JPH0690216B2 - Liquid dispensing method - Google Patents

Liquid dispensing method

Info

Publication number
JPH0690216B2
JPH0690216B2 JP63114086A JP11408688A JPH0690216B2 JP H0690216 B2 JPH0690216 B2 JP H0690216B2 JP 63114086 A JP63114086 A JP 63114086A JP 11408688 A JP11408688 A JP 11408688A JP H0690216 B2 JPH0690216 B2 JP H0690216B2
Authority
JP
Japan
Prior art keywords
sample
liquid
dummy
dispensing
amount
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP63114086A
Other languages
Japanese (ja)
Other versions
JPH01284761A (en
Inventor
浩二 松本
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.)
Toshiba Corp
Original Assignee
Toshiba 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 Toshiba Corp filed Critical Toshiba Corp
Priority to JP63114086A priority Critical patent/JPH0690216B2/en
Publication of JPH01284761A publication Critical patent/JPH01284761A/en
Publication of JPH0690216B2 publication Critical patent/JPH0690216B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Description

【発明の詳細な説明】 [発明の目的] (産業上の利用分野) 本発明は、試料に試薬を反応させこの反応液内の特定成
分の濃度を測定することにより所望項目の化学分析を行
う際に、前記試料を反応容器に分注する場合等に適用さ
れる液体分注方法に関する。
DETAILED DESCRIPTION OF THE INVENTION [Object of the Invention] (Field of Industrial Application) The present invention performs a chemical analysis of a desired item by reacting a sample with a reagent and measuring the concentration of a specific component in the reaction solution. At this time, the present invention relates to a liquid dispensing method applied when the sample is dispensed into a reaction container.

(従来の技術) 例えば人体から採取した血清を試料(サンプル)として
用いこれに所望の試薬を反応させ、この反応液内の特定
成分の濃度を例えば比色法により測定して所望の項目例
として総蛋白(TP),尿酸(UA),中性脂肪(TG)等を
分析するようにした自動化学分析装置が知られている。
(Prior Art) For example, serum collected from a human body is used as a sample (sample), and a desired reagent is reacted with the sample, and the concentration of a specific component in the reaction solution is measured by, for example, a colorimetric method to obtain desired items. An automatic chemical analyzer that analyzes total protein (TP), uric acid (UA), neutral fat (TG), etc. is known.

第8図はこのような分析装置の構成の一例を示す概略平
面図で、円形の恒温槽1内には複数の反応容器2が配置
され、これらの反応容器2は図示しない駆動源によって
矢印方向に一定のサイクルで間欠移動される。恒温槽1
の周囲のA位置には試料分注用ノズル3が配置され、B
位置には試薬分注用ノズル4が配置され、C位置には撹
拌子5が配置されている。反応容器2が停止している状
態で、A位置の反応容器2には試料分注用ノズル3によ
って分析すべき所望の試料が分注され、B位置の反応容
器2には試料分注用ノズル4によって前記試料と反応す
る所望の試薬が分注され、C位置においては攪拌子5に
よって反応容器2内の試料と試薬から成る反応液の攪拌
が行われる。また反応容器2の移動経路の途中位置には
反応容器2を介して配置された光源7,光検出器8を含む
測光系6が設けられ、反応容器2内の反応液内の特定成
分の濃度が比色法によって測定されることにより所望項
目の化学分析が行われるように構成されている。
FIG. 8 is a schematic plan view showing an example of the configuration of such an analyzer, in which a plurality of reaction vessels 2 are arranged in a circular thermostat 1, and these reaction vessels 2 are moved in the direction of the arrow by a drive source (not shown). It is moved intermittently in a certain cycle. Constant temperature bath 1
A sample dispensing nozzle 3 is arranged at a position A around the
The reagent dispensing nozzle 4 is arranged at the position, and the stirring bar 5 is arranged at the position C. While the reaction container 2 is stopped, a desired sample to be analyzed is dispensed by the sample dispensing nozzle 3 into the reaction container 2 in the A position, and a sample dispensing nozzle in the reaction container 2 in the B position. A desired reagent that reacts with the sample is dispensed by 4, and a stirring bar 5 stirs the reaction liquid consisting of the sample and the reagent in the reaction container 2 at the C position. Further, a photometric system 6 including a light source 7 and a photodetector 8 arranged via the reaction container 2 is provided at an intermediate position on the moving path of the reaction container 2, and the concentration of a specific component in the reaction liquid in the reaction container 2 is provided. Is measured by a colorimetric method so that a chemical analysis of a desired item is performed.

