EP3559630A1 - Dispositif et procédé de mouillage de matériel biologique - Google Patents

Dispositif et procédé de mouillage de matériel biologique

Info

Publication number
EP3559630A1
EP3559630A1 EP17840557.7A EP17840557A EP3559630A1 EP 3559630 A1 EP3559630 A1 EP 3559630A1 EP 17840557 A EP17840557 A EP 17840557A EP 3559630 A1 EP3559630 A1 EP 3559630A1
Authority
EP
European Patent Office
Prior art keywords
slide
platform
liquid
deflection
mixing
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Withdrawn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
EP17840557.7A
Other languages
German (de)
English (en)
Inventor
Xaver Einsle
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.)
Prime23 GmbH
Original Assignee
Prime23 GmbH
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 Prime23 GmbH filed Critical Prime23 GmbH
Publication of EP3559630A1 publication Critical patent/EP3559630A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00—Sampling; Preparing specimens for investigation
    • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/30—Staining; Impregnating ; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis
    • G01N1/31—Apparatus therefor
    • G01N1/312—Apparatus therefor for samples mounted on planar substrates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L1/00—Enclosures; Chambers
    • B01L1/02—Air-pressure chambers; Air-locks therefor
    • B01L1/025—Environmental chambers
    • 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
    • B01L3/52—Containers specially adapted for storing or dispensing a reagent
    • 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
    • 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
    • B01L2200/0684—Venting, avoiding backpressure, avoid gas bubbles
    • 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
    • B01L2300/02—Identification, exchange or storage of information
    • B01L2300/021—Identification, e.g. bar codes
    • 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
    • B01L2300/042—Caps; Plugs
    • 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
    • B01L2300/046—Function or devices integrated in the closure
    • 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
    • B01L2300/06—Auxiliary integrated devices, integrated components
    • B01L2300/0609—Holders integrated in container to position an object
    • 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
    • B01L2300/0848—Specific forms of parts of containers
    • B01L2300/0851—Bottom walls
    • 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
    • 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
    • B01L2300/16—Surface properties and coatings
    • 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

Definitions

  • the present invention relates to a device for wetting biological material with at least one liquid.
  • the invention relates to a method for wetting biological material with at least one liquid using a corresponding device.
  • Devices for wetting biological material have been known in practice for many years and exist in a wide variety of embodiments.
  • the device of DE 102 18 988 C1 which comprises a device for supporting a slide. This is designed so that the slide is spaced from a platform.
  • the illustrated incubation chamber is configured such that the slide can be raised or lowered within the incubation chamber by means of a further device relative to the platform.
  • the side of the slide on which the material to be examined is applied faces the platform, and the space between the slide and the platform can be filled, within the chamber, with a liquid reagent.
  • US Patent 5,338,358 B2 discloses a device for wetting biological material.
  • This device also includes means for carrying a slide. However, this is designed so that the slide is objected to in a non-parallel position of a plateau. To ensure that the biological material is completely and sufficiently wetted with a liquid reagent, the wedge-shaped space between the slide and plateau must be filled with a relatively large volume of reagent.
  • US Patent 8,877,485 B2 discloses a method and apparatus for processing biological samples. In the machine, at least one staining unit is provided which includes an array of slides and a corresponding array of lids.
  • the likewise known device of US Pat. No. 8,337,786 B2 represents an incubation chamber which is produced by pushing a cover onto a slide, whereby a space closed off from the cover is formed above the material located on the slide. This space in turn be filled with Einwirk79.
  • the introduction of the monolayer into the incubation chamber takes place in the known device by means of a liquid reservoir located outside the chamber, from which the chamber chamber can be filled passively due to the resulting capillary forces.
  • the lid must be pressed by means of a clamping action on the slide to ensure the tightness of the incubation during the Einwirkluies. To empty the chamber, the clamping action is released and the liquid is sucked off at the opposite end of the liquid reservoir of the chamber.
  • the present invention has for its object to design a device and a method for wetting biological material in such a way and further that is optimized with simple design means the introduction and removal of the necessary liquids for wetting.
  • the device according to the invention comprises a deflection device and a platform for receiving a at least approximately triangular, preferably approximately square, the biological material comprising the slide, wherein the slide of the deflection of a relatively parallel to the platform engagement position in a non-parallel to the platform Collective position is deflected, with only a corner region of the slide in the collection position is not or only slightly raised, such that the liquid collects in this corner region.
  • exposure position is to be understood in the broadest sense and describes, in particular, a position of the slide parallel to the platform, in which a capillary gap can form between the platform and the slide, which capillary gap can be filled with the single-solution
  • the capillary gap-facing side of the slide can, regardless of the spatial orientation of the slide, as "bottom" of the slide to be called.
  • selection position is also to be understood in the broadest sense and describes in particular a position of the slide in the exclusively one Corner of the slide is not or only slightly raised. In this, thus in comparison to the other corner regions of the slide lying lower corner region, the liquid for wetting the biological material is collectable and advantageously removable.
  • silica is also to be understood in the broadest sense and describes an element that can be designed so that it has a surface on which the biological material to be wetted can be applied and which form a parallel capillary gap with a corresponding surface
  • the term thus includes both commercially available square microscope slides known from the field of microscopy and microscope slides present in other geometric forms.
  • the underlying object can be achieved by a suitable deflection device of the device in a surprisingly simple manner.
  • the movement of the slide that can be generated by the device according to the invention is particularly well suited for wetting biological material on a slide with the liquid reagents necessary for immunohistochemical tissue examinations or staining
  • the device according to the invention is also particularly suitable for efficiently and completely mixing the reagents, so that the chemical and biochemical reactions in such tissue examinations or dyeings can be accelerated.
  • both the so-called pre-treatment steps of "de-waxing” and “antigen retrieval” in immunohistochemical staining and “de-waxing” in an in-sf hybridization study as well as the actual tissue staining in detection methods such as
  • biochemical binding reactions in the device according to the invention can be accelerated accelerate.
  • the wetting of biological material on slides, in particular protein and / or RNA-containing material on so-called biochips can be realized particularly efficiently in the incubation chamber according to the invention.
  • substrate solutions are often used to wet biological material which must be prepared from two or more components immediately prior to use.
  • substrate solutions are not only expensive but very often also unstable, so that they can disintegrate and become worthless in a short time.
  • solutions in the device according to the invention if designed as an incubation chamber, can be produced directly in a mixing zone of the incubation chamber. Consequently, such solutions can thus be prepared immediately prior to their use.
  • hydrophobic regions are often formed, for example by the retention of wax or paraffin in the material to be wetted.
  • a further inventive manner can be obtained by the deflection of the slide, a fluid movement of the liquid, which allows a particularly uniform wetting of biological material, even if the biological material has hydrophobic areas.
  • the deflection device can have a deflection means, which in turn comprises a support for the slide and, preferably, an anchor element.
  • the deflection device may be a rocker.
  • the deflection means or the rocker can be moved by at least one lifting means in a raised position and in a tilted position. In the raised position at least two corner regions of the slide are not or only slightly raised, wherein the slide is then in the tilted position in the collection position.
  • slides that are to be used in the device according to the invention may comprise a labeling field in the labeling part of the slide.
  • the label field may be provided with a barcode that allows identification of the slide and the biological material thereon.
  • the inscription field can be located on the side of the inscription part of the object carrier facing away from the capillary gap. The side facing away from the capillary, the labeling field comprehensive side of the slide can, regardless of the spatial orientation of the slide, be referred to as the "top" of the slide.
  • the deflection means comprises a receiving area for the at least one lifting means.
  • the lifting means may be formed as a plunger which projects into the receiving area.
  • the receiving region comprises an anchoring element for the lifting means, so that the anchoring element defines an axis of the deflection means about which the deflection means is rotatable to the tilted position.
