The present invention relates to droplet microfluidic devices, and more specifically to Active Matrix Electrowetting-On-Dielectric (AM-EWOD) devices, and to methods for the manipulation and separation of magnetically responsive particles from droplets of fluid in a microfluidic device.
Electrowetting on dilectric (EWOD) is a well-known technique for manipulating droplets of fluid by application of an electric field. Active Matrix EWOD (AM-EWOD) refers to implementation of EWOD in an active matrix array incorporating transistors, for example by using thin film transistors (TFTs). It is thus a candidate technology for digital microfluidics for lab-on-a-chip technology. An introduction to the basic principles of the technology can be found in “Digital microfluidics: is a true lab-on-a-chip possible?”, R. B. Fair, Microfluid Nanofluid (2007) 3:245-281).
The microfluidic system further may include a control system configured to control actuation voltages applied to the electrode array of the microfluidic device to perform manipulation operations to the fluid droplets. For example, the reader 32 may contain such a control system configured as control electronics 38 and a storage device 40 that may store any application software and any data associated with the system. The control electronics 38 may include suitable circuitry and/or processing devices that are configured to carry out various control operations relating to control of the AM-EWOD device 36, such as a CPU, microcontroller or microprocessor.
In the example of
In the AM-EWOD device 36, a non-polar fluid 60 (e.g. oil) may be used to occupy the volume not occupied by the liquid droplet 52. An insulator layer 62 may be disposed upon the lower substrate 44 that separates the conductive element electrodes 48A and 48B from a first hydrophobic coating 64 upon which the liquid droplet 52 sits with a contact angle 66 represented by θ. The hydrophobic coating is formed from a hydrophobic material (commonly, but not necessarily, a fluoropolymer). On the top substrate 54 is a second hydrophobic coating 68 with which the liquid droplet 52 may come into contact. The reference electrode 58 is interposed between the top substrate 54 and the second hydrophobic coating 68.
The contact angle θ for the liquid droplet is defined as shown in
In operation, voltages termed the EW drive voltages, (e.g. VT, V0 and V00 in
For the purposes of driving and sensing the array elements, the electrical load 70A/70B overall functions in effect as a capacitor, whose value depends on whether a liquid droplet 52 is present or not at a given element electrode 48. In the case where a droplet is present, the capacitance is relatively high (typically of order pico-Farads), whereas if there is no liquid droplet present the capacitance is low (typically of order femto-Farads). If a droplet partially covers a given electrode 48 then the capacitance may approximately represent the extent of coverage of the element electrode 48 by the liquid droplet 52.
U.S. Pat. No. 7,163,612 (Sterling et al., issued Jan. 16, 2007) describes how TFT based thin film electronics may be used to control the addressing of voltage pulses to an EWOD array by using circuit arrangements very similar to those employed in active matrix display technologies. The approach of U.S. Pat. No. 7,163,612 may be termed “Active Matrix Electrowetting on Dielectric” (AM-EWOD). There are several advantages in using TFT based thin film electronics to control an EWOD array, namely:
A serial interface 82 may also be provided to process a serial input data stream and facilitate the programming of the required voltages to the element electrodes 48 in the array 50. A voltage supply interface 84 provides the corresponding supply voltages, top substrate drive voltages, and other requisite voltage inputs as further described herein. A number of connecting wires 86 between the lower substrate 44 and external control electronics, power supplies and any other components can be made relatively few, even for large array sizes. Optionally, the serial data input may be partially parallelized. For example, if two data input lines are used the first may supply data for columns 1 to X/2, and the second for columns (1+X/2) to M with minor modifications to the column driver circuits 76. In this way the rate at which data can be programmed to the array is increased, which is a standard technique used in liquid crystal display driving circuitry.
The array element circuit 72 may typically perform the functions of:
Various methods of controlling an AM-EWOD device to sense droplets and perform desired droplet manipulations have been described. For example, US 2017/0056887 (Hadwen et al., published Mar. 2, 2017) describes the use of capacitance detection to sense dynamic properties of reagents as a way for determining the output of an assay. Such disclosure incorporates an integrated impedance sensor circuit that is incorporated specifically into the array element circuitry of each array element. Accordingly, attempts have been made to optimize integrated impedance sensing circuitry 90 of
The use of functionalized magnetically responsive particles as solid phases in bio-affinity assays, or for the removal of contaminants from sample droplets, has been documented. Magnetically responsive particles may be derivatized or bound with target particles such as antibodies, receptors, nucleic acids and the like. Typically, such magnetically responsive particles may be paramagnetic or super paramagnetic and will typically have no magnetic memory in the sense that the particles are magnetically responsive while a magnetic field is applied, but do not remain magnetized once the magnetic field is removed. Under the influence of a magnetic field, the magnetically responsive particles become magnetic and as a result have a tendency to aggregate, which can be used to aggregate target species or particles that may be associated with or bound to the magnetically responsive particles.
