JPH03245049A - Liquid-sample analyzing disk - Google Patents
Liquid-sample analyzing diskInfo
- Publication number
- JPH03245049A JPH03245049A JP4227590A JP4227590A JPH03245049A JP H03245049 A JPH03245049 A JP H03245049A JP 4227590 A JP4227590 A JP 4227590A JP 4227590 A JP4227590 A JP 4227590A JP H03245049 A JPH03245049 A JP H03245049A
- Authority
- JP
- Japan
- Prior art keywords
- disk
- electrodes
- analysis
- sample
- liquid sample
- 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
- 238000004458 analytical method Methods 0.000 claims abstract description 42
- 239000007788 liquid Substances 0.000 claims abstract description 29
- 239000000758 substrate Substances 0.000 claims abstract description 21
- 238000011161 development Methods 0.000 claims description 8
- 230000003287 optical effect Effects 0.000 abstract description 19
- 230000008859 change Effects 0.000 abstract description 4
- 238000000034 method Methods 0.000 description 11
- 238000005259 measurement Methods 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 5
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 239000012212 insulator Substances 0.000 description 4
- 229910052946 acanthite Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- -1 graphite Chemical class 0.000 description 3
- 229940056910 silver sulfide Drugs 0.000 description 3
- XUARKZBEFFVFRG-UHFFFAOYSA-N silver sulfide Chemical compound [S-2].[Ag+].[Ag+] XUARKZBEFFVFRG-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000012491 analyte Substances 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000004451 qualitative analysis Methods 0.000 description 2
- 238000004445 quantitative analysis Methods 0.000 description 2
- 230000001235 sensitizing effect Effects 0.000 description 2
- 230000007480 spreading Effects 0.000 description 2
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 230000005374 Kerr effect Effects 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 229910021612 Silver iodide Inorganic materials 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000000427 antigen Substances 0.000 description 1
- 230000000890 antigenic effect Effects 0.000 description 1
- 102000036639 antigens Human genes 0.000 description 1
- 108091007433 antigens Proteins 0.000 description 1
- 238000010876 biochemical test Methods 0.000 description 1
- 239000000337 buffer salt Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 150000002843 nonmetals Chemical class 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- SWZDQOUHBYYPJD-UHFFFAOYSA-N tridodecylamine Chemical compound CCCCCCCCCCCCN(CCCCCCCCCCCC)CCCCCCCCCCCC SWZDQOUHBYYPJD-UHFFFAOYSA-N 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
Landscapes
- Optical Measuring Cells (AREA)
- Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、液体試料の分析、例えば液体試料中の特定成
分を定量する際に用いる分析用ディスクに関し、特に光
学的方法て検出てきない対象物の測定を行なえるように
した液体試料分析用ディスクに関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to an analytical disk used for analyzing a liquid sample, for example, quantifying a specific component in a liquid sample, and in particular for analyzing a target that cannot be detected by optical methods. This invention relates to a liquid sample analysis disk that can be used to measure objects.
[従来の技術]
血清などの液体試料を分析して、各種の物質、例えば、
ホルモン、ビタミン、脂質、酵素、含窒′業物質、糖類
、抗原性物質などの存在及び/または濃度を測定するこ
とは、各種の疾病の早期発見の観点からますます重要に
なってきている。[Prior Art] A liquid sample such as serum is analyzed to detect various substances, e.g.
BACKGROUND OF THE INVENTION Measuring the presence and/or concentration of hormones, vitamins, lipids, enzymes, nitrogen-containing substances, sugars, antigenic substances, etc. is becoming increasingly important from the perspective of early detection of various diseases.
そこで近年、液体試料の分析を高精度かつ効率よく行な
うことか強く望まれるようになり、これに応していくつ
かの提案かなされている。Therefore, in recent years, there has been a strong desire to analyze liquid samples with high precision and efficiency, and several proposals have been made in response to this demand.
本発明者らもこのような観点から鋭意研究を重ねた結果
、ディスク上にあらかしめ試薬を塗布しておき、ディス
クとにおいて、液体試料と試薬の反応を行なわせるとと
もに、反応生成物の物質の測定を行なうことにより、液
体試料の分析を高精度かつ効率よく行なえることを知見
して、ディスクを用いた液体試料の分析方法の発明を完
成し、特願平1−92367号等において開示している
。As a result of extensive research from this perspective, the inventors of the present invention have applied a preconditioning reagent onto the disk, and allowed the reaction between the liquid sample and the reagent to occur on the disk. After discovering that liquid samples could be analyzed with high precision and efficiency through measurements, he completed the invention of a method for analyzing liquid samples using a disk, and disclosed this in Japanese Patent Application No. 1-92367 and other documents. ing.
