JPH01203940A - Cover film for optical microscope observation and its manufacture - Google Patents
Cover film for optical microscope observation and its manufactureInfo
- Publication number
- JPH01203940A JPH01203940A JP2975888A JP2975888A JPH01203940A JP H01203940 A JPH01203940 A JP H01203940A JP 2975888 A JP2975888 A JP 2975888A JP 2975888 A JP2975888 A JP 2975888A JP H01203940 A JPH01203940 A JP H01203940A
- Authority
- JP
- Japan
- Prior art keywords
- cover film
- silicone oil
- amount
- adhesive layer
- solvent
- 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.)
- Pending
Links
- 239000013039 cover film Substances 0.000 title claims abstract description 27
- 230000003287 optical effect Effects 0.000 title claims description 15
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 229920002545 silicone oil Polymers 0.000 claims abstract description 29
- 239000012790 adhesive layer Substances 0.000 claims abstract description 17
- 239000011248 coating agent Substances 0.000 claims abstract description 13
- 238000000576 coating method Methods 0.000 claims abstract description 13
- 239000002904 solvent Substances 0.000 claims abstract description 10
- 239000010410 layer Substances 0.000 claims abstract description 8
- 239000010408 film Substances 0.000 claims abstract description 7
- 239000004014 plasticizer Substances 0.000 claims abstract description 4
- 229920002678 cellulose Polymers 0.000 claims description 10
- 239000001913 cellulose Substances 0.000 claims description 10
- 238000000399 optical microscopy Methods 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 abstract description 17
- 238000000034 method Methods 0.000 abstract description 8
- 238000003860 storage Methods 0.000 abstract description 6
- 229920001296 polysiloxane Polymers 0.000 abstract description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000000853 adhesive Substances 0.000 description 16
- 230000001070 adhesive effect Effects 0.000 description 16
- 239000011521 glass Substances 0.000 description 14
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 230000000903 blocking effect Effects 0.000 description 8
- 239000007787 solid Substances 0.000 description 6
- 238000005538 encapsulation Methods 0.000 description 4
- 239000012046 mixed solvent Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000006059 cover glass Substances 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 235000007173 Abies balsamea Nutrition 0.000 description 2
- 239000004857 Balsam Substances 0.000 description 2
- 229920001747 Cellulose diacetate Polymers 0.000 description 2
- 229920002284 Cellulose triacetate Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 244000018716 Impatiens biflora Species 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000008393 encapsulating agent Substances 0.000 description 2
- 239000012120 mounting media Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 241000134884 Ericales Species 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- -1 dimethylsiloxane Chemical class 0.000 description 1
- KSCFJBIXMNOVSH-UHFFFAOYSA-N dyphylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1N(CC(O)CO)C=N2 KSCFJBIXMNOVSH-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
Landscapes
- Sampling And Sample Adjustment (AREA)
- Microscoopes, Condenser (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はとくに、自動封入に適した光学顕微鏡観察用カ
バーフィルムおよびその製造法に関する。DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention particularly relates to a cover film for optical microscope observation suitable for automatic encapsulation and a method for producing the same.
(従来の技術)
従来、光学顕微鏡観察は被検体をカバーガラスとスライ
ドガラスではさみ、カバーガラスが対物レンズ側になる
ように置いてなされている。しかしながら被検体を2枚
のガラス板で単にはさむだけでは、後日再び同一被検体
を観察することが困難なことが多い。この問題を解決す
るために2枚のガラス板の間にミクロン単位の被検体の
薄片をサンドウィッチにして、光学顕微鏡観察した時の
状態のままで長期間保存するための接着剤が考案され、
この接着剤は封入剤と称されている。(Prior Art) Conventionally, optical microscopic observation has been carried out by sandwiching a subject between a cover glass and a slide glass, with the cover glass facing toward the objective lens. However, simply sandwiching the subject between two glass plates often makes it difficult to observe the same subject again at a later date. To solve this problem, an adhesive was devised to sandwich a micron-sized thin slice of the specimen between two glass plates and preserve it for a long period of time in the same state as when observed with an optical microscope.
This adhesive is called an encapsulant.
