JPS58156856A - Chemical analysis and measurement device - Google Patents

Chemical analysis and measurement device

Info

Publication number
JPS58156856A
JPS58156856A JP3939282A JP3939282A JPS58156856A JP S58156856 A JPS58156856 A JP S58156856A JP 3939282 A JP3939282 A JP 3939282A JP 3939282 A JP3939282 A JP 3939282A JP S58156856 A JPS58156856 A JP S58156856A
Authority
JP
Japan
Prior art keywords
chamber
liquid sample
analytical
measurement
arranged along
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.)
Granted
Application number
JP3939282A
Other languages
Japanese (ja)
Other versions
JPH0156706B2 (en
Inventor
Masashi Azuma
我妻 将士
Tadashi Nakamura
正 中村
Tsuneo Narushima
鳴島 恒雄
Takeshi Katsuta
剛 勝田
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.)
Konica Minolta Inc
Original Assignee
Konica Minolta Inc
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 Konica Minolta Inc filed Critical Konica Minolta Inc
Priority to JP3939282A priority Critical patent/JPS58156856A/en
Publication of JPS58156856A publication Critical patent/JPS58156856A/en
Publication of JPH0156706B2 publication Critical patent/JPH0156706B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N35/00Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor

Landscapes

  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)

Abstract

PURPOSE:To raise efficiency, by providing a reaction thermostat contg. a rotary disc having plural liquid sample holders arranged along the periphery, and a rotary support having plural partitioned sample chambers arranged along the periphery of said disc. CONSTITUTION:A rotary disc 3 having plural liquid sample holders 2 arranged along the periphery is installed in a reaction thermostat 1, and a rotary ring 42 for supporting plural partitioned sample chambers 100 arranged along the periphery of the disc 3, etc. are provided in a measurement device. In such a constitution, optional samples in the thermostat 1 can be fed to an optional position continuously, and their measurement can be made after an optional time elapsed from that time, so a number of samples capable of being treated for analysis at the same time can be increased, and chemical analysis can be executed with high efficiency.

Description

【発明の詳細な説明】 薬が含浸された分析素子により液体試料を化学的に分析
し測定するための装置に関するものである〇一般に、人
体の体液その他の液体試料について、当該液体試料にお
ける特定の成分の含有の有無或( 2 ) いはその含有蓋等を知るべき場合が多く、このために反
応試薬による化学分析が行なわれる。液体試料の化学分
析法としては、乾式法と湿式法とがあるが、このうち乾
式法は、特定の試薬が含浸された薄板をマウントに挾み
込んで成る液体試料分析素子を用い、この分析素子に分
析すべき液体試料を滴下して供給し、これを反応用恒温
槽内に置いて液体試料と試薬とを反応せしめ、その反応
の進行状態又は結果を、例えば反応による色の濃度変化
を光学式濃度測定器により測定する手段、その仲の手段
により測定検出する方法であり、液体試料を実際上固体
として取り扱うことができる点で非常に便利である。
[Detailed Description of the Invention] This relates to a device for chemically analyzing and measuring a liquid sample using an analytical element impregnated with a drug. In general, for human body fluids and other liquid samples, specific In many cases, it is necessary to know the presence or absence of a component (2) or its content, and for this purpose chemical analysis using a reaction reagent is performed. There are two methods for chemical analysis of liquid samples: the dry method and the wet method. Of these, the dry method uses a liquid sample analysis element consisting of a thin plate impregnated with a specific reagent inserted into a mount. A liquid sample to be analyzed is supplied dropwise to the element, placed in a thermostatic chamber for reaction, and the liquid sample is allowed to react with the reagent. This is a method of measuring and detecting using an optical concentration meter or other means, and is very convenient in that a liquid sample can actually be treated as a solid.

而して斯かる液体試料の分析においては、各液体試料を
多数の項目について分析することが通常必妾とされ、又
多数の液体試料についてそのような分析を高い効率で行
なわれることが望ましい。
Therefore, in the analysis of such liquid samples, it is usually necessary to analyze each liquid sample for a large number of items, and it is desirable to perform such analysis on a large number of liquid samples with high efficiency.

