EP3653304B1 - Probenbehältnis - Google Patents

Probenbehältnis Download PDF

Info

Publication number
EP3653304B1
EP3653304B1 EP19212880.9A EP19212880A EP3653304B1 EP 3653304 B1 EP3653304 B1 EP 3653304B1 EP 19212880 A EP19212880 A EP 19212880A EP 3653304 B1 EP3653304 B1 EP 3653304B1
Authority
EP
European Patent Office
Prior art keywords
closure
section
sample container
closure element
housing
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.)
Active
Application number
EP19212880.9A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP3653304A1 (de
Inventor
Daniel SIMONS
Dirk LEBER
Harald Quintel
Sasa Lazevski
Bruno Walder
Andreas Bretscher
Thomas Voit
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.)
Hombrechtikon Systems Engineering AG
Original Assignee
Hombrechtikon Systems Engineering AG
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 Hombrechtikon Systems Engineering AG filed Critical Hombrechtikon Systems Engineering AG
Publication of EP3653304A1 publication Critical patent/EP3653304A1/de
Application granted granted Critical
Publication of EP3653304B1 publication Critical patent/EP3653304B1/de
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/508—Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above
    • B01L3/5082—Test tubes per se
    • B01L3/50825—Closing or opening means, corks, bungs
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D39/00—Closures arranged within necks or pouring openings or in discharge apertures, e.g. stoppers
    • B65D39/06—Balls
    • 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
    • B01L2300/045—Connecting closures to device or container whereby the whole cover is slidable

