WO2000051736A1 - Dual manifold system and method for parallel fluid transfer - Google Patents

Dual manifold system and method for parallel fluid transfer Download PDF

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Publication number
WO2000051736A1
WO2000051736A1 PCT/US2000/003922 US0003922W WO0051736A1 WO 2000051736 A1 WO2000051736 A1 WO 2000051736A1 US 0003922 W US0003922 W US 0003922W WO 0051736 A1 WO0051736 A1 WO 0051736A1
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WO
WIPO (PCT)
Prior art keywords
manifold
dual
liquid
recited
aspiration
Prior art date
Application number
PCT/US2000/003922
Other languages
French (fr)
Inventor
Mitchel J. Doktycz
William Louis Bryan
Reid Kress
Original Assignee
Ut-Battelle, Llc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ut-Battelle, Llc. filed Critical Ut-Battelle, Llc.
Priority to JP2000602395A priority Critical patent/JP4128336B2/en
Priority to DE60024973T priority patent/DE60024973T2/en
Priority to CA002364021A priority patent/CA2364021C/en
Priority to AU34924/00A priority patent/AU3492400A/en
Priority to AT00913483T priority patent/ATE313379T1/en
Priority to EP00913483A priority patent/EP1159072B1/en
Publication of WO2000051736A1 publication Critical patent/WO2000051736A1/en

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/02Burettes; Pipettes
    • B01L3/0241Drop counters; Drop formers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/0046Sequential or parallel reactions, e.g. for the synthesis of polypeptides or polynucleotides; Apparatus and devices for combinatorial chemistry or for making molecular arrays
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00277Apparatus
    • B01J2219/00279Features relating to reactor vessels
    • B01J2219/00306Reactor vessels in a multiple arrangement
    • B01J2219/00313Reactor vessels in a multiple arrangement the reactor vessels being formed by arrays of wells in blocks
    • B01J2219/00315Microtiter plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00277Apparatus
    • B01J2219/00351Means for dispensing and evacuation of reagents
    • B01J2219/00378Piezo-electric or ink jet dispensers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00583Features relative to the processes being carried out
    • B01J2219/00603Making arrays on substantially continuous surfaces
    • B01J2219/00659Two-dimensional arrays
    • CCHEMISTRY; METALLURGY
    • C40COMBINATORIAL TECHNOLOGY
    • C40BCOMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B60/00Apparatus specially adapted for use in combinatorial chemistry or with libraries
    • C40B60/14Apparatus specially adapted for use in combinatorial chemistry or with libraries for creating libraries
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N35/00Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
    • G01N35/02Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations
    • G01N35/028Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations having reaction cells in the form of microtitration plates
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/25Chemistry: analytical and immunological testing including sample preparation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/25Chemistry: analytical and immunological testing including sample preparation
    • Y10T436/2575Volumetric liquid transfer

