JP2805463B2 - Liquid mixer - Google Patents

Liquid mixer

Info

Publication number
JP2805463B2
JP2805463B2 JP7294930A JP29493095A JP2805463B2 JP 2805463 B2 JP2805463 B2 JP 2805463B2 JP 7294930 A JP7294930 A JP 7294930A JP 29493095 A JP29493095 A JP 29493095A JP 2805463 B2 JP2805463 B2 JP 2805463B2
Authority
JP
Japan
Prior art keywords
mixing container
sample
capillary
liquid mixer
seal
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
JP7294930A
Other languages
Japanese (ja)
Other versions
JPH09113421A (en
Inventor
和久 矢野
恵一 池田
哲士 石本
務 臼井
Original Assignee
株式会社国宗工業所
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 株式会社国宗工業所 filed Critical 株式会社国宗工業所
Priority to JP7294930A priority Critical patent/JP2805463B2/en
Publication of JPH09113421A publication Critical patent/JPH09113421A/en
Application granted granted Critical
Publication of JP2805463B2 publication Critical patent/JP2805463B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】この発明は、主として臨床検
査や理化学試験において、血液や薬品や試料等の各種液
体を、希釈液等の別の液体と所定割合で希釈や反応さ
せ、いずれかの理化学分析装置等の前処理用として利用
される液体同士の液体混合器に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention mainly relates to a method of diluting or reacting various liquids such as blood, medicines and samples with another liquid such as a diluent at a predetermined ratio in a clinical test or a physicochemical test. The present invention relates to a liquid mixer for liquids used for pretreatment of an analyzer or the like.

【0002】[0002]

【従来の技術】従来、二液を所定割合で希釈等させるに
は、ピペットや毛細管やマイクロピペット等によって一
定量のサンプルを採取し、そのサンプルに対して所定倍
率の量の希釈液等と混ぜ合わせて行っていた。
2. Description of the Related Art Conventionally, in order to dilute two liquids at a predetermined ratio, a predetermined amount of a sample is collected by a pipette, a capillary, a micropipette, or the like, and the sample is mixed with a diluent at a predetermined magnification. We went together.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、従来の
方法では、サンプルは、一旦容器に取られた後、そこか
らピペット等によって一定量を採取する必要があったた
め、手間を要しただけでなく、容器が別に必要という不
都合があった。また、従来の方法は、ピペット等を用い
て行われるので、正確な希釈を行うには、高度のテクニ
ックと高価な器具を要するという問題があった。さら
に、従来の方法は、希釈や反応等を実験室や病院の検査
室等の設備が整った場所でしか行うことができなかっ
た。このため、屋外はもちろん、ベッドサイドや、訪問
診療、町の医院や診療所等で行うことができなかった。
すなわち、サンプルの採取場所で反応結果を見たりする
ことができず不便であり、またサンプルの保存や管理に
手間を要するという問題があった。
However, in the conventional method, it is necessary to collect a certain amount of a sample from the container once by a pipette or the like after the sample is once taken in a container. There was a disadvantage that a separate container was required. In addition, since the conventional method is performed using a pipette or the like, there is a problem that accurate techniques require sophisticated techniques and expensive equipment. Furthermore, the conventional method can perform dilution, reaction, and the like only in a well-equipped place such as a laboratory or a hospital laboratory. For this reason, it was not possible to perform the treatment not only outdoors, but also at the bedside, on-site consultation, at a clinic or clinic in the town.
That is, there is a problem in that it is inconvenient to see the reaction result at the place where the sample is collected, and there is a problem that it takes time to save and manage the sample.

【0004】また、最近では使い捨ての使用器材が多く
なったとはいえ、再度洗浄して使用する器材もまだある
のに対し、従来の方法では前記いずれの場合でも不都合
があった。つまり、従来の方法では上記したように部材
数が多くなるので、使い捨てとすると、コストが高くな
るという欠点があり、逆に再利用するにしても洗浄等に
手間を要するという欠点があった。その上、従来の方法
では、サンプル数が一検体の場合でも、一通りの器具、
器材が必要であったので、サンプル数が少数の場合には
手間がかかり過ぎるといった欠点があった。この発明
は、これらの課題を解決するためになされたものであ
る。
In recent years, although the number of disposable equipment has increased, some equipment has been used after being washed again, whereas the conventional method has disadvantages in any of the above cases. That is, in the conventional method, the number of members is increased as described above, so that if it is disposable, there is a disadvantage that the cost increases, and conversely, even if it is reused, there is a disadvantage that cleaning and the like require time and effort. In addition, in the conventional method, even if the number of samples is one sample, a single instrument,
Since equipment was required, there was a disadvantage that it took too much time when the number of samples was small. The present invention has been made to solve these problems.

