WO1997015394A1 - Microwell plates - Google Patents

Microwell plates Download PDF

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Publication number
WO1997015394A1
WO1997015394A1 PCT/US1996/017072 US9617072W WO9715394A1 WO 1997015394 A1 WO1997015394 A1 WO 1997015394A1 US 9617072 W US9617072 W US 9617072W WO 9715394 A1 WO9715394 A1 WO 9715394A1
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WO
WIPO (PCT)
Prior art keywords
plate
wells
multiwell plate
liquid
well
Prior art date
Application number
PCT/US1996/017072
Other languages
French (fr)
Other versions
WO1997015394A9 (en
Inventor
William Arthur Bains
Peter John Houzego
Original Assignee
Smithkline Beecham Corporation
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 Smithkline Beecham Corporation filed Critical Smithkline Beecham Corporation
Priority to JP9516786A priority Critical patent/JP2000500567A/en
Priority to EP96936933A priority patent/EP0862497A4/en
Publication of WO1997015394A1 publication Critical patent/WO1997015394A1/en
Publication of WO1997015394A9 publication Critical patent/WO1997015394A9/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
    • B01L3/0268Drop counters; Drop formers using pulse dispensing or spraying, eg. inkjet type, piezo actuated ejection of droplets from capillaries
    • 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
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5025Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures for parallel transport of multiple samples
    • 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
    • B01J2219/00317Microwell devices, i.e. having large numbers of wells
    • 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
    • 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
    • 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
    • G01N2035/00178Special arrangements of analysers
    • G01N2035/00237Handling microquantities of analyte, e.g. microvalves, capillary networks

