Mouth-nose aerosol administration device
By designing an oral and nasal aerosol doser including a connecting ring, a connecting tube and an oral-containing fixed delivery assembly, the problem that the mist storage tank cannot monitor the respiratory rate of the atomized inhaler is solved, ensuring the effect of atomization treatment, which is especially suitable for the treatment of young children and children.
Patent Information
- Application Number
- CN202420613452.6
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-03-28
- Publication Date
- 2025-04-15
- Estimated Expiration
- 2034-03-28
AI Technical Summary
The existing mist storage tanks cannot monitor the respiratory rate of the atomized inhaler. Especially when giving atomized treatment to young children and children, it is impossible to know whether they refuse to inhale the drug mist of the drug liquid by holding their breath, resulting in the inability to ensure the effectiveness of the atomized treatment.
An oral and nasal aerosol doser is designed, including a connecting ring, a connecting tube and an oral-containing fixed drug delivery assembly. The oral-containing fixed drug delivery assembly is added through the connecting tube to form a sealed space to monitor and ensure the inhalation of the drug mist.
It effectively solves the problem that the mist storage tank cannot monitor the respiratory rate, and ensures the effectiveness of atomization treatment, especially in the treatment of young children and children.
Smart Images

Figure CN222752382U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of medical devices, in particular to an oral and nasal aerosol dispenser. Background Art
[0002] The pressurized metered-dose inhaler (pMDI) is currently the most widely used inhalation drug delivery device in clinical practice. It has the advantages of being small and portable, quick-acting, easy to use, and capable of administering multiple doses. When using a pMDI, critically ill patients inhale very little each time, and it is difficult for the elderly, children, and patients with low education to master its operation. In view of the shortcomings of pMDI, the Canadian Asthma Society recommends that any patient using a pMDI, regardless of age, should consider using a spacer as an auxiliary tool. The use of a pMDI plus a spacer has low requirements for synergy in inhaling drugs, a wide age range, and reduces the stress response in the airways caused by propellants.
[0003] However, the existing spacer cannot monitor the breathing rate of the aerosol inhaler, especially when aerosol therapy is given to infants and children, it is impossible to know whether the infants and children refuse to inhale the drug mist with added drug solution by holding their breath, and the effect of the aerosol therapy cannot be guaranteed.
[0004] Therefore, there is an urgent need for a controllable oral and nasal aerosol dispenser that can ensure the atomization treatment effect. Utility Model Content
[0005] The utility model aims to provide an oral and nasal aerosol dispenser, which solves the problem that the existing aerosol storage tank cannot guarantee the atomization treatment effect.
[0006] To achieve the above-mentioned purpose, the utility model adopts an oral and nasal aerosol dispenser, comprising a connecting ring, a connecting tube and an oral fixed dosing component, the oral fixed dosing component comprising a hand-held tube, a pressurizing chamber and an air outlet, the connecting tube is detachably connected to the connecting ring and is located below the connecting ring, the hand-held tube is detachably connected to the connecting tube and is located at one end of the connecting tube away from the connecting ring, the pressurizing chamber is fixedly connected to the hand-held tube and is located inside the hand-held tube, and the air outlet is detachably connected to the hand-held tube and is located at one end of the hand-held tube away from the connecting tube.
[0007] Among them, the oral fixed medication assembly also includes a fixing ring and a positioning hole, the fixing ring is detachably connected to the air outlet and is located on the outer surface of the air outlet, and the positioning hole is detachably connected to the fixing ring and is located inside the fixing ring.
[0008] Among them, the oral fixed medication assembly also includes an extension tube and an oral rod, the extension tube is detachably connected to the air outlet and is located at the end of the air outlet away from the hand-held tube, and the extension tube is arranged inside the fixed ring, and the oral rod is detachably connected to the extension tube and is located inside the extension tube.
[0009] Among them, the oral fixed medication assembly also includes a leak-proof sleeve and an air outlet. The leak-proof sleeve is detachably connected to the extension tube and is located at one end of the extension tube away from the air outlet. The air outlet is fixedly connected to the oral rod and is located inside the oral rod.
[0010] Among them, the oral and nasal aerosol dispenser also includes a friction protection component, which includes a protection ring, a rubber pad and a friction groove. The protection ring is detachably connected to the hand-held tube and is located on the outer surface of the hand-held tube. The rubber pad is detachably connected to the protection ring and is located on the side of the protection ring away from the hand-held tube. The friction groove is fixedly connected to the rubber pad and is detachably connected to the rubber pad and is located inside the rubber pad.
