir configurations and methods of using same.
Microfluidics systems and devices are used in a variety of applications to manipulate, process and/or analyze biological materials. Examples of microfluidics devices include droplet actuators, microfluidics cartridges, digital microfluidics (DMF) devices, DMF cartridges, droplet actuators, flow cell devices, and the like. Microfluidics devices generally include two substrates arranged with a gap therebetween. In DMF applications, electrodes are associated with the substrates and arranged to conduct droplet operations via electrowetting.
Certain drawbacks exist with respect to microfluidics devices. For example, as time goes on, there is greater demand to process more and more samples on a single microfluidics device. Accordingly, as the number of samples increases, there is need to increase proportionally the amount of other liquids needed to support the biological processes. Unfortunately, the amount of real-estate on a microfluidics device is limited and adding wells (or reservoirs) for meeting these additional requirements for liquids is challenging. Accordingly, there is a need for improved systems and devices to accommodate high sample throughput.
In some aspects, the present disclosure provides a microfluidic device including: a top substrate; a bottom substrate; a gap between the top substrate and the bottom substrate; and an electrode array disposed near the gap for performing droplet operations within the gap. In some embodiments, the electrode array may include one or more arrays of reservoir electrodes, each of the one or more arrays of reservoir electrodes configured to individually manipulate more than one large-volume droplets within the gap. In some embodiments, the electrode array may include one or more arrays of priming electrodes for priming at least one of the more than one large-volume droplets. In some embodiments, the electrode array may include one or more arrays of dispensing electrodes for dispensing into the gap a small-volume droplet from a primed large-volume droplet.
In some embodiments, priming at least one of the more than one large-volume droplets includes forming one or more medium-volume droplets.
In some embodiments, dispensing into the gap includes separating the small-volume droplet from any one of the one or more medium-volume droplets.
In some embodiments, the one or more arrays of reservoir electrodes and the one or more arrays of priming electrodes are the same.
In some embodiments, the electrode array further includes more than one array of reservoir electrodes.
In some embodiments, the electrode array further includes one or more arrays of bridging electrodes between each of the more than one array of reservoir electrodes for manipulating any one of the more than one large-volume droplets between each of the more than one array of reservoir electrodes.
In some embodiments, the electrode array includes at least one of the one or more arrays of reservoir electrodes is in a linear configuration.
In some embodiments, the electrode array includes at least one of the one or more arrays of reservoir electrodes is in a loop configuration.
In some embodiments, a gap height of the gap is from about 50 μm to about 3000 μm.
In some embodiments, a gap height of the gap is greater near the one or more arrays of reservoir electrodes when compared with the gap height of the gap near the one or more arrays of dispensing electrodes.
In some embodiments, the gap height of the gap near the one or more arrays of reservoir electrodes is from about 300 μm to about 3000 μm.
In some embodiments, the gap height of the gap near the one or more arrays of dispensing electrodes is from about 50 μm to about 500 μm.
In some embodiments, the one or more large-volume droplets has a volume from about 20 μL to about 5000 μL.
In some embodiments, the small-volume droplet has a volume from about 1 μL to about 10 μL.
In some embodiments, the top plate includes one or more loading ports for providing the more than one large-volume droplets.
In some embodiments, the one or more loading ports is configured to interface with a micropipette.
In some embodiments, the electrode array further includes an array of processing electrodes for manipulating the small-volume droplet.
In some embodiments, manipulating the small-volume droplet includes either i) mixing the small-volume droplet with one or more additional droplets; ii) splitting the small-volume droplet into one or more additional droplets; or iii) sensing one or more reagents, analytes, or samples of the small-volume droplet.
In some embodiments, the electrode array further includes an array of waste electrodes for disposing of an unused portion of any one of the more than one large-volume droplets.
In some embodiments, the electrode array further includes an array of mixing electrodes for mixing two or more large-volume droplets.
In some embodiments, at least one of the top plate or bottom plate further includes a boundary feature to prevent migration of the more than one large-volume droplets.
In some embodiments, the boundary feature includes a protrusion disposed on either the top substrate or bottom substrate.
In some embodiments, the microfluidic device is a microfluidic cartridge.
In some aspects, the present disclosure provides a method for fluid manipulation. The method includes the steps of providing a microfluidic device, separating a fluid into more than one large-volume droplets, priming one of the more than one large-volume droplets, and dispensing into the gap a small-volume droplet from a primed large-volume droplet.
In some embodiments, the microfluidic device may include a top substrate, a bottom substrate, a gap between the top substrate and the bottom substrate, and an electrode array disposed near the gap for performing droplet operations within the gap.
In some embodiments, the electrode array may include one or more arrays of reservoir electrodes. In some embodiments, each of the one or more arrays of reservoir electrodes is configured to individually manipulate more than one large-volume droplets within the gap. In some embodiments, the electrode array may include one or more arrays of priming electrodes for priming at least one of the more than one large-volume droplets. In some embodiments, the electrode array may include one or more arrays of dispensing electrodes for dispensing into the gap a small-volume droplet from a primed large-volume droplet; loading a fluid onto the microfluidic device.
In some embodiments, priming at least one of the more than one large-volume droplets includes forming one or more medium-volume droplets.
In some embodiments, dispensing into the gap includes separating the small-volume droplet from any one of the one or more medium-volume droplets.