これらの分析方法においては、主に光学的な測定手段を
用いて反応現象を測定し分析を行なっている。例えば、
レーザー光を利用すると、微細箇所に検出用の光を集光
することができ、通常のレーザーディスク方式て多成分
の信号を処理することか可能になるとともに、時々刻々
変化する多成分系の微量分析をリアルタイムで行なうこ
とかてきる。In these analytical methods, reaction phenomena are mainly measured and analyzed using optical measuring means. for example,
Using laser light, it is possible to focus the detection light on a minute spot, making it possible to process multi-component signals using the normal laser disc method, and also to process minute amounts of multi-component systems that change from moment to moment. Analysis can be performed in real time.
また、分析対象によっては、レーザー光に限らず、その
他の光源等を用いた光学的な手段によって分析を行なっ
ている。Furthermore, depending on the object to be analyzed, analysis is performed not only by laser light but also by optical means using other light sources.
[発明か解決しようとする課題]
しかしながら、上記した従来の光学的測定手段を利用し
た分析法においては、試料中の分析対象物と試料の展開
液あるいはディスク基板等のバックグラウンドとの間に
、反射率、屈折率、特定波長の光の吸収率、蛍光強度あ
るいは旋光度等の光学的性質に何らかの差異かなければ
光学的な測定を行なえなかった。[Problems to be Solved by the Invention] However, in the above-mentioned analysis method using the conventional optical measurement means, there is a possibility that there is a problem between the analyte in the sample and the background of the sample developing solution or disk substrate. Optical measurements cannot be made unless there is some difference in optical properties such as reflectance, refractive index, absorption of light at a specific wavelength, fluorescence intensity, or optical rotation.
したかって、従来、バックグラウンドに対して光学的な
特徴を有しない対象物は、光学的な測定手段を利用した
分析方法によっては分析を行なうことかできなかった。Therefore, in the past, it has not been possible to analyze objects that have no optical characteristics relative to the background using analysis methods that utilize optical measurement means.
一方、特公表昭51−502419号公報ては、毛細管
セルキャビティ内に電気的特性を測定しうる電極を設け
、この毛細管セルキャビティ内に試料を供給して、試料
の電気的特性にもとづく分析を行なえるようにした分析
用デイバイスか提案されている。また、同分析用デイバ
イスには、必要に応し光学的測定をも行なえることか示
されている。On the other hand, in Japanese Patent Publication No. 51-502419, an electrode capable of measuring electrical characteristics is provided in a capillary cell cavity, a sample is supplied into the capillary cell cavity, and analysis based on the electrical characteristics of the sample is performed. Analytical devices have been proposed to enable this. The analytical device has also been shown to be capable of performing optical measurements if necessary.
しかしながら、特公表昭61−502419号公報で提
案されている分析用デイバイスは、シート上に複数のキ
ャビティを設け、毛細管現象を利用してキャビティ内に
試料を供給するものであるため試料の注入、試料展開の
自動化及び分析精度の向上を図ることか困難てあった。However, the analytical device proposed in Japanese Patent Publication No. 61-502419 has multiple cavities on a sheet and supplies the sample into the cavities using capillary action. It has been difficult to automate sample development and improve analysis accuracy.
本発明は上述した問題点にかんがみてなされたちのて、
バックグラウンドに対し光学的特徴を右しない対象物の
分析を、自動的にしかも精度よく行なえるようにした液
体試料分析用ディスクの提供を目的とする。The present invention has been made in view of the above-mentioned problems.
The purpose of the present invention is to provide a liquid sample analysis disk capable of automatically and accurately analyzing an object whose optical characteristics are not influenced by the background.
[課題を解決するための手段]
」二足目的を達成するため、本発明の液体試料分析用デ
ィスクは、ディスク基板上に、液体試料の展開部と、こ
の展開部における電気的特性を測定する電極を、上記展
開部に所定の間隙をもって配置した構成としである。[Means for Solving the Problems] In order to achieve the two objectives, the liquid sample analysis disk of the present invention has a liquid sample development area on a disk substrate and a measurement area for electrical characteristics in this development area. The electrodes are arranged in the expanded portion with a predetermined gap.