For example, U.S. Pat. No. 5,523,231 (Reeve, issued Jun. 4, 1996) describes a method to isolate macromolecules using magnetically attractable beads, although in such processing the beads do not specifically bind to the macromolecules. U.S. Pat. No. 7,439,014 (Pamula et al., issued Oct. 21, 2008) describes a method of droplet-based surface modification and washing using magnetically responsive beads. The step of separating the magnetically responsive beads from a liquid droplet is performed by gathering the beads within a region of a liquid droplet using a magnetic field, and then splitting the droplet by electrowetting operations to isolate the portion of the droplets containing the beads. U.S. Pat. No. 8,093,064 (Shah et al., issued Jan. 10, 2012) describes a similar method, with the additional feature that the meniscus of the droplet is moved back and forth to lift beads from the surface. The process described in U.S. Pat. No. 7,439,014, and comparable conventional processes, are deficient. Because magnetic particle separation is performed by splitting the droplet with an electrowetting operation, such conventional methods result in a significant volume of the liquid from the droplet accompanying the beads after splitting, which is undesirable as maximum isolation of the beads (and any associated target particles) is desired. In addition, the washing and separating process requires a substantial footprint on the EWOD device array relative to the overall array area. This limits the space that can be used for other EWOD operations, and this reduces the overall efficiency and usefulness of the EWOD device.
There is a need in the art, therefore, for an improved system and method for AM-EWOD or EWOD device operation that achieves the selective separation of magnetically responsive particles from a liquid droplet within a microfluidic device, while simultaneously ensuring a large proportion of the magnetically responsive particles are effectively separated from the droplet (high bead capture efficiency), and the magnetically responsive particles are separated combined with a minimal volume of liquid. The present application describes methods for separating magnetically responsive beads or particles from a liquid droplet that achieves such results in an enhanced manner as compared to conventional configurations. In embodiments of the present application, the bead separation step is performed by varying a magnetic field in time, so as to remove the beads from the liquid droplet by applying a magnetic field to apply a force to move the beads from the liquid droplets, rather than using the electrowetting forces to achieve separation by splitting the liquid droplet as done in conventional processes.
An aspect of the invention is a method of operating an EWOD device to employ a magnetic field to separate magnetically responsive particles from a polar liquid droplet. In exemplary embodiments, the method includes the steps of dispensing a liquid droplet onto an element array of the EWOD device, wherein the liquid droplet includes magnetically responsive particles; performing an electrowetting operation to move the liquid droplet along the element array to a location relative to a magnet element in proximity to that location of the EWOD device; operating the magnet element to apply a magnetic field to the liquid droplet, wherein at least a portion of the magnetically responsive particles aggregate within the liquid droplet in response to the magnetic field; and separating the aggregated magnetically responsive particles from the liquid droplet with the magnetic field, wherein the aggregated magnetically responsive particles move in response to the magnetic field to a location on the element array in proximity to the magnet element. (As described below, separating the aggregated magnetically responsive particles from the liquid droplet with the magnetic field may occur either before or after the aggregated magnetically responsive particles move in response to the magnetic field to a location on the element array in proximity to the magnet element.) Embodiments of the methods of the present application may be performed by an EWOD control system executing program code stored on a non-transitory computer readable medium.
Embodiments of the present application have significant advantages over conventional processing. The described embodiments selectively separate magnetically responsive particles from a droplet of polar fluid with a minimal volume of polar fluid accompanying the magnetically responsive particles. Enhanced efficiency of collection of magnetically responsive particles may be achieved by the capability to perform repeated magnetic capture steps. Minimized surface area, i.e., a minimal number of array elements occupied by the separation step, within the microfluidic cartridge is used to achieve successful separation of the magnetically responsive particles. There also is a reduced likelihood of any magnetically responsive particles becoming irreversibly embedded in the microfluidic device surfaces.
These and further features of the present invention will be apparent with reference to the following description and attached drawings. In the description and drawings, particular embodiments of the invention have been disclosed in detail as being indicative of some of the ways in which the principles of the invention may be employed, but it is understood that the invention is not limited correspondingly in scope. Rather, the invention includes all changes, modifications and equivalents coming within the spirit and terms of the claims appended hereto. Features that are described and/or illustrated with respect to one embodiment may be used in the same way or in a similar way in one or more other embodiments and/or in combination with or instead of the features of the other embodiments.
Embodiments of the present invention will now be described with reference to the drawings, wherein like reference numerals are used to refer to like elements throughout. It will be understood that the figures are not necessarily to scale.
