JP2000235028A - Blood component measuring device and blood component measuring method - Google Patents
Blood component measuring device and blood component measuring methodInfo
- Publication number
- JP2000235028A JP2000235028A JP11037882A JP3788299A JP2000235028A JP 2000235028 A JP2000235028 A JP 2000235028A JP 11037882 A JP11037882 A JP 11037882A JP 3788299 A JP3788299 A JP 3788299A JP 2000235028 A JP2000235028 A JP 2000235028A
- Authority
- JP
- Japan
- Prior art keywords
- intensity
- reflected light
- light
- transmitted light
- end time
- 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
Links
- 239000012503 blood component Substances 0.000 title claims abstract description 70
- 238000000034 method Methods 0.000 title claims description 18
- 238000005259 measurement Methods 0.000 claims abstract description 79
- 239000008280 blood Substances 0.000 claims abstract description 40
- 210000004369 blood Anatomy 0.000 claims abstract description 40
- 238000002835 absorbance Methods 0.000 claims abstract description 37
- 238000012360 testing method Methods 0.000 claims abstract description 34
- 238000011088 calibration curve Methods 0.000 claims abstract description 11
- 238000004364 calculation method Methods 0.000 claims description 25
- 230000001678 irradiating effect Effects 0.000 claims description 20
- 230000002123 temporal effect Effects 0.000 claims description 18
- 239000003153 chemical reaction reagent Substances 0.000 claims description 11
- 239000000306 component Substances 0.000 claims description 7
- 238000000611 regression analysis Methods 0.000 claims description 5
- 238000012937 correction Methods 0.000 claims description 4
- 238000000691 measurement method Methods 0.000 claims description 4
- 238000001514 detection method Methods 0.000 claims description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract description 19
- 239000008103 glucose Substances 0.000 abstract description 19
- 238000012790 confirmation Methods 0.000 abstract 1
- 238000013500 data storage Methods 0.000 description 8
- 238000010187 selection method Methods 0.000 description 3
- 238000009529 body temperature measurement Methods 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000005534 hematocrit Methods 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
Landscapes
- Investigating Or Analysing Biological Materials (AREA)
- Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、例えば指先のよう
な生体表面を穿刺して採取した微量の血液の成分の濃度
を測定するための、血液成分測定装置および血液成分測
定方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a blood component measuring apparatus and a blood component measuring method for measuring the concentration of a minute amount of blood components collected by puncturing a living body surface such as a fingertip.
【0002】[0002]
【従来の技術】近年、糖尿病患者の増加に伴い、日常の
血糖値の変動を患者自身がモニターする自己血糖測定が
推奨されてきている。現在、この血糖値測定法の一つと
して、血中のブドウ糖量に応じて呈色する試験紙を装着
し、該試験紙に血液を供給、展開させ、その呈色の度合
いを光学的に測定(測色)して血糖値を定量化する血糖
測定装置を用いる方法が行われている。この呈色を基に
血糖値を検出するには、血液中のグルコースと試験紙中
の試薬の呈色反応が終了する状態まで待った後、その呈
色の度合いを光学的に測定し血糖値を計算する。このた
め現在市販されている血糖測定装置は測定時間に20秒
前後またはそれ以上の時間を要するため、より早く測定
できる血糖測定装置ことが望まれていた。2. Description of the Related Art In recent years, with the increase in the number of diabetic patients, autologous blood glucose measurement in which patients monitor daily fluctuations in blood glucose levels has been recommended. At present, as one of the methods of measuring blood glucose level, a test paper that develops a color according to the amount of glucose in blood is mounted, blood is supplied to the test paper, developed, and the degree of color development is measured optically. 2. Description of the Related Art A method of using a blood glucose measuring device for quantifying a blood glucose level by performing (color measurement) has been performed. To detect the blood glucose level based on this coloration, wait until the color reaction between glucose in blood and the reagent in the test paper is completed, and then optically measure the degree of coloration to measure the blood glucose level. calculate. For this reason, currently available blood glucose measuring devices require a measuring time of about 20 seconds or more, and therefore a blood glucose measuring device capable of performing measurement more quickly has been desired.
【0003】[0003]
【発明が解決しようとする課題】本発明は、上述した従
来技術の問題点を鑑みて、短時間で高精度に血糖値を測
定する血液成分測定装置および血液成分測定方法を提供
することを目的とする。SUMMARY OF THE INVENTION An object of the present invention is to provide a blood component measuring apparatus and a blood component measuring method for measuring a blood glucose level in a short time and with high accuracy in view of the above-mentioned problems of the prior art. And
【0004】[0004]
【課題を解決するための手段】上記目的は、以下の本発
明により達成される。 (1)本発明は、皮膚を穿刺して採取した微量の血液の
成分を測定する血液成分測定装置において、前記血液成
分測定装置に着脱可能に設けられ、血液中の特定成分と
呈色反応する試薬を含む試験紙を備えたチップと、前記
試験紙に光を照射する照射手段と、前記照射手段から前
記試験紙に照射された光の反射光または透過光の強度を
検出する測定手段と、前記血液成分測定装置に電源が入
力されると、一定の時間間隔ごとに、前記照射手段に光
の照射および前記測定手段に反射光または透過光の強度
の検出を行わせる制御手段と、前記測定手段により検出
した前記反射光または透過光の強度を記憶する記憶手段
と、前記反射光または透過光の強度の経時変化から測定
終了時間を決定する測定終了時間決定手段と、前記反射
光または透過光の強度の経時変化から前記測定終了時間
決定手段により決定された測定終了時間後の反射光また
は透過光の強度を予測するための予測係数を求める手段
と、前記予測係数と前記反射光または透過光の強度の経
時変化から、前記測定終了時間決定手段により決定され
た測定終了時間後の反射光または透過光の強度を予測す
る予測演算手段と、前記予測演算手段により予測された
反射光または透過光の強度から血液成分濃度を求める濃
度演算手段とを有することを特徴とする血液成分測定装
置である。The above object is achieved by the present invention described below. (1) The present invention relates to a blood component measuring device that measures a minute amount of blood collected by puncturing the skin, which is detachably provided to the blood component measuring device and performs a color reaction with a specific component in blood. A chip provided with a test paper containing a reagent, irradiation means for irradiating the test paper with light, and measurement means for detecting the intensity of reflected light or transmitted light of light applied to the test paper from the irradiation means, When power is supplied to the blood component measuring device, at regular time intervals, control means for causing the irradiating means to irradiate light and cause the measuring means to detect the intensity of reflected light or transmitted light; and Storage means for storing the intensity of the reflected light or transmitted light detected by the means; measurement end time determining means for determining a measurement end time from a temporal change in the intensity of the reflected light or transmitted light; and the reflected light or transmitted light. of Means for calculating a prediction coefficient for predicting the intensity of the reflected light or transmitted light after the measurement end time determined by the measurement end time determination means from the temporal change of the degree, and the prediction coefficient and the reflected light or transmitted light. Prediction calculation means for predicting the intensity of the reflected light or transmitted light after the measurement end time determined by the measurement end time determination means from the change over time of the intensity; and the reflected light or transmitted light predicted by the prediction calculation means. A blood component measuring device comprising: a concentration calculating means for obtaining a blood component concentration from intensity.
