CN214408319U - Automatic staining device for biological tissue sample section - Google Patents
Automatic staining device for biological tissue sample section Download PDFInfo
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- CN214408319U CN214408319U CN202022972849.9U CN202022972849U CN214408319U CN 214408319 U CN214408319 U CN 214408319U CN 202022972849 U CN202022972849 U CN 202022972849U CN 214408319 U CN214408319 U CN 214408319U
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Abstract
An automatic staining device for biological tissue sample slices comprises a fluid middle-end device, a fluid end device, a glass slide tray and a glass slide tray holding device, wherein the glass slide tray is used for bearing glass slides and is held by the glass slide tray holding device, the fluid middle-end device is connected with the fluid end device through a fluid pipeline, staining liquid input from the outside is distributed to the fluid end device by the fluid middle-end device, a liquid outlet and a waste liquid recovery hole are formed in the fluid end device, the staining liquid is applied to the glass slides borne by the glass slide tray through the liquid outlet, and a negative pressure chamber is recovered through the waste liquid recovery hole in a negative pressure suction mode after a sample on the glass slide is stained. The automatic dyeing device improves the dyeing treatment efficiency of the samples, reduces labor intensity, and simultaneously reduces the possibility of cross contamination among the samples, so that the sample treatment process has consistency and controllability.
Description
Technical Field
The utility model relates to a biological tissue sample section is handled, especially relates to an automatic dyeing apparatus of biological tissue sample section.
Background
The automatic staining treatment technology of biological tissue sample slices is an important step in the whole automatic staining, drying and sealing process of the biological tissue sample, and is an indispensable step, so that the treated biological tissue sample has a convenient observed appearance, the consistency and the high efficiency of the treatment process can be kept, and the staining step is an object which must be strictly controlled in the treatment process of the biological tissue sample.
The purpose of staining is to make different structures within the tissue appear differently colored for easy viewing. The classic Hematoxylin and Eosin staining method is the conventional staining of histological specimens and pathological section specimens, referred to as HE staining for short. After staining, the nuclei were stained violet-blue with hematoxylin, and most of the cytoplasmic and acellular components were stained pink with eosin.
Various techniques may be used to analyze biological samples. Examples of analytical techniques include microscopy, microarray analysis (e.g., protein and nucleic acid microarray analysis), and mass spectrometry. Preparing samples for these and other types of analysis typically includes: the sample is contacted with a series of treatment liquids. Some of these treatment liquids (e.g., staining and counterstaining reagents) may add color and, in contrast or otherwise, alter the visual characteristics of sample components (e.g., at least some types of cells and intracellular structures) that are not visible or difficult to see. Other treatment liquids (e.g., de-paraffinized liquids) may be used to achieve other treatment objectives. If multiple processing liquids are used to process the sample, the application and subsequent removal of the various processing liquids may be important to produce a sample suitable for analysis. In some cases, treating the sample with a plurality of treatment liquids comprises: the processing liquid is manually applied to the microscope slides that each carry a sample. This method of processing samples tends to be labor intensive and inaccurate.
Automatic immersion dyeing machines are available, which can replace manual dyeing. These machines automatically process samples by immersing racks carrying microscope slides in open baths of processing liquid. Unfortunately, the operation of immersion method machines inevitably results in the movement of the rack carrying the microscope slides from one bath to another, leading to the intersection of the liquids of the different baths. Over time, this movement causes degradation of the treatment liquid. Also, when the sample is immersed in a common bath, there is a possibility of cross-contamination. For example, cells may leave a specimen on one slide and be transported to another slide in a common bath. This form of contamination greatly reduces the accuracy of certain types of sample analysis. To alleviate this problem and to address the degradation of the treatment liquid caused by movement, it is often necessary to frequently replace the bath of treatment liquid in the immersion method machine. As a result, these machines tend to consume relatively large volumes of treatment liquid, which increases the costs associated with operating these machines. These open baths of treatment liquids are prone to evaporative loss and oxidative degradation of some of the treatment liquid components. For example, oxidation of certain components of the staining reagent can alter the staining properties of these components and thus reduce the precision of the staining operation.
The above background disclosure is only for the purpose of assisting understanding of the inventive concepts and technical solutions of the present invention, and does not necessarily belong to the prior art of the present patent application, and should not be used for evaluating the novelty and inventive step of the present application in the case that there is no clear evidence that the above contents are disclosed at the filing date of the present patent application.
SUMMERY OF THE UTILITY MODEL
The main object of the present invention is to overcome the problems of the prior art and to provide an automatic staining device for biological tissue sample slices.
