JP4416579B2 - Automatic analyzer - Google Patents

Automatic analyzer Download PDF

Info

Publication number
JP4416579B2
JP4416579B2 JP2004184384A JP2004184384A JP4416579B2 JP 4416579 B2 JP4416579 B2 JP 4416579B2 JP 2004184384 A JP2004184384 A JP 2004184384A JP 2004184384 A JP2004184384 A JP 2004184384A JP 4416579 B2 JP4416579 B2 JP 4416579B2
Authority
JP
Japan
Prior art keywords
sample
dispensing
automatic analyzer
analysis
abnormality
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.)
Active
Application number
JP2004184384A
Other languages
Japanese (ja)
Other versions
JP2006010363A (en
Inventor
雅人 石沢
一啓 田中
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.)
Hitachi High Tech Corp
Original Assignee
Hitachi High Technologies 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 Hitachi High Technologies Corp filed Critical Hitachi High Technologies Corp
Priority to JP2004184384A priority Critical patent/JP4416579B2/en
Publication of JP2006010363A publication Critical patent/JP2006010363A/en
Application granted granted Critical
Publication of JP4416579B2 publication Critical patent/JP4416579B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Description

本発明は血液,尿等の生体サンプルの定性・定量分析を行う自動分析装置に係り、特に搬送装置を介して複数の分析ユニット間でサンプルを移送させる機能を備えた自動分析装置に関する。   The present invention relates to an automatic analyzer that performs qualitative and quantitative analysis of biological samples such as blood and urine, and more particularly to an automatic analyzer that has a function of transferring a sample between a plurality of analysis units via a transport device.

自動分析装置は、血液や尿などの生体試料からなるサンプルと試薬を反応容器に分注し、サンプルと試薬の混合液を光度計の如き測定手段によって測定する。   The automatic analyzer dispenses a sample made of a biological sample such as blood or urine and a reagent into a reaction container, and measures a mixed solution of the sample and the reagent by a measuring means such as a photometer.

特に血液サンプルではサンプル中に凝固成分を含むため、ピペッター等のサンプル分注機構の流路に詰まりが生じる可能性がある。そのため、近年の自動分析装置には、分注動作時にサンプル吸引動作が正常に実行されたかどうかを認識するため、分注流路内の圧力を圧力センサを用いて測定する手段を備えたものも存在する。例えば特許文献1にはこのような圧力センサを用いたつまり検知手段を備えた自動分析装置が開示されている。   In particular, a blood sample contains a coagulation component in the sample, and therefore there is a possibility that the flow path of a sample dispensing mechanism such as a pipetter will be clogged. Therefore, some recent automatic analyzers are provided with means for measuring the pressure in the dispensing flow path using a pressure sensor in order to recognize whether or not the sample suction operation has been normally performed during the dispensing operation. Exists. For example, Patent Document 1 discloses an automatic analyzer using such a pressure sensor, that is, having a detection means.

一方で、複数の分析ユニットが搬送機構を介して接続され分析ユニット間で同一検体の相互搬送を可能とする機能を持つ自動分析装置も存在する。このような自動分析装置は、例えば特許文献2に開示されている。   On the other hand, there is also an automatic analyzer having a function in which a plurality of analysis units are connected via a transport mechanism to enable mutual transport of the same sample between the analysis units. Such an automatic analyzer is disclosed in Patent Document 2, for example.

特開2001−242182号公報JP 2001-242182 A 特開平10−325839号公報Japanese Patent Laid-Open No. 10-325839

ここで、特許文献2に開示されたような構成を持つ自動分析装置において、同一の試料に対して複数の分析ユニットにおいて分析を行う必要がある場合を想定する。もし、最初に分析依頼された分析ユニットの試料分注動作において定量吸引異常と認識された場合であっても、現状のシステムでは試料を以降の分析ユニットに搬送し前述同様に試料分注動作を実施する。この場合、以降の分析ユニットにおいても当初の分析ユニット同様に定量吸引異常が発生する可能性がある。何故なら、分注機構での試料の吸引異常は、試料中の凝固性物質が原因である可能性が高く、同一の試料を分注した場合は、いずれの分注手段を用いても吸引流路に詰まりを発生させる可能性があるからである(もちろん分注機構の定量吸引異常は、分注機構の誤動作による単発的なものである可能性もある)。   Here, in the automatic analyzer having the configuration as disclosed in Patent Document 2, it is assumed that it is necessary to perform analysis in a plurality of analysis units on the same sample. Even if the sample dispensing operation of the analysis unit requested for analysis at first is recognized as an abnormal quantitative suction, the current system transports the sample to the subsequent analysis units and performs the sample dispensing operation in the same way as described above. carry out. In this case, in the subsequent analysis units, there is a possibility that the quantitative suction abnormality may occur as in the initial analysis unit. This is because abnormal suction of the sample in the dispensing mechanism is most likely caused by a coagulant substance in the sample. If the same sample is dispensed, the suction flow is not affected by any dispensing means. This is because clogging may occur in the path (of course, the quantitative suction abnormality of the dispensing mechanism may be a single occurrence due to malfunction of the dispensing mechanism).

