JPS5928252B2 - Method for detecting coagulation state of blood, etc. - Google Patents
Method for detecting coagulation state of blood, etc.Info
- Publication number
- JPS5928252B2 JPS5928252B2 JP10917876A JP10917876A JPS5928252B2 JP S5928252 B2 JPS5928252 B2 JP S5928252B2 JP 10917876 A JP10917876 A JP 10917876A JP 10917876 A JP10917876 A JP 10917876A JP S5928252 B2 JPS5928252 B2 JP S5928252B2
- Authority
- JP
- Japan
- Prior art keywords
- signal
- time
- electrical signal
- reference value
- specimen
- 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
- 210000004369 blood Anatomy 0.000 title claims description 4
- 239000008280 blood Substances 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 4
- 230000015271 coagulation Effects 0.000 title 1
- 238000005345 coagulation Methods 0.000 title 1
- 238000004220 aggregation Methods 0.000 claims description 10
- 230000002776 aggregation Effects 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 10
- 230000004520 agglutination Effects 0.000 claims description 4
- 230000001186 cumulative effect Effects 0.000 claims description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 239000012491 analyte Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 210000000601 blood cell Anatomy 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010339 medical test Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Landscapes
- Investigating Or Analysing Biological Materials (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Description
【発明の詳細な説明】
この発明は血液等の凝集状態を光学的、電気的に検出す
る方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for optically and electrically detecting the state of aggregation of blood or the like.
医学的な諸検差の中には、検体中に各種試薬または、血
清等を混入して、該検体に凝集が起るか否か、または凝
集の状態を調べて各種病状や血液型等を判定する場合が
多い。Among various medical tests, various reagents or serum etc. are mixed into the sample to check whether or not agglutination occurs in the sample, or to check the state of agglutination to determine various medical conditions, blood types, etc. Often judged.
従来はこの判定作業を肉眼により行なうものであるから
、判定に個人差があり、誤判定を招く危険が多かつた。
本発明は上記不都合がなく、正確な凝集の有無を判定す
ることのできる方法を提供することを目的として発明さ
れたものである。Conventionally, this judgment work was performed with the naked eye, so there were individual differences in the judgment, and there was a high risk of erroneous judgments.
The present invention was invented with the object of providing a method that does not have the above-mentioned disadvantages and can accurately determine the presence or absence of aggregation.
次に本発明の原理を説明する。Next, the principle of the present invention will be explained.
ガラス板上に載せ試薬と反応させた検体を、微小断面積
の光束で走査し、その透過光量を調べると、ハ検体が凝
集状態である時は、血球等の局在化した凝集部の透過光
量は小さく、凝集部以外の背景部の透過光量は大きい。When a sample placed on a glass plate and reacted with a reagent is scanned with a beam of light with a small cross-sectional area and the amount of transmitted light is examined, (c) if the sample is in an aggregated state, the transmission of localized aggregates such as blood cells. The amount of light is small, and the amount of transmitted light in the background area other than the agglomerated area is large.
2)検体が非凝集状態である時は、透過光量は反応域全
体に亘つて中程度である。2) When the analyte is in a non-aggregated state, the amount of transmitted light is moderate throughout the reaction zone.
という特性が現われる。This characteristic appears.
従つて透過光量の小さいことによつて判別される凝集部
の全面積および透過光量が大きいことによつて判別され
る背景部の全面積と検体反応域とのそれぞれの割合が一
定値以上である時は凝集ありと判定することができる。Therefore, the respective ratios of the total area of the aggregation area, which is determined by a small amount of transmitted light, and the total area of the background area, which is determined by a large amount of transmitted light, to the sample reaction area are greater than a certain value. At this time, it can be determined that there is aggregation.
本発明はこの原理に基づいて構成したものである。The present invention is constructed based on this principle.
