KR102515617B1 - Apparatus for Infusing medical liquid - Google Patents

Abstract

The present invention provides a chemical solution injection device, comprising: a base body, a reservoir mounted on the base body and having a plunger disposed therein, a rod connected to the plunger, and a connecting member into which the rod is inserted; It includes a driving wheel disposed spaced apart from one end of the burr and transmitting a driving force to the connecting member, and a resistance member inserted into the connecting member and disposed between the reservoir and the driving wheel.

Description

Medicine liquid injection device {Apparatus for Infusing medical liquid}

The present invention relates to a device for injecting a liquid medicine.

In general, a drug solution injection device such as an insulin injection device is used to inject a drug solution into a patient's body. Such a liquid injection device is also used by professional medical personnel such as doctors and nurses, but in most cases, it is used by ordinary people such as patients themselves or their guardians.

In the case of a diabetic patient, especially a pediatric diabetic patient, it is necessary to inject a drug solution such as insulin into the human body at regular intervals. A drug injection device in the form of a patch attached to the human body for a certain period of time is being developed, and this drug injection device can be used while being attached to the body such as the abdomen or waist of a patient for a certain period of time.

In order to increase the effect through drug injection, the drug injection device needs to control the precise injection of the drug into the patient's body, and it is important to precisely inject a small amount of the drug through the small drug injection device.

When attached to the human body, the drug injection device needs to be comfortable to wear, convenient to use, durable, and driven with low power. In particular, since the drug injection device is used by being directly attached to the patient's skin, it is important for the user to drive the drug injection device conveniently and safely.

US Patent Publication US10420883 (published on September 24, 2019)

The present invention provides a drug solution injection device that is safely driven and can accurately deliver a drug.

One aspect of the present invention is a base body, a reservoir mounted on the base body and having a plunger disposed therein, a rod connected to the plunger, a connecting member into which the rod is inserted, and one end of the reservoir. Provided is a drug injection device including a driving wheel disposed spaced apart from the connecting member and transmitting a driving force to the connecting member, and a resistance member inserted into the connecting member and disposed between the reservoir and the driving wheel.

In addition, one side of the resistance member may be supported by the driving wheel when the plunger and the connecting member move toward the rear of the reservoir.

Also, the resistance member may generate frictional force with the outer circumferential surface of the connecting member.

The resistance member may have an insertion opening into which the connection member is inserted, and a minimum diameter of the insertion opening may be smaller than a diameter of the connection member.

In addition, the resistance member may have a base portion extending outwardly of an insertion opening into which the connecting member is inserted, and a cutout portion cut at one side of the base portion and connected to the insertion opening.

The chemical solution injection device according to the present invention may store a high-pressure chemical solution in a reservoir. Since the chemical liquid stored in the reservoir is stored at a high pressure, even if a small amount of driving force acts on the plunger, the chemical liquid can be rapidly and quantitatively discharged while the plunger moves forward.

The drug solution injection device according to the present invention can quickly inject the drug solution into a user without delaying the discharge time of the drug solution through the needle. The chemical solution stored at high pressure can be discharged through the needle even when a small driving force is applied to the plunger. Accordingly, when the device for injecting the liquid medicine is attached to the user, the liquid medicine may be immediately injected into the user. Of course, the scope of the present invention is not limited by these effects.

1 is a block diagram showing a liquid medicine injection system according to an embodiment of the present invention.
2 is a perspective view showing a chemical solution injection device according to an embodiment of the present invention.
3 is an exploded perspective view of the chemical solution injection device of FIG. 2;
FIG. 4 is a perspective view showing some configurations of FIG. 3 .
5 to 8 are cross-sectional views illustrating a drive for injecting a chemical solution into a reservoir, storing the chemical solution, and discharging the chemical solution through a needle.
FIG. 9 is a perspective view showing a part of the structure of FIG. 3 in which a resistance member is assembled;
Fig. 10 is a perspective view showing the resistance member of Fig. 9;
Fig. 11 is a perspective view showing a modified example of the resistance member of Fig. 10;
12 is a graph showing a change in the amount of chemical liquid and a change in driving mode according to driving of the chemical liquid injection device.

Since the present invention can apply various transformations and have various embodiments, specific embodiments will be illustrated in the drawings and described in detail in the detailed description. Effects and features of the present invention, and methods for achieving them will become clear with reference to the embodiments described later in detail together with the drawings. However, the present invention is not limited to the embodiments disclosed below and may be implemented in various forms.

Hereinafter, embodiments of the present invention will be described in detail with reference to the accompanying drawings, and when describing with reference to the drawings, the same or corresponding components are assigned the same reference numerals, and overlapping descriptions thereof will be omitted. .

In the following examples, expressions in the singular number include plural expressions unless the context clearly dictates otherwise.

In the following embodiments, terms such as include or have mean that features or components described in the specification exist, and do not preclude the possibility that one or more other features or components may be added.

When an embodiment is otherwise implementable, a specific process sequence may be performed differently from the described sequence. For example, two processes described in succession may be performed substantially simultaneously, or may be performed in an order reverse to the order described.

In the drawings, the size of components may be exaggerated or reduced for convenience of explanation. For example, since the size and thickness of each component shown in the drawings are arbitrarily shown for convenience of description, the following embodiments are not necessarily limited to those shown.

1 is a block diagram showing a chemical solution injection system 1 according to an embodiment of the present invention.

Referring to FIG. 1 , the drug injection system 1 may include a drug injection device 10 , a user terminal 20 , a controller 30 and a biometric sensor 40 . In the drug injection system 1, a user can drive and control the system using the user terminal 20, and based on blood sugar information monitored by the biometric information sensor 40, the drug solution injection device 10 administers the drug solution. It can be injected periodically.

The drug injection device 10 injects drugs to be injected into the user, such as insulin, glucagon, anesthetics, painkillers, dopamine, growth hormone, and smoking cessation aids, based on data sensed by the biometric sensor 40. also perform a function.

In addition, the liquid medicine injection device 10 may transmit a device status message including information on the remaining battery capacity of the device, whether or not booting of the device was successful, whether injection was successful, etc. to the controller 30 . Messages delivered to the controller may be delivered to the user terminal 20 via the controller 30 . Alternatively, the controller 30 may transmit improved data obtained by processing the received messages to the user terminal 20 .

In one embodiment, the drug injection device 10 is provided separately from the biometric information sensor 40 and may be installed to be spaced apart from the target object. In another embodiment, the drug injection device 10 and the biometric information sensor 40 may be provided in one device.

In one embodiment, the drug solution injection device 10 may be mounted on the user's body. Also, in another embodiment, the drug solution injection device 10 may be mounted on an animal to inject the drug solution.

The user terminal 20 may receive an input signal from a user in order to drive and control the drug solution injection system 1 . The user terminal 20 may generate a signal for driving the controller 30 and control the controller 30 to drive the drug injection device 10 . In addition, the user terminal 20 may display biometric information measured by the biometric information sensor 40 and state information of the drug injection device 10 .