一旦分注機構に詰まりが発生すると、定量吸引異常と認識した試料に対する洗浄動作の追加、既分注済み試薬の無駄な使用など装置として非効率的な動作を実行する必要がある。従来の自動分析装置では、単一の分析ユニットのみならず複数の全分析ユニットでこのような非効率的な動作を実行しなくてはならない可能性があった。   Once the dispensing mechanism is clogged, it is necessary to perform inefficient operations as an apparatus, such as adding a washing operation to a sample that has been recognized as a quantitative suction abnormality, and wasteful use of already dispensed reagents. In the conventional automatic analyzer, there is a possibility that such an inefficient operation has to be executed not only in a single analysis unit but also in a plurality of all analysis units.

本発明は、定量吸引異常時に伴い発生する非効率的な動作を本異常が認識された当該分析ユニットのみに留め、自動分析装置を構成する他の複数の分析ユニットで同じ異常が発生する可能性を低減することによる、分析速度の向上,無駄な試薬の消費を抑えることによるコスト低減を目的とする。   In the present invention, the inefficient operation that occurs in the event of a quantitative suction abnormality is limited to the analysis unit in which the abnormality is recognized, and the same abnormality may occur in a plurality of other analysis units constituting the automatic analyzer. The purpose is to improve the analysis speed by reducing the cost and to reduce the cost by suppressing the consumption of useless reagents.

上記目的を達成するための本発明の構成は以下の通りである。   The configuration of the present invention for achieving the above object is as follows.

試料容器から反応容器へ試料を分注する分注装置であって、該分注装置で試料の分注が正常に実行されたかどうかを検知する分注検知機構を備えた分析ユニットと、同一の試料を、複数の前記分析ユニット間で搬送する搬送機構と、を備えた自動分析装置において、いずれかの前記分析ユニットの分注検知機構が異常を検知した場合、異常が発生した試料に関し、登録されている試料情報に分注異常が発生した旨の情報を付加する機能を備えた自動分析装置。   A dispensing apparatus for dispensing a sample from a sample container to a reaction container, the same as an analysis unit having a dispensing detection mechanism for detecting whether or not the dispensing of the sample has been normally executed by the dispensing apparatus. In an automatic analyzer equipped with a transport mechanism for transporting a sample between a plurality of the analysis units, if the dispensing detection mechanism of any of the analysis units detects an abnormality, registration is performed regarding the sample in which the abnormality has occurred. An automatic analyzer with a function to add information indicating that a dispensing abnormality has occurred to the sample information.

反応容器は試料と試薬を混合する容器を意味する。自動分析装置は通常、反応容器中の混合液の物性(吸光度,発光強度等)を測定することにより試料中の目的成分の濃度を測定する。分注装置はシリンジ,ベローズ等の(負の)圧力発生手段により発生させた圧力変化により分注装置の流路に液体を吸引させることにより液体を吸引または吐出させる装置である。圧力発生手段は上記に限定されるものではなく、液体の吸引/吐出が可能な圧力差を発生させ得るものであればどのようなものであっても良い。   The reaction container means a container for mixing a sample and a reagent. The automatic analyzer usually measures the concentration of the target component in the sample by measuring the physical properties (absorbance, luminescence intensity, etc.) of the mixed solution in the reaction vessel. The dispensing device is a device that sucks or discharges liquid by sucking the liquid into the flow path of the dispensing device by a pressure change generated by a (negative) pressure generating means such as a syringe or bellows. The pressure generating means is not limited to the above, and any pressure generating means may be used as long as it can generate a pressure difference capable of sucking / discharging the liquid.

分析ユニットとは少なくとも1つの試料分注機構を備え、少なくとも1種の分析項目に関し分析結果を算出できる分析装置の単位を意味する。複数の分析ユニットとは筐体が別々に存在することを必ずしも意味しない。同一の筐体内に配置されていてもそれぞれ別の分注装置(分注機構)を備え、別の分析項目の分析結果を出力することができれば、それらは複数の分析ユニットである。例えば、生化学分析項目を分析する分析ユニットと免疫分析項目を分析する分析ユニットが同一の筐体中に配置されていても、それら分析ユニットがそれぞれ分注機構を備えていれば本発明の分析ユニットに該当する。   The analysis unit means a unit of an analyzer that includes at least one sample dispensing mechanism and can calculate an analysis result for at least one type of analysis item. A plurality of analysis units does not necessarily mean that the casings exist separately. Even if they are arranged in the same casing, if they have different dispensing devices (dispensing mechanisms) and can output analysis results of different analysis items, they are a plurality of analysis units. For example, even if an analysis unit for analyzing biochemical analysis items and an analysis unit for analyzing immune analysis items are arranged in the same casing, the analysis unit according to the present invention can be used as long as each analysis unit has a dispensing mechanism. Corresponds to the unit.

