JPH0328759A - Wick for optical train - Google Patents

Wick for optical train

Info

Publication number
JPH0328759A
JPH0328759A JP16485989A JP16485989A JPH0328759A JP H0328759 A JPH0328759 A JP H0328759A JP 16485989 A JP16485989 A JP 16485989A JP 16485989 A JP16485989 A JP 16485989A JP H0328759 A JPH0328759 A JP H0328759A
Authority
JP
Japan
Prior art keywords
sample
wick
cup
area
optical train
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
Application number
JP16485989A
Other languages
Japanese (ja)
Inventor
Hiroshi Terajima
博 寺嶋
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jeol Ltd
Original Assignee
Jeol Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Jeol Ltd filed Critical Jeol Ltd
Priority to JP16485989A priority Critical patent/JPH0328759A/en
Publication of JPH0328759A publication Critical patent/JPH0328759A/en
Pending legal-status Critical Current

Links

Landscapes

  • Investigating Or Analysing Materials By Optical Means (AREA)

Abstract

PURPOSE:To improve the detection sensitivity of an analysis by reducing the size of the shape of the wick for the optical train used when the analysis is taken by thin layer chromatography (TLC). CONSTITUTION:The wick 1 is arranged in the optical train 2 and the area of the tip part where the wick 1 abuts on a sample cup 3 is set smaller than the area of any other end part. Respective samples expanded on a TLC plate for a qualitative analyzing method spreads over the surface of the cup 3 eventually, but the amount of the samples is extremely small, the sample amount per unit area becomes small, so the detection sensitivity becomes inferior as a result. For the purpose, the tip part of the wick 1 on the side of the sample cup 3 is made, for example, conic and then the area of the cup 3 can be made small to concentrate the sample in a narrow range, so the samples can be analyzed with good sensitivity even when the amount is extremely small.

Description

【発明の詳細な説明】 [産業上の利用分野コ 本発明は、ンンレイヤクロマトグラフィー(ThIn 
Layer Chromatography:以下、T
LCと称す)と赤外線分光計とを組み合わせて定性分析
を行う場合に使用するオブチトレインに係り、特に、T
LCプレートと試料カップとの間に介在するウィックの
形状に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention is directed to thin layer chromatography (ThIn
Layer Chromatography: Hereafter, T
In particular, T
This relates to the shape of the wick interposed between the LC plate and the sample cup.

[従来の技術コ 従来、TLCと赤外線分光計とを組み合わせて定性分析
を行うことが知られている。その概略を第2図、第3図
、第4図および第5図を参照して説明する。
[Prior Art] Conventionally, it has been known to perform qualitative analysis by combining TLC and an infrared spectrometer. The outline thereof will be explained with reference to FIGS. 2, 3, 4, and 5.

まず、第2図に示すように、2.5cmX40cm程度
の大きさのTLCプレート11にサンプル13を付着さ
せ、展開槽10の中で適当な有機溶媒からなる展開溶媒
12に浸す。これにより、サンプル13中の各成分(以
下、これを試料と称す)は図中の矢印の方向に移動し、
14、15、18で示すように各試料毎に分離される。
First, as shown in FIG. 2, a sample 13 is attached to a TLC plate 11 having a size of about 2.5 cm x 40 cm, and immersed in a developing solvent 12 made of a suitable organic solvent in a developing tank 10. As a result, each component in the sample 13 (hereinafter referred to as the sample) moves in the direction of the arrow in the figure.
Each sample is separated as shown by 14, 15, and 18.

これが1回目の展開である。なお、TLCプレート11
は、通常、ガラス基板にンリカゲルを塗布して形成され
る。
This is the first development. In addition, TLC plate 11
is usually formed by coating a glass substrate with linica gel.

試料の展開が終了すると、TLCプレー}11は展開槽
10から取り出され、第3図に示すようにオプチトレイ
ン17にネジ19により取り付けられ、固定される。オ
プチトレイン17の上面には、直径が約1 mmの開口
が約1.61Imlのピッチで複数個形成されている。
When the development of the sample is completed, the TLC plate 11 is taken out from the development tank 10, and as shown in FIG. 3, it is attached and fixed to the Optitrain 17 with screws 19. A plurality of openings each having a diameter of approximately 1 mm are formed on the upper surface of the OptiTrain 17 at a pitch of approximately 1.61 Iml.

