JP6790556B2 - Inspection unit - Google Patents

Inspection unit Download PDF

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JP6790556B2
JP6790556B2 JP2016151309A JP2016151309A JP6790556B2 JP 6790556 B2 JP6790556 B2 JP 6790556B2 JP 2016151309 A JP2016151309 A JP 2016151309A JP 2016151309 A JP2016151309 A JP 2016151309A JP 6790556 B2 JP6790556 B2 JP 6790556B2
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storage container
inspection unit
fitting portion
blood
container
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JP2018019765A (en
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福島 英夫
英夫 福島
野口 裕雄
野口  裕雄
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Toppan Inc
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Toppan Inc
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Description

本発明は、検査ユニットに関し、特に自宅等において血液検査を簡易に行うための血液検査ユニットに関する。 The present invention relates to a test unit, and more particularly to a blood test unit for easily performing a blood test at home or the like.

簡易の採血キットを用いて自宅等において採血を行い、それを検査機関に送り、血液検査を行うことが一般的になりつつある。特許文献1及び2には、このような自己採血による血液検査ユニットの一例が開示されている。 It is becoming common to collect blood at home or the like using a simple blood collection kit, send it to a laboratory, and perform a blood test. Patent Documents 1 and 2 disclose an example of such a self-collecting blood test unit.

特開2001−321364号公報Japanese Unexamined Patent Publication No. 2001-321364 特表2011−515171号公報Japanese Patent Publication No. 2011-515171 特許第2805463号公報Japanese Patent No. 2805463

しかしながら、特許文献1及び2に記載の自己採血キットでは、一度採取した血液等の検査対象流体を採取部材から収容容器に移し替える際、採取部材を収容容器に装着した後に、これらをひっくり返す作業を行ったり、または採取部材の先端側に収容容器の口を配置して、検査対象流体がこぼれないように配慮しながら移し替えたり、といった作業をしなければならなかった。また、特許文献1に記載の自己採血キットでは、採血の際に血液が飛び散り、使用時に汚れを発生させる虞もあった。 However, in the self-collection kits described in Patent Documents 1 and 2, when the fluid to be inspected such as blood once collected is transferred from the collection member to the storage container, the work of turning over the collection member after attaching the collection member to the storage container is performed. It was necessary to do the work, or to place the mouth of the storage container on the tip side of the sampling member and transfer it while taking care not to spill the fluid to be inspected. Further, in the self-collecting kit described in Patent Document 1, there is a possibility that blood may be scattered at the time of blood collection and stain may be generated at the time of use.

そこで、本発明では、血液等の検査対象流体の採取後に検査対象流体を採取部材から収容容器に容易に移し替えることが可能な検査ユニットを提供することを目的とする。 Therefore, an object of the present invention is to provide an inspection unit capable of easily transferring the inspection target fluid from the collection member to the storage container after collecting the inspection target fluid such as blood.

本発明は、その一側面として、検査ユニットに関する。この検査ユニットは、検査対象流体を採取するための採取部材と、採取部材により採取された検査対象流体を収容する収容容器とを備え、採取部材は、先端から基端に向かって延びる中空の細管部と、当該細管部の基端側に設けられる中空の嵌合部とを有し、収容容器は、一端が開口する有底筒形状の容器本体と、容器本体の当該開口を開閉自在な蓋体とを有し、採取部材の嵌合部は、収容容器の一端に嵌合可能となるように構成され、収容容器内の空気を外部に逃がすための空隙が採取部材と収容容器との嵌合領域に設けられている。 The present invention relates to an inspection unit as one aspect thereof. This inspection unit includes a sampling member for collecting the fluid to be inspected and a storage container for accommodating the fluid to be inspected collected by the sampling member, and the sampling member is a hollow thin tube extending from the tip to the base end. It has a portion and a hollow fitting portion provided on the base end side of the thin tube portion, and the storage container has a bottomed tubular container body having an opening at one end and a lid that can open and close the opening of the container body. It has a body, and the fitting portion of the collection member is configured so that it can be fitted to one end of the storage container, and a gap for letting air in the storage container escape to the outside is fitted between the collection member and the storage container. It is provided in the joint area.

この検査ユニットでは、採取部材の嵌合部が収容容器の一端に嵌合可能となるように構成されており、しかも、収容容器内の空気を外部に逃がすための空隙が採取部材と収容容器との嵌合領域に設けられている。この場合、血液等の検査対象液体を毛細管現象等を利用して採取部材の細管部によって採取した後、所定の力を細管部又は検査対象流体に加えることで細管部内の検査対象流体を収容容器が位置する下方に移動させようとした際、収容容器内の空気が検査対象流体の移動に応じてそれらの中間にある嵌合領域の空隙から外部に向かってスムーズに逃げることができる。このため、この検査ユニットによれば、細管部で採取した検査対象流体を収容容器内に容易に移動させることができる。この結果、本検査ユニットによれば、血液等の検査対象流体の採取後に検査対象流体を採取部材から収容容器に容易に移し替えることが可能となる。なお、この空隙については、収容容器内の空気の一部を外部に逃がすためのものであるため、過大な空隙である必要はないことから、このような空隙が設けられていても、検査対象流体への影響は軽微なものとすることが可能である。 In this inspection unit, the fitting portion of the sampling member is configured so that it can be fitted to one end of the storage container, and moreover, a gap for letting air in the storage container escape to the outside is formed between the sampling member and the storage container. It is provided in the fitting area of. In this case, after the liquid to be inspected such as blood is collected by the capillary part of the collecting member by using the capillary phenomenon or the like, a predetermined force is applied to the thin tube part or the fluid to be inspected to store the fluid to be inspected in the capillary part. The air in the containment vessel can smoothly escape outward from the gap in the fitting region in the middle as the fluid to be inspected moves when it is attempted to move downward. Therefore, according to this inspection unit, the fluid to be inspected collected in the thin tube portion can be easily moved into the storage container. As a result, according to this inspection unit, it is possible to easily transfer the inspection target fluid from the collection member to the storage container after collecting the inspection target fluid such as blood. It should be noted that this gap is intended to allow a part of the air in the storage container to escape to the outside, and therefore does not need to be an excessive gap. Therefore, even if such a gap is provided, it is subject to inspection. The effect on the fluid can be minor.

上記の検査ユニットにおいて、採取部材は、嵌合部が収容容器の開口の内周部に接合するように収容容器に取り付け可能であってもよい。この場合、採取部材と収容容器との嵌合領域に位置する空隙を設け易くなり、また、収容容器の外周側に嵌合部が配置されないので、蓋体を容器本体に連結するような連結部材を容器本体の外周に設けやすくなる。 In the above inspection unit, the sampling member may be attached to the storage container so that the fitting portion is joined to the inner peripheral portion of the opening of the storage container. In this case, it becomes easy to provide a gap located in the fitting region between the collecting member and the storage container, and since the fitting portion is not arranged on the outer peripheral side of the storage container, a connecting member that connects the lid to the container body. Can be easily provided on the outer circumference of the container body.

上記の検査ユニットにおいて、採取部材は、細管部と嵌合部との間にフランジ部を更に有し、当該フランジ部の嵌合部側の面に突起が設けられ、当該突起により空隙が画定されてもよい。また、嵌合部の外周には周方向と交差する方向に延びる溝が形成され、当該溝が空隙の少なくとも一部を構成するようにしてもよい。このように、空隙又はそれを画定する部材を採取部材(嵌合部)側に設けることにより、収容容器側、特に嵌合部と嵌合する部分の形状を単純又は平坦面状なものとすることができる。このため、例えば、自己採血等の検査を行う場合、検査液収容後の収容容器は、蓋体を開口に嵌めてしっかりと密封した上で検査機関に送る必要があるが、上述したように、収容容器の開口側をスムーズ(平坦面)な形状とすることができることにより、蓋体による収容容器の密封性を容易に高めることができる。 In the above inspection unit, the sampling member further has a flange portion between the thin tube portion and the fitting portion, a protrusion is provided on the surface of the flange portion on the fitting portion side, and the gap is defined by the protrusion. You may. Further, a groove extending in a direction intersecting the circumferential direction may be formed on the outer periphery of the fitting portion, and the groove may form at least a part of the gap. By providing the gap or the member defining the gap on the sampling member (fitting portion) side in this way, the shape of the storage container side, particularly the portion to be fitted with the fitting portion, is made simple or flat. be able to. For this reason, for example, when performing a test such as self-collection of blood, it is necessary to fit the lid into the opening of the container after storing the test solution and tightly seal it before sending it to the testing institution. Since the opening side of the storage container can be formed into a smooth (flat surface) shape, the sealing property of the storage container by the lid can be easily improved.

