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JPH0733986B2 - Blood biochemical substance continuous measuring device - Google Patents
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JPH0733986B2 - Blood biochemical substance continuous measuring device - Google Patents

Blood biochemical substance continuous measuring device

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Publication number
JPH0733986B2
JPH0733986B2 JP60130748A JP13074885A JPH0733986B2 JP H0733986 B2 JPH0733986 B2 JP H0733986B2 JP 60130748 A JP60130748 A JP 60130748A JP 13074885 A JP13074885 A JP 13074885A JP H0733986 B2 JPH0733986 B2 JP H0733986B2
Authority
JP
Japan
Prior art keywords
blood
sample
measuring
biochemical substance
sensor
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP60130748A
Other languages
Japanese (ja)
Other versions
JPS61290363A (en
Inventor
耕一 滝澤
三樹男 高田
聡 中嶋
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.)
Omron Corp
Original Assignee
Omron Corp
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 Omron Corp filed Critical Omron Corp
Priority to JP60130748A priority Critical patent/JPH0733986B2/en
Publication of JPS61290363A publication Critical patent/JPS61290363A/en
Publication of JPH0733986B2 publication Critical patent/JPH0733986B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Investigating Or Analysing Biological Materials (AREA)
  • Sampling And Sample Adjustment (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)

Description

【発明の詳細な説明】 《産業上の利用分野》 この発明は、血液を連続的に採取しながら血中の生化学
物質を測定する血中生化学物質連続測定装置に関する。
Description: TECHNICAL FIELD The present invention relates to a continuous blood biochemical substance measuring device for measuring a biochemical substance in blood while continuously collecting blood.

《従来の技術》 この種の血中生化学物質連続測定装置としては、従来、
次のような構成のグルコース測定装置が知られている。
<Prior art> As a continuous biochemical substance measuring device in this type,
A glucose measuring device having the following configuration is known.

血管内に留置された2重管カテーテルおよびこれに連結
された採血ポンプにより、ヘパリン溶液で希釈しながら
血液を連続的に採取する。その血液試料は、緩衝液と混
合され、グルコース電極の感応部を通過し、ドレンボト
ルへと別のポンプで送給される。グルコース電極にて試
料液中のグルコース濃度が検出される。また、グルコー
ス濃度の既知な標準液についても上記グルコース電極で
測定する構成を有し、測定系を較正するようになってい
る。
Blood is continuously collected while being diluted with a heparin solution by a double-tube catheter placed in a blood vessel and a blood collection pump connected thereto. The blood sample is mixed with the buffer solution, passes through the sensitive part of the glucose electrode, and is pumped to the drain bottle by another pump. The glucose concentration in the sample solution is detected by the glucose electrode. Further, a standard solution having a known glucose concentration is also measured by the glucose electrode, and the measurement system is calibrated.

《発明が解決しようとする問題点》 この装置は患者から採血しながら使用するものであるか
ら、正しい測定を阻害する異常の発生を極力少なくする
ことと、もし異常が発生しても原因究明と回復処置が容
易であることが非常に重要である。従来の装置はこの点
で不十分である。
<Problems to be solved by the invention> Since this device is used while collecting blood from a patient, it is necessary to minimize the occurrence of abnormalities that obstruct correct measurement, and to investigate the cause even if abnormalities occur. It is very important that the recovery procedure is easy. Conventional devices are deficient in this respect.

代表的な異常の1つに、酵素電極(グルコース電極)の
出力レベルが異常に低いという事態がある。この異常を
分析すれば、所定濃度以上の被測定物質(グルコース)
を含んだ試料液が電極感応部を通過しているのに電極出
力レベルが異常に低い場合と、電極感応部を通過してい
る試料液の被測定物質濃度が異常に低い場合とがある。
One of the typical abnormalities is a situation where the output level of the enzyme electrode (glucose electrode) is abnormally low. If this abnormality is analyzed, the substance to be measured (glucose) above a certain concentration
There are cases in which the sample liquid containing the element is passing through the electrode sensitive section but the electrode output level is abnormally low, and cases in which the sample solution passing through the electrode sensitive section has an abnormally low concentration of the substance to be measured.

前者の場合は、電極それ自体、あるいは電極出力の処理
系が異常原因となっており、酵素膜の交換とか、回路動
作のチエツクなどの対策をとることになる。
In the former case, the electrode itself or the processing system of the electrode output is the cause of abnormality, and countermeasures such as replacement of the enzyme membrane and checking of circuit operation will be taken.