これが試料カップ18である。This is the sample cup 18.

第3図のA−Aにおける断面を第4図に示すが、試料カ
ップ18の内部には、例えばTIガラス(G e2es
 b+2s eae)等の赤外透過性粉体が充填されて
いる。また、試料カップ18の底部には、その一端が赤
外透過性粉体に接するように、多孔質のステンレスから
なる円柱状のウィック22が配置されている。TLCプ
レート11の試料が展開された側はネジl9により当該
ウィック22の側壁に接触するように固定されている。
FIG. 4 shows a cross section taken along line A-A in FIG.
It is filled with infrared transparent powder such as b+2s eae). Further, a cylindrical wick 22 made of porous stainless steel is arranged at the bottom of the sample cup 18 so that one end thereof is in contact with the infrared transparent powder. The side of the TLC plate 11 on which the sample was developed is fixed by screws 19 so as to be in contact with the side wall of the wick 22.

さて、第3図に示す状態で2回目の展開を行う。Now, the second expansion is performed in the state shown in FIG.

即ち、TLCプレート11をオプチトレイン17に取り
付けた状態で、第5図に示すように、展開槽20の中に
TLCプレート11を横倒の状態で配置し、適当な展開
溶媒21に浸すことによって試料を1回目の展開の方向
と直角方向に展開するのである。このことにより、TL
Cプレート11に展開された各試料は展開溶媒と共に第
5図の矢印の方向に移動し、最終的には、第4図のウィ
ック22を通って試料カップ18に充増された粉体に浸
透する。なお、試料の展開速度は展開溶媒2■を適宜選
択することで制御することができる。
That is, with the TLC plate 11 attached to the Optitrain 17, as shown in FIG. The sample is developed in a direction perpendicular to the direction of the first development. By this, T.L.
Each sample developed on the C plate 11 moves in the direction of the arrow in FIG. 5 together with the developing solvent, and finally penetrates into the powder filled in the sample cup 18 through the wick 22 in FIG. do. Incidentally, the developing speed of the sample can be controlled by appropriately selecting the developing solvent 2.

2回目の展開が終了した後、試料カップ18の表面に乾
燥空気あるいは窒素ガス等を吹き付けて展開溶媒を除去
し、試料だけを残した状態で各試料カップ18に順次赤
外線を照射し、その反射光を検出、分析することで各試
料の定性分析を行うことができる。
After the second development is completed, dry air or nitrogen gas is blown onto the surface of the sample cup 18 to remove the developing solvent, and each sample cup 18 is sequentially irradiated with infrared rays, leaving only the sample, and its reflection is measured. Qualitative analysis of each sample can be performed by detecting and analyzing light.

[発明が解決しようとする課題コ 以上のようにして試料の定性分析を行うことができるの
であるが、微量な試料に対しては感度よく分析できない
という問題があり、実際、上述した方法においては、試
料の検出限界は100〜200ng程度である。
[Problems to be Solved by the Invention] Qualitative analysis of a sample can be performed in the above manner, but there is a problem that it is not possible to analyze a minute amount of sample with high sensitivity. , the detection limit of the sample is about 100 to 200 ng.

本発明は、上記の課題を解決するものであって、感度よ
く定性分析を行うことができるオプチトレイン用ウィッ
クを提供することを目的とするものである。
The present invention solves the above-mentioned problems, and aims to provide a wick for OptiTrain that allows qualitative analysis to be performed with high sensitivity.

[課題を解決するための手段] 」二記の目的を達成するために、本発明のオプチトレイ
ン用ウィックは、オプチトレイン内部に配置され、試料
が展開されたプレートと試料力・ノブとの間に介在する
オプチトレイン用ウィックにおいて、当該ウィソクの試
料カップに当接する先端部の面積が他端部の面積より小
さくなされていることを特徴とする。
[Means for Solving the Problems] In order to achieve the above two objects, the wick for OptiTrain of the present invention is arranged inside the OptiTrain, and is arranged between the plate on which the sample is developed and the sample force/knob. A wick for OptiTrain interposed therein is characterized in that the area of the tip of the wick that comes into contact with the sample cup of the wick is smaller than the area of the other end.

