Micro-emulsion medicament spray head
By designing a microemulsion spray head including a sealing cap, a positioning shell and a bottle body, using the hand-pinching airbag booster and ball valve body control, the problems of uneven flow and fatigue during the delivery of the microemulsion spray head in the prior art are solved, and a more stable and convenient drug delivery operation is achieved.
Patent Information
- Application Number
- CN202421031078.5
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-05-13
- Publication Date
- 2025-03-04
- Estimated Expiration
- 2034-05-13
AI Technical Summary
The existing microemulsion spray heads need to be repeatedly pressed during the administration process, resulting in uneven flow during the spraying of the liquid, which may cause the spraying of the liquid to be interrupted or overflowed, and the operator is prone to feel hand fatigue, affecting the comfort and accuracy of the operation.
A microemulsion spray head is designed, including a sealing cap, a positioning shell and a medicine bottle body. A funnel-shaped partition is provided on the inside of the sealing cap, and a ball valve body and a diaphragm body are provided in the positioning shell. By pinching the airbag to boost the body of the medicine bottle by hand, the ball valve body is turned to realize the injection and administration of medicine liquid.
It realizes simpler, continuous and stable spraying and drug delivery operations of microemulsion agents, reduces waste of medicine and improves user's operation convenience and safety.
Smart Images

Figure CN222549881U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of microemulsion drug administration, in particular to a microemulsion drug spray head. Background Art
[0002] Microemulsion spray nozzle is a device or apparatus for spraying or spraying microemulsion. Microemulsion is a micellar system composed of oil phase and water phase, with small particle size and high stability, and has broad application prospects in drug delivery and application.
[0003] Compared with conventional nozzles, microemulsion nozzles have the following differences: microemulsion nozzles can more accurately control the injection volume and spray range of the drug solution, as well as parameters such as injection speed and flow rate. This precise control helps to achieve personalized and accurate drug delivery in drug treatment; because microemulsion nozzles can produce fine droplet sizes, they can improve the injection efficiency of drugs. Smaller droplet sizes are conducive to the uniform distribution of drugs in local areas, improving drug absorption and utilization efficiency; microemulsion nozzles can help maintain the stability of microemulsion drugs and reduce the decomposition and inactivation of drugs during injection. Microemulsion drugs usually have a long shelf life and can maintain the stability of their chemical and physical properties before injection; microemulsion nozzles are usually used for local drug delivery, such as skin, eyes, nasal cavity, etc. They can be widely used in the fields of skin disease treatment, ophthalmic medication, nasal administration, etc. In short, compared with conventional nozzles, microemulsion nozzles have higher accuracy, efficiency and stability in drug delivery, can meet some specific drug delivery needs, and have broad application prospects in related fields.
[0004] However, when administering the drug, the conventional microemulsion drug nozzle needs to extract the drug liquid by pressing, so as to spray the drug. However, in order to adapt to the microemulsion drug, the microemulsion drug nozzles currently used mostly use a thin film channel to spray the drug. In this process, the drug liquid is pressed against the film under the action of an external force. When the pressure on the film reaches a critical point, the drug passes through the thin film channel to form droplets and sprays out. In this process, the operator needs to press repeatedly continuously, and it is difficult to ensure that the force of each press is consistent, resulting in uneven flow during the drug liquid spraying process, and may even cause the drug liquid spraying to be interrupted or the drug liquid to overflow. At the same time, due to the need for continuous and repeated pressing, the operator may feel hand fatigue, especially when performing a large number of spraying operations. This not only affects the comfort of the operation, but also may reduce the accuracy and stability of the operation. Utility Model Content
[0005] The purpose of the utility model is to provide a microemulsion medicine spray head, which can effectively solve the problems in the background technology.
[0006] To achieve the above-mentioned purpose, the utility model provides the following technical solutions: a microemulsion medicine spray head, comprising a sealing cover, a positioning shell and a medicine bottle body, a partition is provided on the inner side of the sealing cover, and the partition adopts a funnel-shaped structure design, a positioning shell is threadedly installed on the upper inner side of the sealing cover, a ball valve body is movably inserted in the positioning shell, an external thread is provided at the lower part of the outer wall of the positioning shell and is threadedly connected to the top inner side of the sealing cover, a diaphragm body is movably installed on the inner side of the positioning shell at the top of the ball valve body, a limiting tube is fixedly installed in the middle of the top of the diaphragm body, and a film channel is provided on the diaphragm body inside the limiting tube.
