TWI846581B - Nasal placement breathing trainer - Google Patents

Abstract

A nasal placement breathing trainer, which is disposed in a human nasal cavity, and the nasal placement breathing trainer comprises two inserts and a connecting unit. The two inserts have a main body and a ring of fins on the surface of the main body, and the main body is divided into a connecting part and an extension by means of the fins, and the fins are made of soft material; The two ends of the connecting unit are connected to the connection parts of the two inserts, so that the extension and the fins are placed in the human nasal cavity and then clamped and fixed. Therefore, the present application can reduce the air flow inhaled by a nasal cavity, further reduce the free radicals formed when oxygen exchanges nutrients with a human body, thereby reducing the damage of free radicals to the human body; In addition, the present application can also reduce a nasal inhalation of external allergens, thereby avoiding patients from causing allergic symptoms.

Description

Nasal placement breathing trainer

This application is related to a breathing trainer, in particular a nasal placement breathing trainer.

Studies have shown that when the human body exchanges nutrients with oxygen, free radicals are generated in the human body. The free radicals are highly active and react with cells in the human body (e.g., proteins, lipids, DNA, RNA) to destroy the structure and function of cells in the human body, causing cell damage. When the amount of free radicals is higher than the amount of antioxidants in the body, it will cause damage to the cell structure, thus causing aging of the human body, commonly known as oxidative stress. Therefore, if too much oxygen is inhaled, the following adverse consequences will occur to the human body:

1. It will increase the production of free radicals in the human body, causing damage to cells in the body, resulting in irreversible damage, thereby accelerating the aging of the body.

2. Increase the risk of cancer, cardiovascular disease, respiratory disease and neurological disease.

To solve this problem, people start with diet, try to take in as many antioxidant substances as possible, and look for antioxidant products that can remove free radicals in the body. However, people breathe in a lot of oxygen every day. If the body's dependence on oxygen can be effectively reduced, according to clinical evidence, it can also effectively improve the body's aging and oxidation problems.

On the other hand, what we generally call allergy patients are those who overreact to allergens in the inhaled environment, such as dust mites, dust, and suspended particles in the air, causing the human immune system to become abnormal and release antibodies excessively, resulting in nasal polyps swelling and compressing the respiratory tract. Usually, when patients have the above symptoms, they will inhale air vigorously to allow the body to obtain enough oxygen. However, this will only make it easier for allergens to enter the nasal cavity due to air flow, and will not solve the symptoms. If you want to further treat allergic symptoms, you also need to take anti-allergic drugs and use nasal sprays to achieve effective improvement.

The main purpose of this application is to reduce the amount of air inhaled by the human body and reduce the damage of free radicals to the human body.

Another purpose of this application is to improve the problem of severe allergic symptoms caused by the rapid entry of allergens into the nasal cavity of allergic patients.

The above purpose does not prevent the existence of other purposes. If a person with ordinary knowledge in the relevant technical field can derive the purpose from the description of the specification, patent application scope or drawings, it is also included in the purpose of this application. Therefore, the purpose of this application is not limited to the above listed purposes.

To achieve the above purpose, the present application provides a nasal placement breathing trainer, which is arranged in a human nasal cavity. The nasal placement breathing trainer includes two inserts and a connecting unit. The two inserts respectively have a main body and a wing arranged around the surface of the main body, and the main body is divided into a connecting part and an extending part by the wing. The extending part and the wing are used to be arranged in the human nasal cavity, and the wing is made of soft material; the two ends of the connecting unit are respectively connected to the connecting parts of the two inserts, so that the extending parts and the wing of the two inserts are respectively inserted into the human nasal cavity and fixed by clamping.

Based on the above technical features, this application has the following characteristics:

1. This application can significantly reduce the air flow rate of nasal inhalation through two implants placed in the human nasal cavity, allowing users to perform breathing training for a longer period of time, reducing the free radicals formed when oxygen exchanges nutrients with the human body, thereby reducing the damage of free radicals to the human body.

2. This application inserts two implants into the human nasal cavity respectively and fixes them with a connecting unit to reduce the air flow rate in the nasal cavity, thereby preventing the nasal cavity from rapidly inhaling too many external allergens, thereby reducing the allergic symptoms induced by the patient.

3. This application can be fixed to the nasal cavity shape of different users by setting the wing to meet the needs of use.

4. Because the wing of this application is made of soft material, when the insert is inserted into the human nasal cavity, it not only makes the user feel more comfortable, but also reduces the oxygen flow rate inhaled by the nasal cavity.

100: Nasal placement breathing trainer

1: Human nasal cavity

10: Inserts

11: Subject

111: Connection part

112: Extension

12: Wings

121: Groove

13: Filling the surface

20: Connection unit

Figure 1 is a three-dimensional schematic diagram of the nasal cavity placement breathing training device of the first embodiment of this application.

Figure 2 is a schematic diagram of the front side of the nasal cavity placement breathing trainer of the first embodiment of this application.