  • the receiving area may be as a corresponding with the shape of the plunger recess, wherein the anchoring element, preferably in the form of a pin, projects into the recess.
  • the corresponding with the shape of the recess plunger may preferably in turn contain a corresponding with the shape of the pin opening so that plunger and Pin can be brought into a relatively rotatable connection.
  • the lifting means may also come into direct contact with the slide.
  • the deflection means and / or the anchor element of the deflection means can be designed so that it can be brought into contact with a corresponding anchor surface.
  • the anchor member may be formed as a protruding portion, preferably as an abutment lip of the deflection means.
  • the corresponding armature surface may be formed as a material projection of the device, in particular as a stop. The stop may in turn preferably be designed as a protruding edge of a side wall of the deflection device, preferably an inner side wall of the deflection device.
  • the device according to the invention comprises a deflection device which on the one hand may comprise on a inner side wall a protruding edge and on the other hand a liftable and rotatable deflection means with a abutment lip.
  • abutment lip of the deflection means comes into contact with the corresponding stop of the deflection, the movement of the lifting means can lead to a movement of the deflection, which deflects the slide from the acting parallel to the platform position in the relatively non-parallel to the platform collection position.
  • the corresponding anchor surface may be curved.
  • the armature surface may be configured as a side surface of a substantially cylindrically shaped abutment.
  • the device according to the invention comprises, on the one hand, a stop provided by a curved surface and, on the other hand, a liftable and rotatable deflection means which can come into contact with the essentially cylindrically shaped stop.
  • the deflection means can continue to rotate over the curved side surface of the stop, so that the slide is deflected from the operative position to the collection position.
  • the receiving area for the at least one lifting means may be a recess of the deflection means configured as a guide rail.
  • the lifting means is a plunger which projects into the guide rail.
  • a movement of the plunger within the guide rail can lead to a predetermined by the shape of the guide rail movement of the deflection.
  • this movement may be a multi-directional movement.
  • This predetermined by the guide rail movement can in turn cause the deflection of the slide from the operative position to the collection position.
  • the deflection of the slide from the exposure position to the collection position corresponds to a three-dimensional movement (3-D movement) of the slide.
  • the 3-D movement includes raising and lowering the slide along the Y-axis, sliding the slide laterally along the X-axis, and tilting the slide about the Z-axis.
  • the sequence of the respective movements along one of the three geometric axes mentioned above need not be defined and can be combined as desired.
  • the deflection of the slide by means of the device according to the invention can be carried out continuously or discontinuously. For example, an upward movement of the lifting means may cause the deflection of the slide from the operative position to the collecting position, the counter-downward movement of the lifting means returning the slide back from the collecting position to the operative position.
  • the deflection of the slide can thus also be controlled and, if appropriate, stopped at an arbitrary position between the acting position and the collecting position.
  • the controlled 3-D movement of the slide allows precise control of the liquid, with the the biological material on the slide can be wetted in the device.
  • a capillary gap can be formed between the slide and the platform in the operative position.
  • a targeted steering of a liquid located in the capillary gap can be made possible.
  • the liquid can be directed to the complete collection in the not in the collection position or only slightly raised corner region of the slide.
  • a repeated mixing of the slide from the exposure position into the collection position advantageously enables thorough mixing of the liquid in the capillary gap, removal of bubbles from the capillary gap and / or acceleration of biochemical reactions in the capillary gap.
  • the capillary gap may be formed between the platform, which may be a bottom plate of the device, and the surface of the slide on which the biological material is applied, i. the active area of the slide.
  • the active area of a slide may include the total area of one side of the slide minus the area of the label portion.
  • the volume of the capillary gap can be determined by the distance of the slide to the platform or base plate.
  • the device has special spacers which space the slide in the parallel operative position of the platform or bottom plate.
  • the spacers may be formed as projections or elevations of the platform. In other embodiments, the spacers may be formed as protrusions of one or more side walls of the device. In particular, the spacers form support points or surfaces on which the slide rests in the parallel engagement position.
  • the spacers may be configured such that the gap between the slide and the platform in the parallel engagement position has a height that is at least greater than the thickness of the biological material applied to the slide.
  • the spacers can be designed such that the gap between the slide and the platform or base plate in the parallel engagement position has a height of 0.005 mm 0.5 mm, in particular 0.01 mm to 0.3 mm, in particular 0, 05 mm to 0.2 mm.
  • any other constructions which space the slide from the platform so that a parallel capillary gap extending over the entire active area of the slide can be formed are conceivable here.
  • the at least one liquid with which the slide is to be wetted there are several possibilities.
  • the at least one liquid is a Einwirkslosung, which preferably from the
  • Antibody solutions Washings; staining solutions; Cleaning solutions; Entwachsungsaten; Deparaffinization solutions, alcohol solutions;
  • the controlled 3-D movement of the slide can be used to mix several reagents in a liquid.
  • the device may comprise an outlet.
  • the outlet may be an opening for the liquid, wherein the outlet may be configured to be in fluid communication with the only non-elevated or only slightly raised corner region of the slide in the collection position.
  • the liquid can be removed from the device through the outlet, in particular can be sucked out.
  • the liquid can be completely removed through the outlet. In a particularly advantageous manner, the liquid can be completely sucked out through the outlet.
  • the device For deflecting the slide from the operative position to the collecting position, it is further advantageous that the device comprises an abutment.
  • the abutment can be brought into contact with the slide, preferably on the surface facing away from the support.
  • the contact of the slide with the abutment supports the deflection of the slide from the exposure position to the collection position.
  • the device according to the invention may be an incubation chamber for slides, in particular an incubation chamber for immunohistochemical examinations, in s / fu hybridization studies, tissue stains, biochip stains or the like of the biological material.
  • the biological material may be tissue or cell sections. Such tissue sections may be, for example, sections of tumor tissue.
  • this may comprise a base body with a bottom plate and a deflection device with a rocker housing and a rocker according to the invention for the three-dimensional deflection of the slide located in the chamber.
  • the incubation chamber can advantageously comprise a lid so that a closed atmosphere in the interior of the chamber, a saturated atmosphere can be generated.
  • the lid may include a reading window which is arranged so that it is associated with the labeling field of the slide in the closed state of the chamber, so that a barcode is readable by the reading window.
  • the material of the barcode reading window is designed such that it does not or only slightly deflects laser or infrared rays for reading the barcode on the labeling field, so that the barcode readability through the barcode reading window has a bearing.
  • the base body and the rocker housing of the incubation chamber are constructed as separate components, which can be locked by the cover when closing the chamber relative to each other.
  • the rocker housing can be fastened on a base plate, so that the base body of the chamber by closing the lid not only relative to the rocker housing but also relative to the Base plate is lockable.
  • the base plate can preferably be the base plate of an instrument, in particular of a stainer, on which the base body can be locked so that the platform or base plate of the incubation chamber can be brought into contact with a temperature element of the stainer.
  • the temperature element may be a cooling element and / or a heat source.
  • the temperature element can be designed so that it can both heat and cool the platform or base plate.
  • the heat source may be a heating plate or a heating block.
  • the saturated atmosphere in the closed incubation chamber can be generated in particular by the action of heat, preferably by the action of heat via the platform.
  • the saturated atmosphere can be generated by the slight evaporation of the inactive solutions and / or by the evaporation of a non-reactive liquid.
  • the non-reactive liquid can be, for example, water, which can additionally be introduced into the incubation chamber.
  • the incubation chamber may comprise one or more fluid reservoirs, which may be filled by slight overfilling of the capillary gap with monovalent solution and remain in fluid communication with the monolayer solution in the capillary gap. From these reservoirs, a possible, low evaporation loss of Einwirk79 is compensated in the capillary gap.
  • the total amount of valuable and expensive Einwirksen can be reduced by the generated steam atmosphere in the incubation chamber according to the invention, since overall lower evaporation A / sdampfungsutze be recorded. Especially in reaction steps that require high temperatures.
