An ultrasonic atomization nanometer lauric acid photodynamic rhinitis therapeutic instrument

Abstract

The application provides a kind of ultrasonic atomization nanometer lauric acid photodynamic rhinitis therapeutic instrument based on fog, effectively increase the absorption efficiency of drug, including protective shell, the lower side of the rear end of the protective shell is fixedly installed with connecting plate, the left and right sides of the upper end of the connecting plate are respectively fixedly connected with mounting base, the middle part of each mounting base is respectively fixedly installed with thermostat tube, the upper end of each mounting base is respectively detachably installed with and sleeved on the medicament cylinder on thermostat tube, the inside of each mounting base is respectively fixedly installed with ultrasonic atomizer located at the lower end of thermostat tube, the inside of each thermostat tube is respectively rotatably installed with horizontal adjusting rod, the upper end of each horizontal adjusting rod is respectively rotatably installed with pitch adjusting rod, the application is novel in structure, ingenious in design, easy to operate, effectively achieves the purpose of individualization, accuracy treatment for different patients' rhinitis, shortens the treatment cycle.

Description

Technical Field

[0001] This invention relates to the field of rhinitis treatment equipment technology, and in particular to a rhinitis treatment device based on ultrasonic atomization nano-lauric acid photodynamic therapy. Background Technology

[0002] Photodynamic therapy (PDT) is a medical technique that treats various diseases and conditions by combining a specific light source and a photosensitizer, utilizing light irradiation at specific frequencies and intensities. The working principle of PDT is as follows: first, a photosensitizer is injected or applied topically to the patient, and then the patient is irradiated with a light source of a specific wavelength, such as a laser or LED light. The photosensitizer is activated under the irradiation of this specific wavelength of light, producing a series of chemical reactions that achieve a therapeutic effect. The specific mechanism of PDT mainly includes two aspects: the activation of the photosensitizer and the generation of photochemical reactions. A photosensitizer is a special molecule that can absorb light of a specific wavelength and transform it into an active substance. When light irradiates the photosensitizer, it undergoes a photochemical reaction, producing a series of biological effects. These biological effects can destroy abnormal cells, inhibit inflammatory responses, and promote tissue repair, among others.

[0003] Traditional nasal treatment devices may have the following drawbacks:

[0004] 1. Poor deep treatment capability: Traditional rhinitis devices can usually only treat the surface of the nasal cavity and cannot reach the depths of the nasal cavity and sinuses. The nasal cavity and sinuses are the main sites of rhinitis. If only the surface of the nasal cavity can be treated and the inflammation cannot be penetrated to the depths of the inflammation, the root cause of rhinitis cannot be completely eliminated.

[0005] 2. Relatively slow treatment effect: Traditional nasal devices may require long-term use to achieve satisfactory treatment results, and the drug adhesion is weak and the drug is not long-lasting.

[0006] 3. Weak local stimulation: Traditional rhinitis device treatments mainly use local heat, cold and hot therapy or saline washing, which result in relatively weak local stimulation.

[0007] Chinese Patent No. 202111151363 discloses an ultrasonic electronic rhinitis treatment device that uses far-infrared atomized coconut meat essential oil. The device includes a nasal plug and a nasal wing portion. The nasal plug includes an insertion post placed inside the nostril, containing coconut meat powder, with a far-infrared generating tube inside the coconut meat powder. The nasal wing portion contains an ultrasonic generator and fits snugly against the outer side of the nasal wing. This invention utilizes far-infrared light to atomize the oils and acidic substances in the coconut meat powder, allowing them to be inhaled into the nasal cavity and sinuses with the aid of pulsed ultrasound. The combination of pulsed ultrasound and far-infrared light accelerates tissue recovery and enhances the therapeutic effect, making it suitable for treating chronic rhinitis, acute rhinitis, sinusitis, nasal polyps, etc.

[0008] Regarding the relevant technology patent, the inventor believes that: the device uses far-infrared technology to stimulate the oils and acidic substances in coconut meat powder to treat the internal tissues of the patient's nasal cavity and sinuses. However, the content of substances that can treat rhinitis in coconut meat powder is low, so it cannot effectively achieve the purpose of targeted treatment. Furthermore, the absorption effect in the nasal cavity is poor, resulting in low treatment efficiency. In addition, when the ultrasound is applied to the nasal cavity, the ultrasound waves generated will be severely attenuated when propagating in the air, resulting in only average effects.

