JPH05123188A - Transfer and detection of collected cell specimen and transfer and detection vessel therefor - Google Patents

Transfer and detection of collected cell specimen and transfer and detection vessel therefor

Info

Publication number
JPH05123188A
JPH05123188A JP34928891A JP34928891A JPH05123188A JP H05123188 A JPH05123188 A JP H05123188A JP 34928891 A JP34928891 A JP 34928891A JP 34928891 A JP34928891 A JP 34928891A JP H05123188 A JPH05123188 A JP H05123188A
Authority
JP
Japan
Prior art keywords
urine
activated carbon
examination
detection
vessel
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
JP34928891A
Other languages
Japanese (ja)
Other versions
JPH06104076B2 (en
Inventor
Kiyoshi Hoshina
清 保科
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.)
TOYO KIZAI KAGAKU KK
Original Assignee
TOYO KIZAI 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 TOYO KIZAI KAGAKU KK filed Critical TOYO KIZAI KAGAKU KK
Priority to JP34928891A priority Critical patent/JPH06104076B2/en
Publication of JPH05123188A publication Critical patent/JPH05123188A/en
Publication of JPH06104076B2 publication Critical patent/JPH06104076B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To easily and correctly detect a carrier in patients without using internal examination by adsorbing the urine of a patient to activated carbon using a specific method, transporting the adsorbed material to an examination organization and reacting a culture liquid with bacteria in the urine adsorbed to the activated carbon. CONSTITUTION:The urine of a patient is collected in an examination vessel containing an activated carbon 4 to effect the adsorption of the urine to the activated carbon 4. After discharging the urine from the vessel, the opening of the vessel is closed and the vessel is transported to an examination organization. A culture liquid is introduced into the examination vessel in the examination organization to effect the reaction of the culture liquid with the bacteria in the urine adsorbed to the activated carbon 4. The examination vessel is produced from a thermoplastic resin by integrally forming a thin tube 3 connected to the top 2 of a body tube 1, putting a piece of activated carbon 4 larger than the inner diameter of the thin tube 3 and pressing the lower part of the body tube 1 under heating to integrate the front part 6 and the back part of the body bottom 5 to form a flat face and make the bottom part 8 and the right and left side faces 9, 10 to lie on a straight line.

Description

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

【0001】[0001]

【産業上の利用分野】新生児B群溶連菌(GBS)感染
症の発症予防に際しては、妊婦が産道にGBSを保菌し
ているか否かが問題になる。この発明は、上記患者が保
菌しているかの有無についての集菌検体の輸送検出方法
及びその方法に使用する輸送用検出容器に関するもので
ある。
[Industrial field of application] In preventing the onset of neonatal group B streptococcal (GBS) infection, whether or not a pregnant woman carries GBS in the birth canal becomes a problem. The present invention relates to a method for detecting the transport of a collected specimen for determining whether or not the patient is carrying a bacterium, and a transport detection container used in the method.

【0002】[0002]

【従来の技術】妊婦の産道に生息するGBSを検出する
ためには、従来から膣培養を行なうことが一般的であっ
た。そして、このような膣培養によるよりも、尿沈渣培
養による方が検出率が高いことも知られている。
2. Description of the Related Art In order to detect GBS inhabiting a pregnant woman's birth canal, it has been customary to perform vaginal culture. It is also known that urine sediment culture has a higher detection rate than such vaginal culture.

【0003】[0003]

【発明が解決しようとする課題】前記従来の膣培養検出
によると、綿棒による擦過部位の違いや、擦過圧の違い
等によっては陽性率が異なってくる。さらに、培養する
べき妊娠週数の26週から36週頃迄は、妊婦検診で内
診をしない機関・施設が多いので、一定、かつ、適正な
結果を得ることが困難であった。
According to the above-mentioned conventional vaginal culture detection, the positive rate varies depending on the difference in the rubbing site with the cotton swab, the difference in the rubbing pressure, and the like. Further, from the 26th to the 36th week of the gestational weeks to be cultivated, it is difficult to obtain a constant and appropriate result because there are many institutions / facilities that do not undergo a pelvic examination during the pregnancy screening.