従来の化学分析測定装置においては、互に巣なる種類の
液体試料分析素子を夫々収納せしめた複数の収納器を、
反応用恒温室と独立して並べて配(3) 役し、前記し数の液体試料分析素子から特定の液体試料
分析素子を選択して選択された液体試料分析素子を前記
恒温槽内に供給すると共に、この恒温槽内で液体試料と
試薬との反応を進行せしめ、分析素子の各々において必
要とされる反応時間が経過した分析素子を移送機構によ
り測定領域に移送して当該ff1ll定領域に配設した
測定器によって当該分析素子についての測定を行なうよ
うにしている0 然るに分析素子に必要とされる反応時間は当該分析素子
の試薬の種類によって異なる固有の時間であってしかも
In度の厳密さが必要とされるものであること、及び反
応の進行状態を測定検出するためには、同一の分析素子
について1回の測定のみでなくその測定から再び所定時
間の間反応せしめた後第2回の測定を行うことが必要で
あること、並びに複数の測定器を用いることは、測定器
には固有の微妙な特性があってそれが測定器毎に異なる
ため測定(1tiのは頼性か失われることとなり、従っ
てずべての分析素子について同一の測定器により測定す
ることが必要であること等の(lj山から、従来の方法
においては、同時に分析り(坤を施すことの可能な分析
素子の数が少数に制限され、従って高い効率で分析を行
うことができなかった。そして上述の化学分析法におい
ては、収る種の分析素子について、測定器により測定す
る前に例えば冷却等の処理を行う場合かあるか、従来の
方法によりこのような特別な処理を行う場合には、冷却
室等の処理室を別途設けると共に恒温槽内からυ処理室
までの移送系を必要とし、しかもその移送系を制御する
制1iIlI系を必要とする等装置aが極めて複雑にな
る。更に従来の装置では、検査r白目が多くなると分析
素子の収納器の数が増えることによって大きな設置H面
積を必要とし、特【こ病院で臨床検査を行う場合には不
便なものになるという欠点があった。
In conventional chemical analysis and measurement equipment, multiple containers are used to store liquid sample analysis elements of mutually nested types.
(3) A specific liquid sample analysis element is selected from the above-mentioned number of liquid sample analysis elements, and the selected liquid sample analysis element is supplied into the constant temperature chamber. At the same time, the reaction between the liquid sample and the reagent is allowed to proceed in this constant temperature bath, and the analytical elements, after which the reaction time required for each analytical element has elapsed, are transferred to the measurement area by the transfer mechanism and placed in the ff1ll constant area. However, the reaction time required for an analytical element is a unique time that differs depending on the type of reagent for the analytical element, and the precision of In degree is required. In order to measure and detect the progress of the reaction, it is necessary to conduct not only one measurement on the same analytical element, but also a second reaction after the first measurement for a predetermined period of time. It is necessary to perform measurements of Therefore, in the conventional method, it is necessary to measure all the analytical elements with the same measuring device. The number of analytical elements is limited to a small number, and therefore analysis cannot be performed with high efficiency.In addition, in the above chemical analysis method, the analytical elements that can be accommodated are subjected to treatment such as cooling before being measured with a measuring instrument. If such special treatment is carried out using conventional methods, a separate treatment chamber such as a cooling chamber is required, as well as a transfer system from the thermostatic chamber to the υ treatment chamber. The device a becomes extremely complex as it requires a control system to control the transfer system.Furthermore, in conventional devices, as the number of whites increases, the number of storage containers for analytical elements increases, requiring a large installation area. However, it had the disadvantage of being inconvenient especially when conducting clinical tests at this hospital.

本発明は小型にして篩い効率で液体試料の化学分析を達
成することのできる化学分析測定装置を提供することを
目的とする。
SUMMARY OF THE INVENTION An object of the present invention is to provide a chemical analysis and measurement device that is compact and can perform chemical analysis of a liquid sample with high sieving efficiency.