Definitions

  • This invention relates generally to an apparatus and method for fabricating microarrays of biological samples on a support substrate, and more particularly to a dual manifold system for the rapid, parallel transfer of reagents to test substrates for large-scale screening assays.
  • DNA microarrays such as genosensors allow thousands of samples to be assessed simultaneously on a microelectronic test chip that is less than one- quarter of an inch in length per side. Typical test sites on such a chip are on the order of about 1 00 microns ( ⁇ m) in diameter.
  • the multiple degrees of freedom associated with the movement of individual system components significantly limits the positional accuracy of samples deposited on a target substrate.
  • the equipment is adapted for contact dispensing (i.e., where the dispense elements of the system physically contact the target substrate to effect transfer of the fluid to the target substrate) such limitations may be magnified.
  • dispense tip deformation can lead to irregular sample spacing and, in some instances, cross-contamination of adjacent test sites.
  • a dual-manifold assembly generally includes an aspiration manifold 1 0, a dispense manifold 20, and fluid transfer elements 80 for the parallel transfer of fluids therebetween.
  • the apparatus and method are adaptable for use transferring a variety of liquids to a variety of target substrates, in the preferred embodiment of the invention the apparatus is particularly suited for transferring chemical or biochemical reagents from an array of microtiter plate wells to an array of test sites on a chip-based biological sensor.
  • the aspiration manifold 10 is positioned above a source plate 50, such as a microtiter plate, and is adapted for simultaneously aspirating liquid, such as a chemical reagent, from an array of reservoirs 52.
  • the aspiration manifold includes an array of aspiration manifold subassemblies extending through a base plate 1 7 and adapted for being received by an array of reagent-filled wells 52.
  • each subassembly seals a single well such that fluid communication to and from the well is limited to a pair of conduits 1 2, 1 4 extending into the well.
  • each well is pressurized by a pressure source 40 through conduit 1 2 which urges the liquid 54 through conduit 1 4 toward dispense manifold 20.
  • the aspiration manifold has a gasket element 23 for sealing against the periphery of the microtiter plate 50 during operation, precluding the need to pressurize the wells individually.
  • pressurization of the wells 52 is accomplished through a single pressure conduit 1 2 extending through base plate 1 7.
  • a plurality of aspiration conduits communicate with the dispense manifold side of the assembly through a modular connector 90.
  • the modular connector includes a male component 94 which releasably engages a female component 92.
  • the aspiration conduits 1 4 terminate at component 94 which has integral tips 95 adapted for receipt by female component 92.
  • the female component 92 of the modular connector is integrated into valve assembly 21 .
  • Conduits 24, 26 and 38, of valve assembly 21 can also be adapted for modular connection with other subassemblies of the dual manifold system. For instance, although dispense manifold 20 can be directly integrated into valve assembly 21 , in the preferred embodiment of the invention dispense manifold 20 is adapted for modular connection to valve assembly 21 .
  • volumes of reagent in the range of about ( 1 0) "12 to about ( 1 0) "6 liters are ejected from the dispense manifold through an array of dispense manifold orifices 1 06 upon application of a force, such as a pressure pulse.
  • a pressure pulse is provided by a valve 28 incorporating ink jet style drop-on- demand technology.
  • Valve 28 may be adapted for modular connection to valve assembly 21 or, alternatively, valve 28 may be directly integrated into the valve assembly.
  • the dispense manifold 20 comprises a standard ink-jet style printing head having micro-machined channels each terminating at an orifice 1 06.
  • a purging apparatus 30 is provided for periodically purging the assembly.
  • Purging apparatus 30 includes gas and cleaning liquid inlets, 32 and 34 respectively, controllable through a solenoid or other suitable valve 36.
  • purging apparatus 30 is adapted for modular connection to valve assembly 21 .
  • apparatus 30 can be directly integrated into the valve assembly.
  • auxiliary features are included for improving registration and alignment of reagent samples deposited on the test chip.
  • fiducial pins and/or marks are integrated into the target substrate. The integrated features are sensed by a conventional vision system for ensuring proper alignment and orientation during operation.
  • detection means are provided for detecting the passage of a droplet 1 04 of reagent from a dispense orifice 1 06.
  • the detection means may comprise optoelectronic devices, such as a photodiode 1 00 / photodetector 1 02 pair positioned near each orifice.
  • electronic conduction-based sensors can be integrated into the dispense manifold.
  • microtiter plate 50 is positioned below the aspiration manifold 1 0 and the aspiration manifold is subsequently seated onto the plate such that an air-tight seal is formed between the aspiration manifold and the plate.
  • Microtiter plate wells 52 are pressurized by a pressure source 40 through at least one conduit 1 2 to effect the transfer of reagent through a plurality of conduits 1 4 and into dispense manifold 20 positioned above target substrate 60. Subsequently, a pressure pulse from valve 28 is communicated to the dispense manifold 20, effecting the transfer of a desired volume of reagent through orifice
  • test sites 64 on target substrate 60 Further embodiments of the method include aligning the target substrate to ensure proper positioning of the reagent deposits, detecting the passage of reagent samples from the orifices of the dispense manifold, and purging the system between deposition, or printing, operations.
  • FIG. 1 is a schematic of the major components of a dual manifold assembly in accordance with the present invention
  • FIG. 2 is a schematic of a particular arrangement of subcomponents of a dual-manifold assembly in accordance with a preferred embodiment of the present invention
  • FIG. 3 is a side view, partially in cross-section, of an aspiration manifold in accordance with a preferred embodiment of the present invention
  • FIG. 4 is a side view, partially in cross-section, of an aspiration manifold in accordance with an alternate embodiment of the present invention
  • FIG. 5 is a top view, partially cut away, of a preferred modular fluid connector in accordance with the present invention.
  • FIG. 6 is a front view of a female connector element of the modular fluid connector in FIG. 5;
  • FIG . 7 is a cross-sectional view of a droplet ejection detection apparatus in accordance with an alternate embodiment of the present invention.
  • a dual manifold assembly is provided for the rapid, parallel transfer of liquid from an array of reservoirs 52 to a target substrate 60. It will be apparent to one skilled in the art of microarray printing that the apparatus of the present invention lends itself to a variety of applications. Generally, the assembly is capable of transferring liquids from virtually any type of reservoir - including tubes, bottles and other liquid containers - to virtually any type of substrate.
  • the assembly is particularly suited for transferring chemical or biochemical reagents from an array of wells 52 of a conventional microtiter plate to an array of test sites 64 on a chip-based biological sensor (commonly referred to in the art as a "microarray") for performing screening assays.
  • the assembly is adaptable for printing arrays wherein the distance between adjacent test sites, or test site pitch, is in the range of about 1 micron ( ⁇ m) to about 1 0,000 microns ( ⁇ m).
  • the assembly includes aspiration and dispense manifolds, 1 0 and 20 respectively, separated by fluid transfer elements (generally denoted by reference numeral 80) .
  • the dual-manifold assembly is adapted for the automated printing of multiple analytical chips in succession.
  • a conventional microtiter plate feeder 70 is employed for advancing a series of microtiter plates beneath the aspiration manifold 1 0, and a target chip track 72 is employed for advancing test substrates 60 beneath the dispense manifold 20.
  • advancing is used to describe movement of the tracks 70,
  • the invention is not intended to be so limited.
  • either or both of the tracks can be adapted for movement in multiple directions.
  • the assembly is adapted for transferring reagent from a given number of reservoirs 52 to an equal number of test sites 64 and, accordingly, the assembly is designed for the one-to-one transfer of liquid, i.e., from each reagent reservoir to a designated test site.
  • the assembly can be configured for transferring liquid from a given number of reservoirs to a different number of test sites.
  • the dispense manifold 20 can be designed such that liquid samples from multiple aspiration reservoirs are combined and dispensed on a single test site.
  • the manifolding can be adapted for depositing liquid from a single reservoir to multiple test sites.
  • FIG. 2 A preferred embodiment of the dual-manifold assembly of the present invention is schematically illustrated in Figure 2. Although the assembly is adapted for simultaneously transferring multiple volumes of liquid reagent to multiple chip test sites, a clearer understanding of the invention can be gained through a description of the operation of the assembly with respect to the transfer of reagent from a single reservoir 52 to a single test site on target substrate surface 62. Accordingly, Figure 2 intentionally depicts a single set of fluid transfer elements.
  • a pneumatic source 40 provides controlled pressure to reservoir 52 through a conduit 1 2 extending into the reservoir, with conduit 1 2 terminating at a position above liquid level 56. The magnitude and duration of the pressure supplied to the reservoir can be adjusted by aspiration manifold valve 1 3.
  • Valve 1 3 is preferably a solenoid valve; however, other suitable valves are contemplated. For instance, other suitable valves may include shear valves, flat face valves and pinch valves, actuated by mechanical, electrical or pneumatic means.
  • conduits 1 2 and 1 4 comprise narrow-bore plastic tubing having an inner diameter preferably ranging from about .020 mm to about 2.0 mm.
  • conduits can be manufactured from other suitable materials capable of transferring the desired fluids without being degraded, including, but not limited to, metals and glass.
  • the aspiration manifold and dispense manifold sides of the assembly communicate through at least one modular fluid connector 90.
  • aspiration conduits 1 4 are bundled together and combined in a male component, or plug 94, adapted for releasably engaging a female connector portion 92.
  • the aspiration conduits could be combined in a female plug adaptable for connection with a male component.
  • the structure of a preferred modular connection is described in more detail below; however, numerous variations are possible without departing from the spirit and scope of the invention.
  • the modular connector 90 is depicted attached to a conduit 1 5 extending away from valve assembly 21 , it is preferred that the female connector portion 92 is integrated directly into valve assembly 21 . In this manner, the assembly of the present invention is adaptable for the simple and efficient attachment to myriad different aspiration manifold designs.
  • valve assembly 21 regardless of the structure of the aspiration manifold, the aspiration conduits are combined in a standard connector or plug 94 adapted for releasably engaging female connector portion 92.
  • connector 92 By integrating connector 92 into the valve assembly 21 , a single valve assembly 21 can be modularly connected to a variety of aspiration manifolds having different geometries, dimensions, and structures.
  • Valve assembly 21 includes a dispense manifold switching valve 22 which is preferably a flat face valve; however, other suitable valves are contemplated including, but not limited to, shear valves, solenoid valves and pinch valves, actuated by mechanical, electrical or pneumatic means.
  • Switching valve 22 is fluidly connected to an ejection means 28 for advancing liquid through channels (not shown) in the dispense manifold 20, to effect the ejection of a desired volume of the liquid onto the test substrate.
  • the ejection means delivers a pressure pulse having a pressure ranging from about 6.9(1 0) 3 N/m 2 to about 1 38(1 0) 3 N/m 2 , and having a duration ranging from about ( 1 0) ⁇ 6 seconds to about (1 0) "2 seconds.