In order to achieve the above purpose, the utility model adopts the following technical scheme:
an automatic staining device for biological tissue sample slices comprises a fluid middle-end device, a fluid end device, a glass slide tray and a glass slide tray holding device, wherein the glass slide tray is used for bearing glass slides and is held by the glass slide tray holding device, the fluid middle-end device is connected with the fluid end device through a fluid pipeline, staining liquid input from the outside is distributed to the fluid end device by the fluid middle-end device, a liquid outlet and a waste liquid recovery hole are formed in the fluid end device, the staining liquid is applied to the glass slides borne by the glass slide tray through the liquid outlet, and a negative pressure chamber is recovered through the waste liquid recovery hole in a negative pressure suction mode after a sample on the glass slide is stained.
In some embodiments, a power device coupled to the slide tray holding device for driving the slide tray holding device to rotate in a working position to position slides to be stained relative to the fluid end device; preferably, the power means is also for driving linear movement of the slide tray holding means to switch between the active and inactive positions.
In some embodiments, the fluid end unit comprises a liquid inlet head connected to the liquid outlet via a common manifold, the liquid inlet head being connected to the fluid middle unit via a fluid line, and a high pressure gas connector for receiving high pressure gas during waste liquid recovery, wherein the plurality of waste liquid recovery holes are distributed around the liquid outlet.
In some embodiments, the liquid outlet comprises a dropping needle, and the plurality of waste liquid recovery holes are distributed in rows on two sides of the dropping needle.
In some embodiments, a pump is also included between the fluid middle-end device and the fluid end-device.
In some embodiments, the fluid center-end device comprises a liquid storage chamber providing a fluid inlet for inputting a staining liquid, a fluid outlet for dispensing liquid to the fluid end-device, and at least one of: a negative pressure suction port for creating a negative pressure in the liquid storage chamber for the input of staining liquid, a liquid overflow port for overflowing liquid when the liquid input is excessive, an atmospheric connection port for communicating with the atmosphere when the liquid is dispensed to the fluid end device, and a discharge port for discharging liquid after the staining of the sample is finished, preferably the negative pressure suction port, i.e. the discharge port.
In some embodiments, the liquid storage chamber is provided with a plurality of fluid inlets.
In some embodiments, one or more of the fluid inlets is provided with a fluid switch.
In some embodiments, the fluid middle device comprises a combination of a top, at least one waist and a bottom stacked together in a square shape, the fluid storage chamber is formed by the combination, a plurality of sides of the top and a bottom connected to the waist are respectively provided with an opening, a plurality of sides of the at least one waist are respectively provided with an opening, a top surface of the waist connected to the top is provided with an opening, a bottom surface of the waist connected to the bottom is provided with an opening, a plurality of sides of the bottom and a top connected to the waist are respectively provided with an opening, the opening of the top is used for liquid or air ventilation, and the openings of the waist and the bottom are used for liquid ventilation.
In some embodiments, the fluid middle-end device is provided with a negative pressure conduit connected to the negative pressure suction port and extending to the bottom of the liquid storage chamber.
In some embodiments, the dyeing apparatus further comprises a temperature maintaining device for maintaining the temperature in the dyeing apparatus within a set temperature range or value.
In some embodiments, an automated apparatus for dispensing a liquid onto a biological tissue sample on one or more microscope slides that can perform processing operations on the slides bearing the biological tissue sample to achieve fully automated staining of the biological tissue sample, the apparatus comprising: a fluid middle-end device comprising a central chamber; a fluid tip device comprising a fluid tip head assembly; a slide tray holding device including a rack; a power device comprising a motor coupled to the slide tray holding device and configured to rotate the slide tray holding device to position a slide relative to the fluid end device; a fluid line, a fluid switch, a pump, and a temperature maintenance device may also be included.
Some embodiments may store liquid from a liquid source where the storage is not a long term storage. When the liquid is stored, a negative pressure state is formed in the central cavity, and the liquid in the pipeline is forced to flow into the central cavity under the action of the atmospheric pressure.
Some embodiments may dispense stored liquid. When dispensing the liquid, the liquid in the central chamber may be pumped away under the action of the pump.
Some embodiments may process a specimen carried by a slide. The treatment process comprises the following steps: liquid pumped from the central chamber by the pump is delivered to the slide. The liquid coming out will form a liquid pool due to the effect of surface tension. The collected liquid has an at least partially retained shape and completely covers the sample due to surface tension. The liquid is then removed from the specimen and the volume of liquid remaining on the slide is at least ten percent less than the previously mentioned volume of the collected liquid to expose the specimen for cleaning and subsequent staining. The above operations may be repeated and the applied liquid may be of different kinds.
