JPH0117705B2 - - Google Patents
Info
- Publication number
- JPH0117705B2 JPH0117705B2 JP58067834A JP6783483A JPH0117705B2 JP H0117705 B2 JPH0117705 B2 JP H0117705B2 JP 58067834 A JP58067834 A JP 58067834A JP 6783483 A JP6783483 A JP 6783483A JP H0117705 B2 JPH0117705 B2 JP H0117705B2
- Authority
- JP
- Japan
- Prior art keywords
- dropper
- nozzle
- bottle
- filler
- drop
- 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
Links
- 239000000945 filler Substances 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 11
- -1 polypropylene Polymers 0.000 claims description 10
- 239000011148 porous material Substances 0.000 claims description 7
- 239000004743 Polypropylene Substances 0.000 claims description 5
- 229920001155 polypropylene Polymers 0.000 claims description 5
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- 239000002657 fibrous material Substances 0.000 claims description 3
- 238000003825 pressing Methods 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 11
- 239000004816 latex Substances 0.000 description 7
- 229920000126 latex Polymers 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 229920003002 synthetic resin Polymers 0.000 description 6
- 239000000057 synthetic resin Substances 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- 238000005259 measurement Methods 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 230000004520 agglutination Effects 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000001900 immune effect Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 239000000427 antigen Substances 0.000 description 1
- 102000036639 antigens Human genes 0.000 description 1
- 108091007433 antigens Proteins 0.000 description 1
- 239000004019 antithrombin Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000011491 glass wool Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Landscapes
- Media Introduction/Drainage Providing Device (AREA)
- Coating Apparatus (AREA)
- Devices For Use In Laboratory Experiments (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
Description
本発明は改良された機能を有する滴瓶に関す
る。
従来の滴瓶は少量の液体を迅速かつ正確に取り
出すのに用いられているが、ノズル内に液が残り
やすいという欠点がある。このため、一度滴瓶内
の液体を滴下したのち、続けて滴下するとノズル
内に液切れが起こつたり、末端開口部の外側に液
滴が残つたりして、1滴の滴下量が不正確とな
り、また末端開口部の周囲についた液滴のため汚
れることが多い。
最近、抗原又は抗体を感作したラテツクス試薬
を用い凝集又は凝集阻止反応を利用した生体内物
質等の定量する免疫学的定量方法が広く用いられ
ている。この際、ラテツクス試薬を含有する滴瓶
から滴下される試薬の量は常に一定となることが
必要であり、滴下量にバラツキがあると測定結果
を誤らせ、誤診に導く原因となる。また使用時滴
瓶を強振するとノズル内に液が浸入し、これが内
部空気の膨脹のため、試薬が押し出されるため、
使用時に液滴を拭きとつて使用している。これら
の現象は冷所保存を要するもの、もしくは常温保
存でも夏季など高温時に使用した時に発生するこ
とが多い。また医薬、医薬部外品などの医療用品
の懸濁液は、内容物を均一化するために容器を振
つて使用することがあり、その際キヤツプをはず
したときに内容物がノズルから噴出し、あるいは
キヤツプに内容物が付着して商品価値を低下させ
る。
さらに一試料ごとに滴下量の正確さを期すため
に、末端開口部を拭きながら、プレート上に滴下
するため操作が煩雑である。
本発明はこれらの欠点を除くため、鋭意研究し
た結果完成されたものであつて、ノズル基底部な
いしノズル中央部に、瓶本体の押圧によつて内容
液が容易に通過しうるように充填材を内臓したノ
ズルを有する免疫学的診断又は定量用滴瓶であ
る。
本発明の滴瓶は、充填されている溶液を外部か
