CA2065890C - Quantitative analysis method and its system using a disposable sensor - Google Patents

Quantitative analysis method and its system using a disposable sensor

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Publication number
CA2065890C
CA2065890C CA002065890A CA2065890A CA2065890C CA 2065890 C CA2065890 C CA 2065890C CA 002065890 A CA002065890 A CA 002065890A CA 2065890 A CA2065890 A CA 2065890A CA 2065890 C CA2065890 C CA 2065890C
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Canada
Prior art keywords
chip
sensor
quantitative analysis
voltage
analysis system
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
CA002065890A
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French (fr)
Other versions
CA2065890A1 (en
Inventor
Shiro Nankai
Mariko Kawaguri
Toshihiko Yoshioka
Haruhiro Tsutsumi
Kyozo Terao
Naoki Tanimoto
Masahiro Yoshioka
Hiroshi Hyodo
Takatoshi Uchigaki
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.)
Arkray Inc
Panasonic Holdings Corp
Original Assignee
Kyoto Daiichi Kagaku KK
Matsushita Electric Industrial Co Ltd
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27426909&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CA2065890(C) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to JP3173737A priority Critical patent/JPH0820412B2/en
Priority to EP94115175A priority patent/EP0636880B1/en
Priority to US07/733,130 priority patent/US5266179A/en
Priority to EP91112100A priority patent/EP0471986B1/en
Application filed by Kyoto Daiichi Kagaku KK, Matsushita Electric Industrial Co Ltd filed Critical Kyoto Daiichi Kagaku KK
Priority to CA002065890A priority patent/CA2065890C/en
Publication of CA2065890A1 publication Critical patent/CA2065890A1/en
Application granted granted Critical
Publication of CA2065890C publication Critical patent/CA2065890C/en
Anticipated expiration legal-status Critical
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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
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/4875Details of handling test elements, e.g. dispensing or storage, not specific to a particular test method
    • G01N33/48771Coding of information, e.g. calibration data, lot number
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N35/00Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
    • G01N35/00584Control arrangements for automatic analysers
    • G01N35/00722Communications; Identification
    • G01N2035/00891Displaying information to the operator
    • G01N2035/009Displaying information to the operator alarms, e.g. audible

Abstract

In a quantitative analyzer for a biological fluid, e.g. a blood glucose level analysis, a sensor is inserted into a connector. A constant voltage required to obtain a response current is applied across the connector from a source 15 at required timings. The response current of the sensor is converted into a voltage by a current-to-voltage converter, and the value thereof is determined by a microcomputer.
The analysis results are displayed on a display unit. The system provides more reliable results than prior systems.

