JPH0543065B2 - - Google Patents
Info
- Publication number
- JPH0543065B2 JPH0543065B2 JP5659585A JP5659585A JPH0543065B2 JP H0543065 B2 JPH0543065 B2 JP H0543065B2 JP 5659585 A JP5659585 A JP 5659585A JP 5659585 A JP5659585 A JP 5659585A JP H0543065 B2 JPH0543065 B2 JP H0543065B2
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- storage space
- outer tube
- latex
- double
- 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
- 238000006243 chemical reaction Methods 0.000 claims description 46
- 239000004816 latex Substances 0.000 claims description 35
- 229920000126 latex Polymers 0.000 claims description 35
- 230000004520 agglutination Effects 0.000 claims description 26
- 238000003860 storage Methods 0.000 claims description 26
- 239000012295 chemical reaction liquid Substances 0.000 claims description 22
- 239000003153 chemical reaction reagent Substances 0.000 claims description 20
- 239000013013 elastic material Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 description 15
- 239000012085 test solution Substances 0.000 description 13
- 238000012360 testing method Methods 0.000 description 8
- 239000000427 antigen Substances 0.000 description 6
- 102000036639 antigens Human genes 0.000 description 6
- 108091007433 antigens Proteins 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 5
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000002776 aggregation Effects 0.000 description 3
- 230000001235 sensitizing effect Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- HVYWMOMLDIMFJA-UHFFFAOYSA-N 3-cholesterol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 HVYWMOMLDIMFJA-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000004220 aggregation Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001900 immune effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- -1 LE factor Substances 0.000 description 1
- 206010049190 Red blood cell agglutination Diseases 0.000 description 1
- 241000194017 Streptococcus Species 0.000 description 1
- 241000223996 Toxoplasma Species 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 229940011871 estrogen Drugs 0.000 description 1
- 239000000262 estrogen Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000002949 hemolytic effect Effects 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000008105 immune reaction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 230000002485 urinary effect Effects 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
Landscapes
- Health & Medical Sciences (AREA)
- Immunology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Cell Biology (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、簡単な操作で迅速且つ確実に検査を
行なうことができるコンパクトなラテツクス凝集
反応測定用装置に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a compact device for measuring latex agglutination reaction, which allows quick and reliable testing with simple operations.
[従来の技術]
免疫血清学的検査法中でも間接凝集反応法と呼
ばれるものには、(1)赤血球凝集反応法、(2)ラテツ
クス凝集反応法、(3)コレステリン凝集反応法等が
ある。これらのうち(2)のラテツクス凝集反応法
は、最初慢性関節リウマチの検査に用いられて以
来、現在ではHCG、リウマチ因子、溶血性連鎖
球菌、尿中エストロゲン、CRP、LE因子、血中
FDP、トキソプラズマ、HBs等といつた検査に
応用されており、特にそのラテツクス試薬が製
法、特異性、安定性、コスト等の点で有利であり
又取り扱い易いという特徴を有している為急速に
普及しつつある。[Prior Art] Among immunoserological testing methods, those called indirect agglutination methods include (1) red blood cell agglutination method, (2) latex agglutination method, and (3) cholesterin agglutination method. Of these, (2) the latex agglutination reaction method was first used to test for rheumatoid arthritis, and has since been used to test HCG, rheumatoid factor, hemolytic streptococcus, urinary estrogen, CRP, LE factor, blood
It has been applied to tests for FDP, Toxoplasma, HBs, etc., and is rapidly gaining popularity because its latex reagent has advantages in terms of manufacturing method, specificity, stability, cost, etc., and is easy to handle. It is becoming popular.