ら圧力をかけ一滴ずつ排出することができるもの
であれば、いずれの形状のものも使用することが
できる。滴瓶に用いられる材料としては、例えば
ポリエチレンその他の合成樹脂、ゴムなどの軟質
樹脂が適しており、これらは単独で又は適宜組み
合わせて用いられる。また両端に開口部を有する
ガラス製容器の一方開口部にゴム製キヤツプを装
着し、他方の開口にノズル体を装着したものも用
いられる。
充填材としては、使用する溶媒に不溶性で、瓶
本体の押圧により溶液を容易に通過することので
きる多孔質体又は繊維状物質が好ましい。多孔質
体としては、例えば合成樹脂の発泡体、焼結体さ
らに詳しくはポリビニルホルマールを基質とする
発泡多孔質体、融着もしくは焼結したポリエチレ
ン、ポリプロピレン、ポリアミドなどが挙げられ
る。繊維状物質としてはポリプロピレン、ポリエ
ステル、ビニロン、ナイロン、ポリエチレン等の
合成繊維、グラスウール、脱脂綿などが挙げられ
る。合成樹脂多孔質体は連続気孔及び高い気孔率
を有しており特に好ましい。これらの充填材は単
独で又は適宜組み合わせて用いることができる。
充填材はノズルの形状により任意の形状、例え
ばブロツク状、円柱状、シート状、板状その他の
形で用いることができる。例えば合成樹脂多孔質
体を充填材として使用する場合は、充填材をノズ
ル下部の中央中空部とほぼ同じ直径を有する形に
成形して、この中空部内に密接に挿入することが
好ましい。
さらにこの充填材の上部及び/又は下部に、ノ
ズル細管に対応する孔を有する補助体を挿入する
こともできる。この補助体はアクリル樹脂、フエ
ノール樹脂、シリコーン樹脂、尿素樹脂、弗素樹
脂等で造られる。
以下、本発明滴瓶の1例を図面により説明す
る。
第1図は本発明滴瓶の1例を示す側面図、第2
図及び第3図はその縦断面図である。瓶本体1は
軟質合成樹脂製の円筒形容器であつて、側面を押
圧すると変形して内圧が上昇する。同じく合成樹
脂製のノズル体2は瓶本体の開口部1に好ましく
はネジ構造により嵌合して載置され、中央中空部
4及び細管5を有し、中央中空部4に充填材6が
充填されている。第3図は充填材6の上部に中心
細孔を有する補助体7を挿入した態様を示すもの
である。キヤツプ3はノズル体2に着脱自在に冠
着され、キヤツプ3とノズル体2は、ネジ構造に
より結合されてもよい。
本発明の滴瓶を使用する場合は、キヤツプ3を
取りはずしたのち、ノズルの細管5を下方に向
け、容器本体1の側部を指により押圧すると、瓶
内の液体が充填材6を通過して細管5の末端開口
から小滴として落下する。滴下終了後、容器本体
への加圧を除くと、容器は元の形状に戻り、容器
内部は陰圧となる。
従来の滴瓶では、容器内部が陰圧になると、細
管5から急激に空気が流入するため、細管5に液
体が残留し、再度滴下する場合に、1滴の量が不
正確となることが多かつた。これに対して本発明
の滴瓶は、空気の急激な流入が起こらないため、
細管5内に液が残留することがない。また滴瓶を
強く振つても、液が細管5内に進入することがな
いため、滴下量が常に一定に保たれる。
実験例
先端開口部2mmを有する滴瓶5本に抗ヒトアン
チトロンビン抗体感作ラテツクス試薬を入れ、
この滴瓶から滴下するラテツクス試薬の一滴の重
量を1本の滴瓶につき10回ずつ測定した。測定は
下記のとおり行つた。A:ノズルの先端開口部を
拭きとりながらラテツクス試薬を滴下する。B:
先端開口部を拭きとらずラテツクス試薬を滴下す
る。C:4.5mmのポリビニルホルマール多孔質体
(PVF:カネボウスポンジベルイーターA―3420
鐘紡合成化学(株)製)を充填した滴瓶からラテツク
ス試薬(本発明方法)を滴下する。その結果をま
とめた平均値を次表に示す。
The present invention relates to a dropper with improved functionality. Although conventional dropper bottles are used to dispense small amounts of liquid quickly and accurately, they have the disadvantage that liquid tends to remain in the nozzle. For this reason, if you drop the liquid in the dropper bottle once and then continue dropping it, the liquid may run out in the nozzle, or droplets may remain outside the end opening, resulting in an insufficient amount of each drop. It is accurate and often dirty due to droplets around the distal opening. BACKGROUND ART Recently, immunological quantitative methods have been widely used for quantifying substances in living organisms using agglutination or agglutination inhibition reactions using latex reagents sensitized with antigens or antibodies. At this time, it is necessary that the amount of reagent dripped from the dropper bottle containing the latex reagent is always constant, and any variation in the amount dropped may lead to erroneous measurement results and misdiagnosis. Also, if you shake the dropper bottle vigorously during use, the liquid will seep into the nozzle, and this will cause the internal air to expand, pushing out the reagent.
