JPS5983031A - Liquid sampling and transferring apparatus - Google Patents

Liquid sampling and transferring apparatus

Info

Publication number
JPS5983031A
JPS5983031A JP57192567A JP19256782A JPS5983031A JP S5983031 A JPS5983031 A JP S5983031A JP 57192567 A JP57192567 A JP 57192567A JP 19256782 A JP19256782 A JP 19256782A JP S5983031 A JPS5983031 A JP S5983031A
Authority
JP
Japan
Prior art keywords
liquid
tube
sample
sampling
air
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
JP57192567A
Other languages
Japanese (ja)
Inventor
Yoshiro Kubo
久保 嘉郎
Shinji Kiyofuji
真次 清藤
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.)
Fuji Electric Co Ltd
Original Assignee
Fuji Electric Corporate Research and Development 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
Priority to JP57192896A priority Critical patent/JPS5983032A/en
Application filed by Fuji Electric Corporate Research and Development Ltd filed Critical Fuji Electric Corporate Research and Development Ltd
Priority to JP57192567A priority patent/JPS5983031A/en
Publication of JPS5983031A publication Critical patent/JPS5983031A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/155Devices specially adapted for continuous or multiple sampling, e.g. at predetermined intervals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150015Source of blood
    • A61B5/15003Source of blood for venous or arterial blood
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150206Construction or design features not otherwise provided for; manufacturing or production; packages; sterilisation of piercing element, piercing device or sampling device
    • A61B5/150221Valves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150206Construction or design features not otherwise provided for; manufacturing or production; packages; sterilisation of piercing element, piercing device or sampling device
    • A61B5/150229Pumps for assisting the blood sampling
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150206Construction or design features not otherwise provided for; manufacturing or production; packages; sterilisation of piercing element, piercing device or sampling device
    • A61B5/150267Modular design or construction, i.e. subunits are assembled separately before being joined together or the device comprises interchangeable or detachable modules
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150946Means for varying, regulating, indicating or limiting the speed or time of blood collection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/153Devices specially adapted for taking samples of venous or arterial blood, e.g. with syringes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150992Blood sampling from a fluid line external to a patient, such as a catheter line, combined with an infusion line; blood sampling from indwelling needle sets, e.g. sealable ports, luer couplings, valves

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Medical Informatics (AREA)
  • Hematology (AREA)
  • Biophysics (AREA)
  • Pathology (AREA)
  • Veterinary Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Physics & Mathematics (AREA)
  • Molecular Biology (AREA)
  • Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Manufacturing & Machinery (AREA)
  • Sampling And Sample Adjustment (AREA)

Abstract

PURPOSE:To draw a sample liquid at every specified time interval and to make it possible to perform transferring, by providing a liquid withdrawing part, a liquid holding container part, a sucking and injecting part, and a control means, which monitors and controls the operation of a liquid sampling and transferring apparatus. CONSTITUTION:A liquid sampling and transferring apparatus is constituted by a liquid withdrawing part A, a liquid holding container part B, a sucking and injecting part C, and a control means, which monitors and controls the operation of the liquid sampling and transferring apparatus. The liquid withdrawing part A has the following devices; a constant quantity sampling tube 3, which contains a specified amount of a sample liquid from a blood vessel 1 of a living body or a sample holding container through a blood withdrawing tube 2 and a supplying port 3A; a syringe port 5A, which is connected to said tube 3; and the like. In this constitution, the sample substance can be withdrawn at every specified time interval, and the transferring can be performed.