後者の場合は、採血が正しく行なわれていないと考えて
良い。例えば、カテーテルの装着が適切でなかつたり、
装着後に患者が動いたりし、血液がまつたく採取されな
かつたり、採血量が規定量に満たなかつたりし、試料液
の希釈率が増え、電極に達する試料液の被測定物質濃度
が異常低下する。また、採血系統の試料チユーブが非常
に細いので、抗凝固剤を用いているにもかかわらず、血
液試料が凝固して詰まり、上記と同じことが起こる。
In the latter case, it may be considered that blood collection is not performed properly. For example, when the catheter is worn properly,
The patient may move after wearing the device, blood may not be collected rapidly, or the amount of blood collected may not reach the specified amount, the dilution rate of the sample solution may increase, and the concentration of the measured substance in the sample solution reaching the electrode may abnormally decrease. . Further, since the sample tube of the blood collection system is very thin, the blood sample coagulates and becomes clogged even though the anticoagulant is used, and the same as above occurs.

後者の異常は装置異常ではなく、採血系統の取り扱いの
不適切さが原因で、異常回復の処置も前者の場合とはま
つたく異なる。
The latter abnormality is not a device abnormality but is caused by inadequate handling of the blood collection system, and the abnormality recovery procedure is also different from the former case.

前述した従来の装置においては、標準液を電極感応部に
供給する較正モードにて、電極出力レベルが異常に低い
と警報を発するようになつていた。この異常診断機能は
前者の異常の発見に有効であるが、血液試料の測定モー
ドで生じる後者の異常についてはまつたく役立たない。
In the above-mentioned conventional apparatus, an alarm is issued when the electrode output level is abnormally low in the calibration mode in which the standard solution is supplied to the electrode sensitive section. This abnormality diagnosis function is effective for finding the former abnormality, but is not useful for the latter abnormality that occurs in the blood sample measurement mode.

そのため従来の装置は、採血ミスや血液の詰まりなどの
異常を発見するのに非常に時間がかかり、実際面での使
い勝手が良くなかつた。
Therefore, the conventional device takes a very long time to detect an abnormality such as a blood sampling error or blood clogging, and is not easy to use in actual use.

この発明は上述した従来の問題点に鑑みなされたもの
で、その目的は、採血ミスや血液の詰まりなどによつて
生じる異常を速やかに発見できるようにした血中生化学
物質連続測定装置を提供することにある。
The present invention has been made in view of the above-mentioned conventional problems, and an object thereof is to provide a blood biochemical continuous measurement device capable of promptly discovering an abnormality caused by a blood sampling error or blood clogging. To do.

《問題点を解決するための手段》 そこでこの発明では、抗凝固剤を混入させながら血液を
連続的に採取する採血手段と、採取された血液を希釈し
て流送する流送手段と、希釈された血液と連続的に接触
して生化学物質を測定する測定手段と、この測定手段に
上記血液試料に代って標準液を供給する較正手段とを備
えるものにおいて、上記採血手段あるいは上記流送手段
における血液試料の流路途中に、この流路中の血液が所
定濃度以上か否かを検知する血液センサを設けると共
に、この血液センサの検知結果を表示する表示手段を備
え構成した。
<< Means for Solving Problems >> Accordingly, in the present invention, a blood collecting means for continuously collecting blood while mixing an anticoagulant, a sending means for diluting and sending the collected blood, and a diluting means. The blood collecting means or the flow means, which comprises a measuring means for continuously measuring the biochemical substance by continuous contact with the collected blood and a calibrating means for supplying a standard solution to the measuring means instead of the blood sample. A blood sensor for detecting whether or not the blood in the flow passage has a predetermined concentration or more is provided in the middle of the flow path of the blood sample in the sending means, and a display means for displaying the detection result of the blood sensor is provided.

《作用》 カテーテルの装着が適切でなかつたり、採血口近くの細
いチユーブで血液が詰まつたりすると、上記流路を流れ
る試料液中の血液濃度が急激に低下あるいはゼロにな
り、そのことが上記血液センサで速やかに検出される。
<Operation> If the catheter is not properly attached or blood is clogged with a thin tube near the blood collection port, the blood concentration in the sample liquid flowing through the flow channel will suddenly decrease or become zero. Quickly detected by blood sensor.