In some embodiments, the one or more arrays of reservoir electrodes and the one or more arrays of priming electrodes are the same.
In some embodiments, the electrode array further includes more than one array of reservoir electrodes.
In some embodiments, the electrode array further includes one or more arrays of bridging electrodes between each of the more than one array of reservoir electrodes for manipulating any one of the more than one large-volume droplets between each of the more than one array of reservoir electrodes.
In some embodiments, at least one of the one or more arrays of reservoir electrodes is in a linear configuration.
In some embodiments, at least one of the one or more arrays of reservoir electrodes is in a loop configuration.
In some embodiments, a gap height of the gap is from about 50 μm to about 3000 μm.
In some embodiments, a gap height of the gap is greater near the one or more arrays of reservoir electrodes when compared with the gap height of the gap near the one or more arrays of dispensing electrodes.
In some embodiments, the gap height of the gap near the one or more arrays of reservoir electrodes is from about 300 μm to about 3000 μm.
In some embodiments, the gap height of the gap near the one or more arrays of dispensing electrodes is from about 50 μm to about 500 μm.
In some embodiments, the one or more large-volume droplets has a volume from about 20 μL to about 5000 μL.
In some embodiments, the small-volume droplet has a volume from about 1 μL to about 10 μL.
In some embodiments, the top plate includes one or more loading ports for providing the more than one large-volume droplets.
In some embodiments, the one or more loading ports is configured to interface with a micropipette.
In some embodiments, the electrode array further includes an array of processing electrodes for manipulating the small-volume droplet.
In some embodiments, manipulating the small-volume droplet includes either i) mixing the small-volume droplet with one or more additional droplets; ii) splitting the small-volume droplet into one or more additional droplets; or iii) sensing one or more reagents, analytes, or samples of the small-volume droplet.
In some embodiments, the electrode array further includes an array of waste electrodes for disposing of an unused portion of any one of the more than one large-volume droplets.
In some embodiments, the electrode array further includes an array of mixing electrodes for mixing two or more large-volume droplets.
In some embodiments, at least one of the top plate or bottom plate further includes a boundary feature to prevent migration of the more than one large-volume droplets.
In some embodiments, the boundary feature includes a protrusion disposed on either the top substrate or bottom substrate.
In some embodiments, the microfluidic device is a microfluidic cartridge.
The novel features of the disclosure are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present disclosure will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the disclosure are utilized, and the accompanying drawings of which:
In the following detailed description, reference is made to the accompanying figures, which form a part hereof. In the figures, similar symbols typically identify similar components, unless context dictates otherwise. The illustrative embodiments described in the detailed description, figures, and claims are not meant to be limiting. Other embodiments may be utilized, and other changes may be made, without departing from the scope of the subject matter presented herein. It will be readily understood that the aspects of the present disclosure, as generally described herein, and illustrated in the figures, can be arranged, substituted, combined, separated, and designed in a wide variety of different configurations, all of which are explicitly contemplated herein.
Although certain embodiments and examples are disclosed below, inventive subject matter extends beyond the specifically disclosed embodiments to other alternative embodiments and/or uses, and to modifications and equivalents thereof. Thus, the scope of the claims appended hereto is not limited by any of the particular embodiments described below. For example, in any method or process disclosed herein, the acts or operations of the method or process may be performed in any suitable sequence and are not necessarily limited to any particular disclosed sequence. Various operations may be described as multiple discrete operations in turn, in a manner that may be helpful in understanding certain embodiments, however, the order of description should not be construed to imply that these operations are order dependent. Additionally, the structures, systems, and/or devices described herein may be embodied as integrated components or as separate components.
For purposes of comparing various embodiments, certain aspects and advantages of these embodiments are described. Not necessarily all such aspects or advantages are achieved by any particular embodiment. Thus, for example, various embodiments may be carried out in a manner that achieves or optimizes one advantage or group of advantages as taught herein without necessarily achieving other aspects or advantages as may also be taught or suggested herein.
In some embodiments, the subject matter provides a microfluidics device including ganged (or extended) reservoir configurations and methods of using same.
In some embodiments, the ganged (or extended) reservoir configurations and methods may provide a dispenser portion, a primer portion, and a reservoir portion and wherein the reservoir portion may include any arrangement of two or more liquid storage locations.
In some embodiments, the ganged (or extended) reservoir configurations and methods may be provided wherein a reservoir portion including two or more liquid storage locations supplies liquid to a primer portion and wherein the primer portion supplies liquid to a dispenser portion.
In some embodiments, the ganged (or extended) reservoir configurations and methods may provide a reservoir portion including two or more liquid storage locations and wherein the liquid storage locations may be arranged linearly (i.e., one-dimensionally (1D)).
In some embodiments, the ganged (or extended) reservoir configurations and methods may provide a reservoir portion including two or more liquid storage locations and wherein the liquid storage locations may be arranged in an array (i.e., two-dimensionally (2D)).
In some embodiments, the ganged (or extended) reservoir configurations and methods may provide a reservoir portion including two or more liquid storage locations and wherein the liquid storage locations may be arranged in a loop (i.e., 2D).
In some embodiments, the ganged (or extended) reservoir configurations and methods may provide a reservoir portion including any arrangement of two or more liquid storage locations for holding and managing large-volume droplets and wherein the large-volume droplets may be the same type of droplets or different types of droplets.