封入剤としてよく知られているものとして、バルサム(
Balsam )が挙げられる。しかしながらこれは天
然物であるために産地、精製度、保存条件等によって材
質の不均一性は免れないという欠点がある。このため封
入剤としての合成ポリマー接着剤の検討が試みられてい
る(例えば、秋山太−部、上野部子、臨床検査・196
6年11月)。Balsam (
Balsam). However, since it is a natural product, it has the disadvantage that its quality is inevitably non-uniform depending on the place of production, degree of purification, storage conditions, etc. For this reason, attempts have been made to investigate synthetic polymer adhesives as mounting media (e.g., Taibe Akiyama, Beko Ueno, Clinical Examination, 196
(November 6).
また最近では医学、薬学、生物学、農学および工学上の
要求から数多(の被検体を光学顕微鏡観察する頻度が高
くなってきている。2枚のガラス板の間を薄い封入剤層
で満して固定するための作業は従来殆んど人力で行なわ
れているが、この方式では上記要求に数量的にも時間的
にも対応できない状況になりつつある。この問題を解決
するために、例えば米国特許第4.146.414号、
同第4、203.797号等に記載せる如く、予め透明
支持体上に接着剤を塗布したフィルムを、数滴の有機溶
剤(該接着剤を膨潤あるいは溶解しうるちの)を既に滴
下され、且つ被検体が載せられているスライドガラスに
自動的に重ね合わせて接着させることにより、光学顕微
鏡観察用標本を自動的につくる方法が考案されている。Recently, due to medical, pharmaceutical, biological, agricultural, and engineering requirements, it has become increasingly common to observe a large number of specimens with an optical microscope. Traditionally, most of the fixing work has been done manually, but this method is becoming unable to meet the above requirements both in quantity and time.In order to solve this problem, for example, in the United States, Patent No. 4.146.414,
As described in No. 4, 203.797, etc., a film coated with an adhesive on a transparent support is coated with several drops of an organic solvent (which can swell or dissolve the adhesive). In addition, a method has been devised to automatically create a specimen for optical microscopic observation by automatically superimposing and adhering the specimen to a slide glass on which the specimen is placed.
即ち上記フィルムは従来のカバーガラスの機能と封入剤
の機能を兼ね備えており、以下このようなものをカバー
フィルムと呼ぶ。That is, the above-mentioned film has both the function of a conventional cover glass and the function of a mounting medium, and such a film is hereinafter referred to as a cover film.
(発明が解決しようとする課題)
しかしながら、透明支持体上に予め接着剤を塗布したこ
のカバーフィルムはユーザーがいつでも、どこでも安心
して使用できるためには新たな工夫が必要である。即ち
カバーフィルムはロール状態で保存中に接着剤層とフィ
ルムの裏面(接着剤層と反対側の支持体表面)との間で
いわゆるブロッキングが生じやすい。−旦ブロッキング
が生じると接着剤層がフィルムの裏面に転移したり、接
着剤層表面が不均一になって、顕微鏡観察に必要な充分
な封入が達成できなくなる。(Problems to be Solved by the Invention) However, new innovations are required in order for users to be able to use this cover film, which is a transparent support coated with an adhesive in advance, anytime and anywhere with peace of mind. That is, when the cover film is stored in a roll state, so-called blocking tends to occur between the adhesive layer and the back surface of the film (the surface of the support opposite to the adhesive layer). - Once blocking occurs, the adhesive layer may transfer to the back side of the film or the surface of the adhesive layer may become uneven, making it impossible to achieve sufficient encapsulation necessary for microscopic observation.
このような問題点を解決するため、例えば特開昭62−
38408号にはガラス転移温度が50℃以上のポリマ
ー接着剤を使用することによりブロッキングを防止する
方法が提案されている。確かにこの方法によりある程度
までブロッキングを防止できるが充分とは言えない場合
がある。In order to solve such problems, for example,
No. 38408 proposes a method of preventing blocking by using a polymer adhesive having a glass transition temperature of 50° C. or higher. It is true that this method can prevent blocking to some extent, but it may not be sufficient.
