KR20200075512A - Non-invasive biometric measurement based calibration system and method using multiple sensors - Google Patents

Abstract

According to an embodiment of the present invention, provided is a non-invasive biometric information measurement based calibration system using multiple sensors. The non-invasive biometric information measurement based calibration system using multiple sensors comprises: transmission and reflection based multiple sensors; a biometric information measuring unit which measures biometric information in blood of a user based on a received voltage value measured from the multiple sensors; a calibration unit which calculates a calibration value for calibrating output voltages of the multiple sensors by comparing the measured biometric information with invasive data prepared in advance; and an output unit which increases or decreases the output voltages of the multiple sensors based on the calculated calibration value.

Description

Non-invasive biometric information-based correction system and method using multiple sensors{NON-INVASIVE BIOMETRIC MEASUREMENT BASED CALIBRATION SYSTEM AND METHOD USING MULTIPLE SENSORS}

The present invention relates to a non-invasive biometric information-based correction system and method using multiple sensors.

Recently, non-invasive technology is not only used by IT companies such as Apple, Google, and Samsung, but also medical leaders such as Medtronics, Dexcom, GE, and Philips, as well as companies such as GlucoTrack, KlucoWage, and CNOGA Medical. Research and development of invasive medical devices have been actively conducted.

In this regard, the light-based non-invasive field has been continuously researching a wide range of wavelengths, such as 580~900nm, 850~1380nm, since the early 2000s. And recently, the reliability has been increased by using a plurality of light sources having a wide wavelength band. However, since the complexity of post-processing is increased due to noise reduction between measured data, there is a need for a narrow-band-based multiple light source processing technology capable of minimizing noise.

On the other hand, different people have different skin thicknesses and characteristics, and there is a problem in that a lot of noise processing is generated due to the'fluctuation circle' through external light interference and the fracturing phenomenon of the measurement source. Research is being conducted to minimize noise using various complex sensor sources such as thermoelectric.

Recently, a method of overcoming this has been proposed and commercialized, focusing on ultrasound, thermoelectricity, and skin conductivity, and is being sold domestically. However, it requires frequent correction based on invasiveness, and the sensor has a consumable characteristic, which has a limitation to be universalized.

Particularly, in the case of the cheapest light source-based blood sugar measurement method, a method for overcoming the above limitation is insufficient.

The noise, which has the greatest influence on the measurement and analysis problems, is dependent on the thickness and characteristics of the skin, which vary from person to person. In the past, many studies using information measured by human fingers and ear balls have been conducted, but a separate study for correcting the aforementioned noises is very insufficient.

In order to correct skin characteristics such as the finger and ear of a person having 100 color characteristics of 100 people, a large amount of data is required, and one of the fastest methods is a method of verifying the deviation using a light source made of a recent MEMS LED Array. .

However, these MEMS LED Arrays have different specificities such as individual LED wavelength length, narrowband range, and lens characteristics for each manufacturer, and the photodiode of the receiver also has specificity according to the manufacturer. A calibration method through verification is required. In addition, there is a problem that the blood glucose level is not constantly measured according to the amount of other components in the blood.

According to an exemplary embodiment of the present invention, bioinformation in a user's blood is measured based on a voltage value measured from multiple sensors based on transmissive and reflective methods, and the output voltage of multiple sensors is based on a result of comparison with previously prepared non-invasive data. Provided is a non-invasive biometric information-based correction system and method capable of correcting a value.

However, the technical problem to be achieved by the present embodiment is not limited to the technical problem as described above, and other technical problems may exist.

As a technical means for achieving the above-described technical problem, a non-invasive biometric information-based correction system using multiple sensors according to the first aspect of the present invention includes transmission and reflection-based multiple sensors, and measurements received from the multiple sensors. A bio-information measurement unit that measures bio-information in a user's blood based on a voltage value, and a correction unit that compares the measured bio-information with previously prepared invasive data to calculate a correction value for correcting the output voltage of the multiple sensors And an output unit that increases or decreases the output voltage of the multiple sensors based on the calculated correction value.