Some embodiments control the pump's operating power during the application of the liquid so that the liquid does not splash when it reaches the slide after leaving the fluid tip device.
In some embodiments, the liquid remaining in the central chamber may be recovered. The recovery method comprises the following steps: a pipe which is directly communicated with the cavity bottom is arranged in the central cavity, negative pressure is formed in the pipe, and the air pressure in the central cavity is kept balanced with the atmospheric pressure. The remaining liquid in the central chamber is forced into the conduit by the gas pressure and exits the central chamber.
A method of processing a specimen on an upper surface of a microscope slide comprising: the microscope slide is moved to a processing position. Moving a microscope slide to a processing position refers to receiving a tray carrying the microscope slide from the outside and moving the tray to a position such that the slide carried on the tray is facing the fluid end device. By directly facing is meant that the sample on the slide is located just below the fluid outlet with a positional error within a 3mm radius. The central axis of the longer length of the slide is toward the center of the slide tray. The shorter length of the slide coincides with the width of the fluid tip device. After the sample processing on the previous microscope slide is completed, the next microscope slide can reach the location.
A method of processing a specimen on a microscope slide comprising: reagent is dispensed from an outlet of the fluid dispensing mechanism opposite the upper surface of the microscope slide, forming a layer of reagent in contact with the sample at the mounting area.
In some embodiments, the staining apparatus comprises one or more fluid conduits and a fluid tip device, the fluid tip device being stationary. The fluid tip device may be coupled to the fluid center device and configured to dispense reagents from one or both of the fluid center device. Meanwhile, the fluid end device has the functions of removing liquid and pumping. In some embodiments, the fluid tip device may be configured to blow air to facilitate movement of liquid to the low pressure region. In some embodiments, a fluid tip device comprises: a fluid inlet, a waste outlet, a waste recovery hole, a gas inlet, and a common manifold. The fluid may be delivered through a manifold and dispensed from a head of a fluid tip device.
In some embodiments, the staining apparatus is configured to receive a microscope slide tray carrying microscope slides from the transporter apparatus. The stainer module includes: a microscope slide tray holder, a rotating device and a linear motion device. The microscope slide tray retainer can drive the microscope slide tray to rotate, and the rotating angle and precision can be controlled. The control of the positional accuracy of the microscope slide tray is already achieved on the transport mechanism and is transferred to the staining apparatus when the staining begins with the microscope slide tray being received from the transport apparatus.
In some embodiments, a method of processing a sample on a microscope slide comprises: a liquid is applied to the slide and a high pressure gas is directed toward the upper surface of the slide to diffuse the applied liquid toward the two weeks of the slide.
In some embodiments, a method of processing a sample on a microscope slide comprises: the temperature of the whole dyeing device can be controlled within a certain range, so that the temperature of the sample is kept approximately constant in the dyeing process. The method of controlling the temperature is to create a steady flow of gas at a constant temperature within the device, particularly on a microscope slide tray, which can be achieved by a heating device and a fan.
In some embodiments, a method of processing a sample on a microscope slide comprises: the fluid end device is checked for a slide underneath and can be detected by a scanner. If there is no slide, no staining procedure is performed.
In a particular embodiment, a method of processing a sample on a microscope slide includes: the slides are transported into a stainer module. A liquid is applied to the slide to bring the sample into contact with the liquid. The liquid is blown along and removed from the upper surface of the slide. The slide can then be removed from the stainer module.
The beneficial effects of the utility model are that:
the utility model provides an automatic dyeing apparatus of biological tissue sample section can handle the operation to the slide glass that bears biological tissue sample. The automatic dyeing device improves the dyeing treatment efficiency of the samples, reduces labor intensity, and simultaneously reduces the possibility of cross contamination among the samples, so that the sample treatment process has consistency and controllability. The utility model discloses be favorable to realizing automatic dyeing of batchization, high efficiency, simple and easy, accurate full-automatic biological tissue sample and handle.
Drawings
Fig. 1 is a logic diagram of an automatic dyeing apparatus according to an embodiment of the present invention.
Fig. 2 is a perspective view of an automatic dyeing apparatus according to an embodiment of the present invention.
Fig. 3 is an isometric view of a fluid middle end device.
Fig. 4 is a top view of a fluidic middle-end device.
Figure 5 is an isometric view of a central chamber.
Figure 6 is a top view of the central chamber.
Figure 7 is a cross-sectional view B-B of the central chamber.
Fig. 8 is an isometric view of a fluid tip device.
Fig. 9 is a bottom view of the fluid tip device.
