CN118045287B - An implantable peripheral nerve electrical stimulation zinc oxygen battery and its implantation device - Google Patents

Abstract

The invention provides an implanted peripheral nerve electrical stimulation zinc-oxygen battery and implantation equipment thereof, and belongs to the technical field of medical appliances. The device comprises a mounting base, wherein grooves are formed in the edges of two sides of the mounting base, a rotating handle is nested and rotated at the edge of the outer surface of one side of each groove, and one end of each rotating handle is rotatably connected with a first bevel gear; the device comprises an adjusting component which is arranged on the inner wall of the slot in a sliding way and is used for adjusting the implantation catheter before the device starts to be implanted; the driving component is arranged on one side of the adjusting component and is used for driving the cleaning component and the spraying component; the cleaning assembly is arranged on one side of the driving assembly, and the cleaning assembly is matched with the cleaning assembly and the spraying assembly at the same time, so that function distinction is realized according to different conditions of wounds before and after implantation, one machine of the equipment is multifunctional, and the operation efficiency of the equipment during implantation is improved.

Description

An implantable peripheral nerve electrical stimulation zinc oxygen battery and its implantation device

Technical Field

The present invention relates to the technical field of medical devices, and in particular to an implantable peripheral nerve electrical stimulation zinc-oxygen battery and an implantation device thereof.

Background technique

Peripheral nerve injury is a common consequence of limb trauma or chronic compression. Many studies have found that the application of electrical stimulation can accelerate peripheral nerve regeneration, thereby shortening the growth time of peripheral nerves and reducing care costs. Electrical nerve stimulation can be used to treat one or more diseases, such as chronic or acute pain, epilepsy, depression, bladder diseases or inflammatory diseases. In actual use, minimally invasive surgery is often used to implant a peripheral nerve electrical stimulation zinc oxygen battery into the peripheral nerve through a catheter. The zinc oxygen battery wraps the peripheral nerve to discharge, thereby stimulating the peripheral nerve.

In actual use, before the implant device enters the human body, the wound of the user needs to be disinfected. After the implantation is completed, the wound of the user needs to be treated to avoid the wound from worsening. Existing implant devices mostly use manual disinfection before implantation, and also use manual smearing after the implantation. The manual smearing efficiency is low, and there is uneven smearing resulting in incomplete disinfection, which leads to secondary infection of the wound. Therefore, the present application provides an implantable peripheral nerve electrical stimulation zinc oxygen battery and its implantation device to meet the needs.

Summary of the invention

The technical problem to be solved by the present invention is to provide an implantable peripheral nerve electrical stimulation zinc oxygen battery and its implantation device, so as to solve the problem that the existing implantation device needs to process the wound and apply the medicine manually during implantation, which is inefficient and there is a problem of secondary infection of the wound due to incomplete disinfection.

In order to solve the above technical problems, the present invention provides the following technical solutions:

An implantation device for an implantable zinc-oxygen battery for peripheral nerve electrical stimulation, comprising a mounting base, grooves being arranged at the edges of both sides of the mounting base, a handle being nested and rotatably arranged at the edge of the outer surface of one side of the groove, one end of the handle being rotatably connected to a bevel gear, an implantation catheter being arranged at the top of the adjustment component, and also comprising an adjustment component, the adjustment component being slidably arranged on the inner wall of the groove, the adjustment component being used to adjust the implantation catheter before the device begins to be implanted; a driving component, the driving component being arranged at one side of the adjustment component, the driving component being used to drive a cleaning component and a spraying component; a cleaning component, the cleaning component being arranged at one side of the driving component, the cleaning component being used to clean the skin of a user when the device is implanted; and a spraying component, the spraying component being arranged at one side of the bottom end of the cleaning component, the spraying component being used to spray a wound repair gel on the implantation wound after the implantation is completed.

Optionally, the adjustment component includes a bevel gear 2, which is rotatably arranged on one side of the inner wall of the slot, and is meshed with the bevel gear 1. A screw 1 is rotatably installed on one end of the bevel gear 2, and a bracket is threadedly sleeved on the outer surface of the screw 1, and the outer surface of the bottom end of the bracket slides in contact with the inner wall of the slot.