上記の検査ユニットにおいて、細管部の内孔は、採取部材の先端から基端に向かってテーパ状に広がっていてもよい。上述した検査ユニットの採取部材は、いわゆる毛細管現象を利用して細管部の内孔に検査対象液体が入り込むことを想定して設計されうるが、基端(収容容器)側の内径が先端側よりも広がるように形成しておくことにより、細管部や検査対象流体に対して所定の力を加えた際に、細管部内の検査対象流体が重力等により下方の収容容器へ移動しやすくなる。より具体的には、細管部の基端側の内孔の内径を大きくしておくことにより、その領域における毛細管現象を弱め、一旦、採取された検査対象流体を収容容器側に移動しやすくしておくことが可能となる。このように、上記構成によれば、血液等の検査対象流体の採取後に検査対象流体を採取部材から収容容器に更に容易に移し替えることが可能となる。なお、この場合において、細管部の内孔は、その基端側の最小内径がその先端側の最小内径の2倍以上であることが、移し替えの容易性の観点では好ましい。 In the above inspection unit, the inner hole of the thin tube portion may be tapered from the tip end to the base end of the sampling member. The sampling member of the inspection unit described above can be designed on the assumption that the fluid to be inspected enters the inner hole of the capillary portion by utilizing the so-called capillary phenomenon, but the inner diameter on the base end (containment container) side is from the tip side. By forming the fluid so as to spread, when a predetermined force is applied to the capillary portion or the fluid to be inspected, the fluid to be inspected in the capillary portion can easily move to the lower storage container due to gravity or the like. More specifically, by increasing the inner diameter of the inner hole on the proximal end side of the capillary portion, the capillary phenomenon in that region is weakened, and the fluid to be inspected once collected can be easily moved to the storage container side. It will be possible to keep it. As described above, according to the above configuration, it is possible to more easily transfer the test target fluid from the collection member to the storage container after collecting the test target fluid such as blood. In this case, it is preferable that the minimum inner diameter of the inner hole of the thin tube portion is twice or more the minimum inner diameter of the tip end side thereof from the viewpoint of ease of transfer.

上記の検査ユニットにおいて、収容容器の容器本体の内周面には、周方向と交差する長手方向に延びる少なくとも1つの第1誘導リブが設けられ、当該第1誘導リブは開口の手前まで伸びていてもよい。この場合、採取部材に採取保持されている検査対象流体の一部、例えばその下端が、収容容器内に第1誘導リブに触れると、表面張力等の吸引により、第1誘導リブに沿って収容容器の中へと誘導されやくなる。このため、このような誘導リブを設けておくことにより、血液等の検査対象流体の採取後に検査対象流体を採取部材から収容容器に更に容易に移し替えることが可能となる。この場合において、収容容器側に位置する嵌合部の内周面に、周方向と交差する長手方向に延びる少なくとも1つの第2誘導リブが設けられ、第2誘導リブが、採取部材と収容容器とが嵌合された際に第1誘導リブと接触可能であることが好ましい。この場合、採取部材内の検査対象流体がまずは第1誘導リブにより収容容器側に誘導され、その後、第2誘導リブにより収容容器内へと誘導されることになるため、採取部材から収容容器に更に一層、容易に移し替えることが可能となる。なお、この場合、第1誘導リブ及び第2誘導リブは、互いに異なる数がそれぞれ設けられていることが好ましい。このような構成により、第1誘導リブと第2誘導リブとが接触又は近接する場合と接触又は近接しない場合とを切り替えることが容易に行えるため、採取部材から収容容器への移し替えのタイミングをリブの位置合わせにより調整することが可能となる。 In the above inspection unit, at least one first guide rib extending in the longitudinal direction intersecting the circumferential direction is provided on the inner peripheral surface of the container body of the container, and the first guide rib extends to the front of the opening. You may. In this case, when a part of the fluid to be inspected collected and held by the sampling member, for example, the lower end thereof touches the first guide rib in the container, it is stored along the first guide rib by suction of surface tension or the like. It becomes easy to be guided into the container. Therefore, by providing such an induction rib, it becomes possible to more easily transfer the test target fluid from the collection member to the storage container after collecting the test target fluid such as blood. In this case, at least one second guide rib extending in the longitudinal direction intersecting the circumferential direction is provided on the inner peripheral surface of the fitting portion located on the storage container side, and the second guide rib is the collecting member and the storage container. It is preferable that the first guide rib can be contacted when the and is fitted. In this case, the fluid to be inspected in the sampling member is first guided to the storage container side by the first guide rib, and then guided into the storage container by the second guide rib, so that the sampling member is guided to the storage container. Even more easily, it can be transferred. In this case, it is preferable that the first lead rib and the second lead rib are provided with different numbers. With such a configuration, it is possible to easily switch between the case where the first guide rib and the second guide rib are in contact with or close to each other and the case where the first guide rib and the second guide rib are not in contact with each other. It can be adjusted by aligning the ribs.

なお、上記の検査ユニットは、血液検査に限られず、尿やその他の検査対象流体に用いることが可能であるが、血液検査に用いられる場合にあっては、収容容器には、血液検査のための血漿分離剤が収容されていることが好ましい。この場合、検査前に予め血液から血漿のみを分離することで、検査の迅速性及び精度を向上させることができる。 The above test unit is not limited to blood tests, and can be used for urine and other fluids to be tested. However, when used for blood tests, the storage container is used for blood tests. It is preferable that the plasma separating agent of the above is contained. In this case, the speed and accuracy of the test can be improved by separating only plasma from the blood in advance before the test.

本発明によれば、血液等の検査対象流体の採取後に検査対象流体を採取部材から収容容器に容易に移し替えることが可能な検査ユニットを提供することができる。 According to the present invention, it is possible to provide an inspection unit capable of easily transferring the inspection target fluid from the collection member to the storage container after collecting the inspection target fluid such as blood.

図1は、本発明の第1実施形態に係る検査ユニットを示す斜視図である。FIG. 1 is a perspective view showing an inspection unit according to the first embodiment of the present invention. 図2は、図1に示す検査ユニットの断面図である。FIG. 2 is a cross-sectional view of the inspection unit shown in FIG. 図3は、図1に示す検査ユニットを構成する採取部材を下方から示す斜視図である。FIG. 3 is a perspective view showing a sampling member constituting the inspection unit shown in FIG. 1 from below. 図4は、図1に示す検査ユニットを構成する収容容器を示す斜視図であり、(a)は蓋体を開放した際の状態を示し、(b)は蓋体を閉じた際の状態を示す。4A and 4B are perspective views showing a storage container constituting the inspection unit shown in FIG. 1, where FIG. 4A shows a state when the lid is opened, and FIG. 4B shows a state when the lid is closed. Shown. 図5は、図1に示す検査ユニットの使用例を示す図であり、(a)は血液の採取時の方法を示し、(b)は採取した血液を収容容器に移し替える際の方法を示す。5A and 5B are views showing a usage example of the test unit shown in FIG. 1, in which FIG. 5A shows a method for collecting blood and FIG. 5B shows a method for transferring the collected blood to a storage container. .. 図6は、本発明の第2実施形態に係る検査ユニットを示す斜視図である。FIG. 6 is a perspective view showing an inspection unit according to a second embodiment of the present invention. 図7は、図6に示す検査ユニットを構成する採取部材を示し、(a)は側面図を示し、(b)は下面図を示し、(c)は下方からの斜視図を示す。7A and 7B show a sampling member constituting the inspection unit shown in FIG. 6, FIG. 7A shows a side view, FIG. 7B shows a bottom view, and FIG. 7C shows a perspective view from below. 図8は、図6に示す検査ユニットを構成する収容容器を示し、(a)は上面図を示し、(b)は断面図を示す。8A and 8B show a storage container constituting the inspection unit shown in FIG. 6, FIG. 8A shows a top view, and FIG. 8B shows a cross-sectional view. 図9は、図6に示す検査ユニットの使用例を示す断面図であり、(a)は、血液が採取された状態を示し、(b)は、採取された血液を収容容器に移し替える際の状態を示す。9A and 9B are cross-sectional views showing a usage example of the inspection unit shown in FIG. 6, where FIG. 9A shows a state in which blood has been collected, and FIG. 9B shows a state in which the collected blood is transferred to a storage container. Indicates the state of. 図10は、図6に示す検査ユニットの使用例を示す一部分解図であり、(a)は、血液が採取された状態を示し、(b)は、採取された血液を収容容器に移し替える際の状態を示す。10A and 10B are partially exploded views showing an example of use of the test unit shown in FIG. 6, in which FIG. 10A shows a state in which blood has been collected, and FIG. 10B shows the collected blood being transferred to a storage container. Indicates the state at the time. 図11は、検査ユニットの採取部材の先端形状の変形例を示す部分拡大図であり、(a)は、先端内孔がテーパ形状である例を示す図であり、(b)は、先端内孔がR形状である例を示す図である。FIG. 11 is a partially enlarged view showing a modified example of the tip shape of the sampling member of the inspection unit, FIG. 11A is a view showing an example in which the tip inner hole has a tapered shape, and FIG. 11B is a view inside the tip. It is a figure which shows the example which the hole has an R shape.