Description

1- 2065~90 OUANTITATIVE ANALYSIS METHOD AND ITS SYSTEM USING A DISPOSABLE
SENSOR
The present invention relates to a quantitative analyzer and method for measuring such quantities as the glucose level of a biological fluid, particularly a body fluid.
Various biosensors utilizing a specific catalytic action possessed by enzymes have recently been developed and applied, in particular, to the clinical field. Development of biosensors having an ability to provide rapid and yet precise analytical results has long been desired in view of the increasing number of samples and the increasing number of items to be tested.
Diabetes mellitus is a disease from which the patient cannot be completely cured. However, the patient can live a normal life by keeping the concentration of glucose in the blood at a normal level. Accordingly, constant retention of the normal glucose level is essential as a treatment for diabetes mellitus. The retention of the normal glucose level can be easily carried out on inpatients under physician's observation.
However, outpatients must conduct self-management in order to keep their blood glucose at a constant normal level.
Such self-management includes dietary therapy, ergotherapy, and drug therapy, and the patients usually conduct the self-management on the above-noted two or more items under a physician's directions. It is known that if patients can check by themselves if their blood glucose level is within the normal range or not, self-management is more effective.
In the treatment of insulin-dependent diabetes mellitus 3 0 ( IDDM), the normal blood glucose level is maintained by repeated insulin injections effected by the patients them-selves. However, the blood glucose level varies rapidly and considerably, depending on the caloric intake, dietary time, and injection time, and, therefore, it is essential that the patients be able to conduct the measurement of the glucose level by themselves.
Under such circumstances, various portable measurement ~ 2 - 2065890 systems have long been commercially available, that enable diabetic patients to conduct the glucose level measurement by themselves. This level is generally determined using a conventional measurement system in the following manner:
whole blood which has been taken from a fingertip or ear lobe using a needle is caused to contact a test paper containing an enzyme that specifically reacts with glucose and a color-producing reagent that develops a color based on the oxidation-reduction reaction. In this way, the reagent and blood glucose react together and produce color, the density of which is measured using an exclusive mini-reflectometer analyzer attached to the system. The blood glucose level is determined on the basis of a calibration curve previously prepared and memorized in the analyzer.
However, it has been found that the blood glucose levels determined according to this system vary greatly depending on the patients' manipulation of the measurement. Accordingly, Diabetes Associations in many countries have counselled improvement of the measurement systems. The most important factor causing the above-noted variation of test results is associated with the manipulation needed for removing excess blood from the test paper after a predetermined time. The removal of excess blood is usually conducted by wiping with absorbent cotton, removing with a filter paper or rinsing with water, and such procedures bring about test errors in the following manner.
(i) Blood remaining on the test paper due to incomplete removal gives a greater value than the real one.
(ii) Excessive wiping or rinsing damages the test paper or washes out the colored reagent, which gives a smaller value than the real one.
(iii) Inadequate manipulation, resulting in shortage of reaction time causes insufficient coloration of the reagent, and mistimed manipulation makes it impossible to completely remove the blood because of clotting or drying, whereby erroneous test results are obtained.
Moreover, when blood contacts the test paper, the command ` ~ ~ 3 ~ 2065890 (key input) of the timing for starting the measurement should be effected within a tolerance of only +2 to 3 seconds. In actual cases (of some patients), however, this mistiming may be 30 seconds to one minute, which can be another factor causing variation of test results and less reliability of the measured values.
In the last few years there has been commercially available a new measurement system (manufactured by Medisense Inc., trade name: Exactech) which has solved a main part of the above problems. This system is a pen type system that displays the measured results 30 seconds after the start switch has been pressed the moment blood is fed onto its test electrode chip. This system has obviated the need for removing excess blood and other factors causing test errors.
Diabetics, in some cases, have poor blood circulation, and are therefore susceptible to infectious diseases. This means that a slight wound on their hands or feet may cause suppuration, thus demanding that the diabetics keep themselves clean. Accordingly, the equipment and a sensor for collecting blood in the measurement of blood glucose level are preferably provided in a disposable form for reasons of hygienic control, rather than be used a plurality of times after having been sterilized and stored. This will ensure safety in hygiene and alleviate the patients' burden.
As a method that allows a sensor to be disposable, a biosensor that has already been proposed is disclosed in the Japanese Patent Laid Open 61-294351.
To enable this prior art to be described with the aid of a diagram, the figures of the drawings will first be listed.
Fig. 1 is an exploded perspective view showing an example of the sensor of a conventional measurement system;
Fig. 2 is a perspective view of an embodiment of a measurement system according to the present invention;
Fig. 3 is a perspective view of a sensor used in the measurement system in Fig. 2;
Fig. 4 is a block diagram showing an embodiment of a control unit used in the measurement system in Fig. 2;

