EP1979094A1 - Mikrofilterplatte, herstellungsverfahren dafür und satz - Google Patents

Mikrofilterplatte, herstellungsverfahren dafür und satz

Info

Publication number
EP1979094A1
EP1979094A1 EP07700277A EP07700277A EP1979094A1 EP 1979094 A1 EP1979094 A1 EP 1979094A1 EP 07700277 A EP07700277 A EP 07700277A EP 07700277 A EP07700277 A EP 07700277A EP 1979094 A1 EP1979094 A1 EP 1979094A1
Authority
EP
European Patent Office
Prior art keywords
wells
well
vessel
sample
ribs
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Withdrawn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
EP07700277A
Other languages
English (en)
French (fr)
Other versions
EP1979094A4 (de
Inventor
David A. Cohen
Michael J. Mortillaro
Bruce R. Turner
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.)
Thermo Fisher Scientific Oy
Original Assignee
Finnzymes Instruments Oy
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 Finnzymes Instruments Oy filed Critical Finnzymes Instruments Oy
Publication of EP1979094A1 publication Critical patent/EP1979094A1/de
Publication of EP1979094A4 publication Critical patent/EP1979094A4/de
Withdrawn legal-status Critical Current

Links

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
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/508Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above
    • B01L3/5085Containers 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
    • B01L3/50851Containers 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 specially adapted for heating or cooling samples
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C45/00Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
    • B29C45/17Component parts, details or accessories; Auxiliary operations
    • B29C45/26Moulds
    • B29C45/2624Moulds provided with a multiplicity of wall-like cavities connected to a common cavity, e.g. for battery cases
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C45/00Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
    • B29C45/17Component parts, details or accessories; Auxiliary operations
    • B29C45/46Means for plasticising or homogenising the moulding material or forcing it into the mould
    • B29C45/56Means for plasticising or homogenising the moulding material or forcing it into the mould using mould parts movable during or after injection, e.g. injection-compression moulding
    • B29C45/561Injection-compression moulding
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/12Specific details about manufacturing devices
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/08Geometry, shape and general structure
    • B01L2300/0809Geometry, shape and general structure rectangular shaped
    • B01L2300/0829Multi-well plates; Microtitration plates
    • 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
    • B01L3/508Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above
    • B01L3/5085Containers 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
    • B01L3/50855Containers 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 using modular assemblies of strips or of individual wells