このようにして化学分析を行う場合、第9図のように前
記試料分注ノズル3によって予め分析すべき所望の試料
9が収納されている試料容器10からその試料が吸引され
て反応容器2に分注されいわゆるサンプリングが行われ
るが、通常一つの試料について複数の項目の分析が行わ
れる場合がほとんどであり、この場合は複数の反応容器
2a,2b,2c…2nに各々試料が必要な量サンプリングされる
ことになる。
When performing the chemical analysis in this way, the sample is drawn into the reaction container 2 from the sample container 10 in which the desired sample 9 to be analyzed in advance is stored by the sample dispensing nozzle 3 as shown in FIG. Dispensing and so-called sampling are usually performed, but in most cases analysis of multiple items is performed for one sample.In this case, multiple reaction vessels are used.
The required amount of sample is sampled in each of 2a, 2b, 2c ... 2n.

このように多項目に対応した試料の分注を行う場合従来
において2つの方法が行われている。以下一例としてA
乃至Pの16項目の分析を行う場合を対象とした分注方法
について説明する。第1の方法は第6図(a)のように
A乃至Pの16項目を分析するのに必要な試料9A乃至9Pの
総量をノズル3によって一度に吸引し、続いて各項目に
対応した容器2a乃至2pに対して第6図(b)のように順
次各試料を分注していく方法である。なおこのように試
料の吸引を行う場合は、予めノズル3に水11を満たして
おきこの水11を吸引したときの負圧によって試料9を吸
引するようにしているが、水11と試料9が接触して試料
9が希釈されるのを防止するため両者間に空気槽12を介
在させることが行われている。しかしこれでも水11がノ
ズル3の内壁面を伝わることによって試料9が希釈され
てしまうので、さらに試料9と空気槽12との間に分析に
用いない試料いわゆるダミー試料13を分析試料量に見合
った量だけ予め一度に吸引して介在させることが行われ
ている。このダミー試料13は全ての試料の分注が終了し
た後、所定の位置で排出される。
As described above, in the case of dispensing a sample corresponding to many items, two methods have been conventionally used. As an example, A
The dispensing method for the case of analyzing 16 items from P to P will be described. In the first method, as shown in FIG. 6 (a), the total amount of the samples 9A to 9P necessary for analyzing 16 items A to P is sucked at once by the nozzle 3, and then the container corresponding to each item is drawn. This is a method of sequentially dispensing each sample into 2a to 2p as shown in FIG. 6 (b). When the sample is sucked in this way, the nozzle 3 is filled with water 11 in advance, and the sample 9 is sucked by the negative pressure when the water 11 is sucked. In order to prevent the sample 9 from being contacted and diluted, an air tank 12 is interposed between the two. However, since the sample 9 is diluted by the water 11 traveling on the inner wall surface of the nozzle 3 even in this case, a sample not used for analysis between the sample 9 and the air tank 12, a so-called dummy sample 13, is commensurate with the amount of the sample to be analyzed. It is practiced to suck and intervene by a certain amount in advance. The dummy sample 13 is discharged at a predetermined position after all the samples have been dispensed.