In some embodiments, the ganged (or extended) reservoir configurations and methods may provide a reservoir portion including any arrangement of two or more liquid storage locations for dispensing mid-volume droplets to a primer portion.
In some embodiments, the ganged (or extended) reservoir configurations and methods may provide a primer portion for dispensing small-volume droplets to a dispenser portion.
In some embodiments, the ganged (or extended) reservoir configurations and methods may provide a dispenser portion for dispensing small-volume droplets to the processing area of a microfluidics device.
In some embodiments, the ganged (or extended) reservoir configurations and methods may provide a process by which multiple large-volume droplets at multiple storage locations may be used to resupply mid-volume droplets to one primer portion and then resupply small-volume droplets to one dispenser portion.
Unless otherwise defined, all technical terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs.
The term “activate,” with reference to one or more electrodes, means affecting a change in the electrical state of the one or more electrodes which, in the presence of a droplet, results in a droplet operation. Activation of an electrode can be accomplished using alternating current (AC) or direct current (DC). Any suitable voltage may be used. For example, an electrode may be activated using a voltage which is greater than about 5 V, or greater than about 20 V, or greater than about 40 V, or greater than about 100 V, or greater than about 200 V or greater than about 300 V. Further, electrode may be activated using a positive and/or negative voltage relative to system ground. Further, deactivated electrodes may be held at ground or floated. The suitable voltage being a function of the dielectric's properties such as thickness and dielectric constant, liquid properties such as viscosity and many other factors as well. Where an AC signal is used, any suitable frequency may be employed. For example, an electrode may be activated using an AC signal having a frequency from about 1 Hz to about 10 MHz, or from about 1 Hz and 10 KHz, or from about 10 Hz to about 240 Hz, or about 60 Hz.
The term “droplet” means a volume of liquid on a droplet actuator. Typically, a droplet is at least partially bounded by a filler fluid. For example, a droplet may be completely surrounded by a filler fluid or may be bounded by filler fluid and one or more surfaces of the droplet actuator. As another example, a droplet may be bounded by filler fluid, one or more surfaces of the droplet actuator, and/or the atmosphere. As yet another example, a droplet may be bounded by filler fluid and the atmosphere. Droplets may, for example, be aqueous or non-aqueous or may be mixtures or emulsions including aqueous and non-aqueous components.
The term “droplet actuator” means a device for manipulating droplets. Microfluidics devices, microfluidics cartridges, digital microfluidics (DMF) devices, and DMF cartridges are examples of droplet actuators. Certain droplet actuators will include one or more substrates arranged with a droplet operations gap therebetween and electrodes associated with (e.g., patterned on, layered on, attached to, and/or embedded in) the one or more substrates and arranged to conduct one or more droplet operations. For example, certain droplet actuators will include a base (or bottom) substrate, droplet operations electrodes associated with the substrate, one or more dielectric layers atop the substrate and/or electrodes, and optionally one or more hydrophobic layers atop the substrate, dielectric layers and/or the electrodes forming a droplet operations surface. A top substrate may also be provided, which is separated from the droplet operations surface by a gap, commonly referred to as a droplet operations gap. Droplet actuators will include various electrode arrangements on the bottom and/or top substrates. During droplet operations it is preferred that droplets remain in continuous contact or frequent contact with a ground or reference electrode. A ground or reference electrode may be associated with the top substrate facing the gap, the bottom substrate facing the gap, or within the gap itself. Where electrodes are provided on both substrates, electrical contacts for coupling the electrodes to a droplet actuator instrument for controlling or monitoring the electrodes may be associated with one or both plates. In some cases, electrodes on one substrate are electrically coupled to the other substrate so that only one substrate is in contact with the droplet actuator. Where multiple substrates are used, a spacer may be provided between the substrates to determine the height of the gap therebetween and define on-actuator dispensing reservoirs. The spacer height may, for example, be from about 5 μm to about 1000 μm, or about 100 μm to about 400 μm, or about 200 μm to about 350 μm, or about 250 μm to about 300 μm, or about 275 μm. The spacer may, for example, be formed of features or layers projecting from the top or bottom substrates, and/or a material inserted between the top and bottom substrates. One or more openings may be provided in the one or more substrates for forming a fluid path through which liquid may be delivered into the droplet operations gap.
In some cases, the top and/or bottom substrate of a droplet actuator includes a PCB substrate that is coated with a dielectric, such as a polyimide dielectric, which may in some cases also be coated or otherwise treated to make the droplet operations surface hydrophobic. Various materials are also suitable for use as the dielectric component of the droplet actuator. In some cases, the top and/or bottom substrate of a droplet actuator includes a glass or silicon substrate on which features have been patterned using process technology borrowed from semiconductor device fabrication including the deposition and etching of thin layers of materials using microlithography. The top and/or bottom substrate may consist of a semiconductor backplane (i.e., a thin-film transistor (TFT) active-matrix controller) on which droplet operations electrodes have been formed.
Electrodes of a droplet actuator are typically controlled by a controller or a processor, which is itself provided as part of a system, which may include processing functions as well as data and software storage and input and output capabilities. Reagents may be provided on the droplet actuator in the droplet operations gap or in a reservoir fluidly coupled to the droplet operations gap. The reagents may be in liquid form, e.g., droplets, or they may be provided in a reconstitutable form in the droplet operations gap or in a reservoir fluidly coupled to the droplet operations gap. Reconstitutable reagents may typically be combined with liquids for reconstitution.