Figure 3 is a schematic diagram of the implementation of the nasal cavity placement breathing training device of the first embodiment of this application.

Figure 4 is a three-dimensional schematic diagram of the nasal cavity placement breathing training device of the second embodiment of this application.

Figure 5 is a three-dimensional schematic diagram of the nasal cavity placement breathing training device of the third embodiment of this application.

Figure 6 is a schematic diagram of the front side of the nasal cavity placement breathing trainer of the third embodiment of this application.

Figure 7 is a three-dimensional schematic diagram of the nasal cavity placement breathing training device of the fourth embodiment of this application.

Figure 8 is a schematic diagram of the front side of the nasal cavity placement breathing trainer of the fourth embodiment of this application.

In order to facilitate the explanation of the central idea of this application in the above invention content column, it is expressed in a specific embodiment. The various objects in the embodiment are depicted according to the proportions, sizes, deformations or displacements suitable for the description, rather than being drawn according to the proportions of the actual components, which should be explained in advance.

The following describes in detail exemplary embodiments of the present application with reference to the accompanying drawings, and is not intended to limit the technical principles of the present application to a specific disclosed embodiment. The scope of the present application is limited only by the scope of the patent application, covering substitutions, modifications and equivalents.

Please refer to Figures 1 to 6. This application provides a nasal placement breathing trainer 100, which is arranged in a human nasal cavity 1. The nasal placement breathing trainer 100 includes two insertion parts 10 and a connecting unit 20.

Please refer to FIG. 2 to observe the features of the implant 10 from the front and side view. The two implants 10 respectively have a main body 11 and a wing 12 arranged around the surface of the main body 11. The main body 11 is divided into a connecting portion 111 and an extension portion 112 by the wing 12. The extension portion 112 and the wing 12 are used to be arranged in the human nasal cavity 1 (as shown in FIG. 3).

The material of the insert 10 can be selected from any one of algin, rubber, resin and silicone; the material of the wing 12 can be selected from any one of algin, rubber, resin and silicone. Because the materials have soft properties, when the extension 112 of the insert 10 and the wing 12 are inserted into the human nasal cavity 1, the user can feel comfortable and less likely to feel a lump.

The extension portion 112 gradually contracts from the main body 11 away from the connecting portion 111 to form a pyramidal structure. The pyramidal structure can better fit the user's nasal structure, making it more comfortable for the user to use.

The wing 12 is located between the connecting portion 111 and the extending portion 112, and the wing 12 is made of a soft material. Through the provision of the wing 12, the present application can be fastened to fit and conform to the nasal shapes of different users to meet the needs of use.

Preferably, the wing 12 can be made by extending the insert 10 as a whole. The end of the wing 12 away from the main body surface is bent toward the connecting portion 111 to form a groove 121, which can be more conducive to fitting and conforming to the nasal shape of different users for fastening.

The two ends of the connecting unit 20 are respectively connected to the connecting parts 111 of the two inserts 10, and please refer to FIG. 3 so that the extension parts 112 and the wing pieces 12 of the two inserts 10 can be respectively inserted into the human nasal cavity 1 and then clamped and fixed to block the air inhaled by the human nasal cavity 1.

Please refer to FIG. 4 , the insert 10 has a filling surface 13. The filling surface 13 may be roughened on the entire or partial surface of the connecting portion 111 of the insert 10. Of course, the filling surface 13 may also be provided on the extension portion 112, and the filling surface 13 is used to fill a diffusion fluid. In more detail, the surface roughness (Ra) of the filling surface 13 may be between 0.8 microns and 4.5 microns, so that the diffusion fluid can be better filled on the filling surface 13.

Assuming that the surface roughness (Ra) of the filling surface 13 is lower than 0.8 microns, the result of too small surface roughness will make the diffused fluid unable to be effectively filled in the filling surface 13; and if the surface roughness (Ra) of the filling surface 13 is higher than 4.5 microns, it may cause the diffused fluid to flow out along the filling surface 13, and it is also impossible to better absorb the diffused fluid. The material of the diffused fluid can be made of essential oil with aromatic smell, so that the diffused fluid can emit fragrance in the human nasal cavity 1 to boost the user's spirit and change his physical and mental state; or a medicinal fluid that relieves nasal allergies can be used to reduce the chance of allergic symptoms in patients. In addition, through the use of the filling surface 13 and the diffused fluid, the purpose of slowly releasing the diffused fluid can also be achieved, and the effect of long-term use can be achieved.

This application can adjust the shape of the connecting portion 111 according to the actual use situation, such as a rectangle, a pentagonal column, a hexagonal column, or other polygonal shapes. In this way, the gap when the insert 10 is inserted into the human nasal cavity 1 can be adjusted, thereby changing the air flow rate inhaled by the user. In addition, the setting of the insert 10 with convex corners can better achieve the purpose of stable placement in the nasal cavity.

