JPS602234A - Color concentration measuring apparatus - Google Patents

Color concentration measuring apparatus

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Publication number
JPS602234A
JPS602234A JP58109974A JP10997483A JPS602234A JP S602234 A JPS602234 A JP S602234A JP 58109974 A JP58109974 A JP 58109974A JP 10997483 A JP10997483 A JP 10997483A JP S602234 A JPS602234 A JP S602234A
Authority
JP
Japan
Prior art keywords
light
optical fiber
concentration
reflected
measurement
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.)
Pending
Application number
JP58109974A
Other languages
Japanese (ja)
Inventor
聡一 橋本
伊知郎 祖川
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.)
Sumitomo Electric Industries Ltd
Original Assignee
Sumitomo Electric Industries 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 Sumitomo Electric Industries Ltd filed Critical Sumitomo Electric Industries Ltd
Priority to JP58109974A priority Critical patent/JPS602234A/en
Publication of JPS602234A publication Critical patent/JPS602234A/en
Pending legal-status Critical Current

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  • Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 [11技術分野 本発明は色素希釈法による心拍量測定等の血液の循環量
に係わる測定を行うために生体血液中に注入された色素
の濃度を無侵I!測定する色素濃度測定装置に関する。
DETAILED DESCRIPTION OF THE INVENTION [11 Technical Field] The present invention is a non-invasive method for measuring the concentration of a dye injected into the blood of a living body in order to measure blood circulation volume such as heart rate measurement using a dye dilution method. The present invention relates to a dye concentration measuring device for measuring.

[21従来技術とその問題点 心拍出量の測定を例にとって従来技術について説明する
。この測定法の原理と特徴についてはい(つかの刊行物
によって説明されているが、(例えば「指示薬希釈法の
臨床応用」第4章67〜68頁(中村、香取、渡部共著
、中白書店ン、以下略述する。
[21 Prior Art and Its Problems The prior art will be explained by taking the measurement of cardiac output as an example. The principles and characteristics of this measurement method are explained in some publications (for example, "Clinical Application of Indicator Dilution Method", Chapter 4, pp. 67-68, co-authored by Nakamura, Katori, and Watanabe, published by Nakahaku Shoten). , will be briefly described below.

心拍出量の測定法として、現在臨床で通常用いられてい
る方法は指示薬希釈法である。指示薬希釈法は、用いら
れる指示薬によっていくつかに分けられるが、それらの
中で良(用いられているのは熱希釈法と、色素希釈法で
ある。
The method currently commonly used in clinical practice to measure cardiac output is the indicator dilution method. Indicator dilution methods can be divided into several types depending on the indicator used, but the two most commonly used are the thermodilution method and the dye dilution method.

熱希釈法は、指示薬として体温よりも高温あるいは、低
温の液体を用いる方法であるが、その液体を注入部位で
ある肺動脈に力゛チーチルを用いて注入する際、体温に
よって液温が変化してしまうため、その補正が必要であ
り、精度を上げにくいという問題点がある。さらに、こ
の方法は、上述のようにカテーテルを用いた侵襲的な測
定法である、という点も問題である。
The thermodilution method is a method that uses a liquid that is hotter or colder than body temperature as an indicator. Therefore, there is a problem that correction is necessary and it is difficult to improve accuracy. Another problem is that this method is an invasive measurement method using a catheter as described above.

色素希釈法は、指示薬として色素を用いる方法であり、
色素の血中濃度測定法の違いによってキュベツト法とイ
ヤピース法に分けられる。キュベツト法は、連続的に採
血される血液から直接に色素濃度を測定するため、精度
は良いが、侵襲的測定法である。一方、イヤピース法は
、耳朶で、その透過光を測定することによって血中色素
濃度を測定する方法であり、無侵襲的測定法であるが、
耳朶の皮膚表面からかなり深いところにある血管中の色
素濃度を経皮的に測定するため精度が悪い。
The dye dilution method is a method that uses a dye as an indicator.
It can be divided into the cuvette method and the earpiece method depending on the method used to measure the blood concentration of the dye. The cuvette method measures dye concentration directly from blood that is continuously collected, so although it has good accuracy, it is an invasive measurement method. On the other hand, the earpiece method is a non-invasive measurement method that measures the blood pigment concentration by measuring the transmitted light in the earlobe.
Accuracy is low because it transcutaneously measures the pigment concentration in the blood vessels located quite deep below the skin surface of the earlobe.