またカバーフィルムを長期間ロール状態で保存すると長
尺方向のカール(いわゆる巻きぐせ〉あるいは幅方向の
カールが生じ、このカーリングの程度が大きいと前記米
国特許第4.146.414号、同第4、203.79
7号等に記載されている自動封入機内でカバーフィルム
がつかえて正常に搬送されなくなったり、カバーフィル
ムとスライドガラスとの接触が不充分で被検体を封入で
きなくなる場合がある。Furthermore, when a cover film is stored in a roll for a long period of time, curling in the longitudinal direction (so-called curling) or curling in the width direction occurs, and if the degree of curling is large, the above-mentioned U.S. Pat. , 203.79
In some cases, the cover film gets stuck in the automatic coverslippers machine described in No. 7, etc. and cannot be transported properly, or the cover film and the slide glass do not come into sufficient contact, making it impossible to cover the specimen.
したがって本発明の目的の一つは保存中にブロッキング
することがなく、しかも少量の有機溶剤に接したときに
迅速に接着するカバーフィルムを提供することにある。Therefore, one of the objects of the present invention is to provide a cover film which does not block during storage and which quickly adheres when it comes into contact with a small amount of organic solvent.
さらに本発明の目的の一つはロール状態で保存された場
合にもカーリングの生じにくいカバーフィルムを提供す
ることにある。Furthermore, one of the objects of the present invention is to provide a cover film that is resistant to curling even when stored in a roll state.
さらに本発明のもう一つの目的は、上記カバーフィルム
の製造法を提供することにある。Furthermore, another object of the present invention is to provide a method for manufacturing the above-mentioned cover film.
(課題を解決するための手段)
上記目的はセルロース系透明支持体の一方の面に接着剤
層を設けてなる光学顕微鏡観察用カバーフィルムにおい
て、他方の面にシリコーンオイル層を3〜10mg/m
″の量で塗設したことを特徴とする光学顕微鏡観察用カ
バーフィルムにより達成できることが分った。上記カバ
ーフィルムは、たとえばセルロース系透明支持体の一方
の面に接着剤層を塗設する工程と、該セルロース系透明
支持体中に含まれる可塑剤を溶解することができ、かつ
シリコーンオイルを溶解することができる溶剤に該シリ
コーンオイルを溶解した溶液を、該シリコーンオイルの
塗布量が3〜Long/m2、該溶剤の塗布量が10〜
25rnl/m″となるように塗布する工程とを含む方
法により製造される。(Means for Solving the Problems) The above object is to provide a cover film for optical microscopy comprising an adhesive layer on one side of a cellulose-based transparent support, and a silicone oil layer of 3 to 10 mg/m on the other side.
It has been found that this can be achieved by a cover film for optical microscopic observation characterized in that it is coated in an amount of Then, a solution of the silicone oil in a solvent that can dissolve the plasticizer contained in the cellulose-based transparent support and can also dissolve the silicone oil is added, so that the coating amount of the silicone oil is 3 to 3. Long/m2, the coating amount of the solvent is 10~
25 rnl/m''.
シリコーンオイルとしては例えば特開昭62−2691
39号に記載されている如きオルガノポリシロキサン、
信越シリコーン■(7)product dataに記
載されている如きジメチルシロキサンに各種の有機基を
導入した変性シリコーンオイル等が挙げられる。これら
シリコーンオイルはアセトン、メチルエチルケトン、メ
タノールとアセトンあるいはメチルエチルケトンとの混
合溶剤、エタノールとアセトンあるいはメチルエチルケ
トンとの混合溶剤等比較的低沸点の有機溶剤に溶解する
ものが好ましい。これらシリコーンオイルの塗布量が少
なすぎるともう一方の面の接着剤層とのブロッキングを
防止する効果が発揮できなくなることがある。またシリ
コーンオイルの塗布量が多すぎるとカバーフィルムをロ
ール状態で保存中にシリコーンオイルがもう一方の面の
接着剤層に転移して、被検体をのせたスライドガラスと
充分に接着する(すなわち被検体を封入する)ことがで
きなくなることがある。シリコーンオイルの塗布量が3
mg/m′〜10mg/rn’であればロール状態で保
存中にブロッキングせず、且つ封入性がよいことが分っ
た。更に好ましいシリコーンオイルの塗布量は51T1
g/コ〜8mg/m′テアル。Examples of silicone oil include JP-A-62-2691
organopolysiloxanes as described in No. 39;
Examples include modified silicone oils in which various organic groups are introduced into dimethylsiloxane as described in Shin-Etsu Silicone (7) Product data. These silicone oils are preferably those that are soluble in organic solvents with relatively low boiling points, such as acetone, methyl ethyl ketone, mixed solvents of methanol and acetone or methyl ethyl ketone, and mixed solvents of ethanol and acetone or methyl ethyl ketone. If the amount of silicone oil applied is too small, the effect of preventing blocking with the adhesive layer on the other side may not be exhibited. In addition, if too much silicone oil is applied, the silicone oil will transfer to the adhesive layer on the other side while the cover film is stored in a roll, resulting in sufficient adhesion to the glass slide on which the subject is placed (i.e., It may become impossible to enclose the specimen. The amount of silicone oil applied is 3
It was found that if the concentration was between mg/m' and 10 mg/rn', no blocking occurred during storage in a roll state, and the encapsulation properties were good. A more preferable coating amount of silicone oil is 51T1.
