KR20230113241A - Multi-device system, and formulation dispensing method using a plurality of devices - Google Patents

Abstract

The present invention relates to a method for dispensing a formulation using a plurality of devices and a multi-device system including the plurality of devices.
An example of a method of dispensing a formulation by a plurality of devices according to the present invention is performed by the first device at the first division time of the first period, and having a plurality of nutritional components according to the formulation composition information at the first division time point. A first device dosage form discharging step of discharging a plurality of dosage forms; and a second device different from the first device at the time of the second division of the first period, dispensing a plurality of formulations having a plurality of nutritional components according to the formulation composition information at the time of the second division. 2 device formulation dispensing step; wherein, each of the formulation composition information at the time of the first and second division divides the daily serving amount reflecting the base volume information for the plurality of nutritional components according to preset division ratio information It is calculated, and when the first formulation among the plurality of formulations is provided in only one device of the first device and the second device, the preset division is performed so that the first formulation is discharged only from the any one device. The dose information of the first dosage form in the dosage form composition information at the time of the first or second division calculated according to the ratio information may be adjusted.

Description

Formulation dispensing method using a plurality of devices, and a multi-device system

The present invention relates to a method for dispensing a formulation using a plurality of devices and a multi-device system including the plurality of devices.

As the nutritional supplement market grows and users' needs diversify, personalized nutritional supplement services that analyze users' health conditions and provide a combination of appropriate nutritional supplements accordingly are being activated. This personalized nutritional supplement service collects health information of users through questionnaires, etc., analyzes the collected health information of users, derives nutritional components that are deemed necessary, and provides a combination of nutritional supplements that satisfy the nutritional components. being done in a way

In the provision of the third of these, nutritional supplements, conventionally, the nutritional supplements were combined and packaged in small portions at the factory and operated in a manner that was provided. However, in the case of customized nutritional products produced in factories, the collection and analysis of health information is not performed in real time, so there is a disadvantage that the user's health information that changes on a daily basis cannot be immediately reflected. In addition, due to the minimum production quantity of the factory, there was no choice but to provide customized nutritional supplements as a unit for a considerable period of time (for example, one month).

JP 2020-016959 A KR 10-2020-0025756 A JP 2017-221752 A

An object of the present invention is to provide a method for dispensing a formulation using a plurality of devices and a multi-device system including the plurality of devices.

An example of a method of dispensing a formulation by a plurality of devices according to the present invention is performed by the first device at the first division time of the first period, and has a plurality of nutritional components according to the formulation composition information at the first division time point. A first device dosage form discharging step of discharging a plurality of dosage forms; and a second device different from the first device at the time of the second division of the first period, dispensing a plurality of formulations having a plurality of nutritional components according to the formulation composition information at the time of the second division. 2 device formulation dispensing step; wherein, each of the formulation composition information at the time of the first and second division divides the daily serving amount reflecting the base volume information for the plurality of nutritional components according to preset division ratio information It is calculated, and when the first formulation among the plurality of formulations is provided in only one device of the first device and the second device, the preset division is performed so that the first formulation is discharged only from the any one device. The dose information of the first dosage form in the dosage form composition information at the time of the first or second division calculated according to the ratio information may be adjusted.

Alternatively, according to the formulation dispensing method, when the second formulation among the plurality of formulations is provided in both the first device and the second device, the first or second division calculated according to the preset division ratio information Dose information of the second dosage form in the dosage form composition information at the time may be maintained.

Alternatively, according to the formulation dispensing method, it is performed by the first device before the first device dispensing step, and the first division is performed from an electronic device connected to the first device and the second device through a network. Receiving formulation composition information at the time; and receiving the formulation composition information at the time of the second division from the electronic device, which is performed by the second device prior to the dispensing of the second device formulation.

Alternatively, according to the dosage form dispensing method, the base capacity information is calculated based on personal health information including at least one of identification information, medical examination result information, or medical information about the user, and the plurality of nutritional components may have a capacitance value for

Alternatively, according to the dosage form dispensing method, when calculating each of the dosage form composition information at the time of the first and second division, the base volume information calculated before the time of the first division may be commonly used.

Alternatively, according to the dosage form dispensing method, it is performed by the first device after the first device dosage dispensing step, and the first division into an electronic device connected to the first device and the second device through a network. Transmitting discharge amount information corresponding to a point in time; and transmitting the discharge amount information corresponding to the second division time point to the electronic device, which is performed by the second device after the dosage form dispensing step to the second device.

Alternatively, according to the dosage form dispensing method, it is performed by the first device before the first dividing time point, and is stored in the first device as an electronic device connected to the first device and the second device through a network. Transmitting first cartridge information about the dosage form; and transmitting, performed by the second device before the first dividing time point, second cartridge information about the formulation stored in the second device to the electronic device.

Alternatively, according to the dosage form dispensing method, the daily serving amount at the time of the first division is calculated by reflecting the first current state information of the user at the time of the first division together with the base capacity information, The daily serving amount at the time of the second division may be calculated by reflecting the second current state information of the user at the time of the second division together with the base capacity information.

Alternatively, according to the dosage form dispensing method, the first current state information or the second current state information is the first device, the second device, a user terminal of the user, or an external device that collects the user's biometric information. It is collected from at least one of the devices, and may include information on at least one of the user's mental health condition or symptom, physical health condition or symptom, mood or behavior of the user, and biometric information of the user.

An example of a multi-device system including a plurality of devices according to the present invention includes a first device for dispensing a plurality of formulations having a plurality of nutritional components according to the formulation composition information at the time of the first division of the first period; and a second device for dispensing a plurality of dosage forms having a plurality of nutritional components according to the dosage form composition information at the second division time point of the first period, wherein each of the formulation composition information at the first and second division time points , It is calculated by dividing the daily serving amount reflecting the base capacity information for the plurality of nutritional components according to preset division ratio information, and the first formulation among the plurality of formulations is any one of the first device and the second device When provided in only one device, the first formulation in the formulation composition information at the time of the first or second division calculated according to the preset division ratio information so that the first formulation is discharged from only one of the devices Capacity information can be adjusted.

An embodiment according to the present invention can provide a combination of dosage forms optimized for the user's health condition at each point in time by reflecting the current state information on the user's health condition when the combination of dosage forms is provided to the user.

1 is a diagram illustrating an example of a network environment according to an embodiment of the present invention.
FIG. 2 is a diagram for explaining an example of a user terminal shown in FIG. 1 .
FIG. 3 is a diagram for explaining an example of the configuration of the server shown in FIG. 1 and an example of processing formulation composition information.
4 is a diagram for explaining an example of a method of calculating base capacity information in the present invention.
5 is a diagram for explaining an example in which personal health variable value information is applied for each nutritional component when calculating base dose information in the present invention.
6 is a diagram for explaining an example in which current state information is reflected in base capacity information in the present invention.
FIG. 7 is a diagram for explaining an example of a physical structure of the device shown in FIG. 1;
FIG. 8 is a diagram for explaining an example of a circuit configuration of the device shown in FIG. 7 and an example of a configuration of a device terminal.
FIG. 9 is a diagram for explaining an example of a method of operating the device shown in FIG. 7 .
10A and 10B are diagrams for explaining a first embodiment of a method for operating a service providing server, a user terminal, and a device shown in FIG. 1 .
FIG. 11 is a diagram for explaining an example of a method for obtaining user-specific information by a device in the first and second periods of FIGS. 10A and 10B.
12 is a diagram for explaining an example of a method for a device to obtain current state information in the first and second periods of FIGS. 10A and 10B.
13A is a diagram for explaining an example in which a user terminal displays a daily serving amount customized for each nutritional component in response to current state information.
13B is a diagram for explaining an example in which a user terminal displays whether or not to take a customized nutritional component, insufficient amount, etc. based on cumulative dose information.
13C is an example in which the user terminal displays current state information acquired from the user.
FIG. 16 is a diagram for explaining a first modified example of the first embodiment described in FIGS. 10A and 10B.
FIG. 17 is a diagram for explaining a second modified example of the first embodiment described in FIGS. 10A and 10B.
FIG. 18 is a diagram for explaining a third modified example of the first embodiment described in FIGS. 10A and 10B.
19 is a diagram for explaining a second embodiment of a method for operating the service providing server, user terminal, and device shown in FIG. 1;
FIG. 20 is a diagram for explaining a first modified example of the second embodiment described in FIG. 19 .
21A and 21B are diagrams for explaining a third embodiment of a method for operating a service providing server, a user terminal, and a device shown in FIG. 1 .
FIG. 22A is a diagram for explaining an example of setting divided doses through the user terminal and an example of displaying the number of divided doses by the user terminal in FIG. 21A .
FIG. 23 is a diagram for explaining a first modified example of the third embodiment described in FIGS. 21A and 21B.
24a and 24b are diagrams for explaining a fourth embodiment of a method for operating the service providing server, user terminal, and device shown in FIG. 1;

The following merely illustrates the principles of the present invention. Therefore, those skilled in the art can invent various devices that embody the principles of the present invention and fall within the concept and scope of the present invention, even though not explicitly described or shown herein. In addition, it is to be understood that all conditional terms and embodiments listed herein are, in principle, expressly intended only for the purpose of making the concept of the present invention understood, and not limited to such specifically listed embodiments and conditions. It should be.

Further, it should be understood that all detailed descriptions reciting specific embodiments, as well as principles, aspects and embodiments of the present invention, are intended to encompass both structural and functional equivalents of these matters. In addition, it should be understood that such equivalents include not only currently known equivalents but also equivalents developed in the future, that is, all devices invented to perform the same function regardless of structure.

Thus, for example, the block diagrams herein are to be understood as representing conceptual views of exemplary circuits embodying the principles of the present invention. Similarly, all flowcharts, state transition diagrams, pseudo code, etc., are meant to be tangibly represented on computer readable media and represent various processes performed by a computer or processor, whether or not the computer or processor is explicitly depicted. It should be.

The functions of various elements shown in the drawings including functional blocks represented by processors or similar concepts may be provided using dedicated hardware as well as hardware capable of executing software in conjunction with appropriate software. When provided by a processor, the functionality may be provided by a single dedicated processor, a single shared processor, or a plurality of separate processors, some of which may be shared.

In addition, the explicit use of terms presented as processor, control, or similar concepts should not be construed as exclusively citing hardware capable of executing software, but without limitation, digital signal processor (DSP) hardware, ROM for storing software (ROM), random access memory (RAM) and non-volatile memory. Other hardware for the governor's use may also be included.

In the claims of this specification, components expressed as means for performing the functions described in the detailed description include, for example, a combination of circuit elements performing the functions or all types of software including firmware/microcode, etc. It is intended to include any method that performs the function of performing the function, combined with suitable circuitry for executing the software to perform the function. Since the invention defined by these claims combines the functions provided by the various enumerated means and is combined in the manner required by the claims, any means capable of providing such functions is equivalent to that discerned from this disclosure. should be understood as

The above objects, features and advantages will become more apparent through the following detailed description in conjunction with the accompanying drawings, and accordingly, those skilled in the art to which the present invention belongs can easily implement the technical idea of the present invention. There will be. In addition, in describing the present invention, if it is determined that a detailed description of a known technology related to the present invention may unnecessarily obscure the subject matter of the present invention, the detailed description will be omitted.

Hereinafter, a preferred embodiment according to the present invention will be described in detail with reference to the accompanying drawings.

1 is a diagram illustrating an example of a network environment according to an embodiment of the present invention.

As shown in FIG. 1, a network environment according to an embodiment of the present invention includes a service providing server 100, a dispensing device 200, a user terminal 300, an external device 400, and a medical institution server 500. ) may be included.

The network is not limited in communication method, and may include not only a communication method utilizing a communication network (eg, a mobile communication network, wired Internet, wireless Internet, and broadcasting network) that the network may include, but also short-distance wireless communication.

As an example, the network may include a Local Area Network (LAN), a Wide Area Network (WAN), a Value Added Network (VAN), a Personal Area Network (PAN), and a mobile communication network ( It can be implemented in all types of wired/wireless networks, such as a mobile radiocommunication network) or a satellite communication network.

The service providing server 100 shown in FIG. 1 may be connected to the user terminal 300 and the device 200 through a network.

In addition, the service providing server 100 may receive information provided from the medical institution server 500 and the external device 400 through the user terminal 300 . However, the present invention is not limited thereto, and information provided from the medical institution server 500 and the external device 400 may be directly received without going through the user terminal 300 in some cases.

The service providing server 100 (hereinafter referred to as 'server') will be implemented as a computer device that communicates with the user terminal 300 and the device 200 through a network to provide commands, codes, files, contents, services, and the like. can

For example, the server 100 of the present invention may provide the device 200 with information about a combination of formulations optimized for changes in the user's health condition at the time the user receives the formulation through the device 200. .

To this end, the server 100 calculates base dose information for each nutritional component based on the user's personal health information, and information on the current state related to the user's health during the period to which the user is provided with the formulation (hereinafter, It is possible to calculate information on a combination of formulations to be provided to the user through the device 200 by receiving the 'current state information') and reflecting the base volume information in real time.

The period to which the user receives the dosage form may mean a date or a predetermined length of time to which the user receives the dosage form. For example, if the user is provided with a formulation at 7:00 am on December 24, the period to which the formulation is provided may mean the length of time from 0:00 to 24:00 on December 24 or December 24. there is.

Therefore, the server 100 of the present invention provides information on the combination of formulations optimized for the user's health condition, and reflects the user's current state information in real time, thereby providing a formulation optimized for the user's health condition based on the current time. can provide information on combinations of

Formulation refers to substances in various forms, such as solid form, powder form, or liquid form, including various nutritional components that can be absorbed by the user's body, for example, health functional food, pharmaceuticals , It is processed into general food, etc., and is taken for the purpose of normal functioning and health promotion of the human body, such as tablets, capsules, pills, powders, granules, jelly or It may have at least one form among various forms such as liquid.

When the formulation includes nutrients, the formulation may include, for example, nutritional components such as vitamin B, vitamin C, omega 3, magnesium, milk thistle, red ginseng, and the like.

If the formulation contains pharmaceuticals or specialized drugs, the formulation may contain drugs or specialty drugs that are effective for chronic diseases, such as aspirin or metformin that are effective in preventing cardiovascular disease or heart attack. there is.

The user's personal health information may include information about a chronic or chronic physical or mental disease, symptom, or condition of the user. The user's personal health information may be extracted from at least one of identification information about the user, medical examination result information, or medical information received by the server 100 from the user terminal 300 or the device 200 .

The base dose information may be information in which personal health variable value information extracted from personal health information of the user is reflected for each nutritional component. That is, the base dose information may be information on the dose for each nutritional component optimized for the user's personal health information. A method of calculating such base capacity information will be described later with reference to FIG. 4 or later.

The user's current state information may be information about a mental or physical health state or life state related to the user's physical state that is temporarily generated in relation to the user's health for a specific period of time.

Specifically, current state information is (1) information about the user's mental state or symptoms (eg, depression, tension, anxiety, fatigue, stress, etc.) or (2) information about physical conditions or symptoms (eg, dysmenorrhea, menstruation) pre-syndrome (PMS), diarrhea, constipation, cold, stomatitis, migraine, etc.) After exercise, etc.) and mood (eg, feeling good, not feeling well, etc.) and severity of symptoms (eg, severe dysmenorrhea, moderate dysmenorrhea, etc.) may be further included.

In addition, as the current state information, any information may be used as long as it is information capable of knowing the user's temporary physical state change. For example, current state information may further include biometric information collected from user biometric signals. For example, information about the amount of exercise of the user obtained by various sensors, blood pressure information, electrocardiogram information, etc. can also be used as current state information, and voice information input from the user and image information generated by photographing the user can be used as current state information. can be used as

The current state information of the user may be received by the server 100 from the device 200 or the user terminal 300 .

In the present invention, when the user receives the formulation from the device 200, the user's current state information is reflected in the base volume information in real time, so that the device 200 is a combination of formulations optimized for the user's real-time body condition change. Can be provided as daily serving amount information. As described above, a method of reflecting current state information to base capacity information will be described later with reference to FIG. 6 or later.

Here, the daily serving amount information refers to the serving amount for each nutritional component provided by the device 200 for a predetermined period (eg, 1 day or 24 hours), and can be calculated by reflecting the current state information of the user in the base amount information. there is.

Here, the user's current state information can be used to calculate the daily serving amount of the period to which the current state information is obtained, and is used to calculate the daily serving amount of the period to which the current state information is obtained does not belong. It may not be.

For example, when first current status information of a user is collected in a first period and second current status information of a user is collected in a second period, the first current status information calculates a serving amount per day in the first period. and the second current state information may be used to calculate the daily serving amount of the second period.

The server 100 of the present invention may also receive, from the device 200 , discharge amount information about a dosage form dispensed through the device 200 or taken by the user. The server 100 may continuously monitor discharge amount information from at least one device 200 and provide the information to the user terminal 300 . For example, the server 100 receives the discharge amount information from the first device 200A or receives the discharge amount information from a plurality of devices including the first and second devices 200A and 200B to form one user terminal 300. It is also possible to transmit discharge amount information to .

The configuration and basic functions of the server 100 will be described in more detail with reference to FIGS. 3 to 6 .

The dispensing device 200 (hereinafter referred to as 'device') may perform a function of dispensing a plurality of formulations to a user. Specifically, the device 200 interworks with the server 100 through a network, obtains various information, data, commands, etc. including current state information from the user through user interaction, and forms a formulation reflecting the current state information. A plurality of formulations combined according to the information may be provided to the user.

To this end, the device 200 may include a plurality of formulations containing various nutritional components.

At the time when the user receives the formulation through the device 200, the device 200 may discharge the number of formulations combined according to the formulation composition information based on the current state information. Accordingly, the device 200 may provide the user with a formulation optimized for the user's health according to the user's real-time change in body condition.

In addition, by counting the number of formulations provided to the user for each type of formulation, discharge amount information on the number of formulations may be generated and provided to the server 100 .

A detailed description of the device 200 will be described later with reference to FIG. 8 or less.

The user terminal 300 may be a fixed terminal implemented as a computer device or a mobile terminal. As an example, the user terminal 300 may include a smart phone, a mobile phone, a tablet PC, a computer, a laptop computer, and personal digital assistants (PDAs).

The user terminal 300 may be used by a user. The term "user" may refer to a user of the user terminal 300 or a user of an account registered for a service provided by the server 100 . Therefore, the meaning that the server 100 transmits or provides certain information to the user may mean that certain information is transmitted to the user terminal 300 of an account registered in the server 100 and provided to the user.

The user terminal 300 may be linked to the server 100 through a network using a wireless or wired communication method, and at least one of the above-described base capacity information, current state information, or daily serving information is used as dosage management information by the server. It can be received from (100) and provided to the user.

The user terminal 300 may receive medical examination information from the server 100, perform a medical examination of the user, and then transmit medical examination result information, which is information about a medical examination result value, to the server 100.

The user terminal 300 may request medical information of the user from the medical institution server 500 and provide the medical information received from the medical institution server 500 to the server 100 in response. Medical information may include, for example, a user's disease history and examination information.

When the user terminal 300 obtains current state information from the user through user interaction, it may transmit the obtained current state information to the server 100 . User interaction may mean that the user inputs information reflecting the user's selection or intention to the user terminal 300 by manipulating an input means. The input means may include at least one of a touch screen provided in or connected to the user terminal 300 , a keyboard, a mouse, physical buttons, a camera, and a microphone.

The user terminal 300 detects the user's sensing information (eg, momentum information obtained by an acceleration sensor and a position sensor included in the user terminal 300) detected by a sensor provided therein or the user terminal 300. The user's sensing information (eg, blood pressure information obtained by a sensor linked to the user terminal 300, oxygen saturation information, etc.) detected from the interlocked external device 400 may be transmitted to the server 100 as current state information. there is.