Embodiments of the present application provide for an improved system and method for AM-EWOD or EWOD device operation that achieves the selective separation of magnetically responsive beads or particles from a liquid droplet within a microfluidic device, while simultaneously ensuring a large proportion of the beads are effectively separated from the droplet (high bead capture efficiency), and the magnetically responsive particles or beads are separated combined with a minimal volume of liquid from the droplet. The present application describes a method for separating magnetically responsive beads or particles from a liquid droplet that achieves such results in an enhanced manner as compared to conventional configurations. In embodiments of the present application, the separation step is performed by varying a magnetic field in time, so as to remove the magnetically responsive particles from the liquid droplet by applying a magnetic field to apply a force to move the beads from the liquid droplets, rather than using the electrowetting forces to achieve separation by splitting the liquid droplet as done in conventional processes.
The microfluidic instrument 104 is configured to receive the microfluidic cartridge 102 and is designed to make insertion and removal of a microfluidic cartridge straightforward for the user. The microfluidic instrument 104 includes a second electrical connector 114 that mates with the first electrical connector 112 to permit the electrical signals to be exchanged between the microfluidic cartridge 102 and the microfluidic instrument 104. The microfluidic instrument 104 further includes docking features 116a and 116b for mechanically supporting and positioning the microfluidic cartridge 102 during insertion and removal. The docking features may interact with housing features 118 of the microfluidic cartridge 102 to aid in the insertion, removal, and positioning of the microfluidic cartridge 102 within the microfluidic instrument 104. It will be appreciated that any suitable configuration of docking features and cooperating housing features may be employed. Docking may be achieved by sliding insertion, clamping, or any other mechanical means suitable for positioning the microfluidic cartridge within the instrument.
The microfluidic instrument 104 may have a benchtop format, that for example is designed for use in an analytical laboratory. The microfluidic instrument 104 also may be miniaturized into a hand-held format that for example is appropriate for point-of-care applications in medical treatment facilities. The microfluidic instrument 104 includes components that permit control of the microfluidic cartridge 102 to perform a variety of chemical and biochemical reaction protocols and scripts by AM-EWOD operation. The microfluidic instrument 104, therefore, may include the following components: control electronics for supplying voltage supplies and timing signals for controlling actuation and de-actuation of the AM-EWOD array elements; heater elements 120 for heating portions of the AM-EWOD array elements to control the temperature of the liquid droplets, which is desired or required for certain reaction protocols; optical components or sensors 122 that measure optical properties of droplets on the AM-EWOD element array; magnet elements 124 for applying magnetic fields to the liquid droplets and the AM-EWOD element array; and features for liquid input or extraction, such as for example pipettes incorporated into the microfluidic instrument. The optical components 122 may include both light sources, such as for example light-emitting diodes (LEDs) or laser diodes, for illuminating liquid droplets, and also detection elements, such as for example photodiodes or other image sensors for detecting the optical signals returned from the liquid droplet. Optical measurements of liquid droplets may employ sensing techniques such as absorbance, fluorescence, chemiluminescence, and the like.
As to the magnets 124, as referenced above many reaction protocols employ the use of magnetically responsive particles, such as magnetic beads, within liquid droplets to perform purification or “washing” steps. By using magnetic fields applied from magnets in the microfluidic instrument, magnetic beads may be clumped together or released and be moved through the body of the liquid droplet to perform such washing steps. More specifically, the use of functionalized magnetically responsive particles may be used as solid phases in bio-affinity assays, or for the removal of contaminants from sample droplets. Magnetically responsive particles may be derivatized or bound with target particles such as antibodies, receptors, nucleic acids and the like. Typically, such magnetically responsive particles are paramagnetic or super-paramagnetic and have no magnetic memory in the sense that the particles are magnetically responsive while a magnetic field is applied, but do not remain magnetized once the magnetic field is removed. Under the influence of a magnetic field, the magnetically responsive particles become magnetic and as a result have a tendency to aggregate, which can be used to aggregate target species or particles that may be associated with or bound to the magnetically responsive particles. The size and materials used for the beads used is application dependent. Typically beads will have diameters in the range 5 nm-100 nm, though in some applications larger beads may be employed (diameters in the micron range). Typically, beads include a magnetic core (e.g. iron oxide) surrounded by a polymer, and are coated with bio-molecules designed to capture a species of interest, for example streptavidin for an immunoassay or oligonucleotide capture probes if the bead is designed to capture DNA.
The magnets 124 may be permanent magnets that are moveable in a direction perpendicular to the microfluidic cartridge 102 so as to be closer to or withdrawn from the microfluidic cartridge 102. When in the close or elevated position, a magnetic field is applied to the microfluidic cartridge 102 and any droplets located on the microfluidic cartridge in the area of one of the magnets. When the magnets are withdrawn away from the microfluidic cartridge 102, the magnetic field becomes insignificant and thus no significant magnetic force is applied to any magnetic beads residing within any liquid droplets within the microfluidic cartridge. The magnets may be moved between the elevated close position and the withdrawn position by any suitable driving mechanism 125. In an alternative embodiment, the magnets may be electromagnets that are turned on or off to selectively apply a magnetic field to the microfluidic cartridge.
