JPH0213959Y2 - - Google Patents
Info
- Publication number
- JPH0213959Y2 JPH0213959Y2 JP1983087295U JP8729583U JPH0213959Y2 JP H0213959 Y2 JPH0213959 Y2 JP H0213959Y2 JP 1983087295 U JP1983087295 U JP 1983087295U JP 8729583 U JP8729583 U JP 8729583U JP H0213959 Y2 JPH0213959 Y2 JP H0213959Y2
- Authority
- JP
- Japan
- Prior art keywords
- sample
- tip
- liquid
- sensor
- tip cover
- 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
Links
- 239000007788 liquid Substances 0.000 claims description 20
- 239000000523 sample Substances 0.000 description 27
- 238000005259 measurement Methods 0.000 description 10
- 239000003085 diluting agent Substances 0.000 description 5
- 150000002500 ions Chemical class 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000012488 sample solution Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- -1 Na + Chemical class 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 108010046334 Urease Proteins 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 239000012482 calibration solution Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 230000001795 light effect Effects 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Sampling And Sample Adjustment (AREA)
- Devices For Use In Laboratory Experiments (AREA)
Description
【考案の詳細な説明】
本考案は微量サンプル測定装置に関し、微量サ
ンプルの測定を簡易且つ迅速に行ない得るものを
提供することを目的とする。[Detailed Description of the Invention] The present invention relates to a micro-sample measuring device, and an object of the present invention is to provide an apparatus that can easily and quickly measure a micro-sample.
まずこの考案の実施例を図面に基づき詳述す
る。第1図において微量サンプル吸引器具1は市
販のマイクロピペツタと類似構造を有し、プラン
ジヤノブ2を押すことにより内蔵するピストン・
シリンダが働き、次に述べる先端部1aに吸引力
が作用するようになされている。即ち、該先端部
1aにはイオン選択性FETセンサ3が取着され、
且つ比較電極4が装備される一方、不透明の且つ
導電体製の円錘状チツプカバー5が上記先端部1
aに着脱自在に圧嵌もしくはねじ結合、または接
着して取着され、このチツプカバー5にてFET
センサ3および比較電極4が包覆されると共に、
チツプカバー5内部に微量サンプル測定小室6が
形成され、且つチツプカバー5の先端に吸液口7
が開設されている。尚、図中10はコネクタであ
る。 First, an embodiment of this invention will be described in detail based on the drawings. In FIG. 1, a micro sample suction device 1 has a structure similar to a commercially available micropipette, and by pressing a plunger knob 2, a built-in piston
The cylinder works so that a suction force is applied to the tip 1a, which will be described next. That is, the ion-selective FET sensor 3 is attached to the tip 1a,
In addition, a comparison electrode 4 is provided, and an opaque conical tip cover 5 made of a conductive material is attached to the tip 1.
FET
While the sensor 3 and the reference electrode 4 are covered,
A small sample measurement chamber 6 is formed inside the tip cover 5, and a liquid suction port 7 is formed at the tip of the tip cover 5.
has been established. In addition, 10 in the figure is a connector.
従つて、この微量サンプル測定装置を被検液中
に浸け、プランジヤノブ2を下圧するならば、吸
気路8を経る吸引力でたとえば10〜100μの被
検液が吸液口7から微量サンプル測定小室6に流
入し、そのサンプル液がFETセンサ3の先端感
応部3aに接し、その測定値が器具1の側面に設
けられた表示部9に表示される。この場合、プラ
ンジヤノブ2に連動するピストンストロークを一
定にすることで、微量サンプル測定小室6に流入
するサンプル液を定量に設定し、且つ液位を一定
に保つことにより先端感応部3aが確実に、そし
て最小限接するようにできる。このようにすれ
ば、サンプル量は微量で済み、FETセンサ3の
汚れを最小限に抑えることができる。また、チツ
プカバー5は機械的強度において難点がある
FETセンサ3を機械的、物理的に保護すること
は勿論であつて、その他不透明体構造により光に
弱いFETセンサ3への光影響をなくし、その導
電体構造故に静電破壊をなくすことができる。 Therefore, if this micro sample measuring device is immersed in a test liquid and the plunger knob 2 is lowered, the suction force passing through the suction path 8 will cause a micro sample of the test liquid to be measured from the liquid suction port 7. The sample liquid flows into the small chamber 6 and comes into contact with the tip sensing section 3a of the FET sensor 3, and the measured value is displayed on the display section 9 provided on the side of the instrument 1. In this case, by keeping the piston stroke linked to the plunger knob 2 constant, the sample liquid flowing into the small sample measurement chamber 6 can be set at a fixed amount, and by keeping the liquid level constant, the tip sensing part 3a can be reliably , and can be made to be minimally touching. In this way, only a small amount of sample is required, and contamination of the FET sensor 3 can be minimized. Additionally, the chip cover 5 has a drawback in terms of mechanical strength.