[実施例]
以下、本発明液体試料分析用ディスクの実施例について
、図面を参照しつつ詳細に説明する。[Example] Hereinafter, an example of the liquid sample analysis disk of the present invention will be described in detail with reference to the drawings.
第1図(a)及び(b)は、本発明の第一実施例に係る
液体試料分析用ディスクの平面図(他の区画における電
極は省略しである)及び部分断面図を示している。FIGS. 1(a) and 1(b) show a plan view (electrodes in other sections are omitted) and a partial sectional view of a liquid sample analysis disk according to a first embodiment of the present invention.
これらの図面に示す分析用ディスクは、ディスク基板l
の上面に展開部2を形成するとともに、この展開部2に
三組の電極31a−31b。The analysis disk shown in these drawings has a disk substrate l.
A developed part 2 is formed on the upper surface of the , and three sets of electrodes 31a-31b are provided in this developed part 2.
32a−32b、33a−33bを設けた構成としであ
る。32a-32b and 33a-33b are provided.
ここで、ディスク基板lは円板状の形状をしており、基
板平面上には、中心部より放射状に凸状部5か形成しで
ある。これにより、ディスク基板1の円周方向には、凹
状をした展開部2か複数形成される。ディスク基板lの
大きさ(半径)、厚さ等は分析の目的、態様等によって
適宜選択される。Here, the disk substrate l has a disk shape, and convex portions 5 are formed radially from the center on the plane of the substrate. As a result, a plurality of concave expanded portions 2 are formed in the circumferential direction of the disk substrate 1. The size (radius), thickness, etc. of the disk substrate l are appropriately selected depending on the purpose and mode of analysis.
ディスク基板lを形成する材料としては、ポリカーボネ
ート、ポリメチルメタクリレート、ポリスチレン、ポリ
塩化ビニル、ポリ酢酸ビニル、ポリウレタン、エポキシ
樹脂等のプラスチック材料やガラス等が挙げられる。非
導電(伝導)性材料てあればいずれのものも使用可能で
あるか、後述する光学的分析を併せて行なう場合には、
透明材料を用いる必要かある。Examples of the material forming the disk substrate 1 include plastic materials such as polycarbonate, polymethyl methacrylate, polystyrene, polyvinyl chloride, polyvinyl acetate, polyurethane, and epoxy resin, and glass. Is it possible to use any non-conductive (conductive) material? If you are also performing the optical analysis described below,
Is it necessary to use a transparent material?
ディスク基板1の中心部には、ディスクを回転チーフル
の回転軸に挿着するための軸穴6が設けられており、こ
の軸穴6を介して回転テーブルに搭載され回転か行なわ
れる。A shaft hole 6 is provided in the center of the disk substrate 1 for inserting the disk into the rotation shaft of the rotary chiffle, and the disk is mounted on a rotary table through the shaft hole 6 and rotated.
展開部2は、液体試料か満たされ展開される部分であり
、ディスク基板lの基板平面上に凹状に形成されている
。この展開部2は、通常、ディスク基板lを射出成形あ
るいは射出圧縮成形等する際に同時に成形される。The developing portion 2 is a portion filled with a liquid sample and expanded, and is formed in a concave shape on the substrate plane of the disk substrate l. This expanded portion 2 is usually molded at the same time as injection molding or injection compression molding the disk substrate l.
電極31.32.33は、展開部2内に所定の間隙でそ
れぞれa、bを一組として、半径方向に三組配置されて
いる。この三組の電極のうち、電極31と32はリード
部を介してディスク基板lの周縁に信号端子を形成し、
また電極33はその端部な信号端子としている。これら
信号端子は、スリップリンク10等を介し電気信号供給
装置(図示せず)と接続されている(第1図(ν)及び
(b)参照)。Three sets of electrodes 31, 32, and 33 are arranged in the radial direction within the expanded portion 2, with a and b serving as one set, respectively, at predetermined intervals. Of these three sets of electrodes, electrodes 31 and 32 form signal terminals on the periphery of the disk substrate l via lead portions,
Further, the electrode 33 is used as a signal terminal at the end thereof. These signal terminals are connected to an electric signal supply device (not shown) via a slip link 10 or the like (see FIGS. 1(v) and (b)).