[0009] Therefore, the present invention provides a photodynamic rhinitis treatment device based on ultrasonic atomization nano-lauric acid to solve the above problems. Summary of the Invention

[0010] In view of the above situation and to overcome the defects of the prior art, the present invention provides a rhinitis treatment device based on ultrasonic atomization nano-lauric acid photodynamic therapy. The present invention has a novel structure, ingenious design, and simple and convenient operation. It effectively increases the absorption efficiency of drugs, achieves the goal of personalized and accurate treatment of rhinitis in different patients, and shortens the treatment cycle.

[0011] To achieve the above objectives, the present invention provides the following technical solution:

[0012] A photodynamic rhinitis treatment device based on ultrasonic atomization nano-lauric acid includes a protective shell. A connecting plate is fixedly installed on the lower rear side of the protective shell. Mounting bases are fixedly connected to the left and right sides of the upper part of the connecting plate. A constant temperature tube is fixedly installed in the middle of each mounting base. A medicine cylinder is detachably installed and fitted onto the constant temperature tube at the upper end of each mounting base. An ultrasonic atomizer located at the lower end of the constant temperature tube is fixedly installed inside each mounting base. A horizontal adjustment rod is rotatably installed on the inner side of each constant temperature tube. A tilt adjustment rod is rotatably installed at the upper end of each horizontal adjustment rod. A laser activation probe is fixedly installed at one end of each tilt adjustment rod. A tilt adjustment sleeve is slidably installed up and down at the upper end of each constant temperature tube. An adjustment handle is fixedly connected to and slidably installed inside the tilt adjustment sleeve at the other end of each tilt adjustment rod.

[0013] Preferably, each of the reagent cartridges contains lauric acid solvent, a rubber ring is fixedly installed at the bottom of each reagent cartridge, and a rubber sleeve is fitted on the outside of each reagent cartridge.

[0014] Preferably, each of the mounting bases has a needle that communicates with the ultrasonic atomizer fixedly installed on its inner side, and each needle has an air intake channel communicating with air on one side, and a dust filter is fixedly installed at the end of each air intake channel.

[0015] Preferably, a passive cylindrical gear disk is coaxially fixedly mounted on the lower end of each of the horizontal adjustment rods, an active cylindrical gear disk that meshes with the passive cylindrical gear disk is rotatably mounted on the inner side of each of the mounting bases, and a horizontal adjustment drive mechanism is coaxially fixedly mounted on the front end of each of the active cylindrical gear disks.

[0016] Preferably, each of the pitch adjustment sleeves has a fixedly connected adjusting rack at its lower end, which is slidably mounted up and down inside the constant temperature tube. Each of the mounting bases has an adjusting spur gear rotatably mounted on its inner side, which meshes with the adjusting rack. Each adjusting spur gear has a pitch adjustment drive mechanism coaxially fixedly mounted at its front end.

[0017] Preferably, the protective shell has symmetrical physiotherapy mechanisms on its left and right sides. Only the physiotherapy mechanism on the right side is described. The physiotherapy mechanism includes an adjusting block that slides left and right on the rear end of the protective shell. An adjusting screw threadedly connected to the adjusting block is rotatably mounted on the protective shell. A kneading head is rotatably mounted on the rear end of the adjusting block. A rubber pad is fixedly mounted on and fitted onto the kneading head at the rear end of the adjusting block. A passive bevel gear is coaxially fixedly mounted on the front end of the kneading head. An active bevel gear meshing with the passive bevel gear is rotatably mounted on the front end of the adjusting block. A sliding plate slides left and right on the left end of the active bevel gear. A physiotherapy motor is coaxially fixedly mounted on the left end of the sliding plate.

[0018] Preferably, each of the thermostatic tubes is fitted with a protective sleeve at its upper end.

[0019] Preferably, a sponge pad is fixedly installed at the rear end of the protective shell.

