JPH01156665A - Hermetic sealing method for specimen - Google Patents

Hermetic sealing method for specimen

Info

Publication number
JPH01156665A
JPH01156665A JP62316911A JP31691187A JPH01156665A JP H01156665 A JPH01156665 A JP H01156665A JP 62316911 A JP62316911 A JP 62316911A JP 31691187 A JP31691187 A JP 31691187A JP H01156665 A JPH01156665 A JP H01156665A
Authority
JP
Japan
Prior art keywords
specimen
specimens
low
temperature
sealing
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.)
Granted
Application number
JP62316911A
Other languages
Japanese (ja)
Other versions
JP2567885B2 (en
Inventor
Osamu Minoo
箕尾 治
Satoshi Nakamura
聰 中村
Seiji Kagawa
清二 加川
Hideaki Toda
英明 戸田
Genji Suganuma
菅沼 源二
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.)
Tonen Chemical Corp
Original Assignee
Tonen Sekiyu Kagaku KK
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 Tonen Sekiyu Kagaku KK filed Critical Tonen Sekiyu Kagaku KK
Priority to JP62316911A priority Critical patent/JP2567885B2/en
Publication of JPH01156665A publication Critical patent/JPH01156665A/en
Application granted granted Critical
Publication of JP2567885B2 publication Critical patent/JP2567885B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Medical Preparation Storing Or Oral Administration Devices (AREA)
  • Investigating Or Analysing Biological Materials (AREA)

Abstract

PURPOSE:To prevent pollution of ambient environment by specimens and contamination of the specimens themselves and to enhance the transport efficiency of taking vessels by hermetically packaging the taking vessels into which the specimens are taken with heat shrinkable films. CONSTITUTION:The taking vessels 4 into which the specimens 2 such as blood or urine are taken are capped 6. Such vessels 4 are covered with packages 8 consisting of two sheets of the low-temp. shrinkable films. After the low-temp. shrinkable films are heated and adhered to each other in sealing parts 10 of the packages 8, the packages 8 are thermally shrunk at a low temp. (30-60 deg.C) and are brought into tight contact with the taking vessels. The specimens 2 and the ambient environment are thereby satisfactorily shut off, by which the contamination of the specimens 2 themselves and the pollution of a handling person or the ambient environment are prevented. Since such packages 8 can be efficiently piled in a preserving box 15, the safe transportation of the specimens 2 in a large quantity is possible.

Description

【発明の詳細な説明】 光皿Ω技土分盟 本発明は、体液等の検体自体もしくはこの検体が収容さ
れた採取容器を、安全かつ簡便に、管理ないし輸送させ
ることができ、各種体液検査に対して、検体の分離、取
り扱いが容易な検体の密封方法に関する。
[Detailed Description of the Invention] The present invention enables the safe and simple management or transportation of a specimen such as a body fluid or a collection container containing the specimen, and is suitable for various body fluid tests. The present invention relates to a method for sealing a specimen that facilitates separation and handling of the specimen.

日の ・、白、ゴjLt  びに のurI占従来より
、健常人もしくは患者から血液、尿、胸水、腹水、脳を
髄液等の体液を採取する場合、主としてガラス製または
プラスチック製の採取容器を用いて、その中に検体とし
ての体液等を採取している。体液等の検体が収容された
例えば採液管等の採取容器は、何も被覆されないまま、
何本かの単位で試験管立てに立てられ、生化学検査等に
供される。
Traditionally, when collecting body fluids such as blood, urine, pleural effusion, ascites, and brain cerebrospinal fluid from healthy people or patients, collection containers made of glass or plastic are typically used. It is used to collect body fluids, etc., as specimens. Collection containers such as liquid collection tubes containing samples such as body fluids are left uncovered.
Several units are placed in a test tube stand and used for biochemical tests.

そして、体液の採取後、前記採取容器が設置された試験
管立ては、断熱材から成るボックスあるいは定温ボック
ス等に収納されて、保管かつ運搬される。
After the body fluid is collected, the test tube rack in which the collection container is installed is stored and transported in a box made of a heat insulating material, a constant temperature box, or the like.