さらに、測定前になんらかの手段で耳朶の血行を盛んに
しておく必要があり、面倒である。
Furthermore, it is necessary to stimulate blood circulation in the earlobe by some means before measurement, which is troublesome.

(3)発明の目的 本発明は、上記測定法の間阻点を解決し、色素希釈法を
用いて無侵襲で、簡便に1かつ精度良く、心拍出量を測
定するためになされたものである。
(3) Purpose of the Invention The present invention has been made in order to solve the obstacles between the above measurement methods and to measure cardiac output non-invasively, simply, and with high precision using the dye dilution method. It is.

このために口腔粘膜上で経皮的に光学的方法で一色素濃
度を測定することを特徴とする。
For this purpose, the method is characterized by measuring the concentration of a single pigment transcutaneously on the oral mucosa using an optical method.

口腔粘膜においては、上皮に色素がなく、透明度が高い
ため、血管の分布している下層部tζ光が到達しヤす(
、高精度の測定を行うことができるわけである。
In the oral mucosa, the epithelium has no pigment and is highly transparent, so light can reach the lower layer where blood vessels are distributed (
, it is possible to perform highly accurate measurements.

(4]発明の内容 第1図は、本測定装置に用いる光フアイバセンナの先端
部分の措造を例示した図で、第1図(1)はその断面図
である。本図tζおける1はセンサの先端部である。2
は光ファイバ束で、その一部を口腔粘atζ測定光を照
射するために使用し、残りを粘膜からの反射散乱光を受
光素子に導び(ために使用する。3は光7アイ2束の外
被である。口腔粘膜を必要以上に圧迫することによる血
行阻害を防ぐため、センサ先端部lの粘膜に密着する側
の表面1asga は第1図(2)に示したような、な
めらかに連続した面積の広い曲面となっていることが望
ましい。
(4) Contents of the invention Fig. 1 is a diagram illustrating the structure of the tip portion of the optical fiber sensor used in this measuring device, and Fig. 1 (1) is a sectional view thereof.1 in tζ in this figure is a sensor. This is the tip of 2.
is an optical fiber bundle, a part of which is used to irradiate the oral viscosity measurement light, and the rest is used to guide reflected and scattered light from the mucous membrane to the light receiving element. 3 is a 7-eye 2 bundle of optical fibers. In order to prevent blood circulation from being obstructed by unnecessarily compressing the oral mucosa, the surface 1asga of the sensor tip l on the side that comes into close contact with the mucous membrane is smooth as shown in Figure 1 (2). It is desirable that the surface be a continuous curved surface with a wide area.

第2図は、本測定装置全体の槽成例を示したものである
。センサ先端部1は口腔内、頬の内側の粘II%18と
歯茎14および歯15の間に、センサ表面la e 2
 a が粘膜に密着するように設置される。
FIG. 2 shows an example of the tank configuration of the entire measuring device. The sensor tip 1 is placed in the oral cavity, between the inner cheek viscosity 18, the gums 14 and the teeth 15, and the sensor surface la e 2
a is placed in close contact with the mucous membrane.

光ファイバ束2は、分岐部18で2本の送光用光ファイ
バ束4.5と1本の受光用光ファイバ束6に分岐される
。この分岐は例えば、7アイμ束の開口端面2a にお
ける送受光ファイバの配列がランダムになるよう処分け
る、といったように粘膜からの反射散乱光をできるだけ
広範囲にむらなく受光できるような適切な方法でなされ
ることが望ましい。7a、7b は、それぞれ送光用光
ファイバ束4.5と結合されたJ′i4なった波長の発
光素子(例えばレーザ・ダイオード)であり、駆動用回
路8a、8b によって発光出力を制御される。これら
の発光素子は中央り皿部11からの制御信号によって交
互に点滅される。測定光の口腔粘膜上での反射散乱光は
、受光用光ファイバ束6によって受光素子9(例えばフ
ォト・ダイオード)に導びかれる。受光素子9からの信
号は、増幅回路lOによって増幅され、中央処理部11
に送られる。
The optical fiber bundle 2 is branched into two light transmitting optical fiber bundles 4.5 and one light receiving optical fiber bundle 6 at the branching part 18. This branching can be done in an appropriate manner so that the reflected and scattered light from the mucous membrane can be received evenly over as wide a range as possible, such as by disposing the transmitting and receiving fibers at the opening end surface 2a of the 7-eye μ bundle so that the arrangement is random. It is desirable that this be done. 7a and 7b are light emitting elements (for example, laser diodes) having a wavelength of J'i4, which are coupled to the optical fiber bundle 4.5 for transmitting light, and whose light emitting outputs are controlled by driving circuits 8a and 8b. . These light emitting elements are alternately turned on and off by a control signal from the central tray section 11. The reflected and scattered light of the measurement light on the oral mucosa is guided to a light receiving element 9 (for example, a photo diode) by a light receiving optical fiber bundle 6. The signal from the light-receiving element 9 is amplified by the amplifier circuit lO, and then sent to the central processing unit 11.
sent to.