【0005】(2)本発明は、前記血液成分測定装置の
電源を入力し、前記制御手段によって一定の時間間隔ご
とに、前記照射手段による前記試験紙への光の照射およ
び前記測定手段による前記試験紙からの反射光または透
過光の強度の検出を行いながら、採取した血液を前記試
験紙に展開させ前記試薬と呈色反応させて、検出した前
記反射光または透過光の強度を記憶手段に記憶し、記憶
した前記反射光または透過光の強度の経時変化から前記
測定終了時間決定手段により測定終了時間を決定し、記
憶した前記反射光または透過光の強度の経時変化から前
記予測係数を求める手段により、前記決定された測定終
了時間後の反射光または透過光の強度を予測するための
予測係数を求めた後、前記予測演算手段によって、前記
予測係数と前記反射光または透過光の強度の経時変化か
ら、前記測定終了時間決定手段により決定された測定終
了時間後の反射光または透過光の強度を予測し、前記濃
度演算手段によって、前記予測演算手段により予測され
た反射光または透過光の強度から血液成分の濃度を測定
する上記(1)に記載の血液成分測定装置である。(2) According to the present invention, a power supply of the blood component measuring device is inputted, and the control means controls the irradiation of the test paper with the light by the irradiating means and the measuring means by the measuring means at regular time intervals. While detecting the intensity of the reflected light or transmitted light from the test paper, the collected blood is developed on the test paper and subjected to a color reaction with the reagent, and the detected intensity of the reflected light or transmitted light is stored in storage means. The measurement end time is determined by the measured end time determining means from the stored temporal change of the reflected light or transmitted light intensity, and the prediction coefficient is obtained from the stored temporal change of the reflected light or transmitted light intensity. Means for determining a prediction coefficient for predicting the intensity of the reflected light or transmitted light after the determined measurement end time, and then, by the prediction calculation means, calculates the prediction coefficient and the counter value. The intensity of reflected light or transmitted light after the measurement end time determined by the measurement end time determination means is predicted from the temporal change in the intensity of light or transmitted light, and is predicted by the concentration calculation means by the prediction calculation means. The blood component measuring device according to the above (1), wherein the concentration of the blood component is measured from the intensity of the reflected light or transmitted light.
【0006】(3)本発明は、前記反射光または透過光
の強度を吸光度として記憶手段に記憶し、前記決定され
た測定終了時間後の反射光または透過光の強度として吸
光度(ab(t))を、予測演算手段において、下記式1
によって求める上記(1)乃至(2)に記載の血液成分
測定装置である。(3) According to the present invention, the intensity of the reflected light or transmitted light is stored in a storage means as an absorbance, and the absorbance (ab (t)) is obtained as the intensity of the reflected light or transmitted light after the determined measurement end time. ) Is calculated by the following equation 1
The blood component measuring device according to the above (1) or (2), which is obtained by:
【0007】[0007]
【数5】 (Equation 5)
【0008】[0008]
【数6】 (Equation 6)
【0009】bは、式2から求める。式中のAB(1)、
AB(2)、AB(3)は、前記測定終了時間決定手段にお
いて、記憶手段に記憶された一定の時間間隔(T)ごと
の前記反射光または透過光の強度を吸光度から、一定時
間間隔後(m、ここでm=1,2,3,・・・(整数)で
ある)の吸光度(ab(m))とその一つ前の間隔(m−
1)の吸光度(ab(m−1))の変化率(V(m)=(a
b(m)−ab(m−1))/T)およびさらにその変化率
差(A(l)=(V(l)−V(l−1))/T、ここでl=
m+1である)を求め、A(l)−A(l−1)<0となる
時をAB(1)として、前記AB(1)が決定した以降にさ
らにA(l)−A(l−1)>0かつA(l)*A(l−2)>
5となる時をAB(2)(=ab(l1))として、ab
(l2+(l2−l1))となる時を測定終了時間AB(3)
として求める。M=l2−l1とする。k,aは、前記
予測係数を求める手段において、bとab(0)からAB
(3)までの吸光度データを用い式1において重回帰分析
を行い求める。[0009] b is obtained from equation (2). AB (1) in the formula,
AB (2) and AB (3) measure the intensity of the reflected light or transmitted light at a certain time interval (T) stored in the storage means from the absorbance after a predetermined time interval in the measurement end time determination means. (M, where m = 1, 2, 3,... (Integer)) absorbance (ab (m)) and the immediately preceding interval (m−
The change rate (V (m) = (a) of the absorbance (ab (m-1)) of 1)
b (m) -ab (m-1)) / T) and its rate of change (A (l) = (V (l) -V (1-1)) / T, where l =
m + 1), and when A (l) -A (l-1) <0 is defined as AB (1), A (l) -A (l-) is determined after AB (1) is determined. 1)> 0 and A (l) * A (l-2)>
When the value is 5, AB (2) (= ab (11)) is defined as ab
Measurement end time AB (3) when (l2 + (l2-l1))
Asking. Let M = l2-l1. k and a are AB from b and ab (0) in the means for calculating the prediction coefficient.
Using the absorbance data up to (3), a multiple regression analysis is performed in Equation 1 to determine the value.
【0010】(4)本発明は、前記制御手段が、前記照
射手段に光の照射および前記測定手段に反射光または透
過光の強度の検出を行わせる一定の時間間隔を検出中に
可変できるものである上記(1)乃至(3)に記載の血
液成分測定装置である。(4) The present invention is such that the control means can change a fixed time interval for causing the irradiating means to irradiate light and the measuring means to detect the intensity of reflected light or transmitted light during detection. The blood component measurement device according to any one of (1) to (3) above.
【0011】(5)本発明は、前記予測演算手段が、ロ
ジスティック曲線を使用するものである上記(1)乃至
(4)に記載の血液成分測定装置である。(5) The present invention is the blood component measuring device according to any one of the above (1) to (4), wherein the prediction calculation means uses a logistic curve.
【0012】(6)本発明は、前記濃度演算手段が、血
液成分濃度の変化から実測された反射光または透過光の
強度の変化により描かれた検量線と、それを補正する補
正項を用いて血液成分濃度を求めるものである上記
(1)乃至(5)に記載の血液成分測定装置である。(6) According to the present invention, the concentration calculating means uses a calibration curve drawn by a change in intensity of reflected light or transmitted light actually measured from a change in blood component concentration, and a correction term for correcting the calibration curve. The blood component measuring device according to any one of the above (1) to (5), wherein the blood component concentration is determined by the following method.