【0004】このようなことから、本発明者は、より簡
便な検体の採取方法を研究・検討してきた。上述のよう
に、妊婦検診時の尿を使って尿沈渣を培養すれば、陽性
率が高いと云うことが知られており、本発明者も綿棒に
よる産道培養と尿沈渣培養の比較を行なった結果、尿沈
渣培養の方が陽性率が高いことは既に確認した。
Under the circumstances described above, the present inventor has studied and studied a simpler method for collecting a specimen. As described above, it is known that the positivity rate is high if the urine sediment is cultured using urine at the time of pregnant woman screening, and the present inventor also compared the birth canal culture with the swab and the urine sediment culture. As a result, it was already confirmed that urine sediment culture had a higher positive rate.

【0005】しかし、スクリーニングを行なうために
は、検出したGBSの血清型別をも行なう必要があり、
或る一定の機関・施設での、一定の判定者による判定を
しなければならない。そのためには、各機関・施設から
一定の検査機関に尿沈渣を届けることが煩雑になるし、
培養のための尿沈渣を採取するためには、それらの技師
や看護婦等の手を煩わすことになる。多くの施設で検査
を外注するようになっているために、遠沈器を常備使用
している施設も少なくなっているし、また、患者におい
ても内診のために検査機関へ出向かねばならなかった。
However, in order to perform screening, it is necessary to perform serotyping of the detected GBS,
Judgment must be made by a certain judge at a certain institution / facility. For that purpose, it becomes complicated to deliver the urine sediment from each institution to a certain inspection institution,
In order to collect the urine sediment for culture, the hands of those technicians and nurses are troublesome. Since many of the facilities outsource testing, fewer facilities use a centrifuge permanently, and patients also have to go to a laboratory for internal examination. It was

【0006】このように、尿中の細菌を検出するために
は、尿をそのまま届けるか、または尿を培地に入れて輸
送する以外は方法がなかった。尿をそのまま輸送すれ
ば、輸送中に尿の漏洩の危険性があり、しかも輸送期間
中に増殖能力の強い細菌がはびこり、増殖能力の弱い細
菌は死滅してしまう恐れがあった。この発明は、前記従
来技術の問題点に鑑みて、内診せずに検体の輸送によっ
て患者内の保菌者を簡便、かつ、適正に検出すべきこと
を考慮したものである。
As described above, the only method for detecting bacteria in urine was to deliver urine as it is or to transport urine in a medium. If urine is transported as it is, there is a risk of leakage of urine during transportation, and during the transportation period, bacteria having a strong proliferation ability may spread and bacteria having a weak proliferation ability may be killed. In view of the above-mentioned problems of the prior art, the present invention considers that a carrier in a patient should be easily and properly detected by transporting a sample without performing an internal examination.

【0007】[0007]

【課題を解決するための手段】この発明は、尿中の細菌
を活性炭に吸着してなる検体を検査機関に輸送し、この
検体を培養液によって反応させることにより、その目的
を達成しようとするものである。
The present invention is intended to achieve the object by transporting a sample obtained by adsorbing bacteria in urine to activated carbon to a laboratory and reacting the sample with a culture solution. It is a thing.