以下、図面を参照しつつ、本発明の実施形態に係る検査ユニットについて詳細に説明する。説明において、同一要素又は同一機能を有する要素には、同一符号を用いる場合があり、重複する説明は省略する。 Hereinafter, the inspection unit according to the embodiment of the present invention will be described in detail with reference to the drawings. In the description, the same reference numerals may be used for the same elements or elements having the same function, and duplicate description will be omitted.

[第1実施形態]
図1は、本発明の第1実施形態に係る検査ユニットを示す斜視図である。図2は、図1に示す検査ユニットの断面図である。図1及び図2に示すように、検査ユニット10は、血液などの検査対象流体を採取するための採取部材20と、採取部材20により採取された検査対象流体を収容する収容容器30と、を備えて構成されている。検査ユニット10は、例えば、検査希望者が自身の指などに採血針を指して出てきた血液などの検査対象流体を採取部材20により採取し、採取した血液を収容容器30に収容して検査機関に送り、検査してもらうための自己検査ユニットである(図5参照)。なお、図1及び図2では、採取部材20が収容容器30に嵌め込まれた使用状態が示されているが、これら検査ユニットを郵送などにより使用者に送る際には、採取部材20と収容容器30とは嵌め込まれずに別々に1つの箱に収納されている。また、採血針などを検査ユニット10に含めるようにしてもよい。
[First Embodiment]
FIG. 1 is a perspective view showing an inspection unit according to the first embodiment of the present invention. FIG. 2 is a cross-sectional view of the inspection unit shown in FIG. As shown in FIGS. 1 and 2, the inspection unit 10 includes a collection member 20 for collecting a fluid to be inspected such as blood, and a storage container 30 for accommodating the fluid to be inspected collected by the collection member 20. It is configured to prepare. The inspection unit 10 collects, for example, a fluid to be inspected such as blood that comes out by a person who wants to inspect points a blood collection needle at his / her own finger or the like by a collecting member 20, and stores the collected blood in a storage container 30 for inspection. It is a self-inspection unit for sending to an institution for inspection (see Fig. 5). In addition, although FIG. 1 and FIG. 2 show the usage state in which the collection member 20 is fitted in the storage container 30, when these inspection units are sent to the user by mail or the like, the collection member 20 and the storage container are shown. It is stored separately in one box without being fitted with the 30. Further, a blood collection needle or the like may be included in the test unit 10.

図3は、図1に示す検査ユニットを構成する採取部材を下方から示す斜視図である。採取部材20は、図1〜図3に示すように、その全体がノズル形状を呈しており、細管部21と、嵌合部22と、フランジ部23とを主に備えている。このような採取部材20は、透明なポリプロピレン(PP)、ポリスチレン(PS)、アクリロニトリルスチレン(AS)、又はポリエチレン(PE)等の樹脂を射出成型することにより、一体的に形成することができる。 FIG. 3 is a perspective view showing a sampling member constituting the inspection unit shown in FIG. 1 from below. As shown in FIGS. 1 to 3, the collecting member 20 has a nozzle shape as a whole, and mainly includes a thin tube portion 21, a fitting portion 22, and a flange portion 23. Such a sampling member 20 can be integrally formed by injection molding a transparent resin such as polypropylene (PP), polystyrene (PS), acrylonitrile styrene (AS), or polyethylene (PE).

細管部21は、内孔21aを有する中空の略円錐筒形状であり、先端21bから基端21cに向かって延びるように形成された細管である。細管部21は、その外形がテーパ形状となっているが、ストレート形状であってもよい。細管部21の内孔21aは、検査対象流体を毛細管現象によって採取できるように、その内径が例えば0.5mm〜5mmとされており、先端21bの内径は例えば0.5mm〜2mmの範囲となっている。また、細管部21の内孔21aは、先端21bから基端21cに向かってテーパ状に広がるように形成されており、内孔21aの基端21c側の内径が先端21b側の内径よりも大きくなっている。より好ましくは、内孔21aの基端21c側の内径が先端21b側の内径の2倍以上であり、例えば、内孔21aの先端21b側の内径が1mmである場合、内孔21aの基端21c側の内径は2mm又は3mm以上である。なお、細管部21によって一度に採取される血液等は、例えば100μL〜150μL程度である。 The thin tube portion 21 has a hollow substantially conical tubular shape having an inner hole 21a, and is a thin tube formed so as to extend from the tip end 21b toward the base end 21c. The thin tube portion 21 has a tapered outer shape, but may have a straight shape. The inner diameter of the inner hole 21a of the thin tube portion 21 is, for example, 0.5 mm to 5 mm so that the fluid to be inspected can be collected by the capillary phenomenon, and the inner diameter of the tip 21b is, for example, in the range of 0.5 mm to 2 mm. ing. Further, the inner hole 21a of the thin tube portion 21 is formed so as to taper from the tip 21b toward the base end 21c, and the inner diameter of the inner hole 21a on the base end 21c side is larger than the inner diameter of the tip 21b side. It has become. More preferably, when the inner diameter of the inner hole 21a on the base end 21c side is twice or more the inner diameter of the tip 21b side, for example, when the inner diameter of the inner hole 21a on the tip 21b side is 1 mm, the base end of the inner hole 21a The inner diameter on the 21c side is 2 mm or 3 mm or more. The amount of blood or the like collected at one time by the capillary portion 21 is, for example, about 100 μL to 150 μL.

嵌合部22は、細管部21の基端21c側に設けられた中空の略円筒形状の部材であり、収容容器30の開口部33に嵌合され、採取部材20を収容容器30に取り付けるための部分である。嵌合部22は、細管部21の内孔21aよりも径が大きい内孔22aを有している。この内孔22aは、細管部21の内孔21aと流体的に連通するように連続して構成されている。つまり、細管部21の内孔21aで採取された検査対象流体が内孔22aを介して収容容器30へと移動可能となっている。嵌合部22の外周面上には、複数のリブ25(本実施形態では3つのリブ、図3参照)が均等間隔(均等角度)で設けられており、これらのリブ25の頂部が収容容器30の開口部33の内周に接合することで、嵌合部22が収容容器30に嵌め合わされる。なお、このようなリブが周方向に設けられていることから、嵌合部22の外周面(リブ25の形成領域除く)と収容容器30の内周面との間に空隙26が画定され、この空隙26を介して、収容容器30内の空気が外部に逃げることができるようになっている。 The fitting portion 22 is a hollow substantially cylindrical member provided on the base end 21c side of the thin tube portion 21 and is fitted into the opening 33 of the storage container 30 to attach the sampling member 20 to the storage container 30. Is the part of. The fitting portion 22 has an inner hole 22a having a diameter larger than that of the inner hole 21a of the thin tube portion 21. The inner hole 22a is continuously configured so as to be fluidly communicated with the inner hole 21a of the thin tube portion 21. That is, the fluid to be inspected collected in the inner hole 21a of the thin tube portion 21 can move to the storage container 30 through the inner hole 22a. A plurality of ribs 25 (three ribs in this embodiment, see FIG. 3) are provided at equal intervals (equal angles) on the outer peripheral surface of the fitting portion 22, and the tops of these ribs 25 are storage containers. By joining to the inner circumference of the opening 33 of 30, the fitting portion 22 is fitted into the storage container 30. Since such ribs are provided in the circumferential direction, a gap 26 is defined between the outer peripheral surface of the fitting portion 22 (excluding the rib 25 forming region) and the inner peripheral surface of the storage container 30. The air in the storage container 30 can escape to the outside through the gap 26.