Definitions

  • the invention relates to a sample container with a housing which forms a sample space for receiving a sample and has at least one circular opening, as well as with a spherical closure element.
  • sample containers are used in particular in biotechnological processes to process a biological sample or a sample containing biological material such as nucleic acids. They are used, for example, to replicate nucleic acids in vitro in amplification reactions such as a polymerase chain reaction (PCR).
  • PCR polymerase chain reaction
  • the sample containers serve to hold the sample containing the nucleic acid.
  • sample containers are known from the state of the art and are regularly used as disposable products in corresponding biotechnological processes such as PCR.
  • the sample containers are first filled with the sample, then sealed hermetically and finally fed into the PCR process.
  • High demands are placed on the sealing of the sample containers.
  • the sample containers must be reliably sealed so that the result of the PCR process is not affected by the unwanted entry or exit of sample material.
  • a large number of sample containers are regularly used in a PCR process and must be filled and sealed for this purpose. This should therefore be done as automatically as possible.
  • the sample containers must be cost-effective to produce, particularly because they are required in large numbers and are used as disposable products.
  • a sample container of this type is known in which one end of a cylindrical housing, which forms a sample chamber, is provided with a circular opening that extends into the sample chamber in the form of a channel.
  • the opening channel tapers shortly before the transition into the sample chamber and thereby forms a sealing seat for a spherical closure element. After the closure element has been placed on the sealing seat, it is fixed in place using a closure plug.
  • the EP 0 449 425 A2 The known sample container is a three-part system that is not only relatively complex and therefore expensive, but can also only be closed automatically with relatively great effort.
  • EP 0 264 181 A2 discloses a packaging container in which a spherical closure element can be inserted into an opening channel of a bottle.
  • the spherical closure element has elastic properties and can be fixed in the opening channel in a force-fitting manner in contact with the housing.
  • the opening channel of the bottle forms a projection on the outside opening which reduces the opening cross-section of the opening channel compared to the opening cross-section in which the closure element is fixed in a force-fitting manner for closing.
  • the diameter of the closure element is in the range from 16 to 25 mm.
  • the inner diameter of the opening channel has a dimension in the range from 13 to 14 mm. Due to this significant difference between the inner diameter of the opening channel and the diameter of the spherical closure element, longitudinal axial force components are generated to a not inconsiderable extent when the closure element is fixed in the opening channel in a force-fitting manner.
  • EP 0 503 867 A2 and US 2,367,883 A reveal a multi-part closure.
  • the invention was based on the object of specifying an improved sample container.
  • the sample container according to the invention should be inexpensive to manufacture and be able to be closed automatically with relatively little effort.
  • the sample container according to the invention should have a reliable sealing effect.
  • the essence of the invention lies in the sample container according to the EP 0 449 425 A2
  • the aim is to achieve the functions of sealing and fixing the closure element, which are achieved by two different functional elements, by only one functional element, namely the closure element itself.
  • This is achieved by clamping a spherical closure element in an opening channel of a housing of the sample container according to the invention in such a way that not only a good sealing effect but also a process-safe fixation can be achieved.
  • an additional closure plug for fixing the closure body can be dispensed with.
  • a sample container according to claim 1 is created.
  • the sample container has a housing that forms a sample space for receiving a sample and a circular opening that extends in the form of a channel into the sample space.
  • the sample container according to the invention also has a spherical closure element.
  • the (largest) diameter of the closure element is selected such that it exceeds the diameter of the opening channel in at least one (closure) section of the opening channel, but only to a degree that allows the closure element to be inserted into the closure section of the opening channel so far that the force-fitting fixation is achieved by contact of an area comprising the largest circumference of the closure element with the closure section.
  • the spherical closure element is in contact with the housing.
  • the opening channel between the closure section and the inside opening forms a (first) projection that reduces the opening cross section of the opening channel compared to the opening cross section in the closure section.
  • a one-piece closure is formed by the direct contact of the closure element with the housing.
  • the force-fitting fixation of the closure element by contact of an area comprising the largest circumference of the spherical closure element with the wall of the opening channel is important in order to achieve a secure fixation.
  • the resulting forces in this type of force-fitting fixation have no or only a relatively small (and thus negligible) force component in the longitudinal axial direction of the opening channel; rather, they are directed (largely) radially towards the center of the spherical closure element.
  • sufficient fixation and at the same time a good sealing effect can be achieved with only a relatively small (preferably elastic) deformation of the closure element and the wall of the opening channel.
  • a small deformation then requires only relatively small forces to introduce the closure element into the opening channel. This can simplify the automation of closing the sample container and also enable manual closing of the sample container.
  • the requirements for the materials used for the closure element and the housing are reduced, which keeps the manufacturing costs for the sample container low.
  • the sample container of the EP 0 449 425 A2 the diameter of the closure element exceeds the smallest diameter of the opening channel, but intentionally so much that a sealing seat is formed on which the closure element sits.
  • a sealing seat is well known in terms of its good sealing effect, but requires an additional closure element that generates sufficiently high forces in the longitudinal axial direction of the opening channel in order to press the spherical closure element into the sealing seat and thus achieve the desired sealing effect.
  • This longitudinal axial force component is also directed in such a way that - if it exceeds the frictional forces of the closure element with the opening channel in the area of the ball seat, for example due to an additional effect of excess pressure within the sample chamber - it lifts the closure element off the sealing seat, thus causing the sample container to open unintentionally.