【0005】[0005]

【課題を解決するための手段】上記課題を解決するため
に、この発明の液体混合器は、希釈液等が入れられ、減
圧状態にて開口部をシールで密閉された混合容器と、
の混合容器に進退可能に螺合され、前記希釈液等に対し
て所定量のサンプルを採取する毛細管が形成され、この
毛細管の下端部に前記混合容器への螺進によって前記混
合容器のシールを破る突起が形成されてなる採取部材と
を備えてなり、前記採取部材が、シリンジの先端部に取
り付け可能とされてなることを特徴とする。また、この
発明の液体混合器は、希釈液等が入れられ、減圧状態に
て開口部をシールで密閉された混合容器と、この混合容
器に押し嵌め可能とされ、前記希釈液等に対して所定量
のサンプルを採取する毛細管が形成され、この毛細管の
下端部に前記混合容器への押し嵌めによって前記混合容
器のシールを破る突起が形成されてなる採取部材とを備
えてなり、前記採取部材が、シリンジの先端部に取り付
け可能とされてなることを特徴とする液体混合器であ
る。
In order to solve the above problems SUMMARY OF THE INVENTION The liquid mixer of the present invention, the diluent or the like is placed, and sealed mixing vessel opening in the seal at reduced pressure, this
A capillary tube is formed so as to be able to advance and retreat to the mixing container, and a predetermined amount of a sample is collected with respect to the diluting liquid and the like. The mixing tube is screwed into the mixing container at the lower end of the capillary tube.
A sampling member formed with a projection that breaks the seal of the container
The sampling member is attached to the tip of the syringe.
It is characterized in that it can be attached . In addition, the liquid mixer of the present invention is filled with a diluting liquid or the like, and a mixing container whose opening is sealed with a seal in a decompressed state, and is capable of being press-fitted into the mixing container. A capillary member for collecting a predetermined amount of sample is formed, and a collection member having a projection formed at the lower end of the capillary tube to break the seal of the mixing container by press-fitting the mixing container.
The sampling member is attached to the tip of the syringe.
The liquid mixer is characterized in that the liquid mixer can be used.

【0006】ここで、希釈とは、液体を一定量採取し、
それを一定量の液体に混ぜ合わせ、その併せた量の対比
によって採取した液体を一定の倍率に薄めることをい
う。反応とは、異なる性質の液体同士を混ぜ合わせ、新
たな性質の液体に変えることをいう。サンプルとは、採
取する液体をいう。減圧状態とは、大気圧よりも低い気
圧下におかれている状態をいう。
Here, the term "dilution" means that a certain amount of liquid is collected,
It means that it is mixed with a certain amount of liquid, and the collected liquid is diluted to a certain magnification by comparing the combined amount. The reaction means that liquids having different properties are mixed together and changed to a liquid having new properties. The sample refers to a liquid to be collected. The reduced pressure state refers to a state where the pressure is lower than the atmospheric pressure.

【0007】[0007]

【発明の実施の形態】以下、この発明の液体混合器1に
ついて、さらに詳細に説明する。図1は、この発明の液
体混合器1の一実施例を示す断面図である。この実施例
の液体混合器1は、希釈液5等が入れられた混合容器2
と、この混合容器2に進退可能に螺合される採取部材3
と、この採取部材3に被せられるキャップ4とからな
る。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, the liquid mixer 1 of the present invention will be described in more detail. FIG. 1 is a sectional view showing one embodiment of a liquid mixer 1 of the present invention. The liquid mixer 1 of this embodiment includes a mixing vessel 2 containing a diluent 5 and the like.
And a sampling member 3 screwed into the mixing container 2 so as to be able to advance and retreat.
And a cap 4 placed on the sampling member 3.

【0008】この実施例の混合容器2は、ポリエチレン
のブロー成形により形成されてなり、上部が縮径された
首状に形成され、その首部の上部が開口して形成されて
いる。また、首部の周囲には、採取部材3を螺合するた
めのネジ山が形成されてネジ部21とされている。混合
容器2には、前処理液5として生理食塩水やpH調整液
の他、サンプル6中の検出したい物質に反応する一定濃
度の色素や指示薬が所定量入れられている。この所定量
は、サンプル6の希釈倍率や、指示薬の濃度等により決
定される。そして、希釈液5等が入れられた混合容器2
は、大気圧よりも低い減圧状態とされて、開口部をアル
ミシール20等によって密閉される。
The mixing container 2 of this embodiment is formed by blow molding of polyethylene, has an upper part formed in a neck shape with a reduced diameter, and has an opening at the upper part of the neck part. In addition, a screw thread for screwing the sampling member 3 is formed around the neck to form a screw portion 21. In the mixing container 2, a predetermined amount of a dye or indicator having a constant concentration that reacts with a substance to be detected in the sample 6 is put in addition to a physiological saline solution and a pH adjusting solution as the pretreatment liquid 5. This predetermined amount is determined by the dilution ratio of the sample 6, the concentration of the indicator, and the like. And a mixing container 2 containing the diluent 5 and the like.
Is set in a reduced pressure state lower than the atmospheric pressure, and the opening is sealed with an aluminum seal 20 or the like.