The multi-sensor is disposed on the other side of the first light source array sensor, the first light source array sensor based on the transmissive type, the light source is arranged to penetrate the user's skin, and in the first light source array sensor A first photo array sensor that receives the light source that is output and transmitted through the skin, and is arranged to be spaced apart from the second light source array sensor and the second light source array sensor based on the reflective type, the light source being arranged to reflect the skin of the user And a second photo array sensor that receives a light source reflected from the skin and output from the second light source array sensor, wherein the output unit increases or decreases the output voltage of the first light source array sensor based on the correction value. It may include a first output unit and a second output unit for increasing or decreasing the output voltage of the second light source array sensor.

The bio-information measuring unit measures hemoglobin value in the blood with the bio-information based on the received voltage value respectively measured through the first and second photo array sensors, and converts the hemoglobin value in the blood into a glucose value based on the hemoglobin value. Can.

The bio-information measurement unit may measure the hemoglobin value with the bio-information by analyzing a difference in light variation due to absorption of electromagnetic waves of at least three wavelengths from the received voltage values from the first and second photo array sensors.

The bio-information measurement unit may measure the hemoglobin value by analyzing a fluorescence spectrum from the received voltage value.

The bio-information measurement unit may measure the hemoglobin value by analyzing the fluorescence spectrum based on the received power signal using Raman spectrum and via spectrum techniques.

The bio-information measurement unit may remove elements other than the hemoglobin value and the glucose value from among the bio-information that can be calculated from the measured received voltage value of hemoglobin that reacts according to light in plasma and blood cells that are variously composed in blood. have.

The correction unit may calculate a correction value of one or more output voltages of the first and second light source array sensors by comparing the previously prepared invasive data, hemoglobin value, glucose value, and the glucose value obtained by the bioinformation measurement unit. have.

The correction unit may calculate a correction value for correcting one or more optical wavelength timings of the first and second light source arrays in addition to the correction value of the output voltage based on the comparison result.

In addition, the method for locating non-invasive biometric information using multiple sensors according to the second aspect of the present invention includes measuring voltage-based biometric information through transmissive and reflective based light and photodiode based multiple sensors; Comparing the measured bio-information with previously prepared invasive data; And increasing or decreasing the output voltage of the multiple sensors based on the comparison result.

The step of measuring the voltage-based bio-information through the transmissive and reflective-based multi-sensors is received by the first photo array sensor as the light source in the transmissive-based first light source array sensor penetrates the user's skin. Being a step; Receiving light from a second photo array sensor as the light source from the reflection-based second light source array sensor is reflected from the user's skin; Measuring hemoglobin values in the blood with the bio-information based on the received voltage values respectively measured by the first and second photo array sensors; Controlling reaction factors other than the heloglobin value in the blood; Finally, it may include the step of converting to a glucose value based on the hemoglobin value.

The step of increasing or decreasing the output voltage of the multiple sensors based on the comparison result may include comparing the first and second hemoglobin values, glucose values, and glucose values converted based on the hemoglobin values, which are the invasive data prepared in advance. Calculating a correction value of one or more output voltages of the second light source array sensors; And increasing or decreasing the output voltage of one or more of the first and second light source array sensors based on the calculated correction value.

According to the above-described exemplary embodiment of the present invention, accurate light transmission, absorption, and transmittance can be expected by performing an output voltage correction process of multiple sensors in order to control the intensity of a light source optimized for the skin.

In addition, it is possible to minimize measurement errors that may occur when a single sensor is used by having multiple sensors based on a transmission type and a reflection type having multiple wavelengths.

1 is a view for explaining a relationship between a reflective light source and skin characteristics.
2 is a block diagram of a non-invasive biometric information-based correction system according to an embodiment of the present invention.
3 is a view for explaining multiple sensors.
4A is an exemplary view for explaining the absorption rate of the transmissive light source, and FIG. 4B is an exemplary view for explaining the reaction frequency by the reflective light source.
5 is a block diagram for explaining the correction unit and the output unit.
6 is a flow chart of a non-invasive biometric information positioning method according to an embodiment of the present invention.