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、全血、血漿、血清等の検体液を検査または分
析するに当り、採取された所定量の検体液を分析計等の
測定部に連続的に転輸する採液・転輸装置に関する。 この種の装置は、分析計等の測定部への検体液の注入量
が均一で、再現性がよく、注入系統の洗浄が容易である
と共に、一連の動作が自動的でしかも確実に行い得るこ
と等が要望される。従来、このような採液はシリンジと
、注射針等の採取口とを組合わせて、その都度血管また
は検体液保存容器に採液口を挿入し、シリンジを手動的
または機械的に動かして採液し、採液の後再びシリンジ
により、分析計等の測定部に注入または転注するという
方法が採用さf’していた。7.’C:I’o、この注
入量は1回当り最小で、約数10μ6程度の徹少量であ
る。 まだ、生体より連続的に採血する方法と1−て、人工卑
臓による血液透析装置mがある。この装置の採血系統に
は洗浄機能が通常具備されていない。 すなわち、測定部により連続的7.cデータが得られる
ことが必要であるが、通常、生体の変化は時間的にそれ
程太ぎた変化をし7fい。一般的には数分程度の間欠的
なi11+1定を繰返すことができれば十分で、その測
定結果を連続的なデータとみなすことができる。また、
上述の拙液透析装置が通用される特別な場合を除き、連
続的に検体液を採取することは、当然その採取量が増加
するから、生体の安全上の問題が発生するおそれがある
。 本発明は、上述の点に鑑み、従来技術の問題点である生
体に接続されて所定の時間間隔毎に繰返し採取される所
定量の検体液が転輪さJ′1.ると共に、検体液の経路
内の自動的な洗浄が可能である採液転輸装置を提供する
ことを目的とする。 このような目的は本発明によれば、検体液を採取する採
液チューブと、前記検体液の所定量をサンプリングして
収容する定量サンプリングチューブと、この定量サンプ
リングチューブに残液吸入チューブを介して接続された
サンプリングシリンジと、前記定量サンプリングチュー
ブに接続されたエアポンプと、このエアポンプと並列し
て前記定量サンブリングチューブに接続された洗浄液ポ
ンプとを有する採液部と; 前記定量サンプリングチューブに接続された1次転送チ
ューブと、この1次転送チューブを経て前記エアポンプ
により前記定量サンプリングチューブ内に収容された前
記検体液が転送され収容される液溜容器とを有する液溜
容器部と;前記液溜容器に接続された2次転送チューブ
を介して前記液溜容器内の検体液の所定量を吸引し、注
入チューブを経て測定部に注入するシリンジを有する吸
引・注入部と: 前記シリンジにより前記測定部に前記検体液の所定量が
注入さilて測尼が終了した後、6+1記採危部、液溜
容器(718j6よび吸引・注入部のそれぞilの検体
液の経路に前記洗浄液ポンプより洗浄液を送出して洗浄
し、さらに前記エアポンプにより空気を送用1−て前記
い一浄液を排出することを連n的に繰返す制御手段とを
備えることにより箭(成すiする。 沈圧、本発明の一実施例を図面に基づき、詳細に説ψJ
する。 第1図は本発明の一実施例の計(4,陥構成IM+、第
2図は第1図のa=b作タイミングチャートを7J<す
。第1図および第2図に?いてこの採液・転輪装置幌は
、例えば閉ループ式全血尾連続自動皿糖分析装置用とし
て用いられ、採液部A、1rIl溜谷器部B、11゛(
引・注入部Cおよびこの採液・転輸装置の動作′ff:
!ii、L視し制御する制御手段(図示δれていない)
から構成される。採液部Aは生体、rlll管】または
し17トされていない試料容器より、検体液を採取1−
る採血チューブ2、この採血チューブ2;「dよび世相
「」3Aを経て、所定量の検体液を収容する定、1tツ
ンプリングチューブ3、この定量サンプリングチューブ
3の残液吸入口3Bに残液吸入チューブ6を経て接続さ
れるシリンシロ5Aならびに移動自在なシリンジロッド
5Bを有するサンプリングシリンジ5、定量サンプリン
グチューブ3の残液吸入口3Bに2次エアチューブ7な
らびに1次エアチューブ12を介して接続されたエアポ
ンプLIMよび残液吸入口3Bに2次エアチューブ7な
らびに洗浄液チューブ10を介して接続された洗浄液ボ
ンダ9とからなる。また、大口弁4は採血チューブ2の
液経路に設けられ、エア開口弁8は2次エアチューブ7
に設けられる。なお、31.32はサンプリングシリン
ジに設けられる採血終了検知スイッチ、残液検出検知ス
イッチである。ナユーブ接続部35は2次エアチューブ
7を1次エアチューブ】2に接続し、かつ逆上弁34を
経て洗浄液チューブ】0に接続するT形接続管で、エア
ポンプ11および洗浄液ポンプ9を並列に配置する。 また、液溜答器部Bは、定量サンプリングチューブ3の
供給[(3人に接続され検体液、洗浄液、空気を転送す
る1次転送チューブ14、供給1コ3Aと1次転送チュ
ーブ14との間に設けられた転送側弁15および採赦部
Aより1次転送チューブ14を経て転送される液を、流
入口13Aを経て収容する液溜容器13、g溜容器13
の排出口13Bに1次転送チューブ14より供給される
検体液輸送のだめの空気と洗浄のための洗浄液とを外部
へ放出する排出チューン16J6よび1シ「量弁17か
らなる。 なお、吸引・注入部Cは、液溜容器13の底部に設けら
れた試料供給口13Cに接続さfLる2次転送チューブ
22j6よび2次転送開閉弁36と、十字管接続部21
を経て液溜容器13内の検体液を吸引して注入液溜管1
8内に採取し、十字管接続部21、注入チューブ19お
よび注入弁23を経て測定部(分析計)33に検体液を
注入するシリンシロ20Aを有するシリンジ20と、廃
液弁24を経て廃液タンク25に廃液を排出する廃液チ
ューブ26等力)らなる。また、シリンジ20にはシリ
ンジロッド20Bの位置を検出する吸引終了検知スイッ
チ27.1次注入検知スイッチ28、定量注入停止スイ
ッチ29によび注入終了検知スイッチ30が具備されて
いる。 上述の栴・成により本発明の詳細な説明する。採取部A
において、エア開閉弁8と転送側弁15を閉状態に保持
し、大口弁4を開とし、サンプリングシリンジ5のサン
プリングシリンジロッド5Bの吸引動作により、採血チ
ューブ2、定量サンプリングチューブ3および残液吸入
チューブ6の液経路内を減圧し、生体血管1との圧力差
に基つぎ、採血チューブ2を経て血液(検体液)が定量
サンプリングチューブ3に円滑に供給される。また、採
血チューブ2内に残っていた古い残液は定量サンプリン
グチューブ3を経
The present invention provides a liquid collection/transfer device that continuously transfers a predetermined amount of sample liquid to a measuring section of an analyzer when testing or analyzing sample liquids such as whole blood, plasma, and serum. Regarding. This type of device injects a uniform amount of sample liquid into the measuring section of an analyzer, etc., has good reproducibility, makes cleaning the injection system easy, and can perform a series of operations automatically and reliably. This is requested. Conventionally, such liquid collection has been performed by combining a syringe and a collection port such as an injection needle, inserting the liquid collection port into a blood vessel or sample liquid storage container each time, and moving the syringe manually or mechanically to collect the sample. A method has been adopted in which the liquid is drained, and after the liquid is collected, it is again injected or transferred into the measuring section of an analyzer or the like using a syringe. 7. 'C: I'o, this injection amount is the minimum per injection, which is about several tens of μ6. There is still a method for continuously collecting blood from a living body, and there is a hemodialysis device using an artificial kidney. The blood collection system of this device usually does not have a cleaning function. That is, the measuring section continuously measures 7. Although it is necessary to obtain c data, normally biological changes occur over time and are 7f long. Generally, it is sufficient to repeat intermittent i11+1 constants of several minutes, and the measurement results can be regarded as continuous data. Also,
Except for special cases where the above-mentioned liquid dialysis apparatus is used, continuous collection of specimen fluid naturally increases the amount of specimen fluid collected, which may pose a safety problem for the living body. In view of the above-mentioned points, the present invention solves the problems of the prior art, in which a predetermined amount of sample fluid connected to a living body and repeatedly collected at predetermined time intervals is transferred to a rolling wheel J'1. It is an object of the present invention to provide a liquid sampling transfer device that is capable of automatically cleaning the passage of a sample liquid. According to the present invention, such a purpose is achieved by providing a liquid collection tube for collecting a sample liquid, a quantitative sampling tube for sampling and storing a predetermined amount of the sample liquid, and a residual liquid suction tube connected to the quantitative sampling tube. a liquid sampling section having a sampling syringe connected thereto, an air pump connected to the quantitative sampling tube, and a washing liquid pump connected to the quantitative sampling tube in parallel with the air pump; a liquid reservoir portion having a primary transfer tube, and a liquid reservoir container into which the sample liquid contained in the quantitative sampling tube is transferred and stored by the air pump via the primary transfer tube; a suction/injection unit having a syringe that aspirates a predetermined amount of the sample liquid in the liquid storage container via a secondary transfer tube connected to the container and injects it into the measurement unit via the injection tube; After the predetermined amount of the sample liquid is injected into the 6+1 collection unit, the liquid storage container (718j6, and the suction/injection unit) are injected into the sample liquid path from the cleaning liquid pump. By providing a control means for sending out the cleaning liquid for cleaning, and further repeating the steps of sending air by the air pump and discharging the cleaning liquid continuously, An embodiment of the present invention will be explained in detail based on the drawings ψJ
do. FIG. 1 shows the total configuration of one embodiment of the present invention (4, IM+), and FIG. 2 shows the a=b operation timing chart of FIG. 1. The liquid/roller device hood is used, for example, for a closed-loop whole blood tail continuous automatic dish sugar analyzer.
Operation of the suction/injection part C and this liquid collection/transfer device'ff:
! ii. Control means for viewing and controlling the L (not shown in the figure)
It consists of The liquid sampling section A collects the sample liquid from a living body, rllll tube] or an unfilled sample container.
A blood sampling tube 2, this blood sampling tube 2; a fixed, 1t tumpling tube 3 that accommodates a predetermined amount of sample liquid through 3A, and a residual liquid in the residual liquid inlet 3B of this quantitative sampling tube 3. A sampling syringe 5 having a syringe barrel 5A and a movable syringe rod 5B is connected via a suction tube 6, and a sampling syringe 5 is connected to a residual liquid inlet 3B of a quantitative sampling tube 3 via a secondary air tube 7 and a primary air tube 12. It consists of an air pump LIM and a cleaning liquid bonder 9 connected to the residual liquid suction port 3B via a secondary air tube 7 and a cleaning liquid tube 10. Further, the large mouth valve 4 is provided in the liquid path of the blood collection tube 2, and the air opening valve 8 is provided in the secondary air tube 7.
established in Note that 31 and 32 are a blood collection end detection switch and a residual liquid detection switch provided on the sampling syringe. The naube connection part 35 is a T-shaped connecting pipe that connects the secondary air tube 7 to the primary air tube 2 and then to the cleaning liquid tube 0 via the reverse valve 34, and connects the air pump 11 and the cleaning liquid pump 9 in parallel. Deploy. In addition, the liquid reservoir section B is connected to the supply of the quantitative sampling tube 3 [(the primary transfer tube 14 which is connected to three people and transfers the sample liquid, washing liquid, and air; the supply 1 tube 3A and the primary transfer tube 14 A liquid storage container 13 and a g storage container 13 that accommodate the liquid transferred through the primary transfer tube 14 from the transfer side valve 15 provided in between and the collecting section A through the inflow port 13A.
It consists of a discharge tune 16J6 and a volume valve 17 for discharging to the outside the sample liquid transport tank air and the washing liquid for washing supplied from the primary transfer tube 14 to the discharge port 13B of the pipe. Section C includes a secondary transfer tube 22j6 and a secondary transfer on/off valve 36 connected to the sample supply port 13C provided at the bottom of the liquid storage container 13, and a cross tube connection section 21.
The sample liquid in the liquid reservoir 13 is aspirated through the injection liquid reservoir tube 1.
A syringe 20 having a syringe cap 20A for injecting sample liquid into the measuring section (analyzer) 33 through a cross tube connection 21, an injection tube 19 and an injection valve 23, and a waste liquid tank 25 via a waste liquid valve 24. It consists of a waste liquid tube 26 for discharging waste liquid. The syringe 20 is also equipped with a suction end detection switch 27, a primary injection detection switch 28, a quantitative injection stop switch 29, and an injection end detection switch 30 for detecting the position of the syringe rod 20B. The present invention will be described in detail by Shiba and Sei, mentioned above. Collection part A
At this time, the air on-off valve 8 and the transfer side valve 15 are kept closed, the large mouth valve 4 is opened, and the sampling syringe rod 5B of the sampling syringe 5 is suctioned to aspirate the blood collection tube 2, quantitative sampling tube 3, and residual liquid. The pressure inside the fluid path of the tube 6 is reduced, and based on the pressure difference with the biological blood vessel 1, blood (specimen fluid) is smoothly supplied to the quantitative sampling tube 3 via the blood collection tube 2. In addition, the old residual liquid remaining in the blood collection tube 2 is passed through the quantitative sampling tube 3.

【、残液吸入チューブ6内に収容され
ながら、この残液に引続いて新しい検体液が定量サンブ
リングチューブ3内に収容される。なお、採血チューブ
z内の残液が吸引され排除されると同時に、流入する新
しい検体液の一部少量液は、採血チューブ2および定量
サンプリングチューブ3の内壁罠付着する残液を洗い流
しながら、残液吸入チューブ6に残液と共に収容される
。従って、定量サンプリングチューブ3内には、汚染さ
れない新しい検体液が収容される。 なお、エア開閉弁8、転送側弁15および入口弁4をい
ずれも閉状態に保持した11で、ザングリングロツド5
Bによる吸引動作を行い、所定時間が経過した後、大口
弁4を開とするように制御すれは、減圧度が高くなり、
空気か採血チューブ2を経て生体血管1内に逆流混入す
るという危険を防止することができる。 サンプリングシリンジロッド5Bld、採厘終了検知ス
イッチ31により、所定量の検体液を採血した状態で停
止し、大口弁4を閉とし、エア開閉弁8と転送側弁15
と排出弁17とを開とする。 この状態で、エアポンプ11を作動し、送出される空気
圧により定量サンブリングチューブ3内の検体液を、Y
L溜容器部Bの1次転送チューブ14を経て、液溜容器
13に空気輸送する。この空気輸送による検体液の転送
時間tユ短く、第2図に示す測定サイクルLが大幅に短
縮される。検体液は流入口13Aより液溜容器13内に
流入して底部に収容される。一方、液溜容器13の内部
に充満した余剰の空気は、排出口13Bより1次排出チ
ューブ16を経て、外部に放出される。 吸引・注入部Cにおいて、注入弁23および廃液弁24
を閉に保持し、転送開閉弁36を開とし、シリンジ20
のシリンジロッド20Bの吸引動作により、2次転送チ
ューブ22どよび注入液溜管18の液経路を、液溜容器
13の内部より減圧状態にする。この圧力差に基づき、
液溜容器13の底部に収容された検体液を試料供給口1
3Cより、2次転送チューブ22を経て、注入液溜管1
8に吸引し収容する。シリンジロッドzOB&1:所足
量の検体液を注入液溜管18内に収容し終わると、吸引
終了検知スイッチ27の作動により停止すると共に、転
送開閉弁36を閉とし、注入弁z3i開とする。 次に、転送開閉弁36および廃液弁24を閉状態に、注
入弁23を開状態に保持すると、シリンジロッド20B
の注入動作により、シリンジ20内の空気層は高圧状態
となり、この空気層の圧力により注入チューブ19を紅
て乙ト人液溜’y(1sに収容されている検体液を、分
析計33へ注入する。 この注入動作の際に、注入チューブ19内に残留する空
気(気泡)は、注入される検体液により分析計33に押
出され、注入チューブ19内に(lま検体液が充満する
。それと共に、分析計33は注入される空気により、分
析計33内に発生する気泡を洗浄排出する洗浄動作が行
わtし、従って引続ぎ分析のために注入さノシろ検体液
には、分析精度に悪影響を与える気泡のυ[0人が防l
−されろ。シリンジロッド20Bは引続き注入動作を行
い、分析に心太な所定片の検体成金、注入チューブ19
を経て分析計33に注入し、定量注入停止スイッチ29
の作動により、注入動作を停止する。 なお、吸引終了検知スイッチ27の位置と、1次注入検
知スイッチ28の位置との間を、シリンジロッド20B
が移動する際のシリンジ20の内容積は、注入チューブ
190内谷積よりも太きくなるように、1次注入検知ス
イッチ28の位置が設定されろ。また、定量注入停止ス
イッチ290位1ん−は、1次注入検知スイッチ28の
位置から、分析に供される検体液の所定量の内容積に応
じて設定される。なお、注入終了検知スイッチ30の位
FI4.は、シリンジロッド20Bの先端がシリンジ1
−’] 20 Aに近接した位置であり、シリンジロッ
ド20Bが足鑵注入停止した時点でも、注入テニL−ブ
19内に少量の期成が残留し、分析中に注入チューブ1
9より分析計33内に気泡が流入する危険を防止する。 さらに、注入動作の際に(・jl、転送開閉弁36が閉
で、大口弁4を閉状態に保持し、エア開閉弁8、転送側
弁15J6よび排出弁17を開と(2て、サンプリング
シリンジロッド5Bは残液吸入チューブ6内の残液を、
定量サンプリングチューブ3に排出する。このとぎ、残
液排出検知スイッチ32は排出終了の後のサンプリング
シリンジロッド5Bの動作を停止さぜる。このサンプリ
ングシリンジロッド5Bが停止すると共に、洗浄液ポン
プ9およびエアボングエ1が作動し、洗浄液および空気
は2次エアチューブ7を経て、定量サンプリンタチュー
13月よひ1次転送チューブ14内の残液を洗浄し、流
入I] I 3 Aをね・て教溜容器13に充満し洗浄
し、その余剰液および空気はわl出口13Bより、排出
チューブ16を経て外部の廃液タンク25に放出さh−
ろ。予め設定された洗浄時間の後、洗浄液ポンプ9は停
止するも、エアポンプ11は空気の供給を続けて、抹v
1.部人および液溜容器部I3内の液経過を洗浄し、洗
浄液を排出1−1清掃する。このように、吸引・注入部
Cの注入・分析が行われる際に、採液部A j6よび液
溜容器部13か洗浄されるから、第2図に71”<す′
6111定サイクル時間りの短縮か可能である。 分析終了の後、転送開閉弁36を閉とし、注入弁23、
廃液弁24を開とし、シリンジロッド2Bは再び注入動
作をt2て、注入液溜管18、十字管接続部2】ゴdよ
び注入チューブ10の故紅A’fS内の残液を、廃液チ
ューブ26 :r6よび注入チコーーブ19を経て、廃
液タンク25によび分相泊33に排出する。注入終了検
知スイッチ30の作動により、この注入動作は停止する
。この停止と共に、転送開閉弁36、注入弁23お↓び
廃液弁24を開とし、排出弁17を閉とすることにより
、液溜容器13に残留する洗浄液は空気圧により、試料
供給口13 Cから2次転送チューブ22および注入チ
ューブ19を経て分析計33にまたは廃液チューブ26
を経て廃液タンク26にそれぞれの液経過を洗浄し排出
される。 このように、採液部り、fi、溜谷器部B、吸引・注入
部Cおよび分析計33全自動的に動作させる制御手段(
図示されていない)が設りられたことにより、検体液が
採血され、転送されて分析された後、液経路を洗浄し、
次の採血・転送・分析への連続的な移行が可能である。 また、定量サンプリングチューブ3において、分析に必
要な検体液量と、この装置全体の液経路内に炒成として
残存する残存液量とから、検体液の採取量が選定され、
この採取量と同量の定量サンプリングチューブ3の内容
積が設定さizる。このように構成されたことにより、
ザングリンクシリンジ5の精度に影響されず、常に一定
の採取量が再現されるから、高性能なザンノリンクンリ
ンジ5であることを要しない。な2、定量サンプリング
チューブ30両側總の残液吸入口3Bおよび供給口3A
には、2次エアチューブ7左よび1次転送チューブ14
かそれぞれ接続され、屋!−!7−7ノリングチユーブ
3と共に直線状に形成すJL、空気圧による検体液の転
送が円滑に行われる。芒らに、残液吸入チューブ6と残
液吸入口3Bとの接続部J((よび採血チューブ2と供
給口3Aとの接続部は、定量サンプリングナユーブ3と
2次エアチューブ7 J6よび1次転送チューブ14と
により形成されだ液経路と、直線状態を形成しl工い所
定角度に接続されろ。従って、空気圧により定ht−丈
ンプリンタチューブ3内の検体液を転送する除qこ、残
液吸入チューブ6丑たけ採血チューブ2内の液が空気圧
により、巻込ま〕1.て転送するのを避りることができ
、転送される検体液の汚染が減少する。 また、洗浄液ポンプ9が休止した後、エアポンプ11に
より空気清浄する際K、2次エアチューブ7と洗浄液チ
ューブ10との接続部1−Eよびエア開閉弁8との接続
部において、エアポンプ11より2次エアチューブ7に
送られた空気が、洗浄液チューブ10内の残存洗浄液を
巻込み転送して、液経路全体の壁気による残液排出清浄
時間が長(茂ると共に、清浄が不十分になるおそれがあ
る。 このだめに、2次エアチューブ7と洗浄液ナユーブlO
との間に逆止弁34が設けられ、検体液を空気により転
送する際に発生する洗浄液チューブ10内の洗浄液の巻
込み混合が防止さfLる。また、洗浄液による液経路洗
浄後の空気による洗浄液排出が容易となり、その構成が
簡易化される。 吸引・注入部Cの十字管接続部21は、2次転送チュー
ブ22と廃液チューブ26とを直線的に接続し、液溜容
器13内の洗浄液を、エアポンプ11による空気圧によ
り、試料供給口13Cj6よび2次転送チューブ22を
経て、廃液チューブ26より外部に放出する際に、直線
的で流れ抵尻が少7.【い。喝に、100μl以下の微
少量の検体液を扱う際に、2次転送チューブ22、廃液
チューブ26等の内径は特に細く、1mm以下にする必
要がある。この際にも、流れ抵抗が少ないから、洗浄液
の流れは低圧のエアポンプ11で十分である。同様に、
注入液溜管18と注入ナユーブ19とは、十字管接続部
21により、ia線的に接続され、シリンジロッド20
Bの注入動作にて発生する検体液の注入流れの抵抗が少
な(、注入は容易である。 すylわち、例えば生体血管1にシリコンチューブ叫か
らなる採血チューブ2を接続し、予め制御手段のタイマ
に設定さtした所定の時間間隔で、検体液約90μl程
度を自動採血し、液溜容器部BJdよび吸引・注入部C
を経て、分析計33に注入し、分析計33で所定の分析
を行い、その結果がディジタル表示されると共に、アナ
ログ・ホールド値としで出力さtl、る。また、第2図
に示すLU1ザイクルの時間で、最小3分間隔程度のメ
ーダから、所要の時間まで任意に調整oJ能であるが、
通常、採血から測定値出力までの時間りは約3分程度の
短時間とすることができる。なお、連、続的な閉ループ
を形成するこの測定システムは、自動的に動作するのみ
でなく、外部からの所定の信号によっても動作し得る。 以上に説明するように本発明によれは、採液部は採血チ
ューブ、定量サンプリングチューブ、ザンフリングシリ
ンジおよび弁間からなり、A突に減圧状態で採血される
から、生体血管内への空気の混入の危険がない。定量サ
ンプリングチューブの内容積に応じた採血が可能で、ザ
ンプリンタシリンジの精度に関係1工く、採血量の再現
性が良好で、その内容積を適宜選択することにより、微
少定量の採血が可能である。1だ、液溜容器部は液溜容
器、排出チューブおよび排出弁を有し、空気による採血
の圧送および洗浄液による転送・圧入ごとの洗浄が容易
であり、しかも分析中に採血部、液溜容器部の洗浄が可
能で、測定ザイクル時間の短縮が可能である。°なお、
吸引・注入部は液溜容器に接続する注入液溜管、シリン
ジおよび弁間を組合わせて、シリンジの動作過程におい
てシリンジロッドの設定される動作位置をスイッチ類に
て検出し、所定の休止時間を与える制御手段により、採
液量が多少変動しても、かつ依少量の検体液に対する管
内径の小さい液経路でも、分析計への均一1工注入量の
再現化が確保されると共に、1lllj定後の洗浄も確
実である。さらに、採液部のチューブ接続部およびI紋
別・注入部の十字管接続部は七わ。 ぞiLの液経路?直線的に接続するから、0.経路の流
体抵抗が減少し、小容量のエアポンプ2よび6シ。 浄液ポンプによる空気輸送、液体洗浄2よひ空気による
洗浄液排出が■」能で、その@成〃≦l」・形化される
[, while being accommodated in the residual liquid suction tube 6, a new sample liquid is subsequently accommodated in the quantitative sampling tube 3 following this residual liquid. Note that at the same time that the residual liquid in the blood collection tube z is suctioned and removed, a small amount of the new sample liquid flowing in is removed while washing away the residual liquid adhering to the inner wall traps of the blood collection tube 2 and the quantitative sampling tube 3. It is accommodated in the liquid suction tube 6 together with the remaining liquid. Therefore, the quantitative sampling tube 3 contains fresh, uncontaminated sample liquid. In addition, when the air opening/closing valve 8, the transfer side valve 15, and the inlet valve 4 are all held closed, the zangling rod 5
If the suction operation by B is performed and the large mouth valve 4 is controlled to be opened after a predetermined period of time has elapsed, the degree of pressure reduction will be high.
It is possible to prevent the risk of air backflowing into the living blood vessel 1 through the blood collection tube 2. The sampling syringe rod 5Bld stops after a predetermined amount of sample liquid has been collected by the sampling end detection switch 31, closes the large mouth valve 4, and closes the air on/off valve 8 and the transfer side valve 15.
and discharge valve 17 are opened. In this state, the air pump 11 is operated and the sample liquid in the quantitative sampling tube 3 is pumped by the air pressure sent out.
The liquid is pneumatically transported to the liquid storage container 13 through the primary transfer tube 14 of the L storage container section B. The transfer time of the sample liquid by this pneumatic transportation is shortened, and the measurement cycle L shown in FIG. 2 is significantly shortened. The sample liquid flows into the liquid reservoir 13 from the inlet 13A and is stored at the bottom. On the other hand, excess air filling the inside of the liquid storage container 13 is discharged to the outside through the primary discharge tube 16 from the discharge port 13B. In the suction/injection part C, the injection valve 23 and the waste liquid valve 24
is held closed, the transfer on-off valve 36 is opened, and the syringe 20
By the suction operation of the syringe rod 20B, the secondary transfer tube 22 and the liquid path of the injection liquid reservoir tube 18 are brought into a reduced pressure state from the inside of the liquid reservoir container 13. Based on this pressure difference,
The sample liquid stored in the bottom of the liquid storage container 13 is transferred to the sample supply port 1.
From 3C, via the secondary transfer tube 22, the injection liquid reservoir tube 1
8 and contain it. Syringe rod zOB&1: When a sufficient amount of sample liquid is stored in the injection liquid reservoir tube 18, the suction end detection switch 27 is activated to stop the rod, the transfer opening/closing valve 36 is closed, and the injection valve z3i is opened. Next, when the transfer on-off valve 36 and the waste liquid valve 24 are kept closed and the injection valve 23 is kept open, the syringe rod 20B
Due to the injection operation, the air layer inside the syringe 20 becomes under high pressure, and the pressure of this air layer causes the injection tube 19 to open and transfer the sample liquid contained in the liquid reservoir (1s) to the analyzer 33. Inject. During this injection operation, the air (bubbles) remaining in the injection tube 19 is pushed out to the analyzer 33 by the sample liquid to be injected, and the injection tube 19 is filled with the sample liquid. At the same time, the analyzer 33 performs a cleaning operation to clean and discharge air bubbles generated inside the analyzer 33 by using the injected air. Air bubbles that have a negative impact on
- Be done. The syringe rod 20B continues to perform the injection operation, and the injection tube 19
, into the analyzer 33, and then press the quantitative injection stop switch 29.
The injection operation is stopped by the operation of . Note that the syringe rod 20B is connected between the position of the suction end detection switch 27 and the position of the primary injection detection switch 28.
The position of the primary injection detection switch 28 should be set so that the internal volume of the syringe 20 when it moves is larger than the internal volume of the injection tube 190. Further, the fixed amount injection stop switch 290 position 1 is set according to the position of the primary injection detection switch 28 according to the internal volume of the predetermined amount of sample liquid to be analyzed. Note that the position of the injection end detection switch 30 is FI4. In this case, the tip of syringe rod 20B is connected to syringe 1.
-'] 20A, and even when the syringe rod 20B stops injecting the tube, a small amount of precipitate remains in the injection tube 19, and the injection tube 1
9 to prevent the risk of air bubbles flowing into the analyzer 33. Furthermore, during the injection operation (・jl, the transfer on-off valve 36 is closed, the large mouth valve 4 is held in the closed state, and the air on-off valve 8, the transfer side valve 15J6, and the discharge valve 17 are opened (2), the sampling The syringe rod 5B removes the residual liquid in the residual liquid suction tube 6.
Discharge into quantitative sampling tube 3. At this point, the residual liquid discharge detection switch 32 stops the operation of the sampling syringe rod 5B after the discharge is completed. When the sampling syringe rod 5B stops, the cleaning liquid pump 9 and the air bong 1 are activated, and the cleaning liquid and air pass through the secondary air tube 7 and remove the residual liquid in the primary transfer tube 14. The inflow I] I 3 A is filled into the teaching chamber 13 for cleaning, and the surplus liquid and air are discharged from the outlet 13B through the discharge tube 16 to the external waste liquid tank 25.
reactor. After the preset cleaning time, the cleaning liquid pump 9 stops, but the air pump 11 continues to supply air and
1. The liquid inside the tank and the liquid storage container I3 are cleaned, and the cleaning liquid is discharged and cleaned 1-1. In this way, when the suction/injection part C is injected/analyzed, the liquid collection part Aj6 and the liquid reservoir part 13 are cleaned.
6111 It is possible to shorten the constant cycle time. After the analysis is completed, the transfer on-off valve 36 is closed, and the injection valve 23,
The waste liquid valve 24 is opened, and the syringe rod 2B performs the injection operation again at t2, and the remaining liquid in the injection liquid reservoir tube 18, the cross tube connection part 2 and the waste liquid A'fS of the injection tube 10 is drained into the waste liquid tube. 26: Discharge to the waste liquid tank 25 and the separation tank 33 through the r6 and the injection pipe 19. This injection operation is stopped by the operation of the injection end detection switch 30. Along with this stop, the transfer on/off valve 36, the injection valve 23, and the waste liquid valve 24 are opened, and the discharge valve 17 is closed, so that the cleaning liquid remaining in the liquid storage container 13 is discharged from the sample supply port 13C by air pressure. via secondary transfer tube 22 and injection tube 19 to analyzer 33 or waste tube 26
The respective liquids are washed and discharged to a waste liquid tank 26 through the process. In this way, the control means (
(not shown) is installed to clean the fluid path after the sample fluid is collected, transferred, and analyzed.
Continuous transition to the next blood collection, transfer, and analysis is possible. In addition, in the quantitative sampling tube 3, the amount of sample liquid to be collected is selected from the amount of sample liquid required for analysis and the amount of residual liquid remaining as a result of stirring in the liquid path of the entire device,
The internal volume of the quantitative sampling tube 3 is set to be the same as this sampling amount. With this configuration,
Since a constant sampling amount is always reproduced without being affected by the accuracy of the Zannolink syringe 5, a high-performance Zannolink syringe 5 is not required. 2. Residual liquid suction port 3B and supply port 3A on both sides of quantitative sampling tube 30
includes secondary air tube 7 left and primary transfer tube 14
Or each connected, ya! -! 7-7 The JL is formed in a straight line with the Noring tube 3, and the sample liquid is transferred smoothly by air pressure. At the awn, the connection part J between the residual liquid suction tube 6 and the residual liquid suction port 3B (and the connection part between the blood collection tube 2 and the supply port 3A is connected to the quantitative sampling naive 3 and the secondary air tube 7 J6 and 1 Next, the liquid passage formed by the transfer tube 14 should be connected in a straight line and at a predetermined angle.Therefore, it is possible to transfer the sample liquid in the printer tube 3 of a fixed length by air pressure. It is possible to avoid the liquid in the residual liquid suction tube 6 and the blood collection tube 2 from being entangled by air pressure and transferred, reducing contamination of the transferred sample liquid.In addition, the cleaning liquid pump 9 After the air pump 11 has stopped, when cleaning the air with the air pump 11, the air pump 11 connects the secondary air tube 7 with The sent air entrains and transfers the remaining cleaning liquid in the cleaning liquid tube 10, and the cleaning time for cleaning the remaining liquid due to the wall air throughout the liquid path becomes long (there is a risk that the cleaning will become insufficient as the air grows thicker). , the secondary air tube 7 and the cleaning liquid naublO
A check valve 34 is provided between the cleaning liquid tube 10 and the cleaning liquid tube 10 to prevent mixing of the cleaning liquid in the cleaning liquid tube 10, which occurs when the sample liquid is transferred by air. Further, after cleaning the liquid path with the cleaning liquid, the cleaning liquid can be easily discharged with air, and the configuration thereof is simplified. The cross tube connection part 21 of the suction/injection part C linearly connects the secondary transfer tube 22 and the waste liquid tube 26, and uses the air pressure of the air pump 11 to transfer the cleaning liquid in the liquid storage container 13 to the sample supply port 13Cj6 and 7. When discharging the liquid from the waste tube 26 to the outside through the secondary transfer tube 22, the flow is linear and has little resistance.7. 【stomach. In particular, when handling a very small amount of sample liquid of 100 μl or less, the inner diameter of the secondary transfer tube 22, waste liquid tube 26, etc. must be particularly thin, 1 mm or less. Also in this case, since the flow resistance is small, the low pressure air pump 11 is sufficient for the flow of the cleaning liquid. Similarly,
The injection liquid reservoir pipe 18 and the injection naube 19 are connected in an IA line through a cross tube connection part 21, and the syringe rod 20
There is little resistance to the injection flow of the sample liquid (injection is easy) that occurs during the injection operation of B. In other words, for example, the blood collection tube 2 made of a silicone tube is connected to the biological blood vessel 1, and the control means is Approximately 90 μl of sample liquid is automatically collected at predetermined time intervals set on the timer of
After that, it is injected into the analyzer 33, where it performs a predetermined analysis, and the results are displayed digitally and output as an analog hold value. In addition, the time of LU1 cycle shown in Fig. 2 can be adjusted arbitrarily from the minimum interval of about 3 minutes to the required time.
Normally, the time from blood collection to measurement value output can be a short time of about 3 minutes. Note that this measurement system forming a continuous closed loop can operate not only automatically but also by a predetermined external signal. As explained above, according to the present invention, the liquid collection section consists of a blood collection tube, a quantitative sampling tube, a Zanfling syringe, and a valve gap, and blood is collected in a reduced pressure state in an A-shaped manner, so that air does not enter the living blood vessel. There is no risk of contamination. It is possible to collect blood according to the internal volume of the quantitative sampling tube, and the reproducibility of the amount of blood collected is good, although it is related to the accuracy of the Zamprer syringe, and by selecting the internal volume appropriately, it is possible to collect a very small amount of blood. It is. 1. The liquid collection container has a liquid collection container, a discharge tube, and a discharge valve, and it is easy to pump the blood sample with air, transfer it with cleaning liquid, and wash it after each press-in. The measurement cycle time can be shortened. °In addition,
The suction/injection part combines the injection liquid reservoir pipe connected to the liquid reservoir container, the syringe, and the valve, and uses switches to detect the operating position of the syringe rod during the syringe operation process, and to set the specified pause time. Even if the amount of liquid to be sampled changes slightly, and even if the liquid path has a small inner diameter for a small amount of sample liquid, it is possible to ensure the reproducibility of a uniform one-time injection amount to the analyzer. Cleaning after cleaning is also reliable. Furthermore, the tube connection part of the liquid collection part and the cross tube connection part of the I-monbetsu/injection part are 7-way. The iL liquid route? Since it is connected in a straight line, 0. Air pumps 2 and 6 with reduced flow resistance and small capacity. Pneumatic transport by a purifying liquid pump, liquid cleaning 2 and cleaning liquid discharge by air are possible, and the form is realized.

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

第1図は本発明の一実施例の概略構成図、第2図は第1
図の動作タイミンクチャートでわろ。 A:採液部、B:液溜容器部、C′吸引注入部、2:採
血チューブ、3:定量サンプリングチューブ、5:+)
−ングリンクシリンジ、9:洗浄液ポンプ、11:エア
ポンプ、13;液溜容器、14:1次転送テユーフ、1
8:注入液溜管、19:注入チューブ、20:シリンジ
、33:分析計。 代理人 弁理士横屋赳夫
FIG. 1 is a schematic configuration diagram of an embodiment of the present invention, and FIG.
See the operation timing chart in the figure. A: Liquid collection part, B: Liquid reservoir part, C' suction injection part, 2: Blood collection tube, 3: Quantitative sampling tube, 5: +)
- Link syringe, 9: Cleaning liquid pump, 11: Air pump, 13; Liquid storage container, 14: Primary transfer tube, 1
8: Injection liquid reservoir tube, 19: Injection tube, 20: Syringe, 33: Analyzer. Agent: Takeo Yokoya, patent attorney

Claims (1)

【特許請求の範囲】 (リ 検体液を採取する採血チューブと、前記採血チュ
ーブに接続された定量サンプリングチューブと、この定
量サンプリングチューブに残液吸入チューブを介して接
続され前記定量サンプリングチューブに所定量の前記検
体液を収容させるサンプリングシリンジと、前記定量サ
ンプリングチューブに接続されたエアポンプと、このエ
アポンプと並列して前記定量サンプリングチューブに接
続された洗浄液ポンプとを有する採液部と:前記定量サ
ンプリングチューブに接続された1次転送チューブと、
この1次転送チューブを経て前記エアポンプにより前記
定量サンプリンタチューブ内に収容された前記検体液が
転送され収容される液溜容器とを有する液溜容器部と;
前記液溜容器に2次転送チューブを介して接続され前記
液溜容器内の検体液の所定量を吸引して注入チューブを
介して測定部に注入するシリンジを有する吸引・注入部
と; 前記シリンジにより前記測定部に前記検体液の所定量が
注入されて測定が終了した後、前記採液部、液溜容器部
Rよび吸引・注入部のそれぞれの検体液経路に前記洗浄
液ポンプにより洗浄液を送出して洗浄し、さらに前記エ
アポンプにより空気を送出して前記洗浄液を排出するこ
とを連続的に繰返す制御手段とを備えだことを特徴とす
る採液・転輪装置。 (2)特Ff稍3<の範囲第1項に記載の装置において
、採液チューブに設りら7した大口弁と、エアd<ンプ
および洗浄液ポンプと定量サンプリングチューブとの間
に設けられたエア開閉弁と、前記定量サンプリングチュ
ーブと液溜容器部との間に設置/jられた転送側弁との
いずれも閉にして前記リンプリングシリンジの吸引動作
により前記定量−シンブリングチクーーブ同を減圧した
後、前記入口弁を開として所定量の検体液を採取するだ
めの時限を設定する制御手段を備えたことを特徴とする
採液・転輪装置。 (3)特許請求の範囲第1項または第2項に記載の装置
ににいて、採液チューブ内に残溜した空気および残液を
サンプリングシリンジの吸引動作により残液吸入チュー
ブ内に収容した後、引続いて検体液を前記採液チューブ
を介して定量サンプ1フングチユーブ内に収容するため
の時限を設定する制御手段を備えたことを特徴とする採
液・転輪装置。
[Scope of Claims] (2) A blood collection tube for collecting a sample liquid, a quantitative sampling tube connected to the blood sampling tube, and a predetermined amount of blood connected to the quantitative sampling tube via a residual liquid suction tube to the quantitative sampling tube. a sampling syringe for containing the sample liquid, an air pump connected to the quantitative sampling tube, and a cleaning liquid pump connected to the quantitative sampling tube in parallel with the air pump: the quantitative sampling tube; a primary transfer tube connected to the
a liquid reservoir unit having a liquid reservoir in which the sample liquid contained in the quantitative sampler tube is transferred and stored by the air pump via the primary transfer tube;
a suction/injection unit having a syringe that is connected to the liquid storage container via a secondary transfer tube and aspirates a predetermined amount of the sample liquid in the liquid storage container and injects it into the measurement unit via the injection tube; the syringe; After a predetermined amount of the sample liquid is injected into the measurement unit and the measurement is completed, the cleaning liquid pump sends out the cleaning liquid to each of the sample liquid paths of the liquid collection unit, the liquid storage container R, and the suction/injection unit. A liquid sampling/wheel rolling device characterized by comprising: a control means for continuously repeating the steps of cleaning the cleaning liquid by using the air pump, and discharging the cleaning liquid by sending out air using the air pump. (2) Range of special Ff 3< In the device described in paragraph 1, the air provided between the large mouth valve provided on the liquid sampling tube, the air pump and the cleaning liquid pump, and the quantitative sampling tube. The opening/closing valve and the transfer side valve installed between the quantitative sampling tube and the liquid storage container section are both closed, and the quantitative sampling tube is closed by the suction operation of the limp ring syringe. A liquid sampling and wheel rolling device characterized by comprising a control means for setting a time limit for opening the inlet valve and collecting a predetermined amount of sample liquid after the pressure is reduced. (3) In the device according to claim 1 or 2, after the air and residual liquid remaining in the liquid sampling tube are contained in the residual liquid suction tube by the suction operation of the sampling syringe. . A liquid sampling and wheel rolling device, characterized in that it is equipped with a control means for setting a time limit for subsequently storing the sample liquid into the quantitative sample tube via the liquid sampling tube.
JP57192567A 1982-11-02 1982-11-04 Liquid sampling and transferring apparatus Pending JPS5983031A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP57192896A JPS5983032A (en) 1982-11-02 1982-11-02 Liquid sampling and transferring apparatus
JP57192567A JPS5983031A (en) 1982-11-02 1982-11-04 Liquid sampling and transferring apparatus

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP57192896A JPS5983032A (en) 1982-11-02 1982-11-02 Liquid sampling and transferring apparatus
JP57192567A JPS5983031A (en) 1982-11-02 1982-11-04 Liquid sampling and transferring apparatus

Publications (1)

Publication Number Publication Date
JPS5983031A true JPS5983031A (en) 1984-05-14

Family

ID=46721517

Family Applications (2)

Application Number Title Priority Date Filing Date
JP57192896A Pending JPS5983032A (en) 1982-11-02 1982-11-02 Liquid sampling and transferring apparatus
JP57192567A Pending JPS5983031A (en) 1982-11-02 1982-11-04 Liquid sampling and transferring apparatus

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP57192896A Pending JPS5983032A (en) 1982-11-02 1982-11-02 Liquid sampling and transferring apparatus

Country Status (1)

Country Link
JP (2) JPS5983032A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6458241A (en) * 1987-07-31 1989-03-06 Ee Rin Roorensu Assembly and method for suction of blood

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2132270A1 (en) * 1993-10-28 1995-04-29 Erich Lerch Automatic pipetting apparatus having a cleaning device

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6458241A (en) * 1987-07-31 1989-03-06 Ee Rin Roorensu Assembly and method for suction of blood

Also Published As

Publication number Publication date
JPS5983032A (en) 1984-05-14

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