Definitions

  • This invention relates to microwell plates.
  • HTS High Throughput Screening
  • CC Combinatorial Chemistry
  • This patent application describes a system specifically designed for the parallel synthesis or assay of tens of thousands of compounds.
  • the heart of the concept is a special well structure, called a JetWell in which the wells are arranged as a matrix within the flat plate as is conventional for microwell plates.
  • the novel feature of this concept is that the wells are fabricated with large open areas at one end to accept liquid and integral nozzles at the other end from which liquid can be jet dispensed.
  • These arrays might be made compatible with conventional 96 or 384 microwell plates but advantageously could be higher density (eg 60 x 40 or 120 x 80).
  • the walls of the lower end of the cell may be coated with a binding surface on which the compounds to be synthesised can be attached.
  • JetWell The design of the JetWell enables it to receive and deliver accurate micro volumes of fluid.
  • Dispensing of fluids required for the synthesis into each JetWell would preferably be made without contact of the dispenser to the liquid in the well by using a multinozzle ink-jet head firing into the large end of the wells.
  • a multinozzle approach is necessary to ensure the dispense time for the complete array is short compared to the typical reaction time for each stage of the processing.
  • Liquid removal from the cells is achieved through the integral nozzle in the bottom of the well. During normal operation liquid is prevented from flowing out the cell through the nozzle by surface tension or even a physical plug. Liquid is ejected from the nozzle by applying pressure to the liquid in the wells causing it to jet cleanly out of the hole away from the lower surface.
  • the volume to be removed from the well can be controlled by the pressure applied and time for which it is applied. To achieve clean jetting of the fluid pressure typically in the range 0.1 to 10.0 bar gauge is used and the pressure is applied and removed rapidly to prevent any dribbling of liquid out of the nozzle. If a matching JetWell array is positioned beneath the first array transfer of an accurate volume of liquid from one array to the other occurs in a few milliseconds.
  • the approach provides an accurate system for the parallel dispensing into and from very small JetWell arrays. This enables the volume of the wells to be reduced and the number per plate increased thus greatly increasing the throughput of HTS or CC systems.
  • JetWell Array Structure The specific feature of a JetWell which is different from other forms of microwell plate is that each well has one or more nozzles in the base through which liquid in the well will jet when pressure is applied to the top surface.
  • the diameter of the nozzle controls the rate of liquid flow and is chosen to optimise for speed and accuracy. For example, if the pressure duration is controlled to 1 millisecond accuracy and the volumetric control requirement is 1 nanolitre the flow rate through the hole must be less than 1 microlitre/second. Assuming a jet velocity of 5 metres/second the nozzle would be around 50 microns in diameter which is comparable with that used in conventional ink jet printers.
  • each well depends upon the user requirements.
  • a system might be designed to be compatible with conventional 384 well plates which have a well volume around 20 microlitres arranged on a 4.5mm pitch.
  • well volumes around 20 microlitres arranged on a 4.5mm pitch.
  • a plate of similar size to a conventional microwell plate (either 96 or 384) with wells at 1mm pitch would contain a 96 x 64 array. Taking this size as an example the diameter at the top might be 0.8mm and the hole at the base 30 microns in diameter.
  • Figure 1 shows an example of the basic structure of the JetWell concept and Figure IA is a detailed view, to an enlarged scale of part of that structure.
  • This application, as well as describing the concept and example JetWell designs also addresses suitable manufacturing techniques for the plate and for the associated system components.
  • each line of wells by bonding two strips together with etched structures in them to form the wells.
  • the complete array could be formed etched into the surface of a plate which is then cut into strips and laminated together to form the finished structure.
  • Such a structure could be manufactured for example in glass using a low temperature glass enamel bonding.
  • a single crystal silicon wafer substrate is appropriate with the wells formed by crystallographic etching which can be used to form the nozzle hole with a precision of a few microns.
  • the JetWell concept has many wells in an array on a plate each with a nozzle hole in the base. It is possible to transfer a measured dose from all wells on a JetWell plate to a second receiver JetWell plate in one operation. This is achieved by placing the receiver plate directly below the plate containing the liquid to be dispensed and applying a pressure pulse to all wells of the top plate. Liquid is then jetted from each well on the top plate to the corresponding well on the bottom plate. To jet the fluid cleanly from the nozzle hole the pressure in the fluid must rise quickly and fall sufficiently fast to prevent dribbling from the nozzle. The dynamics of this are well understood from ink-jet experience and it is known that it requires rates in excess of 10 s Pa s "1 (ie 1 bar/ms) for typical dimensions.
  • the pressure rise of a few bar can then be achieved by moving the piston a few millimetres at speeds of a few metres per second.
  • electromagnetic actuators are the simplest.
  • the force required to reach 10 bar is 10 4 Newton's (— 1 ton) which is more difficult to achieve using a simple solenoid drives.
  • an impact actuator can be used.
  • the piston is sealed to the dispense JetWell plate using a compliant seal which permits sufficient travel to reach the desired pressure and then prevents over pressure by limiting the motion using a physical stop.
  • the receiver JetWell plate is fitted directly below the dispense plate.
  • the piston and the two JetWell plates are mounted together on a spring support.
  • the back of the piston is then struck by a mass at a predetermined velocity.
  • the mass striking the piston back moves the piston towards the plate until it reaches the stop. This compresses the air volume above the wells to the desired pressure very quickly. Both the impact mass and the plates continue to move compressing the support spring.
  • the spring decelerates the assembly and then accelerates it back-up.
  • FIG 3 shows two JetWell plates, each of the type shown in Figure 1, mounted in the impact actuator.
  • JWL is the JetWell plate containing the liquid to be dispensed and
  • JW2 is the JetWell plate into which the aliquots are to be dispensed.
  • JW1 and JW2 are mounted rigidly together with JW1 above JW2.
  • the piston plate PP is mounted with a small gap above JW1 on a compressible gas tight edge gasket EG.
  • JW1, JW2 and PP are all supported on spring support SS.
  • mass M is accelerated towards PP so that it impacts at a specified velocity.
  • the piston plate PP and mass M move towards JW1 compressing the edge gasket (EG) until the motion stop (MSI) stops it at a preset gap.
  • EG edge gasket
  • MSI motion stop
  • the dispense pressure is a function of air volume and the distance to the forward stop and the dispense time is a function of the spring constants, masses and initial impact velocity.
  • the technique therefore provides the ability to independently set time and pressure for dispensing over a wide range.
  • a small area piston pump can be located over the specific well.
  • lines, or rectangular sections of the plate can be addressed by specifically shaped actuators.
  • the use of a minimal volume positive displacement air pressure generator has important advantages as has the impact technique described to implement it.
  • the technique for dispensing from a JetWell plate can also be used for dispensing to a JetWell plate providing the same volume is required in each well. This is applicable in some, but not all instances. Where different amounts are required in each well, alternative approaches can be used.
  • Nozzle plates could be selected from a library and cleaned for re-use
  • programmable nozzle arrays including but not restricted to solenoid, piezo, mechanically and thermal drives for ball, plate, disc or poppet mechamsms.
  • nozzles in the sub 0.1mm diameter range with minimal dead volume and implementable in arrays of many thousand is a challenge.
  • One approach is to use cone shaped nozzles which are produced as an array in a ferro magnetic material.
  • the nozzle plate is removable from the pressure generating head.
  • To programme the array to the required pattern magnetic beads are placed in those nozzles to be closed. The magnetic attraction to the plate holds them in place whilst the plate is replaced in the dispense head.
  • the nozzles are then filled with the liquid to be dispensed and a pressure pulse applied for the required time.
  • the ball in cone arrangement ensures a good seal against the dispense pressure.
  • the magnetic beads may be disposable or reusable depending upon application. By using several plates which can be programmed whilst other operations are being performed the system will be rapid and flexible.
  • JetWells of the dispense plate are prefilled with the volume and type of liquids required using an accurate but not necessarily fast technique.
  • the liquid is held in the wells by surface tension.
  • the plate is ready for use. It is positioned over the reaction JetWell plate, and all the content of each well is jet dispensed by a pressure pulse as described previously.
  • JetWell dispensing approaches In some cases neither of these JetWell dispensing approaches will be appropriate. For these instances it may be necessary to use a precision dispensing head.
  • the technique most suitable for this is based upon drop-on-demand ink-jet systems where the dose in each well can be set by dispensing a measured number of drops.
  • All material in contact with the fluid must be inert to a wide range of acids, alkalis and solvents. Preferably it should be restricted to silicon dioxide, stainless steel, and inert polymers
  • the system must be easy to fill and to flush as it must be used many times with a wide range of fluids
  • the nozzle diameter is chosen to match the well size. Typically the drop size is selected to be in the range 10° to IO "4 of the well volume
  • Typical delivery rates are in the range IO 3 to 10 4 drops per second
  • Actuation will preferably be by a thin piezo layer bonded to a silicon or silicon dioxide membrane.
  • the piezo drivers may be integrated on to the head.
  • the head would have gold contacts deposited enabling it to make electrical contact to off head drivers.
  • the application lends itself to implementation of the head using silicon crystallographic etching techniques to form the structure and either silicon to glass or silicon to silicon bonding for assembly.
  • top shooter or side shooter forms could be implemented at typical pitches required (-*0.5mm).
  • the best approach for achieving precision is therefore to include a technique for the calibration of each device prior to use.
  • a technique for the calibration of each device prior to use For example, for JetWell plates there may be a distribution of nozzle diameters coupled with a pressure variation which leads to different volumes being dispensed for each well. If a quantative assay is being performed on part-samples from each well, volume variation would influence the result.
  • the system could be calibrated before use by dispensing a reagent which can be used in a simple standard assay test for volume.
  • a reagent which can be used in a simple standard assay test for volume.
  • This for example could be a colour change reaction which is convenient for automated measurement.
  • the calibration would be used to correct the results of the real assay rather than to control the volumes dispensed.

Abstract

A multiwell plate where the wells have a large opening at the top and small nozzle hole in the base which is chosen so that a jet of liquid is emitted when a pressure pulse is applied to the surface such that by selecting a time for the pressure pulse a precise amount of volume in the well can be dispensed.

