阅读说明：本技术 一种干粉吸入器 (Dry powder inhaler ) 是由 崔岩 单彬彬 于 2021-08-18 设计创作，主要内容包括：本发明公开了一种干粉吸入器,属于医药技术领域,包括分离式药物贮存室、颗粒旋转碰撞室、对称气流入口管道部件、网筛部件以及口含气流出口部件,其中所述可分离式药物贮存室可以实现快速供药；药物颗粒在所述颗粒旋转碰撞室中分离；所述对称气流入口管道部件作为空气进入的通道；药物颗粒通过所述网筛部件,最终经由所述口含气流出口部件进入人体呼吸道。干粉吸入器在采用该内部流动区域后,可显著提高药物颗粒从载体颗粒表面分离的效率,并能有效的将大多数载体颗粒保留在干粉吸入器内,进而可极大地提升用户的使用体验。(The invention discloses a dry powder inhaler, which belongs to the technical field of medicines and comprises a separated medicine storage chamber, a particle rotation collision chamber, a symmetrical airflow inlet pipeline component, a mesh screen component and an oral airflow outlet component, wherein the separated medicine storage chamber can realize quick medicine supply; the drug particles are separated in the particle rotating collision chamber; the symmetrical air flow inlet duct part serves as a passage for air to enter; the medicament particles pass through the mesh screen component and finally enter the respiratory tract of the human body through the buccal airflow outlet component. After the dry powder inhaler adopts the internal flow area, the efficiency of separating the drug particles from the surface of the carrier particles can be obviously improved, most of the carrier particles can be effectively retained in the dry powder inhaler, and the use experience of a user can be greatly improved.)

1. A dry powder inhaler, characterized by comprising a separate drug storage chamber (1), a particle rotation collision chamber (2), an airflow inlet pipe (3), a mesh screen (4) and a buccal airflow outlet pipe (5);

a first opening is arranged above the particle rotating collision chamber (2), and a second opening is arranged below the particle rotating collision chamber; the buccal airflow outlet pipe (5) is assembled at the upper part of the particle rotating collision chamber (2) through the first opening, and the separated medicine storage chamber is assembled at the bottom of the particle rotating collision chamber (2) through the second opening; the mesh screen piece (4) is arranged at the first opening; the airflow inlet pipe fittings (3) are symmetrically arranged on the side wall of the particle rotating collision chamber (2) and are communicated with the particle rotating collision chamber (2);

the wall surface of the particle rotating collision chamber (2) has an inclination angle, and the section of the particle rotating collision chamber (2) in the vertical direction is an isosceles trapezoid;

when the user passes through when inhaling the medicine of dosing in sucking air flow outlet pipe (5), the air is followed air current inflow mouth pipe fitting (3) gets into, drives numerous granule aggregates from disconnect-type medicine storage chamber (1) rises to rotatory collision room (2) of granule, and the granule aggregate is in under the effect of fluid stress rotatory collision room (2) rotary motion of granule to with the inhaler internal face and take place reciprocating collision, thereby realize the separation between medicine granule and the carrier particle in the granule aggregate, the medicine granule after the separation passes through mesh screen spare (4), finally the warp inhale air flow outlet pipe (5) and get into human respiratory track.

2. A dry powder inhaler according to claim 1, characterized in that the angle between the side wall surface and the bottom surface of the particle rotating collision chamber (2) is in the range of 45 ° to 89 °.

3. A dry powder inhaler according to claim 1, characterized in that the wall surface of the air flow inlet fitting (3) is tangential to the side wall surface of the particle rotating collision chamber (2).

4. A dry powder inhaler according to claim 3, characterized in that the two air flow inlet fittings (3) are arranged symmetrically opposite to the center of the particle rotating collision chamber (2).

5. A dry powder inhaler according to claim 1, characterized in that the buccal airflow outlet tube (5) comprises a first tube segment and a second tube segment; the second pipe section is of an L-shaped structure, and the mouth of the first pipe section has a downward inclined angle.

6. A dry powder inhaler according to claim 5, wherein the downward angle of inclination is from-45 ° to 0 °.

7. A dry powder inhaler according to claim 1, wherein the separate medicament storage compartment (1) is a blister pack of medicament, engaging the bottom of the particle rotating collision chamber (2).

Technical Field

The invention belongs to the technical field of medicines, and particularly relates to a dry powder inhaler.

Background

In the treatment of respiratory diseases such as chronic obstructive pulmonary disease, asthma and local infection of the lung, Dry Powder Inhalers (DPI) have advantages of high drug dose carrying capacity, high drug stability, low bio-contamination, small volume, no need for the user to breathe in cooperation and the like compared with liquid-based nebulizers, and thus have high competitiveness in the market.

