The application is filing date on April 23rd, 2014, Application No. 201410166957.3, invention name
It is referred to as the divisional application of " automatically preparing the devices and methods therefor of cell block ".
Background technology
Medically process body fluid cell usually the cell with liquid to be coated directly on sheet glass, then pass through
Microscope is observed.Along with the most cytopathologic development, it is general that above this routine techniques makes
The limitation of logical smear is more and more obvious, such as smear Existence and uniquenss, it is impossible to replicate;Can not forever retain;
Hinder the application that such as SABC, molecular pathology learn a skill of emerging pathological technique.
Cell block is then to fix carrying out paraffin after the cell extraction in liquid, is formed like tissue after fixing
The form of section.This method solve above-mentioned common smear exist problem, also can avoid because of smear damage,
The doctor-patient dispute that loss etc. may cause.Make cell block is also the basis preparing organization chip simultaneously, should
Technology will be widely used in cytopathology field.
Making cell block at present substantially uses manual method to process, and the body fluid cell of process can include
Hydrothorax, ascites, cervical exfoliated cell, dropsy of serous cavity, cerebrospinal fluid, sputum etc..Make by hand briefly
Step as follows: pour the body fluid of extraction into test tube, by the test tube high speed centrifugation some time, remove on test tube
Portion contains the supernatant of the interference components such as blood, makes the liquid cell of collection form cell mass;Careful stripping
From lower complete cell mass, wrap with permeable filter paper, go through fixing, dehydration, transparent, dye, soak
Wax, cool down, the series of steps such as embedding, then embedded wax stone is cut under microtome about 5 μm
Thin slice, thus it is finally completed cell block.
In above step, dehydration, transparent, waxdip can be automatically performed in tissue processor, but remaining
Step is the most all by having been manually done, and is time-consumingly about 7~8 hours, after certain step of period completes, and behaviour
Make personnel and manual intervention just must can carry out next step, time-consuming, laborious.And make cell block by hand,
It is directly associated with the experience level of operator, is otherwise likely to that the uneven situation of wax stone quality occurs;
Additionally manual operations is also possible to contact with the reagent such as formalin, dimethylbenzene, and careless slightly will giving is grasped
The health making personnel brings injury.
Summary of the invention
The present invention has been manually done to overcome existing cell block to make to use, and not only performance accuracy is low and pole
Easily give the problem that the health of operator brings injury, it is provided that a kind of cell block with pressurization, extract function
Preparation facilities.
To achieve these goals, the present invention provide a kind of there is pressurization, prepared by the cell block of extract function
Device, including rotating disk, test tube, semipermeable membrane, liquid taking device, draw-out device and pressue device.Rotating disk has
There is multiple first fixing hole.The quantity of test tube is at least one, and is fixed on the first fixing hole, and test tube includes
First body and the second body, the first body and the second body are detachable connection, the bottom of the second body
Having perforate, the second body is the rounding mesa-shaped of hollow, and the area being positioned at the perforate of the second its bottom is little
Area in the second its bottom.Semipermeable membrane is arranged between the first body and the second body, the upper table of semipermeable membrane
Face and lower surface are all covered with wire netting, and wire netting and semipermeable membrane are arranged at the first body and second
Between body.
Liquid taking device is that test tube adds cellular liquid, reagent and liquid paraffin, it include mechanical arm, suction pipe,
First conduit, working barrel and draw-out device.Mechanical arm includes bottom, rotation section and clamping part, and bottom has
Having multiple through hole, mechanical arm is to be provided with controller in hollow structure, and rotation section.Suction pipe is arranged at clamping
Portion.First conduit via through holes and mechanical arm inside are connected with suction pipe, and for the circulation of liquid, first leads
Being provided with electromagnetic valve on pipe, first conduit is correspondingly arranged on an electromagnetic valve, and electromagnetic valve and controller
It is electrically connected with.Working barrel is arranged at the first conduit, and the reagent aspiration that will be located in the reagent bottle below suction pipe arrives
In suction pipe, and first conduit is correspondingly arranged on a working barrel;Wherein working barrel electrically connects with controller
Connect.