[0020] Preferably, positioning straps are fixedly installed at the left and right ends of the protective shell.

[0021] Preferably, a connector plug is inserted into the lower end of the connecting plate.

[0022] Compared with the prior art, the present invention has the following advantages:

[0023] 1. This device includes an ultrasonic nebulizer, a laser activation probe, a thermostatic tube, a medication cartridge, and lauric acid solvent. In use, the medication cartridge is fitted onto the thermostatic tube, and the lauric acid solvent is atomized by the ultrasonic nebulizer. After passing through the thermostatic tube, it enters the nasal cavity and is absorbed by the nasal mucosa. Then, the laser activation probe is activated to irradiate the inflamed area, specifically activating the medication. This not only effectively increases the absorption efficiency of the medication but also achieves personalized and accurate treatment for different patients' rhinitis conditions. The laser activation probe offers flexible control, improving the accuracy of the treatment location.

[0024] 2. This device has a physiotherapy mechanism. By massaging the Yingxiang acupoint, it stimulates blood circulation in the nasal cavity, which can alleviate rhinitis symptoms to a certain extent. Attached Figure Description

[0025] The accompanying drawings are provided to further illustrate the invention and form part of the specification. They are used in conjunction with embodiments of the invention to explain the invention and do not constitute a limitation thereof. In the drawings:

[0026] Figure 1 This is a schematic diagram of the three-dimensional structure of the present invention. Figure 1 .

[0027] Figure 2 This is a schematic diagram of the three-dimensional structure of the present invention. Figure 2 .

[0028] Figure 3 This is a schematic diagram showing the position of the ultrasonic atomizer in this invention.

[0029] Figure 4 This is a schematic diagram illustrating the rotation adjustment principle of the laser-activated probe in this invention.

[0030] Figure 5 This is a schematic diagram of the physiotherapy device in this invention.

[0031] Figure label:

[0032] 1. Protective shell; 2. Connecting plate; 3. Mounting base; 4. Thermostatic tube; 5. Medicine cylinder; 6. Ultrasonic nebulizer; 7. Horizontal adjustment rod; 8. Pitch adjustment rod; 9. Laser activation probe; 10. Pitch adjustment sleeve; 11. Adjustment handle; 13. Rubber ring; 14. Rubber sleeve; 15. Needle; 16. Air inlet channel; 17. Dust filter; 18. Passive cylindrical gear disc; 19. Active cylindrical gear disc; 20. Horizontal adjustment drive mechanism; 21. Adjusting spur rack; 22. Adjusting spur gear; 23. Pitch adjustment drive mechanism; 24. Physiotherapy mechanism; 25. Adjusting block; 26. Adjusting screw; 27. Kneading head; 28. Rubber pad; 29. ​​Passive bevel gear; 30. Active bevel gear; 31. Sliding plate; 32. Physiotherapy motor; 33. Protective sleeve; 34. Sponge pad; 35. Positioning strap; 36. Connecting plug. Detailed Implementation

[0033] The foregoing and other technical contents, features and effects of the present invention are described in conjunction with the appendix below. Figures 1 to 5 The detailed description of the embodiments will make this clear. All references to the following embodiments are made with reference to the accompanying drawings.

[0034] Exemplary embodiments of the present invention will now be described with reference to the accompanying drawings.