分注検知機構は圧力センサ,光学的センサ,液面検知センサから得られた液面高さの情報に基づき、液面高さの変化に基づくもの等、どのようなものであっても良い。試料が分注機構の流路等に詰まって、分注不能になったり、規定の分注量を分注できない状態であることを検知できるような機構であれば良い。   The dispensing detection mechanism may be anything such as a pressure sensor, an optical sensor, a liquid level detection information obtained from a liquid level detection sensor, and a mechanism based on a change in liquid level. Any mechanism may be used as long as it can detect that the sample is clogged in the flow path or the like of the dispensing mechanism and cannot be dispensed, or that the specified dispensing amount cannot be dispensed.

分注異常が発生した試料にフラグを立て、装置オペレータをそれを認識できる機能があることが望ましい。またフラグの立った試料に関しては、他の分析ユニットで分注が行われた場合は、最初の分析ユニットで発生したのと同様に分注異常が発生する可能性が高いので、他の分析ユニットでの同一試料の分注が行われないように制御する制御手段があることが望ましい。同一の試料とは分注異常が発生したものと同一の試料容器に入っている試料である場合もあるし、同一の試料を複数の試料容器に分けた場合は、それぞれの試料容器中の試料である場合もある。もちろん、分注異常の発生が試料そのものに起因するものでない場合もありえる。試料そのものが原因でなく、特定の分注装置に原因があることが判明した場合には、試料の情報を登録した試料情報データベースにおいて、以前登録した分注異常が発生したとのフラグを削除する機能があることが望ましい。分析ユニットは、試料情報データベースに分注異常が発生したとのフラグがあるかどうかに基づいて、当該試料の分注を行うか中止するかの判断をすることができる。   It is desirable to have a function of setting a flag on a sample in which dispensing abnormality has occurred and recognizing the apparatus operator. For a flagged sample, if dispensing is performed in another analysis unit, there is a high possibility that a dispensing error will occur in the same way as in the first analysis unit. It is desirable to have a control means for controlling so that the same sample is not dispensed. The same sample may be a sample contained in the same sample container as the one in which dispensing abnormality has occurred, or when the same sample is divided into multiple sample containers, the sample in each sample container Can be. Of course, the occurrence of dispensing abnormality may not be caused by the sample itself. When it is determined that the cause is not the sample itself but the specific dispensing device, the flag indicating that a previously registered dispensing abnormality has occurred is deleted from the sample information database in which the sample information is registered. It is desirable to have a function. The analysis unit can determine whether or not to dispense the sample based on whether or not there is a flag indicating that a dispensing abnormality has occurred in the sample information database.

どの試料に分注異常が発生したかを容易に確認できるよう試料の一覧表示と該一覧表示中にフラグの有無が一目でわかるような表示があることが望ましい。オペレータが表示装置に表示された試料一覧から分注異常発生を示すフラグ(識別表示,マーク等)を追加したり、削除したりできる機能があっても良い。   It is desirable to have a list display of samples and a display that allows the presence / absence of a flag to be known at a glance during the list display so that it can be easily confirmed in which sample the dispensing abnormality has occurred. There may be a function that allows the operator to add or delete a flag (identification display, mark, etc.) indicating the occurrence of dispensing abnormality from the sample list displayed on the display device.

本発明の効果としては、当該試料の分注動作において定量吸引異常と認識した分析ユニット以降の当該試料に対する分析動作を自動的に回避し、洗浄動作追加に伴う処理能力低減などの非効率的動作の回避、更には当該試料に対する試薬の分注など装置として非経済的な動作を回避することが可能となる。   As an effect of the present invention, an inefficient operation such as automatically reducing the analysis operation for the sample after the analysis unit recognized as a quantitative suction abnormality in the dispensing operation of the sample and reducing the processing capacity accompanying the addition of the cleaning operation In addition, it is possible to avoid uneconomical operation of the apparatus, such as dispensing of reagents to the sample.

以下図面を用いて本発明の実施例を説明する。   Embodiments of the present invention will be described below with reference to the drawings.

以下に本発明の実施例を図1から順を追って説明する。   Embodiments of the present invention will be described below in order from FIG.

