A human brain photostimulation device and system

By using the delivery and implantation mechanism of the human brain light stimulation device, near-infrared light sources are used to stimulate the deep brain, solving the problems of cumbersome and costly craniotomy in the treatment of degenerative diseases of the central nervous system, and achieving a simple treatment effect.

CN115245629BActive Publication Date: 2025-10-31WUHAN YIRUIDE MEDICAL EQUIP
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Patent Information

Application Number
CN202210643624.X
Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2022-06-08
Publication Date
2025-10-31
Estimated Expiration
2042-06-08

AI Technical Summary

Technical Problem

Current treatments for degenerative diseases of the central nervous system require craniotomy, which is a complicated and expensive procedure.

Method used

The device employs a human brain light stimulation device, which is delivered into the sphenoid sinus via a delivery mechanism. It uses a near-infrared light source to stimulate the deep brain, avoiding craniotomy. The device consists of a delivery mechanism, an implant, a camera, a communication module, and a host computer.

Benefits of technology

It achieves a simple operation without craniotomy, reduces treatment costs, and provides rapid and stable treatment results through effective stimulation of the central nervous system by near-infrared light.

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Abstract

This application provides a human brain photostimulation device, comprising: a delivery mechanism including a piston rod, a push rod, and a guide; the output end of the piston rod is connected to the input end of the push rod, and the guide has a through hole in the middle, through which the output end of the push rod passes; and an implantation mechanism including a housing, a light source, a power supply, and a control module; the input end of the light source is connected to the output end of the control module, and the output end of the power supply is connected to the input end of the control module. The human brain photostimulation device provided by this application delivers the light source system in the implantation mechanism into the patient's sphenoid sinus cavity via the delivery mechanism. Then, the push rod in the delivery mechanism is removed from the implantation mechanism, causing the implantation mechanism to abut against the sphenoid sinus cavity. Subsequently, near-infrared light is continuously emitted deep into the brain, thereby stimulating and treating the brain. The entire process does not require craniotomy. This device is easy to operate and can reduce treatment costs for patients.
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Description

Technical Field

[0001] This application belongs to the field of medical device technology, and in particular relates to a human brain photostimulation device and system. Background Technology

[0002] With the rapid development of semiconductor technology, the application of light sources of various wavelengths in medical devices is expanding. Currently, my country's aging population is becoming increasingly serious, and the incidence of central nervous system degenerative diseases is high among the elderly. The number of patients is expected to continue to grow in the foreseeable future, remaining at a high level for a long time, placing a heavy burden on families and society. Treatment for central nervous system degenerative diseases typically involves medication, but long-term use of drugs can lead to reduced efficacy and side effects, and may even worsen disease symptoms.

[0003] In recent years, non-drug treatments have been attempted in clinical practice to improve disease symptoms, such as deep brain stimulation surgery, exercise therapy, and gene-targeted therapy for central nervous system diseases. However, these methods require craniotomy to implant the treatment device in the brain, which is complicated and expensive. Summary of the Invention

[0004] This application provides a human brain photostimulation device and system to solve the problem that existing treatments for degenerative diseases of the central nervous system require craniotomy, which is cumbersome and expensive.

[0005] This application provides a human brain optical stimulation device, comprising:

[0006] A conveying mechanism, comprising a piston rod, a push rod, and a guide member, wherein the output end of the piston rod is connected to the input end of the push rod, and the guide member has a through hole in the middle, through which the output end of the push rod passes.

[0007] An implantation mechanism includes a housing, a light source, a power supply, and a control module. The housing has an internal cavity. The control module and the power supply are both connected to the inner wall of the cavity. The input terminal of the light source is electrically connected to the output terminal of the control module. The output terminal of the power supply is electrically connected to both the input terminal of the light source and the input terminal of the control module.

[0008] One end of the outer shell is detachably connected to the output end of the push rod, and the other end of the outer shell is used to connect to the inner wall of the sphenoid sinus; the maximum cross-sectional dimension of the implantation mechanism is larger than the cross-sectional dimension of the through hole at the output end of the push rod; the light source is used to emit near-infrared light into the depths of the brain.