In addition to mechanically and physically protecting the FET sensor 3, the opaque structure also eliminates light effects on the FET sensor 3, which is sensitive to light, and its conductive structure eliminates electrostatic damage. .
尚、比較電極4はFETセンサ3と一体モール
ドしても良いし、図のように此等を並設しても良
い。 Note that the comparison electrode 4 may be integrally molded with the FET sensor 3, or they may be arranged side by side as shown in the figure.
又、チツプカバー5を使い捨てとすれば、装置
全体としての汚れも少なく抑えられ、且つ被検液
を汚染することがない。 Furthermore, if the tip cover 5 is disposable, the amount of dirt on the entire device can be kept to a minimum, and the sample liquid will not be contaminated.
第2図および第3図は生体、細胞等の超微小領
域、超微量サンプル用として、チツプカバー5の
先端に針子10を取着したり、あるいはガラスキ
ヤピラリ(先端径1〜10μφ)11を取着した実
施例を示し、此等針子10、ガラスキヤピラリ1
1を目的物の所要部位に突き刺してサンプルを採
取する。 Figures 2 and 3 show a case in which a needle 10 is attached to the tip of a tip cover 5, or a glass capillary (tip diameter 1 to 10 μφ) 11 is used for ultra-micro regions such as living organisms and cells, and ultra-micro samples. This shows an example in which a needle 10 and a glass capillary 1 are attached.
1 into the desired part of the target object to collect the sample.
また、図示しないが第3図と同様な構成で、チ
ツプカバー5の吸液口7を細長いパイプ状のもの
とすれば、NMR(核磁気共鳴)試料管中のサン
プル、オイルパン中のオイルサンプル等のように
従来センサーの入りにくい箇所においても、
FETセンサー3を汚染せずに容易に測定ができ
る。 Although not shown, if the liquid suction port 7 of the tip cover 5 is made into an elongated pipe-like structure with the same configuration as shown in FIG. 3, samples in NMR (nuclear magnetic resonance) sample tubes, oil samples in oil pans, etc. Even in places where conventional sensors are difficult to enter, such as
Measurement can be easily performed without contaminating the FET sensor 3.
又、チツプカバー5がその微量サンプル測定小
室6にサンプル液を定量吸引する使い捨てタイプ
のサンプルセルであることを利用し、第4図の如
く上記小室6の内壁に予め試薬12を定量だけ水
溶性バインダで塗布しておけば、サンプル液の吸
引時にこれを混入させて測定に先立つ前処理工程
を自動的に、そして吸液という一動作で簡便に施
こすことができる。たとえば、Na+等イオン測定
時用にトリスバツフア等PH調整剤を塗布するこ
と、酵素を塗布しておいてサンプル液をFETセ
ンサで測定し得る物質に変換すること(たとえば
尿素を測定する場合、酵素としてウレアーゼを用
い、尿素濃度をPH値に変換する。ジアミン測定す
る場合、ジアミンオキシダーゼでジアミン濃度を
NH3値に変換することなど)、校正液用の薬品を
塗布しておいてイオン交換水を吸引することで測
定系を校正することがあげられる。尚、この種測
定装置では温度補償素子を必要とすることが多
く、たとえば前記FETセンサでは温度補償素子
内蔵を原則としているが、それだけでは不充分な
場合、あるいは酵素を利用していて温度要因が大
きい場合には、ピペツタスタンドを恒温槽とし
て、サンプリングしたまゝの状態で本考案の測定
装置を該槽に立てて測定できるようにすることも
できる。 Furthermore, by utilizing the fact that the tip cover 5 is a disposable type sample cell that sucks a fixed amount of sample liquid into the small sample measurement chamber 6, as shown in FIG. If the sample solution is coated with the solution, it can be mixed into the sample solution when it is aspirated, and the pretreatment step prior to measurement can be automatically and conveniently carried out in a single action of absorbing the solution. For example, applying a pH adjuster such as Tris buffer when measuring ions such as Na + , or applying an enzyme to convert the sample liquid into a substance that can be measured with an FET sensor (for example, when measuring urea, enzyme Convert the urea concentration to a pH value using urease as
(converting to NH3 value, etc.), and calibrating the measurement system by applying chemicals for calibration solution and sucking in ion-exchanged water. Note that this type of measuring device often requires a temperature compensation element. For example, the above-mentioned FET sensor basically has a built-in temperature compensation element, but there are cases where that alone is insufficient, or where enzymes are used and the temperature factor is If the sample is large, the pipette stand can be used as a constant temperature bath, and the measuring device of the present invention can be placed in the bath to perform measurements while sampling.