Draw-out device includes fixture and the second conduit, and fixture is hollow structure, the open top of fixture
Perforate with the second its bottom is fixedly connected, and the bottom opening of fixture and one end of the second conduit are solid mutually
Fixed connection, the top of fixture is provided with the groove corresponding with the second body of hollow rounding mesa-shaped, and recessed
The both sides of groove are provided with working arm, and the sidewall of groove is provided with bolster.Pressue device and the second conduit another
One end is connected, by the second conduit for providing malleation or negative pressure bottom test tube.
In sum, the cell block preparation facilities with pressurization, extract function that the present invention provides, take liquid
The first conduit in device and working barrel are by cellular liquid to be prepared and be positioned at the reagent of reagent bottle and lead to
Cross mechanical arm and suction pipe adds in test tube.Machinery takes liquid and instead of and traditional manually take liquid, reagent not with
Operator contacts, and operator's health will not come to harm.Also control reagent is can reach by controlling working barrel
Addition, precision is higher compared with manual operation.By arrange pressue device soak formalin, dehydration,
It is dyeing, transparent and soak and the step such as paraffin constantly repeats to increasing malleation or negative pressure bottom test tube so that
The cell being positioned on semipermeable membrane sufficiently with the reagent reacting added.User only need to set pressurization on demand
Device adds the time of malleation and negative pressure, can be automatically performed said process.
Additionally, upper surface and lower surface at semipermeable membrane are respectively provided with wire netting, when heater is to paraffin pipe
When road and test tube, wire netting has good heat conduction function and can be delivered on semipermeable membrane by the heat on test tube,
The paraffin on semipermeable membrane is made to keep liquid during soaking paraffin.
For above and other objects of the present invention, feature and advantage can be become apparent, cited below particularly preferably
Embodiment, and coordinate accompanying drawing, it is described in detail below.
Detailed description of the invention
Fig. 1 show the cell block preparation dress with pressurization, extract function that one embodiment of the invention provides
Put schematic diagram;Fig. 2 show the schematic cross-section of test tube in Fig. 1, fixture and pressue device;Fig. 3 institute
It is shown as the workflow diagram of the cell block preparation facilities with pressurization, extract function shown in Fig. 1.Please one
And refering to Fig. 1 to Fig. 3.
The present invention provides a kind of cell block preparation facilities with pressurization, extract function, including rotating disk 1, examination
Pipe 2, semipermeable membrane 3, liquid taking device 4, draw-out device 5 and pressue device 6.Rotating disk 1 has multiple
One fixing hole 11.The quantity of test tube 2 is at least one, and is fixed on the first fixing hole 11.Test tube 2 includes
First body 21 and the second body 22, the first body 21 and the second body 22 are detachable connection, second
The bottom of body 22 has perforate 221.Semipermeable membrane 3 is arranged between the first body 21 and the second body 22.
Liquid taking device 4 includes mechanical arm 41, suction pipe the 42, first conduit 43 and working barrel 44.Wherein mechanical arm
41 add reagent or liquid paraffin for test tube 2.Mechanical arm 41 includes bottom 411, rotation section 412 and folder
Holding portion 413, bottom 411 has multiple through hole.Mechanical arm 41 is to set in hollow structure, and rotation section 412
It is equipped with controller 8.Suction pipe 42 is arranged at clamping part 413.First conduit 43 via through holes and mechanical arm 41
Inside is connected with suction pipe 42, for the circulation of liquid.Working barrel 44 is arranged at the first conduit 43, by position
The reagent aspiration in reagent bottle below suction pipe 42 is in suction pipe 42, and first conduit 43 correspondence sets
It is equipped with a working barrel 44.Draw-out device 5 includes fixture 51 and the second conduit 52, during fixture 51 is
Hollow structure, the perforate 221 bottom the open top of fixture 51 and the second body 22 is fixedly connected, Gu
The bottom opening of locking member 51 and one end of the second conduit 52 are fixedly connected.Pressue device 6 and the second conduit
The other end of 52 is connected, by the second conduit 52 for providing malleation or negative pressure bottom test tube 2.Wherein,
It is additionally provided with electromagnetic valve 45 on one conduit 43, and first conduit 43 is correspondingly arranged on an electromagnetic valve 45.