しかしながら、このような従来の方法では、血液等の体
液を採取容器に採取後に、この採取容器を管理する場合
に、被検者もしくは検査項目毎の採取容器の分類が煩雑
で、しかも採取容器相互(すなわち、検体相互)の混同
が生じ易いという不都合を有している。また、体液の検
査に供するための体液を採取するに際して採取容器の外
側を体液によって汚染したり、又は、これらの体液が収
容された採取容器を運搬する場合に、輸送中の振動や衝
撃によって、採取容器が破損したり、採取容器を封止す
るゴムキャップが脱離したりして、採取容器の周囲が血
液等の体液で汚染され、場合によっては、体液中のウィ
ルス(たとえばHBSもしくはAIDS等)や菌等が取
扱者、輸送者、ないしは検査者等の皮膚に付着し、これ
らの者が感染する虞があり、極めて危険であるという不
都合も有している。さらに、輸送時に採取容器を破損し
ないように収納する必要があることから、収納作業が煩
雑であり、運搬効率が良くないという不都合も有してい
る。
However, in such conventional methods, when managing blood and other body fluids in collection containers after collecting them, it is complicated to classify the collection containers by subject or test item, and furthermore, the collection containers cannot be exchanged with each other. This method has the disadvantage that confusion between samples (that is, mutual samples) is likely to occur. In addition, when collecting body fluids for body fluid testing, the outside of the collection container may become contaminated with body fluids, or when transporting the collection container containing these body fluids, vibrations and shocks during transportation may cause damage. If the collection container is damaged or the rubber cap that seals it comes off, the area around the collection container may be contaminated with blood or other body fluids, and in some cases, viruses (such as HBS or AIDS) in the body fluids may occur. It also has the disadvantage that it is extremely dangerous, as there is a risk that bacteria and bacteria may adhere to the skin of the handler, transporter, or examiner, resulting in infection. Furthermore, since it is necessary to store the collection container so as not to damage it during transportation, there are also disadvantages in that the storage operation is complicated and transportation efficiency is poor.

光咀例且旬 本発明は、このような不都合を解消するためになされ、
体液等の採取から検査終了までの全工程を通じて、検体
としての体液等と周囲環境とが良好に遮断され、したが
って取扱者及び周囲環境への検体による汚染ないし感染
を防止すると共に、検体そのものが周囲環境から汚染さ
れるのを防止し、検体の取扱いないし管理が容易であり
、しかも輸送効率が良く、検体の採取ないし検査システ
ムの省力化ならびに信頼性を高めることができる検体の
密封方法を提供することを目的とする。
The present invention has been made to eliminate such inconveniences,
Throughout the entire process from the collection of body fluids, etc. to the completion of the test, the body fluids, etc. as a specimen are well isolated from the surrounding environment, thus preventing the specimen from contaminating or infecting the handler and the surrounding environment, as well as preventing the specimen itself from being exposed to the surrounding environment. To provide a method for sealing a specimen, which prevents contamination from the environment, facilitates handling and management of the specimen, has good transport efficiency, and can save labor and improve the reliability of a specimen collection or testing system. The purpose is to

光皿ム且五 かかる目的を達成するなめに、本発明は、体液等の検体
を採取容器内に採取した後、この採取容器を、低温収縮
性フィルムから成る包装体で被覆すると共に、この包装
体内を密封させて当該包装体を熱収縮させることを特徴
としている。
In order to achieve the above object, the present invention covers a sample such as a body fluid in a collection container, covers the collection container with a packaging body made of a low-temperature shrink film, and It is characterized by sealing the inside of the body and heat-shrinking the package.

ごのような本発明に係る検体の密封方法によれば、検体
が収容された採取容器を低温収縮性フィルムから成る包
装体で被覆し、この包装体内を密封させて当該包装体を
熱収縮させるようにしなので、検体と周囲環境とが良好
に遮断され、検体自体が汚染されることもなければ、周
囲環境ないしは取扱者が汚染ないし感染されることもな
い。しかも、低温収縮性フィルム相互を熱収縮させるた
めには、高温を必要とせずに低温で十分であるなめ、検
3体を温度によって変質させることもない。
According to the sample sealing method of the present invention, a collection container containing a sample is covered with a package made of a low-temperature shrinkable film, the inside of the package is sealed, and the package is heat-shrinked. Therefore, the specimen and the surrounding environment are well isolated, and the specimen itself is not contaminated, and the surrounding environment or the person handling it is not contaminated or infected. Moreover, in order to heat-shrink the low-temperature shrinkable films, a low temperature is sufficient without requiring a high temperature, so that the specimen is not altered in quality by temperature.

