EP2222832A2 - Support de puits de picolitres et leur procédé de fabrication - Google Patents

Support de puits de picolitres et leur procédé de fabrication

Info

Publication number
EP2222832A2
EP2222832A2 EP08848869A EP08848869A EP2222832A2 EP 2222832 A2 EP2222832 A2 EP 2222832A2 EP 08848869 A EP08848869 A EP 08848869A EP 08848869 A EP08848869 A EP 08848869A EP 2222832 A2 EP2222832 A2 EP 2222832A2
Authority
EP
European Patent Office
Prior art keywords
substrate
holding device
adhesive
pico liter
optionally
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP08848869A
Other languages
German (de)
English (en)
Other versions
EP2222832A4 (fr
Inventor
Mordechai Deutsch
Assaf Deutsch
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Seng Enterprises Ltd
Original Assignee
Seng Enterprises Ltd
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
Priority claimed from US11/940,996 external-priority patent/US7888110B2/en
Application filed by Seng Enterprises Ltd filed Critical Seng Enterprises Ltd
Publication of EP2222832A2 publication Critical patent/EP2222832A2/fr
Publication of EP2222832A4 publication Critical patent/EP2222832A4/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M23/00—Constructional details, e.g. recesses, hinges
    • C12M23/02—Form or structure of the vessel
    • C12M23/12—Well or multiwell plates
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M23/00—Constructional details, e.g. recesses, hinges
    • C12M23/22—Transparent or translucent parts
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/02—Adapting objects or devices to another
    • B01L2200/026—Fluid interfacing between devices or objects, e.g. connectors, inlet details
    • B01L2200/027—Fluid interfacing between devices or objects, e.g. connectors, inlet details for microfluidic devices
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/06—Fluid handling related problems
    • B01L2200/0647—Handling flowable solids, e.g. microscopic beads, cells, particles
    • B01L2200/0668—Trapping microscopic beads
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/04—Closures and closing means
    • B01L2300/041—Connecting closures to device or container
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0809—Geometry, shape and general structure rectangular shaped
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0809—Geometry, shape and general structure rectangular shaped
    • B01L2300/0822—Slides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0887—Laminated structure
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0893—Geometry, shape and general structure having a very large number of wells, microfabricated wells
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/12—Specific details about materials
    • B01L2300/123—Flexible; Elastomeric
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00—Moving or stopping fluids
    • B01L2400/04—Moving fluids with specific forces or mechanical means
    • B01L2400/0403—Moving fluids with specific forces or mechanical means specific forces
    • B01L2400/0406—Moving fluids with specific forces or mechanical means specific forces capillary forces
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/502715—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/508—Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above
    • B01L3/5085—Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above for multiple samples, e.g. microtitration plates
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00—Metal working
    • Y10T29/49—Method of mechanical manufacture
    • Y10T29/49826—Assembling or joining

Definitions

  • the present invention in some embodiments thereof, relates to devices that include pico liter wells used in the study of cellular biology. More specifically, in some embodiments, there are provided holding devices having a multiplicity of pico liter wells formed in a substrate having a refractive index similar to that of water, and methods of making the same. In some embodiments, there are provided embossing or embossing-like methods.
  • optical artifacts may be caused by the differences between the refractive indices of the medium (typically an aqueous buffer composed largely of water) carrying the cells and the material forming the pico liter wells. Such artifacts may be caused by the refraction of light passing from the substrate to the cell carrying medium.
  • the medium typically an aqueous buffer composed largely of water
  • An aspect of some embodiments of the invention relates to a method of forming a cell holder by embossing.
  • a base is covered with an optionally liquid substrate, contacted with a die and the substrate is at least partially hardened.
  • the die defines a plurality of pico liter wells in the substrate.
  • the substrate is adhesive to the base, but not to the die, optionally in spite of the substrate being smooth and the die having small features.
  • the die and adhesive and base materials are selected to afford such differential adhesion.
  • the die is removed before the substrate hardens.
  • at least two areas on the substrate are patterned, each with a different final pattern.
  • one or more walls or barriers are added to the cell holder before, during or after embossing.
  • the base is not mechanically prepared for the substrate.
  • the die is assembled from individual well forming die elements.
  • a handle with a plurality of clamps to hold the die elements is used.
  • other means to hold die elements together into a template are used.
  • the die also serves as a template for non-well embossed elements.
  • the picowell arrays are separated by barriers which may have selected blocking ability, for example, being fluid blocking or cell blocking or fluid passing.
  • a holding device for studying cells in a medium in accordance with an exemplary embodiment of this invention comprises at least one cavity defined by generally inert wall surrounding a substrate.
  • the substrate has a surface in which a plurality of pico liter wells is formed.
  • the substrate is translucent and has a refractive index substantially equal to the refractive index of the medium.
  • An exemplary holding device for studying cells in accordance with an exemplary embodiment of this invention comprises a substantially transparent substrate having a refractive index of 1.33.
  • the substrate has a multiplicity of pico liter wells formed in an upper surface and a wall structure attached thereto.
  • an exemplary embodiment of the present invention includes a holding device for studying cells comprising a substantially transparent carrier plate having a plurality of cavities surrounded by walls formed in a first surface of the carrier plate, a layer of adhesive, which is known to those skilled in the art, disposed on a bottom surface of each cavity, a layer of substantially transparent substrate material having a refractive index of 1.33 and having a multiplicity of pico liter wells formed in an upper surface thereof disposed on the adhesive layer.
  • MY- 133 is known to have a refractive index close to that of water, heretofore MY-133 has apparently not been considered suitable for use as an inert substrate for holding live cells in a medium.
  • other adhesive materials possibly with other refractive indexes are used for embossing.
  • the invention in some embodiments thereof, includes a method of making a holding device for studying cells comprising providing a layer of curable substrate, disposing a wall structure on the layer of curable substrate, embossing a multiplicity of pico liter wells in a surface of the curable substrate, and curing the substrate.