フランジ部23は、細管部21と嵌合部22との間に設けられた円板上の部材であり、細管部21及び嵌合部22の外周よりも大きな径の外周を有している。フランジ部23の外周は、例えば、収容容器30の外周と略同じであり、嵌合部22が収容容器30の開口部33に嵌合された際、収容容器30の図示上端上にその外周部分が引っかかるように配置される。フランジ部23の下面23aには、複数の突起24(本実施形態では3つの突起)が周方向に均等間隔に設けられており、フランジ部23は、これらの突起24を介して、収容容器30の上端に配置される。なお、このような突起24がフランジ部23の下面23aに設けられていることから、フランジ部23の下面23a(突起24の形成領域除く)と収容容器30の上端との間に空隙26が画定され、この空隙26を介して、収容容器30内の空気が外部に逃げることができるようになっている。 The flange portion 23 is a member on a disk provided between the thin tube portion 21 and the fitting portion 22, and has an outer circumference having a diameter larger than the outer circumference of the thin tube portion 21 and the fitting portion 22. The outer circumference of the flange portion 23 is, for example, substantially the same as the outer circumference of the storage container 30, and when the fitting portion 22 is fitted into the opening 33 of the storage container 30, the outer peripheral portion thereof is on the upper end of the drawing of the storage container 30. Is arranged so that it is caught. A plurality of protrusions 24 (three protrusions in the present embodiment) are provided on the lower surface 23a of the flange portion 23 at equal intervals in the circumferential direction, and the flange portion 23 is provided with the accommodation container 30 via these protrusions 24. It is placed at the top of. Since such a protrusion 24 is provided on the lower surface 23a of the flange portion 23, a gap 26 is defined between the lower surface 23a of the flange portion 23 (excluding the region where the protrusion 24 is formed) and the upper end of the storage container 30. Then, the air in the storage container 30 can escape to the outside through the gap 26.

図4は、図1に示す検査ユニットを構成する収容容器を示す斜視図であり、(a)は蓋体を開放した際の状態を示し、(b)は蓋体を閉じた際の状態を示す。収容容器30は、図1、図2及び図4に示すように、容器本体31と蓋体32とを備えて構成されている。収容容器30の容器本体31や蓋体32は、透明なポリプロピレン(PP)、ポリスチレン(PS)、アクリロニトリルスチレン(AS)、又はポリエチレン(PE)等の樹脂を射出成型することにより、それぞれ形成することができる。収容容器30では、蓋体32の紛失等を防止するため、容器本体31や蓋体32を連結部材34で互いに連結するようにしてもよく、この連結部材34が蓋体32と一体成型されていてもよい。 4A and 4B are perspective views showing a storage container constituting the inspection unit shown in FIG. 1, where FIG. 4A shows a state when the lid is opened, and FIG. 4B shows a state when the lid is closed. Shown. As shown in FIGS. 1, 2 and 4, the storage container 30 includes a container body 31 and a lid 32. The container body 31 and the lid 32 of the storage container 30 are each formed by injection molding a resin such as transparent polypropylene (PP), polystyrene (PS), acrylonitrile styrene (AS), or polyethylene (PE). Can be done. In the storage container 30, in order to prevent the lid 32 from being lost, the container body 31 and the lid 32 may be connected to each other by a connecting member 34, and the connecting member 34 is integrally molded with the lid 32. You may.

容器本体31は、一端が開口する有底筒形状の容器であり、例えば円筒形状の容器から構成される。容器本体31の開口部33は、その内周面が平坦になっており、蓋体32が閉じた際に、当該蓋体32により容易に密封できるように構成されている。つまり、蓋体32は、この開口部33を開閉自在とすることができるように構成されている。なお、容器本体31は、検査対象液体(例えば血液)が収容できる大きさであれば特にその大きさに限定はない。 The container body 31 is a bottomed cylindrical container having one end open, and is composed of, for example, a cylindrical container. The inner peripheral surface of the opening 33 of the container body 31 is flat so that when the lid 32 is closed, the opening 33 can be easily sealed by the lid 32. That is, the lid 32 is configured so that the opening 33 can be opened and closed. The size of the container body 31 is not particularly limited as long as it can accommodate the liquid to be inspected (for example, blood).

続いて、このような構成を有する採取部材20と収容容器30とから構成される検査ユニットによる採血作業について、図5を参照して説明する。図5は、図1に示す検査ユニットの使用例を示す図であり、(a)は、血液の採取時の方法を示し、(b)は採取した血液を収容容器に移し替える際の方法を示す。 Subsequently, the blood collection operation by the inspection unit composed of the collection member 20 having such a configuration and the storage container 30 will be described with reference to FIG. 5A and 5B are views showing an example of use of the test unit shown in FIG. 1, FIG. 5A shows a method for collecting blood, and FIG. 5B shows a method for transferring the collected blood to a storage container. Shown.

図5(a)に示すように、検査対象である血液を採取するには、まず検査対象者の指等に採血針(不図示)を指して、血液が出た状態にし、検査ユニット10の採取部材20の先端をその血液Bに接するように検査ユニット10を配置する。このような配置により、毛細管現象で血液Bが採取部材20の細管部21の内孔21a内を基端21c側に進むように採取される。検査ユニット10では、毛細管現象を利用して血液Bを採取しているため、スポイトのようにその一端に設けられた袋を用いて中を負圧にする必要はない。 As shown in FIG. 5A, in order to collect blood to be tested, first, a blood sampling needle (not shown) is pointed at the finger or the like of the test subject to make blood flow, and then the test unit 10 is used. The test unit 10 is arranged so that the tip of the collection member 20 is in contact with the blood B. With such an arrangement, blood B is collected so as to advance in the inner hole 21a of the capillary portion 21 of the collection member 20 toward the proximal end 21c due to the capillary phenomenon. Since the test unit 10 collects blood B by utilizing the capillary phenomenon, it is not necessary to use a bag provided at one end of the blood B like a dropper to create a negative pressure inside.

続いて、採取部材20の細管部21内に検査対象である血液Bが採取されると、検査ユニット10をその収容容器30が下にくるように机等の上に配置する。そして、図5(b)に示すように、採取部材20の上方に小型のゴム袋等からなる送出し部材であるエアーキャップSを被せ、エアーキャップSを指で押圧することで、細管部21内の血液Bを下方に押し出し、収容容器30へと血液Bを移動させる。この際、収容容器30内の空気が採取部材20と収容容器30との間に位置する空隙26から外部に逃げ出すため、採取部材20から収容容器30への血液の移動がスムーズに行われる。また、空隙26は、嵌合部22の外側上方に設けられているため、嵌合部22の内孔22a内を流れる血液によって塞がれることもない。このような空隙26の配置構成により、血液等の移動作業が損なわれないようにすることが可能となる。なお、収容容器30には、血液検査のため、アクリル樹脂ゲルやポリエステルゲルといった血漿分離剤Lが収容されていてもよい(図4及び図5参照)。この場合、検査前に予め血液から血漿のみを分離することで、検査の迅速性及び精度を向上させることができる。 Subsequently, when blood B to be inspected is collected in the thin tube portion 21 of the collection member 20, the inspection unit 10 is arranged on a desk or the like so that the storage container 30 is on the bottom. Then, as shown in FIG. 5B, the thin tube portion 21 is covered with an air cap S, which is a sending member made of a small rubber bag or the like, on the sampling member 20, and the air cap S is pressed with a finger. The blood B inside is pushed downward, and the blood B is moved to the storage container 30. At this time, since the air in the storage container 30 escapes to the outside from the gap 26 located between the collection member 20 and the storage container 30, blood is smoothly transferred from the collection member 20 to the storage container 30. Further, since the gap 26 is provided above the outer side of the fitting portion 22, the gap 26 is not blocked by the blood flowing in the inner hole 22a of the fitting portion 22. With such an arrangement of the voids 26, it is possible to prevent the movement work of blood and the like from being impaired. The storage container 30 may contain a plasma separating agent L such as an acrylic resin gel or a polyester gel for a blood test (see FIGS. 4 and 5). In this case, the speed and accuracy of the test can be improved by separating only plasma from the blood in advance before the test.