The microfluidic cartridge 102 includes a two-dimensional active matrix array of array elements having electrodes on which the droplets are manipulated, such as described above with respect to
Accordingly, the control system 126 may execute program code embodied as a control application stored within the storage device 138. It will be apparent to a person having ordinary skill in the art of computer programming, and specifically in application programming for electronic control devices, how to program the control system to operate and carry out logical functions associated with the stored control application. Accordingly, details as to specific programming code have been left out for the sake of brevity. The storage device 138 may be configured as a non-transitory computer readable medium, such as a random access memory (RAM), a read-only memory (ROM), an erasable programmable read-only memory (EPROM or Flash memory), or any other suitable medium. Also, while the code may be executed by control system 126 in accordance with an exemplary embodiment, such control system functionality could also be carried out via dedicated hardware, firmware, software, or combinations thereof, without departing from the scope of the invention.
The control system may be configured to perform some or all of the following functions:
The control system 126, such as via the instrument electronics 128, may supply and control the actuation voltages applied to the electrode array of the microfluidic cartridge 102, such as required voltage and timing signals to perform droplet manipulation operations and sense liquid droplets on the AM-EWOD element array. The control system further may execute the application software to generate and output control voltages for droplet sensing and performing sensing operations.
The various methods described herein pertaining to enhanced microfluidic operation may be performed using AM-EWOD structures and devices described with respect to
As referenced above, the microfluidic instrument includes at least one magnet element 160 that is either physically moveable or electromagnetically operable to selectively apply a magnetic field to the microfluidic cartridge 102.
In use, the microfluidic cartridge 102 is operated to manipulate droplets of polar fluid 156 dispersed within the non-polar fluid 154 within the reaction chamber 152 by a process of electrowetting. In general, when a droplet of polar fluid 156 is caused to move by electrowetting, the droplet will adopt a nominally square edged profile (although other shape profiles may be achieved according to the activation pattern of respective TFT array elements), which is influenced by the generally square shaped profile of each TFT element within the device array. Thus, when a droplet of polar fluid 156 is caused to move by electrowetting, the droplet tends to adopt an edge profile shape according to the pattern of TFT elements that are actuated during the electrowetting process. In the absence of any actuated TFT elements, a droplet of polar fluid 156 typically adopts a nominally circular profile within the non-polar fluid 154. This “relaxed” shape profile is influenced by the relative surface tension difference between the respective fluids within the microfluidic cartridge 102.
As referenced above, the magnetic element 160 may be moved by any suitable driving mechanism (e.g., element 125 of
An aspect of the invention is a method of operating an EWOD device to employ a magnetic field to separate magnetically response particles from a polar liquid droplet. In exemplary embodiments, the method includes the steps of dispensing a liquid droplet onto an element array of the EWOD device, wherein the liquid droplet includes magnetically responsive particles; performing an electrowetting operation to move the liquid droplet along the element array to a location relative to a magnet element of the EWOD device; operating the magnet element to apply a magnetic field to the liquid droplet, wherein at least a portion of the magnetically responsive particles aggregate within the liquid droplet in response to the magnetic field; and separating the aggregated magnetically responsive particles from the liquid droplet with the magnetic field, wherein the aggregated magnetically responsive particles move in response to the magnetic field to a location on the element array in proximity to the magnet element. Embodiments of the methods of the present application may be performed by an EWOD control system executing program code stored on a non-transitory computer readable medium.
When magnet element 160 is vertically farthest from the surface of the TFT substrate, the magnet element 160 has little or no influence on any magnetically responsive particles 158 present within droplet of polar fluid 156 present in reaction chamber 152. This is so even when the droplet of polar fluid 156 containing the magnetically responsive particles 158 is directly over the location of magnet element 160. When magnet element 160 is about 7 mm in a vertical plane below the surface of the TFT substrate, the magnet element is about 8 mm on the diagonal from a droplet of polar fluid 156 that is located 4 mm horizontally away from the position of magnet element 160 on which the TFT array elements are disposed. Under such arrangement, no aggregation of magnetically responsive particles 158 within droplet of polar fluid 156 is observed.
When magnet element 160 is in the elevated or close position, such that the magnet element is brought into proximity with the external surface of microfluidic cartridge 102, the influence of the magnetic field creates a force on the magnetic particles, the force being related to the gradient of the magnetic field in the locality of the bead. This force is sufficient to cause magnetically responsive particles 158 within droplet of polar fluid 156 to initially aggregate at the edge of droplet of polar fluid 156 that is closest to the location of magnet element 160, and ultimately “jump” from the droplet 156 to be directly above and in proximity to the location of magnet element 160 on the element array 162. As referenced above, magnet element 160 alternatively may be configured as an electromagnet, which may be operated to produce a time variable magnetic field which may facilitate control over the lateral distance over which the magnetically responsive particles 158 may be caused to move under the influence of the magnetic field. The magnet element 160 may be a permanent magnet located on an actuator that raises and lowers the tip of the magnet to bring the magnet sufficiently close to the TFT element array 162 so that the magnetically responsive particles 158 may be moved from a droplet to the position in proximity to the magnet element. When a permanent magnet is used, the magnet may be shaped to control the field line pattern. To maximize the magnetic field strength/field strength gradient, a permanent magnet made from a material of high magnetic strength, such as for example neodymium, may be employed.