The drug particles (1-5 microns, also called Active Pharmaceutical Ingredient, API particles) used in the dry powder inhaler are usually attached to the surface of larger carrier particles (50-500 microns, mostly lactose) to form a particle aggregate (as shown in fig. 4), and the surface modification of the carrier particles can effectively reduce the adhesion between the drug particles and the carrier particles. The working principle is that by means of the design of the internal flow area of the inhaler, the particle polymer can realize the separation of the drug particles from the surface of the carrier particles in the inhaler under the combined action of fluid stress and wall collision, and then enter the respiratory tract of a human body, thereby achieving the treatment effect.

The excellence of the performance of the dry powder inhaler is mainly reflected in the efficiency of the separation of the drug particles from the surface of the carrier particles, and the appearance may vary greatly since the key to the efficiency of the drug separation of the dry powder inhaler is the design of the internal flow area thereof, so the patent focuses on the design of the internal flow area of the dry powder inhaler.

To be provided withFor example, the internal flow area design of current commercial dry powder inhalers is generally shown in fig. 1 and includes: the device comprises a medicine storage chamber (I), a particle rotating collision chamber (II), an airflow inlet pipe fitting (III), a mesh screen fitting (IV) and a buccal airflow outlet pipe (V). The main characteristics of each part are as follows: in the drug reservoir (I), the user has to manually load and unload the capsule and manually puncture the capsule with a probe, exposing the particulate aggregates to the flow area inside the inhaler; the wall surface of the particle rotating collision chamber (II) is vertical to the bottom surface; the section of the air inlet pipe fitting (III) is rectangular; the end of the buccal airflow outlet pipe (V) is vertical to the gravity direction when the buccal airflow outlet pipe is used by a user.

There are three major problems with current dry powder inhalers:

1. when in use, a user needs to put the capsule into the capsule, puncture the capsule and take out the capsule after inhaling. After being separated from the carrier particles, the medicine particles and the carrier particles enter the respiratory tract of a human body together, and are deposited in the oral cavity of the human body under the action of inertia due to the large carrier particles, so that a user needs to spit the medicine particles in a spitting mode after inhaling the medicine particles. In addition, because the carrier particles mostly use lactose, the carrier particles can pose a safety threat to diabetic users after entering human bodies. The above inconvenience of use and security risks constitute a significant negative impact on the user experience.

2. At present, the separation efficiency of medicine particles from the surface of carrier particles of a dry powder inhaler is low and is only 10-30%, and the fundamental reason is that the retention time of particle aggregates in the dry powder inhaler is short (about 0.1 second), and the collision between the particle aggregates and the wall surface is insufficient. Drug particles are very expensive and low drug separation efficiency can dramatically increase the medical costs to the user.

3. Because of the angle between the mouth and the airway, dry powder inhalers are recommended for use in which the user raises his head to hold the mouthpiece airflow outlet tube (V) for inhalation. The user has difficulty in mastering the correct using mode, and needs to be trained before using, so that the time and the training cost are increased. The user will often experience deviations when using the device at a later date, and the doctor has no opportunity to correct the deviations due to the difficulty of medical follow-up.

Therefore, there is a need for a dry powder inhaler with high drug separation efficiency, good user experience, and automatic error correction.

Disclosure of Invention

In view of the above drawbacks and needs of the prior art, the present invention provides a dry powder inhaler, which aims to optimize the structural design of the internal flow area of the dry powder inhaler, thereby solving the technical problems of low drug separation efficiency of the dry powder inhaler, poor user experience, and the like.

The technical principle is as follows:

1. the movement of the particle polymer in the flow field in the dry powder inhaler is a small-angle spiral rising trend in the particle rotating collision chamber, and the particle polymer continuously collides with the wall surface in the movement process, and the drug particles are separated from the surface of the carrier particles under the action of inertia force. Therefore, if the wall surface and the bottom surface in the particle rotating collision chamber are kept at an inclined angle (see fig. 6), the rebound angle of the particle aggregate can be effectively controlled to be swirled but not to rise in the particle rotating collision chamber. The principle can effectively increase the retention time of the particle aggregate in the dry powder inhaler, greatly improve the collision frequency of the particle aggregate and the wall surface, and further effectively improve the medicine separation efficiency in the dry powder inhaler.