In the present embodiment, liquid taking device 4 has two sets, the most a set of for extracting cellular liquid to be produced
With the bottom 411 of mechanical arm 41 in the liquid, and this set liquid taking device such as formalin, ethanol and dimethylbenzene
There are four through holes, have four the first conduits 43 to pass on this corresponding through hole and this liquid taking device 4 respectively
Suction pipe 42 is connected, and being respectively used to draw formalin, concentration is 95% ethanol, anhydrous alcohol and diformazan
Benzene, another set of liquid taking device 4 is used for extracting paraffin.But, this is not limited in any way by the present invention.Yu Qi
In its embodiment, a set of liquid taking device 4 can be used, but more than five logical is set in the bottom of mechanical arm 41
Hole, and two clamping parts 413 and two suction pipes 42 are set, one of them suction pipe 42 is used for drawing formal
The reagent such as woods and cellular liquid to be prepared, and another suction pipe 42 is used for drawing paraffin.
Below in conjunction with Fig. 1 and Fig. 3, offer of the present invention is had pressurization, prepared by the cell block of extract function
The workflow of device is described in detail.
This process originates in sampling, it would be desirable to produces the cellular liquid of cell block and draws into and have semipermeable membrane 3
Test tube 2 in (step S101).After having drawn, suction pipe is rinsed.
Soak formalin (step S102).User opens be connected with the reagent bottle holding formalin
Working barrel 44 on one conduit 43 and electromagnetic valve 45, the neutral good fortune that 5ml concentration is 10% drawn by suction pipe 42
Your Malin is in the test tube 2 being placed with cellular liquid.
Open pressue device 6, bottom test tube, increase negative pressure by the second conduit 52 so that moisture, little point
Son and formalin liquid are by semipermeable membrane 3, and the cell in cellular liquid is then trapped on semipermeable membrane 3.
When on semipermeable membrane 3 accumulation cell more block semipermeable membrane 3 time.Arranging pressue device 6, reversion controls pump,
Bottom test tube, increase malleation, the cell got lodged on semipermeable membrane 3 is pushed back in cellular liquid again.The most again
Again increase negative pressure, the liquid of mix reagent is sucked in waste liquid bottle by semipermeable membrane 3.Constantly repeat above-mentioned
Process so that all cells on semipermeable membrane 3 the most fully soaks formalin, this process lasts 2 hours,
Cross punching must assure that the formalin liquid of at least more than 2ml in test tube at this.
In order to ensure the formalin liquid of at least more than 2ml in test tube, in the present embodiment, by examination
Arranging sensor on the sidewall of pipe 2, this sensor is electrically connected with controller.The real-time test tubes of controller 2
Interior liquid level, when the liquid level in test tube 2 is less than 2ml, controller output control signal is opened
Working barrel 44 and electromagnetic valve 45, suction pipe 42 draws formalin in test tube, it is achieved automatic soaking Fu Er
The process of Malin.
Dehydration (step S103), this dehydration includes primary dewatering and second dehydration, primary dewatering and secondary
The process of dehydration is identical with the process soaking formalin, and reagent simply used in primary dewatering is that concentration is
The ethanol of 95%, dewatering time is 1.5 hours.And the reagent used by second dehydration is anhydrous alcohol, and it is dehydrated
Time is also 1.5 hours.
Dyeing (step S104), adds 0.8ml Yihong in test tube 2 and contaminates the cell of second dehydration
Color, constantly repeats increasing negative pressure, malleation and negative pressure bottom test tube so that is detained on semipermeable membrane 3 is thin
Born of the same parents fully dye, and this process lasts 10 minutes.
Transparent (step S105), in vitro adds dimethylbenzene and the cell after dyed is carried out transparent processing,
Constantly repeating increasing negative pressure, malleation and negative pressure bottom test tube 2, this process lasts 30 minutes.
