JP3192217B2 - Medical tubing - Google Patents
Medical tubingInfo
- Publication number
- JP3192217B2 JP3192217B2 JP14184192A JP14184192A JP3192217B2 JP 3192217 B2 JP3192217 B2 JP 3192217B2 JP 14184192 A JP14184192 A JP 14184192A JP 14184192 A JP14184192 A JP 14184192A JP 3192217 B2 JP3192217 B2 JP 3192217B2
- Authority
- JP
- Japan
- Prior art keywords
- tube
- weight
- parts
- fatty acid
- flow rate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Landscapes
- Infusion, Injection, And Reservoir Apparatuses (AREA)
- Materials For Medical Uses (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は輸血や輸液などに用いる
常に安定した流量設定ができる医療用チューブに関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a medical tube used for blood transfusion, transfusion, etc., which can always set a stable flow rate.
【0002】[0002]
【従来の技術】従来、輸血や輸液に際しては塩化ビニル
製のチューブが使用されているが、ニトログリセリンな
どの脂溶性の高い薬剤が輸液剤に含まれている場合、薬
剤がチューブ内壁に吸着するなどの問題があり、設定し
た量の薬剤が人体に供給されないことがある。2. Description of the Related Art Conventionally, a tube made of vinyl chloride has been used for blood transfusion or infusion. However, when a highly lipid-soluble drug such as nitroglycerin is contained in an infusion solution, the drug adsorbs to the inner wall of the tube. For example, the set amount of medicine may not be supplied to the human body.
【0003】このため、薬剤吸着を起こりにくくするた
め疎水性の高いポリオレフィン系の樹脂を用いたチュー
ブが使われるようになっている。[0003] For this reason, a tube using a polyolefin resin having high hydrophobicity has been used in order to make it difficult for drug adsorption to occur.
【0004】ところが、チューブの疎水性が高くなると
濡れ性が悪くなり、一旦気泡が付着するとなかなか取れ
にくくなるなど問題が生じてきた。[0004] However, when the hydrophobicity of the tube is increased, the wettability is deteriorated, and once the air bubbles adhere, there have been problems such as difficulty in removing the air bubbles.
【0005】例えば、プライミング操作においては、チ
ューブ内に気泡が付着しないように注意深く行わなけれ
ばならず、一旦、チューブ内壁に付着した場合取り去る
のに手間取ることがあった。[0005] For example, in the priming operation, care must be taken to prevent air bubbles from adhering to the inside of the tube, and once it adheres to the inner wall of the tube, it sometimes takes time to remove it.
【0006】また、クレンメなどを用いて流量を調節す
る場合チューブが変形し、流路が非常に狭くなってい
る。その流路が狭くなりつつある付近に特に気泡が付着
しやすくなり、そのためクレンメにより流量を正確に調
節しても、その部分に気泡が付着した場合、流れが妨害
され流量が変化する虞れがあった。Further, when the flow rate is adjusted by using a clamp or the like, the tube is deformed, and the flow path is extremely narrow. In the vicinity where the flow path is narrowing, air bubbles are particularly likely to adhere. Therefore, even if the flow rate is accurately adjusted by using a clamp, if air bubbles adhere to that portion, the flow may be obstructed and the flow rate may change. there were.
【0007】このために疎水性チューブ内壁に界面活性
剤等の親水性の物質をその溶液に浸漬し乾燥するなどし
てコーティングすることにより濡れ性を高める処理が施
されるものが開発されている。[0007] For this purpose, a process has been developed in which a hydrophilic substance such as a surfactant is coated on the inner wall of a hydrophobic tube by dipping in a solution thereof and drying the coating to increase wettability. .
【0008】[0008]
【発明が解決しようとする問題点】ところが、チューブ
内壁にコーティングした場合、コーティングした親水性
物質が溶出したりする虞れがあり、また、コーティング
の工程が複雑となり大量生産できないなど、改善が望ま
れていた。また、輸液を長時間続けるとコーティングが
剥げ落ちるために濡れ性が経時的に変化することがあっ
た。However, when coated on the inner wall of the tube, there is a possibility that the coated hydrophilic substance may be eluted, and furthermore, the coating process becomes complicated and mass production is not possible, and improvement is desired. Was rare. In addition, if the infusion is continued for a long time, the wettability may change with time because the coating peels off.