第2の方法は第7図(a)のようにA乃至Pの16項目の
分析に必要な各試料9A乃至9Pをノズル3によってその都
度吸引,分注を繰返して第7図(b)のように各容器に
分注していく方法である。この場合ダミー試料13A乃至1
3Pもその都度吸引,排出される動作が繰返される。
The second method is as shown in Fig. 7 (a), in which each sample 9A to 9P required for analysis of 16 items A to P is sucked and dispensed by the nozzle 3 each time, and the sample 9A to 9P is repeated. It is a method of dispensing into each container. In this case, dummy samples 13A to 1
The operation of sucking and discharging 3P is repeated each time.

(発明が解決しようとする課題) ところで従来の各試料分注方法では、ダミー試料を多量
に必要とすると共にノズル内において分析すべき試料が
依然として希釈されてしまうという問題がある。ダミー
試料は分析すべき試料と同様に患者から採取されるの
で、患者に与える負担及びコストを考慮すると少ないこ
とが望ましい。しかしながら実際の分注においては分析
試料の約半分の量を必要としている。例えば16項目の各
々が10μの試料量を必要としている(総量は10μ×
16=160μ)とすると、ダミー試料はその総量の半分
の80μ程度必要となる。また試料の希釈の度合につい
て示すと、第6図(a),(b)の分注方法の場合で試
料量として160μ,ダミー試料量として80μ用いる
例では、ノズル3先端からの距離Lと希釈率Dとの関係
は第5図のようになる。試料9及びダミー試料13はいず
れも水11に近い位置のもの程水の影響を受けて希釈率は
高くなっている。このような試料9の希釈は水11がノズ
ル3内壁面を伝わってダミー試料13及び試料9に浸入
し、これが試料内に拡散する結果生ずるものである。
(Problems to be Solved by the Invention) However, each of the conventional sample dispensing methods has a problem that a large amount of dummy sample is required and the sample to be analyzed is still diluted in the nozzle. Since the dummy sample is collected from the patient in the same manner as the sample to be analyzed, it is desirable that the dummy sample is small in consideration of the burden and the cost on the patient. However, the actual dispensing requires about half the amount of the analytical sample. For example, each of the 16 items requires a sample volume of 10μ (total volume 10μ ×
16 = 160μ), the dummy sample needs to be about 80μ, which is half of the total amount. Regarding the degree of dilution of the sample, in the case of the dispensing method of FIGS. 6 (a) and 6 (b), the sample amount of 160 μ and the dummy sample amount of 80 μ are used, the distance L from the tip of the nozzle 3 and the dilution The relationship with the rate D is as shown in FIG. In both the sample 9 and the dummy sample 13, the closer to the water 11, the higher the dilution rate due to the influence of water. Such dilution of the sample 9 occurs as a result of water 11 penetrating the dummy sample 13 and the sample 9 along the inner wall surface of the nozzle 3 and diffusing into the sample.

本発明は以上のような事情に対処してなされたもので、
少ないダミー試料で試料の希釈率を低下させることがで
きる液体分注方法を提供することを目的とするものであ
る。
The present invention has been made in response to the above circumstances,
An object of the present invention is to provide a liquid dispensing method capable of reducing the dilution rate of a sample with a small number of dummy samples.

[発明の構成] (課題を解決するための手段) 上記目的を達成するために本発明は、最初に吸引したダ
ミー液体の少なくとも一部を残した状態で2回目以降の
所望液体の吸引,分注動作を繰返すようにしたものであ
る。
[Structure of the Invention] (Means for Solving the Problems) In order to achieve the above-mentioned object, the present invention has a second and subsequent suction and separation of a desired liquid while leaving at least a part of the first sucked dummy liquid. The injection operation is repeated.

(作 用) 液体を複数の容器に分注することによりこの液体の複数
項目に関する化学分析を行う場合であっても、この液体
の希釈率を低下させることなく分析精度を向上させるこ
とができ、しかも測定項目が多項目に渡る場合であって
も少ないダミー液で多項目に対応した分注を行うことが
できるので、無駄な試料の浪費をなくすことができる。
(Operation) Even when performing chemical analysis on multiple items of this liquid by dispensing the liquid into multiple containers, it is possible to improve the analysis accuracy without decreasing the dilution rate of this liquid. In addition, even if the number of measurement items is large, it is possible to dispense with a large number of items with a small amount of dummy liquid, so that it is possible to eliminate unnecessary waste of the sample.