Fig. 10 is a front view of a fluid tip device.
Fig. 11 is a stepped cross-sectional view G-G in an elevation view of a fluid tip device.
Figure 12 is an isometric view of a portion of an apparatus for dyeing modules.
Figure 13 is an isometric view of a slide tray holding device and a power device.
Figure 14 is a front view of the slide tray holding device and the power device.
Detailed Description
The embodiments of the present invention will be described in detail below. It should be emphasized that the following description is merely exemplary in nature and is not intended to limit the scope of the invention or its application.
It will be understood that when an element is referred to as being "secured to" or "disposed on" another element, it can be directly on the other element or be indirectly on the other element. When an element is referred to as being "connected to" another element, it can be directly connected to the other element or be indirectly connected to the other element. In addition, the connection may be for either a fixed or coupled or communicating function.
It is to be understood that the terms "length," "width," "upper," "lower," "front," "rear," "left," "right," "vertical," "horizontal," "top," "bottom," "inner," "outer," and the like are used in the orientation or positional relationship indicated in the drawings for convenience in describing the embodiments of the present invention and to simplify the description, and are not intended to indicate or imply that the referenced device or element must have a particular orientation, be constructed and operated in a particular orientation, and are not to be construed as limiting the invention.
Furthermore, the terms "first", "second" and "first" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance or implicitly indicating the number of technical features indicated. Thus, a feature defined as "first" or "second" may explicitly or implicitly include one or more of that feature. In the description of the embodiments of the present invention, "a plurality" means two or more unless specifically limited otherwise.
Referring to fig. 1 to 14, in one embodiment, an automatic staining apparatus for biological tissue sample section comprises a fluid middle device 2200, fluid end devices 2300A-2300D, a slide tray 2700 and a slide tray holding device 2400, wherein the slide tray 2700 is used for carrying slides, the slide tray 2700 is held by the slide tray holding device 2400, the fluid middle device 2200 is connected with the fluid end devices 2300A-2300D through fluid pipelines, the fluid middle device 2200 distributes externally input staining liquid to the fluid end devices 2300A-2300D, the fluid end devices 2300A-2300D are provided with liquid outlets and waste liquid recovery holes 2304, the staining liquid is applied to the slides carried by the slide tray 2700, and after staining samples on the slides is finished, the staining liquid is recovered to a negative pressure chamber (2) through the waste liquid recovery holes 2304 in a negative pressure suction mode Not shown).
In a preferred embodiment, a power device 2500 is further included, the power device 2500 being coupled to the slide tray holding device 2400 for driving the slide tray holding device 2400 to rotate in a working position to position slides to be stained relative to the fluid end device 2300A-2300D; preferably, the power device 2500 is also used to drive the linear movement of the slide tray holding device 2400 to switch between the working position and the non-working position.
In a preferred embodiment, the fluid end unit 2300A-2300D comprises a liquid inlet header 2301 and a high pressure gas connector 2303 connected to the liquid outlet via a common manifold 2308, the liquid inlet header 2301 is connected to the fluid middle unit 2200 via a fluid line, the high pressure gas connector 2303 is used for introducing high pressure gas during waste liquid recovery, and a plurality of waste liquid recovery holes 2304 are distributed around the liquid outlet. The high pressure gas forces liquid on the slide to spread from the exit port toward effluent port 2304 and forces liquid in the channel to exit fluid tip assembly 2300A-2300D from inlet header 2301 and back to fluid tip assembly 2200.
In a preferred embodiment, the liquid outlet comprises a dropping needle 2305, and a plurality of waste liquid recovery holes 2304 are distributed in a row on both sides of the dropping needle 2305.
In a preferred embodiment, pumps 2800A-2800D are also included between the fluid middle end device 2200 and the fluid end devices 2300A-2300D to apply motive forces to the liquid.
In a preferred embodiment, the fluid middle-end device 2200 includes a liquid storage chamber (e.g., central chamber 2202) configured with a fluid inlet for inputting a staining liquid, a fluid outlet for dispensing liquid to the fluid end device 2300A-2300D, and at least one of: a negative pressure suction port for forming a negative pressure in the liquid storage chamber to input a staining liquid, a liquid overflow port for overflowing the liquid when the liquid input is excessive, an atmospheric connection port for communicating the atmosphere when the liquid is dispensed to the fluid end device 2300A-2300D, and a discharge port for discharging the liquid after the staining of the sample is completed, preferably, the negative pressure suction port, i.e., the discharge port.
In a preferred embodiment, the liquid storage chamber is provided with a plurality of fluid inlets.
In a preferred embodiment, one or more of said fluid inlets is provided with a fluid switch.