また、検査指示書と検体との識別は、同一包装体に付さ
れる、たとえば識別表示用ラベルによって明確かつ簡単
に行なうことができるため、検体の取り違えを防ぎ、管
理が容易である。又熱収縮で包装体の体積を縮少でき、
採取容器を包装体中に固定でき、又採取容器に付された
表示用ラベルが見やすくなる。
In addition, since the test instructions and the specimen can be clearly and easily identified by, for example, an identification label attached to the same package, the specimens can be easily managed and prevented from being mixed up. Also, the volume of the package can be reduced by heat shrinking.
The collection container can be fixed in the package, and the display label attached to the collection container can be easily seen.

さらに、このような包装体を効率良く積みがさねするこ
とができるので、この包装体内に収容された検体を安全
かつ大量に輸送できる。さらにまた、検体の採取後にお
ける遠心分離操作等を包装体のまま行なうこともできる
ので都合が良い。したがって、検体の採取ないし検査シ
ステムの効率化と省力化とを大幅に促進し、検査システ
ムの信頼性を高めることが可能になる。
Furthermore, since such packages can be stacked efficiently, the specimens contained in the packages can be safely transported in large quantities. Furthermore, it is convenient because centrifugation operations and the like can be performed in the packaged state after the sample is collected. Therefore, efficiency and labor saving of the sample collection or testing system can be greatly promoted, and the reliability of the testing system can be improved.

光叫例且体迫韮朋 以下、本発明を図面に示す実施例に基づき詳細に説明す
る。
EMBODIMENT OF THE INVENTION Hereinafter, the present invention will be explained in detail based on embodiments shown in the drawings.

第1図は本発明の一実施例に係る検体の密封方法を示す
正面図、第2図は同実施例に用いる採取容器の正面図、
第3図は第1図に示す■−■線に沿う断面図、第4図は
検体の輸送方法を示す断面図、第5図は本発明の他の実
施例を示す側面図、第6〜8図は本発明のその他の実施
例をそれぞれ示す正面図である。
FIG. 1 is a front view showing a specimen sealing method according to an embodiment of the present invention, FIG. 2 is a front view of a collection container used in the same embodiment,
FIG. 3 is a sectional view taken along the line ■-■ shown in FIG. 1, FIG. 4 is a sectional view showing a method of transporting a specimen, FIG. FIG. 8 is a front view showing other embodiments of the present invention.

第1〜3図に示す本発明に係る実施例では、第2図に示
すように、まず、人間の血液、尿、胸水、腹水、脳を髄
液等の体液を検体2として採取容器4内に採取した後、
この採取容器4の開口部6−にキャップ6を挿入し、こ
の開口部6″を封止する。なお、検体採取容器は、必ず
しも第2図に示すようなチューブとキャップが装着され
たものに限らずキャップに代るパラフィルムのものも使
用できる。次に、このようにして検体2が収容された採
取容器4を、第1図に示すように、複数本(図示上、5
本)平行に配置し、これらを包装体8で被覆する。なお
、採取容器4を1本毎に包装体8で被覆しても良い。こ
の包装体8は、たとえば2枚の低温収縮性フィルムから
成り、シール部10で熱融着又は高周波シール等により
接着されるようになっている。特に本実施例にあっては
、この包装体8に、検体2を識別するための識別表示用
ラベル12を付すと共に、吊り下げ用のハンギングホー
ル14を形成しである。識別表示用ラベル12を包装体
8に付すのは、各検体2を識別し、取り扱い操作時に誤
って他の検体2と取り違えないようにするためである。
In the embodiment according to the present invention shown in FIGS. 1 to 3, as shown in FIG. After sampling,
A cap 6 is inserted into the opening 6- of this collection container 4, and this opening 6'' is sealed.The specimen collection container does not necessarily have to be equipped with a tube and a cap as shown in FIG. However, parafilm can also be used in place of the cap.Next, as shown in FIG.
books) are placed in parallel and covered with a packaging body 8. Incidentally, each collection container 4 may be covered with a packaging body 8. The package 8 is made of, for example, two low-temperature shrinkable films, which are bonded together at a sealing portion 10 by heat sealing, high-frequency sealing, or the like. Particularly in this embodiment, the package 8 is provided with an identification label 12 for identifying the sample 2, and a hanging hole 14 for hanging the sample 2. The purpose of attaching the identification label 12 to the package 8 is to identify each specimen 2 and to prevent the specimen 2 from being mistakenly confused with another specimen 2 during handling operations.