_ _ 4 _ 2065~90 Fig. 5 is a block diagram showing another embodiment of a control unit used in the measurement system in Fig. 2;
Fig. 6 is an exploded perspective view showing another example of a sensor used in the measurement system in Fig. 2;
Fig. 7 is an exploded perspective view showing a further example of a sensor used in a measurement system of the present invention;
Fig. 8 is a perspective view in which the sensor of Fig. 7 is assembled; and Fig. 9 is a block diagram of a control unit used in combination with the sensor in Fig. 7.
The biosensor referred to in the above-mentioned Japanese application and shown in Fig. 1, is so constructed that electrode systems 136(136'), 137(137'), and 138(138') made of carbon or the like are formed on an insulating substrate 135 by a method of screen printing or the like. An insulating layer 139 is provided on the substrate and the electrode systems are covered with a porous body 141 carrying oxido-reductase and electron acceptors, and all these parts are integrated with a retaining frame 140 and a cover 142. When a sample liquid is dropped onto the porous body, the oxido-reductase and electron acceptors carried by the porous body are dissolved in the sample liquid, causing a reaction to proceed between the enzyme and the substrate in the liquid and the electron acceptors to be reduced. After completion of the reaction, the reduced electron acceptors are electrochemically oxidized, and the resulting value of the oxidation current is used to determine the concentration in the sample liquid.
However, in the Exactech, it is necessary to press a measurement start switch, which risks mistiming of the measurement. Moreover, its analyzer, being of the pen type, has its switch formed in one. As a result, since the calibration and adjustment of the analyzer must be carried out using this switch, the key operation involved has been made complex. Also, since the blood is placed on the test electrode chips tipped by the pin and the measurement is conducted without wiping the blood off, the patient is `~ - 5 - 2065890 required to keep holding the analyzer during the measurement so that the blood will not spill out. The system has therefore been inconvenient for use by patients.
As described heretofore, since the self-management measurement system of blood glucose level conventionally available requires patients to start the measurement themselves, it has been accompanied by the defect that the correctness of the test results depends on the patients' manipulation. Moreover, a complex key operation has been involved in achieving calibration and testing of the analyzer.
Conventional disposable systems, on the other hand, have had the problems that the test results may vary or that patients are required to determine whether a sensor has already been used or not.
An object of the present invention is to provide a measurement system that is capable of minimizing variations in the test results.
To these ends, the invention in one aspect provides a quantitative analysis system for measuring a specific component in biological body fluid by an amperometric method, comprising: a disposable sensor mounting portion, including a disposable sensor for receiving a sample of the biological body fluid for analysis; and means for automatically determining whether a chip mounted on said disposable sensor mounting portion is a sensor for measuring the sample, or an adjustment chip, depending on a measured current value flowing through said system when said chip is mounted on said disposable sensor mounting portion.
In another aspect, the invention provides a quantitative analysis system for measuring a specific component in biological body fluid by an amperometric method, comprising:
a disposable sensor for receiving a sample of the biological body fluid for analysis; and means for automatically distinguishing whether the disposable sensor is used depending on a stability of a measured current value of said disposable sensor.