即ち先ず透過光量を光量変換して電気信号に変えると共
に面積を時間に置換する。次いで該電気信号を二つの基
準Λ、B(A>B)と大小を比較して検体がどの状態に
あるかを区別する。電気信号が一方の基準値Aより大き
いときは背景部を示し、他方の基準値Bより小さいとき
は凝集部を示し、二つの基準値A、Bの中間のときは非
凝集を示す。次いで、電気信号が基準値Aより大きい場
合および基準値Bより小さい場合の全時間をそれぞれ積
算し、双方の積算時間が共にそれぞれの基準時間を越え
たとき凝集ありと判定するものである。以下本発明を実
施するように構成した装置を示す図面について本発明を
説明する。That is, first, the amount of transmitted light is converted into an electrical signal, and the area is replaced with time. Next, the electrical signal is compared in magnitude with two standards Λ and B (A>B) to distinguish which state the specimen is in. When the electric signal is larger than one reference value A, it indicates a background part, when it is smaller than the other reference value B, it indicates an agglomerated part, and when it is between the two reference values A and B, it indicates a non-agglomerated part. Next, the total time when the electrical signal is larger than the reference value A and when it is smaller than the reference value B is respectively integrated, and when both integrated times exceed the respective reference times, it is determined that aggregation has occurred. The invention will now be described with reference to the drawings, which show apparatus configured to carry out the invention.
検体の走査および光電変換は第1図に示す装置により行
なう。Scanning of the specimen and photoelectric conversion are performed using the apparatus shown in FIG.
ガラス等の透明基板1の上に検体を載せ試薬を注入して
反応域5を作る。コンデンサレンズ3を通した光源2か
らの光で反応域5を一様に下から照らす0該反応域5の
微小面積のスポツト6を通る透過光による実像を、レン
ズ系4により暗箱8に内装した光導電素子7上に結像さ
せる。該暗箱8を駆動装置(図示せず)により矢印9の
ように水平面内を平行移動させて、スポツト6による走
査を行なう0光導電素子7は結像が明るく(即ち透過光
量が大きく)なるに従つて内部抵抗が小さくなる性質を
有する0今該光導電素子7、直流電源10、固定抵抗1
1により直列閉回路を形成してあるから、該固定抵抗1
1の両端電圧は透過光量に応じた第一の電気信号12と
して取出される0透過光量が大きくなると光導電素子7
の内部抵抗が小さくなるから、電気信号12は大きくな
る。次に第一の電気信号12は第2図に示す識別装置に
おいて並列接続された2つの比較器13,14の入力信
号となるo一方の比較器13は、透過光量が基準値Aよ
り大きい場合、即ち凝集状態における背景部を区別する
0比較器13には基準値Aに相当する電圧からなる比較
基準値15を付与してあり、入力信号が該基準値15よ
り大きい時間中一定電圧のパルス信号16を発する0該
パルス信号16は積分器17の入力信号となり、該積分
器17においてパルス信号16の発生している時間が逐
次積算され積算時間信号18として発せられる。A reaction area 5 is created by placing a specimen on a transparent substrate 1 such as glass and injecting a reagent. The reaction area 5 is uniformly illuminated from below by light from the light source 2 that passes through the condenser lens 3. A real image of the light transmitted through a spot 6 with a minute area in the reaction area 5 is placed in a dark box 8 using the lens system 4. An image is formed on the photoconductive element 7. The dark box 8 is moved in parallel in a horizontal plane in the direction of an arrow 9 by a driving device (not shown), and the photoconductive element 7 scans the spot 6 as the image becomes brighter (that is, the amount of transmitted light increases). Therefore, the photoconductive element 7, the DC power source 10, and the fixed resistor 1 have a property of decreasing internal resistance.
1 forms a series closed circuit, the fixed resistor 1
The voltage across the terminal 1 is taken out as the first electric signal 12 according to the amount of transmitted light.0 When the amount of transmitted light increases, the photoconductive element 7
The electrical signal 12 becomes larger because the internal resistance of the electrical signal 12 becomes smaller. Next, the first electrical signal 12 becomes an input signal to two comparators 13 and 14 connected in parallel in the identification device shown in FIG. That is, the zero comparator 13 for distinguishing the background part in the agglomerated state is provided with a comparison reference value 15 consisting of a voltage corresponding to the reference value A, and a constant voltage pulse is generated during the time when the input signal is greater than the reference value 15. The pulse signal 16 that generates the signal 16 becomes an input signal to an integrator 17, and the time during which the pulse signal 16 is generated is successively integrated in the integrator 17 and is output as an integrated time signal 18.
