Method and system for monitoring failure of medicine bag of traditional Chinese medicine packaging therapeutic apparatus
By designing a Chinese medicine package failure monitoring system for the Chinese medicine package, using high-precision pressure sensors and drug package failure judgment model, the problem of inaccurate monitoring of the existing Chinese medicine package failure is solved, and accurate and real-time monitoring and early warning of the status of the drug package is achieved, and the safety and effectiveness of the treatment are improved.
Patent Information
- Application Number
- CN202411725780.6
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2024-11-28
- Publication Date
- 2025-03-04
- Estimated Expiration
- Not applicable · inactive patent
AI Technical Summary
When monitoring the use of drug packages, the existing traditional Chinese medicine packet therapy device is less intelligent and cannot accurately and in real time reflect the actual status of the drug package, resulting in inaccurate monitoring of the failure of the drug package and affecting the treatment effect.
A Chinese medicine package failure monitoring system was designed, including a drug package initial pressure data acquisition module, a drug package sealing performance analysis matching module, a drug package failure judgment model establishment module, a pressure attenuation trend prediction module and a drug package monitoring result output module. The initial data is collected through high-precision pressure sensors, the sealing performance is evaluated, the drug effect is judged, and the pressure attenuation risk is predicted.
Accurate and real-time monitoring of drug package failure is achieved, and the accuracy of drug package monitoring is improved. Through real-time monitoring and early warning mechanisms, users can help timely replace failed drug packages, ensure the normal use and treatment effect of the treatment device, and strengthen the safety and effectiveness of the treatment.
Smart Images
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Abstract
Description
Technical Field
[0001] The present invention relates to the field of intelligent monitoring technology, and more specifically to a method and system for monitoring failure of medicine packages of a traditional Chinese medicine sealing therapeutic instrument. Background Art
[0002] The Chinese medicine sealing and therapeutic instrument is a therapeutic device that combines traditional Chinese medicine theory with modern scientific and technological means. It utilizes the drug penetration, thermal stimulation and other effects produced by the Chinese medicine bag, combined with the physical effects of physical therapy instruments, to achieve the purpose of treating diseases. The device has multiple functions such as anti-inflammatory, analgesic, and promoting blood circulation. It is suitable for the treatment of cervical spondylosis, periarthritis of the shoulder, arthritis, lumbar disc herniation and other diseases. With the continuous development of Chinese medicine and the improvement of people's demand for health, the Chinese medicine sealing and therapeutic instrument is becoming more and more widely used in medical institutions, health care institutions and families.
[0003] However, in the existing traditional Chinese medicine sealing package therapeutic instruments, the use of medicine packages is monitored by built-in sensors and other methods, but these methods often have a low degree of intelligence and cannot accurately and real-time reflect the actual status of the medicine packages. There is a problem of inaccurate monitoring of medicine package failure, resulting in poor treatment effects or treatment interruptions. Medicine package failure may be due to a variety of reasons. For example, the medicine package may be affected by environmental factors such as temperature and humidity during use, and the sealing performance and efficacy of the medicine package may change. Traditional monitoring methods are difficult to detect these problems in a timely manner. Therefore, it is particularly important to develop a system that can automatically and accurately monitor the failure of medicine packages. Summary of the invention
[0004] In order to overcome the above-mentioned defects of the prior art, the present invention provides a medicine package failure monitoring system for a traditional Chinese medicine sealing therapy instrument to solve the problems existing in the above-mentioned background technology.