Definitions

  • the invention relates to processing of biological samples.
  • the invention concerns microtiter plates, which are commonly used for performing Polymerase Chain Reaction (PCR) Processes.
  • PCR Polymerase Chain Reaction
  • Such plates have a plurality of wells arranged in a grid, each of the wells being capable of holding a small amount of biological sample.
  • the invention concerns also a method of manufacturing such plates, use of such a method and a kit including such plates.
  • Biological samples are processed in industrial and clinical diagnostics, pharmaceutical and research applications, and as processes have improved, the need for increasing the number and speed of samples processed has also increased.
  • Microfuge tubes come in several, usually non-interchangeable sizes based on the desired volume of the sample to be processed, and are usually used for liquid samples volumes of between 10 ul to 1,500 ul.
  • Microscope slides are utilized for tissues samples and very high density arrays of tiny samples that can be bound to the surface of the slide.
  • Microtiter plates are built like arrays of small microfuge tubes, and are available in a multitude of formats with varying materials, well geometries and sample densities, but all share the same basic footprint and they are typically used for liquid samples that are between 10 ul and 1,500 ul in volume.
  • microfuge tube offers relatively high volume of reactants and low number of biological samples
  • the trend for clinical diagnostics, industrial microbial detection, and pharmaceutical and academic research has been to reduce the reaction volume and increase the throughput of these processes.
  • higher density microtiter plates and slide- based microarrays have become more commonly used. These formats are of particular interest because they offer the ability to perform parallel experiments, reduce reagent consumption, and utilize smaller, relatively less expensive laboratory and analytical instrumentation.
  • microtiter plates in use conform to a set of standards codified by the Society for Biomolecular Screening (SBS) over the last decade.
  • the plates typically have 6, 24, 96, 384 or even 1536 sample wells arranged in a 2:3 rectangular matrix.
  • 96-well and 384-well formats are, by far, the most commonly used.
  • 96-well microtiter plates typically consist of an 8 x 12 array of wells of 9 mm center- to- center pitch and an inner diameter of 5.5 mm. Depending on the variety of plate, each well can hold a maximum of between 100 ul and 200 ul of reaction volume.
  • 384-well plates halve the spacing, such that the plates now offer a 16 x 32 format, with 4.5 mm pitch, 3.0 mm inner diameters, and maximum sample volumes of 40 ul to 60 ul.
  • the geometries of the wells vary depending upon the application - from square- shaped wells with flat bottoms to round wells with conical bottoms. Most biological chemistries performed in a microtiter plate are solution-based, but surfaced based chemistries can also be performed.
  • US 6340589 discloses a microtiter plate which is comprised of two separate parts formed of different materials. Wells are contained in the upper part (deck portion) of the plate and is supported by the lower part (skirt portion). Instead of a complete deck, the upper part may include a meshwork of links, which connect the wells at their upper ends to each other.
  • a major drawback of such a plate is that it has to be manufactured in several steps and the parts need to be attached together before use. Moreover, the rigidity of the upper portion, and consequently the whole plate is low due to the structural non-integrity.
  • US 5922266 discloses an injection molding method and apparatus, which may be modified to suit for producing the plates according to the present invention. As such, the document concerns manufacturing of optical devices, such as lenses.
  • microtiter plate which enables increasing the throughput of multiple-sample high temperature thermal cycling processes.
  • the invention is based on the idea of providing a microtiter plate having a plurality of wells in the form of a grid and further providing ribs between the walls of the wells.
  • the ribs are typically provided in two dimensions such that they connect each well to two, three or four adjacent wells, depending on the position of the well in the grid.
  • the ribs lie generally in a plane perpendicular to the plane of the grid defining the well positions. In such a manner the structure of the plate can be reinforced so as to still allow for considerable portion of the wall of each well to contact a sample holder so that efficient heat transfer to the sample within well can occur.
  • the well walls at the open ends of the wells are shared between adjacent wells.
  • the wells are otherwise round-shaped in cross section, but the interiors of the wells are shaped roughly rectangular in cross section at their open ends in order to achieve higher density of wells in the grid but still maintaining high internal volume of the wells.
  • a microtiter plate comprising a plurality of thin- walled wells in the form of a grid is produced by injection molding by injecting molten mold material to an oversized injection mold comprising several well-forming cavities having an initial volume, at least one of the well-forming cavities being connected to at least one other well-forming cavity by a planar flow channel having a general direction perpendicular to the plane of the well grid, the method comprising a step of reducing the volume of the mold for displacing said mold material in the well-forming cavities and in the flow channels in order to produce a thermally stable microtiter plate having at least one of the wells connected to at least one another well by a rib.