【0009】この実施例の採取部材3は、ポリプロピレ
ンやポリスチレンやポリエチレン等の射出成形により形
成されてなる。採取部材3は、先端部が先細の略円錐形
状に形成されてなり、下部に前記混合容器2のネジ部に
螺合されるネジ穴31が形成されてなる。また、採取部
材3の中心部には、毛細管32が上下方向に貫通して形
成されている。この毛細管32は、採取部材3の上端部
に開口すると共に、前記ネジ穴31に開口して形成され
ている。毛細管32は、毛細管現象を発生させる程度に
細い径の細長い丸穴に形成されている。毛細管32の下
端部、つまりネジ穴31の上部には突起33が下方に突
出して形成されている。この突起33は、毛細管32の
下端部の開口の周囲に略円錐形状に形成されてなる。ま
た、採取部材3の前記突起33の基端部と対応する位置
には、ネジ穴31の周囲の外壁を貫通して、採取部材3
の内外を連通する空気穴34が形成されている。この空
気穴34は、水平方向と平行か、又は、径方向外側に行
くに従ってやや上方に傾斜した小さな丸穴からなる。
The sampling member 3 of this embodiment is formed by injection molding of polypropylene, polystyrene, polyethylene or the like. The sampling member 3 has a tip portion formed in a tapered substantially conical shape, and a screw hole 31 screwed into a screw portion of the mixing container 2 at a lower portion. A capillary 32 is formed in the center of the sampling member 3 so as to penetrate in the vertical direction. The capillary 32 is formed to open at the upper end of the sampling member 3 and to open into the screw hole 31. The capillary 32 is formed in an elongated round hole having a diameter small enough to cause a capillary phenomenon. At the lower end of the capillary tube 32, that is, at the upper portion of the screw hole 31, a projection 33 is formed to protrude downward. The projection 33 is formed in a substantially conical shape around the opening at the lower end of the capillary tube 32. Further, at a position corresponding to the base end of the projection 33 of the collecting member 3, the collecting member 3 penetrates an outer wall around the screw hole 31.
Is formed with an air hole 34 communicating the inside and the outside of the inside. The air hole 34 is formed of a small round hole that is parallel to the horizontal direction or slightly inclined upward toward the outside in the radial direction.

【0010】採取部材3は、図1に示すように、突起3
3の下端部が混合容器2のシール20に当接しない位置
で、混合容器2のネジ部31に進退可能に螺合されて設
けられる。採取部材3の上部には、キャップ4が装着さ
れる。キャップ4は、採取部材3の上部の形状に対応し
た帽子形状に形成されており、内周部の一部が径方向内
側に断面半円形状に突出して凸部41が形成されてお
り、採取部材3の前記凸部41と対応した位置に形成さ
れた凹部35に前記凸部41が係合されてキャップ4を
嵌めることができる構成である。キャップ4をした状態
では、図1に示すように、キャップ4の内面上端部から
突出形成された半球状部42が、毛細管32の上部の開
口に係合されることとなる。
[0010] As shown in FIG.
At the position where the lower end of 3 is not in contact with the seal 20 of the mixing container 2, the lower end 3 is screwed to the screw portion 31 of the mixing container 2 so as to be able to advance and retreat. A cap 4 is mounted on the upper part of the sampling member 3. The cap 4 is formed in a hat shape corresponding to the shape of the upper part of the collecting member 3, and a part of the inner peripheral portion projects radially inward in a semicircular cross section to form a convex portion 41. The projections 41 are engaged with recesses 35 formed at positions corresponding to the projections 41 of the member 3 so that the cap 4 can be fitted. With the cap 4 attached, as shown in FIG. 1, the hemispherical portion 42 formed so as to protrude from the upper end of the inner surface of the cap 4 is engaged with the upper opening of the capillary tube 32.

【0011】次に、この実施例の液体混合器1の使用状
態について説明する。図2から図4は、この実施例の液
体混合器1の使用状態を示す断面図である。液体混合器
1の使用に際しては、図2に示すように、まず採取部材
3からキャップ4を外す。これには、採取部材3からキ
ャップ4を引き抜くように引っ張ることより、キャップ
4を径方向外側に広がるように弾性変形させて、キャッ
プ4の凸部41と採取部材3の凹部35との係合を解除
することにより行われる。
Next, the use state of the liquid mixer 1 of this embodiment will be described. FIG. 2 to FIG. 4 are cross-sectional views showing the use state of the liquid mixer 1 of this embodiment. When using the liquid mixer 1, the cap 4 is first removed from the sampling member 3, as shown in FIG. To do this, the cap 4 is elastically deformed so as to spread radially outward by pulling the cap 4 out of the collection member 3, so that the projection 41 of the cap 4 engages with the recess 35 of the collection member 3. Is performed by canceling.