以上、上述した検査ユニット10によれば、採取部材20の嵌合部22が収容容器30の一端の開口部33に嵌合可能となるように構成されており、しかも、収容容器30内の空気を外部に逃がすための空隙26が採取部材20と収容容器30との嵌合領域に設けられている。このため、血液等の検査対象液体を毛細管現象等を利用して採取部材20の細管部21によって採取した後、所定の力を細管部21又は検査対象流体に加えることで細管部21内の検査対象流体を収容容器30が位置する下方に移動させようとした際、収容容器30内の空気が検査対象流体の移動に応じてそれらの中間に位置する嵌合領域の空隙26から外部に向かってスムーズに逃げることができる。その結果、検査ユニット10によれば、細管部21で採取した検査対象流体の血液B等を収容容器30内に容易に移動させることができ、血液B等の検査対象流体の採取後に検査対象流体を採取部材20から収容容器30に容易に移し替えることが可能となる。なお、この空隙26については、図からも明らかであるが、収容容器30内の空気の一部(微量な空気)を外部に逃がすためのものであるため、過大な空隙である必要はないことから、このような空隙26が設けられていても、検査対象流体への影響は軽微なものとすることが可能である。 As described above, according to the inspection unit 10 described above, the fitting portion 22 of the sampling member 20 is configured to be able to be fitted into the opening 33 at one end of the storage container 30, and the air in the storage container 30. A gap 26 is provided in the fitting region between the sampling member 20 and the storage container 30 to allow the air to escape to the outside. Therefore, after the liquid to be inspected such as blood is collected by the thin tube portion 21 of the collecting member 20 by utilizing the capillary phenomenon or the like, a predetermined force is applied to the thin tube portion 21 or the fluid to be inspected to inspect the inside of the thin tube portion 21. When the target fluid is to be moved downward where the storage container 30 is located, the air in the storage container 30 moves outward from the gap 26 of the fitting region located in the middle of the target fluid according to the movement of the target fluid. You can escape smoothly. As a result, according to the inspection unit 10, the blood B or the like of the inspection target fluid collected in the capillary portion 21 can be easily moved into the storage container 30, and the inspection target fluid after the inspection target fluid such as the blood B is collected. Can be easily transferred from the sampling member 20 to the storage container 30. As is clear from the figure, the void 26 does not need to be an excessive void because it is for allowing a part of the air (a trace amount of air) in the storage container 30 to escape to the outside. Therefore, even if such a gap 26 is provided, the influence on the fluid to be inspected can be made minor.

また、検査ユニット10では、採取部材20は、嵌合部22が収容容器30の開口部33の内周部に接合するように収容容器30に取り付けられている。このため、採取部材20と収容容器30との嵌合領域に位置する空隙26を設け易くなり、また、収容容器30の外周側に嵌合部が配置されないので、蓋体32を容器本体31に連結するような連結部材34を容器本体31の外周に設けやすくなる。 Further, in the inspection unit 10, the sampling member 20 is attached to the storage container 30 so that the fitting portion 22 is joined to the inner peripheral portion of the opening 33 of the storage container 30. Therefore, it becomes easy to provide a gap 26 located in the fitting region between the collecting member 20 and the storage container 30, and since the fitting portion is not arranged on the outer peripheral side of the storage container 30, the lid 32 is attached to the container body 31. It becomes easy to provide a connecting member 34 for connecting to the outer periphery of the container body 31.

また、検査ユニット10では、採取部材20は、細管部21と嵌合部22との間にフランジ部23を更に有し、当該フランジ部23の嵌合部22側の下面23aに複数の突起24が設けられ、当該突起24により空隙26が画定されている。このように、空隙26を画定する部材(突起24やリブ25等)を採取部材20(嵌合部22)側に設けることにより、収容容器30側、特に嵌合部22と嵌合する部分(開口部33)の内周形状を単純又は平坦面状なものとすることができる。このため、例えば、自己採血等の検査を行う場合、検査液収容後の収容容器30は、蓋体32を開口部33に嵌めてしっかりと密封した上で検査機関に送る必要があるが(図4(b)参照)、上述したように、収容容器30の開口部33側をスムーズ(平坦面)な形状とできることにより、蓋体32による収容容器30の密封性を容易に高めることができる。 Further, in the inspection unit 10, the sampling member 20 further has a flange portion 23 between the thin tube portion 21 and the fitting portion 22, and a plurality of protrusions 24 on the lower surface 23a of the flange portion 23 on the fitting portion 22 side. Is provided, and the gap 26 is defined by the protrusion 24. In this way, by providing the member (projection 24, rib 25, etc.) that defines the gap 26 on the collection member 20 (fitting portion 22) side, the portion that fits with the storage container 30 side, particularly the fitting portion 22 (the fitting portion 22). The inner peripheral shape of the opening 33) can be a simple or flat surface. Therefore, for example, when performing a test such as self-collection of blood, the storage container 30 after storing the test solution needs to be sent to the testing institution after the lid 32 is fitted into the opening 33 and tightly sealed (Fig. 4 (b)), as described above, since the opening 33 side of the storage container 30 can be formed into a smooth (flat surface) shape, the sealing property of the storage container 30 by the lid 32 can be easily improved.

また、検査ユニット10では、細管部21の内孔21aは、採取部材20の先端21bから基端21cに向かってテーパ状に広がっている。上述した検査ユニット10の採取部材20は、いわゆる毛細管現象を利用して細管部21の内孔21aに検査対象液体が入り込むことを想定して設計されうるが、基端21c(収容容器)側の内径が先端21b側よりも広がるように形成しておくことにより、細管部21や検査対象流体に対して所定の力を加えた際に、細管部21内の検査対象流体が重力等により下方の収容容器30へ移動しやすくなる。より具体的には、細管部21の基端21c側の内孔の内径を大きくしておくことにより、その領域における毛細管現象による力を弱め、採取された検査対象流体を収容容器30側に移動しやすくしておくことが可能となる。このように、上記構成によれば、血液等の検査対象流体の採取後に検査対象流体を採取部材20から収容容器30に更に容易に移し替えることが可能となる。なお、この場合において、細管部21の内孔21aは、その基端21c側の内径がその先端21b側の内径の2倍以上であることが、移し替えの容易性の観点では好ましい。 Further, in the inspection unit 10, the inner hole 21a of the thin tube portion 21 extends in a tapered shape from the tip end 21b of the sampling member 20 toward the base end 21c. The sampling member 20 of the inspection unit 10 described above can be designed on the assumption that the fluid to be inspected enters the inner hole 21a of the capillary portion 21 by utilizing the so-called capillary phenomenon, but the sampling member 20 on the base end 21c (container container) side. By forming the inner diameter so as to be wider than the tip 21b side, when a predetermined force is applied to the capillary portion 21 and the fluid to be inspected, the fluid to be inspected in the capillary portion 21 is lowered due to gravity or the like. It becomes easy to move to the storage container 30. More specifically, by increasing the inner diameter of the inner hole on the base end 21c side of the capillary portion 21, the force due to the capillary phenomenon in that region is weakened, and the collected fluid to be inspected is moved to the storage container 30 side. It becomes possible to make it easy. As described above, according to the above configuration, it is possible to more easily transfer the test target fluid from the collection member 20 to the storage container 30 after collecting the test target fluid such as blood. In this case, it is preferable that the inner diameter of the inner hole 21a of the thin tube portion 21 on the base end 21c side is twice or more the inner diameter on the tip end 21b side from the viewpoint of ease of transfer.

