DEVICE AND METHOD FOR THE DISSOCIATION OF TISSUE

Abstract

The invention relates to a device and a method for the dissociation of tissue. In one embodiment, the device has at least one dissociation unit, for receiving a tissue sample, which is disposed at least partially in a pot-shaped cell strainer. In addition, the invention relates, in one embodiment, to a device and a method for the dissociation of tissue, the tissue being dissociated by a grinder having mutually movable rows of teeth which cut the tissue when moving past each other in the one direction and grind the tissue when moving past each other in the opposite direction.

Claims

1. A device for the dissociation of tissue, having at least one dissociation unit for receiving a tissue sample, at least one pot-shaped cell strainer, the at least one dissociation unit being disposed at least partially in the pot-shaped cell strainer.

2. The device according to claim 1, the dissociation unit having at least one vessel for receiving the tissue sample, and also a grinder which is disposed in the vessel, the grinder having at least one first row of teeth with a plurality of teeth and at least one second row of teeth with a plurality of teeth, the at least one first of the rows of teeth being disposed on a base of the vessel and the at least one second of the rows of teeth being disposed on a cover of the vessel, the at least one first row of teeth being movable relative to the at least one second row of teeth so that the teeth of the first row of teeth are able to move past the teeth of the second row of teeth, respectively one of the at least one first rows of teeth and one of the at least one second rows of teeth being disposed at such a spacing adjacent to each other that the teeth of these respectively adjacent rows of teeth, if they are moved past each other, effect a dissociation of a part of the tissue sample in a spacing region by their minimum spacing relative to each other.

3. The device according to claim 2, the teeth being configured such that, if they move past each other in one direction, they cut the part of the tissue sample, and if they move past each other in a direction opposite to this direction, grind the part of the tissue sample.

4. The device according to claim 1, having furthermore a reagent vessel, the cell strainer and the dissociation unit being disposed in an opening of the reagent vessel.

5. The device according to claim 2, the rows of teeth disposed in the cover of the vessel being movable relative to the reagent vessel and the rows of teeth disposed in the base of the vessel being fixed relative to the reagent vessel.

6. A device for the dissociation of tissue, having at least one vessel for receiving a tissue sample, and also a grinder disposed in the vessel, the grinder having at least two mutually movable rows of teeth, each of the rows of teeth having a plurality of teeth, adjacent ones of the rows of teeth being disposed at such a spacing relative to each other that the teeth of these respectively adjacent rows of teeth effect a dissociation of a part of the tissue sample in a spacing region by their minimum spacing relative to each other, the teeth being configured such that, if they move past each other in one direction, they cut the part of the tissue sample and, if they move past each other in the direction opposite to this direction, grind the pail of the tissue sample.

7. The device according to claim 6, having furthermore a reagent vessel, the vessel and the grinder being disposed in an opening of the reagent vessel, the rows of teeth disposed in the cover of the vessel being movable relative to the reagent vessel and the rows of teeth disposed in the base of the vessel being fixed relative to the reagent vessel.

8. The device according to claim 1, the cell strainer and the dissociation unit or the vessel and the grinder being disposed at least partially inside a closing cap of the reagent vessel, the closing cap surrounding the opening of the reagent vessel.

9. The device according to claim 2, the rows of teeth extending circularly and concentrically to each other.

10. The device according to claim 2, the rows of teeth extending in a common plane and being mutually movable in this plane.

11. The device according to claim 2, the teeth respectively having a cross-section parallel to the common plane, which has a pointed corner and a rounded side situated opposite the pointed corner, the pointed corners of teeth of adjacent rows of teeth being directed in opposite directions.

12. The device according to claim 2, those edges of the cross-section of the teeth which connect the tip to the rounded side being curved in the direction of a line along which the row of teeth, to which the corresponding tooth belongs, extends.

13. The device according to claim 2, a side wall delimiting the vessel having at least one or more projections in the direction of the rows of teeth, that row of teeth situated closest to the side wall having such a spacing from this side wall that the teeth of this closest row of teeth effect a dissociation of a part of the tissue sample in a spacing region by their minimum spacing from the projections.

14. The device according to claim 2, the vessel having a base element which is surrounded by rows of teeth, the base element having one or more projections in the direction of the rows of teeth, that row of teeth closest to the base element being disposed at such a spacing from this base element that the teeth of this closest row of teeth effect a dissociation of a part of the tissue sample in a spacing region by their minimum spacing from the projections.