【0013】(7)本発明は、皮膚を穿刺して採取した
微量の血液の成分を測定する方法であって、血液中の特
定成分と呈色反応する試薬を含む試験紙と、前記試験紙
に光を照射する照射手段と、前記照射手段から前記試験
紙に照射された光の反射光または透過光の強度を検出す
る測定手段と、一定の時間間隔ごとに、前記照射手段に
光の照射および前記測定手段に反射光または透過光の強
度の検出を行わせる制御手段と、前記測定手段により検
出した前記反射光または透過光の強度を記憶する記憶手
段と、前記反射光または透過光の強度の経時変化から測
定終了時間を決定する測定終了時間決定手段と、前記反
射光または透過光の強度の経時変化から前記測定終了時
間決定手段により決定された測定終了時間後の反射光ま
たは透過光の強度を予測するための予測係数を求める手
段と、前記予測係数と前記反射光または透過光の強度の
経時変化から、前記測定終了時間決定手段により決定さ
れた測定終了時間後の反射光または透過光の強度を予測
する予測演算手段と、前記予測演算手段により予測され
た反射光または透過光の強度から血液成分濃度を求める
濃度演算手段とにより、前記各手段を作動させるための
電源を入力し、前記制御手段によって一定の時間間隔ご
とに、前記照射手段による前記試験紙への光の照射およ
び前記測定手段による前記試験紙からの反射光または透
過光の強度の検出を行いながら、採取した血液を前記試
験紙に展開させ前記試薬と呈色反応させて、検出した前
記反射光または透過光の強度を記憶手段に記憶し、記憶
した前記反射光または透過光の強度の経時変化から前記
測定終了時間決定手段により測定終了時間を決定し、記
憶した前記反射光または透過光の強度の経時変化から前
記予測係数を求める手段により、前記決定された測定終
了時間後の反射光または透過光の強度を予測するための
予測係数を求めた後、前記予測演算手段によって、前記
予測係数と前記反射光または透過光の強度の経時変化か
ら、前記測定終了時間決定手段により決定された測定終
了時間後の反射光または透過光の強度を予測し、前記濃
度演算手段によって、前記予測演算手段により予測され
た反射光または透過光の強度から血液成分の濃度を測定
する血液成分測定方法である。(7) The present invention relates to a method for measuring a small amount of blood components collected by puncturing the skin, comprising: a test paper containing a reagent that causes a color reaction with a specific component in blood; Irradiating means for irradiating the test paper with light, measuring means for detecting the intensity of reflected light or transmitted light of the light irradiating the test paper from the irradiating means, and irradiating the irradiating means with light at regular time intervals. And control means for causing the measuring means to detect the intensity of the reflected light or transmitted light; storage means for storing the intensity of the reflected light or transmitted light detected by the measuring means; and the intensity of the reflected light or transmitted light Measurement end time determining means for determining the measurement end time from the change over time of the reflected light or transmitted light after the measurement end time determined by the measurement end time determination means from the change over time of the intensity of the reflected light or transmitted light. Strength Means for obtaining a prediction coefficient for prediction, and the intensity of the reflected light or transmitted light after the measurement end time determined by the measurement end time determination means, based on the change over time of the prediction coefficient and the intensity of the reflected light or transmitted light. Inputting a power supply for operating each of the means by the prediction operation means for predicting the above, and a concentration operation means for obtaining the blood component concentration from the intensity of the reflected light or transmitted light predicted by the prediction operation means; The blood collected is subjected to the test while irradiating the test paper with light by the irradiating means and detecting the intensity of reflected light or transmitted light from the test paper by the measuring means at regular time intervals by the means. The intensity of the reflected light or transmitted light is stored in storage means, and the intensity of the stored reflected light or transmitted light is stored in storage means. The measurement end time is determined by the measurement end time determining means from the temporal change, and the reflected light after the determined measurement end time is determined by the means for determining the prediction coefficient from the stored temporal change of the intensity of the reflected light or transmitted light. Or, after obtaining a prediction coefficient for predicting the intensity of the transmitted light, the prediction operation means determines the prediction coefficient and the intensity of the reflected light or transmitted light over time, and the measurement end time determining means determines the time. A blood component measurement method for predicting the intensity of reflected light or transmitted light after the measurement end time and measuring the concentration of blood components from the intensity of reflected light or transmitted light predicted by the prediction operation means by the concentration calculation means. is there.
【0014】(8)本発明は、前記反射光または透過光
の強度を吸光度として記憶手段に記憶し、前記決定され
た測定終了時間後の反射光の強度を吸光度(ab(t))
を、予測演算手段において、下記式1によって求める上
記(7)に記載の血液成分測定方法である。(8) In the present invention, the intensity of the reflected light or the transmitted light is stored in a storage means as an absorbance, and the intensity of the reflected light after the determined measurement end time is determined as an absorbance (ab (t)).
Is a blood component measurement method according to the above (7), which is obtained by the predictive calculation means by the following equation 1.
【0015】[0015]
【数7】 (Equation 7)
【0016】[0016]
【数8】 (Equation 8)
【0017】bは式2から求める。式中のAB(1)、A
B(2)、AB(3)は、前記測定終了時間決定手段におい
て、記憶手段に記憶された一定の時間間隔(T)ごとの
前記反射光または透過光の強度を吸光度から、一定時間
間隔後(m、ここでm=1,2,3,・・・(整数)であ
る)の吸光度(ab(m))とその一つ前の間隔(m−
1)の吸光度(ab(m−1))の変化率(V(m)=(a
b(m)−ab(m−1))/T)およびさらにその変化率
差(A(l)=(V(l)−V(l−1))/T、ここでl=
m+1である)を求め、A(l)−A(l−1)<0となる
時をAB(1)として、前記AB(1)が決定した以降にさ
らにA(l)−A(l−1)>0かつA(l)*A(l−2)>
5となる時をAB(2)(=ab(l1))として、ab
(l2+(l2−l1))となる時を測定終了時間AB
(3)として求める。M=l2−l1とする。k,aは、
前記予測係数を求める手段において、bとab(0)から
AB(3)までの吸光度データを用い式1において重回帰
分析を行い求める。B is obtained from equation (2). AB (1) in the formula, A
B (2) and AB (3) are obtained by measuring the intensity of the reflected light or transmitted light at a certain time interval (T) stored in the storage means from the absorbance at a predetermined time interval in the measurement end time determining means. (M, where m = 1, 2, 3,... (Integer)) absorbance (ab (m)) and the immediately preceding interval (m−
The change rate (V (m) = (a) of the absorbance (ab (m-1)) of 1)
b (m) -ab (m-1)) / T) and its rate of change (A (l) = (V (l) -V (1-1)) / T, where l =
m + 1), and when A (l) -A (l-1) <0 is defined as AB (1), A (l) -A (l-) is determined after AB (1) is determined. 1)> 0 and A (l) * A (l-2)>
When the value is 5, AB (2) (= ab (11)) is defined as ab
The time when (l2 + (l2-l1)) is reached is the measurement end time AB
Calculate as (3). Let M = l2-l1. k and a are
In the means for calculating the prediction coefficient, multiple regression analysis is performed in Equation 1 using the absorbance data from b and ab (0) to AB (3).
【0018】(9)本発明は、前記予測演算手段が、ロ
ジスティック曲線を使用する上記(7)乃至(8)に記
載の血液成分測定方法である。(9) The present invention is the blood component measuring method according to any one of (7) to (8), wherein said prediction calculation means uses a logistic curve.
【0019】(10)本発明は、前記濃度演算手段が、
血液成分濃度の変化から実測された反射光または透過光
の強度の変化により描かれた検量線と、それを補正する
補正項を用いて血液成分濃度を求めるものである上記
(7)乃至(9)に記載の血液成分測定方法である。(10) In the present invention, the density calculation means includes:
The above (7) to (9) are obtained by using a calibration curve drawn by a change in intensity of reflected light or transmitted light actually measured from a change in blood component concentration and a correction term for correcting the calibration curve. )).
【0020】[0020]
【発明の実施の形態】[1]以下、添付図面を参照して
本発明の実施形態の一例を詳細に説明する。図1は、本
発明の一例である血液成分測定装置1の構成を示すブロ
ック図、図2は血液成分測定装置1の動作の一例を示す
フローチャートである。DESCRIPTION OF THE PREFERRED EMBODIMENTS [1] Hereinafter, an example of an embodiment of the present invention will be described in detail with reference to the accompanying drawings. FIG. 1 is a block diagram showing a configuration of a blood component measuring device 1 which is an example of the present invention, and FIG. 2 is a flowchart showing an example of an operation of the blood component measuring device 1.