《実施例》 第1図はこの発明の一実施例装置のフローシステムの概
要を示している。同図において、11は採血口であるカテ
ーテル、12は抗凝固剤としてヘパリンを含んだ生理食塩
水(以下、ヘパリン生食水と称す)の容器、13と16は採
血用ポンプ、14は血液とヘパリン生食水との混合器で、
これらは採血手段を構成しており、この採血手段の血液
試料の流路中に本発明の要部となる血液センサ15を設け
ている。カテーテル11を患者に正しく装着し、ポンプ1
3,16とを所定速度(流量)で作動させることにより、カ
テーテル11から所定流量の血液が吸引されるとともに容
器12から所定流量のヘパリン生食水が吸引され、これら
が混合器14で混合され、血液センサ15を通つて切換弁18
側へ流送される。
<< Embodiment >> FIG. 1 shows an outline of a flow system of an embodiment of the present invention. In the figure, 11 is a catheter as a blood sampling port, 12 is a container of physiological saline containing heparin (hereinafter referred to as heparin saline) as an anticoagulant, 13 and 16 are blood sampling pumps, 14 is blood and heparin. Mixer with raw water,
These constitute blood collecting means, and a blood sensor 15 which is an essential part of the present invention is provided in the blood sample flow path of the blood collecting means. Correctly attach the catheter 11 to the patient and pump 1
By operating 3, 16 and 16 at a predetermined speed (flow rate), a predetermined flow rate of blood is sucked from the catheter 11 and a predetermined flow rate of heparin saline is suctioned from the container 12, and these are mixed in the mixer 14, Switching valve 18 through blood sensor 15
Sent to the side.

切換弁18は、上記採血手段による血液試料(ヘパリン生
食水で希釈された血液)と、容器17の標準液とを選択的
にポンプ20側へ導く。このポンプ20ともう1つのポンプ
23とが流送手段の主要部であり、血液試料または標準液
を緩衝液で希釈し、酵素電極27による測定手段を通過さ
せ、ドレン容器(図示省略)に排出する。
The switching valve 18 selectively guides the blood sample (blood diluted with heparin saline) and the standard solution in the container 17 to the pump 20 side by the blood collecting means. This pump 20 and another pump
Reference numeral 23 is a main part of the sending means, and the blood sample or the standard solution is diluted with a buffer solution, passed through the measuring means by the enzyme electrode 27, and discharged into a drain container (not shown).

22は緩衝液の容器、21は血液試料(または標準液)に上
記緩衝液と開放ライン24からの気泡を混合する混合器、
25はこれらの混合を促進するミキシングコイル、26は混
入された気泡を除去する脱泡器である。脱泡器26を経た
溶液の一部を酵素電極27の感応部に流送し、残りは廃棄
する。なお21,25,26,27からなる部分はヒーテイングブ
ロツク28で加熱されている。
22 is a container for buffer solution, 21 is a mixer for mixing the buffer solution and air bubbles from the open line 24 with a blood sample (or standard solution),
Reference numeral 25 is a mixing coil that promotes mixing of these, and 26 is a defoaming device that removes mixed air bubbles. A part of the solution passed through the defoamer 26 is sent to the sensitive part of the enzyme electrode 27, and the rest is discarded. The part consisting of 21, 25, 26, 27 is heated by a heating block 28.

上記のフローシステムはマイクロコンピユータによつて
制御され、通常は測定モードで、比較的長い一定周期で
較正モードが行なわれる。測定モードでは上記のように
採血手段が作動し、血液試料が酵素電極27を通過し、特
定の生化学物質の濃度が検出される。較正モードでは切
換弁18が容器17側に切換わり、標準液が酵素電極27を通
過し、このときの検出値でもつて測定系が較正される。
なお較正モードでは、ポンプ16は停止し、ポンプ13は低
速で駆動される。ポンプ13によつてヘパリン生食水をカ
テーテル11,混合器14,血液センサ15に流入させ、非採血
中の血液の凝固を防ぐ。
The above-mentioned flow system is controlled by a microcomputer, and is normally in a measurement mode and a calibration mode with a relatively long constant period. In the measurement mode, the blood collecting means operates as described above, the blood sample passes through the enzyme electrode 27, and the concentration of the specific biochemical substance is detected. In the calibration mode, the switching valve 18 is switched to the container 17 side, the standard solution passes through the enzyme electrode 27, and the measurement system is calibrated with the detection value at this time.
In the calibration mode, the pump 16 is stopped and the pump 13 is driven at a low speed. Heparin saline is caused to flow into the catheter 11, the mixer 14, and the blood sensor 15 by the pump 13 to prevent coagulation of blood during non-blood sampling.

