JPS60261505A - Filtration device - Google Patents
Filtration deviceInfo
- Publication number
- JPS60261505A JPS60261505A JP59115558A JP11555884A JPS60261505A JP S60261505 A JPS60261505 A JP S60261505A JP 59115558 A JP59115558 A JP 59115558A JP 11555884 A JP11555884 A JP 11555884A JP S60261505 A JPS60261505 A JP S60261505A
- Authority
- JP
- Japan
- Prior art keywords
- filtration
- bottle
- filtrate
- adapter
- injection needle
- 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
Links
- 238000001914 filtration Methods 0.000 title claims description 30
- 238000002347 injection Methods 0.000 claims description 7
- 239000007924 injection Substances 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- 239000012528 membrane Substances 0.000 claims description 7
- 239000000706 filtrate Substances 0.000 claims description 4
- 238000000108 ultra-filtration Methods 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 238000000605 extraction Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 229940121896 radiopharmaceutical Drugs 0.000 description 2
- 239000012217 radiopharmaceutical Substances 0.000 description 2
- 230000002799 radiopharmaceutical effect Effects 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 206010062717 Increased upper airway secretion Diseases 0.000 description 1
- 240000002853 Nelumbo nucifera Species 0.000 description 1
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 1
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- QTCANKDTWWSCMR-UHFFFAOYSA-N costic aldehyde Natural products C1CCC(=C)C2CC(C(=C)C=O)CCC21C QTCANKDTWWSCMR-UHFFFAOYSA-N 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- ISTFUJWTQAMRGA-UHFFFAOYSA-N iso-beta-costal Natural products C1C(C(=C)C=O)CCC2(C)CCCC(C)=C21 ISTFUJWTQAMRGA-UHFFFAOYSA-N 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 description 1
- 238000009206 nuclear medicine Methods 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 208000026435 phlegm Diseases 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000012857 radioactive material Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
Landscapes
- Infusion, Injection, And Reservoir Apparatuses (AREA)
- External Artificial Organs (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
Description
【発明の詳細な説明】
(離業上の利用分!1lIf)
この発明Fi各撫化合物の自動合成装置の端末装置とし
て■濾過装置、特に層院内で1整される蝮寿命アイソト
ープwm化会物の靜脈江射可能秦削化のための限外濾過
に好適な限外濾過装置に関する。Detailed Description of the Invention (Aside from work! 1lIf) This invention is used as a terminal device for an automatic synthesis device for various compounds. The present invention relates to an ultrafiltration device suitable for ultrafiltration for ultrafiltration in which water can be irradiated.
(背景技術)
近年、千減期が数分から数十分の短千減ルJアイソトー
プが核医学分野で重装な地位を占めてきており、こハら
については従来のような装架会社による供給体制では対
応小OT能となっている。このため、一般病院、研究り
[など、k用場所でサイクロトロンを用いて短半減肋核
横を作り、自動8−爪装置itを用いて6稙の裸緑化合
物を合成し、靜汁業に調整することが必蒙小可欠となっ
てきた。サイクロトロンによって生産される短千減期核
褌としては150(半減M2分)、13N(同10分)
、+10 (同20分)、”Ft同110分)等があ
るが、母核様が繊業蝦者吟から供給され、その崩廐生成
物として得られる99mTCのように決仕既に一般病院
で広く匠用されているものについても、よシ尚鍵な放射
性医薬品のむ賊とそのむ注系化が強くめられている。(Background technology) In recent years, short-depletion J isotopes with a depletion period of several minutes to several tens of minutes have come to occupy an important position in the field of nuclear medicine, and these are currently being handled by mounting companies. The supply system has a small OT capacity. For this purpose, we used a cyclotron to create a short half-reduced costal nucleus at a general hospital, research laboratory, etc., and synthesized a 6-terminal naked green compound using an automatic 8-claw device IT, and used it in the soup industry. Adjustment has become essential. Short-life nuclear loincloths produced by a cyclotron are 150 (halved in M2 minutes) and 13N (halved in 10 minutes).
, +10 (20 minutes at the same time), "Ft at 110 minutes), etc., but the mother nucleus is supplied from the textile industry Eshagin, and the final product is already available in general hospitals, such as 99mTC obtained as its decay product. Even in the case of widely used radiopharmaceuticals, there are strong calls for thieves to steal radiopharmaceuticals and to make them available for purchase.
