Intelligent detection method and system for chemical solution

Abstract

The application discloses an intelligent detection method for liquid medicine, which comprises the following steps: detecting reaction information for requesting detection of liquid medicine triggered by the liquid medicine; controlling a control valve to be opened, so that target liquid medicine flows from a liquid medicine container to a reagent container containing reagents to react; collecting a reaction image of the target liquid medicine and the reagents; and analyzing the reaction image to obtain reaction information of the liquid medicine. It can be seen that when reaction information of liquid medicine needing to be detected is detected, the liquid medicine is automatically flowed into the reagent container to react with the reagents, the reaction image of the target liquid medicine and the reagents is automatically collected through an image processing device, and the image is analyzed through a data analysis module, so that the reaction information of the liquid medicine, such as a discoloration curve and a color change value of the reagents, can be quickly determined, which is beneficial to quickly determining accurate analysis results of the liquid medicine, such as pH value and / or osmotic pressure, and is also beneficial to improving training accuracy and efficiency of liquid medicine dispensing.

Description

TECHNICAL FIELD

[0001] The present application relates to the technical field of liquid medicine detection, and in particular to an intelligent detection method and system for liquid medicine. BACKGROUND

[0002] Since the beginning of intravenous infusion treatment for human beings, the way of mixing and configuring medicines has not been fundamentally changed. The medicines are always dissolved in a solvent and then added to a basic infusion, such as glucose injection, sodium chloride injection or glucose sodium chloride injection, to add therapeutic medicines to obtain a complete infusion after adding medicines.

[0003] With the rapid development of intelligent technology, automatic medicine dispensing technology has emerged, that is, medicines are automatically dispensed by a mechanical hand. The appearance of the mechanical hand significantly reduces the working intensity and accuracy of clinical medicine dispensing. However, it is found in practice that the problems solved by the existing automatic medicine dispensing technology still remain in the nature of replacing hands with machines to perform repetitive work, that is, the hands of dispensers are only liberated to a certain extent, and the reaction of the liquid medicine and the reagent after the medicine is dispensed cannot be known. SUMMARY

[0004] The present application provides an intelligent detection method and system for liquid medicine, which can accurately know the reaction of the liquid medicine and the reagent after the medicine is dispensed.

[0005] To solve the above technical problems, the present application discloses an intelligent detection method for liquid medicine in the first aspect, which comprises:

[0006] The liquid medicine detection module detects a detection request triggered by a user for a target liquid medicine, and the detection request is used to request detection of reaction information of the target liquid medicine;

[0007] The liquid medicine sampling component controls the control valve of the liquid medicine sampling component to open according to the detection request, so that the target liquid medicine flows from a liquid medicine container to a reagent container containing a reagent, and the reagent is used to react with the target liquid medicine;

[0008] The image processing device collects a reaction image of the target liquid medicine and the reagent;

[0009] The data analysis module analyzes the reaction image to obtain reaction information of the target liquid medicine.

[0010] As an optional implementation, in the first aspect of the present application, the detection request comprises identification information of the target liquid medicine;

[0011] After the data analysis module analyzes the reaction image to obtain reaction information of the target liquid medicine, the method further comprises:

[0012] The data analysis module screens standard information of the target drug liquid from a pre-stored drug liquid information database according to identification information of the target drug liquid, and analyzes reaction information of the target drug liquid and the screened standard information of the target drug liquid to obtain an analysis result of the target drug liquid, wherein the analysis result of the target drug liquid includes reaction parameters of the target drug liquid, and the reaction parameters of the target drug liquid include pH value of the target drug liquid and / or osmotic pressure of the target drug liquid.

[0013] The drug liquid result display displays the analysis result of the target drug liquid.

[0014] As an optional implementation, in the first aspect of the present application, the detection request further includes a use purpose of the target drug liquid.

[0015] The method further includes:

[0016] The drug liquid sampling component obtains information of the reagent, wherein the information of the reagent includes identification information of the reagent and storage condition of the reagent in the reagent container, and the storage condition of the reagent includes storage amount of the reagent.

[0017] The drug liquid sampling component determines a target drug liquid amount required for the reaction between the target drug liquid and the reagent according to the content included in the detection request and the information of the reagent.

[0018] The drug liquid sampling component controls the control valve of the drug liquid sampling component to be opened to make the target drug liquid flow from the drug liquid container to the reagent container containing the reagent according to the detection request, and the method includes:

[0019] The drug liquid sampling component controls the control valve of the drug liquid sampling component to be opened to make the target drug liquid flow from the drug liquid container to the reagent container containing the reagent by the target drug liquid amount.

[0020] As an optional implementation, in the first aspect of the present application, the type of the reagent includes a solid type or a liquid type, and the solid type includes a test paper type.

[0021] The method further includes:

[0022] When the type of the reagent is the liquid type, the data analysis module analyzes an influence degree of a speed of the target drug liquid flowing to the reagent container on the reaction information of the target drug liquid and the reagent before the storage amount of the target drug liquid in the reagent container reaches the target drug liquid amount according to the content included in the detection request and the information of the reagent.

[0023] The data analysis module determines whether the influence degree is greater than or equal to the determined influence degree threshold. When the determination result is yes, the target speed required for the target drug solution to flow into the reagent container is determined based on the influence degree and the storage amount of the target drug solution in the reagent container.

[0024] The drug sampler generates control parameters for the control valve based on the target speed and the pressure exerted by the target drug container on the control valve. The control parameters include the opening size of the control valve.

[0025] The drug sampler controls the opening of its control valve to allow the target drug solution to flow from the drug container to the reagent container, including:

[0026] The drug sampler controls the control valve of the drug sampler to open according to the control parameters of the control valve, so that the target drug solution flows from the drug container to the reagent container.

[0027] As an optional implementation, in the first aspect of the invention, before the image processing device acquires the reaction image of the target drug solution and the reagent, the method further includes:

[0028] The image processing device corrects the vision of the image processing device;

[0029] The image processing device corrects the vision of the image processing device, including:

[0030] The image processing device identifies the reaction process of each group of sample drug solutions and the corresponding sample reagent in multiple groups of sample drug solutions based on the image acquisition module on the image processing device, and obtains the reaction information of each group of sample drug solutions and the corresponding sample reagent. Each group of sample drug solutions consists of at least one sample drug solution, the reaction parameters of each sample drug solution in each group of sample drug solutions are known, and the pH of each group of sample drug solutions is different. The reaction information of each group of sample drug solutions includes the color corresponding to the pH of the group of sample drug solutions and the image corresponding to the pH of the sample drug solutions.

[0031] The image processing device establishes the correlation between the reaction parameters of each group of sample solutions, the reaction information corresponding to the group of sample solutions, and the sample reagents corresponding to the group of sample solutions, and corrects the image acquisition module based on the correlation between each group of sample solutions.

[0032] As an optional implementation, in the first aspect of the present application, after the data analysis module analyzes the reaction information of the target drug liquid and the screened information of the target drug liquid to obtain the analysis result of the target drug liquid, the method further comprises:

[0033] The data analysis module analyzes the analysis result of the target drug liquid and the pre-stored all medicinal parameters of the target drug liquid to obtain the medicinal parameter analysis result of the target drug liquid;

[0034] When the medicinal parameter analysis result of the target drug liquid is used to indicate that the analysis result of the target drug liquid is a certain medicinal parameter among all medicinal parameters of the target drug liquid, the data analysis module acquires the use suggestion of the target drug liquid according to the medicinal parameter analysis result;

[0035] The drug liquid result display displays the use suggestion of the target drug liquid and the analysis result of the target drug liquid;

[0036] When the medicinal parameter analysis result of the target drug liquid is used to indicate that the analysis result of the target drug liquid is not a certain medicinal parameter among all medicinal parameters of the target drug liquid, the data analysis module determines the medicinal adjustment suggestion of the target drug liquid according to the medicinal parameter analysis result and the medicinal parameter analysis result of the target drug liquid;

[0037] The target drug liquid result display displays the medicinal adjustment suggestion of the target drug liquid.

[0038] As an optional implementation, in the first aspect of the present application, the method further comprises:

[0039] The image processing device queries the spectral type of the current light source, and the spectral type of the current light source is a visible spectral type or an ultraviolet spectral type;

[0040] The data analysis module acquires the type of the reagent and determines whether the spectral type of the current light source and the type of the reagent are matched;

[0041] When it is determined that they are not matched, the data analysis module determines a target light source type matched with the type of the reagent;

[0042] The image processing device switches the current light source to a light source matched with the target light source type.