Optionally, the driving assembly includes a flat gear one, which is rotatably arranged at the bottom end of the internal cavity of the bracket, a rack is meshedly arranged on one side of the flat gear one, and the rack is arranged at the top end of the slotted side, a helical gear three is rotatably arranged on the top end of the flat gear one, a helical gear group is meshed and rotatably arranged on one side of the top end of the helical gear three, a one-way gear is rotatably sleeved on the outer surface of the middle part of the helical gear group, and the helical gear group is rotatably installed on the top end of the bracket.

Optionally, the bottom of the helical gear set is meshed and rotated with teeth, the bottom of the teeth is rotatably provided with a rotating ring, the rotating ring is nested and rotatably provided at the center of the top end of the bracket, and a gear ring is sleeved on the upper edge of the outer surface of the rotating ring.

Optionally, one side of the one-way gear is meshed and rotated with a flat gear 2, the flat gear 2 is rotatably installed at an edge of one side of the top end of the bracket, and one end of the flat gear 2 is rotatably provided with a bevel gear 4.

Optionally, the cleaning component includes a liquid storage barrel, which is arranged at the center edge of the top end of the bracket, and a screw rod 2 is rotatably arranged in the internal cavity of the liquid storage barrel. A piston plate is threadedly sleeved on the outer surface of the screw rod 2, and the piston plate slides and fits in the internal cavity of the liquid storage barrel. A flat gear 3 is rotatably arranged at one end of the screw rod 2, and the flat gear 3 is rotatably arranged at the bottom edge of the bracket, and the flat gear 3 is meshed with the gear ring.

Optionally, a nozzle is provided through one side of the outer surface of the liquid storage barrel, the liquid storage barrels are arranged in a circular array at the bottom end of the bracket, the angle between the liquid storage barrels is set to 120 degrees, and an infusion hose is connected through the outer surfaces of the liquid storage barrels.

Optionally, a collar is provided on one side of the nozzle, a guide groove is provided at the top edge of the collar, the top of the guide groove is connected to the bottom end of the rotating ring, and a sponge sheet is provided through the bottom end of the collar.

Optionally, the spray assembly includes a spray head, which is arranged at the bottom edge of the bracket, one end of the spray head is connected with an infusion catheter, one end of the infusion catheter is connected with a liquid storage box, the liquid storage box is arranged at the edge of one side of the bracket, a screw three is rotatably arranged in the internal cavity of the liquid storage box, one end of the screw three is provided with a bevel gear five, the bevel gear five is meshed with the bevel gear four, a piston disk is threadedly sleeved on the outer surface of the screw three, and the piston disk slides and squeezes in the internal cavity of the liquid storage box.

Optionally, the peripheral nerve electrical stimulation zinc oxygen battery includes an inner core PLGA, one end of the inner core PLGA is set to Aligned PLGA, one end of the inner core PLGA is set to Random PLGA, a zinc anode is sleeved on the outer surface of one end of the inner core PLGA, and a CNT/PT pole is sleeved on the outer surface of one end of the inner core PLGA.

Compared with the prior art, the present invention has at least the following beneficial effects:

In the above scheme, by setting up an adjustment component, in actual use, the bracket can be driven to change its position in real time by turning the handle. When the implant device is implanted, it can be adjusted in real time in actual use according to the different implantation positions of the users, so that the device as a whole has a certain adaptability. At the same time, the linkage between the adjustment component and the drive component is utilized. When the adjustment component makes real-time adjustments to the implanted catheter, the force of the adjustment component is converted into a power source for the drive component, and the structure is simple.

By setting up a driving component and cooperating with a cleaning component and a spraying component, the functions of cleaning and restoring the implant wound can be differentiated. When the adjusting component drives the implant catheter to adjust, the cleaning component is driven by the linkage driving component to disinfect and clean the wound skin and the implant catheter. At the same time, after the implantation is completed, the spraying component is driven in the reverse direction to spray the wound with wound repair gel, so as to achieve functional differentiation according to the different conditions of the wound before and after the implantation, realize multi-functionality of the equipment, and improve the operation efficiency of the equipment during implantation.

By setting up a three-meshing linkage of a toothed ring and a flat gear, the force applied when the handle is turned is used to trigger the cleaning component to spray alcohol on the skin at the wound and the implanted catheter for cleaning and disinfection. At the same time, with the diversion effect of the diversion groove, a part of the sprayed alcohol is directed to the sponge sheet, so that the implanted catheter can be disinfected and cleaned while the skin at the wound of the user is cleaned at the same time. The rotation effect of the rotating ring can further improve the cleaning and disinfection efficiency of the cleaning component.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated herein and constitute a part of the specification, illustrate embodiments of the present disclosure and, together with the description, further serve to explain the principles of the present disclosure and to enable those skilled in the relevant art to make and use the present disclosure.