To this end, the user terminal 300 may have an application for performing the above-described functions, and may be interlocked with the service providing server 100 through the application.

The configuration of the user terminal 300 will be described in more detail with reference to FIG. 2 below.

The external device 400 interworks with the user terminal 300 to collect health-related information about the user of the user terminal 300, and sends the collected health-related information to the server 100 through the user terminal 300. It may be a delivery device.

For example, the external device 400 may include a device capable of collecting and detecting bio-signals from the user. For example, a smart watch equipped with a sensor for collecting and detecting bio-signals, smart glasses, and a smart bracelet. It may include various healthcare devices such as

The external device 400 may collect various health-related sensing information, such as heart rate information, electrocardiogram information, blood pressure information, and blood sugar information corresponding to user information, as current state information. Current state information collected by the external device 400 may be transmitted to the server 100 through the user terminal 300 .

The medical institution server 500 may be a server such as a hospital, medical center, health examination institution, or other national medical institution database that receives and provides medical information from the user terminal 300 .

When the medical institution server 500 receives a request for medical information of a user from the user terminal 300 , it may provide the medical information to the user terminal 300 or the server 100 .

An embodiment of the present invention including the server 100, device 200, and user terminal 300 calculates base amount information for each nutritional component based on the user's personal health information, and when the user receives the formulation The user's current state information is reflected in the base dose information in real time to calculate the formulation composition information, and the type and dose of the formulation optimized according to the formulation composition information can be provided to the user.

Therefore, the present invention optimizes a plurality of formulations and doses according to the user's personal health information and provides them to the user, and provides the user with a formulation more optimized for the user's current body condition by reflecting the current real-time current condition information of the user in the personal health information. can provide

Hereinafter, the present invention will be described in more detail.

FIG. 2 is a diagram for explaining an example of the user terminal 300 shown in FIG. 1 .

As shown in FIG. 2 , the user terminal 300 includes a communication unit 310, a memory 320, a processor 330, an input unit 340 and an output unit 350, and a user terminal sensor 360. can include more.

The communication unit 310 provided in the user terminal 300 transmits information generated by the user terminal 300 to the server 100, external device 400 or medical institution server 500, or the server 100 or external device 400 or information generated by the medical institution server 500 may be received.

The memory 320 may store applications for the user terminal 300 to perform services provided by the server 100, various commands or execution programs necessary for performing the services provided by the server 100, and Various health-related information related to the user may be stored.

The processor 330 executes an application stored in the memory 320 to conduct a medical examination for the user, collect health-related information (eg, personal health information or current condition information, etc.) of the user, or obtain a medical examination result. Information or health-related information of the user may be controlled to be transmitted to the server 100 through the communication unit 310 .

Also, the processor 330 may control the user's health-related information provided from the server 100 to be output as information recognizable by the user.

The input unit 340 may collect or obtain various information input from the user through user interaction according to the execution of the application. The input unit 340 may include, for example, a keyboard, a mouse, a camera, and a microphone.

The output unit 350 may output health-related information of the user provided from the server 100 according to the execution of the application. The output unit 350 may include, for example, a speaker and a display module displaying an image.

If the user terminal 300 has the form of a mobile terminal such as a smart phone, the user terminal 300 may further include a touch screen module capable of input and output as one module.

The user terminal 300, for example, executes a medical examination for the user through the input unit 340 and the output unit 350 to collect medical examination result information from the user, or the user's personal health information or current condition information. can output

The user terminal sensor 360 may detect information related to the user's health, and may include, for example, an acceleration sensor and a location sensor. Accordingly, the user terminal 300 may acquire the user's exercise amount information through the user terminal sensor 360, for example.

FIG. 3 is a diagram for explaining an example of a configuration of the server 100 shown in FIG. 1 and an example of processing formulation composition information.

3(a) is a diagram for explaining the configuration of the server 100, and FIG. 3(b) is a diagram for explaining how the server 100 calculates formulation composition information by receiving current state information am.

In the following descriptions of FIG. 3 , detailed descriptions of overlapping contents with those previously described in FIGS. 1 and 2 will be omitted.

As shown in (a) of FIG. 3 , the server 100 may include a communication unit 110 , a memory 120 and a processor 130 .

The communication unit 110 communicates with the device 200 and the user terminal 300 through a network under the control of the processor 130, thereby providing information necessary for the service provided by the server 100 to the device 200 and the user. It can be transmitted to the terminal 300 or received from the device 200 and the user terminal 300 .

The processor 130 may control overall operations of the server 100 . Specifically, the processor 130 may calculate the base dose information for each nutritional component from the user's personal health information, and the device 200 may use the current state information obtained from the user during the period or time of providing the formulation to the user as the base dose information. Formulation composition information can be calculated by reflecting the information.

The memory 120 may store application information for driving a service provided by the server 100, information received from the user terminal 300 or device 200, and information generated during operation of the processor 130. Such a memory 120 is provided in the form of various storage devices such as ROM, RAM, EPROM, flash drive, hard drive, etc. in terms of hardware, or web storage (which performs the storage function of the memory 120 on the Internet). It may be provided in the form of webstorage or storage in the cloud.

As shown in (b) of FIG. 3, the driving method of the server 100 according to an example of the present invention includes receiving first current state information (S111), calculating first dosage form composition information (S112), Transmitting first dosage form composition information (S113), receiving second current state information (S114), calculating second dosage form composition information (S115), and transmitting second dosage form composition information (S116) can include

In the step of receiving the first current state information (S111), the processor 130 controls the communication unit 110 to receive the first current state information about the user at a first time point, which is any one of the first time periods. can

In the step of calculating the first dosage form composition information (S112), the processor 130 may calculate the first dosage form composition information by reflecting the first current state information.

More specifically, in the step of calculating the first dosage form composition information (S112), the processor 130 adds change amount information according to the first current state information to the base amount information for each nutritional component for the user, The serving amount information may be calculated, and the first dosage form composition information may be calculated by converting the daily serving amount of the first period into the number of dosage forms to be dispensed for each cartridge in the device 200 .

In the step of transmitting the first dosage form composition information ( S113 ), the processor 130 may control the communication unit 110 to transmit the first dosage form composition information to the device 200 dispensing the dosage form.

In the step of receiving the second current state information (S114), the processor 130 controls the communication unit 110 to receive the second current state information about the user at a second point in time, which is any one of the second periods. can

In the step of calculating the second dosage form composition information (S115), the processor 130 may calculate the second dosage form composition information by reflecting the second current state information.

More specifically, in the step of calculating the second dosage form composition information (S115), the processor 130 calculates the amount of change according to the second current state information in the base amount information for each nutritional component for the user, and then calculates the second period information. The daily serving amount information of can be calculated, and the second dosage form composition information can be calculated by converting the daily serving amount of the second period into the number of dosage forms to be dispensed for each cartridge in the device 200.

In the step of transmitting the second dosage form composition information ( S116 ), the processor 130 may control the communication unit 110 to transmit the second dosage form composition information to the device 200 .

In each of the steps of receiving the first and second current state information (S111 and S114), each of the first period and the second period may mean a length of a period predetermined by the server 100. For example, the first period , 2 periods each can have a time length of 24 hours or a day length of 1 day.

The second period may refer to a period continuing after the first period. For example, if the first period means January 1, 22 years, the second period may mean January 2, 22 years. Or as another example, if the first period is from 2:00 on January 1, 22 to 2:00 on January 2, the second period may be from 2:00 on January 2, 22 to 2:00 on January 3. .

Accordingly, each of the first and second points of time may refer to points of time selected by the user in each of the first period and the second period. For example, the first time point may be 8:00 AM on January 1st, which is the first period, and the second time point may be 7:00 PM on January 2nd, which is the second period.

The first current state information may refer to current state information received by the server 100 during a first period or a first time point, and second current state information is received by the server 100 during a second period or second time point. It may mean current state information that

Here, as described above with reference to FIG. 1 , each piece of current state information may include information on at least one of (1) information on a user's mental state or symptom or (2) information on a physical state or symptom of the user. . Specific details are replaced with those described above in FIG. 1 .

In addition, when there is no change in the user's body condition, the user may select “none” as the current state information, and in this case, the server 100 may receive “none” as the current state information.

The server 100 may receive the first and second current state information from the device 200 at the first and second points in time, respectively. However, in some cases, it is also possible for the server 100 to receive the first and second current state information from the user terminal 300 prior to the first and second time points of the first and second periods.

In each of the steps of calculating the first and second formulation composition information (S112 and S115), the base dose information may be dose information for each nutritional component calculated according to the user's personal health information. A method of calculating the base capacity information will be described later in detail with reference to FIG. 4 .

In each of the steps of calculating the first and second dosage form composition information (S112 and S115), the change amount information according to the current state information may be dose information for each nutritional component in which the current state information is converted for each nutritional component. Variation information may be included in the base capacity information and calculated as daily serving amount information. A method of calculating the amount of change information will be described later in detail with reference to FIG. 5 .

In each of the steps of calculating the first and second dosage form composition information (S112 and S115), the daily serving amount information is information obtained by adding the change amount information for each nutritional component at the first or second time point to the base amount information, and the user It may be dose information for each nutritional component provided to the user during the first period or the second period based on the personal health information and the current state information.

Each of the first and second dosage form composition information may include information on the type and number of dosage forms to be ejected from the device 200 corresponding to the first time point or the second time point.

Here, during the first and second periods, each of the base dose information used to calculate the first and second dosage form composition information is information based on the user's personal health information, may be identical to each other, and is obtained from the user at the first time point. Daily serving amount information for the first period according to the first current state information and daily serving amount information for the second period according to the second current state information acquired from the user at the second time point may differ from each other.

Accordingly, when the second current state information is different from the first current state information, the second formulation composition information may be different from the first formulation composition information. That is, when the second current state information is different from the first current state information, at least one of the type and number of dosage forms according to the second dosage form composition information of the second time point is the dosage form according to the first dosage form composition information of the first time point. It may be different from at least one of the type and number of.

Alternatively, when the second current state information is the same as the first current state information, the content of the second dosage form composition information may be the same as the content of the first dosage form composition information, and the type of dosage form according to the first dosage form composition information. and number and type and number of formulations according to the second formulation composition information may be the same.

More specifically, there may be a case where the server 100 receives fatigue as the first current state information at a first time point and stress as the second current state information at a second time point.

In this case, the number of discharged first dosage forms containing the first nutritional component (eg, vitamin B) associated with fatigue may be different from each other at the first and second time points, and the second nutritional component associated with stress may be different. The number of second dosage forms containing the component (eg, lactic acid bacteria) discharged at each of the first and second points in time may be different.

However, among the plurality of formulations, the number of third formulations containing a third nutritional component (eg, omega 3) not related to fatigue and stress may be the same as each other at the first and second points in time.

Hereinafter, a method of calculating the aforementioned base capacity information will be described in more detail with reference to FIGS. 4 and 5 .

4 is a diagram for explaining an example of a method for calculating base capacity information in the present invention. 5 is a diagram for explaining an example in which personal health variable value information is applied for each nutritional component when calculating base dose information in the present invention.

In the present invention, the base capacity information may be basically calculated by the server 100, but in some cases, the device 200 may also calculate the base capacity information.

In the following description of FIG. 4 , a method of calculating the base capacity information by the server 100 is described as an example, but a method of calculating the base capacity information by the device 200 may be similarly applied to FIG. 4 .

As shown in FIG. 4 , the server 100 calculates base capacity information in a step of extracting initial variable value information (S121), setting first base capacity information (S122), and personal health variable values. Extracting information (S123), calculating second base capacity information (S124), calculating third base capacity information (S125), and calculating fourth base capacity information (S126). can

A program for performing the method of calculating the base capacity information may be provided in the form of a program module or an artificial intelligence (AI) program module in the memory of the server 100 or the device 200 terminal.

In addition, although FIG. 4 shows the case in which each step is sequentially performed as an example, the present invention is not limited thereto, and the step of extracting initial variable value information (S121) and the step of extracting personal health variable value information (S121) S123) may be performed in advance before calculating the base capacity information.

Also, among the steps shown in FIG. 4 , the step of calculating the capacity information of the second and third bases may be omitted depending on the case. However, if the step of calculating the second and third base dose information is included, the base dose for each nutritional component can be more accurately calculated for the user's personal health. Hereinafter, the step of calculating the second and third base dose information A case in which is included will be described as an example.

In the step of extracting initial variable value information ( S121 ), at least one piece of initial variable value information may be extracted from the personal health information received by the server 100 .

Here, the personal health information may be extracted from at least one of user identification information, medical examination result information, and medical information. Hereinafter, as an example, a case in which identification information about a user, medical examination result information, and medical information are all extracted will be described as an example.

Identification information about the user may include, for example, information about the user's subscription ID, name, contact information, gender, and age. Such user identification information may be collected when a user signs up for a service provided by the server 100 .

The medical examination result information may refer to information about a result of the user terminal 300 or device 200 performing a medical examination of the user. To this end, the server 100 may transmit medical examination information to the user terminal 300 or the device 200 so that the user terminal 300 or the device 200 may perform the medical examination.

Questionnaire information may consist of basic query information and detailed query information. Query information may include, for example, detailed items classified by category.

For example, detailed query information may include first, second, and third categories, and each of the first, second, and third categories may include detailed items.

For example, the detailed items of the first category include questions about drinking, smoking, exercise, sleep habits, eating habits, etc., or the detailed items of the second category include self-efficacy, work-related, immune-related (allergies, etc.), family history, and medications. Including questions about medications (e.g. pharmaceuticals or nutritional supplements), etc., or detailed items in the third category include questions about various kinds of physical or mental illnesses, symptoms, or indications (or indications), etc. can do. For example, detailed items in the third category include questions related to physical indications such as cardiovascular disease, liver disease, cancer-related diseases, nervous system diseases, immunity, and stress, and questions related to mental indications such as depression, insomnia, and anxiety. can include

Further, the detailed query information of the medical examination information may include additional query information when there is a selection response corresponding to a specific category, and the additional query information may include additional query information for the selected indication. For example, when a user responds to an indication of cardiovascular disease, the duration of disease, treatment method, current or past history, complications, severity of symptoms, etc. Additional query information may be further included.

Using the questionnaire information as described above, the user terminal 300 or the device 200 may perform a questionnaire for the user.

When conducting a medical examination, the user terminal 300 or device 200, for example, displays information about the medical examination through a touch screen module capable of input and output as a single module, and examines the value input through the user's interaction. After saving as result information, it can be transmitted to the server 100. Alternatively, as another example, the user terminal 300 or device 200 may output medical examination inquiry information by voice and receive the user's voice as medical examination result information.

Medical information is information received by the server 100 from the medical institution server 500, for example, medical record information, imaging information, medication taking information, or health examination result information that a user has examined, examined, or diagnosed at a medical institution. may include at least one of them.

The server 100 may extract initial variable value information from personal health information extracted from at least one of the aforementioned user identification information, medical examination result information, or medical information.

Here, the initial variable value information includes the user's gender and age, and may optionally further include whether the user is pregnant or breastfeeding.

In step S122 of setting the first base quantity information, the server 100 may set the first base quantity information as the minimum quantity information for each nutritional component based on the initial variable value information extracted from the personal health information.

Specifically, the server 100 may set the minimum dosage for each nutritional component for the user by inputting initial variable value information for the user into a basic dosage table (or basic dosage algorithm) as an input value.

For example, the server 100 may calculate minimum dosage information for each nutritional component by inputting variable value information about the user's gender, age, pregnancy, and lactation status into a basic dosage table.

In the step of extracting personal health variable value information (S123), the server 100 performs at least one of indication variable value information, factor variable value information, and limitation variable value information from the personal health information. It is possible to extract personal health variable value information including For example, personal health variable value information includes indication variable value information and factor variable value information, but may optionally include limit variable value information.

The indication variable may be a variable for an indication indicating a physical disease, symptom or condition, mental disease, symptom or condition, or energy state affected by nutritional component, and the indication variable value information is obtained from the user's personal health information. It may be information about values of extracted indication variables.

As shown in FIG. 5 , such indication variables may include a plurality of indication variables (eg, a first indication variable to an nth indication variable) for each nutritional component. Examples of such indication variables include cardiovascular disease, liver disease, and depression.

The factor variable is a variable that affects the indication variable, and may be a variable for a detailed factor that forms or changes the value of the indication variable. Factor variable value information may be information on factor variable values for a specific indication variable.

Factor variables may be set for each indication variable. Accordingly, a plurality of factor variables may be dependent on one indication variable, and information on a plurality of factor variable values may be summed with a weight to form an indication variable value.

As shown in FIG. 5, when the first indication variable is, for example, cardiovascular disease, the factor variable is a variable that affects or forms the degree of cardiovascular disease, for example, the user's BMI index value, waist circumference Value, smoking level, family history level, etc. can be used as factor variables.

Such indication variables and factor variables may increase the first base dose information calculated for each nutritional component. For example, for the first nutritional component shown in FIG. 5 , a plurality of indication variables may be calculated with a weight and used to increase the first base dose of the first nutritional component.

As shown in FIG. 5, the limiting variable may be a variable for an element that is prohibited or restricted from taking each nutritional component according to the user's health condition, corresponding to the indication variable, and the limiting variable value information is obtained from the user's personal health information. It may be information about values of extracted limiting variables.

These limiting variables are the user's (1) lifestyle (eg, smoking, sleeping hours, etc.) or diet (eg, mackerel consumption, etc.), (2) user's condition (eg, pregnancy, lactation, etc.), (3) There may be a drug taken by the user or (4) a disease or disease of the user, and the first base dose of the corresponding nutritional component may be reduced by a limiting variable.

For example, in relation to the limiting variable, the present invention considers the interaction between the specific formulation provided by the device 200 and the specific drug when the user takes a specific drug, so that the server 100 determines the specific formulation. Servings may be limited.

In addition, when the user has a specific disease or disease, the server 100 may limit the amount of the specific formulation provided by the device 200 in consideration of the interaction between the specific formulation provided by the device 200 and the specific disease or disease.

In the present invention, a case in which all indication variable value information, factor variable value information, and limit variable value information are applied is described as an example, but unlike this, only indication variable value information and factor variable value information are applied, and limited variable value information may not apply. However, when all are applied, it is possible to provide a more precisely customized formulation to the user's personal health information, and the case where all are applied will be described as an example.

Such indication variable value information, factor variable value information, and limit variable value information may be expressed as numerical values extracted from user's personal health information.

For example, in the user's personal health information including at least one of user identification information, medical information, and medical examination result information about the user, when it is recognized that cardiovascular disease exists, an indication variable for cardiovascular disease is selected, Factor variable value information may be extracted according to a numerical value of a body mass index (BMI), a numerical value of a waist circumference, a numerical value of a smoking amount, a numerical value of a family history, and the like that affect cardiovascular disease.

In step S124 of calculating the second base capacity information, the server 100 may calculate the second base capacity information by reflecting the personal health variable value information extracted from the personal health information to the first base capacity information.

In the step of calculating the second base capacity information (S124) of the present invention, (1) the interaction between the user's body information (eg, height, weight, body surface area, pregnancy, genetic information, etc.) action, (2) interaction between the drug being administered and the nutritional component to be provided, (3) interaction between the nutritional component being taken and the nutritional component to be provided, (4) the disease and Interactions between nutritional components to be provided, (5) interactions between lifestyle and nutritional components to be provided, and (6) interactions between symptoms present and nutritional components to be provided. Taking this into account, the second base amount information for each nutritional component may be calculated.

To this end, the server 100 may calculate the second base dose information by varying the first base dose information for each nutritional component according to personal health variable value information.

More specifically, the server 100 reflects the factor variable value information dependent on each indication variable as an input value to the variable value-nutrient component mapping table based on the variable value-nutrient component mapping table stored in the memory 120, , Calculate the detailed rate of change according to the value information of each factor variable, and apply multiplication or summation to the detailed rate of change of each factor variable through the program module or artificial intelligence (AI) program module. The rate of change can be calculated.