I wipe off the droplets before use. These phenomena often occur when products require storage in a cool place, or when they are stored at room temperature but used during high temperatures such as summer. In addition, suspensions of medical supplies such as drugs and quasi-drugs are sometimes used by shaking the container to homogenize the contents, and when the cap is removed, the contents may spray out from the nozzle. Otherwise, the contents may adhere to the cap, reducing the product value. Furthermore, in order to ensure the accuracy of the amount of drops for each sample, the operation is complicated as the end opening must be wiped while dropping onto the plate. In order to eliminate these drawbacks, the present invention was completed as a result of intensive research, and includes a filler material at the base of the nozzle or the center of the nozzle so that the content liquid can easily pass through when pressed by the bottle body. This is a drop bottle for immunological diagnosis or quantitative measurement that has a nozzle with a built-in nozzle. The dropper of the present invention can be of any shape as long as it can discharge the filled solution drop by drop by applying pressure from the outside. Suitable materials for the dropper include, for example, polyethylene and other synthetic resins, and soft resins such as rubber, which may be used alone or in appropriate combinations. Also used is a glass container having openings at both ends, with a rubber cap attached to one opening and a nozzle body attached to the other opening. The filler is preferably a porous material or a fibrous material that is insoluble in the solvent used and allows the solution to pass through easily by pressing the bottle body. Examples of the porous body include synthetic resin foams, sintered bodies, more specifically, foamed porous bodies having polyvinyl formal as a substrate, fused or sintered polyethylene, polypropylene, polyamide, and the like. Examples of the fibrous material include synthetic fibers such as polypropylene, polyester, vinylon, nylon, and polyethylene, glass wool, and absorbent cotton. Synthetic resin porous bodies have continuous pores and high porosity, and are particularly preferred. These fillers can be used alone or in appropriate combinations. The filler can be used in any shape depending on the shape of the nozzle, such as a block, cylinder, sheet, plate, or other shape. For example, when a porous synthetic resin material is used as a filler, it is preferable that the filler be formed into a shape having approximately the same diameter as the central hollow part at the bottom of the nozzle and tightly inserted into this hollow part. Furthermore, an auxiliary body having a hole corresponding to the nozzle capillary can be inserted into the upper and/or lower part of the filling material. This auxiliary body is made of acrylic resin, phenolic resin, silicone resin, urea resin, fluororesin, etc. Hereinafter, one example of the dropper of the present invention will be explained with reference to the drawings. Fig. 1 is a side view showing one example of the dropper bottle of the present invention;
The figure and FIG. 3 are longitudinal sectional views thereof. The bottle body 1 is a cylindrical container made of soft synthetic resin, and when the side surface is pressed, it deforms and the internal pressure increases. The nozzle body 2, also made of synthetic resin, is fitted into the opening 1 of the bottle body, preferably with a threaded structure, and placed thereon, and has a central hollow part 4 and a thin tube 5, and the central hollow part 4 is filled with a filler material 6. has been done. FIG. 3 shows an embodiment in which an auxiliary body 7 having a central pore is inserted above the filler 6. The cap 3 is detachably attached to the nozzle body 2, and the cap 3 and the nozzle body 2 may be connected by a screw structure. When using the dropper bottle of the present invention, after removing the cap 3, point the thin tube 5 of the nozzle downward and press the side of the container body 1 with your finger, so that the liquid in the bottle passes through the filler 6. and falls from the end opening of the capillary tube 5 as a droplet. When the pressure on the container body is removed after dropping, the container returns to its original shape and the inside of the container becomes negative pressure. In conventional drop bottles, when the inside of the container becomes negative pressure, air suddenly flows in from the thin tube 5, so liquid remains in the thin tube 5, and when dripping again, the amount of one drop may be inaccurate. It was a lot. On the other hand, the dropper of the present invention does not cause a sudden inflow of air, so
No liquid remains in the thin tube 5. Further, even if the dropper is shaken strongly, the liquid does not enter the thin tube 5, so the amount of the droplet is always kept constant. Experimental example: Put anti-human antithrombin antibody sensitizing latex reagent into five dropper bottles with a 2 mm tip opening.
The weight of each drop of latex reagent dropped from this dropper was measured 10 times for each dropper. The measurements were performed as follows. A: Drop the latex reagent while wiping the opening at the tip of the nozzle. B:
Drop the latex reagent without wiping the tip opening. C: 4.5mm polyvinyl formal porous material (PVF: Kanebo Sponge Bell Eater A-3420
A latex reagent (method of the present invention) is dripped from a dropper bottle filled with a dropper (manufactured by Kanebo Synthetic Chemical Co., Ltd.). The average values of the results are shown in the table below.