[0009] Optionally, the housing includes a light-transmitting shell, a gripper, and a spring plate. The cavity is located inside the light-transmitting shell. The gripper is connected to the outer wall of the light-transmitting shell through the spring plate. The bottom end of the gripper is inserted into the output end of the push rod. The gripper portion passes through the through hole of the guide member.

[0010] Optionally, a light source cover is connected to the outer wall of the light source, and the light source cover is used to converge or diverge light.

[0011] Optionally, the guide includes an empty cylinder and a flexible hose. The output end of the empty cylinder is connected to the input end of the flexible hose. Both the empty cylinder and the flexible hose have a through hole in the middle. The output end of the push rod enters from the input end of the empty cylinder and exits sequentially from the through hole of the empty cylinder and the through hole of the flexible hose.

[0012] Optionally, the output end of the flexible hose is provided with an opening, and the gripper portion extends into the opening.

[0013] Optionally, the outer wall of the gripper is provided with a protrusion, which abuts against the inner wall of the opening.

[0014] Optionally, the piston rod has a groove on the outer wall of its output end and a block on the outer wall of its input end, the block being engaged in the groove.

[0015] Optionally, the housing includes a light-transmitting shell, grippers, and a telescopic rod. The cavity is located inside the light-transmitting shell. The inner wall of the grippers is connected to the outer wall of the light-transmitting shell via the telescopic rod. The bottom end of the grippers is inserted into the output end of the push rod. The telescopic rod is electrically connected to the control module. The grippers are partially inserted into the through hole of the guide.

[0016] This application also provides a human brain optical stimulation system, including:

[0017] The human brain optical stimulation device as described in any of the above;

[0018] A camera, which is connected to the bottom outer wall of the housing, is used to acquire image information of the sphenoid sinus cavity;

[0019] A communication module is connected to the inner wall of the outer shell. The communication module is electrically connected to the control module and the camera, and is used to transmit image information of the sphenoid sinus cavity to the outside.

[0020] The host computer is located outside the human brain and is wirelessly connected to the communication module. It is used to receive image information from the sphenoid sinus cavity and to provide feedback control commands based on the image information from the sphenoid sinus cavity.

[0021] Optionally, the host computer includes a processing module and a display module, the processing module being wirelessly connected to the communication module, and the communication module being electrically connected to the display module.

[0022] The human brain photostimulation device provided in this application delivers a light source from the implantation mechanism into the patient's sphenoid sinus cavity via a piston rod, guide, and push rod in the delivery mechanism. Then, the push rod is disassembled from the implantation mechanism, so that the outer shell of the implantation mechanism abuts against the sphenoid sinus cavity. Subsequently, the control module controls the light source to continuously emit near-infrared light deep into the brain, so that the near-infrared light stimulates and treats the central nervous system of the brain. The entire process does not require craniotomy; the implantation mechanism only needs to be inserted from the nose into the sphenoid sinus cavity. This device is easy to operate and can reduce the treatment cost for patients. Attached Figure Description

[0023] To more clearly illustrate the technical solutions in the embodiments of this application, the accompanying drawings used in the description of the embodiments will be briefly introduced below. Obviously, the drawings described below are only some embodiments of this application, and those skilled in the art can obtain other drawings based on these drawings without creative effort.

[0024] To gain a more complete understanding of this application and its beneficial effects, the following description will be provided in conjunction with the accompanying drawings. In the following description, the same reference numerals denote the same parts.

[0025] Figure 1 This is a schematic diagram of the structure of the human brain photostimulation device provided in the embodiments of this application;

[0026] Figure 2 An exploded view of the human brain photostimulation device provided in the embodiments of this application;

[0027] Figure 3 This is a schematic diagram of the implantation mechanism in the human brain photostimulation device provided in the embodiments of this application;

[0028] Figure 4 A schematic diagram of a first structure of the implantation mechanism in the human brain photostimulation device provided in this application embodiment;

[0029] Figure 5 This is a schematic diagram of a second structure of the implantation mechanism in the human brain photostimulation device provided in the embodiments of this application;

[0030] Figure 6 This is a schematic diagram of a third structure of the implantation mechanism in the human brain photostimulation device provided in the embodiments of this application.