この′7tL極の数や配設パターンは、分析の[]的。The number and arrangement pattern of these '7tL poles are the subject of analysis.
態様等によって適宜変更することかてきる。It may be changed as appropriate depending on the aspect etc.
電極31,32.33は、ディスク基板1 hに基若、
スパッタリンク、メツキ、スクリーン印刷等のf−段に
よって、金属専の導電性材料を付着させて形成される。The electrodes 31, 32, 33 are arranged on the disk substrate 1h,
It is formed by depositing a metal-only conductive material by f-steps such as sputter linking, plating, and screen printing.
ここて、導電性材料としては金、銀、flI4.プラチ
ナ及びその化合物等の金属や、クラファイト等の非金属
か挙げられ、これらの粒子等を含むベヒクル等も含まれ
る。Here, the conductive materials include gold, silver, flI4. Examples include metals such as platinum and its compounds, and non-metals such as graphite, and vehicles containing particles of these particles are also included.
また、導電性材料には、特定の分析物に対して′#、極
を敏感にするための増感成分を含ませてもよい。増感成
分としては、例えば、カルシウムジイソオクチルフェニ
ルホスフェート(カルシウム感受性電極用)、ハリノマ
イシン(カリウム感受性電極用)、トリドデシルアミン
(水素イオン感受性電極用)、塩化銀、臭化銀またはヨ
ウ化銀粒子(ハロゲン化物感受性電極用)、硫化銀粒子
(硫化物感受性電極用)、硫化銀と硫化銀の粒子の混合
物(硫化物と銅に感受性の電極用)か挙げられる。The conductive material may also contain a sensitizing component to make the pole sensitive to a particular analyte. Sensitizing components include, for example, calcium diisooctylphenyl phosphate (for calcium-sensitive electrodes), halinomycin (for potassium-sensitive electrodes), tridodecylamine (for hydrogen ion-sensitive electrodes), silver chloride, silver bromide or silver iodide. particles (for halide-sensitive electrodes), silver sulfide particles (for sulfide-sensitive electrodes), and mixtures of silver sulfide and silver sulfide particles (for sulfide- and copper-sensitive electrodes).
なお、第1[2(a)においては、一つの展開部2にの
み電極31,32.33を設けた例を示しているか、円
周方向に分割した各展開部2にも、任意の数の電極を設
けることは勿論可能である。In addition, in 1 [2 (a), an example is shown in which the electrodes 31, 32, 33 are provided only in one expanded portion 2, or an arbitrary number of electrodes 31, 32, 33 are provided in each expanded portion 2 divided in the circumferential direction. Of course, it is possible to provide electrodes of.
また、第1図(C)に示すように、−組の電極の一方ま
たは両方をディスク基板lに設けた貫通孔7を介して基
板下部に導き、ここてスリップリンクIOと接触させる
ことも可能である。さらに、it気信号の取り出しは、
ディスクの上面から行なうこともてきる。Furthermore, as shown in FIG. 1(C), it is also possible to guide one or both of the electrodes of the - group to the lower part of the substrate through the through hole 7 provided in the disk substrate l, and make them contact with the slip link IO here. It is. Furthermore, the extraction of the IT signal is
You can also do this from the top of the disc.
次に、本発明の第二実施例について説明する。Next, a second embodiment of the present invention will be described.
第2図は、本発明の第二実施例に係る液体試料分析用デ
ィスクを示す断面図である。FIG. 2 is a sectional view showing a liquid sample analysis disk according to a second embodiment of the present invention.
同図に示す分析用ディスクは、ディスク基板l上に、第
一の電極3a、展開層2及び第二の電極3bを順次積層
した構成としである。The analysis disk shown in the figure has a structure in which a first electrode 3a, a spreading layer 2, and a second electrode 3b are sequentially laminated on a disk substrate l.
ここて、ディスク基板lは1円板状の平面板となってお
り、その材料には上述した第一実施例のものと回しもの
を用いている。Here, the disk substrate l is a flat plate in the form of a circular plate, and its material is the same as that of the first embodiment described above and a rotating material.