なお、この識別表示用ラベル12は、バーコードに収っ
て変わることもできる。包装体8を構成する低温収縮性
フィルム相互をシール部10で接着するための手段とし
ては、電熱による加熱、高周波による加熱、もしくは超
音波による加熱等の手段を採用し得る。
Note that the identification label 12 can also be changed to match the barcode. As a means for bonding the low-temperature shrinkable films constituting the package 8 to each other at the seal portion 10, heating by electric heat, heating by high frequency, heating by ultrasonic waves, or the like may be employed.

シール部10を形成した後、もしくはそれと同時に熱収
縮性フィルムから成る包装体8を低温(30〜60℃)
で熱収縮させ、採取容器4に密着させる。いずれにして
も、低温収縮性フィルム相互をシール部10で接着させ
るため及び熱収縮させるためには、高温を必要とぜずに
低温で十分であるため、検体2を温度によって変質させ
ることもない。
After forming the seal portion 10 or at the same time, the package 8 made of a heat-shrinkable film is heated at a low temperature (30 to 60°C).
heat-shrink it and bring it into close contact with the collection container 4. In any case, in order to bond the low-temperature shrinkable films to each other at the sealing part 10 and to cause heat shrinkage, a low temperature is sufficient without requiring high temperatures, so the specimen 2 will not be altered by temperature. .

包装体8を構成する低温収縮性フィルムのフィルム収縮
温度は、常温での取扱いができてしかも検体2を変質さ
せない低温収縮をさせるために、30〜60℃が好まし
く、特に好ましくは、40〜50℃が良い。
The film shrinkage temperature of the low-temperature shrinkable film constituting the package 8 is preferably 30 to 60°C, particularly preferably 40 to 50°C, in order to be able to handle it at room temperature and to perform low-temperature shrinkage that does not alter the quality of the specimen 2. ℃ is good.

このような30〜60℃の加熱で収縮する低温収縮性フ
ィルムを製造するには、たとえば次のようにして行う。
To produce such a low-temperature shrinkable film that shrinks when heated at 30 to 60°C, the following procedure is performed, for example.

すなわち、下記(A>に記載する割合のEPDMまたは
EPM、EVA、及びタルクを原料として得られる重合
体フィルムを、下記(B)に記載する温度条件で少なく
とも一方向に1.5倍以上、好ましくは2〜5倍に延伸
成形することにより、本発明方法で用いる低温収縮性フ
ィルムを得る。
That is, a polymer film obtained using EPDM or EPM, EVA, and talc as raw materials in the proportions described in (A> below) is heated at least 1.5 times in one direction, preferably at least 1.5 times, under the temperature conditions described in (B) below. By stretching 2 to 5 times, the low-temperature shrinkable film used in the method of the present invention is obtained.

(A)EPDMまたはEPM、EVA、タルクの配合割
合 EPDMまたはEPM:   40〜70重量%EVA
 (VA含量10重量%以上):30〜60重量% タルク:            5〜15重量%(B
)温度条件 予備加熱温度       :40〜50℃加熱延伸温
度       :45〜55℃冷却温度(熱固定、ア
ニーリング) 加熱延伸温度よりも低く、具体的には20〜40℃程度
(A) Blending ratio of EPDM or EPM, EVA, and talc EPDM or EPM: 40 to 70% by weight EVA
(VA content 10% by weight or more): 30-60% by weight Talc: 5-15% by weight (B
) Temperature conditions Preheating temperature: 40-50°C Heating and stretching temperature: 45-55°C Cooling temperature (heat setting, annealing) Lower than the heating and stretching temperature, specifically about 20-40°C.

上記EPDMとは、エチレン−プロピレン−ジエンエラ
ストマーターポリマー(Ethylene−Propy
lene−Dicne Rubber>である。またE
PMとはエチレンープロピレンエラストマーコボリマー
である。
The above EPDM refers to ethylene-propylene-diene elastomer terpolymer (Ethylene-Propylene).
lene-Dicne Rubber>. Also E
PM is an ethylene-propylene elastomer copolymer.

なおEPDMを形成する際に用いられる非共役ジエンと
しては、ヘキサジエン、ジシクロペンタジェン、エチリ
デンノルボルネン、メチレンノルボルネン、プロピリデ
ンノルボルネン、メチルテトラヒドロインデンなどが用
いられる。
Note that as the non-conjugated diene used when forming EPDM, hexadiene, dicyclopentadiene, ethylidene norbornene, methylene norbornene, propylidene norbornene, methyltetrahydroindene, etc. are used.