[0043] As an optional implementation, in the first aspect of the present application, the data analysis module determines whether the spectral type of the current light source and the type of the reagent are matched comprises:

[0044] When the type of the reagent is a liquid type, the data analysis module determines whether the spectral type of the current light source is an ultraviolet spectral type;

[0045] When it is determined that the spectral type of the current light source is not the ultraviolet spectral type, the data analysis module determines that the spectral type of the current light source does not match the type of the reagent; or,

[0046] When the type of the reagent is a test paper type, the data analysis module determines whether the spectral type of the current light source is a visible spectral type;

[0047] When it is determined that the spectral type of the current light source is the visible spectral type, the data analysis module determines a detection speed required for reaction information of the target reagent according to content included in the detection request, and determines whether the detection speed is greater than or equal to a determined detection speed threshold value, when the determination result is yes, the data analysis module determines that the spectral type of the current light source does not match the type of the reagent;

[0048] When the type of the reagent is a liquid type, the target light source type matched with the type of the reagent is the ultraviolet spectral type;

[0049] When the type of the reagent is a test paper type, the target light source type matched with the type of the reagent is the visible spectral type;

[0050] When the type of the reagent is a test paper type and the detection speed of the target reagent is greater than or equal to the detection speed threshold value, the target light source type matched with the type of the reagent is the ultraviolet spectral type.

[0051] The second aspect of the present application discloses an intelligent detection system of a reagent, the intelligent detection system comprises:

[0052] A reagent detection module is configured to detect a detection request triggered by a user for a target reagent, the detection request is configured to request to detect reaction information of the target reagent;

[0053] A reagent sampling component is configured to control a control valve of the reagent sampling component to be opened according to the detection request, so that the target reagent flows from a reagent container to a reagent container containing a reagent, the reagent is configured to react with the target reagent;

[0054] An image processing device is configured to acquire a reaction image of the target reagent and the reagent;

[0055] A data analysis module is configured to analyze the reaction image to obtain reaction information of the target reagent.

[0056] As an optional implementation, in the second aspect of the present application, the detection request comprises identification information of the target drug solution.

[0057] The data analysis module is further configured to, after analyzing the reaction image to obtain reaction information of the target drug solution, filter standard information of the target drug solution from a pre-stored drug solution information database according to the identification information of the target drug solution, and analyze the reaction information of the target drug solution and the filtered standard information of the target drug solution to obtain an analysis result of the target drug solution, wherein the analysis result of the target drug solution comprises reaction parameters of the target drug solution, and the reaction parameters of the target drug solution comprise pH of the target drug solution and / or osmotic pressure of the target drug solution.

[0058] The intelligent detection system comprises:

[0059] A drug solution result display is configured to display the analysis result of the target drug solution.

[0060] As an optional implementation, in the second aspect of the present application, the detection request further comprises a use purpose of the target drug solution.

[0061] The drug solution sampling component is further configured to obtain information of the reagent, wherein the information of the reagent comprises identification information of the reagent and storage condition of the reagent in the reagent container, and the storage condition of the reagent comprises a storage amount of the reagent.

[0062] The drug solution sampling component is further configured to determine a target drug solution amount required for the reaction between the target drug solution and the reagent according to the content included in the detection request and the information of the reagent.

[0063] The drug solution sampling component controls the control valve of the drug solution sampling component to open to enable the target drug solution to flow from the drug solution container to the reagent container containing the reagent according to the detection request.

[0064] The drug solution sampling component controls the control valve of the drug solution sampling component to open to enable the target drug solution to flow from the drug solution container to the reagent container containing the reagent by the target drug solution amount.

[0065] As an optional implementation, in the second aspect of the present application, the type of the reagent comprises a solid type or a liquid type, and the solid type comprises a test paper type.

[0066] The data analysis module is further configured to, when the type of the reagent is the liquid type, analyze, according to the content included in the detection request and the information of the reagent, an influence degree of a speed of the target drug liquid flowing to the reagent container before the storage amount of the target drug liquid in the reagent container reaches the target drug amount on reaction information of the target drug liquid and the reagent;

[0067] The data analysis module is further configured to determine whether the influence degree is greater than or equal to a determined influence degree threshold, and when the determination result is yes, determine a target speed required for the target drug liquid to flow to the reagent container according to the influence degree and the storage amount of the target drug liquid in the reagent container.

[0068] The drug liquid sampling component is further configured to generate a control parameter of the control valve according to the target speed and the pressure of the target drug liquid container on the control valve, and the control parameter of the control valve includes an opening size of the control valve.

[0069] The drug liquid sampling component controls the control valve of the drug liquid sampling component to open, so that the target drug liquid flows from the drug liquid container to the reagent container in the target drug liquid amount.

[0070] The drug liquid sampling component controls the control valve of the drug liquid sampling component to open according to the control parameter of the control valve, so that the target drug liquid flows from the drug liquid container to the reagent container in the target drug liquid amount.

[0071] As an optional implementation, in the second aspect of the present application, the image processing device is further configured to correct the vision of the image processing device before collecting the reaction image of the target drug liquid and the reagent.

[0072] The image processing device corrects the vision of the image processing device in the following manner:

[0073] The image processing device identifies the reaction process of each group of sample drug liquids and sample reagents corresponding to the sample drug liquids in the plurality of groups of sample drug liquids based on an image collection module on the image processing device, to obtain reaction information of each group of sample drug liquids and sample reagents corresponding to the sample drug liquids in the group, wherein each group of sample drug liquids is composed of at least one sample drug liquid, the reaction parameters of each sample drug liquid in each group of sample drug liquids are known, the pH values of each group of sample drug liquids are different from each other, and the reaction information of each group of sample drug liquids includes a color corresponding to the pH value of the sample drug liquid in the group and an image corresponding to the pH value of the sample drug liquid.

[0074] The data analysis module is further configured to establish a reaction parameter of each group of the sample liquid, reaction information corresponding to the group of the sample liquid, and an association relationship between the group of the sample liquid and a sample reagent corresponding to the group of the sample liquid, and correct the image acquisition module based on the association relationship corresponding to each group of the sample liquid.

[0075] As an optional implementation, in the second aspect, the data analysis module is further configured to, after analyzing the reaction information of the target liquid and the information of the target liquid screened out to obtain an analysis result of the target liquid, analyze the analysis result of the target liquid and all the pharmaceutical parameters of the target liquid stored in advance to obtain a pharmaceutical parameter analysis result of the target liquid.

[0076] The data analysis module is further configured to, when the pharmaceutical parameter analysis result of the target liquid indicates that the analysis result of the target liquid is a certain pharmaceutical parameter of all the pharmaceutical parameters of the target liquid, acquire a use suggestion of the target liquid according to the pharmaceutical parameter analysis result.

[0077] A liquid result display is configured to display the use suggestion of the target liquid and the analysis result of the target liquid.

[0078] The data analysis module is further configured to, when the pharmaceutical parameter analysis result of the target liquid indicates that the analysis result of the target liquid is not a certain pharmaceutical parameter of all the pharmaceutical parameters of the target liquid, determine a pharmaceutical adjustment suggestion of the target liquid according to the pharmaceutical parameter analysis result and the pharmaceutical parameter analysis result of the target liquid.

[0079] The target liquid result display is further configured to display the pharmaceutical adjustment suggestion of the target liquid.

[0080] As an optional implementation, in the second aspect, the method further includes:

[0081] The image processing device is further configured to query a spectral type of a current light source, the spectral type of the current light source being a visible spectral type or an ultraviolet spectral type.

[0082] The data analysis module is further configured to acquire a type of the reagent, and determine whether the spectral type of the current light source matches the type of the reagent; when it is determined that the spectral type of the current light source does not match the type of the reagent, determine a target light source type that matches the type of the reagent.

[0083] The image processing device is further configured to switch the current light source to a light source that matches the target light source type.

[0084] As an optional implementation, in the second aspect of the present application, the manner that the data analysis module determines whether the spectral type of the current light source matches the type of the reagent specifically includes:

[0085] When the type of the reagent is the liquid type, it is determined whether the spectral type of the current light source is the ultraviolet spectral type;

[0086] When it is determined that the spectral type of the current light source is not the ultraviolet spectral type, it is determined that the spectral type of the current light source does not match the type of the reagent; or,

[0087] When the type of the reagent is the test paper type, it is determined whether the spectral type of the current light source is the visible spectral type;

[0088] When it is determined that the spectral type of the current light source is the visible spectral type, the detection speed required for the reaction information of the target reagent is determined according to the content included in the detection request, and it is determined whether the detection speed is greater than or equal to the determined detection speed threshold value, when the determination result is yes, it is determined that the spectral type of the current light source does not match the type of the reagent;

[0089] When the type of the reagent is the liquid type, the target light source type that matches the type of the reagent is the ultraviolet spectral type;

[0090] When the type of the reagent is the test paper type, the target light source type that matches the type of the reagent is the visible spectral type;

[0091] When the type of the reagent is the test paper type and the detection speed of the target reagent is greater than or equal to the detection speed threshold value, the target light source type that matches the type of the reagent is the ultraviolet spectral type.

[0092] The third aspect of the present application discloses another intelligent detection system for reagent, the intelligent detection system comprises:

[0093] A memory storing executable program codes;

[0094] A processor coupled with the memory;

[0095] The processor invokes the executable program codes stored in the memory to execute part or all steps of any one of the intelligent detection methods for reagent disclosed in the first aspect of the present application.