液体試料の展開層2は、アルミナ、シリカ、不織布等の
材料によって形成されており、デイスペンサ等の注入手
段によって試料を注入した後、遠心力により試料を展開
するものである。この展開層2を形成する方法としては
、ロールコータ−スピンコーターを用いたコーティング
あるいはインクシェツトによる描画法等か例示される。The liquid sample spreading layer 2 is formed of a material such as alumina, silica, or nonwoven fabric, and is used to spread the sample by centrifugal force after injecting the sample with an injection means such as a dispenser. Examples of the method for forming the spread layer 2 include coating using a roll coater/spin coater, drawing method using an ink jet, and the like.
なお、この展開層2は、中空状のものとすることもてき
、この場合は、遠心力により試料中の成分か比重差に応
して分離、分画される。また展開層2に、分析に適する
酵素、染料分子、抗原、抗体または緩衝塩その他の試薬
等を含有あるいは塗布させることもてきる。The developing layer 2 may be hollow, and in this case, the components in the sample are separated and fractionated by centrifugal force according to the difference in specific gravity. Further, the developing layer 2 may contain or be coated with enzymes, dye molecules, antigens, antibodies, buffer salts, and other reagents suitable for analysis.
第−及び第二の電極3a、3bは、上記第一実施例にお
ける電極と同様の材料、方法等によって構成してあり、
展開層2を挟むようにして設けられている。The first and second electrodes 3a, 3b are constructed using the same materials, methods, etc. as the electrodes in the first embodiment,
They are provided so as to sandwich the development layer 2 therebetween.
ここで、ディスク基板l上における電極の3a、3bの
配設パターンは、例えば、第4図(a)及び(b)に示
すような放射状に配設した形状あるいは円周方向に配設
した形状としである。そして通常は、第一もしくは第二
電極として、第4図(a)、(b)に示すような配設パ
ターンの電極を用い、これらを展開層2を介して積層す
る。Here, the arrangement pattern of the electrodes 3a and 3b on the disk substrate l is, for example, a radially arranged shape or a circumferentially arranged shape as shown in FIGS. 4(a) and 4(b). It's Toshide. Usually, electrodes having a layout pattern as shown in FIGS. 4(a) and 4(b) are used as the first or second electrodes, and these are laminated with the spread layer 2 in between.
例えば、第一電極3aに第4図(a)に示す電極を用い
、第二電極3bに第4図(b)に示す電極を用いると、
これらを組み合せた場合、第4図(c)に示すようなデ
ィスクとなる。For example, if the electrode shown in FIG. 4(a) is used as the first electrode 3a and the electrode shown in FIG. 4(b) is used as the second electrode 3b,
When these are combined, a disk as shown in FIG. 4(c) is obtained.
なお、配設パターンは、第4図(C)に示すように、デ
ィスク面上における分析部分と対応した部分で交差した
状態とする必要がある。Note that the arrangement pattern must intersect at a portion corresponding to the analysis portion on the disk surface, as shown in FIG. 4(C).
このようにパターン化された電極は、非電極部分の遮蔽
(マスキング)や非電極部分の食刻(エツチング)等、
公知技術によって容易に得ることかてきる。Electrodes patterned in this way can be used to mask the non-electrode portions, to etch the non-electrode portions, etc.
It can be easily obtained by known techniques.
また、電極を腐蝕させる恐れのある試料あるいは導電性
の高い液体を用いる場合には、第3I7Iに示すように
電極3と展開層2との間にインシュレーター(lnsu
later) 4を設けることか好ましい。このインシ
ュレーター4は、セラミックス等の材料を用い、蒸着、
スパッタリング、スピンコード等の方法て形成される。In addition, when using a sample that may corrode the electrode or a highly conductive liquid, an insulator (lnsu) is placed between the electrode 3 and the developing layer 2 as shown in No.
later) It is preferable to provide 4. This insulator 4 is made of a material such as ceramics, and is made by vapor deposition,
It is formed by methods such as sputtering and spin code.
また、樹脂薄膜て電極を被覆してもよい。Alternatively, the electrode may be covered with a resin thin film.
なお、上記実施例においては、ディスクの形状か円板状
である場合の例を示したか、ディスクの形状は円板状の
ものに限定されない。In the above embodiments, an example is shown in which the disk shape is a disk shape, but the shape of the disk is not limited to the disk shape.