  • An increase in the frictional forces without a simultaneous increase in the longitudinal axial force component is not possible, so that the EP 0 449 425 A2 known sample container cannot be securely closed without the additional sealing plug.
  • a ball that is softer than the housing can have advantages in terms of sealing. However, this advantage may be offset by disadvantages in terms of positioning (checking) and material selection.
  • a ball that is harder than the housing is easier to handle during insertion and enables easier positioning and position checking, but can bring with it the risk of overstretching the housing (up to the plastic range).
  • the opening channel between the closure section and the outside opening forms a (second or further) projection, which reduces the opening cross-section of the opening channel compared to the opening cross-section in the closure section.
  • a projection which can be formed, for example, in a (closed) ring shape or by one or more individual projections arranged next to one another, preferably in a ring shape, can be used in particular as a safety stop to prevent the closure element from accidentally coming loose from the closure section of the opening channel, for example as a result of an unexpectedly high pressure increase in the sample chamber, which can be caused, for example, by heating during the PCR process.
  • the closure element can - possibly after a slight displacement within the closure section of the opening channel - support itself on the projection, whereby a secure and, in particular, tight closure of the sample container can still be achieved.
  • the closure element Since the (second or further) projection must be passed by the closure element when closing the sample container, it can be designed in such a way that the closure element is inserted into the closure section by exerting a defined pressing force, which should not be so high that it causes damage to the closure element or the housing of the sample container as a result of excessive deformation, but greater than the maximum force to be expected due to an increase in pressure in the sample chamber.
  • the opening cross-section of the opening channel is larger in the region of the (second) projection than in the region of the first projection. This makes it possible to ensure that the force applied to press the closure element into the opening channel is sufficiently high for the closure element to pass the second projection, but not so high that it can also pass the first projection.
  • the distance between the first and the second closure element is dimensioned depending on the dimensions of the closure element such that a positioning tolerance of the closure element within the closure section of a maximum of 5 mm and in particular a maximum of 0.7 mm is given.
  • a displacement of the closure element over this maximum distance in particular due to an increase in pressure within the sample space, usually still leads to a tolerable change in the process conditions, for example of a PCR process.
  • the opening channel is cylindrical in the area of the closure section. This means that a substantially equal level of force-locking fixation and sealing effect is always achieved, regardless of the actual position of the closure element in the closure section.
  • the opening channel can be designed to be slightly conical (for example with an angle of inclination of 0.1 to 0.5°) in the closure section as well, which can facilitate demolding during casting and in particular injection molding of the housing.
  • the angle of inclination can be chosen to be so small that it has no significant (negative) influence on the fixation and sealing effect of the clamped closure element.
  • the housing of the sample container according to the invention can preferably be tubular (also stepped), with the opening being arranged at one (longitudinal) end of the housing. Furthermore, the housing can preferably be tapered at the second end, whereby even very small sample quantities can be easily concentrated in the sample space, which can facilitate the implementation of the biotechnological process, such as a PCR process.
  • the housing of the sample container is at least partially made of an optically transparent material.
  • the tapered end can be optically transparent, as this is preferably used to hold the sample.
  • the housing in the area that serves to hold the sample has a thinner wall thickness than (at least) a second area of the housing that forms the sample chamber.
  • a wall thickness that is as thin as possible can simplify the examination of the sample using optical methods, while a thicker wall thickness, in particular in a dead space in the sample chamber that is not filled with the sample, can prevent or reduce evaporation through the housing, which is preferably made of plastic.
  • the housing in the closure section of the opening channel is made of an (optically) transparent material.
  • This enables the position of the closure element in the closure section and also the sealing effect to be checked by optical means (also purely visual inspection).
  • optical means also purely visual inspection.
  • a change in the refractive index can be used, which is based on the fact that there is no total reflection of the light at the transition from a first solid (wall of the opening channel) to a second solid (closure element). inner wall, whereas when a solid (wall of the opening channel) changes to air, the inside of the opening channel partially reflects.
  • the housing can preferably form a shoulder to form a support surface.
  • the forces that are applied to press in the closure element can be supported on a holder that supports the sample container via this support surface.
  • the support surface can be formed at a point on the housing that is located near the closure section of the opening channel. This can prevent the forces from being transmitted via other sections of the housing, which may have thinner walls and are therefore more sensitive (in particular the wall of the housing surrounding the sample space).
  • the housing of the sample container, at least in the closure section of the opening channel, and the closure element itself are made of a material with an equally large coefficient of expansion. This prevents the pressure in the contact surface between the closure element and the wall of the opening channel from changing as a result of heating, for example during a PCR process, which could potentially change not only the fixation of the closure element but also its sealing effect to the same extent.
  • the closure element can be made of an electrically conductive material. This not only prevents electrostatic charging of the ball, which could make handling the sample container more difficult, but the conductivity can also allow contact-based or contactless, for example capacitive or inductive, detection of the position of the closure element within the opening channel and/or the sealing effects.
  • the closure element of the sample container according to the invention is made of a material that does not exhibit any inherent fluorescence. This can prevent a negative impact on monitoring of the biotechnological process, such as the PCR process, based on measuring the fluorescence of the sample.
  • the sample container can be provided with a predetermined breaking point at which the housing is split by a defined force.
  • This type of opening is suitable particularly for sample containers that are only to be used once (disposable sample container).