[0096] The fourth aspect of the present application discloses a computer storage medium storing computer instructions, when the computer instructions are invoked, part or all steps of any one of the intelligent detection methods for reagent disclosed in the first aspect of the present application are executed.

[0097] Compared with the prior art, the embodiment of the present application has the following beneficial effects:

[0098] In the embodiment of the present application, the liquid medicine detection module detects a detection request triggered by a user for a target liquid medicine, and the detection request is used to request detection of reaction information of the target liquid medicine; the liquid medicine sampling component controls the control valve of the liquid medicine sampling component to open according to the detection request, so that the target liquid medicine flows from the liquid medicine container to the reagent container containing the reagent, the reagent is used to react with the target liquid medicine; the image processing device collects a reaction image of the target liquid medicine and the reagent; and the data analysis module analyzes the reaction image to obtain the reaction information of the liquid medicine. It can be seen that when the reaction information of the liquid medicine to be detected is detected, the liquid medicine is automatically flowed into the reagent container to react with the reagent, the reaction image of the target liquid medicine and the reagent is automatically collected by the image processing device, and the image is analyzed by the data analysis module, so that the reaction information of the liquid medicine, such as the discoloration curve of the reagent and the color change value, can be quickly determined, which is beneficial to quickly determine the accurate analysis result of the liquid medicine, such as the pH value and / or the osmotic pressure; and is conducive to the research and development of the intelligent detection system of the liquid medicine, and when the present application is applied to training, it is also beneficial to improve the training accuracy and efficiency of the liquid medicine dispensing. BRIEF DESCRIPTION OF DRAWINGS

[0099] In order to more clearly illustrate the technical solutions in the embodiments of the present application, the drawings needed in the embodiment description will be briefly introduced as follows. Obviously, the drawings in the following description are only some embodiments of the present application, and other drawings can be obtained by those skilled in the art without creative labor.

[0100] Figure 1 is a flow diagram of an intelligent detection method of liquid medicine disclosed by the embodiment of the present application;

[0101] Figure 2 is a flow diagram of another intelligent detection method of liquid medicine disclosed by the embodiment of the present application;

[0102] Figure 3 is a structural diagram of an intelligent detection system of liquid medicine disclosed by the embodiment of the present application;

[0103] Figure 4 is a structural diagram of another intelligent detection system of liquid medicine disclosed by the embodiment of the present application;

[0104] Figure 5 is a structural diagram of another intelligent detection system of liquid medicine disclosed by the embodiment of the present application;

[0105] Figure 6 is a discoloration curve of the pH value of a sample liquid medicine disclosed by the embodiment of the present application. DETAILED DESCRIPTION

[0106] In order to better understand the technical scheme of the present application, the technical scheme in the embodiments of the present application will be described clearly and completely below with reference to the drawings in the embodiments of the present application. Obviously, the described embodiments are only some of the embodiments of the present application, but not all the embodiments. Based on the embodiments in the present application, all other embodiments obtained by those skilled in the art without creative efforts belong to the scope of protection of the present application.

[0107] The terms "first", "second", and the like in the specification and claims of the present application and the above-described drawings are used to distinguish different objects, and are not used to describe a particular order. In addition, the terms "include" and "have" and any variations thereof are intended to cover non-exclusive inclusion. For example, a process, method, intelligent detection system, product or end including a series of steps or units is not limited to the listed steps or units, but can optionally include steps or units not listed, or can optionally include other steps or units inherent to the process, method, product or end.

[0108] Reference herein to "an embodiment" means that a particular feature, structure, or characteristic described in connection with the embodiment can be included in at least one embodiment of the application. The appearance of the phrase in various places in the specification does not necessarily all refer to the same embodiment, nor is it necessarily mutually exclusive of other embodiments. It is explicitly and implicitly understood that the embodiments described herein can be combined with other embodiments.

[0109] The present application discloses an intelligent detection method for liquid medicine, which can automatically flow the liquid medicine into the reagent container to react with the reagent when detecting the reaction information of the liquid medicine to be detected, automatically collect the reaction image of the target liquid medicine and the reagent through an image processing device, and analyze the image through a data analysis module, so as to quickly determine the reaction information of the liquid medicine, such as the color change curve and color change value of the reagent, which is beneficial to quickly determine the accurate analysis result of the liquid medicine, such as pH value and / or osmotic pressure, and is conducive to the research and development of the intelligent detection system for liquid medicine, and when the present application is applied in training, it is also beneficial to improve the training accuracy and efficiency of liquid medicine dispensing. The intelligent detection method for liquid medicine described in the present application will be described in detail below.

[0110] Embodiment one

[0111] Please refer to Figure 1 , Figure 1 is a flowchart of an intelligent detection method for liquid medicine disclosed by the embodiments of the present application. Among them, Figure 1 The described method can be applied to an intelligent detection system. For example Figure 1As shown, the intelligent detection method of the drug solution can include the following operations:

[0112] 101. The drug solution detection module detects a detection request triggered by a user for the target drug solution, the detection request being used to request detection of reaction information of the target drug solution.

[0113] In the embodiment of the application, the target drug solution is any drug solution whose reaction information needs to be detected, wherein the reaction information of the drug solution includes a color change curve of the reagent and / or a color change of the reagent during the reaction of the drug solution and the reagent. Further, the reaction information of the drug solution can also include a reaction temperature of the drug solution and the reagent, and further, when the type of the reagent is a test paper type, the reaction information of the drug solution can also include a texture change of the reagent. Further, the reaction information of the drug solution can also include one or more of a reaction bubble of the drug solution and the reagent, a reaction mist of the drug solution and the reagent, and a reaction odor of the drug solution and the reagent. The more the reaction information of the drug solution includes, the more beneficial it is to improve the analysis accuracy and reliability of the analysis result of the drug solution.

[0114] In the embodiment of the application, optionally, the detection request includes identification information of the target drug solution. Further optionally, the detection request also includes a use purpose of the target drug solution. Further, the detection request also includes a detection time of the target drug solution and / or an efficacy of the target drug solution. Further, the detection request also includes information of a user of the target drug solution, wherein the information of the user includes a disease condition of the user. Further, the information of the user also includes a gender of the user and / or an age of the user. The more the detection request includes, the more beneficial it is to improve the acquisition or adjustment of the drug use suggestion, thereby more beneficial to improve the research and development accuracy and reliability of the intelligent detection system of the drug solution and the use training accuracy and reliability of the intelligent detection system of the drug solution.

[0115] 102. The drug solution sampling component controls the control valve of the drug solution sampling component to open according to the detection request, so that the target drug solution flows from the drug solution container to the reagent container containing the reagent for reaction with the target drug solution.

[0116] In the embodiment of the application, the type of the reagent includes a solid type or a liquid type, and the solid type includes a test paper type or other non-test paper type.

[0117] In the embodiment of the application, optionally, one side of the reagent container facing the image acquisition module can be made of a high-transmittance and low-refraction material such as plastic or quartz, and the other sides are designed to be non-transmittance to reduce the occurrence of external light entering the reagent container and reduce the influence of environmental light and environmental noise such as acidity and alkalinity on the reaction of the drug solution and the reagent.

[0118] Optionally, the control valve of the liquid sampling component can be understood as an anti-reverse flow needle group, and further, the anti-reverse flow needle group has a corresponding valve for controlling the liquid to flow into the reagent container and / or preventing the liquid from flowing reversely from the reagent container to the liquid container. In this way, through the control valve, the occurrence of the mixed liquid in the reagent container or the liquid flowing out of the liquid container into the liquid container can be reduced, and the possibility of the liquid in the liquid container being contaminated can be reduced.

[0119] Optionally, in the embodiment of the present application, the reagent can be placed in a specified position of the reagent container, such as a test paper placed at the uppermost part of the reagent container, and when the liquid reaches the upper part of the reagent container and contacts the reagent, a reaction occurs.

[0120] 103. The image processing device acquires a reaction image of the target liquid and the reagent.

[0121] Optionally, in the embodiment of the present application, the image processing device includes at least one image acquisition module, wherein the number of image acquisition modules can be determined according to the number of reaction regions of the target liquid and the reagent in the reagent container, for example, if the number of reaction regions is 2, the number of image acquisition modules is 2.

[0122] 104. The data analysis module analyzes the reaction image to obtain reaction information of the target liquid.

[0123] Optionally, in the embodiment of the present application, the data analysis module compares the color change curve, color change and texture change in the reaction image with the stored color and color value to obtain a color change value.

[0124] It can be seen that, when the reaction information of the liquid to be detected is detected, the method described in the embodiment of the present application automatically causes the liquid to flow into the reagent container to react with the reagent, and automatically acquires the reaction image of the target liquid and the reagent through the image processing device, and analyzes the image through the data analysis module, which can quickly determine the reaction information of the liquid, such as the color change curve and color change value of the reagent, which is beneficial to quickly determine the accurate analysis result of the liquid, such as pH and / or osmotic pressure, and is conducive to the research and development of the intelligent detection system of the liquid, and when the present scheme is applied in training, it is also beneficial to improve the training accuracy and efficiency of liquid dispensing.