  • the invention in some embodiments thereof, includes a method of making a holding device for studying cells comprising providing a carrier plate, applying a first adhesive layer to the carrier plate, depositing a curable substrate on the adhesive layer, applying a second layer of adhesive to the substrate, attaching a wall structure to the second layer of the adhesive, forming a multiplicity of pico liter wells in the substrate with a template, curing the substrate, and removing the template.
  • the invention in some embodiments thereof, also includes a method of making a holding device comprising providing a carrier plate having a plurality of cavities surrounded by walls, depositing a curable substrate in each cavity, embossing a multiplicity of pico liter wells in the curable substrate with a die, and curing the substrate.
  • the term "embossing” includes contacting a substrate with a die and then causing the substrate to set in its new form, for example, by UV curing, radiation curing, chemical curing, hardening and/or cooling.
  • the setting is at room temperature using UV curing, which optionally reduces distortions.
  • a holding device for studying cells comprising a plurality of spaced apart pico liter well arrays.
  • said pico liter well arrays comprise embossed regions.
  • the device comprises at least one barrier between two pico liter well arrays.
  • said arrays are arranged in a two dimensional repeating pattern.
  • said arrays include at least two different well array designs.
  • said device includes at least one non- well embossed region fluidically connected to at least one of said arrays.
  • a holding device for studying cells comprising at least two defined regions:
  • a pico liter well array region including a plurality of pico liter wells; and (b) a non cell holding region in fluid communication with said pico liter well region, wherein fluid can be one or both of added and removed from said non cell holding region without disturbing cells in said picowells.
  • the device comprises at least one fluid permeable barrier between said regions.
  • said non-cell holding array has an embossed design.
  • said pico liter well array is embossed.
  • the device comprises a plurality of pico liter well array regions.
  • a method of forming a template for a picowell array comprising:
  • the method comprises assembling a plurality of said set material into a composite template for embossing a cell holding device.
  • the method comprises further hardening said hardening material after removal of said die.
  • the method comprises priming said base before covering with said hardening material.
  • said hardening material is a liquid UV curable adhesive.
  • said UV curable adhesive has an index of refraction within 5% of that of water.
  • said base is not mechanically abraded under said substrate.
  • the method comprises forming at least one barrier between said region and other parts of said base.
  • said barrier is formed on said base before said contacting.
  • said barrier is formed on said base during said contacting.
  • said die defines a plurality of spaced apart pico well regions.
  • said die defines a plurality of different embossing patterns to be embossed on said hardening material simultaneously.
  • a holding device for studying cells comprising: at least one cavity adapted to receive a sample of cells in a medium consisting essentially of water, the cavity having a substrate and a generally inert wall, wherein the substrate includes a surface for receiving the medium, and wherein the surface includes a multiplicity of pico liter wells and is characterized in that the substrate is substantially translucent and has a refractive index equal to the refractive index of the medium.
  • the medium comprises water and wherein the substrate has a Refractive Index of 1.33.
  • the substrate is moldable.
  • the substrate is inert.
  • the holding device is a carrier plate, and wherein a first adhesive is disposed between the carrier plate and the substrate.
  • the device comprises a second adhesive disposed between the generally inert wall and the substrate.
  • at least one of the substrate, the first adhesive and the second adhesive are UV-light curable.
  • the first adhesive and the second adhesive are acrylic.
  • the device comprises a light source transmitting the UV-light through a bottom surface of the at least one cavity.
  • the substrate is exposed to the UV- light under vacuum pressure.
  • the vacuum pressure is in the range of 0.3 - 0.5 mmHg.
  • the substrate is exposed to the UV- light under inert gas.
  • a method of making a holding device for studying cells comprising: providing a carrier plate; applying a first adhesive layer to the carrier plate; depositing a curable substrate on the adhesive layer; applying a second layer of adhesive to the substrate; attaching a wall structure to the second layer of adhesive; forming a multiplicity of pico liter wells in the substrate with a template; curing the substrate; and removing the template.
  • curing the substrate includes exposing the substrate to UV-light through the carrier plate.
  • the method comprises repeating curing the substrate after removing the template, wherein curing the substrate after removing the template includes exposing the substrate to UV-light under a vacuum pressure through the carrier plate.
  • forming a multiplicity of pico liter wells in the substrate with a template further comprises embossing a surface of the substrate with a die.
  • a method of making a holding device comprising: providing a layer of curable substrate; disposing a wall structure on the layer of curable substrate; embossing a multiplicity of pico liter wells in a surface of the curable substrate; and curing the substrate.
  • the method comprises disposing a first adhesive between the curable substrate and the wall structure.
  • curing the substrate comprises exposing the substrate to the UV-light through the carrier.
  • a method of making a holding device for studying cells comprising: providing a carrier plate having a plurality of cavities surrounded by walls; depositing a curable substrate in each cavity; embossing a multiplicity of pico liter wells in the curable substrate with a die; and curing the substrate.
  • the method comprises applying a first adhesive layer in each cavity before depositing the curable substrate in each cavity.
  • curing the substrate comprises exposing the substrate and the first adhesive to UV-light through the carrier plate when the die is in place.
  • the method comprises removing the die and exposing the substrate to UV-light under a vacuum or inert gas through the carrier plate.
  • a holding device for studying cells comprising: a layer of substantially transparent substrate material having a multiplicity of pico liter wells having a refractive index of 1.33; and, a wall structure attached to the substrate.
  • the substrate is UV-light curable.
  • the device comprises a first adhesive disposed between the wall structure and the substrate.
  • the device comprises a substantially transparent carrier plate having a plurality of cavities surrounded by walls formed in a first surface of the carrier plate, wherein the layer of substantially transparent substrate material is disposed on the carrier plate.