  • the generated vapor atmosphere advantageously enables the above-described repeated deflection can be carried out from the exposure to the Sannnnelposition even in a high-temperature phase of the investigation method of the slide without the water content of valuable and required for the biochemical reactions Einwirkaten evaporates unfavorably quickly.
  • the device according to the invention can be designed as an incubation chamber, comprising:
  • a deflection device which can be brought into contact with the base body in a positive and non-positive connection and by which the slide can be deflected from a position of engagement parallel to the platform of the base body into a collection position not parallel to the platform of the base body, wherein only one corner region of the slide in FIG the collection position is not or only slightly raised, such that the liquid collects in this corner region, and
  • the base body can be designed in one piece or in several parts.
  • a one-piece base body can also comprise a liquid reservoir, which can be configured as a collecting or overflow basin for liquids introduced in excess.
  • the one-piece base body may comprise a coupling element, which may allow a movement of the main body in a positive and non-positive connection with a holding block of the lid.
  • the device according to the invention may comprise a multi-part main body, which may be composed of a plurality of units positively and non-positively.
  • a multi-part body of a designed as a catchment or overflow basin first unit, as a Platform configured second unit and configured as a coupling element third unit be composable.
  • the platform may be formed as a bottom plate of the device, wherein the bottom plate may consist of an inert material or at least on the side facing the slide may be coated with an inert material.
  • the inert material ensures that the in vivo solutions react only with the biological material applied to the slide.
  • the bottom plate can be formed as an inert film of polyimide, in particular Kapton, or polyether ketone (PEEK) or, preferably, be an inertly coated aluminum plate.
  • the bottom plate may be configured such that it enables most efficient temperature transfer between a temperature element located under the bottom plate and the liquid in the capillary gap between the bottom plate and the active surface of the slide.
  • the bottom plate can be designed so that temperature changes of the temperature element can be forwarded with minimum delay to the liquid in the capillary gap.
  • this delay both during heating and during cooling can be between 1 and 5 ° C / second.
  • the temperature delay should not exceed a value of 5 ° C / second.
  • the thermal conductivity of the platform or base plate can be influenced by the material thickness of the base plate, on the other hand by the material properties per se.
  • the material thickness in the region of the bottom plate can be between 0.01 mm and 2 mm.
  • the material thickness in the region of the bottom plate can be between 0.03 mm and 0.8 mm.
  • the material thickness in the region of the bottom plate can be between 0.3 mm and 0.6 mm, in particular 0.55 mm.
  • the bottom plate is an inert polyimide film, especially Kapton, polyether ketone (PEEK) or another inert material may be formed, a material thickness of the film of 0.1 mm should not be exceeded.
  • the platform or base plate should have a high evenness in order to be able to produce a parallel capillary gap between the slide and the platform or base plate on the one hand, and on the other hand to be able to produce a connection with the temperature element that is as positive as possible, thus ensuring temperature transfer between the platform or bottom plate and the liquid located in the capillary gap advantageous to be able to influence.
  • Flatness is according to "Tolerance Management" by Prof. Bernd Klein, University of Kassel, FB15, FG lightweight construction, Mönchbergstr 7, 34109 Kassel, 201 1, pages 40-45, the disclosure of which is fully included in the present application a claim for a surface "in itself".
  • the flatness deviation is the largest distance between an adjacent plane and the real surface.
  • the tolerance zone is limited by two parallel planes at a distance tE. All points of the real surface or derived midplane lie between the two parallel planes with the tolerance distance tE.
  • the real surface of the platform or base plate may have production-related unevenness.
  • the platform or bottom plate can be designed so that it has no bumps whose height could prevent the formation of the parallel capillary gap.
  • the platform or base plate can be designed such that it has elevations of less than 0.1 mm, in particular less than 0.05 mm, in particular less than 0.03 mm.
  • the platform or bottom plate can be made according to the invention include inert temperature-conductive materials and / or materials which may be provided with an inert coating.
  • the platform or bottom plate made of aluminum, stainless steel, a copper alloy or an iron sheet can be made.
  • the platform or base plate may be made of aluminum, in particular of anodized aluminum. It is known to the person skilled in the art that the oxidic layer produced by the anodization process is provided by a conversion of the uppermost layer of the aluminum into an oxide or hydroxide.
  • the term "coating" as used herein is thus to be understood in the broadest sense and includes both a layer of the material of the platform or base plate produced by anodizing process and a coating by a coating, for example a galvanic coating method, on the material of the platform
  • the entire device may be formed from the material of the platform, particularly aluminum
  • the platform or base plate may be incorporated into another material, for example Parts of the device, in particular a main body of the device, made of an inert plastic, which has a temperature resistance of at least 130 ° C, are prepared, in which the platform or bottom plate is incorporated d polyether ketone (PEEK) or polyoxymethylene (POM).
  • PEEK polyether ketone
  • POM polyoxymethylene
  • the materials have suitable resistance under the operating conditions of the device.
  • the material of the device on the one hand should have resistance to the partly highly reactive monolayer solutions, on the other hand to ensure resistance under strongly fluctuating temperature effects.
  • the volume of the capillary gap can be kept surprisingly low.
  • the device may be designed such that the capillary gap can be filled with a liquid volume of at least 50 ⁇ in such a way that a parallel capillary gap extending over the entire active surface of the specimen slide can be formed.
  • the volume of liquid needed to fill the capillary gap should be between 50 ⁇ and 400 ⁇ , advantageously between 50 ⁇ and 150 ⁇ .
  • the bottom plate of the device according to the invention can be designed so that it can bring about an effective limitation of the capillary gap volume.
  • the bottom plate may have an edge, which may preferably adjoin the collecting or overflow basin.
  • this edge can form a borderline for the propagating fluid meniscus when the capillary gap is filled with an adequate volume of fluid.
  • This effect can be enhanced by the fact that the edge of the bottom plate is designed as a collection.
  • a volume of liquid which does not significantly exceed the intended volume of the capillary gap here represents an adequate volume of liquid.
  • the platform or bottom plate may comprise an overflow lip for directing any excess liquid from the capillary gap into the collection or overflow basin.
  • the overflow basin of the apparatus may also be used to provide a small amount of non-reactive liquid, for example water, in the incubation chamber so that the vapor atmosphere may be generated largely by evaporation of the non-reactive liquid.
  • a particularly advantageous manner is defined by an edge of the bottom plate a boundary line for the meniscus of the liquid located in the capillary gap.
  • the capillary gap can be delimited by the edge of the bottom plate, so that a tear-off edge can form for the liquid present in the capillary gap.
  • the precise confinement of the liquid propagating in the capillary gap within the device or incubation chamber can be the same Significantly reduce the risk of contamination. For example, it can be ensured that only the active surface of the slide comes into contact with the respective single-acting solutions. Contamination of the label portion of the slide, however, can be avoided. This can substantially reduce the risk of contamination with potentially mutagenic, carcinogenic, or otherwise toxic liquids and reagents to a user of the device and manipulators of the slides.
  • the device according to the invention may preferably be a sealable incubation chamber into which a slide with biological material can be introduced and deflected according to the invention so that all process steps of an examination protocol, for example an immunohistochemical (IHC) tissue staining protocol, an in situ hybridization assay or a biochip Coloring, can be carried out as efficiently and inexpensively.
  • an examination protocol for example an immunohistochemical (IHC) tissue staining protocol, an in situ hybridization assay or a biochip Coloring
  • the single-solution solutions required in the respective process steps can be introduced into the incubation chamber, but can also be completely removed again, so that the slide can remain in the incubation chamber during the entire protocol.
  • an examination protocol for example an immunohistochemical (IHC) tissue staining protocol, an in situ hybridization assay or a biochip Coloring
  • the single-solution solutions required in the respective process steps can be introduced into the incubation chamber, but can also be completely removed again, so that the slide can remain in the incubation chamber during the entire protocol
  • the inventive design of the incubation chamber can also advantageously facilitate the elimination of the in-solution solutions / reagents used in the chamber.