FIG1 is a schematic diagram of the three-dimensional structure of an implantable peripheral nerve electrical stimulation zinc-oxygen battery and its implantation device;

Fig. 2 is a schematic diagram of the structure of the adjustment component;

Figure 3 is a schematic diagram of the drive assembly structure;

FIG4 is a schematic diagram of the cleaning component structure;

FIG5 is a schematic diagram of the cleaning assembly structure from a bottom view;

FIG6 is a schematic diagram of the cross-sectional structure of a spray assembly;

FIG7 is a schematic diagram of the linkage structure of the driving assembly, the cleaning assembly and the spraying assembly;

FIG8 is a schematic diagram of the structure of a zinc-oxygen battery for peripheral nerve electrical stimulation.

[reference numerals]

1. Mounting base; 2. Slotting; 3. Turning handle; 4. Bevel gear 1; 5. Adjustment assembly; 51. Bevel gear 2; 52. Screw rod 1; 53. Bracket; 6. Driving assembly; 61. Flat gear 1; 610. Rack; 62. Bevel gear 3; 63. Bevel gear set; 630. One-way gear; 64. Gear; 65. Rotating ring; 66. Gear ring; 67. Flat gear 2; 68. Bevel gear 4; 7. Cleaning assembly; 71. Liquid storage barrel; 72. Screw rod two; 73. Piston plate; 74. Flat gear three; 75. Spray head; 76. Infusion hose; 77. Ring; 78. Guide groove; 79. Sponge sheet; 8. Spray assembly; 81. Spray head; 82. Infusion catheter; 83. Liquid storage box; 84. Screw rod three; 85. Bevel gear five; 86. Piston disk; 9. Implant catheter; 10. Inner core PLGA; 101. Aligned PLGA; 102. Random PLGA; 103. Zinc anode; 104. CNT/PT pole.

As shown in the figure, in order to clearly implement the structure of the embodiment of the present invention, specific structures and devices are marked in the figure, but this is only for illustrative purposes and is not intended to limit the present invention to the specific structure, device and environment. According to specific needs, ordinary technicians in this field can adjust or modify these devices and environments, and the adjustments or modifications made are still included in the scope of the attached claims.

Detailed ways

The following is a detailed description of an implantable peripheral nerve electrical stimulation zinc oxygen battery and its implantation device provided by the present invention in conjunction with the accompanying drawings and specific embodiments. At the same time, it is explained here that in order to make the embodiments more detailed, the following embodiments are the best and preferred embodiments, and those skilled in the art may also adopt other alternative methods to implement some known technologies; and the accompanying drawings are only for a more specific description of the embodiments, and are not intended to specifically limit the present invention.

It should be noted that the references to "one embodiment", "an embodiment", "an exemplary embodiment", "some embodiments" and the like in the specification indicate that the embodiments described may include specific features, structures or characteristics, but not every embodiment may include the specific features, structures or characteristics. In addition, when a specific feature, structure or characteristic is described in conjunction with an embodiment, it should be within the knowledge of a person skilled in the art to implement such feature, structure or characteristic in conjunction with other embodiments (whether or not explicitly described).

In general, a term can be understood, at least in part, from its use in context. For example, depending, at least in part, on the context, the term "one or more" as used herein can be used to describe any feature, structure, or characteristic in the singular sense, or can be used to describe a combination of features, structures, or characteristics in the plural sense. Additionally, the term "based on" can be understood as not necessarily intended to convey an exclusive set of factors, but can instead, depending, at least in part, on the context, allow for the presence of other factors that are not necessarily explicitly described.

It will be understood that the meaning of “on,” “over,” and “above” in this disclosure should be interpreted in the broadest manner, so that “on” means not only “directly on” something, but also includes the meaning of being “on” something with intervening features or layers therebetween, and “on” or “over” means not only “on” or “above” something, but also includes the meaning of being “on” or “above” something with no intervening features or layers therebetween.

Additionally, spatially relative terms such as "under," "beneath," "lower," "above," "upper," and the like may be used herein for descriptive convenience to describe the relationship of one element or feature to another element or features, as shown in the accompanying drawings. Spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the accompanying drawings. The device may be oriented in other ways, and the spatially relative descriptors used herein may be similarly interpreted accordingly.