[作用]
はじめに、上述した第一実施例に係る液体試料分析用デ
ィスクの作用について説明する。[Function] First, the function of the liquid sample analysis disk according to the first embodiment described above will be explained.
まず、二つの電極間に一定電圧の交流を印加し、電流の
モニタを行なう。First, a constant voltage alternating current is applied between two electrodes, and the current is monitored.
そして、液体試料を分析用ディスクに滴下した後、この
ディスクを回転させて試料の展開を行ない展開部2に試
料を供給する。After dropping the liquid sample onto the analytical disk, the disk is rotated to develop the sample and supply the sample to the developing section 2.
展開後、分割された各電極ごとの電位差の変化等を測定
することによって分析を行なう。After development, analysis is performed by measuring changes in potential difference between each divided electrode.
なお、被分析成分か電界の印加等により光学的特性を帯
びるものである場合には、上記電気的分析手段のほかに
、光学的分析手段によっても定性及び/または定量分析
を行なうことかてきる。In addition, if the component to be analyzed has optical characteristics due to the application of an electric field, etc., qualitative and/or quantitative analysis may be performed by optical analysis means in addition to the above-mentioned electrical analysis means. .
例えば、印加した電界の強度に比例して複屈折性を帯び
るカー(Kerr)効果等を利用した光学的分析か可能
である。For example, optical analysis using the Kerr effect, which exhibits birefringence in proportion to the intensity of the applied electric field, is possible.
また、例えば生化学的検査における化学反応等の促a(
あるいは単純化)に、電極による電気化学的作用を適用
し、分析を行なうことも可能である。In addition, for example, the promotion of chemical reactions, etc. in biochemical tests (a)
Alternatively, it is also possible to perform analysis by applying electrochemical action using electrodes (for simplification).
次に、−L述した第二実施例に係る液体試料分析用ディ
スクの作用について説明する。Next, the operation of the liquid sample analysis disk according to the second embodiment described above will be explained.
まず、二つの電極3a及び3bの間に一定電圧の交流を
印加し、電流をモニタする。First, a constant voltage alternating current is applied between the two electrodes 3a and 3b, and the current is monitored.
そして、液体試料をデイスペンサ等の注入手段によって
展開層2に注入した後、ディスクを回転させて遠心力に
より試料を展開層2に展開させる。After the liquid sample is injected into the developing layer 2 by an injection means such as a dispenser, the disk is rotated to spread the sample onto the developing layer 2 by centrifugal force.
展開後、電極3a、3bのそれぞれ一つづつの電極の組
合せを選定し、その間のインピーダンスの変化を交流を
用いて測定することにより各位置ごとの成分の定性/定
量分析を行なう。通常は、電極3aごとに展開部を分割
することにより行なう。After deployment, a combination of electrodes 3a and 3b is selected, and changes in impedance between the electrodes are measured using alternating current to perform qualitative/quantitative analysis of the components at each position. Usually, this is done by dividing the expanded portion for each electrode 3a.
なお、上記電流測定による分析のほか、電位差測定、例
えば容量、電圧等の電気的パラメータの測定によって、
分析を行なってもよい。また、試料中の被分析成分の電
気的特性か時間とともに変化する場合には、この時間変
化を測定しつつ分析することも可能である。In addition to the above-mentioned analysis by current measurement, measurement of electrical parameters such as capacitance and voltage by potential difference measurement,
Analysis may be performed. Furthermore, if the electrical characteristics of the component to be analyzed in the sample change over time, it is also possible to perform analysis while measuring this change over time.
[発明の効果]
以上説明したように、本発明の分析用ディスクによれば
、ディスクに電極を設けているので、光学的な分析か不
可能であった試料の電気的性質にもとづく分析か可能と
なる。[Effects of the Invention] As explained above, according to the analytical disk of the present invention, since the disk is provided with electrodes, analysis based on the electrical properties of the sample, which was previously impossible, is now possible. becomes.
また、ディスク方式を採用しているのて、試料の注入や
展開の自動化か図れるとともに、分析精度の向上を図る
ことか可能となる。In addition, since the disk method is adopted, it is possible to automate sample injection and expansion, and it is also possible to improve analysis accuracy.
さらに、電界等を印加しつつ光学的手段による分析を行
なえるのて、従来の光学的手段ではなしえなかった分析
か可能となる。Furthermore, since analysis can be performed by optical means while applying an electric field or the like, it becomes possible to perform analysis that was not possible with conventional optical means.
