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JPH05157747A - Blood-sampling tube - Google Patents

Blood-sampling tube

Info

Publication number
JPH05157747A
JPH05157747A JP3349130A JP34913091A JPH05157747A JP H05157747 A JPH05157747 A JP H05157747A JP 3349130 A JP3349130 A JP 3349130A JP 34913091 A JP34913091 A JP 34913091A JP H05157747 A JPH05157747 A JP H05157747A
Authority
JP
Japan
Prior art keywords
blood
tube
coagulation
blood coagulation
enzymic
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.)
Pending
Application number
JP3349130A
Other languages
Japanese (ja)
Inventor
Shigeru Sekine
滋 関根
Yoko Horie
葉子 堀江
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nissho Corp
Original Assignee
Nissho Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nissho Corp filed Critical Nissho Corp
Priority to JP3349130A priority Critical patent/JPH05157747A/en
Publication of JPH05157747A publication Critical patent/JPH05157747A/en
Pending legal-status Critical Current

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  • Investigating Or Analysing Biological Materials (AREA)
  • Sampling And Sample Adjustment (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)

Abstract

PURPOSE:To shorten time for coagulation after blood sampling to shorten time for blood inspection thereby and to enable sure execution of separation of clot from serum by a method wherein a blood coagulation accelerating medium impregnated with an enzymic blood coagulation accelerator is held in the central part inside a tube. CONSTITUTION:In this blood-sampling tybe, a blood coagulation accelerating medium which is a carrier having a higher specific gravity than blood and is impregnated with an enzymic blood coagulation accelerator is held in the central part inside the tube. As for the coagulation accelerator, an enzymic agent such as thermobin or venom enzyme is used therefor. The blood-sampling tube may be made of either glass or synthetic resin. In order to make the blood coagulation accelerating medium be held in the central part inside the tube, a support such as nonwoven fabric, filter paper or cloth is used. The nonwoven fabric or the like is used for holding the blood coagulation accelerating medium between tube walls by utilizing the rigidity or elasticity thereof. The support needs to have no hemolytic property, to produce no adverse effect on biochemical inspection, to have such flexibility as to be movable to a hemocyte layer by a stress at the time of centrifugation, and to have such a size as to allow it to sink into the hemocyte layer.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、採血管に関するもので
ある。更に詳しくは血液の凝固を図ることができる採血
管に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a blood collection tube. More specifically, it relates to a blood collection tube capable of coagulating blood.

【0002】[0002]

【従来の技術】採血した全血から血清を遠心分離する場
合、血液凝固が不十分であると遠心分離後いわゆる中間
比重を有する境界面の形成状態が悪く、採血管を横にす
ると血球が血清層に漏れ出たり、フイブリンの発生が多
くなり血清採取量が制限を受けるなどの問題が生じる。
2. Description of the Related Art When serum is centrifuged from collected whole blood, if the blood coagulation is insufficient, a boundary surface having a so-called intermediate specific gravity is formed poorly after centrifugation, and when the blood collection tube is laid down sideways, blood cells become serum. There are problems such as leakage to the layers and generation of fibrin, which limits the amount of serum collected.

【0003】そのため、従来、採血後45分乃至1時間
半をかけて十分に凝固させたのち遠心分離を行っている
が、それでも個体差により、十分な凝固が得られず、フ
イブリンが析出する場合がある。
Therefore, conventionally, 45 minutes to 1 and a half hours after blood collection is sufficiently coagulated and then centrifuged, but still, due to individual differences, sufficient coagulation cannot be obtained and fibrin is deposited. There is.

【0004】このような長時間にわたる凝固時間は血清
分離操作、血液検査の能率上好ましくなく、そのため血
液凝固を促進するための種々の方策が従来提案されてい
る。例えば水溶性ポリマーを用いてガラス粉末を分注し
た容器を採血管内壁にコーテイングする方法、あるいは
ガラス粉末を分注した容器を採血管内に配置させる方法
などが知られている。
Such a long coagulation time is not preferable from the viewpoint of efficiency of serum separation operation and blood test. Therefore, various measures have been conventionally proposed for promoting blood coagulation. For example, a method of coating a container in which glass powder is dispensed with a water-soluble polymer on the inner wall of a blood collection tube, a method of disposing a container in which glass powder is dispensed in a blood collection tube, and the like are known.