[0035] Example 1, by Figure 1-4 The present invention includes a protective shell 1, which is designed according to the structure of the human nose, conforms to ergonomics, and is made of lightweight polyethylene plastic, which is lightweight and has good bending resistance. To achieve precise treatment, a connecting plate 2 is fixedly installed on the lower rear end of the protective shell 1. Mounting bases 3 are fixedly connected to the left and right sides of the upper end of the connecting plate 2, respectively. Each mounting base 3 has a groove on its upper end, and a thermostatic tube 4 is fixedly installed in the middle of each groove. The thermostatic tube 4 is made of glass, is open at both ends, and has an inner layer containing an electric heating wire connected to a power supply and a temperature control system to maintain a certain temperature on the surface of the thermostatic tube. A medicine cylinder 5 is detachably installed on the upper end of each mounting base 3 and fitted onto the thermostatic tube 4. The medicine cylinder 5 is made of plastic and is open at both ends along its central axis for easy fitting onto the thermostatic tube 4. The inner side of the medicine cylinder 5 is hollow for filling with medicine. An ultrasonic nebulizer located at the lower end of the thermostatic tube 4 is fixedly installed inside each mounting base 3. 6. The ultrasonic atomizer 6 is connected to the power supply and control system. The ultrasonic atomizer 6 includes an ultrasonic generator, an ultrasonic coupler, an atomizer device, etc. A cavity is provided between the ultrasonic atomizer 6 and the inner bottom of the mounting base 3. The cavity is used to connect the drug cartridge 5. A horizontal adjustment rod 7 is rotatably installed on the inner side of each thermostatic tube 4. A cylinder is fixedly connected to the upper end of each horizontal adjustment rod 7. An elevation adjustment rod 8 is rotatably installed inside the cylinder. A laser activation probe 9 located above the cylinder is fixedly installed at one end of each elevation adjustment rod 8. The laser activation probe 9 is connected to the power supply and control system. The laser activation probe 9 includes a laser transmitter and a miniature lens. An elevation adjustment sleeve 10 is slidably installed up and down at the upper end of each thermostatic tube 4. A circular groove is opened in the middle of the upper end of the elevation adjustment sleeve 10. An annular groove is opened on the side wall of the circular groove. An adjustment handle 11 is fixedly connected to the other end of each elevation adjustment rod 8 and slidably installed in the annular groove. The adjustment handle 11 consists of a curved rod and an end ball. The end ball is slidably installed in the annular groove.

[0036] In practical use: Medical staff place each medication cartridge 5 onto the thermostatic tube 4, connecting the medication cartridge 5 to the cavity on the lower side of the ultrasonic nebulizer 6. After the medication flows into the cavity, the rhinitis patient inserts the medication cartridges 5 on both sides into their nasal cavity and secures the protective shell 1. Then, the control system powers on the laser activation probe 9, and the miniature lens transmits the image of the nasal cavity to the computer. Medical staff can then rotate the horizontal adjustment rod 7 to rotate the laser activation probe 9 horizontally, thus adjusting the horizontal angle. The adjustment handle 11 rotates around the annular groove, and the tilt adjustment sleeve 10 moves up or down, causing the adjustment handle 11 to swing up or down. This, through the tilt adjustment rod 8, drives the laser activation probe 9 to adjust the tilt angle, allowing medical staff to assess the inflammation inside the patient's nasal cavity through the miniature lens and provide personalized treatment plans for optimal results. Finally, the control system powers on the ultrasonic nebulizer 6.

[0037] At this time, the ultrasonic generator operates and generates high-frequency ultrasonic oscillations. The energy is then transferred to the medication in the lower cavity of the nebulizer 6 via the ultrasonic coupler. The medication is then sprayed upward through the nebulizer device, producing atomized liquid, and exited through the upper end of the thermostatic tube 4, delivering the medication deep into the nasal cavity. Because the surface of the thermostatic tube 4 maintains a certain temperature, it can heat the sprayed atomized liquid, avoiding irritation to the nasal cavity in cold weather, thus affecting the treatment effect. Medication atomization ensures that the medication is better absorbed by the nasal mucosa, improving the bioavailability and therapeutic effect. Then, the laser transmitter is turned on, emitting light of a specific wavelength to the inflamed area inside the patient's nasal cavity. The photosensitive medication is activated under the light irradiation. At the same time, the angle of the laser activation probe 9 can be adjusted horizontally or vertically to specifically activate the medication, concentrating the therapeutic effect of the medication on the lesion site and reducing the impact of the medication on healthy tissue. Laser therapy for rhinitis itself has anti-inflammatory, antibacterial, and tissue repair-promoting effects, which can be enhanced with the effects of the medication to improve the treatment effect.

[0038] Example 2, based on Example 1, is given in 2-3. The drug inside each drug cartridge 5 is lauric acid solvent. Lauric acid solvent is a photosensitive solvent that can be activated by laser. It can undergo a chemical reaction through laser irradiation. Lauric acid solvent is obtained by nano-processing lauric acid compound and incorporating it into an organic solvent, followed by stirring, heating and filtration. Nano-processing has the advantages of enhancing bioavailability, improving drug delivery efficiency, improving drug release and reducing side effects. Each drug cartridge 5 is fixedly installed with a rubber ring 13 at the bottom and a rubber sleeve 14 is fitted on the outside of each drug cartridge 5.