  • Implementation of the method and/or system of embodiments of the invention can involve performing or completing selected tasks manually, automatically, or a combination thereof. Moreover, according to actual instrumentation and equipment of embodiments of the method and/or system of the invention, several selected tasks could be implemented by hardware, by software or by firmware or by a combination thereof using an operating system.
  • a data processor such as a computing platform for executing a plurality of instructions.
  • the data processor includes a volatile memory for storing instructions and/or data and/or a non-volatile storage, for example, a magnetic hard-disk and/or removable media, for storing instructions and/or data.
  • a network connection is provided as well.
  • a display and/or a user input device such as a keyboard or mouse are optionally provided as well.
  • FIG. 1 is a perspective view of a presently preferred embodiment of a holding device
  • FIG. 2 is a cross-sectional view of a carrier plate having a substrate and a plurality of walls
  • FIG. 3 is a cross-sectional view of the carrier plate having a first adhesive and the substrate applied thereon;
  • FIG. 4 is a cross-sectional view of the plurality of walls and templates
  • FIG. 5 is a cross-sectional view of the holding device showing the plurality of walls mounted on the carrier plate and showing dies embossing a plurality of pico liter wells in the substrate;
  • FIG. 6 is a cross-sectional view of the holding device showing the pico liter wells embossed in the substrate;
  • FIG. 7 is a cross-sectional view of the holding device showing the first adhesive and the substrate applied to the bottom of cavities;
  • FIG. 8 is a cross-sectional view of the holding device showing the substrate applied to the bottom of the cavities;
  • FIG. 9 is a perspective view of a Petri-dish having the plurality of pico liter wells formed in the substrate;
  • FIG. 10 is a cross-sectional view of the Petri-dish having the plurality of pico liter wells formed in the substrate;
  • FIGs. 1 IA-11C illustrate a method of forming an embossing die, in accordance with an exemplary embodiment of the invention
  • FIGs. 12A-12C illustrate a method of forming an array of pico liter well arrays, in accordance with an exemplary embodiment of the invention
  • FIGs. 13A and 13B illustrate a Petri-dish with an isolated pico liter well array formed thereon, in accordance with an exemplary embodiment of the invention
  • FIGs. 14A-14C illustrate Petri-dish designs with one or more pico liter well arrays and with a partitioning element, in accordance with an exemplary embodiment of the invention
  • FIGs. 15 A and 15B illustrate Petri-dish designs with multiple partitioning elements, in accordance with an exemplary embodiment of the invention.
  • FIGs. 16A-16B illustrate a microscope slide with a pico liter well array, in a blow-apart view and in an assembled view, in accordance with an exemplary embodiment of the invention.
  • the present invention in some embodiments thereof, relates to devices that include pico liter wells used in the study of cellular biology. More specifically, in some embodiments, there are provided holding devices having a multiplicity of pico liter wells formed in or on a transparent, non-cytotoxic substrate, optionally, but not necessarily having a refractive index similar to that of water, and methods of making the same. In some embodiments, there are provided embossing methods.
  • FIG. 1 is a perspective view of a holding device 10 having at least one cavity 12.
  • Holding device 10 may be a Petri dish or similar device, or an assay plate having 6, 12, 48, 96, 384, or 1536 cavities and a standard 8.5 cm by 12.5 cm footprint.
  • the cavity or plurality of cavities 12 is configured to receive aliquots of cells that are temporarily suspended in a desired medium, such as a buffered medium comprising mostly water.
  • a desired medium such as a buffered medium comprising mostly water.
  • the diameter of the individual cavities 12 depends on the number of wells included on the holding device 10.
  • the cavities 12 of a 1536 well plate have a diameter greater than approximately 250 micrometers.
  • the volume of the cavities 12 also depends on the number of cavities and on the depth of each cavity. In some examples, the volume of each cavity is greater than 5 x 10-6 liters.
  • the Gavities are designed to hold groups of cells, cell clusters, embrionic bodies, interacting cells and/or oocytes, for example, which may affect the desired geometry and/or volume of the picowells.
  • 100 micron diameter wells may be designed as deep wells, in order to accommodate one large cells spheroid, or alternatively, as a shallow pan, in order to explore group of small cells (e.g. lymphocytes, yeast cells) while maintaining them in a same focal plane of a microscope.
  • Exemplary well diameters include 1 micron, 5 microns, 10 microns, 30 microns, 60 microns, 100 microns and 250 microns and smaller, intermediate or large sizes may be provided as well.
  • Exemplary depths include 1 micron, 5 microns, 10 microns, 30 microns, 60 microns, 100 microns and 250 microns and smaller, intermediate or large sizes may be provided as well.
  • the cavities 12 optionally further include generally inert walls 14 (also referred to hereinafter as a plurality of walls or a wall structure) and a bottom substrate 16 having a multiplicity of pico liter wells 18 (as shown in FIG. 9).
  • the pico liter wells 18 are configured to physically confine individual cells or a group of cells, wherein the diameter of the pico liter wells 18 depends on the size of the cells to be used.
  • the cells optionally have a diameter between about 5 and 250 micrometers and the pico liter well size and shape may correspond thereto.
  • the substrate 16 is curable, moldable and inert.
  • the substrate 16 in the cured state has an index of refraction of 1.33, which has the substantially same index of refraction as water and approximately the same index of refraction of most mediums used for suspending cells.
  • the substrate 16 is MY-133, which is a commercially available material and can be purchased at My Polymers LTD at www.mypolymers.com/Default.htm.
  • MY-133 is a commercially available material and can be purchased at My Polymers LTD at www.mypolymers.com/Default.htm.
  • the MY-133 is a UV-curable fluoropolymer.
  • the material used is different and/or does not have the same refractive index as water. However, the same process is optionally applied.
  • the substrate is selected to not adhere to the die. Following are exemplary pairs of substrate/die materials, where the substrate can adhere directly or indirectly to a transparent base and avoid adhering to the die: (a) My-133/glass, Myl33/metal (e,g. nickel),
  • the substrate 16 is applied to a carrier plate 20, optionally by brushing, stamping or printing the substrate 16 thereon.