  • Flow channels may be provided so as to connect each of the wells to at least one another well, preferably to two, three or four neighboring wells in the grid by ribs.
  • microtiter plate according to the invention is characterized by what is stated in the characterizing portion of claim 1.
  • the method according to the invention is characterized by what is stated in the characterizing portion of claim 17 and the use is characterized in claim 26.
  • the kit is characterized by what is stated in the characterizing portion of claim 27.
  • the ribs provide support for the wells, which can therefore be designed thin-walled and placed in a dense grid.
  • the ribbed structure enables manufacturing of plates, wherein ratio of the density of tubes to the wall thickness of the tubes is fundamentally increased in relation to prior plates.
  • the ribs make the molding of small-sized protrusions by injection molding possible in an advantageous manner, as they allow the proper flow of resin in a plastic- injection molding of the wells without the requirement for an unduly high number of air- vents in the mold.
  • the injection mold may comprise a plurality of air- vents such that the number of air- vents is considerably smaller, typically at least 20%, preferably at least 50% smaller, than the number of wells in the microtiter plate.
  • a defined volume of resin sufficient to form the part be injected into the part forming cavity while it is held partly open and then the cavity be closed, thereby compressing the resin such that it fills the cavity and forms the thin wall sections desired.
  • a plate In order to maximize thermal performance a plate must be designed with conical wells in a material suitable for biological reactions. Such a design must take into account thermal transfer characteristics, ability of the plate to handle thermal stresses from cycling and the ability to add and remove biological samples using an automated liquid handler.
  • the present invention is particularly advantageous, when a plate having a dense grid of tubes having a wall thickness of less than 0.0065" (0.17 mm) is desired.
  • a dense grid we mean a grid having a well-to-well spacing (pitch) of 2.25 mm or less.
  • the ribbed-conical well format allows for the potential of: i) high sample density of wells (2.25 mm pitch and less), ii) optimized thermal transfer of heat, iii) easy dispensing of low sample volumes, iv) easy sample recovery at bottom of conical tube, and v) lower reagent usage.
  • Forming the plate further into a reduced-size format (e.g., a slide-sized format having a footprint of roughly 1/4 than that of a standard microtiter plate), as described in detail later in this document further allows for: vi) minimization of warping shrinkage of the plastic plate, and vii) the creation of smaller, less expensive instrumentation to perform biological assays, than are afforded by standard microtiter- sized plates of lower density.
  • a reduced-size format e.g., a slide-sized format having a footprint of roughly 1/4 than that of a standard microtiter plate
  • the shape of the wells is preferably conical. That is, at least the lowermost part of the well is tapering towards the bottom of the well (the wells are most advantageously "v-bottomed”).
  • Heat transfer between the sample within such a conical well and the heating/cooling receptacle is efficient because: i) the conical geometry has a relatively high surface to volume ratio, ii) the walls can be molded in such a fashion that the thickness is even 1/2 that of conventional tubes, thus reducing impedance to thermal conductance caused by the plastic, and iii) heating along the entire height of the sample allows for uniform temperatures from top to bottom - important for enzyme kinetics of the reaction.
  • Small wells in particular, those having inner diameters of less than 2 mm
  • provide lower reagent usage because smaller wells have less surface area (and head space) to lose sample volume via vapor pressure.
  • dispensing and retrieval of samples is made more reliable and repeatable because the wells themselves are cone-shaped allowing small volumes to have enough Z-dimension aspect to allow a pipette tip to operate properly.
  • the stress-free molding process of the plates coupled with a frame assembly (detailed below) allows for small volumes to be retrieved with precision.
  • adjacent or “neighboring” wells, we mean neighboring wells either in the principal grid directions or in the diagonal directions of the grid.
  • Figure 1 shows a partial bottom view of a ribbed microtiter plate according to one embodiment of the invention
  • Figure 2 shows a partial perspective view of the ribbed microtiter plate of Fig. 1,
  • Figure 3 shows a partial side view of the ribbed microtiter plate of Figs. 1 and 2
  • Figure 4 shows a perspective view of the ribbed microtiter plate of the previous Figures
  • Figure 5 shows a partial top view of a ribbed microtiter plate of the previous Figures
  • Figure 6 shows a partial cross-sectional view of a microtiter plate between mold members during the molding process
  • Figure 7 shows a first perspective view of an exemplary sample tray assembly which can be used in order to house ribbed microtiter plates
  • Figure 8 shows a second perspective view of the sample tray assembly of Fig. 7.
  • Figs. 1 to 5 show one embodiment of a microtiter plate having round conical wells 11.
  • the deck of the plate is denoted with a reference numeral 10.