装架会社などでの靜江業駒1ハ大皺の試料を融物な品質
官地下で一豐フる■で特に間組はないが、一般病院や研
究所等での靜注薬調整は蜘めて困難であった。これらの
場所では一般に自動合成装置によって合成されるが、自
動合成装置はホットセル内に設置されるため非常に小型
で、その中に多数のwL磁弁、反応容器、センザ顎がテ
フロンチューブ、ステンレスチューブで接続されており
、台成系路の滅菌は険めて困難である。特に、固定化r
#素を利用した標識法は迅速・筒収率で、短寿命核抽の
棒識法として鍜適であるが、遊陥酵素■混入、固定#素
カラムの滅菌が障害となってその普及が制限されている
。At a mounting company, etc., a specimen with large wrinkles of Jingjiang Industry Co., Ltd. is processed for a few minutes in a quality government underground facility, and there is no special procedure, but it is difficult to adjust the dosage at general hospitals and research institutes. It was difficult. In these places, synthesis is generally carried out using automatic synthesis equipment, but the automatic synthesis equipment is very small because it is installed in a hot cell. Sterilization of the pedestal system is extremely difficult. In particular, immobilized r
The labeling method using # element is rapid and yields well, and is suitable as an identification method for short-lived nuclear extraction, but its widespread use is hampered by the contamination of fugitive enzymes and the sterilization of the fixed # element column. Limited.
一方、細菌のへならず、r#累、発熱’*貿等の高分子
迄を痣in除去できる限外濾過膜が市販されてお如、そ
の利用によって靜注槃隔堅がd易になることがM待され
る。しかし、この濾膜を用いfc従来の濾過装置1tは
、各器内への残存液皺l が′きく・短N*放射性医架
品o J: 5 Vc 1〜10mL円匪の小皺の試料
処理には不同きであった0勿−1小紙のフィルタを用い
れは田の2乗に比例して残存液飯は少なくなるが、濾過
のために時間を要することとなり、短人命核柚の嘔扱い
には不向きとなる。On the other hand, there are commercially available ultrafiltration membranes that can remove bacteria, R# accumulation, fever, and other polymers from scratches. I'm looking forward to it. However, the conventional FC filtration device 1t using this filtration membrane does not allow residual liquid wrinkles in each container. If you use a filter with a size of 0 - 1 small paper, which was not the same, the amount of remaining liquid will be reduced in proportion to the square of the amount of paper, but it will take time to filter, which will shorten your life. It becomes unsuitable for handling.
その上、放射性核抽を取扱うため、試料の合成、濾過は
遮蔽壁内で遠隔操作で行なう必要があり、しかも蘭過終
了後迄を宮めで迅速に敗扱う必要があり、濾過状況を遠
隔的に検知しうろことがめられる。Furthermore, in order to handle radioactive nuclear extraction, sample synthesis and filtration must be performed remotely within a shielding wall, and furthermore, until after the extraction is completed, it is necessary to quickly handle the extraction at the temple, and the filtration status can be monitored remotely. It is detected that scales are detected.
(発明の目的)
この発明は上記の多くの散水を満まため、取扱いが簡嚇
で、遠隔的に濾過状況を踊実に把握できる眠界蓚過装置
を得ようとするものでちる。(Objective of the Invention) The present invention aims to provide a sleeping area filtration device that is easy to handle and can easily and easily grasp the filtration status from a remote location, in order to satisfy the above-mentioned many types of water sprinkling requirements.
(発明の構成) 以下この発明を、図面を鯵照して許仙に直切する。(Structure of the invention) This invention will be described below with reference to the drawings.
第1図はこの発明の跡過装置の1実施しlを示す0蓚過
装置は飾膜を支持し、濾過を付なう撞過谷姦1と蓚過液
を収容する容認を保持し、謙過谷睦に一定位置に収付け
るためのアダプター2からなる。FIG. 1 shows one embodiment of the filtration device of the present invention. The filtration device supports the diaphragm and holds the filtration device 1 with the filtration and the capacity for accommodating the filtration liquid. It consists of an adapter 2 for storing it in a certain position on Mutsumi Kenkatani.