【0021】血液成分測定装置1において、制御手段2
はマイクロコンピュータで構成されており血液成分検査
装置1の諸動作を制御する。この制御手段2には、測光
部10からの信号に基づいて測定目的の血液成分(例え
ばぶどう糖など)の血液中の濃度を算出する演算部が内
蔵されている。In the blood component measuring device 1, the control means 2
Is composed of a microcomputer and controls various operations of the blood component testing apparatus 1. The control means 2 has a built-in arithmetic unit for calculating the concentration of a blood component (eg, glucose) in the blood to be measured based on a signal from the photometric unit 10.
【0022】測光部10は、発光素子8と受光素子9と
を有しており、これらは一つのブロック内に収納保持さ
れている。発光素子8は制御手段2と電気的に接続さ
れ、受光素子9は増幅器11およびA/D変換器12を
介して制御手段2と電気的に接続されている。The photometric section 10 has a light emitting element 8 and a light receiving element 9, which are housed and held in one block. The light emitting element 8 is electrically connected to the control means 2, and the light receiving element 9 is electrically connected to the control means 2 via the amplifier 11 and the A / D converter 12.
【0023】発光素子8は制御手段2からの信号により
作動し、所定の時間間隔でパルス光を発する。このパル
ス光は、例えばその周期が0.5〜3.0msec程度、1パ
ルスの発光時間が0.05〜0.3msec程度とされる。ま
た制御手段2は発光素子8の発光周期を作動中に変える
こともできる。また、このパルス光の波長は好ましくは
500〜720nm程度、より好ましくは580〜650
nm程度とされる。The light emitting element 8 is activated by a signal from the control means 2 and emits pulse light at predetermined time intervals. The pulse light has, for example, a cycle of about 0.5 to 3.0 msec and a light emission time of one pulse of about 0.05 to 0.3 msec. Further, the control means 2 can change the light emission cycle of the light emitting element 8 during operation. The wavelength of the pulse light is preferably about 500 to 720 nm, more preferably 580 to 650 nm.
It is about nm.
【0024】試験紙を備えたチップを血液成分測定装置
1に装着した状態で、発光素子8を点灯させると、発光
素子8から発せられた光は試験紙に照射され、その反射
光は、受光素子9に受光され、光電変換される。受光素
子9からはその受光光量に応じたアナログ信号が出力さ
れ、増幅器11により所望に増幅された後、A/D変換
器12にてデジタル信号に変換され、制御手段2に入力
される。When the light emitting element 8 is turned on with the chip provided with the test paper attached to the blood component measuring device 1, light emitted from the light emitting element 8 is irradiated on the test paper, and the reflected light is received by the light receiving element. The light is received by the element 9 and photoelectrically converted. An analog signal corresponding to the amount of received light is output from the light receiving element 9, amplified as desired by the amplifier 11, converted to a digital signal by the A / D converter 12, and input to the control means 2.
【0025】また、血液成分測定装置1は、電源部4、
電源電圧検出部5、電源スイッチ6、スイッチ回路7、
制御発振部13、時計発振部14、データ記憶部15、
ブザー出力部16、外部出力部17、温度測定部18を
有している。The blood component measuring device 1 includes a power supply unit 4,
Power supply voltage detector 5, power switch 6, switch circuit 7,
A control oscillating unit 13, a clock oscillating unit 14, a data storage unit 15,
It has a buzzer output unit 16, an external output unit 17, and a temperature measurement unit 18.
【0026】電源部4には電池が装填される。電源電圧
検出部5には、この電池の電圧を検出し該検出値を制御
手段2へ出力する。これにより、電池の残量をチェック
することが出来る。The power supply unit 4 is loaded with a battery. The power supply voltage detection unit 5 detects the voltage of the battery and outputs the detected value to the control unit 2. Thereby, the remaining amount of the battery can be checked.
【0027】スイッチ回路7は、電源スイッチ6や、以
下に示す種々のスイッチの入力を検出し、その信号を制
御手段2へ入力する。スイッチの種類としては電源スイ
ッチ、6の他に、記憶データ読出スイッチ、時刻設定・
変更スイッチ、リセットスイッチ、ブザー作動/不作動
スイッチ、50Hz/60Hz商用電源周波数選択スイ
ッチ等が挙げられる。The switch circuit 7 detects the input of the power switch 6 and various switches described below, and inputs the signal to the control means 2. The types of switches include a power switch, a storage data read switch, a time setting /
There are a change switch, a reset switch, a buzzer operation / non-operation switch, a 50 Hz / 60 Hz commercial power frequency selection switch, and the like.
【0028】電源スイッチ6は、操作ボタンの押圧によ
り、入力状態/切断状態を切り替えることができる。ま
たは、例えばチップを血液成分検査装置1に取り付ける
時など、血液成分測定装置1の取り扱い手順のなかで自
動に電源が入力状態なる機構であってもよい。The power switch 6 can switch between an input state and a disconnected state by pressing an operation button. Alternatively, for example, when a chip is attached to the blood component analyzer 1, a mechanism in which power is automatically input in a handling procedure of the blood component analyzer 1 may be used.
【0029】制御発振部13はタイマーを構成するもの
で、一定時間間隔のクロックパルスを発振し、制御手段
2のマイクロコンピュータの動作用基準信号の供給を行
う。The control oscillating unit 13 constitutes a timer, oscillates clock pulses at regular time intervals, and supplies a reference signal for operation of the microcomputer of the control means 2.
【0030】時計発振部14は、絶対時間(日時)を特
定する時計を構成するもので、一定時間間隔のクロック
パルスを発振し、制御手段2が内蔵する時計制御回路の
動作用基準信号の供給を行う。The clock oscillating unit 14 constitutes a clock for specifying an absolute time (date and time), oscillates clock pulses at fixed time intervals, and supplies a reference signal for operation of a clock control circuit incorporated in the control unit 2. I do.
【0031】ブザー出力部16には制御手段2からの信
号に基づいてブザーを作動させ、音を発する。The buzzer output section 16 activates a buzzer based on a signal from the control means 2 and emits a sound.
【0032】外部出力部17は、求められた血糖値等の
データを例えばパソコンのような外部装置へ出力するた
めのものである。この場合、外部出力部17は、例えば
RS232Cのような通信ドライバーを内蔵している。
また、赤外線通信を行う場合には、外部出力部17は、
赤外線発光素子およびその駆動回路を内蔵している。The external output section 17 is for outputting data such as the obtained blood sugar level to an external device such as a personal computer. In this case, the external output unit 17 has a built-in communication driver such as RS232C.
When performing infrared communication, the external output unit 17
It has an infrared light emitting element and a driving circuit for the infrared light emitting element.
【0033】温度測定部18は環境温度を測定し得る温
度センサー(例えばサーミスタ)を備えている。温度測
定部18では随時温度測定がなされ、その温度情報はデ
ータ記憶部15に記憶される。データ記憶部15から読
み出された温度情報は制御手段2に入力され、血糖値の
演算に利用される。The temperature measuring section 18 includes a temperature sensor (for example, a thermistor) that can measure the environmental temperature. The temperature measurement unit 18 measures the temperature as needed, and the temperature information is stored in the data storage unit 15. The temperature information read from the data storage unit 15 is input to the control unit 2 and used for calculating a blood sugar level.