第1図(a)は本発明の一実施例に係る液体試料分析用
ディスクを示す平面図。
第1図(b)は゛第1図(a)のI−I線部分断面図。
第1図(C)は電極の他の取付は状態を示す部分断面図
。
第2図は本発明の他の実施例に係る液体試料分析用ディ
スクを示す部分断面図。
第3図は同しく電極と展開層との間にインシュレーター
を設けた液体試料分析用ディスクを示す部分断面図。
第4図(a)及び(b)は電極の配設パターンの具体例
を示す平面図。
第4図(C)は第4図(a)及び(b)の電極用いた分
析用ディスクの平面図である。
l
ディスク基板
展開部
3 (3a、 3b)、 31a、 31b。
32b、 33a、 33b: 電橋32 a 。
イ
ンシュレータ
凸状部
1L願人
出光石油化学株式会社FIG. 1(a) is a plan view showing a liquid sample analysis disk according to an embodiment of the present invention. FIG. 1(b) is a partial sectional view taken along line I--I in FIG. 1(a). FIG. 1(C) is a partial sectional view showing another mounting state of the electrode. FIG. 2 is a partial sectional view showing a liquid sample analysis disk according to another embodiment of the present invention. FIG. 3 is a partial sectional view showing a liquid sample analysis disk in which an insulator is provided between an electrode and a developing layer. FIGS. 4(a) and 4(b) are plan views showing specific examples of electrode arrangement patterns. FIG. 4(C) is a plan view of an analytical disk using the electrodes of FIGS. 4(a) and 4(b). l Disk board expansion section 3 (3a, 3b), 31a, 31b. 32b, 33a, 33b: Electric bridge 32a. Insulator convex part 1L applicant Idemitsu Petrochemical Co., Ltd.
Claims (1)
所定の間隙をもって配置され、展開部における電気的特
性を測定する電極とを設けたことを特徴とする液体試料
分析用ディスク。1. A liquid sample analysis disk comprising, on a disk substrate, a liquid sample development section and an electrode disposed at a predetermined gap in the development section for measuring electrical characteristics in the development section.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4227590A JPH03245049A (en) | 1990-02-22 | 1990-02-22 | Liquid-sample analyzing disk |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4227590A JPH03245049A (en) | 1990-02-22 | 1990-02-22 | Liquid-sample analyzing disk |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03245049A true JPH03245049A (en) | 1991-10-31 |
Family
ID=12631489
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4227590A Pending JPH03245049A (en) | 1990-02-22 | 1990-02-22 | Liquid-sample analyzing disk |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03245049A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997021090A1 (en) * | 1995-12-05 | 1997-06-12 | Gamera Bioscience | Devices and methods for using centripetal acceleration to drive fluid movement in a microfluidics system with on-board informatics |
US6338820B1 (en) | 1997-08-15 | 2002-01-15 | Alexion Pharmaceuticals, Inc. | Apparatus for performing assays at reaction sites |
KR100359820B1 (en) * | 2000-05-10 | 2002-11-07 | 엘지전자 주식회사 | Apparatus for detection and analysis of bio-material, and method for using the same |
WO2007049607A1 (en) * | 2005-10-28 | 2007-05-03 | Matsushita Electric Industrial Co., Ltd. | Measuring device, measuring instrument and method of measuring |
-
1990
- 1990-02-22 JP JP4227590A patent/JPH03245049A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997021090A1 (en) * | 1995-12-05 | 1997-06-12 | Gamera Bioscience | Devices and methods for using centripetal acceleration to drive fluid movement in a microfluidics system with on-board informatics |
US6338820B1 (en) | 1997-08-15 | 2002-01-15 | Alexion Pharmaceuticals, Inc. | Apparatus for performing assays at reaction sites |
KR100359820B1 (en) * | 2000-05-10 | 2002-11-07 | 엘지전자 주식회사 | Apparatus for detection and analysis of bio-material, and method for using the same |
WO2007049607A1 (en) * | 2005-10-28 | 2007-05-03 | Matsushita Electric Industrial Co., Ltd. | Measuring device, measuring instrument and method of measuring |
US7646474B2 (en) | 2005-10-28 | 2010-01-12 | Panasonic Corporation | Measuring device, measuring apparatus and method of measuring |
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