Disclosure of utility model
The utility model aims to solve the technical problem of providing an intelligent inhalation device which can be adjusted according to the requirement of the dosage of administration, is more accurate in administration and can realize flexible proportioning of medicines.
The utility model is realized by the following technical scheme:
The utility model provides a multi-functional repeatedly usable's intelligent inhalation device, includes the base the internally mounted of base has spouts the medicine device the inside of base is located spout the top of medicine device and be provided with mixed medicine bag, works as spout the medicine device during operation, follow mix medicine bag is interior to draw the liquid medicine the outside of base is provided with the nozzle, the nozzle intercommunication spout the medicine device the top of nozzle is installed and is connected spout the button of medicine device, after pressing the button, spout the medicine device through the nozzle outwards spout the top of mixed medicine bag is provided with three micropump in the annular of top of mixed medicine bag, the top of micropump is provided with connecting device the top of cabin is provided with the correspondence connecting device's medicine hole, through the medicine core has been filled to the medicine hole, the lower extreme butt joint connecting device the internally mounted of cabin has electric core and circuit board, the circuit board is connected the electric core, through circuit board is connected with control panel on the control panel charge the button, charge the button is connected with the electric charge pump, the electric charge control circuit board is connected with the electric charge pump.
Preferably, a light-transmitting plate corresponding to the drug core is provided at a side of the nacelle.
Preferably, the medicine core comprises a medicine tube, the upper end of the medicine tube is closed, a tube orifice is arranged at the lower end of the medicine tube, a rubber sealing film is arranged in the tube orifice, a threaded part is arranged at a position, close to the upper part, of the medicine tube, the medicine tube is in threaded connection with the medicine hole through the threaded part, after the threaded connection, the part of the medicine tube is exposed out of the cabin, and the connecting part is matched with the tube orifice.
Preferably, the portion of the cartridge exposed to the outside of the nacelle is provided with an anti-slip portion.
Preferably, the connecting device comprises a connecting terminal, an insertion hole for inserting the pipe orifice is formed in the middle of the connecting terminal, a puncture needle is arranged at the axis of the insertion hole, the puncture needle upwards punctures the rubber sealing membrane and then is inserted into the medicine pipe, and the connecting terminal is arranged at the suction position of the micropump.
The beneficial effects of the utility model are as follows:
The device can adjust the drug input quantity aiming at each independent drug core, flexibly adjust and proportion according to the actual drug delivery requirement, is more flexible to use and can meet the drug delivery requirements of different patients.
The device is administered only by pressing the button, and compared with the traditional mode of pressing the pump, the device is easier to operate and is suitable for popularization and use.
Detailed Description
All of the features disclosed in this specification, or all of the steps in a method or process disclosed, may be combined in any combination, except for mutually exclusive features and/or steps.
Any feature disclosed in this specification (including any accompanying claims, abstract and drawings), may be replaced by alternative features serving the same, equivalent or similar purpose, unless expressly stated otherwise. That is, each feature is one example only of a generic series of equivalent or similar features, unless expressly stated otherwise.
In the description of the present utility model, it should be understood that the terms "one end," "the other end," "the outer side," "the upper," "the inner side," "the horizontal," "coaxial," "the center," "the end," "the length," "the outer end," and the like indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings, merely to facilitate description of the present utility model and simplify the description, and do not indicate or imply that the device or element being referred to must have a specific orientation, be configured and operated in a specific orientation, and therefore should not be construed as limiting the present utility model.
Furthermore, in the description of the present utility model, the meaning of "plurality" means at least two, for example, two, three, etc., unless specifically defined otherwise.
In the present utility model, unless explicitly stated and limited otherwise, the terms "disposed," "coupled," "connected," "extending through," "connected," and the like are to be construed broadly, and may, for example, be fixedly connected, detachably connected, or integrated, mechanically connected, electrically connected, directly connected, or indirectly connected through an intermediate medium, or in communication between two elements or in an interaction relationship between two elements, unless explicitly stated otherwise. The specific meaning of the above terms in the present utility model can be understood by those of ordinary skill in the art according to the specific circumstances.