15. The device according to claim 2, a diameter of the vessel, in that plane in which the rows of teeth extend, being greater than or equal to 0.5 cm, preferably greater than or equal to 1 cm, preferably greater than or equal to 2 cm and/or less than or equal to 4 cm, preferably less than or equal to 3 cm.

16. The device according to claim 2, the minimum spacing of teeth of adjacent ones of the rows of teeth respectively being greater than or equal to 50 μm, preferably greater than or equal to 100 μm, preferably greater than or equal to 200 μm and/or less than or equal to 500 μm, preferably less than or equal to 400 μm, preferably less than or equal to 300 μm.

17. The device according to claim 2, one half of the rows of teeth being disposed on the cover of the vessel and the other half of the rows of teeth being disposed on the base of the vessel, the rows of teeth disposed on the cover respectively being adjacent to the rows of teeth disposed on the base in a plane in which the rows of teeth extend.

18. The device according to claim 17, the rows of teeth disposed on the cover being movable relative to the cover.

19. The device according to claim 8, the closing cap having an opening in its centre, and the cover of the vessel having an opening which is coaxial to the opening of the closing cap, the openings in the closing cap and in the cover being configured such that a driveshaft can actuate the cover of the vessel for moving the teeth of the at least one second row of teeth relative to the teeth of the at least one first row of teeth.

20. The device according to claim 2, the cover of the vessel having a magnetic element, by means of which the cover is actuatable by means of a magnet for moving the rows of teeth.

21. The device according to claim 8, a septum being disposed in the opening in the closing cap and/or in the opening in the cover of the vessel, through which liquid can be introduced into the vessel and/or the reagent vessel.

22. The device according to claim 2, the cell strainer and/or the base having elements, preferably webs, for preventing a relative movement of the base relative to the cell strainer.

23. The device according to claim 19, the opening in the cover being impermeable relative to the opening in the closing cap.

24. A method for the dissociation of tissue, a tissue sample being introduced into a device according to claim 1, and thereafter, the dissociation unit or the grinder being actuated.

25. The method according to claim 24, the rows of teeth being circular and being moved relative to each other at a speed of rotation of greater than or equal to 60 rpm, preferably greater than or equal to 200 rpm, preferably greater than or equal to 300 rpm and/or less than or equal to 700 rpm, preferably less than or equal to 500 rpm, particularly preferably less than or equal to 400 rpm.

26. The method according to claim 24, after actuation of the dissociation unit or of the grinder, a cell suspension produced by actuation of the dissociation unit or of the grinder being purified.

27. The method according to claim 24, at least one medium being added to the tissue sample, before, during and/or after actuation of the dissociation unit or of the grinder.

28. The method according to claim 24, a direction of rotation and/or a speed of rotation of the actuation of the dissociation unit or of the grinder being able to be controlled on the basis of parameters detected during the actuation, the parameters comprising one or more, selected from a torque, a rheological parameter and/or an optical density.

29. The method according to claim 24, a force transmitted to the dissociation unit or to the grinder being determined by means of one or more sensors, and from the thus measured force, a dissociation degree of the tissue being determined.

30. The method according to claim 24, the rows of teeth, whilst they are moved relative to each other, being moved periodically relative to each other in the direction perpendicular to the direction of the movement.

31. The method according to claim 24, the cell suspension being centrifuged in a reaction vessel, in the opening of which the dissociation unit or the grinder is disposed.

Description

[0068] In the following, the invention is intended to be explained on the basis of some Figures by way of example. The features described in the Figures can thereby be produced independently of the concrete example and be combined amongst the examples. The same reference numbers characterise the same or corresponding features.

[0069] There are shown:

[0070] FIG. 1 an example of a device according to the invention for the dissociation of tissue,

[0071] FIG. 2 a further example of a device according to the invention for the dissociation of tissue,

[0072] FIG. 3 a large number of devices according to the invention for the dissociation of tissue, disposed in a microtiter plate,

[0073] FIG. 4 a device according to the invention for the dissociation of tissue with a dissociation unit and a pot-shaped cell strainer,

[0074] FIG. 5 a device as shown in FIG. 4 with a reagent vessel, and

[0075] FIG. 6 the device shown in FIG. 5 placed on an actuation device for actuation of the dissociation unit.