【0012】次に、図3に示すように、採取部材3の先
端部(毛細管32の先端部)をサンプル6が入れられた
容器7に入れる。毛細管32の他端部はネジ穴31に開
口し、このネジ穴31には採取部材3の内外を連通する
空気穴34が形成されているので、毛細管現象が発生
し、採取部材3の毛細管32がサンプルで満たされるこ
ととなる。また、サンプル6が入れられた容器7から採
取部材3を抜き取っても、毛細管32に入っているサン
プル6は毛細管32に滞留し、流れ落ちてしまうことは
ない。なお、採取するサンプル6(例えば、血液、尿
等)の量は、図2に示すように、毛細管32の直径Dか
ら決定される毛細管32の断面積と、毛細管32の長さ
Lによって決まり、この量は混合容器2に入れられた希
釈液5等の量と一定の関係を有している。つまり、サン
プル6を所定倍率に希釈したい場合には、毛細管32の
大きさによって決定されるサンプル6の採取量(通常、
20μl〜100μl)に対して所定倍率の量の希釈液
5が混合容器2に入れられることとなる。よって、希釈
倍率等を変化させたい場合には、毛細管32の大きさを
変えたり、混合容器2内の希釈液5の量や濃度を変化さ
せたりすることにより行うことができる。
Next, as shown in FIG. 3, the tip of the sampling member 3 (the tip of the capillary 32) is placed in a container 7 in which the sample 6 is placed. The other end of the capillary 32 is opened in a screw hole 31, and an air hole 34 communicating between the inside and the outside of the sampling member 3 is formed in the screw hole 31. Is filled with the sample. Further, even if the sampling member 3 is withdrawn from the container 7 in which the sample 6 is placed, the sample 6 in the capillary 32 stays in the capillary 32 and does not flow down. The amount of the sample 6 (for example, blood, urine, etc.) to be collected is determined by the cross-sectional area of the capillary 32 determined from the diameter D of the capillary 32 and the length L of the capillary 32 as shown in FIG. This amount has a certain relationship with the amount of the diluent 5 and the like put in the mixing container 2. That is, when it is desired to dilute the sample 6 to a predetermined magnification, the amount of the sample 6 to be collected determined by the size of the capillary tube 32 (usually,
20 μl to 100 μl) of the diluent 5 at a predetermined magnification is put into the mixing container 2. Therefore, when it is desired to change the dilution ratio or the like, it can be performed by changing the size of the capillary tube 32 or changing the amount or concentration of the diluent 5 in the mixing container 2.

【0013】次に、図4に示すように、再び採取部材3
を上に向けた状態で、混合容器2に対して採取部材3を
ねじ込んで螺進させる。これにより、採取部材3の毛細
管32の下端部に形成された突起33が、混合容器2を
密閉しているシール20を突き破って混合容器2内に突
入する。混合容器2は、減圧状態とされているので、シ
ール20の破損によって毛細管32内に滞留していたサ
ンプル6を混合容器2内に引き込み、サンプル6は混合
容器2内の液体5と希釈されたり反応したりすることと
なる。
Next, as shown in FIG.
The sampling member 3 is screwed into the mixing container 2 and screwed into the mixing container 2 with the. As a result, the projection 33 formed at the lower end of the capillary 32 of the sampling member 3 breaks through the seal 20 that seals the mixing container 2 and enters the mixing container 2. Since the pressure in the mixing container 2 is reduced, the sample 6 remaining in the capillary tube 32 due to the breakage of the seal 20 is drawn into the mixing container 2, and the sample 6 is diluted with the liquid 5 in the mixing container 2. Or react.

【0014】上記実施例においては、混合容器2に希釈
液5等を入れてシールする製造段階で、既に混合容器2
内を減圧状態とした例を示したが、この場合は、減圧状
態を使用時まで保持する必要から、混合容器2をPET
(ポリエチレンテレフタレート)やAS(スチレンアク
リロニトリル強重合体)、ガラスなどのガスバリア性を
有する材料により形成している。しかし、図5に示すよ
うに、混合容器2(2A)の一部に蛇腹部22を形成し
たり、図6に示すように、混合容器2(2B)の底23
がダイアフラムのように上下に変形可能に形成したりし
て、使用時に混合容器2の容積を大きくすることによっ
て内部を減圧状態にできる構成とした場合には、製造時
に減圧状態にする必要はない。よって、この場合には、
ガスバリア性を有しないプラスチック等の適宜の材料で
製作することができる。
In the above embodiment, the mixing vessel 2 is already filled in the mixing vessel 2 at the manufacturing stage in which the diluent 5 and the like are sealed.
In this case, the inside of the mixing container 2 is set to a reduced pressure state.
(Polyethylene terephthalate), AS (strong styrene acrylonitrile polymer), glass, and other materials having gas barrier properties. However, as shown in FIG. 5, a bellows portion 22 is formed in a part of the mixing container 2 (2A), or as shown in FIG. 6, the bottom 23 of the mixing container 2 (2B).
Is formed to be deformable up and down like a diaphragm, so that the inside of the mixing vessel 2 can be decompressed by increasing the volume of the mixing vessel 2 at the time of use. . So, in this case,
It can be made of an appropriate material such as plastic having no gas barrier property.