[0005] The present invention provides the following technical solutions: a medicine package failure monitoring system for a traditional Chinese medicine sealing treatment instrument, comprising: a medicine package initial pressure data acquisition module, a medicine package sealing performance analysis and matching module, a medicine package failure judgment model establishment module, a pressure decay trend prediction module, and a medicine package monitoring result output module; The medicine package initial pressure data acquisition module acquires and records the initial pressure data inside the medicine package through a high-precision pressure sensor; The medicine package sealing performance analysis and matching module evaluates the medicine package sealing performance based on the initial data of the internal pressure of the medicine package; The drug package failure judgment model establishment module establishes a drug package failure judgment model to judge the efficacy of the drug package when the drug package sealing performance evaluation fails, and outputs the judgment result to the drug package monitoring result output module; The pressure decay trend prediction module, when the evaluation result in the medicine package sealing performance analysis and matching module is that the medicine package sealing performance is qualified, performs pressure decay prediction on the medicine package to determine whether the sealed medicine package has a pressure decay risk, and transmits the judgment result to the medicine package monitoring result output module; The medicine package monitoring result output module outputs the efficacy judgment results of the medicine packages with unqualified packaging sealing performance and the pressure decay risk judgment results of the medicine packages with qualified packaging sealing performance to the human-computer interaction terminal, thereby completing the failure monitoring of the medicine packages.
[0006] Preferably, in the medicine package initial pressure data acquisition module, the initial data of the internal pressure of the medicine package is acquired and recorded as the initial pressure value of the internal pressure of the medicine package by a high-precision pressure sensor.
[0007] Preferably, in the medicine package sealing performance analysis and matching module, the sealing performance of the medicine package packaging is evaluated based on the initial data of the internal pressure of the medicine package packaging: the initial value of the internal pressure of the medicine package packaging is compared with a preset standard pressure evaluation interval; when the initial value of the internal pressure of the medicine package packaging is within the preset standard pressure evaluation interval, the evaluation result is qualified; when the initial value of the internal pressure of the medicine package packaging is not within the preset standard pressure evaluation interval, the evaluation result is unqualified.
[0008] Preferably, in the drug package failure judgment model establishment module, the specific contents of establishing the drug package failure judgment model to judge the efficacy of the drug package are as follows: The thermal expansion analysis of the drug package is carried out using the thermodynamic principle, and the thermal expansion coefficient of the drug package is obtained by combining the initial temperature and temperature change data of the drug package; Establish a drug package failure judgment model, input the thermal expansion coefficient of the drug package into the drug package failure judgment model, analyze the thermal stress of the drug package under temperature cycle, and calculate the drug package failure evaluation index; The efficacy of the medicine package is judged based on the medicine package failure evaluation index. When the medicine package failure evaluation index exceeds a preset failure threshold, the medicine package is judged to be failed; otherwise, the medicine package is judged to be effective.
[0009] Preferably, the specific content of the thermal expansion coefficient of the medicine package obtained by analyzing the initial temperature and temperature change data of the medicine package is: Calculate the initial temperature analysis coefficient of the drug package at the initial temperature. The calculation formula is: ,in represents the initial temperature analysis coefficient of the drug package at the initial temperature, represents the initial analysis constant of the drug package, represents the constant of the drug package at the initial temperature, Indicates the initial temperature of the medicine package; Calculate the temperature change analysis coefficient of the medicine package after the temperature changes. The calculation formula is: ,in It indicates the temperature change analysis coefficient of the medicine package after the temperature changes. Indicates the temperature change analysis constant of the medicine package, It represents the constant of the medicine package after the temperature changes. Indicates the temperature change value of the medicine package; Combined with the change in the volume of the medicine package when the temperature changes, the thermal expansion coefficient of the medicine package is analyzed and the calculation formula is: ,in represents the thermal expansion coefficient of the drug package, It indicates the change in the volume of the medicine package when the temperature changes, and it indicates the volume value of the medicine package at the initial temperature.
[0010] Preferably, the specific content of inputting the thermal expansion coefficient of the drug package into the drug package failure judgment model, analyzing the thermal stress of the drug package under temperature cycle, and calculating the drug package failure evaluation index is: When the temperature of the medicine package changes, the value of the thermal stress of the medicine package is: ,in It indicates the value of thermal stress of the medicine package when the temperature changes. Indicates the elastic modulus of the drug package material; After the medicine package is analyzed through n cycles of temperature changes, the temperature change amount measured each time is the same, and each temperature change amount is recorded as , then the calculation formula of the failure evaluation index of the drug package is: ,in represents the failure evaluation index of the drug package, n represents the number of temperature changes, , and Represents a constant.