  • the carrier plate 20 is optionally made from glass or another optically transmissive material such as polystyrene, polycarbonate, PMMA( Poly-methyl-metacrilate ).
  • a material which has optical transparency at least at wavelengths used for visual and/or florescent inspection (e.g., near IR, far IR or near UV) and/or has a refractive index at those wavelengths that is within 20%, 10%, 5%, 1%, 0.1 or intermediate amounts of the refractive index of the aqueous medium used, for example, of that of water with 0.9% salts and sugars added (e.g., to within those percentages of 1.33).
  • wavelengths used for visual and/or florescent inspection e.g., near IR, far IR or near UV
  • refractive index at those wavelengths that is within 20%, 10%, 5%, 1%, 0.1 or intermediate amounts of the refractive index of the aqueous medium used, for example, of that of water with 0.9% salts and sugars added (e.g., to within those percentages of 1.33).
  • the carrier plate 20 is optionally pre-treated with silane before the substrate 16 is applied.
  • the silanation of the surface of the carrier plate 20 can be performed in a manner known to one skilled in the art. Through such silanation process, acrylic groups are attached by covalent bonds to the glass, improving the adhesion of the substrate 16 to the glass carrier 20.
  • Other intermediate base layers may be applied, especially if substrate 16 is of another formulation.
  • Plasma or Corona treatment e.g., as described at www.tantec.com
  • mechanical abrasion is provided. In an exemplary embodiment of the invention, however, plate 20 is kept smooth.
  • the substrate 16 forms a layer, which may have a thickness of less than 200 microns and more optionally in the range of 80-120 microns. Other thicknesses may be provided as well, for example, as described below: between 10 and 300 microns for example, for example, slightly more than the depth of the pico liter wells or other structures embossed.
  • the plurality of walls 14 is optionally then disposed on the substrate 16.
  • Pico liter well forming templates 26 are disposed between each set of plurality of walls 14 disposed on the substrate 16 layer and are pressed into the substrate 16.
  • the templates 26 are optionally dies capable of embossing the substrate 16 with pico liter sized wells.
  • the layered configuration, including the carrier plate 20, the substrate 16, the templates 26 pressed into the substrate 16, and the plurality of walls 14 is polymerized by UV-radiation to cure the substrate 16.
  • the layered configuration is irradiated with UV-light through the bottom of the translucent carrier plate 20.
  • the templates 26 are then optionally removed and the holding device 10 is cured again by irradiating the holding device 10 with UV-light under a vacuum of 0.3- 0.5 mmHg.
  • the holding device 10 includes at least a first adhesive 22 applied between the carrier plate 20 and the substrate 16 to further improve bonding of the substrate 16 thereto. Additionally, a second adhesive 24 may be applied to further improve bonding of the plurality of walls 14 to the substrate 16.
  • the carrier plate 20 is optionally pre-treated with silane before the first adhesive 22 is applied.
  • the silanation of the surface of the carrier plate 20 can be performed in a manner known to one skilled in the art. Through such silanation process, acrylic groups are attached by covalent bonds to the glass, improving the adhesion of the first adhesive 22 to the glass carrier 20.
  • Other treatments as described herein may be applied as well.
  • a thin coat of the first adhesive 22 is applied to the carrier plate 20, optionally, by brushing the adhesive 22 thereon. It should be apparent, however, that other techniques may be used to apply the first adhesive 22, such as by stamping, printing, spraying, dipping, wiping, or the like.
  • the adhesive 22 is applied to only those locations that correspond to the locations of the plurality of walls 14, such that the transparency of the bottom of each cavity 12 is not affected by the adhesive 22.
  • the adhesive 22 comprises mostly MY- 133 and can be applied to the entire surface of the carrier plate 20 because the adhesive 22 also has substantially the same refractive index as water.
  • the adhesive 22 can be any type of adhesive that bonds to the substrate as described below.
  • the first adhesive is a viscous primer that does not mix into a substrate 16. More specifically, the first adhesive 22 is applied as a dilute solution of 25% solids in a mixture based on a medium boiling solvent, wherein the solvent evaporates leaving a thin, but highly viscous layer of adhesive 22 on the carrier plate 20.
  • the solvent optionally comprises PCBTF (also know by the trade name of Oxsol 100), having a boiling point of 139 degrees, isopropyl alcohol (IPA) and acetone.
  • the adhesive 22 is an ultraviolet (UV) radiation curable formulation which adheres well to the substrate 16 and the carrier plate 20.
  • the adhesive 22 is selected so that it is polymerized together with the substrate 16 when exposed to ultraviolet radiation.
  • the adhesive 22 is applied to the carrier plate 20 and the substrate 16 is applied over the adhesive 22, the combination polymerized by UV-radiation at the same time.
  • the adhesive is a combination of both a fluoropolymer and a acrylic agent.
  • the acrylic agent bonds well to the glass or plastic bottom, whereas the fluoropolymer bonds the MY- 133 layer. Therefore, the adhesive serves as an intermediate layer which connects the My-133 with the bottom later.
  • the layer used is formed of primer- 133 available from My polymers LTD of Rehovot Israel. Primers G and P may also be used, possibly with reduced optical efficacy.
  • Further coats of the adhesive 22 can be applied to the first coat of the adhesive 22 and each coat is allowed to dry for optionally at least 2-4 minutes.
  • this delay is selected to allow for the creation of longer and/or more entangled polymer chains, so bonding becomes stronger.
  • the substrate 16 is applied to the adhesive 22 coated surface of the carrier plate 20 and is formed from a moldable optionally UV curable material optionally having an index of refraction substantially the same as the index of refraction of a buffered, substantially water-based medium, for example, Du-Pont Teflon FEP I or MY-133.
  • the substrate 16 forms a layer, which may have a thickness of less than 200 microns and optionally in the range of 80-120 microns.