The user terminal 20 refers to a communication terminal usable in a wired/wireless communication environment. For example, the user terminal 20 may include a smart phone, a tablet PC, a PC, a smart TV, a mobile phone, a personal digital assistant (PDA), a laptop, a media player, a micro server, a global positioning system (GPS) device, an e-book reader, It may be a terminal for digital broadcasting, a navigation device, a kiosk, an MP3 player, a digital camera, a home appliance, a device equipped with a camera, and other mobile or non-mobile computing devices. Also, the user terminal 2 may be a wearable device having a communication function and a data processing function, such as a watch, glasses, a hair band, and a ring. However, as described above, a terminal equipped with an application capable of internet communication may be borrowed without limitation.

The user terminal 20 may be connected one-to-one with the pre-registered controller 30 . The user terminal 20 may be encrypted and connected to the controller 30 in order to prevent the controller 30 from being driven and controlled by an external device.

In one embodiment, the user terminal 20 and the controller 30 may be separated and provided as separate devices. For example, the controller 30 may be provided to a subject equipped with the drug injection device 10, and the user terminal 20 may be provided to the subject or a third person. Since the user terminal 20 is driven by the guardian, the safety of the drug injection system 1 can be increased.

In another embodiment, the user terminal 20 and the controller 30 may be provided as a single device. The controller 30 provided as one with the user terminal 20 communicates with the drug injection device 10 to control the injection of the drug.

The controller 30 performs a function of transmitting and receiving data to and from the drug injection device 10, transmits a control signal related to the injection of drugs such as insulin to the drug injection device 10, and transmits blood sugar from the biometric information sensor 40. It is possible to receive a control signal related to the measurement of a biometric value such as the like.

For example, the controller 30 may transmit an instruction request to measure the current state of the user to the drug injection device 10 and receive measurement data from the drug injection device 10 in response to the instruction request.

The biometric information sensor 40 may perform a function of measuring biometric values such as a user's blood sugar level, blood pressure, heart rate, etc. according to a purpose. Data measured by the biometric information sensor 40 may be transmitted to the controller 30, and a drug cycle and/or injection amount may be set based on the measured data. Data measured by the biometric information sensor 40 may be transmitted to the user terminal 20 and displayed.

As an example, the biometric information sensor 40 may be a sensor that measures a blood sugar level of an object. It may be a continuous glucose monitoring (CGM) sensor. A continuous blood glucose measurement sensor may be attached to a subject to continuously monitor a blood glucose level.

The user terminal 20 , the controller 30 and the drug injection device 10 may perform communication using a network. For example, the network may include a Local Area Network (LAN), a Wide Area Network (WAN), a Value Added Network (VAN), a mobile radio communication network, a satellite communication network, and any of these It is a comprehensive data communication network that includes mutual combinations and allows each network constituent entity to communicate smoothly with each other, and may include wired Internet, wireless Internet, and mobile wireless communication network. In addition, wireless communication, for example, wireless LAN (Wi-Fi), Bluetooth, Bluetooth low energy (Bluetooth low energy), Zigbee, WFD (Wi-Fi Direct), UWB (ultra wideband), infrared communication (IrDA, infrared Data Association), NFC (Near Field Communication), 5G, etc. may exist, but are not limited thereto.

2 is a perspective view showing a chemical solution injection device 10 according to an embodiment of the present invention, FIG. 3 is an exploded perspective view of the chemical solution injection device 10 of FIG. 2, and FIG. 4 shows a part of the configuration of FIG. It is a perspective that

Referring to FIGS. 2 to 4 , the drug solution injection device 10 is attached to a user to inject the drug solution, and can inject the drug solution stored therein in a predetermined amount to the user.

The drug solution injection device 10 may be used for various purposes depending on the type of the injected drug solution. For example, the drug solution may include an insulin-based drug solution for diabetics, other pancreas drug solutions, and other various types of drug solutions for the heart.

An embodiment of the drug solution injection device 10 may include a housing 11 covering the outside and an attachment portion 12 positioned adjacent to the user's skin. The chemical solution injection device 10 includes a plurality of parts disposed in an inner space between the housing 11 and the attachment part 12 . A separate bonding means may be further interposed between the attachment part 12 and the user's skin, and the drug solution injection device 10 may be fixed to the skin by the bonding means.

The drug injection device 10 includes a needle assembly 100, a reservoir unit 200, a driving module 300, a battery 350, a driving unit 400, a clutch unit 500, a trigger member 600, a needle It may include a cover assembly 700, an alarm unit 800 and a plurality of sensor units.

In the chemical solution injection device 10, the base body may form a frame in which at least one body supports internal components. The base body may have a first body 13, a second body 14, and a third body 15 according to arrangement.

The first body 13 is disposed under the housing 11, and the needle assembly 100, the reservoir unit 200, the driving module 300, the battery 350, etc. may be supported in each opening or groove. there is. The second body 14 is disposed under the first body 13 and may be connected to the attachment part 12 . The second body 14 may cover the lower portion of the chemical solution injection device 10 . The third body 15 is disposed above the first body 13 and supports the reservoir unit 200, the driving module 300, the battery 350, the driving unit 400, etc. in each opening or groove. It can be. In the drawings, the first body 13, the second body 14 and the third body 15 are shown, but are not limited thereto and may be integrally provided or provided in plurality.

A control module 16 may be disposed inside the drug injection device 10 . A control module 16, which is a circuit board, is disposed under the second body 14, and may control overall driving of the liquid injection device 10. The control module 16 may electrically contact the driving module 300, the battery 350, the alarm unit 800, and a plurality of sensor units to control their driving.

The needle assembly 100 may be mounted on the first body 13 . In the needle assembly 100, the needle N and/or the cannula may move in an axial direction by rotation of the sleeve 110.

One end of the needle N may be connected to the reservoir unit 200 to deliver the drug solution, and the other end may be inserted into the cannula and moved along the cannula.

Since the cannula has a conduit shape capable of accommodating the needle (N), the liquid discharged from the needle (N) can be injected into the user.

The cannula remains inserted into the user's skin, but the needle N rises and is separated from the object. However, the cannula and the needle (N) form a path through which the fluid moves, so that the drug solution injected from the reservoir 210 can be injected into the user through the needle (N) and the cannula.

In the drug injection device 10, a user may simply rotate the needle assembly 100 to insert a cannula into a subject and start drug injection.

The reservoir unit 200 is mounted on the first body 13 and the third body 15, and is connected to the needle assembly 100. The reservoir unit 200 stores the chemical solution D in the internal space, and can move the chemical solution to the needle N in a fixed amount according to the movement of the plunger 230 . The reservoir unit 200 may include a reservoir 210, a cap cover 220, a plunger 230, a sealing ring 240, and a connector member 250 (see FIG. 5).

The reservoir 210 may extend to a predetermined length in the longitudinal direction and store the chemical liquid in the internal space. In the reservoir 210, the chemical liquid may be discharged through the needle N by the movement of the plunger 230. A cap cover 220 is mounted at an end of the reservoir 210, and the rod 410 and/or the connecting member 520 can move through an opening (not shown) disposed in the cap cover 220 (FIG. see 5).