[0011] The utility model discloses an oronasal aerosol dispenser, comprising a connecting ring, a connecting tube and an oral fixed medication component, wherein the oral fixed medication component comprises a hand-held tube, a pressurizing chamber and an air outlet, the connecting tube is detachably connected to the connecting ring and is located below the connecting ring, the hand-held tube is detachably connected to the connecting tube and is located at one end of the connecting tube away from the connecting ring, the pressurizing chamber is fixedly connected to the hand-held tube and is located inside the hand-held tube, the air outlet is detachably connected to the hand-held tube and is located at one end of the hand-held tube away from the connecting tube, and the air outlet is detachably connected to the hand-held tube and is located at one end of the hand-held tube away from the connecting tube. The oral fixed medication component is added by using the connecting tube, thereby actively and effectively solving the problem that the existing spacer tank cannot guarantee the atomization treatment effect. BRIEF DESCRIPTION OF THE DRAWINGS
[0012] In order to more clearly illustrate the embodiments of the utility model or the technical solutions in the prior art, the drawings required for use in the embodiments or the description of the prior art will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the utility model. For ordinary technicians in this field, other drawings can be obtained based on these drawings without paying creative work.
[0013] Figure 1 It is a schematic diagram of the overall structure of the first embodiment of the utility model.
[0014] Figure 2 It is an overall front view of the first embodiment of the utility model.
[0015] Figure 3 This utility model Figure 2 AA line structural cross-section view.
[0016] Figure 4 It is a schematic diagram of the overall structure of the second embodiment of the utility model.
[0017] 101-connecting ring, 102-connecting tube, 103-hand-held tube, 104-pressurization chamber, 105-air outlet, 106-fixing ring, 107-positioning hole, 108-extension tube, 109-oral rod, 110-leak-proof sleeve, 111-air outlet, 201-protective ring, 202-rubber pad, 203-friction groove. DETAILED DESCRIPTION
[0018] The embodiments of the present invention are described in detail below, and examples of the embodiments are shown in the accompanying drawings, wherein the same or similar reference numerals throughout represent the same or similar elements or elements having the same or similar functions. The embodiments described below with reference to the accompanying drawings are exemplary and are intended to be used to explain the present invention, and should not be construed as limiting the present invention.
[0019] First embodiment
[0020] See also Figure 1 to Figure 3 , Figure 1 It is a schematic diagram of the overall structure of the first embodiment of the utility model. Figure 2 It is a front view of the whole of the first embodiment of the utility model. Figure 3 This utility model Figure 2 AA line structural cross-section view.
[0021] The utility model provides an oral and nasal aerosol dispenser, comprising a connecting ring 101, a connecting tube 102 and an oral fixed medication component, wherein the oral fixed medication component comprises a hand-held tube 103, a pressurizing chamber 104, an air outlet 105, a fixing ring 106, a positioning hole 107, an extension tube 108, an oral rod 109, a leak-proof sleeve 110 and an air outlet 111. The above-mentioned solution solves the problem that the existing spacer cannot monitor the breathing frequency of the aerosol inhaler, especially when aerosol treatment is performed on infants and children, it is impossible to know whether the infants and children refuse to inhale the medicine mist added with the medicine liquid by holding their breath, and it is impossible to Regarding the problem of ensuring the effectiveness of nebulization therapy, it can be understood that the aforementioned solution can place the oral stick 109 in the child's mouth when the child is undergoing nebulization therapy, and absorb the medicine mist through the air outlet 111, while the leak-proof sleeve 110 will fit the child's face, thereby forming a sealed space to a certain extent, thereby effectively solving the problem that the existing mist storage tank cannot monitor the breathing rate of the nebulizer inhaler, especially when nebulization therapy is performed on infants and children, it is impossible to know whether the infants and children refuse to inhale the medicine mist added with the medicine solution by holding their breath, and the effectiveness of the nebulization therapy cannot be guaranteed.
[0022] According to this specific embodiment, the connecting tube 102 is detachably connected to the connecting ring 101 and is located below the connecting ring 101, the hand-held tube 103 is detachably connected to the connecting tube 102 and is located at the end of the connecting tube 102 away from the connecting ring 101, the boosting chamber 104 is fixedly connected to the hand-held tube 103 and is located inside the hand-held tube 103, and the air outlet 105 is detachably connected to the hand-held tube 103 and is located at the end of the hand-held tube 103 away from the connecting tube 102.
[0023] Among them, the fixing ring 106 is detachably connected to the air outlet 105 and is located on the outer surface of the air outlet 105, and the positioning hole 107 is detachably connected to the fixing ring 106 and is located inside the fixing ring 106. The fixing ring 106 is the main component for fixing the air outlet 105 and the extension tube 108, and the positioning hole 107 is the main component for medical staff to observe whether the extension tube 108 is tightly installed.