これらのEPDMまたはEPMとしては、従来公知のも
のが広く用いられる。
Conventionally known EPDMs or EPMs are widely used.

このようなEPDMまたはEPMの配合量は、前述のよ
うに、40〜70重量%であるが、この配合量が40重
量%未満であると、得られるフィルムにべたつきが生じ
るため好ましくなく、一方70重量%を越えると、得ら
れるフィルムの成形性が低下するため好ましくない。
As mentioned above, the blending amount of EPDM or EPM is 40 to 70% by weight, but if the blending amount is less than 40% by weight, the resulting film will become sticky, which is not preferable. If the amount exceeds % by weight, the moldability of the obtained film will deteriorate, which is not preferable.

上記EVAとは、エチレンと酢酸ビニルとの共重合体(
Ethylene−Vinyl−八cctate Co
polymer)であり、酢酸ビニル(VA)含量が1
0重量%以上のものを使用することが好ましい。酢酸ビ
ニル含量が10重量%未満では、得られるフィルムの低
温延伸性に劣るため好ましくない。
The above EVA is a copolymer of ethylene and vinyl acetate (
Ethylene-Vinyl-8cctate Co
polymer) and has a vinyl acetate (VA) content of 1
It is preferable to use 0% by weight or more. A vinyl acetate content of less than 10% by weight is not preferred because the resulting film has poor low-temperature stretchability.

このようなEVAの配合量は、前述のように、30〜6
0重量%であるが、この配合量が30重量%未満では得
られるフィルムの成形性が低下するなめ好ましくなく、
一方60重景%を越えると得られるフィルムの伸縮性が
低下するため好ましくない。
As mentioned above, the blending amount of EVA is 30 to 6
0% by weight, but if this amount is less than 30% by weight, the moldability of the resulting film will decrease, which is not preferable.
On the other hand, if it exceeds 60 %, the stretchability of the resulting film decreases, which is not preferable.

上記タルクとは、3M(10・4Si 02・H2Oの
組成を有し、フィラー(通常葉片状または鱗片状)の代
表的な物質である。
The above-mentioned talc has a composition of 3M (10.4 Si 0 2 .H 2 O) and is a typical filler (usually leaf-shaped or scale-shaped).

このようなタルクの配合量は、前述のように、5〜15
重量%であるが、この配合量が5重量%未満では得られ
るフィルムのブロッキングを充分に防止することができ
ないため好ましくなく、−方15重量%を越えると得ら
れるフィルムの延伸性が低下するため好ましくない。
As mentioned above, the blending amount of such talc is 5 to 15
If the amount is less than 5% by weight, blocking of the obtained film cannot be sufficiently prevented, which is undesirable, and if it exceeds 15% by weight, the stretchability of the obtained film will decrease. Undesirable.

なお上記タルクの代わり、炭酸カルシウム、硫酸バリウ
ムなどを用いることもできる。
Note that calcium carbonate, barium sulfate, etc. can also be used instead of the above-mentioned talc.

本発明においては、これらのEPDMまたはEPM、E
VA、及びタルクを原料とし、これを特定の割合で配合
して得られる重合体フィルム(未延伸フィルム)を、前
記した(B)の温度条件により延伸加工することにより
、低温収縮性フィルムが得られる。このフィルムは、約
30℃程度の低温からでも熱収縮が得られ、したがって
低温でも大きな熱収縮率、低温での十分な弾性、肌への
フィツト性やソフト感があり、熱収縮時間の短いもので
ある。
In the present invention, these EPDM or EPM, E
A low-temperature shrinkable film is obtained by stretching a polymer film (unstretched film) obtained by blending VA and talc in a specific ratio under the temperature conditions described in (B) above. It will be done. This film can be heat-shrinked even at a low temperature of about 30°C, so it has a high heat-shrinkage rate even at low temperatures, sufficient elasticity at low temperatures, a good skin fit and soft feel, and a short heat-shrink time. It is.