[0011] Preferably, in the pressure decay trend prediction module, the specific content of performing pressure decay prediction on the medicine package to determine whether the sealed medicine package has a pressure decay risk is: The medicine package is continuously pressure monitored at the same time interval, and the pressure monitoring results are expressed as follows: Where m represents the total number of times the continuous pressure monitoring of the medicine package is performed, Indicates the pressure value of the mth pressure monitoring of the medicine package; The pressure change stability coefficient of the medicine package is calculated based on the continuous pressure monitoring results of the medicine package at the same time interval. The calculation formula is: ,in It indicates the stability coefficient of pressure change of the medicine package, i indicates the number of times the medicine package is continuously monitored, represents the pressure value of the i-th pressure monitoring of the medicine package; The decomposition coefficient of the magnetic powder in the medicine package is analyzed according to the mass of the magnetic powder and the mass of the composite magnetic powder in the medicine package parameters. The calculation formula is: Where R represents the decomposition coefficient of the magnetic powder in the medicine package, Indicates the mass of magnetic powder in the medicine package. It represents the mass of composite magnetic powder of the medicine package, and t represents the decomposition constant of magnetic powder of the medicine package at the preset working temperature; The pressure decay prediction of the medicine package is performed, and the calculation formula is expressed as: ,in It represents the pressure decay prediction result; When the pressure decay prediction results When the pressure decay risk threshold is greater than or equal to the preset pressure decay risk threshold, the stability of the medicine package is qualified and there is no pressure decay risk. When the pressure is less than a preset pressure decay risk threshold, the stability performance of the medicine package is unqualified and there is a risk of pressure decay.
[0012] Preferably, the medicine package monitoring result output module receives the efficacy judgment result of the medicine package with unqualified packaging sealing performance and the pressure decay risk judgment result of the medicine package with qualified packaging sealing performance, and issues a failure warning message when the efficacy judgment result indicates that the medicine package is invalid, and issues a risk warning message when the pressure decay risk judgment result indicates that there is a pressure decay risk, and outputs the warning message to the human-computer interaction terminal to complete the failure monitoring of the medicine package.
[0013] A method for monitoring failure of a medicine package of a traditional Chinese medicine sealing treatment instrument comprises the following steps: Step S01: collecting and recording initial data of the internal pressure of the medicine package through a high-precision pressure sensor; Step S02: evaluating the sealing performance of the medicine package according to the initial data of the internal pressure of the medicine package; Step S03: when the sealing performance evaluation of the medicine package fails, a medicine package failure judgment model is established to judge the efficacy of the medicine package; Step S04: when the evaluation result shows that the sealing performance of the medicine package is qualified, a pressure decay prediction is performed on the medicine package to determine whether the sealed medicine package has a pressure decay risk; Step S05: output the efficacy judgment results of the medicine packages with unqualified packaging sealing performance and the pressure decay risk judgment results of the medicine packages with qualified packaging sealing performance to the human-computer interaction terminal to complete the failure monitoring of the medicine packages.
[0014] Technical effects and advantages of the present invention: The present invention is provided with a medicine package initial pressure data acquisition module, a medicine package sealing performance analysis and matching module, a medicine package failure judgment model establishment module, a pressure decay trend prediction module and a medicine package monitoring result output module. The sealing performance of the medicine package packaging is evaluated according to the initial data of the internal pressure of the medicine package packaging. When the sealing performance evaluation of the medicine package packaging is unqualified, the medicine package is subjected to thermal expansion analysis by using the thermodynamic principle. The thermal expansion coefficient of the medicine package is obtained by analyzing the initial temperature and temperature change data of the medicine package, and a medicine package failure judgment model is established to judge the efficacy of the medicine package. When the evaluation result shows that the sealing performance of the medicine package packaging is qualified, the pressure decay prediction is performed on the medicine package to judge whether the sealed medicine package has a pressure decay risk, thereby realizing comprehensive monitoring of the failure of the medicine package. A method and system for monitoring the failure of medicine packages of a traditional Chinese medicine sealed package therapeutic instrument not only improves the accuracy of medicine package monitoring, but also helps users to replace failed medicine packages in time through real-time monitoring and early warning mechanisms, thereby ensuring the normal use and therapeutic effect of the therapeutic instrument and enhancing the safety and effectiveness of the treatment. BRIEF DESCRIPTION OF THE DRAWINGS
[0015] Figure 1 The present invention is a flow chart of a medicine package failure monitoring system for a traditional Chinese medicine sealing therapy instrument.