The reservoir 210 may have an inlet end and an outlet end. A chemical solution is injected into the inlet end, a needle (N) is installed at the outlet end, and the chemical solution can be discharged through the needle (N).

The plunger 230 is disposed inside the reservoir 210 and can move linearly by driving the driving module 300 and the driving unit 400 . As the plunger 230 advances, the chemical liquid may be discharged from the inner space to the needle N.

The plunger 230 may have an end 231 and an inclined surface 232 . The end end 231 may move toward the front 210F of the reservoir 210 to move the liquid medicine. The inclined surface 232 may adhere to the inclined portion of the reservoir 210 .

The plunger 230 may be connected to the connector member 250 extending backward. The connector member 250 may be installed on the plunger 230 and move linearly along with the linear movement of the plunger 230 .

The connector member 250 may be made of a material having electrical conductivity and may have a shaft shape. When the connector member 250 moves and contacts the first sensor unit 910A, the storage amount of the drug may be measured or the drug injection device 10 may be started to operate.

The connector member 250 is connected to the rear end of the plunger 230 and may move along with the movement of the plunger 230 . In the drawings, the connector member 250 is shown to have a shaft shape, but is not limited thereto and may have various shapes that generate electrical signals by contacting the first sensor unit 910A.

When the chemical liquid is stored in the reservoir 210 and the plunger 230 retracts, the connector member 250 may retract together with the plunger 230 . In addition, when the plunger 230 moves forward so that the chemical liquid is discharged from the reservoir 210 to the needle N, the connector member 250 may move forward together with the plunger 230 .

The plunger 230 is provided with a sealing ring 240 at a portion in contact with the inner wall of the reservoir 210 to prevent leakage of the chemical liquid when the plunger 230 moves.

The driving module 300 may generate driving force and transmit the driving force to the driving unit 400 . The driving force transmitted by the driving unit 400 linearly moves the plunger 230 inside the reservoir 210 to discharge the liquid medicine.

When the drive units 400 are engaged with each other by the clutch unit 500, the drive module 300 rotates the drive wheel 420 of the drive unit 400, and the rotation of the drive wheel 420 loads the load. The plunger 230 may move as the 410 linearly moves. When the plunger 230 moves, the connector member 250 may also linearly move.

As the driving module 300 , all types of devices having a power to suck in the chemical solution and to discharge the chemical solution by electricity may be used. For example, all types of pumps such as mechanical displacement type micropumps and electromagnetic motion type micropumps can be used. The mechanical displacement type micropump is a pump that uses the movement of solids or fluids such as gears or diagrams to create a pressure difference to induce fluid flow. Diaphragm displacement pumps, fluid displacement pumps ), and rotary pumps. An electrokinetic micropump is a pump that uses energy in the form of electricity or magnetism directly to move a fluid, and includes an electrohydrodynamic pump (EHD), an electroosmotic pump, and a magnetohydrodynamic pump ( Magneto hydrodynamic pump) and Electro wetting pump.

The battery 350 may supply electricity to the liquid medicine injection device 10 to activate each part. The figure shows a pair of batteries 350, but is not limited thereto, and may be variously set according to the capacity, use range, use time, etc. of the liquid injection device 10.

The battery 350 is disposed adjacent to the driving unit 400 and may supply electricity to the driving unit 400 . In addition, the battery 350 is connected to the control module 16, and based on the electrical signal measured by the sensor unit, the sensor unit determines the number of rotations or the rotational speed of the drive unit 400, and the about stored in the reservoir 210. Data on the amount of liquid and the amount of chemical liquid injected into the user may be measured.

5 to 8 are cross-sectional views illustrating a drive for injecting a chemical solution into a reservoir, storing the chemical solution, and discharging the chemical solution through a needle.

5 to 8, the driving unit 400 is installed between the driving module 300 and the reservoir unit 200, and is placed in the reservoir 210 with driving force generated by the driving module 300. The plunger 230 may be moved. However, the driving unit 400 can move the plunger 230 forward only when the rod 410 and the driving wheel 420 are coupled or connected by the clutch unit 500 .

The rod 410 is connected to the plunger 230 and extends in one direction. The rod 410 is inserted into the opening of the cap cover 220, and the rod 410 can move in the longitudinal direction of the reservoir 210 to move the plunger 230. The rod 410 may have a threaded shape on its surface. The rod 410 is inserted into the connecting member 520 and is connected to the drive wheel 420 by the clutch unit 500 when liquid is discharged in a fixed amount, so that the rod 410 can be moved forward.

The driving wheel 420 is drivingly connected to the driving module 300 and can rotate by driving the driving module 300 . The driving wheel 420 may have a first connection end 421 and a second connection end 422, and may have a space in which the rod 410 can move. Since at least one of the first connection end 421 and the second connection end 422 is always driven and connected to the drive module 300 by the connector CN, the driving module 300 drives the drive wheel 420. ) can rotate.

In one embodiment, the first connection end 421 and the second connection end 422 may have a gear tooth shape. The connector CN connected to the driving module 300 applies gear teeth to rotate the driving wheel 420 .

In detail, the connector CN rotates repeatedly with respect to the rotation axis according to the linear reciprocating motion of the driving module 300 . The end of the connector CN may rotate the driving wheel 420 by applying pressure to at least one of the first connection end 421 and the second connection end 422 . For example, one end of the connector CN may be disposed to apply pressure to the first connection end 421 and the other end of the connector CN may be disposed to apply pressure to the second connection end 422 .

When the connector CN rotates about the rotation axis, the second sensor unit 920 may measure the driving of the connector CN. The second sensor unit 920 may measure whether or not the driving force of the driving module 300 is transmitted to the driving wheel 420 by measuring contact with the connector CN. Also, the second sensor unit 920 may measure the rotated angle of the driving wheel 420 by measuring whether or not it is in contact with the connector CN.

The clutch unit 500 may drively connect the driving module 300 and the driving unit 400 . The clutch unit 500 is disposed between the rod 410 and the driving wheel 420 and may include a coupler 510 and a connecting member 520 .

The coupler 510 is disposed outside the connecting member 520, and is spaced apart from the connecting member 520 at a predetermined interval when inactive (FIGS. 5 and 6), and when activated, the rod 410 and the driving wheel ( 420) can be connected (FIGS. 7 and 8). The coupler 510 is a component capable of applying an elastic force to the outside of the connecting member 520, and is not limited to a specific shape. However, in the following description, for convenience of description, the case of the spring type will be mainly described.

At least a portion of the connection member 520 may be inserted into the rod 410 . The connecting member 520 is disposed to cover the outside of the rod 410 . The connecting member 520 may connect the driving module 300 and the rod 410 according to the operation of the coupler 510 .