このような本発明の一実施例に係る検体の密封方法によ
れば、血液等の検体2を低温収縮性フィルムから成る包
装体8で被覆し、この包装体8を熱収縮させると共に包
装体内を密封するようにしたので、検体2と周囲環境と
が良好に遮断され、検体2自体が汚染されることもなけ
れば、周囲環境ないしは取扱者が汚染ないし感染される
こともない。しかも、低温収縮性フィルム相互をシール
部10で接着させるため及び熱収縮させるためには、高
温を必要とせずに低温で十分であるため、検体2を温度
によって変質させることもない。また、検査指示書と包
装体8との識別は、包装体に付される、たとえば識別表
示用ラベル12によって明確かつ簡単に行なうことがで
きるため、検体の取り違えを防ぎ、管理が容易である。
According to the specimen sealing method according to the embodiment of the present invention, a specimen 2 such as blood is covered with a packaging body 8 made of a low-temperature shrinkable film, and the packaging body 8 is heat-shrinked and the inside of the packaging body is sealed. Since it is sealed, the specimen 2 and the surrounding environment are well isolated, and the specimen 2 itself is not contaminated, and the surrounding environment or the person handling it is not contaminated or infected. Furthermore, since a low temperature is sufficient for bonding the low-temperature shrinkable films to each other at the sealing portion 10 and for heat-shrinking the films without requiring high temperatures, the specimen 2 is not altered in quality by temperature. Further, since the test instructions and the package 8 can be clearly and easily identified by, for example, the identification label 12 attached to the package, it is possible to prevent sample mix-ups and facilitate management.

さらに、第4図に示すように、このような包装体8を保
存箱15内に効率良く積みかさねすることができるので
、この包装体8内に収容された検体2を安全かつ大量に
輸送できる。さらにまた、検体2の採取後における遠心
分離操作等を包装体8のまま行なうことができるので都
合が良い。したがって、検体2の採取ないし検査システ
ムの効率化と省力化とを大幅に促進し、検査システムの
信頼性を高めることが可能になる。
Furthermore, as shown in FIG. 4, since such packages 8 can be efficiently stacked in the storage box 15, the specimens 2 contained in the packages 8 can be transported safely and in large quantities. . Furthermore, centrifugation and other operations after collecting the specimen 2 can be performed in the package 8, which is convenient. Therefore, efficiency and labor saving of the specimen 2 collection or testing system can be greatly promoted, and the reliability of the testing system can be improved.

なお、本発明は、上述した実施例に限定されるものでは
なく、本発明の範囲内で種々に改変することができる。
Note that the present invention is not limited to the embodiments described above, and can be variously modified within the scope of the present invention.

たとえば第5図に示すように、第1図に示すような包装
体8を3個束ねて、一端10aを熱シール等の手段で接
着させるようにしても良い。
For example, as shown in FIG. 5, three packages 8 as shown in FIG. 1 may be bundled together and one end 10a may be bonded together by heat sealing or the like.

また、第6図に示すように、採取容器4を上下に2列平
行に配置し、各列に3個の採取容器4が配置させるよう
にこれら採取容器4を包装体8で被覆するようにしても
良い。
Further, as shown in FIG. 6, the collection containers 4 are arranged vertically in two parallel rows, and the collection containers 4 are covered with the packaging body 8 so that three collection containers 4 are arranged in each row. It's okay.

さらに、第7図に示すように、包装体8に例えばミシン
目16を入れて、各採取容器4を1本づつ分離できるよ
うにしても良い。このような実施例によれば、各採取容
器4毎の分離作業が容易であり、都合が良い。
Further, as shown in FIG. 7, for example, perforations 16 may be provided in the package 8 so that each collection container 4 can be separated one by one. According to such an embodiment, the separation operation for each collection container 4 is easy and convenient.

さらにまた、第8図に示すように、予め採取容器4が入
るチューブ18を連続的にシール成形しておいて、採取
容器4を挿入した後に、一端をシール部10bでシール
すると同時に低温収縮性フィルムから成る包装体8を収
縮させるようにしても良い。
Furthermore, as shown in FIG. 8, the tube 18 into which the collection container 4 is inserted is formed into a continuous seal in advance, and after the collection container 4 is inserted, one end is sealed with the seal part 10b and at the same time, the tube 18 is sealed at a low temperature. The package 8 made of film may be shrunk.

また、上述した実施例では、検体2として体液等を用い
た場合について説明したが、本発明はこれに限らず、検
体2として、たとえば微生物、病理標本あるいはその他
の物質を用いることも可能である。
Further, in the above-mentioned embodiment, a case was explained in which a body fluid or the like was used as the specimen 2, but the present invention is not limited to this, and it is also possible to use, for example, a microorganism, a pathological specimen, or other substances as the specimen 2. .