【0008】次に、本発明の要旨とする具体的な構成を
実施例に対応する図面の符号を用いて説明する。すなわ
ちこの発明は、患者の尿を活性炭入りの検出容器に採取
し、前記尿を該活性炭に吸着させたのち、検出容器内の
尿を排出するとともに、開口部を密閉して検査機関へ輸
送し、かつ、前記検出容器の密閉部を開口して、該検出
容器内に培養液を導入せしめ、活性炭に吸着している尿
中の細菌と反応させたことを特徴とする集菌検体の輸送
検出方法である。そして、その方法に使用するものを、
実施例に対応する図面の符号を用いて説明すると、胴管
1の上端2から上方へ連続する細管3を熱可塑性剛性樹
脂材で一体成形し、前記胴管1内に細管3の内径dより
大なる活性炭4を入れ、かつ、胴底5を熱圧着すること
により、該胴底5の正面部6並びに背面部7を一体扁平
にし、同時に底面部8並びに左側面部9及び右側面部1
0を一直線状に形成したことを特徴とする集菌検体の輸
送用検出容器を提供するにある。なお、前記胴管1の横
断面の輸郭を、ほぼ長楕円形状にすると好都合である。
Next, a specific configuration which is the gist of the present invention will be described using the reference numerals of the drawings corresponding to the embodiments. That is, the present invention collects the urine of a patient in a detection container containing activated carbon, adsorbs the urine on the activated carbon, discharges the urine in the detection container, and seals the opening to transport it to a laboratory. And, the transport detection of the collected specimen characterized by opening the closed part of the detection container, introducing the culture solution into the detection container, and reacting with the bacteria in the urine adsorbed on the activated carbon Is the way. And what to use for that method,
Explaining with reference to the reference numerals of the drawings corresponding to the embodiments, a thin tube 3 continuous upward from the upper end 2 of the body tube 1 is integrally molded with a thermoplastic rigid resin material, and the inner diameter d of the thin tube 3 is larger than the inner diameter d of the thin tube 3 in the body tube 1. By inserting a large amount of activated carbon 4 and thermocompression-bonding the bottom 5 of the body, the front part 6 and the back part 7 of the bottom 5 are made flat, and at the same time, the bottom part 8 and the left side part 9 and the right side part 1 are formed.
Another object is to provide a detection container for transporting a collected specimen, which is characterized in that 0 is formed in a straight line. In addition, it is convenient to make the cross section of the body tube 1 substantially elliptical.

【0009】[0009]

【作用】上記のように構成された検出容器は、自ずから
その下部が徐々に薄くしぼられて胴底に連続するので、
輸送の際に封筒底から封筒全体の膨らみに沿った相似体
形となり、また、胴管の横断面の輪郭を長楕円状に形成
すれば、封筒の立体形状をさらに薄くすることができ
る。
In the detection container configured as described above, the lower part of the detection container is naturally squeezed and continues to the bottom of the body.
The three-dimensional shape of the envelope can be further thinned by forming a similar shape along the bulge of the entire envelope from the bottom of the envelope at the time of transportation and forming the cross-sectional contour of the body tube in an oblong shape.

【0010】そして、胴管は熱可塑性合成樹脂材で製さ
れて柔軟であるから、該胴管を指先で押圧し、細管の開
口部を貯溜した尿中に入れ押圧を止めれば、尿は細管か
ら胴管に導入され、胴管内に散在している活性炭に吸着
される。また、胴管内に残留する尿は、細管の開口部を
下に向けて胴管を押圧することによって排出される。こ
のとき、活性炭は細管の内径より大きい物であるから、
これが尿と共に排出されることはない。従って、活性炭
は尿を吸着したまま胴管内に散在する。また、図1に示
すように、細管を屈折してリング11を嵌めることによ
り、細管の開口部を閉塞できる。このリングは、本体と
同様に熱可塑性合成樹脂材で製すれば柔軟性を有し好都
合であるが、リングとは限らず、紐や輪ゴム等で適宜に
縛ることでもよい。
Since the body tube is made of a thermoplastic synthetic resin material and is flexible, if the body tube is pressed with a fingertip and the opening of the thin tube is put into the stored urine and the pressing is stopped, the urine becomes a thin tube. It is introduced into the body tube from and is adsorbed by the activated carbon scattered in the body tube. Further, the urine remaining in the body tube is discharged by pressing the body tube with the opening of the thin tube facing downward. At this time, the activated carbon is larger than the inner diameter of the thin tube,
It is not excreted with urine. Therefore, the activated carbon is scattered in the body tube while absorbing the urine. Further, as shown in FIG. 1, the opening of the thin tube can be closed by bending the thin tube and fitting the ring 11. This ring is flexible and convenient if it is made of a thermoplastic synthetic resin material like the main body, but is not limited to the ring, and may be appropriately bound with a string or a rubber band.