Soaking paraffin (step S106), heating fills the reagent bottle of paraffin, paraffin suction pipe and test tube,
Paraffin melting by reagent bottle, the paraffin after melting adds to test tube 2, to bottom test tube 2 constantly
Repeating to increase negative pressure, malleation and negative pressure, this process lasts 1.5 hours, will remain on cell after transparent processing
Dimethylbenzene cement out, the temperature of test tube 2 is at 60 DEG C~70 DEG C in this process.In the present embodiment, it is anti-
Paraffin cooled and solidified on semipermeable membrane 3 the most in step s 106, at upper surface and the lower surface of semipermeable membrane 3
It is all covered with wire netting 7, and wire netting 7 and semipermeable membrane 3 is arranged between the first body and the second body,
Wire netting 7 can quickly by the temperature transfer of test tube 2 to semipermeable membrane 3 so that the temperature of semipermeable membrane 3 maintains
60 DEG C~70 DEG C.Additionally, semipermeable membrane 2 also can be played a supporting role by wire netting 5.
In above-mentioned steps S102~step S106, make to be trapped on semipermeable membrane 3 by pressue device 6
The reagent that adds of cell and each step or paraffin repeat reaction, all of process is all automatically performed, user
Time of each step only need to be set and pressue device 6 adds time of malleation or negative pressure.Operator without
Any reagent need to be contacted, the healthy of operator will not be endangered.Further, by increasing electromagnetic valve
45, by controlling the valve opening of electromagnetic valve 45, the accurate absorption of reagent can be realized.And increase sensor
Liquid level in test tubes 2, and the signal detected is passed to controller, controller is according to this inspection
Survey signal and control electromagnetic valve 45 and the duty of working barrel 44, it is achieved automatically control.
Embedding frame is put into when step S106 completes and removed by the cell block on semipermeable membrane 3 after test tube 2 cooling
Inside carry out embedding and embedded cell block being placed under microtome section (step S107).
In the present embodiment, the second body 22 rounding mesa-shaped in hollow, and be positioned at bottom the second body 22
The area of perforate 221 less than the area bottom the second body 22.With this rounding corresponding consolidating of mesa-shaped structure
The top of locking member 51 is provided with groove 511, and the both sides of groove 511 are provided with working arm 512.Inverted round stage
In liquid can be concentrated the fixture 51 flowing into hollow by the second body 22 of shape structure.Meanwhile, the second body
The area of the perforate 221 bottom 22 is less than the area bottom the second body 22, and liquid will not occur any seepage.
Rounding mesa-shaped structure can preferably protect the second body 22, prevents the second body 22 chipping.For entering
Protection second body 22 of one step, not only the sidewall at groove 511 is provided with bolster 513, the most also exists
The lateral wall of the first body 21 is provided with stop block 211, the lower limb of stop block 211 and the first body 21 and
The joint face of the second body 22 is in the same plane.When fixture 51 rises fixing even with the second body 22
When connecing, working arm 512 is stopped by stop block 211, prevents fixture 51 from too rising, so that
The bottom of the second body 22 is squeezed and chipping.
In sum, what the present invention provided has pressurization, the cell block preparation facilities of extract function and side thereof
Method, the first conduit 43 and working barrel 44 in liquid taking device 4 by cellular liquid to be prepared and are positioned at
Reagent in reagent bottle is added in test tube 2 by mechanical arm 41 and suction pipe 42.Machinery takes liquid and instead of
Traditional manually takes liquid, and reagent does not contacts with operator, and operator's health will not come to harm.By controlling
Working barrel 44 also can reach the addition controlling reagent, and precision is higher compared with manual operation.Added by setting
Pressure device 6 soak formalin, be dehydrated, dye, transparent and soak in the steps such as paraffin and constantly repeat
To increasing malleation or negative pressure bottom test tube 2 so that be positioned at the cell on semipermeable membrane 3 sufficiently with added
Reagent reacting.User only need to set pressue device 6 on demand and add the time of malleation and negative pressure, can be automatically
Complete said process.
Additionally, upper surface and lower surface at semipermeable membrane 3 arrange wire netting 7, when heater is to paraffin pipe
When road and test tube, wire netting 7 has good heat conduction function can be delivered to semipermeable membrane 3 by the heat on test tube
On so that the paraffin on semipermeable membrane 3 keeps liquid during soaking paraffin.
Although the present invention is disclosed above by preferred embodiment, but it is not limited to the present invention, any ripe
Know this those skilled in the art, without departing from the spirit and scope of the present invention, a little change and retouching can be made, therefore
Protection scope of the present invention is when being as the criterion depending on claims scope required for protection.