  • the ejection means 28 comprises a conventional ink-jet style printing valve or pump designed for drop-on-demand printing. Ink-jet style printing valves/pumps for drop-on-demand printing, including thermal, solenoid and piezoelectric types, are commercially available and well known in the art. For instance, the Lee
  • valve assembly 21 which is suitable for use with the present invention.
  • ejection means 28 is shown connected to valve assembly 21 via a conduit 24, the ejection means can be adapted for releasable attachment to the valve assembly, via a modular connector 90, in a manner similar to the preferred aspiration manifold connection.
  • alternate valve arrangements are possible. For instance, an ink jet valve/pump 28 can be directly integrated into valve assembly 21 via conduit 26.
  • ink-jet drop-on-demand printing technology provides significant advantages visa-vis known systems for printing microarrays.
  • the ability to deliver the short-duration pressure pulses associated with ink-jet print valves enables the non-contact delivery of reagent sample volumes in the range of about (10) "12 to about ( 1 0) "6 liters.
  • a pressure pulse Upon application of a pressure pulse, at least one droplet of reagent is ejected through dispense manifold orifice 1 06 onto surface 62 of test substrate 60.
  • non-contact refers to the lack of contact between the dispense manifold and the target substrate during deposition.
  • liquid is communicated through channels micro-machined into an ink-jet style printhead - such as those commonly used in desktop and industrial printers - and each terminating at an orifice 1 06.
  • the orifices 1 06 can have diameters ranging from a minimum of about 1 micron ( ⁇ m) to a maximum of about 200 microns ( ⁇ m) .
  • the dispense manifold 20 is adapted for releasable attachment to the valve assembly 21 via a modular connector 90.
  • the modular connector can be integrated directly into switching valve 22. In this manner, the dispense manifold 20 can be fitted with a male connector portion 94 adapted for direct attachment to switching valve 22, precluding the need for conduit 26.
  • liquid transferred from a reservoir on the aspiration side of the liquid transfer assembly can be manifolded in such a manner that the liquid is ejected through multiple orifices on the dispense side of the assembly.
  • liquid from multiple reservoirs on the aspiration side of the assembly can be combined and ejected through a single dispense orifice.
  • the manifold assembly of the present invention also enables liquid to be transferred from a quantity of reservoirs to a quantity of test sites less than, equal to, or greater than the number of reservoirs. Accordingly, the array of printhead orifices can be dimensioned differently, or arranged in a different pattern, than the array of aspiration conduits 1 4 extending through the aspiration manifold 1 0.
  • the assembly can be adapted for transferring liquid from a non-linear array of reservoirs to a linear array of dispense manifold orifices, and vice-versa.
  • the assembly can be adapted for transferring liquid from a rectangular array to a radial array, and vice- versa.
  • array is also intended to encompass a plurality of reservoirs, conduits, orifices or test sites having non-symmetric patterns or variable pitches.
  • the printhead can also be adapted for being rotated during operation. Accordingly, the relative orientations of the aspiration manifold conduits 1 4 and dispense manifold orifices 1 06 can be varied.
  • the manifold structure of the present invention enables liquid to be transferred from an array of sample reservoirs having a minimum pitch on the order of millimeters to an array of orifices having a minimum pitch on the order of microns.
  • Auxiliary apparatus 30 may be provided for cleaning and purging the various fluid transfer conduits of the assembly.
  • a gas pressure conduit 32 and cleaning liquid conduit 34 may be fluidly connected, via conduit 38, to switching valve 22.
  • the introduction of cleaning/purging fluids into the system is controllable through a suitable valve 36, such as solenoid, shear, flat face and pinch valves, actuated by mechanical, electrical or pneumatic means.
  • purging apparatus 30 is fluidly connected to valve assembly 21 through a modular connector 90 integrated into the valve assembly.
  • purging apparatus 30 can be directly integrated into dispense manifold switching valve 22.
  • the aspiration manifold includes an array of aspiration subassemblies extending through a base plate 1 7 and adapted for being received by a corresponding array of liquid filled reservoirs 52 formed in a source plate 50.
  • the reservoirs comprise reagent-filled wells formed in a microtiter plate.
  • Each subassembly includes a guide member 1 6, a cap member 1 8, a pressure conduit 1 2 and an aspiration conduit 1 4.
  • Pressure and aspiration conduits 1 2 and 1 4 preferably comprise narrow-bore tubing constructed from plastic, metal or glass.
  • Guide member 1 6 has a first end adapted for being mechanically fastened to base plate 1 7.
  • mechanical fastening is achieved by providing guide member 1 6 with a first threaded end for easy mechanical insertion, i.e., twisting, into the base plate. It will be apparent to one skilled in the art that alternate mechanical fastening means are possible. Regardless of the fastening means employed, it is important that the guide member snugly engages the base plate to prevent movement of the guide member during operation of the assembly. When fully inserted, a second flanged end 1 1 of the guide member extends downward from a lower surface of the base plate. Guide member 1 6 also has a pair of longitudinally- extending channels (not shown) for snugly-receiving the plastic tubing.
  • Cap member 1 8 has a first end adapted for engaging the flanged end 1 1 of guide member 1 6. An opposite second end of the cap member has a tapered outer surface 1 9 for engaging the perimeter of one of the liquid-filled reservoirs 52.
  • the cap member is manufactured from a suitable polymer, rubber or other compressible material. In this manner, as aspiration manifold 1 0 is seated onto microtiter plate 50, the cap members act to seal the reservoirs.
  • Each cap member 1 8 is provided with longitudinally-extending channels aligning with the channels in a corresponding guide member 1 6 for receiving the plastic tube conduits. Pressure conduit 1 2 extends completely through cap member 1 8, but terminates above liquid level 56.
  • Aspiration conduit 1 4 extends through cap member 1 8, terminating at a position below liquid level 56.
  • aspiration manifold is seated onto microtiter plate 50 such that cap members 1 8 seal against the perimeter of corresponding wells 52.
  • the wells are pressurized by applying pneumatic pressure through pressure tubing 1 2, thereby urging the transfer of liquid reagent 54 from the wells 52, through aspiration tubing 1 4, toward the dispense manifold 20.
  • cap member 1 8 and guide member 1 6 comprise a unitary component, for example, molded from plastic or machined from metal.
  • cap and guide members 1 8 and 1 6, respectively are integrated into base member 1 7 such that the entire aspiration manifold assembly, except for the tubing, comprises a single, unitary component.
  • the entire aspiration manifold assembly can be molded from a suitable polymer or machined from a suitable metal.
  • an alternate embodiment of the aspiration manifold has a single pressure inlet 1 2 for pressurizing the wells 52.
  • a gasket member 23 preferably constructed from a suitable polymer, rubber or other compressible material, is disposed along the periphery of the underside of base plate 1 7.
  • sealing member 23 seals against the periphery of plate 50.
  • Individual aspiration conduits 1 4 extend into each of the liquid-filled reservoirs for transferring reagent from the wells to the dispense manifold.
  • modular connectors 90 provide fluid connection between the valve assembly 21 and various subassemblies of the dual manifold system. It will be apparent to one skilled in the art of connectors that myriad different modular connector designs are possible for use with the present invention. Referring now to Figure 5, a preferred connector design will now be described. For the purpose of simplicity, the following discussion is directed specifically to a single modular connector located between aspiration manifold 1 0 and valve assembly 21 . However, all of the modular connectors 90 can have similar structures and operate in a similar fashion. Modular connector 90 includes female and male components, 92 and 94, respectively.
  • Channels 96 formed in female subconnector 92 are adapted for releasably engaging integral connector tips 95 extending from male component, or plug, 94.
  • the individual channels/fittings 96 of the female unit have integral sealing elements 99, such as ribs, for preventing the leakage of fluids passing through the connector.
  • male connector 94 is fitted in female connector 92 such that the ends of tips 95 contact integral stop mechanisms 98.
  • the geometry of the connectors may vary. However, as illustrated in Figure 6, the individual connector units are preferably designed much like a standard electrical connector. In alternate embodiments of the present invention, auxiliary assembly features are included for improving registration and alignment of reagent samples dispensed on the target substrate and/or for improving quality control.
  • fiducial pins and/or marks are integrated into the target substrate and/or microtiter plate.
  • the integrated features can be directly sensed by a conventional vision system for ensuring proper alignment and orientation during operation.
  • the integrated features can be designed for interaction with position-sensitive detection electronics.
  • detection means are provided for detecting the passage of a droplet of reagent from a dispense orifice 1 06. For instance, referring now to Figure 7, photodiode
  • photodetector 1 02 devices can be positioned proximate to a dispensing orifice 1 06 to sense the passage of a droplet.
  • electronic conduction-based sensors can be incorporated directly into the dispense manifold, for example, by applying a conductive coating to portions of the inner wall of each orifice 1 06 and monitoring electrical current therebetween.
  • a source plate 50 such as a microtiter plate
  • target substrate 60 is advanced on track 72 until it is properly positioned beneath dispense manifold 20.
  • An optional alignment step may be performed to ensure proper positioning and orientation of the source plate, the target substrate or both.
  • cap members 1 8 of the aspiration subassemblies form a seal over the reservoirs.
  • the aspiration manifold 1 0 is vertically-actuated until gasket 23 seals against the periphery of source plate 50.
  • the aspiration and dispense manifolds are limited to vertical movement. With the aspiration manifold properly seated upon the source plate, pressure is introduced to the reservoirs from pressure source 40, via conduit(s) 1 2, to effect liquid transfer through conduits 1 4 toward dispense manifold 20.
  • switching valve 22 is actuated to disable fluid connection between the dispense manifold and the aspiration manifold, while enabling fluid communication between the dispense manifold and liquid ejection means 28.
  • dispense manifold 20 can be vertically positioned to a desired height above target substrate 60.
  • a force such as a pressure pulse, is communicated to the dispense manifold for a period of time to effect the ejection of a precise volume of liquid from the dispense manifold through orifices
  • the dispense manifold is maintained at a constant position during operation of the assembly.
  • a complete array of test sites are printed contemporaneously, and tracks 70 and 72 are each advanced after the printing of a single array.
  • liquid transferred from a single array of reservoirs may be adequate to dispense multiple arrays or sub-arrays of test sites.
  • printing can comprise repeatedly advancing test track 72 to reposition an array or sub-array of test sites beneath dispense manifold 20, while maintaining the position of feeder track 70.
  • other applications may require maintaining the position of test track 72 while advancing feeder track 70.
  • the method can include repositioning the reservoirs and/or test substrate via movement of the tracks 70, 72, such that the tracks are not "advanced " .
  • the step of positioning the dispense manifold can include the sub- step of rotating the printhead.
  • the method includes the additional step of detecting the passage of a droplet, or volume, of liquid from the array of dispense manifold orifices to the array of test sites.
  • the method includes periodically purging fluid transfer conduits of the assembly with a cleaning fluid such as water.