【0034】次に、図2のフローチャートに基づき、血
液成分測定装置1の動作例を説明する。試験紙を備えた
チップを血液成分測定装置1に取り付けた後、電源スイ
ッチ6を入力状態にする。この時、チップの取り付けは
電源を入力状態にした後に行っても良い。なお、電源ス
イッチ6は、チップを血液成分測定装置1に装着するこ
とにより、その手順の前後において自動に電源が入力状
態となる機構からなるものが望ましい。電源が入力され
た後、血液成分測定装置1が正常に動作していることが
確認されたら、測光部10を作動させて反射光量の測定
を行う。反射光量の測定は制御手段2から測定終了の判
断がなされるまで一定時間間隔で継続して行われる。こ
こで一定時間間隔とは1秒以内が望ましい。Next, an example of the operation of the blood component measuring device 1 will be described with reference to the flowchart of FIG. After attaching the chip provided with the test paper to the blood component measuring device 1, the power switch 6 is turned on. At this time, the chip may be attached after the power is turned on. It is desirable that the power switch 6 has a mechanism in which the power is automatically turned on before and after the procedure by mounting the chip on the blood component measuring device 1. After the power is input, if it is confirmed that the blood component measuring device 1 is operating normally, the photometric unit 10 is operated to measure the amount of reflected light. The measurement of the reflected light amount is continuously performed at regular time intervals until the control means 2 determines that the measurement has been completed. Here, the predetermined time interval is preferably within one second.
【0035】血液成分測定装置1の正常動作確認後、最
初に測定した反射光量を基準反射光量(R(0))として
データ記憶部15に記憶する。その後の一定時間間隔ご
とに測定した反射光量(R(n)、n=1,2,・・・で
ある)も随時、データ記憶部15に記憶する。After confirming the normal operation of the blood component measuring device 1, the first measured reflected light amount is stored in the data storage unit 15 as a reference reflected light amount (R (0)). The reflected light amount (R (n), n = 1, 2,...) Measured at regular time intervals thereafter is also stored in the data storage unit 15 as needed.
【0036】制御手段2は、測定開始後、式3に示す基
準反射光量と測定した反射光量との比(ab(n))(以
下、吸光度という)の計算を随時行っていき、その結果
をデータ記憶部15に記憶させる。After the start of the measurement, the control means 2 calculates a ratio (ab (n)) (hereinafter referred to as absorbance) between the reference reflected light amount and the measured reflected light amount shown in Expression 3 as needed, and calculates the result. The data is stored in the data storage unit 15.
【0037】[0037]
【数9】 (Equation 9)
【0038】式中、n=0,1,2,3,・・・である。In the equation, n = 0, 1, 2, 3,...
【0039】abと時間の関係をグラフに描くと、この
グラフは近似的に式1に示す関数で表される。ここで、
kおよびaは係数、eは指数、tは時間を表す。またb
は式2に表される。When the relationship between ab and time is drawn on a graph, this graph is approximately represented by the function shown in Equation 1. here,
k and a are coefficients, e is an index, and t is time. Also b
Is represented by Equation 2.
【0040】[0040]
【数10】 (Equation 10)
【0041】[0041]
【数11】 [Equation 11]
【0042】Mは後述するようにAB(1)、AB(2)
を選択した後に決定する。血液中の特定成分と試薬との
反応が平衡に達し、吸光度がある程度一定の値となるま
で至らなくても、反応途中の点までの吸光度データを用
いて式1を解くことで、吸光度と時間の関係を表す関数
を求めることができる。M is AB (1) and AB (2) as described later.
Is determined after selecting. Even if the reaction between the specific component in the blood and the reagent reaches equilibrium and the absorbance does not reach a certain value, solving equation 1 using the absorbance data up to the point in the middle of the reaction gives the absorbance and time. Can be obtained.
【0043】次に、式1の解法を説明する。始めに式1
中の係数b(式2で求める)を満たす3つのデータAB
(1)、AB(2)、AB(3)を選択する。式3に示すab
(n)の計算、記憶をするとともに式4に示す吸光度の変
化率(V(m))および式5に示すさらにその変化率(A
(l))の計算を行い、得られたV(m)およびA(l)をデ
ータ記憶部15に記憶する。Next, the solution of Equation 1 will be described. Equation 1
Three data AB satisfying the coefficient b (determined by equation 2)
(1), AB (2) and AB (3) are selected. Ab shown in equation 3
(n) is calculated and stored, and the rate of change in absorbance (V (m)) shown in equation 4 and the rate of change (A
(l)) is calculated, and the obtained V (m) and A (l) are stored in the data storage unit 15.
【0044】[0044]
【数12】 (Equation 12)
【0045】[0045]
【数13】 (Equation 13)
【0046】式中、Tは測定時間の間隔、m=1,2,
3,・・・、l=2,3,・・・を示す。In the equation, T is the interval of the measurement time, m = 1, 2,
.., 1 = 2, 3,.
【0047】ここで、A(l)−A(l−1)の計算を行い
最初にA(l)−A(l−1)<0となる時、式2におい
て、AB(1)=ab(l)(=ab(l1))とする。次に
AB(1)が決定した以降の測定データにおいて、A(l)
−A(l−1)>0かつA(l)*A(l−2)>5となる
時、AB(2)=ab(l)(=ab(l2))とする。最後
にAB(3)=ab(l2+(l2−l1))とする。また式
2中のMについて、M=l2−l1とする。AB(3)の
測定点を反射光量の測定終了点とし、反射光量の測定を
AB(3)まで行う。選択したAB(1)、AB(2)、AB
(3)からbを計算する。なお3点、AB(1)、AB
(2)、AB(3)の選択方法は上述した方法でなくとも良
いが、3点の選択方法が予測計算の精度に大きく関わっ
てくるため、試験紙、試薬の種類による、反射光の経時
変化の違いに応じて選択方法は随時変えていく。Here, when A (l) -A (l-1) is calculated and A (l) -A (l-1) <0 for the first time, AB (1) = ab in equation (2). (l) (= ab (l1)). Next, in the measurement data after AB (1) is determined, A (l)
When A (l-1)> 0 and A (l) * A (l-2)> 5, AB (2) = ab (l) (= ab (l2)). Finally, AB (3) = ab (l2 + (l2-l1)). Further, for M in Equation 2, M = 12−11. The measurement point of AB (3) is set as the measurement end point of the reflected light amount, and the measurement of the reflected light amount is performed up to AB (3). Selected AB (1), AB (2), AB
Calculate b from (3). 3 points, AB (1), AB
The selection method of (2) and AB (3) may not be the method described above, but since the selection method of three points greatly affects the accuracy of the prediction calculation, the time of reflected light depending on the type of test paper and reagent The selection method is changed at any time according to the change.
【0048】得られたbとab(0)からAB(3)までの
吸光度データを用いて式1において、重回帰分析を行い
k,aを求める。その結果、式1は時間のみの関数で表
すことができ、その結果、測定点AB(3)以降の任意の
時間(例えば反射光量が一定となるような時間)におけ
る吸光度の予測計算を行うことが出来る。なお上述の式
1に表される関数以外にも、試験紙、試薬の種類による
反射光比の経時変化、反応速度等の違いに応じて、適し
た関数を使用することも可能である。例えば式1のロジ
スティック曲線以外にジグモイド曲線等などが挙げられ
る。Using the obtained b and the absorbance data from ab (0) to AB (3), multiple regression analysis is performed in equation 1 to obtain k and a. As a result, Equation 1 can be expressed as a function of time alone, and as a result, the prediction calculation of the absorbance at an arbitrary time after the measurement point AB (3) (for example, a time at which the amount of reflected light is constant) is performed. Can be done. In addition to the function represented by the above-described formula 1, it is also possible to use an appropriate function in accordance with the change in the reflected light ratio with time, the reaction speed, and the like depending on the type of the test paper and the reagent. For example, a jigmoid curve or the like in addition to the logistic curve of Equation 1 is given.