  • the chamber may allow the complete removal, in particular aspiration, of a single-solution solution used in the chamber without mixing it with other solutions used in previous or subsequent process steps.
  • a prescribed separation and / or elimination be advantageously ensured the resulting chemical waste.
  • suitable single-solution solutions can be effectively recycled.
  • the slide can remain in the chamber during all process steps can also substantially reduce the risk of contamination of the immediate environment, especially for a user of the chamber with one of the inducible solutions. Even in circumstances in which the capillary gap of the chamber should be overfilled, the risk of contamination to the user remains low as the excess fluid is collected in an overflow basin.
  • the platform or bottom plate can be designed so that excess liquid can be preferably passed into the overflow basin, it can further be ensured that only the active surface of the slide, but not the inscription part is wetted with the reactive liquids. This can further reduce the risk of contamination to the user.
  • a spread of the introduced into the chamber liquids can be avoided in the deflection. This can avoid that the deflection can be exposed unfavorable effects of the fluids.
  • time-consuming cleaning of the deflection can be reduced to a minimum, which in addition to the obvious time savings continue to have the advantage of counteracting premature wear.
  • the device according to the invention can comprise an outlet for the fluid, which is in fluid communication with the only one, which is not elevated or only slightly raised, in the collecting position in the collecting position.
  • the liquid can be removed from the device through the outlet.
  • the outlet can be designed as an exhaust pipe guided through the lid of the chamber.
  • the suction nozzle can be anchored in the lid so that it can be brought to a predetermined position of the incubation chamber when closing the lid, which is assigned to the corner region of the slide.
  • the suction nozzle can be designed so that it in the closed state of Incubation chamber with the not or only slightly raised in the collection position corner region of the slide can enter into a positive and non-positive connection and / or the slide can provide a further abutment, which supports the tilting movement of the slide in the collection position.
  • the suction nozzle may be formed of a deformable material such as rubber or silicone, so that the positive and non-positive connection of the suction nozzle is sealed to the slide. Thus, it can be ensured that a negative pressure in the suction can be generated.
  • the suction nozzle can be arranged in the incubation chamber so that the suction opening encloses the corner of the not in the collecting position or only slightly raised corner region of the slide.
  • the end of the suction nozzle which meets the slide can be funneled out like a funnel or trumpet, so that the suction nozzle can be brought into a positive and non-positive connection with the corner region of the slide by closing the lid of the incubation chamber.
  • the funnel or trumpet-like everted end of the suction can be designed so that on the one hand, a fluid connection between the liquid located in the capillary gap and the suction opening of the suction can be generated and the positive and non-positive connection on the other hand can allow the generation of a negative pressure in the suction ,
  • the end of the suction nozzle which meets the object carrier can be provided with a recess which can receive the corner region of the object carrier which is not or only slightly raised in the collecting position in a positive and non-positive connection.
  • the corner of the slide can protrude into the suction opening of the suction nozzle, so that by closing the lid of the incubation on the one hand, a fluid connection between the located in the capillary liquid and the suction opening of the Absaugstutzens can be generated and the positive and non-positive connection on the other hand can allow the generation of a negative pressure in the exhaust.
  • the outlet can be designed so that it can be connected to at least one suction element.
  • the suction element may be part of an exhaust system for the separate disposal of the introduced into the capillary liquid.
  • the suction channel can receive a suction element, in particular a pipette tip or a pipetting needle, so that the liquid can be removed or sucked out of the incubation chamber through the suction nozzle and via the pipette tip or pipetting needle.
  • the suction element may be a suction hose.
  • the suction channel can lead through the lid of the incubation chamber. In such embodiments, the suction channel is usually rectilinear.
  • the suction channel may comprise a bend, which makes it possible to remove or suck the liquid not through the lid of the incubation chamber but through a side wall of the main body from the incubation chamber.
  • the suction channel lead to a passage in a side wall of the main body.
  • the implementation can be designed so that they can accommodate a suction hose. By closing the cover of the incubation chamber, the suction channel can be brought into a non-positive and positive connection with the suction tube.
  • the suction channel leads through the lid of the incubation chamber and can be connected to a suction tube
  • the suction tube must be flexible or movable so that the lid of the incubation can be fully opened and closed without restriction.
  • a flexible or movable configuration of the suction hose is not absolutely necessary. This can bring constructive advantages.
  • the device according to the invention is designed as an incubation chamber for use in a stainer.
  • the slide can be deflected into a mixing position that is not parallel to the platform.
  • the mixing position may be a position between the exposure position and the collection position, in which the space between the slide and the platform can form a flow connection between a mixing zone of the device and the only not completely raised in the collection position corner region of the slide.
  • Reagents that are introduced into a mixing zone while the slide is at the collection position may flow through the flow connection into the non-elevated or slightly elevated corner region as the slide is deflected into the mixing position.
  • the liquid for wetting the biological material may be a highly reactive and short-lived liquid which must be prepared from two or more components immediately prior to their use.
  • the liquid may be a substrate solution for an enzymatic reaction.
  • substrate solutions are often unstable and can disintegrate in a short time and are often usable only in a short time window after their preparation. Because of its short life (low durability) lengthy mixing procedures and / or service lives of such liquids should be avoided after their preparation.
  • such liquids can be advantageously provided directly in the device and thus immediately prior to their use.
  • a 3,3'-diaminobenzidine (DAB) solution and a hydrogen peroxide-containing buffer solution may be introduced into the mixing zone, and then, by repeatedly deflecting the slide from the collection position to the mixing position into a DAB peroxidase substrate solution to wet the biological material to be mixed.
  • the DAB peroxidase substrate solution can be brought into contact with the biological material immediately after its preparation.
  • the mixing position can advantageously be selected so that the reagents to be mixed do not come into contact with the biological material during the mixing process.
  • the mixing position may be farther away from the collection position, the farther away the biological material from the corner region not or only slightly raised in the collection position is applied to the active surface of the slide.
  • the mixing zone can be arranged so that it can be assigned to a first edge of the slide, wherein the first edge is part of the not or only slightly raised corner region of the slide and on the other hand farther away from the biological material than the second edge of the not or only slightly raised corner region.
  • This further method may include the following steps:
  • the non-parallel mixing position may be selectable so that the reagents do not contact the biological material during steps (a) through (c) of the process.
  • the at least two reagents may be a 3,3'-diaminobenzidine (DAB) solution and a hydrogen peroxide-containing buffer solution, such that the by the complete mixing of the two reagents may be a DAB peroxidase substrate solution.
  • DAB 3,3'-diaminobenzidine
  • Fig. 1 in a schematic, perspective view a
  • Fig. 2 shows the device according to the invention according to Figure 1, in which the
  • FIGS. 1 and 2 shows the device according to the invention according to FIGS. 1 and 2 in the closed state
  • FIG. 4 shows a schematic, perspective view of a deflection means of a device according to the invention
  • FIG. 5 in a schematic, perspective view of a
  • Deflection device of a device according to the invention 6 is a schematic, perspective view of a one-piece main body of a device according to the invention.
  • FIG. 7 is a schematic representation of another embodiment of a device according to the invention in the closed state
  • FIG. 8 in a schematic, perspective view another
  • FIG. 9 is a schematic, perspective view of a multipart, in particular three-part body in positive connection with a deflection device of a device according to the invention.
  • FIG. 10 is a schematic perspective view of a coupling element of a multi-part main body of a device according to the invention.
  • FIG. 1 1 in a schematic, perspective view another
  • FIG. 12 is a schematic, perspective view of a deflection means of a device according to the invention.
  • FIG. 13 is a schematic, perspective view of an outlet of a device according to the invention.