Here, the change rate value of each indication variable may have a value increasing the first base capacity.

For reference, the rate of change of each indication variable calculated based on the variable value-nutrient component mapping table may be calculated within the range of the maximum rate of change (R) value set for each indication variable. In addition, the detailed rate of change (r) according to the value of each factor variable may be calculated within a range of the rate of change smaller than the maximum rate of change (R) of each indication variable.

In addition, the limited variable value information may calculate the second base capacity by reducing the first base capacity increased by the indication change rate value by a predetermined capacity or by processing it again as 0 (zero).

Accordingly, the indication variable can be used to calculate the dose of each nutritional component that has a positive effect on physical disease or symptom, mental disease or symptom, or energy state, and the factor variable is used to control the increase in the indication variable. It can be used, and the limiting variable can be used as a variable that reduces or zeroes the dose of each nutritional component.

For example, in the case of the limiting variable, when it is confirmed that sufficient intake of the first nutritional component is obtained through food or outdoor activities, the value may be set as a negative summation, and the indication variable and factor may be determined according to the application of the limiting variable. The dose determined by the variable may be reduced.

Furthermore, the limiting variable is a case that is already taken as a prescription drug or should not be taken due to an interaction with a specific drug being taken according to a prescription, a nutritional component contraindicated according to age, a nutritional component contraindicated for pregnant or lactating women, , In the case of a nutritional component contraindicated in taking due to other health conditions such as an underlying disease, the value may be set as a multiplication operation of 0 (zero), and accordingly, the dose determined by the indication variable and the factor variable is 0 ( zero) and can be limited.

More specifically, for example, omega 3, a nutritional component, is an indicator variable, and physical diseases or symptoms that are positively affected by omega 3 include cardiovascular disease, pregnancy-related diseases or symptoms, lactation-related diseases or symptoms, and liver disease. Mental disorders or symptoms may include cognitive dysfunction, depression, bipolar disorder, etc.

In addition, when the indication variable of omega 3 is cardiovascular disease, the factor variable for cardiovascular disease is the factor affecting cardiovascular disease, such as BMI (body mass index), waist circumference, smoking, drinking, lack of exercise, and interaction with drugs. (Hyper TG-inducing drugs), triglyceride level, family history as a CVD risk factor, and menopause information.

In addition, the limiting variable of omega 3 is a negative variable, for example, a mackerel intake level variable is set, or a variable limiting it to 0 (zero), taking contraindicated prescription drugs (eg, nutritional drug interaction (DNI)), separate omega 3 Information on whether to take or not may be set.

The first base dose according to the user's personal health information, the amount of increase by the indication variable and the factor variable, and the amount of decrease or limit by the limiting variable may be recorded and updated in the variable value-nutritional component mapping table.

The server 100 of the present invention refers to the variable value-nutritional ingredient mapping table and calculates and processes indication variables, factor variables, and limitation variables to determine the second basis from the first base amount information. Base capacity information can be calculated.

Here, the variable value-nutritional component mapping table may be configured by assigning a maximum rate of change (R) corresponding to each sequential variable process.

For example, in the variable value-nutritional component mapping table, the maximum fluctuation rate range (R) for each indication variable is set in correspondence with the first base dose for each nutritional component, and the factor variable is applied within the maximum fluctuation rate range (R). An incremental weight may be assigned.

In addition, when a plurality of indication variables are selected, the second base dose for each nutritional component is individually calculated for each indication variable, and the fluctuation rate values for each indication variable calculated by the variable value-nutritional component mapping table ( The second base dose for each nutritional component may be determined by applying and summing the weights (S1, S2, S3, ..., SN) in the order of higher R1, R2, R3, ... RN.

More specifically, when there are a plurality of indication variable values extracted from the user's personal health information, and the rate of change according to the plurality of indication variables is calculated by the variable value-nutritional component mapping table, the second base for the corresponding nutritional component The capacity is calculated by applying weights (S1, S2, S3, ..., SN) to the fluctuation rate according to a plurality of indication variables and multiplying each weight by the first base capacity, as shown in Equations 1 and 2 below. It can be.

For example, as shown in Equations 1 to 4 below, an increase value of the first base capacity information may be calculated using indication variable value information and factor variable value information. However, the present invention is not necessarily limited to Equations 1 to 4.

Here, D0 may mean the first base amount for each nutritional component, S may mean the sum of the weights for the corresponding nutritional component, and D (raw) may mean the second base amount for each calculated nutritional component.

Here, each of S1, S2, S3, ..., Sn means a weight value for each indication variable, and the sum of the weight values (S) can be calculated by summing the weight values for each indication variable.

Here, each weight value (S1, S2, S3, ..., Sn) for each indication variable is arranged in the order of highest fluctuation rate values (R1, R2, R3, ... RN) for each indication variable. can be a value

Here, weight values (S1, S2, S3, ..., Sn) for each indication variable can be calculated as in Equations 3 and 4 below.

In Equation 3, S1 means the largest weight value among weight values of a plurality of indication variables, and R1 is the rate of change values (R1, R2) according to a plurality of indication variables calculated by the variable value-nutritional component mapping table. , R3, ... RN) may mean the largest change rate value (R1).

Therefore, in the present invention, the nearest change rate value R1 among the change rate values of a plurality of indication variables may be assigned as the largest weight value S1.

Equation 4 may be an equation for determining the weight values of the second ranks (S2, S3, ..., Sn) excluding the largest weight value (S1) among weight values of a plurality of indication variables.

In Equation 4, the n value has a value greater than 2, Rn is the rate of change of each indication variable calculated from the medical information and the result information of the medical examination, and the calculated value of the rate of change of Rn is determined in descending order from the largest value. can Sr means a weight value for each indication variable.

Therefore, for example, the calculated rate of change value for the first indication variable is 115% and has a value of 1.15, the calculated rate of change value for the second indication variable is 220% and has a value of 2.2, and the third indication variable has a value of 2.2. Assuming that the calculated rate of change for the variable has a value of 1.2 as 120% and the calculated rate of change for the fourth indication variable as 150% and has a value of 1.5, R1 is the second indication having the largest value. The variable rate of change value is 2.2, R2 is the next highest rate of change value, 1.5, R3 is 1.2, and R4 is 1.15.

Accordingly, R1 = 2.2, R2 = 1.5, R3 = 1.2, R4 = 1.15 are reflected in Equations 3 and 4, and the weights S1, S2, S3, and S4 of each indication variable are calculated, According to 2, the total sum weight value S can be calculated.

Then, according to Equation 1, the S value, which is the total sum weight value, is reflected in the first base dose for each nutritional component, and the reduction amount according to the limiting variable value information is reflected for each nutritional component, so that the second base dose for each nutritional component is calculated It can be.

In the step of calculating the third base amount information (S125), the server 100 cuts off the amount of nutritional ingredients exceeding the first maximum serving amount of the second base amount information to the first maximum serving amount, thereby providing the third base amount information. can be calculated.

In addition, in the step of calculating the third base amount information (S125), together with the first maximum serving amount correction described above, nutritional ingredients that do not meet the preset minimum serving amount among the second base amount information may be corrected to have a minimum serving amount. there is. However, when performing the correction of the minimum serving amount, correction for nutritional components prohibited from being taken in personal health information may be excluded.

Here, the first maximum serving amount may mean the maximum recommended amount for each nutritional component that the user can take for a predetermined period of time. That is, if a user takes too much of a nutritional component, desired effects may not occur or side effects may occur. To prevent this, a first maximum serving amount may be set for each nutritional component.

The predetermined period may be 1 day or 24 hours, and the first maximum serving amount may be the maximum recommended daily amount for each nutritional component. However, the present invention is not necessarily limited thereto, and it is possible that the predetermined period varies for each nutritional component.

Therefore, in the step of calculating the third base dose information (S125), the server 100 determines whether the second base dose in which the personal health variable value information is reflected for each nutritional component exceeds the maximum recommended daily dose. For nutritional components, the third base dose may be calculated by performing a cut-off correction of the second base dose to the range of the maximum recommended daily amount.

The first maximum serving amount for each nutritional component may be set differently according to demographic group information, health status information, lifestyle information, side effects for each nutritional component, and the like.

More specifically, the first maximum serving amount for each nutritional component may be set differently according to demographic groups (gender, age, pregnancy status, lactation status).

For example, for vitamin C, the first maximum serving amount may be set to 200 mg for men between the ages of 40 and 50, and the first maximum serving amount may be set to 150 mg for women between the ages of 15 and 19 years.

Therefore, when the second base dose for vitamin C for the first user is calculated as 170 mg, when the first user is a male between the ages of 40 and 50, 170 mg is calculated as the third base dose, but the first user is 15 For females between the ages of -19 years, the dose of vitamin C can be corrected for the cut off to 150 mg to yield a third base dose.

In addition, the first maximum serving amount for each nutritional component is set differently according to the user's personal health information (physical or mental disease or condition), lifestyle (smoking status, etc.), or depending on side effects of the corresponding nutritional component. may be set differently.

For example, if the second base dose for vitamin C for the first user is calculated to be 170 mg, but the first user has gastrointestinal disorder, the dose of vitamin C is cut off to 100 mg by the first maximum serving amount according to the gastrointestinal disorder. and can be calculated as the third base capacity. Alternatively, when the first user has urinary stones, the dose of vitamin C may be cut off to 50 mg according to the first maximum serving amount according to the urinary stones, and thus calculated as a third base dose.

If, as described above, if the first maximum serving amount corresponds to a plurality of cases (eg, the first user is a male between the ages of 40 and 50 with gastrointestinal disorders and urinary stones), the first maximum serving amount (eg, , gastrointestinal disorder - 200 mg, urolithiasis - 50 mg) can be selected as the smallest value (eg 50 mg).

In the step of calculating the fourth base capacity information (S126), the server 100 receives the base capacity information of any one of the first to third base capacity information from the device 200, and cartridge information for each of the plurality of cartridges. Based on the above, fourth base capacity information may be calculated for each cartridge by performing redundancy correction while allocating each nutritional component to each cartridge.

Here, the base capacity information of any one of the first to third base capacity information may mean base capacity information calculated before the step of calculating the fourth base capacity information (S126).

That is, when the server 100 has calculated up to the first base capacity information but has not calculated the second and third base capacity information, the first base capacity information can be allocated to each cartridge, and the server 100 can allocate the second base capacity information. When the information is calculated, the second base capacity information can be allocated to each cartridge, and when the server 100 calculates the third base capacity information, the third base capacity information can be allocated to each cartridge.

Cartridge information may be received by the server 100 from the device 200 and stored in the memory 120 of the server 100 prior to calculating the fourth base capacity information (S126).

Such cartridge information may include information on each of a plurality of cartridges currently loaded in the device 200 and information on formulations stored for each cartridge.

For example, if the number of cartridges currently loaded in the device 200 is 8, the cartridge information may include information on formulations provided in each of the 8 cartridges. The information on the dosage form may include information on the type of dosage form provided in the cartridge, the number of remaining amounts of the dosage form, the date of manufacture of the dosage form, and information on the manufacturer.

The information on the type of formulation may include the name or identification number of the formulation, and when the server 100 receives information on the type of formulation, the server 100 queries the DB of the formulation stored in memory to determine the unit weight of the formulation, Information on the nutritional components contained in the formulation and the content of the nutritional components per unit weight of the formulation can be confirmed.

Therefore, the server 100 inquires cartridge information, which nutritional component formulations are currently stored in the device 200 for each cartridge, the content or content ratio of the nutritional components contained in each formulation, and the total formulation Recognize the number and total amount of nutrients.

Accordingly, the server 100 may query cartridge information to recognize nutritional components contained per unit dosage form of formulation provided for each cartridge and the content or content ratio of the corresponding nutritional component.

Redundancy correction means that when the server 100 queries cartridge information and recognizes that the same influencing component exists in a plurality of cartridges, the same influencing component is assigned to at least one of the plurality of cartridges. It can mean deducting the dose of a nutritional component.

For example, the third base capacity calculated for iron powder is 50mg and the third base capacity calculated for magnesium component is 10mg, and as a result of cartridge information inquiry of the server 100, an iron cartridge containing iron powder (100%) and iron powder There may be cases in which multimineral cartridges containing (50%) and magnesium (50%) exist together.

At this time, the server 100 may first allocate 10 mg of the third base for the magnesium component to the multi-mineral cartridge.

Thereafter, the server 100 performs redundancy correction by subtracting 10 mg of the iron component allocated amount generated while allocating 10 mg of the magnesium component to the multi-mineral cartridge from the third base capacity of 50 mg calculated for the iron component, so that the iron content in the iron cartridge is reduced. A fourth base dose of the ingredient yields 40 mg.

For reference, the fourth base capacity information for the multi-mineral cartridge may be calculated as 20 mg, which is a sum of 10 mg of magnesium and 10 mg of iron.

Such redundant corrections can be made between cartridges containing a single nutritional component (eg, containing iron) and cartridges containing a complex nutritional component (eg, containing iron and magnesium) as well as between cartridges containing a first complex nutritional component (eg, containing zinc and vitamin C). ) cartridge and the second complex nutritional component (eg, containing zinc, vitamin C, and vitamin E) cartridge.

After performing the redundancy correction described above, the server 100 may calculate the fourth base capacity information by allocating the third base capacity information to each cartridge.

Here, the above-described first, second, third, and fourth base dose information is a unit value according to each nutritional component, such as IU (international unis), mg (milligram), mcg (microgram), and CFU (Colony Forming Unit). can have

However, the present invention is not necessarily limited thereto, and since the fourth base amount information calculated by the server 100 is information allocated to the nutritional components of the formulation held by each cartridge, the third base amount information for each nutritional component is information assigned to each nutritional component. It is also possible that the fourth base capacity information for the component has a unit value of weight (eg, mg).

Hereinafter, unless otherwise specified, fourth base capacity information calculated for each cartridge is referred to as 'base capacity information'.

As described above, the server 100 of the present invention may calculate the base capacity differently according to the user's personal health information. That is, according to the present invention, the base dosage for each nutritional component may vary according to the user's health condition.

So far, the case where the server 100 calculates the base capacity information has been described as an example, but the present invention is not limited thereto, and the base capacity information may be calculated by the device 200 in some cases.

To this end, a program or algorithm for calculating base capacity information may also be stored in the device 200 .

If the device 200 calculates the base capacity information, the step of calculating the first, second, third, and fourth base capacity information in FIG. 4 is maintained, and the initial variable value information and the personal health variable value information are extracted. Instead, initial variable value information and personal health variable value information may be received from the server 100 .

6 is a diagram for explaining an example in which current state information is reflected in the present invention.

In (a) of FIG. 6, a method for the server 100 to reflect the user's current state information to the base capacity information is described as an example, but the present invention is not necessarily limited thereto, and the device 200 is not limited to the user's current state information. It is also possible to reflect state information to base capacity information.

In order to perform an operation of reflecting the current state information to the base capacity information, a program or artificial intelligence (AI) program may be provided in the form of a module in the memory of the terminal of the server 100 or the device 200 .

The server 100 of the present invention reflects the user's current state information in the base volume information for each cartridge calculated based on the user's personal health information, thereby providing a formulation with a dose more optimized for changes in the user's physical condition. there is.

Here, the time of reflecting the information on the current state of the user in the base capacity information may be the time when the user receives the dosage form.

To this end, the server 100 may receive current state information of the user from the device 200 or the user terminal 300 . The time at which the server 100 receives the user's current state information may be a time when the user is provided with a formulation or a period including a time when the user is provided with a formulation.

Specifically, the time at which the user receives the dosage form may be the above-described first and second time points, or a period from the start of the first period to the first time point, or a period from the start of the second period to the second time point.

As shown in (a) of FIG. 6, the method for the server 100 to reflect the user's current state information to the base capacity information includes inputting (S131), calculating variation information (S132), It may include calculating the serving amount (S133) and converting it into the number of formulations (S134).

In the input step (S131), the current state information received by the server 100 may be input to the state reflection algorithm.

The state reflection algorithm may receive current state information and calculate a variable value for each nutritional component according to the current state information. The state reflection algorithm may be stored in the memory 120 of the server 100, and may be called and used at a necessary time under the control of the processor 130.

In the step of calculating change amount information (S132), the state reflection algorithm provided in the server 100 may calculate change amount information for each nutritional component based on the user's current state information.

For example, the state reflection algorithm may reflect the user's current state information based on the above-described third base amount information to calculate change amount information for each nutritional component.

In the present invention, a case in which variation information according to the current state information is calculated based on the third base capacity information will be described as an example, but the present invention is not necessarily limited to this, and the first base capacity information or the second base capacity information It is also possible to calculate the amount of change information on the basis. However, when the server 100 calculates change amount information based on the third base capacity information for which the first maximum serving amount correction has been performed, the current state information of the user may be more accurately reflected. Hereinafter, a case in which variation information is calculated based on the third base capacity information will be described as an example.

Therefore, in FIG. 3 described above, when the server 100 calculates the change amount information according to the first current state information at the first point in time or the change amount information according to the second current state information at the second point in time, the first , Variation information according to each of the 2 current state information may be calculated differently for each nutritional component according to the third base content information.

Specifically, the device 200 has a plurality of cartridges storing first, second, and third dosage forms containing first, second, and third nutritional ingredients, respectively, and the first nutritional ingredients have first current state information and effects. Assume that the second nutritional component affects the second current state information, and the third nutritional component does not affect the first and second current state information.

In this case, when the server 100 receives the first current condition information at the first time point, the server 100 sets a positive (+) value or a negative (-) value for the amount of change only for the first nutritional component. It is possible to calculate change amount information having, and change amount information in which each change amount is 0 (zero) for the second and third nutritional components.

In addition, when the server 100 receives the second current state information at the second time point, the server 100 provides information having a positive (+) value or a negative (-) value for the amount of change only for the second nutritional component. , and for the first and third nutritional components, information in which the value of change is 0 (zero) can be calculated.

For example, the cartridge of the device 200 has a lactic acid bacteria component, a multi-mineral component, and an omega-3 component, the lactic acid bacteria component affects only 'stress', the multi-mineral component affects only 'exercise', and the omega-3 component Let's assume that the 3 ingredients have no effect on stress and exercise.

In such a state, when the server 100 receives information about 'stress' as the first current state information, the server 100 has a positive (+) value or a negative value only for the lactic acid bacteria component related to the stress. Change amount information having a (-) value can be calculated, and change amount information of 0 (zero) can be calculated for the omega 3 component and the multimineral component.

In addition, when the server 100 receives information about 'exercise' as the second current state information, the server 100 has a positive (+) value or a negative (-) value only for multi-mineral components related to exercise. ) value, and information of a change of 0 (zero) can be calculated for the omega-3 component and the lactic acid bacteria component.

In addition, the amount of change having a positive (+) value in the amount of change information may be calculated differently according to the size value of the third base dose of each nutritional component. For example, the change amount having a positive (+) value may be calculated differently according to the ratio of the third base dose to the second maximum serving amount for each nutritional component.

Here, the second maximum serving amount may be information pre-stored in the memory 120 of the server 100, and may have a value equal to or greater than the first maximum serving amount described above. In the present invention, a case in which the second maximum serving amount for each nutritional component is the same as the first maximum serving amount will be described as an example. As an example, the second maximum serving amount may be set differently according to the demographic group (gender, age, pregnancy, lactation status) and physical or mental disease, symptom, or condition for each nutritional component, as in the first maximum serving amount. there is.

More specifically, (1) when the ratio of the third base dose to the second maximum serving amount is large, the allowable range of the increased amount of change may be relatively small, and (2) the ratio of the third base dose to the second maximum serving amount is If it is small, the allowable range of the change amount to be increased may be relatively large.

For example, when the second maximum serving amount for the user's vitamin C component is 200 mg and the third base dose for the user's vitamin C component is 150 mg, the allowable range of variation in the amount of vitamin C component increased according to the current state information is It can be increased within the range of 50mg or less.