[0039] In practical use: Rubber sleeve 14 is a disposable rubber sleeve, convenient for different patients to replace, thus achieving medical safety and hygiene conditions. Lauric acid is a natural plant secondary metabolite with various biological activities such as antioxidation, anti-inflammation, and anti-cancer. Nano-processing of lauric acid may bring the following advantages:

[0040] Enhanced bioavailability: Nanoparticles can increase the specific surface area of ​​lauric acid particles, thereby improving their solubility and bioavailability, making them easier for the human body to absorb.

[0041] Improving drug delivery efficiency: Nanosized lauryl acid may have better drug delivery performance, enabling more efficient delivery of drugs to the tissues or cells in need.

[0042] Improved drug release: The unique structure of nanoparticles may affect the release kinetics of lauric acid, resulting in more sustained and stable drug release.

[0043] Reduced side effects: Nanosized lauryl acid may be able to target lesions more precisely, reducing the impact on healthy tissues and thus reducing drug side effects.

[0044] Example 3, based on Example 2, by Figure 3 As shown, each mounting base 3 has a needle 15 fixedly installed on its inner side, which is connected to the ultrasonic atomizer 6. The needle 15 is made of stainless steel. Each needle 15 has an air inlet channel 16 connected to the air on one side. Each air inlet channel 16 has a dust filter 17 fixedly installed at its end.

[0045] In practical use: When medical staff install the medicine cartridge 5, they put the medicine cartridge 5 onto the thermostatic tube 4 and move the medicine cartridge 5 downward so that the needle 15 pierces the rubber ring 13. At this time, the inside of the medicine cartridge 5 is connected to the cavity on the lower side of the ultrasonic nebulizer 6. In order to avoid oxidation of the lauric acid solvent in the medicine cartridge 5, the inside of the medicine cartridge 5 is normally set to a vacuum state. After the needle 15 penetrates the rubber ring 13, when the lauric acid solvent flows through the needle 15, air is introduced into the medicine cartridge 5 through the air inlet channel 16. The dust filter 17 can prevent impurities in the air from entering the lauric acid solvent.

[0046] Example 4, based on Example 1, by Figure 4As shown, a passive cylindrical gear disk 18 is coaxially fixedly mounted on the lower end of each horizontal adjustment rod 7, and an active cylindrical gear disk 19 that meshes with the passive cylindrical gear disk 18 is rotatably mounted on the inner side of each mounting base 3. A horizontal adjustment drive mechanism 20 is coaxially fixedly mounted on the front end of each active cylindrical gear disk 19. The horizontal adjustment drive mechanism 20 is fixedly mounted on the inner side of the mounting base 3 and connected to the power supply and control system. The horizontal adjustment drive mechanism 20 includes a horizontal adjustment drive motor and a micro reducer.

[0047] In practical use: When adjusting the angle of the laser activation probe 9, medical staff control the horizontal adjustment drive mechanism 20 to turn on the power through the control system. At the same time, the active cylindrical toothed disk 19 meshes with the passive cylindrical toothed disk 18 and rotates, thereby driving the horizontal adjustment rod 7 to rotate and adjust the horizontal angle of the laser activation probe 9.

[0048] Example 5, based on Example 4, by Figure 4 Each pitch adjustment sleeve 10 has a connecting rod fixedly connected to its lower front end and slidably installed inside the thermostatic tube 4. The lower end of the connecting rod is fixedly connected to an adjusting spur rack 21. Each mounting base 3 has an adjusting spur gear 22 rotatably installed on its inner side, meshing with the adjusting spur rack 21. Each adjusting spur gear 22 has a pitch adjustment drive mechanism 23 coaxially fixedly installed at its front end. The pitch adjustment drive mechanism 23 is fixedly installed on the inner side of the mounting base 3 and connected to the power supply and control system. The pitch adjustment drive mechanism 23 includes a pitch adjustment drive motor and a micro reducer.