Hereinafter, exemplary embodiments of the present invention will be described in detail with reference to the accompanying drawings so that those skilled in the art to which the present invention pertains may easily practice. However, the present invention can be implemented in many different forms and is not limited to the embodiments described herein. In addition, parts not related to the description are omitted in the drawings to clearly describe the present invention.

When a part of the specification "includes" a certain component, it means that other components may be further included instead of excluding other components unless specifically stated otherwise.

1 is a view for explaining a relationship between a reflective light source and skin characteristics.

When non-invasively measuring bioinformation using the light source P1, the refractive index of the subcutaneous tissue and the thickness in the epidermis have a great influence on the measurement result.

And in order to know the accurate light (P1) transmission and absorption rate, the intensity of the light source (P1) is transmitted through the epidermis to enable the analysis of capillaries and arterioles of the papillary dermis in the dermis. It is most important to control.

At this time, when using the light source (P1), it is possible to analyze the capillaries and small arteries of the papillary dermis from the dermis of the person through the reflex expression, the transmission rate of the small arteries can be confirmed through the transmission formula.

However, in the case of using the light source P1, the refractive index of the subcutaneous tissue and the thickness in the epidermis have a great influence on the measurement result. Therefore, in order to know the accurate light transmission and absorption, the tissue has transparency to overcome the noise of the epidermis. The intensity of the optimized light source P1, which does not affect, is important.

In particular, since the thickness of the epidermis and dermis is different for each person, it is necessary to additionally introduce a method for correcting this, and accurately verify the properties of the main component for the reaction of light (P1) in human blood.

An embodiment of the present invention is a non-invasive composite bio-information positioning technique using multiple light sources, a MOSFET-based voltage and current circuit in which a plurality of LEDs are connected with a feedback circuit of an LED light source array and a photodiode in consideration of the reflective and transmissive methods. Through this, it is possible to control the output voltage and provide a correction method of the LED light source array by adjusting the generation cycle through PWM.

On the other hand, an embodiment of the present invention is characterized in that it is possible to non-invasively measure glucose and hemoglobin for body parts such as fingers in contact with a certain instrument and correct the output voltage for the measurement.

Hereinafter, a non-invasive biometric information based correction system 100 according to an embodiment of the present invention will be described with reference to FIGS. 2 to 5.

2 is a block diagram of a non-invasive biometric information based correction system 100 according to an embodiment of the present invention. 3 is a diagram for explaining multiple sensors 110.

The non-invasive biometric information based correction system 100 according to an embodiment of the present invention includes a multi-sensor 110, a biometric information measurement unit 120, a correction unit 130, and an output unit 140.

The multi-sensor 110 is composed of a transmission-based sensor and a reflection-based sensor, specifically, the first and second light source array sensors 111 and 115, and the first and second photo array sensors 113 and 117 It may include.

Referring to FIG. 3, the first light source array sensor 111 is arranged such that the light source penetrates the user's skin on a transmissive basis.

In addition, the first photo array sensor 113 is disposed at regular intervals in a vertical direction on the other side facing the one surface of the first light source array sensor 111, and is output from the first light source array sensor 111 to accurately skin, The light source transmitted through the blood vessel is received.

The second light source array sensor 115 is disposed on a reflective basis so that the light source reflects the user's skin.

In addition, the second photo array sensor 117 is arranged to be spaced apart from the second light source array sensor 115 in a horizontal direction at regular intervals, and receives the light output from the second light source array sensor 115 and reflected from the skin, and precisely blood vessels. do.

Meanwhile, the first and second light source array sensors 111 and 115 may be composed of LED elements capable of generating three or more wavelengths in the range of 480 nm to 1380 nm, for example, IR, RED, GREEN, ORANGE, etc. It can be composed of LED elements.

Further, the first and second light source array sensors 111 and 115 may be provided with a configuration for condensing the generated light sources, for example, a predetermined optical system for focusing the light sources.

For example, the light source generated from the LED may be condensed in the light collecting part and incident on a certain part of the finger through the hole of the device in contact with the finger.

The incident light sources are scattered and reflected by blood components in the user's body part.