Referring more specifically to
As shown in
As shown in
In practice, the first removal of an aggregation 164 of magnetically responsive particles 158 may not include all such particles located within the polar droplet 156, and a substantial number of magnetically responsive particles still may remain within the droplet 156. Accordingly, the process of
When the number of magnetically responsive particles 158 within the polar droplet 156 is or becomes insufficient for the magnetic field to remove an aggregation of said particles from the droplet, in an exemplary embodiment a step may be performed to add more magnetically responsive particles to the droplet. The added magnetically responsive particles may not participate in any of the active processes that the original magnetically responsive particles are intended to perform (i.e., the magnetically responsive particles do not bind to or interact with a target species). Rather the added magnetically responsive particles serve to ensure that the droplet 156 contains a sufficient number of magnetically responsive particles to aggregate, and subsequently move under the influence of the magnetic field from the liquid droplet 156 toward the magnet element 160. Accordingly, the addition of further magnetically responsive particles increases the likelihood of transferring as many of the original magnetically responsive particles as possible out of the droplet 156 under the influence of magnet element 160. An advantageous example adds magnetically responsive particles that are of a relatively large size as compared to the original magnetically responsive particles. Large sized magnetically responsive particles are highly susceptible to the magnetic field, and thus may be used to efficiently aggregate or “mop-up” any remaining original small sized magnetically responsive particles that participate in the reaction activity.
Under certain conditions, it has been observed that the influence of magnet element 160 may be such that rather than cause magnetically responsive particles 160 to break through the meniscus between non-polar fluid 154 and the polar droplet 156, the magnetic field instead may cause the entire droplet 156 to be pulled toward magnet element 156 until the polar droplet 156 rests over the location of magnet element 160, such that the magnetically responsive particles 158 come as close to magnetic element 160 as may be possible. Removal may then result once the droplet 156 is moved to sufficiently close proximity to the magnet element 160.
In an alternative embodiment, prior to commencing the process of removal of magnetically responsive particles 158 from the droplet of polar fluid 156, the droplet 156 may be manipulated within reaction chamber 152 under electrowetting activation while magnet element 160 is in an elevated position. During the manipulation phase, the magnetically responsive particles 158 may be caused to generally aggregate within droplet of polar fluid 156 but are not removed therefrom. Magnet element 160 may then be moved to a lowered position, before the droplet of polar fluid 156 is moved to the location from which magnetic particle removal is intended to occur, and electrowetting activation removed, before magnet element 160 is once again raised to the elevated position shown in
The first magnet element 160a may be employed to aid in aggregating the magnetically responsive particles 158 within the droplet 156. As shown in
As shown in
As shown in
As shown in
There may come a time when removal of the magnetically responsive particles 158 from the polar droplet 156 becomes desirable. As shown in
As shown in
In accordance with such principles, any suitably shaped droplet profile may be formed using electrowetting actuation according to the specific requirements of an assay or reaction protocol being performed. Generally, it is observed that droplet profiles that present a straight edge toward the location of magnet element 160 while actuated result in an accumulation of magnetically responsive particles 158 along the meniscus of droplet of polar fluid 156 closest to the location of magnet element 160 when magnet element is raised into elevated position. With such straight edge orientation toward the magnet element, the magnetically responsive particles 158 typically are unable to overcome the droplet surface tension, and thus are unable to break through the straight edge of an actuated polar droplet 156. This process can be used to perform a prolonged aggregation step to increase the proportion of aggregated magnetically responsive particles. On the other hand, when a droplet of polar fluid 156 is actuated by the electrowetting forces to have a non-straight edge, such as a corner or point, oriented toward the magnet element, then the magnetically responsive particles 158 typically may accumulate and subsequently break through the surface tension of polar droplet 156 at the non-straight edge. Thus, the magnetically responsive particles may be removed through the point or corner of droplet 156 and locate in an aggregation over the location of magnet element 160.
Furthermore, when the population of magnetically responsive particles 158 within a droplet of polar fluid 156 is below a sufficient number, when such a droplet is located at a defined distance from a magnet element 160 in the absence of electrowetting actuation, the magnetically responsive particles 158 initially accumulate along the edge of the droplet closest to the location of magnetic element 160. With such insufficient number, the mass of magnetically responsive particles is insufficient to break through the meniscus to escape droplet of polar fluid 156. Rather, in such circumstances, the magnetic field effect on the accumulated magnetically responsive particles may be such that rather than breaking through the meniscus, the entire droplet of polar fluid 156 is pulled through non-polar fluid 154 toward the location of magnet element 160.