-- - 5a - 206~90 In a further aspect, the invention consists of a quantitative analysis system comprising: means for applying a reaction voltage to a sensor; means for detecting that a sample liquid is supplied to said sensor; means for interrupting the reaction voltage based on said detection;
means for reapplying said reaction voltage to said sensor after a specified time period; means for detecting a reaction state of said sensor due to reapplication of said reaction voltage; and means for displaying the reaction state.
In yet another aspect, the invention provides a quantitative analysis system comprising: disposable sensor means, including a capillary shaped portion and an enzyme portion, for receiving a sample liquid for analysis; control means, including a connector for said disposable sensor means, for allowing enzymes in said enzyme portion and the sample liquid to react in an absence of a reaction voltage, for automatically applying the reaction voltage to the reaction after a specified time period, and for measuring an oxidation current indicative of a concentration of a constituent part of the sample liquid; and calibrating and testing means for calibrating and testing said system without key operation.
The preferred system of the present invention is used as a set with an exclusive sensor. The exclusive sensor is a disposable electrode using the amperometric method, while the system is an amperometric analyzer that displays the - - 6 - 20658~0 calculated concentration of glucose using a calibration curve from a measured current value.
When using this system, with the sensor fitted into a sensor holder of the analyzer, the value of the resistance at the electrode is infinity when no blood is applied.
Accordingly, the analyzer knows that the sensor has been fitted into the holder, awaiting blood.
When blood is applied, the resistance value abruptly drops. The sensor detects this lowering of the resistance, and determines that blood has been supplied, causing the timer of the analyzer to start. After a specified time, a constant voltage is applied to the sensor, and the resulting current is measured and converted into a glucose level using a previously set calibration curve, the converted result being displayed as a measured value.
For adjustment of the analyzer, if a resistive chip (adjustment chip) having a sensor-like shape with a constant resistance value is fitted into the holder of the analyzer, it shows a constant resistance value. Accordingly, the analyzer knows that it is not the sensor but an adjustment chip used for adjustment of the analyzer. Adjustment chips include an adjustment mode switching chip, an instrumental error compensating chip, a calibration chip, a test chip, and a unit switching chip.
Instrumental error compensation for the analyzer can be carried out in the following manner.
If the adjustment mode switching chip is fitted into the holder of the analyzer, the sensor initially shows a constant low resistance within a range assigned to the adjustment mode switching chip. From this fact, the analyzer determines that it is the instrumental error compensating chip, and switches the analyzer to the instrumental error compensation mode.
After adjustment of the applied voltage, one of two types of compensating chips having predetermined different resistance values (RLI RH) can be fitted into the holder of the analyzer, the resulting measured value (R1) being stored in the memory. Then, the other compensating chip is fitted into the ~ 7 ~ 2 0 6 5 8 9 0 holder and the resulting measured value (Rz) is stored in the memory; thereafter, a subsequently measured value Rn is compensated for as a resistance value R according to the following equation 1:
R = R L R + RLRZ-RHR1 ( 1 ) Rz-R1 R2 R1 For calibration of the analyzer, if the calibration chip is fitted into the holder of the analyzer, the sensor initially shows a constant resistance value within a range assigned to the calibration chip. From this fact, the analyzer knows that it is the calibration chip, judging the type of calibration curve from the resulting resistance value.
Whereas a plurality of types of calibration curves are stored in the analyzer, one type of calibration curve selected there-from by the calibration chip is set and this completes the calibration. Since the calibration curve differs depending on the production lot of the sensors, the sensors are supplied with calibration chips corresponding to each other.
For testing the analyzer, when a test chip is fitted into the holder of the analyzer, the sensor initially shows a constant resistance value within a range assigned to the test chip. From this fact, the analyzer knows that it is the test chip and displays the resistance value converted into a glucose level. The operator then can tell whether any abnormality exists in the analyzer. It may also be arranged that a normal range is previously stored in the analyzer so that the existence of any abnormality will be displayed.
When the unit switching chip is fitted into the holder of the analyzer, the sensor initially shows a constant resistance value within a range assigned to the unit switching chip.
From this fact, the analyzer knows that it is the unit switching chip, and sets the unit corresponding to this resistance value.
If a used sensor is fitted into the holder of the analyzer, the sensor initially shows a low resistance value because the sensor has been made wet by a blood sample.