In addition, the transmitted or reflected light source is collected from the light receiving unit in the form of a predetermined optical system and transmitted to the first and second photo array sensors 113 and 117.

On the other hand, the photo array sensor is an individual light-receiving photo sensor that can measure 580nm, 640nm, 830nm, 880nm, 940nm, etc. that match individual narrow-band LED light sources. It is a group of receiving sensors composed of a number of subordinates.

At this time, the first and second photo array sensors 113 and 117 may receive light sources from the first and second light source array sensors 111 and 115 in a predetermined unit.

The first and second photo-array sensors 113 and 117 may be composed of three or more types of photo diodes to correspond to the first and second light source array sensors 111 and 115.

In addition, the first and second photo array sensors 113 and 117 may generate a fluorescence spectrum through a reaction of an electric signal for each light source by spectralizing the received light source, and using the predetermined sensing means It can sense and convert it into a constant electrical signal.

In addition, an analog type electrical signal can be converted into a digital signal, expressed as a voltage value having an accurate level value, and provided to a biological information measuring unit described below for each wavelength.

At this time, the first and second photo array sensors 113 and 117 may include or separately include a configuration for converting the corresponding analog value to a digital value.

The bio-information measurement unit 120 is configured to display bio-information in the user's blood based on the received voltage values measured from the first and second photo arrays 113 and 117, respectively, before and after pressure is applied to the user's body. Measure.

Specifically, in the case of the transmissive type, the bio-information measuring unit 120 is based on the received voltage value measured through the first photo array sensor 113 and the wavelength of the light reflection coefficient due to absorption of the light source at the user's first body part. By analyzing the degree of change, the hemoglobin value in the blood is measured by bioinformation.

Similarly, in the case of the reflection type, the light source is transmitted to and reflected from the user's second body part based on the received voltage value measured by the second photo array sensor 117 and analyzes the change in the amount of polarization of the light to obtain blood as biometric information. The hemoglobin value at is measured.

The hemoglobin values measured as described above may be averaged or converted to glucose values using weight analysis.

At this time, the bio-information measurement unit 120 analyzes the degree of reception according to the light source wavelength from the received voltage value by the transmitted or reflected light source through the fluorescence spectrum, and analyzes the intensity of the fluorescence spectrum, the Raman spectrum, and the via spectrum. Hemoglobin values in the blood can be measured.

4A is an exemplary view for explaining the absorption rate of the transmissive light source, and FIG. 4B is an exemplary diagram for explaining the reaction frequency by the reflective light source.

Typically, before pressure is applied to a body part, such as a finger, blood is filled in blood vessels at the bottom contacting the finger contact mechanism.

In addition to glucose and hemoglobin, water, red blood cells, white blood cells, electrolytes, and cholesterol are present in the blood.

When these blood components are under pressure, most of them are pushed to other places that are not under pressure, and blood components are minimized in blood vessels of the finger region under pressure.

At this time, when analyzing the measurement site by the reflection type and the transmission type, the value of the spectral current is determined by the Ramam characteristic in which the molecules of the fluorescence spectrum received by the light source array sensor are scattered by the light source due to the light source array sensor. It varies by wavelength.

In this way, a plurality of light sources between 480nm and 1380nm of the projected light source array sensor analyzes the scattering of the hemoglobin as the main component by the reaction frequency of light to the main component of the white blood cells in the blood vessel, and various components of the red blood cells are wavelengths in the light. During the reaction, the light-frequency component including the glucose component is scattered, so that the blood glucose level can be predicted through Raman analysis that appears at a specific wavelength.

In this process, the bio-information measurement unit 120 designates and removes the remaining elements excluding hemoglobin and glucose values from the bio-information that can be calculated from the measured received voltage value of red blood cells in the blood as a negative factor, thereby removing the hemoglobin value from the blood and Glucose values can be measured more accurately.

To this end, the bio-information measurement unit 120 accurately measures the hemoglobin value and glucose value by analyzing absorption and reflection differences of light wavelengths of at least three wavelengths from the received voltage values from the first and second photo array sensors 113 and 117 can do. For example, the wavelength of the electromagnetic waves used before and after the pressure is applied to the user's body part may be within 1380 nm, and the upper light source frequency band is excluded because it may affect the cellular tissue inside the human body.