The term “droplet operation” means any manipulation of a droplet on a droplet actuator. A droplet operation may, for example, include: loading a droplet into the droplet actuator; dispensing one or more droplets from a source droplet; splitting, separating or dividing a droplet into two or more droplets; transporting a droplet from one location to another in any direction; merging or combining two or more droplets into a single droplet; diluting a droplet; mixing a droplet; agitating a droplet; deforming a droplet; retaining a droplet in position; incubating a droplet; heating a droplet; vaporizing a droplet; cooling a droplet; disposing of a droplet; transporting a droplet out of a droplet actuator; other droplet operations described herein; and/or any combination of the foregoing. The terms “merge,” “merging,” “combine,” “combining” and the like are used to describe the creation of one droplet from two or more droplets. It should be understood that when such a term is used in reference to two or more droplets, any combination of droplet operations that are sufficient to result in the combination of the two or more droplets into one droplet may be used. For example, “merging droplet A with droplet B,” can be achieved by transporting droplet A into contact with a stationary droplet B, transporting droplet B into contact with a stationary droplet A, or transporting droplets A and B into contact with each other. The terms “splitting,” “separating” and “dividing” are not intended to imply any particular outcome with respect to volume of the resulting droplets (i.e., the volume of the resulting droplets can be the same or different) or number of resulting droplets (the number of resulting droplets may be 2, 3, 4, 5 or more). The term “mixing” refers to droplet operations which result in more homogenous distribution of one or more components within a droplet. Examples of “loading” droplet operations include microdialysis loading, pressure assisted loading, robotic loading, passive loading, and pipette loading. Droplet operations may be electrode-mediated. In some cases, droplet operations are further facilitated by the use of hydrophilic and/or hydrophobic regions on surfaces and/or by physical obstacles. Impedance and/or capacitance sensing and/or imaging techniques may sometimes be used to determine or confirm the outcome of a droplet operation. Generally speaking, the sensing or imaging techniques may be used to confirm the presence or absence of a droplet at a specific electrode. For example, the presence of a dispensed droplet at the destination electrode following a droplet dispensing operation confirms that the droplet dispensing operation was effective. Similarly, the presence of a droplet at a detection spot at an appropriate step in an assay protocol may confirm that a previous set of droplet operations has successfully produced a droplet for detection. Droplet transport time can be quite fast. For example, in various embodiments, transport of a droplet from one electrode to the next may be completed within about 1 sec, or about 0.1 sec, or about 0.01 sec, or about 0.001 sec. In one embodiment, the electrode is operated in AC mode but is switched to DC mode for imaging. It is helpful for conducting droplet operations for the footprint area of droplet to be similar to or larger than the electrowetting area; in other words, 1×-, 2×-3×-droplets are usefully controlled and/or operated using 1, 2, and 3 electrodes, respectively. If the droplet footprint is greater than number of electrodes available for conducting a droplet operation at a given time, the difference between the droplet size and the number of electrodes should typically not be greater than 1; in other words, a 2× droplet is usefully controlled using 1 electrode and a 3× droplet is usefully controlled using 2 electrodes. When droplets include beads, it is useful for droplet size to be equal to the number of electrodes controlling the droplet, e.g., transporting the droplet.
The term “filler fluid” means a fluid associated with a droplet operations substrate of a droplet actuator, which fluid is sufficiently immiscible with a droplet phase to render the droplet phase subject to electrode-mediated droplet operations. For example, the droplet operations gap of a droplet actuator is typically filled with a filler fluid. The filler fluid may, for example, be or include a low-viscosity, low-surface tension oil, such as silicone oil or hexadecane. The filler fluid may be or include a halogenated oil, such as a fluorinated or perfluorinated oil. The filler fluid may fill the entire gap of the droplet actuator or may only coat one or more surfaces of the droplet actuator or may only surround a droplet (i.e., an “oil-shell”) and the droplet brings its own oil with it. Filler fluids may be selected to improve droplet operations and/or reduce loss of reagent or target substances from droplets, reduce formation of unwanted microdroplets, reduce cross contamination between droplets, reduce contamination of droplet actuator surfaces, reduce degradation of droplet actuator materials, reduce evaporation of droplets, and so on. For example, filler fluids may be selected for compatibility with droplet actuator materials. As an example, fluorinated filler fluids may be usefully employed with fluorinated surface coatings. In another example, fluorinated filler fluids may be used to dissolve surface coatings (e.g., Fluorinert fc-40 may be a solvent for Teflon AF). Fluorinated filler fluids are useful to reduce loss of lipophilic compounds, such as umbelliferone substrates like 6-hexadecanoylamido-4-methylumbelliferone substrates (e.g., for use in Krabbe, Niemann-Pick, or other assays); Filler fluids may, for example, be doped with surfactants or other additives. For example, additives may be selected to improve droplet operations and/or reduce loss of reagent or target substances from droplets, formation of microdroplets, cross contamination between droplets, contamination of droplet actuator surfaces, degradation of droplet actuator materials, etc. Composition of the filler fluid, including surfactant doping, may be selected for performance with reagents or samples used in the specific assay protocols and effective interaction or non-interaction with droplet actuator materials. For example, fluorinated oils may in some cases be doped with fluorinated surfactants, e.g., Zonyl FSO-100 (Sigma-Aldrich) and/or others.
