JPH0350972B2 - - Google Patents
Info
- Publication number
- JPH0350972B2 JPH0350972B2 JP58120174A JP12017483A JPH0350972B2 JP H0350972 B2 JPH0350972 B2 JP H0350972B2 JP 58120174 A JP58120174 A JP 58120174A JP 12017483 A JP12017483 A JP 12017483A JP H0350972 B2 JPH0350972 B2 JP H0350972B2
- Authority
- JP
- Japan
- Prior art keywords
- specimen
- specimens
- processing liquid
- holder
- microscopic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/30—Staining; Impregnating ; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis
- G01N1/31—Apparatus therefor
- G01N1/312—Apparatus therefor for samples mounted on planar substrates
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/30—Staining; Impregnating ; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis
- G01N1/31—Apparatus therefor
- G01N2001/317—Apparatus therefor spraying liquids onto surfaces
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Sampling And Sample Adjustment (AREA)
Description
【発明の詳細な説明】
(産業上の利用分野)
この発明に係る顕微鏡標本を染色する方法及び
装置は、病理検体の薄切片をスライドガラスに貼
着した細胞診用顕微鏡標本を染色するために利用
する。Detailed Description of the Invention (Industrial Application Field) The method and apparatus for staining a microscopic specimen according to the present invention are for staining a microscopic specimen for cytodiagnosis in which a thin section of a pathological specimen is attached to a glass slide. Make use of it.
(従来技術)
癌その他の病気診断のため、患部等から採取し
た病理検体の薄切片をスライドガラスに貼着して
顕微鏡標本を作り、これを顕微鏡で観察すること
が広く行なわれている。このような顕微鏡で観察
するための標本は、観察し易くするために、細胞
の組織を異る部分毎に色を変えて予め染色を施さ
れる。(Prior Art) For diagnosis of cancer and other diseases, it is widely practiced to prepare a microscopic specimen by attaching a thin section of a pathological specimen taken from an affected area to a glass slide, and then observe this specimen under a microscope. Specimens to be observed under such a microscope are pre-stained with different colors for different parts of the cell tissue in order to make them easier to observe.
このため従来から、吊下げ式の篭の中に、スラ
イドガラスに病理検体の薄切片を貼着した多数の
標本を、互いの間に間隔をあけて多数収容し、こ
の篭をハリスヘマトキシリン、塩酸、エタノール
等の処理液を入れた複数の処理槽中に順次浸漬し
たり、或は上記のような標本を吊り金具に支持さ
せて複数の処理槽中に順次浸漬したりして、標本
の染色を行なつていた。 For this reason, conventionally, a large number of specimens (thin sections of pathological specimens pasted to glass slides) are housed in a hanging basket, spaced apart from each other, and the basket is filled with Harris hematoxylin, hydrochloric acid , Staining the specimen by sequentially immersing it in multiple processing tanks containing a processing solution such as ethanol, or by supporting the specimen on a hanging bracket and sequentially immersing it in multiple processing tanks. was being carried out.
(発明が解決しようとする課題)
ところが、このようにして顕微鏡標本の染色を
行なう場合は、処理槽中の各種処理液がスライド
ガラスや篭の表面に付着したまま比較的多量に、
次の処理槽にまで送られ、前後の処理槽中の処理
液が混合することが避けられない。このようにし
て異種処理液の混合が生じると、処理液の性能が
劣化し、標本の染色が不鮮明になつてしまう。こ
のため従来も、一定数の標本処理を行なつたなら
ば、処理槽中の処理液を新しいものと交換するよ
うに作業していたが、交換直前の処理液は性能が
劣化しているため、この液で処理された標本の染
色は十分鮮明なものとはなり難かつた。(Problem to be Solved by the Invention) However, when staining a microscopic specimen in this manner, a relatively large amount of various processing solutions in the processing tank remain attached to the surface of the slide glass or cage.
The liquid is sent to the next processing tank, and it is inevitable that the processing liquid in the previous and subsequent processing tanks will mix. When different types of processing liquids are mixed in this way, the performance of the processing liquid deteriorates and the staining of the specimen becomes unclear. For this reason, in the past, once a certain number of specimens had been processed, the processing solution in the processing tank was replaced with a new one, but the performance of the processing solution immediately before replacement had deteriorated. However, the staining of specimens treated with this solution was difficult to be sufficiently clear.