この時間積算は反応域5の全体に亘る走査が完了するま
での全走査時間Tの間行なわれる0積算時間信号18は
比較器19の入力信号となる。該比較器19には凝集状
態における背景部の分量として十分な面積を走査するに
要する時間Ta(T>Ta踏表わす比較基準値20を付
与してあり、積算時間信号18が該基準値20を越える
と第二の電気信号21を発する。他方の比較器14は、
透過光量が基準値Bより小さい場合、即ち凝集状態にお
ける凝集部を区別する0該比較器14には基準値Bに相
当する比較基準値22を付与してあり、電気信号12が
これより小さいときにパルス信号23が発せられる。This time integration is performed for the entire scanning time T until the entire reaction area 5 is scanned. The zero integration time signal 18 becomes an input signal to the comparator 19. The comparator 19 is provided with a comparison reference value 20 representing the time Ta (T>Ta) required to scan an area sufficient for the background portion in the agglomerated state, and the integrated time signal 18 When the voltage is exceeded, a second electrical signal 21 is generated.The other comparator 14 is
When the amount of transmitted light is smaller than the reference value B, that is, the agglomerated portion in the agglomerated state is distinguished.The comparator 14 is provided with a comparison reference value 22 corresponding to the reference value B, and when the electric signal 12 is smaller than this, A pulse signal 23 is emitted.
積分器24はパルス信号23の供給される時間を積算し
た積算時間信号25を発する。比較器26には凝集状態
における凝集部の分量として十分な面積を走査するに要
する時間Tb(T>Ta>Tb)を表わす比較基準値2
7を付与してあり、積算時間信号25がこれを越えると
第三の゛屯気信号28を発する。以上の比較基準値15
,20,22,27は判定の正確さを確保するため重要
な値であるから、それぞれ検体の性質や、判定目的に応
じて適正な大きさに設定するものとする〇上記第二、第
三の電気信号21,28はそれぞれ論理積回路29の人
力信号となる。The integrator 24 generates an integrated time signal 25 that integrates the time during which the pulse signal 23 is supplied. The comparator 26 has a comparison reference value 2 representing the time Tb (T>Ta>Tb) required to scan an area sufficient for the amount of the agglomerated portion in the agglomerated state.
7 is given, and when the cumulative time signal 25 exceeds this, a third pressure signal 28 is generated. The above comparison standard value 15
, 20, 22, and 27 are important values for ensuring accuracy of determination, so they should be set to appropriate sizes depending on the properties of the specimen and the purpose of determination. 〇The above second and third values The electrical signals 21 and 28 become human input signals of the AND circuit 29, respectively.
該論理積回路29は双方の電気信号21,28が共に入
力した時だけ凝集有りの信号30を発する。この論理積
回路29の動作は、検体が凝集状態にあるときは必ず、
第二、第三の信号21,28が得られることに基づいて
いる。これ以外の場合は非凝集と判定する。次に実際の
検体例に本発明を適用した場合を示す第3図A−C列に
ついて更に説明する〇A列、C列は凝集状態を示し、B
列は非凝集状態を示す。The AND circuit 29 generates a signal 30 indicating aggregation only when both electric signals 21 and 28 are input together. The operation of this AND circuit 29 is such that whenever the specimen is in an aggregated state,
This is based on the fact that the second and third signals 21 and 28 are obtained. In other cases, it is determined that there is no aggregation. Next, we will further explain columns A to C in FIG. 3, which show the case where the present invention is applied to an actual specimen example. Columns A and C show the agglutination state, and B
Columns indicate non-agglomerated state.