【0005】しかし、前者の方法は塗布・乾燥などの工
程が複雑であり、また有機溶剤を使用するため作業環境
上好ましくない、また後者の方法はガラス粉末を収容す
る容器を必要とするためコストが高くなり、また適量の
粉末を分注するための管理上の困難をともなうなどの問
題があった。
However, the former method is complicated in the steps of coating and drying, and is not preferable in the working environment because it uses an organic solvent, and the latter method requires a container for containing glass powder, which is costly. However, there is a problem in that it is difficult to manage for dispensing an appropriate amount of powder.

【0006】このような問題を解決するため、管内に血
液凝固促進媒体を収容した採血管であって、該血液凝固
促進媒体が血液より高比重の担体に、血清に可溶性のバ
インダーを介して粉状血液凝固促進剤を担持させた採血
管が、特公昭58−27933号公報で開示されてい
る。
In order to solve such a problem, a blood collection tube containing a blood coagulation accelerating medium in a tube, the blood coagulation accelerating medium being a carrier having a higher specific gravity than blood and powdered through a binder soluble in serum. A blood collection tube carrying a blood coagulation accelerator is disclosed in Japanese Patent Publication No. 58-27933.

【0007】[0007]

【発明が解決しようとする課題】この特公昭58−27
933号公報に開示された凝固促進剤を入れた採血管又
はこの管と分離剤との組合せのものといえども、凝固時
間がいずれも15分程度かかり、透析患者検体などの抗
凝固剤入りの検体についてはいずれも約40分を要し、
血液の迅速検査には不十分であった。
DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention
Even with a blood collection tube containing a coagulation promoter disclosed in Japanese Patent No. 933 or a combination of this tube and a separating agent, the coagulation time takes about 15 minutes, and the coagulation agent containing an anticoagulant such as a dialysis patient sample is included. It takes about 40 minutes for each sample,
Inadequate for rapid blood tests.

【0008】この特公昭58−27933号公報では粉
状血液凝固促進剤にガラス・カオリン・ベントナイト珪
藻土・珪藻珪土・珪砂から選ばれるために、凝固時間が
長くかかるものと考えられる。
In this Japanese Patent Publication No. 58-27933, it is considered that the powdery blood coagulation promoter is selected from glass, kaolin, bentonite diatomaceous earth, diatomaceous earth and silica sand, so that the coagulation time is long.

【0009】また、血液検査をもっと迅速に行うことに
関し、特開昭56−106157号公報・特開昭57−
142561号公報にヒメハブなどの蛇毒を有効成分と
する血清分離用血液凝固促進剤が好ましいとの開示がな
されている。
Further, regarding a more rapid blood test, JP-A-56-106157 and JP-A-57-57
Japanese Patent No. 142561 discloses that a blood coagulation promoter for serum separation containing a venom such as Himehab as an active ingredient is preferable.

【0010】しかしこの場合、採血管内にある血清分離
剤があれば、これが蛇毒酵素を吸着あるいは隠蔽して、
該酵素の分散を悪くするなど該酵素の働きを減退させる
という問題があった。
However, in this case, if there is a serum separating agent in the blood collection tube, this adsorbs or masks the snake venom enzyme,
There has been a problem that the function of the enzyme is diminished, for example, the dispersion of the enzyme is deteriorated.

【0011】本発明は、粉状血液凝固促進剤を使用した
場合よりも短時間で血液を凝固させ、採血管内の血清分
離剤の影響を受けない採血管を提供する。
The present invention provides a blood collection tube that coagulates blood in a shorter time than when a powdery blood coagulation promoter is used and is not affected by the serum separating agent in the blood collection tube.

【0012】[0012]

【課題を解決するための手段】本発明は,血液より高比
重の担体であり、酵素系血液凝固促進剤を含浸させた血
液凝固促進媒体を管内の中央部に収容したことを特徴と
する採血管を要旨とする。
The present invention is a carrier having a specific gravity higher than that of blood, and is characterized in that a blood coagulation promoting medium impregnated with an enzyme-based blood coagulation promoting agent is contained in a central portion of a tube. The main point is blood vessels.

【0013】本発明において、管内の中央部に血液凝固
促進媒体を収容するということは、管内において血液凝
固促進媒体と管底にある血清分離剤を互いに接しないよ
うにするためで、該媒体と該分離剤が互いに接しない位
置にあれば十分である。
In the present invention, the fact that the blood coagulation promoting medium is contained in the central portion of the tube is to prevent the blood coagulation promoting medium and the serum separating agent at the bottom of the tube from contacting each other in the tube. It is sufficient if the separating agents are in a position where they do not contact each other.

