WO2018041264A1

WO2018041264A1 - Screening test paper, and verification system and method therefor

Info

Publication number: WO2018041264A1
Application number: PCT/CN2017/100479
Authority: WO
Inventors: 柯正浩
Original assignee: 柯正浩
Priority date: 2016-09-05
Filing date: 2017-09-05
Publication date: 2018-03-08
Also published as: CN107796806A

Abstract

A screening test paper (30) comprises a recognition area (32), for encoding a screening function by means of a color coordinate model; a calibration area (31), having a specific color, for calibrating an external spectrum analysis device (40); and a reaction area (33), which can chemically react to a specific specimen and change the color of the reaction area. By means of the external spectrum analysis device (40) performing a light splitting processing on a reflected light source of the recognition area (32) and the reaction area (33) on the screening test paper (30), the invention can achieve the effect of automatic recognition and simple and convenient usage.

Description

Screening test paper and system and method thereof

[Technical Field]

The invention relates to a screening test paper, in particular to a screening test paper which can be transmitted through spectral analysis and a system and method for the inspection thereof.

【current technology】

According to, as human beings pay more and more attention to their own physical health, screening, including physiological screening or environmental screening, has become a very hot topic. Fig. 1 is a schematic view of a conventional screening test paper on which a reaction zone 11 is disposed. When the user drops the sample onto the reaction zone 11, the reaction zone 11 chemically reacts with the sample to change the color of the reaction zone 11. The user can analyze the normality of the sample according to the color change of the reaction zone and the contrast color. However, although the screening test paper 10 has the function of screening, it does not have any indication for identification. If there are many types of screening test papers, the user is very easily confused, and misuse of contrast colors may occur. Phenomenon, the result of misjudgment, is therefore difficult to use.

FIG. 2 is a schematic view of another conventional screening test paper. The screening test paper 20 is provided with an identification area 21 and a reaction area 22. The identification area 21 is a two-dimensional barcode. When the user reads the two-dimensional barcode by using an electronic device (not shown), the use of the screening test strip 20 can be known from the electronic device (not shown). When the user drops the corresponding sample onto the reaction zone 22, the reaction zone 22 chemically reacts with the sample to change the color of the reaction zone 22. The user can analyze the normality of the sample according to the color change of the reaction zone and the contrast color.

In the current more sophisticated screening technology, it is common to use a spectrometer to determine the amount of color change in the reaction zone of the test strip to obtain a screening result. However, in addition to being expensive, existing spectrum analyzers have limited spectroscopic effects and can only be designed to detect wavelengths in specific sections. For example, screening urine sugar and hemoglobin must be screened by two spectrum analyzers. Inspection leads to high costs. In addition, in the screening test paper 20 of Fig. 2, in addition to the spectrum analyzer, a two-dimensional bar code reading device is required to be used in combination, which is quite inconvenient and therefore difficult to use.

[Summary of the Invention]

One of the objects of the present invention is to disclose a screening test paper which, in addition to having an identification function, can effectively solve the above problem of inconvenient use.

According to an embodiment of the invention, a screening test paper is disclosed, comprising an identification area, wherein the screening function is encoded by a color coordinate model; and a correction area having a specific color for correcting an external spectrum analysis device; And a reaction zone that chemically reacts to a particular sample and changes its own color.

According to another embodiment of the present invention, a screening test paper inspection system is disclosed, comprising a screening test paper having an identification area, wherein the screening function is encoded by a color coordinate model; and a correction area having a specific color; And a reaction zone, which can chemically react to a specific sample and change its own color; a spectral analysis device can perform spectroscopic correction through the calibration zone and generate color according to the identification zone and the color of the reaction zone. a dichotomy signal; and a display device that determines a screening result based on the dichotomy signal.