図1は一般的な自動分析装置の分注機構周辺部概略図を示す。各部の機能は公知のものである為、詳細についての記述は省略する。サンプリング機構1のサンプリングアーム2は上下すると共に回転し、サンプリングアーム2に取り付けられたプローブ105を用いて、左右に回転するサンプルディスク102に配置されたサンプル容器101内の試料7を吸引し、反応容器106へ吐出するように構成されている。本図からもわかるように試料容器101のサンプルディスク102への配置はサンプルディスク102上へ直接配置する場合や試験管(図示は無い)上にサンプル容器101を載せる事も可能なユニバーサルな配置に対応可能な構造のものが一般的である。   FIG. 1 is a schematic view of the periphery of a dispensing mechanism of a general automatic analyzer. Since the function of each part is well-known, detailed description is omitted. The sampling arm 2 of the sampling mechanism 1 moves up and down and rotates. Using the probe 105 attached to the sampling arm 2, the sample 7 in the sample container 101 arranged on the sample disk 102 rotating left and right is sucked and reacted. It is comprised so that it may discharge to the container 106. FIG. As can be seen from this figure, the sample container 101 is placed on the sample disk 102 in a universal arrangement in which the sample container 101 can be placed directly on the sample disk 102 or on the test tube (not shown). The thing of the structure which can respond is common.

図1における自動分析装置の構成をさらに説明する。回転自在な試薬ディスク125上には分析対象となる複数の分析項目に対応する試薬のボトル112が配置されている。可動アームに取り付けられた試薬分注プローブ110は、試薬ボトル112から反応容器
106へ所定量の試薬を分注する。
The configuration of the automatic analyzer in FIG. 1 will be further described. On the rotatable reagent disk 125, reagent bottles 112 corresponding to a plurality of analysis items to be analyzed are arranged. The reagent dispensing probe 110 attached to the movable arm dispenses a predetermined amount of reagent from the reagent bottle 112 to the reaction container 106.

サンプル分注プローブ105は、サンプル用シリンジポンプ107の動作に伴ってサンプルの吸引動作、及び吐出動作を実行する。試薬分注プローブ110は、試薬用シリンジポンプ111の動作に伴って試薬の吸引動作、及び吐出動作を実行する。各サンプルのために分析すべき分析項目は、キーボード121、又はCRT118の画面のような入力装置から入力される。この自動分析装置における各ユニットの動作は、コンピュータ103により制御される。   The sample dispensing probe 105 performs a sample suction operation and a discharge operation in accordance with the operation of the sample syringe pump 107. The reagent dispensing probe 110 executes a reagent suction operation and a discharge operation in accordance with the operation of the reagent syringe pump 111. The analysis items to be analyzed for each sample are input from an input device such as a keyboard 121 or a CRT 118 screen. The operation of each unit in this automatic analyzer is controlled by the computer 103.

サンプルディスク102の間欠回転に伴ってサンプル容器101はサンプル吸引位置へ移送され、停止中のサンプル容器内にサンプル分注プローブ105が降下される。その下降動作に伴って分注プローブ105の先端がサンプルの液面に接触すると液面検出回路
151から検出信号が出力され、それに基づいてコンピュータ103が可動アーム2の駆動部の下降動作を停止するよう制御する。次に分注プローブ105内に所定量のサンプルを吸引した後、分注プローブ105は上死点まで上昇する。分注プローブ105がサンプルを所定量吸引している間は、分注プローブ105とサンプル用ポンプ107流路間の吸引動作中の流路内圧力変動を圧力センサ152からの信号を用い圧力検出回路153で監視し、吸引中の圧力変動に異常を発見した場合は所定量吸引されていない可能性が高い為、当該分析データに対しアラームを付加する。
As the sample disk 102 rotates intermittently, the sample container 101 is transferred to the sample suction position, and the sample dispensing probe 105 is lowered into the stopped sample container. When the tip of the dispensing probe 105 comes into contact with the liquid level of the sample along with the lowering operation, a detection signal is output from the liquid level detection circuit 151, and the computer 103 stops the lowering operation of the driving unit of the movable arm 2 based on the detection signal. Control as follows. Next, after a predetermined amount of sample is sucked into the dispensing probe 105, the dispensing probe 105 rises to the top dead center. While the dispensing probe 105 is sucking a predetermined amount of sample, the pressure detection circuit uses the signal from the pressure sensor 152 to detect the pressure fluctuation in the flow channel during the suction operation between the dispensing probe 105 and the sample pump 107 flow channel. When monitoring is performed at 153 and an abnormality is found in the pressure fluctuation during suction, an alarm is added to the analysis data because there is a high possibility that a predetermined amount has not been sucked.