In the preferred embodiment, the fluid middle-end device 2200 comprises a combination of a top 2203, at least one waist 2204 and a bottom 2205 stacked together in a square shape, the fluid storage chamber is formed by the combination, a plurality of sides of the top 2203 and a bottom connected with the waist 2204 are respectively provided with openings, a plurality of sides of the at least one waist 2204 are respectively provided with openings, a top surface of the waist 2204 connected with the top 2203 is provided with an opening, a bottom surface of the waist 2204 connected with the bottom 2205 is provided with an opening, namely a fluid outlet 2206A, a plurality of sides of the bottom 2205 and a top surface connected with the waist 2204 are respectively provided with openings, an opening of the top 2203 is used for liquid or air, and an opening of the waist 2204 and an opening of the bottom 2205 are used for liquid.
In a preferred embodiment, the fluid middle-end 2200 is provided with a negative pressure conduit 2207, and the negative pressure conduit 2207 is connected with the negative pressure suction port and extends to the bottom of the liquid storage chamber.
In a preferred embodiment, a temperature maintenance device 2900 is also included for maintaining the temperature within the dyeing device at a set temperature range or value.
Specific embodiments of the present invention are described in further detail below.
An automatic staining device for biological tissue sample slices. The automatic dyeing apparatus includes: fluid lines (not shown), a fluid middle end device 2200, fluid end devices 2300A-2300D, fluid switches, a slide tray holding device 2400, a power device 2500, a temperature maintenance device 2900, pumps 2800A-2800E, and a rack 2600. Fluid lines connect an external source of liquid to the fluid end-device 2200, the fluid lines connect the fluid end-device 2200 with the fluid end-devices 2300A-2300D, and pumps 2800A-2800D are included between the fluid end-device 2200 and the fluid end-devices 2300A-2300D. The fluid line includes a liquid conduit (preferably a flexible, corrosion resistant conduit), a fluid switch, and a port. The fluid center apparatus 2200 includes a fluid switch, a central chamber, and an interface. The end-of-fluid device 2200 can store and dispense liquids. Fluid end devices 2300A-2300D include a plurality of ports, waste recovery apertures 2304, and a plurality of manifolds, enabling liquid application, waste recovery, and blowing operations. The slide tray holding device 2400 includes a slide tray 2700 support. The slide tray holding device 2400 can drive the slides to rotate and translate. The temperature maintaining device can maintain the temperature in the dyeing device to be approximately constant, and the best dyeing effect is realized. The frame holds the various sections.
Dyeing logic of the dyeing apparatus as generally shown in fig. 1, a fluid middle-end apparatus 2200 dispenses an externally inflowing liquid to fluid end-devices 2300A-2300D. The liquid is delivered to the slides of the slide tray 2700 held by the slide tray holding device 2400 by the fluidic tip devices 2300A-2300D. After the task of the fluid is completed, the fluid is again recovered by the fluid end devices 2300A-2300D. The positions of the fluid lines, the fluid middle end device 2200, and the fluid end devices 2300A-2300D are typically held stationary relative to the ground, and the slide tray holding device 2400 rotates the slide tray 2700 to effect a one-by-one staining of the specimen on each slide. The slide tray holding device 2400 can receive the slide tray 2700 when open and is in operation when closed. The temperature maintaining device keeps the temperature in the dyeing device approximately constant.
In FIG. 2, 2200 shows a fluid medium-end device, and 2300A-2300D show a fluid end device. The dyeing module can be provided with a plurality of fluid pipelines, and each fluid pipeline only contains one liquid. The fluid pipeline is inserted with a fluid switch which can be a solenoid valve and controls the liquid to enter the fluid middle-end device. The dyeing module can be provided with a fluid middle-end device, a plurality of fluid inlets are distributed on the device to receive liquid from the outside, and a fluid switch is arranged on each inlet and can be an electromagnetic valve; the device has at least one fluid outlet, which may be provided without a switch. The fluid middle-end device can be regarded as a liquid transfer station. The fluid middle-end device is provided with a liquid storage chamber. The staining module has at least one fluid end device therein. The fluid end device is connected with the fluid middle end device through a fluid pipeline. The fluid end device is in fluid communication with the fluid middle device. When a switch in a fluid pipeline in which a certain liquid exists is opened, the liquid flows into the fluid middle-end device, so that the storage cavity of the fluid middle-end device is filled with the liquid. To allow liquid to flow into the fluidic medium device, the air pressure in the storage chamber of the fluidic medium device may be reduced in some way. This may be done by using a pump 2800E to draw air away from the chamber. When the liquid amount in the storage chamber reaches a certain standard, the switch in the fluid pipeline where the liquid exists is closed, and the liquid is stopped from entering. In order to prevent the fluid middle-end device from sucking excessive liquid, a liquid overflow outlet is arranged in the fluid middle-end device. When the fluid tip device is activated, liquid in the storage chamber flows out of the outlet of the fluid tip device past the fluid tip device onto a slide carried by the slide tray 2700. In order to make the liquid have certain power, a pump is arranged on a pipeline between the fluid middle-end device and the fluid end device to apply power to the liquid. During this process, the air pressure in the fluid storage chamber of the fluid center device is maintained equal to atmospheric pressure by some means. When the amount of liquid on the slide reaches a desired level, the fluid end device changes operating conditions to move the fluid end device and the liquid in the fluid line between the fluid end device and the fluid middle device into the storage chamber of the fluid middle device. The liquid in the storage chamber is discharged by a tube. After a certain amount of time, the fluid tip device removes liquid from the slides carried by the slide tray 2700 and delivers it to a waste recovery site. When the task of the liquid is finished, the liquid middle-end device discharges the liquid which finishes the task out of the storage chamber, and the liquid is discharged out of the dyeing module through the corresponding fluid pipeline.