As shown in FIG1 , an embodiment of the present invention provides an implantable peripheral nerve electrical stimulation zinc oxygen battery implantation device, comprising a mounting base 1: slots 2 are provided at the edges of both sides of the mounting base 1, a handle 3 is nested and rotatably provided at the edge of the outer surface of one side of the slot 2, and one end of the handle 3 is rotatably connected to a bevel gear 4; an adjustment component 5 is also included, the adjustment component 5 is slidably provided on the inner wall of the slot 2, the adjustment component 5 is used to adjust the implantation catheter 9 before the device starts to be implanted, and the implantation catheter 9 is provided at the top of the adjustment component 5; a driving component 6, the driving component 6 is provided on one side of the adjusting component 5, and the driving component 6 is used to drive a cleaning component 7 and a spraying component 8; a cleaning component 7, the cleaning component 7 is provided on one side of the driving component 6, and the cleaning component 7 is used to clean the skin of the user when the device is implanted; a spraying component 8, the spraying component 8 is provided on one side of the bottom end of the cleaning component 7, and the spraying component 8 is used to Afterwards, the wound is sprayed with wound repair gel. By setting the adjustment component 5, in actual use, the operator can drive the adjustment component 5 to operate by the turning handle 3, and drive the implantation catheter 9 to make real-time adjustments before starting the implantation, so that the implantation catheter 9 is aligned with the implantation wound. At the same time, by setting the driving component 6, when the adjustment component 5 is running, the linkage cleaning component 7 disinfects and cleans the implantation catheter 9 and the skin wound of the user, so as to avoid the bacteria from entering the human body through the wound during the implantation, thereby improving the medical safety in the implantation operation. At the same time, after the implantation is completed, when the user turns the turning handle 3 to drive the adjustment component 5 to reset, the wound of the user is sprayed with wound repair gel through the one-way linkage spray component 8 of the driving component 6. After the implant device leaves the human body, the implantation wound is pre-treated during implantation to avoid bacteria from entering and causing wound infection, thereby affecting the wound recovery of the subsequent user.

As shown in FIG. 2 , the adjustment assembly 5 includes a bevel gear 2 51, which is rotatably arranged on one side of the inner wall of the slot 2, and the bevel gear 2 51 meshes with the bevel gear 1 4. A screw 1 52 is rotatably installed at one end of the bevel gear 2 51, and a bracket 53 is threadedly sleeved on the outer surface of the screw 1 52. The outer surface of the bottom end of the bracket 53 slides and fits the inner wall of the slot 2. Before starting the implantation, the operator rotates the handle 3, and the handle 3 drives the bevel gear 1 4 on one side to mesh and rotate, and the bevel gear 1 4 drives the bevel gear 2 51 to mesh and rotate, and the bevel gear 2 51 drives the screw 1 5 at one end. 2 rotates synchronously, and when the screw rod 1 52 rotates, the bracket 53 threadedly sleeved on the outer surface of the screw rod 1 52 slides against the inner wall of the slot 2, and the bracket 53 drives the implantation catheter 9 at the bottom to slide synchronously, so as to achieve real-time adjustment of the implantation position of the implantation catheter 9. By setting the bevel gear 2 51 of the bevel gear 1 4 to mesh, the real-time adjustment of the position of the bracket 53 is achieved by turning the handle 3, so that the implantation catheter 9 set at the top of the bracket 53 can be adjusted in real time in actual use according to the different implantation positions of the users, so that the device as a whole has a certain adaptability.

As shown in Figures 3 and 7, the driving assembly 6 includes a flat gear 1 61, which is rotatably arranged at the bottom end of the internal cavity of the bracket 53, a rack 610 is meshed with one side of the flat gear 61, and the rack 610 is arranged at the top of one side of the slot 2, a bevel gear 3 62 is rotatably arranged at the top of the flat gear 1 61, and a bevel gear set 63 is meshed and rotatably arranged at one side of the top of the bevel gear 3 62, and a one-way gear 630 is rotatably sleeved on the outer surface of the middle part of the bevel gear set 63, the bevel gear set 63 is rotatably installed at the top of the bracket 53, a meshing tooth 64 is meshed and rotatably arranged at the bottom of the bevel gear set 63, and a rotating ring 65 is rotatably arranged at the bottom of the meshing tooth 64, and the rotating ring 65 is nested and rotatably arranged at the center of the top end of the bracket 53, and a gear ring 66 is sleeved on the upper edge of the outer surface of the rotating ring 65, a flat gear 2 67 is meshed and rotatably arranged on one side of the one-way gear 630, the flat gear 2 67 is rotatably installed at the edge of one side of the top end of the bracket 53, and a bevel gear 4 68 is rotatably arranged at one end of the flat gear 2 67.