  • FIG. 14 is a schematic, perspective view of part of a device according to the invention in an enlarged detail
  • 15 is a schematic, perspective view of an outlet of a device according to the invention
  • 16 shows a schematic perspective view of an extraction system that can be connected to the outlet of the device according to the invention.
  • 17 is a schematic, perspective view of a platform for
  • Fig. 18 in a schematic, perspective view of a platform for
  • 19 is a schematic, perspective view of a platform for
  • Fig. 20 is a schematic, perspective view of another
  • Embodiment of a device according to the invention in which the slide is in the operative position.
  • Fig. 21 is a schematic, perspective view of a lid with extended side walls.
  • FIG. 1 shows a device 1 according to the invention, which is designed as an incubation chamber 1 'for a slide 2.
  • the incubation chamber V comprises a deflection device 3, a one-piece base body 4 with a platform for receiving the slide 2 and a cover 5.
  • the platform lies in the incubation chamber 1 'below the slide 2 and is therefore not visible in FIGS. 1 and 2.
  • the incubation chamber V serves to wet biological material deposited on the active surface of the slide 2 with at least one liquid and is particularly useful in immunohistochemistry, s / fu hybridization studies, tissue staining, biochip staining or the like of the biological material. in particular of tissue or cell sections, suitable.
  • the slide 2 is within the incubation chamber 1 'deflected into a collecting position in which a corner region 6 of the slide 2 is not or only slightly raised, so that a liquid for wetting the applied on the slide 2 biological material 6 collects in this corner.
  • the deflection device 3 comprises a deflection means 7, which is designed as a rocker 7 ', and a rocker housing 8.
  • the slide 2 comprises at one end a labeling field 9 with a bar code 10 and lies with this end on the rocker 7' on.
  • the designed as an incubation V, inventive device 1 is shown with an open lid 5, which can be fixed via a support block 1 1 at a designated, not shown in Figure 1, base plate.
  • the cover 5 further comprises an outlet 12, which may be formed as a suction nozzle 12 'and anchored in the lid 5.
  • the impact on the slide 2 end 13 of the suction 12 ' is funnel-shaped or trumpet-like everted and is pressed when closing the lid 5 on the corner region 6 of the slide 2, so that in the suction 12' a negative pressure can be generated.
  • the suction nozzle 12 ' In the collecting position of the slide 2, the suction nozzle 12 'is in fluid communication with the corner region 6 through the connection with the slide 2, so that the liquid for wetting the biological material can be completely sucked by the negative pressure which can be generated in the suction nozzle 12'.
  • the cover 5 comprises a plurality of abutments 14 which, with the cover 5 of the incubation chamber 1 'closed, can come into contact with the surface of the slide 2 facing away from the support 24 of the rocker 7, so that the deflection of the slide 2 from the action position into the collection position is supported becomes.
  • a saturated atmosphere can be generated, in particular by heat, preferably by heat through the platform or bottom plate of the base body 4.
  • a closure 15 is provided, through which the base body 4 with the Deflection device 3 is connected.
  • the closure 15 has a receiving region 16 for a locking element 17.
  • the closure 15 causes when closing the lid 5 not only that the Base 4 is locked relative to the rocker housing 8, but also relative to the base plate.
  • the shutter 15 is provided with a gripping lip 18 which can facilitate the user to open and close the lid 5. All other constructive embodiments of a lid closure, which can provide the described functions, are conceivable.
  • the platform or bottom plate of the base 4 can be exactly and advantageously positioned on an underlying temperature element, for example on a hot plate or on a heating block. Furthermore, depending on the design of the receiving region 16 of the closure 15 and of the corresponding locking element 17, the platform or bottom plate of the base body 4 can be positioned on the temperature element in a force-fitting manner. This enables effective and precise temperature transfer from the temperature element via the platform or bottom plate of the main body 4 into the capillary gap between the slide 2 and the platform or bottom plate 34.
  • the lid 5 of the incubation chamber V comprises a bar code reading window 19 which, in the closed state, can be assigned to the labeling field 9 of the slide 2 resting on the rocker 7 ', so that the bar code 10 also passes through the lid 5 in the closed state of the incubation chamber 1' can be read.
  • the bar code reading window 19 may be made of a transparent plastic, which does not or only slightly deflects the corresponding laser or infrared rays for reading the bar code, so that the bar code readability is enduring.
  • the lid 5 comprises at least one passage 20 for the introduction of liquids into the closed incubation chamber V.
  • a coloring process of the biological material requires the multiple exchange of reagents.
  • the reagents can be introduced through the passage 20 in the lid 5 laterally of the slide 2 into the incubation chamber 1 '.
  • the passage 20 In order to maintain the saturated atmosphere in the closed incubation chamber V, the passage 20 must be on the one hand be closed, on the other hand allow the piercing with a pipette tip or pipetting needle and close again after the introduction of the liquid.
  • the passage 20 may be provided, for example, with a silicone closure with a cross recess, which closes automatically after retraction of the pipette tip or pipetting needle again.
  • the closure can be configured as a displaceable cover, which can initially be pushed aside by the pipette tip or pipetting needle and automatically closes again after retraction of the pipette tip or pipetting needle due to an elastic bias. If the cover has several feedthroughs for introducing liquids into the closed incubation chamber 1 ', then the described closure possibilities of the feedthrough 20 are also conceivable for the further feedthroughs.
  • FIG. 2 shows the incubation chamber 1 'according to FIG. 1, the slide 2 being in the action position. For this purpose, the non-visible rocker 7 'is lowered.
  • FIG. 3 shows the incubation chamber V according to FIGS. 1 and 2 in the closed state. To avoid repetition relating to FIGS. 2 and 3, reference is made to the description of FIG.
  • FIG. 4 shows the deflection means 7, designed as a rocker T, of the deflection device 3.
  • the rocker T may comprise a receiving region 21 for a lifting means, for example a plunger.
  • the plunger can be anchored in the receiving region 21 via an anchoring element 22, for example via the pin 22 ', so that the deflection means 7 configured as a rocker T can be moved from the bottom to the top into a raised position and into a tilted position.
  • the raised position of the rocker 7 ' at least two corner regions of the slide 2 are not or only slightly raised, wherein the slide 2 is present in the tilted position in the collection position.
  • an anchor element 23 of the rocker 7 'designed as abutment lip 23' can come into contact with a corresponding armature surface of the device 1, for example an armature surface of the rocker housing 8, so that the rocker 7 'moves from the raised position into the tilted position turns.
  • the armature surface of the rocker housing 8 can be used as a material projection, for Example be formed as a protruding edge of a side wall of the rocker housing 8, which serves the abutment lip 23 'as a stop.
  • a first lateral rocker wall 25 may limit the sliding movement of the slide 2.
  • the first rocker wall 25 is configured slightly higher than the opposite, second rocker wall 26 so that they can bump in the closed incubation chamber 1 'against the lid 5, the abutment lip 23' in particularly strong inclination of the rocker 7 'contact with the lose corresponding anchor surface of the rocker housing 8.
  • the abutment of the first rocker wall 25 against the cover 5 form another abutment, which can support the tilting movement of the rocker 7 'and thus the deflection of the slide 2 in the collection position.
  • the rocker 7 ' is shown in the tilted position in the rocker housing 8, which is connectable to the main body 4 of the incubation chamber V.
  • the tilting movement of the slide 2 is supported in the closed incubation V as already described above by the abutment 14.
  • the tilting movement of the slide 2 can be supported against the forces acting in the capillary gap adhesion forces.
  • the rocker 7 ' is further provided with a rear wall 27, which prevents the slide 2, the front inner wall 28 of the rocker housing 8 touches and jammed with this when lowering.
  • the rocker housing 8 may be attached to fixing points 29, for example by means of screws to a base plate of an instrument or machine. By attaching the rocker housing 8 to a base plate of the base body 4 may be arranged stationary when closing the shutter 15 relative to the base plate.