The multifunctional reusable intelligent inhalation device shown in fig. 1 and 2 comprises a base 1, wherein a medicine spraying device 2 is installed in the base 1, a mixed medicine bag 3 is arranged above the medicine spraying device 2 in the base 1, medicine liquid is sucked from the mixed medicine bag 3 when the medicine spraying device 2 works, a nozzle 4 is arranged on the outer side of the base 1, the nozzle 4 is communicated with the medicine spraying device 2, a button 41 connected with the medicine spraying device 2 is installed on the top of the nozzle 4, after the button 41 is pressed, the medicine spraying device 2 sprays medicine outwards through the nozzle 4, three micropumps 31 are annularly arranged on the top of the mixed medicine bag 3, a connecting device 32 is arranged on the top of the micropump 31, a cabin 5 is arranged on the top of the cabin 5, a medicine hole 51 corresponding to the connecting device is formed, a6 is formed through the medicine hole 51, the lower end of the medicine core 6 is in butt joint with the connecting device 32, a medicine core 7 is connected with an integrated circuit (not shown) through the electric control panel 73, an electric control panel is connected with the electric control panel 73, and a charge control panel is connected with the electric control panel 73, and the electric control panel is connected with the electric control panel 73.
In the above technical scheme, the medicine spraying device 2 is a combination of a medicine spraying pump and an atomizing nozzle, the medicine liquid is sucked by the medicine spraying pump, the medicine liquid is atomized and sprayed by the atomizing nozzle, and the sprayed atomized medicine liquid is sprayed outwards through the nozzle 4.
In this technical solution, the three independent micro pumps 31 are used to suck the liquid medicine in each drug core 6, the liquid medicine is mixed after being sucked into the mixed drug bag 3, the mixing ratio can be controlled by the dose adjusting button 73, and each time the dose adjusting button 73 is pressed, the micro pump 31 is used to pump 2 milliliters of liquid medicine.
Referring to fig. 1, a light-transmitting plate 551 corresponding to the core 6 is provided at a side of the nacelle 5.
The medicine core 6 is transparent, and whether the medicine amount in the medicine core 6 is sufficient can be determined through the light-transmitting plate 551.
Referring to fig. 1, 2 and 3, the drug core 6 includes a drug tube 61, an upper end of the drug tube 61 is closed, a lower end is provided with a tube orifice 62, a rubber sealing film (not shown) is disposed in the tube orifice 62, a threaded portion 63 is disposed near an upper portion of the drug tube 61, the drug tube 61 is screwed with the drug hole 51 through the threaded portion 63, after the threaded connection, a part of the drug tube 61 is exposed outside the nacelle 5, and the connecting portion 32 is matched with the tube orifice 62.
In the above technical solution, the fixing of the medicine tube 61 is realized by screwing down the thread, so that the medicine tube 61 is more tightly matched with the connecting portion 32.
Referring to fig. 3, the portion of the cartridge exposed to the outside of the nacelle is provided with an anti-slip portion 661.
The anti-slip portion 661 is provided to facilitate the application of rotational torque.
Referring to fig. 3 and 4, the connection device 32 includes a connection terminal 321, an insertion hole 322 for inserting into the orifice is provided in the middle of the connection terminal 321, a puncture needle 323 is provided at the axial center of the insertion hole 322, the puncture needle 323 pierces the rubber sealing film upwards and then is inserted into the medicine tube 61, and the connection terminal is mounted at the suction position of the micro pump.
In the above technical scheme, the design of the puncture needle 323 is adopted, so that the medicine can be taken after penetrating through the rubber sealing film, the tightness during medicine taking is improved, and leakage is avoided.
The foregoing is merely illustrative of specific embodiments of the present utility model, and the scope of the utility model is not limited thereto, but any changes or substitutions that do not undergo the inventive effort should be construed as falling within the scope of the present utility model. Therefore, the protection scope of the present utility model should be subject to the protection scope defined by the claims.