  • the layer is made thinner due to cost considerations and/or for improved optical ability (e.g., limited depth range of microscope), while maintaining a minimal mechanical strength for its intended application.
  • the adhesive comprises a polymer that optionally includes both acrylic groups and highly fluorinated groups that attract the components of the MY-133.
  • a glass carrier plate 20 it may be desirable to modify the first adhesive 22 to increase its affinity for glass.
  • the adhesive 22 thus, may include 1-2% additional silane.
  • a second adhesive 24 (optionally of a mixture of acrylic and fluorocarbon polymer precursors) is optionally applied to the bottom of the plurality of walls 14 arranged to define cavities 12 of the holding device 10 and the plurality of walls 14 are then disposed onto the substrate 16.
  • the second adhesive 24 is allowed to dry for at least 2-4 minutes, or as needed.
  • the second adhesive 24 is also a viscous primer that does not mix into a substrate 16. More specifically, the second adhesive 24 is optionally applied as a dilute solution of 25% solids in a mixture based on a medium boiling solvent, wherein the solvent evaporates leaving a thin, but highly viscous layer of adhesive 24 on the bottom of the plurality of walls 14.
  • the solvent optionally comprises PCBTF (also known by the trade name Oxsol 100), having a boiling point of 139 degrees, isopropyl alcohol (IPA) and acetone.
  • the adhesive 24 is an UV-radiation curable formulation which adheres well to the substrate 16 and the plurality of walls 14.
  • the adhesive 24 is selected so that it is polymerized together with the substrate 16 when exposed to ultraviolet radiation. This permits the adhesive 24 to be applied to the bottom of the plurality of walls 14, which is then attached to the substrate 16 layer adhered to the carrier plate 20 by the first adhesive 22.
  • pico liter well forming templates 26 are disposed between each set of plurality of walls 14 disposed on the substrate 16 layer and are then pressed into the substrate 16.
  • the templates 26 are optionally dies capable of embossing the substrate 16 with pico liter sized wells.
  • the substrate is liquid so the dies need to only be strong enough to support their own weight as little pressure is optionally applied.
  • the use of low pressure is to avoid damage and/or distortion to underlying plate and/or setting substrate.
  • the layered configuration including the carrier plate 20, first adhesive 22, substrate 16, template pressed into the substrate 16, and plurality of walls 14 is polymerized by UV-radiation to cure the substrate 16 and the adhesives 22, 24 at the same time.
  • the layered configuration is irradiated with UV-light through the bottom of the translucent carrier plate 20.
  • this curing is sufficient to set the adhesives so the die can be removed, but does not finish hardening the substrate.
  • the templates 26 are then optionally removed and the holding device 10 is cured again by irradiating the holding device 10 with UV-light under vacuum of 0.3- 0.5 mmHg.
  • the Vacuum is used to avoid chemical interference of oxygen with the setting material.
  • an inert gas is used instead of vacuum.
  • Another method of making some embodiments of the invention includes providing a carrier 20 having at least one cavity 12 surrounded by walls 14. As shown in FIG. 7, a layer of either the first or second adhesive 22, 24, respectively, is deposited at the bottom of the at least one cavity 12. A layer of substrate 16 is then applied to the adhesive layer 22 or 24. The layer of substrate 16 can also be applied directly to the bottom of the at least one cavity 12, without the adhesive 22 or 24 as shown in FIG. 8. The pico liter well templates 26 are then translated between the walls 14 and pressed into the substrate 16 to emboss the pico liter wells 18.
  • the first or second adhesive 22 or 24, if present, and the substrate 16 are cured by UV-radiation through the bottom of the holding device 10. Then, the templates 26 are removed and the holding device 10 undergoes further curing by UV-light under vacuum of 0.3- 0.5 mmHg or inert gas.
  • a separate carrier plate 20 is not utilized. That is, the holding device 10 can include the substrate 16 embossed to form pico liter wells 18 as described above and shown in FIGs. 9 and 10.
  • the substrate 16 optionally has a thickness of less than 200 microns and more optionally in the range of 80-120 microns. Other thicknesses may be used, for example, for mechanical considerations.
  • the walls 14 are disposed on the substrate 16 and templates 26 are pressed into the substrate 16. While the templates remain pressed into the substrate 16, the substrate 16 is cured with UV- radiation. The templates 26 are removed and the substrate 16 can optionally be cured again, but with UV-radiation under vacuum.
  • a plate 20 with a same index of refraction as substrate 16, is used.
  • the walls 14 can be disposed on the substrate 16 after the UV-curing thereof.
  • the walls 14 are then affixed along a perimeter edge of the substrate 16 using any type of strong adhesive known in the art.
  • barriers (see below) and/or walls are dippe din a UV adhesive (or such adhesive is brushed on) and the adhesive set during a same or separate step of UV curing as used for the embossed sections.
  • the perimeter of the walls 14 can be adhered to the edge of the substrate 16 forming a Petri dish-shaped holding device 10.
  • the walls 14 having adhesive 22 or 24 can be applied to a layer of substrate 16, wherein the substrate 16 functions as the bottom of the holding device 10.
  • the templates 26 are pressed into the substrate 16 to emboss the pico liter wells 18 therein.
  • the layered configuration, including the templates 26, is cured using UV-radiation. It should be appreciated by one having ordinary skill in the art that, since the holding device 10 does not include the carrier plate 20 attached to the substrate 16 via adhesive 22 or 24, the holding device 10 can be cured from above the substrate 16 or below the substrate 16. After the first curing step, the template 16 is removed and the holding device 10 is then cured again, using UV-light under vacuum. Thereafter, the pico liter well holding device 10 is optionally sterilized and/or washed for use in biological experiments. Such post-manufacture acts may be carried out with other methods of forming device 10.
  • the walls are pressed against a layer of substrate 16 at a same time as templates 26 are pressed, with the walls adhering and the templates causing embossing.
