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JPH0233096B2 - - Google Patents
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JPH0233096B2 - - Google Patents

Info

Publication number
JPH0233096B2
JPH0233096B2 JP55104061A JP10406180A JPH0233096B2 JP H0233096 B2 JPH0233096 B2 JP H0233096B2 JP 55104061 A JP55104061 A JP 55104061A JP 10406180 A JP10406180 A JP 10406180A JP H0233096 B2 JPH0233096 B2 JP H0233096B2
Authority
JP
Japan
Prior art keywords
blood
amount
tested
light emitted
luminescence
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
Application number
JP55104061A
Other languages
Japanese (ja)
Other versions
JPS5728256A (en
Inventor
Hisashi Kaneko
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tohoku Electronic Industrial Co Ltd
Original Assignee
Tohoku Electronic Industrial Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Tohoku Electronic Industrial Co Ltd filed Critical Tohoku Electronic Industrial Co Ltd
Priority to JP10406180A priority Critical patent/JPS5728256A/en
Publication of JPS5728256A publication Critical patent/JPS5728256A/en
Publication of JPH0233096B2 publication Critical patent/JPH0233096B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/52Use of compounds or compositions for colorimetric, spectrophotometric or fluorometric investigation, e.g. use of reagent paper and including single- and multilayer analytical elements

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hematology (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Urology & Nephrology (AREA)
  • Molecular Biology (AREA)
  • Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Physics & Mathematics (AREA)
  • Biochemistry (AREA)
  • Cell Biology (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Biotechnology (AREA)
  • Analytical Chemistry (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)

Description

【発明の詳細な説明】 この発明は異常な血液を光学的に検出する発光
量による異常血液の検査方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for testing abnormal blood by optically detecting abnormal blood based on the amount of light emitted.

人間の健康を判断する大きな要素として血液検
査があることは周知の通りである。従来、血液検
査として種々の方法があり実用化されている。し
かしながら、この種の検査は一般に試薬等を使用
するものであり、手法が複雑で結果が判明するま
でに時間がかかるものであつた。また、近年輸血
の必要性が急激に増大していることは言うまでも
ない。この際、異常な血液を輸血することは危険
であり、事前に検査を行なうことが必要である。
採血する前に血液に何等かの異常があることを発
見すれば献血者に余分な負担をかけなくてすみ極
めて有利である。しかし、異常血液を簡単、且つ
迅速に判定し得る方法は従来なかつた言わざるを
得ない。
It is well known that blood tests are a major factor in determining a person's health. BACKGROUND ART Conventionally, various methods for blood testing have been put into practical use. However, this type of test generally uses reagents and the like, and the method is complicated and it takes time to obtain results. Furthermore, it goes without saying that the need for blood transfusions has increased rapidly in recent years. At this time, it is dangerous to transfuse abnormal blood, and it is necessary to conduct a test in advance.
If it is discovered that there is some kind of abnormality in the blood before the blood is collected, it is extremely advantageous because there is no need to place an extra burden on the blood donor. However, it must be said that there has never been a method for easily and quickly determining abnormal blood.

この発明は上記事情に基づいてなされたもの
で、被検査血液が発する極く微弱な光の発光量を
測定し、基準となる正常な血液の発光量との相関
関係により小量の血液で異常血液を簡単、且つ迅
速に判定し得る発光量による異常血液の検査方法
を提供しようとするものである。
This invention was made based on the above circumstances, and it measures the amount of extremely weak light emitted by the blood to be tested, and determines the correlation between the amount of light emitted by normal blood as a reference and detects an abnormality in a small amount of blood. It is an object of the present invention to provide a method for testing abnormal blood based on the amount of luminescence, which allows blood to be determined easily and quickly.

食品や高分子化合物等多くの物質がその劣化と
ともに極く微弱な化学発光をすることは周知の通
りである。人間の血液も極く微弱な光を発生する
ことが確認された。しかも、この発光量が正常人
の血液と病人の血液とでは大きな差を有すること
が確認された。したがつて、基準となる正常な血
液の発光量と被検査血液の発光量との相関関係に
よつて異常血液を検査できることが判明したもの
である。
It is well known that many substances such as foods and polymer compounds emit extremely weak chemiluminescence as they deteriorate. It has been confirmed that human blood also emits extremely weak light. Furthermore, it was confirmed that there is a large difference in the amount of luminescence between the blood of a normal person and the blood of a diseased person. Therefore, it has been found that abnormal blood can be tested based on the correlation between the amount of luminescence of normal blood serving as a reference and the amount of luminescence of blood to be tested.