g/co~8mg/m'theal.
シリコーンオイルを溶かすための溶剤は、塗布した溶剤
の一部がセルロース系支持体中に浸透し支持体中の可塑
剤を溶解して支持体表面にこれを移動せしめる。このた
め、該溶剤を塗布しなかった時とはカーリングの程度お
よびカーリングの方向が変化する。通常、セルロース系
透明支持体の一方の面に接着剤が塗布されただけの系で
は接着剤層側が凹になるようにカールする。またセルロ
ース系透明支持体の一方の面に有機溶剤が塗布されただ
けの系では、有機溶剤が塗布された側が凹になるように
カールする。従ってセルロース系透明支持体の一方の面
に接着剤を塗布し、もう一方の面に有機溶剤を塗布する
ことによりカーリングバランスをとることが可能になる
。接着剤層の塗布量によってカーリングバランスをとる
のに必要な有機溶剤の塗布量の適正値は変るので、適宜
選択すればよい。すなわち、封入のために必要な接着剤
の塗布量は被検体の厚みに依存するが、一般に、接着剤
の塗布量は固形分換算で10g/m″〜30 g /
m2、好ましくは15 g/m’ 〜25 g/m”で
あるので、このようなばあい、カーリングバランスをと
るために必要な有機溶剤の塗布量は1〇−/m′〜25
m1/m”の範囲である。A portion of the applied solvent for dissolving the silicone oil penetrates into the cellulose support, dissolves the plasticizer in the support, and transfers it to the surface of the support. Therefore, the degree of curling and the direction of curling change from when the solvent was not applied. Usually, in a system in which an adhesive is applied to only one side of a cellulose-based transparent support, the adhesive layer side curls in a concave manner. Further, in a system in which only one side of a cellulose-based transparent support is coated with an organic solvent, the side coated with the organic solvent curls in a concave manner. Therefore, by applying an adhesive to one side of the cellulose-based transparent support and applying an organic solvent to the other side, it becomes possible to maintain curling balance. The appropriate amount of organic solvent to be applied to maintain curling balance varies depending on the amount of adhesive layer applied, so it may be selected as appropriate. That is, the amount of adhesive required for encapsulation depends on the thickness of the specimen, but in general, the amount of adhesive applied is 10 g/m'' to 30 g/m'' in terms of solid content.
m2, preferably 15 g/m' to 25 g/m'', so in such a case, the amount of organic solvent applied to balance the curling is 10-/m' to 25 g/m'.
m1/m'' range.
カバーフィルムの支持体は原則的には透明な支持体であ
ればよいが、例えば通常入手できるポリエステル系透明
支持体を用いた場合には5〜10倍程度の低倍率光学顕
微鏡観察では問題ないが、それ以上の倍率での光学顕微
鏡観察ではピントが合わなくなる。その理由はよく分っ
てはいないが、二軸延伸による光学異方性のためと考え
られる。In principle, the support for the cover film may be any transparent support, but for example, if a commonly available polyester transparent support is used, there will be no problem when observed with a low magnification optical microscope of about 5 to 10 times. , it becomes out of focus when observed with an optical microscope at higher magnifications. The reason for this is not well understood, but it is thought to be due to optical anisotropy caused by biaxial stretching.