2. However, the angle between the wall surface and the bottom surface in the rotating collision chamber of the particles cannot be infinitely reduced. Because this angle results in a narrowing of the cross-section above the particle spinning collision chamber, the cross-sectional area above the particle spinning collision chamber is smaller according to the equation of continuity in fluid mechanics, and therefore the flow velocity is greater. Also, according to bernoulli's equation, the pressure above it is relatively small compared to below, and the high pressure region pushes the particles toward the low pressure region, rather forcing the particle aggregates to rapidly exit the dry powder inhaler under the influence of fluid stress. This principle is contrary to the above principle, so that the most appropriate angle needs to be calculated by computational fluid dynamics according to the synthesis method of the drug particles and the material properties of the particles, thereby achieving the effect of improving the drug separation efficiency.

3. The size of the drug particles is only 1-5 microns, so the drug particles with the size can be attached to a streamline under the action of a flow field, and can quickly leave the inhaler along the streamline after being separated from carrier particles; and because the carrier particles are large in size (50-500 microns), the carrier particles can be separated from a streamline under the influence of inertia force and continuously collide with the inclined wall surface of the particle rotating collision chamber, and can be effectively retained in the dry powder inhaler without entering the oral cavity of a person.

4. Because of the inclined wall design of the particle rotating collision chamber, the airflow inlet pipe member needs to be tangential to the particle rotating collision chamber, otherwise the airflow inlet pipe member can cause disturbance to the rotation of the particle aggregates in the particle rotating collision chamber, so that the cross section of the airflow inlet pipe member is a quadrangle which is tangential to the particle rotating collision chamber and has a corresponding inclined angle, rather than a rectangle which is used by the existing dry powder inhaler. In addition, the airflow inlet pipe needs to adopt two symmetrical inlet designs, otherwise a stable flow field cannot be generated.

5. The buccal airflow outlet pipe has strong correlation with the head elevation angle of a user when the user uses the inhaler, and the design of the buccal airflow outlet pipe which is inclined downwards is adopted, so that the user can naturally lean the head up to use when the inhaler is used. The correct inhalation mode can be effectively guided to the user by the design. The specific angle at which the buccal airflow outlet tube slopes downward is dependent on the age and gender of the user.

6. The blister type medicine is adopted as a part of the internal flow area of the dry powder inhaler, only one action of peeling is needed by a user, actions of placing a capsule, puncturing the capsule, removing the capsule after inhalation and the like are not needed like the traditional dry powder inhaler, and the use experience of the user can be effectively improved.

To achieve the above objects, according to one aspect of the present invention, there is provided a dry powder inhaler comprising a separate medicine storage chamber, a particle rotation collision chamber, an airflow inlet pipe member, a mesh screen member, and a mouth airflow outlet pipe;

a first opening is arranged above the particle rotating collision chamber, and a second opening is arranged below the particle rotating collision chamber; the buccal airflow outlet pipe is assembled at the upper part of the particle rotating collision chamber through the first opening, and the separated medicine storage chamber is assembled at the bottom of the particle rotating collision chamber through the second opening; the mesh screen piece is arranged at the first opening; the airflow inlet pipe fittings are symmetrically arranged on the side wall of the particle rotating collision chamber and are communicated with the particle rotating collision chamber;

the wall surface of the particle rotating collision chamber is provided with an inclination angle, and the section of the particle rotating collision chamber in the vertical direction is an isosceles trapezoid;

when a user inhales and administers the medicine through the buccal airflow outlet pipe, air enters from the airflow inlet pipe to drive a plurality of particle polymers to ascend from the separated medicine storage chamber to the particle rotating collision chamber, the particle polymers rotate in the particle rotating collision chamber under the action of fluid stress and collide with the inner wall surface of the inhaler in a reciprocating mode, so that the separation between the medicine particles in the particle polymers and the carrier particles is achieved, the separated medicine particles penetrate through the mesh screen piece, and finally enter the respiratory tract of the human body through the buccal airflow outlet pipe.

Preferably, the included angle between the side wall surface and the bottom surface of the particle rotating collision chamber ranges from 45 degrees to 89 degrees.

Preferably, the wall surface of the airflow inlet pipe is tangent to the side wall surface of the particle rotating collision chamber.

Preferably, two of said gas flow inlet pipes are arranged in reverse symmetry with respect to the centre of said particle rotating collision cell.

Preferably, the buccal gas flow outlet tube comprises a first tube segment and a second tube segment; the second pipe section is of an L-shaped structure, and the mouth of the first pipe section has a downward inclined angle.

Preferably, the downward inclination angle is-45 ° to 0 °.

Preferably, the separated medicine storage chamber is a blister package of medicines, is attached to the bottom of the particle rotating collision chamber, and belongs to a part of the internal flow area of the dry powder inhaler.