この様なラテツクス凝集反応に用いられるラテ
ツクス試薬は、粒径0.1〜0.8μmのラテツクス粒
子に抗体(又は抗原)を吸着させて感作ラテツク
ス試薬としたもので、この感作ラテツクス試薬
(以下単に感作ラテツクスという場合もある)が
検液中の抗原(又は抗体)を検出する。すなわち
ラテツクス粒子に吸着されている抗体(又は抗
原)が、これと対応する検液中の抗原(又は抗
体)と抗原抗体反応をするに伴ない該ラテツクス
粒子が凝集して集塊を形成するが、これを目視そ
の他の適当な方法で検知・識別すればよい。一方
検液中に抗原(又は抗体)が存在しない場合に
は、ラテツクス粒子の凝集が起らず依然としてミ
ルク状を呈しているに過ぎない。 The latex reagent used in such a latex agglutination reaction is a sensitized latex reagent made by adsorbing antibodies (or antigens) to latex particles with a particle size of 0.1 to 0.8 μm. (sometimes called latex) detects antigens (or antibodies) in the test solution. In other words, as the antibodies (or antigens) adsorbed on latex particles undergo an antigen-antibody reaction with the corresponding antigens (or antibodies) in the test solution, the latex particles aggregate to form agglomerates. , this may be detected and identified by visual inspection or other appropriate methods. On the other hand, if no antigen (or antibody) is present in the test solution, the latex particles will not aggregate and will still have a milky appearance.
上述の如き感作ラテツクスの凝集反応を検知・
識別する方法としては、(A)分光学的に濁度を測定
する方法、(B)光散乱を利用する方法、(C)感作ラテ
ツクスの感度が大きい場合、凝集反応の結果生成
する前記集塊を肉眼観察によつて定性的に識別し
て判断する方法、等を挙げることができる。中で
も(C)の肉眼によりラテツクス凝集反応を観察する
方法においては、大病院にしか設備されていない
様な特殊な装置や専門家しか修得していない様な
高度な知識やテクニツクを必要としないといつた
利点を有しており、広範な使用が期待されてい
る。とは言えこの方法ではラテツクス凝集反応
を観察すべき反応板上に検液を滴下する、感作
ラテツクス及び緩衝液を検液に滴下する、これ
らを均一に且つ十分に撹拌する、反応板を数分
間ゆつくり揺り動かし照明下でラテツクスの凝集
状態を観察する、判断する、等非常に煩雑で
夫々別個独立した過程を有しているだけでなく凝
集反応により生じる凝集塊の有無を短時間内(数
分以内)に判定しないと反応液が蒸発してしまい
上記判定を見誤る可能性が大きいといつた重大な
欠点を有している。この為上述の如き独立した過
程〜を合理的に行なうことができしかも判定
の見誤りの少ないコンパクトなラテツクス凝集反
応測定用装置が望まれていた。 Detects the agglutination reaction of sensitized latex as described above.
Identification methods include (A) spectroscopic turbidity measurement, (B) light scattering, and (C) when the sensitivity of the sensitized latex is high, the aggregation produced as a result of the agglutination reaction. Examples include a method of qualitatively identifying and determining a mass by visual observation. Among them, the method (C) of observing latex agglutination reactions with the naked eye does not require special equipment that is only available in large hospitals or advanced knowledge and techniques that only experts have acquired. It has many advantages and is expected to be widely used. However, this method requires dropping the test solution onto the reaction plate where the latex agglutination reaction is to be observed, dropping the sensitized latex and buffer onto the test solution, stirring them evenly and thoroughly, and using several reaction plates. Not only does it involve very complicated and separate processes, such as observing and determining the state of agglomeration of the latex by gently shaking it for several minutes under illumination, but also the presence or absence of agglomerates produced by the aggregation reaction can be detected within a short period of time (several times). This method has a serious drawback in that if the determination is not made within 1 minute), the reaction solution will evaporate and there is a high possibility that the above determination will be misjudged. For this reason, there has been a demand for a compact apparatus for measuring latex agglutination reactions, which can rationally carry out the above-mentioned independent processes and is less likely to make misjudgments.