染色作業の度に処理槽中の処理液を新しいもの
と交換することは、高価なものも含まれる処理液
の費用が嵩むため、現実的でない。 It is not practical to replace the processing liquid in the processing tank with a new one every time a dyeing operation is performed because the cost of the processing liquid, which may include expensive ones, increases.
この様な不都合を解消する為の発明として、特
開昭53−43542号公報に記載された顕微鏡標本ス
ライド自動調整方法及び装置がある。 As an invention for solving such inconveniences, there is a method and apparatus for automatically adjusting a microscope specimen slide described in Japanese Patent Application Laid-Open No. 53-43542.
この公報に記載された発明においては、鉛直方
向の軸を中心として回転するターンテーブルの上
面に複数枚のスライドガラスを放射状に載置する
と共に、上記ターンテーブルを回転させつつノズ
ルから処理液を噴射させて、これら複数枚のスラ
イドガラスの表面に処理液を付着させるように構
成している。 In the invention described in this publication, a plurality of slide glasses are placed radially on the top surface of a turntable that rotates around a vertical axis, and processing liquid is injected from a nozzle while rotating the turntable. The processing liquid is then applied to the surfaces of the plurality of slide glasses.
ところが、このように構成される、上記公報に
記載された発明の場合、ノズルから噴出してスラ
イドガラスに付着した処理液は、重力によつてそ
のままスライドガラス表面を流れ落ちるだけとな
るため、必要とする処理時間中、ノズルから処理
液を噴出し続けなければならない。 However, in the case of the invention described in the above-mentioned publication, which is configured in this way, the processing liquid ejected from the nozzle and attached to the slide glass simply flows down the slide glass surface due to gravity. The processing liquid must continue to be ejected from the nozzle during the processing time.
このため、処理時間が長い場合には、処理液の
消費量が過大となり、運転経費が徒に嵩む事が避
けられなかつた。 For this reason, when the processing time is long, the amount of processing liquid consumed becomes excessive, which inevitably increases operating costs unnecessarily.
本発明は上述のような不都合を何れも解消し、
少ない運転経費で、常に鮮明な標本染色を行なう
ことのできる方法と、この方法の実施に直接使用
する装置とを提供することを目的としている。 The present invention solves all of the above-mentioned disadvantages,
It is an object of the present invention to provide a method that allows clear specimen staining at all times with low operating costs, and an apparatus that can be used directly to carry out this method.
(課題を解決する為の手段)
a 標本を染色する方法の発明の構成
本発明の顕微鏡標本を染色する方法は、病理
検体の薄切片をスライドガラスに貼着した複数
枚の顕微鏡標本を、断面が放射状で、全体とし
て円錐台状になるように配列して、水平方向の
軸を中心として緩速回転させつつ、この標本に
一つの処理液を吹き付けた後、この処理液が作
用する間そのまま緩速回転を継続し、その後上
記標本を高速回転させて、各標本の表面に付着
した処理液を遠心力により飛散させて排除し、
その後再び標本を緩く回転させつつ行なう別の
処理液の吹き付けおよび高速回転による余分の
処理液の排除を、所定の処理液についてそれぞ
れ繰り返して、顕微鏡標本の染色を行なうもの
である。(Means for Solving the Problems) a. Structure of the Invention of a Method for Staining a Specimen The method for staining a microscopic specimen of the present invention involves cross-sectional are arranged in a radial pattern, forming a truncated cone shape as a whole, and while rotating slowly around a horizontal axis, one treatment solution is sprayed onto the specimen, and then the sample remains as it is while this treatment solution acts. Continue slow rotation, then rotate the specimens at high speed to scatter and eliminate the processing liquid adhering to the surface of each specimen by centrifugal force.