Abstract

A dual-manifold assembly is provided for the rapid, parallel transfer of liquid reagents from a microtiter plate to a solid state microelectronic device having biological sensors integrated thereon. The assembly includes aspiration and dispense manifolds connected by a plurality of conduits. In operation, the aspiration manifold is actuated such that the aspiration manifold is seated onto an array of reagent-filled wells of the microtiter plate. The wells are pressurized to force reagent through conduits toward the dispense manifold. A pressure pulse provided by a standard ink-jet printhead ejects nanoliter-to-picoliter droplets of reagent through an array of printhead orifices and onto test sites on the surface of the microelectronic device.

Description

DUAL MANIFOLD SYSTEM AND METHOD FOR PARALLEL FLUID TRANSFER
Statement Regarding Federally-Sponsored Research or Development This invention was made with government support under contract DE-AC05-96OR22464, awarded by the United States Department of Energy to
Lockheed Martin Energy Research Corporation, and the United States Government has certain rights in this invention.
Field of the Invention This invention relates generally to an apparatus and method for fabricating microarrays of biological samples on a support substrate, and more particularly to a dual manifold system for the rapid, parallel transfer of reagents to test substrates for large-scale screening assays.
Background of the Invention
In clinical chemistry, it is frequently necessary to carry out the metered application of an analytical liquid to a target. One case which is particularly relevant to the present invention is the application of the analytical liquid to an analysis element such as a chip-based biological sensor in which biological materials are integrated with microelectronic devices. In recent years, rapid technological advances have enabled the use of micro-scale chemical/ biochemical reactions for performing various types of analyses. For instance, DNA microarrays such as genosensors allow thousands of samples to be assessed simultaneously on a microelectronic test chip that is less than one- quarter of an inch in length per side. Typical test sites on such a chip are on the order of about 1 00 microns (μm) in diameter. Conventional applications of chip- based biological sensors include mutation diagnosis, organism identification and gene expression profiling. More recent applications, such as parallel screening of chemical compounds for drug discovery and protein arrays for functional analysis, will soon be routine. Known fluid handling systems for dispensing, or "micro-spotting", arrays of biological materials on a target substrate commonly comprise pick-and-place equipment. Generally, pick-and-place dispense systems include a dispense head adapted for transferring volumes of fluid from a fluid source to a target substrate. The time required to pick up, transfer and deposit a given volume of liquid significantly limits the efficiency of pick-and-place systems for micro- spotting. This lack of efficiency is even more pronounced where the target substrate contains hundreds, or even thousands, of test sites. Efforts have been made to improve the efficiency of pick and place systems for micro-spotting. For instance, systems have been adapted for picking up, transferring and depositing multiple sample volumes simultaneously. However, the time required for dispense head movement remains a significant limitation of such systems.
Furthermore, the multiple degrees of freedom associated with the movement of individual system components, such as the dispense head, significantly limits the positional accuracy of samples deposited on a target substrate. In instances where the equipment is adapted for contact dispensing (i.e., where the dispense elements of the system physically contact the target substrate to effect transfer of the fluid to the target substrate) such limitations may be magnified. In particular, dispense tip deformation can lead to irregular sample spacing and, in some instances, cross-contamination of adjacent test sites.
Due in part to the aforementioned limitations, the positional accuracy and liquid transfer volume capability of conventional pick-and-place dispensing systems can not meet the requirements of many evolving applications. Constructing microarrays having a higher degree of miniaturization will require an increase in test site array density. Realizing such an increase in density will require a reduction in sample spot size and spot pitch (i.e., the center-to-center distance between adjacent deposits) . In order to achieve such miniaturization, a fluid handling system capable of accurately and efficiently depositing chemical and biochemical reagent droplets having volumes on the order of picoliters is required. Technology for dispensing liquid volumes on the order of picoliters exists, but has been primarily limited to the field of ink-jet printing. Many drop-on- demand ink-jet ideas and systems were invented, developed, and produced commercially in the 1 970s and 1 980s. A detailed and comprehensive summary of state-of-the-art drop-on-demand ink-jet printing technologies, including the fabrication of ink-jet valves and printheads, is provided in a published article by Hue P. Le, entitled Progress and Trends in Ink-jet Printing (Journal of Imaging Science and Technology, Volume 42, Number 1 , pp. 49-62)(1 998) .
There is an established need for an apparatus and method for accurately and efficiently transferring and depositing, or printing, microarrays of reagent samples having volumes on the order of picoliters on a test substrate. It would be desirable to have a microarray printing apparatus for performing large-scale chemical/biochemical screening assays, wherein the system incorporates known drop-on-demand ink-jet printing technology and is particularly suited for dispensing chemical and/or biochemical reagents.
Summary of the Invention It is an object of this invention to provide a liquid transfer apparatus capable of accurately and efficiently transferring liquid reagents from an array of reservoirs to an array of sites on a target substrate It is another object of this invention to provide a liquid transfer apparatus capable of accurately and efficiently depositing volumes of liquid reagents in the range of about ( 1 0)~12 to about (1 0)"6 liters.
It is another object of this invention to provide a liquid transfer apparatus capable of effecting such reagent transfer with minimal movement of the apparatus during operation.
It is another object of this invention to provide a liquid transfer apparatus employing non-contact dispensing.
It is another object of this invention to provide a liquid transfer apparatus and method adapted for the automated printing, or micro-spotting, of multiple analytical chips in succession for performing large-scale screening assays. These and other objects are achieved with the assembly and method of the present invention. Briefly, according to the invention, a dual-manifold assembly generally includes an aspiration manifold 1 0, a dispense manifold 20, and fluid transfer elements 80 for the parallel transfer of fluids therebetween. Although the apparatus and method are adaptable for use transferring a variety of liquids to a variety of target substrates, in the preferred embodiment of the invention the apparatus is particularly suited for transferring chemical or biochemical reagents from an array of microtiter plate wells to an array of test sites on a chip-based biological sensor. The aspiration manifold 10 is positioned above a source plate 50, such as a microtiter plate, and is adapted for simultaneously aspirating liquid, such as a chemical reagent, from an array of reservoirs 52. In the preferred embodiment of the present invention, the aspiration manifold includes an array of aspiration manifold subassemblies extending through a base plate 1 7 and adapted for being received by an array of reagent-filled wells 52. When the aspiration manifold is seated onto the microtiter plate 50, each subassembly seals a single well such that fluid communication to and from the well is limited to a pair of conduits 1 2, 1 4 extending into the well. In operation, each well is pressurized by a pressure source 40 through conduit 1 2 which urges the liquid 54 through conduit 1 4 toward dispense manifold 20. In an alternate embodiment of the invention, the aspiration manifold has a gasket element 23 for sealing against the periphery of the microtiter plate 50 during operation, precluding the need to pressurize the wells individually. In this alternate embodiment, pressurization of the wells 52 is accomplished through a single pressure conduit 1 2 extending through base plate 1 7.
In the preferred embodiment of the invention, a plurality of aspiration conduits communicate with the dispense manifold side of the assembly through a modular connector 90. Generally, the modular connector includes a male component 94 which releasably engages a female component 92. Preferably, the aspiration conduits 1 4 terminate at component 94 which has integral tips 95 adapted for receipt by female component 92. Preferably, the female component 92 of the modular connector is integrated into valve assembly 21 . Conduits 24, 26 and 38, of valve assembly 21 , can also be adapted for modular connection with other subassemblies of the dual manifold system. For instance, although dispense manifold 20 can be directly integrated into valve assembly 21 , in the preferred embodiment of the invention dispense manifold 20 is adapted for modular connection to valve assembly 21 .
Volumes of reagent in the range of about ( 1 0)"12 to about ( 1 0)"6 liters are ejected from the dispense manifold through an array of dispense manifold orifices 1 06 upon application of a force, such as a pressure pulse. Preferably, a pressure pulse is provided by a valve 28 incorporating ink jet style drop-on- demand technology. Valve 28 may be adapted for modular connection to valve assembly 21 or, alternatively, valve 28 may be directly integrated into the valve assembly. In the preferred embodiment of the invention, the dispense manifold 20 comprises a standard ink-jet style printing head having micro-machined channels each terminating at an orifice 1 06.
In an alternate embodiment of the invention, a purging apparatus 30 is provided for periodically purging the assembly. Purging apparatus 30 includes gas and cleaning liquid inlets, 32 and 34 respectively, controllable through a solenoid or other suitable valve 36. Preferably, purging apparatus 30 is adapted for modular connection to valve assembly 21 . Alternatively, apparatus 30 can be directly integrated into the valve assembly.
In further embodiments of the invention, auxiliary features are included for improving registration and alignment of reagent samples deposited on the test chip. In particular, fiducial pins and/or marks are integrated into the target substrate. The integrated features are sensed by a conventional vision system for ensuring proper alignment and orientation during operation.
In yet a further embodiment of the invention, detection means are provided for detecting the passage of a droplet 1 04 of reagent from a dispense orifice 1 06. The detection means may comprise optoelectronic devices, such as a photodiode 1 00 / photodetector 1 02 pair positioned near each orifice. Alternatively, electronic conduction-based sensors can be integrated into the dispense manifold.
In operation, microtiter plate 50 is positioned below the aspiration manifold 1 0 and the aspiration manifold is subsequently seated onto the plate such that an air-tight seal is formed between the aspiration manifold and the plate. Microtiter plate wells 52 are pressurized by a pressure source 40 through at least one conduit 1 2 to effect the transfer of reagent through a plurality of conduits 1 4 and into dispense manifold 20 positioned above target substrate 60. Subsequently, a pressure pulse from valve 28 is communicated to the dispense manifold 20, effecting the transfer of a desired volume of reagent through orifice
1 06 to test sites 64 on target substrate 60. Further embodiments of the method include aligning the target substrate to ensure proper positioning of the reagent deposits, detecting the passage of reagent samples from the orifices of the dispense manifold, and purging the system between deposition, or printing, operations.
Brief Description of the Drawings FIG. 1 is a schematic of the major components of a dual manifold assembly in accordance with the present invention;
FIG. 2 is a schematic of a particular arrangement of subcomponents of a dual-manifold assembly in accordance with a preferred embodiment of the present invention;
FIG. 3 is a side view, partially in cross-section, of an aspiration manifold in accordance with a preferred embodiment of the present invention;
FIG. 4 is a side view, partially in cross-section, of an aspiration manifold in accordance with an alternate embodiment of the present invention;
FIG. 5 is a top view, partially cut away, of a preferred modular fluid connector in accordance with the present invention;
FIG. 6 is a front view of a female connector element of the modular fluid connector in FIG. 5; FIG . 7 is a cross-sectional view of a droplet ejection detection apparatus in accordance with an alternate embodiment of the present invention.
Detailed Description of the Preferred Embodiments Referring now to Figures 1 and 2, a dual manifold assembly is provided for the rapid, parallel transfer of liquid from an array of reservoirs 52 to a target substrate 60. It will be apparent to one skilled in the art of microarray printing that the apparatus of the present invention lends itself to a variety of applications. Generally, the assembly is capable of transferring liquids from virtually any type of reservoir - including tubes, bottles and other liquid containers - to virtually any type of substrate. However, in the preferred embodiment of the present invention the assembly is particularly suited for transferring chemical or biochemical reagents from an array of wells 52 of a conventional microtiter plate to an array of test sites 64 on a chip-based biological sensor (commonly referred to in the art as a "microarray") for performing screening assays. The assembly is adaptable for printing arrays wherein the distance between adjacent test sites, or test site pitch, is in the range of about 1 micron (μm) to about 1 0,000 microns (μm).
The assembly includes aspiration and dispense manifolds, 1 0 and 20 respectively, separated by fluid transfer elements (generally denoted by reference numeral 80) . In operation, the dual-manifold assembly is adapted for the automated printing of multiple analytical chips in succession. Preferably, a conventional microtiter plate feeder 70 is employed for advancing a series of microtiter plates beneath the aspiration manifold 1 0, and a target chip track 72 is employed for advancing test substrates 60 beneath the dispense manifold 20. Although the term "advancing" is used to describe movement of the tracks 70,
72, the invention is not intended to be so limited. In particular, either or both of the tracks can be adapted for movement in multiple directions.
In the preferred embodiment of the invention, the assembly is adapted for transferring reagent from a given number of reservoirs 52 to an equal number of test sites 64 and, accordingly, the assembly is designed for the one-to-one transfer of liquid, i.e., from each reagent reservoir to a designated test site. However, the flexibility of the present invention lends itself to numerous variations of the preferred use. In particular, the assembly can be configured for transferring liquid from a given number of reservoirs to a different number of test sites. For instance, the dispense manifold 20 can be designed such that liquid samples from multiple aspiration reservoirs are combined and dispensed on a single test site. Conversely, the manifolding can be adapted for depositing liquid from a single reservoir to multiple test sites.
A preferred embodiment of the dual-manifold assembly of the present invention is schematically illustrated in Figure 2. Although the assembly is adapted for simultaneously transferring multiple volumes of liquid reagent to multiple chip test sites, a clearer understanding of the invention can be gained through a description of the operation of the assembly with respect to the transfer of reagent from a single reservoir 52 to a single test site on target substrate surface 62. Accordingly, Figure 2 intentionally depicts a single set of fluid transfer elements. A pneumatic source 40 provides controlled pressure to reservoir 52 through a conduit 1 2 extending into the reservoir, with conduit 1 2 terminating at a position above liquid level 56. The magnitude and duration of the pressure supplied to the reservoir can be adjusted by aspiration manifold valve 1 3. Valve 1 3 is preferably a solenoid valve; however, other suitable valves are contemplated. For instance, other suitable valves may include shear valves, flat face valves and pinch valves, actuated by mechanical, electrical or pneumatic means. Upon application of pressure to the reservoir, liquid 54 is urged into and through aspiration conduit 1 4. In the preferred embodiment of the invention, conduits 1 2 and 1 4 comprise narrow-bore plastic tubing having an inner diameter preferably ranging from about .020 mm to about 2.0 mm.
However, the conduits can be manufactured from other suitable materials capable of transferring the desired fluids without being degraded, including, but not limited to, metals and glass.
