JP2753340B2 - Preparation of reaction sample - Google Patents

Preparation of reaction sample

Info

Publication number
JP2753340B2
JP2753340B2 JP1227080A JP22708089A JP2753340B2 JP 2753340 B2 JP2753340 B2 JP 2753340B2 JP 1227080 A JP1227080 A JP 1227080A JP 22708089 A JP22708089 A JP 22708089A JP 2753340 B2 JP2753340 B2 JP 2753340B2
Authority
JP
Japan
Prior art keywords
sample
reaction
analysis
diluted sample
diluted
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP1227080A
Other languages
Japanese (ja)
Other versions
JPH0390837A (en
Inventor
杉夫 間部
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.)
Olympus Corp
Original Assignee
Olympus 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 Olympus Corp filed Critical Olympus Corp
Priority to JP1227080A priority Critical patent/JP2753340B2/en
Publication of JPH0390837A publication Critical patent/JPH0390837A/en
Application granted granted Critical
Publication of JP2753340B2 publication Critical patent/JP2753340B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Investigating Or Analysing Biological Materials (AREA)
  • Sampling And Sample Adjustment (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)

Description

【発明の詳細な説明】 [産業上の利用分野] この発明は生化学や免疫学用の分析装置における反応
サンプルの作製方法の改善に関するものである。
Description: TECHNICAL FIELD The present invention relates to an improvement in a method for preparing a reaction sample in an analyzer for biochemistry or immunology.

[従来の技術] 生化学や免疫学的用の自動分析装置で、ある検体のサ
ンプルを分析する場合、分析項目によっては希釈サンプ
ルを使用することがある。また異常高値検体の再検査や
尿の検査にも希釈サンプルが使用されることが多い。
[Prior Art] When analyzing a sample of a certain sample by an automatic analyzer for biochemistry or immunology, a diluted sample may be used depending on an analysis item. Also, diluted samples are often used for re-examination of abnormally high samples and urinalysis.

この従来の自動分析装置による分析方法において、使
用される希釈サンプルは原サンプルと希釈液とをシリン
ジ等の移送装置を介してサンプルカップにそれぞれ定量
分注し、攪拌混和させることにより作製し、次の行程で
サンプルカップに作製された希釈サンプルを所要数の反
応容器に別な移送装置により分注し、さらにそれぞれの
反応容器ごとに所定の試薬を分注し混和反応させた反応
サンプルを作り、これらの反応サンプルを光透過度測定
などにより分析定量化していた。
In this conventional analysis method using an automatic analyzer, a diluted sample to be used is prepared by dispensing a fixed amount of an original sample and a diluent into a sample cup via a transfer device such as a syringe, and mixing them with stirring. The diluted sample prepared in the sample cup in the process of the above is dispensed into a required number of reaction vessels by another transfer device, and further, a predetermined reagent is dispensed into each reaction vessel and a reaction sample is produced by mixing and mixing, These reaction samples were analyzed and quantified by light transmittance measurement or the like.

[発明が解決しようとする課題] しかしながら従来の分析方法には次のような問題があ
った。
[Problems to be Solved by the Invention] However, the conventional analysis method has the following problems.

a.サンプルカップとして原サンプル用のサンプルカップ
と反応サンプル用の反応容器のほか、中間処理としての
希釈用の希釈サンプルカップが必要であり、そのための
スペースと費用を必要としていた。
a. In addition to the sample cup for the original sample and the reaction vessel for the reaction sample as the sample cup, a diluted sample cup for dilution as an intermediate treatment was required, which required space and cost.

b.中間処理としての希釈行程があるので、サンプルカッ
プと希釈サンプルカップ間の移送用と希釈サンプルカッ
プと反応容器間の移送用にそれぞれ別な移送装置が必要
であり、この点に関しても大きなスペースと費用を必要
としていた。このスペースと費用を節約し移送装置を共
通に利用しようとすると動作がシリーズとなるため分析
時間が長くなると言う別の問題がでる。
b.Because there is a dilution process as an intermediate process, separate transfer devices are required for transfer between the sample cup and the diluted sample cup and for transfer between the diluted sample cup and the reaction vessel, and in this regard, a large space is required. And needed expense. Attempting to save space and expense and to use a common transfer device has the further problem of increasing the analysis time due to the series of operations.