The term “reservoir” means an enclosure or partial enclosure configured for holding, storing, or supplying liquid. A droplet actuator system of the disclosure may include on-cartridge reservoirs and/or off-cartridge reservoirs. On-cartridge reservoirs may be (1) on-actuator reservoirs, which are reservoirs in the droplet operations gap or on the droplet operations surface; (2) off-actuator reservoirs, which are reservoirs on the droplet actuator cartridge, but outside the droplet operations gap, and not in contact with the droplet operations surface; or (3) hybrid reservoirs which have on-actuator regions and off-actuator regions. An example of an off-actuator reservoir is a reservoir in the top substrate. An off-actuator reservoir is typically in fluid communication with an opening or flow path arranged for flowing liquid from the off-actuator reservoir into the droplet operations gap, such as into an on-actuator reservoir. An off-cartridge reservoir may be a reservoir that is not part of the droplet actuator cartridge at all, but which flows liquid to some portion of the droplet actuator cartridge. For example, an off-cartridge reservoir may be part of a system or docking station to which the droplet actuator cartridge is coupled during operation. Similarly, an off-cartridge reservoir may be a reagent storage container or syringe which is used to force fluid into an on-cartridge reservoir or into a droplet operations gap. A system using an off-cartridge reservoir will typically include a fluid passage means whereby liquid may be transferred from the off-cartridge reservoir into an on-cartridge reservoir or into a droplet operations gap.
The term “washing” with respect to washing a surface, such as a hydrophilic surface, means reducing the amount and/or concentration of one or more substances in contact with the surface or exposed to the surface from a droplet in contact with the surface. The reduction in the amount and/or concentration of the substance may be partial, substantially complete, or even complete. The substance may be any of a wide variety of substances; examples include target substances for further analysis, and unwanted substances, such as components of a sample, contaminants, and/or excess reagent or buffer.
The terms “top,” “bottom,” “over,” “under,” and “on” are used throughout the description with reference to the relative positions of components of the droplet actuator, such as relative positions of top and bottom substrates of the droplet actuator. It will be appreciated that in many cases the droplet actuator is functional regardless of its orientation in space.
When a liquid in any form (e.g., a droplet or a continuous body, whether moving or stationary) is described as being “on”, “at”, or “over” an electrode, array, matrix or surface, such liquid could be either in direct contact with the electrode/array/matrix/surface, or could be in contact with one or more layers or films that are interposed between the liquid and the electrode/array/matrix/surface. In one example, filler fluid can be considered as a dynamic film between such liquid and the electrode/array/matrix/surface.
When a droplet is described as being “on” or “loaded on” a droplet actuator, it should be understood that the droplet is arranged on the droplet actuator in a manner which facilitates using the droplet actuator to conduct one or more droplet operations on the droplet, the droplet is arranged on the droplet actuator in a manner which facilitates sensing of a property of or a signal from the droplet, and/or the droplet has been subjected to a droplet operation on the droplet actuator.
Following long-standing patent law convention, the terms “a,” “an,” and “the” refer to “one or more” when used in this application, including the claims. Thus, for example, reference to “a subject” includes a plurality of subjects, unless the context clearly is to the contrary (e.g., a plurality of subjects), and so forth.
The terms “comprise,” “comprises,” “comprising,” “have,” “has,” “having” “include,” “includes,” and “including,” are intended to be non-limiting (i.e., open ended), such that recitation of items in a list is not to the exclusion of other like items that may be substituted or added to the listed items (i.e., not closed).
Terms like “preferably,” “commonly,” and “typically” are not utilized herein to limit the scope of the claimed embodiments or to imply that certain features are critical or essential to the structure or function of the claimed embodiments. These terms are intended to highlight alternative or additional features that may or may not be utilized in a particular embodiment of the disclosure.
The term “substantially” is utilized herein to represent the inherent degree of uncertainty that may be attributed to any quantitative comparison, value, measurement, or other representation and to represent the degree by which a quantitative representation may vary from a stated reference without resulting in a change in the basic function of the subject matter at issue.
For the purposes of this specification and appended claims, unless otherwise indicated, all numbers expressing amounts, sizes, dimensions, proportions, shapes, formulations, parameters, percentages, quantities, characteristics, and other numerical values used in the specification and claims, are to be understood as being modified in all instances by the term “about” even though the term “about” may not expressly appear with the value, amount or range. Accordingly, unless indicated to the contrary, the numerical parameters set forth in the following specification and attached claims are not and need not be exact, but may be approximate and/or larger or smaller as desired, reflecting tolerances, conversion factors, rounding off, measurement error and the like, and other factors known to those of skill in the art depending on the desired properties sought to be obtained by the subject matter. For example, the term “about,” when referring to a value can be meant to encompass variations of, in some embodiments ±100%, in some embodiments ±50%, in some embodiments ±20%, in some embodiments ±10%, in some embodiments ±5%, in some embodiments ±1%, in some embodiments ±0.5%, and in some embodiments ±0.1% from the specified amount, as such variations are appropriate to perform the disclosed methods or employ the disclosed compositions.
Further, the term “about” when used in connection with one or more numbers or numerical ranges, should be understood to refer to all such numbers, including all numbers in a range and modifies that range by extending the boundaries above and below the numerical values set forth. The recitation of numerical ranges by endpoints includes all numbers, e.g., whole integers, including fractions thereof, subsumed within that range (for example, the recitation of 1 to 5 includes 1, 2, 3, 4, and 5, as well as fractions thereof, e.g., 1.5, 2.25, 3.75, 4.1, and the like) and any range within that range.