以下、この発明の一実施例について図面を参照
して説明する。
An embodiment of the present invention will be described below with reference to the drawings.

第1図において、11は被検査血液が収容され
る容器である。この容器11には対向して被検査
血液より発生される微弱な光(可視光)を検出す
る光電子増倍管12が設けられる。この光電子増
倍管12と前記容器11との中間部にはシヤツタ
ー13が設けられる。これら容器11、光電子増
倍管12、シヤツター13は暗箱14内に収容さ
れる。前記光電子増倍管12の出力信号は波形整
形回路15においてパルス信号に変換され、計測
部16に供給される。この計測部16はカウンタ
等によつて構成され、このカウンタによつて前記
パルス信号が計数される。この計数出力信号は例
えばデイジタルプリンターやペンレコーダによつ
て構成される記録部17に供給され、記録され
る。
In FIG. 1, 11 is a container in which blood to be tested is stored. A photomultiplier tube 12 is provided opposite to the container 11 to detect weak light (visible light) generated from the blood to be tested. A shutter 13 is provided at an intermediate portion between the photomultiplier tube 12 and the container 11. These container 11, photomultiplier tube 12, and shutter 13 are housed in a dark box 14. The output signal of the photomultiplier tube 12 is converted into a pulse signal by a waveform shaping circuit 15 and supplied to a measuring section 16 . This measuring section 16 is composed of a counter or the like, and the pulse signal is counted by this counter. This counting output signal is supplied to a recording section 17, which is composed of, for example, a digital printer or a pen recorder, and is recorded therein.

上記構成において、容器11には被検査血液が
2ml程度収容される。この血液は実際には恒温装
置によつて体温と同じ温度に保たれる。この状態
において、シヤツター13が例えば10秒程度開か
れ、被検査血液から発生される微弱光が光電子増
倍管12によつて検出される。この検出信号は波
形整形回路15を介して計測部16に供給され発
光量が計数される。この計数出力信号は記録部1
7に供給され、記録される。
In the above configuration, the container 11 contains approximately 2 ml of blood to be tested. This blood is actually kept at the same temperature as body temperature by a thermostat. In this state, the shutter 13 is opened for about 10 seconds, for example, and the photomultiplier tube 12 detects weak light generated from the blood to be tested. This detection signal is supplied to the measuring section 16 via the waveform shaping circuit 15, and the amount of light emission is counted. This counting output signal is
7 and recorded.

このように記録された血液の発光量は、予め上
記と同様の方法により測定された正常人の血液の
発光量と比較され、異常血液の検査が行なわれ
る。
The luminescence amount of blood recorded in this way is compared with the luminescence amount of normal human blood measured in advance by the same method as described above, and abnormal blood is tested.

第2図は上記の方法による測定結果の一例を示
すものであり、Aは正常人、Bは糖尿症患者、C
は癌患者、Dは白血症患者の血液の発光量であ
る。各ポイントは年令や性別によつて異なるもの
であるが正常人Aの場合は発光量が約40カウン
ト/10秒以下であり、その他各罹病者B、C、D
の発光量は殆んどそれ以上の範囲に分布している
ことが認められる。したがつて、病名の判定は難
かしいものの、血液に何らかの異常があれば正常
人より発光量が増すから異常血液を検査すること
ができる。
Figure 2 shows an example of measurement results using the above method, where A is a normal person, B is a diabetic patient, and C is a diabetic patient.
is the luminescence amount of the blood of a cancer patient and D is a leukemia patient. Each point differs depending on age and gender, but in the case of normal person A, the amount of luminescence is approximately 40 counts/10 seconds or less, and for each other affected person B, C, and D.
It is recognized that the amount of light emitted by is distributed over a range larger than that. Therefore, although it is difficult to determine the name of the disease, if there is any abnormality in the blood, the amount of luminescence will be higher than in a normal person, so abnormal blood can be tested.

尚、前記光電子増倍管12は周囲温度等によつ
て変動するため、実用上は装置のダークカウン
ト、正常人の血液のカウント、被検査血液のカウ
ントの比をとつて検査することが有効である。こ
の方法によればカウント数は10〜100秒間の平均
値で充分であり、しかも、一検査に1〜2分程度
しか要さないため迅速な検査を行ない得る。
In addition, since the photomultiplier tube 12 changes depending on the ambient temperature, etc., it is practically effective to perform the test by calculating the ratio of the dark count of the device, the count of normal human blood, and the count of the blood to be tested. be. According to this method, an average count value over 10 to 100 seconds is sufficient, and one test requires only about 1 to 2 minutes, allowing for rapid testing.