次に、この発明の要部である血液センサ15について説明
する。血液センサ15の構造の一例を第2図に示してい
る。
Next, the blood sensor 15, which is a main part of the present invention, will be described. An example of the structure of blood sensor 15 is shown in FIG.

第2図において、31は混合器14につながるチユーブ、32
はポンプ16につながるチユーブで、これらの間に血液セ
ンサ15が接続されている。血液センサ15は、不透明な外
殻体33の内部に、透明な材質(石英など)からなる偏平
な透明管34を内蔵している。この透明管34はチユーブ3
1,32と連通しており、ヘパリン生食水で希釈された血液
試料が透明管34を通つて流れる。
In FIG. 2, 31 is a tube connected to the mixer 14, 32
Is a tube connected to the pump 16, and the blood sensor 15 is connected between them. The blood sensor 15 has a flat transparent tube 34 made of a transparent material (such as quartz) built in an opaque outer shell 33. This transparent tube 34 is a tube 3
In communication with 1, 32, a blood sample diluted with heparin saline is flowed through a transparent tube 34.

透明管34の対向する2平面の外側には発光器35と受光器
36とが設けられており、発光器35から生じた光が透明管
34を横断して受光器36に達するように配置されている。
発光器35から発生する光の波長は、血液の濃度によつて
透過光量が大きく変化するように、540nm程度が好まし
い。発光器35としては例えばハロゲンランプとフイルタ
ーの組合せを使用し、受光器36としては例えばフオトダ
イオードを使用する。
A light emitting device 35 and a light receiving device are provided outside the two opposite planes of the transparent tube 34.
36 is provided, and the light emitted from the light emitter 35 is a transparent tube.
It is positioned so that it crosses 34 and reaches the light receiver 36.
The wavelength of the light emitted from the light emitter 35 is preferably about 540 nm so that the amount of transmitted light greatly changes depending on the blood concentration. As the light emitter 35, for example, a combination of a halogen lamp and a filter is used, and as the light receiver 36, for example, a photodiode is used.

発光器35は発光駆動回路37の出力を受けて発光し、受光
器36の出力は増幅回路38を経てレベル弁別回路39に入力
される。透明管34内を流れる溶液の血液濃度が高い程、
発光器35から受光器36に達する光量が減り、血液濃度が
低いと受光光量が大きくなる。レベル弁別回路39は増幅
された受光出力を受けて、血液濃度が所定値以上か否か
を判定する。その判定結果が表示回路40で表示される。
The light emitter 35 receives the output of the light emission drive circuit 37 and emits light, and the output of the light receiver 36 is input to the level discrimination circuit 39 via the amplifier circuit 38. The higher the blood concentration of the solution flowing in the transparent tube 34,
The amount of light reaching the light receiver 36 from the light emitter 35 decreases, and the amount of light received increases when the blood concentration is low. The level discrimination circuit 39 receives the amplified received light output and determines whether the blood concentration is equal to or higher than a predetermined value. The determination result is displayed on the display circuit 40.

《発明の効果》 以上詳細に説明したように、この発明に係る血中生化学
物質連続測定装置にあつては、正しく採血されているか
否か、または採血された試料が正しく測定手段まで流送
されているか否かが、試料流路中に設けた血液センサに
よつて常時チエツクされているので、採血ミスや詰まり
などを生じても、すぐに適切な回復処置がとれ、円滑な
測定が可能になる。
<< Effects of the Invention >> As described in detail above, in the blood biochemical substance continuous measuring apparatus according to the present invention, whether or not blood is correctly collected, or the collected sample is correctly sent to the measuring means. Whether or not the sample has been collected is constantly checked by the blood sensor provided in the sample flow path, so even if a blood sampling error or clogging occurs, appropriate recovery measures can be taken immediately and smooth measurement can be performed. become.