【0009】[0009]
【発明が解決するための課題】本発明の目的は、簡単に
製造でき、溶出物の発生の虞れがなく内壁に気泡が付着
しにくいか、または付着しても容易に脱離することがで
きる医療用チューブを提供することである。DISCLOSURE OF THE INVENTION An object of the present invention is to make it easy to manufacture, and there is no danger of generation of elutes, and it is difficult for air bubbles to adhere to the inner wall, or even if they adhere, they are easily desorbed. It is to provide a medical tube that can be used.
【0010】[0010]
【課題を解決するための手段】このような目的は以下に
記載の本発明によって達成される。すなわち、1,2−
ポリブタジエン100重量部に脂肪酸エステル系の非イ
オン性界面活性剤を0.02から5.0重量部を配合し
てなる医療用チューブによって達成される。This and other objects are achieved by the invention described hereinafter. That is, 1,2-
This is achieved by a medical tube comprising 100 parts by weight of polybutadiene and 0.02 to 5.0 parts by weight of a fatty acid ester-based nonionic surfactant.
【0011】[0011]
【作用】本発明は1,2−ポリブタジエン100重量部
に脂肪酸エステル系の非イオン性界面活性剤を0.02
から5.0重量部を配合してなる医療用チューブである
ので、チューブ内壁は基材となる樹脂に配合された界面
活性剤の影響で濡れ性が増加しており、したがって、気
泡が付着しにくくなっており、たとえ付着したとしても
容易に離脱してしまう。また、1,2−ポリブタジエン
に脂肪酸エステル系の非イオン性界面活性剤が配合され
ているので、溶出が起こりにくく、経時的にチューブ内
表面の変化が少ない。According to the present invention, a fatty acid ester-based nonionic surfactant is added in an amount of 0.02 to 100 parts by weight of 1,2-polybutadiene.
Is 5.0 parts by weight, the wettability of the inner wall of the tube is increased due to the effect of the surfactant incorporated in the resin serving as the base material. It is difficult to remove even if it adheres. Further, since a fatty acid ester-based nonionic surfactant is blended with 1,2-polybutadiene, elution is unlikely to occur, and there is little change in the inner surface of the tube over time.
【0012】ここで本発明で用いられる脂肪酸エステル
系の非イオン性界面活性剤としてはグリセリンモノステ
アレート、グリセリンモノラウレート、グリセリンモノ
オレート、グリセリンモノパルミテートなどのグリセリ
ンの脂肪酸エステル、プロピレングリコールモノラウレ
ート、プロピレングリコールモノステアレート、プロピ
レングリコールモノオレート、プロピレンモノパルミテ
ートなどのプロピレングリコールの脂肪酸エステル、ソ
ルビタンモノラウレート、ソルビタンモノステアレー
ト、ソルビタンモノオレート、ソルビタンパルミテート
などのソルビタンの脂肪酸エステルなどがある。これら
の界面活性剤は親油性が高いためにオレフィン系樹脂と
非常に混和性が高い。The nonionic surfactants of the fatty acid ester type used in the present invention include fatty acid esters of glycerin such as glycerin monostearate, glycerin monolaurate, glycerin monooleate and glycerin monopalmitate; Fatty acid esters of propylene glycol such as laurate, propylene glycol monostearate, propylene glycol monooleate, and propylene monopalmitate; fatty acid esters of sorbitan such as sorbitan monolaurate, sorbitan monostearate, sorbitan monooleate, and sorbitan palmitate There is. These surfactants are highly miscible with olefin resins because of their high lipophilicity.
【0013】また、本発明に用いられる脂肪酸エステル
系の非イオン性界面活性剤の配合量は1,2−ポリブタ
ジエン100重量部に対して0.02〜5.0重量部、
好ましくは0.03〜4.0重量部である。配合量が
0.02重量部未満であると、チューブ内壁の濡れ性が
悪く、5.0重量部を越えると輸液剤に界面活性剤が溶
出する虞れが生じることとなるので、好ましくない。The amount of the fatty acid ester nonionic surfactant used in the present invention is 0.02 to 5.0 parts by weight based on 100 parts by weight of 1,2-polybutadiene.
Preferably it is 0.03-4.0 parts by weight. If the amount is less than 0.02 parts by weight, the wettability of the inner wall of the tube is poor, and if it exceeds 5.0 parts by weight, the surfactant may be eluted into the infusion solution, which is not preferable.