c.従来の分析方法は希釈サンプルカップ内の希釈サンプ
ルを所要数の反応容器に分注する方式であるので、それ
ぞれの反応容器に供給される希釈サンプルの希釈倍率は
同倍率となり、分析項目毎に異なる希釈倍率の反応サン
プルを必要とする場合は異なる希釈倍率に対応した希釈
サンプルカップをそれぞれに用意する必要があり、装置
も複雑になる。
c. The conventional analysis method dispenses the diluted sample in the diluted sample cup into the required number of reaction vessels, so the dilution ratio of the diluted sample supplied to each reaction vessel is the same, and When reaction samples having different dilution ratios are required, it is necessary to prepare diluted sample cups corresponding to different dilution ratios, and the apparatus becomes complicated.

d.また原サンプルを反応容器内に分注するまでに、定量
分注の行程が二回必要であり、その間に分注器のプロー
ブにおいてキャリオーバーの影響を二度受け、分析精度
を悪くする恐れがあった。
d. In addition, two steps of quantitative dispensing are required before dispensing the original sample into the reaction vessel, during which the probe of the dispenser is affected twice by the carryover, which deteriorates the analysis accuracy. There was fear.

この発明は、上記したような従来の方法の問題点を解
決するためになされたもので、装置の簡易化を可能に
し、かつキャリオーバーの影響を少なくした反応サンプ
ルの作製方法を提供することを目的としている。
The present invention has been made in order to solve the problems of the conventional method as described above, and it is an object of the present invention to provide a method for preparing a reaction sample which enables simplification of an apparatus and reduces the influence of carryover. The purpose is.

[課題を解決するための手段] 生化学や免疫学用の分析装置に使用する検体のサンプ
ルを希釈液で希釈し試薬を加える析用の反応サンプルの
作製方法において、サンプルと希釈液とを所望する分析
項目に対応する希釈倍率に応じてそれぞれの所定量を分
析項目の反応容器に直接供給し混和して所望する希釈倍
率の希釈サンプルを作製し、作製したこの希釈サンプル
のうち分析項目毎に決まる所要量を残して、余分量を反
応容器から排出して、反応容器に残した所要量の希釈サ
ンプルに所定の試薬を加え混和し作成することを特徴と
している。
[Means for Solving the Problems] In a method for preparing a reaction sample for analysis, in which a sample of a sample used in an analyzer for biochemistry or immunology is diluted with a diluent and a reagent is added, a sample and a diluent are desired. In accordance with the dilution factor corresponding to the analysis item to be analyzed, each predetermined amount is directly supplied to the reaction vessel of the analysis item and mixed to prepare a diluted sample having a desired dilution ratio. The method is characterized in that an excess amount is discharged from the reaction vessel while leaving the determined required amount, and a predetermined reagent is added to and mixed with the required amount of the diluted sample left in the reaction vessel.

[作用] このように反応サンプルを直接反応容器に作製するこ
とにより、希釈サンプルカップを省略するとともに、分
注操作に伴うキャリオーバーによる汚染の機会を少なく
することができる。
[Operation] By directly preparing the reaction sample in the reaction vessel, the diluted sample cup can be omitted, and the chance of contamination due to carryover accompanying the dispensing operation can be reduced.

[実施例] 以下図面を参照しながらこの発明の一実施例を説明す
る。第1図(a)〜(g)はこの発明の希釈サンプルの
作製より分析定量化までの方法順序の説明図である。
Embodiment An embodiment of the present invention will be described below with reference to the drawings. FIGS. 1 (a) to 1 (g) are explanatory diagrams of a method sequence from preparation of a diluted sample to analysis and quantification of the present invention.