濾過容認1は第2図にその分解斜視図を示すように、#
液の流下口でおるルアースリップ雄4を下面中央に有す
る浅い円筒形の谷藷底部3、その中にステンレス網で構
成される支持板5と鼠畳された濾膜6を収納し、この濾
膜を周縁で中蓋7で抑圧−矩する。この中蓋はその縁付
フランジ7′を固定ねじ8で緊締する。中蓋7■上縁は
1儲9を螺着して閉じ、中蓋7内は濾液の’d’dWを
形成する。10は臥科尋人口、11は濾過の除の加圧力
ス尋人口、12は密封のためのQ IJングである。こ
れらの部材は、限外濾過のために加えられる読出に耐え
るよう7縁/。m2以上の耐圧に!するようにrl:ら
れる〇谷す底部の詳細を第3図に示す。全体として断面
がH形V)底部3は上側内面には固定ねじ8月の雄ねじ
31を、その底面にf′i誌液のIW寺擲32かV字跡
として形成される。また、蒋33は匪細Oリング12θ
ためのリング鍔であり、リング12はその殆んどかこの
リング纒33中に没入し、固定ねじ8でm付けた挾は支
持板5は底面にはは@着してこの支持板以下に残貿す
。As shown in the exploded perspective view of Fig. 2, filtration acceptance 1 is #
A shallow cylindrical valley bottom part 3 with a lure slip male 4 at the center of the lower surface through which the liquid flows, a support plate 5 made of a stainless steel net and a filter membrane 6 which is folded are housed in the bottom part 3. The membrane is compressed at the periphery with the inner lid 7 - rectangular. This inner lid is tightened at its edge flange 7' with fixing screws 8. The upper edge of the inner lid 7■ is closed by screwing a screw 9, and the inside of the inner lid 7 forms a 'd'dW of the filtrate. 10 is the pressure droplet, 11 is the pressure pressure droplet for filtration removal, and 12 is the pressure droplet for sealing. These members are designed to withstand the readings applied for ultrafiltration. Withstand pressure of m2 or more! Figure 3 shows the details of the bottom of the valley where rl: is made. Overall, the cross section is H-shaped (V) The bottom part 3 has a male screw 31 with a fixing screw on the upper inner surface, and a V-shaped trace of an IW temple 32 of f'i magazine on the bottom surface. In addition, Chiang 33 has a narrow O-ring 12θ
Most of the ring 12 is immersed in this ring string 33, and the clamp attached with the fixing screw 8 is attached to the bottom of the support plate 5 and remains below this support plate. trade
.
る師液蓋を極めて少なくする。Minimize the amount of phlegm liquid required.
下面内周には後で読切する位抽決めアダプタ2■喉付は
雌ねじ34が、そして中央には―液をバイアル瓶に晦入
する江射針】3をt!に合するルアースリップ雄4が設
けられている。On the inner periphery of the lower surface is a drawing adapter 2 for later reading, and a female thread 34 for the throat attachment, and in the center - an injection needle for pouring liquid into a vial] 3. A male luer slip 4 is provided to match the luer slip.
アダプタ2は、嫡4図に斜視図及び3面図を示すように
、バイアル瓶14を収納保持する瓶保持$15及びこれ
と指動可能に鯰合する可動部16で構成される。可動部
16の上部には答益匠部Qねじ34と都合するねじ16
1が設けられ、このねじ161 k 1)ALEするこ
とによシアダプタ2の濾過谷躇1に対する位置が決めら
れる。瓶9f、持8I515は底部はバイアル瓶140
低部と獣合し、その内面Vi町可動16■外周と指動可
能に獣&すると共に、光亀険出ヒル17のための窓15
1を有している。また、必要に応じ、瓶14を肉眼的に
維緒するため、1 tilllに窓152を敗けてもよ
い。As shown in a perspective view and a three-sided view in Figure 4, the adapter 2 is composed of a vial holder 15 that stores and holds a vial 14, and a movable part 16 that is movably engaged with the vial holder 15. At the top of the movable part 16 is a screw 16 that matches the Q screw 34 of the answering section.
1 is provided, and the position of the shear adapter 2 with respect to the filtration valley 1 is determined by this screw 161 k 1) ALE. Bottle 9f, holding 8I515 has a vial bottle 140 at the bottom.
The lower part meets the beast, and its inner surface is movable 16.
1. Further, if necessary, the window 152 may be closed until the bottle 14 is visually maintained.
この蓮過!装置は以下のように肥用される。This lotus pass! The device is used as follows.
この限外語過装fは、第5図にその概念図を承すように
、図示しない機枠に固定金具18によって固定する。次
いで賦科導入口10Fi自動g H1装置と逆止弁19
付テフロンテコーーブを介してルアージヨイントに依り
ワンタッチでihされる。また7111圧力ス導入口1
1は加圧ガス制−バルブ20とテフロンチューブを介し
て裟続される。As shown in the conceptual diagram of FIG. 5, this extralingual overload f is fixed to the machine frame (not shown) with a fixing fitting 18. Next, the feeder inlet 10Fi automatic g H1 device and check valve 19
It can be heated with one touch by using a luage joint through a Teflon tape cove. Also 7111 pressure gas introduction port 1
1 is connected via a pressurized gas control valve 20 and a Teflon tube.