However, unlike the above, when the second maximum serving amount for the user's vitamin C component is 200 mg or the third base dose for the user's vitamin C component is 50 mg, the amount of change in the vitamin C component increased according to the current state information The permissible width can be increased within the range of 150 mg.

As described above, after the change amount information according to the current status information is calculated, the server 100 determines that the sum of the amounts added to the third base amount for each nutritional component exceeds the second maximum serving amount. Correction may be performed to cut off the calculated change amount to a limit of the second maximum serving amount so as not to exceed the maximum serving amount.

That is, the server 100 may adjust the amount of change calculated through the correction of the second maximum serving amount, and the adjusted amount of change information may be used in the daily serving amount calculation step.

In the step of calculating the daily serving amount (S133), the server 100 may calculate the daily serving amount by including the variation information in the base amount information for each nutritional component.

Here, the base capacity information used to calculate the serving amount per day may be fourth base capacity information calculated for each cartridge by applying redundancy correction.

Here, the daily serving amount may be calculated differently for each time point at which the current state information is received, since change amount information reflecting the user's current state information is reflected in the base capacity information.

More specifically, when the first current state information and the second current state information described in FIG. 3 are different from each other, the daily serving amount information for each nutritional component according to the first current state information at the first point in time during the first period is Daily serving amount information for each nutritional component according to the second current state information at a second point in time during the period may be different from each other.

However, unlike the above, when the first current state information and the second current state information are the same, the daily serving amount information for each nutritional component according to the first current state information and the daily serving amount for each nutritional component according to the second current state information Information may be identical to each other.

For example, as shown in (b) of FIG. 6, the cartridge of the device 200 has a lactic acid bacteria component, a multi-mineral component, and an omega-3 component, and the lactic acid bacteria component affects only 'stress', and the multi-mineral component Affects only 'exercise', omega 3 component has no effect on stress and exercise, lactobacillus component is 7 billion CFU, multi-mineral component is 100 mg, omega 3 component is 120 mg as the 4th base dose according to the user's personal health information Suppose this is calculated.

Here, the server 100 receives stress and exercise as the first current state information, the amount of change in lactic acid bacteria component is increased by 3 billion CFU, the amount of change in multimineral component is increased by 50 mg, and the amount of change in omega 3 is calculated as 0 (zero) In one case, the server 100 provides 10 billion (7 billion + 3 billion) CFU of lactobacillus component, 150 mg (100 mg + 50 mg) of multi-mineral component, and omega 3 component as a daily serving amount for each nutritional component according to the first current state information. Silver can yield 120mg (120mg+0mg).

In addition, when the server 100 receives the stress as the second current state information, the amount of change in the lactic acid bacteria component is increased by 3 billion CFU, and the amount of change in the multimineral component and omega 3 is calculated as 0 (zero), the server 100 10 billion (7 billion + 3 billion) CFU for lactobacillus component, 100 mg (100 mg + 0 mg) for multi-mineral component, and 120 mg (120 mg + 0 mg) for omega-3 component according to the second current status information. can be calculated.

In addition, as an example, if the current state information is not obtained from the user terminal 300 or the device 200 or is selected as 'none' and then the server 100 receives it, the server 100 determines the current state information according to the current state information. The value of the change amount can be calculated as 0 (zero).

If the change amount value is 0 (zero), since the change amount information of each nutritional component included in the base amount information for each nutritional component is 0 (zero), the server 100 provides the fourth base amount information and the fourth base amount information for all nutritional components. The same value can be calculated as daily serving amount information. For example, when the server 100 receives 'none' as the current status information, the server 100 has 7 billion CFU of lactic acid bacteria component, 100 mg of multi-mineral component, the same as the fourth base dose in a daily serving amount, The omega 3 component can yield 120 mg.

In addition, when the change amount of a certain nutritional component has a negative (-) value, the server 100 subtracts the amount of change calculated from the fourth base amount information of the corresponding nutritional component or decreases the fourth base amount information by the ratio according to the change amount. This can be used to calculate the daily serving amount.

For example, if the fourth base dose of the vitamin C component causing gastrointestinal disorder is 100 mg, and gastrointestinal disorder is received as the current state information and the amount of change in the vitamin C component is calculated as (-) 50 mg, the server 100 calculates 100 mg 50 mg can be subtracted from 50 mg to yield 50 mg as a daily serving of vitamin C.

In some cases, the daily serving amount of a nutritional component may be calculated as 0 (zero) by deducting the entire fourth base dose of a nutritional component due to change amount information having a negative (-) value.

Here, as an example, the daily serving amount information may be calculated as a unit value for nutritional components of formulations held for each cartridge. However, the present invention is not necessarily limited thereto, and the daily serving amount information may be calculated as a weight (eg, mg) value for nutritional components.

In this way, the server 100 of the present invention calculates the daily serving amount information by including the current condition information according to the change in the user's physical condition into the base amount information for each nutritional component according to the user's personal health information in real time, It is possible to provide information for each nutritional component more precisely tailored to the user's real-time health condition.

In the step of converting into the number of formulations (S134), the server 100 may convert the daily serving amount for each nutritional component for a predetermined period into the number of formulations to be dispensed for each cartridge.

More specifically, in the step of converting into the number of formulations (S134), the server 100 converts the daily serving amount of the first period into the number of formulations to be dispensed for each cartridge to calculate first formulation composition information, , Second dosage form composition information may be calculated by converting the daily serving amount of the second period into the number of dosage forms to be dispensed for each cartridge.

In the step of converting the number of formulations (S134), the server 100 refers to the individual unit weight of the formulation held in each cartridge and the individual unit content of the active ingredient contained in the individual unit formulation from the cartridge information inquired by the server 100, The daily serving amount for each nutritional component can be converted into the number of formulations to be dispensed for each cartridge.

As an example, the calculated daily serving amount for the vitamin B component is 330 mg, and as a result of the server 100 querying the vitamin B cartridge information among the cartridge information, the individual unit weight of the vitamin B formulation is 40 mg, and the vitamin B component When the individual unit content is 30 mg, the server 100 may divide 330 mg by 30 mg and calculate 11 as the number of vitamin B formulations to be ejected from the vitamin B cartridge.

In this way, when the server 100 converts the daily serving amount for each nutritional component into the number of formulations to be dispensed for each cartridge in the step of converting to the number of formulations of the present invention, the server 100 converts the number of formulations substantially contained in individual unit formulations. The number of formulations can be converted based on the individual unit content of the active ingredient.

Accordingly, the present invention can provide a more precise dose of formulation to the user.

For reference, when only the daily serving amount for the vitamin B component calculated under the same conditions as described above is calculated as 335mg, the server 100 divides 330mg by 30mg and then divides 330mg by 30mg, and the remaining 5mg It is not included in the conversion of the number of silver formulations and can be purified through rounding.

Accordingly, even when the daily serving amount of the vitamin B component is 335 mg, the server 100 may calculate 11 as the number of vitamin B formulations to be discharged from the vitamin B cartridge. Accordingly, the present invention can prevent the user from overdosing on nutritional ingredients.

So far, the case where the server 100 reflects the current state information to the base capacity information has been described as an example, but the present invention is not limited thereto, and in some cases, a method of reflecting the current state information to the base capacity information is a device ( 200) may be performed.

To this end, a program or algorithm for reflecting current state information may also be stored in the device 200 .

If the device 200 reflects the current state information to the fourth base capacity information, the device 200 obtains the third base capacity information and the fourth base capacity information from the server 100 before acquiring the current state information from the user. Capacity information may be received.

FIG. 7 is a diagram for explaining an example of a physical structure of the device 200 shown in FIG. 1 .

In an embodiment of the present invention, the device 200 may be configured in a form in which the device terminal 230 is integrally coupled to the hardware 210 for dispensing the dosage form. However, the device terminal 230 may also be provided in a form that is detachable from the hardware 210 . When the device terminal 230 is provided in a detachable form, the device terminal 230 may communicate with the dispensing hardware 210 wirelessly.

The dispensing hardware 210 may control ejection of formulations from the plurality of cartridges 212 storing formulations according to formulation composition information, and may count the number of dispensed formulations.

The device terminal 230 may obtain, for example, current state information from a user, transmit the information to the server 100, receive formulation composition information from the server 100, and transmit the information to the dispensing hardware 210. However, the present invention is not limited thereto, and in some cases, the device terminal 230 may generate formulation composition information and transmit it to the dispensing hardware 210 .

As shown in FIG. 7, the hardware 210 according to an example of the present invention includes a cartridge insertion unit 211, a plurality of cartridges 212, a formulation discharge sensor 213, a formulation discharge passage 214, and an outlet ( 215), and a cup stand 216. In addition, it may further include components of general electronic devices such as a power device such as a dispensing device and an electric motor for dispensing a dosage form, a hardware communication unit, a camera unit, an external communication means, and a power supply unit.

A plurality of cartridges 212 may be inserted into each of the plurality of cartridge insertion units 211 . Formulations containing different nutritional ingredients may be stored in the plurality of cartridges 212 .

In addition, two or more formulations may be mixed and stored in each cartridge 212 . For example, a cartridge 212 storing a multivitamin formulation in which a vitamin B component and a vitamin C component are mixed may be inserted.

Also, a dosage form discharge passage 214 may be formed below the cartridge insertion part 211 . The formulation discharge passage 214 may be in communication with each formulation outlet 215 of the plurality of cartridges 212 . Various types of formulations discharged from the plurality of cartridges 212 may be discharged to the outside of the device 200 through the final discharge port 215 through the formulation discharge passage 214 . A cup stand 216 may be formed below the final discharge port 215 .

According to an embodiment of the present invention, a dosage form dispensing sensor 213 for detecting the discharge amount of the dosage form (ie, the number of dispensed dosage forms) may be provided at the bottom of each of the plurality of cartridges 212 . The dosage form dispensing sensor 213 may detect the number of dosage forms ejected from each cartridge 212 to generate dispensing amount information, and the device 200 may store the dispensing amount information or transmit it to the server 100. For example, a photo interrupter, an ultrasonic sensor, an infrared sensor, a camera sensor, or the like may be applied to the dosage form dispensing sensor 213 .

As shown in FIG. 7 , the formulation discharge passage 214 may have a structure inclined toward the final discharge port 215, and the formulation discharged from the cartridge 212 rolls toward the final discharge port 215 to move into a cup. It can be collected in a cup 201 located on a pedestal 216 .

A device terminal 230 may be provided on an outer portion (eg, upper portion) of the device 200, and the device terminal 230 may provide information to a user and receive data and commands from the user. For example, the device terminal 230 may receive or obtain data related to the user's health, such as current state information. The configuration of the device terminal 230 will be described in detail with reference to FIG. 8(b).

The device terminal 230 may transmit and receive information by communicating with the server 100 . Specifically, the device terminal 230 receives formulation composition information from the server 100 and transmits it to the hardware 210, and the hardware 210 generates a control signal corresponding to the formulation composition information to control the formulation to be dispensed. can

8(a) is a diagram for explaining an example of a circuit configuration of the device 200 shown in FIG. 7, and FIG. 8(b) is a diagram for explaining an example of a configuration of a device terminal.

As shown in (a) of FIG. 8, the circuit configuration of the device 200 according to an example of the present invention includes a cartridge management unit 221, a formulation dispensing unit 222, a dispenser control unit 223, a biosignal sensing unit ( 224) and the device terminal 230. Here, the cartridge management unit 221, the formulation dispensing unit 222, the dispenser control unit 223, and the biosignal sensing unit 224 may be provided in the dispensing hardware 210, and the biosignal sensing unit 224 may be may be omitted depending on

The cartridge management unit 221 may store and manage cartridge information about the cartridges 212 in which formulations having various nutritional components are stored.

Specifically, a memory chip may be provided in each of the plurality of cartridges 212 . When the cartridge 212 storing a specific formulation is inserted into the cartridge insertion unit 211, the cartridge management unit 221 stores the type or name of the corresponding formulation according to nutritional components from the memory 120 provided for each cartridge 212, Cartridge information including at least one of individual unit weight of the dosage form, individual unit content of nutritional ingredients included in the dosage form, storage quantity information, manufacturing date, and manufacturer is received, and through the dispenser control unit 223 and the device terminal 230 It can be transmitted to the server 100.

In addition, the cartridge management unit 221 may monitor the discharge amount information of the formulations (IG1 to IGN) discharged from each cartridge 212 and the remaining amount information of the formulation stored for each cartridge 212, the discharge amount information and the remaining amount information It may be output through the device terminal 230 or transmitted to the server 100 and the user terminal 300 .

The dosage form dispensing unit 222 is a dispensing device coupled to each cartridge 212 to eject the dosage form, a drive motor mechanically coupled to each dispensing device to operate the dispensing device, and a dosage form provided at the bottom of each dispensing device. It may include a formulation discharge sensor 213 for detecting the number of.

Each of the plurality of driving motors may operate the ejection device of each of the plurality of cartridges 212 according to a control signal input from the dispenser control unit 223 to eject the formulation from each cartridge 212 . The dosage form dispensing sensor 213 may count the number of dosage forms dispensed from the cartridge 212 to generate dispensing amount information, and the generated dispensing amount information may be provided to the dispenser control unit 223 .

When the formulation dispensing unit 222 is driven, the formulation dispensing sensor 213 detects and counts the number of formulations discharged from each cartridge 212, and the counted and generated discharge amount information is transmitted to the device through the dispenser control unit 223. It may be transmitted to the terminal 230. Thereafter, the device terminal 230 may transmit discharge amount information to the server 100 .

The dispenser controller 223 may include a printed circuit board (PCB) on which a processor, memory, and communication module for controlling overall operations of the device 200 are mounted.

The dispenser control unit 223 may be electrically connected to the device terminal 230, the cartridge management unit 221, and the formulation dispensing unit 222, and in some cases, the biosignal sensing unit 224 may be connected to the device 200. and controls the cartridge management unit 221 and the formulation dispensing unit 222 according to information provided from the device terminal 230, and transmits information input from the cartridge management unit 221 and the formulation dispensing unit 222 to the device terminal 230. ) can be provided.

Specifically, the dispenser control unit 223 may provide cartridge information provided from the cartridge management unit 221 to the device terminal 230 . The dispenser control unit 223 converts formulation composition information input from the device terminal 230 into a control signal, and controls the formulation to be discharged from each cartridge 212 by inputting the control signal to the formulation dispensing unit 222. .

In addition, the dispenser control unit 223 provides the discharge amount information provided from the formulation dispensing unit 222 to the device terminal 230 and the cartridge management unit 221, and the cartridge management unit 221 subtracts the discharge amount information from the storage quantity information of the formulation Remaining amount information can be generated, tracking the remaining amount information of the dosage form for each cartridge 212, and the remaining amount information can be provided to the device terminal 230 through the dispenser control unit 223.

The bio-signal sensing unit 224 that detects the user's bio-signal may be connected to the dispenser controller 223 by wire or wirelessly.

The biosignal sensing unit 224 may include, for example, a biometric sensor and a sensor for detecting a user's biosignal (e.g., electromyogram, brainwave, etc.), and the biosignal obtained from the user is a dispenser control unit 223. ) may be provided to the device terminal 230 through.

As shown in (b) of FIG. 8 , the device terminal 230 may include a communication unit 231 , a memory 232 , a processor 233 , an input unit 234 and an output unit 235 .

The communication unit 231 of the device terminal 230 may communicate with the dispensing hardware 210 and the server 100 .

The input unit 234 of the device terminal 230 includes various types of input units 234 for receiving user's commands, for example, a touch pad, a keyboard, a microphone (243b in FIG. 7), a camera (243a in FIG. 7), and the like. and may further include various types of sensors (eg, a touch sensor and a motion sensor) for sensing various external physical energies of the device 200 .

When a camera (243a in FIG. 7 ) is provided as the input unit 234 of the device terminal 230 , the camera 243a may capture a user's motion for a period after the dosage form is dispensed. The device 200 may store and transmit the user's photographing information to the server 100 or transmit it to the medical institution server 500 . In this case, the server 100 or the medical institution server 500 may perform image analysis or video analysis on the photographing information to accurately determine whether or not the user actually ingested the formulation discharged from the device 200 .

Alternatively, the device terminal 230 detects a biometric sensor configured to detect a user's biometric information (eg, fingerprint, face, iris, vein, voice, etc.), and a user's biometric signal (eg, electromyogram, brainwave, etc.) A sensor or the like may be further provided.

The output unit 235 of the device terminal 230 may include, for example, a display device, a speaker, and the like for providing information to a user. The output unit 235 is, for example, at least one type of types such as a liquid crystal display (LCD), a light emitting diode (LED), an organic light emitting diode (OLED), and a quantum dot light emitting diode (QLED). A display device may be included.

The device terminal 230 outputs information related to the dispensing hardware 210 through the output unit 235 (eg, information on the remaining amount of the formulation remaining in the cartridge 212), icon information for specifying the user, and the current state of the user. Information, discharge amount information, etc. can be displayed.

For example, the device terminal 230 may include a touch screen module capable of input and output as one module, and information may be received from a user through the touch screen module.

In addition, when the device terminal 230 includes a microphone (243b in FIG. 7 ) and a speaker, the device terminal 230 may perform an interview for the user using the microphone and the speaker. For example, the device terminal 230 may output paperwork question information to the user through a speaker, receive the user's answer through a microphone, and generate paperwork result information.

Also, it is possible for the device terminal 230 to receive current state information as voice input from the user using a microphone and a speaker. At this time, the device terminal 230 may create a face image by photographing the user's face using a camera. After that, the present invention can analyze the user's voice and facial image and use it as the user's current state information.

The memory 232 of the device terminal 230 includes an application program for operating the dispensing hardware 210 in conjunction with the server 100 and an application program for acquiring current state information from the user or interworking with the server 100. , information received from the dispensing hardware 210 or information received from the server 100 may be stored.

The processor 233 of the device terminal 230 controls to obtain current state information from the user at a specific time point, and the formulation dispensing unit 222 responds to the specific time point based on formulation composition information in which the current state information at the specific time point is reflected. It can be controlled to discharge a combination of one dosage form.

An example of a method of operating the device 200 by the processor 233 will be described in more detail with reference to FIG. 9 .

FIG. 9 is a diagram for explaining an example of a method of operating the device 200 shown in FIG. 7 .

In FIG. 9 and below, detailed descriptions of overlapping contents with those previously described are omitted, and are replaced with the above-described contents.

As shown in FIG. 9 , the operating method of the device 200 according to an example of the present invention includes obtaining first current state information (S210) and dispensing a combination of formulations corresponding to a first time point (S220). ), obtaining second current state information (S230), and dispensing a combination of formulations corresponding to the second time point (S240).

In the step of obtaining first current state information ( S210 ), the device 200 may obtain first current state information of the user at a first point in time during a first period.

In the step of dispensing a combination of dosage forms corresponding to the first time point (S220), the device 200 may eject a combination of dosage forms corresponding to the first time point based on the first dosage form composition information in which the first current state information is reflected. can

In obtaining second current state information ( S230 ), the device 200 may obtain second current state information of the user at a second time point among second periods consecutive after the first period.

In the step of dispensing a combination of dosage forms corresponding to the second time point (S240), the device 200 may eject a combination of dosage forms corresponding to the second time point based on the second dosage form composition information in which the second current state information is reflected. can

In each of the steps of acquiring the first and second current state information (S210 and S230), the device 200 receives a first signal from the user through the input unit 234 or the biosignal sensing unit 224 provided in the device terminal 230. , the second current state information may be received or obtained. For example, when the device terminal 230 includes a touch screen module, the device 200 may receive first and second current state information from the user through the touch screen module. This will be described in more detail with reference to FIG. 9 .