同図において1は反応容器で、この反応容器1は被検
体の分析項目およびその分析項目が必要とする希釈倍率
区分に対応させて必要数が用意され、同図(a)に示す
第1の行程で、図示しない分注器によりこれら反応容器
1に生体食塩水等の希釈液2を、必要とする希釈倍率に
応じて所定量を分注する。次に同図(b)に示す第2の
行程で、希釈液2が収容されている反応容器1に、図示
しない分注器により被検体のサンプル3を、必要とする
希釈倍率に応じて所定量を分注し加え、同図(c)に示
す第3の行程で、希釈液2とサンプル3とを攪拌等の操
作により均一に混和して、所要希釈倍率の希釈サンプル
4を作製する。
In the figure, reference numeral 1 denotes a reaction vessel, and a required number of reaction vessels 1 are prepared in correspondence with the analysis items of the specimen and the dilution ratios required by the analysis items, and the first number shown in FIG. In the process, a diluent 2 such as a physiological saline solution is dispensed into these reaction vessels 1 by a dispenser (not shown) in a predetermined amount according to a required dilution ratio. Next, in a second step shown in FIG. 4B, a sample 3 of the subject is placed in a reaction vessel 1 containing a diluent 2 by a dispenser (not shown) in accordance with a required dilution ratio. The diluent is dispensed and added, and in a third step shown in FIG. 3C, the diluent 2 and the sample 3 are uniformly mixed by an operation such as stirring to prepare a diluted sample 4 having a required dilution ratio.

希釈サンプル4を作製し終わったら同図(d)に示す
第4の行程で、反応容器1より分析に必要な量の希釈サ
ンプル4を残し、余分の希釈サンプル4を図示しない分
注器等を使用して排出し、次の同図(e)に示す第5の
行程で、分析項目に応じた所定の試薬5を図示しない分
注器により分注し加え、同図(f)に示す第6の行程
で、希釈サンプル4と試薬5とを攪拌等の操作により均
一に混和し、かつ一定温度下で反応させて反応サンプル
6を作製する。
When the diluted sample 4 has been prepared, in a fourth step shown in FIG. 4D, an amount of the diluted sample 4 necessary for analysis is left from the reaction vessel 1 and an extra diluted sample 4 is dispensed by a dispenser or the like. Then, in a fifth step shown in FIG. 11E, a predetermined reagent 5 corresponding to the analysis item is dispensed by a dispenser (not shown). In step 6, the diluted sample 4 and the reagent 5 are uniformly mixed by an operation such as stirring, and reacted at a constant temperature to prepare a reaction sample 6.

反応サンプル6を作製し終わったら同図(g)に示す
第7の行程で、この反応サンプル6についての光透過度
を測定する測光検査等により被検体サンプル3を分析定
量化する。
When the reaction sample 6 has been prepared, the subject sample 3 is analyzed and quantified by a photometric test or the like for measuring the light transmittance of the reaction sample 6 in a seventh step shown in FIG.

この実施例において、第1の行程と第2の行程の順序
を逆にしても同じ作用効果が得られる。
In this embodiment, the same operation and effect can be obtained even if the order of the first step and the second step is reversed.

なお、この発明は上記実施例に限定されるものでなく
要旨を変更しない範囲で変形して実施できる。
The present invention is not limited to the above-described embodiment, and can be modified and implemented without departing from the scope of the invention.