In one embodiment, the rod 410 and the connecting member 520 may each have the form of a screw and a screw thread. A screw thread is formed on an outer circumferential surface of the rod 410 and a screw thread is formed on an inner circumferential surface of the connection member 520 to be connected in a screw-fitting manner.

In one embodiment, the connecting member 520 has a screw thread formed on the inner circumferential surface at one end, but the screw thread may not be disposed on the other end.

Referring to FIG. 5 , a screw thread is formed on the inner circumferential surface of the first section L1 of the connecting member 520, and the rod 410 is screwed only in the first section L1. In addition, the diameter of the first section L1 corresponds to the rod 410 and may have a size D1.

No thread is formed on the inner circumferential surface of the second section L2 of the connecting member 520 . Also, the diameter D2 of the second section L2 may be set larger than the diameter D1 of the first section L1. In the second section (L2), the connecting member 520 does not contact the rod 410.

The length of the first section L1 may be set to overlap with the coupler 510 when the connecting member 520 moves backward. 6 and 7, when the plunger 230 extends rearward, at least a portion of the first section L1 overlaps the coupler 510, that is, at least a portion faces the coupler 510. do. When the coupler 510 is activated, the length of the first section L1 in the connecting member 520 may be set so that the coupler 510 grips at least a portion of the first section L1.

Since the rod 410 is screwed only in the first section L1 of the connecting member 520, when the connecting member 520 rotates to move the rod 410 forward, the connecting member 520 and the rod ( 410) can reduce the load due to screw coupling.

As shown in FIGS. 7 and 8 , when the coupler 510 is activated, the coupler 510 grips the connecting member 520 and rotates the connecting member 520 as the driving wheel 420 rotates. Since the connecting member 520 and the rod 410 are screwed only in the first section L1, even when the driving wheel 420 rotates with a small torque, the connecting member 520 can move the rod 410 forward. can That is, since the rod 410 and the connecting member 520 are screwed only in the first section L1, the plunger 230 can be moved forward even with a slightly weak force by the driving of the driving unit 400. Therefore, the chemical solution injection device 10 can discharge the chemical solution to the needle N even when a small force is generated in the drive module 300, and relatively small driving force is applied to the drive unit 400 and the clutch unit 500. Therefore, durability of parts can be improved.

Referring back to FIG. 3 , the trigger member 600 may generate a mechanical signal for injecting the chemical solution of the drug solution injection device 10 . The trigger member 600 is rotatably disposed on one side of the third body 15, the trigger member 600 rotates to start driving the driving module 300, and at the same time the clutch unit 500 drives the driving unit ( 400) can be driven and connected.

FIG. 9 is a perspective view showing a part of the structure of FIG. 3 in which the resistance member 530 is assembled, and FIG. 10 is a perspective view showing the resistance member 530 of FIG. 9 .

Referring to FIGS. 9 and 10 , the resistance member 530 may be inserted into the connection member 520 . The resistance member 530 may contact the connecting member 520 and generate frictional force when the connecting member 520 retreats.

The resistance member 530 is inserted into the connection member 520 and may be variously set as a component that generates resistance to the connection member 520 . Although the drawing shows that the resistance member 530 has an opening in the center and has a thin plate shape, it is not limited thereto and may be set in various ways. For example, the resistance member may be formed of silicon inserted outside the connection member 520 . Also, the resistance member may be a spring connecting the cap cover 220 and the connection member 520, and the spring may resist the connection member 520 from retracting. However, hereinafter, for convenience of description, an embodiment in which the resistance member 530 has a plate shape will be mainly described.

The resistance member 530 may have an insertion opening OP through which the connecting member 520 is inserted, and a base portion 531 extending outward of the insertion opening OP. In addition, the resistance member 530 may have a cutout CF connected to the insertion opening OP by being cut at one side of the base portion 531 .

The connection member 520 may be installed to pass through the insertion opening OP of the resistance member 530 . The resistance member 530 may be disposed between the rear end of the reservoir 210 and the driving wheel 420 . The plunger 230 in the reservoir 210 is connected to the rod 410, and the rod 410 is inserted into the connecting member 520. The driving wheel 420 is spaced apart from the rear end of the reservoir 210, and the connecting member 520 may be inserted into the inner space.

When the plunger 230 and the connection member 520 move to the rear of the reservoir 210, one side of the resistance member 530 may be supported by the driving wheel 420. The resistance member 530 is disposed between the reservoir 210 and the driving wheel 420, and the connecting member 520 moves until the connecting member 520 contacts the front end 420F of the driving wheel 420 during movement. can move with When the base portion 531 of the resistance member 530 contacts the front end 420F of the drive wheel 420, when the connecting member 520 moves backward, it does not retreat due to the front end 420F, and the connecting member 520 ) can form resistance (frictional force) in the opposite direction to the moving direction. That is, the resistance member 530 may generate frictional force on the outer circumferential surface of the connection member 520 .

The base portion 531 extends outside the insertion opening OP and may have a predetermined thickness. The base portion 531 may be supported by the driving wheel 420 .

The wing end 532 may be disposed outside the base part 531 . 10 shows two wing stages 532, but is not limited thereto, and may be set to one or three or more. The blade 532 may be supported by the driving wheel 420 and receive resistance from the driving wheel 420 .

The connection end 533 may connect the base part 531 and the wing end 532 . The connection end 533 has a predetermined thickness, so that the resistance force transmitted from the base part 531 and the wing end 532 can be evenly distributed.

The cut end 534 extends outward from the base portion 531, and the cut portion CF may be disposed thereon. The cut ends 534 may be spaced apart from each other to form the cut portion CF.

The connection member 520 is inserted into the insertion opening OP, and as shown in FIG. 10 in one embodiment, the insertion opening OP may be formed in a circular shape. In another embodiment, the insertion opening may be formed in a polygonal shape. In another embodiment, the insertion opening may include a plurality of protrusions protruding from the inner circumferential surface of the base toward the center. A plurality of protrusions may contact the outer circumferential surface of the connecting member.

The minimum diameter M2 of the insertion opening OP may be set smaller than the diameter M1 of the connection member 520 . In order to tightly assemble the insertion opening OP to the connection member 520, the minimum diameter M2 of the insertion opening OP may be set smaller than the diameter M1 of the connection member 520. Accordingly, when the resistance member 530 contacts the driving wheel 420, a resistance force may be generated in the connecting member 520.

The cutout CF is formed by cutting one side of the base portion 531 and may be connected to the insertion opening OP. The cutout CF may form an elastic force in the resistance member 530 .

5 and 6 , when the chemical solution D is injected into the reservoir 210, the plunger 230, the rod 410, and the connecting member 520 are retracted toward the driving wheel 420. When the plunger 230 and the connection member 520 are retracted by the injection of the chemical solution D into the reservoir 210, the resistance member 530 contacts the driving wheel 420 to generate resistance to the connection member 520. do.

Only when the chemical solution D is injected into the reservoir 210 with a greater pressure that overcomes the resistance force, the chemical solution D may be injected into the reservoir 210 while the connecting member 520 is retracted. Since the chemical liquid D is injected and stored in the reservoir 210 at a high pressure that overcomes resistance, the chemical liquid D stored in FIG. 6 has a high pressure.