さらにまた、上述した実施例では検体2として液体を用
いたため、検体2を採取容器4内に採取した後に、この
採取容器4を包装体8で被覆するようにしたが、検体2
として固体を用いる場合等には、検体2を直接包装体8
で被覆するようにしても良い。
Furthermore, in the above embodiment, since a liquid was used as the specimen 2, after the specimen 2 was collected into the collection container 4, the collection container 4 was covered with the packaging body 8, but the specimen 2
When using a solid as
It may be covered with.

主叫五差盟 以上説明してきたように、本発明によれば、体液等の検
体を密封する方法において、低温収縮性フィルムから成
る包装体で前記検体を収容した採取容器を被覆すると共
に、この包装体内を密封させて当該包装体を熱収縮させ
るようにしたので、検体としての体液等の採取から検査
終了までの全工程を通じて、検体と周囲環境とが良好に
遮断され、したがって取扱者及び周囲環境への検体によ
る汚染ないし感染を有効に防止し得ると共に、検体その
ものが周囲環境から汚染されるのを有効に防止し得ると
いう優れた効果を奏する。しかも、熱収縮により該包装
体の体積を縮少できるため、検体の取扱いないし管理が
容易となると共に、輸送効率が大幅に向上し、検体の採
収ないし検査システムの省力化ならびに信頼性を大幅に
高めることが可能になる。さらに、検体の密封時に高い
温度を必要とせず簡単に行い得ることから、検体を変質
させることもなく作業性良く検体を密封できるので都合
が良い。又熱収縮で包装体の体積を縮少でき、採取容器
を包装体中に固定でき、又採取容器に付された表示用ラ
ベルが見やすくなる。
As explained above, according to the present invention, in a method for sealing a specimen such as a body fluid, a collection container containing the specimen is covered with a packaging body made of a low-temperature shrinkable film, and Since the inside of the package is sealed and the package is heat-shrinkable, the sample is well isolated from the surrounding environment throughout the entire process, from the collection of body fluids etc. as a sample to the completion of the test, and therefore the handler and surrounding environment are well isolated. This has the excellent effect of effectively preventing contamination or infection of the environment by the specimen, as well as effectively preventing the specimen itself from being contaminated from the surrounding environment. Moreover, since the volume of the package can be reduced through heat shrinkage, handling and management of specimens becomes easier, transportation efficiency is greatly improved, and labor-saving and reliability of specimen collection and testing systems are greatly improved. It becomes possible to increase the Furthermore, since the sealing of the sample does not require high temperatures and can be easily carried out, the sample can be sealed with good workability without deteriorating the quality of the sample, which is convenient. Furthermore, the volume of the package can be reduced by heat shrinking, the collection container can be fixed in the package, and the display label attached to the collection container can be easily seen.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の一実施例に係る検体の密封方法を示す
正面図、第2図は同実施例に用いる採取容器の正面図、
第3図は第1図に示す■−■線に沿う断面図、第4図は
検体の輸送方法を示す断面図、第5図は本発明の他の実
施例を示す側面図、第6〜8図は本発明のその他の実施
例をそれぞれ示す正面図である。 2・・・検体       4・・・採取容器8・・・
包装体     10・・・シール部代理人  弁理士
  鈴 木 俊一部 第  1  図            第  2  
図第3図 第4図 第  5  図 第6図 第  8  図 ム
FIG. 1 is a front view showing a specimen sealing method according to an embodiment of the present invention, FIG. 2 is a front view of a collection container used in the same embodiment,
FIG. 3 is a sectional view taken along the line ■-■ shown in FIG. 1, FIG. 4 is a sectional view showing a method of transporting a specimen, FIG. FIG. 8 is a front view showing other embodiments of the present invention. 2... Specimen 4... Collection container 8...
Packaging 10... Seal Department Agent Patent Attorney Shunichi Suzuki Figure 1 Figure 2
Figure 3 Figure 4 Figure 5 Figure 6 Figure 8

Claims (1)