[0031] Figure 7 This is a structural block diagram of the signal transmission of components in the human brain photostimulation system provided in the embodiments of this application;

[0032] In the diagram: 1. Conveying mechanism; 11. Piston rod; 111. Slot; 12. Push rod; 121. Block; 13. Guide component; 131. Empty cylinder; 132. Flexible tube; 2. Implantation mechanism; 21. Outer shell; 211. Cavity; 212. Light-transmitting shell; 213. Gripper; 214. Spring; 22. Light source; 221. Light source cover; 23. Power supply; 24. Control module; 3. Camera; 4. Communication module; 5. Host computer; 51. Processing module; 52. Display module. Detailed Implementation

[0033] The technical solutions of the embodiments of this application will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only a part of the embodiments of this application, and not all of them. All other embodiments obtained by those skilled in the art based on the embodiments of this application without creative effort are within the scope of protection of this application.

[0034] This application provides a human brain photostimulation device and system to address the problem that existing treatments for degenerative diseases of the central nervous system require craniotomy, which is cumbersome and expensive. The following description, in conjunction with the accompanying drawings, will illustrate this.

[0035] like Figure 1 As shown, this application provides a human brain photostimulation device. Figure 1 This is a schematic diagram of a human brain photostimulation device. This device can be applied to various degenerative diseases of the central nervous system. Taking Parkinson's disease patients as an example, this device emits near-infrared light deep into the patient's brain. Near-infrared light is an electromagnetic wave between visible and mid-infrared light. For example, near-infrared light with a wavelength of 670nm can activate photoreceptors such as cytochrome C oxidase, thereby regulating human metabolism. Therefore, near-infrared light can penetrate between various tissues in the body, passing through intracranial tissues and reaching deep into the brain. Near-infrared light reaching deep into the brain can stimulate the central nervous system, regulate the patient's metabolism, protect the central nervous system, and thus prevent the onset of Parkinson's symptoms, exhibiting a rapid and stable therapeutic effect.

[0036] like Figure 1-3 As shown, in some implementations, Figure 2 An explosion view of a human brain light stimulation device. Figure 3This is a schematic diagram of the implantation mechanism 2 in a human brain optical stimulation device. The human brain optical stimulation device includes a delivery mechanism 1 and an implantation mechanism 2. The delivery mechanism 1 includes a piston rod 11, a push rod 12, and a guide 13. The output end of the piston rod 11 is connected to the input end of the push rod 12. The guide 13 has a through hole in the middle, through which the output end of the push rod 12 passes. The implantation mechanism 2 includes a housing 21, a light source 22, a power supply 23, and a control module 24. The housing 21 has a cavity 211 inside. The control module 24... Both the light source 22 and the power supply 23 are connected to the inner wall of the cavity 211. The light source 22 is electrically connected to the control module 24. The output end of the power supply 23 is electrically connected to the light source 22 and the control module 24 respectively. One end of the outer shell 21 is detachably connected to the output end of the push rod 12, and the other end of the outer shell 21 is used to connect to the inner wall of the sphenoid sinus cavity. The maximum cross-sectional size of the implantation mechanism 2 is larger than the cross-sectional size of the through hole at the output end of the push rod 12. The light source 22 can emit near-infrared light towards the brain, and the near-infrared light can penetrate the intracranial tissue to reach the depths of the brain.

[0037] During patient treatment, a matching implantation device 2 can be designed based on the patient's symptoms and assembled onto the delivery mechanism 1. The implantation device 2 is then placed inside the patient's nose. Guided by the guide 13, the implantation device 2 is delivered into the patient's sphenoid sinus cavity via the piston rod 11 and push rod 12. Maintaining the position of the guide 13, the piston rod 11 is pulled back, causing the piston rod 11 to move the implantation device 2 outward via the push rod 12. Because the size of the implantation device 2 is larger than the through-hole, the output end of the guide 13 applies a reaction force to the implantation device 2, causing the push rod 12 to separate from the implantation device 2. Finally, the implantation device 2 falls into the patient's sphenoid sinus cavity, and the push rod 12 and guide 13 are removed. During operation, the control module 24 within the implantation device 2 controls the light source 22 to emit near-infrared light. This near-infrared light can penetrate intracranial tissue to reach deep into the brain and stimulate the central nervous system deep within the patient's brain, thereby treating the patient.