【0014】[0014]

【作用】本発明では採血時に、血液凝固を速やかに促進
する酵素系の促進剤が血中に溶解し、血液を速やかに凝
固させる。それも本発明では血液凝固促進剤が支持体に
より血清分離剤から隔てられて管内の中央部に存在して
いるために、血液凝固の機能を十分に発揮させることが
できる。
In the present invention, at the time of collecting blood, an enzyme-based accelerator that promptly promotes blood coagulation is dissolved in the blood to rapidly coagulate the blood. Also, in the present invention, since the blood coagulation promoter is present in the central portion of the tube separated from the serum separating agent by the support, the blood coagulation function can be sufficiently exerted.

【0015】[0015]

【実施例】以下、本発明の実施例について説明する。本
発明は血清分離剤の有する封止剤(例えばゴム栓)付き
採血管として好適であって、凝固促進剤にトロンビン、
蛇毒酵素(レプチラーゼ・クロタローゼ・オーコード)
等の酵素系薬剤を使用する。なお、血清分離剤は公知の
チキソトロピー性ゲル状物質がよく採用され、採血管は
ガラス製でも合成樹脂製でも差支えない。
EXAMPLES Examples of the present invention will be described below. INDUSTRIAL APPLICABILITY The present invention is suitable as a blood collection tube with a sealant (for example, a rubber stopper) that a serum separating agent has, and thrombin as a coagulation accelerator,
Snake venom enzyme (reptilase, crotarose, ocord)
Enzyme-based drugs such as A well-known thixotropic gel-like substance is often used as the serum separating agent, and the blood collection tube may be made of glass or synthetic resin.

【0016】本発明において、血液凝固促進媒体を管内
の中央部に収容させるために、不織布・濾紙・布等の支
持体が用いられ、その支持体に酵素系血液凝固促進剤を
含浸させる。不織布等が支持体として使用されるという
のは、その剛性又は弾性を利用して血液凝固促進媒体を
管壁間に挟持させるためである。また、支持体は剛性又
は弾性を有することの他、溶血性がないこと・生化学検
査に悪影響を与えないこと・遠心分離時の応力により血
球層へ移動し得る柔軟性を有すること・血球層内に沈み
得る大きさであること等が必要である。
In the present invention, a support such as a non-woven fabric, a filter paper or a cloth is used to contain the blood coagulation promoting medium in the central portion of the tube, and the support is impregnated with the enzyme-based blood coagulation promoting agent. The non-woven fabric or the like is used as the support in order to hold the blood coagulation promoting medium between the tube walls by utilizing its rigidity or elasticity. In addition to having rigidity or elasticity, the support does not have hemolytic properties-It does not adversely affect biochemical tests-It has the flexibility to move to the blood cell layer due to the stress during centrifugation-The blood cell layer It is necessary that the size is such that it can sink inside.

【0017】ヒメハブの毒液を有効成分とする血清分離
用血液凝固促進剤を利用するときは特開昭56−106
157号公報を参考にして、次のように作製する。
When a blood coagulation promoter for serum separation containing venom of Himehab as an active ingredient is used, it is disclosed in JP-A-56-106.
With reference to Japanese Patent No. 157, it is manufactured as follows.

【0018】生きたままのヒメハブからシヤーレ上に蛇
毒を吐出させ、これを多量集めて、冷却遠心器により4
℃程度で遠心分離し、その上澄みを凍結乾燥して、この
凍結乾燥物を血液凝固促進剤とする。
A snake venom was discharged from a living Himebu on a sheare, and a large amount of this was collected and cooled by a cooling centrifuge.
Centrifugation is performed at about C, and the supernatant is freeze-dried, and the freeze-dried product is used as a blood coagulation promoter.

【0019】ここに得られる凍結乾燥物は、使用に際し
て、必要量を生理食塩水に溶解し、蛇毒液と同程度の濃
度に調製し、孔径0.45μ程度の濾過膜を通して無菌
凝血酵素液とする。
The lyophilized product obtained here is dissolved in physiological saline in a necessary amount at the time of use, adjusted to a concentration similar to that of the snake venom, and passed through a filter membrane having a pore size of about 0.45 μm to prepare a sterile coagulation enzyme solution. To do.

【0020】無菌凝血酵素液には、安定剤・分散剤等を
添加することもある。このような酵素液に支持体を含浸
させ、検体である血液量1ml当たり0.2NIH単位
/mlを使用する。ここでNIH単位とは0.1%フイ
ブリノーゲン溶液1mlを15秒で凝固させる活性単位
である。
Stabilizers and dispersants may be added to the sterile coagulation enzyme solution. The enzyme solution is impregnated with a support, and 0.2 NIH unit / ml is used per 1 ml of the blood sample. The NIH unit is an active unit for coagulating 1 ml of 0.1% fibrinogen solution in 15 seconds.