[0007] Preferably, an external thread is provided below the inner wall of the sealing cover and the thread is installed on the top of the medicine bottle body.
[0008] Preferably, a first sealing ring is embedded in the top of the medicine bottle body, and the upper end surface of the first sealing ring on the top of the medicine bottle body contacts the outer side of the lower surface of the partition but is not fixedly connected. A hand-pinch airbag is fixedly installed on the outer side of the medicine bottle body, and the air outlet end on the top of the hand-pinch airbag is connected to the medicine bottle body.
[0009] Preferably, the top of the positioning shell is opened and connected to a connecting pipe, a second sealing ring is embedded in the top of the connecting pipe, and a limiting groove is opened below the outer wall of the positioning shell, and the width of the limiting groove matches the valve stem diameter on the ball valve body.
[0010] Preferably, the lower part of the outer wall of the ball valve body is in contact with the inner side of the partition but not fixedly connected, the bottom end of the ball valve body passes through the partition and is provided with an installation groove and embedded with a third sealing ring, the third sealing ring is in contact with the bottom of the partition but not fixedly connected, the bottom of the ball valve body adopts a conical structure design and is connected and installed with a liquid extraction tube, the liquid extraction tube extends into the interior of the medicine bottle body and does not contact the inner bottom of the medicine bottle body.
[0011] Preferably, the upper and lower ends of the diaphragm body are grooved and embedded with a third sealing ring, the third sealing ring on the upper end surface of the diaphragm body contacts but is not fixedly connected to the top of the inner wall of the positioning shell, and the third sealing ring on the lower end surface of the diaphragm body contacts but is not fixedly connected to the top of the ball valve body.
[0012] Preferably, the top of the limiting tube passes through an opening at the top of the positioning shell, and the limiting tube and the diaphragm body adopt an integrally formed structure design.
[0013] Compared with the prior art, the beneficial effects of the utility model are as follows:
[0014] The utility model is operated by an operator with only one hand, which is simpler than repeated pressing operation. The operator only needs to squeeze the air bag in advance to pump air into the medicine bottle body to increase pressure, and then the ball valve body can be rotated in the subsequent operation to realize the spraying and administration of the medicine liquid, avoiding the problem of intermittent spraying of the medicine during repeated pressing operation. At the same time, under the action of high pressure, the microemulsion medicine can be discharged quickly and stably through the thin film channel on the diaphragm body, thereby improving the stability and uniformity of the spraying. Since the spraying and administration of the medicine liquid are realized by controlling the valve stem of the ball valve body The flow rate and injection volume of the medicine liquid can be better controlled, and the overflow and waste of the medicine liquid can be reduced. The operator can directly hold the inverted medicine bottle body, and thus accurately position the medicine liquid to the patient's medication position through the connecting tube, making the medication operation more precise and controllable, and improving the safety and comfort of the user. In short, the utility model places the diaphragm body in the positioning shell, and combines the design of the positioning shell, the ball valve body and the sealing cover to achieve a simpler, continuous and stable microemulsion medicine injection and medication operation, while reducing the waste of medicine liquid and improving the user's operating convenience and safety. BRIEF DESCRIPTION OF THE DRAWINGS
[0015] Figure 1 This is a schematic diagram of the main structure of the utility model;
[0016] Figure 2 It is a schematic diagram of the cross-sectional structure of the utility model;
[0017] Figure 3 For the utility model Figure 2 The structural diagram of the enlarged part in the middle;
[0018] Figure 4 This is a schematic diagram of the diaphragm body structure of the utility model;
[0019] Figure 5 This is a schematic diagram of the positioning housing installation structure of the utility model:
[0020] Figure 6 This is a schematic diagram of the ball valve body structure of the utility model;
[0021] Figure 7 It is a schematic diagram of the sealing cover structure of the utility model.