[0125] In an optional embodiment, after the data analysis module analyzes the reaction image to obtain the reaction information of the target liquid, the method further includes the following steps:

[0126] The data analysis module screens standard information of the target drug liquid from a pre-stored drug liquid information database according to identification information of the target drug liquid, and analyzes reaction information of the target drug liquid and the screened standard information of the target drug liquid to obtain an analysis result of the target drug liquid, the analysis result of the target drug liquid including reaction parameters of the target drug liquid, the reaction parameters of the target drug liquid including pH of the target drug liquid and / or osmotic pressure of the target drug liquid.

[0127] The drug liquid result display displays the analysis result of the target drug liquid.

[0128] In the optional embodiment, the drug liquid information database stores standard information of different drug liquids, wherein the standard information of the drug liquid includes a plurality of reaction standard colors of the drug liquid and corresponding pH and osmotic pressure of each reaction standard color. Further, the higher the grade of the drug liquid, the more the number of reaction standard colors.

[0129] In the optional embodiment, the drug liquid result display can be one display module or composed of two display modules, i.e., a first display module and a second display module, wherein each display module can share one display screen or have an independent display screen.

[0130] It can be seen that the optional embodiment can quickly detect accurate drug liquid analysis results such as pH and / or osmotic pressure by automatically comparing the analyzed drug liquid and reagent discoloration reaction curve, color change value, etc. with the standard information of the drug liquid.

[0131] In another optional embodiment, the method further includes the following steps:

[0132] The drug liquid sampling component obtains information of the reagent, the information of the reagent including identification information of the reagent and storage condition of the reagent in a reagent container, the storage condition of the reagent including storage amount of the reagent;

[0133] The drug liquid sampling component determines a target drug liquid amount required for reaction of the target drug liquid and the reagent according to contents included in the detection request and the information of the reagent;

[0134] The drug liquid sampling component controls the control valve of the drug liquid sampling component to open to make the target drug liquid flow from the drug liquid container to the reagent container containing the reagent according to the detection request, including:

[0135] The drug liquid sampling component controls the control valve of the drug liquid sampling component to open to make the target drug liquid flow from the drug liquid container to the reagent container containing the reagent according to the detection request.

[0136] In the optional embodiment, the storage condition of the reagent further includes temperature of the reagent.

[0137] In the optional embodiment, the target drug liquid amount can be measured by volume.

[0138] It can be seen that the optional embodiment can improve the reaction accuracy and reliability with the reagent by first determining the required amount of reagent for the reagent reaction, and controlling the reagent flow into the reagent container and the reagent reaction corresponding to the reagent amount, thereby facilitating the acquisition of accurate reaction images, and further facilitating the improvement of the accuracy of the reagent reaction information; and by combining and analyzing the identification information of the reagent and the storage condition of the reagent in the reagent container, the determination accuracy and reliability of the required amount of reagent for the reagent reaction can be improved.

[0139] In yet another optional embodiment, the method can further include the following steps:

[0140] When the type of the reagent is a liquid type, the data analysis module analyzes the influence degree of the speed of the target reagent flowing into the reagent container on the reaction information of the target reagent and the reagent before the storage amount of the target reagent in the reagent container reaches the target reagent amount according to the content included in the detection request and the information of the reagent;

[0141] The data analysis module determines whether the influence degree is greater than or equal to the determined influence degree threshold, and when the result is determined to be yes, determines the target speed required for the target reagent to flow into the reagent container according to the influence degree and the storage amount of the target reagent in the reagent container;

[0142] The reagent sampling component generates the control parameter of the control valve according to the target speed and the pressure of the control valve of the target reagent container, and the control parameter of the control valve includes the opening size of the control valve;

[0143] The reagent sampling component controls the opening of the control valve of the reagent sampling component to make the target reagent flow from the reagent container to the reagent container containing the reagent in the target reagent amount, including:

[0144] The reagent sampling component controls the opening of the control valve of the reagent sampling component according to the control parameter of the control valve to make the target reagent flow from the reagent container to the reagent container containing the reagent in the target reagent amount.

[0145] In the optional embodiment, optionally, when the influence degree is determined to be less than the influence degree threshold, the operation of controlling the opening of the control valve of the reagent sampling component to make the target reagent flow from the reagent container to the reagent container containing the reagent in the target reagent amount can be triggered.

[0146] It can be seen that the optional embodiment can improve the control accuracy of the liquid medicine flowing into the reagent container by generating the control parameter of the control valve in advance and controlling the liquid medicine to flow into the reagent container based on the control parameter of the control valve, thereby facilitating to improve the reaction accuracy and reliability of the liquid medicine and the reagent. In addition, the accuracy and reliability of the operation of generating the control parameter of the control valve can be improved by generating the control parameter of the control valve when it is determined that the speed of the liquid medicine flowing into the reagent container has a great influence on the reaction of the liquid medicine and the reagent.

[0147] In yet another optional embodiment, before the image processing device collects the reaction image of the target liquid medicine and the reagent, the method can further include the following steps:

[0148] The image processing device corrects the vision of the image processing device.

[0149] The image processing device corrects the vision of the image processing device, including:

[0150] The image processing device identifies the reaction process of each group of sample liquid medicine and the sample reagent corresponding to the group of sample liquid medicine based on the image acquisition module on the image processing device, and obtains the reaction information of each group of sample liquid medicine and the sample reagent corresponding to the group of sample liquid medicine.

[0151] The image processing device establishes the association relationship between the reaction parameter of each group of sample liquid medicine, the reaction information corresponding to the group of sample liquid medicine, and the sample reagent corresponding to the group of sample liquid medicine, and corrects the image acquisition module based on the association relationship corresponding to each group of sample liquid medicine.

[0152] In the optional embodiment, each group of sample liquid medicine is composed of at least one sample liquid medicine, the reaction parameter of each sample liquid medicine in each group of sample liquid medicine is known, and the pH values of each group of sample liquid medicine are different from each other. The reaction information corresponding to each group of sample liquid medicine includes the color corresponding to the pH value of the group of sample liquid medicine and the image corresponding to the pH value of the sample liquid medicine. Further optionally, the sample liquid medicine of the same type, the same concentration and the same temperature can correspond to reagents of different types and / or the same type, different concentrations and / or different temperatures. In this way, by correcting the image acquisition module based on the sample liquid medicine under different conditions and the reagent under different conditions, the correction comprehensiveness and accuracy of the image acquisition module can be improved, so that the image acquisition module is suitable for detection of different liquid medicines.

[0153] The pH value of the sample liquid medicine is exemplified by taking the test paper reagent as an example, as shown in Figure 6 , and Figure 6 is a color change curve of the pH value of the sample liquid medicine disclosed in the embodiment of the application. As Figure 6As shown, the color change curve reflects the reaction of the sample liquid with different pH values and the reagent at the same temperature, wherein the abscissa is the pH value of the sample liquid, and the ordinate is the image of the reaction of the sample liquid and the reagent, wherein the image contains the color change of the test paper corresponding to each pH value, and further includes the pattern change of the test paper.

[0154] It can be seen that the optional embodiment can improve the accuracy and reliability of the image acquisition of the reaction of the liquid and the reagent by correcting the vision of the image processing device first, thereby further improving the analysis accuracy of the color change curve and the color change value of the liquid.

[0155] In another optional embodiment, before the image processing device corrects the vision of the image processing device, the method can further include the following steps:

[0156] The image processing device determines whether the vision of the image processing device needs to be corrected;

[0157] When it is determined that the vision of the image processing device needs to be corrected, the image processing device performs the above-mentioned operation of correcting the vision of the image processing device;

[0158] The image processing device determines whether the vision of the image processing device needs to be corrected, including:

[0159] The image processing device determines whether the image processing device has a corresponding corrected identifier, and when it is determined that there is no corrected identifier, it is determined that the vision of the image processing device needs to be corrected.

[0160] When it is determined that there is a corrected identifier, the image processing device analyzes the influence level of the liquid on the user according to the information of the liquid and the information of the user, and determines whether the influence level is greater than or equal to the determined influence level threshold; when the result is determined to be yes, it is determined that the vision of the image processing device needs to be corrected.

[0161] It should be noted that the related description of the information of the liquid and the information of the user is described above, and will not be repeated here.

[0162] It can be seen that the optional embodiment can enrich the way of determining the correction of the vision of the image processing device by providing that the vision of the image processing device needs to be corrected when it is determined that the image processing device has a corrected identifier, or even if there is a corrected identifier, but when it is determined that the liquid has a greater influence on the user, thereby improving the determination possibility of the correction of the vision of the image processing device, thereby facilitating the accuracy and efficiency of adjusting the vision of the image processing device.

[0163] In another optional embodiment, the water-blocking and air-permeable filter is optionally present in the reagent container, and before the image processing device collects the reaction image of the target reagent and the reagent, the method can further include the following steps:

[0164] When the target reagent enters the reagent container, the reagent sampling component collects the air condition in the reagent container in real time, and according to the collected air condition, the information of the target reagent and the information of the reagent, judges whether the air in the reagent container will have an adverse effect on the reaction of the target reagent and the reagent.