  • the wells 11 protrude in a parallel manner from the deck 10 such that their upper (open) ends abut on the upper surface of the deck 10.
  • the ribs protrude all the way from the bottom of the deck to the level of the bottoms 16 (closed ends) of the wells, and connect to each other at the bottoms 16 of the wells.
  • An interstitial space 18 bordering on the bottom of the deck and four wells and four respective ribs is formed in the middle of each neighboring four wells set.
  • the wells 11 have the shape of a truncated cone and the ribs are connected from their sides to the wells of the wells 11 in full length, each of the ribs has a triangular shape.
  • Figs. 4 and 5 show the upper surface of the plate. Due to the high density and conical shape of the wells, the interiors of the wells are shaped roughly rectangular in cross-section at their upper ends. This is to prevent overlap of adjacent well cavities and to allow decent sealing of the plate. Thus, extra material is provided at the upper ends of the well walls order to separate the otherwise round- shaped wells from each other. A biological sample 19 is provided in some of the wells.
  • the vessel possesses a plurality of wells having walls consisting of inner and outer surfaces, said wells being generally independent and conical in nature but transitioning, at their open ends, to a more square geometry at which point they interconnect by means of shared wall surfaces at said open ends.
  • the upper surface of the vessel is defined as that which coincides with the open ends of the tubes and whose uppermost surface plane is defined by the ends of open tube.
  • the closed ends of the essentially conical tubes being the furthermost point from the open end of the tubes, define the lower surface plane of the vessel.
  • an array of openings having a female orientation remains between the individual wells.
  • This array of openings allows for the vessel to mate intimately with a corresponding array of male features formed in the thermal control block of the thermal cycling instrument. Since the openings present on the underside of the vessel extend nearly to the upper surface of the vessel, it becomes possible to surround the sample containing area of the well of the vessel nearly completely with the thermal control source, a necessary feature for effective performance of vessels intended for PCR applications.
  • a thin standing wall i.e., rib
  • Said wall extends from the underside of the vessels upper surface to a point corresponding to the tip of the well's closed end.
  • Each wall is aligned with, and parallel to, the centerline of each well and extends perpendicularly in each direction thereby interconnecting each well with it' s neighboring well.
  • a plate is produced by delivering plasticized resin into a mold cavity sufficiently to fill the cavity and evenly displacing a portion of that resin within the cavity by compressing the resin by walls of the cavity, typically by clamping with core pins which form the internal diameter (ID) of the sample tube, to form the desired wall thickness.
  • the resin is then allowed to cool in the pressurized cavity thereby forming a thin-walled vessel having the desired uniform shape and reduced internal stresses.
  • the resin fills evenly the mold cavity, including the well wall portions, rib portions, and a deck portion usually present for binding the upper ends of the tubes firmly to each other.
  • the deck portion could also be left out, because binding of the tubes to each other can be achieved by the ribs, in particular when reinforced from their upper ends by sharing the walls of adjacent wells, as described above.
  • the phases of injection of the molten material and clamping are carried out successively in order to secure as homogeneous structure of the thin-walled vessel as possible.
  • US 5922266 does not include any teachings about using the method for producing thin object portions and, in particular, for producing robust vessels for thermal cycling applications.
  • Closing of the core pins does two things. Firstly, it compresses the tube walls to the desired thickness, and, secondly, evenly displaces the polymer in the mold cavity to produce an equalized packing force on the part prior to cooling.
  • the tubes In traditional injection molding techniques, the tubes must be either filled or vented at each tube in order to flow material such that it will completely fill the tubes. This, however, makes the molding process unduly complex.
  • the present invention allows for filling and/or venting of the tubes at the region of the ribs, whereby reduction of filling/venting points is possible and no undesired molding residues are produced in the tube walls.
  • the method comprises in carried out by injection molding in an injection molding machine using a molten thermoplastic resin, and comprises the steps of:
  • Fig. 6 shows a vessel 64 clamped between mold members.
  • the upper mold member comprises core pins 60, which define the internal diameter (ID) and the internal shape of the wells.
  • the lower mould member 62 defines the outer diameter (OD) and shape of the wells, and the shape of the ribs.
  • the thin wall portion of the wells is denoted with reference numeral 66.
  • the image plane of the cross-section lies slightly off the plane of the ribs in order to show the protrusion of the lower mold member to the interstitial space between the wells more clearly.
  • the process according to the invention allows for increases in the density of wells with much thinner walls associated with the conical bottom portions of the wells.