(実施例) 本発明実施例の説明に先立ち本発明の原理について説明
する。
(Example) The principle of the present invention will be described prior to the description of the examples of the present invention.

従来の2つの分注方法を参照して実験を行った結果次の
ような事実が確められた。先ず第1の方法のようにダミ
ー試料13を分析試料量に見合った量だけ予め一度に吸引
することは、ダミー試料13とノズル3内壁面の接触面積
が大となりこの結果水11の浸入を許し易くするというこ
とである。この点第2の方法のようにダミー試料13をそ
の都度必要量だけ吸引することは、前記接触面積が小と
なるので水の浸入を許し難くする利点がある。この反面
第2の方法のようにダミー試料13の量が常に少なくなっ
ていることは、水が拡散し易くなるという欠点がある。
The following facts were confirmed as a result of experiments conducted with reference to two conventional dispensing methods. First of all, as in the first method, by previously sucking the dummy sample 13 by an amount corresponding to the amount of the analysis sample at one time, the contact area between the dummy sample 13 and the inner wall surface of the nozzle 3 becomes large, and as a result, the infiltration of the water 11 is allowed. It is to make it easier. In this respect, sucking the dummy sample 13 by the required amount each time as in the second method has an advantage that it is difficult to allow water to enter because the contact area becomes small. On the other hand, the fact that the amount of the dummy sample 13 is always small as in the second method has a drawback that water easily diffuses.

しかし総合的に見た場合には次表に示すように希釈率の
点で第2の方法が優れていると判断することができる。
However, when viewed comprehensively, it can be judged that the second method is superior in terms of dilution rate as shown in the following table.

また第4図は試料を10μ吸引し、ダミー試料を10μ
以内で可変した場合のダミー試料量Vと希釈率Dとの関
係を示すものである。Vの減少につれDは増加してくる
ことを示している。従ってダミー試料量Vを試料量との
関係で適量に選ぶことにより希釈率Dを低下させること
が可能となる。
In addition, in Fig. 4, a sample of 10μ is sucked and a dummy sample of 10μ is drawn.
It shows the relationship between the dummy sample amount V and the dilution rate D when it is varied within the range. It is shown that D decreases as V decreases. Therefore, the dilution ratio D can be reduced by selecting the dummy sample amount V in an appropriate amount in relation to the sample amount.

本発明は以上のような原理を基になされたものであり、
以下図面を参照して本発明実施例を説明する。
The present invention is based on the above principle,
Embodiments of the present invention will be described below with reference to the drawings.

第1図(a),(b)は本発明の液体分注方法の第1の
実施例を示す説明図で、第1図(a)のように予めノズ
ル3に水11を満たし空気層12を介在させてダミー試料13
を吸引した状態で、先ずAの項目の分析に必要な試料9A
を吸引した後第1図(b)のように対応した容器2aに試
料9Aを分注する。次にダミー試料13はそのままでBの項
目の分析に必要な試料9Bを吸引した後、第1図(b)の
ように対応した容器2bに試料9Bを分注する。続いてダミ
ー試料13はそのままでCの項目の分析に必要な試料9Cを
吸引した後、第1図(b)のように対応した容器2cに試
料9Cを分注する。以下ダミー試料13はそのままでPの項
目に至る迄同様な吸引,分注動作を繰返す。一例として
A乃至Pの16項目の各々が10μの試料量を選び、ダミ
ー試料量を40μに選んだ。
1 (a) and 1 (b) are explanatory views showing a first embodiment of the liquid dispensing method of the present invention. As shown in FIG. 1 (a), the nozzle 3 is filled with water 11 in advance and the air layer 12 is formed. With dummy sample 13
First, sample 9A necessary for the analysis of item A in the state of sucking
After sucking, the sample 9A is dispensed into the corresponding container 2a as shown in FIG. 1 (b). Next, after the sample 9B necessary for the analysis of the item B is sucked with the dummy sample 13 as it is, the sample 9B is dispensed into the corresponding container 2b as shown in FIG. 1 (b). Subsequently, while the dummy sample 13 is left as it is, the sample 9C necessary for the analysis of the item C is sucked, and then the sample 9C is dispensed into the corresponding container 2c as shown in FIG. 1 (b). Thereafter, the dummy sample 13 is left as it is, and the same suction and dispensing operations are repeated until the item P is reached. As an example, a sample amount of 10 μ was selected for each of the 16 items A to P, and a dummy sample amount of 40 μ was selected.