The physical structure of linear ganged reservoir configuration 100 may be generally that of a microfluidics device, which may be, for example, a digital microfluidics (DMF) device. For example, linear ganged reservoir configuration 100 may include a bottom substrate 120 and a top substrate 122 separated by a droplet operations gap 124. In the case of DMF, droplet operations may occur in the droplet operations gap 124 between bottom substrate 120 and top substrate 122 of linear ganged reservoir configuration 100.
In one example, bottom substrate 120 may be a printed circuit board (PCB)-based substrate, such as a multi-layer PCB. In another example, bottom substrate 120 may be glass or silicon substrate that has patterned electrodes. In one example, top substrate 122 may be formed of glass or plastic. For example, top substrate 122 may be formed of injection molded thermoplastic materials or injection molded glass. Additionally, top substrate 122 may be substantially transparent to light. However, in other embodiments, top substrate 122 may be substantially opaque. Additionally, top substrate 122 may include a ground or reference electrode (not shown). In one example, the ground or reference electrode may be formed of indium tin oxide (ITO). In some embodiments, the ITO ground or reference electrode is substantially transparent to light.
In linear ganged reservoir configuration 100, dispenser portion 110 may include multiple lines, paths, and/or arrays of droplet operations electrodes 126 (e.g., electrowetting electrodes). Additionally, certain droplet operations electrodes 126 may be flanked by electrodes 127. Further, primer portion 112 may include multiple lines, paths, and/or arrays of primer electrodes 128 (e.g., electrowetting electrodes). Further, reservoir portion 114 may include multiple lines, paths, and/or arrays of reservoir electrodes 130 (e.g., electrowetting electrodes). Additionally, reservoir portion 114 may include at least two storage locations 116 up to any number of storage locations 116 (e.g., storage locations 116a through 116n) all ganged together. In this example, storage location 116a may be considered the outlet storage location 116 (i.e., storage location proximal to the primer portion 112). Further, in this example, each of the storage locations 116 has a loading port 118 (e.g., loading ports 118a through 118n). The loading port 118 allows a user of the device to provide a fluid to the storage locations 116, such as, for example, by pipetting. The loading port 118 may have a similar size and or geometry to the wells of a standard microwell plate. In configurations where each storage location 116 has a loading port 118, each storage location 116 may be filled without activating the electrodes to move droplets between storage locations 116. Droplet operations electrodes 126, primer electrodes 128, and reservoir electrodes 130 may be formed, for example, of copper, gold, chromium, or aluminum.
A dielectric layer 132 (e.g., parylene coating, silicon nitride) may be atop the electrodes 126, 128, and 130. Further, a hydrophobic layer (not shown) may be provided on both the top side of bottom substrate 120 and the bottom side of top substrate 122 that is facing droplet operations gap 124. Examples of hydrophobic materials or coatings may include, but are not limited to, polytetrafluoroethylene (PTFE), Cytop, Teflon™ AF (amorphous fluoropolymer) resins, FluoroPel™ coatings, silane, and the like.
In linear ganged reservoir configuration 100, to accommodate different volumes of liquid, the height of droplet operations gap 124 may vary from dispenser portion 110, to primer portion 112, to reservoir portion 114. For example, each storage location 116 of reservoir portion 114 may be designed to hold a discrete large-volume droplet 140 (see
Accordingly, at reservoir portion 114, the gap height of droplet operations gap 124 may be, for example, from about 300 μm to about 3000 μm. At primer portion 112, the gap height of droplet operations gap 124 may be, for example, from about 100 μm to about 1000 μm. At dispenser portion 110, the gap height of droplet operations gap 124 may be, for example, from about 50 μm to about 500 μm.
Further, in linear ganged reservoir configuration 100, primer portion 112 and dispenser portion 110 may be designed or sized optimally for very precise dispensing. For example, each of the droplet operations electrodes 126 may have the following dimensions: 1.25 mm×1.25 mm; 1.25 mm×3 mm; 1 mm×1 mm; 1.25 mm×3.3 mm; or 1.25 mm×3.85 mm.
Each of the storage locations 116 of reservoir portion 114 may be designed to hold, for example, from about 800 μL to about 1000 μL, or from about 1000 μL to about 1500 μL, or from about 2.5 mL to about 5 mL. When, for example, a certain larger volume of liquid is needed, then a line of multiple storage locations 116 may be provided. In one example, linear ganged reservoir configuration 100 may include a line of 1500 μL storage locations 116 to provide some greater volume of liquid. In another example, linear ganged reservoir configuration 100 may include a line of 2-5 μL storage locations 116 to provide some greater volume of liquid.
In operation, each of the storage locations 116a through 116n of reservoir portion 114 may be loaded with a large-volume droplet 140 via the respective loading ports 118a through 118n. The primer portion 112 may prime the large-volume droplet 140 using droplet operations, such that mid-volume droplets 142 may be split off from a large-volume droplet 140 at storage location 116a and dispensed into primer portion 112. Priming may also include manipulating a fluid within the reservoir portion 114 to ensure it is the correct shape and that the exterior of the fluid is equilibrated to a surfactant in the oil phase.