Description

TITLE: MICROWELL PLATES
Introduction
This invention relates to microwell plates.
High Throughput Screening (HTS) and Combinatorial Chemistry (CC) are key technologies in the search for new drugs. HTS addresses the screening of thousands of different compounds for a specific biological activity whereas CC addresses the manufacture of compound libraries by the parallel synthesis of different combinations of side groups on molecules of a particular structural class.
Many of the techniques used in both areas are based around the use of spatial arrays of reaction sites in the form of cells, microwells or immobilisation surfaces. For these approaches there is a requirement to move accurate volumes of liquid into and out of the cells in a short period of time.
One established approach is to use a microwell plate and a robot controlled micro- dispenser to fill and empty each well with its required chemicals in sequence. However, where the goal is to produce thousands of chemicals this approach is limited by the time taken to sequentially dispense to each well.
This patent application describes a system specifically designed for the parallel synthesis or assay of tens of thousands of compounds. The heart of the concept is a special well structure, called a JetWell in which the wells are arranged as a matrix within the flat plate as is conventional for microwell plates. The novel feature of this concept is that the wells are fabricated with large open areas at one end to accept liquid and integral nozzles at the other end from which liquid can be jet dispensed. These arrays might be made compatible with conventional 96 or 384 microwell plates but advantageously could be higher density (eg 60 x 40 or 120 x 80). The walls of the lower end of the cell may be coated with a binding surface on which the compounds to be synthesised can be attached.
The design of the JetWell enables it to receive and deliver accurate micro volumes of fluid.
Dispensing of fluids required for the synthesis into each JetWell would preferably be made without contact of the dispenser to the liquid in the well by using a multinozzle ink-jet head firing into the large end of the wells. A multinozzle approach is necessary to ensure the dispense time for the complete array is short compared to the typical reaction time for each stage of the processing.
Liquid removal from the cells is achieved through the integral nozzle in the bottom of the well. During normal operation liquid is prevented from flowing out the cell through the nozzle by surface tension or even a physical plug. Liquid is ejected from the nozzle by applying pressure to the liquid in the wells causing it to jet cleanly out of the hole away from the lower surface.
The volume to be removed from the well can be controlled by the pressure applied and time for which it is applied. To achieve clean jetting of the fluid pressure typically in the range 0.1 to 10.0 bar gauge is used and the pressure is applied and removed rapidly to prevent any dribbling of liquid out of the nozzle. If a matching JetWell array is positioned beneath the first array transfer of an accurate volume of liquid from one array to the other occurs in a few milliseconds.
The approach provides an accurate system for the parallel dispensing into and from very small JetWell arrays. This enables the volume of the wells to be reduced and the number per plate increased thus greatly increasing the throughput of HTS or CC systems.
This patent application covers the fundamental concept and specific methods of implementing the individual components of the system.
.letWell Array Structure The specific feature of a JetWell which is different from other forms of microwell plate is that each well has one or more nozzles in the base through which liquid in the well will jet when pressure is applied to the top surface.
The diameter of the nozzle controls the rate of liquid flow and is chosen to optimise for speed and accuracy. For example, if the pressure duration is controlled to 1 millisecond accuracy and the volumetric control requirement is 1 nanolitre the flow rate through the hole must be less than 1 microlitre/second. Assuming a jet velocity of 5 metres/second the nozzle would be around 50 microns in diameter which is comparable with that used in conventional ink jet printers.
The overall volume of each well depends upon the user requirements. A system might be designed to be compatible with conventional 384 well plates which have a well volume around 20 microlitres arranged on a 4.5mm pitch. However, there are considerable advantages in using larger arrays with smaller well volumes.
As an example a plate of similar size to a conventional microwell plate (either 96 or 384) with wells at 1mm pitch would contain a 96 x 64 array. Taking this size as an example the diameter at the top might be 0.8mm and the hole at the base 30 microns in diameter.
Figure 1 shows an example of the basic structure of the JetWell concept and Figure IA is a detailed view, to an enlarged scale of part of that structure. This application, as well as describing the concept and example JetWell designs also addresses suitable manufacturing techniques for the plate and for the associated system components.
JetWell Plate Manufacture
Where implementations do not require holes below 0.1mm diameter in the base of the wells, conventional moulded manufacturing approaches may be used. However, as smaller holes are required then other approaches will be required. One approach is to use a moulded structure with a thinned section in the base through which a hole is drilled using a laser. Alternatively, a thin sheet with photolithographically defined holes, created either by etching or electro forming, may be bonded to the bottom of the array.
Another approach is to form each line of wells by bonding two strips together with etched structures in them to form the wells. With this approach the complete array could be formed etched into the surface of a plate which is then cut into strips and laminated together to form the finished structure. Such a structure could be manufactured for example in glass using a low temperature glass enamel bonding.
Where very small wells are required then a single crystal silicon wafer substrate is appropriate with the wells formed by crystallographic etching which can be used to form the nozzle hole with a precision of a few microns.
Examples of these types of construction are shown in Figures 2a, 2b, 2c.
Dispense from the JetWell Plate
The JetWell concept has many wells in an array on a plate each with a nozzle hole in the base. It is possible to transfer a measured dose from all wells on a JetWell plate to a second receiver JetWell plate in one operation. This is achieved by placing the receiver plate directly below the plate containing the liquid to be dispensed and applying a pressure pulse to all wells of the top plate. Liquid is then jetted from each well on the top plate to the corresponding well on the bottom plate. To jet the fluid cleanly from the nozzle hole the pressure in the fluid must rise quickly and fall sufficiently fast to prevent dribbling from the nozzle. The dynamics of this are well understood from ink-jet experience and it is known that it requires rates in excess of 10sPa s"1 (ie 1 bar/ms) for typical dimensions.
Achieving this rate of pressure rise uniformly over the whole area of the plate is not trivial if contact with the liquid in the wells is to be avoided. One approach to achieving this is to use a piston arrangement over the whole area with the initial distance between the plate and the piston small compared to the lateral dimensions of the plate (eg 5mm spacing for a plate 60 x 40mm). This minimises the volume of air being compressed and the distance in air for the pressure waves to travel.
The pressure rise of a few bar can then be achieved by moving the piston a few millimetres at speeds of a few metres per second. There are many options for implementing this motion. Where the areas are small, electromagnetic actuators are the simplest. However, for a plate area of 100 x 100 mm the force required to reach 10 bar is 104Newton's (— 1 ton) which is more difficult to achieve using a simple solenoid drives.
To meet this requirement an impact actuator can be used. In this approach, the piston is sealed to the dispense JetWell plate using a compliant seal which permits sufficient travel to reach the desired pressure and then prevents over pressure by limiting the motion using a physical stop. The receiver JetWell plate is fitted directly below the dispense plate. The piston and the two JetWell plates are mounted together on a spring support. The back of the piston is then struck by a mass at a predetermined velocity. The mass striking the piston back moves the piston towards the plate until it reaches the stop. This compresses the air volume above the wells to the desired pressure very quickly. Both the impact mass and the plates continue to move compressing the support spring. The spring decelerates the assembly and then accelerates it back-up. Both JetWell plates are stopped at the original position but the piston is free to continue. As the piston and impact mass move away from the plates the pressure above the wells falls rapidly. The piston and impact mass are then decelerated, using viscous damping, to a stop. This apparatus is illustrated, by way of example, in Figure 3. It should be noted that there is a temperature rise associated with the rapid air compression which must be accounted for in the design.