In the preferred embodiment of the present invention, the aspiration manifold and dispense manifold sides of the assembly communicate through at least one modular fluid connector 90. In particular, aspiration conduits 1 4 are bundled together and combined in a male component, or plug 94, adapted for releasably engaging a female connector portion 92. Alternatively, as will be apparent to one skilled in the art, the aspiration conduits could be combined in a female plug adaptable for connection with a male component. The structure of a preferred modular connection is described in more detail below; however, numerous variations are possible without departing from the spirit and scope of the invention. Furthermore, although the modular connector 90 is depicted attached to a conduit 1 5 extending away from valve assembly 21 , it is preferred that the female connector portion 92 is integrated directly into valve assembly 21 . In this manner, the assembly of the present invention is adaptable for the simple and efficient attachment to myriad different aspiration manifold designs.
In other words, regardless of the structure of the aspiration manifold, the aspiration conduits are combined in a standard connector or plug 94 adapted for releasably engaging female connector portion 92. Thus, by integrating connector 92 into the valve assembly 21 , a single valve assembly 21 can be modularly connected to a variety of aspiration manifolds having different geometries, dimensions, and structures.
Valve assembly 21 includes a dispense manifold switching valve 22 which is preferably a flat face valve; however, other suitable valves are contemplated including, but not limited to, shear valves, solenoid valves and pinch valves, actuated by mechanical, electrical or pneumatic means. Switching valve 22 is fluidly connected to an ejection means 28 for advancing liquid through channels (not shown) in the dispense manifold 20, to effect the ejection of a desired volume of the liquid onto the test substrate. Preferably, the ejection means delivers a pressure pulse having a pressure ranging from about 6.9(1 0)3 N/m2 to about 1 38(1 0)3 N/m2, and having a duration ranging from about ( 1 0)~6 seconds to about (1 0)"2 seconds. In the preferred embodiment of the invention, the ejection means 28 comprises a conventional ink-jet style printing valve or pump designed for drop-on-demand printing. Ink-jet style printing valves/pumps for drop-on-demand printing, including thermal, solenoid and piezoelectric types, are commercially available and well known in the art. For instance, the Lee
Company of Essex, Connecticut manufactures a solenoid-based ink-jet valve (Model No. INKX0502600AB) which is suitable for use with the present invention. Although ejection means 28 is shown connected to valve assembly 21 via a conduit 24, the ejection means can be adapted for releasable attachment to the valve assembly, via a modular connector 90, in a manner similar to the preferred aspiration manifold connection. Furthermore, alternate valve arrangements are possible. For instance, an ink jet valve/pump 28 can be directly integrated into valve assembly 21 via conduit 26.
The incorporation of ink-jet drop-on-demand printing technology into the dispense assembly of the present invention provides significant advantages visa-vis known systems for printing microarrays. In particular, the ability to deliver the short-duration pressure pulses associated with ink-jet print valves enables the non-contact delivery of reagent sample volumes in the range of about (10)"12 to about ( 1 0)"6 liters. Upon application of a pressure pulse, at least one droplet of reagent is ejected through dispense manifold orifice 1 06 onto surface 62 of test substrate 60. As used herein, the term "non-contact" refers to the lack of contact between the dispense manifold and the target substrate during deposition. In the preferred embodiment of the invention, liquid is communicated through channels micro-machined into an ink-jet style printhead - such as those commonly used in desktop and industrial printers - and each terminating at an orifice 1 06. Depending upon the particular application, the orifices 1 06 can have diameters ranging from a minimum of about 1 micron (μm) to a maximum of about 200 microns (μm) . In the preferred embodiment of the invention, the dispense manifold 20 is adapted for releasable attachment to the valve assembly 21 via a modular connector 90. Furthermore, the modular connector can be integrated directly into switching valve 22. In this manner, the dispense manifold 20 can be fitted with a male connector portion 94 adapted for direct attachment to switching valve 22, precluding the need for conduit 26.
As previously discussed, liquid transferred from a reservoir on the aspiration side of the liquid transfer assembly can be manifolded in such a manner that the liquid is ejected through multiple orifices on the dispense side of the assembly. Conversely, liquid from multiple reservoirs on the aspiration side of the assembly can be combined and ejected through a single dispense orifice. The manifold assembly of the present invention also enables liquid to be transferred from a quantity of reservoirs to a quantity of test sites less than, equal to, or greater than the number of reservoirs. Accordingly, the array of printhead orifices can be dimensioned differently, or arranged in a different pattern, than the array of aspiration conduits 1 4 extending through the aspiration manifold 1 0. For instance, the assembly can be adapted for transferring liquid from a non-linear array of reservoirs to a linear array of dispense manifold orifices, and vice-versa. Similarly, the assembly can be adapted for transferring liquid from a rectangular array to a radial array, and vice- versa. As used herein, the term "array" is also intended to encompass a plurality of reservoirs, conduits, orifices or test sites having non-symmetric patterns or variable pitches. The printhead can also be adapted for being rotated during operation. Accordingly, the relative orientations of the aspiration manifold conduits 1 4 and dispense manifold orifices 1 06 can be varied. Significantly, the manifold structure of the present invention enables liquid to be transferred from an array of sample reservoirs having a minimum pitch on the order of millimeters to an array of orifices having a minimum pitch on the order of microns. For instance, we have employed the present invention to transfer reagents from conventional microtiter plate wells having a pitch in the range of about 2.25 mm to about 9.0 mm, to test sites on a solid state substrate having a pitch in the range of about 1 micron to about 1 0,000 microns.
Auxiliary apparatus 30 may be provided for cleaning and purging the various fluid transfer conduits of the assembly. For example, a gas pressure conduit 32 and cleaning liquid conduit 34 may be fluidly connected, via conduit 38, to switching valve 22. Preferably, the introduction of cleaning/purging fluids into the system is controllable through a suitable valve 36, such as solenoid, shear, flat face and pinch valves, actuated by mechanical, electrical or pneumatic means. Preferably, purging apparatus 30 is fluidly connected to valve assembly 21 through a modular connector 90 integrated into the valve assembly. Alternatively, purging apparatus 30 can be directly integrated into dispense manifold switching valve 22.
Referring now to Figure 3, an aspiration manifold assembly 1 0 is illustrated in accordance with a preferred embodiment of the present invention. The aspiration manifold includes an array of aspiration subassemblies extending through a base plate 1 7 and adapted for being received by a corresponding array of liquid filled reservoirs 52 formed in a source plate 50. In the preferred embodiment of the invention, the reservoirs comprise reagent-filled wells formed in a microtiter plate. Each subassembly includes a guide member 1 6, a cap member 1 8, a pressure conduit 1 2 and an aspiration conduit 1 4. Pressure and aspiration conduits 1 2 and 1 4 preferably comprise narrow-bore tubing constructed from plastic, metal or glass. Guide member 1 6 has a first end adapted for being mechanically fastened to base plate 1 7. Preferably, mechanical fastening is achieved by providing guide member 1 6 with a first threaded end for easy mechanical insertion, i.e., twisting, into the base plate. It will be apparent to one skilled in the art that alternate mechanical fastening means are possible. Regardless of the fastening means employed, it is important that the guide member snugly engages the base plate to prevent movement of the guide member during operation of the assembly. When fully inserted, a second flanged end 1 1 of the guide member extends downward from a lower surface of the base plate. Guide member 1 6 also has a pair of longitudinally- extending channels (not shown) for snugly-receiving the plastic tubing.
Cap member 1 8 has a first end adapted for engaging the flanged end 1 1 of guide member 1 6. An opposite second end of the cap member has a tapered outer surface 1 9 for engaging the perimeter of one of the liquid-filled reservoirs 52. Preferably, the cap member is manufactured from a suitable polymer, rubber or other compressible material. In this manner, as aspiration manifold 1 0 is seated onto microtiter plate 50, the cap members act to seal the reservoirs. Each cap member 1 8 is provided with longitudinally-extending channels aligning with the channels in a corresponding guide member 1 6 for receiving the plastic tube conduits. Pressure conduit 1 2 extends completely through cap member 1 8, but terminates above liquid level 56. Aspiration conduit 1 4 extends through cap member 1 8, terminating at a position below liquid level 56. In operation, aspiration manifold is seated onto microtiter plate 50 such that cap members 1 8 seal against the perimeter of corresponding wells 52. Subsequently, the wells are pressurized by applying pneumatic pressure through pressure tubing 1 2, thereby urging the transfer of liquid reagent 54 from the wells 52, through aspiration tubing 1 4, toward the dispense manifold 20.
Although the various elements of the aspiration manifold assembly are illustrated as individual sub-components, they can be combined. For instance, in an alternate embodiment of the present invention, cap member 1 8 and guide member 1 6 comprise a unitary component, for example, molded from plastic or machined from metal. Taking this integration a step further, in yet a further embodiment of the invention, cap and guide members 1 8 and 1 6, respectively, are integrated into base member 1 7 such that the entire aspiration manifold assembly, except for the tubing, comprises a single, unitary component. For instance, the entire aspiration manifold assembly can be molded from a suitable polymer or machined from a suitable metal.
Referring now to Figure 4, an alternate embodiment of the aspiration manifold has a single pressure inlet 1 2 for pressurizing the wells 52. In lieu of individual cap members for sealing each of the wells, a gasket member 23, preferably constructed from a suitable polymer, rubber or other compressible material, is disposed along the periphery of the underside of base plate 1 7. In this manner, as aspiration manifold 1 0 is seated onto microtiter plate 50, sealing member 23 seals against the periphery of plate 50. Individual aspiration conduits 1 4 extend into each of the liquid-filled reservoirs for transferring reagent from the wells to the dispense manifold.
As illustrated in Figure 2, in the preferred embodiment of the present invention, modular connectors 90 provide fluid connection between the valve assembly 21 and various subassemblies of the dual manifold system. It will be apparent to one skilled in the art of connectors that myriad different modular connector designs are possible for use with the present invention. Referring now to Figure 5, a preferred connector design will now be described. For the purpose of simplicity, the following discussion is directed specifically to a single modular connector located between aspiration manifold 1 0 and valve assembly 21 . However, all of the modular connectors 90 can have similar structures and operate in a similar fashion. Modular connector 90 includes female and male components, 92 and 94, respectively. Channels 96 formed in female subconnector 92 are adapted for releasably engaging integral connector tips 95 extending from male component, or plug, 94. Preferably, the individual channels/fittings 96 of the female unit have integral sealing elements 99, such as ribs, for preventing the leakage of fluids passing through the connector. During operation of the assembly, male connector 94 is fitted in female connector 92 such that the ends of tips 95 contact integral stop mechanisms 98. The geometry of the connectors may vary. However, as illustrated in Figure 6, the individual connector units are preferably designed much like a standard electrical connector. In alternate embodiments of the present invention, auxiliary assembly features are included for improving registration and alignment of reagent samples dispensed on the target substrate and/or for improving quality control. For instance, in one alternate embodiment of the invention, fiducial pins and/or marks are integrated into the target substrate and/or microtiter plate. The integrated features can be directly sensed by a conventional vision system for ensuring proper alignment and orientation during operation. Alternatively, the integrated features can be designed for interaction with position-sensitive detection electronics. In a further embodiment of the present invention, detection means are provided for detecting the passage of a droplet of reagent from a dispense orifice 1 06. For instance, referring now to Figure 7, photodiode
1 00 and photodetector 1 02 devices can be positioned proximate to a dispensing orifice 1 06 to sense the passage of a droplet. Alternatively, electronic conduction-based sensors can be incorporated directly into the dispense manifold, for example, by applying a conductive coating to portions of the inner wall of each orifice 1 06 and monitoring electrical current therebetween.
Referring now to FIGS. 1 -7, the operation of the dual-manifold assembly of the present invention will now be described. Initially, a source plate 50, such as a microtiter plate, is advanced on a feeder track 70 until it is properly positioned beneath aspiration manifold 1 0, and target substrate 60 is advanced on track 72 until it is properly positioned beneath dispense manifold 20. An optional alignment step may be performed to ensure proper positioning and orientation of the source plate, the target substrate or both. With the source plate and aspiration manifold adequately aligned, aspiration manifold 1 0 is vertically-actuated until it is seated onto source plate 50 such that an air-tight seal is formed between the manifold 1 0 and the plate 50. In the preferred embodiment of the invention (Figure 3), cap members 1 8 of the aspiration subassemblies form a seal over the reservoirs. Where the alternate embodiment of the aspiration manifold assembly is employed (Figure 4), the aspiration manifold 1 0 is vertically-actuated until gasket 23 seals against the periphery of source plate 50. Preferably, during operation, the aspiration and dispense manifolds are limited to vertical movement. With the aspiration manifold properly seated upon the source plate, pressure is introduced to the reservoirs from pressure source 40, via conduit(s) 1 2, to effect liquid transfer through conduits 1 4 toward dispense manifold 20. Preferably, once liquid transfer to the dispense manifold has been effected, switching valve 22 is actuated to disable fluid connection between the dispense manifold and the aspiration manifold, while enabling fluid communication between the dispense manifold and liquid ejection means 28. If necessary, dispense manifold 20 can be vertically positioned to a desired height above target substrate 60. Subsequently, a force, such as a pressure pulse, is communicated to the dispense manifold for a period of time to effect the ejection of a precise volume of liquid from the dispense manifold through orifices
1 06 to test sites 64 on target substrate 60. Preferably, the dispense manifold is maintained at a constant position during operation of the assembly.
Preferably, a complete array of test sites are printed contemporaneously, and tracks 70 and 72 are each advanced after the printing of a single array. However, liquid transferred from a single array of reservoirs may be adequate to dispense multiple arrays or sub-arrays of test sites. In that instance, printing can comprise repeatedly advancing test track 72 to reposition an array or sub-array of test sites beneath dispense manifold 20, while maintaining the position of feeder track 70. Conversely, other applications may require maintaining the position of test track 72 while advancing feeder track 70.
It will be apparent to one skilled in the art that further variations of the methods described herein are possible without departing from the scope of the invention. For instance, where track 70 and/or track 72 are adapted for movement in multiple directions, the method can include repositioning the reservoirs and/or test substrate via movement of the tracks 70, 72, such that the tracks are not "advanced " . Similarly, where the printhead is adapted for being rotated, the step of positioning the dispense manifold can include the sub- step of rotating the printhead.
In an alternate embodiment of the present invention, the method includes the additional step of detecting the passage of a droplet, or volume, of liquid from the array of dispense manifold orifices to the array of test sites. In a further embodiment of the invention, the method includes periodically purging fluid transfer conduits of the assembly with a cleaning fluid such as water.
While the preferred embodiments of the invention have been illustrated and described, it will be clear that the invention is not so limited. Numerous modifications, changes, variations, substitutions and equivalents will occur to those skilled in the art without departing from the spirit and scope of the present invention as described in the claims. For instance, it will be apparent to one skilled in the art that various modifications to the preferred valving arrangement are possible.