本発明の特徴と1−るところは、周縁に沿って腹(5) 数の准体試料分析素子保持部を配列した円板状の保持体
を有する反応用恒温室と、前記保持体の外周に沿って複
数の区画された素子室を配列した支持体と、前記保持体
の外周に沿って前記支持体を相対的に移動させる移動機
構と、前記支持体の素子室内に収納し7!′液体試料分
析素子を前記保持体の液体試料分析素子保持部へ出入せ
しめる搬送機構と、前記支持体に素子室と並んで設けた
測定室とを具えて成る点(こある。
The features and first features of the present invention are a constant temperature chamber for reaction having a disc-shaped holder in which (5) anti-substance sample analysis element holders are arranged along the periphery, and an outer periphery of the holder. a support body in which a plurality of divided element chambers are arranged along the holder; a moving mechanism for relatively moving the support body along the outer periphery of the holding body; and 7! 'A transport mechanism for moving the liquid sample analysis element into and out of the liquid sample analysis element holding portion of the holder, and a measurement chamber provided in the support body in parallel with the element chamber.

以下図面によって本発明を説明する。The present invention will be explained below with reference to the drawings.

第1図は本発明に係る化学分析測定装置の縦断側面図、
第2図は第1図の崩断乎面Nであり、図中1は反応用恒
温室を形成する@湯槽(以下「恒温槽」という。)を示
す。この恒温槽lは支柱11に支持さねており、ごの恒
温槽1内には、各々液体試料分析素子(以下「分析素子
」という。)を保持するための複数の分析素子保持部(
以下「保持部」という。)2 (2A〜2ft)をその
外周部に有する円板状の保持体3を設ける。前記保持部
2は、第1図に示すように前記保持体3に形成さく 6
 ) れた凹所81において内方側が下がった状態に置かれる
回動保持板20を有し、この回動保持板2゜は、前記凹
所31の外端における軸Pを中心として上下方向に同動
される。12は分析素子が恒温槽lに出入りするための
給送[1であり、例えばシャッター(図示せず)により
適宜開閉される。
FIG. 1 is a longitudinal sectional side view of a chemical analysis and measurement device according to the present invention;
FIG. 2 shows the collapse plane N of FIG. 1, and 1 in the figure indicates a bath (hereinafter referred to as "thermal chamber") forming a thermostatic chamber for reaction. This thermostatic chamber 1 is supported by a column 11, and inside the thermostatic chamber 1, there are a plurality of analytical element holding parts (hereinafter referred to as "analytical elements") each for holding a liquid sample analytical element (hereinafter referred to as "analytical element").
Hereinafter referred to as the "holding section". ) 2 (2A to 2 ft) on its outer periphery. The holding portion 2 is formed on the holding body 3 as shown in FIG. 1.
) The rotary retaining plate 20 is placed in a state in which the inner side is lowered in the recess 81, and this rotary retaining plate 2° is arranged vertically about the axis P at the outer end of the recess 31. will be moved together. Reference numeral 12 denotes a feeder [1] for moving the analytical element into and out of the thermostatic chamber l, which is opened and closed as appropriate by, for example, a shutter (not shown).

前記恒温槽l外には、前記保持体8の外周に沿って順次
に区画され且つ連結されている複数の区画室4を設ける
。この例では、前記支柱11の中心軸Xを中心とする円
に沿って延びるガイド部材41にガイドされなから、前
記支柱11のまわりに回動される支持体としてのリンク
状の回動体42に、夫々底壁の内方側に切欠部401が
形成された複数の筒状体40を、当該回動体42の外周
に沿って順次に垂立して設け、これら筒状体↓0によっ
て前記区画室4(4A−4H)をfN成する。
A plurality of compartments 4 are provided outside the thermostatic chamber 1, which are sequentially divided and connected along the outer periphery of the holder 8. In this example, it is not guided by a guide member 41 extending along a circle centered on the central axis , a plurality of cylindrical bodies 40 each having a notch 401 formed on the inner side of the bottom wall are sequentially vertically provided along the outer periphery of the rotating body 42, and these cylindrical bodies ↓0 form the partitions. Chamber 4 (4A-4H) is formed fN.