判定操作は先ず、AO,BOに示される光学的パターン
を形成したそれだれの検体を、破線矢印に示す走査線群
32a,32bに沿つて全面積を走査する0今実線矢印
で示すある走査線31a,31bについてみると、固定
抵抗11の両端からAl,Blに示すような第一の電気
信号12a,12bが得られる0A列の第一の電気信号
12aは2つの比較基準値15,22の上下に亘つて変
動するから、比較器13によつてA2に示すパルス信号
16aが発せられ、比較器14によつてA3に示すパル
ス信号23aが発せられる。B列の第一の電気信号12
bは2つの比較基準値15,22の中間にあるから、B
2,B3に示すように比較器13,14によるパルス信
号は発せられない。全走査時間T内に得られるパルス信
号16a,23aはそれぞれCl,C4に示すようにな
る。In the judgment operation, first, each specimen that has formed the optical patterns indicated by AO and BO is scanned over its entire area along scanning line groups 32a and 32b indicated by dashed line arrows. Regarding 31a and 31b, the first electric signal 12a of the 0A column in which the first electric signals 12a and 12b as shown in Al and Bl are obtained from both ends of the fixed resistor 11 is equal to the two comparison reference values 15 and 22. Since it fluctuates vertically, the comparator 13 generates a pulse signal 16a shown at A2, and the comparator 14 generates a pulse signal 23a shown at A3. First electrical signal 12 in row B
Since b is between the two comparison reference values 15 and 22, B
As shown at 2 and B3, the comparators 13 and 14 do not generate pulse signals. Pulse signals 16a and 23a obtained within the total scanning time T are as shown by Cl and C4, respectively.
パルス信号16aは積分器17により積算されてC2に
示すような積算時間信号18となり、走査時間t1時間
経過すると該積算時間信号18が比較基準値20を越え
、比較器19からC3に示すような第二の電気信号21
が発せられる0同様にパルス信号23aは積分器24に
より積算されてC5に示すような積算時間信号25とな
り、走査時間がT2時間経過すると積算時間信号25が
比較基準値27を越え、比較器26からC6に示すよう
な第三の電気信号28が発せられる0今t1〉T2であ
るから走査開始後t1時間経過すると第二、第三の信号
が共に論理積回路29に入り、該論理積回路29からC
7に示すような凝集ありの電気信号30が発せられる〇
B列の場合は、積算時間信号が皆無であるため論理積回
路29から信号30は発せられず、非凝集と判定される
0また、たとえばB列において電気的ノイズが発生して
B2,B3にパルス信号が発生したとしても、該パルス
信号は短時間信号であるから積算時間が比較基準値20
,27より著しく小さいため、信号30は発せられない
〇このように本発明の方法は、全走査時間に亘つて得ら
れた走査信号を凝集状態において全く異なる二つの相対
的画像に応じた基準値により区分して判定するものであ
るから、1)判定精度が従来方法より極めて高く、信頼
性が高い〇2)走査信号と異なる内部雑音信号が混入し
ても、影響されることなく正確な判定をすることができ
る〇3)第二、第三の電気信号の何れか一方のみが発生
した場合には、その検体を疑問検体して判別することが
でき、精密検査に回すことができる。The pulse signal 16a is integrated by the integrator 17 to become an integrated time signal 18 as shown in C2, and when the scanning time t1 elapses, the integrated time signal 18 exceeds the comparison reference value 20, and the integrated time signal 18 is integrated by the comparator 19 as shown in C3. second electrical signal 21
Similarly, the pulse signal 23a is integrated by the integrator 24 to become an integrated time signal 25 as shown in C5, and when the scanning time T2 time elapses, the integrated time signal 25 exceeds the comparison reference value 27, and the comparator 26 A third electric signal 28 as shown in C6 is emitted from 0 now t1>T2, so when t1 time has passed after the start of scanning, both the second and third signals enter the AND circuit 29, and the AND circuit 29 to C
In the case of the 〇B column in which the electric signal 30 with aggregation as shown in 7 is emitted, the signal 30 is not emitted from the AND circuit 29 because there is no integrated time signal, and the signal 30 is determined to be non-aggregation. For example, even if electrical noise occurs in the B row and a pulse signal is generated in B2 and B3, the pulse signal is a short-time signal, so the cumulative time is 20% of the comparison reference value.