[0024] Secondly, the extension tube 108 is detachably connected to the air outlet 105 and is located at one end of the air outlet 105 away from the hand-held tube 103, and the extension tube 108 is arranged inside the fixed ring 106, and the oral rod 109 is detachably connected to the extension tube 108 and is located inside the extension tube 108. The extension tube 108 is a main component connecting the oral rod 109 and the air outlet 105, and the oral rod 109 is a main component to solve the problem of children giving up nebulization treatment due to external factors.
[0025] At the same time, the leak-proof sleeve 110 is detachably connected to the extension tube 108 and is located at an end of the extension tube 108 away from the air outlet 105. The air outlet 111 is fixedly connected to the oral rod 109 and is located inside the oral rod 109. The leak-proof sleeve 110 is the main component for preventing the leakage of medicine mist, and the air outlet 111 is the main component for children to absorb the medicine mist.
[0026] When the utility model is used for aerosol treatment of children, the oral stick 109 is placed in the child's mouth, and the medicine mist is absorbed through the air outlet 111, and the leak-proof sleeve 110 fits the child's face, thereby forming a sealed space to a certain extent, thereby effectively solving the problem that the existing aerosol storage tank cannot monitor the breathing frequency of the aerosol inhaler, especially when aerosol treatment is performed on infants and children, it is impossible to know whether the infants and children refuse to inhale the medicine mist added with the medicine solution by holding their breath, and the effect of the aerosol treatment cannot be guaranteed.
[0027] Second embodiment
[0028] See also Figure 4 , Figure 4 It is a schematic diagram of the overall structure of the second embodiment of the utility model.
[0029] On the basis of the first embodiment, the oral and nasal aerosol dispenser of the utility model further includes a friction protection component, and the friction protection component includes a protection ring 201 , a rubber pad 202 and a friction groove 203 .
[0030] According to this specific embodiment, the protective ring 201 is detachably connected to the hand-held tube 103 and is located on the outer surface of the hand-held tube 103. The rubber pad 202 is detachably connected to the protective ring 201 and is located on the side of the protective ring 201 away from the hand-held tube 103. The friction groove 203 is fixedly connected to the rubber pad 202 and is located on the rubber pad 202. The rubber pad 202 is detachably connected and is located inside the rubber pad 202. The protective ring 201 is the main component for necessary protection of the hand-held tube 103, and the rubber pad 202 is the main component for facilitating children to hold and grasp, and the friction groove 203 is the main component that will increase the friction of the rubber pad 202.
[0031] The above disclosure is only a preferred embodiment of the present invention, and certainly cannot be used to limit the scope of rights of the present invention. Ordinary technicians in this field can understand that all or part of the processes of the above embodiment and equivalent changes made according to the claims of the present invention still fall within the scope covered by the utility model.
Claims
1. An oral and nasal aerosol dispenser, comprising a connecting ring and a connecting tube, wherein the connecting tube is detachably connected to the connecting ring and is located below the connecting ring, characterized in that: It also includes an oral fixed medication component, which includes a hand-held tube, a pressurization chamber, an air outlet, a fixing ring and a positioning hole, an extension tube, an oral rod, a leak-proof sleeve and an air outlet. The hand-held tube is detachably connected to the connecting tube and is located at one end of the connecting tube away from the connecting ring. The pressurization chamber is fixedly connected to the hand-held tube and is located inside the hand-held tube. The air outlet is detachably connected to the hand-held tube and is located at one end of the hand-held tube away from the connecting tube. The fixing ring is detachably connected to the air outlet and is located on the outer surface of the air outlet. The positioning hole is detachably connected to the fixing ring and is located inside the fixing ring. The extension tube is detachably connected to the air outlet and is located at one end of the air outlet away from the hand-held tube, and the extension tube is arranged inside the fixing ring. The oral rod is detachably connected to the extension tube and is located inside the extension tube. The leak-proof sleeve is detachably connected to the extension tube and is located at one end of the extension tube away from the air outlet. The air outlet is fixedly connected to the oral rod and is located inside the oral rod.
2. The oral and nasal aerosol dispenser according to claim 1, characterized in that: The oral and nasal aerosol dispenser also includes a friction protection component, which includes a protection ring, a rubber pad and a friction groove. The protection ring is detachably connected to the hand-held tube and is located on the outer surface of the hand-held tube. The rubber pad is detachably connected to the protection ring and is located on a side of the protection ring away from the hand-held tube. The friction groove is fixedly connected to the rubber pad and is detachably connected to the rubber pad and is located inside the rubber pad.