As shown in FIG. 7 , when the coupler 510 of the clutch unit 500 grips the connecting member 520 and the drive wheel 420 rotates, the chemical solution D can be quickly discharged through the needle N. . Since the chemical liquid D stored in the reservoir 210 is stored at a higher pressure than the external pressure, even if a small driving force is transmitted from the driving module 300, the plunger 230, the rod 410, and the connecting member 520 While moving forward, the chemical solution D may be discharged in a fixed amount through the needle N.

FIG. 11 is a perspective view showing a modified example of the resistance member 530A of FIG. 10 .

Referring to FIG. 11 , the resistance member 530A may have an insertion opening OP, a cutout CF, a base portion 531A, and a cutout end 532A. The connection member 520 is inserted into the insertion opening OP, and the base portion 531A extends along the insertion opening OP, and when the connection member 520 moves, the front end 420F of the driving wheel 420 can contact The cutout CF is cut from the base portion 531 and may be disposed between the cutouts 532A facing each other.

The resistance member 530A is inserted into the connecting member 520 to generate a resisting force in the connecting member 520 when the chemical solution D is injected into the reservoir 210, and the chemical solution D in the reservoir 210. ) is stored at high pressure.

In another embodiment, the resistive member 530A is installed together with the aforementioned resistive member 530 to generate a greater resistance to the connection member 520, and the chemical solution D stored in the reservoir 210 is further reduced. Can be stored at high pressure.

Referring back to FIG. 3 , the trigger member 600 may rotate in one direction about the pivot axis. At this time, the trigger member 600 may apply force to the clutch unit 500 to couple the rod and the driving wheel 420 .

In detail, when the user rotates the needle assembly 100, the knob of the needle assembly 100 presses the end of the trigger member 600, so that rotation of the trigger member 600 may be initiated. When the trigger member 600 rotates, the trigger member 600 presses the end of the coupler 510, the coupler 510 is engaged with the connecting member 520, and the clutch unit 500 is activated.

Needle cover assembly 700 may be mounted below needle assembly 100 . The needle cover assembly 700 may prime air stored in the reservoir unit 200 before injecting the liquid medicine. Through the chemical liquid injector (NI), when the chemical liquid is in the reservoir 210, gas (air) remaining in the reservoir 210 may be discharged to the outside.

The needle cover assembly 700 may have a first cover 710 , a second cover 720 , a filter member 730 and an adhesive layer 740 .

The first cover 710 may be disposed under the chemical solution injection device 10 . The second cover 720 may be inserted and assembled into the opening of the first cover 710 . An insertion protrusion 711 inserted into the second body 14 and fixing the needle cover assembly 700 may be disposed on one side of the first cover 710 .

The second cover 720 is assembled to the first cover 710, and a needle N and/or a cannula may be aligned in the center. The second cover 720 is penetrated in the center in the height direction and may have a storage space in which the chemical solution D is stored.

The first cover 710 has greater rigidity than the second cover 720 . The first cover 710 is a portion exposed to the outside, and is formed of a material with a slightly greater rigidity. The second cover 720 is assembled to the first cover 710 and is formed of a material having less rigidity than the first cover 710 in order to be inserted into the opening of the second body 14 .

A protrusion 721 inserted into the second body 14 may be provided at the center of the second cover 720 . In addition, the second cover 720 has a fixing protrusion 722, and the fixing protrusion 722 is inserted into the first cover 710, so that the first cover 710 and the second cover 720 are assembled. can

The filter member 730 is mounted on the second cover 720 . The filter member 730 is disposed under the storage space of the second cover 720, and gas such as air passes through the filter member 730, but liquid such as chemical does not pass through the filter member 730. Thus, the air discharged from the needle N passes through the filter member 730 and is discharged to the outside, but the chemical discharged from the needle is stored in the storage space defined by the second cover 720 and the filter member 730. can

The shape of the filter member 730 may change according to the amount of liquid medicine stored in the storage space. For example, when the storage space is filled with the chemical solution, the filter member 730 expands downward, so that the user can recognize that the chemical solution has flowed into the needle cover assembly 700 .

The adhesive layer 740 is disposed on one surface of the needle cover assembly 700 and may attach the needle cover assembly 700 to the attachment part 12 .

The alarm unit 800 is disposed inside or outside the chemical solution injection device 10 and can notify a user of normal operation or malfunction of the drug solution injection device 10 .

For example, the alarm unit 800 is disposed below the housing 11 and is connected to a circuit board. The alarm unit 800 may generate a warning sound or generate light to deliver an alarm to an external user.

Referring to FIG. 4 , the plurality of sensor units may measure the driving of the chemical solution injection device 10 . The plurality of sensor units measure the storage amount of the chemical solution in the reservoir 210, whether the drive module 300 is driven, whether the drive unit 400 is driven, the rotation angle of the drive wheel 420, and the plunger 230. You can measure distance, etc.

Each of the sensor units may have a plurality of contact ends. The contact terminal may measure each event or data by measuring electrical contact.

The position of any one end of the contact end may be changed by contact with another part, and may return to its original position by restoring force when contact with the other part is released.

In one embodiment, the contact end may have an elastic spring shape. The contact end may have a first end connected to the control module 16 that is a circuit board, and a second end extending from the first end and contacting the connector member 250 .

A diameter of the first end may be set larger than a diameter of the second end. Since the diameter of the first end is larger than the diameter of the second end, the first end can be firmly supported on the circuit board. The first end is stably supported by the control module 160, and the position or shape of the second end is easily deformed to stably maintain contact with other parts.

A length of the first end may be set smaller than a length of the second end. Since the length of the first end is shorter than the length of the second end, the first end can be firmly supported on the circuit board. The first end is stably supported by the control module 160, and the position or shape of the second end is easily deformed to stably maintain contact with other parts.

In particular, since the diameter of the second end is smaller than the diameter of the first end, or the length of the second end is set to be longer than the length of the first end, the second end is like the connector member 250 or the base cover 933. Even when in contact with other parts, the position or shape of the second end is easily deformed, and contact with other parts can be stably maintained.

The first sensor unit 910A is disposed adjacent to the reservoir unit 200 . The first sensor unit 910A may be disposed on the movement path of the connector member 250 . The first sensor unit 910A may have a plurality of contact ends, and the plurality of contact ends may be mounted in the fixing groove 14A of the second body 14 . While the connector member 250 moves, it may come into contact with at least one of the plurality of contact ends.

In one embodiment, the first sensor unit 910A may include a first contact end 911 and a second contact end 912 . The first contact end 911 and the second contact end 912 are spaced apart from each other, and the connector member 250 linearly moves to contact the first contact end 911 and/or the second contact end 912. can do.

The connector member 250 may contact the first contact end 911 at the first position P1 and contact the second contact end 912 at the second position P2.