図中43は車輪を示す。この例では前記区画室4のうち
4A〜4Fで示した区画室を、分析素子を収納するため
の素子室100として構成すると共に、4Gで示した区
画室を、光学的分析器等が組(7) 込まれた、分析素子の試薬及び液体試料の反応物の濃度
を測定するための測定室200としてPfな成し、史に
4Hで示した区画室を、測定が終了されて不要となった
分析素子を排出するための排出用区画室300として構
成する。
In the figure, 43 indicates a wheel. In this example, the compartments 4A to 4F of the compartments 4 are configured as an element chamber 100 for storing analytical elements, and the compartment 4G is configured to contain optical analyzers, etc. 7) Pf is used as the measurement chamber 200 for measuring the concentration of the reagent of the analytical element and the reactant of the liquid sample. It is configured as a discharge compartment 300 for discharging the analytical elements.

前記回動体42の外側には、当該回動体42をギヤ’F
M’flltを介して回動させるモータ5を設ける。
On the outside of the rotating body 42, the rotating body 42 is connected to a gear 'F
A motor 5 is provided for rotation via M'fllt.

このモータ5は前記回動体42を回動させることにより
前記区画室4を前記保持体8の外周に沿って移動せしめ
る移動@溝を構成する。前記恒温槽lと前記回動体42
との間には、前記区画室4から前記保持部2へ、或いは
前記保持部2から前記区画室4へ分析素子を送る搬送機
構6(第1図、第2図中一点@il線で示す。)を設け
る。この搬送Fli 購eは、モータ61によってギヤ
Fl!Imを介して111J iiL支柱11のまわり
を回動する回動板62に取付けられており、第3図に示
すように、図示しないモータによって回動される一対の
ローラ63゜68’の間に設けられたベルト64と、前
記ローラ68.63’を夫々支持し且つ上下方向に進退
せしめられる支1lilll(15,65’と、この支
軸65.f!5’を進退せしめる駆動部66とより成る
。前記ベルト64は、01)記筒状体4oの切欠部40
1において筒状体Φ0の底壁の内面と等しいレベルに位
置される上昇位置(実線で示す。)と、前記保持体3の
−L面と等しいレベルに位置される下降位置(二点鎖線
で示す。)との間を昇降する。図中7は前記素子100
より前記保持部2に送られる分析素子に、これが送られ
るタイミングに合わせて液体試料を滴下する、前記搬送
機構6の移動に伴って移動される液体試料源である。
This motor 5 constitutes a movement @ groove that moves the compartment 4 along the outer periphery of the holding body 8 by rotating the rotating body 42 . The constant temperature bath l and the rotating body 42
A transport mechanism 6 (indicated by a dot @il line in Figs. .) will be established. This conveyance Fl is carried out by the motor 61 through the gear Fl! It is attached to a rotating plate 62 that rotates around the 111J iiL support column 11 via Im, and as shown in FIG. A belt 64 provided, supports 15, 65' that support the rollers 68 and 63' respectively and are moved forward and backward in the vertical direction, and a drive section 66 that moves the support shafts 65.f!5' forward and backward. The belt 64 consists of: 01) the notch 40 of the cylindrical body 4o;
1, there is a raised position (indicated by a solid line) located at the same level as the inner surface of the bottom wall of the cylindrical body Φ0, and a lowered position (indicated by a two-dot chain line) located at the same level as the −L plane of the holder 3. ). 7 in the figure is the element 100.
This is a liquid sample source that is moved along with the movement of the transport mechanism 6 and drops a liquid sample onto the analysis element that is sent to the holding section 2 at the same timing as the analysis element is sent.