Figure 3 shows two JetWell plates, each of the type shown in Figure 1, mounted in the impact actuator. JWL is the JetWell plate containing the liquid to be dispensed and JW2 is the JetWell plate into which the aliquots are to be dispensed. JW1 and JW2 are mounted rigidly together with JW1 above JW2. The piston plate PP is mounted with a small gap above JW1 on a compressible gas tight edge gasket EG. JW1, JW2 and PP are all supported on spring support SS. In use, mass M is accelerated towards PP so that it impacts at a specified velocity. The piston plate PP and mass M move towards JW1 compressing the edge gasket (EG) until the motion stop (MSI) stops it at a preset gap. This raises the pressure rapidly and uniformly over all of JW1 to the pressure required to jet the liquid from the nozzles in the base of the wells. M, PP, JW1 and JW2 all continue to move down compressing spring support SS. The spring support SS oscillates forcing M, PP, JW1 and JW2 upwards after a time governed by resonant frequency of the spring/mass system. Upward motion of JW1 and JW2 is halted by the stop MS2 with PP and M continuing upwards by their inertia. PP and M are stopped by the stop MS3 at their starting position so that the pressure above JW1 returns rapidly to 1 bar.
The dispense pressure is a function of air volume and the distance to the forward stop and the dispense time is a function of the spring constants, masses and initial impact velocity. The technique therefore provides the ability to independently set time and pressure for dispensing over a wide range.
Where dispensing is required from a single well only then a small area piston pump can be located over the specific well. Similarly lines, or rectangular sections of the plate can be addressed by specifically shaped actuators. The use of a minimal volume positive displacement air pressure generator has important advantages as has the impact technique described to implement it.
Dispense to the JetWell Plate
The technique for dispensing from a JetWell plate can also be used for dispensing to a JetWell plate providing the same volume is required in each well. This is applicable in some, but not all instances. Where different amounts are required in each well, alternative approaches can be used.
Several approaches for this have been developed depending upon specific requirements. One approach is to use the minimal volume pressure generator approach described previously with a patterned nozzle plate which addresses only those wells which are to receive the dose. This can be implemented by:
* Pre-fabricating a nozzle plate having the desired pattern of nozzles which is fitted to the dispenser when required. Nozzle plates could be selected from a library and cleaned for re-use
* A programmable nozzle array.
There are many possible implementations of programmable nozzle arrays including but not restricted to solenoid, piezo, mechanically and thermal drives for ball, plate, disc or poppet mechamsms.
However, implementation for nozzles in the sub 0.1mm diameter range with minimal dead volume and implementable in arrays of many thousand is a challenge. One approach is to use cone shaped nozzles which are produced as an array in a ferro magnetic material. The nozzle plate is removable from the pressure generating head. To programme the array to the required pattern, magnetic beads are placed in those nozzles to be closed. The magnetic attraction to the plate holds them in place whilst the plate is replaced in the dispense head. The nozzles are then filled with the liquid to be dispensed and a pressure pulse applied for the required time. The ball in cone arrangement ensures a good seal against the dispense pressure.
After operation the liquid is removed and the nozzle plate back-flushed to remove the beads before being cleaned for re-use. The magnetic beads may be disposable or reusable depending upon application. By using several plates which can be programmed whilst other operations are being performed the system will be rapid and flexible.
In other cases it may be necessary to dispense different volumes of a range of liquids to the wells. This can be achieved using the JetWell system in a pre-fill capacity. In this approach the JetWells of the dispense plate are prefilled with the volume and type of liquids required using an accurate but not necessarily fast technique. The liquid is held in the wells by surface tension. When all wells have been filled with the predetermined volume of the appropriate liquid, the plate is ready for use. It is positioned over the reaction JetWell plate, and all the content of each well is jet dispensed by a pressure pulse as described previously.
This approach is most appropriate where it is necessary to make the transfer into the wells quickly but there is time between transfers to pre-load the dispenser. Care must be taken to avoid solvent loss by evaporation from the wells between filling and dispensing.
In some cases neither of these JetWell dispensing approaches will be appropriate. For these instances it may be necessary to use a precision dispensing head. The technique most suitable for this is based upon drop-on-demand ink-jet systems where the dose in each well can be set by dispensing a measured number of drops.
The most rapid dispensing would be achieved by having a two dimensional array of nozzles to match the plate. However, this is difficult to construct and hence expensive. The preferred approach is to use a linear array of nozzles which is scanned across the plate. Commercially available ink -jet heads are unlikely to be appropriate, mainly because of the pitch between nozzles and their choice of materials, and a specific implementation is therefore needed. The features of the head which are required are:
* The dead volume of the system must be minimised to avoid wastage of reagents which in some cases may be expensive
* All material in contact with the fluid must be inert to a wide range of acids, alkalis and solvents. Preferably it should be restricted to silicon dioxide, stainless steel, and inert polymers
The system must be easy to fill and to flush as it must be used many times with a wide range of fluids The nozzle diameter is chosen to match the well size. Typically the drop size is selected to be in the range 10° to IO"4 of the well volume
* Each nozzle is operated independently in a drop on demand mode. Typical delivery rates are in the range IO3 to 104 drops per second
* Actuation will preferably be by a thin piezo layer bonded to a silicon or silicon dioxide membrane.
For high density arrays the piezo drivers may be integrated on to the head. Alternatively the head would have gold contacts deposited enabling it to make electrical contact to off head drivers.
The application lends itself to implementation of the head using silicon crystallographic etching techniques to form the structure and either silicon to glass or silicon to silicon bonding for assembly.
Either top shooter or side shooter forms could be implemented at typical pitches required (-*0.5mm).
Calibration
The precision of dispensing achievable either by pressurised jetting or by drop on demand devices depends upon the accurate control of a range of parameters. Where the nozzles become very small it is difficult to achieve precision from the accuracy of manufacture alone. However, by reasonable control of the operating parameters reproducibility can be excellent.
The best approach for achieving precision is therefore to include a technique for the calibration of each device prior to use. Thus, for example, for JetWell plates there may be a distribution of nozzle diameters coupled with a pressure variation which leads to different volumes being dispensed for each well. If a quantative assay is being performed on part-samples from each well, volume variation would influence the result.
The system could be calibrated before use by dispensing a reagent which can be used in a simple standard assay test for volume. This for example could be a colour change reaction which is convenient for automated measurement.
The calibration would be used to correct the results of the real assay rather than to control the volumes dispensed.
The implementation of automated calibration is an important technique for achieving high precision for multinozzle microdispensing systems.