このような本実施例によれば、ダミー試料13としては分
析すべき試料の総量(この例の場合10μ×16=160μ
)に対して比較的少量(40μ)を選んでこの量をノ
ズル3に保持したままで、16項目の試料9A乃至9Pの吸
引,分注動作を繰返すので、水の浸入及び拡散を抑える
ことができる。従って試料の希釈率を低下させることが
でき、0.1乃至1%の希釈率が得られた。
According to this embodiment, the total amount of samples to be analyzed as the dummy sample 13 (10 μ × 16 = 160 μ in this example)
)), A relatively small amount (40μ) is selected, and while holding this amount in the nozzle 3, the suction and dispensing operations of 16 items of samples 9A to 9P are repeated, so that the infiltration and diffusion of water can be suppressed. it can. Therefore, the dilution rate of the sample can be reduced, and the dilution rate of 0.1 to 1% was obtained.

第2図(a),(b)は本発明の第2実施例を示すもの
で、試料の総量として160μを選んだ場合、試料9Aを
吸引するに先立ち第2図(a)のようにダミー試料13を
5μ+32μ(160μ×0.2)吸引し、次に試料9Aを
10μ吸引した後第2図(b)のように容器2aに試料9A
を分注する。以後このようにダミー試料13を37μ保持
したままで項目Pに至る迄同様な吸引,分注動作を繰返
す。なお、32μは一例として試料の総量160μの20
%の目安として選んだものである。本実施例によっても
比較的少量(37μ)のダミー試料を選ぶことにより、
試料9A乃至9Pの吸引,分注動作を繰返すので、前記実施
例と同様な効果を得ることができる。
FIGS. 2 (a) and 2 (b) show a second embodiment of the present invention. When 160 .mu. Is selected as the total amount of the sample, a dummy as shown in FIG. Aspirate sample 13 by 5μ + 32μ (160μ × 0.2), then sample 9A
After aspirating 10μ, sample 9A was placed in container 2a as shown in Fig. 2 (b).
To dispense. Thereafter, similar suction and dispensing operations are repeated until the item P is reached with the dummy sample 13 held at 37 μ in this way. Note that 32μ is an example of 20μ of the total sample 160μ.
It was selected as a measure of%. Also in this embodiment, by selecting a relatively small amount (37μ) of dummy sample,
Since the suction and dispensing operations of the samples 9A to 9P are repeated, it is possible to obtain the same effect as that of the above embodiment.