【0011】このようにして封筒に入れて検査機関に送
られてきた検出容器は、リングによって閉塞された細管
の適宜な個所を切断した後、採尿時と同様の作用にて培
養液を胴管内に導入すれば、これが活性炭に吸着した尿
と反応することになる。従って、この検出容器は前述の
ようにスポイト機能を有するとともに、活性炭を保護
し、尿を採取・排出し、さらに培養液を導入・排出し、
反応をも行なう等の作用・機能を有することになる。
In the detection container thus sent to the inspection facility in the envelope, after cutting an appropriate part of the thin tube closed by the ring, the culture solution is put into the body tube by the same action as when collecting urine. If introduced into, it will react with urine adsorbed on activated carbon. Therefore, this detection container has a dropper function as described above, protects activated carbon, collects and discharges urine, and further introduces and discharges a culture solution,
It has an action / function such as performing a reaction.

【0012】[0012]

【実施例】各検査機関や施設に受診している妊婦につい
て、受診時の尿検査のために採取した尿を検体として基
礎実験に供した。この尿に一定の菌量を添加後、菌数計
算をするとともに、活性炭に吸着させて一晩放置した後
に前記尿を捨てた。このようにして残存した活性炭を4
℃、37℃及び42℃の状態でそれぞれ5日間保存して
SEB培地(日水)を添加し、そして、約10mlの尿
について次の三種類の実施を行なった。 尿を抗生剤入りの選択的血液寒天平板培地に1ml
量を流し込み、1分後に尿を捨てて培養した(直接培
養)。 約7mlの尿を3000回転で10分間遠沈した
後、2mlのSEB培地を添加・撹拌後に培養した(沈
渣培養)。 2mlの尿に活性炭粒子を4粒入れて室温にて一晩
放置した後、尿を捨ててSEB培地を添加後に培養した
(活性炭培養)。 その結果、基礎実験で種々の温度において5日間保存し
ても、10(10の1乗)の菌量が検出可能であっ
た。116例の妊婦から採取した尿において、上記三種
の培養方法により何れか一種でも陽性であったのは58
例であった。その内訳として、直接培養での陽性は18
例(15.5%)、沈渣培養での陽性は53例(45.
7%)、活性炭培養での陽性は27例(23.3%)で
あった。三種ともに陽性は17例、沈渣培養のみが陽性
22例、活性炭のみの陽性が4例、活性炭と沈渣培養の
陽性が5例と云う結果であった。
[Examples] With regard to pregnant women who had been examined at each laboratory or facility, urine collected for urine examination at the time of examination was used as a sample for basic experiments. After adding a certain amount of bacteria to this urine, the number of bacteria was calculated, and the urine was discarded after being adsorbed on activated carbon and left overnight. The activated carbon remaining in this way is
The samples were stored at 5 ° C, 37 ° C and 42 ° C for 5 days, SEB medium (Japanese water) was added thereto, and about 10 ml of urine was subjected to the following three kinds of operations. 1 ml of urine on selective blood agar plate containing antibiotics
The amount was poured, and 1 minute later, the urine was discarded and the cells were cultured (direct culture). Approximately 7 ml of urine was spun down at 3000 rpm for 10 minutes, and then 2 ml of SEB medium was added and stirred and then cultured (sediment culture). Four activated carbon particles were added to 2 ml of urine and allowed to stand overnight at room temperature, and then the urine was discarded and the SEB medium was added to the culture (activated carbon culture). As a result, in the basic experiment, even if the cells were stored at various temperatures for 5 days, a bacterial load of 10 1 (10 to the power of 1) was detectable. Of urine collected from 116 pregnant women, 58 were positive by any one of the above three culture methods.
It was an example. Among them, 18 were positive in direct culture.
Example (15.5%), 53 positive cases in sediment culture (45.
7%), and positive in activated carbon culture was 27 cases (23.3%). The results were 17 positive for all three species, 22 positive for sediment culture only, 4 positive for activated carbon only, and 5 positive for activated carbon and sediment culture.