[発明の効果] この発明によれば次の効果が期待できる。According to the present invention, the following effects can be expected.

a.希釈サンプルを直接反応容器の中に作製するので、希
釈サンプル用のサンプルカップとその設置スペースおよ
び希釈サンプルを反応容器に移送する移送装置が不要に
なる。
a. Since the diluted sample is prepared directly in the reaction vessel, a sample cup for the diluted sample and its installation space and a transfer device for transferring the diluted sample to the reaction vessel are not required.

b.この発明による方法は、希釈サンプルの作製あたって
の操作は排出操作のみであり、吸引、吐出のステップの
ある従来の方法と比べてプローブにおけるキャリオーバ
ーによる汚染の影響を少なくし、分析精度を高めること
ができる。
b. The method according to the present invention requires only the discharge operation to prepare the diluted sample, reduces the influence of contamination due to carry-over in the probe and reduces the analysis accuracy compared to the conventional method having a suction and discharge step. Can be increased.

c.反応容器に直接希釈サンプルを作製するので分析項目
に適した希釈倍率の希釈サンプルを反応容器毎に作製す
ることも容易にできる。
c. Since the diluted sample is prepared directly in the reaction container, it is easy to prepare a diluted sample having a dilution ratio suitable for the analysis item for each reaction container.

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

第1図(a)〜(g)はこの発明の一実施例の希釈サン
プルの作製より分析定量化までの方法順序の説明図であ
る。 1……反応容器、2……希釈液 3……サンプル、4……希釈サンプル 5……試薬、6……反応サンプル
1 (a) to 1 (g) are explanatory diagrams of a method sequence from preparation of a diluted sample to analysis and quantification according to one embodiment of the present invention. 1 ... reaction vessel 2 ... diluent 3 ... sample 4 ... diluted sample 5 ... reagent, 6 ... reaction sample

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】生化学や免疫学用の分析装置に使用する検
体のサンプルを希釈液で希釈し試薬を加える分析用の反
応サンプルの作製方法において、 前記サンプルと前記希釈液とを所望する分析項目に対応
する希釈倍率に応じてそれぞれの所定量を分析項目、希
釈倍率に対応した分析用の反応容器に直接供給し混和し
て前記所望する希釈倍率の希釈サンプルを作製し、作製
したこの希釈サンプルのうち分析項目毎に決まる所要量
を残して、余分量を反応容器から排出して、反応容器に
残した所要量の希釈サンプルに所定の試薬を加え混和し
作成することを特徴とした反応サンプルの作製方法。
1. A method for preparing a reaction sample for analysis, comprising diluting a sample of a specimen to be used in an analyzer for biochemistry and immunology with a diluent and adding a reagent thereto, wherein a desired analysis of the sample and the diluent is performed. According to the dilution ratio corresponding to the item, each predetermined amount is directly supplied to the analysis item corresponding to the analysis item, the reaction container for analysis corresponding to the dilution ratio, and mixed to prepare a diluted sample having the desired dilution ratio. A reaction characterized by leaving a required amount determined for each analysis item in the sample, discharging an excess amount from the reaction vessel, adding a predetermined reagent to a required amount of the diluted sample left in the reaction vessel, and mixing the diluted sample to prepare. Sample preparation method.
JP1227080A 1989-09-01 1989-09-01 Preparation of reaction sample Expired - Fee Related JP2753340B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1227080A JP2753340B2 (en) 1989-09-01 1989-09-01 Preparation of reaction sample

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1227080A JP2753340B2 (en) 1989-09-01 1989-09-01 Preparation of reaction sample

Publications (2)

Publication Number Publication Date
JPH0390837A JPH0390837A (en) 1991-04-16
JP2753340B2 true JP2753340B2 (en) 1998-05-20

Family

ID=16855197

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1227080A Expired - Fee Related JP2753340B2 (en) 1989-09-01 1989-09-01 Preparation of reaction sample

Country Status (1)

Country Link
JP (1) JP2753340B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0995803A3 (en) 1998-10-20 2001-11-07 Matsushita Electric Industrial Co., Ltd. Sample treating kit and sample treating method using the same for analysis with a biosensor
JP6072450B2 (en) * 2012-07-12 2017-02-01 株式会社日立ハイテクノロジーズ Automatic analyzer

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62184356A (en) * 1986-02-07 1987-08-12 Seiko Instr & Electronics Ltd Automatic living body processing device

Also Published As

Publication number Publication date
JPH0390837A (en) 1991-04-16

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