  • One advantage of this design of the sample container according to the invention can be that the process of opening it can be less complicated than removing the closure element fixed in the closure section of the opening channel, which is also possible.
  • a predetermined breaking point it is also possible to design the housing in two parts, with the two parts being connectable to one another, for example, via a plug or snap connection. To open the closed sample container, the housing can then be opened again at this connection point.
  • the sample container can also be opened by pushing the closure element into the sample chamber.
  • the sample chamber should have a larger cross-sectional area than the closure element in at least one section in order to be able to empty the sample chamber.
  • sample containers that are used as part of the respective biotechnological process should not be opened again.
  • the invention can also provide for the closure element to be additionally secured in the closure section, for example by welding it to the wall of the housing (e.g. by ultrasonic welding or thermal welding) with a suitable choice of material or by securing it in a form-fitting manner by flanging an upper edge of the housing.
  • the closure element can also provide for the closure element to be additionally secured in the closure section, for example by welding it to the wall of the housing (e.g. by ultrasonic welding or thermal welding) with a suitable choice of material or by securing it in a form-fitting manner by flanging an upper edge of the housing.
  • any other types of additional form-fitting, force-fitting or material-fitting fixation are possible.
  • sample container in a preferred embodiment, it can also be provided to provide a second closure section for a second closure element, with a second sample space being formed between the two closure elements. All further developments that were previously shown with regard to the first closure section and/or the first closure element can also be provided for the second closure section and/or the second closure element.
  • one bypass channel can be provided in the wall of the housing between the two closure sections of the sample container. This can serve to avoid an overpressure that would otherwise arise in the lower sample chamber as a result of the introduction of one closure element into the lower closure section and to upper sample material into the lower sample chamber by pressing down the upper closure element.
  • a method for preparing or processing a biological sample or a sample containing biological material such as nucleic acids in particular is described, in which the sample container according to the invention is used.
  • the sample container according to the invention is described in detail in the description and the claims. Reference is made to the corresponding disclosure.
  • the method can in particular be a biotechnological method such as an amplification method, in particular a PCR method.
  • the Fig.1 shows a sample container 1 according to the invention in a first embodiment.
  • the sample container 1 has a housing 2 which is designed with a largely cylindrical outer surface in a first (head section 3) and a second (middle section 4) section.
  • the outer surface has only a slight conical taper, which serves to make it easier to demold the plastic housing 2 after injection molding.
  • At the end of the middle section 4 opposite the head section 3 there is an end section 5 in which the housing 2 tapers and is thus tapered in a broader sense.
  • the housing 2 is made of an (optically) transparent material which enables the use of optical measuring elements in the context of a biotechnological process, such as a PCR process, in which the sample container 1 is to be used.
  • the housing 2 On the outside between the head section 3 and the middle section 4, the housing 2 forms a shoulder 6 which serves as a support surface via which the housing 2 can be attached to a sample container carrier 7 (cf. Fig.2 ) is supported.
  • a sample chamber is formed within the middle section 4 and the end section 5 of the housing 2, the wall thickness of the housing 2 being largely constant in these two sections, so that a largely cylindrical sample chamber section is formed within the middle section 4 and a conically tapered sample chamber section with a rounded tip is formed in the end section 5 of the housing 2.
  • An opening channel is formed in the head section 3 of the housing 2, which makes it possible to fill the sample container 1 with the sample to be examined.
  • the sample space is closed by inserting a spherical closure element 8.
  • the closure effect ie both the sealing and the fixing of the closure element 8 in the opening channel, is brought about by the largest outer diameter of the closure element 8 being slightly larger than the opening channel in a defined section (closure section 11) (cf. Fig.2 ) and the closure element 8 is thus clamped in the opening channel.
  • the opening channel is initially provided with an inlet bevel 9, which defines a relatively large opening cross-section (largest diameter: 4.5 mm) (in relation to the outer diameter of the closure element 8).
  • the inlet bevel 9 makes it easier to position the closure element 8 centrally (largest diameter: 4.1 mm to 4.2 mm).
  • the inlet bevel 9 merges into a first annular projection 10, which reduces the opening cross-section (diameter: 3.7 mm) of the opening channel in relation to the opening cross-section in the closure section of the opening channel (diameter: approx. 4.0 mm).
  • a force component
  • the force is so high that it causes a deformation of both the housing 2 in the area of the head section 3 and the closure element 8 itself, which allows the closure element 8 to pass the first projection 10 and be pushed into the closure section 11 of the opening channel.
  • the closure element 8 is fixed, i.e. clamped, in the closure section 11 by its larger (maximum) diameter compared to the diameter of the opening channel.
  • the forces are achieved by a (largely elastic) deformation of the housing 2 in the area of the closure section 11 and the closure element 8.
  • the reaction forces that act from the wall of the opening channel onto the ball - and vice versa - have no component in the longitudinal axial direction of the housing.
  • the closure element 8 is held securely after being introduced into the closure section 11, provided that no significant external forces act on it in the longitudinal axial direction of the housing 2.
  • the first projection 10, which must be passed by the closure element 8 when it is introduced into the closure section 11, serves on the one hand as an end stop which prevents the closure element 8 from being pushed out of the opening channel when excess pressure develops within the closed sample space, for example due to heating during a biotechnological process, such as a PCR process, and the sample container 1 thus opens unintentionally.
  • this projection 10 serves to generate a characteristic force curve when inserting the closure element 8, by means of which an actual insertion of the closure element 8 into the closure section 11 can be detected (in the manner of a snap-in).
  • the transition of the opening channel into the sample chamber of the housing 2 is designed as an annular shoulder.
  • This shoulder represents a second projection 12, which serves as an end stop for the closure element 8 and thus limits the closure section 11 of the opening channel on the side of the sample chamber.