[第2実施形態]
次に、図6〜図8を参照して、本発明に係る検査ユニットの第2実施形態について説明する。図6は、本発明の第2実施形態に係る検査ユニットを示す斜視図である。図7は、図6に示す検査ユニットを構成する採取部材を示し、(a)は側面図を示し、(b)は下面図を示し、(c)は下方からの斜視図を示す。図8は、図6に示す検査ユニットを構成する収容容器を示し、(a)は上面図を示し、(b)は断面図を示す。なお、以下の説明では、第1実施形態に係る検査ユニット10と相違する点について主に説明し、同じ点については、説明を省略する場合がある。
[Second Embodiment]
Next, a second embodiment of the inspection unit according to the present invention will be described with reference to FIGS. 6 to 8. FIG. 6 is a perspective view showing an inspection unit according to a second embodiment of the present invention. 7A and 7B show a sampling member constituting the inspection unit shown in FIG. 6, FIG. 7A shows a side view, FIG. 7B shows a bottom view, and FIG. 7C shows a perspective view from below. 8A and 8B show a storage container constituting the inspection unit shown in FIG. 6, FIG. 8A shows a top view, and FIG. 8B shows a cross-sectional view. In the following description, the differences from the inspection unit 10 according to the first embodiment will be mainly described, and the description may be omitted for the same points.

図6〜図8に示すように、検査ユニット40は、血液などの検査対象流体を採取するための採取部材50と、採取部材50により採取された検査対象流体を収容する収容容器60とを備えて構成されている。検査ユニット40は、第1実施形態と同様に、例えば検査希望者が自身の指などに採血針を指して出てきた血液などの検査対象流体を採取し、採取した検査対象流体を検査機関に送り、検査してもらうための自己検査ユニットである。 As shown in FIGS. 6 to 8, the inspection unit 40 includes a collection member 50 for collecting a fluid to be inspected such as blood, and a storage container 60 for accommodating the fluid to be inspected collected by the collection member 50. It is composed of. Similar to the first embodiment, the inspection unit 40 collects the test target fluid such as blood that comes out by the test applicant pointing the blood collection needle at his / her finger or the like, and sends the collected test target fluid to the test institution. It is a self-inspection unit for sending and inspecting.

採取部材50は、細管部51と、嵌合部52と、フランジ部53と、補強リブ58とを主に備えている。細管部51は、第1実施形態の細管部21と略同様の形状である。また、フランジ部53は、第1実施形態のフランジ部23と略同様の形状であるが、その下面に突起を備えない点で相違している。 The sampling member 50 mainly includes a thin tube portion 51, a fitting portion 52, a flange portion 53, and a reinforcing rib 58. The thin tube portion 51 has substantially the same shape as the thin tube portion 21 of the first embodiment. Further, the flange portion 53 has substantially the same shape as the flange portion 23 of the first embodiment, but is different in that the lower surface thereof is not provided with a protrusion.

嵌合部52は、細管部51の基端21c側に設けられた中空の略円筒形状の部材であり、第1実施形態の嵌合部22と略同様の形状を有しており、収容容器60の開口部63に嵌合され、採取部材50を収容容器60に取り付ける。嵌合部52は、第1実施形態の嵌合部22と異なり、その外周面に断面L字状の溝56が設けられている。この溝56により、収容容器60内の空気が外部に逃げることができるようになっている。また、嵌合部52には、その内周側に複数の誘導リブ57(第2誘導リブ)が設けられている。誘導リブ57は、周方向と直行(交差)する長手方向に延びるように嵌合部52の内孔52aにその略全長に渡って形成されており、誘導リブ57により、細管部51の内孔51a内に採取された血液等が嵌合部52の内孔52a内に移動するように誘導される。 The fitting portion 52 is a hollow substantially cylindrical member provided on the base end 21c side of the thin tube portion 51, and has substantially the same shape as the fitting portion 22 of the first embodiment, and is a storage container. It is fitted into the opening 63 of 60, and the sampling member 50 is attached to the storage container 60. Unlike the fitting portion 22 of the first embodiment, the fitting portion 52 is provided with a groove 56 having an L-shaped cross section on its outer peripheral surface. The groove 56 allows the air in the storage container 60 to escape to the outside. Further, the fitting portion 52 is provided with a plurality of guide ribs 57 (second guide ribs) on the inner peripheral side thereof. The guide rib 57 is formed in the inner hole 52a of the fitting portion 52 so as to extend in the longitudinal direction perpendicular (intersecting) with the circumferential direction over substantially the entire length, and the guide rib 57 forms an inner hole of the thin tube portion 51. The blood or the like collected in the 51a is guided to move into the inner hole 52a of the fitting portion 52.

収容容器60は、図6及び図8に示すように、容器本体61と蓋体62とを備えて構成されている。蓋体62は、連結部材64により容器本体61に取り付けられている。蓋体62は第1実施形態と同様の構成である。 As shown in FIGS. 6 and 8, the storage container 60 includes a container body 61 and a lid 62. The lid 62 is attached to the container body 61 by a connecting member 64. The lid 62 has the same configuration as that of the first embodiment.

容器本体61は、一端が開口する有底筒形状の容器であり、例えば円筒形状の容器から構成される。容器本体61の開口部63は、その内周面が平坦になっており、蓋体62が閉じた際に、当該蓋体62により容易に密封できるように構成されている。また、容器本体61の内周面には、その周方向に直行(交差)する方向に延びる2つの誘導リブ65(第1誘導リブ)が設けられている。誘導リブ65は、嵌合部52の内孔52aまで誘導された血液を更に収容容器60へ誘導して移動させるための部材である。誘導リブ65は、採取部材50が収容容器60に嵌め合わされた際に嵌合部52が開口部63に嵌合する領域の手前まで延びるように形成されており、両者の嵌合を阻害しないように構成されている。一方、誘導リブ65は、採取部材50が収容容器60に嵌め合わされた際には、嵌合部52の誘導リブ57に接触可能である又は検査対象流体を誘導できる程度に近接して配置されていてもよい。 The container body 61 is a bottomed tubular container having one end open, and is composed of, for example, a cylindrical container. The inner peripheral surface of the opening 63 of the container body 61 is flat, and is configured so that when the lid 62 is closed, the opening 63 can be easily sealed by the lid 62. Further, on the inner peripheral surface of the container body 61, two guide ribs 65 (first guide ribs) extending in a direction perpendicular (intersecting) in the circumferential direction are provided. The guide rib 65 is a member for further guiding and moving the blood guided to the inner hole 52a of the fitting portion 52 to the storage container 60. The guide rib 65 is formed so that when the sampling member 50 is fitted into the storage container 60, the fitting portion 52 extends to the front of the region where the fitting portion 52 fits into the opening 63, so as not to hinder the fitting of the two. It is configured in. On the other hand, when the sampling member 50 is fitted into the storage container 60, the guide ribs 65 are arranged so close that they can come into contact with the guide ribs 57 of the fitting portion 52 or can guide the fluid to be inspected. You may.