【0049】またデータ記憶部15記憶されている予め
設定されている検量線と予測した吸光度から血糖値が求
まる。血糖値は表示手段3に表示される。ここで検量線
は予測計算を行う時間において設定を行えば良く、特に
反射光量、吸光度の値が一定となった時に限定するもの
ではない。The blood glucose level is obtained from the preset calibration curve stored in the data storage unit 15 and the predicted absorbance. The blood sugar level is displayed on the display means 3. Here, the calibration curve may be set at the time of performing the prediction calculation, and is not particularly limited to the case where the values of the reflected light amount and the absorbance become constant.
【0050】[2]上述した方法で求めた予測計算値
と、実測値との比較を行った。ある成人男性の血液をグ
ルコース溶液で調整を行い8種類の血糖値の血液試料を
用意した(ヘマトクリット値はすべて40%)。それぞ
れの血液について反射光量を測定(測定時間間隔は1
秒)した。各データに対して式2の計算に使用するAB
1、AB2、AB3と式1から求めた30秒後の吸光度
の予測計算結果を表1に示す。なお、表1中の血糖値
(mg/dl)は、Glucoroder−GXT(株式会
社シノテスト社製)で測定し、実測吸光度および予測計
算を行うための吸光度データはメディセーフ(テルモ株
式会社製)を使用して得られた反射光量データをA/D
変換器を介して取り出したものを用いた。[2] The predicted calculated value obtained by the above-described method was compared with the actually measured value. An adult male's blood was adjusted with a glucose solution to prepare eight types of blood glucose level blood samples (all hematocrit values were 40%). Measure the amount of reflected light for each blood (measurement time interval is 1
Seconds). AB used for calculation of Equation 2 for each data
Table 1 shows the results of the predicted calculation of the absorbance after 30 seconds obtained from 1, AB2, AB3 and Equation 1. In addition, the blood glucose level (mg / dl) in Table 1 was measured by Glucorder-GXT (manufactured by Shinotest Co., Ltd.), and the absorbance data for performing the measured absorbance and the prediction calculation was measured using Medisafe (manufactured by Terumo Corporation). The reflected light quantity data obtained by
The one taken out through the converter was used.
【0051】[0051]
【表1】 [Table 1]
【0052】吸光度の実測値と予測計算値を比較すると
その誤差は±3%以内に収まり、血糖値の高低に関わら
ず精度の高い予測計算が出来た。また測定時間は7〜1
3秒とより短時間で血糖値の測定ができた。When the measured value of the absorbance was compared with the predicted value, the error was within ± 3%, and a highly accurate predicted value could be calculated regardless of the blood sugar level. The measurement time is 7-1
The blood glucose level could be measured in a shorter time of 3 seconds.
【0053】[0053]
【発明の効果】以上、本発明の血液成分測定装置および
血液成分測定方法によれば、反射光量が平衡状態になる
前までの反射光量データを用いて、一定時間後(平衡状
態)の反射光量を予測することができるため、短時間で
高精度に、血液成分濃度を測定できる効果がある。As described above, according to the blood component measuring apparatus and the blood component measuring method of the present invention, the reflected light amount after a certain period of time (equilibrium state) is obtained by using the reflected light amount data before the reflected light amount reaches the equilibrium state. Therefore, the blood component concentration can be measured with high accuracy in a short time.
【図1】血液成分測定装置1の内部構成のブロック図で
ある。FIG. 1 is a block diagram of an internal configuration of a blood component measurement device 1.
【図2】血液成分測定装置1の動作の一例を示すフロー
チャートである。FIG. 2 is a flowchart illustrating an example of the operation of the blood component measurement device 1.
Claims (10)
を測定する血液成分測定装置において、 前記血液成分測定装置に着脱可能に設けられ、血液中の
特定成分と呈色反応する試薬を含む試験紙を備えたチッ
プと、 前記試験紙に光を照射する照射手段と、 前記照射手段から前記試験紙に照射された光の反射光ま
たは透過光の強度を検出する測定手段と、 前記血液成分測定装置に電源が入力されると、一定の時
間間隔ごとに、前記照射手段に光の照射および前記測定
手段に反射光または透過光の強度の検出を行わせる制御
手段と、 前記測定手段により検出した前記反射光または透過光の
強度を記憶する記憶手段と、 前記反射光または透過光の強度の経時変化から測定終了
時間を決定する測定終了時間決定手段と、 前記反射光または透過光の強度の経時変化から前記測定
終了時間決定手段により決定された測定終了時間後の反
射光または透過光の強度を予測するための予測係数を求
める手段と、 前記予測係数と前記反射光または透過光の強度の経時変
化から、前記測定終了時間決定手段により決定された測
定終了時間後の反射光または透過光の強度を予測する予
測演算手段と、 前記予測演算手段により予測された反射光または透過光
の強度から血液成分濃度を求める濃度演算手段とを有す
ることを特徴とする血液成分測定装置。1. A blood component measuring device for measuring a minute amount of blood collected by puncturing the skin, comprising: a reagent which is detachably provided to the blood component measuring device and which performs a color reaction with a specific component in blood. A chip provided with a test paper including: an irradiation unit for irradiating the test paper with light; a measurement unit for detecting an intensity of reflected light or transmitted light of light irradiated on the test paper from the irradiation unit; and the blood. When power is input to the component measuring device, at regular time intervals, control means for causing the irradiating means to perform light irradiation and the measuring means to detect the intensity of reflected light or transmitted light, and the measuring means Storage means for storing the detected intensity of the reflected light or transmitted light; measurement end time determining means for determining a measurement end time from a temporal change in the intensity of the reflected light or transmitted light; Means for obtaining a prediction coefficient for predicting the intensity of the reflected light or transmitted light after the measurement end time determined by the measurement end time determination means from the temporal change of the intensity; and the prediction coefficient and the reflected light or transmitted light. Prediction calculation means for predicting the intensity of the reflected light or transmitted light after the measurement end time determined by the measurement end time determination means from the temporal change of the intensity, and the reflected light or transmitted light predicted by the prediction calculation means A blood component measuring device comprising: a concentration calculating means for obtaining a blood component concentration from intensity.
記制御手段によって一定の時間間隔ごとに、前記照射手
段による前記試験紙への光の照射および前記測定手段に
よる前記試験紙からの反射光または透過光の強度の検出
を行いながら、採取した血液を前記試験紙に展開させ前
記試薬と呈色反応させて、 検出した前記反射光または透過光の強度を記憶手段に記
憶し、 記憶した前記反射光または透過光の強度の経時変化から
前記測定終了時間決定手段により測定終了時間を決定
し、 記憶した前記反射光または透過光の強度の経時変化から
前記予測係数を求める手段により、前記決定された測定
終了時間後の反射光または透過光の強度を予測するため
の予測係数を求めた後、 前記予測演算手段によって、前記予測係数と前記反射光
または透過光の強度の経時変化から、前記測定終了時間
決定手段により決定された測定終了時間後の反射光また
は透過光の強度を予測し、 前記濃度演算手段によって、前記予測演算手段により予
測された反射光または透過光の強度から血液成分の濃度
を測定する請求項1に記載の血液成分測定装置。2. A power supply of the blood component measuring device is inputted, and the control means irradiates the test paper with the light at regular time intervals and reflects the light from the test paper by the measurement means. While detecting the intensity of light or transmitted light, the collected blood is spread on the test paper and caused to undergo a color reaction with the reagent, and the detected intensity of the reflected light or transmitted light is stored in storage means. The measurement end time is determined by the measurement end time determining means from the temporal change in the intensity of the reflected light or the transmitted light, and the determination is performed by the means for obtaining the prediction coefficient from the stored temporal change in the intensity of the reflected light or the transmitted light. After obtaining a prediction coefficient for predicting the intensity of the reflected light or transmitted light after the measured measurement end time, the prediction operation means calculates the prediction coefficient and the reflected light or transmitted light. The intensity of reflected light or transmitted light after the measurement end time determined by the measurement end time determining means is predicted from the temporal change of the light intensity, and the reflected light predicted by the prediction calculation means by the density calculating means. The blood component measuring device according to claim 1, wherein the concentration of the blood component is measured from the intensity of the transmitted light.