[0038] In this embodiment, the cavity 211 is used to house the various components of the device and provides protection for them. The outer shell 21 can be made of non-biodegradable polymers or alloys, such as polyurethane, stainless steel, titanium, etc. The outer shell 21 can also be a one-piece molded structure, with the head of the outer shell 21 designed as a cylinder with a diameter of 3mm, and a cylindrical handle installed at the tail of the outer shell 21. The bottom end of the cylindrical handle has a groove, and the output end of the push rod 12 is inserted into the groove. The power supply 23 uses a micro battery, which powers the control module 24 and the light source 22 through a micro power interface. The light source 22 uses a near-infrared light source with a diameter of 1mm, and the light source 22 can continuously emit near-infrared light in the wavelength range of 650–2500nm deep into the brain.

[0039] like Figure 1-6As shown, based on the above embodiments, this application preferably provides the following embodiments: Figure 4 This is a schematic diagram of the first type of implantable mechanism 2 in a human brain optical stimulation device. Figure 5 This is a schematic diagram of the second structure of the implantable mechanism 2 in the human brain optical stimulation device. Figure 6 This is a schematic diagram of the third structure of implantable mechanism 2 in a human brain photostimulation device.

[0040] In one embodiment, the outer shell 21 includes a light-transmitting shell 212, a gripper 213, and a spring 214. The cavity 211 is located inside the light-transmitting shell 212. The gripper 213 is connected to the outer wall of the light-transmitting shell 212 through the spring 214. The bottom end of the gripper 213 is inserted into the output end of the push rod 12, and part of the gripper 213 passes through the through hole of the guide member 13. A light source cover 221 is connected to the outer wall of the light source 22. The light source cover 221 is used to converge or diverge light. When the delivery mechanism 1 is assembled with the implantation mechanism 2, the gripper 213 is partially placed in the through hole of the guide 13. The gripper 213 will be squeezed by the inner wall of the through hole. At this time, the spring 214 is in a compressed state, and the gripper 213 on the light-transmitting shell 212 is in a contracted state. After the implantation mechanism 2 falls into the sphenoid sinus cavity, the spring 214 recovers its deformation, the gripper 213 is in an unfolded state in the sphenoid sinus cavity and adheres to the inner wall of the sphenoid sinus cavity. The control module 24 controls the light source 22 to emit near-infrared light. The near-infrared light can be transmitted from the light-transmitting shell 212 into the sphenoid sinus cavity and pass through the intracranial tissue to reach the depths of the brain.

[0041] In this embodiment, several grippers 213 can be used, and they are evenly distributed on the bottom sidewall of the light-transmitting housing 212. In specific implementation, the number of grippers 213 can be set to eight, and the eight grippers 213 are evenly installed on the bottom sidewall of the light-transmitting housing 212. The diameter of the patient's sphenoid sinus cavity is about 8 mm, and the diameter of the sphenoid sinus opening is about 5 mm. The cross-sectional size of the through hole at the output end of the push rod 12 can be set to 4.4 mm. When the grippers 213 are compressed, the cross-sectional size of the eight grippers 213 is set to 4.5 mm. When the grippers 213 are naturally unfolded, the cross-sectional size of the outer shell 21 formed by the eight grippers 213 is set to 8.2 mm to 8.4 mm. The light source cover 221 can fix the light source 22 and focus the light emitted by the light source 22 before it is emitted from the light-transmitting housing 212. The light source cover 221 can be made of a reflective metal or alloy, and the light-transmitting surface of the light source cover 221 can be processed into a mirror. Depending on the specific application scenario, the light source cover 221 can focus or disperse near-infrared light, thereby ensuring its transmission effect and performance. The housing 212 can be made of polymethyl methacrylate to ensure the transmission effect of the light source 22.