The processes described above may be employed in connection with sensing structures to enhance the separation of the magnetically responsive particles with the magnet elements. Such sensing structures and methods are described in Applicant's U.S. application Ser. No. 16/298,063 filed on Mar. 11, 2019, the contents of which are incorporated herein by reference. Sensing may sense the location of a droplet of polar fluid 156 and/or magnetic element 160 relative to reaction chamber 152. The microprocessor within the EWOD control system may therefore be programmed to detect and therefore accurately position the polar droplets 156 at any spatial location within reaction chamber 152 by electrowetting operations. The system is thus capable of ensuring droplets of polar fluid 156 are moved to a defined distance both horizontally (x) and vertically (y) within reaction chamber 152 relative to the location of magnet element 160, such that processes performed within different devices can occur with a high degree of reproducibility.
The system also may use real-time sensor feedback regarding the position of a droplet of polar fluid 156 relative to magnet element 160. As described above, under certain circumstances, typically when the number of magnetically responsive particles 158 within a droplet of polar fluid 156 has been reduced following removal of a portion thereof, the entire droplet may begin to be dragged toward the location of magnet element 160. There is a need to prevent the separated magnetically responsive particles 158 from being returned into the droplet of polar fluid 156 from which they were removed. To accomplish such result, when the sensor feedback indicates a droplet of polar fluid 156 is approaching the location of the excised magnetically responsive particles 158, the system may be programmed to either lower magnet element 160, thereby removing the magnetic field and thus preventing further dragging of the droplet, and/or electrowetting actuation may be applied to move the droplet of polar fluid 156 to a location at which the magnetic field has a negligible effect. The position of the magnet element 160 relative to the electrowetting array also may be determined by the sensor structures, as also described in the '063 application.
Another co-owned application of the Applicant is U.S. Publication No. 2018/0284423, which describes a method of controlling the spatial position of a droplet within an EWOD device, through use of selective application of electrowetting activation in combination with sensor feedback. When a droplet that is not actively under electrowetting control has moved beyond a predefined distance from a location within the reaction chamber 152, sensor feedback causes the system to apply electrowetting activation to reposition the droplet to the desired location, before electrowetting actuation is again removed.
As an example of sensor operation,
In the example of
In another exemplary embodiment, a polar droplet is processed to decrease the surface tension with the non-polar fluid, prior to operating the magnet element to apply the electric field for performing the separation step as to the magnetically responsive particles. This increases the ability of the magnetically responsive particles to transfer from the droplet successfully, more easily penetrating the outer meniscus caused by the surface tension. Decreasing the surface tension may be achieved by changing the temperature or adding an additional droplet containing a surfactant to the original droplet before performing the separation operation.
Embodiments of the present application have significant advantages over conventional processing. The described embodiments selectively separate magnetically responsive particles from a droplet of polar fluid with a minimal volume of polar fluid accompanying the separated magnetically responsive particles. Enhanced efficiency of collection of magnetically responsive particles may be achieved by the capability to perform repeated magnetic capture steps. Minimized surface area, i.e., a minimal number of array elements occupied by the separation step, within the microfluidic cartridge is used to achieve successful separation of the magnetically responsive particles, which permits use of other areas of the device for other reaction steps. There also is a reduced likelihood of any magnetically responsive particles becoming irreversibly embedded in the microfluidic device surfaces.
The following describes examples, which are non-limiting, of use of the embodiments of the present application. In one example, embodiments of the present application may be used for isolation of a target nucleic acid. A sample suspected of containing a target nucleic acid of interest is provided within a microfluidic device, for example such as described above with reference to
Magnetically responsive particles are provided within a second droplet, which is dispensed into the reaction chamber of the microfluidic device. The sample droplet is subsequently merged with the magnetically responsive particle containing droplet, and the droplets are mixed to ensure a homogeneous distribution of the magnetically responsive particles within the sample suspected of containing a nucleic acid of interest. The magnetically responsive particles provided in the system are previously prepared such that they will selectively bind to the target nucleic acid of interest, if present in the sample.
Once the magnetically responsive particles have been incubated within the sample for enough time to ensure capture of nucleic acid on the magnetically responsive particles, the droplet is brought into proximity of a magnetic element contained within the microfluidic device. Magnetically responsive particles that have acquired the target nucleic acid are thus aggregated above the location of the magnetic element, and separated away from the initial droplet that may contain contaminants according to any of the embodiments described above.
Following extraction of magnetically responsive particles carrying target nucleic acid from the initial sample droplet, the magnet element may be lowered before a droplet of clean buffer is moved by electrowetting to engulf the aggregated magnetically responsive particles. By a process of agitation, the magnetically responsive particles may then be re-suspended throughout the volume of the droplet. If warranted, as described above according to certain embodiments, a further cycle of aggregating the magnetically responsive particles above the magnetic element, followed by re-dispersion into another droplet of buffer, may be performed.