次にサンプリングアーム2が水平方向に旋回し反応ディスク109上の反応容器106の位置でサンプル分注プローブ105を下降し反応容器106内へ保持していたサンプルを吐出する。サンプルが入った反応容器106が試薬添加位置まで移動された時に、該当する分析項目に対応した試薬が試薬分注プローブ110から添加される。サンプル、及び試薬の分注に伴って試料容器101内のサンプル、及び試薬ボトル112内の試薬の液面が検出される。サンプル、及び試薬が加えられた反応容器内の混合物は、攪拌器113により攪拌される。混合物が収納された反応容器が測定手段162に移送され、同時にアクチュエータ160による遮蔽手段が開口し、各混合物の発光値、或いは吸光度が測定手段としてのフォトマルチプライヤ161、或いは光度計により測定される。発光信号は、A/D変換器116を経由しインターフェース104を介してコンピュータ103に入り、分析項目の濃度が計算される。分析結果は、インターフェース104を介してプリンタ
117に印字出力するか、又はCRT118に画面出力すると共に、メモリとしてのハードディスク122に格納される。測光が終了した反応容器106は、洗浄機構119の位置にて洗浄される。洗浄用ポンプ120は、反応容器へ洗浄水を供給すると共に、反応容器から廃棄を排出する。図1の例では、サンプルディスク102に同心円状に3列のサンプル容器101がセットできるように3列の容器保持部が形成されており、サンプル分注プローブ105によるサンプル吸引位置が各々の列に1個ずつ設定されている。
Next, the sampling arm 2 rotates in the horizontal direction, the sample dispensing probe 105 is lowered at the position of the reaction vessel 106 on the reaction disk 109, and the sample held in the reaction vessel 106 is discharged. When the reaction container 106 containing the sample is moved to the reagent addition position, a reagent corresponding to the corresponding analysis item is added from the reagent dispensing probe 110. As the sample and reagent are dispensed, the liquid level of the sample in the sample container 101 and the reagent in the reagent bottle 112 is detected. The sample and the mixture in the reaction vessel to which the reagent has been added are stirred by the stirrer 113. The reaction container containing the mixture is transferred to the measuring means 162, and simultaneously the shielding means by the actuator 160 is opened, and the luminescence value or absorbance of each mixture is measured by the photomultiplier 161 or the photometer as the measuring means. . The emission signal enters the computer 103 via the interface 104 via the A / D converter 116, and the concentration of the analysis item is calculated. The analysis result is printed out to the printer 117 via the interface 104 or output to the CRT 118 and stored in the hard disk 122 as a memory. After completion of photometry, the reaction vessel 106 is cleaned at the position of the cleaning mechanism 119. The cleaning pump 120 supplies cleaning water to the reaction container and discharges waste from the reaction container. In the example of FIG. 1, three rows of container holding portions are formed so that three rows of sample vessels 101 can be set concentrically on the sample disk 102, and the sample suction position by the sample dispensing probe 105 is in each row. One by one is set.

次に分析ユニットを複数台接続し構成された自動分析装置の一例を図2を用い以下説明する。前述機能を有した分析ユニットを複数台接続し、これら分析ユニット間は試料搬送部18により相互接続される。自動分析装置としてのU/Iは装置操作部16により行われ、自動分析装置内部のインターフェースはイーサーネット(R)などの適当な通信手段により行われる。サンプル容器101は試料投入部14より投入され試料搬送部18により分析依頼された分析ユニットに搬送され、分析完了後にサンプル容器101は試料搬出部15へ適宜搬送される。図2では分析ユニット1 10のみに依頼があった場合、或いは分析ユニット1 10,分析ユニット2 11,分析ユニット4 13に依頼があった場合の試料搬送経路を特定例と図示した。   Next, an example of an automatic analyzer configured by connecting a plurality of analysis units will be described with reference to FIG. A plurality of analysis units having the aforementioned functions are connected, and these analysis units are interconnected by the sample transport unit 18. U / I as an automatic analyzer is performed by the apparatus operation unit 16, and an interface inside the automatic analyzer is performed by an appropriate communication means such as Ethernet (R). The sample container 101 is loaded from the sample loading unit 14 and is transported to the analysis unit requested to be analyzed by the sample transport unit 18, and the sample container 101 is appropriately transported to the sample unloading unit 15 after the analysis is completed. FIG. 2 shows a specific example of the sample transport path when only the analysis unit 110 is requested or when the analysis unit 110, the analysis unit 211, and the analysis unit 413 are requested.