According to still another embodiment of the present invention, a screening test paper inspection method is disclosed, comprising the steps of: providing a screening test paper having an identification area, a correction area, and a reaction area, wherein the identification area is performed by a color coordinate model. a screening function code, the correction zone having a specific color, the reaction zone reacting to a specific sample and changing its own color; contacting a specific sample with the reaction zone; using the calibration zone to The spectral analysis device performs spectroscopic correction; the spectral analysis device splits the identification region and the color of the reflected light source of the reaction region, and generates a dichotomy signal; and provides a display device, and determines a sieve according to the dichotomy signal Check the results and display the screening results on them.

[Description of the Drawings]

Figure 1 is a schematic view of a conventional screening test paper.

Figure 2 is a schematic diagram of another conventional screening test strip.

Figure 3 is a schematic view of the screening test paper of the present invention.

Figure 4 is a color coordinate model diagram used in the present invention.

5A to 5C are views showing an embodiment of the screening test paper inspection system of the present invention.

Figure 6 is a schematic diagram of the wavelength of the splitting light of the present invention.

Figure 7 is a flow chart showing the implementation of the present invention.

[Embodiment]

Certain terms are used throughout the description and following claims to refer to particular components. Those of ordinary skill in the art should understand that hardware manufacturers may refer to the same component by different nouns. This specification and the scope of the subsequent patent application do not use the difference in name as the means of distinguishing components, but the function of the components. Differences come as a criterion for differentiation. The term "including" as used throughout the specification and subsequent claims is an open term and should be interpreted as "including but not limited to".

3 is a schematic view of the screening test paper of the present invention. As shown in the figure, the screening test paper of the present invention mainly comprises a correction zone 31, an identification zone 32 and a reaction zone 33. The correction zone 31 has a particular color and the particular color is typically white. When an external spectrum analyzing device 40 (shown in FIG. 5A) receives the reflected light source of the white correction area 31, it splits and self-corrects the error to improve the accuracy of the splitting. The reaction zone 33 can chemically react to a particular sample and change its own color. After receiving the reflected light source of the reaction zone 33, the external spectrum analyzing device 40 (shown in FIG. 5A) performs splitting and generates a splitting signal.

Figure 4 is a color coordinate model diagram used in the present invention, as shown in the figure: In the color coordinate model diagram, the x chromaticity coordinates correspond to the ratio of the red primary colors, and the y chromaticity coordinates correspond to the proportion of the green primary colors. From the position of each wavelength of the horseshoe-shaped spectral trajectory in the figure, it can be found that the red band of the spectrum is concentrated in the lower right part of the figure, the green band is concentrated in the upper part of the figure, and the blue band is concentrated in the lower left part of the trajectory. The center point has the lowest saturation and the source trajectory has the highest line saturation. If the wavelength points representing the different color lights on the spectral track are connected to the center point of the chromaticity diagram, the chromaticity picture can be divided into various color areas. Therefore, if the chromaticity coordinates x, y of a certain color can be calculated, its color characteristics can be clearly determined in the chromaticity. For example, the surface color chromaticity coordinates of the cyan sample are x=0.1902, y=0.2302, and the like. Of course, different colors have different chromaticity coordinates and occupy different positions in the chromaticity diagram. Referring to FIG. 3, the identification area 32 of the screening test paper 30 of the present invention performs screening function coding via a one-color coordinate model, and provides a screening function code corresponding to different samples to be tested. A wide variety of screening test strips can be classified by the large number of color coordinate model codes.

5A to 5C are diagrams of an embodiment of the screening test paper inspection system of the present invention, as shown in the figure: the screening test paper inspection system of the present invention mainly comprises a screening test paper 30, a spectral analysis device 40 and a The display device 50 is composed of. The spectrum analyzing device 40 performs splitting according to the reflected light source of the identification area 32 on the screening test paper 30, generates a splitting signal, and transmits the splitting signal to the display device 50. The display device 50 determines the type of the sample to be tested according to the split signal, and automatically sets the screening parameters. The spectrum analyzing device 40 splits the reflected light source of the reaction zone 33 on the screening test paper 30 to generate a splitting signal, and transmits the split signal result to the display device 50. The display device 50 compares the split signal result with the set screening parameter to determine whether the screening result of the sample to be tested is normal.