【表】
この結果から明らかなように、本発明の滴瓶を
用いると、滴下ごとにノズルの先端開口部を拭き
とりながら行つていた従来の一滴の滴下量とほと
んど差異がなく、しかも一滴の滴下重量差(又は
標準偏差)が従来法の約半分という極めて優れた
効力が得られる。さらに本発明の滴瓶を用いるこ
とにより、従来のノズルの先端開口部を拭きとり
ながら試薬を滴下した時と比べ、試薬の損失もな
く、試料の測定回数も2〜3回増えることが確認
された。充填材として繊維状態のポリプロピレン
を用いた場合も同様の結果が得られた。
例 1
直経2mmの先端開口部を有するポリエチレン製
滴瓶に、ポリビニルホルマール多孔質体(カネボ
ウスポスジベルイ―ターA―3420鐘紡合成化学(株)
製)を直径4.5mm、高さ8mmの円柱状に形成し、
滴瓶に装着した。
例 2
直径 1.0mmの先端開口部を有するポリエチレ
ン製滴瓶にポリビニルホルマール多孔質体(カネ
ボウスポンジベルイーターAー3410)を直径5.6
mm、高さ3mmの円柱状に形成し、滴瓶に装着し
た。
例 3
直径2mmの先端開口部を有する一部ゴムから成
るガラス製滴瓶にポリプロピレン合成繊維を隙間
なく長さ3mmとなるように密に充填した。[Table] As is clear from the results, when using the dropper of the present invention, there is almost no difference in the amount of each drop from the conventional method, which involves wiping the tip opening of the nozzle after each drop, and moreover, The difference in dropped weight (or standard deviation) of this method is approximately half that of the conventional method, resulting in extremely excellent efficacy. Furthermore, it was confirmed that by using the dropper of the present invention, there was no loss of reagent and the number of sample measurements increased by two to three times compared to the conventional method of dropping reagent while wiping the tip opening of the nozzle. Ta. Similar results were obtained when fibrous polypropylene was used as the filler. Example 1 A polyvinyl formal porous material (Kanebosu Siber Eater A-3420 Kanebo Synthetic Chemical Co., Ltd.) was placed in a polyethylene dropper with a tip opening of 2 mm in diameter.
) was formed into a cylindrical shape with a diameter of 4.5 mm and a height of 8 mm,
It was attached to a drop bottle. Example 2 A polyvinyl formal porous material (Kanebo Sponge Bell Eater A-3410) with a diameter of 5.6 mm was placed in a polyethylene dropper with a tip opening of 1.0 mm in diameter.
It was formed into a cylindrical shape with a height of 3 mm and a height of 3 mm, and was attached to a drop bottle. Example 3 Polypropylene synthetic fibers were tightly packed into a glass dropper bottle made of partially rubber and having a tip opening with a diameter of 2 mm to a length of 3 mm without any gaps.
第1図は本発明の滴瓶の1例を示す側面図、第
2図及び第3図はその2種の態様を示す縦断面図
であつて、図中の記号1は容器本体、2はノズル
体、3はキヤツプ、6は充填材、7は補助体を示
す。
FIG. 1 is a side view showing one example of the dropper bottle of the present invention, and FIGS. 2 and 3 are longitudinal cross-sectional views showing two types of the dropper bottle, in which symbol 1 is the container body, and 2 is the container body. In the nozzle body, 3 is a cap, 6 is a filling material, and 7 is an auxiliary body.
Claims (1)
の押圧によつて内容液が容易に通過しうるように
充填材を内臓したノズルを有する免疫学的診断又
は定量用滴瓶。 2 充填材が多孔質物質又は繊維状物質である、
特許請求の範囲第1項に記載の滴瓶。 3 充填材が多孔質ポリビニルホルマール樹脂又
はポリプロピレン焼結体である、特許請求の範囲
第1項又は第2項に記載の滴瓶。[Scope of Claims] 1. A dropper bottle for immunodiagnosis or metering that has a nozzle with a built-in filler at the base or center of the nozzle so that the liquid can easily pass through by pressing the bottle body. . 2 The filler is a porous material or a fibrous material,
A dropper bottle according to claim 1. 3. The dropper according to claim 1 or 2, wherein the filler is a porous polyvinyl formal resin or a polypropylene sintered body.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58067834A JPS59194751A (en) | 1983-04-19 | 1983-04-19 | Drip bottle |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58067834A JPS59194751A (en) | 1983-04-19 | 1983-04-19 | Drip bottle |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59194751A JPS59194751A (en) | 1984-11-05 |
JPH0117705B2 true JPH0117705B2 (en) | 1989-03-31 |
Family
ID=13356366
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58067834A Granted JPS59194751A (en) | 1983-04-19 | 1983-04-19 | Drip bottle |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59194751A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0752040Y2 (en) * | 1991-04-06 | 1995-11-29 | 東亞合成株式会社 | Adhesive container |
FI108514B (en) * | 1993-06-25 | 2002-02-15 | Cusi Lab | Use of polymer membranes in the distribution of pharmaceutical solutions containing quaternary ammonium compounds as preservatives |
BR102014031869A2 (en) * | 2014-12-18 | 2016-06-21 | Invitra Tecnologia Da Reprodução Assistida Ltda | multi-dose pipettor bottle and its use |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5093496U (en) * | 1973-12-26 | 1975-08-06 | ||
JPS5093495U (en) * | 1973-12-26 | 1975-08-06 |
-
1983
- 1983-04-19 JP JP58067834A patent/JPS59194751A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59194751A (en) | 1984-11-05 |
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