[0042] A camera and a signal transmitter / receiver can be embedded in the outer wall of the gripper 213. An angle adjuster is installed in the through hole at the output end of the guide 13. The camera is connected to the signal transmitter / receiver, which is connected to the control module 24 and an external terminal. The angle adjuster is connected to the control module. Before the implantation mechanism 2 falls, the angle adjuster can adjust the rotation angle of the implantation mechanism 2 so that the light source 22 is aligned with the depth of the brain. After the implantation mechanism 2 falls, the camera can collect the light information emitted by the light source 22 onto the wall of the sphenoid sinus cavity and transmit the collected light information to the external terminal through the signal transmitter / receiver. The external terminal can analyze the collected light information, determine that the light source 22 is aligned with the depth of the brain, and send a control command to the signal transmitter / receiver. The signal transmitter / receiver transmits the control command to the control module 24. The control module 24 controls the angle adjuster to adjust the contact position of the gripper 213 so that the light source 22 is aligned with the depth of the brain, which can improve the treatment effect. At the same time, the light source cover 221 can further focus the light emitted by the light source 22, so that the light can be more concentrated and penetrate into the depth of the brain, improving the treatment effect for the patient.

[0043] In addition, the clamps 213 can also adopt four C-shaped structures and be evenly surrounded on the bottom side wall of the light-transmitting shell 212. After the implantation mechanism 2 is delivered into the sphenoid sinus cavity, the doctor can push the implantation mechanism 2 out through the piston rod 11, so that each clamp 213 unfolds and abuts against the inner wall of the sphenoid sinus cavity; the outer surface of the clamps 213 can also be sanded to increase the friction between the clamps 213 and the inner wall of the sphenoid sinus cavity, thereby preventing the implantation mechanism 2 from shifting position.

[0044] like Figure 4-6 As shown, in this embodiment, the unfolding direction of the gripper 213 can be towards the light source 22, or towards the push rod 12, or towards other mounting directions. This application does not impose any restrictions on this.

[0045] like Figure 1-3 As shown, in one embodiment, the guide member 13 includes a hollow cylinder 131 and a flexible hose 132. The output end of the hollow cylinder 131 is connected to the input end of the flexible hose 132. Both the hollow cylinder 131 and the flexible hose 132 have through holes in the middle. The output end of the push rod 12 passes through the input end of the hollow cylinder 131 and exits sequentially through the through holes of the hollow cylinder 131 and the flexible hose 132. The output end of the flexible hose 132 has an opening, and a portion of the gripper 213 is placed in the opening. The outer wall of the gripper 213 has a protrusion that abuts against the inner wall of the opening. The outer wall of the output end of the piston rod 11 has a slot 111, and the outer wall of the input end of the push rod 12 has a locking block 121 that engages in the slot 111.

[0046] In use, the locking block 121 at the input end of the push rod 12 is engaged in the locking groove 111 on the outer wall of the output end of the piston rod 11. The output end of the push rod 12 is then passed through the through hole of the empty cylinder 131 and the through hole of the flexible tube 132 in sequence. The implantation mechanism 2 is then inserted into the output end of the push rod 12. The gripper 213 part of the implantation mechanism 2 is placed in the through hole of the flexible tube 132, so that the protrusion on the gripper 213 abuts against the inner wall of the opening. Then, guided by the empty cylinder 131 and the flexible tube 132, the push rod 12 is pushed out through the through hole of the piston rod 11. The output end of rod 12 and the implantation mechanism 2 are inserted into the patient's sphenoid sinus cavity. Then, the piston rod 11 is pulled back. Since the maximum cross-sectional size of the implantation mechanism 2 is smaller than the size of the opening, the implantation mechanism 2 will separate from the push rod 12 at the opening. Finally, the control module 24 controls the light source 22 to emit near-infrared light. The near-infrared light can penetrate the sphenoid sinus cavity wall and intracranial tissue and reach the depths of the brain. The near-infrared light can stimulate the central nervous system deep in the patient's brain, thereby achieving a therapeutic effect on the patient.

[0047] like Figure 1-3 As shown, in one embodiment, the outer shell 21 includes a light-transmitting shell 212, a gripper 213, and a telescopic rod. The cavity 211 is located inside the light-transmitting shell 212. The inner wall of the gripper 213 is connected to the outer wall of the light-transmitting shell 212 via the telescopic rod. The bottom end of the gripper 213 is inserted into the output end of the push rod 12. The telescopic rod is electrically connected to the control module 24. Part of the gripper 213 is inserted into the through hole of the guide member 13.