【0014】[0014]
【0015】また、本発明のチューブの樹脂を内部に持
つ積層構造をとってもよい。その際に内壁となる樹脂の
厚みは要求される柔軟性などによって適宜変えることが
できる。Further, a laminated structure having the resin of the tube of the present invention inside may be adopted. At that time, the thickness of the resin serving as the inner wall can be appropriately changed depending on the required flexibility and the like.
【0016】また、本発明の医療用チューブは1,2−
ポリブタジエン100重量部に脂肪酸エステル系の非イ
オン性界面活性剤を配合した後、通常公知のチューブの
製造方法である押出成形が適用できる。[0016] The medical tube of the present invention comprises 1,2-
After blending a fatty acid ester-based nonionic surfactant with 100 parts by weight of polybutadiene, extrusion molding, which is a generally known method for producing a tube, can be applied.
【0017】[0017]
【0018】[0018]
【実施例1〜3】1.2−ポリブタジエン(RB81
0、日本合成ゴム株式会社製)にグリセリンモノステア
レート(リケマール、理化ビタミン製)を表1に示す配
合量に従い配合し、押出成形機を用いて内径2.1m
m、外形3.1mmのチューブを作成した。Examples 1-3: 1.2-polybutadiene (RB81
0, manufactured by Nippon Synthetic Rubber Co., Ltd.) and glycerin monostearate (Riquemar, manufactured by Rika Vitamin Co., Ltd.) according to the compounding amounts shown in Table 1. The inner diameter was 2.1 m using an extruder.
A tube having an outer diameter of 3.1 mm was prepared.
【0019】[0019]
【比較例1】実施例で用いたものと同じ1.2−ポリブ
タジエンを実施例と同じ方法でチューブを作成した。Comparative Example 1 A tube was prepared from the same 1.2-polybutadiene used in the examples by the same method as in the examples.
【0020】[0020]
【表1】 [Table 1]
【0021】[実験例]実施例1〜3と比較例1で作成
したチューブを長さ2mに切断し、一端にビン針付きの
点滴筒を付け、チューブの中央付近にクレンメをセット
し、他端に穿刺針をつなぎ、さらにビン針を輸液バッグ
の薬液導出口に突き刺しチューブ内に輸液剤を導入し
た。この輸液バッグを高所に吊し、点滴筒内の滴下量
(単位時間当たりの滴下数、1分間で60滴ほど滴下す
ると、1時間当たり60mlになる)を見ながらクレン
メにより流量の調節をおこなった。この後約1時間後再
び流量を観測したときの変化率(下記式)を観測した。
その結果を表2に示す。表2から実施例1〜3のチュー
ブは流量の変化がほとんどないことがわかる。[Experimental Example] The tubes prepared in Examples 1 to 3 and Comparative Example 1 were cut to a length of 2 m, a drip tube with a bottle needle was attached to one end, and a clamp was set near the center of the tube. A puncture needle was connected to the end, and a bottle needle was pierced into the drug solution outlet of the infusion bag to introduce the infusion solution into the tube. The infusion bag is suspended at a high place, and the flow rate is adjusted by creme while observing the amount of dripping in the drip tube (the number of drippings per unit time, when about 60 drops are dropped per minute, it becomes 60 ml per hour). Was. About one hour later, the rate of change (the following equation) when the flow rate was observed again was observed.
Table 2 shows the results. From Table 2, it can be seen that the tubes of Examples 1 to 3 have almost no change in the flow rate.
【0022】変化率(%)=100×(1時間後の流
量)−(始めの流量(60ml/時))÷(始めの流量
(60ml/時)) また、目視にてチューブを観測した結果、実施例のチュ
ーブには気泡の付着は見られなかったが、比較例1のも
のはクレンメ付近に気泡の付着が見られた。Rate of change (%) = 100 × (flow rate after 1 hour) − (initial flow rate (60 ml / hour)) ÷ (initial flow rate (60 ml / hour)) Also, the result of visual observation of the tube No air bubbles were observed on the tube of the example, but air bubbles were observed on the tube of Comparative Example 1 near the clamp.
【0023】[0023]
【表2】 [Table 2]
【0024】[試験例]実施例1〜3と比較例1で作成
したチューブについて、薬局法に準じて安全性の試験を
行った。その結果を表3に示す。[Test Example] The tubes prepared in Examples 1 to 3 and Comparative Example 1 were subjected to a safety test according to the pharmacy method. Table 3 shows the results.