Claims

We claim:
1 . A dual-manifold assembly for transferring liquid from an array of reservoirs to an array of test sites on a target substrate, comprising: a liquid aspiration manifold; a liquid dispense manifold having a plurality of orifices; a plurality of conduits for providing fluid connection between said aspiration manifold and said dispense manifold; a controllable pneumatic pressure source for urging the liquid from said reservoirs through said plurality of conduits toward said dispense manifold; and, a means for effecting the ejection of at least one droplet of said liquid through at least one of said plurality of orifices and onto at least one of said test sites.
2. A dual-manifold assembly as recited in claim 1 , further comprising a switching valve integrated into said liquid dispense manifold.
3. A dual-manifold assembly as recited in claim 1 , wherein said ejection means is integrated into said liquid dispense manifold.
4. A dual-manifold assembly as recited in claim 1 , further comprising at least one modular connector for providing fluid connection between lengths of said plurality of conduits.
5. A dual-manifold assembly as recited in claim 1 , wherein said ejection means comprises an ink-jet printing valve incorporating drop-on-demand technology.
6. A dual-manifold assembly as recited in claim 5, wherein said ink-jet valve is one of a thermal ink-jet valve, a solenoid ink-jet valve, and a piezoelectric ink-jet valve.
7. A dual-manifold assembly as recited in claim 5, wherein said ink jet valve is adapted for delivering a pressure pulse having a pressure of about 6.9( 1 0)3 N/m2 to about 1 38( 1 0)3 N/m2, and having a pulse duration ranging from about ( 1 0)"6 seconds to about (1 0)"2 seconds.
8. A dual-manifold assembly as recited in claim 1 , wherein said plurality of conduits comprise plastic tubing.
9. A dual-manifold assembly as recited in claim 1 , wherein said plurality of conduits comprise at least one of metal and glass tubing.
1 0. A dual-manifold assembly as recited in claim 1 , wherein said array of reservoirs comprise microtiter plate wells and said liquid comprises a reagent.
1 1 . A dual-manifold assembly as recited in claim 1 , wherein said array of test sites comprise biological sensors integrated on a microelectronic device.
1 2. A dual-manifold assembly as recited in claim 1 , wherein the minimum distance between adjacent test sites on said target substrate is in the range of about 1 micron (μm) to about 1 0,000 microns (μm) .
1 3. A dual-manifold assembly as recited in claim 1 , wherein said liquid dispense manifold is adapted for dispensing volumes of liquid in the range of about (1 0)"12 to about ( 1 0)~6 liters.
1 4. A dual-manifold assembly as recited in claim 1 , further comprising a conduit cleaning and purging apparatus.
1 5. A dual-manifold assembly as recited in claim 1 , further comprising a means for detecting the passage of a droplet of liquid from a dispense manifold orifice.
1 6. A dual-manifold assembly as recited in claim 1 5, wherein said detection means comprise optoelectronic devices.
1 7. A dual-manifold assembly as recited in claim 1 5, wherein said detection means comprise electronic conduction-based sensors integrated into said dispense manifold.
1 8. A dual-manifold assembly as recited in claim 1 , wherein said aspiration manifold includes an array of aspiration subassemblies extending from a base plate and adapted for being received by said array of liquid-filled reservoirs, each subassembly comprising: a guide member having a first end adapted for being mechanically fastened to said base plate and having a second flanged end extending away from said base plate; a cap member having a first end adapted for engaging the flanged end of said guide member and a second end having a tapered outer surface for engaging the perimeter of one of said liquid-filled reservoirs; and, first and second conduits each extending through aligned apertures in each of said base plate, said guide member and said cap member; wherein said first conduit terminates at a position above a liquid level of the reservoir and said second conduit terminates at a position below a liquid level of the reservoir, said first conduit providing a means for pressurizing said reservoir to urge liquid through said second conduit toward said dispense manifold.
1 9. A dual-manifold assembly as recited in claim 1 8, wherein each of said guide member, said cap member and said base plate are integrated to form a unitary structure.
20. A dual-manifold assembly as recited in claim 1 , wherein said aspiration manifold assembly is adapted for being seated upon a source plate having an array of liquid-filled reservoirs, said aspiration manifold assembly comprising: a base plate; a gasket member disposed along the periphery of a lower surface of said base plate, said gasket dimensioned for sealing against a periphery of said source plate; a pressure conduit extending through said base plate for pressurizing said array of liquid-filled reservoirs; and, a plurality of aspiration conduits extending through said base plate and into said liquid-filled reservoirs for aspirating said liquid from said reservoirs.
21 . A method for transferring liquid reagent from an array of source plate reservoirs to an array of test sites on a target substrate using a dual-manifold assembly, comprising the steps of: positioning said source plate below an aspiration manifold; positioning said target substrate below a dispense manifold having a plurality of channels each terminating at an orifice; seating said aspiration manifold onto said source plate; pressurizing said source plate reservoirs through at least one pressure conduit to effect the aspiration of reagent from said reservoirs via a plurality of aspiration conduits to said dispense manifold; and, communicating a force to reagent in said dispense manifold channels for a period of time, wherein said force effects the ejection of a desired volume of said reagent to each of the test sites.
22. A method as recited in claim 21 , further comprising the step of checking the alignment of said target substrate prior to said step of communicating a force.
23. A method as recited in claim 21 , further comprising the step of detecting the passage of a volume of reagent from each said orifice to each said test site after the step of communicating a force.
24. A method as recited in claim 21 , further comprising the step of purging said dual-manifold system.
25. A method as recited in claim 21 , wherein the step of communicating a force comprises communicating a pressure pulse in the range of about 6.9( 1 0)3 N/m2 to about 1 38( 1 0)3 N/m2, for a period of time in the range of about (10)"6 seconds to about (10)"2 seconds.
PCT/US2000/003922 1999-03-04 2000-02-16 Dual manifold system and method for parallel fluid transfer WO2000051736A1 (en)