[0076] FIG. 1 shows an example of a device according to the invention for the dissociation of tissue. In the illustrated example, the device 1 for the dissociation of tissue is configured to be circular. The device has a base 2 of which, in the plan view of FIG. 1, a circular side wall 2a can be detected. The base 2 is closed by a cover 3 of which, in the sectional image of FIG. 1, a cylindrical side wall 3 can be seen. The elements 2 and 3 together form a vessel 4 for receiving a tissue sample. The vessel 4 here is delimited by the side wall 3 of the cover. The base 2 has a base element about a centre of the housing 2 which has an opening in its interior. A central element of the cover 3 can engage in this opening.

[0077] In the example shown in FIG. 1, the device has a grinder with two mutually movable rows of teeth 5a-5f and 6a-6f. Each of the rows of teeth has a plurality of teeth 5a-5f or 6a-6f. The rows of teeth are disposed relative to each other at such a spacing that the teeth 5a-5f and 6a-6f of these respectively adjacent rows of teeth effect a dissociation of a part of the tissue sample in a spacing region by their minimum spacing relative to each other. The partial images of FIG. 1 show the grinder in a state in which the teeth 5a and 6a to 5f and 6f respectively have a minimum spacing relative to each other.

[0078] In the example shown in FIG. 1, the teeth have a drop shape in a cross-section perpendicular to the axis of rotation about which the rows of teeth rotate. In the direction of a line along which the teeth 5a-5f or 6a-6f are disposed in the corresponding row of teeth, the drop shape has, on the one hand, a tip and, on the other hand, opposite, a rounding. The tips of the teeth 5a-5f of the one row of teeth are directed in the opposite direction to the tips of the teeth 6a-6f of the other row of teeth. Likewise, the roundings of these teeth are directed in opposite directions to each other. As a result, the teeth 5a-5f together with the teeth 6a-6f cut the tissue if they move in the direction of the tips and grind the tissue if they move in the direction of the roundings.

[0079] In order to improve the dissociation result, the wall of the cover 3 has triangular projections 7a-7d which protrude from the wall in the direction of the teeth 5a-5f and 6a-6f and also in the direction of the centre of the vessel 4. If the teeth 6a-6f move past these projections 7a-7d, then tissue is ground between the projections 7a-7d and the teeth 6a-6f.

[0080] Similarly, the base element 2b has triangular teeth 8a-8c which protrude in the direction of the teeth 5a-5f and 6a-6f from the base 2b. If the teeth 5a-5f of the inner row of teeth move past these projections 8a-8c, then tissue is ground between the teeth 5a-5f and the projections 8a-8c.

[0081] The teeth 6a-6f of the inner row of teeth can be disposed on the cover 3 and be moved together with the latter. The teeth 5a-5f of the outer row of teeth are advantageously disposed on the base 2 of the vessel 4 and fixed relative to the latter. Correspondingly, the base element 2b with the projections 8a-8c is advantageously disposed on the underside of the vessel 4 and fixed relative to the latter. If now the cover 3 or an element disposed on the cover 3 and bearing the teeth 6a-6f is rotated, then the teeth 6a-6f move in the circle past the teeth 5a-5f and the projections 8a-8c and effect a dissociation of the tissue. At the same time, the projections 7a-7d on the cover move past the teeth 5a-5f and effect there a dissociation of the tissue.

[0082] FIG. 2 shows a further embodiment of a device according to the invention for the dissociation of tissue. The construction of the device shown in FIG. 2 corresponds to that shown in FIG. 1 so that reference should be made to the description relating to FIG. 1. In the following, only the differences from FIG. 1 are stated.

[0083] In FIG. 2, the teeth 5a-5f and 6a-6f likewise have a drop shape which is bent however, relative to the drop shape shown in FIG. 1, in the direction about the centre and the axis of rotation. As a result, these teeth 5a-5f and 6a-6f likewise have a pointed side and a round side which are connected however, in FIG. 2, differently from in FIG. 1 by curved sides. In the illustrated example, the inner side of the outer teeth 5a-5f are optionally curved parallel to the course of this row of teeth, i.e. essentially has the same radius of curvature. The outsides of the teeth 5a-5f and 6a-6f are optionally curved with a smaller radius of curvature than the row of teeth.

[0084] FIG. 3 shows a large number of devices according to the invention which are disposed in 4×6 cavities 10 of a microtiter plate 9. For each of the cavities 10, a cover 3 is provided which carries the teeth 6a, 6b of one of the rows of teeth. Above that, each cavity 10 forms a vessel 2 in which teeth 5a, 5b, 5c of a further row of teeth sire disposed. The arrangement of the teeth and configuration of the teeth can be achieved as shown in FIGS. 1 and 2. The teeth. 5a, 5b, 5c can also be configured as inserts for the cavities 10 so that they can be inserted in commercially available microtiter plates 9.