第5図は測定装置を簡易フロースルー型とした
もので、プランジヤノブ2を押す動作に伴い先行
して吸液されたサンプル液が排出口14から排出
され、次にノブ2から指を離すと新たなサンプル
液が吸液口7から吸液されるようにしてある。図
中15,16は逆止弁である。これであれば微量
サンプルを連続してサンプリングし、且つ測定で
きる。第6,7図は、本考案の測定装置に、さら
に希釈装置を付設した実施例を示す。こ実施例に
おいて、まず希釈液用ノブ20を操作してチツプ
カバー5内に希釈液を導入し、次に、ノブ2を操
作してサンプル液をチツプカバー5内に導入す
る。そして、軽く全体を振つて撹拌した後、サン
プル液中の所定成分の濃度を測定する。次に、前
記ノブ20を操作して希釈液をチツプカバー5内
に導入して洗浄する。そして、汚れが目立つとチ
ツプカバー5を交換する。 FIG. 5 shows a simple flow-through measuring device, in which the sucked sample liquid is discharged from the discharge port 14 when the plunger knob 2 is pressed, and then when the knob 2 is released, the sample liquid is discharged from the discharge port 14. A new sample liquid is sucked from the liquid suction port 7. In the figure, 15 and 16 are check valves. With this, it is possible to continuously sample and measure trace amounts of samples. FIGS. 6 and 7 show an embodiment in which a diluting device is further attached to the measuring device of the present invention. In this embodiment, first the diluent knob 20 is operated to introduce the diluent into the tip cover 5, and then the knob 2 is operated to introduce the sample liquid into the tip cover 5. Then, after stirring the whole sample by shaking it lightly, the concentration of a predetermined component in the sample liquid is measured. Next, the knob 20 is operated to introduce the diluent into the tip cover 5 for cleaning. Then, when the dirt is noticeable, the tip cover 5 is replaced.
尚、図中、21は希釈液タンク、22,23,
24,25は逆止弁、26,27はピストン、2
8,29はストツパである。又、希釈液中にPH緩
衝成分や妨害物質マスキング剤を溶解させておい
て、イイオン電極による測定をより完全にするこ
とも可能である。このように希釈装置を付設する
ものとしては、酸度計、食塩計等の測定装置があ
る。 In addition, in the figure, 21 is a diluent tank, 22, 23,
24, 25 are check valves, 26, 27 are pistons, 2
8 and 29 are stoppers. Furthermore, it is also possible to dissolve pH buffering components and interfering substance masking agents in the diluent to make the measurement using the ion electrode more complete. Measurement devices such as acidity meters and salt meters are examples of devices that are equipped with dilution devices in this way.
本考案は上述したように微量サンプル測定を簡
易、迅速に行なえ且つチツプカバーにてセンサの
破損、汚染等を防止できる。 As described above, the present invention allows measurement of a small amount of sample to be performed easily and quickly, and the chip cover prevents damage to the sensor, contamination, etc.
尚、前記実施例では、センサとしてFETセン
サを用いたが、本考案はこれに限らず、たとえば
温度計や一般のイオン電極、溶存酸素電極、白金
電極、導電率測定用電極などの種々のセンサを用
いることができる。 In the above embodiments, an FET sensor was used as the sensor, but the present invention is not limited to this, and can be applied to various sensors such as a thermometer, a general ion electrode, a dissolved oxygen electrode, a platinum electrode, an electrode for measuring conductivity, etc. can be used.