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JP2000602395A JP4128336B2 (en) 1999-03-04 2000-02-16 Dual manifold system and liquid parallel transfer method
DE60024973T DE60024973T2 (en) 1999-03-04 2000-02-16 DOUBLE DISTRIBUTION SYSTEM AND METHOD FOR THE SIMULTANEOUS TRANSMISSION OF FLUIDS
CA002364021A CA2364021C (en) 1999-03-04 2000-02-16 Dual manifold system and method for parallel fluid transfer
AU34924/00A AU3492400A (en) 1999-03-04 2000-02-16 Dual manifold system and method for parallel fluid transfer
AT00913483T ATE313379T1 (en) 1999-03-04 2000-02-16 DOUBLE DISTRIBUTOR SYSTEM AND METHOD FOR SIMULTANEOUS TRANSFER OF FLUID
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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002011889A1 (en) * 2000-08-03 2002-02-14 Arrayjet Limited Highly parallel fabrication of microarrays by ink jet printheads
EP1197693A2 (en) * 2000-10-11 2002-04-17 Innovadyne Technologies, Inc. Hybrid valve apparatus, system and method for fluid handling
EP1208912A2 (en) * 2000-11-22 2002-05-29 Xerox Corporation Testing methods and configurations for multi-ejector system
EP1250955A1 (en) * 1998-09-08 2002-10-23 Tibotec N.V. Method for the rapid screening of analytes
FR2827199A1 (en) * 2001-07-10 2003-01-17 Centre Nat Rech Scient Production ex-situ of biochips, comprises projecting micro volumes of reagent containing probes on to a substrate to form a plot ex situ with a low or medium probe integration
WO2003023410A1 (en) * 2001-09-07 2003-03-20 Innovadyne Technologies, Inc. Secondary liquid dispensing module for liquid handling system
WO2002076615A3 (en) * 2001-03-26 2003-11-06 Allegro Technologies Ltd Liquid droplet dispensing
US6983636B2 (en) 2002-01-25 2006-01-10 Innovadyne Technologies, Inc. Apparatus and method for assessing the liquid flow performances through a small dispensing orifice
US7135146B2 (en) 2000-10-11 2006-11-14 Innovadyne Technologies, Inc. Universal non-contact dispense peripheral apparatus and method for a primary liquid handling device
US8598867B2 (en) 2010-06-04 2013-12-03 Allegro Microsystems, Llc Circuits and methods for generating a threshold signal used in a motion detector
US9304141B2 (en) 2007-04-18 2016-04-05 Becton, Dickinson And Company Method and apparatus for determing dispense volume
EP2838659A4 (en) * 2012-04-18 2016-05-25 Biofire Diagnostics Llc Microspotting device

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020006359A1 (en) * 1998-11-25 2002-01-17 Affymetrix, Inc. Microplate sample and reagent loading system
US6656432B1 (en) 1999-10-22 2003-12-02 Ngk Insulators, Ltd. Micropipette and dividedly injectable apparatus
JP2002001092A (en) * 2000-06-22 2002-01-08 Shimadzu Corp Apparatus for discharging liquid
US6864091B1 (en) 2000-08-31 2005-03-08 Symyx Technologies, Inc. Sampling probe
US6887429B1 (en) * 2001-01-26 2005-05-03 Global Fia Apparatus and method for automated medical diagnostic tests
EP1399724B1 (en) * 2001-06-13 2007-08-22 Kenneth F. Uffenheimer Automated fluid handling system and method
US7410615B2 (en) * 2002-01-24 2008-08-12 Perkinelmer Las, Inc. Precision liquid dispensing system
US9283521B2 (en) 2002-06-14 2016-03-15 Parker-Hannifin Corporation Single-use manifold and sensors for automated, aseptic transfer of solutions in bioprocessing applications
USRE49221E1 (en) 2002-06-14 2022-09-27 Parker Intangibles, Llc Single-use manifolds for automated, aseptic handling of solutions in bioprocessing applications
US6712963B2 (en) * 2002-06-14 2004-03-30 Scilog, Llc Single-use manifold for automated, aseptic transfer of solutions in bioprocessing applications
CA2503797A1 (en) * 2002-11-08 2004-05-27 Irm, Llc Systems and methods of sorting samples
US7195026B2 (en) * 2002-12-27 2007-03-27 American Air Liquide, Inc. Micro electromechanical systems for delivering high purity fluids in a chemical delivery system
US20040151635A1 (en) * 2003-01-31 2004-08-05 Leproust Eric M. Array fabrication using deposited drop splat size
US7025935B2 (en) * 2003-04-11 2006-04-11 Illumina, Inc. Apparatus and methods for reformatting liquid samples
EP2322278B1 (en) * 2003-10-24 2017-01-04 Aushon Biosystems, Inc. Apparatus and Method for Dispensing Fluid, Semi-Solid and Solid Samples
US7591287B2 (en) * 2003-12-18 2009-09-22 Weyerhaeuser Nr Company System and method for filling a seedcoat with a liquid to a selected level
AU2005252242A1 (en) * 2004-06-07 2005-12-22 Irm Llc Dispensing systems, software, and related methods
CA2575186A1 (en) * 2004-08-04 2006-02-16 Irm, Llc Object storage devices, systems, and related methods
US20060258011A1 (en) 2005-04-22 2006-11-16 Igor Shvets Cleaning of system for dispensing of liquid droplets
US8383059B2 (en) * 2005-09-30 2013-02-26 University Of Utah Research Foundation Microfluidic interface for highly parallel addressing of sensing arrays
TWI316873B (en) * 2006-08-08 2009-11-11 Ind Tech Res Inst Apparatus of manufacturing biochip and manufacture method of biochip tip array
US20080134806A1 (en) * 2006-12-06 2008-06-12 Agamatrix, Inc. Container system for dispensing a liquid
WO2008089449A2 (en) 2007-01-19 2008-07-24 Biodot, Inc. Systems and methods for high speed array printing and hybridization
AU2011221244B2 (en) 2010-02-23 2014-02-13 Rheonix, Inc. Self-contained biological assay apparatus, methods, and applications
US8236256B2 (en) * 2010-04-27 2012-08-07 Thomas Friedlander Apparatus and method for efficient and precise transfer of liquids
DE102010047384B4 (en) * 2010-10-02 2012-06-28 Karlsruher Institut für Technologie Apparatus and method for generating or depositing a fluid stream from fluid segments and their use
US9068566B2 (en) 2011-01-21 2015-06-30 Biodot, Inc. Piezoelectric dispenser with a longitudinal transducer and replaceable capillary tube
US20130025690A1 (en) * 2011-07-29 2013-01-31 Intermolecular, Inc. No-Contact Wet Processing Tool with Liquid Barrier
JP6967427B2 (en) * 2017-11-06 2021-11-17 Nok株式会社 Gasket and sealing structure
WO2020040728A1 (en) * 2018-08-20 2020-02-27 Hewlett-Packard Development Company, L.P. Collections and measurements of microfluidic samples
US11768215B2 (en) 2019-01-04 2023-09-26 Funai Electric Co., Ltd. Digital dispense system cartridge
US11474007B2 (en) 2019-01-04 2022-10-18 Funai Electric Co., Ltd. Digital dispense system
US11331660B2 (en) 2019-01-04 2022-05-17 Funai Electric Co. Ltd. Digital dispense system
US11471879B2 (en) 2019-01-04 2022-10-18 Funai Electric Co., Ltd. Volume data representation and processing for liquid dispensing devices
CN111013680B (en) * 2019-12-11 2021-09-14 广东顺德工业设计研究院(广东顺德创新设计研究院) Droplet generating device

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2317634A1 (en) * 1975-07-11 1977-02-04 Dynatech Lab METHOD AND APPARATUS DESIGNED FOR TRANSFERRING LIQUIDS
WO1998029736A1 (en) * 1996-12-31 1998-07-09 Genometrix Incorporated Multiplexed molecular analysis apparatus and method
DE19712195A1 (en) * 1997-03-22 1998-09-24 Univ Schiller Jena Off line sample analysis
WO1999055460A1 (en) * 1998-04-27 1999-11-04 Corning Incorporated Redrawn capillary imaging reservoir