In addition, the bio-information measurement unit 120 may predict blood glucose level by analyzing a Raman spectrum that is scattered about glucose and dissolved oxygen components in blood vessels in the fluorescence spectrum and largely displayed at a corresponding wavelength.

The correction unit calculates a correction value for correcting the output voltage of the multi-sensor 110 by comparing the bio-information measured by the bio-information measurement unit 120 with the invasive data D1 prepared in advance.

At this time, an embodiment of the present invention uses the multiple sensors 110 to measure the exact glucose value and hemoglobin value, and at the same time, based on the hemoglobin value and glucose value measured by invasion with the invasive data D1 prepared in advance. It can be used as a value.

The invasive data (D1) may be measured and input by a blood glucose meter, a glucose meter, etc. in advance, and an embodiment of the present invention may be prepared only once or only if necessary for the invasive data (D1) repeatedly It is different from the conventional invasive technology in that it is not required.

The compensator 130 compares the hemoglobin value, glucose value, and the hemoglobin value and glucose value obtained by the bioinformation measurement unit 120, which are pre-prepared invasive data D1, to the first light source array sensor 111 and A correction value for correcting one or more output voltages of the second light source array sensor 115 is calculated.

In addition, the correction unit 130 additionally calculates and outputs a correction value for correcting the timing of at least one of the first and second light source arrays 111 and 115 along with the correction value of the output voltage based on the comparison result. It can be provided to the unit 140.

The output unit 140 controls to increase or decrease the output voltage of the multiple sensors 110 based on the correction values calculated by the correction unit 130.

At this time, when the multiple sensors 110 are composed of the first and second light source array sensors 111 and 115 and the first and second photo array sensors 113 and 117, the output unit 140 is based on the correction value. It may be composed of a first output unit 141 to increase or decrease the output voltage of the first light source array sensor 111, and a second output unit 143 to increase or decrease the output voltage of the second light source array sensor 115. .

Subsequently, the first and second light source array sensors 111 and 115 are driven according to the corrected output voltage, and when measurement results are provided to the correcting unit 130, the correcting unit 130 re-invasive data D1 ), it is possible to determine whether to perform an additional correction process.

Meanwhile, in one embodiment of the present invention, the light source array sensors 111 and 115, the photo array sensors 113 and 117, and the output unit 140 are not necessarily composed of only two pairs, and can be expanded to various numbers as necessary. It is possible.

5 is a block diagram illustrating the correction unit 130 and the output unit 140.

The compensator 130 corrects the output voltage of one or more of the first and second light source array sensors 111 and 115 by comparing the invasive data D1 prepared in advance and the value measured by the bio-information measuring unit 120. A correction value for correction and a correction value for correcting the optical wavelength timing may be calculated, and for this, an LED control unit 131 and an optical wavelength timing control unit 132 may be included.

The optical wavelength timing control unit 132 transmits the calculated optical wavelength timing correction value to the LED control unit 131, and the LED control unit 131 includes the optical wavelength timing information and the output voltage information in the correction values, so that the first and second output units ( 141, 143).

The received first and second output units 141 and 143 receive digital signal-based correction values and convert them into analog signals for driving LEDs, and the first and second light source array sensors through the LED driving driver ( 111, 115) and the timing of the optical wavelength can be controlled.

According to an embodiment of the present invention, through such a correction process and a feedback process, it is possible to more accurately measure bio-information contained in blood by minimizing the effect of different skin thickness for each person.

Meanwhile, in an embodiment of the present invention, components such as the bio-information measurement unit 120 and the correction unit 130 may include a memory and a processor that executes a program stored in the memory.

At this time, the memory refers to a non-volatile storage device and a volatile storage device that keep the stored information even when power is not supplied.

For example, the memory may be a compact flash (CF) card, secure digital (SD) card, memory stick, solid-state drive (SSD), micro SD card, or the like. And a magnetic computer storage device such as a NAND flash memory, a hard disk drive (HDD), and an optical disc drive such as a CD-ROM, DVD-ROM, or the like.