光学異方性のない透明支持体であればカバーフィルムの
支持体として有用であり、比較的容易に入手できる支持
体としてセルロース系透明支持体を用いた系では400
倍以上の高倍率光学顕微鏡観察が可能である。したがっ
て本発明ではセルロース系支持体を使用する。このよう
なセルロース系支持体の例としては、セルローストリア
セテート、セルロースジアセテートおよびセルロースア
セテートブチレート等が挙げられる。これら支持体の厚
さは一般に50μm〜250μm1好ましくは100μ
m〜150μmが適当である。これら支持体には写真感
光材料業界ではよく知られている下びき層が塗設されて
いたり紫外線照射、コロナ放電あるいはグロー放電等の
表面処理がなされていてもよい。A transparent support without optical anisotropy is useful as a support for a cover film, and a system using a cellulose-based transparent support as a relatively easily available support has a
High-magnification optical microscopic observation is possible. Therefore, a cellulosic support is used in the present invention. Examples of such cellulosic supports include cellulose triacetate, cellulose diacetate, cellulose acetate butyrate, and the like. The thickness of these supports is generally 50 μm to 250 μm, preferably 100 μm.
m to 150 μm is suitable. These supports may be coated with a subbing layer well known in the photographic material industry, or may be subjected to surface treatments such as ultraviolet irradiation, corona discharge or glow discharge.
本発明に使用される接着剤の例としては特開昭62−3
8408号に記載されている如きアクリル系ポリマー接
着剤あるいはポリエステル系接着剤が挙げられる。Examples of adhesives used in the present invention include JP-A No. 62-3
Examples include acrylic polymer adhesives or polyester adhesives such as those described in No. 8408.
本発明のカバーフィルムを製造するばあい、接着剤層と
シリコーンオイル層は、いずれか一方を支持体上に塗設
してから他方を塗設してもよいし両者を同時に塗設して
もよい。When producing the cover film of the present invention, either one of the adhesive layer and the silicone oil layer may be coated on the support before the other, or both may be coated at the same time. good.
(発明の効果)
本発明の光学顕微鏡観察用カバーフィルムはロール状態
で保存してもブロッキングを生じることがなく、またカ
ーリングを生じにくい。したがって自動封入機内でつか
えることなく正常に搬送され、またカバーフィルムとス
ライドガラスとの接触が充分に行われるため、被検体の
封入不良を起こすことがほとんどない。(Effects of the Invention) The cover film for optical microscopic observation of the present invention does not cause blocking even when stored in a roll state, and is less likely to curl. Therefore, the specimen is transported normally without getting jammed in the automatic coverslipping machine, and the cover film and the slide glass are sufficiently contacted, so that there is almost no possibility of failure to cover the specimen.
以下実施例により本発明を更に詳細に説明する。The present invention will be explained in more detail with reference to Examples below.
実施例1
130μmの厚さの透明なセルローストリアセテート支
持体の一方の面に、酢酸エチルとトルエンが1=1(容
積比)の混合溶媒に溶かした接着剤アロンS−1017
(ガラス転移温度87℃、東亜合成化学工業株式会社、
日本)とアロンS−1030C(ガラス転移温度52℃
、同)を固型分重量比で4=6の割合でブレンドし、全
固形分塗布量が20g/m゛になるように塗布し試料(
a)を作成した。このときの溶媒塗布量はトルエン
30−/m2、酢酸エチル30m!/m″であった。こ
の試料(a)のもう一方の面に第1表に示されるように
アセトンまたはシリコーンオイル(KF−945(A)
)のアセトン溶液を塗布し、試料(b)、(C)およ
び(d)を作成した。Example 1 Adhesive Aron S-1017 prepared by dissolving ethyl acetate and toluene in a mixed solvent of 1=1 (volume ratio) was applied to one side of a 130 μm thick transparent cellulose triacetate support.
(Glass transition temperature 87℃, Toagosei Chemical Industry Co., Ltd.,
Japan) and Aron S-1030C (glass transition temperature 52℃
, the same) were blended at a solid content weight ratio of 4 = 6 and applied so that the total solid content coating amount was 20 g/m゛.
a) was created. The amount of solvent applied at this time was 30 m2 of toluene and 30 m2 of ethyl acetate! The other side of sample (a) was coated with acetone or silicone oil (KF-945(A)) as shown in Table 1.
) was applied to prepare samples (b), (C) and (d).