Family Cites Families (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2933376A (en) * 1957-01-28 1960-04-19 Roger W Mcbrien Titration apparatus
US3012863A (en) * 1958-09-26 1961-12-12 Thomas V Feichtmeir Apparatus for the preparation of laboratory test samples
GB1051716A (en) * 1962-07-02 1900-01-01
US3492876A (en) * 1968-02-08 1970-02-03 Us Health Education & Welfare Aliquant discharge device
US4342407A (en) * 1975-07-11 1982-08-03 Dynatech Laboratories, Incorporated Liquid dispensing apparatus
US4199013A (en) * 1977-04-01 1980-04-22 Packard Instrument Company, Inc. Liquid sample aspirating and/or dispensing system
US4140020A (en) * 1978-03-24 1979-02-20 Syva Company Seal-free pipette device
US4432470A (en) * 1981-01-21 1984-02-21 Otto Engineering, Inc. Multicomponent liquid mixing and dispensing assembly
US4353243A (en) * 1981-02-02 1982-10-12 Quadrex Corporation Flexible diaphragm controlled valve
DE3410508C2 (en) * 1984-03-22 1986-06-26 Kernforschungsanlage Jülich GmbH, 5170 Jülich Serial filling device for filling the cups of a micro cup plate
FR2582655B1 (en) * 1985-06-03 1988-12-23 Centre Nat Rech Scient SOLID PHASE SEMI-AUTOMATIC PEPTIDE MULTI-SYNTHESIZER
US4809909A (en) * 1985-06-13 1989-03-07 Glas-Craft, Inc. Plural component application system
US5000921A (en) * 1986-10-24 1991-03-19 Hanaway Richard W Multiple pipette samples
US5092184A (en) * 1989-12-22 1992-03-03 Medical Research Institute Of The Mary Imogene Bassett Hospital Cell staining system for flow cytometry
US5316181A (en) * 1990-01-29 1994-05-31 Integrated Designs, Inc. Liquid dispensing system
DE4024545A1 (en) 1990-08-02 1992-02-06 Boehringer Mannheim Gmbh Metered delivery of biochemical analytical soln., esp. reagent
US5341691A (en) * 1992-03-31 1994-08-30 Callis Rex D Dual use pressurized and unpressurized oil sampling apparatus
US5396812A (en) * 1992-06-09 1995-03-14 Peterson; Roger Sample system
US5728351A (en) * 1993-01-21 1998-03-17 Cdc Technologies, Inc. Apparatus for making a plurality of reagent mixtures and analyzing particle distributions of the reagent mixtures
GB9321786D0 (en) 1993-10-22 1993-12-15 Xaar Ltd Droplet deposition apparatus
US5807522A (en) 1994-06-17 1998-09-15 The Board Of Trustees Of The Leland Stanford Junior University Methods for fabricating microarrays of biological samples
JPH0839807A (en) 1994-07-29 1996-02-13 Canon Inc Ink jet printing method and apparatus
US5545531A (en) 1995-06-07 1996-08-13 Affymax Technologies N.V. Methods for making a device for concurrently processing multiple biological chip assays
JPH0932941A (en) * 1995-07-21 1997-02-07 Smc Corp Switching valve connecting body
GB9522056D0 (en) * 1995-10-27 1996-01-03 Dynatech Med Prod Ltd Level sensor and washer unit
US5862832A (en) * 1996-02-29 1999-01-26 Waters Investments Limited Gradient proportioning valve
US5849598A (en) * 1996-03-15 1998-12-15 Washington University Method for transferring micro quantities of liquid samples to discrete locations
US6083762A (en) * 1996-05-31 2000-07-04 Packard Instruments Company Microvolume liquid handling system
US5741554A (en) * 1996-07-26 1998-04-21 Bio Dot, Inc. Method of dispensing a liquid reagent
US6083761A (en) * 1996-12-02 2000-07-04 Glaxo Wellcome Inc. Method and apparatus for transferring and combining reagents
US5964089A (en) * 1997-06-27 1999-10-12 Lynntech, Inc Diagnostics and control of an on board hydrogen generation and delivery system
US6902703B2 (en) * 1999-05-03 2005-06-07 Ljl Biosystems, Inc. Integrated sample-processing system
EP1030736B1 (en) * 1997-11-14 2003-10-01 Gen-Probe Incorporated Assay work station
US6033911A (en) * 1998-02-27 2000-03-07 Hamilton Company Automated assaying device
US6106783A (en) * 1998-06-30 2000-08-22 Microliter Analytical Supplies, Inc. Microplate assembly and closure
US6787111B2 (en) * 1998-07-02 2004-09-07 Amersham Biosciences (Sv) Corp. Apparatus and method for filling and cleaning channels and inlet ports in microchips used for biological analysis
US5988236A (en) * 1998-07-31 1999-11-23 Gilson, Inc. Multiple syringe pump assembly for liquid handler
US6162341A (en) * 1998-09-11 2000-12-19 The Perkin-Elmer Corporation Multi-channel capillary electrophoresis device including sheath-flow cuvette and replacable capillary array
US6039211A (en) * 1998-09-22 2000-03-21 Glaxo Wellcome Inc. Position triggered dispenser and methods
US6152162A (en) * 1998-10-08 2000-11-28 Mott Metallurgical Corporation Fluid flow controlling
US20020006359A1 (en) * 1998-11-25 2002-01-17 Affymetrix, Inc. Microplate sample and reagent loading system
US6159629A (en) * 1998-12-17 2000-12-12 Ballard Power Systems Inc. Volume effecient layered manifold assembly for electrochemical fuel cell stacks
US20020028160A1 (en) * 2000-02-22 2002-03-07 Jianming Xiao Method and apparatus based on bundled capillaries for high throughput screening
JP2002001092A (en) * 2000-06-22 2002-01-08 Shimadzu Corp Apparatus for discharging liquid

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2317634A1 (en) * 1975-07-11 1977-02-04 Dynatech Lab METHOD AND APPARATUS DESIGNED FOR TRANSFERRING LIQUIDS
WO1998029736A1 (en) * 1996-12-31 1998-07-09 Genometrix Incorporated Multiplexed molecular analysis apparatus and method
DE19712195A1 (en) * 1997-03-22 1998-09-24 Univ Schiller Jena Off line sample analysis
WO1999055460A1 (en) * 1998-04-27 1999-11-04 Corning Incorporated Redrawn capillary imaging reservoir

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
LE H P: "PROGRESS AND TRENDS IN INK-JET PRINTING TECHNOLOGY", JOURNAL OF IMAGING SCIENCE AND TECHNOLOGY, US, SOC. FOR IMAGING SCIENCE AND TECHNOLOGY, SPRINGFIELD, VA, vol. 42, no. 1, 1 January 1998 (1998-01-01), pages 49 - 62, XP000735876, ISSN: 1062-3701 *

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1250955A1 (en) * 1998-09-08 2002-10-23 Tibotec N.V. Method for the rapid screening of analytes
WO2002011889A1 (en) * 2000-08-03 2002-02-14 Arrayjet Limited Highly parallel fabrication of microarrays by ink jet printheads
AU2001276486B2 (en) * 2000-08-03 2006-07-27 Arrayjet Limited Highly parallel fabrication of microarrays by ink jet printheads
US7128393B2 (en) 2000-08-03 2006-10-31 Array Jet Limited Highly parallel fabrication of microarrays by ink jet printheads
US6852291B1 (en) 2000-10-11 2005-02-08 Innovadyne Technologies, Inc. Hybrid valve apparatus and method for fluid handling
EP1197693A2 (en) * 2000-10-11 2002-04-17 Innovadyne Technologies, Inc. Hybrid valve apparatus, system and method for fluid handling
US7135146B2 (en) 2000-10-11 2006-11-14 Innovadyne Technologies, Inc. Universal non-contact dispense peripheral apparatus and method for a primary liquid handling device
EP1197693A3 (en) * 2000-10-11 2003-03-26 Innovadyne Technologies, Inc. Hybrid valve apparatus, system and method for fluid handling
US6740530B1 (en) 2000-11-22 2004-05-25 Xerox Corporation Testing method and configurations for multi-ejector system
EP1208912A2 (en) * 2000-11-22 2002-05-29 Xerox Corporation Testing methods and configurations for multi-ejector system
EP1208912A3 (en) * 2000-11-22 2003-08-06 Xerox Corporation Testing methods and configurations for multi-ejector system
WO2002076615A3 (en) * 2001-03-26 2003-11-06 Allegro Technologies Ltd Liquid droplet dispensing
WO2003006153A3 (en) * 2001-07-10 2003-10-16 Centre Nat Rech Scient Method and machine for ex situ production of low and medium integration biochip networks
WO2003006153A2 (en) * 2001-07-10 2003-01-23 Centre National De La Recherche Scientifique Method and machine for ex situ production of low and medium integration biochip networks
FR2827199A1 (en) * 2001-07-10 2003-01-17 Centre Nat Rech Scient Production ex-situ of biochips, comprises projecting micro volumes of reagent containing probes on to a substrate to form a plot ex situ with a low or medium probe integration
WO2003023410A1 (en) * 2001-09-07 2003-03-20 Innovadyne Technologies, Inc. Secondary liquid dispensing module for liquid handling system
US6983636B2 (en) 2002-01-25 2006-01-10 Innovadyne Technologies, Inc. Apparatus and method for assessing the liquid flow performances through a small dispensing orifice
US7169616B2 (en) 2002-01-25 2007-01-30 Innovadyne Technologies, Inc. Method of purging trapped gas from a system fluid contained in an actuation valve
US9304141B2 (en) 2007-04-18 2016-04-05 Becton, Dickinson And Company Method and apparatus for determing dispense volume
US8598867B2 (en) 2010-06-04 2013-12-03 Allegro Microsystems, Llc Circuits and methods for generating a threshold signal used in a motion detector
US9140536B2 (en) 2010-06-04 2015-09-22 Allegro Microsystems, Llc Circuits and methods using a first cycle of a signal to generate a threshold signal used for comparing to a second later cycle of the signal
EP2838659A4 (en) * 2012-04-18 2016-05-25 Biofire Diagnostics Llc Microspotting device
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US11207655B2 (en) 2012-04-18 2021-12-28 Biofire Diagnostics, Llc Microspotting device

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JP4128336B2 (en) 2008-07-30
US20010053337A1 (en) 2001-12-20
US6627157B1 (en) 2003-09-30
AU3492400A (en) 2000-09-21
EP1159072B1 (en) 2005-12-21
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EP1159072A1 (en) 2001-12-05
CA2364021A1 (en) 2000-09-08
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ATE313379T1 (en) 2006-01-15
US6569687B2 (en) 2003-05-27

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