In order to detect the urine sugar value of the patient, if it has been determined that the screening test paper taken for urine sugar is dedicated, the test can be directly performed; if it is not determined, the user must use the correction area 31 on the screening test paper. The spectral analysis device 40 performs spectroscopic correction. After the calibration is completed, the spectral analysis device 40 can be used to receive the reflected light source from the screening test strip identification area. After the splitting, the splitting result is transmitted to the display device 50 by wire or wirelessly. The display device 50 determines the type of the sample to be tested according to the type of the test test paper, and automatically sets the screening parameters. After the screening test paper 30 to be selected is for detecting the urine sugar value, the urine to be tested may be brought into contact with the reaction zone 33 of the screening test paper 30 (usually by dripping or infiltration), and the reaction zone 33 The ingredients inside will chemically react with the urine to be tested and change the color of the reaction zone 33. In addition, the reaction zone 33 can include a plurality of different detection zones 331-333 for detecting glucose, protein, pH, occult blood or other physiological values in the urine to achieve the effect of screening multiple values at a time. The urine to be tested is subjected to a contact reaction with the reaction zone 33 of the screening test paper 30, and the sieve test paper 30 can be placed in the spectrum analyzer 40. The spectrum analyzer 40 performs spectroscopic correction according to the reflected light source of the calibration area 31 of the screening test paper 30, performs splitting according to the reflected light source of the identification area 32, and transmits the splitting signal to the display device 50, and the display device 50 displays the light according to the splitting signal. Screen the test sample type (urine sugar) of the test paper, and automatically set the spectroscopic screening parameters of urine sugar. The color change of the reaction zone 33 may not be visible to the human eye, but after the spectroscopic analysis device 40 is split, the spectral microscopic appearance is significantly different, so the detection result is quite accurate.

Referring to FIG. 6 , it is a schematic diagram of the wavelength of the spectroscopic wavelength of the present invention. When the screening test paper 30 is used for detecting the urine sugar value, it can be clearly found that the reflected light source of the reaction zone 33 is split by the spectrum analyzer 40 and has a wavelength of about 600 nm. The light source has been absorbed (the urine protein is about 450nm), and the degree of absorption, that is, the height of the trough, represents the value of urine sugar. The display device 50 compares the light source according to the degree of absorption of the light source having a wavelength of about 600 nm, and displays the urine sugar value and the normality according to the built-in parameters. The user can know the result of the screening through the display device 50. In this way, automatic identification and ease of use can be achieved.

In the case of physiological screening, the sample to be tested may be saliva, urine, blood or feces, etc., and in the case of environmental screening, the sample to be tested may be water (measuring heavy metal content in water), food, toxic and harmful. There are many kinds of substances or microorganisms, so the color coordinate model of this technology is used for coding and identification, so there is no need to worry about the lack of source code for the classification of the sample to be tested. Because each specific component in the sample to be tested is chemically reacted with the reaction zone of the test strip, after the reflected light of the reaction zone is split, a light source of a specific wavelength is absorbed, so that the absorbed light can be collected. The wavelength parameter corresponds to the parameter to be tested and is made into a parameter truth table, and is stored in the display device 50 to facilitate screening comparison with the spectroscopic signal.

Referring to Figure 7, a flow chart of the implementation of the present invention is shown in the figure. When a physiological value screening is to be performed, first, a screening test paper having an identification area, a correction area and a reaction area must be provided (step S1). ) for reacting with the sample to be tested. The identification zone is coded by a color coordinate model, and the correction zone has a specific color, and the reaction zone can generate a chemical reaction on a specific sample, which actually causes a change in the spectrum (if determined by the human eye) Change its own color). Then, the specific sample can be brought into contact with the reaction zone (step S2), and then the spectral analysis device is subjected to spectral correction using the calibration region (step S3) to calibrate the spectral analysis device. The steps S2 and S3 may be reversed. Thereafter, the identification zone and the reaction can be transmitted through the spectrum analyzer The color of the reflected light source of the area is split, and a dichotomy signal is generated (step S4), which respectively represents the detection item and the detection result of the screening test paper, and finally a display device is provided, and a screening result is determined according to the dichotomy signal. And the screening result is displayed thereon (step S5), and the screening operation is completed.