Then, small-volume droplets 144 may be split off from a mid-volume droplet 142 and dispensed into dispenser portion 110. Then, using droplet operations, small-volume droplets 144 may be transported away for processing. As, for example, the large-volume droplet 140 at storage location 116a is depleted, the next large-volume droplet 140 may be transported (via droplet operations) into storage location 116a from storage location 116b. Then, all other upstream large-volume droplets 140 may also be advanced (via droplet operations) to the next storage location 116 toward primer portion 112. This process may continue until all large-volume droplets 140a through 140n are substantially depleted or consumed.
Further, after substantially depleting and/or consuming large-volume droplets 140a through 140n, there may be some small residue left within any storage location 116. In one example, this residue may be simply left and held within storage location 116. In another example, assuming a large enough volume, this residue may be transported (via droplet operations) out of storage location 116 to waste.
That is, using linear ganged reservoir configuration 100, multiple large-volume droplets 140 at multiple storage locations 116 may be used to resupply mid-volume droplets 142 at the primer portion 112 and then resupply small-volume droplets 144 at the dispenser portion 110. Then, small-volume droplets 144 from dispenser portion 110 may be used to supply any processes of a microfluidics device (not shown).
In microfluidics certain surface forces (e.g., surface tension) and certain volume forces (e.g., gravity) should be balanced to enable electrowetting. Therefore, it is important to note that the maximum volume of any large-volume droplet 140 must be just short of any volume that causes gravity to flood the system. At the same time, if the volume of large-volume droplet 140 is too small, then it may be difficult to split off a mid-volume droplet 142 into primer portion 112 (using droplet operations). Accordingly, large-volume droplet 140 at each storage location 116 may have a certain optimal maximum-minimum volume which may depend in part on the size of the reservoir portion 114 and the size and shape of the reservoir electrodes 148.
Further, the operation of linear ganged reservoir configuration 100 shown in
By way of contrast,
In this example, the use of 4×4-linear ganged reservoir 101 in place of the four conventional wells or reservoirs 202 may result in a space savings of, for example, from about 30% to about 50%. At the same time, 4×4-linear ganged reservoir 101 may store substantially the same volume of liquid as the four conventional wells or reservoirs 202, while requiring less real-estate on the microfluidics device. That is, 4×4-linear ganged reservoir 101 provides substantially the same amount of liquid storage as the four conventional wells or reservoirs 202 while having a smaller footprint than the four conventional wells or reservoirs 202.
In the ganged reservoir configurations described hereinabove, the transport of large-volume droplets 140 from one storage location 116 to a different storage location 116 is limited to linear transport. However, the ganged reservoir configurations are not limited to linear movement only of large-volume droplets 140. In other embodiments, large-volume droplets 140 may be transported linearly and also across lanes of storage locations 116. That is, when, for example, a certain larger volume of liquid is needed, then an array of multiple storage locations 116 may be provided. In one example, linear ganged reservoir configuration 100 may include an array of 1500 μL storage locations 116 to provide some greater volume of liquid. In another example, linear ganged reservoir configuration 100 may include an array of 2-5 μL storage locations 116 to provide some greater volume of liquid. Examples of which are described hereinbelow with reference to
Using droplet operations, large-volume droplets 140 may be moved from one storage location 116 to a different storage location 116. Empty storage locations 116 may be provided to allow movement or shuffling of large-volume droplets 140 to or from different storage locations 116. For example, to minimize contamination between different types of large-volume droplets 140, a large-volume wash droplet 140 may be transported across any shared reservoir electrodes 130 for cleaning purposes. Although, different types of large-volume droplets 140 may be provided, the different types of large-volume droplets 140 should be provided in an order that supports the processes of the microfluidics device and minimizes cross-contamination.
In another example,
In one example, storage location 116d may hold a large-volume droplet 140 that may be from about 1000 μL to about 5000 μL in volume. Storage location 116c may hold a large-volume droplet 140 that may be from about 100 μL to about 500 μL in volume. Storage location 116b may hold a large-volume droplet 140 that may be from about 10 μL to about 50 μL in volume. Storage location 116a may hold a large-volume droplet 140 that may be from about 1 μL to about 5 μL in volume.
Electrode configuration 164 of
Processing area 170 may include any arrangements of any types of electrodes for performing any functions of a microfluidics device. For example, processing area 170 may include mixing regions, sensing regions, detection regions, and the like.
Further, the other side of storage location 116a supplies a waste area 172. In one example, every other storage location 116 may include one type of large-volume sample droplet 180 while the remaining storage locations 116 may include another type of large-volume droplet 182. For example, storage locations 116b, 116d, 116f, and 116h may include large-volume sample droplets 180a, 180b, 180c, and 180d, respectively. Further, storage locations 116c, 116e, and 116g may include other large-volume droplets 182a, 182b, and 182c, respectively.
During processing, any of one type of large-volume sample droplets 180 and/or another type of large-volume droplets 182 may be transported to storage location 116a and dispensed into processing area 170. However, at any given time, the entire volume at any droplet may not be used completely during dispensing. Therefore, there may be reason to move any unused volume to waste area 172. Accordingly, electrode configuration 164 facilitates both the advantages of linear ganged reservoir configuration 100 and the ability to move any unused volume to waste.
Electrode configuration 168 of
Processing area 170 may include any arrangements of any types of electrodes for performing any functions of a microfluidics device. For example, processing area 170 may include further mixing regions or sensing regions, detection regions, and the like.