【0015】図7は、この発明の液体混合器1の他の実
施例の使用状態を示す断面図である。この実施例の液体
混合器1は、図8に示される注射器の注射針11に換え
て、採取部材3(3A)が取り付けられて使用されるも
のである。採取部材3Aが装着されるシリンジ8は、シ
リンダ9にピストン10が摺動可能に嵌挿されてなる。
シリンダ9は、全体として略円筒形状で、外周部にネジ
山が形成されたネジ部91が先端側に突出形成されると
共に、基端部に径方向外側に広がる鍔部92が一体形成
されてなる。ピストン10は、シリンダ9に密嵌されて
摺動するピストン本体10aと、このピストン本体10
aから基端側に延びるピストン棒10bと、このピスト
ン棒10bの基端部に一体形成された円板状の操作部1
0cとからなる。この実施例の採取部材3は、前記した
図1の実施例とほぼ同様の構成であるが、空気穴34が
形成されていない点が異なる。
FIG. 7 is a sectional view showing the use state of another embodiment of the liquid mixer 1 of the present invention. The liquid mixer 1 of this embodiment is used by attaching a sampling member 3 (3A) instead of the injection needle 11 of the syringe shown in FIG. The syringe 8 to which the sampling member 3A is attached has a piston 9 slidably fitted into a cylinder 9.
The cylinder 9 has a substantially cylindrical shape as a whole, and a screw portion 91 having a thread formed on an outer peripheral portion is formed so as to protrude toward the distal end side, and a flange portion 92 that expands radially outward at a base end portion is integrally formed. Become. The piston 10 includes a piston body 10a which is closely fitted to the cylinder 9 and slides, and a piston body 10a.
a piston rod 10b extending proximally from a, and a disc-shaped operating part 1 integrally formed at the proximal end of the piston rod 10b.
0c. The sampling member 3 of this embodiment has substantially the same configuration as that of the embodiment of FIG. 1 described above, except that the air hole 34 is not formed.

【0016】次に、この実施例の液体混合器1の使用状
態について説明する。例えば、図8に示される注射器に
よって人体から血液6等を採取した場合、その先端の注
射針11をシリンダ9から取り外し、その代わりに図7
に示すように、採取部材3をシリンダ9のネジ部91に
螺着する。なお、採取部材3をシリンダ9に取り付ける
際には、採取部材3の先端部には前記キャップ4が装着
されており、採取部材3をシリンダ9に取り付けた後に
キャップ4は取り外される。なお、キャップ4を有さ
ず、採取部剤3のみからなる構成であってもよい。その
後、シリンダ9に対してピストン10を押し進めて採取
部材3の毛細管32の中にシリンダ9内の血液6を送
り、毛細管32の先端部からある程度放出する。そし
て、シリンダ9から採取部材3を取り外すのであるが、
採取部材3を取り外しても、毛細管32に入っている血
液等のサンプル6は毛細管32に滞留し、流れ落ちてし
まうことはない。
Next, the use state of the liquid mixer 1 of this embodiment will be described. For example, when blood 6 or the like is collected from the human body by using the syringe shown in FIG. 8, the injection needle 11 at the tip thereof is removed from the cylinder 9 and, instead, the injection needle 11 shown in FIG.
As shown in (5), the sampling member 3 is screwed to the screw portion 91 of the cylinder 9. When attaching the sampling member 3 to the cylinder 9, the cap 4 is attached to the tip of the sampling member 3, and the cap 4 is removed after attaching the sampling member 3 to the cylinder 9. In addition, the structure which does not have the cap 4 but consists only of the extraction | collection part agent 3 may be sufficient. Thereafter, the piston 10 is pushed against the cylinder 9 to send the blood 6 in the cylinder 9 into the capillary 32 of the sampling member 3 and discharge the blood 6 to some extent from the tip of the capillary 32. Then, the sampling member 3 is removed from the cylinder 9.
Even if the sampling member 3 is removed, the sample 6 such as blood contained in the capillary 32 stays in the capillary 32 and does not flow down.