[0016] Figure 2 The present invention is a flow chart of a method for monitoring failure of medicine packages of a traditional Chinese medicine sealing therapy instrument. DETAILED DESCRIPTION
[0017] The technical solution of the present invention will be clearly and completely described below in conjunction with the accompanying drawings in the present invention. In addition, the forms of the various structures recorded in the following embodiments are merely illustrative. The method and system for monitoring the failure of a medicine package of a traditional Chinese medicine sealing therapy instrument involved in the present invention are not limited to the various structures recorded in the following embodiments. All other implementations obtained by ordinary technicians in this field without making creative work are within the scope of protection of the present invention.
[0018] like Figure 1 As shown, the present invention provides a medicine package failure monitoring system for a traditional Chinese medicine sealing treatment instrument, comprising: a medicine package initial pressure data acquisition module, a medicine package sealing performance analysis and matching module, a medicine package failure judgment model establishment module, a pressure decay trend prediction module, and a medicine package monitoring result output module; The medicine package initial pressure data acquisition module acquires and records the initial pressure data inside the medicine package through a high-precision pressure sensor; The medicine package sealing performance analysis and matching module evaluates the medicine package sealing performance based on the initial data of the internal pressure of the medicine package; The drug package failure judgment model establishment module establishes a drug package failure judgment model to judge the efficacy of the drug package when the drug package sealing performance evaluation fails, and outputs the judgment result to the drug package monitoring result output module; The pressure decay trend prediction module, when the evaluation result in the medicine package sealing performance analysis and matching module is that the medicine package sealing performance is qualified, performs pressure decay prediction on the medicine package to determine whether the sealed medicine package has a pressure decay risk, and transmits the judgment result to the medicine package monitoring result output module; The medicine package monitoring result output module outputs the efficacy judgment results of the medicine packages with unqualified packaging sealing performance and the pressure decay risk judgment results of the medicine packages with qualified packaging sealing performance to the human-computer interaction terminal, thereby completing the failure monitoring of the medicine packages.
[0019] In the present embodiment, it should be specifically explained that in the initial pressure data acquisition module of the medicine package, the initial data of the internal pressure of the medicine package is collected and recorded by a high-precision pressure sensor as the initial pressure value inside the medicine package. The medicine package is installed in a traditional Chinese medicine package comprehensive therapeutic instrument. The traditional Chinese medicine package comprehensive therapeutic instrument consists of a controller, a far-infrared package and a composite magnetic therapy package. The controller consists of a control module, a power module, and a human-computer interaction module. The far-infrared package consists of a carbon-based material heating element, a temperature control switch, a flame retardant sponge, a connecting wire and a connecting part. The composite magnetic therapy package consists of a temperature control chip, a magnetic button, a composite magnetic powder, a non-woven fabric, and a nylon mesh. The composite magnetic powder consists of magnetic powder and moxibustion materials.
[0020] In the present embodiment, it should be specifically explained that, in the medicine package sealing performance analysis and matching module, the sealing performance of the medicine package packaging is evaluated based on the initial data of the internal pressure of the medicine package packaging: the initial value of the internal pressure of the medicine package packaging is compared with a preset standard pressure evaluation interval; when the initial value of the internal pressure of the medicine package packaging is within the preset standard pressure evaluation interval, the evaluation result is qualified; when the initial value of the internal pressure of the medicine package packaging is not within the preset standard pressure evaluation interval, the evaluation result is unqualified.