[0022] In the figure: 1. hand-squeezed air bag; 2. sealing cover; 3. positioning shell; 4. connecting pipe; 5. ball valve body; 6. medicine bottle body; 7. diaphragm body; 8. liquid extraction tube; 9. first sealing ring; 10. limiting tube; 11. second sealing ring; 12. limiting groove; 13. installation groove; 14. third sealing ring; 15. partition. DETAILED DESCRIPTION
[0023] The following will be combined with the drawings in the embodiments of the utility model to clearly and completely describe the technical solutions in the embodiments of the utility model. Obviously, the described embodiments are only part of the embodiments of the utility model, not all of the embodiments. Based on the embodiments in the utility model, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the utility model. Example
[0024] like Figures 1 to 7 As shown, an embodiment provided by the utility model is: a microemulsion medicine spray head, comprising a sealing cover 2, a positioning shell 3 and a medicine bottle body 6, an outer thread is provided at the lower inner wall of the sealing cover 2 and the thread is installed at the top of the medicine bottle body 6. A partition 15 is provided on the inner side of the sealing cover 2, a first sealing ring 9 is embedded and installed at the top of the medicine bottle body 6, the upper end surface of the first sealing ring 9 at the top of the medicine bottle body 6 is in contact with the outer side of the lower surface of the partition 15 but is not fixedly connected, a hand-pinch airbag 1 is fixedly installed on the outer side of the medicine bottle body 6, and the air outlet end at the top of the hand-pinch airbag 1 is connected and installed with the medicine bottle body 6.
[0025] The partition 15 adopts a funnel-shaped structure design, and a positioning shell 3 is threadedly installed on the upper inner side of the sealing cover 2. The positioning shell 3 is movably inserted with a ball valve body 5. A hole is opened on the top of the positioning shell 3 and a connecting pipe 4 is installed in communication with it. A second sealing ring 11 is embedded on the top of the connecting pipe 4. A limiting groove 12 is opened at the bottom of the outer wall of the positioning shell 3, and the width of the limiting groove 12 matches the valve stem diameter on the ball valve body 5.
[0026] The lower part of the outer wall of the ball valve body 5 contacts the inner side of the partition 15 but is not fixedly connected. The lower end of the ball valve body 5 passes through the partition 15 and is provided with a mounting groove 13 and embedded with a third sealing ring 14. The third sealing ring 14 contacts the bottom of the partition 15 but is not fixedly connected. The bottom of the ball valve body 5 adopts a conical structure design and is connected with a liquid extraction tube 8. The liquid extraction tube 8 extends into the inside of the medicine bottle body 6 and does not contact the bottom of the inner side of the medicine bottle body 6. An external thread is provided at the lower part of the outer wall of the positioning shell 3 and is threadedly connected to the top of the inner side of the sealing cover 2. A diaphragm body 7 is movably installed inside the positioning shell 3 at the top of the ball valve body 5. The upper and lower ends of the diaphragm body 7 are grooved and embedded with a third sealing ring 14. The third sealing ring 14 on the upper end face of the diaphragm body 7 contacts the top of the inner wall of the positioning shell 3 but is not fixedly connected. The third sealing ring 14 on the lower end face of the diaphragm body 7 contacts the top of the ball valve body 5 but is not fixedly connected. A limit tube 10 is fixedly installed in the middle of the top of the diaphragm body 7, and a film channel is opened on the diaphragm body 7 inside the limit tube 10. The top of the limit tube 10 passes through the opening at the top of the positioning housing 3, and the limit tube 10 and the diaphragm body 7 adopt an integrally formed structure design.
[0027] When the utility model is used, the diaphragm body 7 is placed in the positioning housing 3, and the ball valve body 5 is inserted into the positioning housing 3 along the limiting groove 12, and the sealing cover 2 is threadedly installed on the bottom of the positioning housing 3, so that the ball valve body 5 is positioned and installed through the sealing cover 2, and then the microemulsion medicine is directly injected into the medicine bottle body 6, and the sealing cover 2 is threadedly installed on the top of the medicine bottle body 6, at this time, the ball valve body 5 is closed, and the hand-kneading airbag 1 is repeatedly squeezed to increase the pressure inside the medicine bottle body 6, at this time, the operator holds the inverted medicine bottle body 6 with one hand, and aligns the connecting tube 4 with the patient's medication position, and rotates the valve stem on the ball valve body 5 with the other hand, so as to open the ball valve body 5, and then under the high pressure inside the medicine bottle body 6, the microemulsion medicine is discharged along the liquid extraction tube 8, and under the high pressure, the microemulsion medicine passes through the thin film channel on the diaphragm body 7, so that the microemulsion medicine is discharged to the patient's medication position inside the connecting tube 4, thereby realizing the medication operation.