Further, the other side of mixing area 174 supplies a waste area 172. In one example, the linear arrangement of storage locations 116 may include one type of large-volume sample droplet 182 while the looped arrangement storage locations 116 may include another type of large-volume droplet 180. For example, storage locations 116a, 116b, 116c, and 116d may include large-volume sample droplets 182a, 182b, 182c, and 182d, respectively. Further, storage locations 116e, 116f, 116g, 116h, 116i and 116j may include other large-volume droplets 180a, 180b, 180c, 180d, 180e and 182f, respectively.
During processing, any of one type of large-volume sample droplets 180 and/or another type of large-volume droplets 182 may be transported to mixing area 174. Mixing area 174 may comprise a distinct electrode layout and/or gap height gradient and may receive large-volume droplets 180 and/or another type of large-volume droplets 182 to be mixed prior to dispensing into the processing area 170. Mixing area 174 allows for mixing of larger volumes of liquid and may enable mixing of air sensitive reagents which may degenerate quickly. However, at any given time, the entire volume at any droplet may not be used completely during dispensing. Therefore, there may be reason to move any unused volume to waste area 172. Accordingly, electrode configuration 168 facilitates both the advantages of linear reservoir configuration 100 and looped reservoir configuration 160 and the ability to move any unused volume to waste.
Referring now to
At step 410, a microfluidics device is provided that includes one or more ganged (or extended) reservoir configurations. For example, a microfluidics device is provided that may include one or more ganged (or extended) reservoir configurations, such as, but not limited to, any of the linear ganged reservoir configurations 100 (see
At step 415, one or more the storage locations are loaded with liquid. For example, the one or more storage locations may be loaded by a user using a micropipette. However, other means may be provided for loading the one or more storage locations including blister packs or reagent plates which interface with the DMF device. In one example, one or more storage locations 116 of linear ganged reservoir configuration 100 (see
At step 420, mid-volume droplets are dispensed using droplet operations into the primer portion of the ganged reservoir from the large-volume droplet in the storage location of the ganged reservoir. For example, mid-volume droplets 142 may be dispensed into primer portion 112 of any of the ganged reservoirs from the large-volume droplet 140 in the outlet storage location 116 of the ganged reservoir. In one example, mid-volume droplets 142 may be dispensed into primer portion 112 of linear ganged reservoir configuration 100 (see
At step 425, small-volume droplets are dispensed into the dispenser portion of the ganged reservoir from the mid-volume droplet in the primer portion of the ganged reservoir using droplet operations. For example, small-volume droplets 144 may be dispensed into dispenser portion 110 of any of the ganged reservoirs from the mid-volume droplet 142 in the outlet storage location 116 of the ganged reservoir. In one example, small-volume droplets 144 may be dispensed into dispenser portion 110 of linear ganged reservoir configuration 100 (see
At step 430, the small-volume droplets may be transported away from the dispenser portion of the ganged reservoir for further processing. For example, small-volume droplets 144 may be transported away from dispenser portion 110 of any of the ganged reservoirs for further processing. In one example, small-volume droplets 144 may be transported away from dispenser portion 110 of linear ganged reservoir configuration 100 (see
At step 435, the large-volume droplets are transported or advanced from one storage location to the next of the ganged reservoir to keep the outlet storage location replenished. For example, in the ganged reservoir or reservoir configuration, large-volume droplets 140 may be transported or advanced from one storage location 116 to the next storage location 116 to keep the outlet storage location 116 replenished for dispensing mid-volume droplets 142 and then small-volume droplets 144. Further to the example, when the large-volume droplet 140 at the outlet storage location 116a is depleted, then the next large-volume droplet 140 may be transported (via droplet operations) into storage location 116a from storage location 116b. Further, all other upstream large-volume droplets 140 may be advanced toward the outlet storage location 116a.
Generally, using method 400 and, for example, linear ganged reservoir configuration 100, multiple large-volume droplets 140 at multiple storage locations 116 may be used to resupply mid-volume droplets 142 to the one primer portion 112 and then resupply small-volume droplets 144 to the one dispenser portion 110. Then, small-volume droplets 144 from dispenser portion 110 may be used to supply any processes of a microfluidics device (not shown).
While preferred embodiments of the present disclosure have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. It is not intended that the disclosure be limited by the specific examples provided within the specification. While the disclosure has been described with reference to the aforementioned specification, the descriptions and illustrations of the embodiments herein are not meant to be construed in a limiting sense. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the disclosure. Furthermore, it shall be understood that all aspects of the disclosure are not limited to the specific depictions, configurations or relative proportions set forth herein which depend upon a variety of conditions and variables. It should be understood that various alternatives to the embodiments of the disclosure described herein may be employed in practicing the disclosure. It is therefore contemplated that the invention shall also cover any such alternatives, modifications, variations or equivalents. It is intended that the following claims define the scope of the disclosure and that methods and structures within the scope of these claims and their equivalents be covered thereby.
This application claims the benefit of U.S. Provisional Application No. 63/405,207, filed Sep. 9, 2022, which is hereby incorporated by reference in its entirety herein.
Filing Document | Filing Date | Country | Kind |
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PCT/CA2023/051186 | 9/8/2023 | WO |
Number | Date | Country | |
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63405207 | Sep 2022 | US |