【0021】本発明の酵素系凝固促進剤を含浸させた媒
体を入れた採血管又はこの管と分離剤との組合せのもの
は、凝固時間がいずれも5分以内であり、透析患者検体
などの抗凝固剤入りの検体についてはいずれも15〜2
0分を要しただけで、血液検査を迅速に行うことができ
た。
The blood collection tube containing the medium impregnated with the enzyme-based coagulation accelerator of the present invention or the combination of this tube and the separating agent has a coagulation time of 5 minutes or less, and is used for dialysis patient specimens and the like. 15 to 2 for samples containing anticoagulant
A blood test could be performed quickly, requiring only 0 minutes.

【0022】[0022]

【発明の効果】本発明の採血管を使用すれば、採血後の
凝固時間が約5分に短縮され、抗凝固剤入り血液に対応
でき、採血後の凝固時間短縮により、血液検査の時間が
短縮される。また、本発明では血液凝固促進媒体を管内
の中央部に有し、血餅と血清の分離が確実に行なえる。
EFFECTS OF THE INVENTION By using the blood collection tube of the present invention, the coagulation time after blood collection can be shortened to about 5 minutes, and blood containing an anticoagulant can be dealt with. Shortened. Further, in the present invention, the blood coagulation promoting medium is provided in the central portion of the tube, and the blood clot and the serum can be reliably separated.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 G01N 33/48 K 7055−2J ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location G01N 33/48 K 7055-2J

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 血液より高比重の担体であり、酵素系血
液凝固促進剤を含浸させた血液凝固促進媒体を管内の中
央部に収容したことを特徴とする採血管。
1. A blood collection tube which is a carrier having a specific gravity higher than that of blood and which contains a blood coagulation promoting medium impregnated with an enzyme-based blood coagulation promoting agent in a central portion of a tube.
JP3349130A 1991-12-06 1991-12-06 Blood-sampling tube Pending JPH05157747A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3349130A JPH05157747A (en) 1991-12-06 1991-12-06 Blood-sampling tube

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3349130A JPH05157747A (en) 1991-12-06 1991-12-06 Blood-sampling tube

Publications (1)

Publication Number Publication Date
JPH05157747A true JPH05157747A (en) 1993-06-25

Family

ID=18401702

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3349130A Pending JPH05157747A (en) 1991-12-06 1991-12-06 Blood-sampling tube

Country Status (1)

Country Link
JP (1) JPH05157747A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2619540A1 (en) * 2010-09-20 2013-07-31 The University of Queensland Serum preparation
JP2015232028A (en) * 2010-03-11 2015-12-24 アントワーヌ テュージィ Method for preparing thrombin serum
WO2020242425A1 (en) * 2019-05-29 2020-12-03 Istanbul Universitesi Rektorlugu Obtaining vitamin/mineral/drug/hormone/enzyme/bio-material composition by means of thrombocyte concentrate

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5838536A (en) * 1981-08-27 1983-03-07 ベクトン・デイツキンソン・アンド・カンパニ− Blood collecting apparatus

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5838536A (en) * 1981-08-27 1983-03-07 ベクトン・デイツキンソン・アンド・カンパニ− Blood collecting apparatus

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015232028A (en) * 2010-03-11 2015-12-24 アントワーヌ テュージィ Method for preparing thrombin serum
JP2017149786A (en) * 2010-03-11 2017-08-31 アントワーヌ テュージィ Thrombin serum preparation, use thereof, and preparation instrument thereof
EP2619540A1 (en) * 2010-09-20 2013-07-31 The University of Queensland Serum preparation
KR20140014071A (en) * 2010-09-20 2014-02-05 더 유니버시티 오브 퀸스랜드 Serum preparation
EP2619540A4 (en) * 2010-09-20 2014-04-09 Univ Queensland Serum preparation
CN107870246A (en) * 2010-09-20 2018-04-03 Q-塞拉有限公司 It is prepared by serum
US10385381B2 (en) 2010-09-20 2019-08-20 Paul Masci Serum preparation
CN107870246B (en) * 2010-09-20 2021-04-09 Q-塞拉有限公司 Serum preparation
WO2020242425A1 (en) * 2019-05-29 2020-12-03 Istanbul Universitesi Rektorlugu Obtaining vitamin/mineral/drug/hormone/enzyme/bio-material composition by means of thrombocyte concentrate

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