Referring to FIGS. 4, 5, and 6, in the process of injecting the chemical liquid D into the reservoir 210, the connector member 250 first contacts the first contact end 911 at the first position P1. (the plunger 230 is at the P-1 position), and then the connector member 250 contacts the second contact end 912 at the second position P2 (the plunger 230 is at the P-2 position).

In one embodiment, the connector member 250 may electrically connect the first contact end 911 and the second contact end 912 . When the first contact end 911 and the second contact end 912 are electrically connected through the connector member 250, the control module 16 may recognize a specific event of the reservoir unit 200.

For example, when the connector member 250 contacts the first contact end 911 and the second contact end 912, the first sensor unit 910A stores the liquid stored in the reservoir 210 in a first reference amount (for example, 10%, 20%, 30%, etc.) can be sensed.

When recognizing that the chemical solution D is stored in the reservoir 210 as the set first reference amount, the control module 16 may wake up the chemical solution injection device 10 (AWAKE). That is, the control module 16 may confirm that a certain amount of liquid medicine is stored in the reservoir 210, and may start partially driving to preheat the chemical liquid injection device 10 (first mode).

In another embodiment, the connector member 250 may contact at least one of the contact ends of the first sensor unit 910A to generate an electrical signal. When the connector member 250 contacts the first contact end 911, the control module 16 recognizes the first event, and when the connector member 250 contacts the second contact end 912, the control module 16 may recognize the second event.

For example, the connector member 250 may contact the first contact end 911 to wake up the chemical solution injection device 10, and contact the second contact end 912 to release the chemical solution stored in the chemical solution injection device 10. The amount of storage can be sensed.

For example, the connector member 250 may contact the first contact end 911 to wake up the chemical solution injection device 10 and primarily sense the amount of the chemical solution stored in the reservoir 210, and the second contact end ( 912), the storage amount of the chemical solution stored in the chemical solution injection device 10 may be sensed secondarily.

As shown in FIGS. 4, 7, and 8, in the process of discharging the chemical solution D to the needle N, the connector member 250 first releases contact with the second contact end 912 at the second position P2, and (The plunger 230 is at the P-2 position), and then the connector member 250 is released from contact with the first contact end 911 at the first position P1 (the plunger 230 is at the P-1 position). .

In one embodiment, when the connector member 250 maintains contact with the first contact end 911 and the second contact end 912 and the contact of the second contact end 912 is separated, the first contact end ( 911) and the second contact end 912 are disconnected electrically. When the first contact terminal 911 and the second contact terminal 912 are electrically disconnected, the control module 16 may recognize a specific event of the reservoir unit 200 .

In detail, when the second contact end 912 is disconnected, the control module 16 may generate a signal indicating that the chemical solution D stored in the reservoir 210 is insufficient. The control module 16 generates an alarm signal and transfers the alarm signal to the controller 30, the user terminal 20, and/or the alarm unit 800 so that the user can recognize the amount of liquid medicine.

In addition, when the third mode is set in the chemical solution injection device 10, the forward distance of the plunger 230 within the reservoir 210 is determined using the second sensor unit 920 and/or the encoder unit 930. It can accurately measure and precisely measure and monitor the amount of chemical solution stored in the reservoir 210.

In another embodiment, different events may be recognized by releasing contact with at least one of the contact ends of the connector member 250 of the first sensor unit 910A. When the connector member 250 releases contact with the second contact end 912, the control module 16 recognizes the third event, and the connector member 250 releases contact with the first contact end 911. If so, the control module 16 may recognize the fourth event.

For example, if the connector member 250 releases contact with the second contact end 912, the control module 16 may transmit an alarm signal to the user, and if contact with the first contact end 911 is released, , The control module 16 may forcibly terminate the chemical solution injection device 10, continuously generate an alarm signal to the user terminal 20, reduce the amount of the chemical solution injected into the user, or increase the injection period.

The second sensor unit 920 may sense whether the driving module 300 and/or the driving unit 400 are driven. The driving module 300 and the driving wheel 420 are drivenly connected by a connector CN. When the drive module 300 moves linearly, the connector rotates repeatedly around the rotation axis, and both ends of the connector CN connect the first connection end 421 and the second connection end 422 of the drive wheel 420. The driving wheel 420 is rotated by applying an alternating force. The second sensor unit 920 may measure whether or not the connector CN rotates about the rotation axis and the number of rotations.

The second sensor unit 920 may measure the moving distance of the plunger 230, the discharge amount of the chemical solution discharged through the needle N, and the amount of the chemical solution remaining in the reservoir 210. The second sensor unit 920 measures how much the connector CN rotates the drive wheel 420 . When the rotational angle of the drive wheel 420 is measured by the second sensor unit 920, the linearly moved distance of the plunger 230 can be calculated, and the discharged from the reservoir 210 through the moving distance can be calculated. The chemical solution and the chemical solution remaining in the reservoir 210 may be measured.

The second sensor unit 920 may have a 1A contact end 921 and a 2A contact end 922 . When the connector CN contacts the 1A contact end 921, the second sensor unit 920 applies the connector CN to either the first connection end 421 or the second connection end 422. to be measured as In the second sensor unit 920, when the connector CN contacts the 2A contact end 922, the connector CN applies the other one of the second connection end 422 and the second connection end 422. to be measured as

The encoder unit 930 may be disposed at one end of the driving unit 400 to measure rotation of the driving unit 400 . The encoder unit 930 may measure rotation of the drive wheel 420 .

The encoder unit 930 may have a base cover 933 having a 1B contact end 931, a 2B contact end 932, a cover end 933A, and a teeth end 933B.

The 1B contact end 931 is disposed at the end of the base cover 933 and can always maintain contact with the base cover 933 . The 1B contact end 931 may selectively maintain contact with the cover end 933A.

In the drawing, the 1B contact end 931 is shown to be disposed on the opposite side of the 2B contact end 932, but is not limited thereto. For example, the 1B contact end 931 and the 2B contact end 932 may be disposed on the same side of the driving wheel 420 . In addition, the 1B contact end 931 may be disposed behind the driving wheel 420 .

The 2B contact end 932 is disposed at the end of the base cover 933 and is spaced apart from the 1B contact end 931 . The 2B contact end 932 is disposed to come into contact with the tooth end 933B, so that contact may be made or released according to rotation of the driving wheel 420 .

The base cover 933 is inserted into one end of the drive wheel 420 . The cover end 933A extends to go around the outer circumferential surface of the drive wheel 420, but the tooth end 933B extends from the cover end 933A and may be spaced apart from each other along the outer circumferential surface of the drive wheel 420. . The tooth end 933B may extend along the longitudinal direction of the driving wheel 420 from the cover end 933A.

The encoder unit 930 may measure whether the second sensor unit 920 is properly driven by sensing the rotation of the driving wheel 420 . If the rotation of the driving wheel 420 is measured by the encoder unit 930 when the drug injection device 10 is normally operating, the second sensor unit 920 should also contact the connector CN. If it is measured by the encoder unit 930 that the driving wheel 420 does not rotate, the second sensor unit 920 should not also contact the connector CN. Therefore, by comparing the signal measured by the encoder unit 930 and the signal measured by the second sensor unit 920, the encoder unit 930 may check the error of the second sensor unit 920.