Fig. 3 is an isometric view of a fluid center device, and fig. 4 is a top view of the fluid center device. 2201A-2201L are fluid switches, which may be solenoid valves. 2202 is the central chamber. The central chamber has one or more inlets and one or more outlets. The fluid switch is connected with a fluid pipeline and/or a negative pressure device (which can be a vacuum pump) and/or atmospheric pressure.
Figure 5 is an isometric view of a central chamber. The central chamber may consist of a top, waist and bottom, each of which carries a different function. The central chamber has a bottom and a waist, but may have one or more waists. The central chamber has a top, a waist, and a bottom. The top of the device is provided with 5 openings, four openings of which are connected with the fluid switch, and one opening of which is connected with the waist. The waist has 6 openings, of which four are connected to the fluid switch, and of which the other two openings can be connected to the top, waist or bottom. The bottom can have 5 openings or 9 openings, wherein 4 openings are necessary for the fluid outlet, and one opening is necessary to be connected with the waist. In this example, 2203 is the top of the central chamber, 2204 is the waist of the central chamber, and 2205 is the bottom of the central chamber. 2206A is a liquid outlet at the bottom 2205 of the central chamber that is connected to a fluid line leading to a fluid terminal device. The top 2205 of the central chamber has two ports connected to the underpressure, one may be a liquid overflow and one needs to be connected to the atmosphere. The central chamber waist 2204 is typically connected to a fluid line for the liquid. When a certain liquid is required, the fluid switch on the fluid line for this liquid is opened, and at the same time the switch connected to the negative pressure is also opened, so that the liquid enters the interior of the central chamber. If the liquid enters too much, the liquid will flow out of the liquid overflow outlet. When it is desired to deliver liquid from the central chamber to the fluid end fitting, the switch to the port for atmospheric connection is opened, the pump is started and liquid flows out of the central chamber 2202.
Figure 6 is a top view of the central chamber. Figure 7 is a cross-sectional view B-B of the central chamber. 2207 is a pipe which is part of the top of the central chamber. One end of the pipe is connected to the top and its length is such that its other end is just below the bottom of the central chamber. The conduit is connected through the top of the central chamber to an external gas pressure controller, which may be a vacuum pump. The fluid middle-end device changes the gas pressure in the liquid storage chamber through the pipeline. Meanwhile, the fluid middle-end device can also discharge the liquid in the storage cavity which is used for completing the task out of the storage cavity through the pipeline. When it is desired to drain the liquid from the central chamber, a negative pressure is created in the conduit 2207 and the port to atmosphere is opened and the liquid in the central chamber can be drained from the fluid center.