【0017】次に、サンプル6が滞留した採取部材3
を、図1の実施例の場合と同様、図4に示すように、所
定量の希釈液5(例えば全血に対して、10〜20倍の
生理食塩水)や指示薬が入れられて減圧状態とされた混
合容器2のネジ部21に螺合し、混合容器2に対して採
取部材3を螺進させて、そのシール20を開封し、毛細
管32内のサンプル6を混合容器2内に吸入させて、希
釈液5等を混ぜ合わせられ、例えば糖尿病や肝炎、肝臓
癌などの抗原抗体検査に使用される。なお、この実施例
の場合でも、図5や図6の混合容器2が使用可能なこと
は言うまでもない。また、本発明の液体混合器1によっ
て、前処理された液体は、抗原抗体反応を見る他、液ク
ロマトグラフィ、ガスクロマトグラフィ、イオンクロマ
トグラフィ、原子吸光度分析装置、IPC分析装置、質
量分析器などの分析機に加えて使用することもできる。
なお、上記各実施例では、混合容器2に採取部材3が螺
合され、混合容器2のネジ部21に対して採取部材3を
螺進させることにより、混合容器2を開封する構成であ
ったが、これは他の構成であってもよい。例えば、両者
2,3を螺合させずに、混合容器2の首部に径方向外側
に突出する係止部を突出形成し、採取部材3は通常、こ
の係止部で係止されて混合容器2の首部に嵌合されるの
が阻止されているが、混合容器2の首部に採取部材3を
押し嵌めることにより、採取部材3が前記係止部を乗り
越えて混合容器2の首部に嵌合し、混合容器2のシール
が破られて開封される構成であってもよい。図9及び図
10には、この構成の場合の液体混合器1の一例を示し
た。これらの図では、採取部剤3にシリンジ8からサン
プル6を採取した後、混合容器2で希釈等する場合につ
いて、(A)から(E)まで時系列に示した。
Next, the sampling member 3 where the sample 6 has stayed
As in the case of the embodiment of FIG. 1, as shown in FIG. 4, a predetermined amount of diluent 5 (for example, physiological saline 10 to 20 times the volume of whole blood) or an indicator is added and the pressure is reduced. The sampling member 3 is screwed into the mixing container 2, the seal 20 is opened, and the sample 6 in the capillary 32 is sucked into the mixing container 2. Then, the diluent 5 and the like are mixed and used for an antigen-antibody test for, for example, diabetes, hepatitis, and liver cancer. Needless to say, even in the case of this embodiment, the mixing container 2 shown in FIGS. 5 and 6 can be used. In addition, the liquid pretreated by the liquid mixer 1 of the present invention is used for analyzing the antigen-antibody reaction, as well as analyzers such as liquid chromatography, gas chromatography, ion chromatography, atomic absorption analyzer, IPC analyzer, and mass analyzer. It can also be used in addition to.
In each of the above embodiments, the collecting member 3 is screwed into the mixing container 2, and the mixing container 2 is opened by screwing the collecting member 3 into the screw portion 21 of the mixing container 2. However, this may be another configuration. For example, a locking portion projecting radially outward is formed at the neck of the mixing container 2 without screwing the two 2 and 3 together, and the sampling member 3 is usually locked by the locking portion to form the mixing container. 2 is prevented from being fitted to the neck of the mixing container 2, but by pressing the collecting member 3 onto the neck of the mixing container 2, the collecting member 3 goes over the locking portion and fits into the neck of the mixing container 2. The seal of the mixing container 2 may be broken and opened. FIGS. 9 and 10 show an example of the liquid mixer 1 having this configuration. In these figures, the case where the sample 6 is collected from the syringe 8 into the collecting agent 3 and then diluted in the mixing container 2 is shown in a time series from (A) to (E).

【0018】[0018]

【発明の効果】以上詳述したように、この発明の液体混
合器によれば、ピペット等を使用せずに、直接サンプル
を採取することができ、作業が容易で、部材も少なくて
済み、コストの低減を図ることもできる。また、サンプ
ルを毛細管現象によって採取し、この毛細管を希釈液等
が減圧状態で密閉された混合容器に突き刺すだけで、毛
細管内のサンプルを混合容器内に吸入して両液を混合す
るので、作業者の個体差や危険性、コンタミネーション
が少なく、採取現場で正確な希釈や反応結果(定性、定
量)を瞬時に知ることができる。よって、実験室以外の
ベッドサイドや診療所等でも希釈等を行うことができ、
またサンプルの保存や管理も不要である。さらに、各部
材を全てプラスチックによって形成する等すれば、使い
捨てとすることができる。この場合でも、本発明の液体
混合器は、基本的に混合容器と採取部材の2つの部材の
みからなり、この2つの部材のみでサンプルの採取から
全てを行うことができるので、コストが高くなってしま
うという不都合はない。その上、前記2つの部材があれ
ばすむので、サンプル数が少数の場合でも、手間がかか
らず、時間の短縮化を図ることができる。
As described in detail above, according to the liquid mixer of the present invention, a sample can be directly collected without using a pipette or the like, the operation is easy, and the number of members is reduced. Cost can also be reduced. In addition, the sample is collected by capillary action, and the diluent or the like is simply pierced into a sealed mixing vessel under reduced pressure, and the sample in the capillary is sucked into the mixing vessel to mix the two liquids. There are few individual differences, dangers, and contaminations among individuals, and accurate dilution and reaction results (qualitative and quantitative) can be instantly known at the sampling site. Therefore, dilution and the like can be performed at a bedside or a clinic other than the laboratory,
There is no need to store or manage samples. Furthermore, if all the members are formed of plastic or the like, they can be disposable. Even in this case, the liquid mixer of the present invention basically includes only two members, ie, the mixing container and the sampling member, and can perform everything from the sampling of the sample with only these two members, which increases the cost. There is no inconvenience. In addition, since only the two members are required, even if the number of samples is small, no labor is required and time can be reduced.

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

【図1】この発明の液体混合器の一実施例を示す断面図
である。
FIG. 1 is a sectional view showing an embodiment of a liquid mixer of the present invention.

【図2】図1の液体混合器の使用状態を示し、キャップ
を取り外した状態を示す断面図である。
FIG. 2 is a sectional view showing a use state of the liquid mixer of FIG. 1 and showing a state where a cap is removed.

【図3】図1の液体混合器の使用状態を示し、採取部材
でサンプルを一定量採取する際の状態を示す断面図であ
る。
FIG. 3 is a sectional view showing a use state of the liquid mixer of FIG. 1 and showing a state when a fixed amount of a sample is collected by a collection member.

【図4】図1の液体混合器の使用状態を示し、サンプル
と希釈液等とを混合する際の状態を示す断面図である。
FIG. 4 is a sectional view showing a use state of the liquid mixer of FIG. 1 and showing a state when a sample is mixed with a diluent or the like.

