JPH0449655B2 - - Google Patents
Info
- Publication number
- JPH0449655B2 JPH0449655B2 JP59104068A JP10406884A JPH0449655B2 JP H0449655 B2 JPH0449655 B2 JP H0449655B2 JP 59104068 A JP59104068 A JP 59104068A JP 10406884 A JP10406884 A JP 10406884A JP H0449655 B2 JPH0449655 B2 JP H0449655B2
- Authority
- JP
- Japan
- Prior art keywords
- plasma
- module
- blood
- component
- separation
- 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 - Lifetime
Links
- 210000000601 blood cell Anatomy 0.000 claims description 10
- 239000012510 hollow fiber Substances 0.000 claims description 9
- 238000012360 testing method Methods 0.000 claims description 7
- 210000004369 blood Anatomy 0.000 description 17
- 239000008280 blood Substances 0.000 description 17
- 238000000926 separation method Methods 0.000 description 13
- 238000005119 centrifugation Methods 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 210000002966 serum Anatomy 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000003146 anticoagulant agent Substances 0.000 description 1
- 229940127219 anticoagulant drug Drugs 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229960002897 heparin Drugs 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
- B01D63/02—Hollow fibre modules
- B01D63/021—Manufacturing thereof
- B01D63/0233—Manufacturing thereof forming the bundle
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/14—Ultrafiltration; Microfiltration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/14—Ultrafiltration; Microfiltration
- B01D61/18—Apparatus therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
- B01D63/02—Hollow fibre modules
- B01D63/024—Hollow fibre modules with a single potted end
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Water Supply & Treatment (AREA)
- Manufacturing & Machinery (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、臨床検査に係わり、検体試料である
採取した全血から血漿を短時間にて分離する装置
に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a clinical test and relates to an apparatus for separating plasma from collected whole blood, which is a specimen sample, in a short time.
従来技術との関係
従来、血液の生化学血清検査等は、患者から真
空採血管或いは、注射器で採血し、血清の場合は
30〜60分間静置後、血漿の場合は、ヘパリン
EDTA当の抗凝固剤を加えた後3000回転/分で、
5〜10分間遠心分離を行い、上清液を試料として
行なつていた。かかる方法に依れば長時間と人手
を要し特に緊急の場合は問題視されてきた。一方
従来の方法では分析値に関しても長時間高速で遠
心分離するため、血球中の酵素類であるLDH、
GOTの血漿への流出、発生熱による凝固検査、
アンモニア検査への影響、気流による蒸発、高分
子の除去など人体中における濃度成分と異なり真
の生体情報が歪められた値として測定されてき
た。又血小板分離が不充分であるという問題もあ
つた。これらの欠点を克服するため、遠心分離の
自動化とか、平膜による分離とかいつた試みがな
されてきているが、まだまだ分析時間の短縮当の
面で解決すべき問題点を内在させていた。Relationship with conventional technology Conventionally, in blood biochemical and serum tests, blood is collected from the patient with a vacuum blood collection tube or syringe, and in the case of serum, blood is collected from the patient using a vacuum blood collection tube or syringe.
After standing for 30-60 minutes, in the case of plasma, add heparin.
After adding anticoagulant such as EDTA, at 3000 rpm,
Centrifugation was performed for 5 to 10 minutes, and the supernatant was used as a sample. This method requires a lot of time and manpower, and has been viewed as a problem, especially in urgent cases. On the other hand, in the conventional method, analysis values are also obtained by centrifugation at high speed for a long time, so LDH, an enzyme in blood cells,
GOT leakage into plasma, coagulation test based on generated heat,
Unlike concentration components in the human body, such as the influence on ammonia tests, evaporation by air currents, and removal of polymers, true biological information has been measured as a distorted value. There was also the problem that platelet separation was insufficient. In order to overcome these drawbacks, attempts have been made to automate centrifugation and separation using flat membranes, but there are still problems that need to be solved in terms of shortening analysis time.
発明の目的
而して本発明者は、上記した従来装置の欠点に
鑑み生体情報を損うことなく簡便に迅速に試料を
得ることを目的とした血漿分離装置を見い出すべ
く鋭意検討した結果本発明に到達した。Purpose of the Invention In view of the above-mentioned shortcomings of conventional devices, the present inventor has conducted intensive studies to find a plasma separation device that can easily and quickly obtain samples without damaging biological information, and as a result has developed the present invention. reached.