In addition, the reason why the spectrum analysis device currently on the market cannot analyze the wavelengths of all the light sources is that the spectral separation effect is not satisfactory, and the reason why the spectral separation effect is not satisfactory is that the components in the spectrum analysis device are mostly not system-on-chip (SOC). In a way, even if a small number of spectral analysis devices are implemented in the form of a system-on-a-chip (SOC), the light source is reflected and the attenuation is too large, which makes it impossible to perform analysis. Therefore, the spectrum analyzing device 40 of the present invention is realized by a system chip (SOC), and its internal components (reflected light receiving portion and grating, etc.) utilize a wavelength range of between 0.01 nm and 100 nm. After the energy source is exposed to the photoresist layer, the unexposed photoresist layer is removed. In this way, not only the spectral analysis device 40 can be reduced in size, but also the surface roughness can be reduced, so that the reflected light source can be totally reflected without being attenuated, thereby achieving the effect of complete splitting.

The above are only the preferred embodiments of the present invention, and all changes and modifications made to the scope of the present invention should be within the scope of the present invention.

【Symbol Description】

10 screening test paper

11 reaction zone

20 screening test paper

21 identification area

22 reaction zone

30 screening test paper

31 calibration area

32 identification area

33 reaction zone

40 Spectral analysis device

50 display device

Claims

A screening test paper characterized by comprising:

An identification zone is coded by a color coordinate model for screening function;

a calibration zone having a specific color for correcting an external spectral analysis device;

A reaction zone that chemically reacts to a particular sample and changes its own color.
The screening test paper according to claim 1, wherein the external spectrum analyzing device performs spectroscopic processing on the identification region and the reflected light source of the reaction region.
The screening test paper according to claim 1, wherein the external spectrum analyzing means performs spectroscopic processing on the reflected light source of the correction area and performs self-correction error.
A screening test paper inspection system, comprising:

A screening test paper with:

An identification zone is coded by a color coordinate model for screening function;

a correction zone having a specific color;

a reaction zone that reacts to a particular sample and changes its own color;

a spectral analysis device for performing spectroscopic correction through the calibration region, and generating a dichotomy signal according to the color of the identification region and the reaction region;

A display device determines a screening result based on the dichotomy signal.
The screening test paper inspection system according to claim 4, wherein a parameter truth table is stored in the display device, and the screening result is compared with the parameter truth table according to the dichotomy signal. Got it.
The screening test paper inspection system according to claim 4, wherein the spectral analysis device is a system chip (SOC), and the internal components thereof have a wavelength range of from 0.01 nm to 100 nm. After the high-energy light source is exposed to a photoresist layer, the unexposed photoresist layer is removed.
A screening test paper inspection method, characterized in that the method comprises the following steps:

Providing a screening test paper having an identification area, a correction area and a reaction area, wherein the identification area is coded by a color coordinate model, the correction area has a specific color, and the reaction area can be used for a specific inspection The body produces a reaction and changes its own color;

Contacting the specific sample with the reaction zone;

Using the calibration area to perform spectroscopic correction on a spectral analysis device;

And illuminating the color of the reflected light source of the identification area and the reaction area through the spectrum analyzing device, and generating a dichotomy signal;

A display device is provided, and a screening result is determined according to the dichotomy signal, and the screening result is displayed thereon.
A method of testing a test strip according to claim 7, wherein the specific color is white.
The method for testing a test strip according to claim 7, further comprising the step of storing a parameter truth table in the display device, and the screening result is based on the dichotomy signal and the parameter. The truth table is obtained.
The method for testing a test strip according to claim 7, wherein the spectroscopic device is a system chip (SOC), and the internal components thereof have a wavelength range of from 0.01 nm to 100 nm. After the high-energy light source is exposed to a photoresist layer, the unexposed photoresist layer is removed.