位fkP:めアダプタ16に収付ねじ161上部の関口
からバイアル瓶14金伸人吠合さ忙、アダプター町動部
16を上方に引出した状態(第6図a)で取付ねじ16
1を谷し区部3の下面O数行ねじ34に綿層することに
より、瓶保持部15中の瓶14と、ルアースリップ雄4
に獣縫させた注射針13との相対位置が決定される。Position fkP: The vial bottle 14-karat gold Nobujin is attached to the female adapter 16 from the upper part of the mounting screw 161, and the mounting screw 16 is attached to the female adapter 16 with the adapter housing moving part 16 pulled upward (Fig. 6a).
1 on the lower surface O of the threaded section 3, the bottle 14 in the bottle holding section 15 and the luer slip male 4 are attached.
The relative position with respect to the injection needle 13 that has been sewn is determined.
次いで瓶保持部15を第6図aの矢印のように摺動させ
れば注射針13はバイアル瓶14の) ゴムキャンプ1
41v中央に画直に伸直され、注射針13!7)先端は
正しく光電検出hQ元路上方に位置される。23は空気
抜きの針である。Next, by sliding the bottle holder 15 in the direction of the arrow in FIG. 6a, the injection needle 13 is attached to the vial 14)
The injection needle 13!7) is re-extended to the center of the image 41v, and the tip of the injection needle 13!7) is correctly positioned above the source of the photoelectric detection hQ. 23 is an air vent needle.
第5図21Fi制(財)パネルを概念的に示したものf
、Thす、Rehlo te 、4.oca l fi
’jJ 懐スイ7 f T hす、LocalViこ
の装置の与に仏る嘔独駆動、Remo L e ij曲
Q機指からの16号に依る遠隔1動を示す。Lo c
a lモードのときは1尤unスイツチに依り濾過が開
始される。T1〜T6はタイマーであり、後述のT、〜
T4の時@をセットするり謙過手Illは、@7図のフ
レーチャー)′f:&照して、Runのスイッチオン(
Remote のときね他V)機kKから■糎号により
)により眩H■移込が開始される。誤動作防止のため1
1秒待った後光−検出622を作動さぜ、緘糾■尚下時
間間隔が12以上になったとき移送終了と刊断し、加圧
ガスを尋人口11から蓚過容lit 1内に尋人し、g
l過を開始する0加圧力スcO舒崩装諏へQ苑入は逆止
弁19で阻止される。蓚過開始汝、a!4動作防止のだ
め13秒狩った仮、元嵐険出b17をr[動させ、隷欣
の部下時間間隔を映出する。この間隔が予め設定した時
間11秒以上になったときU−過終了と刊断して終了信
号を発信する0(発明の効果)
この発明は上記の構成からなり、以下のような顕著な効
果を有する。Figure 5 conceptually shows the 21Fi system (goods) panel f
, Thsu, Rehlo te, 4. ocal fi
'j J Kaisui 7 f Th, LocalVi shows the remote 1 movement based on No. 16 from the German-Japanese drive and the Remo Leij song Q machine finger with this device. Loc
In the al mode, filtration is started by the 1-un switch. T1 to T6 are timers, and T, ~, which will be described later, are timers.
When T4 is set, @ is set, the feature shown in Figure 7)'f:&, and the Run switch is turned on (
The dazzling H■ transfer is started by the Remote Tokine et al. To prevent malfunction 1
Wait 1 second, activate the halo detection 622, and when the time interval becomes 12 or more, it is determined that the transfer is complete, and the pressurized gas is discharged from the tank volume 11 to the tank volume 1. person, g
A check valve 19 prevents the 0 pressurizing force from entering the 0-pressure-pressing system, which starts the flow. Start passing through you, a! 4. If you hunt for 13 seconds to prevent movement, move the former Arashi Danshi b17 to r[ and display the time interval of the slave's subordinate. When this interval reaches a preset time of 11 seconds or more, it is cut off as U-Excess and an end signal is sent.0 (Effects of the Invention) This invention has the above-mentioned configuration, and has the following remarkable effects. has.
■ 急過容器を滅菌して用いれば、試料はバイアル瓶に
貯留される迄全く空気や滅菌Q雌しい泡出d等に触れる
ことなく濾過できる。■ If a sterilized rapid container is used, the sample can be filtered without coming into contact with air or bubbles until it is stored in a vial.
■ 部下状態を常に監視し、滴下時間が一定時間より長
くなれば薄遇終了と判断することによシ、濾過に要する
時間を峡小に止め、短寿砧核袖標識化合物の処理に特に
dしている。■ By constantly monitoring the condition of the subordinates and determining that the treatment is over if the dripping time is longer than a certain time, the time required for filtration can be kept to a minimum, and this method is especially effective when processing short-lived Kinutokusode-labeled compounds. are doing.