このような構成の化学分析測定装置の操作の一例につい
て説明すると、先ず素子室100に夫々同一種類のW数
の分析素子Sを、第1図の一点鎖線で示すように堆櫂し
て収納する。収納された分析素子Sの種類は素子室10
0毎に異なるものとされる。そして例えば−の素子室1
00(4A)の分析素子Sに液体試料を滴下してこれを
−の保持部2人に送り入れ、次いで上記の素子室100
(4A)に隣接する素子室100(ΦB)の分析(9) 素子Sに液体試料を滴下してこれを上記の保持部2人に
隣接した保持部2Bに送り入れ、このようにして円に沿
って鼓ぶ各素子室100内に収納されている分析素子S
に液体試料を順次に滴下してこれを保持部2の各々に送
り入れる。この操作は、先ず−の素子室1.00 (4
A )とこれに対向する−の保持部2Aとの間に搬送機
Il#6を位置せしめ、搬送機構6のベルト64を上昇
位置に置くと共にベルト64を駆動させることによって
上記の素子室100(4A)の最下方に位置されている
分析素子Sがベルト64との摩擦により送り出され、こ
のとき液体試料源7から液体試料が分析素子Sに滴下さ
れ、次いで支軸65.65’を縮退させてベルト64を
下降[&に置くことにより、ベルト64上の分析素子S
が恒温槽1の給送口12を介して回動保持板20上を滑
り落ち、凹所31の壁面に当接されて保持部2人に保持
される。然る後にモータ61を駆動することにより回診
板62を第2図中時計方向に回動させて搬送機構6及び
液体試料源7を、上記の素子室100(4・A)に隣(
l O) 接する素子室100(4B)と、これに対向する保持部
2Bとの間に位置せしめ、同様の操作により当該素子室
1.00 (4B )内の分析素子Sを保持部2Bに保
持せしめ、このような操作を順次に行うことによって各
素子室100内に収納されている分析素子Sを保持部2
の各々に送り入れる。
To explain an example of the operation of a chemical analysis and measurement apparatus having such a configuration, first, analytical elements S of the same type and the same W number are stacked and stored in the element chamber 100 as shown by the dashed line in FIG. . The type of analytical element S stored is element chamber 10.
Each 0 is different. And for example - element chamber 1
A liquid sample is dropped onto the analytical element S of 00 (4A) and sent to the two holding parts of -, and then transferred to the element chamber 100 described above.
Analysis of the element chamber 100 (ΦB) adjacent to (4A) (9) Drop a liquid sample onto the element S and feed it into the holding part 2B adjacent to the two holding parts described above, and form a circle in this way. Analytical elements S housed in each element chamber 100 along the
A liquid sample is sequentially dropped into the holding parts 2 and sent to each of the holding parts 2. This operation first begins with - element chamber 1.00 (4
A) and the opposing holding section 2A, the conveyance machine Il#6 is positioned, the belt 64 of the conveyance mechanism 6 is placed in the raised position, and the belt 64 is driven to move the element chamber 100 ( 4A) is sent out by friction with the belt 64, and at this time, a liquid sample is dripped onto the analysis element S from the liquid sample source 7, and then the support shaft 65.65' is retracted. By lowering the belt 64 and placing it on the
slides down on the rotary holding plate 20 through the supply port 12 of the constant temperature bath 1, comes into contact with the wall surface of the recess 31, and is held by two holding members. Thereafter, by driving the motor 61, the circulation plate 62 is rotated clockwise in FIG.
l O) Position it between the adjacent element chamber 100 (4B) and the holding part 2B facing it, and hold the analytical element S in the element chamber 1.00 (4B) in the holding part 2B by the same operation. By sequentially performing such operations, the analytical elements S stored in each element chamber 100 are transferred to the holding unit 2.
send it to each of them.