[発明が解決しようとする問題点]
本発明は上述の様な事情に着目してなされたも
のであつて、簡単な操作で迅速且つ確実に検査を
行なうことのできるコンパクトなラテツクス凝集
反応測定用装置を提供しようとするものである。[Problems to be Solved by the Invention] The present invention has been made in view of the above-mentioned circumstances, and is a compact device for measuring latex agglutination reaction that can be quickly and reliably tested with simple operations. The aim is to provide equipment.
[問題点を解決するための手段]
本発明に係るラテツクス凝集反応測定用装置
は、透明板と不透明板を両者の間に反応収納空間
を残しつつ貼り合わせると共に該反応液収納空間
には、吸入口、及び内側管と、弾力性を有する材
質で形成された外側管から構成され、且つ該内側
管の上端が外側管の内部と連通され、内側管と外
側管の間に試薬収納空間を形成した2重管状スポ
イドの内側管を夫々連通したものであることに要
旨が存在するものである。[Means for Solving the Problems] The device for measuring latex agglutination reaction according to the present invention has a transparent plate and an opaque plate bonded to each other while leaving a reaction storage space between them, and the reaction liquid storage space has an inlet port. It is composed of a mouth, an inner tube, and an outer tube made of an elastic material, and the upper end of the inner tube communicates with the inside of the outer tube, forming a reagent storage space between the inner tube and the outer tube. The gist lies in that the inner tubes of the double-tubular dropper are connected to each other.
[作用]
本発明に係るラテツクス凝集反応測定用装置
は、上述の如く()透明板と不透明板を貼り合
わせて両者の間に反応液収納空間を形成し、()
該反応液収納空間には吸入口と、及び内側管と、
弾力性を有する材質で形成された外側管から構成
され、且つ該内側管の上端が外側管の内部と連通
されている2重管状スポイドとを夫々連通し、
()2重管状スポイドの内側管と外側管の間に
試薬収納空間を形成し、これら()、()、
()の構成を相乗的に結合させたところに最大
の特長を有するものである。以下上記()、
()、()につき説明を加えつつ本発明の作
用・効果を説明していく。[Function] As described above, the device for measuring latex agglutination reaction according to the present invention comprises () pasting together a transparent plate and an opaque plate to form a reaction liquid storage space between them;
The reaction liquid storage space includes an inlet, an inner pipe,
communicating with a double tubular dropper formed of an outer tube made of an elastic material, the upper end of the inner tube communicating with the inside of the outer tube,
() A reagent storage space is formed between the inner tube and the outer tube of the double-tubular dropper, and these (), (),
The greatest feature lies in the synergistic combination of the configurations in parentheses. Below the above (),
The functions and effects of the present invention will be explained while adding explanations for () and ().
() 透明板と不透明板を貼り合わせて両者の間
に反応収納空間を形成した点について
反応液収納空間を形成することによりここに
反応液を密封状態で収納することができる様な
場所が提供されたことになるから、従来の様に
反応板を用意する必要がなくなるばかりか該反
応液についての判定に若干時間を要したとして
も蒸発等に対する懸念の必要がなくなる。そし
て透明板を用いることによつて該反応液を外部
から観察することが可能となり、しかも対向側
に不透明板を使用しているので該反応液におけ
る色彩や形態等の特徴をひきたてるのに好都合
となつた。() Regarding the fact that a transparent plate and an opaque plate are pasted together to form a reaction storage space between them.By forming a reaction liquid storage space, a place where the reaction liquid can be stored in a sealed state is provided. Therefore, there is no need to prepare a reaction plate as in the conventional method, and there is no need to worry about evaporation or the like even if it takes some time to judge the reaction liquid. By using a transparent plate, it is possible to observe the reaction liquid from the outside, and since an opaque plate is used on the opposite side, it is convenient for highlighting the characteristics of the reaction liquid, such as color and form. Summer.