【図5】図1の液体混合器の混合容器の変形例を示す正
面図である。
FIG. 5 is a front view showing a modification of the mixing container of the liquid mixer of FIG.

【図6】図1の液体混合器の混合容器の別の変形例を示
す正面図である。
FIG. 6 is a front view showing another modification of the mixing container of the liquid mixer of FIG. 1;

【図7】この発明の液体混合器の他の実施例の使用状態
を示し、採取部材をシリンジに装着してサンプルを一定
量採取する際の状態を示す断面図である。
FIG. 7 is a sectional view showing a use state of another embodiment of the liquid mixer of the present invention, showing a state in which a sampling member is attached to a syringe and a predetermined amount of a sample is collected.

【図8】図7のシリンジが使用された注射器を示す断面
図である。
8 is a sectional view showing a syringe using the syringe of FIG. 7;

【図9】この発明の液体混合器の他の実施例の使用状態
を示し、混合容器に採取部材を押し嵌めることにより、
混合容器を開封する構成である。
FIG. 9 shows a use state of another embodiment of the liquid mixer of the present invention.
In this configuration, the mixing container is opened.

【図10】図9の液体混合器の使用状態を示す断面図で
ある。
FIG. 10 is a sectional view showing a use state of the liquid mixer of FIG. 9;

【符号の説明】[Explanation of symbols]

1 液体混合器 2 混合容器 3 採取部材 4 キャップ 5 希釈液等の前処理液 6 血液等のサンプル 7 容器 8 シリンジ 9 シリンダ 10 ピストン 20 シール 21 ネジ部 22 蛇腹部 23 ダイアフラム部(混合容器の底) 31 ネジ穴 32 毛細管 33 開封手段(突起) 34 空気穴 91 シリンダのネジ部(シリンジ先端部) REFERENCE SIGNS LIST 1 liquid mixer 2 mixing container 3 sampling member 4 cap 5 pretreatment liquid such as diluent 6 sample of blood 7 container 8 syringe 9 cylinder 10 piston 20 seal 21 screw part 22 bellows part 23 diaphragm part (bottom of mixing container) Reference Signs List 31 screw hole 32 capillary tube 33 opening means (projection) 34 air hole 91 cylinder screw part (syringe tip)

フロントページの続き (56)参考文献 特表 昭55−500366(JP,A) (58)調査した分野(Int.Cl.6,DB名) G01N 1/00 101 G01N 1/10 G01N 1/28 A61B 5/14 300Continuation of the front page (56) References Special Tables Sho 55-500366 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) G01N 1/00 101 G01N 1/10 G01N 1/28 A61B 5/14 300

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 希釈液等が入れられ、減圧状態にて開口
部をシールで密閉された混合容器と、 この混合容器に進退可能に螺合され、前記希釈液等に対
して所定量のサンプルを採取する毛細管が形成され、こ
の毛細管の下端部に前記混合容器への螺進によって前記
混合容器のシールを破る突起が形成されてなる採取部材
とを備えてなり、 前記採取部材が、シリンジの先端部に取り付け可能とさ
れてなる ことを特徴とする液体混合器。
1. A mixing container in which a diluent or the like is put, and an opening is sealed with a seal in a reduced pressure state; and a predetermined amount of sample is screwed into the mixing container so as to be able to advance and retreat. A sampling member formed by forming a capillary tube for sampling the mixture, and a projection formed at the lower end of the capillary tube to break the seal of the mixing container by screwing into the mixing container.
It includes bets, the collecting member is attachable to the distal end of the syringe
A liquid mixer characterized by being obtained .
【請求項2】 希釈液等が入れられ、減圧状態にて開口
部をシールで密閉された混合容器と、 この混合容器に押し嵌め可能とされ、前記希釈液等に対
して所定量のサンプルを採取する毛細管が形成され、こ
の毛細管の下端部に前記混合容器への押し嵌めによって
前記混合容器のシールを破る突起が形成されてなる採取
部材とを備えてなり、 前記採取部材が、シリンジの先端部に取り付け可能とさ
れてなる ことを特徴とする液体混合器。
Wherein the diluent or the like is placed, and sealed mixing vessel opening in the seal at reduced pressure, is capable push-fit into the mixing container, a sample of a predetermined amount with respect to the diluent, etc. A collecting member formed with a capillary to be collected, and a projection formed at a lower end portion of the capillary so as to break a seal of the mixing container by press-fitting the mixing container , wherein the collecting member includes a tip of a syringe; It can be attached to the part
A liquid mixer characterized by being obtained .
JP7294930A 1995-10-17 1995-10-17 Liquid mixer Expired - Fee Related JP2805463B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7294930A JP2805463B2 (en) 1995-10-17 1995-10-17 Liquid mixer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7294930A JP2805463B2 (en) 1995-10-17 1995-10-17 Liquid mixer

Publications (2)

Publication Number Publication Date
JPH09113421A JPH09113421A (en) 1997-05-02
JP2805463B2 true JP2805463B2 (en) 1998-09-30

