Protein introduction equipment for scar repair

Abstract

The utility model belongs to the technical field of medical apparatus and instruments, and particularly relates to protein leading-in equipment for scar repair, which comprises a cover body, a machine base, a storage container, a separation mechanism and an extraction leading-in component, the cover body is connected to the upper portion of the machine base, and a protection cavity is formed between the cover body and the machine base. The storage container is connected to the interior of the protection cavity; a storage cavity and an extraction cavity are formed in the storage container; the separation mechanism is arranged between the storage cavity and the extraction cavity so as to control conduction or separation between the storage cavity and the extraction cavity; the extracting and leading-in component is connected to the storage container; an extraction channel is arranged in the extraction leading-in part, and the extraction channel is communicated with the extraction cavity; scale marks are arranged on the extracting and leading-in component. According to the utility model, the accuracy of the lead-in amount of the repair protein can be effectively improved, and the phenomena of material waste, excessive damage to a user and the like are reduced.

Description

Technical Field

[0001] This utility model belongs to the field of medical device technology, and in particular relates to a protein delivery device for scar repair. Background Technology

[0002] Collagen, also known as scar repair protein, is a biological macromolecular protein. Collagen possesses excellent biological properties, providing a scaffold for the migration and proliferation of epidermal cells, supplying nutrients, promoting the growth of skin and nerve cells, and facilitating the proliferation and repair of epithelial cells, thereby promoting wound healing. Therefore, it is frequently used in hospitals for wound care to accelerate the recovery of patient scars.

[0003] However, the output of most existing protein delivery devices for scar repair is difficult to control, which can easily lead to waste of recombinant collagen solution and affect the efficiency of use. Utility Model Content

[0004] The purpose of this invention is to provide a protein delivery device for scar repair, which addresses the shortcomings of existing technologies and solves the technical problem that the output volume is difficult to control.

[0005] To achieve the above objectives, the present invention adopts the following technical solution:

[0006] A protein delivery device for scar repair includes a cover, a base, a storage container, a separating mechanism, and an extraction and delivery component. The cover is connected above the base and has a protective cavity between it and the base. The storage container is connected inside the protective cavity. The storage container contains a storage cavity and an extraction cavity. The separating mechanism is disposed between the storage cavity and the extraction cavity to control the connection or separation between the storage cavity and the extraction cavity. The extraction and delivery component is connected to the storage container. The extraction and delivery component has an extraction channel that communicates with the extraction cavity. The extraction and delivery component has graduation lines.

[0007] Preferably, the storage container includes a main shell and a cover plate connected to each other; the main shell and the cover plate form the storage cavity and the extraction cavity; and the separating mechanism is connected to the cover plate; the extraction and inlet component is disposed on the cover plate.

[0008] Preferably, the main housing has a guide slope at the bottom of the extraction cavity; and the inner diameter of the extraction cavity in the direction of the guide slope toward the storage cavity is smaller than the inner diameter of the extraction cavity in the direction of the guide slope toward the extraction cavity.

[0009] Preferably, the extraction and induction component includes a support block, an extraction tube, and a rubber sleeve; the support block is snapped into the opening of the extraction cavity; the outer surface of the extraction tube is connected to the interior of the support block; and the extraction channel is disposed on the inner wall of the extraction tube in the height direction; the scale line is connected to the outer surface of the extraction channel in the height direction; the rubber sleeve is connected to one end of the extraction tube and communicates with the interior of the extraction channel; the other end of the extraction tube communicates with the extraction cavity.

[0010] Preferably, the separating mechanism includes a first baffle, a second baffle, and a blocking component; the first baffle and the second baffle are connected side by side to the bottom of the cover plate; the blocking component is movably disposed between the first baffle and the second baffle; and the bottom of the blocking component can abut against the inner bottom of the main housing.

[0011] Preferably, the blocking component includes a partition block and a support rod; one end of the support rod is connected to the top of the partition block; the other end of the support rod passes through the cover plate and is slidably connected to the cover plate; the two opposite side surfaces of the partition block abut against the first baffle and the second baffle, respectively.

[0012] Preferably, the protein delivery device for scar repair further includes a disinfection mechanism; the disinfection mechanism is disposed inside the protective cavity; and the disinfection mechanism has a disinfection inner cavity; the extraction and delivery component is disposed inside the disinfection inner cavity.