() 該反応液収納空間には吸入口及び2重管状
スポイドの内側管を夫々連通した点について
ここに言う2重管状スポイドとは、例えば第
2図に示す様なものである。すなわち外側管1
5と内側管14から構成され且つ該外側管15
の内部が該内側管14の上端と連通しており更
に該外側管15が弾力性を有する材質のもの
(例えば弾性体等)で形成され、該変形に伴な
い内側管14を通じて流体を外側管15の内部
の試薬収納空間16へ吸入することができると
共にここに該流体を貯留することができ且つ該
貯留された流体を逆に内側管2を通じて押し出
すこともできるものである。この様な2重管状
スポイドの内側管及び吸入口を上記反応液収納
空間に連通し上記2重管スポイドの作用を活用
することによつて、従来においては(a)反応板を
用意し、(b)これに検疫を適下するに当たり該反
応板と独立のスポイドを別途準備して行なうこ
とが必要であつたが、これらのことを必要とし
なくなつた。()2重管状スポイドの内側管
と外側管の間に試薬収納空間を形成した点につ
いて
2重管状スポイドに関する上記説明のところ
で流体を貯留することができる様な空間が外側
管15と内側管14の間に形成される旨記載し
たが、該空間は、試薬を予め収容保持する空間
であると同時に、ここに吸入された検液との混
合・撹拌・反応の場としても利用されることに
なる。しかも該混合・撹拌による反応を行なわ
せるに当たつては、従来の様に検液等の適下さ
れた反応板をゆつくり揺り動かすといつた配慮
を払う必要がないので検査を行なう者にとつて
誠に簡便且つ容易な操作になつたと言うことが
できる。() Regarding the fact that the reaction liquid storage space communicates with the inlet and the inner tube of the double-tubular dropper.The double-tubular dropper referred to herein is, for example, as shown in FIG. 2. i.e. outer tube 1
5 and an inner tube 14, and the outer tube 15
The inside of the inner tube 14 communicates with the upper end of the inner tube 14, and the outer tube 15 is made of an elastic material (for example, an elastic body), and the fluid is transferred to the outer tube through the inner tube 14 as it deforms. The fluid can be sucked into the reagent storage space 16 inside the reagent 15 and can be stored there, and the stored fluid can also be pushed out through the inner tube 2. Conventionally, by communicating the inner pipe and the suction port of such a double-tube dropper with the reaction liquid storage space and utilizing the action of the double-tube dropper, (a) a reaction plate is prepared; b) It was necessary to separately prepare a dropper independent of the reaction plate to apply quarantine to this, but this is no longer necessary. () Regarding the formation of a reagent storage space between the inner tube and the outer tube of the double-tubular dropper In the above explanation regarding the double-tubular dropper, there is a space in the outer tube 15 and the inner tube 14 that can store fluid. As mentioned above, this space is a space for pre-accommodating and holding reagents, and is also used as a place for mixing, stirring, and reaction with the sample solution inhaled. Become. Moreover, when carrying out the reaction by mixing and stirring, there is no need to take precautions such as gently shaking the reaction plate on which the test solution has been applied, as in the past, so it is easy for the person conducting the test to carry out the reaction. It can be said that the operation has become really simple and easy.
上述の如き混合・撹拌・反応を行なつた後の
反応液は、前記2重管状スポイドのところで示
した様に内側管を通して押し出されるから、こ
の押し出された反応液は前記()項で述べた
反応液収納空間に移行収納され、反応結果の判
定に供される。すなわち混合・撹拌・反応が終
つたままスポイド内に貯めておいても反応の進
行具合を正確に判断することはできない。 The reaction liquid after the above-mentioned mixing, stirring, and reaction is extruded through the inner tube as shown in the double-tubular dropper, so this extruded reaction liquid is as described in () above. It is moved and stored in the reaction liquid storage space, and is used for determining the reaction results. In other words, even if the mixture is stored in the dropper after mixing, stirring, and reaction, it is not possible to accurately judge the progress of the reaction.