[作用および発明の効果コ 本発明は、ウイックの試料力・ンプに当接する側の面積
が小さくなされているので、試料を狭い範囲に濃縮する
ことができ、従って試料力・ンプ内の試料の密度を上げ
ることができるので、検出感度を向上させることができ
る。
[Operation and Effects of the Invention] In the present invention, the area of the side of the wick that comes into contact with the sample force/pump is made small, so the sample can be concentrated in a narrow range. Since the density can be increased, detection sensitivity can be improved.

[実施例] 以下、図面を参照しつつ実施例を説明する。[Example] Examples will be described below with reference to the drawings.

第1図は、本発明に係るオプチトレイン用ウイックの1
実施例の構成を示す断面図であり、図中、1はウィック
、2はオプチトレイン、3は試料カップを示す。
FIG. 1 shows one of the wicks for OptiTrain according to the present invention.
1 is a cross-sectional view showing the configuration of an example, in which 1 indicates a wick, 2 indicates an optitrain, and 3 indicates a sample cup.

さて、従来例の定性分析方法において、検出感度がよく
ない原因を考察してみると、試料力・ンプ18の面積が
大きいことが最犬の原因であることが判明した。つまり
、各試料はほぼ均一に試料カップ18の表面に広がるか
ら、試料が微量の場合は試料の密度、即ち単位面積当り
の試料量が非常に少なくなり、その結果検出感度が悪い
ものになってしまうのである。
Now, when we considered the reason why the detection sensitivity was not good in the conventional qualitative analysis method, it was found that the main reason was that the sample force and the area of the pump 18 were large. In other words, since each sample spreads almost uniformly on the surface of the sample cup 18, when the sample is in a small amount, the density of the sample, that is, the amount of sample per unit area, becomes very small, resulting in poor detection sensitivity. It's put away.

そこで、本発明においては、第1図に示すように、ウィ
ソク1の試料カップ3側の先端部の形状を円鉛.状とし
た。
Therefore, in the present invention, as shown in FIG. 1, the tip of the sample cup 3 side of the Wisok 1 is shaped like a circular lead. It was made into a state.

これによって、試料カップ3の面積を、第4図に示す従
来の試料カップ18に比して小さくすることができ、従
って、第4図に示すウィック22に比較して試料の密度
を上げることができる。
As a result, the area of the sample cup 3 can be made smaller compared to the conventional sample cup 18 shown in FIG. 4, and therefore the density of the sample can be increased compared to the wick 22 shown in FIG. can.

つまり、本発明は、試料を狭い範囲に濃縮するものであ
るから、試料が微量な場合にも感度よく分析を行うこと
ができるのである。
In other words, since the present invention concentrates the sample in a narrow range, it is possible to perform analysis with high sensitivity even when the sample is in a trace amount.

以上、本発明の1実施例を説明したが、本発明は上記実
施例に限定されるものではなく、種々の変形が可能であ
る。即ち、上記実施例ではウイ・ンク1の先端部を円錐
状としたが、これは発明の木質ではなく、要するに、試
料力・ソプに当接する先端部の面積が他端部の面積より
小さくなる形状ならどのようなものでもよいことは当業
者に明らかである。
Although one embodiment of the present invention has been described above, the present invention is not limited to the above embodiment, and various modifications are possible. That is, in the above embodiment, the tip of wink 1 is conical, but this is not the wood of the invention, and in short, the area of the tip that comes into contact with the sample force is smaller than the area of the other end. It will be clear to those skilled in the art that any shape may be used.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の1実施例の構成を示す断面図、第2図
、第3図、第4図、第5図はTLCと赤外分光計を組み
合わせた定性分析法を説明するための図であり、第2図
は1回目の展開を説明する図、第3図はTLCプレート
をオプチトレインに固定した状態を示す図、第4図は第
3図のA’−Aにおける断面図、第5図は2回目の展開
を説明する図である。 1・・・ウィック、2・・・オプチトレイン、3・・・
試料カップ。 出  願  人 日本電子株式会社
FIG. 1 is a sectional view showing the configuration of one embodiment of the present invention, and FIGS. 2, 3, 4, and 5 are diagrams for explaining a qualitative analysis method combining TLC and an infrared spectrometer. FIG. 2 is a diagram explaining the first deployment, FIG. 3 is a diagram showing a state in which the TLC plate is fixed to Optitrain, and FIG. 4 is a cross-sectional view taken along A'-A in FIG. 3. FIG. 5 is a diagram illustrating the second development. 1...Wick, 2...Optitrain, 3...
sample cup. Applicant: JEOL Ltd.