そして保持部2に夫々保持されている分析素子Sが恒温
槽l内で一定温度に、各分析素子Sに係る固有の反応時
間維持されてから、各分析素子Sを測定器によって測定
する。この操作は次のようにして行われる。例えば−の
保持部21Gこ保持されている分析素子Sを測定する場
合には、モータ5の駆動により回動体42を回動させて
測定室tGを−の保持部2Aに対向した位1aに停止[
−せしめると共に、モータ61の駆動により回動板62
を回動させて搬送機構6を−の保持部2Aに対向した位
置に停止せしめ、次に当該保持部2Aに係る回動保持板
20を図示しない駆動機構により軸Pを中心に回動して
第3図の二点鎖線の位置まで起立せしめ、これによって
同動保持板2o上の分析素(11) 子Sをスライドさせて搬送機構6に係る下降位置に置か
れたベルト64上に送り出し、その後ベルト64を上昇
位置に置くことにより測定室200に分析素子Sを送り
入れる。ここでの測定が終了すると分析素子Sは搬送機
11176を介して排出用区画室800に排出される。
After each analytical element S held in the holding section 2 is maintained at a constant temperature in the constant temperature bath l for a specific reaction time for each analytical element S, each analytical element S is measured by a measuring instrument. This operation is performed as follows. For example, when measuring the analytical element S held by the - holding part 21G, the rotating body 42 is rotated by driving the motor 5 to stop the measurement chamber tG at a position 1a facing the - holding part 2A. [
- At the same time, the rotating plate 62 is driven by the motor 61.
is rotated to stop the transport mechanism 6 at a position opposite to the - holding part 2A, and then the rotary holding plate 20 associated with the holding part 2A is rotated around the axis P by a drive mechanism (not shown). 3, and thereby slide the analyte (11) S on the co-moving holding plate 2o and feed it onto the belt 64 placed in the lowered position of the transport mechanism 6. Thereafter, the analytical element S is sent into the measurement chamber 200 by placing the belt 64 in the raised position. When the measurement here is completed, the analytical element S is discharged to the discharge compartment 800 via the carrier 11176.

このように回動体42を回動して測定室200を順次に
移動させ且つこれに合わせて搬送@構6を移動させるこ
とによって保持部2に夫々保持されている分析素子Sの
測定が順次に行われ2)ことになる。史に各分析素子S
の夫々について測定を2回以上行う場合には上述の操作
か繰り返して行われることとなる。こうして分析素子S
の測定が終了すると、空になった保持部2には、素子Y
100より新たな分析素子Sが送り入れられる。ここで
素子室100内の分析紫fSを保持部2に送り入れるに
あたっては、上述のように素子室100の並びに対応し
た順番で分析素子Sを各保持部2に位置せしめる代りに
、任意に素子室100を選んでそこから分析素子Sを保
持部2の−に送り入れることもできる。この場合には、
夫々任意に選ばれた素子室100よりの分析素子Sが各
保持部2に位置されることとなり、分析素子Sを各分析
素子Sの固有の反応時間に合わせて夫々測定室200に
送り入れて測定が行われることとなる。
By rotating the rotating body 42 in this way to sequentially move the measurement chambers 200 and moving the transport @ structure 6 accordingly, the analytical elements S held in the holding sections 2 can be measured sequentially. 2) It will happen. Each analytical element S
If measurements are to be made for each of these two or more times, the above-mentioned operations will be repeated. In this way, the analytical element S
When the measurement of the element Y is completed, the empty holding part 2 is filled with the element Y.
A new analysis element S is sent in from 100. Here, when sending the analytical purple fS in the element chamber 100 to the holding part 2, instead of placing the analytical elements S in each holding part 2 in the order corresponding to the arrangement of the element chambers 100 as described above, It is also possible to select the chamber 100 and send the analytical element S to - of the holding section 2 from there. In this case,
Analytical elements S from arbitrarily selected element chambers 100 are placed in each holding section 2, and the analytical elements S are sent into the measurement chambers 200 in accordance with the unique reaction time of each analytical element S. Measurements will be taken.