. 1) The accuracy of the judgment is much higher than that of conventional methods and the reliability is high. 2) The judgment is accurate without being affected even if an internal noise signal different from the scanning signal is mixed in. 〇3) If only one of the second and third electrical signals occurs, the sample can be identified as a questionable sample and sent for detailed testing.
4)比較基準値を変えることにより、判定基準を目的に
応じて適正に定めることができる〇等の大きな効果を有
する。4) By changing the comparison standard value, the judgment standard can be determined appropriately according to the purpose, which has a large effect such as 〇.
第1図〜2図は本発明を実施する装置の概略を示し、第
1図は走査および光電変換装置の概略図、第2図は識別
装置のプロツク図、第3図A−Cは検体例とそれぞれの
検体における走査信号とを示す説明図である。
5:反応域、7:光導電素子、12:第一の電気信号、
18:積算時間信号、21:第二の電気信号、25:積
算時間信号、28:第三の電気信号。1 and 2 schematically show an apparatus for carrying out the present invention, in which FIG. 1 is a schematic diagram of a scanning and photoelectric conversion device, FIG. 2 is a block diagram of an identification device, and FIG. 3 A to C are examples of specimens. FIG. 3 is an explanatory diagram showing the scanning signals for each specimen. 5: reaction zone, 7: photoconductive element, 12: first electrical signal,
18: Accumulated time signal, 21: Second electrical signal, 25: Accumulated time signal, 28: Third electrical signal.
Claims (1)
た光につき光電変換を行なつてその透過光量に応じた大
きさの第一の電気信号を取出し、該第一の電気信号と二
つの基準値A、B(A>B)とを比較して第一の信号が
一方の基準値Aより大きい場合の積算時間が基準時間以
上のとき第二の電気信号を出すと共に第一の信号が他方
の基準値Bより小さい場合の積算時間が基準時間以上の
とき第三の電気信号を出し、全走査時間内に上記第二、
第三の信号が共に発せられた場合に凝集有りと判定する
ことを特徴とする血液等の凝集状態を検出する方法。1 A specimen is scanned with a light beam having a minute cross-sectional area, photoelectric conversion is performed on the light that has passed through the specimen, a first electrical signal having a size corresponding to the amount of transmitted light is extracted, and the second electrical signal is combined with the first electrical signal. Compare the two reference values A and B (A>B), and when the first signal is larger than one of the reference values A, a second electrical signal is output when the cumulative time is equal to or greater than the reference time, and the first signal is output. is smaller than the other reference value B. When the cumulative time is greater than or equal to the reference time, a third electrical signal is output, and the second,
A method for detecting an aggregation state of blood, etc., characterized in that it is determined that there is agglutination when a third signal is emitted at the same time.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10917876A JPS5928252B2 (en) | 1976-09-10 | 1976-09-10 | Method for detecting coagulation state of blood, etc. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10917876A JPS5928252B2 (en) | 1976-09-10 | 1976-09-10 | Method for detecting coagulation state of blood, etc. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5334595A JPS5334595A (en) | 1978-03-31 |
| JPS5928252B2 true JPS5928252B2 (en) | 1984-07-11 |
Family
ID=14503624
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10917876A Expired JPS5928252B2 (en) | 1976-09-10 | 1976-09-10 | Method for detecting coagulation state of blood, etc. |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5928252B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS562559A (en) * | 1979-06-21 | 1981-01-12 | Olympus Optical Co Ltd | Detector for particle coagulation pattern |
| JPS562561A (en) * | 1979-06-21 | 1981-01-12 | Olympus Optical Co Ltd | Deciding method for particle coagulation pattern |
| JPS562563A (en) * | 1979-06-21 | 1981-01-12 | Olympus Optical Co Ltd | Deciding method for particle coagulation pattern |
| JPS59105543A (en) * | 1982-12-08 | 1984-06-18 | Matsushita Electric Ind Co Ltd | Antigen-antibody reaction detector |
-
1976
- 1976-09-10 JP JP10917876A patent/JPS5928252B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5334595A (en) | 1978-03-31 |
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