以下図面を参照しつつ実施態様を説明すること
によつて本発明をより鮮明にしていくが、本発明
は以下の実施態様に限定されるものではなく前後
の記載に基づき本発明の範囲内で種々の変形が可
能である。また上記試薬としては感作ラテツクス
を選定して説明してきたが該試薬はこれのみに限
定する必要はなく、検液を導入することによつて
凝集反応を起こす様な抗原(又は抗体)で感作さ
せた例えば赤血球やコレステリン等の試薬あるい
は検液を導入することによつて発色反応を観察で
きる。試薬であつても良いことは言う迄もない。 The present invention will be made clearer by describing the embodiments below with reference to the drawings, but the present invention is not limited to the following embodiments, and can be understood within the scope of the present invention based on the preceding and following descriptions. Various modifications are possible. In addition, although the above reagent has been explained by selecting a sensitizing latex, it is not necessary to limit the reagent to this only, and it is possible to sensitize with an antigen (or antibody) that causes an agglutination reaction by introducing a test solution. A color reaction can be observed by introducing a reagent or a test solution such as red blood cells or cholesterin. Needless to say, it is good to use it as a reagent.
[実施例]
第1図は本発明の一実施態様を示す断面説明図
であり、aは正面断面図、bは側面断面図を夫々
示す。本発明に係るラテツクス凝集反応測定用装
置3は、フイルター部4、判定プレート5及び2
重管状スポイド6から構成されている。該フイル
ター部4における吸入器7の内部にはフイルター
8が充填され該フイルター8を保護すべくシール
材8aが積層されており、該判定プレート5はb
に示す様に透明板9と不透明板(着色の有無及び
色は問わない)10をこれらの間に反応液収納空
間11を残しつつ貼り合わせることによつて形成
されている。そして該判定プレート5の吸収口1
2に上記フイルター部4の一端が嵌合されてお
り、該判定プレート5の2重管状スポイド側端部
13の内周壁には2重管状スポイド6の内側管1
4が嵌合されている。そして該判定プレート5の
2重管状スポイド側端部13の外周壁には2重管
状スポイド6の外側管15が嵌合されている。そ
して該内側管14と外側管15の間には検液を貯
留すると共に感作ラテツクス試薬を収納すること
のできる試薬収納空間16が形成されている。尚
該感作ラテツクス試薬17は図示する様に2重管
状スポイド6における内側管14と外側管15の
間に形成される空間の下方部に予め収納してお
く。[Example] Fig. 1 is an explanatory cross-sectional view showing one embodiment of the present invention, in which a shows a front sectional view and b shows a side sectional view. The latex agglutination reaction measuring device 3 according to the present invention includes a filter section 4, a determination plate 5 and 2.
It is composed of a heavy tubular dropper 6. A filter 8 is filled inside the inhaler 7 in the filter section 4, and a sealing material 8a is laminated to protect the filter 8.
As shown in FIG. 2, it is formed by pasting together a transparent plate 9 and an opaque plate 10 (colored or uncolored) while leaving a reaction liquid storage space 11 between them. And the absorption port 1 of the determination plate 5
2 is fitted with one end of the filter section 4, and the inner circumferential wall of the double tubular dropper side end 13 of the determination plate 5 is fitted with the inner tube 1 of the double tubular dropper 6.
4 is fitted. The outer tube 15 of the double tubular dropper 6 is fitted into the outer peripheral wall of the double tubular dropper side end 13 of the determination plate 5 . A reagent storage space 16 is formed between the inner tube 14 and the outer tube 15 in which a test solution can be stored and a sensitizing latex reagent can be stored therein. The sensitizing latex reagent 17 is stored in advance in the lower part of the space formed between the inner tube 14 and the outer tube 15 of the double-tubular dropper 6, as shown in the figure.
この様なラテツクス凝集反応測定用装置3の使
用手順は以下の通りであり、説明は箇条書形式と
する。 The procedure for using such a device 3 for measuring latex agglutination reaction is as follows, and the explanation will be in bulleted form.