第 1 表
上記試料を幅24mmにスリットし、径が126mmの
巻芯に、封入剤層が巻芯側に向くように各々60mずつ
巻きつけた。この巻きつけた試料を3日間室温保存した
。この試料を、カバーエイド自動封入装置5CA−18
00(サクラ精機株式会社、日本)を用いてスライドガ
ラスと貼合わせた。全試料とも貼合せは良好であった。Table 1 The above samples were slit to a width of 24 mm, and each sample was wound by 60 m around a core having a diameter of 126 mm, with the encapsulant layer facing toward the core. This wound sample was stored at room temperature for 3 days. This sample was transferred to the CoverAid automatic enclosing device 5CA-18.
00 (Sakura Seiki Co., Ltd., Japan) to attach it to a slide glass. Bonding was good for all samples.
また、上記試料をロール状態で40℃、80%RH(相
対湿度)で3日間保存した後、同様な操作でスライドガ
ラスとの貼合せを試みた。結果を第2表に示す。Further, after storing the above sample in a roll state at 40° C. and 80% RH (relative humidity) for 3 days, lamination with a slide glass was attempted in the same manner. The results are shown in Table 2.
第 2 表 40℃、80%R)l 3日間保存後
の貼合せ結果
第2表から接着剤層と反対側に有機溶剤の塗布量が20
rn1/m’になるようシリコーンオイルの有機溶剤溶
液を塗設したカバーフィルムは高温高湿下で保存されて
もスライドガラスとの貼合せが可能であることが分る。Table 2 Lamination results after storage at 40℃, 80%R)l for 3 days From Table 2, the amount of organic solvent applied on the side opposite to the adhesive layer was
It can be seen that the cover film coated with an organic solvent solution of silicone oil so as to have rn1/m' can be attached to a slide glass even when stored under high temperature and high humidity.
シリコーンオイル層がないとブロッキングが生じ易く、
また有機溶媒を塗布しないばあい、ならびに多量の有機
溶媒を塗布したばあいにはいずれもカーリングのため貼
合せが不良になることが分る。Without a silicone oil layer, blocking is likely to occur,
It is also found that when no organic solvent is applied and when a large amount of organic solvent is applied, bonding becomes poor due to curling.
実施例2
150μmの厚さの透明なセルロースジアセテート支持
体の一方の面の上に、接着剤アロンS−1017とアロ
ンS−1030C(固形分重量比=1:1)を酢酸エチ
ルとトルエンが7:3(容積比)の混合溶媒に溶かした
溶液を、全固形分塗布量が25g/ゴになるように塗布
し試料(e)を作成した。このときトルエンの塗布量は
39mj!/m2、酢酸エチルの塗布量は70mA’/
m″であった。この試料(e)のもう一方の面の上に第
3表に示すように、有機溶媒のみ、またはシリコーンオ
イル(にF−353)の有機溶媒溶液を塗布し、試料(
f)および(母を作成した。Example 2 Adhesives Aron S-1017 and Aron S-1030C (solid weight ratio = 1:1) were coated with ethyl acetate and toluene on one side of a 150 μm thick transparent cellulose diacetate support. A sample (e) was prepared by applying a solution dissolved in a mixed solvent of 7:3 (volume ratio) so that the total solid content coating amount was 25 g/g. At this time, the amount of toluene applied was 39mj! /m2, the amount of ethyl acetate applied is 70mA'/
m''.On the other side of this sample (e), as shown in Table 3, an organic solvent alone or an organic solvent solution of silicone oil (F-353) was applied.
f) and (created mother.
第 3 表
上記試料を作成後ロール状態で50℃、15%RHで2
日間保存した後、カバーエイド自動封入装置でスライド
ガラスとの貼合せを試みた。結果を第4表に示す。Table 3 After preparing the above sample, it was rolled at 50℃ and 15%RH for 2 hours.
After storing it for a day, we attempted to attach it to a glass slide using a CoverAid automatic coverslipper. The results are shown in Table 4.
第4表から接着剤層と反対側にシリコーンオイルの有機
溶剤溶液を塗設したカバーフィルムハ高温下で保存され
てもスライドガラスとの貼合せが可能であることが分る
。Table 4 shows that the cover film coated with an organic solvent solution of silicone oil on the side opposite to the adhesive layer can be bonded to a glass slide even if it is stored at high temperatures.