第3図(a),(b)は本発明の第3実施例を示すもの
で、試料の総量として160μを選んだ場合、試料9Aを
吸引するに先立ち第3図(a)のようダミー試料13を
(5μ+2μ)吸引し、次に試料9Aを10μ吸引し
た後、第3図(b)のよう容器2aに試料9Aを分注する。
続いてダミー試料13として2μ吸引した(計9μ)
後試料9Bを10μ吸引して、第3図(b)のように容器
2bに試料9Bを分注する。さらに続いてダミー試料13とし
て2μ吸引した(計11μ)後試料9Cを10μ吸引し
て、第3図(b)のように容器2cに試料9Cを分注する。
以後このようにダミー試料13を2μずつ追加した後試
料の吸引,分注動作を項目Pに至る迄繰返す。本実施例
によっても比較的少量(37μ=5μ+2μ×16)
のダミー試料13を選ぶようにしたので、前記実施例と同
様な効果を得ることができる。
FIGS. 3 (a) and 3 (b) show a third embodiment of the present invention. When 160 .mu. Is selected as the total amount of the sample, a dummy sample as shown in FIG. After sucking 13 (5 μ + 2 μ) and then sucking 10 μ of the sample 9A, the sample 9A is dispensed into the container 2a as shown in FIG. 3 (b).
Then, 2μ was sucked as a dummy sample 13 (total 9μ)
After that, aspirate 10μ of the sample 9B and place it in a container as shown in Fig. 3 (b).
Dispense sample 9B into 2b. Further, subsequently, 2 μm is sucked as the dummy sample 13 (11 μm in total), 10 μm of the sample 9C is sucked, and the sample 9C is dispensed into the container 2c as shown in FIG. 3 (b).
Thereafter, the dummy sample 13 is added by 2 .mu.m in this way, and then the sample suction and dispensing operations are repeated until the item P is reached. Also in this embodiment, a relatively small amount (37μ = 5μ + 2μ × 16)
Since the dummy sample 13 is selected, it is possible to obtain the same effect as that of the above embodiment.

本発明の第4実施例として試料9A乃至9Pの総量を第2実
施例の半分(160μ×1/2=80μ)に選んだ場合、ダ
ミー試料13を4μ+16μ(80μ×0.2)に選び第
2実施例と同様な吸引,分注動作を繰返すことにより、
ダミー試料をより少量(20μ)用いて同様な効果を得
ることができる。
As the fourth embodiment of the present invention, when the total amount of the samples 9A to 9P is selected to be half (160 μ × 1/2 = 80 μ) of the second embodiment, the dummy sample 13 is selected to be 4 μ + 16 μ (80 μ × 0.2) and the second execution is performed. By repeating suction and dispensing operations similar to the example,
A similar effect can be obtained by using a smaller amount of dummy sample (20μ).

次表は以上の各実施例で得られた各データを従来例と比
較して示すものである。
The following table shows each data obtained in each of the above examples in comparison with the conventional example.

以上の各実施例で示した数値は一例を示したものであ
り、用途,目的等に応じて任意の変更が可能である。ま
た実施例でな分注対象として試料を用いた例で示した
が、何らこれに限らず他の液体例えば試薬等に対しても
同様に適用できるものである。
The numerical values shown in each of the above embodiments are merely examples, and can be arbitrarily changed according to the use, purpose, and the like. Further, although an example in which a sample is used as an object to be dispensed is shown in the examples, the present invention is not limited to this and is similarly applicable to other liquids such as reagents.

このように本実施例によれば試料の希釈率を低下させる
ことができるので、測定すべき項目の選択を自由にでき
また測定データの精度を安定にすることができる。また
少量のダミー液体を用いて目的を達成することができる
ので、患者に与える負担を軽減することができ、さらに
試料のコストダウンを図ることができる。さらに多項目
分注を行う際各項目ごとに試料の吸引,分注を行うので
サンプリング速度を早くすることができ、また複数本の
ノズルを用いた分注方法を採用することによりサンプリ
ング効率を改善することもできる。
As described above, according to the present embodiment, the sample dilution rate can be lowered, so that the items to be measured can be freely selected and the accuracy of the measurement data can be stabilized. Moreover, since the object can be achieved by using a small amount of dummy liquid, the burden on the patient can be reduced, and the cost of the sample can be further reduced. Furthermore, when performing multi-item dispensing, the sample is suctioned and dispensed for each item, so the sampling speed can be increased, and the sampling efficiency is improved by adopting a dispensing method using multiple nozzles. You can also do it.