When the operator turns the handlebar 3 to drive the bracket 53 to slide, the bracket 53 drives the flat gear 1 61 to slide. When the flat gear 1 61 follows the bracket 53, it meshes and rotates with the rack 610 on one side. When the flat gear 1 61 rotates, it drives the bevel gear 3 62 on the top to rotate synchronously. When the bevel gear 3 62 rotates, it drives the bevel gear set 63 on one side of the top to mesh and rotate. When the bevel gear set 63 rotates, it drives the meshing gear 64 to mesh and rotate. The meshing gear 64 drives the rotating ring 65 to rotate in the nested position at the center of the top of the bracket 53. The center of the top of the bracket 53 drives the gear ring 66 to rotate synchronously. Similarly, when the operator turns the handlebar 3 in the opposite direction, the bevel gear set 63 rotates and synchronously drives the one-way gear 630 to rotate. The one-way gear 630 drives the flat gear The second wheel 67 meshes and rotates, and the flat gear 2 67 drives the bevel gear 4 68 to mesh and rotate. By setting the linkage between the flat gear 1 61 and the rack 610, the force generated when the bracket 53 drives the rack 610 to slide is used to drive the flat gear 1 61 to rotate. The mechanism is simple, and the driving function is distinguished by setting the one-way gear 630. When the operator rotates the handle 3 in the positive direction, the driving component 6 drives the cleaning component 7 to spray the implantation wound with alcohol for disinfection. After the implantation is completed, the user rotates the handle 3 in the opposite direction, and the driving component 6 drives the spraying component 8 to spray the wound with wound repair gel, so as to realize functional distinction according to the different conditions of the wound before and after the implantation, realize the multi-function of the equipment, and improve the operation efficiency of the equipment during implantation.

As shown in Figures 4, 5 and 7, the cleaning assembly 7 includes a liquid storage barrel 71, which is arranged at the center edge of the top end of the bracket 53. A screw rod 72 is rotatably arranged in the internal cavity of the liquid storage barrel 71. A piston plate 73 is threadedly sleeved on the outer surface of the screw rod 72. The piston plate 73 slides and fits in the internal cavity of the liquid storage barrel 71. A flat gear 74 is rotatably arranged at one end of the screw rod 72. The flat gear 74 is rotatably arranged at the bottom edge of the bracket 53, and the flat gear 74 meshes with the gear ring 66. The outer surface of the liquid storage barrel 71 is provided with a nozzle 75, and the liquid storage barrels 71 are arranged in a circular array at the bottom of the bracket 53. The angle between the liquid storage barrels 71 is set to 120 degrees. The outer surfaces of the liquid storage barrels 71 are connected with an infusion hose 76. A collar 77 is provided on one side of the nozzle 75. A guide groove 78 is provided at the top edge of the collar 77. The top of the guide groove 78 is connected to the bottom of the rotating ring 65. A sponge sheet 79 is provided at the bottom of the collar 77. When the gear ring 66 rotates, it drives the flat gear The gear 3 74 meshes and rotates, and the flat gear 3 74 drives the screw 2 72 to rotate in the internal cavity of the liquid storage barrel 71. When the screw 2 72 rotates, it drives the piston plate 73 to slide and squeeze on the inner wall of the liquid storage barrel 71, and the alcohol stored in the liquid storage barrel 71 is sprayed out through the nozzle 75 to disinfect the skin at the wound and the implanted catheter 9. At the same time, the rotating ring 65 drives the sleeve ring 77 to rotate synchronously, and the sprayed alcohol is converged to the sponge sheet 79 at the bottom of the sleeve ring 77 through the guide groove 78. Under the rotation of the rotating ring 65, the alcohol on the wound skin is evenly applied, further improving the disinfection effect of the alcohol on the skin near the wound. By setting the gear ring 66 and the flat gear 3 74 meshing and linkage, the cleaning component 7 is triggered to spray alcohol on the skin at the wound and the implanted catheter 9 for cleaning and disinfection by utilizing the force when the handle 3 is rotated. At the same time, with the diversion effect of the guide groove 78, part of the sprayed alcohol is converged to the sponge sheet 79, and then with the rotation effect of the rotating ring 65, the cleaning and disinfection effect of the cleaning component 7 is further improved.