実施例3
120μmの厚さの透明なセルロースアセテートブチレ
ート支持体の一方の面の上に酢酸エチルとトルエンが1
=1(容積比)の混合溶媒に溶かしたバイロン200(
東洋紡績株式会社、日本)を固形分塗布量が15g/r
n’になるように塗布した。このとき溶媒の塗布量は酢
酸エチル40m1!/m゛、トルエン40mA’/m’
であった。この支持体のもう一方の面の上に第5表に示
されるシリコーンオイルの有機溶媒溶液を塗布し、試料
(5)および(1)を作成した。Example 3 Ethyl acetate and toluene were deposited on one side of a 120 μm thick transparent cellulose acetate butyrate support.
Byron 200 (
Toyobo Co., Ltd., Japan) with a solid content coating amount of 15g/r.
It was applied so that it became n'. At this time, the amount of solvent applied was 40ml of ethyl acetate! /m゛, toluene 40mA'/m'
Met. On the other side of this support, a solution of silicone oil in an organic solvent shown in Table 5 was applied to prepare samples (5) and (1).
第 5 表
上記試料(社)および(1)をロール状態で、45℃、
20%RH17日間保存した後カバーエイド自動封入装
置でスライドガラスと貼り合せを試みた。結果を第6表
に示す。Table 5 The above samples (Company) and (1) were rolled at 45°C.
After storing the sample at 20% RH for 17 days, it was attempted to be attached to a slide glass using a CoverAid automatic coverslipper. The results are shown in Table 6.
第 6 表 45℃、20%RH7日間保存後の貼合
せ結果
第6表からシリコーンオイルが多すぎてもスライドガラ
スとの貼合せができないことが分る。Table 6: Lamination results after storage at 45° C. and 20% RH for 7 days From Table 6, it can be seen that even if there is too much silicone oil, the sample cannot be laminated with a glass slide.
**
Claims (2)
設けてなる光学顕微鏡観察用カバーフィルムにおいて、
他方の面にシリコーンオイル層を3〜10mg/m^2
の量で塗設したことを特徴とする光学顕微鏡観察用カバ
ーフィルム。(1) In a cover film for optical microscope observation, which is formed by providing an adhesive layer on one side of a cellulose-based transparent support,
Silicone oil layer on the other side 3~10mg/m^2
A cover film for optical microscope observation, characterized in that it is coated in an amount of .
塗設する工程と、該セルロース系透明支持体中に含まれ
る可塑剤を溶解することができ、かつシリコーンオイル
を溶解することができる溶剤に該シリコーンオイルを溶
解した溶液を、該シリコーンオイルの塗布量が3〜10
mg/m^2、該溶剤の塗布量が10〜25ml/m^
2となるように塗布する工程とを含む、請求項(1)記
載の光学顕微鏡観察用カバーフィルムの製造法。(2) A step of coating an adhesive layer on one side of the cellulose-based transparent support, and a step that can dissolve the plasticizer contained in the cellulose-based transparent support and also dissolve the silicone oil. A solution prepared by dissolving the silicone oil in a solvent that can be applied is applied until the coating amount of the silicone oil is 3-10.