[発明の効果] 以上詳述した通り、本願発明によれば、液体を複数の容
器に分注することによりこの液体の複数項目に関する化
学分析を行う場合であっても、この液体の希釈率を低下
させることなく分析精度を向上させることができ、しか
も測定項目が多項目に渡る場合であっも少ないダミー液
で多項目に対応した分注を行うことができるので、無駄
な試料の浪費のない液体分注方法を提供することができ
るという優れた効果を奏するものである。
[Effects of the Invention] As described in detail above, according to the present invention, even when performing chemical analysis on a plurality of items of this liquid by dispensing the liquid into a plurality of containers, the dilution rate of this liquid can be adjusted. Analytical accuracy can be improved without lowering, and even if there are multiple measurement items, it is possible to dispense with a small number of dummy liquids corresponding to multiple items, so no wasted sample is wasted It has an excellent effect of being able to provide a liquid dispensing method.

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

第1図(a),(b)乃至第3図(a),(b)は本発
明の液体分注方法の異なった実施例を示す説明図、第4
及び第5図は本発明の原理を説明する特性図、第6図
(a),(b)及び第7図(a),(b)は従来例の説
明図、第8図は自動化学分析装置の構成の一例を示す概
略平面図、第9図は試料分注の説明図である。 2……反応容器、3……試料分注ノズル、 9……試料(サンプル)、11……水、 12……空気層、13……ダミー試料。
1 (a), (b) to 3 (a), (b) are explanatory views showing a different embodiment of the liquid dispensing method of the present invention, and FIG.
5 and 5 are characteristic diagrams for explaining the principle of the present invention, FIGS. 6 (a) and 6 (b) and FIGS. 7 (a) and 7 (b) are explanatory diagrams of a conventional example, and FIG. 8 is an automatic chemical analysis. FIG. 9 is a schematic plan view showing an example of the configuration of the apparatus, and FIG. 9 is an explanatory diagram of sample dispensing. 2 ... Reaction container, 3 ... Sample dispensing nozzle, 9 ... Sample (sample), 11 ... Water, 12 ... Air layer, 13 ... Dummy sample.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】所望の液体をダミー液を介してノズルで吸
引して所定の容器に分注することにより該液体の化学分
析を行うための液体分注方法において、前記液体を複数
の容器に分注することにより該液体の複数項目に関する
化学分析を行う際、最初に吸引した前記ダミー液体の少
なくとも一部を残した状態で2回目以降の前記液体の吸
引,分注動作を繰り返すことを特徴とする液体分注方
法。
1. A liquid dispensing method for performing a chemical analysis of a desired liquid by suctioning a desired liquid through a dummy liquid with a nozzle and dispensing the liquid into a predetermined container. When performing chemical analysis on a plurality of items of the liquid by dispensing, the second and subsequent suction and dispensing operations of the liquid are repeated while leaving at least a part of the initially sucked dummy liquid. Liquid dispensing method.
【請求項2】最初に吸引された前記ダミー液体の全体を
残した状態で2回目以降の所望液体の吸引,分注動作を
繰り返す請求項1記載の液体分注方法。
2. The liquid dispensing method according to claim 1, wherein the second and subsequent suction and dispensing operations of the desired liquid are repeated while leaving the whole of the initially sucked dummy liquid.
【請求項3】2回目以降の所望液体の吸引を行なう前に
最初に吸引されたダミー液体に各々所望量のダミー液体
を加える請求項1記載の液体分注方法。
3. The liquid dispensing method according to claim 1, wherein a desired amount of dummy liquid is added to each of the first sucked dummy liquids before the second and subsequent desired liquids are sucked.
【請求項4】ダミー液体が最初に吸引された固定量と2
回目以降の所望液体の吸引前に各々所望液体の吸引量に
応じて決定される可変量とから成る請求項3記載の液体
分注方法。
4. The fixed amount and 2 at which the dummy liquid is first sucked.
4. The liquid dispensing method according to claim 3, comprising a variable amount which is determined according to the suction amount of the desired liquid before the subsequent suction of the desired liquid.
JP63114086A 1988-05-11 1988-05-11 Liquid dispensing method Expired - Lifetime JPH0690216B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63114086A JPH0690216B2 (en) 1988-05-11 1988-05-11 Liquid dispensing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63114086A JPH0690216B2 (en) 1988-05-11 1988-05-11 Liquid dispensing method