However, the present invention is not limited thereto, and the device 200 collects and acquires the user's face image or voice information through a camera or microphone provided in the device terminal 230 and uses it as the first and second current state information. may be

Here, when the second current state information is different from the first current state information, a combination of dosage forms ejected by the device 200 corresponding to the second time point may be different from a combination of dosage forms ejected corresponding to the first time point.

That is, when the second current state information is different from the first current state information, at least one of the type and number of dosage forms that the device 200 dispenses corresponding to the second time point corresponds to the dosage form derived corresponding to the first time point. It may be different from at least one of the type and number.

Alternatively, when the second current state information is the same as the first current state information, the combination of formulations ejected by the device 200 corresponding to the second time point may be the same as the combination of formulations ejected corresponding to the first time point. there is.

That is, when the second current state information is the same as the first current state information, at least one of the type and number of dosage forms ejected by the device 200 corresponding to the second time point is the type of dosage form dispensed corresponding to the first time point. and may be equal to the number.

To this end, each of the first and second dosage form composition information in which the first and second state information is reflected in the base volume information for each nutritional component may include information on the type and number of dosage forms to be dispensed.

Accordingly, when the first and second current state information are different from each other, at least one of the type and number of dosage forms included in the first and second dosage form composition information may be different from each other.

That is, when the second current state information is different from the first current state information, information on at least one of the type and number of dosage forms included in the second dosage form composition information is the type and number of dosage forms included in the first dosage form composition information. It may be different from the information on at least one of them.

For example, when the plurality of cartridges 212 provided in the device 200 include the first, second, and third formulations containing the first, second, and third nutritional ingredients, the first and second formulation composition information is , 2, 3 information on the dosage form may be included.

Here, the first and second current state information are different from each other, the first formulation containing the first nutritional component is related to the first current state information, and the second formulation containing the second nutritional component is related to the second current state information. , and a third formulation containing a third nutritional component has no relevance to the first and second current state information.

In this case, the first dosage form composition information includes information on the number of first dosage forms calculated as a daily serving amount by including the amount of change according to the first current state information in the base amount of the first nutritional component, and the second, 3 dosage forms may include information on the number of second and third dosage forms calculated as a daily serving amount with the base doses of the second and third nutritional ingredients unchanged according to the first current state information.

In addition, the second dosage form composition information includes information on the number of second dosage forms calculated as a daily serving amount by including the amount of change according to the second current state information in the base amount of the second nutritional ingredient, and the first and third dosage forms may include information on the number of first and third dosage forms calculated as a daily serving amount without change according to the second current state information.

Therefore, the number of first and second dosage forms that are related to each of the first and second current state information is different from each other in the number discharged at the first and second time points, and the third dosage form that is not related to each of the first and second current state information is The numbers discharged at the first and second points in time may be the same.

As such, the device 200 according to an example of the present invention obtains current condition information from the user at the time the user intends to take the dosage form, and selects the type and number (or dose) of the dosage form more optimized for the user's current health condition. can provide

Hereinafter, various embodiments and modified examples in which the above-described server 100, device 200, and user terminal 300 are operated in conjunction with each other will be described. In FIG. 10A and below, detailed descriptions of overlapping contents with those described in FIGS. 1 to 9 are replaced with the previous contents.

In addition, the order related to the flow and operation of information shown in FIG. 10A and below is only shown for explanation by way of example, and the present invention is not limited to the order related to the flow and operation of information.

10A and 10B are diagrams for explaining a first embodiment of a method in which the service providing server 100, the user terminal 300, and the device 200 shown in FIG. 1 work in conjunction, and FIG. 11 is FIGS. 10A and 10B are diagrams for explaining an example of a method for obtaining user-specific information by the device 200 in the first and second periods.

FIG. 12 is a diagram for explaining an example of a method for the device 200 to obtain current state information in the first and second periods of FIGS. 10A and 10B.

FIG. 13A is a diagram for explaining an example in which the user terminal 300 displays a daily serving amount tailored to the user for each nutritional component in response to current state information, and FIG. 13B is a diagram showing the user terminal 300 according to the discharge amount information Based on the cumulative dose information, it is a diagram for explaining an example of displaying whether or not to take a customized nutritional ingredient, insufficient amount, etc., and FIG.

FIG. 14 is a table for explaining an example in which change amount information at a first point in time is reflected, and FIG. 15 is a table for explaining an example in which change amount information at a second point in time is reflected.

As shown in FIG. 10A , in the interlocking operation method according to the first embodiment of the present invention, a step of registering user information and device information (S10) may be performed.

In the step of registering user information and device information (S10), the user terminal 300 receives user identification information (eg, the user's name, phone number, e-mail address, etc.) and device identification information (eg, a unique code number of the device 200) may be received and transmitted to the server 100 (S11).

In addition, the device 200 may transmit device identification information to the server 100 in order to register for a service provided by the server 100 (S13).

The server 100 may receive user identification information and device identification information from the user terminal 300 and device identification information from the device 200 . The server 100 registers a user account in the server 100 using the user identification information, and sets the user account and the device 200 to be linked using the device identification information (S15), thereby registering (S10). ) can be performed.

When the registration step (S10) is performed in this way, the server 100 transmits user account information (eg, user's name, nickname or contact information) associated with the device 200 to the device 200, and the device ( 200) may internally store user account information. Thereafter, when the user intends to receive a dosage form through the device 200, the device 200 may use user account information to obtain user-specific information.

Thereafter, the server 100 may request the user's medical information from the medical institution server 500 through the user terminal 300, and the server 100 may send the user's medical information through the user terminal 300 to the medical institution server. It can be received from (500) (S3010). As another example, the server 100 may directly receive medical information of a user from the medical institution server 500 .

In addition, the server 100 may transmit the medical examination information to the user terminal 300 at the request of the user (S1010). Here, a detailed description of the structure of the questionnaire information is replaced with the description of FIG. 4 .

The user terminal 300 performs a medical examination for the user according to the medical examination inquiry information (S3020), receives an answer to each medical examination inquiry information from the user, generates medical examination result information, and transmits the medical examination result information to the server 100. It can be transmitted to (S3021).

When performing a medical examination, the user terminal 300 may display medical examination information through a touch screen module provided in the user terminal 300 and may receive an answer to the medical examination information from the user. Alternatively, the user terminal 300 may output paperweight question information as voice through a speaker and receive an answer from the user through a microphone.

In addition, when a plurality of cartridges 212 storing formulations of different nutritional ingredients are installed in the device 200, the device 200 acquires cartridge information from each of the plurality of cartridges 212 (S2010) to obtain the server 100 ) can be transmitted (S2011). The server 100 may receive cartridge information and use the cartridge information to calculate fourth base capacity information.

The server 100 may calculate base dose information for each nutritional component optimized for the user's personal health condition from the user's personal health information. Here, the user's personal health information may include at least one of user identification information, medical examination result information, and medical information, and a detailed description thereof will be replaced with the foregoing.

In the step of calculating the base capacity information (S1020), the server 100, for example, calculates the first base capacity information (S1021), and reflects the personal health variable value extracted from the personal health information to obtain the second base capacity information. It is possible to calculate (S1022), perform maximum serving amount correction to calculate third base capacity information (S1023), and perform redundancy correction to calculate fourth base capacity information (S1024). Here, the method of calculating the first, second, third, and fourth base capacity information is replaced with the content described in FIG. 4 .

Hereinafter, as shown in the tables of FIGS. 14 and 15, the server 100 calculates the base capacity information (eg, the fourth base capacity information) based on the user's personal health information, and the lactic acid bacteria component is 7 billion CFU, multi A case where 100 mg of mineral components and 120 mg of omega 3 components are calculated will be described as an example.

In this way, after the server 100 calculates the base capacity information for the user, the device 200 may perform an operation of obtaining device input information of the first time (S2110) at a first time point during the first period.

Obtaining device input information at the first time (S2110) may include obtaining user specific information (S2111), obtaining first current state information (S2112), and receiving ejection command information (S2113). can

Here, the first time point is the time point from when the user starts to operate through the device 200 during the first period to take the dosage form until the device 200 specifies the user and completes acquisition of ejection command information. can mean

In the step of acquiring user-specific information (S2111), the device 200 may obtain specific information of a user who intends to take a dosage form through the device 200 at a first time point.

To this end, as shown in FIG. 11 , for example, the device 200 may display a user registered in the device 200 through the device terminal 230 as an icon. At this time, the device terminal 230 may display the user's name (eg, user 1, user 2, etc.) at the bottom of the icon using the user identification information.

The device 200 may obtain user-specific information from the user through user interaction, such as touching an icon. In FIG. 11 , a case in which user 1 is specified as the user of the device 200 at the first time point is illustrated as an example.

In FIG. 11, a case in which the device 200 receives an icon selected from the user and specifies the user as a method for specifying the user is shown as an example, but the present invention is not limited thereto, and the device 200 is the device terminal 230 The user may be identified by detecting the user's voice information through a microphone provided in or acquiring the user's facial image through a camera.

Then, as shown in FIG. 10A , in obtaining first current state information ( S2112 ), the device 200 may obtain first current state information from the user. To this end, as shown in (a) of FIG. 12, the device 200 transmits a plurality of icon images IM1 to IMn including icon images for each of the first current state information through the device terminal 230. If at least one icon (IMs) is selected from among a plurality of icon images through a user's interaction, first current state information corresponding to the at least one icon (IMs) may be obtained.

Here, the first current state information may refer to current state information obtained by the device 200 from the user in response to a first point in time of the first period, and the first current state information is one information about a change in the user's body state. Alternatively, a plurality of pieces of information may be included.

For example, after the user is specified, the device 200 displays examples of various current state information selectable by the user as icon images (IM1 to IMn, drinking, exercise, etc.) as shown in (a) of FIG. 12 . ) can be expressed as

If, as shown in (b) of FIG. 12, when the user selects the stress (IMs) as the first current state information, the device 200 provides the user with a selectable interface for the stress index indicating the degree of stress, , it is possible to receive input from the user about the stress index.

As shown in (a) of FIG. 12 , when the user's biological signal sensing unit 224 is connected to the device 200, the device 200 may display sensing information as an example of current state information selectable by the user.

If the user selects sensing information as the first current state information, as shown in (c) of FIG. 12, the device 200 provides a selectable interface for the type of sensing information (eg, blood pressure, heart rate, electrocardiogram, etc.) may be provided to the user, and corresponding sensing information may be acquired from the user through the biosignal sensing unit 224 .

Then, the device 200 may receive ejection command information from the user. For example, if the user selects the “Start Combination” button after the user completes the input of the first current state information, the device 200 recognizes this as ejection command information, and the device input information at the first point in time. may be transmitted to the server 100.

Here, the device input information of the first time point may include user specific information acquired from the user, first current state information (eg, stress, index 3), and ejection command information.

When transmitting the device input information of the first time point to the server 100, the device 200 transmits, for example, user specific information, first current state information (eg, stress, index 3) and ejection command information to the server 100. It can be converted into usable code information from the algorithm stored in and transmitted (S1114).

The server 100 receiving the device input information at the first time point from the device 200 may perform a step of reflecting the change amount information at the first time point ( S1100 ). In the step of reflecting the change amount information at the first point in time (S1100), the server 100 reflects the first current state information on the base amount information for each nutritional component calculated based on the personal health information of the specified user and discharges the cartridge for each cartridge. The number of formulations to be produced can be calculated.

Specifically, in the step of reflecting the change amount information at the first point in time (S1100), as an example, the server 100 inputs the first current state information at the first point in time to the algorithm (S1110), and the first current state information of the user Change information for each nutritional component is calculated (S1120), change information is reflected in the base volume information for each nutritional component, and daily serving amount information at the first time point is calculated (S1130), and daily serving amount for each nutritional component is calculated for each cartridge. It can be converted into the number of formulations to be dispensed (S1140). Here, since the method of reflecting the variation information is the same as that described above in FIG. 6 , the detailed description is replaced with the previous description.

For example, as shown in FIG. 15, let's assume that the lactic acid bacteria component affects only 'stress', the omega 3 component affects 'premenstrual syndrome', and the multimineral component has no effect on stress and premenstrual syndrome. .

When the server 100 receives the stress as the first current state information, the server 100 inputs the stress at the first point in time into the algorithm (S1110), and changes information for each nutritional component corresponding to the stress as follows: The change in lactic acid bacteria component can be calculated as 3 billion CFU increase, the change in multi-mineral component as 0mg (zero), and the change in omega 3 as 0mg (zero).

Thereafter, in the step of calculating daily serving amount information at the first time point (S1130), the server 100 adds the amount of change (3 billion CFU) according to the first current state information to the base capacity information (eg, 7 billion CFU) of the lactic acid bacteria component. ) to calculate 10 billion CFU as a daily serving amount, multimineral component by incorporating 0mg into 100mg to calculate 100mg into daily serving amount, and omega-3 component by incorporating 120mg into 0mg to calculate 120mg into daily serving amount can be calculated

Subsequently, in the step of converting the daily serving amount information at the first time point into the number of formulations (S1140), the server 100 contains 1 billion CFU of lactic acid bacteria components per lactic acid bacteria formulation, and 20 mg of multimineral components per 1 multimineral formulation. and 10mg of omega-3 component per omega-3 formulation, the server 100 calculates 10 lactic acid bacteria formulations, 5 multimineral formulations, and 12 omega-3 formulations as the first formulation composition information. can do.

Here, information input by a user's interaction or selection, excluding sensing information, among the first current state information may be input in the form of a code usable to an algorithm, and may be directly used by an algorithm used in the step of reflecting the variation information. can

However, when sensing information is included in the first current state information received by the server 100, the server 100 converts the user's sensing information (eg, blood pressure information) into personal health information in order to reflect change information in the sensing information. Among them, a value for the degree of state change may be calculated by comparing with corresponding information (eg, blood pressure information), and the calculated value may be input to an algorithm reflecting the change amount information at the first time point.

For example, in the blood pressure information according to the user's personal health information, the systolic blood pressure (or systolic blood pressure) is 124 mmHg and the diastolic blood pressure (or diastolic blood pressure) is 84 mmHg, and as shown in FIG. 12(c), the first current state When the systolic blood pressure is 134 mmHg and the diastolic blood pressure is 95 mmHg in the blood pressure information according to the information, the server 100 compares the blood pressure information of the personal health information with the blood pressure information of the first current state information, and the value for the degree of change in blood pressure. (eg, blood pressure index 2) can be calculated and input into the algorithm.

The server 100 may store the received first current state information of the user in the memory of the server 100 and continuously track the current state information of the user.

Thereafter, as shown in FIG. 10A , the server 100 may transmit information on the number of formulations to be ejected for each cartridge at the first time point to the device 200 as first formulation composition information (S1170).

The device 200 converts the information on the number of dosage forms for each cartridge received from the server 100 into a control signal for the hardware 210 of the device 200 based on the first dosage form composition information at the first time. Accordingly, the formulation may be discharged for each cartridge (S2180).

The device 200 detects the number of formulations discharged from each cartridge 212 in response to the first time point using the formulation dispensing sensor 213 to generate discharge amount information (S2190), and sends the generated discharge amount information to the server (S2190). 100) may be transmitted (S2191). If the device 200 is equipped with a camera, it is also possible to generate and transmit the user's taking information to the server 100 by photographing whether or not the device 200 is taking the dispensed dosage form.

The server 100 receives discharge amount information on the number of formulations dispensed for each cartridge corresponding to the first time point from the device 200, stores it in the memory 232 of the server 100, and provides the formulation to the user. The type of and the number of formulations for each type can be continuously tracked.

In addition, the server 100 converts the base capacity information for the user, the first current state information at the first time point, the daily serving amount information and the discharge amount information to the user terminal as dosage management information corresponding to the current state information at the first time point ( 300) may be transmitted (S1180).

As shown in FIG. 13A , the user terminal 300 may provide the base amount information as information on the user's customized nutritional components. Such base capacity information may be provided to the user terminal 300 on a regular basis or as needed regardless of a specific event time point such as a first time point or a second time point.

In addition, as shown in FIG. 13B, the user terminal 300 converts the discharge amount information for each nutritional component corresponding to the first time point into information on today's dose (eg, lactic acid bacteria: +42.8%) in preparation for base dose information. and provide the first current state information as today's current state information (eg, stress index 3, blood pressure index 2).

In addition, as shown in FIG. 13C , the server 100 continuously tracks and tracks the user's current state information to provide current state information with a high frequency of user selection for each period through the user terminal 300. .

Thereafter, as shown in FIG. 10B , at a second point in time during the second period, the device 200 may perform an operation of obtaining device input information of the second point (S2210). The method for obtaining device input information at the second point of view may include obtaining user specific information (S2211), acquiring second current state information (S2212), and receiving ejection command information (S2213). The second point in time means a point in time from when the user starts to operate through the device 200 during the second period in order for the user to take the dosage form until the device 200 specifies the user and completes acquisition of ejection command information. can do.

A method of obtaining device input information of the second view is the same as the method of acquiring device input information of the first view except for a different view, so a detailed description thereof will be omitted.

At the second point of view, the device 200 may obtain the same user (eg, user 1) as the user at the first point of view as user specific information, and obtain second current state information different from the first current state information. . Hereinafter, a case in which premenstrual syndrome (PMS) is selected as the second current condition information will be described as an example.

The device 200 may transmit user specific information, second current state information (eg, premenstrual syndrome), and ejection command information to the server 100 as device input information of the second time (S2214).

The server 100 receiving the device input information of the first time point from the device 200 may perform a step of reflecting the change amount information of the second time point ( S1200 ).

In the step of reflecting the change information at the second point in time (S1200), the server 100 specifies the user based on the device input information at the second point of time received from the device 200, and assigns the specified user's personal health information. The number of formulations to be dispensed for each cartridge may be calculated by reflecting the second current condition information (eg, premenstrual syndrome) in the base volume information for each nutritional component calculated based on the base volume.

In the step of reflecting the change amount information at the second time point (S1200), for example, the server 100 inputs the second current state information at the second time point to the algorithm (S1210), and the user's second current state information (eg, Premenstrual Syndrome) is calculated (S1220), and the change information is reflected in the base volume information for each nutritional component to calculate daily serving amount information at the second time point (S1230). The serving amount may be converted into the number of formulations to be dispensed for each cartridge (S1240). Here, since the method of reflecting the variation information is the same as that described above in FIG. 6 , the detailed description is replaced with the previous description.

For example, as shown in FIG. 15 , when the server 100 receives premenstrual syndrome as the second current state information, the server 100 inputs the premenstrual syndrome of the second time point into the algorithm (S1110), Change information for each nutritional component corresponding to all syndromes is calculated as follows: 0 CFU (zero) for lactic acid bacteria, 80 mg increase for omega 3, and 0 mg (zero) for multi-mineral change (S1220) can

Thereafter, in the step of calculating the daily serving amount information at the second time point (S1230), the server 100 adds the second current condition information (eg, premenstrual syndrome) to the base dose information (eg, 120mg) of the omega-3 component. 200mg is calculated as the daily serving amount by including the change (increase by 80mg) according to the amount, 7 billion CFU is calculated as the daily serving amount by including 0CFU (zero) in the change in 7 billion CFU for lactic acid bacteria, and 0mg of multi-mineral ingredient is 100mg can be taken into account to calculate 100 mg as a daily serving.

Subsequently, in the step of converting the daily serving amount information at the second time point into the number of formulations (S1240), the server 100 has 7 lactobacillus formulations, 5 multimineral formulations, and omega 3 formulations as the second formulation composition information. can yield 20 silver.

Thereafter, as shown in FIG. 10B , the server 100 may transmit information on the number of formulations to be ejected for each cartridge at the second time point to the device 200 as second formulation composition information (S1270).

The device 200 may eject the formulation for each cartridge according to the second formulation composition information at the second time (S2280). The device 200 may generate discharge amount information corresponding to the second point in time (S2290) and transmit the discharge amount information of the second point in time to the server 100 (S2291).