  • a wall thickness of less than about 0.0065 inch (less than about 0.17 mm) at the bottom portions of the wells in combination with a small (less or equal than 2.25 mm) well pitch can be achieved, still maintaining the robustness of the plate due to relieved stresses and small variations in the wall thickness.
  • the thinner well walls maximize heat transfer such that high rates of thermal transfer can occur, allowing for overall shorter assay times and higher sample processing rates.
  • the rate at which a sample is heated and cooled during a conventional thermal cycling reaction may account for up to 50% of the total assay time, whereby halving the wall thickness enables reduction of the total assay time by as much as 25%.
  • the thicker walls and other structures associated with the tops and sides of the plates provide additional rigidity and structural integrity to the entire plate. These features will help minimize the shrinking and warping of the plate after repeated exposure to hot and cold temperatures. Minimization of shrinking and warping both before and after thermal cycling is a requirement for automated liquid handlers to repeatedly and reliably dispense or aspirate small volumes of sample at the bottoms of the tube.
  • a microtiter plate format which comprises in combination:
  • a plate comprising a plurality of wells supported by ribs as disclosed above and arranged in a grid having a predetermined pitch
  • a number of wells in a first dimension of the plate which corresponds to the number of wells in a first dimension of an SBS standard plate and the number of wells in a second dimension of the plate, which corresponds to a fraction of the number of wells in a second dimension of an SBS standard plate.
  • such a plate can be designed, for example, in a quarter-sized format of a standard microtiter plate (roughly corresponding to the size of a microscope slide-format).
  • the smaller footprint of the plate further reduces the dimensional stresses of the plate so that warping of the plate as it is ejected from an injection molding machine is minimized.
  • This feature also reduces problems associated with flow dynamics of molten plastic as it fills the cavities of the mold, such that the cavities are more likely to fill at the proper pressures.
  • a tray assembly which is capable of receiving and holding a plurality of reduced- sized plates.
  • Such tray assembly generally comprises a frame 77 having two parallel first frame elements 70 and two parallel second frame elements 72, the frame elements being perpendicularly connected to each other to form a generally rectangularly shaped frame, the inner edges 75 of the frame elements defining a central opening and the frame being capable of accommodating and immobilizing a plurality of adjacent sample plates such that their sample wells at least partially protrude through the central opening of the frame.
  • the outer peripheral dimensions of the frame meet the SBS standards, whereby the present sample plate assembly can be used for processing of biological samples in, e.g., thermal cyclers, which are conventionally operating on SBS standard microtiter plates.
  • thermal cyclers which are conventionally operating on SBS standard microtiter plates.
  • Figs. 7 and 8 show and example of tray designed for a 4 x 96 well plate configuration, but a similar tray may also be manufactured for a 4 x 384 well plate configuration in order to fit together with the most preferred form of the plates according to the invention. Needeless to say, 2 x 768, 3 x 512, 6 x 256 etc. configurations, and all other configurations in which plates can be fitted side-by-side in order to fill a rectangular frame are possible, and may have advantages in some applications.
  • the described frame design combined with the ribbed- well design further helps to accomplish the goals of the invention, and to maintain robust manufacturability and manageability of the plates.
  • Reduced-sized plates can be assembled, side -by-side, on a microtiter- sized frame to allow the manipulation of these plates by standard liquid handling and robotic workstations commonly used in life science research.
  • the ability for two or more, typically four, of these slide-sized plates to be combined into one microtiter- sized tray assembly still maintains some of the key advantages of microtiter- sized plates such as: i) use of standard liquid handling devices, and ii) compatibility with existing laboratory and analytical instrumentation.
  • liquid handlers for molecular biological reactions remove and dispense liquid as either a single tip, a row of 4, 8, or 12 tips, or an array of 96 or 384 tips (in a 8 x 12 or 16 x 24 tip array respectively).
  • Such liquid manipulating instruments are designed to hold a standard, SBS- compatible, microtiter plate in a position relative to the dispensing tips and either move the tips, or the plate (or both) to address the appropriate wells.
  • the key to maintaining the compatibility is to offer a format of correct X-Y dimensions, and a correct well-to-well spacing.
  • common types of laboratory equipment and analytical instrumentation have been designed to work specifically with microtiter plates of particular X-Y dimensions and well-to-well spacing.
  • An exemplary, yet preferred, plate format is based on a slide- sized plate concept with 384 conical wells protruding from the bottom surface of the deck of the plate.
  • the 384-well slide- sized plate preferably has a format of 12 x 32, with a center- to-center pitch for adjacent wells of 2.25 mm.
  • the maximum sample volume will be between 10 ul and 20 ul.
  • the plate can be sealed by any of the following methods which will allow for efficient sealing to as low as 1 ul reaction volume with the application of pressure from the top: i) heat-sealing films, ii) pressure sealing films, and iii) reusable sealing mats.