フイルター部4に設けられたシール8aを剥
がす。 Peel off the seal 8a provided on the filter section 4.
該ラテツクス凝集反応測定用装置3を、2重
管状スポイド6の外側管15を少し押圧しつつ
第1図の垂直姿勢を保持したまま検液収納容器
例えば採尿コツプの上方から降下させていきフ
イルター部4を検液中に含浸させる。次いで外
側管15の押圧を解除すると、検液はフイルタ
ー部4及び前記反応液収納空間11を経て内側
管14内を上昇し上端の通路開放部を矢印で示
す様に越流し、第1図bの状態になる。尚上記
フイルター8により反応並びに反応結果の観察
に妨害となる沈殿物は除去される。 The latex agglutination reaction measuring device 3 is lowered from above the sample liquid storage container, such as a urine collection cup, while maintaining the vertical position shown in FIG. 1 while slightly pressing the outer tube 15 of the double-tubular dropper 6. 4 into the test solution. Next, when the pressure on the outer tube 15 is released, the test liquid passes through the filter section 4 and the reaction liquid storage space 11, rises inside the inner tube 14, and overflows the passage opening at the upper end as shown by the arrow, as shown in FIG. 1b. becomes the state of Note that the filter 8 removes precipitates that may interfere with the reaction and observation of the reaction results.
試薬収納空間16に導かれた検液の量が所定
量になつたことを確認したら直ちにラテツクス
凝集反応測定用装置3を引上げるか、又は更に
該外側管15を再び指で押さえて内側管14、
反応液収納空間11、フイルター8に残存する
過剰の検液を落下除去する。 Immediately after confirming that the amount of the test solution introduced into the reagent storage space 16 has reached a predetermined amount, the device 3 for measuring latex agglutination reaction is pulled up, or the outer tube 15 is pressed again with a finger to remove the inner tube 14. ,
Excess test solution remaining in the reaction solution storage space 11 and filter 8 is removed by dropping.
フイルター部4を脱却するか若しくはフイル
ター部4をつけたままでラテツクス凝集反応測
定用装置3を軽く振とうし感作ラテツクス17
と検液を混合・撹拌してこれらを反応させる。 The sensitized latex 17 is removed by removing the filter part 4 or gently shaking the latex agglutination reaction measuring device 3 with the filter part 4 attached.
Mix and stir the and test solution to react.
一定時間免疫学的凝集反応をさせた後、2重
管状スポイド6が下になる様な状態にして反応
液を外側管15の底部(第1図では上端)へ移
行させ再び外側管15を軽く指で押されると該
移行した反応液が前記反応液収納空間11へ押
し上げられる。 After allowing the immunological agglutination reaction to occur for a certain period of time, the reaction solution is transferred to the bottom of the outer tube 15 (the upper end in FIG. 1) with the double tubular dropper 6 facing down, and the outer tube 15 is gently opened again. When pressed with a finger, the transferred reaction liquid is pushed up into the reaction liquid storage space 11.
ここで外側管15の押圧を解除するとせつか
く反応液収納空間11内に入つた反応液が再び
2重管状スポイド6内へ戻るのでフイルター部
4の上端(フイルター部4を除去した後であれ
ば吸収口12の先端)を指で押えるか又は2重
管状スポイド6を除去して均圧を図る。 When the pressure on the outer tube 15 is released, the reaction liquid that has entered the reaction liquid storage space 11 returns to the double tubular dropper 6. Press the tip of the absorption port 12 with your finger or remove the double tubular dropper 6 to equalize the pressure.
黒色の不透明板10を背景に透明板9を通し
て上記免疫学的凝集反応により生じる凝集塊の
有無を観察することができる。 The presence or absence of aggregates produced by the immunological agglutination reaction can be observed through the transparent plate 9 against the background of the black opaque plate 10.