The server 100 receives the discharge amount information corresponding to the second time point from the device 200, stores it in the memory 232 of the server 100, and continuously displays the type of formulation provided to the user and the number of formulations for each type. can be tracked with

In addition, the server 100 transmits second current state information, daily serving amount information, and discharge amount information of the user at a second time point to the user terminal 300 as dosage management information corresponding to the current state information at the second time point ( S1280).

As such, the present invention may reflect current state information, which is information about a change in the user's temporary physical condition, to the user's personal health information.

For example, as described above, when the user is stressed, the number of lactic acid bacteria formulations is reflected in the base dose information (e.g., lactobacillus formulation-7, multi-mineral formulation-5, omega-3 formulation-12). Only increase (lactic acid bacteria formulation: 7 -> 10) is provided, and if the user has premenstrual syndrome, only the number of omega 3 formulations may be increased (omega 3 formulation: 12 -> 20).

Accordingly, the present invention can provide the user with nutritional components optimized and precisely tailored to the user's personal health information and temporary real-time current status information.

In the first embodiment of the present invention, the case where the device 200 obtains the current state information from the user has been described as an example, but the present invention is not limited thereto, and the user terminal 300 obtains the current state information from the user. It is also possible.

FIG. 16 is a diagram for explaining a first modified example of the first embodiment described in FIGS. 10A and 10B.

In FIG. 16, descriptions of overlapping contents with those described in FIGS. 10A to 13C are replaced with the previous descriptions, and other parts are mainly described.

As shown in FIG. 16, in the first modified example of the first embodiment of the present invention, a step of registering user information and device information (S10) may be performed.

Next, the user terminal 300 receives the medical examination query information from the server 100 (S2010), performs a medical examination (S3020), generates medical examination result information, and transmits the generated medical examination result information to the server 100 (S3021). )can do.

In addition, the server 100 may receive medical information from the user terminal 300 (S3010) and receive cartridge information from the device 200 (S2011).

Thereafter, the server 100 may calculate base dose information for each nutritional component optimized for the user's personal health condition from personal health information including at least one of user identification information, medical examination result information, and medical information (S1020).

Next, after the base capacity information is calculated (S1020), the user terminal 300 may obtain first current state information from the user during the first period (S3120).

To this end, as described above with reference to FIG. 12 , an application capable of executing an interface capable of receiving current state information from a user may be installed and stored in the user terminal 300 in advance.

The user terminal 300 may acquire (S3120) first current state information from the user for a period up to a first point in the first period through an interface, and input the first current state information to the user terminal of the first period. It can be transmitted to the server 100 as information (S3121).

Although not shown, when the server 100 receives the first current state information acquired by the user's interaction from the user terminal 300 during the first period, the first current state information is received from the user terminal 300 Information notifying that it has been received may be transmitted to the device 200 . In this case, when the device obtains the input information at the first time (S2110′), it is also possible to display to the user through the application that there is the first current state information acquired from the user terminal.

In the step of obtaining device input information at the first time (S2110'), since the device 200 receives the first current state information through the user terminal 300, the current state information is excluded as the device input information at the first time. Then, only user-specific information and ejection command information may be received from the user (S2111, S2113) and transmitted to the server 100 (S2114).

However, the present invention is not limited thereto, and the device 200 obtains the current state information as described above with reference to FIGS. It is also possible to perform further steps for this.

Thereafter, the server 100 may perform a step (S1100) of reflecting the change amount information at the first point in time. In the step of reflecting the change amount information at the first point in time (S1100), the first current state information received from the user terminal 300 is input as an input variable to an algorithm for calculating the change amount, and the change amount information at the first point in time is calculated and First dosage form composition information of one time point may be calculated.

Next, the device 200 receives the first dosage form composition information from the server 100 (S1170), ejects the dosage form from each cartridge 212 according to the first dosage form composition information (S2180), and generates discharge amount information ( S2190), and the discharge amount information of the first time point may be transmitted to the server 100 (S2191).

The server 100 may provide the received discharge amount information at the first time point to the user terminal 300 as the dose management information corresponding to the current state information at the first time point (S1180).

Thereafter, during the second period, the user terminal 300 may acquire second current state information from the user (S3220) and transmit it to the server 100 as user terminal input information of the second period (S3221).

Thereafter, in the step of obtaining device input information at the second time (S2210'), the device 200 acquires user specific information and ejection command information excluding the second current state information as device input information (S2211, S2213) to obtain the device input information, and obtain the server input information (S2211, S2213). It can be transmitted to (100) (S2214).

Next, in the step of reflecting the change amount information at the second point in time (S1200), the server 100 inputs the second current state information received from the user terminal 300 as an input variable to an algorithm for calculating the change amount, so that the second point in time The second dosage form composition information at the second time point may be calculated by calculating daily serving amount information by reflecting the change amount information.

The device 200 receives second dosage form composition information from the server 100 (S1270), ejects a dosage form from each cartridge 212 according to the second dosage form composition information (S2280), and generates discharge amount information (S2290) And, the discharge amount information of the second time point may be transmitted to the server 100 (S2291).

The server 100 may provide the received discharge amount information of the second time point to the user terminal 300 as the dose management information corresponding to the current state information of the second time point (S1280).

When the first current state information or the second current state information is obtained through the user terminal 300, it is obtained through the input unit 234 provided in the user terminal 300, for example, a touch screen module, a microphone, or a camera. can

When the first and second current state information is received through the touch screen module of the user terminal 300, similarly to the case where the first and second current state information is received through the device terminal 230, the user determines the current state information. By selecting the icon, the first and second current state information can be input.

In addition, an image of a part of the body such as the user's face is obtained through the camera of the user terminal 300 or an image of an analysis kit (eg, urine kit) used by the user is obtained, and the first , 2 can also be used as current state information.

Alternatively, when the first and second current state information is received through the microphone of the user terminal 300, the user's voice information obtained through the microphone may be analyzed and used as the first and second current state information.

A first modified example of the first embodiment of the present invention is that the user inputs the first current state information or the second current state information of the user in advance through the user terminal 300 without going through the device 200, and the user Since the present invention can further increase user convenience, since the user can be provided with a dosage form by inputting only user-specific information and ejection command information into the device 200 at a desired time.

So far, in the first embodiment of the present invention and the first modified example of the first embodiment, the device 200 or the user terminal 300 transmits information selected by the user through an interface to the first current state information or the second current state information. The case of acquiring current state information has been described as an example.

However, the present invention is not limited thereto, and the sensing information not selected by the user and sensed by the user terminal 300 or the external device 400 interlocked with the user terminal 300 to detect the user's health condition is also used by the user. It can be used as the first current state information or the second current state information of An explanation of this is as follows.

FIG. 17 is a diagram for explaining a second modified example of the first embodiment described in FIGS. 10A and 10B.

As described above with reference to FIGS. 1 and 2 , the user terminal 300 has a user terminal sensor 360 or an external device 400 that collects health-related information about the user by interworking with the user terminal 300 If provided, the server 100 may use the sensing information transmitted from the user terminal 300 or the external device 400 as the first current state information or the second current state information.

As shown in FIG. 17 , in the second modified example of the first embodiment of the present invention, a step of registering user information and device information (S10) may be performed.

Next, the user terminal 300 receives the medical examination inquiry information from the server 100 (S1010), performs a medical examination (S3020), generates medical examination result information, and transmits the generated medical examination result information to the server 100 (S3021). )can do.

Thereafter, the server 100 may calculate base dose information for each nutritional component optimized for the user's personal health condition from personal health information including at least one of user identification information, medical examination result information, and medical information (S1020).

Next, after the base capacity information is calculated, the external device 400 may generate first sensing information by detecting a biosignal from the user's body during a period up to and before a first time point in the first period. Information may be transmitted to the user terminal 300 .

Alternatively, the user terminal sensor 360 provided in the user terminal 300 may detect the user's biological signal during the period up to the first point in time during the first period to generate second sensing information.

Then, the user terminal 300 may transmit the first sensing information or the second sensing information to the server 100 as the first current state information (S3130). To this end, an application that works with the external device 400 and an application capable of transmitting the first sensing information or the second sensing information to the server 100 as the first current state information are installed and stored in the user terminal 300. can

Unlike the foregoing, the user terminal transmits the first sensing information received from the external device 400 to a third server that provides a service according to the function of the external device 400, and the third server analyzes or processes the first sensing information. 1 It is also possible to receive sensing information and transmit it to the server 100 of the present invention.

Such first sensing information or second sensing information may be information generated by sensing a biosignal from the user's body, rather than information selected by a user's selection through a user's interaction operation.

When the server 100 receives the first sensing information or the second sensing information as the first current state information from the user terminal 300 during the first period up to the first point in time, notifying that the first current state information has been received Information may be transmitted to the device 200 .

Thereafter, in the step of obtaining device input information at the first time point (S2110), the device 200 may obtain device input information at the first time point from the user (S2110). At this time, since the device 200 receives the first current state information through the user terminal 300, it may receive only user specific information and ejection command information from the user and transmit them to the server 100.

However, the present invention is not limited thereto, and the device 200 obtains the current state information as described above with reference to FIGS. It is also possible to perform further steps for this.

The server 100 compares the first sensing information or the second sensing information received during the first period with the personal health information of the user, calculates a value for the degree of state change, and calculates the value as the amount of change at the first point in time. You can input that information into an algorithm that reflects it.

Thereafter, the server 100 may perform a step (S1100) of reflecting the change amount information at the first point in time. In the step of reflecting the change amount information at the first time point (S1100), a value according to the first sensing information or the second sensing information may be input as an input variable to an algorithm for calculating the change amount as the first current state information.

Accordingly, in the step of reflecting the change amount information at the first time point (S1100), the change amount information at the first time point is calculated to calculate the first dosage form composition information at the first time point, and the server transmits the first dosage form composition information to the device. (S1170).

Next, the device 200 receives the first dosage form composition information from the server 100, ejects the dosage form from each cartridge 212 according to the first dosage form composition information (S2180), generates discharge amount information (S2190), and , Discharge amount information of the first time point may be transmitted to the server 100 (S2191).

The server 100 may provide the received discharge amount information at the first time point to the user terminal 300 as the dose management information corresponding to the current state information at the first time point (S1180).

Thereafter, the server 100 uses the first sensing information acquired by the external device 400 or the second sensing information acquired by the user terminal 300 during the period from the second period to the second point in time to the second current state. It may be received as information (S3230), and the server 100 may transmit information indicating that the second current state information has been received to the device 200.

Thereafter, in obtaining device input information at the second time point ( S2210 ), the device 200 may obtain device input information at the second time point. At this time, since the device 200 receives the second current state information through the user terminal 300, it may receive only user-specific information and ejection command information from the user and transmit them to the server 100, but the present invention is limited thereto. it is not going to be

The server 100 compares the first sensing information or the second sensing information received during the second period with the user's personal health information, calculates a value for the degree of state change, and calculates the value for the change amount at the second time point. You can input that information into an algorithm that reflects it.

Accordingly, in the step of reflecting the variation information of the second viewpoint (S1200), the variation information of the second viewpoint is calculated to calculate the second formulation composition information of the second viewpoint, and the server transmits the first formulation composition information to the device. (S1270).

Next, the device 200 receives the second dosage form composition information from the server 100, ejects the dosage form from each cartridge 212 according to the second dosage form composition information (S2280), generates discharge amount information (S2290), , Discharge amount information of the second time point may be transmitted to the server 100 (S2291).

The server 100 may provide the received discharge amount information at the first time point to the user terminal 300 as the dose management information corresponding to the current state information at the second time point (S2180).

A second modified example of the first embodiment of the present invention is that even if the user does not take any interaction to input the first or second current state information, the server 100 configures the user's first or second current state information. , and the user can receive the dosage form by simply inputting only user-specific information and ejection command information into the device 200 at a desired time point, and the present invention can further increase user convenience.

In the first embodiment of the present invention and the first and second modified examples of the first embodiment so far, the case where paperweight is performed in the user terminal 300 has been described as an example, but the present invention is not necessarily limited thereto, and the paperweight It is also possible that this is performed in the device 200 . An explanation of this is as follows.

FIG. 18 is a diagram for explaining a third modified example of the first embodiment described in FIGS. 10A and 10B.

In FIG. 18 , except for the contents related to the medical examination, registering user information and device information (S10), receiving medical information by the server 100 (S3010), and receiving cartridge information by the server 100 (S2011), the server 100 calculating the base capacity information (S1020), the device 200 obtaining (S2110, S2210) and transmitting (S2114, S2214) device input information at the first and second time points, respectively. ) step, the server 100 calculates and transmits (S1170, S1270) the first and second dosage form composition information by reflecting the change amount information at the first and second time points (S1100 and S1200), and the device 200 The description of the steps of receiving the composition information of the 1st and 2nd formulations, dispensing the formulation (S2180, S2280), generating the discharge amount information (S2190, S2290) and transmitting the information to the server 100 is the same as described in the first embodiment. Therefore, the contents of this part are replaced with the contents of FIGS. 10A and 10B.

As shown in FIG. 18 , unlike the above-described examples, paperweight may also be performed in the device 200 . In order to provide the convenience of paperweight to the user, the device terminal 230 of the device 200 may be detachably provided from the dispensing hardware 210, and in this case, the device terminal 230 is the dispensing hardware 210 and can perform wireless communication.

In addition, an application for performing paperweight may be pre-installed and stored in the device terminal 230 .

The device 200 may provide an interface for performing a medical examination through the device terminal 230 and obtain user specific information S2020 from the user. Here, a method of obtaining user-specific information may be the same as that described above with reference to FIG. 11 as an example.

Thereafter, when the device 200 receives information on the medical examination request from the user through the device terminal 230 (S2030), the medical examination request information notifying that the medical examination request has been input from the user is transmitted to the server 100 (S2031) can do.

The server 100 may provide medical examination inquiry information to the device terminal 230 in response to the medical examination request information of the device terminal 230 (S1011), and the device terminal 230 may target the user according to the medical examination inquiry information. Paperweight can be performed (S2032).

At this time, the device terminal 230 outputs the questionnaire information as an image to the user through a touch screen module, which is one of the output units 235 of the device 200, and inputs the result of the questionnaire through the user's interaction. Receive and generate information about the results of the questionnaire.

Alternatively, the device terminal 230 may provide the user with questionnaire information through a speaker, receive the user's voice information through a microphone, and generate medical examination result information.

Thereafter, the device terminal 230 transmits the generated medical examination result information to the server 100 (S2033), so that the medical examination result information can be used in the step of calculating the base capacity information by the server 100 (S1020). .

The third modified example of the first embodiment of the present invention is to enable the device terminal 230 to perform a medical examination targeting the user, so that elderly people with poor experience of using the user terminal 300 such as a smartphone, It can make it easier for children, blind or hearing impaired people to carry out paperwork.

Accordingly, the present invention can allow a user with poor experience of using the user terminal 300 to receive a dosage form optimized for personal health information from the device 200, thereby further increasing the usability of the device 200. there is.

In the first embodiment and the first, second, and third modifications to the first embodiment so far, the case where the server 100 reflects the change amount information of the first and second points of view has been described as an example, but this The invention is not limited thereto, and it is possible for the device 200 to reflect the change amount information of the first point of view or the second point of view in some cases. An explanation of this is as follows.

FIG. 19 is a diagram for explaining a second embodiment of a method in which the service providing server 100, the user terminal 300, and the device 200 shown in FIG. 1 work in conjunction with each other.

In FIG. 19 , descriptions of contents overlapping with those described in the first embodiment and various modified examples of the first embodiment are replaced with the previous description, and other parts are mainly described.

As shown in FIG. 19 , in the second embodiment of the present invention, first registering user information and device information (S10) may be performed.

Next, the user terminal 300 receives the medical examination inquiry information from the server 100 (S1010), performs a medical examination (S3020), generates medical examination result information, and transmits the generated medical examination result information to the server 100 (S3021). )can do. In addition, the server 100 may receive medical information from the user terminal 300 (S3010) and receive cartridge information from the device 200 (S2011).

Thereafter, the server 100 may calculate base dose information for each nutritional component optimized for the user's personal health condition from personal health information including at least one of user identification information, medical examination result information, and medical information (S1020).

In order for the server 100 to be used to reflect the variation information in the base capacity information in the device 200, the base capacity information is calculated (S1020), and the third base capacity information for each nutritional component for the user calculated in step S1020 and the third base capacity information 4 base capacity information may be transmitted to the device 200 prior to the first period. Here, the server 100 may transmit third base capacity information and fourth base capacity information to a user registered as a user in the corresponding device 200 (S1015).

Although the case in which the third base capacity information is transmitted to the device 200 has been described as an example in the second embodiment, the first base capacity information or the second base capacity information may be transmitted instead of the third base capacity information.

Thereafter, at a first point in time during the first period, the device 200 may acquire device input information from the user (S2110) to obtain user specific information, first current state information, and ejection command information. . Since this is the same as described in the above-described first embodiment and the third modified example of the first embodiment, a detailed description thereof will be omitted.

Thereafter, the device 200 may perform a step (S2120) of reflecting the change amount information at the first point in time. To this end, an algorithm reflecting the variation information may be pre-stored and installed in the device 200 . A method in which the device 200 reflects the variation information may be substantially the same as that of FIG. 6 except that the subject is the device 200 .

Accordingly, in step S2120 of the device 200 reflecting the change amount information at the first time point, the device 200 may calculate the first dosage form composition information at the first time point by reflecting the first current state information.

To this end, in the step of reflecting the change amount information at the first time point (S2120), the device 200 first inputs the first current state information of the user acquired at the first time point to an algorithm that reflects it (S2121), Variation information for each nutritional component corresponding to the first current state information may be calculated (S2122).

Here, when the device 200 calculates the change information for each nutritional component corresponding to 1 current state information, for example, the third base amount information received from the server 100 may be used.

Thereafter, the device 200 calculates the daily serving amount information of the first period by including the amount of change according to the first current state information in the fourth base amount information for each nutritional component (S2123), and then the daily serving amount of the first period First dosage form composition information may be calculated by converting to the number of dosage forms to be dispensed for each cartridge (S2124).

Next, the device 200 controls the dosage form to be dispensed (S2180) according to the first dosage form composition information and the ejection command information at the first time point, and generates discharge amount information corresponding to the first time point by counting the dosage form to be dispensed (S2190). )can do.

Thereafter, the device 200 transmits the discharge amount information of the first time point to the server 100 (S2191), and the server 100 responds to the first current state information of the first time point by reflecting the discharge amount information of the first time point. Taking management information may be transmitted to the user terminal 300 (S1180).

Then, at a second point in time during the second period, the device 200 may acquire device input information from the user (S2110) to obtain user specific information, second current state information, and ejection command information. .

Thereafter, the device 200 may perform a step of reflecting the change amount information of the second time point (S2220) to calculate the second formulation composition information of the second time point by reflecting the second current state information.

In the step of reflecting the change amount information at the second time point (S2220), first, the device 200 inputs the second current state information of the user obtained at the first time point to an algorithm that reflects it (S2221), Variation information for each nutritional component corresponding to the state information may be calculated (S2222).

Thereafter, the device 200 calculates the daily serving amount information of the second period by calculating the amount of change according to the second current state information in the fourth base amount information for each nutritional component (S2223), and then the daily serving amount of the second period Second dosage form composition information may be calculated by converting to the number of dosage forms to be dispensed for each cartridge (S2224).

Next, the device 200 controls the dosage form to be dispensed (S2280) according to the second dosage form composition information and the ejection command information at the second time point, and generates discharge amount information corresponding to the second time point by counting the dosage form to be dispensed (S2290). )can do.

Thereafter, the device 200 transmits the discharge amount information of the second time point to the server 100 (S2291), and the server 100 responds to the second current state information of the second time point by reflecting the discharge amount information of the second time point. Taking management information to be taken may be transmitted to the user terminal 300 (S1280).