Claims

1. A multiwell plate where the wells have a large opening at the top and a small nozzle hole in the base.
2. A multiwell plate where the diameter of the small hole in the base is chosen so that a jet of liquid is emitted when a pressure pulse is applied to the surface such that by selecting a time for the pressure pulse a precise amount of the volume in the well can be dispensed.
3. A multiwell plate as in (1) which has immobilisation coating on the walls for the purpose of synthesis or assay.
4. A multiwell plate as in (1) in which the nozzle is fabricated by moulding, laser drilling, photolithographic processes, or by etching.
5. A multiwell plate according to claim 1 which is fabricated by stacking layers together which have etched structures which form the wells.
6. The use of an air pressure to eject measured volumes of liquid from the nozzles in the base of the wells described in (1).
7. The generation of the air pressure pulse by the movement of a piston plate in close proximity to the surface of the multiwell plate.
8. The generation of the movement of the piston used in (6) by electrical, hydraulic or mechanical impact means.
PCT/US1996/017072 1995-10-24 1996-10-24 Microwell plates WO1997015394A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP9516786A JP2000500567A (en) 1995-10-24 1996-10-24 Microwell plate
EP96936933A EP0862497A4 (en) 1995-10-24 1996-10-24 Microwell plates

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9521775.8A GB9521775D0 (en) 1995-10-24 1995-10-24 Microwell plates
GB9521775.8 1995-10-24

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WO1997015394A1 true WO1997015394A1 (en) 1997-05-01
WO1997015394A9 WO1997015394A9 (en) 1997-09-25

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Cited By (74)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999001221A1 (en) * 1997-06-30 1999-01-14 INSTITUT FüR MIKROTECHNIK MAINZ GMBH Micro-reaction vessel, arrangement of micro-reaction vessels and method for discharging a liquid therefrom
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US6309828B1 (en) 1998-11-18 2001-10-30 Agilent Technologies, Inc. Method and apparatus for fabricating replicate arrays of nucleic acid molecules
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US6350618B1 (en) 1998-04-27 2002-02-26 Corning Incorporated Redrawn capillary imaging reservoir
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US6436351B1 (en) 1998-07-15 2002-08-20 Deltagen Research Laboratories, L.L.C. Microtitre chemical reaction system
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US6689323B2 (en) 1998-10-30 2004-02-10 Agilent Technologies Method and apparatus for liquid transfer
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WO2004106070A3 (en) * 2003-05-28 2005-02-10 Hoffmann La Roche A device for dispensing drops of a liquid
US6886409B2 (en) 2001-03-13 2005-05-03 Pamgene International B.V. System for controlling the flow of a fluid through a substrate
US6893877B2 (en) 1998-01-12 2005-05-17 Massachusetts Institute Of Technology Methods for screening substances in a microwell array
EP1627680A2 (en) * 2004-08-17 2006-02-22 Samsung Electronics Co., Ltd. Inkjet spotting apparatus and method for manufacturing microarrays
US7037680B2 (en) 1993-09-21 2006-05-02 The United States Of America As Represented By The Secretary Of The Army Recombinant light chains of botulinum neurotoxins and light chain fusion proteins for use in research and clinical therapy
US7063216B2 (en) 2003-09-04 2006-06-20 Millipore Corporation Underdrain useful in the construction of a filtration device
US7081529B2 (en) 1993-09-21 2006-07-25 The United States Of America As Represented By The Secretary Of The Army Recombinant vaccine against botulinum neurotoxin
US7105134B2 (en) 2001-03-13 2006-09-12 Pamgene B.V. Device for holding a substrate
US7211224B2 (en) 2002-05-23 2007-05-01 Millipore Corporation One piece filtration plate
US7227010B2 (en) 1993-09-21 2007-06-05 United States Of America As Represented By The Secretary Of The Army Recombinant light chains of botulinum neurotoxins and light chain fusion proteins for use in research and clinical therapy
US7427379B1 (en) 1999-03-19 2008-09-23 Biotage Ab Liquid dispensing apparatus
DE102007041071A1 (en) * 2007-08-30 2009-03-05 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Fluid reception device for supplying the fluid on sample carrier, comprises recesses, whose base has holes, which are formed so that the capillary pressure in the hole is greater than the pressure produced through the fluid in the recess
US8318479B2 (en) 2004-05-19 2012-11-27 Massachusetts Institute Of Technology Perfused three-dimensional cell/tissue disease models
US8354080B2 (en) 2009-04-10 2013-01-15 Canon U.S. Life Sciences, Inc. Fluid interface cartridge for a microfluidic chip
US8753588B2 (en) 2003-10-15 2014-06-17 Emd Millipore Corporation Support and stand-off ribs for underdrain for multi-well device
US8900856B2 (en) 2004-04-08 2014-12-02 Biomatrica, Inc. Integration of sample storage and sample management for life science
US8906618B2 (en) 2000-02-18 2014-12-09 The Board Of Trustees Of The Leland Stanford Junior University Apparatus and methods for parallel processing of micro-volume liquid reactions
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US9376709B2 (en) 2010-07-26 2016-06-28 Biomatrica, Inc. Compositions for stabilizing DNA and RNA in blood and other biological samples during shipping and storage at ambient temperatures
US9428800B2 (en) 2002-12-20 2016-08-30 Life Technologies Corporation Thermal cycling apparatus and method
US9725703B2 (en) 2012-12-20 2017-08-08 Biomatrica, Inc. Formulations and methods for stabilizing PCR reagents
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US10064404B2 (en) 2014-06-10 2018-09-04 Biomatrica, Inc. Stabilization of thrombocytes at ambient temperatures
US10195579B2 (en) 1999-03-19 2019-02-05 Life Technologies Corporation Multi-through hole testing plate for high throughput screening
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US10568317B2 (en) 2015-12-08 2020-02-25 Biomatrica, Inc. Reduction of erythrocyte sedimentation rate
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Families Citing this family (5)

* Cited by examiner, † Cited by third party
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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4111754A (en) * 1976-11-29 1978-09-05 Hydow Park Immunological testing devices and methods
US4304865A (en) * 1978-08-31 1981-12-08 National Research Development Corporation Harvesting material from micro-culture plates
US4483925A (en) * 1982-12-30 1984-11-20 Becton, Dickinson And Company Liquid removal device
US4493815A (en) * 1983-07-28 1985-01-15 Bio-Rad Laboratories, Inc. Supporting and filtering biochemical test plate assembly
US4787988A (en) * 1987-02-20 1988-11-29 Biomedical Research And Development Laboratories, Inc. Cell harvester
US5039493A (en) * 1990-05-04 1991-08-13 The United States Of America As Represented By The Secretary Of The Navy Positive pressure blotting apparatus with hydropholic filter means
US5395594A (en) * 1991-08-26 1995-03-07 Shimadzu Corporation Simultaneous multiple chemical synthesizer