In general, compared with the prior art, the above technical solution contemplated by the present invention can achieve the following beneficial effects:

1. the dry powder inhaler provided by the invention adopts the particle rotating collision chamber with the wall surface with the inclination angle and the two airflow inlet pipe fittings tangent to the particle rotating collision chamber, and the particle polymer can continuously rotate in the particle rotating collision chamber and collide with the wall surface due to the inclination angle of the wall surface, so that the collision frequency of the wall surface can be greatly improved, and the separation efficiency of the medicine particles from the carrier particles is effectively improved. Smaller sized drug particles will follow streamlines and exit the dry powder inhaler and enter the body, producing a therapeutic effect. In addition, because the carrier granule receives the rotatory impact chamber's of the granule of inclination wall influence, can be incessantly at the rotatory indoor spiral of granule impact to avoided the carrier granule (great lactose granule promptly) to get into human respiratory track, promotion user's that can be very big use is experienced, and can be applicable to the user that has blood sugar diseases such as diabetes.

2. The buccal airflow outlet pipe adopted by the dry powder inhaler provided by the invention is of a front-section bent structure and a rear-section L-shaped structure, so that a user can actively adopt a correct inhalation posture in the using process of the inhaler, the deposition of inhaled medicines at the throat is effectively avoided, and the inhalation administration efficiency can be effectively improved.

3. The dry powder inhalation proposed by the present invention removes the drug reservoir of a conventional dry powder inhaler and uses a blister type drug with a blister shell as part of the internal flow area of the dry powder inhaler, reducing the three actions required for using a conventional dry powder inhaler to one action of peeling, thereby improving the user experience.

Drawings

FIG. 1 is a schematic diagram of a prior art dry powder inhaler;

FIG. 2 is a schematic diagram of the structure of the dry powder inhaler of the present invention;

FIG. 3 is a schematic view of the dry powder inhaler of the present invention during use;

FIG. 4 is a schematic diagram of the structure of a particulate polymer body used in the dry powder inhaler of the present invention;

FIG. 5 is a schematic diagram of the structure of the separate drug reservoir of the dry powder inhaler of the present invention;

FIG. 6 is a cross-sectional view of a particle rotating collision cell of the dry powder inhaler of the present invention;

FIG. 7 is a schematic diagram of the construction of the mesh of the dry powder inhaler of the present invention;

FIG. 8 is a schematic diagram of the structure of the buccal airflow outlet tube of the dry powder inhaler of the present invention;

figure 9 is a graph comparing the number of particle agglomeration collisions with the data for particle agglomeration residence time for the present invention and prior art inhalers.

The same reference numbers will be used throughout the drawings to refer to the same or like elements or structures, wherein: 1-a separate drug reservoir; 2-a particle rotating collision chamber; 3-an air flow inlet fitting; 4-a mesh screen; 5-buccal airflow exit tube.

Detailed Description

In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention is described in further detail below with reference to the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention. In addition, the technical features involved in the embodiments of the present invention described below may be combined with each other as long as they do not conflict with each other.

Referring to fig. 2, the present invention provides a dry powder inhaler, which comprises a separated drug storage chamber 1, a particle rotation collision chamber 2, an airflow inlet pipe 3, a mesh screen 4 and a buccal airflow outlet pipe 5. Specifically, a first opening is arranged above the particle rotating collision chamber 2, and a second opening is arranged below the particle rotating collision chamber; the buccal airflow outlet pipe 5 is assembled at the upper part of the particle rotating collision chamber 2 through the first opening, and the separated medicine storage chamber is assembled at the bottom of the particle rotating collision chamber 2 through the second opening; the mesh screen 4 is arranged at the first opening; the airflow inlet pipe fittings 3 are symmetrically arranged on the side wall of the particle rotating collision chamber 2 and are communicated with the particle rotating collision chamber 2.

Before using the dry powder inhaler, the separate drug reservoir 1, i.e. the blister pack of the drug, will hold a dose of particulate aggregates and accumulate at the bottom due to gravity; the airflow inlet pipe fittings 3 are respectively in tangential symmetry distribution with the particle rotation collision chamber 2 and are communicated with the atmosphere, so that the pressure at the tail ends of the two inlets is one atmospheric pressure, when a user uses the dry powder inhaler, negative pressure is applied to the tail end of the buccal airflow outlet pipe 5 through inhalation action, in this case, the particle polymer can be in rotation collision in the particle rotation collision chamber 2, under the combined action of fluid stress and wall collision, the separation of drug particles from the surfaces of carrier particles is realized, and because the wall surface of the particle rotation collision chamber 2 has an inclined angle, the carrier particles can continuously rotate in the particle rotation collision chamber and collide with the wall surface, and finally stay in the rotation chamber, so that the drug particles are prevented from entering the oral cavity of a person, and under the action of fluid stress, the drug particles pass through the mesh screen fittings 4 along a streamline, finally enters the respiratory tract of the human body through the buccal airflow outlet pipe 5, and the specific process is shown in figure 3.