[0049] In practical use: When adjusting the pitch angle of the laser activation probe 9, medical staff control the pitch adjustment drive mechanism 23 to turn on the power through the control system, which drives the adjusting spur gear 22 to mesh with the adjusting spur rack 21 and slide up or down. This drives the pitch adjustment sleeve 10 to move up or down through the connecting rod, thereby adjusting the pitch angle of the laser activation probe 9.

[0050] When adjusting the horizontal and vertical angles of the laser activation probe 9, the horizontal adjustment drive mechanism 20 and the vertical adjustment drive mechanism 23 do not affect each other and can be adjusted simultaneously.

[0051] Example 6, based on Example 1, by Figure 2 and Figure 5As shown, the protective shell 1 has sliding grooves on its left and right rear ends, and symmetrical physiotherapy mechanisms 24 are provided in the two sliding grooves respectively. Therefore, only the physiotherapy mechanism 24 located on the right side is described. The physiotherapy mechanism 24 includes an adjusting block 25 that is slidably installed in the sliding groove. An adjusting screw 26 that is threadedly connected to the adjusting block 25 is rotatably installed on the right end of the protective shell 1. A knob is coaxially fixedly installed on the right end of the adjusting screw 26. A kneading head 27 is rotatably installed on the rear end of the adjusting block 25. The kneading head 27 includes a circular plate and a protrusion fixedly connected to the eccentric rear end of the circular plate. A knob is coaxially fixedly connected to and rotatably installed on the front end of the kneading head 27. The passive spindle on the adjusting block 25 has a rubber pad 28 fixedly installed at the rear end of the adjusting block 25 and fitted onto the kneading head 27. A passive bevel gear 29 is coaxially fixedly installed at the front end of the passive spindle. An active bevel gear 30 that meshes with the passive bevel gear 29 is rotatably installed at the front end of the adjusting block 25. An active spindle is coaxially fixedly connected to the left end of the active bevel gear 30. A strip groove is opened at the left end of the active spindle. A sliding plate 31 is slidably installed in the strip groove. A physiotherapy motor 32 is coaxially fixedly installed at the left end of the sliding plate 31. The physiotherapy motor 32 is fixedly installed at the rear end of the protective shell 1 and connected to the power supply and control system.

[0052] In practical use: When a rhinitis patient wears this device, the two physiotherapy units 24 are roughly located at the Yingxiang acupoints on both sides of the patient's nose. Then, depending on the different locations of the Yingxiang acupoints for different patients, the knob is turned, which causes the adjustment block 25 to slide left or right in the groove. The strip groove slides left or right along the sliding plate 31, so that the rubber pad 28 is accurately moved to the Yingxiang acupoint position. This is determined by the medical staff based on observation. Then, when treating rhinitis, each physiotherapy motor 32 is powered on, which simultaneously drives the active bevel gear 30 to mesh with the passive bevel gear 29 and rotate, which in turn drives the kneading head 27 to rotate, massaging the patient's Yingxiang acupoints, stimulating nasal blood circulation, and relieving rhinitis symptoms to a certain extent.

[0053] Example 7, based on Example 1, by Figure 2-3 Each thermostatic tube 4 is fitted with a protective sleeve 33 at its upper end. When the device is not in use, the protective sleeve 33 is fitted on the upper end of the thermostatic tube 4 to effectively prevent impurities in the air from entering the thermostatic tube 4. At the same time, when installing the medicine cylinder 5 on the thermostatic tube 4, the protective sleeve 33 can protect the laser activation probe 9 from damage caused by collision. After inserting the medicine cylinder 5, the protective sleeve 33 can be removed upwards when performing treatment.

[0054] Example 8, based on Example 1, by Figure 4 As shown, a sponge pad 34 is fixedly installed at the rear end of the protective shell 1. The sponge pad 34 is concave in the shape of a nose. When wearing this device, it effectively improves the patient's comfort and can also keep the nose warm, thereby reducing nasal congestion and improving breathing.