[0013] Preferably, the disinfection mechanism includes a placement housing, at least one heating tube, and at least one ultraviolet disinfection lamp; the disinfection cavity is disposed inside the placement housing; the heating tube is connected to the inside of the placement housing, and the heating direction of the heating tube is directed toward the placement housing; the ultraviolet disinfection lamp is connected to the inside of the placement housing, and the light direction of the ultraviolet disinfection lamp is directed toward the placement housing.

[0014] The beneficial effects of this utility model are as follows: This technical solution adds a storage cavity and an extraction cavity inside the storage container, and controls the delivery of repair proteins in the storage cavity to the extraction cavity according to certain requirements through a separation mechanism; combined with an extraction and introduction component with graduation lines and extraction channels, it achieves precise extraction of repair proteins, thereby effectively improving the accuracy of the amount of repair proteins introduced, reducing material waste and the risk of harm to the user from excessive amounts; thus improving efficiency; in addition, the external isolation protection provided by the cover and base prevents accidental contact with the extraction and introduction component when not in use, thus avoiding waste of recombinant collagen repair fluid, thereby improving protective performance. Attached Figure Description

[0015] The following will refer to the appendix.Figures 1-4 This section describes the features, advantages, and technical effects of exemplary embodiments of the present invention.

[0016] Figure 1 This is a schematic diagram of the structure of a protein delivery device for scar repair according to an embodiment of the present invention;

[0017] Figure 2 This is a schematic diagram of the structure of a protein delivery device for scar repair according to an embodiment of the present invention;

[0018] Figure 3 This is a schematic diagram of the extraction and introduction component of a protein introduction device for scar repair according to an embodiment of the present invention.

[0019] Figure 4 This is a schematic diagram of the sterilization mechanism of a protein delivery device for scar repair according to an embodiment of the present invention.

[0020] In the diagram: 1-Cover; 2-Base; 101-Protective cavity; 3-Storage container; 31-Main shell; 32-Cover plate; 301-Storage cavity; 302-Extraction cavity; 303-Guide slope; 4-Separation mechanism; 41-First baffle; 42-Second baffle; 43-Separation block; 44-Support rod; 5-Extraction guide component; 51-Support block; 501-Extraction channel; 52-Extraction tube; 521-Graduation line; 53-Rubber sleeve; 6-Disinfection mechanism; 601-Disinfection cavity; 61-Placement shell; 62-Heating tube; 63-Ultraviolet disinfection lamp. Detailed Implementation

[0021] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this application pertains; the terminology used herein is for the purpose of describing particular embodiments only and is not intended to limit the application; the terms “comprising” and “having”, and any variations thereof, in the specification, claims, and foregoing description of the drawings are intended to cover non-exclusive inclusion.

[0022] In the description of the embodiments of this application, technical terms such as "first" and "second" are used only to distinguish different objects and should not be construed as indicating or implying relative importance or implicitly specifying the number, specific order, or primary and secondary relationship of the indicated technical features. In the description of the embodiments of this application, "multiple" means two or more, unless otherwise explicitly defined.

[0023] In this document, the term "embodiment" means that a particular feature, structure, or characteristic described in connection with an embodiment may be included in at least one embodiment of this application. The appearance of this phrase in various places throughout the specification does not necessarily refer to the same embodiment, nor is it a separate or alternative embodiment mutually exclusive with other embodiments. It will be explicitly and implicitly understood by those skilled in the art that the embodiments described herein can be combined with other embodiments.

[0024] In the description of the embodiments in this application, the term "and / or" is merely a description of the relationship between related objects, indicating that three relationships can exist. For example, A and / or B can represent: A existing alone, A and B existing simultaneously, or multiple situations existing alone. In addition, the character " / " in this document generally indicates that the related objects before and after are in an "or" relationship.

[0025] In the description of the embodiments of this application, unless otherwise expressly specified and limited, technical terms such as "installation," "connection," "joining," and "fixing" should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral part; they can refer to a mechanical connection or an electrical connection; they can refer to a direct connection or an indirect connection through an intermediate medium; they can refer to the internal communication of two components or the interaction between two components. For those skilled in the art, the specific meaning of the above terms in the embodiments of this application can be understood according to the specific circumstances.

[0026] The following is in conjunction with the appendix Figures 1-4 The present invention will be described in further detail, but this is not intended to limit the scope of the present invention.

[0027] like Figure 1 and 3 As shown in one embodiment of this utility model, the protein delivery device for scar repair includes a cover 1, a base 2, a storage container 3, a separating mechanism 4, and an extraction and delivery component 5. The cover 1 is connected above the base 2, and a protective cavity 101 is provided between the cover 1 and the base 2. The storage container 3 is connected inside the protective cavity 101. The storage container 3 has a storage cavity 301 and an extraction cavity 302. The separating mechanism 4 is disposed between the storage cavity 301 and the extraction cavity 302 to control the connection or separation between the storage cavity 301 and the extraction cavity 302. The extraction and delivery component 5 is connected to the storage container 3. The extraction and delivery component 5 has an extraction channel 501, and the extraction channel 501 communicates with the extraction cavity 302. The extraction and delivery component 5 has a scale line 521.

[0028] The technical solution of this utility model adds a storage cavity and an extraction cavity inside the storage container, and controls the delivery of repair proteins in the storage cavity to the extraction cavity according to certain requirements through a separation mechanism; combined with an extraction and introduction component with scale lines and extraction channels, it achieves precise extraction of repair proteins, thereby effectively improving the accuracy of the amount of repair proteins introduced, reducing material waste and harm to the user from excessive amounts, and thus improving efficiency; in addition, the external isolation protection provided by the cover and base prevents accidental contact with the extraction and introduction component when not in use, thus avoiding waste of recombinant collagen repair fluid, thereby improving protection performance.

[0029] Specifically, in some implementations, such as Figure 1 and 2 As shown, the storage container 3 includes a main shell 31 and a cover plate 32 connected to each other; the main shell 31 and the cover plate 32 form the storage cavity 301 and the extraction cavity 302; and the separating mechanism 4 is connected to the cover plate 32; the extraction and inlet component 5 is disposed on the cover plate 32. The cover plate 32 is provided with at least one feeding pipe, which communicates with the storage cavity 301 to achieve rapid replenishment. The cover plate 32 is provided with a mounting groove, and the extraction and inlet component 5 is snapped into the mounting groove.

[0030] Specifically, in some implementations, such as Figure 1 and 2 As shown, the main housing 31 has a guide slope 303 at the bottom of the extraction cavity 302; and the inner diameter of the guide slope 303 near the storage cavity 301 of the extraction cavity 302 is smaller than the inner diameter of the guide slope 303 near the extraction cavity 302. In other words, the guide slope 303, which is recessed and inclined downwards from the storage cavity 301 towards the extraction cavity 302, can improve the delivery speed of the repair protein, thereby improving the introduction efficiency.

[0031] Specifically, in some implementations, such as Figure 1 and 3As shown, the extraction and introduction component 5 includes a support block 51, an extraction tube 52, and a rubber sleeve 53. The support block 51 is snapped into the opening of the extraction cavity 302 (within the mounting groove on the middle cover plate 32). The outer surface of the extraction tube 52 is connected to the interior of the support block 51. The extraction channel 501 is located on the inner wall of the extraction tube 52 in the height direction. The scale line 521 is connected to the outer surface of the extraction channel 501 in the height direction. The rubber sleeve 53 is connected to one end of the extraction tube 52 and communicates with the interior of the extraction channel 501. The other end of the extraction tube 52 communicates with the extraction cavity 302. This structure, through the squeezing action of the rubber sleeve 53, creates a negative pressure inside the extraction channel 501, thereby adsorbing the repair protein into its interior, thus achieving precise extraction.

[0032] Specifically, in some implementations, such as Figure 1 and 2 As shown, the separating mechanism 4 includes a first baffle 41, a second baffle 42, and a blocking component; the first baffle 41 and the second baffle 42 are connected side-by-side to the bottom of the cover plate 32; the blocking component is movably disposed between the first baffle 41 and the second baffle 42; and the bottom of the blocking component can abut against the inner bottom of the main housing 31. Wherein, as... Figure 1 and 2 As shown, the blocking component includes a separator 43 and a support rod 44; one end of the support rod 44 is connected to the top of the separator 43; the other end of the support rod 44 passes through the cover plate 32 and is slidably connected to the cover plate 32; the two opposite side surfaces of the separator 43 respectively abut against the first baffle 41 and the second baffle 42. That is, by separating the two cavities from above through the first baffle 41 and the second baffle 42, the repair protein is prevented from entering the extraction cavity during non-introduction operations; thereby reducing corrosion of the outer wall of the extraction tube 52 of the extraction and introduction component 5, and reducing adhesion to the outer wall of the extraction tube 52 causing loss; further reducing material waste and potential harm to the user; and improving efficiency.