As shown in FIG. 4, the particle aggregate used in the present invention is composed of carrier particles and drug particles on the surface thereof.

To be further described, the separate medicament storage chamber 1, i.e. the blister pack of the medicament, only needs to take one action of peeling off during use, instead of three actions required by the conventional dry powder inhaler, as shown in fig. 5, so that the efficiency of changing the medicament is improved, the use by the user is more convenient, and the use experience of the user is improved.

To be more specific, the particle rotating collision chamber 2 has a wall surface with an inclined angle, so that after the inhalation action of the user, the particle aggregates enter the particle rotating collision chamber 2 under the action of the fluid stress to collide with the wall surface, and the wall surface with the inclined angle can effectively control the rebound angle of the particle aggregates to make the particle aggregates circle in the particle rotating collision chamber 2 but not rise, so that the particle aggregates continuously collide with the wall surface of the particle rotating collision chamber 2, thereby effectively increasing the retention time of the particle aggregates in the dry powder inhaler, greatly increasing the collision frequency of the particle aggregates with the wall surface, and further effectively improving the separation efficiency of the drug particles from the carrier particles in the dry powder inhaler under the combined action of the fluid stress and the wall surface collision. The section of the particle rotating collision chamber 2 in the vertical direction is isosceles trapezoid.

As shown in fig. 6, as a preferred embodiment of the present invention, the angle range of the included angle between the isosceles trapezoid waist and the long base is 45 ° to 89 °.

To explain further, the airflow inlet pipe 3 is tangent to the wall of the particle rotation collision chamber 2, so as to avoid disturbance to the rotation of particle aggregates in the particle rotation collision chamber 2, and therefore, the cross section of the airflow inlet pipe 3 is a quadrilateral tangent to the particle rotation collision chamber 2 and having a corresponding inclination angle, and the two airflow inlet pipes are in reverse symmetry with respect to the center of the particle rotation collision chamber 2, and the tangent position is not fixed, so that when a user inhales drug particles through the airflow outlet pipe 5, the symmetrical airflow inlet is more beneficial to the generation of stable flow, thereby enabling the particles to rotate in the symmetrical flow field in the particle rotation collision chamber 2, increasing the collision time, and thus being beneficial to the improvement of the separation efficiency of the drug particles.

Furthermore, as shown in fig. 8, the buccal airflow outlet pipe 5 has a structure with a curved front section and an L-shaped rear section, so that a user can actively adopt a correct inhalation posture during the use of the inhaler, the deposition of inhaled medicine on the throat is effectively avoided, and the inhalation administration efficiency can be effectively improved.

As a preferred embodiment of the present invention, the front section of the buccal airflow outlet pipe 5 is inclined downwards in a negative direction compared with the horizontal part of the rear section, and the included angle of the front section of the buccal airflow outlet pipe 5 ranges from-45 ° to 0 °.

In order to make the excellent performance of the internal flow area structure of the dry powder inhaler according to the present invention more clear, the technical solution of the present invention is further illustrated by the following specific examples.

Referring to fig. 1 to 8, the inclined angle of the wall surface of the particle rotating collision chamber 2 is 85 °, the included angle between the front section and the horizontal section of the rear section of the buccal airflow outlet pipe 5 is-20 °, and the diameter of the particle aggregate is 104.9 μm. The movement of 2000 particle aggregates in the internal flow region of the dry powder inhaler was simulated by computational fluid dynamics in 0.5 second and the average number of collisions of the particle aggregates with the wall of the particle rotating collision cell 2 and the average residence time in the dry powder inhaler were recorded and compared withIn contrast, the average number of particle aggregates collided with by the dry powder inhaler was from 4 kPa52.22 lifts to 273.34 lifts, the average residence time of the particle aggregates is fromThe 0.084 second rise to 0.4989 seconds, which is close to the total inhalation time of 0.5 seconds. It can be seen that the dry powder inhaler using the internal flow region structure of the present invention has a larger improvement in key parameters affecting the drug separation efficiency than the current commercial dry powder inhalers, and can significantly improve the separation efficiency of drug particles, as shown in fig. 9 (the dry powder inhaler using the internal flow region structure of the present invention is annotated as a self-grinding DPI).

It will be understood by those skilled in the art that the foregoing is only a preferred embodiment of the present invention, and is not intended to limit the invention, and that any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the scope of the present invention.