According to the second embodiment of the present invention, communication between the device 200 and the server 100 is temporarily interrupted at a first time point of the first period or a second time point of the second period when the user wants to receive a dosage form from the device 200. This may be performed when the device 200 is operated in offline mode due to a power outage or when the device 200 needs to reflect the change amount information of the first time point or the second time point.

In the second embodiment of the present invention, the case where the device 200 reflects the change amount information of the first or second time points has been described as an example, but the device 200 may also calculate base capacity information. A more detailed description of this is as follows.

FIG. 20 is a diagram for explaining a first modified example of the second embodiment described in FIG. 19 .

In FIG. 20 , the description of the contents overlapping with the contents described in the first embodiment, its modified example, and the second embodiment is replaced with the previous description, and the other parts are mainly described.

As shown in FIG. 20, in the first third modified example of the second embodiment of the present invention, user information and device information are first registered (S10), and the server 100 receives medical information (S3010). can

20, when the device 200 performs a medical examination, as described in the third modified example of the first embodiment, the device 200 acquires user specific information (S2020), and requests a medical examination from the user. When information about is input (S2030), the user's medical examination request information may be transmitted to the server 100 (S2031).

The server 100 may provide medical examination inquiry information to the device terminal 230 in response to the medical examination request information of the device terminal 230 (S1011), and the device terminal 230 may target the user according to the medical examination inquiry information. A medical examination result information may be generated by performing a medical examination (S2032).

The device terminal 230 may store the generated medical examination result information in the memory 232 of the device 200 and transmit it to the server 100 (S2033). In addition, the device terminal 230 may receive user medical information S1034 from the server 100 to use in calculating the base capacity information.

Thereafter, the device terminal 230 may calculate base capacity information based on personal health information including at least one of user identification information, medical examination result information, and medical information (S2040).

Here, a method in which the device terminal 230 calculates the base capacity information (S2040) may be substantially the same as that of FIG. 4 except that the subject is the device 200.

Specifically, the method for the device terminal 230 to calculate the base capacity information (S2040) includes the step of the device 200 calculating the first base capacity information (S2041), the device 200 reflecting the personal health variable value, Calculating the second base capacity information (S2042), the device 200 performing the maximum serving amount correction and calculating the third base capacity information (S2043), and the device 200 performing redundant correction to the fourth base A step of calculating capacity information (S2044) may be included.

Thereafter, at a first point in time during the first period, the device 200 may acquire device input information from the user (S2110) to obtain user specific information, first current state information, and ejection command information. .

Thereafter, the device 200 may perform a step of reflecting the change amount information at the first time point ( S2120 ) to calculate the first formulation composition information at the first time point by reflecting the first current state information.

Next, the device 200 controls the dosage form to be dispensed (S2180) according to the first dosage form composition information and the ejection command information at the first time point, and generates discharge amount information corresponding to the first time point by counting the dosage form to be dispensed (S2190). )can do.

Thereafter, the device 200 transmits the discharge amount information of the first time point to the server 100 (S2191), and the server 100 responds to the first current state information of the first time point by reflecting the discharge amount information of the first time point. Taking management information may be transmitted to the user terminal 300 (S1180).

Then, at a second point in time during the second period, the device 200 may acquire device input information from the user (S2110) to obtain user specific information, second current state information, and ejection command information. .

Thereafter, the device 200 may perform a step of reflecting the change amount information of the second time point (S2220) to calculate the second formulation composition information of the second time point by reflecting the second current state information.

Next, the device 200 controls the dosage form to be dispensed (S2280) according to the second dosage form composition information and the ejection command information at the second time point, and generates discharge amount information corresponding to the second time point by counting the dosage form to be dispensed (S2290). )can do.

Thereafter, the device 200 transmits the discharge amount information of the second time point to the server 100 (S2291), and the server 100 responds to the second current state information of the second time point by reflecting the discharge amount information of the second time point. Taking management information to be taken may be transmitted to the user terminal 300 (S1280).

In the first and second embodiments so far, a case in which a user receives a formulation from the device 200 at a first time point or a second time point, which is either a first time period or a second time period, will be described as an example. However, it is also possible for the user to receive the formulation from the device 200 at a plurality of times during the first period and to receive the formulation from the device 200 at a plurality of times during the second period.

That is, in the present invention, the device 200 may divide and provide a time point at which the formulation is provided to the user into a plurality of divided time points in the first period or the second period. That is, each of the first time point of the first period and the second time point of the second period may include a first division time point and a second division time point in each of the first or second period.

Hereinafter, as described above, a case in which the device 200 divides and provides a dosage form according to the present invention will be described in detail.

21a and 21b are diagrams for explaining a third embodiment of a method in which the service providing server 100, the user terminal 300, and the device 200 shown in FIG. 1 work in conjunction, and FIG. 22a is FIG. 21A is a diagram for explaining an example of setting divided doses through the user terminal 300 and an example of displaying the number of divided doses by the user terminal 300, and FIG. 22B is a view for explaining first and second doses in FIGS. It is a diagram for explaining an example of a method of reflecting variation information at the time of division.

In the description of the third embodiment of the present invention, the contents overlapping with the contents described in the first and second embodiments are replaced with the above contents, and the other parts are mainly described.

Hereinafter, the dividing time point means a time point at which the device 200 receives current state information from the user in order to provide the dosage form for each session according to the divided dose setting information during either the first period or the second period. can do.

In addition, the first and second division time points may refer to specific points in time included in any one period, and the second division points in time may mean time points temporally spaced apart from the first division point in time.

As shown in FIG. 21A , in the third embodiment of the present invention, first registering user information and device information (S10) may be performed.

Next, the user terminal 300 receives the medical examination inquiry information from the server 100 (S1010), performs a medical examination (S3020), generates medical examination result information, and transmits the generated medical examination result information to the server 100 (S3021). )can do.

In addition, the server 100 may further receive medical information in addition to the medical examination result information from the user terminal 300 (S3010), and may receive cartridge information from the device 200 (S2011). The server 100 may determine the type of dosage form currently possessed by the device 200 using the cartridge information, and the cartridge information may be used later when calculating base capacity information (S1020) or calculating a division ratio. there is.

Thereafter, the server 100 may calculate base dose information for each nutritional component optimized for the user's personal health condition from personal health information including at least one of user identification information, medical examination result information, and medical information (S1020).

The user terminal 300 may provide an interface for setting divided doses and receive setting information for divided doses from the user (S3030).

Here, the divided dose means that the device 200 provides the user with the dosage form at a plurality of times in any one period, rather than providing the dosage form to the user only at any one time in any one of the first and second periods. can mean To this end, an application for dividing and providing dosage forms may be pre-stored and installed in the user terminal 300 .

The user terminal 300 may provide an interface as shown in (a) of FIG. 22A in order to receive setting information for divided doses from the user. As shown in (a) of FIG. 22A, the user terminal 300 sets the number of divided doses (eg, twice) selected by the user (eg, user 1) on the interface page for divided dose setting as divided dose setting information. Input can be received, and divided dose setting information can be transmitted to the server 100 (S3031).

In addition, although not shown, the user terminal 300 may receive alarm setting information from the user for each division number.

Next, as shown in FIG. 21A , the server 100 may calculate the division ratio for each dosage form for each divided dose by reflecting the divided dose setting information (S1030). The server 100 may determine the type of dosage form currently possessed by the device 200 by using the cartridge information in the process of calculating the division ratio. In the third embodiment of the present invention, a case in which the first division time point is the time point of the first division episode and the second division time point is the time point of the second division episode is described as an example.

When calculating the division ratio, the server 100 considers the cartridge information, the characteristics of nutritional components, and the alarm setting information for each number of divisions together, and according to the characteristics of the nutritional components contained in the formulation possessed by the device 200, each formulation Different split ratios can be calculated.

For example, from the cartridge information, the device 200 provides a first formulation that is well absorbed on an empty stomach (eg, contains lactic acid bacteria component) and a second formulation that causes gastrointestinal disturbances on an empty stomach (eg, contains multimineral component), It is understood that a third dosage form with good absorption rate (eg, containing omega 3 ingredients) is provided, and the number of divisions can be set to 2 times (1st round: 7:00 am, 2nd round: 7:00 pm).

In this case, as shown in (a) and (b) of FIG. 22B, the server 100 reflects the good fasting absorption rate of the first formulation (eg, containing lactic acid bacteria component), and the first formulation (eg, containing lactic acid bacteria component) ), the split ratio can be calculated as 70% for the first round (eg, 7:00 am) and 30% for the second round (eg, 7 pm).

In addition, as shown in (a) and (b) of FIG. 22B, the server 100 causes gastrointestinal disorders in the fasting state and reflects the fact that the absorption rate in the body after eating is good, and the second formulation (eg, containing multi-mineral ingredients) And for the third formulation (eg, containing omega 3 component), the split ratio can be calculated as 30% in the first round (eg, 7 am) and 70% in the second round (eg, 7 pm in the evening).

The above-described calculation of the division ratio may be calculated prior to the first period by entering device information and division ratio setting information in the division ratio setting table, and at the time when the user receives the formulation from the device 200, the division ratio Depending on the dosage (i.e., the number) of the dosage form can be divided.

If the user has a chronic disease and there is a dosage rule for a specific dosage form related to the chronic disease, the user may set a division ratio for the specific dosage form according to the dosage rule through the user terminal 300 .

Thereafter, at the first division time of any one of the first period and the second period, the device 200 performs the device input information acquisition step (SA2110) to obtain the device input information at the first division time. As an example, User specific information, current state information at the time of the first division, and ejection command information may be acquired and transmitted to the server 100 (SA2114).

Upon receiving the device input information at the time of the first division, the server 100 performs a step (SA1100) of reflecting the change amount information at the time of the first division to calculate formulation composition information at the time of the first division, and then the first division The number of formulations may be divided according to the division ratio of the time point.

More specifically, in the step of reflecting the change amount information at the time of the first division (SA1100), the server 100 first inputs the current state information at the time of the first division into the algorithm (SA1110), Change information for each nutritional component corresponding to the current state information at the time of the first division may be calculated (SA1120).

Next, the server 100 calculates the daily serving amount at the time of the first division by including the amount of change according to the current state information at the time of the first division in the fourth base amount for each nutritional component (SA1130), The serving amount can be converted into the number of formulations to be dispensed for each cartridge (SA1140). A more detailed description of each step of the method of reflecting the variation information is the same as described above, and thus an additional description will be omitted.

Thereafter, the server 100 may divide and calculate (SA1150) the type and number of formulations for each nutritional component according to the daily serving amount at the first division time according to the division ratio at the first division time.

The server 100 may generate formulation composition information at the time of the first division using the number of formulations calculated by division and transmit the information to the device 200 (SA1170).

Next, the device 200 discharges the formulation from each cartridge 212 according to the formulation composition information at the time of the first division (SA2180), and counts the number of formulations discharged from each cartridge 212 to generate discharge amount information ( SA2190) and transmitted to the server (SA2191).

Thereafter, the server 100 receives discharge amount information on the type and number of dispensed formulations corresponding to the first division time point from the device 200, and then converts the discharge amount information at the first division time point to an accumulation during any one period. It may be stored as discharge amount information (SA1180), and cumulative discharge amount information for any one period may be transmitted to the user terminal 300 (SA1190).

The user terminal 300 may provide information on the number of divided doses of the user, as shown in FIG. 22A (b), using the user's cumulative discharge amount information, and the discharge amount for each dosage form dispensed at the first division time point. By using the information, it is possible to provide information on the dosage of each nutritional component taken by the user up to the time of the first division.

Thereafter, the device 200 performs a device input information obtaining step (SA2210) at a second division time point of any one of the periods to which the first division time period belongs, and user-specific information and second Current state information and ejection command information at the time of division into two parts may be acquired and transmitted to the server 100 (SA2214).

Upon receiving the device input information at the time of the second division, the server 100 performs the step of reflecting the change amount information at the time of the second division (SA1200) to calculate formulation composition information at the time of the second division, and then the second division The number of formulations may be divided according to the division ratio of the time point.

More specifically, in the step of reflecting change information at the time of the second division (SA1200), the server 100 first inputs the current state information at the time of the second division into the algorithm (SA1210), and then the current state at the time of the first division It is possible to calculate change amount information for each nutritional component corresponding to the information (SA1220).

Next, the server 100 calculates the daily serving amount at the time of the second division by including the amount of change according to the current state information at the time of the second division into the base capacity for each nutritional component (SA1230), and calculates the daily serving amount for each nutritional component. It can be converted into the number of formulations to be dispensed for each cartridge (SA1240).

Thereafter, the server 100 may divide and calculate (SA1250) the type and number of formulations for each nutritional component according to the daily serving amount at the second division time point according to the division ratio at the second division time point.

The server 100 may generate formulation composition information at the time of the second division by using the number of formulations calculated by division, and then transmit the information to the device 200 (SA1270).

Next, the device 200 discharges the formulation from each cartridge 212 according to the formulation composition information at the time of the second division (SA2280), and counts the number of formulations discharged from each cartridge 212 to generate discharge amount information ( SA2290) and then transmitted to the server (SA2291).

Thereafter, the server 100 receives discharge amount information about the type and number of dispensed formulations corresponding to the second division time point from the device 200, and then provides the cumulative discharge amount information including the discharge amount information at the first division time point. The cumulative discharge amount information for any one period may be updated (SA1280) by summing the discharge amount information at the time of the second division, and the accumulated discharge amount information up to the second division time point may be transmitted to the user terminal 300 (SA1290). .

Here, when the server 100 divides the number of formulations according to the division ratio by the number of formulations according to the daily serving amount, the number of formulations according to the daily serving amount is multiplied by the division ratio for each time, and divided into each time The number of formulations can be calculated.

If the number of formulations divided according to the division ratio occurs as a value below the decimal point rather than an integer, the number below the decimal point may be rounded down to make it an integer.

In addition, when a shortage occurs in the number of formulations according to the daily serving amount due to the lowering process according to the division ratio, the formulation may be provided by allocating the shortage to the first round.

For example, if the number of formulations according to the daily serving amount is 11 and the split ratio for each round is set to 30% for the first round and 70% for the second round, the split ratio can be calculated as 3.3 for the first round and 7.7 for the second round. can In this case, the server 100 may allocate the number of formulations for each round by dividing the number of formulations into 4 in the first round and 7 in the second round.

As such, each of the dosage form composition information at the time of the first and second divisions provided by the server 100 may have a value assigned according to a division ratio of daily serving amount information for each formulation to be dispensed during any one period.

At each of the first and second division time points, the base doses for each nutritional component applied to reflect the change information at the first and second division time points may be the same.

For example, as shown in (a) and (b) of FIG. 22B, the device 200 is a lactic acid bacteria formulation (eg, containing lactic acid bacteria component-affects stress), a multi-mineral formulation (eg, containing multi-mineral component-affects exercise) ), let's assume that you have an omega 3 formulation (eg, containing omega 3 ingredients-affecting premenstrual syndrome).

In this case, as shown in (a) and (b) of FIG. 22B, the server 100 is the fourth base capacity information for calculating the amount of change information at each of the first and second division time points, for example, the lactic acid bacteria component 7 billion CFU, multi-mineral ingredient 100mg, omega 3 ingredient 120mg can be used in common.

In addition, the daily serving amount may have a value calculated by reflecting the amount of change according to the current state information at the time of the first division or the current state information at the time of the second division in the base amount information for each nutritional component.

Therefore, when the current state information at the time of the first division is different from the current state information at the time of the second division, the daily serving amount at the time of the first division and the daily serving amount at the time of the second division are different for each nutritional component, or can be the same

For example, as shown in (a) and (b) of FIG. 22B, in the division ratio for each formulation, the lactic acid bacteria formulation is divided into 70% at the first division time (first round) and 30% at the second division time (second round). Assume that it is set, and the multimineral formulation and the omega-3 formulation are each set at the first split time point (1st round) -30%, and the second split time point (2nd round) -70%.

As shown in (a) of FIG. 22B, after, for example, when stress is obtained as current state information at the time of the first division, the server 100 changes the amount of change for each nutritional component, increases the lactic acid bacteria component by 3 billion CFU, and omega 3 Ingredients can yield 0mg (zero), and multi-mineral ingredients can yield 0mg (zero).

In this case, the server 100 calculates 10 billion CFU for the lactic acid bacteria component, 100 mg for the multi-mineral component, and 120 mg for the omega-3 component as the daily serving amount for each nutritional component at the time of the first division, By converting the serving amount into the number of formulations, 10 lactic acid bacteria formulations, 5 multimineral formulations, and 12 omega 3 formulations can be obtained.

Here, as shown in (a) of FIG. 22B, the server 100 divides the number of each formulation according to the division ratio at the time of the first division, but the lactic acid bacteria formulation is 7 (10 * 70%), and the multimineral formulation is 1.5 pieces (5 pieces * 30%), Omega 3 formulations are divided into 3.6 pieces (12 pieces * 30%), and purification treatment is performed to reflect the shortfall caused by the lowering process in the first round, and the lactic acid bacteria formulation is 7 pieces , By allocating 2 multimineral formulations and 4 omega 3 formulations, it can be calculated with formulation composition information at the time of the first division.

In addition, for example, as shown in (b) of FIG. 22B, when premenstrual syndrome is obtained as the current state information at the time of the second division, the server 100 changes the amount of change for each nutritional component, and the lactic acid bacteria component is 0 CFU (zero ), 80 mg increase in omega 3, and 0 mg (zero) in multi-mineral ingredients.

In this case, as shown in (b) of FIG. 22B, the server 100 provides 7 billion CFU of lactic acid bacteria component, 100mg of multimineral component, and 200mg of omega 3 component as a daily serving amount for each nutritional component at the time of the second division. 2.1 for lactic acid bacteria formulation, 3.5 for multimineral formulation, and 14 for omega 3 formulation by converting the daily serving amount of each nutritional component into the number of formulations 3 mineral formulations and 14 omega 3 formulations can be allocated.

As such, if the current state information at the time of the first division and the current state information at the time of the second division are different, the daily serving amount for each nutritional component at the time of the first division (e.g., lactic acid bacteria component is 10 billion CFU, multi-mineral component is 10 billion CFU) 100mg, omega 3 component 120mg) and the daily serving amount by nutritional component at the time of the second split (e.g., lactobacillus component is 7 billion CFU, multimineral component is 100mg, and omega-3 component is 200mg) at the time of the first and second split, respectively Since it is calculated by reflecting the current state information of , it may have different values for each nutritional component.

However, differently from this, if the current state information at the time of the first division and the current state information at the time of the second division are the same or have no effect on the current state information at the time of the first and second division, The daily serving amount for each nutritional component may be the same (eg, multimineral component).

In addition, unlike the example of FIG. 22B, the daily serving amount for each nutritional component according to the current status information obtained at the first and second division time points during any one period is It may be substantially the same as the daily serving amount when all the same information as the current state information obtained at the time of the 2nd division is obtained.

For example, if stress is acquired as current state information at the first division time point during the first period and premenstrual syndrome is acquired as current state information at the second division time point, the daily serving amount for each nutritional component at each division time point Selective combination (e.g., lactobacillus-10 billion, multi-mineral-100mg, omega-3-200mg) is the same as the daily serving amount for each nutritional component when stress and premenstrual syndrome were acquired together with the current status information during the first period. can

As such, the third embodiment of the present invention allows the user to take a plurality of dosage forms at a desired time, rather than taking a plurality of dosage forms at once, so that the user's convenience can be further increased.

For example, if a user has a chronic disease and needs to take a dosage form related to the chronic disease multiple times a day, the device 200 may take multiple times a day according to the prescription of the dosage form related to the chronic disease. A dosage form can be provided, so that the convenience of users suffering from chronic diseases can be further increased.

FIG. 23 is a diagram for explaining a first modified example of the third embodiment described in FIGS. 21A and 21B.

In the first modified example of the third embodiment of the present invention, descriptions of overlapping contents of the first to third embodiments are replaced with the above-described contents, and other contents are mainly described.