  • the rocker housing 8 comprises a positioning element, which is designed as a depression / bulge 30, and can receive a corresponding positioning element of the base body 4.
  • the circumferential walls 31, 32 and 33 of the rocker housing 8 are designed so that they can be connected to a corresponding recess of the lid 5.
  • the inner sides 31 'of the peripheral wall 31 of the rocker housing 8 may be correspondingly far away from each other, as corresponding lateral boundary elements of the base body 4.
  • the inner sides of the rocker walls 25 and 26 a Limit lateral slippage of the slide 2.
  • FIG. 6 shows a one-piece basic body 4 of the device designed as incubation chamber 1 '.
  • the main body 4 comprises the platform or bottom plate 34, which consists of an inert material, or at least on the side facing the slide 2 with an inert material is coated.
  • the bottom plate 34 is an inert film of polyimide, especially Kapton, or polyether ketone (PEEK), or a coated aluminum plate.
  • PEEK polyether ketone
  • a capillary gap is formed between the slide 2 and the platform or bottom plate 34, which may be filled by the liquid for wetting the biological material applied to the slide 2.
  • the deflection of the slide 2 by the deflection device 3 allows a targeted steering of the liquid in the corner region 6, which is associated with a suction point 35 of the base body 4.
  • the base body 4 comprises spacers 36.
  • the spacers 36 may have, in particular, a height of 0.05 mm to 0.2 mm relative to the platform or base plate 34.
  • the base body 4 comprises limiting elements 37, 38, 39, which can limit the lateral movement or the slippage of the slide 2 in the incubation chamber 1 '.
  • the delimiting element 39 can prevent the possibly sharp-edged slide 2 from being moved out of the action position into the collecting position on the inner rear wall 40 of the Can block body 4, the deflection of the slide 2 would affect.
  • direct pressure can be exerted on the surrounding walls 41, 42, 43 of the main body 4 as well as on the peripheral walls 31, 32, 33 of the rocker housing 8 by closing the cover 5, which pressure is indirectly applied to the housing Platform or bottom plate 34 of the base body 4 results.
  • the indirect pressure supports the most direct possible temperature transfer from a temperature element lying below the platform or bottom plate 34 to the platform or bottom plate 34.
  • the main body 4 comprises a positioning element designed as a material projection 44, which can be connected to the depression / bulge 30 of the rocker housing 8. Furthermore, the main body 4 comprises an overflow basin 45. A wall of the overflow basin 45 defines a tear-off edge 46 for the liquid in the capillary gap, so that the liquid can flow into the overflow basin 45 only when the capillary gap is overfilled.
  • the main body 4 shown in FIG. 6 has a region 47 into which liquids can be introduced.
  • the region 47 may be in fluid communication with the outlet 12 of the device 1, preferably via the capillary gap.
  • the main body 4 comprises a further indentation 48 which is assigned to the region 47 and can facilitate the introduction, for example the pipetting in, of a liquid into the region 47.
  • the region 47 may also be located in other locations in other embodiments of the device 1 according to the invention. If, however, the region 47 also functions as a mixing zone 47 'in a method according to the invention, it is to be arranged in the base body 4 such that a flow connection between the region 47 and the corner region 6 can be formed in a non-parallel mixing position of the slide 2.
  • reagents which are introduced into the mixing zone 47 'and flow through the flow connection into the corner region 6 can be completely mixed by repeatedly deflecting the slide 2 from the collection position into the mixing position.
  • the liquid for wetting the biological material can be provided.
  • a 3,3'-dianninobenzidine (DAB) solution and a hydrogen peroxide-containing buffer solution may be introduced into the mixing zone 47 'such that a DAB peroxidase substrate solution for wetting the biological material directly into the incubation chamber 1' may be prepared by a mixing method of the present invention.
  • FIG. 7 shows a schematic representation of the possible arrangement of the region 47 and of the mixing zone 47 'relative to the slide 2 in the closed device 1 designed as incubation chamber 1'.
  • the incubation chamber 1 ' in particular the lid 5, the slide 2 and the base 4, are shown.
  • both the lid 5 and the slide 2 are shown transparently so that underlying features are visible in the figure.
  • FIG. 7 shows a passage 20 'assigned to the mixing zone 47' for introducing liquids to be mixed into the incubation chamber 1 '.
  • the mixing zone 47 ' can be arranged so that it is associated with the first edge 49 of the slide, on the one hand part of the not or only slightly raised corner portion 6 of the slide 2 and on the other hand is further away from the biological material than the second edge 50 of the no or only slightly raised corner region 6. This ensures that contact of the reagents to be mixed with the applied on the underside of the slide 2 biological material 51 can be prevented during mixing.
  • FIG. 7 shows a passage 20 'assigned to the mixing zone 47' for introducing liquids to be mixed into the incubation chamber 1 '.
  • the mixing zone 47 ' can be arranged so that it is associated with the first edge 49 of the slide, on the one hand part of the not or only slightly raised corner portion 6 of the slide 2 and on the other hand is further away from the biological material than the second edge 50 of the no or only slightly raised corner region 6.
  • FIG. 8 shows a device 1 according to the invention designed as an incubation chamber 1 'with a design of the cover 5 deviating from the incubation chambers of FIGS. 1 to 3.
  • the cover 5 also comprises a passage for a suction nozzle 12', an abutment 14, a bar code reading window 19 and at least one passage 20 for introducing liquids into the closed incubation chamber 1 '.
  • the lid 5 of the In the incubation chamber 1 'shown in FIGS. 1 to 3 several passages for introducing liquids into the closed incubation chamber 1' are conceivable for the cover 5 of the incubation chamber 1 'shown in FIG. 8, for example corresponding to the passages 20 and 20' as shown in FIG ,
  • a pressure exerted on the cover 5 on the base body 4 that a platform or bottom plate 34 of the base body 4 is pressed onto an underlying heating element and so a direct and improved temperature transfer via the platform or bottom plate 34 in the capillary gap feasible is.
  • the cover construction of Figure 7 provides this effect by means of a locking arm 52 ready.
  • the locking arm 52 is in turn fixable via a holding block 1 1 to a base plate of an instrument or a machine, not shown.
  • the hinge of the locking arm 52 in the holding block 1 1 is designed such that it is biased to urge the lid 5 in a closed position. This can be achieved for example by a spring in the holding block 1 1. Due to the bias of the locking arm 52, the cover 5 of the incubation chamber V exerts a pressure both on the main body 4 and on the rocker housing 8 in the closed state of the chamber.
  • FIG. 9 shows a device 1 designed as an incubation chamber V with a multipart base body 4.
  • the base body 4 consists of an overflow basin 45, a platform 34 and a coupling element 53.
  • the apparatus 1 shown includes a deflection device 3 according to the figure 5.
  • the units of the multi-part base body 4 can over the already described construction possibilities of the lid 5 with each other and with the Deflection device 3 are connected.
  • the platform 34 may be formed as a bottom plate of the device 1.
  • the bottom plate 34 shown in Figure 9 may be an inertly coated aluminum plate, wherein the spacers 36, the limiting elements 37, 38, 39 and the trailing edge 46 may be an integral part of the bottom plate 34. This has the advantage that the entire platform 34 can be produced as a single workpiece, giving the required evenness the platform 34 can ensure.
  • the platform or bottom plate 34 is incorporated in a base body 4, the resulting forces on the platform or bottom plate 34 must be compensated so that the flatness of the platform or bottom plate 34 remains.
  • FIG. 10 shows a coupling element 53 of a multipart base body 4, in which the suction channel 54 of the device 1 passes through the peripheral wall 42 of the main body 4 and can be connected to a suction hose. Furthermore, the coupling element 53 comprises bearing surfaces 55 for the platform 34 so that it can be connected to the coupling element 53.