[0165] When it is judged that an adverse effect occurs, the reagent sampling component generates an exhaust control parameter according to the collected air condition, and controls the exhaust component (such as a water-blocking and air-permeable filter, or a combination of a water-blocking and air-permeable filter and other components) corresponding to the reagent container to exhaust the air in the reagent container according to the exhaust control parameter, and triggers the image processing device to perform the above-mentioned operation of collecting the reaction image of the target reagent and the reagent.

[0166] In the optional embodiment, the air condition in the reagent container includes the air pressure and / or the components of the air in the reagent container.

[0167] In the optional embodiment, the adverse effect includes the adverse effect of the pH of the air on the reaction of the target reagent and the reagent, and the adverse effect of the components such as carbon dioxide and / or nitrogen in the air on the reaction of the target reagent and the reagent. The adverse effect is used to represent the reduction of the detection accuracy of the reaction of the reagent and the reagent.

[0168] It can be seen that, after the reagent enters the reagent container, the optional embodiment can reduce the adverse effect of the air pressure and / or the components of the air on the reaction of the reagent and the reagent by exhausting the air in the reagent container, and can improve the accuracy and reliability of the subsequent operation of collecting the reaction image of the reagent and the reagent, thereby further improving the analysis accuracy and reliability of the analysis result of the reagent.

[0169] Embodiment Two

[0170] Please refer to Figure 2 , Figure 2 is another flowchart of the intelligent detection method of the reagent disclosed by the embodiment of the present application. Among them, Figure 2 The method described can be applied to an intelligent detection system. As Figure 2 shown, the intelligent detection method of the reagent can include the following operations:

[0171] 201, the reagent detection module detects the detection request triggered by the user for the target reagent, and the detection request is used to request to detect the reaction information of the target reagent.

[0172] Optionally, the detection request comprises identification information of the target liquid medicine. Further optionally, the detection request further comprises a use purpose of the target liquid medicine.

[0173] 202. The liquid medicine sampling component controls a control valve of the liquid medicine sampling component to open according to the detection request, so that the target liquid medicine flows from the liquid medicine container to a reagent container containing a reagent for reacting with the target liquid medicine.

[0174] In the embodiment of the present application, the type of the reagent includes a solid type or a liquid type, and the type of the test paper includes a test paper type or a non-test paper type.

[0175] 203. The image processing device acquires a reaction image of the target liquid medicine and the reagent.

[0176] 204. The data analysis module analyzes the reaction image to obtain reaction information of the target liquid medicine.

[0177] 205. The data analysis module screens standard information of the target liquid medicine from a pre-stored liquid medicine information database according to the identification information of the target liquid medicine, and analyzes the reaction information of the target liquid medicine and the screened standard information of the target liquid medicine to obtain an analysis result of the target liquid medicine, wherein the analysis result of the target liquid medicine comprises reaction parameters of the target liquid medicine, and the reaction parameters of the target liquid medicine include pH value and / or osmotic pressure of the target liquid medicine.

[0178] 206. The liquid medicine result display displays the analysis result of the target liquid medicine.

[0179] 207. The data analysis module analyzes the analysis result of the target liquid medicine and all medicinal parameters of the pre-stored liquid medicine to obtain a medicinal parameter analysis result of the target liquid medicine.

[0180] 208. When the medicinal parameter analysis result of the target liquid medicine is used to indicate that the analysis result of the target liquid medicine is a certain medicinal parameter in all medicinal parameters of the target liquid medicine, the data analysis module obtains a use suggestion of the target liquid medicine according to the medicinal parameter analysis result.

[0181] 209. The liquid medicine result display displays the use suggestion of the target liquid medicine and the analysis result of the target liquid medicine.

[0182] 210. When the medicinal parameter analysis result of the target liquid medicine is used to indicate that the analysis result of the target liquid medicine is not a certain medicinal parameter in all medicinal parameters of the target liquid medicine, the data analysis module determines a medicinal adjustment suggestion of the target liquid medicine according to the medicinal parameter analysis result and the medicinal parameter analysis result of the target liquid medicine.

[0183] 211. The liquid medicine result display displays the medicinal adjustment suggestion of the target liquid medicine.

[0184] When the analysis result of the medicinal parameter of the target medicinal liquid is used to indicate that the analysis result of the target medicinal liquid is not a certain medicinal parameter in all medicinal parameters of the target medicinal liquid, the first display module of the medicinal liquid result display is used to display the analysis result of the target medicinal liquid, and the second display module is used to display the medicinal adjustment suggestion of the target medicinal liquid.

[0185] For example, the pH of the sodium chloride injection produced by the A factory is 5, and the range specified in the pharmacopoeia is 4-6. Under the pharmacopoeia specification, this drug is qualified. If an acidic medicinal liquid is added, the pH may decrease sharply to below 4. Under the prior art scheme, it is impossible to quickly and efficiently understand the pH quantitative index of the configured medicinal liquid in the clinic. However, the present scheme can give the use adjustment suggestion of the medicinal liquid after detecting that the pH is below 4, so as to effectively neutralize the medicinal liquid to make the final medicinal liquid meet the safety requirements specified in the pharmacopoeia, thereby improving the training efficiency and accuracy of medicinal liquid detection.

[0186] In the embodiment of the present application, for the related description of steps 201-206, please refer to the detailed description of steps 101-104 and other related embodiments in Embodiment One. The present embodiment will not be repeated here.

[0187] It can be seen that, when the reaction information of the medicinal liquid to be detected is detected, the present embodiment automatically flows the medicinal liquid into the reagent container to react with the reagent, automatically collects the reaction image of the target medicinal liquid and the reagent through the image processing device, and analyzes the image through the data analysis module, so as to quickly determine the reaction information of the medicinal liquid, such as the discoloration curve and color change value of the reagent, which is conducive to quickly determining the accurate analysis result of the medicinal liquid, such as the pH and / or osmotic pressure, and is conducive to the research and development of the intelligent medicinal liquid detection system. When the present scheme is applied in training, it is also conducive to improving the training accuracy and efficiency of medicinal liquid dispensing. In addition, after analyzing the pH and / or osmotic pressure and other parameters of the medicinal liquid, the present embodiment further compares the parameters with the stored medicinal parameters, and when the required parameter range is compared, directly outputs the use suggestion of the medicinal liquid through the display, or when the parameter range is not compared, directly outputs the medicinal adjustment suggestion, which is conducive to improving the training accuracy and reliability of medicinal liquid detection, and is conducive to improving the research and development accuracy and reliability of the intelligent medicinal liquid detection system.

[0188] In an optional embodiment, the method can further include the following steps:

[0189] The image processing device queries the spectral type of the current light source, and the spectral type of the current light source is a visible spectral type or an ultraviolet spectral type or other spectral type;

[0190] The data analysis module acquires the type of the reagent, and determines whether the spectral type of the current light source matches the type of the reagent;

[0191] When it is determined that the matching is not matched, the data analysis module determines a target light source type matched with the type of the reagent;

[0192] The image processing device switches the current light source to a light source matched with the target light source type.

[0193] In the optional embodiment, when it is determined that the spectral type of the current light source is matched with the type of the reagent, step 103 is directly executed.

[0194] It can be seen that, in the optional embodiment, the spectral type of the current light source of the image processing device is compared with the type of the reagent, and when the matching is not matched, the light source is automatically switched to a light source matched with the type of the reagent, so as to reduce the influence of the light source on the reaction of the reagent and the reagent, and facilitate to improve the acquisition accuracy of the reaction image of the reagent and the reagent, thereby facilitating to improve the analysis accuracy and reliability of the reagent.

[0195] In another optional embodiment, the data analysis module determines whether the spectral type of the current light source is matched with the type of the reagent, comprising:

[0196] When the type of the reagent is a liquid type, the data analysis module determines whether the spectral type of the current light source is an ultraviolet spectral type;

[0197] When it is determined that the spectral type is not an ultraviolet spectral type, the data analysis module determines that the spectral type of the current light source is not matched with the type of the reagent; or,

[0198] When the type of the reagent is a test paper type, the data analysis module determines whether the spectral type of the current light source is a visible spectral type;

[0199] When it is determined that the spectral type is a visible spectral type, the data analysis module determines a detection speed required for detecting the reaction information of the target reagent according to the content included in the detection request, and determines whether the detection speed is greater than or equal to the determined detection speed threshold value, and when the determination result is yes, it is determined that the spectral type of the current light source is not matched with the type of the reagent;

[0200] When the type of the reagent is a liquid type, the target light source type matched with the type of the reagent is an ultraviolet spectral type;

[0201] When the type of the reagent is a test paper type, the target light source type matched with the type of the reagent is a visible spectral type;

[0202] When the type of the reagent is a test paper type and the detection speed of the target reagent is greater than or equal to the detection speed threshold value, the target light source type matched with the type of the reagent is an ultraviolet spectral type.