Publications (2)

Publication Number Publication Date
JPH01284761A JPH01284761A (en) 1989-11-16
JPH0690216B2 true JPH0690216B2 (en) 1994-11-14

Family

ID=14628734

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63114086A Expired - Lifetime JPH0690216B2 (en) 1988-05-11 1988-05-11 Liquid dispensing method

Country Status (1)

Country Link
JP (1) JPH0690216B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009243969A (en) * 2008-03-28 2009-10-22 Olympus Corp Apparatus and method for automatic analysis

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5183765A (en) * 1990-10-11 1993-02-02 Drd Diluter Corporation Means and method of measuring and dispensing
JP2006266789A (en) * 2005-03-23 2006-10-05 Ebara Corp Spotting method and spotting device
JP5210692B2 (en) * 2008-04-11 2013-06-12 株式会社東芝 Automatic analyzer and its dispensing method
JP5180710B2 (en) * 2008-07-11 2013-04-10 株式会社東芝 Automatic analyzer
JP5305988B2 (en) * 2009-03-05 2013-10-02 株式会社東芝 Automatic analyzer
JP6027742B2 (en) * 2011-12-28 2016-11-16 シスメックス株式会社 Blood cell analyzer, blood cell analysis method, and computer program
WO2014033797A1 (en) * 2012-09-03 2014-03-06 株式会社島津製作所 Liquid dripping method

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0625771B2 (en) * 1987-01-07 1994-04-06 株式会社日立製作所 Sample dispensing method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009243969A (en) * 2008-03-28 2009-10-22 Olympus Corp Apparatus and method for automatic analysis

Also Published As

Publication number Publication date
JPH01284761A (en) 1989-11-16

Similar Documents

Publication Publication Date Title
EP0047130B1 (en) Flow analysis
US5773305A (en) Sample dilution module
JP2731613B2 (en) Cartridge for enzyme immunoassay, measuring method and measuring apparatus using the same
US5316726A (en) Automated immunoassay analyzer with pictorial display of assay information
US4608231A (en) Self-contained reagent package device for an assay
JPS5992356A (en) Weighing method and weigher
JPS63259468A (en) Automatic patient sample analyzer
JPH0148511B2 (en)
EP0089346A1 (en) Automated immunoassay system.
JPH08506893A (en) Solid phase immunoassay with a carrier that conforms to the shape of the sample well
EP0103268A2 (en) Sampling apparatus
JPH0690216B2 (en) Liquid dispensing method
US4002269A (en) Liquid proportioning system in a liquid sample analyzer
JP4101466B2 (en) Biological sample analyzer
JP4153171B2 (en) Analysis method of biological sample
JP3380542B2 (en) Biological sample analysis method
JP3194601B2 (en) Automatic analysis method and automatic analyzer
JP4537472B2 (en) Analysis equipment
JPH07119670B2 (en) Separation liquid control device and container
CA2299911A1 (en) An automated method for rapidly performing multiple immunoassays by different membrane-eia test kit combinations in one operation
JPH0477670A (en) Quantitative analysis using antigen/antibody reaction
JPS6249259A (en) Automatic analyzer
EP0497019B1 (en) Automatic immunological analysing system
JP2973125B2 (en) Automatic chemical analyzer
JPH0219421B2 (en)

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20071114

Year of fee payment: 13

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

Free format text: PAYMENT UNTIL: 20081114

Year of fee payment: 14

EXPY Cancellation because of completion of term
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081114

Year of fee payment: 14