  • a base 20 has a layer of picowells formed thereon, for example, by embossing a layer of substrate 16 thereon.
  • embossing is uses an embossing cylinder.
  • the walls 14 are attached onto substrate 16, in some cases, possibly covering existing picowells thereon.
  • the bottom of the walls are coated with an adhesive layer of sufficient volume to fill in such picowells.
  • spreading of substrate 16 on base 20 depends on the area being embossed.
  • substrate 16 is optionally applied as drops to the center of the areas to be embossed. If a larger area, substrate 16 is optionally spread using a draw bar or rollercoater. Methods known in the art for spreading such adhesives (and for bonding to other materials) may be used. In an alternative layer, walls 14 are applied while templates 26 are embossing layer
  • the embossing methods described herein are applied on fragile bases so little temperature and/or pressure changes are applied. Rather the embossing is optionally at low pressure and at room temperature (e.g., 15-35 degrees Celsius).
  • the embossed substrate is non- reversibly deformed by the embossing.
  • the embossed substrate is set by one or more of chemical setting, light setting, radiation based setting and/or other cross-linking or hardening or setting methods known in the art and as appropriate for the specific materials used.
  • the thickness of the embossed layer is minimal, for example, being 15, 5%, 20%, 60%, 100%, 300%, 100% or intermediate percentages of the depth of the picowell and/or other embossed feature.
  • the additional thickness below the well is 1, 10, 20, 30, 100 microns or intermediate amounts.
  • the template can have attached thereto patterns for the walls between the picowells, medicaments and chemicals for attachment to the picowells or walls between them, small beads for such transfer and/or electrode wires.
  • portions that are not for picowells electronics, valves and/or other items may be impressed on the substrate during embossing.
  • device 10 can be further processed in various ways, for example, washing to remove toxic residues, hole drilling (e.g., using laser, e-beam) and/or sterilization.
  • holding device 10 is optionally seeded with cells, for example by injecting cells suspended in a medium, such as an aqueous buffered medium, into at least a first cavity of the holding device 10.
  • the device 10 is optionally agitated to ensure that the cells settle in the pico liter wells 18.
  • the cells are then observed from below, for example, using a confocal microscope or brightfield microscope with or without deconvolution image processing software.
  • fluorescent imaging methods are used. Because the substrate 16 has a refractive index of water, optical artifacts, which would otherwise be caused by the differences between the refractive indices of the medium carrying the cells and the substrate 16, are essentially eliminated. This gives the viewer the ability to observe the cells being studying more precisely as if there were no microstructures on the substrate.
  • One potential advantage of a cell holder with multiple picowell arrays is that multiple experiments which require some similar conditions and some different conditions can be conducted simultaneously. For example, incubation can be same for all well areas, while cell type and/or reagents (e.g., drugs) added could be different. Optionally or alternatively, a same experiment can be repeated in separate well areas, so that cells metabolites from one cell do not affect others. Optionally, the wells themselves are different between areas, which may also affect the outcome of such an experiment. Other materials may also serve as the polymerizing agent as well and used to form the pico liter wells array.
  • the difference in index of refraction yields to the observation of the pico liter wells contours when observed in brightfield microscopy; in fluorescence microscopy the fluorescence cells or other microscopic particles emits new intrinsic light in certain range of wavelengths which is out of the range of the excitation light, and therefore the pico liter wells are merely visually observable.
  • multi-location structures can also be formed using non-embossing methods.
  • wells can be heat and/or pressure stamped unto a suitable substrate.
  • a plurality of elements defining picowells may be attached (e.g., using adhesive or an interference method) into wells of a multi-well device.
  • the array is injected under pressure against a die and maintained in such manner until set.
  • other structures can be formed as well in like manner, instead of picowells and/or to support picowell operation.
  • such structures can include landmarks to assist in user orientation (e.g., patterned clusters of non-etched areas or other singularities or markings to enhance user's orientation when the array is used).
  • some such markings are particularly visible under a microscope (e.g., pico well address and/or a well address).
  • micro-fluidics structures such as reservoirs, channels, mixers, filters and flow regulators are embossed (e.g., with the embossing defining 3D structures that affect flow.
  • embossed preparation for various structures is embossed (and/or additional elements mounted on the die),f or example, pumps, electronics, conductors, sensor mountings and/or valves.
  • the embossing process may change in accordance with the specific material or precursor used for substrate 16. For example, some materials require the application of a primer layer to strengthen the bonding to the base layer, whereas, additionally or independently, other materials require a detoxification process in order to extract biologically toxic residues such as un-cured monomers in the embossed layer.
  • a typical precursor may be a UV-curable adhesive such as NOA-61 or NOA-81 or the low self-fluorescence NOA-63 (Norland Products Inc., Cranbury, NJ, USA, USA). Embossing is performed, for example, by applying a drop of the fluid precursor of the adhesive on glass or plastic base, and curing the fluid precursor while in contact with a die (made, for example, from a metal such as nickel, glass, PDMS or silicone rubber) having a negative geometry of the well array. The drop of adhesive disperses between the slide and the die and forms a thin layer (e.g., 10-100 micrometers thick). After the adhesive has set, the die is peeled away or otherwise removed.
  • a UV-curable adhesive such as NOA-61 or NOA-81 or the low self-fluorescence NOA-63 (Norland Products Inc., Cranbury, NJ, USA, USA). Embossing is performed, for example, by applying a drop of the fluid precursor of the adhesive on glass or plastic base,
  • Additional acts are optionally made to stabilize the structure and its adhesion to the base and/or to extract and/or remove non-polymerized residues of the adhesive which may harm cells.
  • Such acts can include annealing at a mild temperature ( ⁇ 60°C) for at least one hour.
  • the bases are soaked in 90% ethanol (or other suitable solvent, depending on materials used for construction) for 5 days. This can extract toxic un- cured agents from the polymerized adhesive.