As shown in Figures 6 and 7, the spray assembly 8 includes a spray head 81, which is arranged at the bottom edge of the bracket 53. One end of the spray head 81 is connected with an infusion catheter 82, and one end of the infusion catheter 82 is connected with a liquid storage box 83. The liquid storage box 83 is arranged at the edge of one side of the bracket 53. A screw three 84 is rotatably arranged in the internal cavity of the liquid storage box 83. One end of the screw three 84 is provided with a bevel gear five 85, which is meshed with the bevel gear four 68. A piston disk 86 is threadedly sleeved on the outer surface of the screw three 84, and the piston disk 86 slides and squeezes in the internal cavity of the liquid storage box 83.

In this embodiment, when the user turns the handle 3 in the opposite direction to drive the one-way gear 630 to rotate, the bevel gear four 68 drives the bevel gear five 85 to engage and rotate, and the bevel gear five 85 drives the screw three 84 to rotate in the internal thread of the liquid storage box 83, driving the piston plate 86 to slide and squeeze in the liquid storage box 83, and the wound repair gel stored in the liquid storage box 83 is squeezed into the spray head 81 through the infusion catheter 82 and sprayed out. At this time, because the user turns the handle 3 in the opposite direction to drive the adjustment component 5 to reset, the spray head 81 passes over the wound driven by the adjustment component 5, and the sprayed wound repair gel gradually covers the implanted wound, thereby achieving the protective effect of the device on the wound after the implantation is completed.

As shown in Figure 8, the peripheral nerve electrical stimulation zinc oxygen battery includes an inner core PLGA10, one end of the inner core PLGA10 is set to Aligned PLGA101, one end of the inner core PLGA10 is set to Random PLGA102, a zinc anode 103 is sleeved on the outer surface of one end of the inner core PLGA10, and a CNT/PT pole 104 is sleeved on the outer surface of one end of the inner core PLGA10.

The technical solution provided by the present invention, by setting an adjustment component, in actual use, the bracket can be driven to change its position in real time by turning the handle. When the implant device is implanted, real-time adjustment can be made in actual use according to the different implantation positions of the users, so that the device as a whole has a certain adaptability. At the same time, the linkage between the adjustment component and the drive component is utilized. When the adjustment component makes real-time adjustment to the implant catheter, the force of the adjustment component is converted into a power source of the drive component, and the structure is simple.

By setting up a driving component and cooperating with a cleaning component and a spraying component, the functions of cleaning and restoring the implant wound can be differentiated. When the adjusting component drives the implant catheter to adjust, the cleaning component is driven by the linkage driving component to disinfect and clean the wound skin and the implant catheter. At the same time, after the implantation is completed, the spraying component is driven in the reverse direction to spray the wound with wound repair gel, so as to achieve functional differentiation according to the different conditions of the wound before and after the implantation, realize multi-functionality of the equipment, and improve the operation efficiency of the equipment during implantation.

By setting up a three-meshing linkage of a toothed ring and a flat gear, the force applied when the handle is turned is used to trigger the cleaning component to spray alcohol on the skin at the wound and the implanted catheter for cleaning and disinfection. At the same time, with the diversion effect of the diversion groove, a part of the sprayed alcohol is directed to the sponge sheet, so that the implanted catheter can be disinfected and cleaned while the skin at the wound of the user is cleaned at the same time. The rotation effect of the rotating ring can further improve the cleaning and disinfection efficiency of the cleaning component.

The present invention covers any substitution, modification, equivalent method and scheme made on the essence and scope of the present invention. In order to make the public have a thorough understanding of the present invention, specific details are described in detail in the following preferred embodiments of the present invention, and those skilled in the art can fully understand the present invention without the description of these details. In addition, in order to avoid unnecessary confusion about the essence of the present invention, well-known methods, processes, procedures, components and circuits are not described in detail.

The above is only a preferred embodiment of the present invention. It should be pointed out that for ordinary technicians in this technical field, several improvements and modifications can be made without departing from the principle of the present invention. These improvements and modifications should also be regarded as the scope of protection of the present invention.