  • the length of the closure section 11 of the opening channel is dimensioned such that the closure element 8 can be displaced over a certain distance x therein before it strikes one of the two projections 11, 12 (cf. Fig.3 ). In the present case, this distance is limited to a maximum of 0.7 mm, since experience has shown that with such a displacement of the closure element 8, the process parameters (in particular pressure, temperature) within the sample space change so little that no significant (negative) effects on the biotechnological process, such as the PCR process, are to be feared.
  • This positioning tolerance of the closure element 8 within the closure section 11 also has the advantage that relatively large tolerances can be specified when manufacturing the housing 2 and the closure element 8, which means that lower demands can be placed on the corresponding tools.
  • the Figures 4 to 6 show the use of a plunger 13 (in two embodiments) to push the closure element 8 into the opening channel.
  • the plunger 13 has an outer diameter of 3.6 mm (or smaller), which is thus smaller than the inner diameter of the opening channel in the area of the first projection 11.
  • the plunger 13 can thus be immersed in the opening channel.
  • the movement of the plunger should be precisely controllable in order to prevent it from pressing the closure element 8 against the second projection serving as an end stop with a force that could lead to damage to the housing 2 or the closure element 8.
  • the Figure 7a shows an example force curve (force F over the plunger path I) for a closing process using a plunger according to Fig.4 .
  • force F force over the plunger path I
  • a first section (a) of the force curve the force is almost zero; this section defines the displacement of the plunger 13 until it comes into contact with the closure element 8.
  • This is followed in a second section by a sharp increase in the force up to a first maximum value (b) (first extreme point of the curves) which is required to allow the closure element to pass the first projection 10.
  • This force drops down to a second extreme point (c) which defines the force (which then only increases slightly due to the slightly conical design of the opening channel, see section (d)) which is required to displace the ball in the closure section 11.
  • This force corresponds essentially to the force which results from the friction between the wall of the opening channel in the closure section 11 and the section of the closure element 8 which is in contact with it. If the closure process is carried out correctly, the application of force ends somewhere in section (d) of the Fig.7 .
  • the Fig. 7b shows a corresponding exemplary force curve for the use of a ram according to the Fig. 5 and 6 .
  • the force curve in sections (a) and (d) and in between corresponds to that of the Fig. 7a .
  • section (d) there is then a force increase (h), which is even stronger than in the course according to the Fig. 7a This is caused by the impact of the plunger 13 on the edge of the sample container 1.
  • the plunger 13 should then only be moved a relatively small distance further in order to avoid overloading the sample container 1 (or the To control the stroke of the ram, the force curve can be evaluated so that, for example, when the end of section (h) is reached, a (force) limit value is reached, which can, for example, lead to a ram drive being switched off.
  • a (force) limit value is reached, which can, for example, lead to a ram drive being switched off.
  • the further force progression is also shown in dashed lines, which leads to a break in the sample container due to overloading. This is marked by a continuation of section (h) (section (i)), at the end of which the break occurs. This is marked by a direct drop in the force to a level close to zero (section (k)).
  • the Fig. 20a to 20f show examples of deviations from the previously described "normal" force curves. From these deviations, the corresponding source of error can be deduced.
  • the deviating force curve is shown with a solid line, while the "normal" force curve is shown with a dashed line.
  • the Fig. 20a shows two different force curves where the dimensions or the material properties of the sample container in the area of the opening channel and/or the closure element are not correct.
  • Fig. 20b shows two different force curves where the vertical alignment of the locking element, ie the distance between the locking element and the plunger, is too small or too large. In the case of the different force curve according to the Fig.
  • the horizontal alignment is not correct, ie there is insufficient alignment of the longitudinal axes of the sample container and the plunger. This can lead to an obstruction of the movement of the closure element.
  • the Fig. 20d shows a different force curve, which occurs when the closure element is missing and the movement of the plunger takes place without significant force until a collision with the sample container.
  • the Fig. 20e The deviating force curve shown may occur if the contact surfaces of the closure element and/or the sample container do not meet the requirements.
  • Fig. 20f shows, however, a different force curve that can result from the breakage of a sample container.
  • the Fig. 8a and 8b show a second embodiment of a sample container 1, in which two closure elements 8 are fixed in a force-fitting manner in a common closure section 11 of the housing 2. This creates a second sample space between the two closure elements 8.
  • the corresponding design of the opening channel can - unlike the representation in the Fig.8 - any according to the embodiment according to the Figures 1 to 3 , ie in particular be provided with one or more projections.
  • a bypass channel 14 is also introduced into the wall of the housing.
  • the upper bypass channel 14 serves to prevent excess pressure in the two sample chambers
  • the lower bypass channel 14 is intended, however, to transfer a sample contained in the upper sample chamber into the lower sample chamber, for example as part of the PCR process, as is shown in the Fig. 8a is shown.
  • the lower closure element 8 is pushed by means of the upper closure element 8 into the section of the opening channel/sample chamber having the lower bypass channel 14, so that the sample can flow from the upper sample chamber via the lower bypass channel 14 past the lower closure element 8 into the lower sample chamber.
  • Fig. 9a to 9b show a sample container 1 in a further embodiment, in which it is intended to be opened again by the closure element 8 being pushed completely into the sample chamber up to the closed end by means of a plunger 13.
  • the sample liquid displaced in this way can flow out via a bypass channel 14 introduced into the wall of the housing 2 on one side and thus be removed from the sample container 1.
  • the Fig.10 shows a sample container 1 in which the housing 2 is provided with a varying wall thickness in the area of the sample chamber.
  • the housing 2 In the area of the sample chamber that holds the sample, the housing 2 has the smallest possible wall thickness of e.g. 0.2 to 0.3 mm.
  • a small wall thickness simplifies the examination of the sample using optical methods.