  • the slides are rinsed in distilled water to wash away debris and/or residues of the extracted undesired foreign materials.
  • the materials chosen and/or washing are selected to allow long term life of biological cells without toxic effects form the cell holder.
  • Exemplary base plates for any of the embossing methods described herein include any substantially transparent glass (or plastic) surface, such as a microscope slide (0.17mm - lmm thick, 2.54 cm wide, 7.62 cm long), a Petri dish (either monolithic plastic dish or a plastic dish with a thin glass or polymer sheet bottom, designed for high resolution microscopy) or the bottom of microtitter plates (either monolithic plastic plate or plate having a thin glass or polymer sheet bottom, designed for high resolution microscopy).
  • a microscope slide (0.17mm - lmm thick, 2.54 cm wide, 7.62 cm long
  • a Petri dish either monolithic plastic dish or a plastic dish with a thin glass or polymer sheet bottom, designed for high resolution microscopy
  • microtitter plates either monolithic plastic plate or plate having a thin glass or polymer sheet bottom, designed for high resolution microscopy.
  • the Petri dish or any other pico liter wells bearing device may include a partitioning element, such as a plastic or fabric barrier, to distinguish between several areas in the same device.
  • the partitioning element single or plural, if made or include mesh, slits or perforated parts can also act as a flow regulator, to damp and control (by selecting proper size and pitch of the openings) fluid transfer between partitions.
  • a barrier can block or reduce fluid flow or block or reduce cellular or particle flow (e.g., of certain sizes), for example, acting as a filter.
  • the barrier serves to reduce flow rates to levels which would not remove cells/particles from picowells.
  • Such barriers may be attached by any method known in the art.
  • the barriers are attached by dipping in a UV curable adhesive as used herein.
  • such barriers include a base ring for mechanically aligning said barriers on said substrate.
  • a cylindrical or cone mesh element 1402 made for example from Polyester or Nylon, with openings of sizes 5-10um, or 10-50um, or 50-100um, or 100-200um or 200-500um, surrounds an embossed area 1404 (and/or is surrounded by an area 1406) in the center (or other location) of a Petri dish 1400
  • FIG. 13A shows a Petri dish (or other holder) 1300 having a picowell array 1304 defined in one location thereof, for example, a center, surrounded by a non-embossed region 1302.
  • FIG. 13B is an isometric view of Petri dish 1300.
  • FIG. 15A shows a Petri dish (or other holder) 1500, which defines a plurality of picowell areas 1502, some or all of which are surrounded by corresponding barriers 1504. Not all barriers need be of same type. Not all picowells or other embossed areas need be of same design and/or size. One or more optional free spaces 1506 may also be defined, with optional barriers surrounding, for example, for insertion or removal of fluids and/or for optically analyzing chemical properties of fluids.
  • FIG. 15B shows an alternative design 1520, having a large embossed area 1522 separated by one or more barriers 1526 from a clear area 1524. Optionally, a space 1528 is formed between the barriers.
  • the coverage of the carrier by picowell and/or other embossed regions can be, for example, 1%, 5%, 10%, 20%, 50%, 70%, 90%, 100% or intermediate amounts, for example, depending on the application.
  • multiple sizes and/or types of pico liter wells are provided on a same substrate, for example, 2, 4, 6, 10, 20 or intermediate numbers of types of pico wells may be provided.
  • a pico well bearing microtitter plate can be made of, for example, a monolithic plastic structure or from a glass or transparent plastic bottom and an upper structure.
  • the die is optionally formed made as an array of "fingers" which match the pitch of the wells in the microtitter plate.
  • a die/template may be made using the following method. As shown in FIG. 1 IA, a plate 1100 having a desired embossing pattern
  • FIG. HB shows the parts assembled, at which point silicon or other setting material 1108 may be inserted into matching apertures 1107.
  • the top spacer 1106 is removed (or a separate base 1114 is applied over spacer 1106) and serves as a based 1114 of a template 1126.
  • a plurality of silicone fingers 1110, with a negative embossing pattern 1112 at their tips is therefore created.
  • the template is a 2D template and not a ID template as shown for clarity.
  • fingers 1110 engage spacer 1106 via inner hollows (not shown) inside spacer 1106.
  • spacer 1106 is treated to adhere to the silicone and/or spacers 1104 and 1102 are treated to not adhere.
  • precursor is optionally applied into each well, the die (1126) is then embedded in the microtitter plate and then UV radiated.
  • the pico liter wells structure is thereby created in each well separately. Since this process is performed on ready-made monolithic plates, no leaks are expected between well areas.
  • FIGs. 12A-12C An example of this process is illustrated in FIGs. 12A-12C.
  • precursor material .1204 is placed in a plurality of well regions 1202 of a plate 1200, for example, using a one dimensional well filling device, for example, as known in the art of manipulating such wells with biological materials.
  • template 1126 for example
  • UV radiation 1208 is provided for curing.
  • the length of fingers 1110 is matched to the amount of precursor provided and to the clearance between template 1126 and plate 1200, so no precursor is wasted or lacking.
  • FIG. 12C shows the result after template 1126 is removed, in which a picowell array or other embossed design 1210 is formed in those wells which were impressed by template 1126.
  • the fingers are of different length and define different heights for wells.
  • the design at the tips 1112 is different, providing multiple well types and/or arrangements.
  • the diameter of the tips is different.
  • the tips emboss structures other than wells.
  • the tips emboss wells of different depth.
  • a mix of well types/sizes/number and micro fluidics constructs and fluid reservoirs is selected and made into a cell holding device.
  • a plurality of "standard" such cell holder designs are made and optionally mass-produced.
  • a non-uniform cell holder is manufactured using a configurable die.
  • a plurality of fingers 1110 are manufactured, for example, each with a different plate 1100 having different patterns or on parts of the plate with different patterns.
  • a die may be constructed by assembling the desired fingers in the desired arrangement to provide a template.
  • the fingers are reusable as they do not stick to the adhesive.