■ 位置決めアダプターにより極めて容易にバイアル瓶
○瞬定の位置に注射針を挿通出来、濾過状態の監視が隋
実である。■ The positioning adapter makes it extremely easy to insert the injection needle into the instant position of the vial, making it very easy to monitor the filtration status.
■ 操作が総て自動化され、遠隔珠作が可能なので放射
性物質を安全に取扱うことができる。■ All operations are automated and remote production is possible, allowing safe handling of radioactive materials.
■ この濾過装置は限外簿過装置として病院ΦhJF死
所等で靜注粂を調整するのに特に適しているが、■〜■
の幼果は特にこの目的に限定されることなく、濾過装置
として広い応用範囲會有している。■ This filtration device is particularly suitable as an ultrafiltration device for adjusting the filtration in hospitals, etc., but ■〜■
The young fruits are not limited to this purpose in particular, and have a wide range of applications as filter devices.
(9)(9)
第1図はこの発明の濾過装置の1笑踊卸υ1部断囲図、
第2図は濾過容器の分11#斜視図、第3図は濾過容器
底部の旺細図、第4図はアダプタV斜視図及び3if1
図、第5図は濾過装置及び制岬装f&f7)概念図、第
6図はアダツタの作動直切図、第7図は濾過装置の作動
子j社のフローチャートである。
1:諸過容臣 2:瓶数行アメ゛ブタ 3:dIg低部
5:濾膜支持板 6:細膜 7:中蓋8:固定ねじ
9:上蓋 10:臥科辱人口11 : 7J11比力ス
専人口 12;0リング13:注射針 14:バイアル
瓶 15:瓶保持部 16:可動部 17.22:yt
、凰11d18:固定金八 19:逆止弁 20:加圧
力スルリ両バルブ 21:制岬パネル 23:璧気払ぎ
針
%吐出願人 科学技術庁放射称医学総「研冗er長油嘔
敏之
(l tlJ
綜 臣
ワ
27一Figure 1 is a cross-sectional view of one part of the filtration device of this invention.
Figure 2 is a perspective view of the filtration container 11#, Figure 3 is a detailed view of the bottom of the filtration container, and Figure 4 is a perspective view of the adapter V and 3if1.
Fig. 5 is a conceptual diagram of the filtration device and cape f&f7), Fig. 6 is a direct cut diagram of the operation of the adapter, and Fig. 7 is a flowchart of the operator of the filtration device. 1: Various lines 2: Several lines of the bottle 3: dIg lower part 5: Filter membrane support plate 6: Thin membrane 7: Inner lid 8: Fixing screw
9: Top lid 10: Obesity 11: 7J11 special force 12; 0 ring 13: Syringe needle 14: Vial 15: Bottle holding part 16: Movable part 17.22: yt
, 凰11d18: Fixed gold eight 19: Check valve 20: Pressurized pressure smooth double valve 21: Control cape panel 23: Percentage needle Applicant: Science and Technology Agency, Medical Research Institute (l tlJ Somiwa 271
Claims (1)
する容器を内蔵し、上記濾過容器の一定位置に固定され
る位置決めアダプターがらなり、上記濾過容器の濾液導
出口は注射針区会部を有し、上記アダプターは濾過容器
への取付部分に対して摺動しうる各器保持器が濾液の滴
下を検出するための非接触咲出すを有することを%歇と
する濾過装置It has a built-in membrane, a filtration container into which the sample is introduced, a container for storing liquid, and a positioning adapter that is fixed at a certain position on the filtration container, and the filtrate outlet of the filtration container is connected to the injection needle area. A filtration device, wherein the adapter has a non-contact opening for detecting dripping of filtrate, and each container holder that can slide against the attachment part to the filtration container has a non-contact opening for detecting dripping of filtrate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59115558A JPS60261505A (en) | 1984-06-07 | 1984-06-07 | Filtration device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59115558A JPS60261505A (en) | 1984-06-07 | 1984-06-07 | Filtration device |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60261505A true JPS60261505A (en) | 1985-12-24 |
JPH0516890B2 JPH0516890B2 (en) | 1993-03-05 |
Family
ID=14665511
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59115558A Granted JPS60261505A (en) | 1984-06-07 | 1984-06-07 | Filtration device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60261505A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2305204A1 (en) * | 2009-09-30 | 2011-04-06 | Fresenius Medical Care Deutschland GmbH | Tubing set having an insert for the infusion of drugs |
-
1984
- 1984-06-07 JP JP59115558A patent/JPS60261505A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0516890B2 (en) | 1993-03-05 |
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