【0013】上記結果に示したように、直接培養した例
の検出率が最も悪く、次に活性炭培養、沈渣培養の順で
あった。しかし、沈渣培養では陽性率が非常に高くな
り、僅かな菌量でも遠沈操作で集菌したために陽性率が
高くなったものと考えられる。検出された菌の血清型を
分別すると、同一人からは如何なる培養方法を採っても
同じ血清型が検出されているが、同じ検査施設からは或
る一定の血清型が特に多く検出されているわけではな
く、今までの報告にある血清型別分布と類似していて、
一般の尿採取からの培養でも十分に対応できることが判
明した。
As shown in the above results, the detection rate was the worst in the case of direct culture, followed by activated carbon culture and sediment culture. However, it is considered that the positive rate was extremely high in the sediment culture, and the positive rate was high because the cells were collected by the centrifugation operation even with a small amount of bacteria. When the serotypes of the detected bacteria are separated, the same serotype is detected from the same person regardless of which culture method is used, but a certain serotype is particularly often detected from the same laboratory. However, it is similar to the serotype distributions reported so far,
It was found that culture from general urine collection can also be adequately applied.

【0014】[0014]

【発明の効果】この発明によると、検体である尿は活性
炭に吸着され、さらに、一定の容器に密閉されて輸送さ
れるので、輸送中に尿の漏洩並びに蒸発が十分に防止さ
れ、しかも、尿は数日間の温度変化に対しても極めて安
定状態を保つ。従って、輸送中においても細菌の繁殖並
びに死滅がなく、検体に付した場合に、結果として常に
一定の陽性率が得られる。また、内診によるものではな
いから、患者並びに検査機関や施設の関係者に対しても
煩雑な手数を省くことができる。そして、本発明による
輸送用容器は、材質が熱可塑性合成樹脂による一体成形
であるから、頗る生産性に富み、いわゆる「使い捨て」
に適応でき、かつ、衛生的であるとともに、輸送の際に
破損しにくく安全性にも富む。また、そのままの形態で
採尿と培養液導入を行なうことができる。さらに、その
材質並びに形状とが結合し、軽量で嵩張りがなく、細管
を折り曲げて固定すれば簡便に密閉ができる。しかも、
封筒内に極めて良好にフィットするので、封筒内での移
動やガタつきがなく輸送に適合する。
According to the present invention, urine, which is a sample, is adsorbed by activated carbon and further transported while being sealed in a fixed container, so that leakage and evaporation of urine during transportation can be sufficiently prevented, and Urine remains extremely stable even when the temperature changes for several days. Therefore, even if the bacteria are not propagated or killed even during transportation, a constant positive rate can always be obtained as a result when attached to a sample. Moreover, since it is not based on an internal examination, it is possible to save a troublesome procedure for a patient and a person involved in a laboratory or facility. The shipping container according to the present invention, which is integrally molded of thermoplastic synthetic resin, has excellent productivity and is so-called “disposable”.
It is adaptable to, and is hygienic, and is not easily damaged during transportation and is highly safe. Further, urine collection and culture solution introduction can be performed in the same form. Further, the material and the shape are combined to make it lightweight and not bulky, and it can be easily sealed by bending and fixing the thin tube. Moreover,
Since it fits very well in the envelope, there is no movement or rattling inside the envelope and it is suitable for transportation.

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

【図1】本発明の一実施例を示した斜視図である。FIG. 1 is a perspective view showing an embodiment of the present invention.

【図2】本発明の一実施例を示した正面図である。FIG. 2 is a front view showing an embodiment of the present invention.

【図3】本発明の一実施例を示した縦断面図である。FIG. 3 is a vertical sectional view showing an embodiment of the present invention.