Fig. 8 is an isometric view of a fluid tip device. Fig. 9 is a bottom view of the fluid tip device. Fig. 10 is a front view of a fluid tip device. Fig. 11 is a stepped cross-sectional view G-G in an elevation view of a fluid tip device. 2301 is a liquid inlet head of a fluid terminal device, and 2301 is connected to a fluid middle device through a fluid pipeline. When a switch in a fluid pipeline in which a certain liquid exists is opened, the liquid flows into the fluid middle-end device, so that the storage cavity of the fluid middle-end device is filled with the liquid. When the liquid amount in the storage chamber reaches a certain standard, the switch in the fluid pipeline where the liquid exists is closed, and the liquid is stopped from entering. Subsequently, the fluid end device is operated and the liquid in the storage chamber flows out of the outlet of the fluid end device through the fluid line to the fluid end device inlet header 2301 into the fluid end device. 2302 is the waste outlet head of the fluid end set. The task-performed liquid recovered from the slide eventually exits the fluidic terminal device through a waste outlet header 2302 of the fluidic terminal device. 2303 is a high pressure gas connection of the fluid end unit, through which high pressure gas enters. The conduits of the inlet header 2301 and the conduits of the high pressure gas connection 2303 merge into a common manifold 2308. Attached to the end of the common manifold is a drip needle 2305. In FIG. 9, 2304 denotes a waste liquid recovery hole. Waste recovery holes 2304 are distributed in rows on both sides of dropping needles 2305. The number of each row of waste liquid recovery holes is between 5 and 15. The waste liquid recovery hole is connected with the negative pressure chamber. The negative pressure chamber is connected to a negative pressure source through waste outlet header 2302, which can draw negative pressure via tubing to draw fluid out of the negative pressure chamber. When liquid is distributed, the waste liquid recovery hole 2304 and the high-pressure gas connector 2303 are in a non-operating state, and the liquid passes through the liquid inlet head 2301 and the common manifold 2308 and finally goes out of the dropping needle 2305 to reach the slide glass. After the liquid finishes the coloring task, the waste liquid recovery hole 2304 and the high pressure gas joint 2303 start to work. High pressure gas enters the common manifold 2308 from the high pressure gas connection 2303 and then travels in both directions. And upward, to displace liquid in the conduit from the inlet header 2301 out of the fluid end device to the fluid middle device. Flows downward, out of common manifold 2308 to drip needle 2305, and blows liquid onto the slide. The high pressure forces the liquid on the slide to spread from the center to the two sides of the waste liquid recovery hole. At the same time, the low air pressure in the waste liquid recovery hole sucks the liquid into the negative pressure chamber, thereby completing the waste liquid removal work.
Figure 12 is an isometric view of a portion of an apparatus for dyeing modules. Figure 13 is an isometric view of a slide tray holding device and a power device. Figure 14 is a front view of the slide tray holding device and the power device. In fig. 12, 2900 denotes a temperature maintaining device which radiates or radiates heat to maintain the temperature inside the dyeing apparatus within a set temperature range or value. 2700 denotes a slide tray carrying slides circumferentially distributed on the slide tray with their long side axes aligned with the center of the tray. The center region of the slide tray 2700 has a convex spatial geometry with corresponding draft features on the bottom surface of the slide tray corresponding to these shapes. The fluid end devices 2300A-2300D can precisely align slides carried on the slide tray during the staining process. After the end of a staining process, the slide tray holding device 2400 rotates the slide tray 2700 at an angle so that the next slide adjacent to the slide that ended the staining process is properly aligned with the fluid end device 2300A-2300D. The slide tray is coupled to the slide tray support in a manner that maintains the relative position unchanged. 2401 in fig. 13 shows a slide tray holder. The slide tray support 2401 also has raised dimensional geometry that can be precisely matched to the draft features on the underside of the slide tray. A power source 2501 on the power unit 2500 rotates the slide tray support 2401. The power source may be an electric motor. The power source 2500 and slide tray support 2401 can be connected by a timing belt to a timing pulley. The power source 2500 can also be connected with the slide tray holding device 2400 through a lead screw to realize linear motion of the slide tray holding device 2400.
In fig. 14, 2400 denotes a slide tray holding device, 2500 denotes a power device, and 2600 denotes a rack of a staining apparatus. The slide tray holding device has at least one of linear movement in one direction relative to the frame of the staining apparatus and circular movement in one direction relative to the frame of the staining apparatus. The slide tray holding device has two states of open and working. In the open state, the slide tray holding device does not perform circular motion. The slide tray holding device only moves linearly during opening and during returning. In the operating state, the slide tray holding device only performs a circular motion. In fig. 2, the slide tray holding device is in an operative state. In an operative condition, the slide tray holding device is capable of holding at least one slide on the slide tray of the slide tray holding device against the fluid tip device after each of the circular movements of the slide tray holding device has ceased. Meanwhile, a device is arranged on the frame of the dyeing device to detect whether the position of the slide glass tray holding device is accurate or not. A power device powers the slide tray holding device. In fig. 14, the slide tray holding device is in an open state.
The background section of the present invention may contain background information related to the problems or the environment of the present invention and is not necessarily descriptive of the prior art. Accordingly, the inclusion in the background section is not an admission of prior art by the applicant.