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

第1図はこの発明の一実施例装置のフローシステムの概
要を示すブロツク図、第2図は同上装置における血液セ
ンサの構成例を示す図である。 11……カテーテル、12……ヘパリン生食水容器、13……
ポンプ、14……混合器、15……血液センサ、16……ポン
プ、17……標準液容器、18……切換弁、20……ポンプ、
21……混合器、22……緩衝液容器、23……ポンプ、24…
…開放ライン、25……ミキシングコイル、26……脱泡
器、27……酵素電極、28……ヒーテイングブロツク、3
1,32……チユーブ、33……外殻体、34……透明管、35…
…発光器、36……受光器。
FIG. 1 is a block diagram showing an outline of a flow system of an apparatus according to an embodiment of the present invention, and FIG. 2 is a diagram showing a configuration example of a blood sensor in the apparatus. 11 …… Catheter, 12 …… Heparin saline container, 13 ……
Pump, 14 ... Mixer, 15 ... Blood sensor, 16 ... Pump, 17 ... Standard solution container, 18 ... Switching valve, 20 ... Pump,
21 ... Mixer, 22 ... Buffer container, 23 ... Pump, 24 ...
… Open line, 25 …… Mixing coil, 26 …… Deaerator, 27 …… Enzyme electrode, 28 …… Heating block, 3
1,32 …… Chuube, 33 …… Outer shell, 34 …… Transparent tube, 35…
… Light emitter, 36 …… light receiver.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 中嶋 聡 京都府京都市右京区花園中御門町3番地 株式会社立石ライフサイエンス研究所内 (56)参考文献 特開 昭58−38856(JP,A) 実開 昭60−79145(JP,U) 実開 昭57−101981(JP,U) 特公 昭58−11018(JP,B2) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Satoshi Nakajima Satoshi Nakajima, No. 3 Nakamimon-cho, Hanazono, Ukyo-ku, Kyoto Prefecture, Japan Tateishi Life Science Laboratory Co., Ltd. (56) Reference JP-A-58-38856 (JP, A) Actual Kai 60-79145 (JP, U) Actual Kai 57-101981 (JP, U) Japanese Patent Sho 58-11018 (JP, B2)

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】抗凝固剤を混入させながら血液を連続的に
採取する採血手段と、採取された血液を希釈して流送す
る流送手段と、希釈された血液と連続的に接触して生化
学物質を測定する測定手段と、この測定手段に上記血液
試料に代って標準液を供給する較正手段とを備えるもの
において、上記採血手段あるいは上記流送手段における
血液試料の流路途中に、この流路中の血液が所定濃度以
上か否かを検知する血液センサを設けると共に、この血
液センサの検知結果を表示する表示手段を備えたことを
特徴とする血中化学物質連続測定装置。
1. A blood collecting means for continuously collecting blood while mixing an anticoagulant, a sending means for diluting and sending the collected blood, and a continuous contact with the diluted blood. A measuring means for measuring a biochemical substance and a calibrating means for supplying a standard solution to the measuring means instead of the blood sample, wherein the blood collecting means or the sending means has a blood sample in the middle of the flow path. An apparatus for continuously measuring chemical substances in blood, comprising: a blood sensor for detecting whether or not blood in the flow channel has a predetermined concentration or more, and display means for displaying a detection result of the blood sensor.
JP60130748A 1985-06-18 1985-06-18 Blood biochemical substance continuous measuring device Expired - Lifetime JPH0733986B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60130748A JPH0733986B2 (en) 1985-06-18 1985-06-18 Blood biochemical substance continuous measuring device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60130748A JPH0733986B2 (en) 1985-06-18 1985-06-18 Blood biochemical substance continuous measuring device

Publications (2)

Publication Number Publication Date
JPS61290363A JPS61290363A (en) 1986-12-20
JPH0733986B2 true JPH0733986B2 (en) 1995-04-12

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP60130748A Expired - Lifetime JPH0733986B2 (en) 1985-06-18 1985-06-18 Blood biochemical substance continuous measuring device

Country Status (1)

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JP (1) JPH0733986B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3126507A1 (en) * 1981-07-04 1983-01-20 Surculus AG, Vaduz "ARMATURE"
JPS5838856A (en) * 1981-08-31 1983-03-07 Kyoto Daiichi Kagaku:Kk Automatic liquid chromatograph apparatus

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JPS61290363A (en) 1986-12-20

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