Family

ID=17814115

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7294930A Expired - Fee Related JP2805463B2 (en) 1995-10-17 1995-10-17 Liquid mixer

Country Status (1)

Country Link
JP (1) JP2805463B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101957273B (en) * 2009-07-15 2012-09-19 英科新创(厦门)科技有限公司 Device for collecting and diluting trace liquid sample at fixed ratio and use method thereof

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE0001175L (en) * 2000-03-31 2001-08-27 Boule Medical Ab Device for dilution and mixing of a liquid sample
JP3869810B2 (en) * 2003-02-24 2007-01-17 株式会社堀場製作所 Micro blood cell counter
US7588724B2 (en) * 2004-03-05 2009-09-15 Bayer Healthcare Llc Mechanical device for mixing a fluid sample with a treatment solution
WO2006045749A1 (en) * 2004-10-20 2006-05-04 Dsm Ip Assets B.V. Device for sampling a fluid and detecting an analyte therein
JP5048762B2 (en) * 2007-04-27 2012-10-17 国立大学法人京都工芸繊維大学 Blood quantitative mixer
SE531873C2 (en) * 2007-11-12 2009-09-01 Lifeassays Ab Device for biochemical processing and analysis of sample liquid
KR101009447B1 (en) * 2007-11-12 2011-01-19 바디텍메드 주식회사 Device for sampling and preprocessing biological fluids and method thereof
CA2719813C (en) * 2008-03-28 2019-03-12 Orion Diagnostica Oy Sampling and dispensing device
CN109730697A (en) * 2012-12-05 2019-05-10 赛拉诺斯知识产权有限责任公司 For collecting the device of humoral sample
FR3008792B1 (en) * 2013-07-17 2017-03-24 Horiba Abx Sas DEVICE AND METHOD FOR SAMPLING AND DISPENSING A BIOLOGICAL FLUID USING A CAPILLARY TUBE, AND BIOLOGICAL ANALYSIS APPARATUS
US11448571B2 (en) * 2016-07-06 2022-09-20 Nipro Corporation Specimen collection tip, specimen preparation container and specimen preparation kit
JP6819111B2 (en) * 2016-07-21 2021-01-27 Dicプラスチック株式会社 Specimen test kit
CN107569240A (en) * 2017-08-30 2018-01-12 台州市黄岩方野科技发展有限公司 A kind of micro blood-taking tube of preset reagent and blood sampling and the method for adding reagent
WO2024024039A1 (en) * 2022-07-28 2024-02-01 ナッジヘルステック株式会社 Blood storage container and blood collection instrument

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55500366A (en) * 1978-05-26 1980-06-26

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101957273B (en) * 2009-07-15 2012-09-19 英科新创(厦门)科技有限公司 Device for collecting and diluting trace liquid sample at fixed ratio and use method thereof

Also Published As

Publication number Publication date
JPH09113421A (en) 1997-05-02

Similar Documents

Publication Publication Date Title
JP2805463B2 (en) Liquid mixer
US6203503B1 (en) Collection container assembly
AU765875B2 (en) Disposable test vial with sample delivery device
US4022576A (en) Method and apparatus for preparation of liquids containing suspended material for examination
AU8301598A (en) Collection container assembly
AU2021200665B2 (en) Device and method for collecting and detecting samples
JP6474347B2 (en) Sample preparation container
CN107036848B (en) Sample collection and detection device
EP4012408B1 (en) Sample collection and detection device and method
WO2004043601A1 (en) Test tube with insert
AU8301198A (en) Collection container assembly
AU747043B2 (en) Collection container assembly
CN110477958B (en) Method for collecting and detecting sample
CA2245126C (en) Collection container assembly
US20220250053A1 (en) Apparatus and method for collecting and testing sample
CN210401424U (en) Sample collection member
CA3131957A1 (en) Blood collection structure and whole blood and fingertip blood testing device and testing method
CN215078596U (en) Blood sampling structure
JP3234519U (en) Blood collection structure, whole blood and fingertip blood detector
CN210401425U (en) Sample collecting and detecting device
EP0412225A1 (en) A device for measuring by displacement, an exact micro dose of a fluid to be analysed from a totally filled capillary tube closed at one end and flushing such dose into a cuvette by means of an exactly measured dose of a reagent fluid

Legal Events

Date Code Title Description
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 19980526

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

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

Free format text: PAYMENT UNTIL: 20080724

Year of fee payment: 10

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

Free format text: PAYMENT UNTIL: 20080724

Year of fee payment: 10

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

Free format text: PAYMENT UNTIL: 20090724

Year of fee payment: 11

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

Free format text: PAYMENT UNTIL: 20100724

Year of fee payment: 12

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

Free format text: PAYMENT UNTIL: 20100724

Year of fee payment: 12

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

Free format text: PAYMENT UNTIL: 20110724

Year of fee payment: 13

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

Free format text: PAYMENT UNTIL: 20110724

Year of fee payment: 13

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

Free format text: PAYMENT UNTIL: 20120724

Year of fee payment: 14

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

Free format text: PAYMENT UNTIL: 20130724

Year of fee payment: 15

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees