MICRONEEDLE ASSEMBLY

Abstract

The microneedle assembly of the present invention includes: a main body (110) opened at one side thereof and including a solution reservoir (111) formed in the opened side thereof; a dispensing unit (120) disposed at the other side of the main body (110) in such a manner as to fluidically communicate with the solution reservoir (111); a needle supports (130) positioned at a front portion of each of the dispensing units (120), and protrudingly formed at the other end of the main body (110); a microneedles (140) engaged with the front end of the needle support (130); and a first solution release flow channel (150) formed to penetrate through a portion extending outwardly from a front end of the dispensing unit (120) to the front end of the needle support (130).

Claims

1. A microneedle assembly comprising: a main body (110) opened at one side thereof, and including a solution reservoir (111) formed in the opened side thereof to allow a functional solution to be contained therein; a dispensing unit (120) disposed at the other side of the main body (110), which is a front side of the solution reservoir (111), in such a manner as to fluidically communicate with the solution reservoir (111), wherein the dispensing unit (120) is provided in plural numbers in such a manner as to be disposed at a central portion and a peripheral portion of the main body 110 so as to be circumferentially arranged spaced apart from each other at equal radial angles so that the dispensing unit (120) dispense the functional solution contained in the solution reservoir (111); a needle supports (130) positioned at a front portion of each of the dispensing units (120), and protrudingly formed at the other end of the main body (110) so that when the needle support (130) comes into close contact with the skin, a front end thereof presses the subcutaneous fat of the skin; a microneedles (140) engaged with the front end of the needle support (130) so that when the microneedle (140) comes into close contact with the skin, it is inserted into the skin; and a first solution release flow channel (150) formed to penetrate through a portion extending outwardly from a front end of the dispensing unit (120) to the front end of the needle support (130), and configured to allow the functional solution received in the dispensing unit (120) to be delivered to the front end of the needle support (130) therethrough so that the delivered functional solution is released to the skin tissue from the front end of the needle support (130) therethrogh via a gap formed between an outer circumference of the microneedle 140 and the skin along the microneedle (140).

2. The microneedle assembly according to claim 1, wherein the first solution release flow channel (150) is formed extending obliquely from the front end of the dispensing unit (120) to an outer circumferential portion of the front end of the needle support (130).

3. The microneedle assembly according to claim 1, wherein the microneedle (140) may be formed in a conical shape and has a hollow flow channel (141) formed therein to penetrate vertically therethrough, and the needle support (130) further comprises a second solution release flow channel (131) formed therein so as to fluidically communicate with the hollow flow channel (141) of the microneedle (140) to allow the functional solution to be delivered to the skin therefrom through the hollow flow channel (141) of the microneedle (140).

4. The microneedle assembly according to claim 3, further comprising a guide (160) engaged with the outer circumference of the main body and having a height that is lower than a front end of the microneedle (140) and higher than a front end of the main body (110), the guide being configured to support the main body 110 to ensure that the microneedle 140 is stably inserted into the skin.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0029] The above and other objects, features and advantages of the present invention will be apparent from the following detailed description of the preferred embodiments of the invention when taken in conjunction with the accompanying drawings, in which:

[0030] FIGS. 1 and 2 are cross-sectional and top perspective views showing a conventional microneedle according to the prior art;

[0031] FIG. 3 is a perspective views showing a microneedle assembly according to the present invention;

[0032] FIG. 4 is an exploded perspective view showing a microneedle assembly according to the present invention; and

[0033] FIGS. 5 and 6 are cross-sectional views showing a microneedle assembly according to the present invention.

DESCRIPTION OF REFERENCE NUMERALS

[0034] 110: main body

[0035] 111: solution reservoir

[0036] 112: protrusion

[0037] 120: dispensing unit

[0038] 130: needle support

[0039] 131: second solution release flow channel

[0040] 140: microneedle

[0041] 141: hollow flow channel

[0042] 150: first solution release flow channel

[0043] 160: guide

[0044] 161: grooved recess

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0045] Hereinafter, a monoblock brake caliper and manufacturing method thereof according to the present invention will be described in detail with reference to the accompanying drawings.

[0046] FIG. 3 is a perspective views showing a microneedle assembly according to the present invention, FIG. 4 is an exploded perspective view showing a microneedle assembly according to the present invention, and FIGS. 5 and 6 are cross-sectional views showing a microneedle assembly according to the present invention.

[0047] The microneedle assembly according to the present invention includes a main body 110; a dispensing unit 120; a needle support 130; a microneedle 140; and a first solution release flow channel 150.

[0048] The main body 110 is opened at one side thereof, and includes a solution reservoir 111 formed in the opened side thereof to allow a functional solution to be contained therein. A release means is disposed at a rear portion of the solution reservoir 111 of the main body 110 so as to allow the functional solution contained in the solution reservoir 111 to be released thereby to the dispensing unit 120 and the first solution release flow channel 150, which will be described later. As the release means, a cylinder and a piston rod described in Korean Patent Laid-Open Publication No. 10-2019-0111682 entitled “Hollow Microneedle Array for Injector, Injector Including the Same, and Manufacture Method of Microneedle Array for Injector” may be used, and any other release means known in the art may be used to release the solution.

[0049] The solution reservoir 111 fluidically communicates with a plurality of dispensing units 120 which will be described later. The solution reservoir is provided in single number and fluidically communicates, at a front end thereof, with the plurality of dispensing units 120 (see FIGS. 5 and 6).

[0050] An inner circumferential surface of the solution reservoir 111 is preferably formed in a tapered shape which is gradually reduced in diameter as it goes in a direction where the solution is released (see FIGS. 5 and 6).

[0051] The dispensing unit 120 is disposed at the other side of the main body 110, which is a front side of the solution reservoir 111, in such a manner as to fluidically communicate with the solution reservoir 111. The dispensing unit 120 is provided in plural numbers in such a manner that two or fifteen dispensing units are disposed at a central portion and a peripheral portion of the main body 110 so as to be circumferentially arranged spaced apart from each other at equal radial angles so that the dispensing unit 120 can serve to dispense the functional solution contained in the solution reservoir 111. The dispensing unit 120 is formed in a cylindrical shape so as to fluidically communicate with the solution reservoir 111, and a front end of a portion of the dispensing unit 120 fluidically communicating with the solution reservoir 111 is formed in a sharp conical shape like the needle support 130 which will be described as shown in FIGS. 5 and 6 so that the functional solution delivered thereto from the solution reservoir 111 is received in the dispensing unit 120 so as to be dispensed in a direction in which the needle support 130 is positioned

[0052] The needle support 130 is positioned at a front portion of each of the dispensing unit 120 in such a manner as to be protrudingly formed at the other end of the main body 110 so that when the needle support 130 comes into close contact with the skin, a front end thereof presses the subcutaneous fat of the skin. The microneedle 140 is engaged with a front end of the needle support 130. When the needle support 130 is caused to press the skin, the skin insertion depth of the microneedle 140 can be increased.

[0053] The microneedle 140 is engaged with the front end of the needle support 130 so that when the microneedle 140 comes into close contact with the skin, it is inserted into the skin. The needle support 130 is preferably made of a synthetic resin material, and the microneedle 140 is preferably formed integrally with the needle support 130.

[0054] The first solution release flow channel 150 is formed to penetrate through a portion extending outwardly from a front end of the dispensing unit 120 to the front end of the needle support 130, and allows the functional solution received in the dispensing unit 120 to be delivered to the front end of the needle support 130 therethrough so that the delivered functional solution is released to the skin tissue from the front end of the needle support 130 therethrough via a gap formed between an outer circumference of the microneedle 140 and the skin along the microneedle 140.

[0055] The functional solution released to the skin tissue through the first solution release flow channel 150 is absorbed into the skin tissue via a gap formed between the microneedle 140 and the skin tissue perforated by the microneedle 140 along the microneedle 140.

[0056] As such, the functional solution released through the first solution release flow channel 150 is absorbed into the skin tissue via the gap formed between the microneedle 140 and the skin tissue perforated by the microneedle 140 along the microneedle 140, the cosmetic or medical treatment effect on the skin tissue around the microneedle 140 occur.

[0057] In this case, in order to facilitate the release of the functional solution through the first solution release flow channel 150, the first solution release flow channel 150 is preferably formed extending obliquely from the front end of the dispensing unit 120 to an outer circumferential portion of the front end of the needle support 130 as shown in FIGS. 5 and 6.

[0058] The first solution release flow channel 150 may be provided in single number. In order for the functional solution to be uniformly absorbed into the skin tissue around the microneedle 140 upon the release of the functional solution through the first solution release flow channel 150, the first solution release flow channel 150 may be provided in plural numbers (two or four) to extend radially at equal angles from the front end of the dispensing unit 120 to the outer circumferential portion of the front end of the needle support 130.

[0059] In this case where the number of the first solution release flow channels 150 provided is 1, the functional solution may be delivered to the microneedle 140 positioned at an opposite side to the release direction of the functional solution in a less amount compared to the case where the first solution release flow channel 150 is provided in plural numbers.

[0060] If the number of the first solution release flow channels 150 extending radially at equal angles from the front end of the dispensing unit 120 to the outer circumferential portion of the front end of the needle support 130 exceeds four, the strength of the needle support 130 that supports the microneedle 140 becomes relatively low due to a very great increase in the number of the first solution release flow channels 150, and thus there is a high risk that the needle support 130 will be collapsed. Therefore, it is desirable to limit the number of the first solution release flow channels 150.

[0061] The present invention enables the functional solution to be absorbed into the surrounding tissue of the skin perforated by the microneedle 140 through the first solution release flow channel 150, as well as enables the functional solution to be absorbed into the surrounding tissue of the skin positioned at a front of the microneedle 140 through the microneedle 140.

[0062] To this end, as shown in FIG. 6, the microneedle 140 is formed in a conical shape and has a hollow flow channel 141 formed therein to penetrate vertically therethrough, and the needle support 130 further include a second solution release flow channel 131 formed therein so as to fluidically communicate with the hollow flow channel 141 of the microneedle 140 to allow the functional solution to be delivered to the skin therefrom through the hollow flow channel 141 of the microneedle 140.

[0063] The main body 110 may be formed in various shapes, preferably may have any one selected from among a cylindrical shape, a quadrangular prism shape, a cylindroid shape, a rectangular prism shape, and a polygonal prism shape. Among them, in the case where the main body 110 has the cylindroid shape or the rectangular prism shape, the microneedles 140 are also arranged in a row according to the arrangement of the needle supports 130 in a row so that the microneedles 140 can be applied to the skin care or treatment of a skin site with a narrow width.

[0064] Preferably, the needle support 130 has any one selected from between a conical shape and a polygonal pyramid shape. The reason why the needle support 130 is formed in the conical shape is that the needle support 130 easily presses the subcutaneous fat.

[0065] When the skin is perforated by the microneedle 140 of the microneedle assembly to deliver the functional solution to the skin tissue, the microneedle 140 is preferably oriented perpendicular to the skin surface. In addition, when the skin is perforated by the microneedle 140 of the microneedle assembly, the main body 110 is caused to come into close contact with the skin surface or the front end of the needle support 130 is caused to press the skin surface so that the functional solution can be delivered into the skin tissue.

[0066] In this case, in the case where the skin surface is flat, there is caused no problem, but in most case, the skin surface is not in a flat state. When the skin is perforated by the microneedles 140 during the use of the microneedle assembly and when the main body 110 comes into close contact with skin surface or the front end of the needle support 130 presses the skin surface, there occurs a problem in that the main body 110 of the microneedle assembly is not stably supported. In addition, when the functional solution is delivered to the skin after the perforation of the skin by the microneedle 140, there also occurs a problem in that the main body 110 of the microneedle assembly may shake.

[0067] In order to solve such problems, the microneedle assembly of the present invention adopts a guide 160 engaged with the main body 110 to support the main body 110 (see FIGS. 3 and 4).

[0068] The guide 160 is engaged with the outer circumference of the main body, has a height that is lower than a front end of the microneedle 140 and higher than a front end of the main body 110, and support the main body 110 while coming into close contact with the skin to ensure that the microneedle 140 is stably inserted into the skin.

[0069] In this case, preferably, the guide 160 enables to control the height of engagement between the guide 160 and the main body 110 so that the skin insertion depth of the microneedle 140 can be controlled.

[0070] The guide 160 and the main body 110 may be engaged with each other, for example, in a screw-engagement manner.

[0071] Alternatively, the engagement between the guide 160 and the main body 110 may be achieved, for example, by the cooperative operation between a protrusion 112 formed longitudinally on the outer circumferential surface of the main body 110 and a grooved recess 161 formed longitudinally on the inner circumferential surface of the guide 160 so as to be engaged with the protrusion 112 (see FIG. 4).

[0072] The guide 160 may be made of an elastic material so as to cause less skin irritation upon contact between the guide 160 and the skin.

[0073] The technical spirit of the present invention should not be construed by limiting the present invention to the above-mentioned embodiments. The application range thereof is of course varied, and various modifications thereof may be made by those skilled in the art without departing from the gist of the present invention. Therefore, as long as these modifications and changes are apparent to those skilled in the art, they fall within the protection scope of the present invention.