  • a precursor is optionally uniformly applied to the transparent bottom prior to placing the die and irradiating.
  • pico liter wells are created on the whole bottom area (e.g., using a flat and uniform die).
  • the bottom plate is then bonded to the upper structure as it is usually done in this type of plates (for example, based on utilizing NOA as a cementable adhesive).
  • pico liter wells may be created only at desired locations, such as those areas which will become the bottom of wells, excluding inter-wells areas. This can be controlled, for example, by applying aliquots of precursor instead of a uniform layer.
  • Embossing, using MY- 133 or NOA or materials may be practiced on a microscope slide, either on the whole glass or selected parts and may serve as a base plate for various single or multi cavity devices.
  • the embossed glass can be covered with adhesive spacers and covers already used in laboratory practice, such as those made by Grace Biolabs (Bend, OR, USA) www.gracebio.com/Products/Imaging Microscopy/Cover Well_Perfusion_Chambers and enhance the practice to include pico liter wells bottoms instead of a plain glass surface.
  • these covers can form a water-tight, multiwell cell incubation or cytochemistry chamber when pressed to coverslips or microscope slides.
  • reagents can be quickly added and removed through access ports without disturbing or cross- contaminating specimens in adjacent wells, while cells remain in their picowells.
  • Various devices useful for microscopy can be built based on an embossed microscope slide, for example a slide 0.17-lmm thick.
  • the glass is then covered with a spacing layer which has a hole just above the embossed area. The diameter of the hole may be smaller than the embossed area.
  • This structure creates an open chamber, which can be useful for accommodating a cell suspension.
  • This structure may be covered by a cover slip and cells can be observed by an upright and/or inverted microscope.
  • a slide structure supports one or more of exchanging cells media, staining, and/or other manipulations of the cells within their picowells.
  • an additional "flow" layer is cured to form a flow channel above the cells chamber and a reservoir.
  • This flow layer is sticky on both surfaces, thus can be bonded to the spacer layer beneath it, and to the cover layer above.
  • a flexible transparent cover such as made of polycarbonate film, is bonded only on the distal edge of the flow channel.
  • a pinhole or larger hole
  • a non-sticky removable liner is optionally provided keeps the cover from bonding to the rest of the flow channel.
  • FIGs. 16A and 16B An exemplary such device 1600 is shown in FIGs. 16A and 16B, with FIG. 16A being a blow-apart view.
  • a glass slide 1602 has embossed (or otherwise attached) thereon a picowell array 1604.
  • a spacer layer 1606 with an aperture 1608 is attached above, for example, layer 1606 being a two sided adhesive layer.
  • a flow layer 1610 including a flow channel 1612 and a reservoir 1614 is provided above, optionally as a two sided adhesive layer.
  • a cover layer 1616 with an optional air hole 1624 and slot 1618 are provided above.
  • a non-adhesive layer 1620 is provided between layers 1616 and 1610 and includes a tip 1622 which is temporarily attached to layer 1610.
  • the length of layer 1620 is shorter than layers 1616 and 1610, so layers 1616 and 1610 can be adhered to each other at their tip.
  • Other structures may also be built up by layering shaped layers of double-sided adhesive, on microscope slides and/or other bases.
  • flexible covers 1620 and 1616 are pulled back and expose the chamber formed by aperture 1618 and wells area 1604. Cells are loaded into the chamber and removeable liner layer 1620 is peeled off. Flexible cover 1616 is released and bonds to the rest of upper surface of flow layer 1616.
  • Layer 1610 optionally defines a capillary channel between layers 1616 and 1606. Aliquots of fluid can be presented to the capillary slit 1618 created between the cover and the opening of the flow channel. Capillary force pulls the fluid into the channel, the fluid replaces and/or flows over the cell media, and the excessive fluid is gradually accumulated in the reservoir 1614. Additional fluid can be presented to the flow channel, basically until the reservoir is full. Optionally, fluid can be removed from reservoir 1614
  • Double sided adhesive tapes may be used to bond the layers and/or to form the layers.
  • the layers are optionally bonded while wet. This can eliminate air and prevent such air from being trapping between the layers, possibly minimizing the appearance of air bubbles in the suspension along incubation time.
  • the devices are manufactured and/or packed under vacuum, to prevent repeated air penetration between the layers before the device is used.
  • range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the invention. Accordingly, the description of a range should be considered to have specifically disclosed all the possible subranges as well as individual numerical values within that range. For example, description of a range such as from 1 to 6 should be considered to have specifically disclosed subranges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numbers within that range, for example, 1, 2, 3, 4, 5, and 6. This applies regardless of the breadth of the range.

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Abstract

L'invention porte sur des méthodes d'embossage permettant de former des réseaux de puits de picolitres (ou d'autres structures) ou des arrangements de tels réseaux par exemple disposés en réseaux de zones de picolitres, et sur des méthodes de formation de gabarits d'embossage. L'invention porte également sur des puits dont l'indice de réfraction est similaire à celui du milieu porteur de cellules des puits.
EP08848869A 2007-11-15 2008-11-13 Support de puits de picolitres et leur procédé de fabrication Withdrawn EP2222832A4 (fr)

Applications Claiming Priority (2)

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US11/940,996 US7888110B2 (en) 2003-06-26 2007-11-15 Pico liter well holding device and method of making the same
US613007P 2007-12-26 2007-12-26

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EP2222832A2 true EP2222832A2 (fr) 2010-09-01
EP2222832A4 EP2222832A4 (fr) 2012-08-29

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108636465A (zh) * 2018-05-15 2018-10-12 中国科学院化学研究所 图案化流体阵列及其制备方法和应用
CN108636465B (zh) * 2018-05-15 2020-08-14 中国科学院化学研究所 图案化流体阵列及其制备方法和应用

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EP2222832A4 (fr) 2012-08-29
WO2009063462A3 (fr) 2010-03-11

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