- 8 - 2 0 ~5 890 value of current flowing through the sensor will vary with the resistance value gradually varying on account of polarization after the voltage is applied. Accordingly, the analyzer determines that it is a used sensor on the basis of the time S stability of the current value (resistance value), and displays this fact on its display unit.
The analyzer can automatically detect if the sensor has been fitted in the wrong position and interrupts the voltage source until corrected. This enables battery consumption to be minimized.
According to the present invention, since the reaction voltage is applied after the reaction has become stabilized, variation of test results is minimized.
Furthermore, under the condition of high humidity, some sensors (for example, if the porous body 141 seen in Fig. l is made of any hygroscopic material) can be made wet due to humidification even though unused. The sensor then initially shows a low resistance value, which further gradually varies on account of polarization after the voltage is applied. Due to this, the sensor may be erroneously determined to be a used sensor. To prevent this, the above-noted disposable sensor is further provided with an electrode for detection of a liquid junction, so that the sensor will show a low resistance value when fitted into the sensor holder of the analyzer. The circuit checks whether or not any liquid junction exists when the resistance value gradually varies. If a liquid junction exists, it indicates that a used sensor has been fitted, while if not, an unused sensor has been fitted, such sensor awaiting blood for measurement.
An electrode for detection of a liquid junction can also be used in the above-mentioned adjustment chip or test chip.
A first embodiment of the present invention will now be described with reference to Figs. 2 to 6. Fig. 2 shows an example of a sensor to be used in combination with the system of the present invention.
The primary constituents contained in the reagent layer of the sensor are oxidoreductase which is specific for an - 9 - 2 0 6 ~ 89 (3 objective substance in biological body fluid and a redox compound that makes an electron carrier of the enzyme.
As an example, the reaction measurement principle is described below in the case of measuring a glucose level.
Glucose oxidase (hereinafter referred to as GOD) is used as an oxidase, and potassium ferrocyanide is used as a mediator. When a test sample containing glucose is provided and contacts the sensor, an enzyme reaction occurs between the mediator and the glucose in the presence of GOD, as shown in reaction 2, whereby potassium ferrocyanide is produced in an amount corresponding to the glucose level. Then, after elapse of a specified time, a constant voltage is applied across leads 8a, 8b (Fig. 3) of the sensor. Since the oxidation current obtained is proportional to the concentration of potassium ferrocyanide produced by the enzyme reaction, i.e. the glucose level, the glucose level in the subject body can be determined by measuring the response current.
D - Glucose + 2Fe(CN)63 + H20 GOD
Gluconic acid + 2H+ + 2Fe(CN) 64-2Fe(CN)64~ ~ 2Fe(CN)63~ + 2e~ (2) Constant voltage Fig. 4 shows a preferred embodiment of the present inven-tion. A sensor 13 is inserted into a connector 14. When this insertion of the sensor 13 is detected by a switch 20, a switch 21 is closed so that the constant voltage required to obtain a response current is applied across the terminals of the connector 14 from a battery 15 serving as a voltage source. The response current of the sensor 13 inserted into the connector 14 is converted into a voltage by a current-to-voltage converter 16, and further inputted into an A/D
converter 17.
A microcomputer 18 receives and reads an output signal from the A/D converter 17 and calculates the glucose concentration. The sensor 13, enzyme electrode as it is, can be considered to be a type of resistor. For example, if the - 10 - 206~i890 resistance value of the sensor 13 is Rs, the amplification resistance of the current-to-voltage converter 16 is Rf, and the applied voltage is E, then the output voltage Eo of the current-to-voltage converter 16 can be determined by the following calculation:
Eo = E + i x Rf = E + (E/Rs) x Rf Without a sample applied, since the resistance value Rs of the sensor 13 is extremely high and nearly infinity, the resulting current value i is accordingly extremely low, so that the output voltage Eo of the current-to-voltage converter 16 becomes nearly equal to E (Eo E).
On the other hand, with a sample applied to the sensor 13, since the resistance value Rs of the sensor 13 is abruptly lowered, the value of Eo is abruptly increased, so that the result can be detected by continuously monitoring the output voltage Eo~
As a result, the measuring timer is automatically started by discerning this variation of the output voltage Eo of the converter 16 by the computer 18. With this operation, the switch 21 is simultaneously opened and, after elapse of a specified time, closed, thereby allowing the measured result to be obtained.
In order to adjust the analyzer, there is used an adjustment chip 22 having a shape similar to that of the sensor 13 and having a very small constant resistance value that is not to be compared with that of a new sensor (equal to infinity). Since the adjustment chip 22 initially shows a stable, constant measured voltage, the computer 18 can identify the adjustment chip 22, which can be of various types, from the amount of the voltage.
Adjustment chips 22 include ones that can be used for adjustment mode switching, instrumental error compensating, calibration, testing, unit switching, and the like. When the chip is determined to be an adjustment mode switching chip, the analyzer is switched into the adjustment mode, the resistance value of the instrumental error compensating chip is stored, and the measured values obtained thereafter are - 11 - 2065~90 compensated accordingly. Normally, the adjustment mode switching chip is used when the analyzer is manufactured or repaired. For example, if the chip is seen to be a calib-ration chip, the computer 18 automatically identifies and selects a calibration curve depending on the resistance value (voltage value) from a plurality of calibration curves previously stored in the analyzer.
If the chip is seen to be a test chip, the computer 18 converts the voltage value into a concentration and displays the result on a display 2, allowing it to be judged from the displayed amount whether any abnormality in the equipment exists or not.
If the chip is seen to be a unit switching chip, the computer 18 changes and converts the concentration value into respective concentration units (for instance, mg/dl or mmol/L), then displays it.
Table 1 shows the case of using calibration chips.