次に、現状の自動分析装置が有す問題点を図3を用い以下説明する。試料搬送経路は図2で前述した通り分析ユニット1 10,分析ユニット2 11,分析ユニット4 13に依頼があった場合とする。装置操作部16により分析依頼されたサンプル容器101は試料投入部14より投入され分析ユニット1 10へ搬入され当該サンプルの分析を行う。搬入されたサンプルは前述のごとくサンプル容器101内にサンプル分注プローブ105が降下され、可動アーム2の駆動部の下降動作を停止後に分注プローブ105内に所定量のサンプルを吸引する。本吸引動作において圧力検出回路153で所定量の吸引動作で異常を認識した場合は現状の自動分析装置では分析ユニット1 10において吸引したサンプルの排出動作,サンプル分注プローブ105の洗剤を用いた洗浄動作、或いは当該サンプル分析用試薬の排出動作等、吸引動作異常の認識に伴い複数の付加動作が発生し自動分析全体として処理能力を低下させる結果となる。図3に示すように分析ユニット1 10で上記吸引動作異常が認識された場合、現状の自動分析装置ではサンプル容器101は分析依頼されたごとく分析ユニット2 11,分析ユニット4 13に搬入され上記吸引動作を行う。つまり分析ユニット1 10と同様に吸引動作異常の認識される可能性が非常に高く、前述処理能力を更に低下させる可能性を持ち合わせていた。   Next, the problems of the current automatic analyzer will be described below with reference to FIG. The sample transport path is assumed to be a request from the analysis unit 110, the analysis unit 211, and the analysis unit 413 as described above with reference to FIG. The sample container 101 requested to be analyzed by the apparatus operation unit 16 is input from the sample input unit 14 and is carried into the analysis unit 110 to analyze the sample. As described above, the sample dispensing probe 105 is lowered into the sample container 101, and a predetermined amount of sample is sucked into the dispensing probe 105 after stopping the lowering operation of the drive unit of the movable arm 2. In this suction operation, when the pressure detection circuit 153 recognizes an abnormality by a predetermined amount of suction operation, the current automatic analyzer discharges the sample sucked in the analysis unit 110 and cleans the sample dispensing probe 105 with a detergent. A plurality of additional operations are generated in accordance with the recognition of the abnormal suction operation such as the operation or the discharge operation of the sample analysis reagent, resulting in a reduction in processing capacity as a whole automatic analysis. As shown in FIG. 3, when the abnormal suction operation is recognized in the analysis unit 110, the sample container 101 is carried into the analysis unit 211 and the analysis unit 413 as requested for analysis in the current automatic analyzer, and the suction is performed. Perform the action. That is, as with the analysis unit 110, there is a very high possibility that a suction operation abnormality will be recognized, and there is a possibility of further reducing the processing capability.

次に、本発明を適用した自動分析装置の動作を図4を用い以下説明する。前述図3と同様に試料搬送経路は分析ユニット1 10,分析ユニット2 11,分析ユニット4
13に依頼があった場合とする。分析ユニット1 10でサンプル所定量吸引動作において圧力検出回路153で異常を認識した場合、本発明を適用した自動分析装置では分析ユニット1で認識された所定量吸引動作異常のステータスを当該サンプル容器101に付加し、分析依頼されている以降の当該サンプルの分析においても分析ユニット1の分析結果と同様に所定量吸引動作異常と認識される可能性が高いと判断し、分析ユニット2 11,分析ユニット4 13への当該サンプル容器101の搬入、及び分析を自動的に中止し、前述吸引動作異常の認識に伴う付加動作の発生を未然に防ぎ、処理能力低減などの非効率的動作、及び非経済的な動作の発生を回避し、自動分析装置として最適な動作環境の提供に寄与することが可能となる。
Next, the operation of the automatic analyzer to which the present invention is applied will be described below with reference to FIG. As in FIG. 3, the sample transport path is the analysis unit 110, the analysis unit 2 11, and the analysis unit 4.
It is assumed that 13 is requested. When an abnormality is recognized by the pressure detection circuit 153 in the sample predetermined amount suction operation in the analysis unit 110, the automatic analyzer to which the present invention is applied displays the status of the predetermined amount suction operation abnormality recognized in the analysis unit 1 in the sample container 101. In the analysis of the sample after being requested to be analyzed, it is determined that there is a high possibility that it is recognized that the predetermined amount of suction operation is abnormal in the same manner as the analysis result of the analysis unit 1, and the analysis unit 211, analysis unit 413 automatically cancels the loading and analysis of the sample container 101, prevents the occurrence of an additional operation associated with the recognition of the abnormal suction operation, inefficient operation such as processing capacity reduction, and inexpensive It is possible to avoid the occurrence of a typical operation and contribute to the provision of an optimal operating environment as an automatic analyzer.

上記実施例ではサンプル所定量吸引動作の異常を認識する手段として圧力センサ152からの信号を圧力検出回路153で監視する手段を一例として挙げたが、別異常認識手段としてはサンプル用ポンプ107流路内の特定位置の光学的な屈折量を監視する手段、或いはサンプル吸引前の液面停止位置、つまりサンプル分注プローブ105停止位置高さと前回分注時のサンプル分注プローブ105停止位置高さの推移から推移高さが期待値未満であった場合に異常と認識する手段など複数の有効な手段が考えられるが本発明内で前述手段を詳細説明は省略する。   In the above embodiment, the means for monitoring the signal from the pressure sensor 152 by the pressure detection circuit 153 is taken as an example as means for recognizing the abnormality of the sample predetermined amount suction operation. Means for monitoring the amount of optical refraction at a specific position, or the liquid surface stop position before sample suction, that is, the height of the sample dispensing probe 105 stop position and the height of the sample dispensing probe 105 stop position at the previous dispensing. A plurality of effective means such as a means for recognizing an abnormality when the transition height is less than the expected value from the transition can be considered, but the detailed description of the above means will be omitted in the present invention.