Claims (1)

【特許請求の範囲】[Claims] (1)オプチトレイン内部に配置され、試料が展開され
たプレートと試料カップとの間に介在するオプチトレイ
ン用ウィックにおいて、当該ウィックの試料カップに当
接する先端部の面積が他端部の面積より小さくなされて
いることを特徴とするオプチトレイン用ウィック。
(1) In the OptiTrain wick that is placed inside the OptiTrain and interposed between the plate on which the sample is spread and the sample cup, the area of the tip of the wick that comes into contact with the sample cup is larger than the area of the other end. A wick for OptiTrain that is characterized by its small size.
JP16485989A 1989-06-26 1989-06-26 Wick for optical train Pending JPH0328759A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16485989A JPH0328759A (en) 1989-06-26 1989-06-26 Wick for optical train

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16485989A JPH0328759A (en) 1989-06-26 1989-06-26 Wick for optical train

Publications (1)

Publication Number Publication Date
JPH0328759A true JPH0328759A (en) 1991-02-06

Family

ID=15801275

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16485989A Pending JPH0328759A (en) 1989-06-26 1989-06-26 Wick for optical train

Country Status (1)

Country Link
JP (1) JPH0328759A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8491148B2 (en) 2007-10-27 2013-07-23 Osram Sylvania Inc. Chambered waterproof lamp assembly having a transparent cover switch activator

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8491148B2 (en) 2007-10-27 2013-07-23 Osram Sylvania Inc. Chambered waterproof lamp assembly having a transparent cover switch activator

Similar Documents

Publication Publication Date Title
EP0348006B2 (en) Liquid transport device and diagnostic assay device
Schmalzing et al. Immunoassay for thyroxine (T4) in serum using capillary electrophoresis and micromachined devices
SE7902734L (en) METHOD AND APPARATUS FOR ANALYSIS OF BLOOD
ATE425450T1 (en) METHOD FOR PHOTOMETRIC EVALUATION OF TEST ELEMENTS
DE69718438D1 (en) METHOD AND DEVICE FOR MALDI ANALYSIS
JPS5571942A (en) Ionic sample activating measuring device
JPS589040A (en) Selective analyzing method for separate trace quantity component in gas and liquid
ES549194A0 (en) BLOOD ANALYSIS METHOD AND CORRESPONDING DEVICE
IT7921220A0 (en) PROCESS AND REAGENT FOR THE DETERMINATION OF BIOLOGICALLY ACTIVE HEPARIN IN PLASMA.
ES489644A0 (en) A METHOD OF DETERMINING THE QUANTITY OR CONCENTRATION OF AN ANALYTE IN A SAMPLE
CN100347547C (en) Chromatogrphy quantitative measurement device, chromatography, quantitative measurement method, and chromatography test piece used therefor
EP0113118A3 (en) Photometric measurement and cuvette for carrying out the measurement
DE3850249D1 (en) DETECTION OF ANALYTES IN SAMPLE CONTAINING PARTICLES.
JPH0328759A (en) Wick for optical train
US4812241A (en) Sample transfer for infrared analysis in thin layer chromatography-structure & method
JPH05157699A (en) Light emitting sample testing apparatus
EP0123443A3 (en) Method of analyzing whole blood sample
TW429312B (en) Method and apparatus for the rapid screening of analytes
WO1992013229A3 (en) Analysis method by capillary electrophoresis with fluorescence detection
US20020024018A1 (en) Method of measuring phosphorescence or fluorescence
JPH1164279A (en) Microchip electrophoresis apparatus
JP3405162B2 (en) Microchip electrophoresis device
CN209764812U (en) High-sensitivity thin-layer chromatographic plate
JPH0363567A (en) Transfer method for choromatograph
JPH11326274A (en) Member for electrophoresis