For reference, the components shown in FIGS. 2 and 5 according to an embodiment of the present invention may be implemented in software or in a hardware form such as a field programmable gate array (FPGA) or an application specific integrated circuit (ASIC). Roles can be played.

However,'components' are not limited to software or hardware, and each component may be configured to be in an addressable storage medium or may be configured to reproduce one or more processors.

Thus, as an example, a component is a component, such as software components, object-oriented software components, class components and task components, processes, functions, attributes, procedures, sub Includes routines, segments of program code, drivers, firmware, microcode, circuitry, data, database, data structures, tables, arrays and variables.

Components and functions provided within those components may be combined into a smaller number of components or further separated into additional components.

Hereinafter, a method performed in the non-invasive biometric information based correction system 100 according to an embodiment of the present invention will be described with reference to FIG. 6.

6 is a flow chart of a non-invasive biometric information positioning method according to an embodiment of the present invention.

In the non-invasive biometric information positioning method according to an embodiment of the present invention, voltage-based biometric information is measured through multiple sensors 110 based on transmissive and reflective (S110).

At this time, according to an embodiment of the present invention, the light source in the first light source array sensor based on the transmissive light is received by the first photo array sensor as it passes through the user's skin, and the light source in the light source array sensor based on the reflection type is the user. The light is received by the second photo array sensor as it is reflected from the skin.

In addition, hemoglobin values in the blood may be measured as bioinformation based on the received voltage values respectively measured through the first and second photo array sensors, and the biomolecule information may be measured by converting the measured hemoglobin values into glucose values.

Next, the measured bio-information is compared with previously prepared invasive data D1 (S120), and the output voltage of the multiple sensors 110 is increased or decreased based on the comparison result (S130).

That is, one embodiment of the present invention is a process of calibrating the output voltage, and compares the hemoglobin value, glucose value, which is the invasive data D1, which is prepared in advance, and the glucose value obtained as a result of the measurement. A correction value of the above output voltage may be calculated, and one or more output voltages of the first and second light source array sensors may be increased or decreased based on the calculated correction value.

Meanwhile, in the above description, steps S110 to S130 may be further divided into additional steps or combined into fewer steps according to an embodiment of the present invention. In addition, some steps may be omitted if necessary, and the order between the steps may be changed. In addition, even if omitted, the contents already described with respect to the non-invasive biometric information positioning-based correction system 100 in FIGS. 1 to 5 are also applied to the non-invasive biometric information positioning method of FIG. 6.

Meanwhile, an embodiment of the present invention may also be implemented in the form of a computer program stored in a medium executed by a computer or a recording medium including instructions executable by a computer. Computer readable media can be any available media that can be accessed by a computer and includes both volatile and nonvolatile media, removable and non-removable media. In addition, computer readable media may include both computer storage media and communication media. Computer storage media includes both volatile and nonvolatile, removable and non-removable media implemented in any method or technology for storage of information such as computer readable instructions, data structures, program modules or other data. Communication media typically includes computer readable instructions, data structures, program modules, or other data in a modulated data signal such as a carrier wave, or other transport mechanism, and includes any information delivery media.

Although the methods and systems of the present invention have been described in connection with specific embodiments, some or all of their components or operations may be implemented using a computer system having a general purpose hardware architecture.

The above description of the present invention is for illustration only, and a person having ordinary knowledge in the technical field to which the present invention pertains can understand that it can be easily modified into other specific forms without changing the technical spirit or essential features of the present invention. will be. Therefore, it should be understood that the embodiments described above are illustrative in all respects and not restrictive. For example, each component described as a single type may be implemented in a distributed manner, and similarly, components described as distributed may be implemented in a combined form.

The scope of the present invention is indicated by the following claims rather than the above detailed description, and it should be interpreted that all changes or modified forms derived from the meaning and scope of the claims and equivalent concepts thereof are included in the scope of the present invention. do.