このような構成の検査ユニットによれば、第1実施形態と同様に、検査ユニットによる採血作業を行うことができるが、特に図9及び図10に示すように、採取部材50から収容容器60への検査対象流体の移動を更に容易に行うことが可能である。より具体的には、本実施形態に係る検査ユニット40によれば、まず図9(a)及び図10(a)に示すように、採取部材50と収容容器60との嵌め合わせがやや不完全な状態(両者間に多少の隙間がある状態)で、血液等の採取を行う。そして、採取が終了した後、図9(b)及び図10(b)に示すように、採取部材50を収容容器60に向かって押し込み、両者を嵌合させる。その際、採取部材50の誘導リブ57と収容容器60の誘導リブ65とが接触するようにさせることで、両誘導リブ57,65による誘導により、採取部材50内の血液等が収容容器60内へと誘導される。なお、本実施形態では、嵌合部52の誘導リブ57と容器本体61の誘導リブ65とはその数が異なっているが、このように数が異なることにより、誘導リブ57と誘導リブ65とが接触していない状態も容易に作り出すことができ、接触しない位置関係で血液の採取を行い、その後、採取部材を回転させながら押し込むことで両誘導リブ57,65が接触するようにすることで、採取部材50から収容容器60への血液等の移動を開始させることができる。なお、第2実施形態の検査ユニット40では、上述したように誘導リブを用いて採取部材50から収容容器60への血液等の移動を行うようにしているが、第1実施形態のように、ゴム状のエアーキャップS(図5(b)参照)を更に用いてもよい。 According to the inspection unit having such a configuration, the blood collection operation can be performed by the inspection unit as in the first embodiment, but as shown in FIGS. 9 and 10, the collection member 50 is transferred to the storage container 60. It is possible to move the fluid to be inspected more easily. More specifically, according to the inspection unit 40 according to the present embodiment, first, as shown in FIGS. 9A and 10A, the fitting of the collecting member 50 and the storage container 60 is slightly incomplete. Collect blood, etc. in a normal state (with some gap between the two). Then, after the collection is completed, as shown in FIGS. 9 (b) and 10 (b), the collection member 50 is pushed toward the storage container 60 to fit the two. At that time, the guide ribs 57 of the collection member 50 and the guide ribs 65 of the storage container 60 are brought into contact with each other, so that the blood and the like in the collection member 50 can be brought into the storage container 60 by the guidance by both guide ribs 57 and 65. Is guided to. In the present embodiment, the number of the guide ribs 57 of the fitting portion 52 and the number of the guide ribs 65 of the container body 61 are different, but due to the difference in the numbers, the guide ribs 57 and the guide ribs 65 It is possible to easily create a state in which the blood is not in contact with each other. Blood is collected in a positional relationship where the blood is not in contact with each other, and then the blood collection members are pushed in while rotating so that the both guide ribs 57 and 65 come into contact with each other. , The movement of blood or the like from the collection member 50 to the storage container 60 can be started. In the inspection unit 40 of the second embodiment, as described above, the guide rib is used to move the blood or the like from the collection member 50 to the storage container 60, but as in the first embodiment, A rubber-like air cap S (see FIG. 5B) may be further used.

以上、上述した検査ユニット40によれば、第1実施形態の検査ユニット10と同様に、細管部51で採取した検査対象流体の血液B等を収容容器60内に容易に移動させることができ、血液B等の検査対象流体の採取後に検査対象流体を採取部材50から収容容器60に容易に移し替えることが可能となる。 As described above, according to the above-mentioned inspection unit 40, the blood B or the like of the fluid to be inspected collected in the capillary tube 51 can be easily moved into the storage container 60 as in the inspection unit 10 of the first embodiment. After collecting the test target fluid such as blood B, the test target fluid can be easily transferred from the collection member 50 to the storage container 60.

また、検査ユニット40では、嵌合部52の外周に周方向と直行する方向に延びる溝56が形成され、溝56が収容容器60内の空気を外に逃がす空隙の少なくとも一部を構成するようになっている。このように、空隙に相当する溝56を採取部材50(嵌合部52)側に設けることにより、収容容器60側、特に嵌合部52と嵌合する部分の形状を単純又は平坦面状なものとすることができる。このため、例えば、自己採血等の検査を行う場合、検査液収容後の収容容器60は、蓋体62を開口部63に嵌めてしっかりと密封した上で検査機関に送る必要があるが、上述したように、収容容器60の開口部63をスムーズ(平坦面)な形状とすることができることにより、蓋体62による収容容器60の密封性を容易に高めることができる。 Further, in the inspection unit 40, a groove 56 extending in a direction perpendicular to the circumferential direction is formed on the outer periphery of the fitting portion 52, and the groove 56 constitutes at least a part of a gap for allowing air in the storage container 60 to escape to the outside. It has become. By providing the groove 56 corresponding to the gap on the sampling member 50 (fitting portion 52) side in this way, the shape of the storage container 60 side, particularly the portion to be fitted with the fitting portion 52, is simple or flat. Can be. Therefore, for example, when performing a test such as self-collection of blood, the storage container 60 after storing the test liquid needs to be sent to the testing institution after the lid 62 is fitted into the opening 63 and tightly sealed. As described above, since the opening 63 of the storage container 60 can be formed into a smooth (flat surface) shape, the sealing property of the storage container 60 by the lid 62 can be easily improved.

また、検査ユニット40では、収容容器60の容器本体61の内周面に、周方向と直行する長手方向に延びる誘導リブ65が設けられ、誘導リブ65は開口部63の手前まで伸びている。このため、採取部材50に採取保持されている検査対象流体の一部、例えばその下端が、収容容器60内の誘導リブ65に触れると、表面張力等の吸引により、誘導リブ65に沿って収容容器60の中へと誘導されやくなる。このため、誘導リブ65を設けておくことにより、血液等の検査対象流体の採取後に検査対象流体を採取部材50から収容容器60に更に容易に移し替えることが可能となる。この場合において、収容容器60側に位置する嵌合部52の内周面に、周方向と直行する長手方向に延びる誘導リブ57が更に設けられ、誘導リブ57が、採取部材50と収容容器60とが嵌合された際に誘導リブ65と接触可能となっている。このため、採取部材50内の検査対象流体がまずは誘導リブ57により収容容器60側に誘導され、その後、誘導リブ65により収容容器60内へと誘導されることになるため、採取部材50から収容容器60に更に一層、容易に移し替えることが可能となる。 Further, in the inspection unit 40, a guide rib 65 extending in the longitudinal direction perpendicular to the circumferential direction is provided on the inner peripheral surface of the container body 61 of the container 60, and the guide rib 65 extends to the front of the opening 63. Therefore, when a part of the fluid to be inspected collected and held by the sampling member 50, for example, the lower end thereof touches the guide rib 65 in the storage container 60, it is stored along the guide rib 65 by suction of surface tension or the like. It becomes easy to be guided into the container 60. Therefore, by providing the guide rib 65, it is possible to more easily transfer the test target fluid from the collection member 50 to the storage container 60 after collecting the test target fluid such as blood. In this case, a guide rib 57 extending in the longitudinal direction perpendicular to the circumferential direction is further provided on the inner peripheral surface of the fitting portion 52 located on the storage container 60 side, and the guide rib 57 is the collecting member 50 and the storage container 60. When and are fitted, they can come into contact with the induction rib 65. Therefore, the fluid to be inspected in the sampling member 50 is first guided to the storage container 60 side by the guide rib 57, and then guided into the storage container 60 by the guide rib 65, so that the fluid is housed from the sampling member 50. It can be even more easily transferred to the container 60.

なお、本実施形態では、誘導リブ57,65は、互いに異なる数がそれぞれ設けられている。このような構成により、誘導リブ57と誘導リブ65とが接触する場合と接触しない場合とを採取部材50の回転等により切り替えることが容易に行えるため、採取部材50から収容容器60への移し替えのタイミングをリブの位置合わせにより調整することが可能となる。 In the present embodiment, the guide ribs 57 and 65 are provided with different numbers. With such a configuration, it is possible to easily switch between the case where the guide rib 57 and the guide rib 65 are in contact with each other and the case where the guide rib 65 is not in contact with each other by rotating the collecting member 50 or the like. Therefore, the collection member 50 is transferred to the storage container 60. It is possible to adjust the timing of the above by aligning the ribs.

以上、本発明の好適な実施形態について説明したが、本発明は上記実施形態に限定されるものではなく、種々の変形を適用できる。例えば、上記第2実施形態では、嵌合部52の外周面に1つの溝56を設け、これを空隙とするようにしたが、第1実施形態において空隙26を構成する突起24やリブ25を第2実施形態の嵌合部52に更に設けるようにして、空隙を広げるようにしてもよいし、また複数の溝56を設けるようにしてもよい。また、上述した実施形態では、空隙26や溝56に特に何らかの部材を設けていなかったが、これらの空隙等を介して外部から内部への汚染粒子等の浸入が気になる検査分野においては、当該部分に気体が通過可能なフィルタなどを設けるようにしてもよい。また、上記実施形態では、採取部材20,50と収容容器30,60とは郵送時に別々に箱に収容されており、使用時に採取部材20,50を収容容器30,60に嵌合させて両者を一体化させて採取していたが、用途によっては、採取部材20,50と収容容器30,60とを予め嵌合して一体化させておき、それをそのまま郵送して使用するようにしてもよい。 Although the preferred embodiment of the present invention has been described above, the present invention is not limited to the above embodiment, and various modifications can be applied. For example, in the second embodiment, one groove 56 is provided on the outer peripheral surface of the fitting portion 52 to form a gap, but in the first embodiment, the protrusions 24 and ribs 25 forming the gap 26 are provided. The fitting portion 52 of the second embodiment may be further provided to widen the gap, or a plurality of grooves 56 may be provided. Further, in the above-described embodiment, no particular member is provided in the gap 26 or the groove 56, but in the inspection field where infiltration of contaminated particles or the like from the outside to the inside through these gaps or the like is a concern. A filter or the like through which gas can pass may be provided in the portion. Further, in the above embodiment, the collection members 20, 50 and the storage containers 30, 60 are separately housed in a box at the time of mailing, and the collection members 20, 50 are fitted into the storage containers 30, 60 at the time of use, and both are used. However, depending on the application, the collection members 20 and 50 and the storage containers 30 and 60 are previously fitted and integrated, and the collection members 20 and 50 are mailed as they are for use. May be good.