Thereafter, the microscopic specimen is stained by spraying another treatment liquid while rotating the specimen slowly again and removing the excess treatment liquid by high-speed rotation for each predetermined treatment liquid.
b 標本を染色する装置の発明の構成
本発明の顕微鏡標本を染色する装置は、病理
検体の薄切片をスライドガラスに貼着した複数
枚の顕微鏡標本を、断面が放射状で、全体とし
て円錐台状となるように装着でき、中心部に挿
入される水平方向の回転軸に結合させる保持部
と、この保持器を回転させるための速度変換自
在なモータと、上記保持器の外周を覆い、下端
に排出口を有するカバーと、このカバー内にお
いて保持器に装着された標本に処理液を吹き付
けるための噴霧器とから構成される。b. Structure of the invention of apparatus for staining specimens The apparatus for staining microscopic specimens of the present invention is capable of staining multiple microscope specimens, each of which has a radial cross-section and a truncated conical shape as a whole, in which thin sections of pathological specimens are pasted onto glass slides. It can be installed so that It consists of a cover having a discharge port, and a sprayer inside the cover for spraying a processing liquid onto a specimen mounted on a holder.
(作 用)
上述の様に構成される本発明の顕微鏡標本を染
色する方法及び装置の場合、断面放射状で全体を
円錐台状に配列された複数枚の顕微鏡標本を水平
方向の回転軸を中心として緩速で回転させつつ、
ノズルから所定量の処理液を噴霧し、標本の表面
に付着させると、この処理液は、水平方向の回転
軸の周囲を公転しつつ自転する標本の検体薄切片
およびスライドガラスの表面を、長さ方向並びに
幅方向に亙り、往復するように流れて、この表面
をまんべんなく濡らす。(Function) In the method and apparatus for staining microscopic specimens of the present invention configured as described above, a plurality of microscopic specimens arranged in a truncated conical shape with a radial cross section are rotated about a horizontal axis of rotation. While rotating slowly as
When a predetermined amount of processing liquid is sprayed from the nozzle and deposited on the surface of the specimen, this processing liquid will spray a thin section of the specimen and the surface of the slide glass, which rotate around the horizontal axis of rotation, over a long distance. It flows back and forth in both the length and width directions, evenly wetting the surface.
検体薄切片に付着した処理液が十分作用するま
での間、回転軸を緩速で回転させたならば、次い
で上記回転軸を急速回転させれば、標本の表面に
付着している処理液が遠心力により振り飛ばされ
る。 If the rotating shaft is rotated slowly until the processing liquid attached to the specimen thin section is sufficiently affected, then the rotating shaft can be rapidly rotated to remove the processing liquid attached to the surface of the specimen. It is blown away by centrifugal force.
それまで付着していた処理液が総て振り飛ばさ
れたならば、再び回転軸を緩速で回転させ、次の
処理液を噴霧して標本に付着させ、上述の行程を
各処理液について繰り返せば、所定の標本の染色
が行なわれる。 Once all the processing solution that had been attached up to that point has been shaken off, rotate the rotating shaft slowly again, spray the next processing solution to adhere to the specimen, and repeat the above process for each processing solution. For example, a predetermined specimen is stained.
(実施例)
次に、図示の実施例を説明しつつ本発明を更に
詳しく説明する。(Example) Next, the present invention will be explained in more detail by explaining the illustrated embodiment.
第1〜2図は、本発明により病理検体の薄切片
をスライドガラスに貼着した顕微鏡標本を染色す
る装置の全体構成を示しており、第1図は縦断側
面図、第2図は第1図のA−A断面図である。基
台1の上面には、緩速と高速とに速度変換自在な
モータ2が固定されており、このモータ2の、基
台1の側方に大きく突出した回転軸3には、病理
検体の薄切片をスライドガラスに貼着した複数枚
(図示の例では16枚)の標本4,4を、断面放射
状かつ全体を円錐台状に装着する保持器5が、こ
の回転軸3との相対的回転を不能として、取付け
られている。 Figures 1 and 2 show the overall configuration of an apparatus for staining a microscopic specimen in which a thin section of a pathological specimen is attached to a slide glass according to the present invention. It is an AA sectional view of the figure. A motor 2 that can freely change the speed between slow and high speeds is fixed on the top surface of the base 1. A rotary shaft 3 of this motor 2, which protrudes largely to the side of the base 1, is connected to a rotary shaft 3 for carrying the pathological specimen. A holder 5 holds a plurality of specimens 4 (16 specimens in the illustrated example) with thin sections pasted on glass slides in a radial cross-section and a truncated conical shape relative to the rotating shaft 3. It is installed so that it cannot rotate.