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6433070U (en) * 1987-08-22 1989-03-01
US5159197A (en) * 1988-02-16 1992-10-27 Difco Laboratories Luminescence test and exposure apparatus
SE9002579D0 (en) * 1990-08-07 1990-08-07 Pharmacia Ab METHOD AND APPARATUS FOR CARRYING OUT BIOCHEMICAL REACTIONS
US5472672A (en) * 1993-10-22 1995-12-05 The Board Of Trustees Of The Leland Stanford Junior University Apparatus and method for polymer synthesis using arrays

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4111754A (en) * 1976-11-29 1978-09-05 Hydow Park Immunological testing devices and methods
US4304865A (en) * 1978-08-31 1981-12-08 National Research Development Corporation Harvesting material from micro-culture plates
US4483925A (en) * 1982-12-30 1984-11-20 Becton, Dickinson And Company Liquid removal device
US4493815A (en) * 1983-07-28 1985-01-15 Bio-Rad Laboratories, Inc. Supporting and filtering biochemical test plate assembly
US4787988A (en) * 1987-02-20 1988-11-29 Biomedical Research And Development Laboratories, Inc. Cell harvester
US5039493A (en) * 1990-05-04 1991-08-13 The United States Of America As Represented By The Secretary Of The Navy Positive pressure blotting apparatus with hydropholic filter means
US5395594A (en) * 1991-08-26 1995-03-07 Shimadzu Corporation Simultaneous multiple chemical synthesizer