When the magnetically responsive particles populated with the target nucleic acid of interest have been sufficiently washed, the magnetically responsive may then be transferred into an elution droplet. Initially the magnetically responsive particles are again aggregated above the magnetic element before being re-suspended into a droplet of elution buffer, which contains an agent that will release the target nucleic acid from the surface of the magnetically responsive particles. The particles are again aggregated above the magnetic element to yield a droplet that contains only the target nucleic acid of interest, diluted in elution buffer. The droplet containing purified nucleic acid subsequently may be subjected to a range of processes, including but not limited to, nucleotide sequencing, polymerase chain reaction, isothermal amplification, and the like.
In another example, embodiments of the present application may be used for performing an immunoassay. A sample suspected of containing a target of interest may be subjected to an immunoassay within a microfluidic device, for example such as described above with reference to
Sample droplets suspected of containing the target of interest are introduced into the reaction chamber. Sample droplets are subsequently mixed with droplets containing the capture antibody modified magnetically responsive particles, along with labelling antibodies. Droplets are then mixed and allowed to incubate to ensure capture of target species on the magnetically responsive particle immobilized antibody, and subsequent labelling thereof. After sufficient incubation, the sample droplet is moved into proximity of a magnetic element contained within the microfluidic device to separate the magnetically responsive particle target complexes, away from the remainder of the sample and any unbound labelling antibodies, according to any of the embodiments described above. The magnetically responsive particles are subsequently re-suspended in a buffer, and a further aggregation step is performed before the magnetically responsive particles with associated target and labelling antibody are subsequently taken up into a detection droplet.
Detection may be performed in a number of ways as are known in the art, including for example fluorescence detection, luminescence detection, or electrochemical detection. When fluorescence detection is used, it is possible to perform multiplex assays, in which labelling antibodies against different targets are prepared with distinct fluorescent labels, which may be determined together in the same sample without interference. When electrochemical detection is used, an enzyme such as horse radish peroxidase, which converts a non-electrochemically active species, such as 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) in the presence of hydrogen peroxide to oxidized-ABTS, which can be determined electrochemically. The process of capture, washing and detection may thus be performed in multiplicate within the microfluidic device, using significantly lower total sample volume than might otherwise be achieved using more traditional assay formats, thereby increasing statistical confidence in the measurement result.
An aspect of the invention, therefore, is a method of operating an EWOD device to employ a magnetic field to separate magnetically responsive particles from a polar liquid droplet. In exemplary embodiments, the method includes the steps of dispensing a liquid droplet onto an element array of the EWOD device, wherein the liquid droplet includes magnetically responsive particles; performing an electrowetting operation to move the liquid droplet along the element array to a location relative to a magnet element of the EWOD device; operating the magnet element to apply a magnetic field to the liquid droplet, wherein at least a portion of the magnetically responsive particles aggregate within the liquid droplet in response to the magnetic field; and separating the aggregated magnetically responsive particles from the liquid droplet with the magnetic field, wherein the aggregated magnetically responsive particles move in response to the magnetic field to a location on the element array in proximity to the magnet element. The method of operating may include one or more of the following features, either individually or in combination.
In an exemplary embodiment of the method of operating, the method further includes removing an electrowetting force of the electrowetting operation from the liquid droplet prior to operating the magnet element to apply the magnetic field.
In an exemplary embodiment of the method of operating, the method further includes maintaining an electrowetting force on the liquid droplet to maintain the liquid droplet in an actuated state prior to operating the magnet element; performing an electrowetting operation to orient the actuated droplet with a straight edge facing the magnet element; operating the magnet element to apply the magnetic field to the liquid droplet, wherein at least a portion of the magnetically responsive particles aggregate within the liquid droplet in response to the magnetic field along the straight edge; and removing the electrowetting force to de-actuate the liquid droplet to separate the aggregated magnetically responsive particles from the liquid droplet with the magnetic field.
In an exemplary embodiment of the method of operating, the method further includes maintaining an electrowetting force on the liquid droplet to maintain the liquid droplet in an actuated state prior to operating the magnet element; performing an electrowetting operation to orient the actuated droplet with a non-straight edge facing the magnet element; and operating the magnet element to apply the magnetic field to the liquid droplet, wherein at least a portion of the magnetically responsive particles aggregate within the liquid droplet in response to the magnetic field along the non-straight edge; wherein the aggregated magnetically responsive particles separate from the liquid droplet at the non-straight edge in response to the magnetic field.
In an exemplary embodiment of the method of operating, the method further includes performing an electrowetting operation to move the liquid droplet along the element array to a location relative to a first magnet element and a second magnet element of the EWOD device; operating the first magnet element to apply a first magnetic field to the liquid droplet, wherein a portion of the magnetically responsive particles aggregate within the liquid droplet in response to the first magnetic field; performing another electrowetting operation to move the liquid droplet along the element array relative to the first magnet element, wherein additional magnetically responsive particles aggregate within the liquid droplet in response to the first magnetic field as the liquid droplet is moved relative to the first magnet element; operating the first magnet element to remove the first magnetic field from the liquid droplet; operating the second magnet element to apply a second magnetic field to the liquid droplet; and separating the aggregated magnetically responsive particles from the liquid droplet with the second magnetic field, wherein the aggregated magnetically responsive particles move in response to the second magnetic field to a location on the element array in proximity to the second magnet element.