而して本発明においては、恒温室内において膜数の保持
部を保持体の外周部に並べて配置すると共に、保持体の
外周に沿って素子室及び測定室を保持体に対して相対的
に移動自在に設けてこれら区画室と保持部との間で分析
素子を出入させる構成としているため、任意の分析素子
を選んで恒温室内の任意の保持部に送り入れることがで
きると共に、恒温室内に置かれている分析素子のうち任
意の分析素子を任意の時間に測定室に送り入れることが
でき、しかも分析素子の測定か終了して空になった保持
部に、選ばれた新たな分析素子を直ちに位置せしめるこ
とができる。従って恒温室内に任意の分析素子を任意の
位置に連続的に供給しながら、これらの分析素子の測定
を任意の反応時間が経過した時点で測定することができ
ることと(18) なるから、同時に分析処理を施すことの可能な分析素子
の数を多くすることができて高い効率で液体試料の化学
分析を達成することができる。また素子室を保持体の外
周に沿って順次に配置した構成としているため、素子室
の数を多くしながら装置の設置a面積を小ざいものとす
ることができ、従って例えば検査項目の数が増noして
分析素子の数が多くなっても装置の小型化を図ることが
できる。
Therefore, in the present invention, the holding parts for the number of membranes are arranged side by side on the outer periphery of the holder in a constant temperature room, and the element chamber and the measurement chamber are moved relative to the holder along the outer periphery of the holder. Since the analytical elements can be freely installed and moved in and out between these compartments and the holding part, it is possible to select any analytical element and send it to any holding part in the thermostatic chamber, and also to place it in the thermostatic chamber. You can send any analytical element out of the existing analytical elements to the measurement chamber at any time, and you can also place a new selected analytical element into the empty holding section after the measurement of the analytical element has been completed. It can be positioned immediately. Therefore, it is possible to continuously supply arbitrary analytical elements to arbitrary positions in a thermostatic chamber and measure these analytical elements after an arbitrary reaction time has elapsed (18).This means that simultaneous analysis can be performed. The number of analytical elements that can be processed can be increased, and chemical analysis of liquid samples can be achieved with high efficiency. Furthermore, since the element chambers are arranged sequentially along the outer periphery of the holder, the installation area of the device can be made small while increasing the number of element chambers. Therefore, for example, the number of inspection items can be reduced. Even if the number of analytical elements increases, the device can be made smaller.

更に上述の実施例では恒温槽内において分析素子が移動
されないため、分析素子が相対的な空気の流れにより冷
却されることを避けることができるので分析素子の温度
を一定の温度に維持することができ、従って信頼性の高
い測定結果を得ることができる。
Furthermore, in the above embodiment, since the analytical element is not moved within the thermostatic chamber, the analytical element can be prevented from being cooled by relative air flow, and the temperature of the analytical element can be maintained at a constant temperature. Therefore, highly reliable measurement results can be obtained.

そして本発明においては、膜数の区画室のいくつかを、
恒温室内の温度と異なる温度の雰囲気とされた冷却等の
処理用区画室として構成してもよく、このようにすれば
装置の構成を簡単なものとしながら恒温室内の任意の分
析素子を任意の時間に前記処理用区画室に送り入れ或い
はここから取(14) 出すことができて分析素子について種々の処理を高い効
率をもって行うことができる。
In the present invention, some of the membrane compartments are
It may also be configured as a compartment for processing such as cooling with an atmosphere at a temperature different from the temperature inside the constant temperature chamber.In this way, the configuration of the apparatus can be simplified and any analytical element inside the constant temperature chamber can be connected to any The analytical element can be fed into or taken out from the processing compartment (14) at any time, and various treatments can be performed on the analytical element with high efficiency.

尚本発明においては、膜数の搬送機構を設けてもよく、
このような構成によれは区画室の数が多い場合により一
層高い効率をもって分析処理を行うことができる。
In the present invention, a conveyance mechanism for the number of membranes may be provided,
With such a configuration, analysis processing can be performed with higher efficiency when the number of compartments is large.

以上のように本発明によれば、小型にして高い効率で液
体試料の化学分析を達成することのできる化学分析測定
装置を提供することができる。
As described above, according to the present invention, it is possible to provide a chemical analysis and measurement device that is small in size and can perform chemical analysis of a liquid sample with high efficiency.

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

第1図は本発明に係る化学分析測定装置を示す縦断側面
図、第2図は第1図の横断平面図、第8図は第11の一
部を拡大して搬送機構の具体的構成を示す説明図である
。 1・・・恒温槽      2・・・分析素子保持部3
・・・保持体      81・・・凹所4.4l−4
H・・・区画室  40・・・筒状体t2・・・回動体
     5・・・モータ6・・・搬送機構     
62・・・回動板100・・・素子室    200・
・・測定室(15) 300・・・排出用区画室 S・・・分析素子代理人弁
理士  大  井  止  彦特開BH5B−1568
56(5) 莱3図
FIG. 1 is a vertical cross-sectional side view showing a chemical analysis and measurement device according to the present invention, FIG. 2 is a cross-sectional plan view of FIG. 1, and FIG. 8 is a partially enlarged view of FIG. FIG. 1... Constant temperature chamber 2... Analytical element holding part 3
... Holding body 81 ... Recess 4.4l-4
H... Compartment chamber 40... Cylindrical body t2... Rotating body 5... Motor 6... Transport mechanism
62... Rotating plate 100... Element chamber 200.
...Measurement room (15) 300...Discharge compartment S...Analytical element agent Patent attorney Tomohiko Ooi JP-A BH5B-1568
56(5) Lai 3 figure