  • the wells are designed to allow for efficient heat transfer of samples and removal of low reaction volumes with standard pipeting tools.
  • the material of the plates will be of polypropylene, or like material, that offers good thermal conductivity, hydrophobicity and low interference with molecular biological reactions.
  • ribs connect the sides of the wall of each conical well.
  • the ribs can be in any of a number of different configurations, but the preferred embodiment is to have the ribs arranged in a standard square grid configuration with the sides of each square equivalent to the pitch used and the intersection of the four ribs will meet at the bottom of each well.
  • the height of each rib will be defined as starting at the bottom surface of the plate deck and stretch at least halfway down the well depth axis, preferably all the way to the bottom of each well, thus making an "egg crate" appearance to the bottom of the plate.
  • each rib can be optimized for proper flow of resin in the mold, and maximized exposed surface area of the tube wall to contact the heating/cooling receptacle.
  • a typical thickness of a rib is between 0.008 and 0.020 inches as measured at the lower surface of the rib.
  • the walls of the wells, at points in which the ribs are not joined, will be of a thickness of less than 6/1000ths of inch.
  • Ribs are typically of generally planar form and lie perpendicularly to the upper plane of the vessel. They may, however, exhibit a gently sloping (tapering) or patterned form. Ribs may also be provided in configurations not explained here in detail, for example, in oblique manner (diagonally in the grid from well to well). In that case, the ribs connecting four wells in a square-like vertices of the well grid would form an X-shaped interconnecting structure. A multi-facetedly (i.e., between nearest neighbors and between diagonal neighbors) ribbed structure would even further add to the rigidity of the product, however, at the expense of usable heat transfer area. In the case of large plates (e.g., standard- sized high-density plates), this may, however, be beneficial.
  • large plates e.g., standard- sized high-density plates
  • the conical wells themselves preferably have an inner draft angle of between 3° and up to 10°.
  • the cones protrude between 4.0 mm and 7.0 mm from the bottom of the deck.
  • the tubes thicken gradually from bottom to top such that the thinnest portion of less than or equal to 6/1000ths of inch will be maintained at all points in direct contact with the heating/cooling receptacle and increase thereafter to give the wells added strength.
  • the rims of the wells are preferably shared between wells. Regardless of the configuration the rims preferably have a curvature along the top surface so that pressure-based sealing films will form a vapor-tight contact along the entire periphery of the well rim.
  • the overall format of the mated frame/plate assemblies will be 32 x 48 wells (equivalent to a 1,536-well microtiter plate).
  • the frame itself will be of SBS standards, and made of a material that is both rigid and heat-resistant, so that it holds the slide-sized plates in a regular and repeatable position, even after stresses caused by standard laboratory processes and conditions.
  • the addition or removal of a plate, or series of plates from the frame assembly can be accomplished manually, without the aid of tools, or alternatively can be incorporated into a robotic system, which will perform such tasks in an automated fashion.
  • the mated frame/plate assembly will be compatible with general laboratory equipment and analytical instrumentation.
  • general lab equipment includes centrifuges adapted to spin individual and stacked microliter plates; thermal cyclers that accommodate v-bottom micro titer plates; simple heaters and chillers that accept micro titer plates; and liquid handlers that are designed to manipulate reactions in wells configured within a microtiter plate format.
  • analytical instrumentation that will accept microtiter- sized plates are DNA automated sequencing systems, florescence and colorimetric plate readers, and real-time, quantitative PCR instruments.
  • the described frame/plate assembly provides a convenient way of achieving an ultra thin walled densely designed vessel for increased thermal performance and sample throughput.
  • a 1,536-well plate can also be manufactured as a single piece by means of the described process utilizing ribs between the tubes.
  • the vessel is provided with an integral deck part having an upper surface facing to the direction of the open ends of the wells and a lower surface facing to the direction of the closed ends of the wells and being connected to the well walls in the vicinity of the open ends of wells.
  • an integral deck part having an upper surface facing to the direction of the open ends of the wells and a lower surface facing to the direction of the closed ends of the wells and being connected to the well walls in the vicinity of the open ends of wells.
  • the walls of the wells are shared between the wells at their upper ends in order to provide a more dense grid, whereby the deck in these shared areas is inherently formed of the rims of the wells and usually has no distinguishable lower surface at the locations where the walls of the adjacent wells meet.
  • the plate preferably consists of a single and structurally integral unit made from a biocompatible material.
  • the material of the plate is most advantageously suitable for the temperature range of PCR processes.