中央処理部11は、この信号を217]類の波長の測定
光それぞれに対する反射散乱光の強度信号に分離、色素
濃度を算出し、その値を用いて心拍出量をめる。12は
データの表示部であり、色素濃度曲線、その他のデータ
(例えば心拍出量)を表示する。反射散乱光強度から、
血中色素濃度をめるための原理の概略を以下に述べる。
The central processing unit 11 separates this signal into intensity signals of reflected and scattered light for each of the measurement lights having wavelengths of 217], calculates the pigment concentration, and calculates the cardiac output using this value. A data display section 12 displays a dye concentration curve and other data (for example, cardiac output). From the reflected and scattered light intensity,
An outline of the principle for determining blood pigment concentration is described below.

口腔粘膜上に測定光を照射し、その反射散乱光強度を測
定するならば、その強度は粘膜下層部に分布する血管中
を流れる血液中の色素濃度の増大に対して指数関数的に
低下する。この関係を利用して反射散乱光強度の変化か
ら、血中色素濃度をめることができる。また、測定光の
波長に、色素濃度変化による吸光度の変化が大きな波長
と、はとんど変化しない波長の2波長を選び、それぞれ
に対する反射散乱光強度を測定し、それらの比を取るこ
とによって、色素濃度変化による以外の反射散乱光強度
の変化を相殺することができる。
If the measurement light is irradiated onto the oral mucosa and the intensity of the reflected and scattered light is measured, the intensity will decrease exponentially as the pigment concentration in the blood flowing through the blood vessels distributed in the submucosa increases. . Using this relationship, the blood pigment concentration can be estimated from changes in the intensity of reflected and scattered light. In addition, by selecting two wavelengths for the measurement light, one for which the absorbance changes significantly due to changes in dye concentration, and another for which the absorbance hardly changes, measuring the reflected and scattered light intensity for each, and taking the ratio. , changes in reflected and scattered light intensity other than those caused by changes in dye concentration can be offset.

さて、静脈にI(nv)の色素を両開的に注入した時に
第3図に示したような色素希釈曲縁が得られたものとす
る。この曲線の初回?7!環部分の面積をS (nV・
min// )としたとき、心拍出量Q (//min
)は次式によってめられる。
Now, suppose that when the dye I(nv) is injected bilaterally into a vein, a dye dilution curve as shown in FIG. 3 is obtained. The first time this curve? 7! The area of the ring part is S (nV・
min// ), cardiac output Q (//min
) is determined by the following formula.

Q=I/S (//m1n) 以上、本発明を心拍出量測定に用いる際の措成について
述べたが、本発明の色素濃度測定装置は、心拍出量測定
に限らず、例えば肝機能検査のような、やけ秒色素を用
いた検査に使用することが可能である。
Q=I/S (//m1n) The configuration for using the present invention to measure cardiac output has been described above, but the dye concentration measuring device of the present invention is not limited to measuring cardiac output, but can also be used, for example. It can be used for tests that use burn second dyes, such as liver function tests.

(5)発明の効果 本発明の色素濃度測定装置を用いれば、被験者に侵襲を
加えることす<、光フアイバセンサの先端部を口に含ん
でもらうだけで、簡便に稍度良(血中色素濃度を測定す
ることができる。
(5) Effects of the Invention By using the pigment concentration measuring device of the present invention, it is possible to easily detect a good color (blood pigment concentration) by simply holding the tip of the optical fiber sensor in the subject's mouth without causing any invasive treatment to the subject. Concentration can be measured.