In an exemplary embodiment of the method of operating, the method further includes removing an electrowetting force of the electrowetting operation prior to operating the second magnet element to apply the second magnetic field.
In an exemplary embodiment of the method of operating, multiple iterations of aggregation and separation of the magnetically responsive particles are performed in response to applying the magnetic field.
In an exemplary embodiment of the method of operating, the method further includes, when a number of remaining magnetically responsive particles is insufficient to separate from the liquid droplet in response to the magnetic field, adding additional magnetically responsive particles to the liquid droplet, wherein the aggregated magnetically responsive particles including the additional magnetically responsive particles separate from the liquid droplet in response to the magnetic field.
In an exemplary embodiment of the method of operating, aggregating the magnetically responsive particles within the liquid droplet in response to the magnetic field does not induce bulk movement of the liquid droplet. In an exemplary embodiment of the method of operating, the liquid droplet includes a polar liquid, and the liquid droplet is dispensed into a non-polar liquid on the element array of the EWOD device.
In an exemplary embodiment of the method of operating, the magnet element is a permanent magnet, and the magnet element is moved by an actuator 5 in the EWOD device relative to the element array from a withdrawn position to an elevated position to apply the magnetic field.
In an exemplary embodiment of the method of operating, the magnet element is an electromagnet, and the magnet element is operated from an off state to an on state to apply the magnetic field.
In an exemplary embodiment of the method of operating, the EWOD device further includes sensing circuitry, and the method further comprises reading the output of the sensing circuitry to determine a location of the magnet element and/or the liquid droplet to position the liquid droplet relative to the magnet element.
In an exemplary embodiment of the method of operating, the method further includes applying a voltage perturbation to the magnet element, and reading the output from the sensing circuitry in response to the voltage perturbation applied to the magnet element.
In an exemplary embodiment of the method of operating, the method further includes preventing return of the separated magnetically responsive particles to the liquid droplet by the steps of: employing sensor feedback to determine whether the liquid droplet has moved toward the magnet element; and performing an electrowetting operation to move the liquid droplet away from the magnet element and/or operating the magnet element to remove the electric field.
In an exemplary embodiment of the method of operating, the method further includes, prior to operating the magnet element, incubating the magnetically responsive particles for a sufficient time to bind the magnetically responsive particles to target particles.
In an exemplary embodiment of the method of operating, the method further includes increasing a viscosity of the liquid droplet prior to operating the magnet element to apply the magnetic field.
In an exemplary embodiment of the method of operating, the method further includes decreasing a surface tension of the liquid droplet prior to operating the magnet element to apply the magnetic field.
Another aspect of the invention is a microfluidic system that includes an electrowetting on dielectric (EWOD) device comprising an element array configured to receive a liquid droplet, the element array comprising a plurality of individual array elements; a magnet element operable to apply an electric field to the element array; and a control system configured to control actuation voltages applied to the element array to perform droplet manipulation operations, and to control operation of the magnet element to apply the electric field, to perform the method of operating an EWOD device according to any of the embodiments.
Another aspect of the invention is a non-transitory computer-readable medium storing program code which is executed by a processing device for controlling operation of an electrowetting on dielectric (EWOD) device, the program code being executable by the processing device to perform the method of operating an EWOD device according to any of the embodiments
Although the invention has been shown and described with respect to a certain embodiment or embodiments, equivalent alterations and modifications may occur to others skilled in the art upon the reading and understanding of this specification and the annexed drawings. In particular regard to the various functions performed by the above described elements (components, assemblies, devices, compositions, etc.), the terms (including a reference to a “means”) used to describe such elements are intended to correspond, unless otherwise indicated, to any element which performs the specified function of the described element (i.e., that is functionally equivalent), even though not structurally equivalent to the disclosed structure which performs the function in the herein exemplary embodiment or embodiments of the invention. In addition, while a particular feature of the invention may have been described above with respect to only one or more of several embodiments, such feature may be combined with one or more other features of the other embodiments, as may be desired and advantageous for any given or particular application.
The described embodiments could be used to provide an enhanced AM-EWOD device. The AM-EWOD device could form a part of a lab-on-a-chip system. Such devices could be used for optical detection of biochemical or physiological materials, such as for cell detection and cell counting. Applications include healthcare diagnostic testing, material testing, chemical or biochemical material synthesis, proteomics, tools for research in life sciences and forensic science.
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/EP2020/066408 | 6/12/2020 | WO | 00 |
Number | Date | Country | |
---|---|---|---|
62861536 | Jun 2019 | US |