  • the wall thickness In a section of the sample chamber that forms a dead space (ie without a sample contained therein), the wall thickness is, however, thicker (e.g. twice as thick, e.g. 0.4 to 0.6 mm), which not only increases the mechanical stability of the housing 2, but also reduces evaporation of the sample through the housing 2.
  • FIGS 11 and 12 show individual components of an automated closing device (cf. Figure 17 ) which are to be used in a device for carrying out a PCR process (cf. Figure 18 ).
  • the Figure 11 a storage container 15 in which an elongated spiral guide 16 is arranged, which serves to receive and guide a plurality of closure elements 13 of a sample container 1.
  • the lower end of the guide 16 ends in an outlet opening, via which the closure elements of a closure unit 17, as partially shown in the Figure 12 shown.
  • the storage container 15, which can be sold as a filled disposable container, can be attached to the front end of the closing unit 17 for this purpose.
  • the closing unit 17 comprises an electric motor arranged in a housing 18, via which a drive disk 19 can be driven in rotation.
  • the drive disk 19 is provided with a bolt 20 in a decentralized manner, which is guided in an elongated hole 21 of a tappet guide 22.
  • the guidance of the bolt 20 in the elongated hole 21 translates the rotary movement of the drive disk 19 into a cyclical upward and downward movement of the tappet guide 22 including a tappet 13 attached to it, as is basically the case in the Figure 13 is shown.
  • a closure element 8 held in a transfer position is taken along and is guided via an outlet opening of the closure unit into the opening channel of a housing 2 of a sample container 1 arranged underneath (in the Fig. 13 not shown).
  • This embodiment can also be further developed in such a way that the cyclical movement of the plunger 13 is basically realized by a continuous rotation of the drive disk 19 and the drive motor only stops the movement and reverses its direction of movement when there is a risk of exceeding the permissible force.
  • the Fig. 14 shows a storage container 15a for a plurality of closure elements 8 in an alternative embodiment.
  • the essential differences to the storage container 15 according to the Fig. 11 are that, on the one hand, the closure elements 8 are stored unsorted in a storage space of the storage container 15a, ie as a bulk material, and, on the other hand, a plunger 13a is integrated for the individual dispensing of the closure elements 8 from the storage container 15a.
  • the bottom and wall surfaces of the storage container 15a are designed in such a way that the closure elements located at the bottom in the bulk material are fed to a dispensing channel 29, the inner diameter of which is only slightly larger than the outer diameter of the closure elements. This ensures that the closure elements are individually moved into a transfer position where they can be grasped and taken away by the plunger 13a.
  • the Fig. 15 shows the use of the storage container according to the Fig. 14 in combination with an alternative closing unit 17a (only partially shown).
  • a special feature of this combination is the use of a total of two plungers, firstly the plunger 13a integrated in the storage container 15a, which serves to individually dispense the closure elements 8 from the storage container, whereby these are placed on a sample container 1 located underneath.
  • a second plunger 13 integrated in the closing unit 17a serves to drive the closure element 8 previously placed on a (different) sample container 1 into the closure section of the opening channel of this sample container.
  • the main advantage of using two plungers is improved hygiene when the storage container 17a including the plunger 13a is used as a disposable container, which is thus disposed of after use.
  • the movements of the two tappets 13, 13a are coupled to one another.
  • the movement of the tappet 13 is thus transferred to the tappet 13a.
  • the tappet 13 itself is constructed in several parts and comprises a tappet element 31, which is axially displaceably mounted in the lower end of a base body 32 of the tappet 13.
  • the tappet element 31 is connected to a threaded pin 33, which is part of a force limiting unit, via a central bore with an internal thread.
  • the force limiting unit also comprises a spring 34 (cylindrical coil spring), which is preloaded by two contact plates 35.
  • the preload forces are supported by the upper support plate 35 and an annular projection of the tappet element 31 on corresponding contact surfaces of the base body 32.
  • the preload of the coil spring can be changed by the depth of screwing the threaded bolt 33 into the tappet element 31 and thus a limit value for the force exerted by the tappet element 31 on the closure element 8 can be set. As soon as this force is exceeded, the tappet stroke is (partially) compensated by the tappet element 13 moving back.
  • the Fig. 16 shows a closing unit 17b, which is functionally essentially the same as that of the Fig. 15 corresponds, but is structurally simpler.
  • a (mechanical) force limiting unit is not provided there, rather this is achieved electronically, by a corresponding control of a tappet drive.
  • the tappet element 31a is therefore axially immovably integrated in the base body 32a of the tappet 13 and also the bolt 30a for driving the tappet 13a of the
  • the storage container 15a is not spring-mounted.
  • the storage container 15a corresponds to that of the Fig. 15 .
  • the closing units 17, 17a, 17b and storage containers 15, 15a can be integrated into an automatic closing device 25 as shown in the Figure 17 is shown. There, the unit comprising the closing unit 17 and the storage container 15 can be moved along a first axis (in the transverse direction) via a linear drive 26.
  • the automatic closing device according to the Figure 17 is in turn integrated into a device for carrying out a PCR process according to Figure 18 integrated in such a way that the entire closing device 25 can be moved via a second linear drive 27 to a second axis (in the longitudinal direction) which is aligned perpendicular to the first axis (the travel axis of the linear drive 26 of the closing device).
  • the ability of the unit comprising the closing unit 17 and the storage container 15 to move in two axes aligned perpendicular to one another makes it possible to move a large number of housings 2 of sample containers 1, which are positioned in several rows in a total of three sample container carriers 7, and to close each one with a closure element 8.
  • the correct placement of the closure element 8 in the individual housings 2 is checked with the aid of a laser distance sensor (not shown).
  • the Fig. 19 shows in a schematic representation the possibility of releasably fixing the closure elements 8 in a conveyor belt (blister belt) 28 and of positioning them one after the other in the transfer position by moving the conveyor belt 28, from which they can then be introduced into the opening channel of a sample container 1 by means of a plunger 13.
  • the conveyor belt 28 has a base belt 36 provided with openings arranged at regular intervals, wherein in the area of each of the openings a closure element 8 rests on one side of the base belt 26 and is surrounded there by a holding band 37 and thus held.
  • the individual closure elements can be released from the conveyor belt 28 through the respective opening by means of the plunger 13 and driven into the opening channel of the sample container 1.