[0055] Example 9, based on Example 1, by Figure 1 As shown, positioning straps 35 are fixedly installed at the left and right ends of the protective shell 1, and the ends of the positioning straps 35 are provided with adjustment buckles. When the device is worn, the two positioning straps 35 can be wrapped around the back of the head and locked to effectively fix the device and prevent it from slipping off during treatment.

[0056] Example 10, based on Example 1, is... Figure 1 As shown, a connector 36 is inserted into the lower end of the connector plate 2. One end of the connector 36 is connected to this device, and the other end is connected to a calculator via a connecting cable. The calculator controls this device to treat the patient's rhinitis. After the treatment is completed, the connector 36 can be pulled down and removed.

[0057] Working principle:

[0058] In use, medical personnel first attach each medication cartridge 5 to the thermostatic tube 4 and move the medication cartridge 5 downwards so that the needle 15 pierces the rubber ring 13. At this time, the lauric acid solvent inside the medication cartridge 5 flows into the cavity below the ultrasonic nebulizer 6. Then, the protective cover 33 is removed, and the rhinitis patient inserts the medication cartridges 5 on both sides into the nasal cavity. The two positioning straps 35 are wrapped around the back of the head and secured. After wearing, the position of the physiotherapy mechanism 24 is manually adjusted to the patient's Yingxiang acupoint, and the connecting plug 36 is connected to the device and the calculator. At this time, the calculator displays the real-time image of the patient's nasal cavity taken by the laser activation probe 9. The laser activation probe is adjusted by controlling the horizontal adjustment drive mechanism 20 and the vertical adjustment drive mechanism 23 to rotate forward or backward. The horizontal and vertical angles of probe 9 are used to assess the inflammation within the patient's nasal cavity, providing a personalized treatment plan. Then, the ultrasonic nebulizer 6 is powered on, atomizing lauric acid solvent and spraying it upwards, exiting through the upper end of the thermostatic tube 4 to deliver the medication deep into the nasal cavity. Next, the laser transmitter is activated, emitting light of a specific wavelength to the inflamed area within the patient's nasal cavity. The photosensitive medication is activated under light irradiation. Simultaneously, the angle of the laser activation probe 9 can be adjusted horizontally or vertically to specifically activate the medication, concentrating the therapeutic effect on the lesion site and reducing the impact of the medication on healthy tissue. At the same time, the physiotherapy motor 32 is powered on, and the kneading head 27 rotates to massage the patient's Yingxiang acupoint, achieving a better therapeutic effect.

[0059] Compared with the prior art, the present invention has the following advantages:

[0060] 1. This device includes an ultrasonic nebulizer, a laser activation probe, a thermostatic tube, a medication cartridge, and lauric acid solvent. In use, the medication cartridge is fitted onto the thermostatic tube, and the lauric acid solvent is atomized by the ultrasonic nebulizer. After passing through the thermostatic tube, it enters the nasal cavity and is absorbed by the nasal mucosa. Then, the laser activation probe is activated to irradiate the inflamed area, specifically activating the medication. This not only effectively increases the absorption efficiency of the medication but also achieves personalized and accurate treatment for different patients' rhinitis conditions. The laser activation probe offers flexible control, improving the accuracy of the treatment location.

[0061] 2. This device has a physiotherapy mechanism. By massaging the Yingxiang acupoint, it stimulates blood circulation in the nasal cavity, which can alleviate rhinitis symptoms to a certain extent.

[0062] Although the present invention has been described in detail through the preferred embodiments above, it should be understood that the above description should not be considered as a limitation of the present invention. Various modifications and substitutions to the present invention will be apparent to those skilled in the art after reading the above description. Therefore, the scope of protection of the present invention should be defined by the appended claims.