更に、この保持器5の周囲には、この保持器5
の外径よりも十分に大きな内径を有する、有底短
円筒状のカバー6が設けられている。このカバー
6のモータ2と反対側の端部は、回転軸3に保持
器5を着脱できるように開口しているが、後述す
るように、カバー6内に噴霧されたり、標本から
振り飛ばされる処理液が外部に拡散しないよう
に、開閉自在な蓋を設けることもできる。 Furthermore, around this cage 5, this cage 5
A short cylindrical cover 6 with a bottom and an inner diameter sufficiently larger than an outer diameter is provided. The end of the cover 6 opposite to the motor 2 is open so that the holder 5 can be attached to and detached from the rotating shaft 3, but as will be described later, spray may be sprayed into the cover 6 or shaken off from the specimen. A lid that can be opened and closed may be provided to prevent the processing liquid from diffusing to the outside.
カバー6の側面には、処理液噴霧用のノズル7
が設けられており、ホース8を送られて来る処理
液を圧縮空気によつて、又は無気式にカバー6内
に霧状に吹込み、保持器5に装着された標本4,
4のほぼ中央部に貼着された検体の薄切片に吹き
付けるようにしている。 On the side of the cover 6, there is a nozzle 7 for spraying the processing liquid.
The processing liquid sent through the hose 8 is blown into the cover 6 in the form of a mist using compressed air or in an airless manner, and the specimen 4, which is attached to the holder 5, is
The sample is sprayed onto the thin section of the specimen attached to the approximately central part of the sample.
更に、カバー6の下端には、標本4,4から振
り飛ばされた用済又は余分の処理液を排出するた
めの、排出口9が設けられている。 Furthermore, a discharge port 9 is provided at the lower end of the cover 6 for discharging the used or excess processing liquid that has been shaken off from the specimens 4, 4.
一方、複数の標本4,4を装着するための保持
器5は、第3図に示すような主体10と、第4図
に示すような抑え板11と、両部材10,11を
結合するためのナツト片12(第1図)とから成
つている。 On the other hand, a holder 5 for mounting a plurality of specimens 4, 4 is made up of a main body 10 as shown in FIG. 3, a holding plate 11 as shown in FIG. It consists of a nut piece 12 (Fig. 1).
第3図に示した主体10は、円板状の基板部1
3の上面(上下は図面による。)中央部に、前記
回転軸3を挿通できる円管部14を垂直に植立
し、この円管部14の上部に上記基板部13と平
行で、この基板部13よりもやや小径の円板状の
支持板部15を設け、円管部14の上端部の、支
持部15よりも上方に突出した部分の外周面には
雄ねじ16を形成している。 The main body 10 shown in FIG.
A circular tube section 14 through which the rotating shaft 3 can be inserted is vertically planted in the center of the upper surface of 3 (the top and bottom are according to the drawings), and a circular tube section 14 that is parallel to the substrate section 13 is placed above the circular tube section 14. A disk-shaped support plate portion 15 having a slightly smaller diameter than the portion 13 is provided, and a male thread 16 is formed on the outer circumferential surface of a portion of the upper end of the circular tube portion 14 that protrudes above the support portion 15.
基板部13の上面外周縁部には立壁17が形成
されており、この立壁17の内側部分には、保持
器5に装着すべき標本の枚数と同数の、放射状の
溝18,18が、環状に配列されて形成されてい
る。各溝18,18は、外周寄り部分よりも内周
寄り部分が深くなるように形成されている。 A standing wall 17 is formed on the outer peripheral edge of the upper surface of the substrate section 13, and on the inner side of this standing wall 17, radial grooves 18, 18, the same number as the number of specimens to be mounted on the holder 5, are formed in an annular shape. It is arranged and formed. Each of the grooves 18, 18 is formed so that a portion closer to the inner periphery is deeper than a portion closer to the outer periphery.
基板部13と平行な支持板部15には、標本の
下端を上記溝18,18に嵌合させた際に、内周
側に倒れようとするこの標本4の上端部を支持す
るための複数の切込み19,19が、溝18,1
8に対応して溝18,18と同方向に同数形成さ
れている。 A support plate section 15 parallel to the substrate section 13 has a plurality of plates for supporting the upper end of the specimen 4 which tends to fall toward the inner circumference when the lower end of the specimen is fitted into the grooves 18, 18. The cuts 19, 19 are the grooves 18, 1
The same number of grooves are formed in the same direction as the grooves 18 and 18 corresponding to the grooves 8.