Please refer to FIG. 5 . The difference between FIG. 5 and FIG. 1 to FIG. 4 is that in the embodiment of FIG. 1 to FIG. 4 , the overall shape of the insert 10 is roughly cylindrical, and the wing 12 is arranged to be circular and surround the shape of the insert 10; while in the embodiment of FIG. 5 , the overall shape of the insert 10 is roughly square, and the wing 12 is arranged to be square and surround the shape of the insert 10; in this embodiment, and in conjunction with FIG. 6 , the extension portion 112 can also gradually shrink from the main body 11 away from the connecting portion 111 to form a quadrangular pyramid-like structure.

Please refer to Figures 7 and 8. The difference between this embodiment and the embodiments of Figures 1 to 6 is that the overall shape of the insert 10 of this embodiment is roughly hexagonal, so that the wing 12 can be arranged in a hexagonal shape to match the shape of the insert 10, and the extension 112 can gradually shrink from the main body 11 away from the connecting portion 111 to form a hexagonal pyramid-like structure.

Combining the above technical features, this application has the following characteristics:

1. By inserting two inserts 10 into the human nasal cavity 1, the oxygen flow rate inhaled into the nasal cavity can be significantly reduced, allowing users to perform breathing training for a longer period of time, reducing the free radicals formed when oxygen exchanges nutrients with the human body, thereby reducing the damage of free radicals to the human body.

2. The two inserts 10 are respectively inserted into the human nasal cavity 1 and fixed with the connecting unit 20. In this way, the insert 10 can reduce the air flow rate in the nasal cavity, prevent the nasal cavity from quickly inhaling too many external allergens, and thus reduce the allergic symptoms induced by the patient.

3. The present application can be fixed to the nasal cavity shape of different users by setting the wing 12 to meet the needs of use.

4. The wing 12 of the present application is made of a soft material, so that when the insert 10 is inserted into the human nasal cavity 1, it not only makes the user feel more comfortable, but also reduces the oxygen flow rate inhaled by the nasal cavity.

5. The present application forms a pyramidal structure through the extension portion 112 to conform to the user's nasal structure, making it comfortable when used.

6. This application fills the filling surface 13 with a diffusion fluid, so that the diffusion fluid can emit fragrance in the human nasal cavity 1 to boost the user's spirit and change his or her physical and mental state; or provides a diffusion fluid for medicinal herbs to achieve the purpose of reducing allergies.

7. This application can also achieve the purpose of slowly releasing the diffused fluid through the use of the filling surface 13 and the diffused fluid, thereby achieving the effect of long-term use.

8. This application can be used in different usage scenarios, so that the wing 12 can be arranged in a circular, square or hexagonal shape to match the shape of the insert 10, so as to adjust the gap between the inner wall of the human nasal cavity 1 and the insert 10, thereby changing the air flow inhaled by the user.

9. Since the overall shape of the insert 10 is roughly square or hexagonal, the insert 10 can be stably placed in the nasal cavity by setting the convex corners.

The aforementioned effects do not preclude the existence of other effects. If a person with ordinary knowledge in the relevant technical field can derive the effects from the description of the specification, the scope of the patent application, or the drawings, they are also included in the effects of this application. Therefore, the effects of this application are not limited to the aforementioned effects.

The above examples are only used to illustrate this application and are not intended to limit the scope of this application. Any modifications or changes that do not violate the spirit of this application are within the scope of protection intended by this application.

100: Nasal placement breathing trainer

10: Inserts

11: Subject

111: Connection part

112: Extension

12: Wings

20: Connection unit

Claims (8)

A nasal placement breathing trainer is arranged in a human nasal cavity. The nasal placement breathing trainer comprises: two inserts, each having a main body and a wing arranged around the surface of the main body, and the main body is divided into a connecting part and an extending part by the wing, the extending part and the wing are used to be arranged in the human nasal cavity, and the wing is made of soft material; and a connecting unit, the two ends of which are respectively connected to the connecting parts of the two inserts, so that the extending parts and the wing of the two inserts are respectively inserted into the human nasal cavity for clamping and fixing. A nasal placement breathing trainer as described in claim 1, wherein the end of the wing away from the main body surface is bent toward the connecting portion to form a groove. The nasal placement breathing trainer as described in claim 1, wherein the wing is arranged in a circular, square or hexagonal shape to match the shape of the insert. As described in claim 1, the nasal placement breathing trainer, wherein the extension portion gradually contracts from the main body away from the connecting portion to form a cone-shaped structure. The nasal placement breathing trainer as described in claim 1, wherein the material of the insert is selected from any one of alginate, rubber, resin and silicone; the material of the wing is selected from any one of alginate, rubber, resin and silicone. A nasal placement breathing trainer as described in claim 5, wherein the wing is made by extending the insert as a whole. A nasal placement breathing trainer as described in claim 1, wherein the insert has a filling surface, and the filling surface is used to fill a diffusion fluid. A nasal placement breathing trainer as described in claim 7, wherein the surface roughness (Ra) of the filling surface is between 0.8 microns and 4.5 microns.

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