[0021] In this embodiment, it should be specifically explained that in the drug package failure judgment model establishment module, the specific contents of establishing the drug package failure judgment model to judge the efficacy of the drug package are as follows: The thermal expansion analysis of the medicine package is carried out using the principles of thermodynamics. Combined with the initial temperature and temperature change data of the medicine package, the thermal expansion coefficient of the medicine package is analyzed and obtained. When the traditional Chinese medicine sealing package comprehensive therapeutic instrument reaches a steady-state state, the temperature in the effective heating area should not be lower than 37°C. The output temperature of the traditional Chinese medicine sealing package comprehensive therapeutic instrument is adjustable within the range of 38°C to 48°C, with an error of no more than ±3°C, the temperature adjustment step is 1°C, and the maximum temperature is less than 60°C.
[0022] Establish a drug package failure judgment model, input the thermal expansion coefficient of the drug package into the drug package failure judgment model, analyze the thermal stress of the drug package under temperature cycle, and calculate the drug package failure evaluation index; The efficacy of the medicine package is judged based on the medicine package failure evaluation index. When the medicine package failure evaluation index exceeds a preset failure threshold, the medicine package is judged to be failed; otherwise, the medicine package is judged to be effective.
[0023] In this embodiment, it should be specifically explained that the specific content of the thermal expansion coefficient of the medicine package obtained by analyzing the initial temperature and temperature change data of the medicine package is: Calculate the initial temperature analysis coefficient of the drug package at the initial temperature. The calculation formula is: ,in represents the initial temperature analysis coefficient of the drug package at the initial temperature, represents the initial analysis constant of the drug package, represents the constant of the drug package at the initial temperature, Indicates the initial temperature of the medicine package; Calculate the temperature change analysis coefficient of the medicine package after the temperature changes. The calculation formula is: ,in It indicates the temperature change analysis coefficient of the medicine package after the temperature changes. Indicates the temperature change analysis constant of the medicine package, It represents the constant of the medicine package after the temperature changes. Indicates the temperature change value of the medicine package; Combined with the change in the volume of the medicine package when the temperature changes, the thermal expansion coefficient of the medicine package is analyzed and the calculation formula is: ,in represents the thermal expansion coefficient of the drug package, It indicates the change in the volume of the medicine package when the temperature changes, and it indicates the volume value of the medicine package at the initial temperature.
[0024] Preferably, the specific content of inputting the thermal expansion coefficient of the drug package into the drug package failure judgment model, analyzing the thermal stress of the drug package under temperature cycle, and calculating the drug package failure evaluation index is: When the temperature of the medicine package changes, the value of the thermal stress of the medicine package is: ,in It indicates the value of thermal stress of the medicine package when the temperature changes. Indicates the elastic modulus of the drug package material; After the medicine package is analyzed through n cycles of temperature changes, the temperature change amount measured each time is the same, and each temperature change amount is recorded as , then the calculation formula of the failure evaluation index of the drug package is: ,in represents the failure evaluation index of the drug package, n represents the number of temperature changes, , and Represents a constant.
[0025] Preferably, in the pressure decay trend prediction module, the specific content of performing pressure decay prediction on the medicine package to determine whether the sealed medicine package has a pressure decay risk is: The medicine package is continuously pressure monitored at the same time interval, and the pressure monitoring results are expressed as follows: Where m represents the total number of times the continuous pressure monitoring of the medicine package is performed, Indicates the pressure value of the mth pressure monitoring of the medicine package; The pressure change stability coefficient of the medicine package is calculated based on the continuous pressure monitoring results of the medicine package at the same time interval. The calculation formula is: ,in It indicates the stability coefficient of pressure change of the medicine package, i indicates the number of times the medicine package is continuously monitored, represents the pressure value of the i-th pressure monitoring of the medicine package; The decomposition coefficient of the magnetic powder in the medicine package is analyzed according to the mass of the magnetic powder and the mass of the composite magnetic powder in the medicine package parameters. The calculation formula is: Where R represents the decomposition coefficient of the magnetic powder in the medicine package, Indicates the mass of magnetic powder in the medicine package. It represents the mass of composite magnetic powder of the medicine package, and t represents the decomposition constant of magnetic powder of the medicine package at the preset working temperature; The pressure decay prediction of the medicine package is performed, and the calculation formula is expressed as: ,in It represents the pressure decay prediction result; When the pressure decay prediction results When the pressure decay risk threshold is greater than or equal to the preset pressure decay risk threshold, the stability of the medicine package is qualified and there is no pressure decay risk. When the pressure is less than a preset pressure decay risk threshold, the stability performance of the medicine package is unqualified and there is a risk of pressure decay.