[0085] A tissue processing can take place for example as follows in the examples of FIGS. 1 to 3. 24 cavities can be provided as shown in FIG. 3. An inner diameter of the cavities can be for example 2 cm. The teeth 5a-5f can be rotated relative to the teeth 6a-6f, for example with a speed of rotation of 60-700 rpm. In the case of other scales of the cavities and of the grinder, the speed of rotation can be adapted correspondingly. The duration of the dissociation can be chosen for example between 1 and 10 min. During this time, one or more changes of direction can be undertaken. In this way, for example pieces of tissue of a mass of 50 mg to 3 g can be dissociated, A minimum spacing of the teeth of adjacent rows of teeth can be for example between 50 and 500 μm.

[0086] FIG. 4 shows, as exploded drawing, a device according to the invention for the dissociation of tissue with a dissociation unit 1 which is configured here with a cover 1a and a base 1b. The dissociation unit is disposed, in FIG. 4, at least partially in the interior of a closing cap 41 of a reagent vessel, which is shown in FIG. 5. The device has in addition a pot-shaped cell strainer 42 in which the dissociation unit 1 is disposed. The closing cap 41, the cover 1a, the base 1b and the cell strainer 42 are disposed, in FIG. 4, cylindrically and with coaxial cylindrical axes. In FIG. 4, the components are shown separated in the direction of the cylindrical axis, in the assembled state they are all situated however one in the other.

[0087] The cell strainer 42, in the illustrated example, is configured to be pot-shaped, and in fact in the form of a circular cylinder which is closed on one side. The cell strainer 42 thereby has four cell strainer surfaces 44 in the cylindrical surface. Furthermore, that end-side 43 of the cell strainer which is orientated towards the dissociation unit 1 is closed by a cell strainer surface 45, That end-side of the pot-shaped cell strainer, which is situated opposite the cell strainer surface 45, is open.

[0088] The dissociation unit has, on the one hand, the cover 1a and, on the other hand, the base 1b. The cover 1a thereby has an end-side which cannot be detected in the Figure, on which a plurality of teeth 5a, 5b are disposed such that they are parallel to the cylindrical axis of the cover. The teeth of the cover 1a are surrounded by the jacket face 1c which extends along an edge of the end-side of the cover on which the teeth 5a, 5b sire disposed. The jacket face 1c here is a cylindrical surface, the cylindrical axis of which coincides with the cylindrical axis of the dissociation unit 1 and also of the cell strainer 42.

[0089] The base 1b of the dissociation unit 1 has teeth 6a which cooperate with the teeth of the cover for the dissociation.

[0090] In the illustrated example 1a, the cover 1a has in addition a central through-opening 1d which extends in the centre of the end-face which cannot be detected and is surrounded by the teeth 5a, 5b. This opening 1d allows, on the one hand, coupling of a motor for actuation of the cover 1a and furthermore also the introduction of liquids into the dissociation unit 1. Advantageously, the opening can thereby have a septum at its end orientated towards the cell strainer 42. The opening 1d can be configured as a tubular channel which extends from the end-face of the cover 1a up to the end of the jacket face 1c of the cover.

[0091] Advantageously, the closing cap 41 also has an opening which is coaxial to the opening 1d and sealed relative to the opening 1d.

[0092] FIG. 5 shows the dissociation unit shown in FIG. 4 as an exploded drawing with a reagent vessel 51. As in FIG. 4, the dissociation unit 1 is disposed with a cover 1a and a base 1b in the closing cap 41 and is surrounded by the ceil strainer 42. With respect to these elements, reference should be made to the description relating to FIG. 4.

[0093] The reagent vessel 51 has a circular-cylindrical shape with a tapered closed end and an opening 52 in that end-face of the cylindrical shape which is situated opposite the tip. The closing cap 41 can be screwed onto the opening 52 and surrounds or encloses the opening 52. The dissociation unit 1 and the cell strainer 42, in the screwed-on state, are disposed in the closing cap 41 and in the opening 52 or shortly behind the opening 52 in the interior of the reagent vessel 51. FIG. 5A shows the device in a perspective illustration. FIG. 5B shows the device in connection with an actuation device 53 as a perspective illustration and FIG. 5C shows the device shown in FIG. 5B assembled in a sectional view.