抑え板11は、上記主体10の支持板部15よ
りもやや大径の円板で、中央には上記円管部14
の上端の雄ねじ16を形成した部分を挿通できる
円孔20が、下面周縁部には垂下壁21が、それ
ぞれ形成されている。ナツト片12は、上記雄ね
じ16に螺合するものである。 The holding plate 11 is a circular plate having a slightly larger diameter than the support plate portion 15 of the main body 10, and the circular tube portion 14 is located in the center.
A circular hole 20 through which the male thread 16 at the upper end can be inserted is formed, and a hanging wall 21 is formed at the peripheral edge of the lower surface. The nut piece 12 is screwed onto the male thread 16.
このように構成される保持器5に標本4,4を
装着するには、各標本4の下端縁を基板部上面の
溝18に嵌合させ、上端部を支持板部15の切込
み19に挿入する。溝18は内周寄り部分が外周
寄り部分よりも深いため、溝18に下端縁を嵌合
させた標本4の上端部は内周側に倒れようとし、
切込み19にしつかりと保持される。 To attach the specimens 4 to the holder 5 configured in this manner, the lower edge of each specimen 4 is fitted into the groove 18 on the top surface of the base plate, and the upper end is inserted into the notch 19 of the support plate 15. do. Since the groove 18 is deeper in the inner circumference than in the outer circumference, the upper end of the specimen 4 whose lower edge is fitted into the groove 18 tends to fall toward the inner circumference.
It is firmly held in the notch 19.
このため、主体10を第3図の状態で机上等に
置き、標本4,4を装着する作業を、先に装着済
の標本4,4の倒れ防止を考慮することなく、容
易に行なうことができる。 Therefore, it is possible to easily place the main body 10 on a desk or the like in the state shown in FIG. can.
各溝18,18並びに切込み19,19に標本
を装着したならば、抑え板11を支持板部15に
被せ、ナツト片12を円管部14上端の雄ねじ1
6に螺合させて、抑え板11を主体10に結合す
る。 Once the specimens are mounted in the grooves 18, 18 and the notches 19, 19, the holding plate 11 is placed over the support plate 15, and the nut piece 12 is attached to the male screw 1 at the upper end of the circular tube 14.
6 to connect the holding plate 11 to the main body 10.
これにより、各標本4,4は外縁部上下端をそ
れぞれ立壁17と垂下壁21とによつて支持され
て、保持器5を回転させても外れないようにな
る。 As a result, the upper and lower outer edges of each specimen 4, 4 are supported by the standing wall 17 and the hanging wall 21, respectively, so that they will not come off even if the holder 5 is rotated.
このようにして、保持器5に複数の標本4を装
着し、各標本4に貼着された検体の薄切片を染色
するには、保持器5を横にして、その主体10の
中心の円管部14内にモータ2の回転軸3を挿通
し、円管部14内の通孔に形成した非円形断面部
分と回転軸3に形成した非円形断面部分とを嵌合
させ、次いで円管部14から突出した回転軸3の
先端に形成した雄ねじにナツト片22を螺合させ
て、保持器5をこのナツト片22と回転軸3の基
部外周に形成したフランジ23との間で挟持す
る。 In this way, in order to attach a plurality of specimens 4 to the holder 5 and stain the thin section of the specimen affixed to each specimen 4, the holder 5 is placed horizontally, and a circle at the center of the main body 10 is The rotary shaft 3 of the motor 2 is inserted into the tube portion 14, the non-circular cross-sectional portion formed in the through hole in the circular tube portion 14 and the non-circular cross-sectional portion formed in the rotary shaft 3 are fitted, and then the circular tube A nut piece 22 is screwed onto a male thread formed at the tip of the rotating shaft 3 protruding from the portion 14, and the retainer 5 is held between the nut piece 22 and a flange 23 formed on the outer periphery of the base of the rotating shaft 3. .