Claims (1)

【特許請求の範囲】[Claims] 1)周縁に沿って複数の液体試料分析素子保持部を配列
した円板状の保持体を有する反応用恒温室と、前記保持
体の外周に沿って、複数の区画された素子室を配列した
支持体と、前記保持体の外周に沿って前記支持体を相対
的に移動させる移動機構と、前記支持体の素子室内に収
納した液体試料分析素子を前記保持体の液体試料分析素
子保持部へ出入せしめる搬送機溝と、前記支持体に素子
室と並んで設けた測定室とを具えて成ることを詩歌とす
る化学分析測定装置。
1) A thermostatic reaction chamber including a disk-shaped holder in which a plurality of liquid sample analysis element holders are arranged along the periphery, and a plurality of divided element chambers arranged along the outer periphery of the holder. a support, a moving mechanism for relatively moving the support along the outer periphery of the holder, and a liquid sample analysis element stored in an element chamber of the support to a liquid sample analysis element holding part of the holder. A chemical analysis and measurement device characterized by comprising a conveyor groove for entry and exit, and a measurement chamber provided in the support body in parallel with an element chamber.
JP3939282A 1982-03-15 1982-03-15 Chemical analysis and measurement device Granted JPS58156856A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3939282A JPS58156856A (en) 1982-03-15 1982-03-15 Chemical analysis and measurement device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3939282A JPS58156856A (en) 1982-03-15 1982-03-15 Chemical analysis and measurement device

Publications (2)

Publication Number Publication Date
JPS58156856A true JPS58156856A (en) 1983-09-17
JPH0156706B2 JPH0156706B2 (en) 1989-12-01

Family

ID=12551722

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3939282A Granted JPS58156856A (en) 1982-03-15 1982-03-15 Chemical analysis and measurement device

Country Status (1)

Country Link
JP (1) JPS58156856A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6180055A (en) * 1984-09-28 1986-04-23 Shimadzu Corp Method and apparatus for automatic analysis of multiple items
JPS61209341A (en) * 1985-03-13 1986-09-17 Konishiroku Photo Ind Co Ltd Biochemical analyser
JPS61259142A (en) * 1985-05-14 1986-11-17 Konishiroku Photo Ind Co Ltd Biochemical analysis apparatus
JPS621168U (en) * 1985-06-19 1987-01-07
JPS62157551A (en) * 1985-12-30 1987-07-13 Konishiroku Photo Ind Co Ltd Boichemical analysis method
JPH06506622A (en) * 1991-10-02 1994-07-28 ターゲット セラピューティクス,インコーポレイテッド Vasoocclusive coil with attached fibrous member

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6180055A (en) * 1984-09-28 1986-04-23 Shimadzu Corp Method and apparatus for automatic analysis of multiple items
JPS61209341A (en) * 1985-03-13 1986-09-17 Konishiroku Photo Ind Co Ltd Biochemical analyser
JPS61259142A (en) * 1985-05-14 1986-11-17 Konishiroku Photo Ind Co Ltd Biochemical analysis apparatus
JPS621168U (en) * 1985-06-19 1987-01-07
JPH0413655Y2 (en) * 1985-06-19 1992-03-30
JPS62157551A (en) * 1985-12-30 1987-07-13 Konishiroku Photo Ind Co Ltd Boichemical analysis method
JPH06506622A (en) * 1991-10-02 1994-07-28 ターゲット セラピューティクス,インコーポレイテッド Vasoocclusive coil with attached fibrous member

Also Published As

Publication number Publication date
JPH0156706B2 (en) 1989-12-01

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