[0203] It can be seen that the optional embodiment can improve the determination accuracy of the spectrum type, improve the determination accuracy and reliability of the light source, and further reduce the influence of the non-corresponding spectrum on the reaction image of the reagent and the reagent, thereby improving the acquisition accuracy and reliability of the reaction image of the reagent and the reagent.

[0204] In yet another optional embodiment, the method can further include the following steps:

[0205] The image processing device acquires the ambient light condition of the current environment, wherein the ambient light condition of the current environment includes one or more of ambient light brightness, ambient light intensity, and ambient light wavelength;

[0206] The image processing device switches the current light source to a light source matched with the target light source type, including:

[0207] The image processing device switches the current light source to a light source matched with the target light source type according to the ambient light condition of the current environment, to emit a light source with a wavelength matched with the target reagent and the reagent.

[0208] It can be seen that the optional embodiment can improve the accuracy and reliability of switching to a matched light source by switching the light source in combination with the ambient light condition of the current environment, thereby further improving the reaction accuracy of the reagent and the reagent, and further improving the analysis accuracy and reliability of the reagent.

[0209] Embodiment three

[0210] Please refer to Figure 3 , Figure 3 is a structural schematic diagram of an intelligent detection system for reagent disclosed by the embodiment of the present application. As shown in Figure 3 , the intelligent detection system for reagent can include:

[0211] The reagent detection module 301 is configured to detect a detection request triggered by a user for a target reagent, and the detection request is configured to request to detect reaction information of the target reagent;

[0212] The reagent sampling component 302 is configured to control the control valve of the reagent sampling component to open according to the detection request, so that the target reagent flows from the reagent container to the reagent container containing the reagent, and the reagent is configured to react with the target reagent;

[0213] The image processing device 303 is configured to acquire a reaction image of the target reagent and the reagent;

[0214] The data analysis module 304 is configured to analyze the reaction image to obtain the reaction information of the target reagent.

[0215] It can be seen that the implementation Figure 3 The described intelligent detection system can automatically flow the drug liquid into the reagent container to react with the reagent when detecting the reaction information of the drug liquid, and automatically collect the reaction image of the target drug liquid and the reagent through the image processing device, and analyze the image through the data analysis module, so as to quickly determine the reaction information of the drug liquid, such as the color change curve of the reagent and the color change value, etc., which is beneficial to quickly determine the accurate analysis result of the drug liquid, such as the pH value and / or the osmotic pressure, etc.; and is conducive to the research and development of the intelligent detection system of the drug liquid, and when the scheme is applied in training, it is also beneficial to improve the training accuracy and efficiency of the drug liquid dispensing.

[0216] In an optional embodiment, the detection request includes identification information of the target drug liquid; and as Figure 3 As shown, the data analysis module 304 is also used to, after analyzing the reaction image to obtain the reaction information of the target drug liquid, screen the standard information of the target drug liquid from the pre-stored drug liquid information database according to the identification information of the target drug liquid, and analyze the reaction information of the target drug liquid and the screened standard information of the target drug liquid to obtain the analysis result of the target drug liquid, the analysis result of the target drug liquid including the reaction parameters of the target drug liquid, the reaction parameters of the target drug liquid including the pH value of the target drug liquid and / or the osmotic pressure of the target drug liquid;

[0217] And, as Figure 4 shown, the intelligent detection system includes:

[0218] The drug liquid result display 305 is used to display the analysis result of the target drug liquid.

[0219] It can be seen that the implementation Figure 4 The described intelligent detection system can compare the analyzed color change reaction curve, color change value, etc. of the drug liquid and the standard information of the drug liquid, and quickly detect the accurate analysis result of the drug liquid, such as the pH value and / or the osmotic pressure, etc.

[0220] In another optional embodiment, the detection request further includes the use purpose of the target drug liquid; and, as Figure 4 shown, the drug liquid sampling component 302 is also used to obtain the information of the reagent, the information of the reagent including the identification information of the reagent, the storage condition of the reagent in the reagent container, and the storage condition of the reagent including the storage amount of the reagent;

[0221] The drug liquid sampling component 302 is also used to determine the target drug liquid amount required for the reaction of the target drug liquid and the reagent according to the content included in the detection request and the information of the reagent;

[0222] The control valve of the liquid sampling component 302 is controlled to open, so that the target liquid flows from the liquid container to the reagent container containing the reagent in a manner that the target liquid quantity reaches the reagent container.

[0223] The control valve of the liquid sampling component 302 is controlled to open, so that the target liquid flows from the liquid container to the reagent container containing the reagent in a manner that the target liquid quantity reaches the reagent container.

[0224] It can be seen that the implementation Figure 4 The intelligent detection system described can also improve the accuracy and reliability of the reaction of the liquid and the reagent by first determining the required liquid quantity for the reaction of the liquid and the reagent, and controlling the liquid corresponding to the liquid quantity to flow into the reagent container to react with the reagent, thereby facilitating the acquisition of accurate reaction images, and further facilitating the improvement of the accuracy of the reaction information of the liquid. The identification information of the liquid and the like is combined and analyzed with the identification information of the reagent and the storage condition of the reagent in the reagent container, thereby improving the determination accuracy and reliability of the required liquid quantity for the reaction of the liquid and the reagent.

[0225] In another optional embodiment, the type of reagent includes a solid type or a liquid type, and the solid type includes a test paper type.

[0226] The data analysis module 304 is also configured to, when the type of reagent is a liquid type, analyze the influence degree of the speed of the target liquid flowing into the reagent container on the reaction information of the target liquid and the reagent before the storage quantity of the target liquid in the reagent container reaches the target liquid quantity, according to the content included in the detection request and the information of the reagent.

[0227] The data analysis module 304 is also configured to determine whether the influence degree is greater than or equal to the determined influence degree threshold, and when the result of the determination is yes, determine the target speed required for the target liquid to flow into the reagent container according to the influence degree and the storage quantity of the target liquid in the reagent container.

[0228] The liquid sampling component 302 is also configured to generate a control parameter of the control valve according to the target speed and the pressure of the control valve of the target liquid container, and the control parameter of the control valve includes the opening size of the control valve.

[0229] The control valve of the liquid sampling component 302 is controlled to open, so that the target liquid flows from the liquid container to the reagent container containing the reagent in a manner that the target liquid quantity reaches the reagent container.

[0230] The control valve of the liquid sampling component 302 is controlled to open, so that the target liquid flows from the liquid container to the reagent container containing the reagent in a manner that the target liquid quantity reaches the reagent container.

[0231] It can be seen that the implementation Figure 4The intelligent detection system described can also improve the control accuracy of the flow of the liquid medicine into the reagent container by first generating the control parameter of the control valve and controlling the flow of the liquid medicine into the reagent container based on the control parameter of the control valve, thereby facilitating the improvement of the reaction accuracy and reliability of the liquid medicine and the reagent. In addition, the generation of the control parameter of the control valve can be performed when it is determined that the speed of the flow of the liquid medicine into the reagent container has a great influence on the reaction of the liquid medicine and the reagent, thereby improving the accuracy and reliability of the generation operation of the control parameter of the control valve.

[0232] In yet another optional embodiment, the image processing device 303 is also configured to correct the vision of the image processing device before collecting the reaction image of the target liquid medicine and the reagent.

[0233] The manner in which the image processing device 303 corrects the vision of the image processing device specifically includes:

[0234] The reaction information of each group of sample liquid medicine and the sample reagent corresponding to the group of sample liquid medicine is obtained by identifying the reaction process of each group of sample liquid medicine and the sample reagent corresponding to the group of sample liquid medicine based on the image acquisition module on the image processing device, and the correlation between the reaction parameter of each group of sample liquid medicine, the reaction information corresponding to the group of sample liquid medicine, and the sample reagent corresponding to the group of sample liquid medicine is established, and the image acquisition module is corrected based on the correlation corresponding to each group of sample liquid medicine.

[0235] In this optional embodiment, each group of sample liquid medicine is composed of at least one sample liquid medicine, the reaction parameter of each sample liquid medicine in each group of sample liquid medicine is known, and the pH values of each group of sample liquid medicine are different from each other. The reaction information corresponding to each group of sample liquid medicine includes the color corresponding to the pH value of the group of sample liquid medicine and the image corresponding to the pH value of the sample liquid medicine. Further optionally, sample liquid medicines of the same type, the same concentration, and the same temperature can correspond to reagents of different types and / or the same type, different concentrations, and / or different temperatures. In this way, the correction comprehensiveness and accuracy of the image acquisition module can be improved by correcting the image acquisition module based on sample liquid medicines under different conditions and reagents under different conditions, so as to facilitate the detection of different liquid medicines by the image acquisition module.