【特許請求の範囲】 1)体液等の検体を採取容器内に採取した後、この採取
容器を、低温収縮性フィルムから成る包装体で被覆する
と共に、この包装体内を密封させて当該包装体を熱収縮
させることを特徴とする検体の密封方法。 2)前記低温収縮性フィルムは、フィルム収縮温度が3
0〜60℃の範囲にある特性を有するフィルムであるこ
とを特徴とする特許請求の範囲第1項に記載の検体の密
封方法。 3)前記採取容器を、複数まとめて、前記低温収縮性フ
ィルムから成る包装体で、同時かつ一体に被覆したこと
を特徴とする特許請求の範囲第1項または第2項に記載
の検体の密封方法。 4)前記低温収縮性フィルムから成る包装体内を密封さ
せるための手段が、電熱による加熱、高周波による加熱
、もしくは超音波による加熱のいずれかであることを特
徴とする特許請求の範囲第1項から第3項のいずれかに
記載の検体の密封方法。
[Scope of Claims] 1) After collecting a sample such as a body fluid into a collection container, the collection container is covered with a packaging made of a low-temperature shrinkable film, and the inside of the packaging is sealed to close the packaging. A method for sealing a specimen characterized by heat shrinking. 2) The low temperature shrinkable film has a film shrinkage temperature of 3
The method for sealing a specimen according to claim 1, wherein the film is a film having characteristics in the range of 0 to 60°C. 3) Sealing of a specimen according to claim 1 or 2, wherein a plurality of the collection containers are simultaneously and integrally covered with a packaging body made of the low-temperature shrinkable film. Method. 4) The means for sealing the inside of the package made of the low-temperature shrinkable film is any one of electric heating, high frequency heating, or ultrasonic heating. The method for sealing a specimen according to any of paragraph 3.
JP62316911A 1987-12-15 1987-12-15 Sample sealing method Expired - Lifetime JP2567885B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62316911A JP2567885B2 (en) 1987-12-15 1987-12-15 Sample sealing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62316911A JP2567885B2 (en) 1987-12-15 1987-12-15 Sample sealing method

Publications (2)

Publication Number Publication Date
JPH01156665A true JPH01156665A (en) 1989-06-20
JP2567885B2 JP2567885B2 (en) 1996-12-25

Family

ID=18082283

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62316911A Expired - Lifetime JP2567885B2 (en) 1987-12-15 1987-12-15 Sample sealing method

Country Status (1)

Country Link
JP (1) JP2567885B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008228612A (en) * 2007-03-19 2008-10-02 Nikken Seibutsu Igaku Kenkyusho:Kk Tool for wipe test of environmental microorganism

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102488848B1 (en) 2015-02-27 2023-01-17 도레이 카부시키가이샤 Cyclic amine derivative and pharmaceutical use thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58102762A (en) * 1981-12-15 1983-06-18 旭化成株式会社 Low-temperature heat-shrinkable multilayer barrier film and its manufacture

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58102762A (en) * 1981-12-15 1983-06-18 旭化成株式会社 Low-temperature heat-shrinkable multilayer barrier film and its manufacture

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008228612A (en) * 2007-03-19 2008-10-02 Nikken Seibutsu Igaku Kenkyusho:Kk Tool for wipe test of environmental microorganism

Also Published As

Publication number Publication date
JP2567885B2 (en) 1996-12-25

Similar Documents

Publication Publication Date Title
KR900005729B1 (en) Body fluid sample collection tube composite
US4469227A (en) Package for cryogenically frozen liquids
EP0173811B1 (en) Biological specimen collection device
US4910147A (en) Cell culture media flexible container
US4637061A (en) Specimen, sample collection and transport container
US5000804A (en) Process for making body fluid sample collection tube composite
US4283498A (en) Biological specimen collection and transport system
US4706839A (en) Closures and methods of closure for a sterilization container system
US4150950A (en) Transport system for clinical specimens
EP1006359A2 (en) Device and method for separating components of a liquid sample
US7350669B2 (en) Closure device for flexible pouches
JP2019505232A (en) Cryogenic analyte carrier and related methods
US3783104A (en) Testing and culturing transport system and method of making same
US20040081601A1 (en) Integrity testable autoclavable, sterile transfer bag
EP0039947A1 (en) A container having thin, uncharged, transparent, flexible wall structure for storing and transporting biogenic fluid
EP0512803A1 (en) Transparent package with a low moisture vapor transmission rate and method of making such a package
JPH01156665A (en) Hermetic sealing method for specimen
US4066511A (en) Analytic device and method
KR900004140B1 (en) Body fluid sample collection tube composite
CA1236396A (en) Endotoxin-detecting device
EP1663496B1 (en) Heat-sealed cap for resealing test tubes in clinical analyses
GB2059992A (en) Culture-collecting kit and a method of taking a culture sample utilising it
Dyne et al. Toluene, 1-butanol, ethylbenzene and xylene from Sarstedt Monovette serum gel blood collection tubes
CN220340236U (en) Low density lipoprotein cholesterol detection kit
CA1300409C (en) Unitary specimen collection tube and microscope slide device