次いで、モータ2を緩速で回転させつつ、ノズ
ル7から所定量の処理液をケース6内に噴霧す
る。噴霧された処理液は、標本4の表面に付着す
るが、この標本4は回転軸3の周囲を公転しつつ
自転するため、上記付着した処理液は、標本4の
検体薄切片およびスライドガラスの表面を往復す
るように流れて、この表面をまんべんなく濡ら
す。 Next, a predetermined amount of processing liquid is sprayed into the case 6 from the nozzle 7 while rotating the motor 2 at a slow speed. The sprayed processing liquid adheres to the surface of the specimen 4, but since the specimen 4 rotates while revolving around the rotation axis 3, the attached processing liquid adheres to the specimen thin section of the specimen 4 and the slide glass. It flows back and forth across the surface, evenly wetting this surface.
この場合に於いて、標本4は断面放射状で全体
を円錐台状に配列されている為、各標本4の表面
に付着した処理液は、幅方向(放射方向)だけで
なく、長さ方向(第1図の左右方向)にも往復し
て流れ、特に処理液の噴霧量を多くしなくても、
表面に付着した検体薄切片をまんべんなく濡ら
し、この検体薄切片の処理が均一に行なわれる様
になる。 In this case, since the specimens 4 are arranged in a truncated cone shape with a radial cross section, the processing liquid attached to the surface of each specimen 4 is distributed not only in the width direction (radial direction) but also in the length direction ( The flow also reciprocates in the left-right direction (in Fig. 1), and the process liquid can be sprayed without increasing the amount of spray.
The specimen thin section attached to the surface is evenly wetted, so that the specimen thin section can be processed uniformly.
検体薄切片に付着した処理液が十分作用するま
での間、モータ2を緩速で回転させたならば、次
いでモータ2を高速回転させ、標本4,4の表面
に付着している処理液を遠心力により振り飛ば
す。振り飛ばされた用済または余分の処理液は、
カバー6の内面で捕捉されてカバー下端の排出口
9から排出される。 The motor 2 is rotated at a slow speed until the processing liquid adhering to the specimen thin section is sufficiently acted upon, and then the motor 2 is rotated at a high speed to remove the processing liquid adhering to the surface of the specimens 4. It is blown away by centrifugal force. Spent or excess processing liquid that has been shaken off is
It is captured by the inner surface of the cover 6 and discharged from the discharge port 9 at the lower end of the cover.
それまで付着していた処理液が総て振り飛ばさ
れたならば、モータを再び緩速で回転させ、次の
処理液を噴霧して標本4,4に付着させる。この
ようにして、上述の行程を各処理液について繰り
返し、標本の染色を行なう。 When all the processing liquid that had adhered up to that point has been shaken off, the motor is rotated at a slow speed again, and the next processing liquid is sprayed and adhered to the specimens 4, 4. In this way, the above steps are repeated for each treatment solution to stain the specimen.
(発明の効果)
本発明の顕微鏡標本を染色する方法及び装置
は、以上に述べたように構成されかつ実施される
ため、異種の処理液同士が混合して劣化を起すこ
とがなく、常に新鮮な処理液により鮮明な染色処
理を行なうことができる。(Effects of the Invention) Since the method and apparatus for staining a microscopic specimen of the present invention are configured and carried out as described above, different types of processing solutions do not mix with each other and cause deterioration, and are always kept fresh. Clear dyeing can be performed using a clear processing solution.
しかも、標本に噴霧する処理液の量を特に多く
しなくても、標本に付着した薄切片を十分均一に
濡らすことができる為、染色を行なう場合に於け
る運転経費が徒に嵩む事もない。 In addition, the thin sections attached to the specimen can be sufficiently evenly wetted without particularly increasing the amount of processing solution sprayed onto the specimen, so there is no unnecessary increase in operating costs when staining. .
第1〜2図は本発明の装置の実施例を示してお
り、第1図は縦断側面図、第2図は第1図のA−
A断面図、第3図は保持器の主体を示す斜視図、
第4図は同じく抑え板の斜視図である。
1:基台、2:モータ:3:回転軸、4:標
本、5:保持器、6:カバー、7:ノズル、8:
ホース、9:排出口、10:主体、11:抑え
板、12:ナツト片、13:基板部、13:円管
部、15:支持板部、16:雄ねじ、17:立
壁、18:溝、19:切込み、20:円孔、2
1:垂下壁、22:ナツト片、23:フランジ。
Figures 1 and 2 show an embodiment of the device of the present invention, with Figure 1 being a longitudinal sectional side view and Figure 2 being A--A in Figure 1.