尚上記不透明板としてここでは黒色のものを用
いたが白色板を使用すれば免疫反応や酵素反応の
結果生じる色原体の発色の有無を観察することが
でき、この様にするとラテツクス凝集反応を利用
した診断試薬だけでなく、他の色原体を用いるラ
テツクス凝集反応測定用装置としての応用も可能
である。いずれにせよ不透明板の色は特定されな
い。 Although a black plate was used as the above-mentioned opaque plate, if a white plate is used, it is possible to observe the presence or absence of color development of the chromogen resulting from the immune reaction or enzyme reaction.In this way, the latex agglutination reaction can be observed. In addition to the diagnostic reagent used, it can also be applied as a device for measuring latex agglutination reactions using other chromogens. In any case, the color of the opaque plate is not specified.
[発明の効果]
本発明は上述の様に構成されているので、簡単
な操作で迅速且つ確実に検査を行なうことができ
るコンパクトなラテツクス凝集反応測定用装置を
提供することができる。[Effects of the Invention] Since the present invention is configured as described above, it is possible to provide a compact device for measuring latex agglutination reaction that can perform tests quickly and reliably with simple operations.
第1図は本発明の一実施態様を示す断面説明図
[aは正面断面説明図、bは側面断面説明図]、第
2図は2重管状スポイドを示す説明図である。
6……2重管状スポイド、9……透明板、10
……不透明板、11……反応液収納空間、12…
…吸入口、14……内側管、15……外側管、1
6……試薬収納空間。
FIG. 1 is an explanatory sectional view showing one embodiment of the present invention [a is an explanatory front sectional view, b is an explanatory side sectional view], and FIG. 2 is an explanatory view showing a double tubular dropper. 6...Double tubular dropper, 9...Transparent plate, 10
... Opaque plate, 11 ... Reaction liquid storage space, 12 ...
...Suction port, 14...Inner pipe, 15...Outer pipe, 1
6...Reagent storage space.
Claims (1)
間を残しつつ貼り合せると共に該反応液収納空間
には、 吸入口、及び 内側管と、弾力性を有する材質で形成された外
側管から構成され、且つ該内側管の上端が外側管
の内部と連通され、内側管と外側管の間に試薬収
納空間を形成した2重管状スポイドの内側管 を夫々連通したものであることを特徴とするラテ
ツクス凝集反応測定用装置。[Scope of Claims] 1. A transparent plate and an opaque plate are bonded together while leaving a reaction liquid storage space between them, and the reaction liquid storage space includes: an inlet, and an inner pipe formed of an elastic material. The inner tube of a double-tubular dropper is composed of an outer tube, the upper end of which is in communication with the inside of the outer tube, and a reagent storage space is formed between the inner tube and the outer tube. A device for measuring latex agglutination reaction, characterized by the following.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5659585A JPS61213770A (en) | 1985-03-20 | 1985-03-20 | Diagnostic reagent kit |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5659585A JPS61213770A (en) | 1985-03-20 | 1985-03-20 | Diagnostic reagent kit |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61213770A JPS61213770A (en) | 1986-09-22 |
| JPH0543065B2 true JPH0543065B2 (en) | 1993-06-30 |
Family
ID=13031553
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5659585A Granted JPS61213770A (en) | 1985-03-20 | 1985-03-20 | Diagnostic reagent kit |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61213770A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2586815B1 (en) * | 1985-09-04 | 1989-04-21 | Lacaille Yves | DEVICE FOR DETERMINING A BLOOD GROUP |
| US4775515A (en) * | 1986-11-18 | 1988-10-04 | Cottingham Hugh V | Agglutinographic slide |
| WO1990007716A1 (en) * | 1988-12-23 | 1990-07-12 | Toray Industries, Inc. | Immunological inspection tube |
-
1985
- 1985-03-20 JP JP5659585A patent/JPS61213770A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61213770A (en) | 1986-09-22 |
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