No. of calibration Resistance No. of calibration chip value (KQ) curve Also, the number of terminals of the connector can be increased as shown in Fig. 5, so that a calibration chip or a test chip can be inserted into a terminal other than that into which the sensor 13 is inserted.
However, it is possible that, if the identification of calibration chips and test chips is carried out based merely on the amount of the resistance value, the chip may be misinterpreted as a calibration chip or a test chip if a used sensor is inserted. This is due to the fact that the resistance value of a used sensor is so low that it may be of the same level as a calibration or test chip.
To prevent this misidentification, the following method is adopted: Voltage value Eo1 is measured at the time when the power supply is turned ON with any electrode inserted into a connector of the system, and the voltage value Eo2 is measured again after several seconds. The resulting rate of voltage change ~E is calculated, and, if it shows a change in voltage above a specified level, the chip is determined to be a used sensor, which fact is displayed on the display unit. Other-wise, the chip is determined to be a calibration chip or a test chip.
¦ E -E 2 If the sensor, even though unused, has a property showing a behaviour similar to that of a used sensor due to humidific-ation under a high humidity condition, electrodes 9a, 9b for detection of a liquid junction are provided in the sensor, as shown in Fig. 6. If, when using this sensor having electrodes for detection of a liquid junction and the circuit shown in Fig. 5, it is found that the resistance between the electrodes 9a and 9b is infinity, there is no liquid junction, so that it can be concluded that the inserted sensor is an unused one.
On the other hand, if the resistance between the electrodes 9a, 9b is low, the sensor is a used one. The A/D converter 17 is used for turning ON and OFF the switches 21, 21' through the computer 18.
Fig. 7 is a detailed exploded perspective view of the sensor of the measurement system, which is a second embodiment of the present invention, and Fig. 8 is an outline perspective view of the same.
On a substrate plate 31 there are a counter electrode 34 and a measuring electrode 35, with leads 33, 32 connected thereto, and an insulating layer 36. Also, although not shown, there is a reaction layer containing an enzyme and a mediator formed to cover the counter electrode and measuring ~ 13 - 2065890 electrode. On the substrate plate 31 there is a fixed cover 39 with a spacer 37 interposed therebetween. Numeral 38 denotes a sample supply hole, through which a sample liquid is introduced onto the counter electrode 34 and the measuring electrode 35 by capillary action. Reference numeral 40 denotes an air hole. In order not to mistake the front and back of the sensor, there is an inverse-insertion preventing protrusion 41 extending from one side of the sensor. Only when the sensor is correctly oriented the protrusion 41 passes through a gap of a connector 51 (Fig. 9).
Fig. 9 is a block diagram of a control unit embodying the invention. Initially the whole system is put in a standby state by starting up a CPU 50.
When the sensor 30 is inserted into the connector 51 of the system, a circuit 52 detects the insertion of the sensor, turning on a current-to-voltage converter 53, and A/D
converter 54, a temperature sensor 55, and other components through the CPU 50.
Next, when a sample liquid is supplied to the sensor to interconnect the measuring electrode 35 and the counter electrode 34, the initial resistance will vary to a large extent. This variation is distinguished by the CPU 50 through the A/D converter 54, turning off the current-to-voltage converter 53, with the result that no reaction voltage is supplied. The reaction between the enzyme and sample liquid is then allowed to proceed for approximately 55 seconds.
During this period, a countdown is displayed on an LCD display 56. Thereafter, a reaction voltage is applied for approxi-mately 5 seconds, and the current is measured. This measured value is also displayed on the display 56.
The voltage of a battery 57 is checked by the CPU 50 through a battery checker 58 for each sequence of the measurement, so that the voltage, if lower than a specified level, will be displayed on the display 56. A buzzer indicated by numeral 59 notifies that the sensor 30 has been inserted. An oscillator 60 generates pulses for clocking the operation of the system.