Claims (2)

1. An implantable peripheral nerve electrical stimulation zinc oxygen battery implantation device, characterized in that it comprises a mounting base, grooves are arranged at the edges of both sides of the mounting base, a handle is nested and rotatably arranged at the edge of the outer surface of one side of the groove, one end of the handle is rotatably connected to a bevel gear, an implantation catheter is arranged at the top of the adjustment component, and also comprises an adjustment component, the adjustment component is slidably arranged on the inner wall of the groove, and the adjustment component is used to adjust the implantation catheter before the device starts to be implanted; A driving assembly, the driving assembly is arranged on one side of the adjusting assembly, and the driving assembly is used to drive the cleaning assembly and the spraying assembly; A cleaning component, which is arranged on one side of the driving component and is used to clean the skin of a user when the device is implanted; A spraying assembly, which is arranged on one side of the bottom end of the cleaning assembly and is used to spray wound repair gel on the implantation wound after the implantation is completed; The adjustment assembly includes a second bevel gear, which is rotatably arranged on one side of the inner wall of the slot, and is meshed with the first bevel gear. A screw rod is rotatably mounted on one end of the second bevel gear, and a bracket is threadedly sleeved on the outer surface of the screw rod, and the outer surface of the bottom end of the bracket slides in contact with the inner wall of the slot; The driving assembly includes a flat gear 1, which is rotatably arranged at the bottom of the inner cavity of the bracket, a rack is meshed on one side of the flat gear 1, and the rack is arranged on the top of one side of the slot, a helical gear 3 is rotatably arranged on the top of the flat gear 1, a helical gear set is meshed and rotatably arranged on one side of the top of the helical gear 3, a one-way gear is rotatably sleeved on the outer surface of the middle part of the helical gear set, and the helical gear set is rotatably installed on the top of the bracket; The bottom of the helical gear set is meshed and rotated with meshing teeth, the bottom of the meshing teeth is rotatably provided with a rotating ring, the rotating ring is nested and rotatably provided at the center of the top end of the bracket, and a gear ring is sleeved on the upper edge of the outer surface of the rotating ring; One side of the one-way gear is meshed and rotated with a flat gear 2, the flat gear 2 is rotatably mounted on the edge of one side of the top end of the bracket, and one end of the flat gear 2 is rotatably provided with a helical gear 4; The cleaning assembly includes a liquid storage barrel, which is arranged at the center edge of the top end of the bracket, a screw rod 2 is rotatably arranged in the internal cavity of the liquid storage barrel, a piston plate is threadedly sleeved on the outer surface of the screw rod 2, and the piston plate slides and fits in the internal cavity of the liquid storage barrel, a flat gear 3 is rotatably arranged at one end of the screw rod 2, and the flat gear 3 is rotatably arranged at the bottom edge of the bracket, and the flat gear 3 is meshed with a gear ring; A nozzle is provided through one side of the outer surface of the liquid storage barrel, the liquid storage barrels are arranged in a circular array at the bottom end of the bracket, the angle between the liquid storage barrels is set to 120 degrees, and an infusion hose is connected through the outer surfaces of the liquid storage barrels; A collar is provided on one side of the nozzle, a guide groove is provided at the top edge of the collar, the top of the guide groove is connected to the bottom of the rotating ring, and a sponge sheet is provided through the bottom of the collar; The spray assembly includes a spray head, which is arranged at the bottom edge of the bracket, one end of the spray head is connected with an infusion catheter, one end of the infusion catheter is connected with a liquid storage box, the liquid storage box is arranged at the edge of one side of the bracket, a screw rod three is rotatably arranged in the internal cavity of the liquid storage box, one end of the screw rod three is provided with a bevel gear five, the bevel gear five is meshed with the bevel gear four, a piston disk is threadedly sleeved on the outer surface of the screw rod three, and the piston disk slides and squeezes in the internal cavity of the liquid storage box. 2. An implantable peripheral nerve electrical stimulation zinc oxygen battery, which is implanted using the implantable peripheral nerve electrical stimulation zinc oxygen battery implantation device described in claim 1, characterized in that the peripheral nerve electrical stimulation zinc oxygen battery includes an inner core PLGA, one end of the inner core PLGA is set as Aligned PLGA, one end of the inner core PLGA is set as Random PLGA, a zinc anode is sleeved on the outer surface of one end of the inner core PLGA, and a CNT/PT pole is sleeved on the outer surface of one end of the inner core PLGA.