【0025】[0025]
【0026】[0026]
【表3】 [Table 3]
【0027】また、実施例1〜3の実験例で流した輸液
剤を分析したが、界面活性剤はほとんど検出されなかっ
た。Further, when the infusion solution that was flowed in the experimental examples of Examples 1 to 3 was analyzed, almost no surfactant was detected.
【0028】[0028]
【発明の効果】本発明は1,2−ポリブタジエン100
重量部に脂肪酸エステル系の非イオン性界面活性剤を
0.02から5.0重量部を配合してなる医療用チュー
ブであって、1,2−ポリブタジエンに界面活性剤が配
合されているためにチューブ内壁の濡れ性が配合してい
ないものに比べ向上しており、輸血、輸液の途中で気泡
が付着しても容易に脱離させることができる。さらに、
クレンメによる流量の調節を行っていても流路に気泡が
付着することがなく、流量の変化が起きず安定した流量
を確保することができる。また、コーティングしたもの
と同様な気泡付着防止の効果があり、界面活性剤が溶出
する虞れがないなどの利点がある。The present invention relates to 1,2-polybutadiene 100
This is a medical tube in which 0.02 to 5.0 parts by weight of a fatty acid ester-based nonionic surfactant is blended in parts by weight, and the surfactant is blended in 1,2-polybutadiene. In addition, the wettability of the inner wall of the tube is improved as compared with the case where the tube is not blended, and even if air bubbles adhere during blood transfusion or transfusion, the tube can be easily removed. further,
Even when the flow rate is adjusted by the clamp, no air bubbles adhere to the flow path, and a stable flow rate can be secured without a change in the flow rate. Further, it has the same effect of preventing air bubble adhesion as the coated one, and has the advantage that there is no fear that the surfactant is eluted.
Claims (3)
肪酸エステル系の非イオン性界面活性剤を0.02〜
5.0重量部配合してなる樹脂からなる医療用チュー
ブ。1. A fatty acid ester-based nonionic surfactant is used in an amount of 0.02 to 100 parts by weight of 1,2-polybutadiene.
A medical tube made of a resin mixed with 5.0 parts by weight.
の配合量が0.03〜4.0重量部である請求項1記載
の医療用チューブ。2. The medical tube according to claim 1, wherein the amount of the fatty acid ester-based nonionic surfactant is 0.03 to 4.0 parts by weight.
がグリセリンモノステアレートである請求項1記載の医
療用チューブ。3. The medical tube according to claim 1, wherein the fatty acid ester nonionic surfactant is glycerin monostearate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14184192A JP3192217B2 (en) | 1992-06-03 | 1992-06-03 | Medical tubing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14184192A JP3192217B2 (en) | 1992-06-03 | 1992-06-03 | Medical tubing |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05329202A JPH05329202A (en) | 1993-12-14 |
JP3192217B2 true JP3192217B2 (en) | 2001-07-23 |
Family
ID=15301403
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14184192A Expired - Fee Related JP3192217B2 (en) | 1992-06-03 | 1992-06-03 | Medical tubing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3192217B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101320166B (en) * | 2007-06-08 | 2012-02-22 | 斯坦雷电气株式会社 | Monochromatic liquid crystal display with high contrast |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4806890B2 (en) * | 2003-10-02 | 2011-11-02 | 株式会社ジェイ・エム・エス | Medical molded parts |
JP2005124690A (en) * | 2003-10-22 | 2005-05-19 | Jms Co Ltd | Most suitable base material for medical conduit |
JP2005152039A (en) * | 2003-11-20 | 2005-06-16 | Jms Co Ltd | Medical molded member |
JP6172422B1 (en) * | 2015-10-23 | 2017-08-02 | 株式会社村田製作所 | Infusion tube and infusion set |
EP3960221B1 (en) | 2016-06-17 | 2024-06-12 | Becton, Dickinson and Company | Method and apparatus for wetting internal fluid path surfaces of a fluid port to increase ultrasonic signal transmission |
-
1992
- 1992-06-03 JP JP14184192A patent/JP3192217B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101320166B (en) * | 2007-06-08 | 2012-02-22 | 斯坦雷电气株式会社 | Monochromatic liquid crystal display with high contrast |
Also Published As
Publication number | Publication date |
---|---|
JPH05329202A (en) | 1993-12-14 |
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