[0236] It can be seen that the implementation Figure 4 The intelligent detection system described can also improve the control accuracy of the flow of the liquid medicine into the reagent container by first generating the control parameter of the control valve and controlling the flow of the liquid medicine into the reagent container based on the control parameter of the control valve, thereby facilitating the improvement of the reaction accuracy and reliability of the liquid medicine and the reagent. In addition, the generation of the control parameter of the control valve can be performed when it is determined that the speed of the flow of the liquid medicine into the reagent container has a great influence on the reaction of the liquid medicine and the reagent, thereby improving the accuracy and reliability of the generation operation of the control parameter of the control valve.

[0237] In yet another optional embodiment, as Figure 4As shown, the data analysis module 304 is further configured to, after obtaining the analysis result of the target drug liquid by analyzing the reaction information of the target drug liquid and the information of the screened target drug liquid, analyze the analysis result of the target drug liquid and all the medicinal parameters of the drug liquid stored in advance to obtain a medicinal parameter analysis result of the target drug liquid.

[0238] The data analysis module 304 is further configured to, when the medicinal parameter analysis result of the target drug liquid indicates that the analysis result of the target drug liquid is a certain medicinal parameter among all the medicinal parameters of the target drug liquid, obtain a use suggestion of the target drug liquid according to the medicinal parameter analysis result.

[0239] The drug liquid result display 305 is configured to display the use suggestion of the target drug liquid and the analysis result of the target drug liquid.

[0240] The data analysis module 304 is further configured to, when the medicinal parameter analysis result of the target drug liquid indicates that the analysis result of the target drug liquid is not a certain medicinal parameter among all the medicinal parameters of the target drug liquid, determine a medicinal adjustment suggestion of the target drug liquid according to the medicinal parameter analysis result and the medicinal parameter analysis result of the target drug liquid.

[0241] The drug liquid result display 305 is further configured to display the medicinal adjustment suggestion of the target drug liquid.

[0242] It can be seen that, by implementing the above technical solutions, Figure 4 The described intelligent detection system can further compare the obtained parameters such as the pH value and / or the osmotic pressure of the drug liquid with the stored medicinal parameters, and when the required parameter range is compared, directly output the use suggestion of the drug liquid through the display, or when the required parameter range is not compared, directly output the medicinal adjustment suggestion, which is beneficial to improve the training accuracy and reliability of the drug liquid detection, and is beneficial to improve the research and development accuracy and reliability of the intelligent detection system of the drug liquid.

[0243] In another optional embodiment, as shown in Figure 4 The image processing device 303 is further configured to query the spectral type of the current light source, and the spectral type of the current light source is a visible spectral type or an ultraviolet spectral type.

[0244] The data analysis module 304 is further configured to obtain the type of the reagent, and determine whether the spectral type of the current light source matches the type of the reagent, and when it is determined that the spectral type of the current light source does not match the type of the reagent, determine a target light source type that matches the type of the reagent.

[0245] The image processing device 303 is further configured to switch the current light source to a light source that matches the target light source type.

[0246] It can be seen that, by implementing the above technical solutions, Figure 4The intelligent detection system described can also automatically switch the light source to a light source matching the type of reagent by comparing the spectral type of the current light source of the image processing device with the type of reagent and, when there is no match, so as to reduce the influence of the light source on the reaction of the drug liquid with the reagent and facilitate the improvement of the collection accuracy of the reaction image of the drug liquid with the reagent, thereby facilitating the improvement of the analysis accuracy and reliability of the drug liquid.

[0247] In yet another optional embodiment, the manner in which the data analysis module 304 determines whether the spectral type of the current light source matches the type of reagent specifically includes:

[0248] When the type of reagent is a liquid type, it is determined whether the spectral type of the current light source is an ultraviolet spectral type;

[0249] When it is determined that it is not an ultraviolet spectral type, it is determined that the spectral type of the current light source does not match the type of reagent; or,

[0250] When the type of reagent is a test paper type, it is determined whether the spectral type of the current light source is a visible spectral type;

[0251] When it is determined that it is a visible spectral type, the detection speed required for the reaction information of the target drug liquid according to the content included in the detection request is determined, and it is determined whether the detection speed is greater than or equal to the determined detection speed threshold, and when the determination result is yes, it is determined that the spectral type of the current light source does not match the type of reagent;

[0252] When the type of reagent is a liquid type, the target light source type matching the type of reagent is an ultraviolet spectral type;

[0253] When the type of reagent is a test paper type, the target light source type matching the type of reagent is a visible spectral type;

[0254] When the type of reagent is a test paper type and the detection speed of the target drug liquid is greater than or equal to the detection speed threshold, the target light source type matching the type of reagent is an ultraviolet spectral type.

[0255] It can be seen that the implementation Figure 4 The intelligent detection system described can also determine the corresponding spectral type required according to the reagent of the test paper type or the reagent of the liquid type and the detection speed required by the drug liquid, which can improve the determination accuracy of the spectral type, thereby improving the determination accuracy and reliability of the light source, and further reducing the influence of non-corresponding spectra on the reaction image of the drug liquid with the reagent, thereby improving the collection accuracy and reliability of the reaction image of the drug liquid with the reagent.

[0256] In yet another optional embodiment, optionally, there is a water-blocking and air-permeable filter film in the reagent container, and, for example, Figure 5As shown, the liquid sampling component 302 is also configured to collect the air condition in the reagent container in real time before the image processing device 303 collects the reaction image of the target liquid and the reagent, and after the target liquid enters the reagent container, and determine whether the air in the reagent container will have an adverse effect on the reaction of the target liquid and the reagent according to the collected air condition, the information of the target liquid and the information of the reagent.

[0257] The liquid sampling component 302 is also configured to generate an exhaust control parameter according to the collected air condition when it is determined that an adverse effect occurs, and control the exhaust component (such as a water-blocking and air-permeable filter membrane, or a combination of a water-blocking and air-permeable filter membrane and other components) corresponding to the reagent container to exhaust the air in the reagent container according to the exhaust control parameter, and trigger the image processing device 303 to perform the above-mentioned operation of collecting the reaction image of the target liquid and the reagent.

[0258] It can be seen that the implementation of the above-mentioned intelligent detection system can reduce the adverse effect of the air pressure and / or the air composition on the reaction of the liquid and the reagent, and can improve the accuracy and reliability of the subsequent operation of collecting the reaction image of the liquid and the reagent, thereby further improving the analysis accuracy and reliability of the analysis result of the liquid. Figure 5 The intelligent detection system described above can also reduce the adverse effect of the air pressure and / or the air composition on the reaction of the liquid and the reagent by exhausting the air in the reagent container after the liquid enters the reagent container, and can improve the accuracy and reliability of the subsequent operation of collecting the reaction image of the liquid and the reagent, thereby further improving the analysis accuracy and reliability of the analysis result of the liquid.

[0259] Embodiment Four

[0260] Please refer to Figure 5 , ​ is another structure diagram of the intelligent detection system of the liquid disclosed by the embodiment of the present application. As shown in the figure, ​ The intelligent detection system of the liquid can include:

[0261] a memory 401 storing executable program codes;

[0262] a processor 402 coupled with the memory 401;

[0263] Further, it can also include an input interface 403 and an output interface 404 coupled with the processor 402;

[0264] The processor 402 calls the executable program codes stored in the memory 402 to execute part or all of the steps of the intelligent detection method of the liquid disclosed in the embodiment one or the embodiment two.

[0265] Embodiment Five

[0266] The embodiment of the present application discloses a computer storage medium, which stores computer instructions, and when the computer instructions are invoked, part or all of the steps of the intelligent detection method of the chemical liquid disclosed in the embodiment one or the embodiment two are executed.

[0267] The above-described intelligent detection system embodiment is only illustrative, wherein the modules described as separate components can or can not be physically separated, and the components displayed as modules can or can not be physical modules, i.e., can be located in one place or can be distributed to multiple network modules. Part or all of the modules can be selected to achieve the purpose of the embodiment scheme according to actual needs. Those skilled in the art can understand and implement without creative labor.

[0268] Through the specific description of the above embodiments, those skilled in the art can clearly understand that each embodiment can be realized by means of software and the necessary general hardware platform, and of course, can also be realized by hardware. Based on such understanding, the above technical solutions can be embodied in the form of a software product, and the computer software product can be stored in a computer readable storage medium, including a read-only memory (ROM), a random access memory (RAM), a programmable read-only memory (PROM), an erasable programmable read-only memory (EPROM), a one-time programmable read-only memory (OTPROM), an electrically erasable programmable read-only memory (EEPROM), a compact disc read-only memory (CD-ROM) or other optical disk storage, a magnetic disk storage, a magnetic tape storage, or any other computer readable medium that can be used to carry or store data.

[0269] It should be finally pointed out that: the disclosed intelligent detection method and system of the drug solution disclosed in the embodiments of the present application are only the preferred embodiments of the present application, and are only used to illustrate the technical solutions of the present application, but not to limit them; although the present application has been described in detail with reference to the foregoing embodiments, those skilled in the art should understand that; it can still modify the technical solutions recorded in the foregoing embodiments, or make equivalent replacement for part of the technical features; and these modifications or replacements do not make the essence of the corresponding technical solutions deviate from the spirit and scope of the technical solutions of the embodiments of the present application.