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  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Clinical Laboratory Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
EP07700277A 2006-01-13 2007-01-12 Mikrofilterplatte, herstellungsverfahren dafür und satz Withdrawn EP1979094A4 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FI20060031A FI20060031A0 (fi) 2006-01-13 2006-01-13 Mikrotiitterilevy, menetelmä sen valmistamiseksi ja sarja
PCT/FI2007/050012 WO2007080230A1 (en) 2006-01-13 2007-01-12 Microtiter plate, method of manufacturing thereof and kit

Publications (2)

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US8222048B2 (en) 2007-11-05 2012-07-17 Abbott Laboratories Automated analyzer for clinical laboratory
US20170182489A1 (en) * 2014-04-09 2017-06-29 Greiner Bio-One Gmbh Receiver container and receiver unit for receiving body fluid
JP7059725B2 (ja) * 2018-03-19 2022-04-26 凸版印刷株式会社 収容容器
JP7003763B2 (ja) * 2018-03-19 2022-02-04 凸版印刷株式会社 試薬カートリッジ
CN111902722A (zh) * 2018-03-19 2020-11-06 凸版印刷株式会社 收容容器、试剂容器用盖材料、试剂容器及试剂盒

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US5922266A (en) * 1992-10-08 1999-07-13 Grove; Dale Injection molding
US20050058578A1 (en) * 2000-06-08 2005-03-17 Eppendorf Ag Microtitration plate
US20020022263A1 (en) * 2000-07-10 2002-02-21 Corning Incorporated Microplate having a lubricious surface and methods for making and using such microplates
GB2396317A (en) * 2002-12-20 2004-06-23 Advanced Biotech Ltd Microtitration plate assembly and method of manufacture

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EP1979094A4 (de) 2010-10-13
WO2007080230A1 (en) 2007-07-19
FI20060031A0 (fi) 2006-01-13

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