発明の構成
本発明の検査用血漿分離装置は、微細孔を有す
る中空繊維束よりなる両端が開放された血漿過
部と血漿成分流路部を有する血球成分受槽とが直
列に一体化したモジユール及び該モジユールに着
脱可能な血漿成分受槽を接続可能とした構造を有
してなるものである。Structure of the Invention The plasma separation device for testing of the present invention includes a module in which a plasma filtering section made of a hollow fiber bundle having micropores and having both ends open and a blood cell component receiving tank having a plasma component flow path section are integrated in series. It has a structure in which a removable plasma component receiver can be connected to the module.
以下本発明を図面に基づき説明する。 The present invention will be explained below based on the drawings.
第1図は本発明の一実施例を示すもので、患者
から真空採血管2により採血した全血1の入つた
該真空採血管に対し、分離モジユールケース6に
ネジ込み接合した血漿成分受槽8を上方より挿入
する。全血中の血漿を過する分離モジユール中
空繊維束3は、端部シール帯4の接着剤により固
着されているが端面では各々の中空繊維は開口し
ている。一方下方の端部シール帯4′は過側に
開口した血漿成分流路5を有している。分離モジ
ユールケースは上部に血漿を下方に流出せしめる
ための空気孔13を有している。血球成分受槽は
上部の端部シール帯4′から血漿成分流路5が中
央に位置し、下部受底12に接続している。該流
路は上部過側と下部血漿成分受槽とで通じてい
る。 FIG. 1 shows an embodiment of the present invention, in which a plasma component receiver is screwed and connected to a separation module case 6 for a vacuum blood collection tube containing whole blood 1 collected from a patient using a vacuum blood collection tube 2. Insert 8 from above. The separation module hollow fiber bundle 3, which passes through the plasma in whole blood, is fixed by the adhesive of the end seal band 4, but each hollow fiber is open at the end face. On the other hand, the lower end sealing band 4' has a plasma component flow path 5 open to the rear side. The separation module case has an air hole 13 in the upper part for allowing plasma to flow downward. In the blood cell component receiving tank, a plasma component channel 5 is located in the center from the upper end seal band 4' and connected to the lower receiving bottom 12. The flow path communicates between the upper side and the lower plasma component receiver.
該受槽の端部シール帯4′から中空繊維束中を
通過した血球成分は血球成分受槽に溜る。そのた
めにケースは同様に上方に空気孔13′を有して
いる。血漿成分受槽8は過された血漿成分を血
漿成分流路5を介して貯溜する。過後分離モジ
ユールと切離しが可能である。又他部と同様に上
方に空気孔13′を有する。 The blood cell components that have passed through the hollow fiber bundle from the end seal band 4' of the receiver are collected in the blood cell component receiver. For this purpose, the housing likewise has air holes 13' in the upper part. The plasma component receiving tank 8 stores the filtered plasma components via the plasma component flow path 5. It can be separated from the separation module after separation. Also, like the other parts, there is an air hole 13' in the upper part.
以上を操作順に要約すると真空採血管2に上方
より分離モジユール6を挿入後、上下を反転させ
真空採血管2とモジユール6をピストンとシリン
ダーの関係で各々上下せしめて過を行い全血中
の血球成分7は、中空繊維を通り血球受槽7に貯
る。一方血漿成分は中空繊維3で過され、流路
5を通り受槽8に貯る。第2図は、検体を注射器
で採取した場合を示す。ここでは手動により分離
する方法についてであるが該分離モジユールを用
いて自動化することもできる。又用いる中空繊維
は膜過型のものが採用される。 To summarize the above steps in the order of operation, after inserting the separation module 6 into the vacuum blood collection tube 2 from above, turn it upside down and move the vacuum blood collection tube 2 and module 6 up and down in a piston-cylinder relationship to collect the blood cells in the whole blood. Component 7 passes through the hollow fibers and accumulates in the blood cell receptor 7. On the other hand, the plasma component is filtered through the hollow fiber 3, passes through the channel 5, and is stored in the receiving tank 8. FIG. 2 shows a case where a specimen is collected with a syringe. Although the manual separation method is described here, it can also be automated using the separation module. Also, the hollow fibers used are membrane type.