[0028] It is obvious to those skilled in the art that the present invention is not limited to the details of the exemplary embodiments described above, and that the present invention can be implemented in other specific forms without departing from the spirit or essential features of the present invention. Therefore, the embodiments should be regarded as exemplary and non-restrictive from any point of view, and the scope of the present invention is defined by the appended claims rather than the above description, and it is intended that all changes falling within the meaning and scope of the equivalent elements of the claims be included in the present invention. Any reference numeral in a claim should not be regarded as limiting the claim to which it relates.
Claims
1. A microemulsion medicine spray head, comprising a sealing cover (2), a positioning shell (3) and a medicine bottle body (6), characterized in that: A partition (15) is provided on the inner side of the sealing cover (2), and the partition (15) is designed with a funnel-shaped structure. A positioning housing (3) is threadedly installed on the upper inner side of the sealing cover (2), and a ball valve body (5) is movably inserted into the positioning housing (3). An external thread is provided on the lower outer wall of the positioning housing (3) and is threadedly connected to the top inner side of the sealing cover (2). A diaphragm body (7) is movably installed on the inner side of the positioning housing (3) at the top of the ball valve body (5), and a limiting tube (10) is fixedly installed in the middle of the top of the diaphragm body (7), and a film channel is provided on the diaphragm body (7) inside the limiting tube (10).
2. A microemulsion medicine spray nozzle according to claim 1, characterized in that: An external thread is provided at the lower part of the inner wall of the sealing cover (2), and the thread is mounted on the top of the medicine bottle body (6).
3. A microemulsion medicine spray nozzle according to claim 1, characterized in that: A first sealing ring (9) is embedded and installed on the top of the medicine bottle body (6); the upper end surface of the first sealing ring (9) on the top of the medicine bottle body (6) contacts the outer side of the lower surface of the partition (15) but is not fixedly connected; a hand-pinch airbag (1) is fixedly installed on the outer side of the medicine bottle body (6); and the air outlet end of the top of the hand-pinch airbag (1) is connected and installed with the medicine bottle body (6).
4. A microemulsion medicine spray nozzle according to claim 1, characterized in that: The top of the positioning housing (3) is opened and connected to a connecting pipe (4) installed thereon. A second sealing ring (11) is embedded and installed on the top of the connecting pipe (4). A limiting groove (12) is provided below the outer wall of the positioning housing (3). The width of the limiting groove (12) matches the diameter of the valve stem on the ball valve body (5).
5. A microemulsion medicine spray nozzle according to claim 1, characterized in that: The lower part of the outer wall of the ball valve body (5) contacts the inner side of the partition (15) but is not fixedly connected. The lower end of the ball valve body (5) passes through the partition (15) and is provided with a mounting groove (13) and is embedded with a third sealing ring (14). The third sealing ring (14) contacts the bottom of the partition (15) but is not fixedly connected. The bottom of the ball valve body (5) adopts a conical structure design and is connected to a liquid extraction tube (8). The liquid extraction tube (8) extends into the interior of the medicine bottle body (6) and does not contact the inner bottom of the medicine bottle body (6).
6. A microemulsion medicine spray nozzle according to claim 1, characterized in that: The diaphragm body (7) is grooved at both upper and lower ends and is embedded with a third sealing ring (14); the third sealing ring (14) on the upper end surface of the diaphragm body (7) contacts the top of the inner wall of the positioning housing (3) but is not fixedly connected; the third sealing ring (14) on the lower end surface of the diaphragm body (7) contacts the top of the ball valve body (5) but is not fixedly connected.
7. A microemulsion medicine spray nozzle according to claim 1, characterized in that: The top of the limiting tube (10) passes through an opening at the top of the positioning shell (3), and the limiting tube (10) and the diaphragm body (7) adopt an integrally formed structural design.