Landscapes

  • 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)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Sampling And Sample Adjustment (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Devices For Use In Laboratory Experiments (AREA)
EP19212880.9A 2011-03-11 2012-03-09 Probenbehältnis Active EP3653304B1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP11157906 2011-03-11
PCT/EP2012/054165 WO2012123375A1 (de) 2011-03-11 2012-03-09 Probenbehältnis
EP12712599.5A EP2683485B1 (de) 2011-03-11 2012-03-09 Probenbehältnis

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
EPPCT/EP2012/712599 Previously-Filed-Application 2012-03-09
EP12712599.5A Division EP2683485B1 (de) 2011-03-11 2012-03-09 Probenbehältnis

Publications (2)

Publication Number Publication Date
EP3653304A1 EP3653304A1 (de) 2020-05-20
EP3653304B1 true EP3653304B1 (de) 2024-05-01

Family

ID=44327213

Family Applications (2)

Application Number Title Priority Date Filing Date
EP12712599.5A Active EP2683485B1 (de) 2011-03-11 2012-03-09 Probenbehältnis
EP19212880.9A Active EP3653304B1 (de) 2011-03-11 2012-03-09 Probenbehältnis

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP12712599.5A Active EP2683485B1 (de) 2011-03-11 2012-03-09 Probenbehältnis

Country Status (9)

Country Link
US (1) US9242246B2 (zh)
EP (2) EP2683485B1 (zh)
JP (1) JP2014513927A (zh)
CN (1) CN103459037B (zh)
AU (1) AU2012228412B2 (zh)
BR (1) BR112013023055A2 (zh)
CA (1) CA2829703A1 (zh)
ES (2) ES2769308T3 (zh)
WO (1) WO2012123375A1 (zh)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI20155107A (fi) 2015-02-19 2016-08-20 Thermo Fisher Scientific Oy Näyteastia
US10537892B2 (en) * 2017-01-03 2020-01-21 Illumina, Inc. Sample tube with integrated mixing plunger head
WO2021213636A1 (de) * 2020-04-21 2021-10-28 Hombrechtikon Systems Engineering Ag Probenbehältnis und verfahren zur analyse einer probe
DE102020131098A1 (de) * 2020-11-24 2022-05-25 Syntegon Technology Gmbh Vorrichtung zum Verschließen von pharmazeutischen Behältnissen

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2367883A (en) * 1942-09-21 1945-01-23 Frankfort Distilleries Inc Bottle closure
JPS5241990Y2 (zh) * 1973-06-29 1977-09-22
JPS6388960U (zh) * 1986-05-30 1988-06-09
EP0264181A3 (en) * 1986-10-13 1989-01-11 Nihon Taisanbin Kogyo Kabushiki Kaisha Packing container
FI895113A0 (fi) * 1989-10-27 1989-10-27 Bo Kultti Tillslutningsanordning foer behaollare.
US5127895A (en) 1990-03-30 1992-07-07 Beckman Instruments, Inc. Self-seal centrifuge tube
DE69217261T2 (de) 1991-03-08 1997-08-21 Shinsozai Sogo Kenkyusho Kk Apparat zum Lagern und Mischen
AU7237696A (en) * 1995-09-15 1997-04-01 Egon Erlich Tamper-evident container
FR2758799B1 (fr) * 1997-01-24 1999-04-02 Stago Diagnostica Bouchage pour flacon de reactif utilisable par un automate d'analyse
EP1847461A3 (de) * 2006-04-18 2008-01-02 Terxo AG Kunststoffbehälter
ITTO20070714A1 (it) 2007-10-10 2008-01-09 Bisio Progetti Spa Fiala monodose richiudibile.
DE102008010402B3 (de) * 2008-02-21 2009-04-09 Bruker Biospin Ag System zur Bereitstellung einer Vielzahl von Probengefäßen, insbesondere NMR-Probenröhrchen, und Verwendung des Systems