[0048] In this embodiment, the telescopic rod can be an electrically operated telescopic rod. Before the implantation mechanism 2 falls into the sphenoid sinus cavity, the electrically operated telescopic rod and the gripper 213 are in a retracted state and are installed at the output end of the push rod 12. After the implantation mechanism 2 falls into the sphenoid sinus cavity, the control module 24 controls the extension of the electrically operated telescopic rod according to the size of the patient's sphenoid sinus cavity. The electrically operated telescopic rod can cause the gripper 213 to unfold, so that the gripper 213 abuts against the inner wall of the patient's sphenoid sinus cavity, thereby preventing the implantation mechanism 2 from sliding in the patient's sphenoid sinus cavity.

[0049] like Figure 1 , 2 As shown in 3 and 7, Figure 7This is a structural block diagram of signal transmission of components in a human brain photostimulation system. This application also provides a human brain photostimulation system, including the human brain photostimulation device, camera 3, communication module 4, and host computer 5 as described above. The camera 3 can be connected to the outer wall of the gripper 213, and can acquire image information of the sphenoid sinus cavity. The communication module 4 is connected to the inner wall of the outer shell 21, and is electrically connected to the control module 24 and the camera 3. The communication module 4 can transmit the image information of the sphenoid sinus cavity to the outside. The host computer 5 is located outside the human brain and is wirelessly connected to the communication module 4. The host computer 5 can receive the image information of the sphenoid sinus cavity and provide feedback control commands based on the image information. After receiving the control commands sent by the host computer 5, the communication module 4 can transmit the control commands to the control module 24. The control module 24 can adjust the wavelength of the light source 22 in the human brain photostimulation device according to the commands. Different wavelengths of infrared light can provide appropriate treatment according to the different symptoms of the patient, thereby achieving the best treatment effect. The power supply 23 can provide power to the camera 3 and the communication module 4.

[0050] In this embodiment, the host computer 5 includes a processing module 51 and a display module 52. The processing module 51 is wirelessly connected to the communication module 4, and the communication module 4 is electrically connected to the display module 52.

[0051] In use, the locking block 121 at the input end of the push rod 12 is engaged in the locking groove 111 on the outer wall of the output end of the piston rod 11. The output end of the push rod 12 is then passed through the through hole of the empty cylinder 131 and the through hole of the flexible tube 132 in sequence. The implantation mechanism 2 is then inserted into the output end of the push rod 12. The clamp 213 part of the implantation mechanism 2 is inserted into the through hole of the flexible tube 132, so that the protrusion on the clamp 213 abuts against the inner wall of the opening. Then, guided by the empty cylinder 131 and the flexible tube 132, the output end of the push rod 12 and the implantation mechanism 2 are inserted into the patient's sphenoid sinus cavity. After that, the piston rod 11 is pulled back. Since the maximum cross-sectional size of the implantation mechanism 2 is smaller than the size of the opening, the implantation mechanism 2 will separate from the push rod 12 at the opening. Finally, the control module 24 controls the light source 22 to emit near-infrared light. The near-infrared light can penetrate the intracranial tissue to reach the depths of the brain and stimulate the central nervous system deep in the patient's brain, thereby treating the patient. During operation, camera 3 can acquire real-time image information of the patient's sphenoid sinus cavity. This image information can be transmitted to an external host computer 5 via communication module 4. The processing module 51 in the host computer 5 can analyze the received image information. After analysis, the processing module 51 can wirelessly transmit control commands to the communication module 4 in the implantation device 2. The communication module 4 transmits the control commands to the control module 24, which adjusts the human brain light stimulation device appropriately, thereby improving the patient's treatment effect. At the same time, the image information acquired by camera 3 can also be wirelessly transmitted to the display module 52 in the host computer 5 via communication module 4, thus facilitating the doctor's diagnosis.

[0052] In the above embodiments, the descriptions of each embodiment have different focuses. For parts not described in detail in a certain embodiment, please refer to the relevant descriptions in other embodiments.

[0053] In the description of this application, the terms "first" and "second" are used for descriptive purposes only and should not be construed as indicating or implying relative importance or implicitly specifying the number of technical features indicated. Thus, features defined with "first" and "second" may explicitly or implicitly include one or more features.