The foregoing is a more detailed description of the present invention, taken in conjunction with the specific/preferred embodiments thereof, and it is not intended that the invention be limited to the specific embodiments shown and described. For those skilled in the art to which the invention pertains, a plurality of alternatives or modifications can be made to the described embodiments without departing from the concept of the invention, and these alternatives or modifications should be considered as belonging to the protection scope of the invention. In the description herein, references to the description of the term "one embodiment," "some embodiments," "preferred embodiments," "an example," "a specific example," or "some examples" or the like, mean that a particular feature, structure, material, or characteristic described in connection with the embodiment or example is included in at least one embodiment or example of the invention. In this specification, the schematic representations of the terms used above are not necessarily intended to refer to the same embodiment or example. Furthermore, the particular features, structures, materials, or characteristics described may be combined in any suitable manner in any one or more embodiments or examples. Various embodiments or examples and features of various embodiments or examples described in this specification can be combined and combined by one skilled in the art without contradiction. Although the embodiments of the present invention and their advantages have been described in detail, it should be understood that various changes, substitutions and alterations can be made herein without departing from the scope of the claims.
Claims (10)
1. An automatic staining device for biological tissue sample slices is characterized by comprising a fluid middle-end device, a fluid tail-end device, a glass slide tray holding device and a temperature holding device, the slide tray is used for carrying slides, the slide tray is held by the slide tray holding device, the fluid middle-end device is connected with the fluid end device through a fluid pipeline, the fluid middle-end device distributes externally input dyeing liquid to the fluid end device, the fluid end device is provided with a liquid outlet and a waste liquid recovery hole, the staining liquid is applied to the glass slide carried by the glass slide tray from the liquid outlet, and after the sample on the glass slide is dyed, the sample is recovered to a negative pressure chamber through the waste liquid recovery hole in a negative pressure suction mode, the temperature maintaining device is used for maintaining the temperature in the dyeing device in a set temperature range or a set temperature value.
2. The automated staining apparatus of claim 1, further comprising a power device coupled to the slide tray holding device for driving the slide tray holding device to rotate in a working position to position slides to be stained relative to the fluid end device; the power device is also used for driving the linear motion of the slide glass tray holding device for switching between the working position and the non-working position.
3. The automatic dyeing apparatus according to claim 1 or 2, wherein said fluid terminal means comprises a liquid inlet header connected to said liquid outlet via a common manifold, said liquid inlet header being connected to said fluid terminal means via a fluid line, and a high-pressure gas connection for supplying high-pressure gas during effluent recovery, said effluent recovery holes being distributed around said liquid outlet.
4. The automatic dyeing apparatus according to claim 3, wherein said liquid outlet comprises a dropping needle, and a plurality of said effluent collecting holes are arranged in a row on both sides of the dropping needle.
5. The automatic staining apparatus of any one of claims 1 to 2, further comprising a pump between the fluid middle-end device and the fluid end-device.
6. The automated staining apparatus of any one of claims 1 to 2, wherein the fluid medium-end device comprises a liquid storage chamber provided with a fluid inlet for inputting a staining liquid, a fluid outlet for dispensing the liquid to the fluid end device, and at least one of: a negative pressure suction port for creating a negative pressure in the liquid storage chamber for the input of staining liquid, a liquid overflow port for overflowing liquid when the liquid input is excessive, an atmospheric connection port for communicating with the atmosphere when dispensing liquid to the fluid end device, and a discharge port for discharging liquid after the staining of the sample is finished.
7. The automatic dyeing apparatus according to claim 6, wherein said negative pressure suction port and said discharge port are the same port.
8. The automatic dyeing apparatus according to claim 6, wherein said liquid storage chamber is provided with a plurality of fluid inlets provided with fluid switches.
9. The automatic dyeing device according to claim 6, characterized in that said fluid middle-end means comprises a combination of a top portion, at least one waist portion and a bottom portion stacked together in a block shape, said fluid storage chamber is formed by said combination, a plurality of side surfaces of said top portion and a bottom surface connected to said waist portion are respectively provided with openings, a plurality of side surfaces of said at least one waist portion are respectively provided with openings, and a top surface of said waist portion connected to said top portion is provided with an opening, a bottom surface of said waist portion connected to said bottom portion is provided with an opening, a plurality of side surfaces of said bottom portion and a top surface connected to said waist portion are respectively provided with openings, said opening of said top portion is used for passing liquid or air, and said openings of said waist portion and said bottom portion are used for passing liquid.
10. The automatic dyeing apparatus according to claim 6, characterized in that said fluid middle-end device is provided with a negative pressure conduit connected to said negative pressure suction port and extending to the bottom of said liquid storage chamber.
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