また、上記の実施形態では、検査ユニット10,40の採取部材20,50の先端21b等の内孔形状については特に限定していないが、図11(a)及び(b)に示すように、採取部材71の先端71aが内側テーパ形状となっていてもよいし、採取部材81の先端81aが内側R形状となっていてもよい。図11(a)に示す先端71aの内側テーパ形状の傾斜角は、採取部材71の外周面と平行な線に対してその傾斜角が例えば45°以下であってもよい。また、図11(b)に示す先端81aの内側テーパ形状のR部は、そのRが1mm〜10mmの範囲であってもよい。このような先端形状とすることにより、検査ユニット(採取部材)による血液等の採取吸引をより行い易くすることが可能となる。 Further, in the above embodiment, the inner hole shape of the tips 21b and the like of the sampling members 20 and 50 of the inspection units 10 and 40 is not particularly limited, but as shown in FIGS. 11A and 11B, The tip 71a of the sampling member 71 may have an inner tapered shape, or the tip 81a of the sampling member 81 may have an inner R shape. The inclination angle of the inner tapered shape of the tip 71a shown in FIG. 11A may be, for example, 45 ° or less with respect to a line parallel to the outer peripheral surface of the sampling member 71. Further, the R portion of the inner tapered shape of the tip 81a shown in FIG. 11B may have an R portion in the range of 1 mm to 10 mm. With such a tip shape, it becomes possible to facilitate the collection and suction of blood or the like by the inspection unit (collection member).

10,40…検査ユニット、20,50…採取部材、21,51…細管部、21a…内孔、21b…先端、21c…基端、22,52…嵌合部、22a,52a…内孔、23,53…フランジ部、23a…下面、24…突起、25…リブ、26…空隙、30,60…収容容器、31,61…容器本体、32,62…蓋体、33,63…開口部、56…溝(空隙)、57…誘導リブ(第2誘導リブ)、58…補強リブ、65…誘導リブ(第1誘導リブ)、B…血液(検査対象流体)。 10,40 ... Inspection unit, 20,50 ... Collecting member, 21,51 ... Thin tube part, 21a ... Inner hole, 21b ... Tip, 21c ... Base end, 22,52 ... Fitting part, 22a, 52a ... Inner hole, 23, 53 ... Flange, 23a ... Bottom surface, 24 ... Protrusion, 25 ... Rib, 26 ... Void, 30, 60 ... Storage container, 31, 61 ... Container body, 32, 62 ... Lid, 33, 63 ... Opening , 56 ... Groove (void), 57 ... Induction rib (second induction rib), 58 ... Reinforcing rib, 65 ... Induction rib (first induction rib), B ... Blood (fluid to be inspected).

Claims (10)

検査対象流体を採取するための採取部材と、
前記採取部材により採取された前記検査対象流体を収容する収容容器と、を備え、
前記採取部材は、先端から基端に向かって延びる中空の細管部と、当該細管部の基端側に設けられる中空の嵌合部とを有し、
前記収容容器は、一端が開口する有底筒形状の容器本体と、前記容器本体の当該開口を開閉自在な蓋体とを有し、
前記採取部材の前記嵌合部は、前記収容容器の前記一端に嵌合可能となるように構成され、前記収容容器内の空気を外部に逃がすための空隙が前記採取部材と前記収容容器との嵌合領域に設けられており、
前記採取部材は、前記細管部と前記嵌合部との間にフランジ部を更に有し、当該フランジ部の前記嵌合部側の面に突起又は溝が設けられ、当該突起又は溝により前記空隙が画定される、検査ユニット。
A sampling member for sampling the fluid to be inspected, and
A storage container for accommodating the fluid to be inspected collected by the collection member is provided.
The collecting member has a hollow thin tube portion extending from the tip toward the proximal end and a hollow fitting portion provided on the proximal end side of the thin tube portion.
The storage container has a bottomed cylindrical container body having one end opened and a lid body capable of opening and closing the opening of the container body.
The fitting portion of the collecting member is configured so as to be able to be fitted to the one end of the containing container, and a gap for letting air in the containing container escape to the outside is formed between the collecting member and the containing container. It is provided in the mating area and
The collecting member further has a flange portion between the thin tube portion and the fitting portion, and a protrusion or groove is provided on the surface of the flange portion on the fitting portion side, and the gap is formed by the protrusion or groove. Is defined, the inspection unit.
前記採取部材は、前記嵌合部が前記収容容器の前記開口の内周部に接合するように前記収容容器に取り付け可能である、請求項1に記載の検査ユニット。 The inspection unit according to claim 1, wherein the sampling member can be attached to the storage container so that the fitting portion is joined to the inner peripheral portion of the opening of the storage container. 前記空隙は、少なくとも一部が前記フランジ部の前記嵌合部側の面に沿って延びる、請求項1又は2に記載の検査ユニット。The inspection unit according to claim 1 or 2, wherein at least a part of the gap extends along a surface of the flange portion on the fitting portion side. 前記溝は、前記嵌合部の外周において周方向と交差する方向に延び、当該溝が前記空隙の少なくとも一部を構成する、請求項1〜3の何れか一項に記載の検査ユニット。 The groove extends in a direction crossing the Oite circumferential direction on the outer periphery of the fitting portion, the groove constitutes at least a part of the gap, the inspection unit according to any one of claims 1 to 3 .. 前記細管部の内孔は、前記先端から前記基端に向かってテーパ状に広がっている、請求項1〜4の何れか一項に記載の検査ユニット。 The inspection unit according to any one of claims 1 to 4, wherein the inner hole of the thin tube portion extends in a taper shape from the tip end to the base end. 前記細管部の内孔は、前記基端側の内径が前記先端側の内径の2倍以上である、請求項5に記載の検査ユニット。 The inspection unit according to claim 5, wherein the inner hole of the thin tube portion has an inner diameter on the base end side that is at least twice the inner diameter on the tip end side. 前記収容容器の前記容器本体の内周面には、周方向と交差する長手方向に延びる少なくとも1つの第1誘導リブが設けられ、当該第1誘導リブは前記開口の手前まで伸びている、請求項1〜6の何れか一項に記載の検査ユニット。 The inner peripheral surface of the container body of the container is provided with at least one first guide rib extending in the longitudinal direction intersecting the circumferential direction, and the first guide rib extends to the front of the opening. The inspection unit according to any one of Items 1 to 6. 前記嵌合部の内周面には、周方向と交差する長手方向に延びる少なくとも1つの第2誘導リブが設けられ、前記第2誘導リブは、前記採取部材と前記収容容器とが嵌合された際に前記第1誘導リブと接触可能である、請求項7に記載の検査ユニット。 At least one second guide rib extending in the longitudinal direction intersecting the circumferential direction is provided on the inner peripheral surface of the fitting portion, and the collecting member and the storage container are fitted to the second guide rib. The inspection unit according to claim 7, which can come into contact with the first guide rib at the time. 前記第1誘導リブ及び前記第2誘導リブは、互いに異なる数がそれぞれ設けられている、請求項8に記載の検査ユニット。 The inspection unit according to claim 8, wherein the first lead rib and the second lead rib are provided with different numbers of each. 前記収容容器には、血液検査のための血漿分離剤が収容されている、請求項1〜9の何れか一項に記載の検査ユニット。 The test unit according to any one of claims 1 to 9, wherein the storage container contains a plasma separating agent for a blood test.
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