本発明が適用される分析ユニットの全体構成を示す概略図。Schematic which shows the whole structure of the analysis unit to which this invention is applied. 分析ユニットが複数台で構成された自動分析装置の全体構成概略図。1 is a schematic diagram of the overall configuration of an automatic analyzer including a plurality of analysis units. 本発明が解決すべき課題。Problems to be solved by the present invention. 本発明を適用した自動分析装置の試料ワークフロー。The sample workflow of the automatic analyzer which applied this invention.

符号の説明Explanation of symbols

1…サンプリング機構、10…分析ユニット1、11…分析ユニット2、12…分析ユニット3、13…分析ユニット4、14…試料投入部、15…試料搬出部、18…試料搬送部、101…サンプル容器(試料容器)、152…圧力センサ、153…圧力検知回路。
DESCRIPTION OF SYMBOLS 1 ... Sampling mechanism, 10 ... Analysis unit 1, 11 ... Analysis unit 2, 12 ... Analysis unit 3, 13 ... Analysis unit 4, 14 ... Sample input part, 15 ... Sample unloading part, 18 ... Sample conveyance part, 101 ... Sample Container (sample container), 152 ... pressure sensor, 153 ... pressure detection circuit.

Claims (5)

試料容器から反応容器へ試料を分注する少なくとも1つの試料分注機構と、該分注機構において試料の分注が正常に実行されたかどうかを検知する分注検知機構と、を備えた、複数の分析ユニットと、
前記複数の分析ユニットの間で、試料を搬送する試料搬送機構と、
試料情報を記憶する記憶部と、
いずれかの前記分析ユニットが備える前記分注検知機構が前記試料分注機構の詰まり異常を検知した場合、詰まり異常が発生した試料に関し、前記記憶部に登録されている試料情報に詰まり異常が発生した旨の情報を付加する情報付加部と、を備え、
前記分析ユニットは、前記記憶部に登録されている試料情報に詰り異常が発生した旨の情報があるかどうかに基づいて、当該分析ユニットで当該試料の分注を行うか中止するかの判断をする判断部を備えたことを特徴とする自動分析装置。
At least one sample dispensing mechanism to dispense the specimen into the reaction vessel from a sample container, a dispensing detection mechanism for detecting whether the dispensing of the sample was successful in dispensing mechanism, comprising a plurality With an analysis unit of
A sample transport mechanism for transporting a sample between the plurality of analysis units;
A storage unit for storing sample information;
When the dispensing detection mechanism provided in any of the analysis units detects a clogging abnormality in the sample dispensing mechanism, a clogging abnormality occurs in the sample information registered in the storage unit regarding the sample in which the clogging abnormality has occurred. An information adding unit for adding information indicating that
The analysis unit determines whether to dispense or stop the sample in the analysis unit based on whether there is information indicating that a clogging abnormality has occurred in the sample information registered in the storage unit. An automatic analyzer characterized by comprising a determination unit that performs the operation .
請求項1記載の自動分析装置において、The automatic analyzer according to claim 1, wherein
前記分注検知機構が異常を検知した場合、アラームを出力するアラーム出力手段を備えたことを特徴とする自動分析装置。An automatic analyzer comprising alarm output means for outputting an alarm when the dispensing detection mechanism detects an abnormality.
請求項1に記載の自動分析装置において、The automatic analyzer according to claim 1,
前記分注検知機構は分注流路内の圧力値に基づいて分注の異常を検知するものであることを特徴とする自動分析装置。The automatic analyzer is characterized in that the dispensing detection mechanism detects an abnormality of dispensing based on a pressure value in the dispensing flow path.
請求項1に記載の自動分析装置において、The automatic analyzer according to claim 1,
前記分注検知機構は液体の持つ光学的な屈折率の変動値を利用し分注の異常を検知するものであることを特徴とする自動分析装置。An automatic analyzer characterized in that the dispensing detection mechanism detects an abnormality in dispensing by using a fluctuation value of an optical refractive index of a liquid.
請求項1記載の自動分析装置において、The automatic analyzer according to claim 1, wherein
複数の試料容器に同一の試料が収容され、The same sample is stored in multiple sample containers,
前記複数の試料容器のうちの一つに収容された試料に対して前記情報付加部によって前記記憶部に詰まり異常が生じた旨の情報が付加された場合、When information indicating that a clogging abnormality has occurred in the storage unit by the information adding unit is added to the sample stored in one of the plurality of sample containers,
前記情報付加部は前記複数の試料容器のうち他の試料容器に収容された試料に対しても前記記憶部に前記情報を付加することを特徴とする自動分析装置。The automatic analysis apparatus, wherein the information adding unit adds the information to the storage unit even for a sample stored in another sample container among the plurality of sample containers.
JP2004184384A 2004-06-23 2004-06-23 Automatic analyzer Active JP4416579B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2004184384A JP4416579B2 (en) 2004-06-23 2004-06-23 Automatic analyzer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2004184384A JP4416579B2 (en) 2004-06-23 2004-06-23 Automatic analyzer

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2008317805A Division JP4713629B2 (en) 2008-12-15 2008-12-15 Automatic analyzer

Publications (2)

Publication Number Publication Date
JP2006010363A JP2006010363A (en) 2006-01-12
JP4416579B2 true JP4416579B2 (en) 2010-02-17

Family

ID=35777799

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004184384A Active JP4416579B2 (en) 2004-06-23 2004-06-23 Automatic analyzer

Country Status (1)

Country Link
JP (1) JP4416579B2 (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008224385A (en) * 2007-03-12 2008-09-25 Olympus Corp Analyzer and analytical method
JP4538478B2 (en) 2007-08-31 2010-09-08 株式会社日立ハイテクノロジーズ Automatic analyzer
CA3170924A1 (en) 2007-10-02 2009-04-09 Labrador Diagnostics Llc Modular point-of-care devices and uses thereof
JP2010223638A (en) * 2009-03-19 2010-10-07 Beckman Coulter Inc Dispensing device, automatic analyzer, and dispensation monitoring method of dispensing device
US8943909B2 (en) * 2009-04-20 2015-02-03 Hitachi High-Technologies Corporation Automatic analyzer
JP5255590B2 (en) * 2010-03-29 2013-08-07 富士フイルム株式会社 Analysis apparatus and method
BR112013018656B1 (en) 2011-01-21 2021-03-02 Labrador Diagnostics Llc method for detecting the presence or concentration of an analyte in a sample of fluid contained in a container, and, method of measuring the concentration of analyte in a sample of fluid
US8475739B2 (en) 2011-09-25 2013-07-02 Theranos, Inc. Systems and methods for fluid handling
US20140170735A1 (en) 2011-09-25 2014-06-19 Elizabeth A. Holmes Systems and methods for multi-analysis
US9632102B2 (en) 2011-09-25 2017-04-25 Theranos, Inc. Systems and methods for multi-purpose analysis
US9664702B2 (en) 2011-09-25 2017-05-30 Theranos, Inc. Fluid handling apparatus and configurations
US10012664B2 (en) 2011-09-25 2018-07-03 Theranos Ip Company, Llc Systems and methods for fluid and component handling
US9810704B2 (en) 2013-02-18 2017-11-07 Theranos, Inc. Systems and methods for multi-analysis
MX342267B (en) * 2013-02-18 2016-09-23 Theranos Inc Systems and methods for multi-analysis.

Also Published As

Publication number Publication date
JP2006010363A (en) 2006-01-12

Similar Documents

Publication Publication Date Title
JP5178830B2 (en) Automatic analyzer
JP3990944B2 (en) Automatic analyzer
JP3156550B2 (en) Reagent management method and apparatus
JP4416579B2 (en) Automatic analyzer
JP4949389B2 (en) Automatic analyzer
JP5331056B2 (en) Automatic analyzer
JP2004170279A (en) Automatic analyzer
US9513305B2 (en) Multiple cleaning stations for a dispensing probe
JP3140422B2 (en) Automatic analyzer
US20230204609A1 (en) Automatic analysis apparatus and maintenance method in automatic analysis apparatus
JP5487275B2 (en) Automatic analyzer
JP6863708B2 (en) Automatic analyzer
JPH10232234A (en) Automatic analyzer
US8889069B2 (en) Sample processing apparatus and a method of controlling a sample processing apparatus
JP7461963B2 (en) Automatic analyzer and reagent dispensing method
JP5485014B2 (en) Automatic analyzer
JP4713629B2 (en) Automatic analyzer
JP4110082B2 (en) Automatic analyzer
JP6711690B2 (en) Automatic analyzer
JP5258090B2 (en) Automatic analyzer
JP5174930B2 (en) Automatic analyzer
JP2010217047A (en) Automatic analysis device and its specimen carrying method thereof
JP6675162B2 (en) Automatic analyzer
US20190369130A1 (en) Automatic Analyzer
CN115769079A (en) Automatic analyzer

Legal Events

Date Code Title Description
RD04 Notification of resignation of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7424

Effective date: 20060509

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20060913

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20060913

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20080918

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20081014

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20081215

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20081215

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20090310

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20090427

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20090915

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20091019

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20091110

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20091124

R150 Certificate of patent or registration of utility model

Ref document number: 4416579

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121204

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20131204

Year of fee payment: 4

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350