[0026] In the present embodiment, it should be specifically explained that, in the medicine package monitoring result output module, the efficacy judgment result of the medicine package with unqualified packaging sealing performance and the pressure decay risk judgment result of the medicine package with qualified packaging sealing performance are received, and a failure warning message is issued when the efficacy judgment result is that the medicine package is invalid, and a risk warning message is issued when the pressure decay risk judgment result is that there is a pressure decay risk, and the warning message is output to the human-computer interaction terminal to complete the failure monitoring of the medicine package.
[0027] like Figure 2 As shown, in this embodiment, it should be specifically explained that a method for monitoring the failure of a medicine package of a traditional Chinese medicine sealing treatment instrument includes the following steps: Step S01: collecting and recording initial data of the internal pressure of the medicine package through a high-precision pressure sensor; Step S02: evaluating the sealing performance of the medicine package according to the initial data of the internal pressure of the medicine package; Step S03: when the sealing performance evaluation of the medicine package fails, a medicine package failure judgment model is established to judge the efficacy of the medicine package; Step S04: when the evaluation result shows that the sealing performance of the medicine package is qualified, a pressure decay prediction is performed on the medicine package to determine whether the sealed medicine package has a pressure decay risk; Step S05: output the efficacy judgment results of the medicine packages with unqualified packaging sealing performance and the pressure decay risk judgment results of the medicine packages with qualified packaging sealing performance to the human-computer interaction terminal to complete the failure monitoring of the medicine packages.
[0028] In the present embodiment, it should be specifically explained that the difference between the present embodiment and the prior art lies mainly in that the present embodiment is provided with a medicine package initial pressure data acquisition module, a medicine package sealing performance analysis and matching module, a medicine package failure judgment model establishment module, a pressure decay trend prediction module and a medicine package monitoring result output module, and collects and records the initial data of the internal pressure of the medicine package through a high-precision pressure sensor, and evaluates the sealing performance of the medicine package according to the initial data of the internal pressure of the medicine package. When the evaluation of the sealing performance of the medicine package is unqualified, a medicine package failure judgment model is established to judge the efficacy of the medicine package, and when the evaluation result shows that the sealing performance of the medicine package is qualified, the pressure decay prediction is performed on the medicine package, so as to realize comprehensive monitoring of the failure of the medicine package; The thermal expansion analysis of the medicine package is carried out using the principles of thermodynamics. The thermal expansion coefficient of the medicine package is analyzed based on the initial temperature and temperature change data of the medicine package. A medicine package failure judgment model is established to judge the efficacy of the medicine package. The pressure decay of the medicine package is predicted to determine whether the sealed medicine package has a pressure decay risk. This not only improves the accuracy of medicine package monitoring, but also helps users to replace failed medicine packages in time through real-time monitoring and early warning mechanisms, ensuring the normal use and treatment effect of the therapeutic device, and enhancing the safety and effectiveness of the treatment.
[0029] Finally: The above description is only a preferred embodiment of the present invention and is not intended to limit the present invention. Any modifications, equivalent substitutions, improvements, etc. made within the spirit and principles of the present invention should be included in the protection scope of the present invention.
[0030] The above is only a specific implementation of the present application, but the protection scope of the present application is not limited thereto. Any technician familiar with the technical field can easily think of changes or substitutions within the technical scope disclosed in the present application, which should be included in the protection scope of the present application. Therefore, the protection scope of the present application should be based on the protection scope of the claims.