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP0862497A4 *

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Publication number Priority date Publication date Assignee Title
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DE19828995B4 (en) * 1997-06-30 2006-01-12 INSTITUT FüR MIKROTECHNIK MAINZ GMBH Arrangement of microreaction vessels and method for dispensing a liquid from an array of microreaction vessels
WO1999001221A1 (en) * 1997-06-30 1999-01-14 INSTITUT FüR MIKROTECHNIK MAINZ GMBH Micro-reaction vessel, arrangement of micro-reaction vessels and method for discharging a liquid therefrom
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EP1019696A1 (en) * 1997-09-19 2000-07-19 Aclara BioSciences, Inc. Apparatus and method for transferring liquids
WO1999019067A1 (en) * 1997-10-10 1999-04-22 Biosepra, Inc. Aligned multiwell multiplate stack and method for processing biological/chemical samples using the same
US7273759B2 (en) 1997-10-10 2007-09-25 Pall Corporation Plate alignment and sample transfer indicia for a multiwell multiplate stack and method for processing biological/chemical samples using the same
US6464942B2 (en) 1997-10-10 2002-10-15 Ciphergen Biosystems, Inc. Plate alignment and sample transfer indicia for a multiwell multiplate stack and method for processing biological/chemical samples using the same
US6387331B1 (en) 1998-01-12 2002-05-14 Massachusetts Institute Of Technology Method and apparatus for performing microassays
US6893877B2 (en) 1998-01-12 2005-05-17 Massachusetts Institute Of Technology Methods for screening substances in a microwell array
JP2009244271A (en) * 1998-01-12 2009-10-22 Massachusetts Inst Of Technol <Mit> Method and apparatus for performing microassays
JP4668334B2 (en) * 1998-01-12 2011-04-13 マサチューセッツ インスティテュート オブ テクノロジー Trace analysis method and apparatus
WO1999034920A1 (en) * 1998-01-12 1999-07-15 Massachusetts Institute Of Technology Method and apparatus for performing microassays
US6743633B1 (en) 1998-01-12 2004-06-01 Massachusetts Institute Of Technology Method for performing microassays
US6401769B1 (en) 1998-01-17 2002-06-11 Central Research Laboratories Limited Apparatus for dispensing a predetermined volume of a liquid
WO1999036176A1 (en) 1998-01-17 1999-07-22 Central Research Laboratories Limited Apparatus for dispensing a predetermined volume of a liquid
US6197575B1 (en) * 1998-03-18 2001-03-06 Massachusetts Institute Of Technology Vascularized perfused microtissue/micro-organ arrays
GB2336908A (en) * 1998-04-17 1999-11-03 Merck & Co Inc Multiwell plate
EP1075327A1 (en) * 1998-04-27 2001-02-14 Corning Incorporated Redrawn capillary imaging reservoir
US6596237B1 (en) 1998-04-27 2003-07-22 Nicholas F. Borrelli Redrawn capillary imaging reservoir
US6350618B1 (en) 1998-04-27 2002-02-26 Corning Incorporated Redrawn capillary imaging reservoir
EP1075327A4 (en) * 1998-04-27 2006-01-25 Corning Inc Redrawn capillary imaging reservoir
EP0955084A1 (en) * 1998-04-27 1999-11-10 Corning Incorporated Redrawn capillary imaging reservoir
WO1999060373A1 (en) * 1998-05-20 1999-11-25 Nanomont Gesellschaft Für Nanotechnologie Mbh Method and device for fixing micro- and/or nano-objects
US6762061B1 (en) 1998-07-03 2004-07-13 Corning Incorporated Redrawn capillary imaging reservoir
US6436351B1 (en) 1998-07-15 2002-08-20 Deltagen Research Laboratories, L.L.C. Microtitre chemical reaction system
EP1250955A1 (en) * 1998-09-08 2002-10-23 Tibotec N.V. Method for the rapid screening of analytes
US6103199A (en) * 1998-09-15 2000-08-15 Aclara Biosciences, Inc. Capillary electroflow apparatus and method
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EP1113850A1 (en) * 1998-09-17 2001-07-11 Advion BioSciences, Inc. Integrated monolithic microfabricated electrospray and liquid chromatography system and method
WO2000020117A2 (en) * 1998-10-02 2000-04-13 Central Research Laboratories Limited Method of and apparatus for removing a substance from a container
WO2000020117A3 (en) * 1998-10-02 2003-04-17 Central Research Lab Ltd Method of and apparatus for removing a substance from a container
WO2000024511A1 (en) * 1998-10-26 2000-05-04 The Regents Of The University Of California An integrated titer plate-injector head for microdrop array preparation, storage and transfer
US6165417A (en) * 1998-10-26 2000-12-26 The Regents Of The University Of California Integrated titer plate-injector head for microdrop array preparation, storage and transfer
DE19950809B4 (en) * 1998-10-30 2007-11-15 Agilent Technologies, Inc. (n.d.Ges.d. Staates Delaware), Santa Clara Method and apparatus for fluid transfer
US6689323B2 (en) 1998-10-30 2004-02-10 Agilent Technologies Method and apparatus for liquid transfer
US6309828B1 (en) 1998-11-18 2001-10-30 Agilent Technologies, Inc. Method and apparatus for fabricating replicate arrays of nucleic acid molecules
US10195579B2 (en) 1999-03-19 2019-02-05 Life Technologies Corporation Multi-through hole testing plate for high throughput screening
US7427379B1 (en) 1999-03-19 2008-09-23 Biotage Ab Liquid dispensing apparatus
WO2001018539A3 (en) * 1999-09-06 2001-09-27 Amersham Pharm Biotech Uk Ltd Mixing chamber
US6955462B1 (en) 1999-09-06 2005-10-18 Amersham Plc Mixing chamber
WO2001018539A2 (en) * 1999-09-06 2001-03-15 Amersham Biosciences Uk Ltd. Mixing chamber
WO2001019517A1 (en) * 1999-09-14 2001-03-22 Pamgene, B.V. Analytical test device with substrate having oriented through going channels and improved methods and apparatus for using same
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US6849408B2 (en) 1999-09-14 2005-02-01 Pamgene B.V. Analytical test device with substrate having oriented through going channels and improved methods and apparatus for using same
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WO2001019502A3 (en) * 1999-09-17 2001-08-09 Millipore Corp High throughput screening card
US6544480B1 (en) 1999-10-26 2003-04-08 Tibotec Bvba Device and related method for dispensing small volumes of liquid
WO2001030499A1 (en) * 1999-10-26 2001-05-03 Tibotec Nv Device and related method for delivering small volumes of liquid
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EP1103305A1 (en) * 1999-11-26 2001-05-30 F.Hoffmann-La Roche Ag Macroactuator coupling system contained in a pipetting module
US7125519B1 (en) 1999-11-26 2006-10-24 Roche Diagnostics Corporation Actuator coupling system and a pipetting module comprising such a coupling system
WO2001037996A1 (en) * 1999-11-26 2001-05-31 F. Hoffmann-La Roche Ag Actuator coupling system and a pipetting module comprising such a coupling system
EP1269518A1 (en) * 1999-12-30 2003-01-02 Advion BioSciences, Inc. Multiple electrospray device, systems and methods
EP1269518A4 (en) * 1999-12-30 2006-06-28 Advion Biosciences Inc Multiple electrospray device, systems and methods
EP1248949A4 (en) * 2000-01-18 2007-07-25 Advion Biosciences Inc Separation media, multiple electrospray nozzle system and method
EP1248949A1 (en) * 2000-01-18 2002-10-16 Advion BioSciences, Inc. Separation media, multiple electrospray nozzle system and method
US8906618B2 (en) 2000-02-18 2014-12-09 The Board Of Trustees Of The Leland Stanford Junior University Apparatus and methods for parallel processing of micro-volume liquid reactions
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EP1142641A1 (en) * 2000-04-04 2001-10-10 CSEM Centre Suisse d'Electronique et de Microtechnique SA Preparation of biological samples by means of a micro-nozzle matrix
WO2001089694A1 (en) * 2000-05-22 2001-11-29 Biorobotics Limited Liquid transfer device
US7731904B2 (en) 2000-09-19 2010-06-08 Canon Kabushiki Kaisha Method for making probe support and apparatus used for the method
US9248445B2 (en) 2000-09-19 2016-02-02 Canon Kabushiki Kaisha Method for making probe support and apparatus used for the method
EP1188475A3 (en) * 2000-09-19 2003-07-23 Canon Kabushiki Kaisha Method for making probe support and apparatus used for the method