上記実施例によれば、異常血液を血液の発光量
によつて検査している。このため従来に比べて検
査に要する時間を大幅に短縮することが可能であ
る。
According to the above embodiment, abnormal blood is tested based on the amount of light emitted from the blood. Therefore, the time required for inspection can be significantly shortened compared to the conventional method.

また、被検査血液は約2ml程度であるため検査
に要する採血が少なくてすみ、採血者の負担を軽
減することが可能である。
Further, since the amount of blood to be tested is about 2 ml, less blood is required for the test, and the burden on the person collecting the blood can be reduced.

尚、この発明は上記実施例に限定されるもので
はなく、例えば前記ダークカウントおよび正常人
の血液のカウント等を例えばマイクロコンピユー
タ等に予じめ記憶しておき、このマイクロコンピ
ユータによつて被検査血液のカウントと前記正常
人のカウントとの比を求め、これが所定値以下の
場合正常、それ以上の場合異常の信号を出力する
ようにすればさらに検査時間を短縮し得る。
It should be noted that the present invention is not limited to the above-mentioned embodiments. For example, the dark count and the blood count of a normal person may be stored in advance in, for example, a microcomputer, and the microcomputer may be used to perform the test. The test time can be further shortened by determining the ratio between the blood count and the normal person's count, and outputting a normal signal if the ratio is less than a predetermined value, and an abnormal signal if it is more than that.

その他、この発明の要旨を変えない範囲で種々
変形実施可能なことは勿論である。
It goes without saying that various other modifications can be made without departing from the gist of the invention.

以上、詳述したようにこの発明によれば、被検
査血液が発する極く微弱な光の発光量を測定し、
基準となる正常な血液の発光量との相関関係によ
り小量の血液で異常血液を簡単、且つ迅速に検査
し得る発光量による血液の検査方法を提供でき
る。
As detailed above, according to the present invention, the amount of extremely weak light emitted by the blood to be tested is measured,
It is possible to provide a method for testing blood based on the amount of light emitted by which abnormal blood can be tested simply and quickly using a small amount of blood based on the correlation with the amount of light emitted by normal blood as a reference.

【図面の簡単な説明】[Brief explanation of drawings]

第1図はこの発明に係わる発光量による血液の
検査方法の一実施例を示す構成図、第2図はこの
検査方法による測定値の一例を示す図である。 11……容器、12……光電子増倍管、13…
…シヤツター、14……暗箱、15……波形整形
回路、16……計測部、17……記録部。
FIG. 1 is a block diagram showing an embodiment of a blood testing method based on luminescence intensity according to the present invention, and FIG. 2 is a diagram showing an example of measured values by this testing method. 11... Container, 12... Photomultiplier tube, 13...
...Shutter, 14...Dark box, 15...Waveform shaping circuit, 16...Measuring section, 17...Recording section.

Claims (1)

【特許請求の範囲】[Claims] 1 検査容器に収容された被検査血液の発光量を
測定し、この発光量と基準となる正常な血液の発
光量との相関関係により、異常血液を検出するこ
とを特徴とする発光量による異常血液の検査方
法。
1 Abnormal blood is detected by measuring the amount of light emitted from blood to be tested contained in a test container, and detecting abnormal blood based on the correlation between this amount of light and the amount of light emitted from normal blood as a reference. How to test blood.
JP10406180A 1980-07-29 1980-07-29 Inspection of blood depending on light emission Granted JPS5728256A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10406180A JPS5728256A (en) 1980-07-29 1980-07-29 Inspection of blood depending on light emission

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10406180A JPS5728256A (en) 1980-07-29 1980-07-29 Inspection of blood depending on light emission

Publications (2)

Publication Number Publication Date
JPS5728256A JPS5728256A (en) 1982-02-15
JPH0233096B2 true JPH0233096B2 (en) 1990-07-25

Family

ID=14370659

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10406180A Granted JPS5728256A (en) 1980-07-29 1980-07-29 Inspection of blood depending on light emission

Country Status (1)

Country Link
JP (1) JPS5728256A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6175239A (en) * 1984-09-20 1986-04-17 Advance Res & Dev Co Ltd Detection of mutagen-oriented substance
JPH0194249A (en) * 1987-10-07 1989-04-12 Tohoku Denshi Sangyo Kk Organ failure foretelling apparatus

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54100793A (en) * 1978-01-25 1979-08-08 Mitsubishi Heavy Ind Ltd Material deterioration meter
JPS54127386A (en) * 1978-03-27 1979-10-03 Mitsubishi Heavy Ind Ltd Material deterioration measuring apparatus

Also Published As

Publication number Publication date
JPS5728256A (en) 1982-02-15

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