第1図はこの考案の一実施例を示す一部破断正
面図、第2図および第3図は生体用等として使用
する場合の応用例で、第2図は要部断面図、第3
図は外観図であり、第4図は前処理用としての試
薬を塗布する場合の応用例を示す要部断面図、第
5図は簡易型フローフルーとした変形例を示す
図、第6,7図は本考案の別実施例である希釈装
置付測定装置を示す側面図と概略断面図である。
1……微量サンプル吸引器具、3……センサ、
5……チツプカバー、7……吸液口。
Fig. 1 is a partially cutaway front view showing one embodiment of this invention, Figs. 2 and 3 are application examples when used for biological purposes, etc. Fig. 2 is a sectional view of the main part, and Fig. 3 is a sectional view of the main part.
The figure is an external view, Figure 4 is a sectional view of the main part showing an application example when applying a reagent for pre-treatment, Figure 5 is a diagram showing a modified example of a simplified flow fluid, FIG. 7 is a side view and a schematic sectional view showing a measuring device with a diluting device, which is another embodiment of the present invention. 1... Trace sample suction device, 3... Sensor,
5... Chip cover, 7... Liquid suction port.
Claims (1)
を特定するためのセンサを設けると共に、吸液口
を備え前記センサを包覆するチツプカバーを前記
先端部に着脱自在に設けたことを特徴とする微量
サンプル測定装置。 A sensor for specifying the properties of the test liquid is provided at the tip of the micro sample suction device, and a tip cover having a liquid suction port and covering the sensor is detachably provided at the tip. Micro sample measuring device.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8729583U JPS59191638U (en) | 1983-06-07 | 1983-06-07 | Micro sample measuring device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8729583U JPS59191638U (en) | 1983-06-07 | 1983-06-07 | Micro sample measuring device |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59191638U JPS59191638U (en) | 1984-12-19 |
JPH0213959Y2 true JPH0213959Y2 (en) | 1990-04-17 |
Family
ID=30217207
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8729583U Granted JPS59191638U (en) | 1983-06-07 | 1983-06-07 | Micro sample measuring device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59191638U (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001286771A (en) * | 2000-04-07 | 2001-10-16 | Arkray Inc | Multiple pipette |
JP2005522246A (en) * | 2002-04-08 | 2005-07-28 | ディジム,テュンサー | A method for measuring blood urea concentration by reverse iontophoresis. |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009018473A1 (en) * | 2007-07-31 | 2009-02-05 | Micronics, Inc. | Sanitary swab collection system, microfluidic assay device, and methods for diagnostic assays |
TWI631337B (en) * | 2012-10-29 | 2018-08-01 | 榮研化學股份有限公司 | Sample inspection device |
JP6668477B2 (en) * | 2017-06-28 | 2020-03-18 | 佳則 山口 | Measuring pipette tip, measuring device and measuring method using the measuring pipette tip |
EP3995210A4 (en) * | 2019-09-03 | 2022-08-31 | Kyocera Corporation | Pipette tip and pipette |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5260684A (en) * | 1975-11-14 | 1977-05-19 | Hitachi Ltd | Sample dispenser |
JPS5326144U (en) * | 1976-08-12 | 1978-03-06 | ||
JPS5668429A (en) * | 1979-11-07 | 1981-06-09 | Olympus Optical Co | Ion concentration measuring apparatus |
-
1983
- 1983-06-07 JP JP8729583U patent/JPS59191638U/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5260684A (en) * | 1975-11-14 | 1977-05-19 | Hitachi Ltd | Sample dispenser |
JPS5326144U (en) * | 1976-08-12 | 1978-03-06 | ||
JPS5668429A (en) * | 1979-11-07 | 1981-06-09 | Olympus Optical Co | Ion concentration measuring apparatus |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001286771A (en) * | 2000-04-07 | 2001-10-16 | Arkray Inc | Multiple pipette |
WO2001076754A1 (en) * | 2000-04-07 | 2001-10-18 | Arkray, Inc. | Multiple pipette and method of using the same |
JP4576502B2 (en) * | 2000-04-07 | 2010-11-10 | アークレイ株式会社 | Multiple pipette |
JP2005522246A (en) * | 2002-04-08 | 2005-07-28 | ディジム,テュンサー | A method for measuring blood urea concentration by reverse iontophoresis. |
Also Published As
Publication number | Publication date |
---|---|
JPS59191638U (en) | 1984-12-19 |
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