[0094] It can be detected in FIG. 5C that the closing cap 41 is screwed or fitted on the reagent vessel 51 and thereby clamps the cell strainer 42 between an edge around the opening 52 of the reagent vessel 51 and the closing cap 41. As a result, the cell strainer 42 is retained in the opening 52 in the interior of the reagent vessel 51, directly behind the opening 52. A shaft 54 of the actuation device 53 engages in the cover 1a of the dissociation unit, as a result of which the latter is rotatable. The base 1b of the dissociation unit 1 is fixed relative to the cell strainer and the reagent vessel 51 and is not jointly rotated when rotating the cover 1a. As a result, the teeth 5a of the cover 1a move relative to the teeth 6a of the base 1b and thus effect a dissociation of tissue introduced into the dissociation unit 1. The cover 1a and the base 1b of the dissociation unit 1 form a housing, within which the tissue is dissociated. In the illustrated example, the housing is however not fluid-impermeable so that the cell suspension can flow out of the dissociation unit 1 if the device is rotated such that the reagent vessel 51 is pointing downwards or if the device is introduced into a centrifuge in which the centrifugal force acts in the direction of the reagent vessel 51.

[0095] The reagent vessel 51 can advantageously be a standard laboratory vessel, and also the cover 41 can be a standard laboratory vessel cover. The cover can also be fixed by means of a circumferentially situated clamping ring.

[0096] The duct of the coupling of the actuator 53 to the base 1b of the dissociation unit 1 can be fitted with sliding bearings in order to ensure a low-resistance rotation and simultaneous impermeability.

[0097] FIG. 6 shows the device shown in FIG. 5, fitted on a tissue grinder device which acts here as actuation device 53. The tissue grinder device 53 can hereby have in turn a shaft 54 which engages in the cover 1a of the dissociation unit 1 and can rotate the latter.

[0098] In the following, a course of a method according to the invention is intended to be described by way of example, in which the described device can be used.

[0099] In a first step of the tissue processing, a tissue sample to be examined is introduced into the dissociation unit 1 or the housing of the dissociation unit 1. For this purpose, the cover 1a can be filled with the tissue and a liquid, e.g. medium or enzyme solution, and be brought together with the base 1b in the cell strainer 42 via a coupling ring or closing cap 41. By rotation, preferably in both directions, and optionally linear up and down movement of the dissociation unit 1, now the tissue is processed by cutting and/or grinding processes. Optionally, the cutting unit can be operated also uncoupled from the cover 1a, e.g. by an integrated magnet. In this case, the cover 1a and the dissociation unit 1 can be uncoupled and the cover 1a can be actuated by rotation of a magnet above the cover.

[0100] During the desintegration process, the cover 1a of the cutting unit is connected to the actuator 53, and is actuated by the latter. The base 1b of the dissociation unit 1 or of the housing 1 is stationary here and can be inserted directly into the cell strainer 42. In order to produce a closed system, the base 1b of the dissociation unit 1, which can be integrated in the cell strainer 42, is screwed with the cover 1a of the dissociation unit 1 by the closing cap 41 on the reagent vessel 51.

[0101] After ending the desintegration process, the cell suspension is separated from the tissue residues, for example by means of centrifugation. Further washing steps to increase the cell output can be effected through a septum which can be integrated in the opening 1d in the cover 1b. In the reagent vessel 51, the cell suspension can be collected and hence can remain in a closed system from introducing the tissue sample via the desintegration until continuing analysis, which reduces the danger of contamination significantly and simultaneously increases the user friendliness.

[0102] The tissue processing with the described rows of teeth can be effected, during use for centrifugal tubes 51 and cell filters (with for example a mesh width between 10 and 200 μm) with a cutting unit inner diameter of for example 2 cm and a speed of rotation of for example 10 to 700 rpm. Other scales are possible, then the speed of rotation being adapted preferably. According to the type of tissue, a rotation time of for example 1 to 10 minutes and one or more changes in direction of rotation can be sensible. With suitable adaptation of the size of the housing, a dissociation of tissue pieces from a mass of e.g. 50 mg to 3 g is achievable. The minimum spacing between teeth of adjacent rows of teeth is preferably between 50 and 500 μm.