[0054] The above provides a detailed description of the human brain photostimulation device provided in the embodiments of this application. Specific examples have been used to illustrate the principles and implementation methods of this application. The description of the above embodiments is only for the purpose of helping to understand the method and core ideas of this application. At the same time, for those skilled in the art, there will be changes in the specific implementation methods and application scope based on the ideas of this application. Therefore, the content of this specification should not be construed as a limitation of this application.

Claims

1. A human brain photostimulation device, characterized in that, include: The conveying mechanism (1) includes a piston rod (11), a push rod (12) and a guide (13). The output end of the piston rod (11) is connected to the input end of the push rod (12). The guide (13) has a through hole in the middle. The output end of the push rod (12) passes through the through hole of the guide (13). The guide (13) includes a hollow cylinder (131) and a flexible hose (132). An implantation mechanism (2) is provided, comprising a housing (21), a light source (22), a power supply (23), and a control module (24). The housing (21) has an internal cavity (211), a gripper (213), and a telescopic rod. The control module (24) and the power supply (23) are both connected to the inner wall of the cavity (211). The input end of the light source (22) is electrically connected to the output end of the control module (24), and the output end of the power supply (23) is electrically connected to the input end of the light source (22) and the input end of the control module (24). One end of the outer shell (21) is detachably connected to the output end of the push rod (12), and the other end of the outer shell (21) is used to connect to the inner wall of the sphenoid sinus; the maximum cross-sectional dimension of the implantation mechanism (2) is larger than the cross-sectional dimension of the through hole at the output end of the push rod (12); the light source (22) is used to emit near-infrared light into the depths of the brain; The flexible tube (132) has an opening at its output end, and the clamp (213) is partially inserted into the opening. The outer wall of the clamp (213) has a protrusion that abuts against the inner wall of the opening. In use, the implantation mechanism is inserted from the nose into the patient's sphenoid sinus cavity, so that the output end of the push rod (12) is inserted into the patient's sphenoid sinus cavity. Then, the piston rod (11) is pulled back, and the implantation mechanism will separate from the opening and the output end of the push rod and fall into the sphenoid sinus cavity. The telescopic rod is connected to the control module (24). When the implantation mechanism (2) falls, the control module (24) controls the telescopic rod to extend, causing the clamp (213) to unfold and abut against the inner wall of the patient's sphenoid sinus cavity, thereby preventing the implantation mechanism from sliding in the patient's sphenoid sinus cavity.

2. The human brain photostimulation device according to claim 1, characterized in that, A light source cover (221) is connected to the outer wall of the light source (22), and the light source cover (221) is used to converge or disperse light.

3. The human brain photostimulation device according to claim 1, characterized in that, The piston rod (11) has a slot (111) on the outer wall of the output end, and the push rod (12) has a block (121) on the outer wall of the input end, and the block (121) is engaged in the slot (111).

4. The human brain photostimulation device according to claim 1, characterized in that, The outer shell (21) also includes a light-transmitting shell (212), the cavity (211) is located inside the light-transmitting shell (212), the inner wall of the gripper (213) is connected to the outer wall of the light-transmitting shell (212) through the telescopic rod, the bottom end of the gripper (213) is inserted into the output end of the push rod (12), the telescopic rod is electrically connected to the control module (24), and part of the gripper (213) is inserted into the through hole of the guide (13).

5. A human brain photostimulation system, characterized in that, include: The human brain photostimulation device as described in any one of claims 1-4; Camera (3), which is connected to the bottom outer wall of the outer shell (21), is used to collect image information of the sphenoid sinus cavity; The communication module (4) is connected to the inner wall of the outer shell (21). The communication module (4) is electrically connected to the control module (24) and the camera (3) and is used to transmit image information of the sphenoid sinus cavity to the outside. The host computer (5) is located outside the human brain. The host computer (5) is wirelessly connected to the communication module (4) to receive image information of the sphenoid sinus cavity and to feed back control commands based on the image information of the sphenoid sinus cavity. The power supply (23) is also electrically connected to the camera (3) and the communication module (4).

6. The human brain photostimulation system according to claim 5, characterized in that, The host computer (5) includes a processing module (51) and a display module (52). The processing module (51) is wirelessly connected to the communication module (4), and the communication module (4) is electrically connected to the display module (52).

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