【図4】本発明の一実施例を示した平面図である。FIG. 4 is a plan view showing an embodiment of the present invention.

【図5】本発明の一実施例を示した底面図である。FIG. 5 is a bottom view showing an embodiment of the present invention.

【図6】本発明の一実施例を示した横断面図である。FIG. 6 is a cross-sectional view showing an embodiment of the present invention.

【符号の説明】[Explanation of symbols]

1 胴管 2 上端 3 細管 4 活性炭 5 胴底 6 正面部 7 背面部 8 底面部 9 左側面部 10 右側面部 11 リング d 内径 1 Body tube 2 Upper end 3 Thin tube 4 Activated carbon 5 Body bottom 6 Front part 7 Back part 8 Bottom part 9 Left side part 10 Right side part 11 Ring d Inner diameter

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 患者の尿を活性炭入りの検出容器に採
取し、前記尿を該活性炭に吸着させたのち、検出容器内
の尿を排出するとともに、開口部を密閉して検査機関へ
輸送し、かつ、前記検出容器の密閉部を開口して、該検
出容器内に培養液を導入せしめ、活性炭に吸着している
尿中の細菌と反応させたことを特徴とする集菌検体の輸
送検出方法。
1. The urine of a patient is collected in a detection container containing activated carbon, the urine is adsorbed on the activated carbon, the urine in the detection container is discharged, and the opening is sealed and transported to a laboratory. And, the transport detection of the collected specimen characterized by opening the closed part of the detection container, introducing the culture solution into the detection container, and reacting with the bacteria in the urine adsorbed on the activated carbon Method.
【請求項2】 胴管(1)の上端(2)から上方へ連
続する細管(3)を熱可塑性合成樹脂材で一体成形し、
前記胴管(1)内に細管(3)の内径(d)より大なる
活性炭(4)を入れ、かつ、胴底(5)を熱圧着するこ
とにより、該胴底(5)の正面部(6)並びに背面部
(7)を一体扁平にし、同時に底面部(8)並びに左側
面部(9)及び右側面部(10)を一直線状に形成した
ことを特徴とする集菌検体の輸送用検出容器。
2. A thin tube (3) continuous upward from the upper end (2) of the body tube (1) is integrally molded with a thermoplastic synthetic resin material,
By inserting activated carbon (4) larger than the inner diameter (d) of the thin tube (3) into the body tube (1) and thermocompressing the body bottom (5), the front part of the body bottom (5). (6) and the back surface part (7) are integrally flattened, and at the same time, the bottom surface part (8) and the left side surface part (9) and the right side surface part (10) are formed in a straight line. container.
【請求項3】 胴管(1)の横断面の輪郭が、ほぼ長
楕円形状を呈する請求項2記載の集菌検体の輸送用検出
容器。
3. The container for transporting a collected specimen according to claim 2, wherein the profile of the cross section of the body tube (1) is substantially elliptical.
JP34928891A 1991-10-31 1991-10-31 Method for detecting transport of collected specimen and detection container for transportation used in the method Expired - Fee Related JPH06104076B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP34928891A JPH06104076B2 (en) 1991-10-31 1991-10-31 Method for detecting transport of collected specimen and detection container for transportation used in the method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP34928891A JPH06104076B2 (en) 1991-10-31 1991-10-31 Method for detecting transport of collected specimen and detection container for transportation used in the method

Publications (2)

Publication Number Publication Date
JPH05123188A true JPH05123188A (en) 1993-05-21
JPH06104076B2 JPH06104076B2 (en) 1994-12-21

Family

ID=18402747

Family Applications (1)

Application Number Title Priority Date Filing Date
JP34928891A Expired - Fee Related JPH06104076B2 (en) 1991-10-31 1991-10-31 Method for detecting transport of collected specimen and detection container for transportation used in the method

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Country Link
JP (1) JPH06104076B2 (en)

Also Published As

Publication number Publication date
JPH06104076B2 (en) 1994-12-21

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