The chemical solution injection device 10 according to the present invention may store the high-pressure drug solution D in the reservoir 210 . Since the chemical liquid (D) stored in the reservoir 210 is stored at a high pressure, even if a small amount of driving force acts on the plunger 230, the plunger 230 can rapidly and quantitatively discharge the chemical liquid (D) while moving forward. can

The chemical solution injection device 10 stores the chemical solution in the reservoir 210 using an external injection device (not shown), then transfers the driving force generated by the driving module 300 to the plunger 230, ) is discharged by a needle (N). At this time, a strong force for advancing the plunger 230 is transmitted and the internal pressure of the chemical solution D is discharged through the needle N only when the internal pressure is high enough to be discharged. If the pressure of the chemical liquid (D) stored in the reservoir 210 is not high enough, the chemical liquid (D) is not discharged to the needle (N) at the beginning of the operation of the chemical liquid injection device 10, and the driving force is applied to the reservoir 210 ) It is used to increase the pressure of the chemical solution (D) stored in.

When the chemical solution is stored in the reservoir 210, the resistance member 530 generates resistance and can be stored at a high pressure. Since the resistance member 530 generates a force that resists the movement of the connection member 520 when the connection member 520 is retracted, the pressure of the injected chemical solution must overcome the resistance force to be injected into the reservoir 210. there is. Therefore, the chemical liquid D stored in the reservoir 210 can be maintained at a high pressure enough to overcome the resistance.

The drug solution injection device 10 according to the present invention can quickly inject the drug solution into the user without delaying the time the drug solution is discharged through the needle N. The chemical liquid D stored at high pressure can be discharged through the needle N even when a small driving force is applied to the plunger 230 . Therefore, when the chemical solution injection device 10 is attached to the user, the drug solution can be immediately injected into the user.

FIG. 12 is a graph showing a change in the amount of chemical liquid and a change in driving mode according to driving of the chemical liquid injection device 10 .

5 to 8 and 17, before attaching the chemical solution injection device 10 to the user, the chemical solution D is stored in the reservoir 210, and then the reservoir 210 is transferred to the needle N. A process of discharging the chemical solution D and injecting the chemical solution D to the user will be described as follows.

<Drug Storage Step>

A user injects a chemical solution into the reservoir unit 200 of the chemical solution injection device 10 using an external chemical solution injector (not shown). Referring to FIG. 5 , prior to injecting the chemical solution, the plunger 230 is disposed at the front end of the reservoir 210, and the rod 410 is assembled to the connecting member 520 at the rear end of the plunger 230. At this time, since the coupler 510 does not grip the connecting member 520, the driving wheel 420 is not connected to the rod 410.

The user puts the drug D to be injected into a drug injector (not shown) and inserts the drug injector into the inlet end of the reservoir unit 200 . When the chemical solution D is injected, the plunger 230 retracts together with the connecting member 520 . At this time, the resistance member 530 attached to the connection member 520 collides with the front end 420F of the driving wheel 420 and generates resistance in a direction opposite to the moving direction of the connection member 520 . The chemical solution D is injected into the reservoir 210 only when a pressure high enough to overcome the resistance is generated. In addition, the chemical solution D injected into the reservoir 210 maintains a high pressure.

When the chemical liquid is injected, air remaining inside the reservoir 210 may be primed. In detail, during the assembly process of the reservoir unit 200, air remains between the reservoir 210 and the plunger 230. If the chemical solution is injected while air remains in the reservoir 210, there is a risk that the air will also be injected into the user, so an operation to remove the air (priming operation) is required.

When the chemical liquid starts to flow into the reservoir 210 from the chemical liquid injector, the remaining gas is pushed out through the needle N while being introduced between the inner surface of the reservoir 210 and the plunger 230 . At this time, the gas may move along the guide groove 211 . That is, the gas remaining inside the reservoir 210 may be discharged to the needle N along the guide of the guide groove 211 by the flowing chemical liquid D. The gas passing through the needle N moves to the needle cover assembly 700 and passes through the filter member 730 of the needle cover assembly 700 to be discharged to the outside. Gas remaining inside the reservoir 210 is quickly discharged to the outside by the guide of the guide groove 211, and the gas in the reservoir 210 can be removed.

The first sensor unit 910A may be driven according to the amount of the chemical liquid D injected into the reservoir 210 .

When the plunger 230 passes the point P-1 according to the injection of the chemical solution D, the connector member 250 contacts the first contact end 911 at the first position P1. Then, when the plunger 230 passes the point P-2, the connector member 250 contacts the second contact end 912 at the second position P2.

In one embodiment, when the connector member 250 electrically connects the first contact end 911 and the second contact end 912, the first mode is driven. The first mode is an AWAKE mode of the chemical solution injection device 10, and then, when the drug solution injection device 10 is attached to a user, the chemical solution injection device 10 may be preheated so as to be immediately driven. In addition, the user may be notified through the user terminal 20 that the preset first reference amount of the chemical solution D is stored in the reservoir 210, thereby informing the user to use the chemical solution injection device 10 in advance.

In another embodiment, when the connector member 250 is connected to the first contact end 911, the control module 16 recognizes it as a first event, and when connected to the second contact end 912, the control module 16 It can be recognized as the second event. That is, when the connector member 250 contacts different contact ends, different events may be recognized and the events may be transmitted to the user.

<Attach step>

6, when the drug (D) is stored in the reservoir 210, the drug solution injection device 10 is attached to the user. Since gas in the reservoir 210 is removed (priming operation is completed) through the needle cover assembly 700 in the above-described drug storage step, the needle cover assembly 700 is removed from the drug injection device 10.

The user attaches the drug solution injection device 10 to the user, rotates the needle assembly 100, and inserts the needle N and the cannula into the skin. The needle (N) is inserted into the skin together with the cannula, and can lead the cannula to be inserted into the skin.

Then, the needle (N) is withdrawn from the skin, but remains connected to the cannula. When the user further rotates the needle assembly 100, the needle N moves upward while the cannula is inserted into the skin. At least a part of the cannula and the needle N is connected, and forms and maintains a path through which the liquid medicine moves.

<Drug Injection Step-Second Mode>

The driving module 300 and the driving unit 400 are driven at substantially the same time as the cannula and the needle N are inserted into the user. In the second mode, the chemical solution injection device 10 may inject the chemical solution D into the user according to the set cycle and injection amount.

When the user rotates the needle assembly 100 to insert the needle N and the cannula into the skin, the trigger member 600 drives the driving module 300. When the driving module 300 is driven, the connector CN rotates the driving wheel 420 while rotating about the pivot axis. The connector CN may rotate the driving wheel 420 in units of 1 tooth while alternately applying pressure to the first connection end 421 and the second connection end 422 .