して記憶手段に記憶し、前記決定された測定終了時間後
の反射光または透過光の強度として吸光度(ab(t))
を、予測演算手段において、下記式1によって求める請
求項1乃至2に記載の血液成分測定装置。 【数1】 【数2】 bは式2から求める。式中のAB(1)、AB(2)、AB
(3)は、前記測定終了時間決定手段において、記憶手段
に記憶された一定の時間間隔(T)ごとの前記反射光ま
たは透過光の強度を吸光度から、一定時間間隔後(m、
ここでm=1,2,3,・・・(整数)である)の吸光度
(ab(m))とその一つ前の間隔(m−1)の吸光度
(ab(m−1))の変化率(V(m)=(ab(m)−ab
(m−1))/T)およびさらにその変化率差(A(l)=
(V(l)−V(l−1))/T、ここでl=m+1であ
る)を求め、A(l)−A(l−1)<0となる時をAB
(1)として、前記AB(1)が決定した以降にさらにA
(l)−A(l−1)>0かつA(l)*A(l−2)>5とな
る時をAB(2)(=ab(l1))として、ab(l2+
(l2−l1))となる時を測定終了時間AB(3)として
求める。M=l2−l1とする。k,aは、前記予測係
数を求める手段において、bとab(0)からAB(3)ま
での吸光度データを用い式1において重回帰分析を行い
求める。3. The intensity of the reflected light or transmitted light is stored in a storage means as an absorbance, and the absorbance (ab (t)) is obtained as the intensity of the reflected light or transmitted light after the determined measurement end time.
The blood component measuring apparatus according to claim 1, wherein the following formula (1) is obtained by the predictive calculation means. (Equation 1) (Equation 2) b is obtained from Equation 2. AB (1), AB (2), AB
(3) In the measurement end time determining means, the intensity of the reflected light or the transmitted light at each fixed time interval (T) stored in the storage means is calculated from the absorbance after a predetermined time interval (m,
Here, m = 1, 2, 3,... (Integer)) and the absorbance (ab (m-1)) at the preceding interval (m-1). Change rate (V (m) = (ab (m) -ab
(m-1)) / T) and the difference in the rate of change (A (l) =
(V (l) -V (l-1)) / T, where l = m + 1) is obtained, and when A (l) -A (l-1) <0, AB
As (1), after AB (1) is determined, A
When (l) -A (l-1)> 0 and A (l) * A (l-2)> 5, AB (2) (= ab (l1)) is defined as ab (l2 +
The time when (l2-l1)) is obtained as the measurement end time AB (3). Let M = l2-l1. k and a are obtained by performing a multiple regression analysis in Equation 1 using the absorbance data from b and ab (0) to AB (3) in the means for obtaining the prediction coefficient.
および前記測定手段に反射光または透過光の強度の検出
を行わせる一定の時間間隔を検出中に可変できるもので
ある請求項1乃至3に記載の血液成分測定装置。4. The apparatus according to claim 1, wherein said control means is capable of changing a fixed time interval for causing said irradiation means to irradiate light and said measuring means to detect the intensity of reflected light or transmitted light during detection. 4. The blood component measurement device according to any one of items 1 to 3.
を使用するものである請求項1乃至4に記載の血液成分
測定装置。5. The blood component measuring device according to claim 1, wherein said predictive calculation means uses a logistic curve.
から実測された反射光または透過光の強度の変化により
描かれた検量線と、それを補正する補正項を用いて血液
成分濃度を求めるものである請求項1乃至5に記載の血
液成分測定装置。6. A method according to claim 1, wherein said concentration calculating means calculates a blood component concentration using a calibration curve drawn by a change in intensity of reflected light or transmitted light measured from a change in blood component concentration and a correction term for correcting the calibration curve. 6. The blood component measuring device according to claim 1, which is to be obtained.
を測定する方法であって、 血液中の特定成分と呈色反応する試薬を含む試験紙と、 前記試験紙に光を照射する照射手段と、 前記照射手段から前記試験紙に照射された光の反射光ま
たは透過光の強度を検出する測定手段と、 一定の時間間隔ごとに、前記照射手段に光の照射および
前記測定手段に反射光または透過光の強度の検出を行わ
せる制御手段と、 前記測定手段により検出した前記反射光または透過光の
強度を記憶する記憶手段と、 前記反射光または透過光の強度の経時変化から測定終了
時間を決定する測定終了時間決定手段と、 前記反射光または透過光の強度の経時変化から前記測定
終了時間決定手段により決定された測定終了時間後の反
射光または透過光の強度を予測するための予測係数を求
める手段と、 前記予測係数と前記反射光または透過光の強度の経時変
化から、前記測定終了時間決定手段により決定された測
定終了時間後の反射光または透過光の強度を予測する予
測演算手段と、 前記予測演算手段により予測された反射光または透過光
の強度から血液成分濃度を求める濃度演算手段とによ
り、 前記制御手段によって一定の時間間隔ごとに、前記照射
手段による前記試験紙への光の照射および前記測定手段
による前記試験紙からの反射光または透過光の強度の検
出を行いながら、採取した血液を前記試験紙に展開させ
前記試薬と呈色反応させて、 検出した前記反射光または透過光の強度を記憶手段に記
憶し、 記憶した前記反射光または透過光の強度の経時変化から
前記測定終了時間決定手段により測定終了時間を決定
し、 記憶した前記反射光または透過光の強度の経時変化から
前記予測係数を求める手段により、前記決定された測定
終了時間後の反射光または透過光の強度を予測するため
の予測係数を求めた後、 前記予測演算手段によって、前記予測係数と前記反射光
または透過光の強度の経時変化から、前記測定終了時間
決定手段により決定された測定終了時間後の反射光また
は透過光の強度を予測し、 前記濃度演算手段によって、前記予測演算手段により予
測された反射光または透過光の強度から血液成分の濃度
を測定する血液成分測定方法。7. A method for measuring a component of a trace amount of blood collected by puncturing skin, comprising: a test paper containing a reagent that undergoes a color reaction with a specific component in blood; and irradiating the test paper with light. Irradiating means, measuring means for detecting the intensity of reflected light or transmitted light of the light radiated on the test paper from the irradiating means, and irradiating the irradiating means with light and measuring the light at predetermined time intervals. Control means for detecting the intensity of the reflected light or transmitted light; storage means for storing the intensity of the reflected light or transmitted light detected by the measuring means; and measurement from the temporal change in the intensity of the reflected light or transmitted light A measurement end time determining means for determining an end time, and the intensity of the reflected light or the transmitted light after the measurement end time determined by the measurement end time determining means is predicted from the temporal change of the intensity of the reflected light or the transmitted light. Means for determining a prediction coefficient for predicting the intensity of the reflected light or transmitted light after the measurement end time determined by the measurement end time determination means from the temporal change of the prediction coefficient and the intensity of the reflected light or transmitted light. And a concentration calculating means for obtaining a blood component concentration from the intensity of the reflected light or transmitted light predicted by the predicting calculation means, wherein the control means controls the test by the irradiation means at regular time intervals. While irradiating the paper with light and detecting the intensity of the reflected light or transmitted light from the test paper by the measuring means, the collected blood was developed on the test paper and caused to undergo a color reaction with the reagent to detect the blood. The intensity of the reflected light or the transmitted light is stored in a storage unit, and the measurement end time determination unit determines the end of the measurement from the stored temporal change of the intensity of the reflected light or the transmitted light. A prediction coefficient for predicting the intensity of the reflected light or transmitted light after the determined measurement end time by means for determining a time and calculating the prediction coefficient from the stored temporal change of the intensity of the reflected light or transmitted light. Is calculated by the prediction calculation means, and the intensity of the reflected light or transmitted light after the measurement end time determined by the measurement end time determination means is determined from the change over time of the prediction coefficient and the intensity of the reflected light or transmitted light. A blood component measuring method for measuring the concentration of the blood component from the intensity of the reflected light or transmitted light predicted by the concentration calculating means.