As shown in FIG. 22A, in the first modification to the third embodiment, the device terminal 230, not the server 100, reflects the change information at the first and second division time points, and divides the first division time point. It is different from the third embodiment in that the number of formulations is divided according to the ratio, and the remaining parts may be substantially the same as those of the third embodiment.

In a first modification to the third embodiment, a step of registering user information and device information (S10) may be performed.

Next, the user terminal 300 receives the medical examination inquiry information from the server 100 (S1010), performs a medical examination (S3020), generates medical examination result information, and transmits the generated medical examination result information to the server 100 (S3021). )can do.

The server 100 may further receive medical information from the user terminal 300 in addition to the medical examination result information (S3010), and may receive cartridge information from the device 200 (S2011).

Thereafter, the server 100 may calculate base dose information for each nutritional component optimized for the user's personal health condition from personal health information including at least one of user identification information, medical examination result information, and medical information (S1020).

The user terminal 300 may receive setting information for divided doses from the user (S3030) and transmit it to the server 100 (S3031), and the server 100 may reflect the divided dose setting information for each division. The division ratio for the formulation can be calculated (S1030).

The server 100 may transmit base capacity information of users registered in the device 200 and information about a split ratio to the device 200 . Here, the base capacity information transmitted to the device 200 may include any one of first to third base capacity information and fourth base capacity information. In the first modified example of the third embodiment, a case in which the third base capacity information and the fourth base capacity information are included in the base capacity information transmitted to the device 200 will be described as an example.

The device 200 may acquire device input information from the user at the first division time of any one of the first period and the second period (SA2110). Here, the device input information at the time of the first division may include, for example, user specific information, current state information at the time of the first division, and ejection command information.

Thereafter, in the step of reflecting the change amount information at the time of the first division (SA2120), the device 200 calculates change information for each nutritional component based on the third base capacity using the current state information at the time of the first division, The amount of change according to the current state information at the time of the first division is included in the fourth base volume for each nutritional component to calculate the daily serving amount for each nutritional component at the time of the first division, and the daily serving amount is converted into the number of formulations to be dispensed for each cartridge. can be converted

Next, in the step of dividing the number of formulations according to the division ratio at the first division time (SA2130), the device 200 divides the number of formulations according to the daily serving amount at the first division time according to the division ratio at the first division time. It is possible to calculate formulation composition information at the time of the first division by dividing according to.

Thereafter, the device 200 discharges the formulation from each cartridge 212 according to the formulation composition information at the time of the first division (SA2180), and counts the number of formulations discharged from each cartridge 212 to generate discharge amount information ( After S2190), it can be transmitted to the server (SA2191).

The server 100 receives discharge amount information on the type and number of dispensed formulations corresponding to the first division time point from the device 200, and then converts the discharge amount information at the first division time point into cumulative discharge amount information for any one period. It can be stored as (SA1180), and the cumulative discharge amount information for any one period can be transmitted to the user terminal 300 (SA1190).

The device 200 may obtain device input information SA2210 from the user at a second division time point among any one period to which the first division time point belongs. Here, the device input information at the time of the second division may include, for example, user specific information, current state information at the time of the second division, and ejection command information.

Thereafter, in the step of reflecting change information at the time of the second division (SA2220), the device 200 calculates change information for each nutritional component based on the third base amount using the current state information at the time of the second division, and The amount of change according to the current state information at the time of the second division is included in the fourth base volume for each component to calculate the daily serving amount for each nutritional component at the time of the second division, and the daily serving amount is converted into the number of formulations to be dispensed for each cartridge can do.

Next, in the step of dividing the number of formulations according to the division ratio at the time of the second division (SA2230), the device 200 divides the number of formulations according to the daily serving amount at the time of the second division by the division ratio at the time of the second division. It is possible to calculate formulation composition information at the time of the second division by dividing according to.

Thereafter, the device 200 discharges the formulation from each cartridge 212 according to the formulation composition information at the time of the second division (SA2280), and counts the number of formulations discharged from each cartridge 212 to generate discharge amount information ( After SA2290), it can be transmitted to the server (SA2291).

The server 100 receives discharge amount information about the type and number of dispensed formulations corresponding to the second division time point from the device 200, and then divides the second division into the cumulative discharge amount information including the discharge amount information at the first division time point. The cumulative discharge amount information for any one period may be updated (SA1280) by summing the discharge amount information at each point in time, and the accumulated discharge amount information up to the second division time point may be transmitted to the user terminal 300 (SA1290).

Here, when the current state information at the time of the first division and the second division are different from each other, the amount of daily serving at the time of the first division calculated by the device 200 and the amount of daily serving at the time of the second division may be different from each other.

In addition, when the current state information at the time of the first division and the second division are identical to each other, the daily serving amount at the first division time point and the daily serving amount at the second division time point calculated by the device 200 may be the same.

In the third embodiment and modified examples of the third embodiment according to the present invention so far, one device 200 divides the formulation according to the division ratio within any one period at the first division time point and the second division time point. The provided case has been described as an example.

However, the present invention is not limited thereto, and it is also possible for the plurality of devices 200 to provide formulations according to the division ratio at each division time point. An explanation of this is as follows.

24a and 24b are diagrams for explaining a fourth embodiment of a method in which the service providing server 100, the user terminal 300, and the device 200 shown in FIG. 1 work in conjunction with each other.

In the fourth embodiment of the present invention, descriptions of overlapping contents with those described in the first to third embodiments are replaced with the above contents, and other parts are mainly explained.

As shown in the fourth embodiment, the device 200 may include a first device 200A and a second device 200B. Here, the first device 200A and the second device 200B may be provided at locations spaced apart from each other. For example, when the first device 200A is installed in the user's home, the second device 200B may be installed in the user's company.

In the present invention, as in the fourth embodiment, when a plurality of devices 200 register the same user, all of the plurality of devices 200 may provide formulations to the user. Specifically, the plurality of devices 200 may provide the formulation to the user in the divided provision method described in the third embodiment or the first modified example of the third embodiment.

In the fourth embodiment of the present invention, as shown in FIG. 24A, first registering user information and device information (S10) may be performed.

In the step of registering user information and device information (S10), the server 100 receives user identification information and identification information of each of the first and second devices 200A and 200B from the user terminal 300, and the first, After receiving identification information of each of the first and second devices 200A and 200B from each of the two devices 200A and 200B, the registered user account and the first and second devices 200A and 200B may be set to work together. .

Next, the user terminal 300 receives the medical examination inquiry information from the server 100 (S1010), performs a medical examination (S3020), generates medical examination result information, and transmits the generated medical examination result information to the server 100 (S3021). )can do.

The server 100 may further receive medical information from the user terminal 300 in addition to the medical examination result information (S3010), receive first cartridge information from the first device 200A (SA2011), and the second device 200B ), second cartridge information may be received (SB2011). Accordingly, the server 100 may determine the formulation for each nutritional component possessed by the first device 200A and the formulation for each nutritional component possessed by the second device 200B.

Thereafter, the server 100 calculates base capacity information for each nutritional component optimized for the user's personal health condition from personal health information including at least one of user identification information, medical examination result information, or medical information, and first and second cartridge information. (S1020).

The user terminal 300 may receive divided dose setting information from the user (S3030) and transmit it to the server 100 (S3031), and the server 100 may receive divided dose setting information and first and second cartridge information. It is possible to calculate the division ratio for each dosage form possessed by the first and second devices 200A and 200B for each division by reflecting. The division ratio may be calculated differently depending on the characteristics of the nutritional components contained in the formulation. Regarding the divided rounds, a case in which the first division time point is the first division time point and the second division time point is the second division time point will be described as an example.

Next, the first device 200A may acquire input information of the first device 200A at the first division time during any one of the first period and the second period (SA2110). For example, the first device 200A may obtain user specific information, current state information at the time of the first division, and ejection command information from the user as input information of the first device 200A, and Input information of may be transmitted to the server 100 (SA2114).

The server 100 may perform a step SA1100 of reflecting change amount information at the first division time point by using the input information of the first device 200A obtained at the first division time point.

Specifically, the server 100 inputs (SA1110) the current state information at the first division point received from the first device 200A into an algorithm to reflect the change amount information at the first division point in time to the third base capacity. Based on the first division, change information for each nutritional component corresponding to the current state information at the time of the first division is calculated (SA1120), and the change according to the current state information at the time of the first division is calculated in the fourth base dose for each nutritional component. A daily serving amount for each nutritional component at the time of division may be calculated (SA1130), and the daily serving amount may be converted into the number of formulations to be dispensed for each cartridge (SA1140).

Next, the server 100 may divide (SA1150) the number of formulations according to the daily serving amount at the time of the first division according to the division ratio at the time of the first division.

Thereafter, the server 100 adjusts the number of divided formulations according to the division ratio at the first division time by applying a multi-device algorithm to calculate formulation composition information at the first division time (SA1160), and the first device 200A ), formulation composition information at the time of the first division may be transmitted (SA1170).

Specifically, in the multi-device algorithm, as a result of the server 100 referring to the first and second cartridge information, when the first dosage form is identified as being provided only in any one device 200 among the plurality of devices 200, the first formulation The number of divided first formulations may be adjusted according to the division ratio so that the entire daily serving amount of the formulation is discharged from only one device 200 .

As an example, as a result of the server 100 referring to the first and second cartridge information, the first device 200A has a lactic acid bacteria formulation, a multimineral formulation, and a vitamin B formulation, and the second Bidice has a multimineral formulation and vitamin B formulation. There may be instances where it is identified as having a formulation and an omega 3 formulation.

In this case, the multi-device algorithm adjusts the number of lactic acid bacteria formulations calculated according to the division ratio so that the entire daily serving amount of the lactic acid bacteria formulation is discharged at the time of the first division for the lactic acid bacteria formulation having only the first device 200A. can

In addition, the multi-device algorithm adjusts the number of lactic acid bacteria formulations calculated according to the division ratio to 0 (zero) so that the omega-3 formulation is not discharged at the time of the first division for the omega-3 formulation equipped with only the second device 200B. can

In addition, the multi-device algorithm may maintain the number of multi-mineral formulations and vitamin B formulations commonly provided by the first and second devices 200A and 200B according to the division ratio at the time of the first division.

Thereafter, the first device 200A discharges the formulation from each cartridge 212 of the first device 200A according to the formulation composition information at the time of the first division (SA2180), and the number of formulations discharged from each cartridge 212 Discharge amount information may be generated by counting the number (SA2190) and then transmitted to the server (SA2191).

The server 100 receives discharge amount information on the type and number of dispensed formulations corresponding to the first division time point from the first device 200A, and then converts the discharge amount information at the first division time point to an accumulation during any one period. It may be stored as discharge amount information (SA1180), and cumulative discharge amount information for any one period may be transmitted to the user terminal 300 (SA1190).

Next, the second device 200B may acquire input information of the second device 200B at a second division time point during any one period (SB2210). For example, the second device 200B may obtain user specific information, current state information at the time of the second division, and ejection command information from the user as input information of the second device 200B, and Input information of may be transmitted to the server 100.

The server 100 may perform a step SA1200 of reflecting change amount information at the time of the second division by using the input information of the second device 200B obtained at the time of the second division.

Specifically, the server 100 inputs (SA1210) the current state information received from the second device 200B into an algorithm in order to reflect (SA1200) the change amount information at the second division time to the algorithm. Based on the 3 base dose, the amount of change for each nutritional component corresponding to the current state information at the time of the second division is calculated (SA1220), and the change according to the current state information at the time of the second division is included in the fourth base dose for each nutritional component. The daily serving amount for each nutritional component at the time of the second division may be calculated (SA1230), and the daily serving amount may be converted into the number of formulations to be dispensed for each cartridge (SA1240).

Next, the server 100 may divide (SA1250) the number of formulations according to the daily serving amount at the time of the second division according to the division ratio at the time of the second division.

Thereafter, the server 100 applies a multi-device algorithm to adjust the number of divided formulations according to the division ratio at the second division time (SA1260) to calculate formulation composition information at the second division time, and the second device 200B ), formulation composition information at the time of the second division may be transmitted (SA1270).

For example, the multi-device algorithm, when the cumulative discharge amount of the previous round (eg, the first division time) for the first dosage form is equal to the number of servings per day at the first division time, the current cycle (eg, the second division time) In ), the number of divided first dosage forms may be adjusted to 0 (zero) according to the division ratio so that the first dosage form is not discharged.

In addition, the multi-device algorithm, when the cumulative discharge amount up to the previous round (eg, the first division time point) for the second formulation is 0 (zero), the current round (eg, the second division time point) for the second formulation The number of divided formulations may be adjusted according to the division ratio so that the entire daily serving amount is discharged.

For example, for the lactic acid bacteria formulation, when all of the daily serving amount is discharged in the previous round (eg, at the time of the first division), and the cumulative serving amount up to the previous round is equal to the daily serving amount of the lactic acid bacteria formulation, the current round (eg, The number of divided lactic acid bacteria formulations may be adjusted to 0 (zero) according to the division ratio so that the lactic acid bacteria formulation is not discharged at the time of the second division).

In addition, for the omega-3 formulation, if the cumulative discharge amount up to the previous round (eg, at the time of the first division) is zero, the entire daily serving amount for omega 3 in the current round (eg, at the time of the second division) The number of divided formulations can be adjusted according to the division ratio so as to be dispensed.

In addition, the multi-device algorithm maintains the number according to the split ratio at each of the first and second split points when the first and second devices 200A and 200B have a multi-mineral formulation and a vitamin B formulation in common. can do.

In addition, the server 100, if due to insufficient remaining amount or failure of the corresponding cartridge 212, information on the discharge amount in the previous round (eg, first division time) for the second formulation (eg, multi-mineral formulation) If it is insufficient compared to the number of second formulations (eg, multi-mineral formulations) according to the formulation composition information at the time of the first division, the insufficient amount that was not discharged in the previous round (eg, at the time of the first division) It can be replenished at the time of division 2).

Specifically, the server 100 calculates the number of the insufficient amount that was not dispensed in the previous round (eg, at the time of the first division) according to the division ratio, and the second dosage form (eg, at the time of the second division) of the current round (eg, at the time of the second division) For example, the number of second dosage forms to be discharged in the current round (eg, the time of the second division) can be adjusted by counting the number of second dosage forms (eg, multimineral dosage forms).

For example, if the number to be dispensed is 10 according to the formulation composition information of the previous round (e.g., the time of the first division) for the multi-mineral formulation, but the actual discharge amount is 8, the server 100 calculates the number according to the division ratio. It can be calculated as formulation composition information at the time of the second division by adding two to the number of multimineral formulations (eg, multimineral formulations) of the current round (eg, the time of the second division).

Thereafter, the second device 200B ejects (SB2280) the formulation from each cartridge 212 of the second device 200B according to the formulation composition information at the time of the second division, and the amount of the formulation discharged from each cartridge 212 Discharge amount information may be generated by counting the number (SB2290) and then transmitted to the server (SB2291).

The server 100 receives discharge amount information on the type and number of dispensed formulations corresponding to the second division time point from the second device 200B, and then provides the cumulative discharge amount information including the discharge amount information at the first division time point. The cumulative discharge amount information for any one period may be updated (SA1280) by summing the discharge amount information at the time of the second division, and the accumulated discharge amount information up to the second division time point may be transmitted to the user terminal 300 (SA1290). .

In the fourth embodiment of the present invention, the user can receive the dosage form through the plurality of devices 200, so the user's convenience can be further increased.

As such, one embodiment according to the present invention provides a combination of formulations optimized for the user's health condition at each point in time by reflecting the current state information on the user's health condition at the time when the combination of formulations is provided to the user. can

The technical features disclosed in each embodiment and modified example of the present invention are not limited to the corresponding embodiment, and may be incorporated or modified and applied to other embodiments or modified examples unless incompatible with each other.

Therefore, in each embodiment, each technical feature is mainly described, but each technical feature may be merged and applied to each other unless incompatible with each other.

The present invention is not limited to the above-described embodiments and accompanying drawings, and various modifications and variations will be possible from the viewpoint of those skilled in the art to which the present invention belongs. Therefore, the scope of the present invention should be defined by not only the claims of this specification but also those equivalent to these claims.

Claims (10)

A method in which a plurality of devices acquiring user's ejection command information ejects a formulation,
a first device dosage form dispensing step performed by a first device at a first division time point of a first period and discharging a plurality of formulations having a plurality of nutritional components according to formulation composition information at the first division time point; and
A second division performed by a second device different from the first device at the time of the second division of the first period and dispensing a plurality of formulations having a plurality of nutritional components according to the formulation composition information at the time of the second division. Including; device formulation dispensing step,
Each of the formulation composition information at the time of the first and second division,
It is calculated by dividing the daily serving amount reflecting the base amount information for the plurality of nutritional components according to preset division ratio information,
When the first formulation among the plurality of formulations is provided in only one device of the first device and the second device,
The capacity information of the first dosage form in the dosage form composition information at the time of the first or second division calculated according to the preset division ratio information is adjusted so that the first formulation is discharged only from the one device,
Formulation dispensing method. According to claim 1,
When the second formulation among the plurality of formulations is provided in both the first device and the second device,
The capacity information of the second formulation in the formulation composition information at the time of the first or second division calculated according to the preset division ratio information is maintained,
Method of dispensing the formulation. According to claim 1,
Receiving dosage form composition information at the time of the first division from an electronic device connected to the first device and the second device through a network, which is performed by the first device before the first device dosage dispensing step; and
Performed by the second device before the step of dispensing the second device formulation, receiving formulation composition information at the time of the second division from the electronic device; further comprising,
Method of dispensing the formulation. According to claim 1,
The base capacity information,
Calculated based on personal health information including at least one of identification information, medical examination result information, or medical information for the user, and having a dose value for the plurality of nutritional components,
Method of dispensing the formulation. According to claim 4,
When calculating each of the formulation composition information at the time of the first and second division,
The base capacity information calculated before the first division time point is commonly used,
Formulation dispensing method. According to claim 1,
Transmitting discharge amount information corresponding to the first division time point to an electronic device connected to the first device and the second device through a network, performed by the first device after the first device dosage dispensing step; ; and
Performed by the second device after the step of dispensing the formulation to the second device, and transmitting the discharge amount information corresponding to the second division time point to the electronic device; further comprising,
Method of dispensing the formulation. According to claim 1,
It is performed by the first device before the first division time and transmits first cartridge information for a formulation contained in the first device to an electronic device connected to the first device and the second device through a network step; and
Performed by the second device before the first division time point, transmitting second cartridge information for the formulation contained in the second device to the electronic device; further comprising,
Formulation dispensing method. According to claim 1,
The daily serving amount at the time of the first division is calculated by reflecting the first current state information of the user at the time of the first division together with the base capacity information,
The daily serving amount at the time of the second division is calculated by reflecting the second current state information of the user at the time of the second division together with the base capacity information.
Method of dispensing the formulation. According to claim 8,
The first current state information or the second current state information,
Collected from at least one of the first device, the second device, a user terminal of the user, or an external device that collects the user's biometric information,
Including information on at least one of the user's mental health condition or symptom, physical health condition or symptom, the user's mood or behavior, and the user's biometric information,
Method of dispensing the formulation. In a multi-device system including a plurality of devices,
a first device for dispensing a plurality of dosage forms having a plurality of nutritional components according to the dosage form composition information at the time of the first division of the first period; and
A second device for discharging a plurality of formulations having a plurality of nutritional components according to the formulation composition information at the time of the second division of the first period;
Each of the formulation composition information at the time of the first and second division,
It is calculated by dividing the daily serving amount reflecting the base amount information for the plurality of nutritional components according to preset division ratio information,
When the first formulation among the plurality of formulations is provided in only one device of the first device and the second device,
The capacity information of the first dosage form in the dosage form composition information at the time of the first or second division calculated according to the preset division ratio information is adjusted so that the first formulation is discharged only from the one device,
Multi-device system.