Claims

1. An ultrasonic atomization nanometerization lauric acid photodynamic rhinitis treatment instrument based on, comprising a protective shell (1), characterized in that, The lower end of the protection shell (1) is fixedly installed with a connecting plate (2), the left and right sides of the upper end of the connecting plate (2) are fixedly connected with mounting bases (3), respectively, the middle parts of each mounting base (3) are fixedly installed with constant temperature tubes (4), respectively, the upper ends of each mounting base (3) are detachably installed with and sleeved on the constant temperature tubes (4), respectively, the inner parts of each mounting base (3) are fixedly installed with ultrasonic atomizers (6) located at the lower ends of the constant temperature tubes (4), respectively, the inner sides of each constant temperature tube (4) are rotatably installed with horizontal adjusting rods (7), respectively, the upper ends of each horizontal adjusting rod (7) are rotatably installed with pitch adjusting rods (8), respectively, one end of each pitch adjusting rod (8) is fixedly installed with a laser activation probe (9), respectively, the upper ends of each constant temperature tube (4) are slidably installed with pitch adjusting sleeves (10), respectively, the other end of each pitch adjusting rod (8) is fixedly connected with and slidably installed in the pitch adjusting sleeve (10), respectively. The lower end of each horizontal adjusting rod (7) is coaxially fixedly installed with a driven cylindrical gear (18), respectively, the inner side of each mounting base (3) is rotatably installed with a driving cylindrical gear (19) engaged with the driven cylindrical gear (18), respectively, the front end of each driving cylindrical gear (19) is coaxially fixedly installed with a horizontal adjusting drive mechanism (20), respectively. The lower end of each pitch adjusting sleeve (10) is fixedly connected with and slidably installed in the constant temperature tube (4) in a up-down direction, respectively, the inner side of each mounting base (3) is rotatably installed with a pitch adjusting spur gear (22) engaged with the pitch adjusting spur gear (21), respectively, the front end of each pitch adjusting spur gear (22) is coaxially fixedly installed with a pitch adjusting drive mechanism (23), respectively.

2. The ultrasonic atomization nanometer lauric acid photodynamic rhinitis treatment instrument based on claim 1, characterized in that, The inside of each medicament cylinder (5) is filled with lauric acid solvent, the bottom of each medicament cylinder (5) is fixedly installed with a rubber ring (13), respectively, the outer side of each medicament cylinder (5) is sleeved with a rubber sleeve (14), respectively.

3. The ultrasonic atomization nanometer lauric acid photodynamic rhinitis treatment instrument based on claim 2, characterized in that, The inner side of each mounting base (3) is fixedly installed with a needle (15) communicated with the ultrasonic atomizer (6), respectively, one side of each needle (15) is provided with an air inlet channel (16) communicated with air, respectively, the end of each air inlet channel (16) is fixedly installed with a dustproof filter (17), respectively.

4. The ultrasonic atomization nanometer lauric acid photodynamic rhinitis treatment instrument based on claim 1, characterized in that, The left and right sides of the protective shell (1) are respectively provided with mutually symmetrical physiotherapy mechanisms (24), the physiotherapy mechanism (24) on the right side comprises an adjusting block (25) slidably installed on the rear end of the protective shell (1), a adjusting screw rod (26) is rotatably installed on the protective shell (1) and is in threaded connection with the adjusting block (25), a kneading head (27) is rotatably installed on the rear end of the adjusting block (25), a rubber pad (28) is fixedly installed on the rear end of the adjusting block (25) and is sleeved on the kneading head (27), a driven bevel gear (29) is coaxially fixedly installed on the front end of the kneading head (27), a driving bevel gear (30) is rotatably installed on the front end of the adjusting block (25) and is in engagement with the driven bevel gear (29), a sliding plate (31) is slidably installed on the left end of the driving bevel gear (30), and a physiotherapy motor (32) is coaxially fixedly installed on the left end of the sliding plate (31).

5. The ultrasonic atomization nanometer lauric acid photodynamic rhinitis treatment instrument based on claim 1, characterized in that, The upper end of each constant-temperature tube (4) is sleeved with a protective sleeve (33).

6. The ultrasonic atomization nanometer lauric acid photodynamic rhinitis treatment instrument based on claim 1, characterized in that, The rear end of the protective shell (1) is fixedly installed with a sponge pad (34).

7. The ultrasonic atomization nanometer lauric acid photodynamic rhinitis treatment instrument based on claim 1, characterized in that, The left and right ends of the protective shell (1) are respectively fixedly installed with positioning bands (35).

8. The ultrasonic atomization nanometer lauric acid photodynamic rhinitis treatment instrument based on claim 1, characterized in that, The lower end of the connecting plate (2) is inserted with a connecting plug (36).

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