A sectional view, FIG. 3 is a perspective view showing the main body of the cage,
FIG. 4 is a perspective view of the holding plate. 1: Base, 2: Motor, 3: Rotating shaft, 4: Specimen, 5: Holder, 6: Cover, 7: Nozzle, 8:
Hose, 9: Discharge port, 10: Main body, 11: Holding plate, 12: Nut piece, 13: Base part, 13: Circular pipe part, 15: Support plate part, 16: Male thread, 17: Vertical wall, 18: Groove, 19: Notch, 20: Circular hole, 2
1: hanging wall, 22: nut piece, 23: flange.
Claims (1)
た複数枚の顕微鏡標本を、断面が放射状で、全体
として円錐台状となるように配列して、水平方向
の軸を中心として緩速回転させつつ、この標本に
一つの処理液を吹き付けた後、この処理液が作用
する間そのまま緩速回転を継続し、その後上記標
本を高速回転させて各標本の表面に付着した処理
液を遠心力により飛散させて排除し、その後再び
標本を緩く回転させつつ行なう別の処理液の吹き
付けおよび高速回転による余分の処理液の排除
を、所定の処理液についてそれぞれ繰り返すこと
を特徴とする顕微鏡標本を染色する方法。 2 病理検体の薄切片をスライドガラスに貼着し
た複数枚の顕微鏡標本を、断面が放射状で、全体
として円錐台状となるように装着でき、中心部に
挿入される水平方向の回転軸に結合される保持器
と、この保持器を回転させるための速度変換自在
なモータと、上記保持器の外周を覆い、下端に排
出口を有するカバーと、このカバー内において保
持器に装着された標本に処理液を吹き付けるため
の噴霧器とから成る顕微鏡標本を染色する装置。[Scope of Claims] 1. A plurality of microscopic specimens in which thin sections of pathological specimens are pasted onto glass slides are arranged so that the cross section is radial and the whole has a truncated conical shape, and the horizontal axis is the center. After spraying one treatment liquid onto this specimen while rotating slowly as shown in FIG. The method is characterized in that the liquid is scattered and removed by centrifugal force, and then the spraying of another processing liquid while gently rotating the specimen and the removal of excess processing liquid by high-speed rotation are repeated for each predetermined processing liquid. How to stain microscopic specimens. 2 Multiple microscopic specimens with thin sections of pathological specimens pasted onto glass slides can be mounted so that the cross section is radial and the whole has a truncated cone shape, and is connected to a horizontal rotating shaft that is inserted into the center. a holder for rotation, a variable speed motor for rotating the holder, a cover that covers the outer periphery of the holder and has a discharge port at the lower end; A device for staining microscopic specimens, consisting of a sprayer for spraying a processing solution.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58120174A JPS6011136A (en) | 1983-06-30 | 1983-06-30 | Method and device for dyeing microscope specimen |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58120174A JPS6011136A (en) | 1983-06-30 | 1983-06-30 | Method and device for dyeing microscope specimen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6011136A JPS6011136A (en) | 1985-01-21 |
| JPH0350972B2 true JPH0350972B2 (en) | 1991-08-05 |
Family
ID=14779748
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58120174A Granted JPS6011136A (en) | 1983-06-30 | 1983-06-30 | Method and device for dyeing microscope specimen |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6011136A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11402305B2 (en) | 2016-01-29 | 2022-08-02 | Sysmex Corporation | Smear staining apparatus, smear preparing apparatus, and smear staining method |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0866748A4 (en) * | 1995-07-24 | 2000-03-01 | Fisher Scient Company Llc | Automated slide staining system |
| JP3667599B2 (en) * | 2000-06-26 | 2005-07-06 | 独立行政法人科学技術振興機構 | Tissue staining device |
| CN104568557A (en) * | 2014-12-22 | 2015-04-29 | 珠海迪尔生物工程有限公司 | Clamp for fixing slide |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6027944B2 (en) * | 1976-10-01 | 1985-07-02 | ロナルド・ダニエル・ホワイト | Microscope specimen slide automatic preparation method and device |
-
1983
- 1983-06-30 JP JP58120174A patent/JPS6011136A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11402305B2 (en) | 2016-01-29 | 2022-08-02 | Sysmex Corporation | Smear staining apparatus, smear preparing apparatus, and smear staining method |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6011136A (en) | 1985-01-21 |
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