WO2002040164A1 (en) * 2000-11-15 2002-05-23 Biomerieux S.A. Method for depositing an analyte solution, device therefor, solid support produced by the method and diagnosis kit comprising such a solid support
FR2816711A1 (en) * 2000-11-15 2002-05-17 Biomerieux Sa Analyte solution droplet maker e.g. for manufacture of bio-chips uses container with base outlet and side projection applied with impact to support surface
US6824024B2 (en) 2000-11-17 2004-11-30 Tecan Trading Ag Device for the take-up and/or release of liquid samples
US6869571B2 (en) 2000-11-17 2005-03-22 Tecan Trading Ag Device for aspirating and dispensing liquid samples
CH695544A5 (en) * 2000-11-17 2006-06-30 Tecan Trading Ag Apparatus for dispensing or aspirating / dispensing liquid samples.
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WO2002040163A1 (en) * 2000-11-17 2002-05-23 Tecan Trading Ag Device for the take-up and/or release of liquid samples
US7105134B2 (en) 2001-03-13 2006-09-12 Pamgene B.V. Device for holding a substrate
US6886409B2 (en) 2001-03-13 2005-05-03 Pamgene International B.V. System for controlling the flow of a fluid through a substrate
EP1442135A2 (en) * 2001-10-11 2004-08-04 Xerox Corporation Devices and methods for detecting genetic sequences
EP1442135A4 (en) * 2001-10-11 2006-09-13 Xerox Corp Devices and methods for detecting genetic sequences
EP1466144A1 (en) * 2001-12-19 2004-10-13 Sau Lan Tang Staats Interface members and holders for microfluidic array devices
EP1466144A4 (en) * 2001-12-19 2007-09-05 Sau Lan Tang Staats Interface members and holders for microfluidic array devices
WO2003074166A3 (en) * 2002-02-28 2004-04-29 Edc Biosystems Inc Apparatus and method for composing high density materials onto target substrates by a rapid sequence
WO2003074166A2 (en) * 2002-02-28 2003-09-12 Edc Biosystems, Inc. Apparatus and method for composing high density materials onto target substrates by a rapid sequence
WO2003079030A1 (en) * 2002-03-14 2003-09-25 Cybio Ag Method for characterizing a highly parallelized liquid handling technique using microplates and test kit for carrying out the method
GB2403535B (en) * 2002-03-14 2005-05-11 Cybio Ag Method for characterizing a highly parallelized liquid handling technique using microplates and test kit for carying out the method
US7504264B2 (en) 2002-03-14 2009-03-17 Cybio Ag Method for characterizing a highly parallelized liquid handling technique using microplates and test kit for carrying out the method
GB2403535A (en) * 2002-03-14 2005-01-05 Cybio Ag Method for characterizing a highly parallelized liquid handling technique using microplates and test kit for carrying out the method
US7211224B2 (en) 2002-05-23 2007-05-01 Millipore Corporation One piece filtration plate
US9428800B2 (en) 2002-12-20 2016-08-30 Life Technologies Corporation Thermal cycling apparatus and method
WO2004106070A3 (en) * 2003-05-28 2005-02-10 Hoffmann La Roche A device for dispensing drops of a liquid
US7063216B2 (en) 2003-09-04 2006-06-20 Millipore Corporation Underdrain useful in the construction of a filtration device
US8753588B2 (en) 2003-10-15 2014-06-17 Emd Millipore Corporation Support and stand-off ribs for underdrain for multi-well device
US9266108B2 (en) 2004-03-12 2016-02-23 Life Technologies Corporation Nanoliter array loading
US10974247B2 (en) 2004-03-12 2021-04-13 Life Technologies Corporation Nanoliter array loading
US10065189B2 (en) 2004-03-12 2018-09-04 Life Technologies Corporation Nanoliter array loading
US9078426B2 (en) 2004-04-08 2015-07-14 Biomatrica, Inc. Integration of sample storage and sample management for life science
US8900856B2 (en) 2004-04-08 2014-12-02 Biomatrica, Inc. Integration of sample storage and sample management for life science
US8318479B2 (en) 2004-05-19 2012-11-27 Massachusetts Institute Of Technology Perfused three-dimensional cell/tissue disease models
US11154834B2 (en) 2004-08-04 2021-10-26 Life Technologies Corporation Coating process for microfluidic sample arrays
US10213761B2 (en) 2004-08-04 2019-02-26 Life Technologies Corporation Coating process for microfluidic sample arrays
EP1627680A3 (en) * 2004-08-17 2006-10-11 Samsung Electronics Co., Ltd. Inkjet spotting apparatus and method for manufacturing microarrays
EP1627680A2 (en) * 2004-08-17 2006-02-22 Samsung Electronics Co., Ltd. Inkjet spotting apparatus and method for manufacturing microarrays
DE102007041071B4 (en) * 2007-08-30 2010-02-04 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Device for holding a liquid and device for applying liquids to sample carriers and method for this purpose
DE102007041071A1 (en) * 2007-08-30 2009-03-05 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Fluid reception device for supplying the fluid on sample carrier, comprises recesses, whose base has holes, which are formed so that the capillary pressure in the hole is greater than the pressure produced through the fluid in the recess
US8354080B2 (en) 2009-04-10 2013-01-15 Canon U.S. Life Sciences, Inc. Fluid interface cartridge for a microfluidic chip
US8871156B2 (en) 2009-04-10 2014-10-28 Canon U.S. Life Sciences, Inc. Fluid interface cartridge for a microfluidic chip
US10092902B2 (en) 2009-04-10 2018-10-09 Canon U.S. Life Sciences, Inc. Fluid interface cartridge for a microfluidic chip
US9138744B2 (en) 2009-04-10 2015-09-22 Canon U.S. Life Sciences, Inc. Fluid interface cartridge for a microfluidic chip
US9376709B2 (en) 2010-07-26 2016-06-28 Biomatrica, Inc. Compositions for stabilizing DNA and RNA in blood and other biological samples during shipping and storage at ambient temperatures
US9845489B2 (en) 2010-07-26 2017-12-19 Biomatrica, Inc. Compositions for stabilizing DNA, RNA and proteins in saliva and other biological samples during shipping and storage at ambient temperatures
US9999217B2 (en) 2010-07-26 2018-06-19 Biomatrica, Inc. Compositions for stabilizing DNA, RNA, and proteins in blood and other biological samples during shipping and storage at ambient temperatures
US9725703B2 (en) 2012-12-20 2017-08-08 Biomatrica, Inc. Formulations and methods for stabilizing PCR reagents
US10772319B2 (en) 2014-06-10 2020-09-15 Biomatrica, Inc. Stabilization of thrombocytes at ambient temperatures
US10064404B2 (en) 2014-06-10 2018-09-04 Biomatrica, Inc. Stabilization of thrombocytes at ambient temperatures
US11672247B2 (en) 2014-06-10 2023-06-13 Biomatrica, Inc. Stabilization of thrombocytes at ambient temperatures
CN110042060A (en) * 2014-08-05 2019-07-23 雅马哈发动机株式会社 Plate
US10568317B2 (en) 2015-12-08 2020-02-25 Biomatrica, Inc. Reduction of erythrocyte sedimentation rate
US11116205B2 (en) 2015-12-08 2021-09-14 Biomatrica, Inc. Reduction of erythrocyte sedimentation rate
LU501475B1 (en) * 2022-02-15 2023-08-16 Dispendix Gmbh Method for determining a function for determining a volume of liquid to be dispensed
LU501476B1 (en) * 2022-02-15 2023-08-16 Dispendix Gmbh Method for determining a function for determining a volume of liquid to be dispensed
LU501473B1 (en) * 2022-02-15 2023-08-16 Dispendix Gmbh Method for setting a volume of liquid to be dispensed
LU501474B1 (en) * 2022-02-15 2023-08-17 Dispendix Gmbh Method for determining a volume of liquid arranged in a receptacle
WO2023156354A1 (en) * 2022-02-15 2023-08-24 Dispendix Gmbh Method for determining a volume of liquid arranged in a receptacle
LU501663B1 (en) * 2022-03-15 2023-09-20 Dispendix Gmbh Method for determining a function for determining a volume of liquid to be dispensed
LU501825B1 (en) * 2022-04-10 2023-10-10 Dispendix Gmbh Method for setting a volume of liquid to be dispensed by using a function
LU501823B1 (en) * 2022-04-10 2023-10-10 Dispendix Gmbh Method for determining a function for determining a volume of liquid to be dispensed
LU501824B1 (en) * 2022-04-10 2023-10-10 Dispendix Gmbh Method for setting a volume of liquid to be dispensed from a receptacle
LU502213B1 (en) * 2022-06-02 2023-12-04 Dispendix Gmbh Method for Determining a Volume of Liquid dispensed from a Receptacle

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GB9521775D0 (en) 1996-01-03

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