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

第1図は、本測定装置に用いる光7アイパ七ンサの先端
部の桁造の1例を示したもので、(1)はその横断面図
、(2)は(1)を左方から見た図である。第2図は本
測定装置全体の桁成を示した図である。 第8vAは、色素濃度の時間的変化を示す希釈曲線であ
り、Sは初回循環部分の面積である。 l・・・光フアイバセンナ先端部本体 1a・・・光フアイバセンサ先端部本体表面2 ・・・
送受光用光ファイバ束 2a・・・送受光用光ファイバ束間口端面8 ・・・光
ファイバ束の外被 4.5・・・送光用光ファイバ束 6 ・・・受光用光ファイバ来 7 a e 7 b・・・発光素子 8at8b・・・発光素子駆動用回路 9 ・・・受光素子 10 ・・・増幅回路 11 ・・・中央処理部 12 ・・・表示部 代理人弁理士 上代 哲 司 (f) 第1図 ] 素 支 箒3目
Figure 1 shows an example of the girder structure at the tip of the optical 7-eye sensor used in this measuring device. (1) is its cross-sectional view, and (2) is (1) viewed from the left. This is a view. FIG. 2 is a diagram showing the order of magnitude of the entire measuring device. The 8th vA is a dilution curve showing the temporal change in dye concentration, and S is the area of the first circulation part. l... Optical fiber sensor tip body 1a... Optical fiber sensor tip body surface 2...
Optical fiber bundle for transmitting and receiving light 2a ... Optical fiber bundle for transmitting and receiving light end face 8 ... Outer cover of optical fiber bundle 4.5 ... Optical fiber bundle for transmitting light 6 ... Optical fiber for receiving light 7 a e 7 b...Light emitting element 8at8b...Light emitting element driving circuit 9...Light receiving element 10...Amplifying circuit 11...Central processing unit 12...Patent attorney representing the display department Satoshi Ushiro (f) Figure 1] Suboshibroom 3 eyes

Claims (1)

【特許請求の範囲】[Claims] 中の色素濃度を測定する装置であって、交互に点滅する
29類の波長の発光素子からの測定光を測定部位に導(
第1の光ファイバ来と、前記部位からの反射散乱光を受
光素子へ導く第2の光ファイバ東とを具え、前記受光素
子が受光した光信号を前記測定光に含まれているそれぞ
れの波長ごとに分離して強度をめ5る手段、得られた各
波長に対する反射散乱光の強度から色素濃度を算出する
手段と、前記の色素濃度の時間変化曲線をめ、色素注入
による初回体内循環量と対比して心拍出量を算出するこ
とを特徴とする色素濃度測定装置。
This is a device that measures the concentration of pigment in the body, and it guides measurement light from a light-emitting element with 29 wavelengths that flashes alternately to the measurement site (
A first optical fiber is provided, and a second optical fiber is provided that guides the reflected and scattered light from the portion to the light receiving element, and the light signal received by the light receiving element is transmitted to the light receiving element at each wavelength included in the measurement light. A method for calculating the dye concentration from the intensity of the reflected and scattered light for each wavelength obtained, and a means for calculating the dye concentration from the intensity of the reflected and scattered light for each wavelength, and a means for calculating the dye concentration time change curve. A pigment concentration measuring device characterized in that it calculates cardiac output in comparison with.
JP58109974A 1983-06-17 1983-06-17 Color concentration measuring apparatus Pending JPS602234A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58109974A JPS602234A (en) 1983-06-17 1983-06-17 Color concentration measuring apparatus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58109974A JPS602234A (en) 1983-06-17 1983-06-17 Color concentration measuring apparatus

Publications (1)

Publication Number Publication Date
JPS602234A true JPS602234A (en) 1985-01-08

Family

ID=14523867

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58109974A Pending JPS602234A (en) 1983-06-17 1983-06-17 Color concentration measuring apparatus

Country Status (1)

Country Link
JP (1) JPS602234A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63216540A (en) * 1987-03-05 1988-09-08 テルモ株式会社 Apparatus for measuring heart rate output quantity
JPS6470024A (en) * 1987-03-05 1989-03-15 Terumo Corp Cardiac output measuring apparatus equipped with automatic starting function of measurement

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5764044A (en) * 1980-10-02 1982-04-17 Hajime Yokosuga Inspection device for liver function
JPS57115232A (en) * 1980-07-09 1982-07-17 Deyuuku Univ Inc Apparatus for measuring metabolic action in internal organ

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57115232A (en) * 1980-07-09 1982-07-17 Deyuuku Univ Inc Apparatus for measuring metabolic action in internal organ
JPS5764044A (en) * 1980-10-02 1982-04-17 Hajime Yokosuga Inspection device for liver function

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63216540A (en) * 1987-03-05 1988-09-08 テルモ株式会社 Apparatus for measuring heart rate output quantity
JPS6470024A (en) * 1987-03-05 1989-03-15 Terumo Corp Cardiac output measuring apparatus equipped with automatic starting function of measurement

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