Also Published As

Publication number Publication date
US20140056784A1 (en) 2014-02-27
EP3653304A1 (de) 2020-05-20
US9242246B2 (en) 2016-01-26
AU2012228412A9 (en) 2015-12-03
BR112013023055A2 (pt) 2016-12-13
CA2829703A1 (en) 2012-09-20
ES2979386T3 (es) 2024-09-25
EP2683485B1 (de) 2019-12-04
WO2012123375A1 (de) 2012-09-20
ES2769308T3 (es) 2020-06-25
AU2012228412B2 (en) 2016-01-07
CN103459037B (zh) 2016-11-02
EP2683485A1 (de) 2014-01-15
CN103459037A (zh) 2013-12-18
AU2012228412A1 (en) 2013-10-03
JP2014513927A (ja) 2014-06-19

Similar Documents

Publication Publication Date Title
EP2118542B1 (de) Mikroventil
EP3479129B1 (de) Dosierkopf, dosiervorrichtung umfassend einen dosierkopf und verfahren zum dosieren mittels eines dosierkopfes
EP1171240B1 (de) Pipettenspitze, pipettiervorrichtung und kombination aus pipettenspitze und pipettiervorrichtung
DE102009013778B4 (de) Positioniereinrichtung für einen Probenträger
WO2018002254A1 (de) Dosierkopf, dosiervorrichtung umfassend einen dosierkopf und verfahren zum dosieren mittels eines dosierkopfes
EP0478905B1 (de) Vorrichtung zur Einführung von Pipettiereinsätzen durch Probegefäss-Stopfen
DE60131735T2 (de) Vorrichtung zur abgabe von genau kontrollierten kleinen flüssigkeitsmengen
EP3653304B1 (de) Probenbehältnis
EP3162443B1 (de) Nadelführung mit zentrierung für septum-piercing
EP2105074A1 (de) Vorrichtung und Anordnung zum Zubereiten eines flüssigen Lebens- oder Genussmittels sowie Portionsverpackung
WO2014166635A1 (de) Pipettiervorrichtung mit einer mikrodosiereinheit
DE102004057450A1 (de) Automatisches Pipetier- und Analysegerät
EP2659978B1 (de) Pipette mit Verriegelungssystem
DE102013106534B4 (de) Chromatographiepipettenspitze
WO2019228682A1 (de) Pipettenspitze
EP2683486A1 (de) Vorrichtung zum verschliessen eines probenbehältnisses mit einem kugelförmigen verschlusselement
EP0331912A2 (de) Befüllbares Probenaufnahmegefäss zur Handhabung einer flüssigen Probe
EP1432787A2 (de) Vorrichtung und verfahren zur selektion von selbstbeweglichen biologischen spezies, insbesondere von samenzellen
EP3489693B1 (de) Verfahren zum steuern einer pipettiervorrichtung
EP3450020B1 (de) Mikrodosiereinrichtung zur dosierung von kleinsten fluidproben
EP3498376B1 (de) Spritze, spritzenfamilie und dosiervorrichtung
DE102010022552B4 (de) Vorrichtung und Verfahren zur restlosen Aufnahme von Flüssigkeiten aus Gefäßen
DE19917029A1 (de) Verfahren und Vorrichtung zur dosierten Ausgabe von Flüssigkeitsmengen im Bereich von 0,1 nl bis 100 mul
WO2022148785A1 (de) Kartuschenaufnahme, kartuschensystem, getränkezubereitungssystem und verfahren zur zubereitung eines getränks
CH712234A2 (de) Pipettiervorrichtung mit automatisiert wechselbarem Funktionsbauteil, insbesondere Filter, und Verfahren zur ausrichtungsfreien Aufnahme eines Funktionsbauteils in einem Pipettierkanal.

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN PUBLISHED

AC Divisional application: reference to earlier application

Ref document number: 2683485

Country of ref document: EP

Kind code of ref document: P

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

RIN1 Information on inventor provided before grant (corrected)

Inventor name: VOIT, THOMAS

Inventor name: QUINTEL, HARALD

Inventor name: SIMONS, DANIEL

Inventor name: BRETSCHER, ANDREAS

Inventor name: WALDER, BRUNO

Inventor name: LAZEVSKI, SASA

Inventor name: LEBER, DIRK

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20201120

RBV Designated contracting states (corrected)

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20230913

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20231030

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20240221

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AC Divisional application: reference to earlier application

Ref document number: 2683485

Country of ref document: EP

Kind code of ref document: P

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

Free format text: NOT ENGLISH

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Free format text: LANGUAGE OF EP DOCUMENT: GERMAN

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 502012017259

Country of ref document: DE

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20240501

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2979386

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20240925

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20240901

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20240501

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20240501

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20240501

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20240802

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20240902

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20240501