When the user rotates the needle assembly 100, the trigger member 600 can activate the coupler 510 as shown in FIG. When the coupler 510 grips the outside of the connecting member 520, the driving wheel 420, the coupler 510, and the connecting member 520 are integrated into one body. Therefore, when the driving wheel 420 rotates, the connecting member 520 also rotates, and the rod 410 moves forward.

When the rod 410 moves forward, the plunger 230 may also move forward, and the liquid medicine may be discharged through the needle N. Therefore, the drug may be injected into the user according to the set driving cycle and driving speed of the driving module 300 .

At this time, the second sensor unit 920 may measure rotation of the connector CN. The 1A contact end 921 and the 2A contact end 922 of the second sensor unit 920 alternately contact the corresponding ends of the connector CN. The second sensor unit 920 senses contact between the 1A contact end 921 and one end of the connector CN, and senses contact between the 2A contact end 922 and the other end of the connector CN.

In one embodiment, when the contact end of the second sensor unit 920 and the connector CN come into contact, the second sensor unit 920 may sense an electrical signal. In another embodiment, when the contact end of the second sensor unit 920 and the connector CN come into contact, the second sensor unit 920 may sense an impact signal according to the contact.

The second sensor unit 920 measures whether the driving module 300 and the connector CN are driven based on data obtained by measuring the rotation of the connector, or determines whether the driving wheel 420 is driven by the connector CN. It is possible to measure the rotational angle and/or rotational speed of the drive wheel 420, or measure the movement distance of the plunger 230 and the injection amount of the chemical solution by the rotation of the drive wheel 420.

When the drive wheel 420 rotates, the encoder unit 930 may measure the rotation angle and rotation speed of the drive wheel 420 . The 1B contact end 931 maintains electrical contact with the cover end 933A, but the 2B contact end 932 maintains electrical contact with the tooth end 933B, but is in electrical contact with the tooth end 933B. this can be released.

The encoder unit 930 may measure data related to rotation of the drive wheel 420 by electrically measuring a connection signal and/or an electrical release signal. The control module 16 calculates the rotation angle and rotation speed of the drive wheel 420 based on the data measured by the encoder unit 930, and calculates the movement distance of the plunger 230 and the discharge amount of the chemical solution based on this. there is.

<Drug Injection Step-Third Mode>

When the plunger 230 is located at the P-2 position and the connector member 250 is located at the second position P2, the first contact end 911 and the second contact end 912 in the first sensor unit 910A ) are electrically isolated. The control module 16 may activate the third mode when the first sensor unit 910A is electrically released.

In the third mode, the control module 16 may transmit an alarm signal indicating that the amount of stored chemical solution corresponds to the second reference amount to the user through the user terminal 20, the controller 30, and/or the alarm unit 800. . The second reference amount may be defined as the amount of liquid chemical recognized by the driving module 300 at the time of driving in the third mode. The control module 16 may inform the user that the amount of liquid medicine remaining in the reservoir 210 is a preset second reference amount, so that the user may prepare to replace the liquid medicine injection device 10 .

In one embodiment, the first reference amount may be set to the same chemical storage amount as the second reference amount. When the plunger 230 moves forward or backward, and when the connector member 250 contacts or releases contact with the second contact end 912, the position of the plunger 230 in the reservoir 210 is the same. The first reference amount and the second reference amount may be set identically.

In another embodiment, the first reference amount may be set as a chemical storage amount greater than the second reference amount. The first reference amount is a reference value set for driving in the first mode, and may be set to be substantially equal to the amount of liquid chemical stored in the reservoir 210 . The second reference amount is the amount of chemical liquid recognized by the driving module 300 at the start of the third mode, and may be set to be smaller than the amount of chemical liquid actually remaining in the reservoir 210 to have a margin.

Since the second reference amount is set smaller than the amount of chemical liquid stored in the actual reservoir 210, the actual reservoir 210 has a margin corresponding to the difference between the actual remaining amount of the chemical liquid and the second reference amount. Even if the chemical solution injection device 10 informs that there is no chemical solution, the chemical solution left in the reservoir 210 can be further used, thereby eliminating a sudden disconnection of the chemical solution or an accident, thereby increasing the safety of the chemical solution injection device 10. there is.

Since the remaining amount of the chemical solution is important in the third mode, the control module 16 can calculate the injected amount of the chemical solution and the remaining amount of the chemical solution in the reservoir 210 very precisely in the third mode. In the third mode, based on the data obtained from the second sensor unit 920 and the encoder unit 930, the control module 16 accurately determines the rotation angle of the drive wheel 420 and the movement distance of the plunger 230. By measuring, the discharge amount of the chemical liquid and the amount of the chemical liquid remaining in the reservoir 210 can be strictly calculated. The residual amount of the chemical solution accurately calculated in the third mode is transmitted to the user in real time, so that the user can recognize the danger.

In one embodiment, the drug solution injection device 10 may accurately count the amount of the drug solution left in the reservoir 210 only in the third mode. In the second mode, since the amount of the chemical solution stored in the reservoir 210 exceeds a preset range (ie, the second reference amount), the amount of the chemical solution in the reservoir 210 is not precisely counted, but in the third mode, the reservoir The amount of the chemical solution stored in 210 can be counted quantitatively. Since the amount of chemical solution stored in the chemical solution injection device 10 is accurately counted only at the level at which an alarm is required, the control load of the chemical solution injection device 10 can be reduced.

The spirit of the present invention should not be limited to the above-described embodiments and should not be determined, and not only the claims to be described later, but also all ranges equivalent to or equivalently changed to these claims fall within the scope of the spirit of the present invention. would be said to belong.

1: liquid medicine injection system
10: chemical solution injection device
100: needle assembly
200: reservoir unit
300: drive module
400: drive unit
500: clutch unit
600: trigger absence
700: needle cover assembly
800: alarm unit

Claims (5)

base body;
a reservoir mounted on the base body and having a plunger disposed therein;
a rod connected to the plunger;
a connecting member into which the rod is inserted;
a driving wheel disposed spaced apart from one end of the reservoir and transmitting a driving force to the connecting member;
a coupler disposed outside the connecting member, spaced apart from the connecting member when inactive, and connecting the rod and the drive wheel when activated; and
and a resistance member inserted into the connection member, disposed between the reservoir and the drive wheel, and resisting a retreating movement of the connection member when the coupler is deactivated. According to claim 1,
The resistance member is
When the plunger and the connecting member move toward the rear of the reservoir, one side thereof is supported by the driving wheel. According to claim 2,
The resistance member is
A chemical solution injection device that generates frictional force with an outer circumferential surface of the connecting member. According to claim 1,
The resistance member is
The drug injection device having an insertion opening into which the connecting member is inserted, wherein a minimum diameter of the insertion opening is smaller than a diameter of the connecting member. According to claim 1,
The resistance member is
a base portion extending outwardly of the insertion opening into which the connection member is inserted; and
A drug solution injection device having a cutout portion cut at one side of the base portion and connected to the insertion opening.

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