100: non-invasive biometric information based correction system
110: multiple sensors
111: first light source array sensor
113: first photo array sensor
115: second light source array sensor
117: second photo array sensor
120: biometric information measurement unit
130: correction unit
140: output
141: first output
143: second output

Claims (12)

In a non-invasive biometric information-based correction system using multiple sensors,
Transmissive and reflective based multiple sensors,
A bio-information measuring unit for measuring bio-information in the user's blood based on the received voltage value measured from the multiple sensors,
A correction unit for comparing the measured bio-information with previously prepared invasive data and calculating a correction value for correcting the output voltage of the multiple sensors;
A non-invasive biometric information-based correction system including an output unit that increases or decreases the output voltage of the multiple sensors based on the calculated correction value. According to claim 1,
The multiple sensors,
The transmission-based first light source array sensor is arranged so that the light source penetrates the user's skin,
A first photo array sensor disposed on one side of the first light source array sensor facing the other side, and receiving the light source output from the first light source array sensor and transmitted through the skin;
A second light source array sensor based on the reflective type, wherein a light source is arranged to reflect the skin of the user;
And a second photo array sensor arranged to be spaced apart from the second light source array sensor, and receiving a light source output from the second light source array sensor and reflected from the skin.
The output unit includes a first output unit that increases or decreases the output voltage of the first light source array sensor based on the correction value and a second output unit which increases or decreases the output voltage of the second light source array sensor. Correction system. According to claim 2,
The bio-information measurement unit measures hemoglobin value in the blood with the bio-information based on the received voltage value respectively measured through the first and second photo array sensors, and converts the hemoglobin value in the blood into a glucose value based on the hemoglobin value. A non-invasive biometric information based correction system. The method of claim 3,
The bio-information measuring unit measures the hemoglobin value using the bio-information by analyzing absorption and reflection differences of light wavelengths of at least three wavelengths or more from the received voltage values from the first and second photo array sensors. Based correction system. The method of claim 4,
The bio-information measurement unit is a non-invasive bio-information positioning-based correction system that measures the hemoglobin value by analyzing a fluorescence spectrum from the received voltage value. The method of claim 5,
The bio-information measuring unit is a non-invasive bio-information positioning-based correction system that measures the hemoglobin value by analyzing the Raman spectrum and the Beer spectrum using the fluorescence spectrum based on the received power signal. The method of claim 3,
The bio-information measurement unit is a non-invasive bio-information positioning-based correction system that removes the remaining elements excluding the hemoglobin value and the glucose value from the bio information that can be calculated from the measured received voltage value. The method of claim 3,
The compensator calculates a correction value of one or more output voltages of the first and second light source array sensors by comparing the previously prepared invasive data, the hemoglobin value, the glucose value and the glucose value obtained by the bioinformation measurement unit Non-invasive biometric information based correction system. The method of claim 8,
The correction unit calculates a correction value for correcting one or more optical wavelength timings of the first and second light source arrays in addition to a correction value of the output voltage based on the comparison result. In the non-invasive biometric information positioning method using multiple sensors,
Measuring voltage-based bio-information through transmissive and reflective-based multiple sensors;
Comparing the measured bio-information with previously prepared invasive data; And
And increasing or decreasing the output voltage of the multiple sensors based on the comparison result. The method of claim 10,
The step of measuring the voltage-based biometric information through the transmissive and reflective-based multiple sensors,
Receiving light from the first photo array sensor as the light source from the transmission-based first light source array sensor penetrates the user's skin;
Receiving light from a second photo array sensor as the light source from the reflection-based second light source array sensor is reflected from the user's skin;
Measuring hemoglobin values in the blood with the bio-information based on the received voltage values respectively measured by the first and second photo array sensors;
Controlling reaction perceptions other than the hemoglobin value in the blood; And
Non-invasive bioinformation positioning method comprising the step of converting to a glucose value based on the hemoglobin value. The method of claim 11,
The step of increasing or decreasing the output voltage of the multiple sensors based on the comparison result,
Calculating a correction value of one or more output voltages of the first and second light source array sensors by comparing the hemoglobin values, glucose values, and glucose values converted based on the hemoglobin values, which are the previously prepared invasive data; And
And increasing or decreasing the output voltage of one or more of the first and second light source array sensors based on the calculated correction value.

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