mg/m^2, the coating amount of the solvent is 10 to 25 ml/m^
2. The method for producing a cover film for optical microscopy according to claim 1, comprising the step of applying the film in such a manner that the amount of the cover film becomes 2.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2975888A JPH01203940A (en) | 1988-02-10 | 1988-02-10 | Cover film for optical microscope observation and its manufacture |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2975888A JPH01203940A (en) | 1988-02-10 | 1988-02-10 | Cover film for optical microscope observation and its manufacture |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01203940A true JPH01203940A (en) | 1989-08-16 |
Family
ID=12284978
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2975888A Pending JPH01203940A (en) | 1988-02-10 | 1988-02-10 | Cover film for optical microscope observation and its manufacture |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01203940A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH049009U (en) * | 1990-05-11 | 1992-01-27 | ||
WO2021251424A1 (en) * | 2020-06-12 | 2021-12-16 | 富士フイルム株式会社 | Encapsulation method |
WO2023054048A1 (en) * | 2021-09-30 | 2023-04-06 | 富士フイルム株式会社 | Cover film |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4828542A (en) * | 1971-08-18 | 1973-04-16 | ||
JPS53144761A (en) * | 1977-05-23 | 1978-12-16 | Saitorogisuka Sentoraruraborat | Method and equipment of fixing piece of cover on slide holding microscope specimen |
JPS60206842A (en) * | 1984-03-30 | 1985-10-18 | Uchiyama Mfg Corp | Surface treating liquid |
JPS6238408A (en) * | 1985-08-13 | 1987-02-19 | Fuji Photo Film Co Ltd | Cover film for microscope |
JPS6273941A (en) * | 1985-09-26 | 1987-04-04 | モ−ビル オイル コ−ポレ−ション | Heat sealable film laminate |
JPS62269139A (en) * | 1986-05-16 | 1987-11-21 | Konika Corp | Photographic sensitive material improved in transferability of organopolysiloxane |
-
1988
- 1988-02-10 JP JP2975888A patent/JPH01203940A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4828542A (en) * | 1971-08-18 | 1973-04-16 | ||
JPS53144761A (en) * | 1977-05-23 | 1978-12-16 | Saitorogisuka Sentoraruraborat | Method and equipment of fixing piece of cover on slide holding microscope specimen |
JPS60206842A (en) * | 1984-03-30 | 1985-10-18 | Uchiyama Mfg Corp | Surface treating liquid |
JPS6238408A (en) * | 1985-08-13 | 1987-02-19 | Fuji Photo Film Co Ltd | Cover film for microscope |
JPS6273941A (en) * | 1985-09-26 | 1987-04-04 | モ−ビル オイル コ−ポレ−ション | Heat sealable film laminate |
JPS62269139A (en) * | 1986-05-16 | 1987-11-21 | Konika Corp | Photographic sensitive material improved in transferability of organopolysiloxane |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH049009U (en) * | 1990-05-11 | 1992-01-27 | ||
WO2021251424A1 (en) * | 2020-06-12 | 2021-12-16 | 富士フイルム株式会社 | Encapsulation method |
WO2023054048A1 (en) * | 2021-09-30 | 2023-04-06 | 富士フイルム株式会社 | Cover film |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH0519684B2 (en) | ||
US4545831A (en) | Method for transferring a thin tissue section | |
JPH0142041Y2 (en) | ||
Blackstad | Electron microscopy of Golgi preparations for the study of neuronal relations | |
Nakamura et al. | Experimental studies of the shape and structure of isolated cardiac jelly | |
EP3313918A1 (en) | High-transparency coated cellulose triacetate film and dissolver medium | |
PT99045B (en) | ELECTRIC CONDENSER AND PROCESS FOR THEIR MANUFACTURE | |
JP5608282B2 (en) | Polymer membrane with human skin-like permeability and use thereof | |
JPH01203940A (en) | Cover film for optical microscope observation and its manufacture | |
Kunz et al. | Downregulation of extraembryonic tension controls body axis formation in avian embryos | |
Lengerer et al. | The structural and chemical basis of temporary adhesion in the sea star Asterina gibbosa | |
JPH11101943A (en) | Cover film for microscope | |
Sawaguchi et al. | Direct attachment of cell suspensions to high‐pressure freezing specimen planchettes | |
Matthaei et al. | Tissue microarray analysis of cyclin-dependent kinase inhibitors p21 and p16 in Fuchs dystrophy | |
RU2386137C1 (en) | Coat of slides for immunocytochemical and histological studies | |
GB2163866A (en) | Grating film for quantitative or semi-quantitative microscopic evaluation of biological specimens | |
JPH02210265A (en) | Analysis element | |
Zientara et al. | How to test adhesive strength: a biomechanical testing for aortic glue used in type a dissection repair | |
Mazzarella et al. | Cardiovascular prosthetic surgery: an analysis of cellular and molecular patterns underlying valve implantation failure | |
US3673037A (en) | Method of making a laminated article comprising blood or skin tissue samples | |
Lamberger et al. | Streamlining the Highly Reproducible Fabrication of Fibrous Biomedical Specimens toward Standardization and High Throughput | |
Sayk et al. | Significant damage of the conduction system during cardioplegic arrest is due to necrosis not apoptosis | |
JPS58170499A (en) | Analytical element for measuring lap | |
CN115219308A (en) | Slice making method and imaging method for high-resolution imaging of complete thick biological tissue | |
Allt et al. | Distribution of filipin-sterol complexes in the myelinated nerve fiber |