- - 14 - 2065~9~
A memory 61 for storing compensation values for each system serves to compensate for variations among systems.
Numeral 62 denotes a voltage regulator circuit. A circuit 63 serves to set a reaction voltage to be applied to the sensor.
A circuit 64 serves to reset the CPU when, for example, a measurement in progress has been stopped, or the battery changed. A circuit 65 is a gain control circuit.
Although in the above-described embodiments the measurement system is normally in the standby state so that actions such as applying the reaction voltage are not started until the sensor is inserted into the system, thereby mini-mizing the number of parts of the system, the present invention is not limited to such an arrangement and includes a system in which a standby switch is provided separately.
As described heretofore, the introduction of samples can be automatically detected, and, further, stable measurement with less variation of the results can be realized.

Claims (22)

1. A quantitative analysis system for measuring a specific component in biological body fluid by an amperometric method, comprising:
a disposable sensor mounting portion, including a disposable sensor for receiving a sample of the biological body fluid for analysis; and means for automatically determining whether a chip mounted on said disposable sensor mounting portion is a sensor for measuring the sample, or an adjustment chip, depending on a measured current value flowing through said system when said chip is mounted on said disposable sensor mounting portion.
2. A quantitative analysis system for measuring a specific component in biological body fluid by an amperometric method, comprising:
a disposable sensor for receiving a sample of the biological body fluid for analysis; and means for automatically distinguishing whether the disposable sensor is used depending on a stability of a measured current value of said disposable sensor.
3. The quantitative analysis system of claim 2, wherein said disposable sensor including an electrode for detecting a liquid junction.
4. A quantitative analysis system comprising:
means for applying a reaction voltage to a sensor;
means for detecting that a sample liquid is supplied to said sensor;
means for interrupting the reaction voltage based on said detection;
means for reapplying said reaction voltage to said sensor after a specified time period;
means for detecting a reaction state of said sensor due to reapplication of said reaction voltage; and means for displaying the reaction state.
5. The quantitative analysis system of claim 4, said system further comprising means for detecting that said sensor has been mounted on the system, wherein said reaction voltage application means is initiated by said detection.
6. The quantitative analysis system of claim 4 or 5, wherein said reaction voltage application means includes a current-to-voltage converter, for generating a voltage depending on a current generated in said sensor as a result of the application voltage and said reaction state detection means includes a CPU and detects said reaction state based on an output of said current-to-voltage converter and converts said reaction state to a digital value.
7. A quantitative analysis system comprising:
disposable sensor means, including a capillary shaped portion and an enzyme portion, for receiving a sample liquid for analysis;
control means, including a connector for said disposable sensor means, for allowing enzymes in said enzyme portion and the sample liquid to react in an absence of a reaction voltage, for automatically applying the reaction voltage to the reaction after a specified time period, and for measuring an oxidation current indicative of a concentration of a constituent part of the sample liquid; and calibrating and testing means for calibrating and testing said system without key operation.
8. The quantitative analysis system of claim 7, wherein said system is portable.
9. The quantitative analysis system of claim 7, said calibrating and testing means including, means for automatically distinguishing whether said disposable sensor means has been placed in said connector with the sample liquid or without the sample liquid and for distinguishing whether an adjustment chip has been placed in said connector, depending on the measured current.
10. The quantitative analysis system of claim 9, wherein the adjustment chip is an adjustment mode switching chip, an instrumental error compensating chip, a calibration chip, a test chip, or a unit switching chip.
11. The quantitative analysis system of claim 10, wherein when the adjustment chip is the adjustment mode switching chip, which has a constant low resistance with a range assigned to the adjustment mode switching chip in order to adjust the reaction voltage.
12. The quantitative analysis system of claim 11, wherein two instrumental error compensating chips are sequentially inserted in said connector after the adjustment mode switching chip in order to compensate a resistance of said system.
13. The quantitative analysis system of claim 9, wherein the adjustment chip is the calibration chip and said system generates a constant resistance with a range assigned to the calibration chip in order to select an appropriate calibration curve.
14. The quantitative analysis system of claim 9, wherein the adjustment chip is the test chip and said system generates a constant resistance with a range assigned to the test chip in order to identify and abnormalities in said system.
15. The quantitative analysis system of claim 9, wherein the adjustment chip is the unit switching chip and said system generates a constant resistance with a range assigned to the unit switching chip in order to set a unit corresponding to the measured current.
16. The quantitative analysis system of claim 7, said disposable sensing means including a liquid junction detection electrode, said control means monitoring said liquid detection electrode in order to determine whether a liquid junction exists.
17. The quantitative analysis system of claim 10, said disposable sensing means including a mediator, and said mediator contacts blood glucose in the presence of glucose oxidase to produce potassium ferrocyanide, and after the predetermined time, the reaction voltage is applied to said disposable sensing means to produce the oxidation current which is proportional to the potassium ferrocyanide level and representative of the blood glucose level.
18. The quantitative analysis system of claim 10, wherein said enzyme portion acts as a resistor, said control means including, means for determining whether said disposable sensing means or said adjustment chip has been inserted in said connector, voltage means for applying the reaction voltage across said connector, and correcting means for converting the oxidation current into a voltage, said voltage represented by:

E0 = E + i x Rf = E + (E/Rs) x Rf where:
E0 = said voltage, E = the reaction voltage, Rf = an amplification resistance of said converting means, and Rs = a resistance value of said enzyme portion.
19. The quantitative analysis system of claim 18, said calibrating and testing means including means for automatically determining the type of adjustment chip according to said voltage.
20. The quantitative analysis system of claim 10, said control means including a second connector for receiving the adjustment chip.
21. The quantitative analysis system of claim 7, said disposable sensing means including, a substrate, including a counter electrode, a measuring electrode, and at least one lead, an insulating layer, a reaction layer, including an enzyme and a mediator which cover said counter electrode and said measuring electrode, a spacer, with longitudinal groove, a cover, with an air hole through which the sample liquid is placed on the reaction layer, and an inverse-inserting preventing protrusion for ensuring said disposable sensing means is correctly oriented in said connector.
22. The quantitative analysis system of claim 7, wherein said control means includes a standby switch for initiating the specified time period.
CA002065890A 1990-07-20 1992-04-13 Quantitative analysis method and its system using a disposable sensor Expired - Lifetime CA2065890C (en)

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JP3173737A JPH0820412B2 (en) 1990-07-20 1991-07-15 Quantitative analysis method and device using disposable sensor
EP94115175A EP0636880B1 (en) 1990-07-20 1991-07-19 Quantitative analyzing apparatus
US07/733,130 US5266179A (en) 1990-07-20 1991-07-19 Quantitative analysis method and its system using a disposable sensor
EP91112100A EP0471986B1 (en) 1990-07-20 1991-07-19 Quantitative analysis method and its system using a disposable sensor
CA002065890A CA2065890C (en) 1990-07-20 1992-04-13 Quantitative analysis method and its system using a disposable sensor

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