Claims
1. A medicine package failure monitoring system for a traditional Chinese medicine package treatment instrument, characterized in that: include: Drug package initial pressure data acquisition module, drug package sealing performance analysis and matching module, drug package failure judgment model establishment module, pressure decay trend prediction module and drug package monitoring result output module; The medicine package initial pressure data acquisition module acquires and records the initial pressure data inside the medicine package through a high-precision pressure sensor; The medicine package sealing performance analysis and matching module evaluates the medicine package sealing performance based on the initial data of the internal pressure of the medicine package; The drug package failure judgment model establishment module establishes a drug package failure judgment model to judge the efficacy of the drug package when the drug package sealing performance evaluation fails, and outputs the judgment result to the drug package monitoring result output module; The pressure decay trend prediction module, when the evaluation result in the medicine package sealing performance analysis and matching module is that the medicine package sealing performance is qualified, performs pressure decay prediction on the medicine package to determine whether the sealed medicine package has a pressure decay risk, and transmits the judgment result to the medicine package monitoring result output module; The medicine package monitoring result output module outputs the efficacy judgment results of the medicine packages with unqualified packaging sealing performance and the pressure decay risk judgment results of the medicine packages with qualified packaging sealing performance to the human-computer interaction terminal, thereby completing the failure monitoring of the medicine packages.
2. A medicine package failure monitoring system for a traditional Chinese medicine package therapy instrument according to claim 1, characterized in that: In the medicine package initial pressure data acquisition module, the initial data of the internal pressure of the medicine package is acquired and recorded as the initial pressure value of the internal pressure of the medicine package through a high-precision pressure sensor.
3. A medicine package failure monitoring system for a traditional Chinese medicine package therapy instrument according to claim 1, characterized in that: In the medicine package sealing performance analysis and matching module, the medicine package sealing performance is evaluated based on the initial data of the internal pressure of the medicine package: the initial value of the internal pressure of the medicine package is compared with a preset standard pressure evaluation interval. When the initial value of the internal pressure of the medicine package is within the preset standard pressure evaluation interval, the evaluation result is qualified; when the initial value of the internal pressure of the medicine package is not within the preset standard pressure evaluation interval, the evaluation result is unqualified.
4. The Chinese medicine package treatment instrument failure monitoring system according to claim 1 is characterized by: In the drug package failure judgment model establishment module, the specific contents of establishing the drug package failure judgment model to judge the efficacy of the drug package are as follows: The thermal expansion analysis of the drug package is carried out using the thermodynamic principle, and the thermal expansion coefficient of the drug package is obtained by combining the initial temperature and temperature change data of the drug package; Establish a drug package failure judgment model, input the thermal expansion coefficient of the drug package into the drug package failure judgment model, analyze the thermal stress of the drug package under temperature cycle, and calculate the drug package failure evaluation index; The efficacy of the medicine package is judged based on the medicine package failure evaluation index. When the medicine package failure evaluation index exceeds a preset failure threshold, the medicine package is judged to be failed; otherwise, the medicine package is judged to be effective.
5. A medicine package failure monitoring system for a traditional Chinese medicine package therapy instrument according to claim 4, characterized in that: The specific content of the thermal expansion coefficient of the medicine package obtained by analyzing the initial temperature and temperature change data of the medicine package is: Calculate the initial temperature analysis coefficient of the drug package at the initial temperature. The calculation formula is: ,in represents the initial temperature analysis coefficient of the drug package at the initial temperature, represents the initial analysis constant of the drug package, represents the constant of the drug package at the initial temperature, Indicates the initial temperature of the medicine package; Calculate the temperature change analysis coefficient of the medicine package after the temperature changes. The calculation formula is: ,in It indicates the temperature change analysis coefficient of the medicine package after the temperature changes. Indicates the temperature change analysis constant of the medicine package, It represents the constant of the medicine package after the temperature changes. Indicates the temperature change value of the medicine package; Combined with the change in the volume of the medicine package when the temperature changes, the thermal expansion coefficient of the medicine package is analyzed and the calculation formula is: ,in represents the thermal expansion coefficient of the drug package, It indicates the change in the volume of the medicine package when the temperature changes, and it indicates the volume value of the medicine package at the initial temperature.