  • Figure 1 1 shows an alternative embodiment of the device 1 according to the invention, which comprises a deflection device 3 and a base body 4. Due to the shown position of the deflection device 3, the slide 2 is in the collection position.
  • the rocker 7 'on a designed as a guide rail recess which serves as a receiving area 21 for the lifting means.
  • the lifting means which may be designed as a plunger, may protrude into the receiving region 21 and deflect the rocker 7 'into a predetermined by the shape of the guide rail movement.
  • the deflection of the object carrier 2 from the engagement position into the collection position can be achieved by the shape of the receiving region 21 designed as a guide rail.
  • the liquid in the capillary gap between the slide 2 and the platform 34 can be deflected in such a way that it collects in the corner region 6.
  • FIG. 12 shows the rocker 7 'of the device 1 of Figure 1 1 in detail, which is referred to the description of Figure 1 1.
  • FIG. 13 shows a suction nozzle 12 'which is designed in such a way that the suction channel 50 is guided through the lid 5 of an incubation chamber V.
  • the suction nozzle 12 ' comprises a recess 56 which can receive the corner region 6 of the slide 2.
  • both the suction opening 57 and the suction channel 54 of the suction nozzle 12 ' can be brought into fluid communication with the liquid present in the capillary gap.
  • FIG. 14 shows the suction nozzle 12 'according to FIG. 13 in a suction position as it may be in the closed state of an incubation chamber 1'.
  • the slide 2 can be present in the incubation chamber 1 'and how the recess 56 can receive the corner region 6 of the slide 2 so that both the suction opening 57 and the suction channel 54 of the suction nozzle 12' are in fluid communication with that in the capillary gap Liquid can be brought.
  • FIG. 15 shows an alternative embodiment of the suction nozzle 12 'in which the suction channel 54 is guided by the peripheral wall 42 of the base body 4.
  • the suction channel 54 in the intake 12 thus includes a bend.
  • the suction tube In embodiments in which the suction channel 54 leads through the lid 5 of the incubation chamber 1 '(as shown in FIGS. 12 and 13), the suction tube must be designed such that the lid 5 of the incubation chamber V can be fully opened and closed without restriction.
  • the suction channel 54 leads through the circumferential wall 42 of the main body 4 and can be connected to a suction hose, a flexible or movable configuration of the suction hose is not absolutely necessary.
  • FIG. 16 schematically shows an exhaust system 58 which can be connected to the outlet 12 or the exhaust pipe 12 'via a suction element 59.
  • the suction element 59 is shown as the pipette tip 59 ', which may be anchored in a pipette tip holder 60.
  • the suction system 58 serves for the separate disposal of the liquids used in the capillary gap of the device 1 designed as an incubation chamber V according to the invention. Therefore, as shown, a plurality of pipette tips 59 'in the Pipette tip holder 60 be anchored, which are each intended for sucking a liquid from the device 1.
  • a negative pressure can be generated in the suction hoses 61 and the waste containers 63.
  • the negative pressure may be generated by a vacuum pump 64 in communication with the waste containers 63.
  • the connection of the vacuum pump 64 with the waste containers 63 is ensured in the illustrated suction system 58 via a central vacuum tank 65, which in turn can be connected via hose connections 66 to the respective waste containers 63.
  • a negative pressure in all suction hoses 61 can be generated via a single vacuum pump 64, which enables the suction of the liquids located in the capillary gap via the pipette tips 59 '.
  • the suction can be performed by one of the pipette tips 59 '.
  • a suction element 59 which is associated with a liquid to be sucked off and is connected to the corresponding waste container 63 for this liquid, must be connected to the outlet 12 or the suction nozzle 12 'and the corresponding valve 67 to be opened, if this liquid flows out of the Incubation chamber V should be removed.
  • the suction system 58 described here can be a unit of a stainer for the device according to the invention, and the steps described can be part of an automated process, which run in conjunction with the wetting of the biological material 51 applied to the slide 2 in the incubation chamber 1 ' can.
  • the steps described can be part of an automated process, which run in conjunction with the wetting of the biological material 51 applied to the slide 2 in the incubation chamber 1 ' can.
  • the complete removal, in particular suction, of the single-solution solutions used can be possible so that a prescribed separation and / or removal of the resulting waste solutions is advantageously possible.
  • 58 suitable Einwirktheen can be effectively recycled with appropriate design of the extraction system.
  • FIG. 17 to 19 show further exemplary embodiments of a platform 34 which can each be used with a device 1 having a multipart base body 4 designed as an incubation chamber 1 '.
  • FIG. 17 shows a platform 34, wherein the spacers 36, the limiting elements 37, 38, 39 and the tear-off edge 46 are an integral part of the platform 34.
  • the limiting elements 37, 38, 39 are formed by a deformation of the material, for example by bending, of the circumferential side walls 41, 42, 43.
  • a platform 34 can be provided by simple means and thus extremely cost-efficient, which meets the requirements with respect to a planar design.
  • the limiting elements 37, 38, 39 do not extend to the surface of the base plate 34. This has the advantage that adhesion and / or capillary effects are avoided or minimized by contact of the boundary elements 37, 38, 39 with the liquid reagents.
  • the limiting elements 37, 38, 39 ensures that slipping of the slide 2 is limited. Furthermore, jamming of the slide 2 under one of the limiting elements 37, 38 or 39 is effectively prevented.
  • the limiting element (s) 38 the distance of the slide 2 to the vertical or oblique side wall 43 is defined, this distance allows the insertion of a pipetting needle or pipette tip.
  • the limiting elements 37 and 39 ensure that the non-recessed parts of a suction nozzle 12, 12 ', shown for example in FIG. 15, have sufficient space to form-fit around a corner of the slide 2, thereby allowing the aspiration of liquid reagents.
  • FIG. 17 shows that the peripheral walls 41, 43 of the platform 34 are configured obliquely or at an angle of more than 90 ° to the surface of the bottom plate 34.
  • This facilitates the insertion of a pipetting needle or pipette tip through a passage 20 provided in the opening 20 so that liquids or reagents are easier to introduce into the incubation chamber 1 '.
  • the angle of more than 90 ° between the surface of the platform 34 and the sidewalls 41, 43 prevents the liquid reagents from initially spreading along the edge before passing under the light In the experiment, it has been found that this cornering effect is reduced when the side walls 41, 43 are inclined obliquely outwards as in FIGS. 17 and 18.
  • the angle between the surface of the platform 34 and the side walls 41, 43 between 95 and 120 °, in particular between 95 and 1 15 °, in particular between 95 and 1 10 °, in particular between 100 and 1 10 ° , in particular between 105 and 110 ° C.
  • the platform 34 according to Figure 17 is shown in Figure 18, the limiting element 38 is not present, however, by tilting the side wall 43 even without limiting element 38 a sufficient distance to a liquid reagent is introduced along the inside of the side wall 43 into the incubation chamber V.
  • the reagent is at approximately half the height of the side wall d 43 can be introduced into the incubation chamber 1 'so that it flows into the non-rectangular edge between the surface of the bottom plate 34 and the side wall 43 and from there can flow directly under the slightly raised or parallel slides 36 lying on the spacers 36.
  • the area of the platform 34 shown in Figure 18 is reduced in width such that the freedom of movement of the slide 2 is limited to the same extent as in a platform 34, which has a limiting element 38.
  • FIG. 19 shows a further embodiment of the platform 34, in which the spacers 36, the delimiting elements 37, 38, 39 and the tear-off edge 46 are an integral part of the platform 34.
  • the limiting elements 37, 38, 39 are likewise formed by forming the material of the circumferential side walls 41, 42, 43.
  • the limiting elements 37, 38, 39 are formed as material projections (bulges).
  • a platform 34 can be provided by simple means and thus extremely cost-efficient, which meets the requirements with respect to a planar design.
  • the limiting elements 37, 38, 39 ensures that slipping of the slide 2 is limited.