発明の効果
本発明は、遠心分離器を用いることなく、使い
捨てができる分離膜モジユールにより簡便にかつ
迅速に、試料を損うことなく血漿を分離すること
ができる。又自動機に組み込むことにより採血し
た試料を注入するだけで、今まで遠心分離で途切
れていた工程を無くすことが可能となる。分離器
で得られた血漿は自動分析器に導かれ、分析結果
を計算機に出力するといつた完全自動化が可能と
なる。一方では緊急検査に速やかに対応できるの
みならず他面分析値としてはより真の生体情報を
提供でき臨床データとしての信頼性を高める効果
も大きい有意義なものである。Effects of the Invention According to the present invention, plasma can be easily and quickly separated using a disposable separation membrane module without using a centrifugal separator and without damaging the sample. In addition, by incorporating it into an automatic machine, it becomes possible to eliminate the process that was previously interrupted by centrifugation by simply injecting the collected blood sample. The plasma obtained by the separator is led to an automatic analyzer, and the analysis results are output to a computer, allowing for complete automation. On the one hand, it not only allows us to respond quickly to emergency tests, but on the other hand, it is also very meaningful in that it provides truer biological information as analysis values and increases the reliability of clinical data.
第1図は本発明の一実施態様を示すもので真空
採血管を用いた場合、第2図は注射器を用いた場
合を示す。
1……全血試料、2……真空採血管、3……中
空繊維膜、4……端部シール帯、5……血漿成分
流路、6……ケース、7……血球成分、8……血
漿成分受槽、9……血漿、10……採血シリン
ジ、11……接続ノズル、12……血球成分受
底、13……空気孔。
FIG. 1 shows an embodiment of the present invention in which a vacuum blood collection tube is used, and FIG. 2 shows a case in which a syringe is used. DESCRIPTION OF SYMBOLS 1... Whole blood sample, 2... Vacuum blood collection tube, 3... Hollow fiber membrane, 4... End seal band, 5... Plasma component flow path, 6... Case, 7... Blood cell component, 8... ...Plasma component receiver, 9...Plasma, 10...Blood collection syringe, 11...Connection nozzle, 12...Blood cell component receiver, 13...Air hole.
Claims (1)
よりなる過部と血漿成分流路部を有する血球成
分受槽とが直列に一体化されたモジユール及び該
モジユールに着脱可能に接続した血漿成分受槽よ
りなる検査用血漿分離器。1. A module in which a filter section made of a hollow fiber bundle with micropores and open ends and a blood cell component receiving tank having a plasma component flow path section are integrated in series, and a plasma component detachably connected to the module. A plasma separator for testing consisting of a receiving tank.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59104068A JPS60247163A (en) | 1984-05-22 | 1984-05-22 | Serum separator for examination |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59104068A JPS60247163A (en) | 1984-05-22 | 1984-05-22 | Serum separator for examination |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60247163A JPS60247163A (en) | 1985-12-06 |
JPH0449655B2 true JPH0449655B2 (en) | 1992-08-12 |
Family
ID=14370843
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59104068A Granted JPS60247163A (en) | 1984-05-22 | 1984-05-22 | Serum separator for examination |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60247163A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11856757B2 (en) * | 2020-08-04 | 2023-12-26 | Changxin Memory Technologies, Inc. | Method for manufacturing semiconductor structure with capacitor wires |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05188053A (en) * | 1992-01-10 | 1993-07-27 | Sanwa Kagaku Kenkyusho Co Ltd | Instrument for separating serum or plasma component from blood |
CN1116919C (en) * | 1998-04-07 | 2003-08-06 | 成都迪康血液科技有限公司 | Small area hollow fibre membrane plasma separation filter |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5521098B2 (en) * | 1977-12-15 | 1980-06-07 | ||
JPS5774637A (en) * | 1980-10-20 | 1982-05-10 | Unitika Ltd | Separator for blood collecting plasma |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5521098U (en) * | 1978-07-31 | 1980-02-09 |
-
1984
- 1984-05-22 JP JP59104068A patent/JPS60247163A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5521098B2 (en) * | 1977-12-15 | 1980-06-07 | ||
JPS5774637A (en) * | 1980-10-20 | 1982-05-10 | Unitika Ltd | Separator for blood collecting plasma |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11856757B2 (en) * | 2020-08-04 | 2023-12-26 | Changxin Memory Technologies, Inc. | Method for manufacturing semiconductor structure with capacitor wires |
Also Published As
Publication number | Publication date |
---|---|
JPS60247163A (en) | 1985-12-06 |
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