6. A medicine package failure monitoring system for a traditional Chinese medicine package therapy instrument according to claim 4, characterized in that: The specific content of inputting the thermal expansion coefficient of the drug package into the drug package failure judgment model, analyzing the thermal stress of the drug package under temperature cycle, and calculating the drug package failure evaluation index is: When the temperature of the medicine package changes, the value of the thermal stress of the medicine package is: ,in It indicates the value of thermal stress of the medicine package when the temperature changes. Indicates the elastic modulus of the drug package material; After the medicine package is analyzed for n temperature changes, the temperature change amount measured each time is the same, and each temperature change amount is recorded as , then the calculation formula of the failure evaluation index of the drug package is: ,in represents the failure evaluation index of the drug package, n represents the number of temperature changes, , and Represents a constant.
7. The Chinese medicine package treatment instrument failure monitoring system according to claim 1 is characterized by: In the pressure decay trend prediction module, the specific contents of performing pressure decay prediction on the medicine package to determine whether the sealed medicine package has a pressure decay risk are as follows: The medicine package is continuously pressure monitored at the same time interval, and the pressure monitoring results are expressed as follows: Where m represents the total number of times the continuous pressure monitoring of the medicine package is performed, Indicates the pressure value of the mth pressure monitoring of the medicine package; The pressure change stability coefficient of the medicine package is calculated based on the continuous pressure monitoring results of the medicine package at the same time interval. The calculation formula is: ,in It indicates the stability coefficient of pressure change of the medicine package, i indicates the number of times the medicine package is continuously monitored, represents the pressure value of the pressure monitoring of the medicine package for the i-th time; The decomposition coefficient of the magnetic powder in the medicine package is analyzed according to the mass of the magnetic powder and the mass of the composite magnetic powder in the medicine package parameters. The calculation formula is: Where R represents the decomposition coefficient of the magnetic powder in the medicine package, Indicates the mass of magnetic powder in the medicine package. It represents the mass of composite magnetic powder of the medicine package, and t represents the decomposition constant of magnetic powder of the medicine package at the preset working temperature; The pressure decay prediction of the medicine package is performed, and the calculation formula is expressed as: ,in It represents the pressure decay prediction result; When the pressure decay prediction results When the pressure decay risk threshold is greater than or equal to the preset pressure decay risk threshold, the stability of the medicine package is qualified and there is no pressure decay risk. When the pressure is less than a preset pressure decay risk threshold, the stability performance of the medicine package is unqualified and there is a risk of pressure decay.
8. The Chinese medicine package treatment instrument failure monitoring system according to claim 1 is characterized by: In the medicine package monitoring result output module, the efficacy judgment results of the medicine packages with unqualified packaging sealing performance and the pressure decay risk judgment results of the medicine packages with qualified packaging sealing performance are received, and when the efficacy judgment result is that the medicine package is invalid, failure warning information is issued, and when the pressure decay risk judgment result is that there is a pressure decay risk, risk warning information is issued, and the warning information is output to the human-computer interaction terminal to complete the failure monitoring of the medicine package.
9. A method for monitoring failure of a medicine package of a traditional Chinese medicine package therapeutic instrument, used for using a monitoring system for failure of a medicine package of a traditional Chinese medicine package therapeutic instrument as claimed in any one of claims 1 to 8, characterized in that: The following steps are involved: Step S01: collecting and recording initial data of the internal pressure of the medicine package through a high-precision pressure sensor; Step S02: evaluating the sealing performance of the medicine package according to the initial data of the internal pressure of the medicine package; Step S03: when the sealing performance evaluation of the medicine package fails, a medicine package failure judgment model is established to judge the efficacy of the medicine package; Step S04: when the evaluation result shows that the sealing performance of the medicine package is qualified, a pressure decay prediction is performed on the medicine package to determine whether the sealed medicine package has a pressure decay risk; Step S05: output the efficacy judgment results of the medicine packages with unqualified packaging sealing performance and the pressure decay risk judgment results of the medicine packages with qualified packaging sealing performance to the human-computer interaction terminal to complete the failure monitoring of the medicine packages.