  • FIG. 20 shows a device 1 according to the invention, which is designed as an incubation chamber 1 'for a slide 2.
  • the incubation chamber 1 ' comprises a deflection device 3, a platform 34 as shown in FIG. 17 for receiving the slide 2 and a cover 5.
  • the device 1 according to the invention designed as an incubation chamber V, is shown in FIG. 20 with an open lid 5, which has a holding block 1 1 is fixed to a designated base plate 69.
  • the platform 34 rests directly on the heating block 70 provided on the base plate 69.
  • the lid 5 further comprises extended sidewalls 71, which extend down to the base plate 69 when the lid is closed and thus seal the incubation chamber without requiring a seal running along the underside of the lid 5.
  • This has particular constructive advantages in incubation chambers 1 'with multi-part basic bodies 4, as shown for example in FIGS. 9 and 20.
  • FIGS. 9 and 20 In the case of the deck constructions illustrated in FIGS.
  • the sealing of the incubation chambers V is realized by a silicone seal or a form-fitting connection between the underside of the cover 5 with the base body 4 and the deflection device 3.
  • 3 corresponding surfaces may be formed on the base body 4 and on the deflection device.
  • the cover 5 of the incubation chamber V from FIG. 20 is shown separately.
  • the side walls 71 are fastened by screws 72 on the sides of the lid 5.
  • mounting holes 73 which are connected to a corresponding fastener of the Holding block 1 1 are connectable.
  • the bushing closure 74 of the bushing 20 is shown.
  • this feedthrough closure 74 can be made of silicone and have a cross slot so that a pipetting needle or pipette tip can be pushed through the passage while maintaining the saturated atmosphere in the incubation chamber 1 '.
  • the cover 5 shown in FIG. 21 can be produced, for example, as a separate workpiece by injection molding.
  • the cover 5 may have a barcode reading window 19 for reading the barcode 10 of the slide 2.
  • the bar code reading window 19 may be made of transparent material, for. As glass or macro ion exist. Alternatively, the entire cover 5 can be made of a transparent material, for example a macroion.

Abstract

La présente invention concerne un dispositif de mouillage de matériel biologique avec au moins un liquide. L'invention concerne également un procédé de mouillage de matériel biologique avec au moins un liquide à l'aide à un dispositif correspondant.
EP17840557.7A 2016-12-21 2017-12-20 Dispositif et procédé de mouillage de matériel biologique Withdrawn EP3559630A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102016225885.0A DE102016225885B4 (de) 2016-12-21 2016-12-21 Vorrichtung und Verfahren zum Benetzen von biologischem Material
PCT/EP2017/083860 WO2018115145A1 (fr) 2016-12-21 2017-12-20 Dispositif et procédé de mouillage de matériel biologique

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EP3559630A1 true EP3559630A1 (fr) 2019-10-30

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EP17840557.7A Withdrawn EP3559630A1 (fr) 2016-12-21 2017-12-20 Dispositif et procédé de mouillage de matériel biologique

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US (1) US20190368983A1 (fr)
EP (1) EP3559630A1 (fr)
DE (1) DE102016225885B4 (fr)
WO (1) WO2018115145A1 (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10596574B2 (en) * 2015-04-24 2020-03-24 Euroimmun Medizinische Labordiagnostika Ag Incubation tray
CN108353890B (zh) * 2018-02-13 2021-01-26 京东方科技集团股份有限公司 一种生物片材固定装置
US11169073B2 (en) * 2019-05-24 2021-11-09 Essen Instruments, Inc. Apparatus for supplying reagents to a flow cytometry system
DE102019215577B3 (de) 2019-10-10 2020-11-05 Prime23 GmbH Vorrichtung und Verfahren zur Benetzung von biologischem Material
DE102020204670A1 (de) 2020-04-14 2021-10-14 Prime23 GmbH Vorrichtung und Verfahren zum Benetzen von biologischen Material mit wenigstens einer Flüssigkeit sowie eine Halteeinrichtung

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1088421A (en) 1964-01-07 1967-10-25 Harshaw Chemicals Ltd A method and apparatus for depositing a coating on the internal walls of capillary or smallbore tubes
US4034700A (en) 1976-05-25 1977-07-12 Honeywell Inc. Slide preparation station
AU6156780A (en) 1979-08-24 1981-04-09 G.D. Searle & Co. Stack plate culture
US5595707A (en) * 1990-03-02 1997-01-21 Ventana Medical Systems, Inc. Automated biological reaction apparatus
CA2299118C (fr) * 1990-03-02 2006-08-08 Ventana Medical Systems, Inc. Appareil de reaction biologique automatise
JP3320444B2 (ja) 1992-04-06 2002-09-03 株式会社千代田製作所 染色装置用ノズル洗浄装置
DE10016554A1 (de) 2000-04-03 2001-10-18 Rootec Ges Fuer Bioaktive Wirk Vorrichtung zum Kultivieren von pflanzlichen oder tierischen Gewebekulturen
DE10218988C1 (de) 2002-04-24 2003-11-20 Horst Dieter Becker Vorrichtung und Verfahren zum Benetzen von Objekten
AUPS309002A0 (en) 2002-06-20 2002-07-11 Vision Biosystems Limited A covertile for a substrate
DE10352716A1 (de) * 2003-11-05 2005-06-16 Einsle, Xaver Plattform
US7195394B2 (en) 2004-07-19 2007-03-27 Vijay Singh Method for resonant wave mixing in closed containers
DE102004054125B4 (de) 2004-11-08 2011-01-05 Minucells And Minutissue Vertriebs Gmbh Gradientenkammer zum Kultivieren und/oder Differenzieren von Zellen/Geweben
ATE529732T1 (de) * 2006-10-30 2011-11-15 Ventana Med Syst Inc Dünnfilmvorrichtung und -verfahren
CN101809142A (zh) 2007-09-26 2010-08-18 通用电气医疗集团生物科学生物方法公司 三维可用后即弃生物反应器
US8501115B2 (en) * 2008-10-24 2013-08-06 Statspin, Inc. Modular system for performing laboratory protocols and associated methods
CN102687023B (zh) * 2009-11-13 2016-01-06 文塔纳医疗系统公司 用于可调容纳体积的薄膜处理装置
US8877485B2 (en) 2009-12-09 2014-11-04 Dako Denmark A/S Apparatus and method for processing biological samples
CN101966435B (zh) 2010-09-27 2012-08-29 四川南格尔生物医学股份有限公司 医用三轴摇摆机
DK2625502T3 (en) 2010-10-06 2018-12-17 Biocare Medical Llc Method and system for efficient processing of biological samples
US8580568B2 (en) * 2011-09-21 2013-11-12 Sakura Finetek U.S.A., Inc. Traceability for automated staining system
US8932543B2 (en) 2011-09-21 2015-01-13 Sakura Finetek U.S.A., Inc. Automated staining system and reaction chamber
CA2866854C (fr) * 2012-03-09 2020-08-18 Leica Biosystems Richmond, Inc. Dispositif et procede pour controler la temperature dans un fluide mobile dans un systeme de traitement d'echantillons de laboratoire
US9284521B2 (en) 2012-03-24 2016-03-15 Therapeutic Proteins International, LLC Pivoting pressurized single-use bioreactor
US10035116B2 (en) 2012-06-15 2018-07-31 Life Technologies Corporation Fluid mixing system with tiltable support housing
GB2519961A (en) * 2013-11-01 2015-05-13 Cellect Biotech Ltd Particle identification apparatus, system, and method
DE202017101988U1 (de) 2017-04-04 2017-08-09 Tecan Trading Ag Automatisiertes System zur Kultivierung und Differenzierung pluripotenter Stammzellen

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US20190368983A1 (en) 2019-12-05
DE102016225885B4 (de) 2023-12-21
DE102016225885A1 (de) 2018-06-21
WO2018115145A1 (fr) 2018-06-28

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