して記憶手段に記憶し、前記決定された測定終了時間後
の反射光の強度を吸光度(ab(t))を、予測演算手段
において、下記式1によって求める請求項7に記載の血
液成分測定方法。 【数3】 【数4】 bは式2から求める。式中のAB(1)、AB(2)、AB
(3)は、前記測定終了時間決定手段において、記憶手段
に記憶された一定の時間間隔(T)ごとの前記反射光ま
たは透過光の強度を吸光度から、一定時間間隔後(m、
ここでm=1,2,3,・・・(整数)である)の吸光度
(ab(m))とその一つ前の間隔(m−1)の吸光度
(ab(m−1))の変化率(V(m)=(ab(m)−ab
(m−1))/T)およびさらにその変化率差(A(l)=
(V(l)−V(l−1))/T、ここでl=m+1であ
る)を求め、A(l)−A(l−1)<0となる時をAB
(1)として、前記AB(1)が決定した以降にさらにA
(l)−A(l−1)>0かつA(l)*A(l−2)>5とな
る時をAB(2)(=ab(l1))として、ab(l2+
(l2−l1))となる時を測定終了時間AB(3)として
求める。M=l2−l1とする。k,aは、前記予測係
数を求める手段において、bとab(0)からAB(3)ま
での吸光度データを用い式1において重回帰分析を行い
求める。8. The prediction calculation means stores the intensity of the reflected light or transmitted light in a storage means as an absorbance, and calculates the absorbance (ab (t)) of the reflected light intensity after the determined measurement end time. The blood component measurement method according to claim 7, wherein the blood component measurement method is obtained by the following equation (1). (Equation 3) (Equation 4) b is obtained from Equation 2. AB (1), AB (2), AB
(3) In the measurement end time determining means, the intensity of the reflected light or the transmitted light at each fixed time interval (T) stored in the storage means is calculated from the absorbance after a predetermined time interval (m,
Here, m = 1, 2, 3,... (Integer)) and the absorbance (ab (m-1)) at the preceding interval (m-1). Change rate (V (m) = (ab (m) -ab
(m-1)) / T) and the difference in the rate of change (A (l) =
(V (l) -V (l-1)) / T, where l = m + 1) is obtained, and when A (l) -A (l-1) <0, AB
As (1), after AB (1) is determined, A
When (l) -A (l-1)> 0 and A (l) * A (l-2)> 5, AB (2) (= ab (l1)) is defined as ab (l2 +
The time when (l2-l1)) is obtained as the measurement end time AB (3). Let M = l2-l1. k and a are obtained by performing a multiple regression analysis in Equation 1 using the absorbance data from b and ab (0) to AB (3) in the means for obtaining the prediction coefficient.
を使用する請求項7乃至8に記載の血液成分測定方法。9. The blood component measuring method according to claim 7, wherein said prediction calculation means uses a logistic curve.
化から実測された反射光または透過光の強度の変化によ
り描かれた検量線と、それを補正する補正項を用いて血
液成分濃度を求めるものである請求項7乃至9に記載の
血液成分測定方法。10. The concentration calculating means calculates a blood component concentration using a calibration curve drawn by a change in intensity of reflected light or transmitted light actually measured from a change in blood component concentration, and a correction term for correcting the calibration curve. The blood component measuring method according to claim 7, which is obtained.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11037882A JP2000235028A (en) | 1999-02-16 | 1999-02-16 | Blood component measuring device and blood component measuring method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11037882A JP2000235028A (en) | 1999-02-16 | 1999-02-16 | Blood component measuring device and blood component measuring method |
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| Publication Number | Publication Date |
|---|---|
| JP2000235028A true JP2000235028A (en) | 2000-08-29 |
Family
ID=12509922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11037882A Pending JP2000235028A (en) | 1999-02-16 | 1999-02-16 | Blood component measuring device and blood component measuring method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2000235028A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003098062A (en) * | 2001-09-21 | 2003-04-03 | Sefa Technology Kk | Sedimentation velocity measuring method and its device |
| JP2009524832A (en) * | 2006-01-24 | 2009-07-02 | ライフ テクノロジーズ コーポレーション | Device and method for quantifying analytes |
| CN101587117A (en) * | 2008-05-20 | 2009-11-25 | 瑞鼎科技股份有限公司 | Continuous detection device and continuous detection system |
| JP2011174865A (en) * | 2010-02-25 | 2011-09-08 | Fujifilm Corp | Device and method for measuring coloration |
| WO2023002581A1 (en) * | 2021-07-20 | 2023-01-26 | 株式会社日立ハイテク | Analysis method and analysis device |
| WO2024176658A1 (en) * | 2023-02-22 | 2024-08-29 | テルモ株式会社 | Component measurement device, component measurement device set, and component measurement method |
-
1999
- 1999-02-16 JP JP11037882A patent/JP2000235028A/en active Pending
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003098062A (en) * | 2001-09-21 | 2003-04-03 | Sefa Technology Kk | Sedimentation velocity measuring method and its device |
| JP2009524832A (en) * | 2006-01-24 | 2009-07-02 | ライフ テクノロジーズ コーポレーション | Device and method for quantifying analytes |
| CN101587117A (en) * | 2008-05-20 | 2009-11-25 | 瑞鼎科技股份有限公司 | Continuous detection device and continuous detection system |
| CN101587117B (en) * | 2008-05-20 | 2013-08-14 | 瑞鼎科技股份有限公司 | Continuous detection device and continuous detection system |
| JP2011174865A (en) * | 2010-02-25 | 2011-09-08 | Fujifilm Corp | Device and method for measuring coloration |
| WO2023002581A1 (en) * | 2021-07-20 | 2023-01-26 | 株式会社日立ハイテク | Analysis method and analysis device |
| JPWO2023002581A1 (en) * | 2021-07-20 | 2023-01-26 | ||
| JP7712365B2 (en) | 2021-07-20 | 2025-07-23 | 株式会社日立ハイテク | Analysis method and analysis device |
| WO2024176658A1 (en) * | 2023-02-22 | 2024-08-29 | テルモ株式会社 | Component measurement device, component measurement device set, and component measurement method |
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