[0103] A reagent vessel 51 is suitable for the processing of a tissue sample or a plurality of tissue samples at the same time. Advantageously, seals, e.g. in the form of sliding bearings, can be provided in order to ensure a lower-resistance rotation and simultaneous impermeability. In particular the opening in the closing cap 41 and in the cover 1a can hereby be sealed relative to each other. By providing the cell filter 42, tissue residues of individual cells in the closed system can be separated.

[0104] It is particularly advantageous if the breakdown degree, i.e. the dissociation efficiency, is effected via an online process control. The breakdown of the tissue sample can thereby be effected by means of sensors, e.g. by means of a measurement of turbidity, via an optical sensor and/or a torque measurement and/or rheological measurements of the breakdown tools. The received parameters can be analysed and converted into a generally valid differential equation for describing the viability and yield of the target cells with different process parameters. On the basis of the online process control, an intelligent control of the direction of rotation and speed of rotation of the grinder and also of the duration of the tissue dissociation can be effected. As a result, any tissue sample can be processed individually in order to ensure an optimum cell yield.

[0105] The method according to the invention can be effected for example by firstly the dissociation unit 1 being loaded with a tissue sample and the weight of the tissue sample being determined. In addition, medium can be added. For the dissociation, the direction of rotation, speed of rotation and/or duration of the dissociation can be controlled by the online detection of process parameters, such as torque, and rheological parameters and optical density. The received parameters can be analysed and transferred by means of degradation equations to a feedback system of the motor control of the actuator 53. The feedback system can allow an individual dissociation of each tissue sample in order to increase the efficiency and yield.

[0106] Purification of the generated cell suspension is possible. For this purpose, the reagent vessel 51 can be placed in a centrifuge. After a first centrifugation, an arbitrary number of washing steps, for example by renewed addition of medium via the integrated septum in the motor coupling, can be effected. The purified cells then collect on the base of the reagent vessel 51.

[0107] The device according to the invention and the method according to the invention allow a very specific dissociation of tissue with which a desired end state of the dissociation can be achieved very precisely. By suitable combination of geometries of the teeth, if necessary cell strainers and dissociation units and intelligent control, prescribed dissociation degrees can be adjusted precisely. The described combination of tissue dissociation and centrifugation in a closed system allows complete processing of a tissue sample without the danger of contamination. By means of the described drop shapes and bent shapes of the teeth, the tissue can be cut and/or ground in a particularly sparing manner, a choice being able to be made between cutting and grinding according to requirements. By control of the direction of rotation, the predominant force effect can be determined. In comparison to processes according to the state of the art, tissue samples are processed not only in a more sparing manner for the cells but also in a time-saving manner. The tissue need no longer be cut with a scalpel into very small pieces but rather can be processed as a whole or in a few pieces. By integration of a cell strainer, the tissue sample can be purified directly without further pipetting steps. The process is partially automatable, as a result of which a higher reproducibility and standardisation is provided. The technology can be included in automated processes.

[0108] A further advantage of the system is the ability to operate in parallel. Because of the possibility of the simultaneous use of a plurality of centrifugal tubes, the tissue processing can be achieved in parallel so that a plurality of samples can be processed at the same time. The advantage resides, on the one hand, in the time saving, on the other hand, sources of error are minimised. During the processing of a plurality of samples, all the necessary preparatory operating steps can thus be implemented simultaneously for all samples and need no longer be integrated. An improved comparability of the results is thus provided. An example of this is a specific incubation time with an enzyme solution which can be maintained only when samples are mixed with the enzyme precisely this time before the dissociation.

[0109] Because of the centrifugal tube format, the system can be integrated in an automated process. Automation prevents differences in the processing as would be the case when implemented by different colleagues. This leads to an improved reproduction and comparability of the results.

[0110] Since the device, in the centrifugal tube variant thereof, concerns disposable articles, the contamination probability and auxiliaries expenditure can be minimised very greatly.

[0111] The device is suitable both for cell breakdown and for generation of single cells made from tissue.

[0112] A cell breakdown precedes for example a protein isolation or nucleic acid isolation and also other processes which include an analysis of cell components.

[0113] The more sparing dissociation of tissue is advantageous when single cells are required. This is for example the case when testing tumour cells with mass spectrometry, infrared spectroscopy or ELISA. Potential tumour tissue can be dissociated for histological tests. In addition, the production of single-cell suspensions is important for generation of 2D-cultures, 3D-cultures, single-cell characterisation, high-throughput drug screening and organ-on-chip technology. The system is not restricted to use on tumour tissue but rather can be adapted theoretically to any type of tissue.