Claims

1. An intelligent detection method of a chemical liquid, characterized by, The method comprises: The liquid medicine detection module detects a detection request triggered by a user for a target liquid medicine, and the detection request is used to request to detect reaction information of the target liquid medicine; The liquid medicine sampling component controls a control valve of the liquid medicine sampling component to open according to the detection request, so that the target liquid medicine flows from a liquid medicine container to a reagent container containing a reagent used for reaction with the target liquid medicine; An image processing device collects a reaction image of the target liquid medicine and the reagent; A data analysis module analyzes the reaction image to obtain reaction information of the target liquid medicine; Before the image processing device collects the reaction image of the target liquid medicine and the reagent, the method further comprises: The image processing device judges whether the vision of the image processing device needs to be corrected; When it is judged that the vision of the image processing device needs to be corrected, the image processing device corrects the vision of the image processing device; The image processing device judges whether the vision of the image processing device needs to be corrected, comprising: When it is judged that there is no corrected identification, it is determined that the vision of the image processing device needs to be corrected; When it is judged that there is a corrected identification, the image processing device analyzes an influence level of the target liquid medicine on a user according to information of the target liquid medicine and information of the user, and judges whether the influence level is greater than or equal to a determined influence level threshold; when the result is yes, it is determined that the vision of the image processing device needs to be corrected, wherein the information of the user includes disease conditions, gender and / or age; The image processing device corrects the vision of the image processing device, comprising: The image processing device identifies a reaction process of each group of sample liquid medicine and sample reagent corresponding to the group of sample liquid medicine in a plurality of groups of sample liquid medicine based on an image collection module on the image processing device, to obtain reaction information of each group of sample liquid medicine and sample reagent corresponding to the group of sample liquid medicine, wherein each group of sample liquid medicine is composed of at least one sample liquid medicine, the reaction parameters of each sample liquid medicine in each group of sample liquid medicine are known, the pH values corresponding to each group of sample liquid medicine are different from each other, the reaction information corresponding to each group of sample liquid medicine includes a color corresponding to the pH value of the group of sample liquid medicine and an image corresponding to the pH value of the sample liquid medicine, and sample liquid medicines of the same type, same concentration and same temperature correspond to reagents of different types and / or the same type, different concentrations and / or different temperatures; The image processing device establishes an association relationship between the reaction parameters of each group of sample liquid medicine, the reaction information corresponding to the group of sample liquid medicine and the sample reagent corresponding to the group of sample liquid medicine, and corrects the image collection module based on the association relationship corresponding to each group of sample liquid medicine.

2. The method of claim 1, wherein the method is characterized by, The detection request includes identification information of the target liquid medicine; After the data analysis module analyzes the reaction image to obtain the reaction information of the target liquid medicine, the method further comprises: The data analysis module screens standard information of the target chemical liquid from a pre-stored chemical liquid information database according to identification information of the target chemical liquid, and analyzes reaction information of the target chemical liquid and the screened standard information of the target chemical liquid to obtain an analysis result of the target chemical liquid, the analysis result of the target chemical liquid including reaction parameters of the target chemical liquid, the reaction parameters of the target chemical liquid including pH of the target chemical liquid; The chemical liquid result display displays the analysis result of the target chemical liquid.

3. The method of claim 2, wherein the step of detecting the liquid is performed by using a camera. The detection request further includes a use purpose of the target chemical liquid; And the method further includes: The chemical liquid sampling component obtains information of the reagent, the information of the reagent including identification information of the reagent and storage condition of the reagent in the reagent container, the storage condition of the reagent including storage amount of the reagent; The chemical liquid sampling component determines a target chemical liquid amount required for the reaction of the target chemical liquid and the reagent according to contents included in the detection request and the information of the reagent; The chemical liquid sampling component controls the control valve of the chemical liquid sampling component to open to make the target chemical liquid flow from the chemical liquid container to the reagent container containing the reagent, including: The chemical liquid sampling component controls the control valve of the chemical liquid sampling component to open to make the target chemical liquid flow from the chemical liquid container to the reagent container containing the reagent.

4. The method of claim 3, wherein the step of detecting the liquid is performed by using a camera. The type of the reagent includes a solid type or a liquid type, and the solid type includes a test paper type; The method further includes: When the type of the reagent is the liquid type, the data analysis module analyzes an influence degree of a speed of the target chemical liquid flowing to the reagent container before the storage amount of the target chemical liquid in the reagent container reaches the target chemical liquid amount on the reaction information of the target chemical liquid and the reagent according to the contents included in the detection request and the information of the reagent; The data analysis module determines whether the influence degree is greater than or equal to a determined influence degree threshold value, and determines a target speed of the target chemical liquid flowing to the reagent container according to the influence degree and the storage amount of the target chemical liquid in the reagent container when the determination result is yes; The chemical liquid sampling component generates control parameters of the control valve according to the target speed and pressure of the control valve of the chemical liquid container, the control parameters of the control valve including an opening size of the control valve; The chemical liquid sampling component controls the control valve of the chemical liquid sampling component to open to make the target chemical liquid flow from the chemical liquid container to the reagent container containing the reagent, including: The chemical liquid sampling component controls the control valve of the chemical liquid sampling component to open according to the control parameters of the control valve to make the target chemical liquid flow from the chemical liquid container to the reagent container containing the reagent.

5. The method of claim 2-4, wherein, The method further includes: The data analysis module analyzes the analysis result of the target drug liquid with all the drug parameters of the target drug liquid stored in advance to obtain a drug parameter analysis result of the target drug liquid; When the drug parameter analysis result of the target drug liquid indicates that the analysis result of the target drug liquid is a certain drug parameter among all the drug parameters of the target drug liquid, the data analysis module obtains a use suggestion of the target drug liquid according to the drug parameter analysis result; A drug liquid result display displays the use suggestion of the target drug liquid and the analysis result of the target drug liquid; When the drug parameter analysis result of the target drug liquid indicates that the analysis result of the target drug liquid is not a certain drug parameter among all the drug parameters of the target drug liquid, the data analysis module determines a drug adjustment suggestion of the target drug liquid according to the drug parameter analysis result and the drug parameter analysis result of the target drug liquid; The drug liquid result display displays the drug adjustment suggestion of the target drug liquid.

6. The intelligent medical liquid detection method according to claim 5, wherein The method further comprises: The image processing device queries a spectrum type of a current light source, and the spectrum type of the current light source is a visible spectrum type or an ultraviolet spectrum type; The data analysis module obtains a type of the reagent and determines whether the spectrum type of the current light source matches the type of the reagent; When it is determined that the spectrum type of the current light source does not match the type of the reagent, the data analysis module determines a target light source type that matches the type of the reagent; The image processing device switches the current light source to a light source that matches the target light source type.

7. The method of claim 6, wherein the method is characterized by, The data analysis module determines whether the spectrum type of the current light source matches the type of the reagent, comprising: When the type of the reagent is a liquid type, the data analysis module determines whether the spectrum type of the current light source is an ultraviolet spectrum type; When it is determined that the spectrum type of the current light source is not the ultraviolet spectrum type, the data analysis module determines that the spectrum type of the current light source does not match the type of the reagent; or When the type of the reagent is a test paper type, the data analysis module determines whether the spectrum type of the current light source is a visible spectrum type; When it is determined that the spectrum type of the current light source is the visible spectrum type, the data analysis module determines a detection speed required for reaction information of the target drug liquid according to the content included in the detection request, and determines whether the detection speed is greater than or equal to a determined detection speed threshold value, and when the determination result is yes, it is determined that the spectrum type of the current light source does not match the type of the reagent; When the type of the reagent is a liquid type, the target light source type that matches the type of the reagent is the ultraviolet spectrum type; When the type of the reagent is a test paper type, the target light source type that matches the type of the reagent is the visible spectrum type; When the type of the reagent is a test paper type and the detection speed of the target drug liquid is greater than or equal to the detection speed threshold value, the target light source type that matches the type of the reagent is the ultraviolet spectrum type.

8. An intelligent detection system for a medical liquid, characterized by, The intelligent detection system is used to execute the intelligent detection method of the medical fluid as claimed in any one of claims 1-7, and the intelligent detection system comprises: a medical fluid detection module, configured to detect a detection request triggered by a user for a target medical fluid, the detection request being used to request detection of reaction information of the target medical fluid; a medical fluid sampling component, configured to control a control valve of the medical fluid sampling component to open according to the detection request, so as to make the target medical fluid flow from a medical fluid container to a reagent container containing a reagent, the reagent being used to react with the target medical fluid; an image processing device, configured to acquire a reaction image of the target medical fluid and the reagent; a data analysis module, configured to analyze the reaction image to obtain reaction information of the target medical fluid.

9. An intelligent detection system for a medical liquid, characterized by, The intelligent detection system comprises: a memory storing executable program codes; a processor coupled with the memory; the processor invokes the executable program codes stored in the memory to execute the intelligent detection method of the medical fluid as claimed in any one of claims 1-7.

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