[0033] Specifically, in some implementations, such as Figure 1 and 2 As shown, the protein delivery device for scar repair also includes a disinfection mechanism 6; the disinfection mechanism 6 is disposed inside the protective cavity 101; and the disinfection mechanism 6 has a disinfection inner cavity 601; the extraction and delivery component 5 (with extraction tube 52) is disposed inside the disinfection inner cavity 601. Wherein, as Figure 4As shown, the disinfection mechanism 6 includes a housing 61, at least one heating tube 62, and at least one ultraviolet disinfection lamp 63; the disinfection cavity 601 is disposed inside the housing 61; the heating tube 62 is connected to the inside of the housing 61, and the heating direction of the heating tube 62 is oriented towards the housing 61; the ultraviolet disinfection lamp 63 is connected to the inside of the housing 61, and the light direction of the ultraviolet disinfection lamp 63 is oriented towards the housing 61.

[0034] Furthermore, it should be understood that although this specification describes embodiments, not every embodiment contains only one independent technical solution. This narrative style of the specification is merely for clarity. Those skilled in the art should regard the specification as a whole, and the technical solutions in each embodiment can also be appropriately combined to form other embodiments that can be understood by those skilled in the art.

[0035] Based on the disclosure and teachings of the above specification, those skilled in the art can make changes and modifications to the above embodiments. Therefore, this utility model is not limited to the specific embodiments described above, and any obvious improvements, substitutions, or modifications made by those skilled in the art based on this utility model are within the protection scope of this utility model. Furthermore, although some specific terms are used in this specification, these terms are only for convenience of explanation and do not constitute any limitation on this utility model.

Claims

1. A protein delivery device for scar repair, characterized in that: The device includes a cover, a base, a storage container, a separating mechanism, and an extraction / introduction component. The cover is connected above the base and has a protective cavity between it and the base. The storage container is connected inside the protective cavity. The storage container contains a storage cavity and an extraction cavity. The separating mechanism is located between the storage cavity and the extraction cavity to control the connection or separation between them. The extraction / introduction component is connected to the storage container and has an extraction channel that communicates with the extraction cavity. The extraction / introduction component has graduation lines.

2. The protein delivery device for scar repair according to claim 1, characterized in that: The storage container includes a main shell and a cover plate connected to each other; the main shell and the cover plate form the storage cavity and the extraction cavity; and the separating mechanism is connected to the cover plate; the extraction and inlet component is disposed on the cover plate.

3. The protein delivery device for scar repair according to claim 2, characterized in that: The main housing is provided with a guide slope at the bottom of the extraction cavity; and the inner diameter of the extraction cavity in the direction of the guide slope near the storage cavity is smaller than the inner diameter of the extraction cavity in the direction of the guide slope near the extraction cavity.

4. The protein delivery device for scar repair according to claim 1, characterized in that: The extraction and induction component includes a support block, an extraction tube, and a rubber sleeve; the support block is snapped into the opening of the extraction cavity; the outer surface of the extraction tube is connected to the interior of the support block; and the extraction channel is disposed on the inner wall of the extraction tube in the height direction; the scale line is connected to the outer surface of the extraction channel in the height direction; the rubber sleeve is connected to one end of the extraction tube and communicates with the interior of the extraction channel; the other end of the extraction tube communicates with the extraction cavity.

5. The protein delivery device for scar repair according to claim 2, characterized in that: The separating mechanism includes a first baffle, a second baffle, and a blocking component; the first baffle and the second baffle are connected side by side to the bottom of the cover plate; the blocking component is movably disposed between the first baffle and the second baffle; and the bottom of the blocking component can abut against the inner bottom of the main housing.

6. The protein delivery device for scar repair according to claim 5, characterized in that: The blocking component includes a partition block and a support rod; one end of the support rod is connected to the top of the partition block; the other end of the support rod passes through the cover plate and is slidably connected to the cover plate; the two opposite side surfaces of the partition block abut against the first baffle and the second baffle, respectively.

7. The protein delivery device for scar repair according to claim 1, characterized in that: The protein delivery device for scar repair also includes a disinfection mechanism; the disinfection mechanism is located inside the protective cavity; and the disinfection mechanism has a disinfection inner cavity; the extraction and delivery component is located inside the disinfection inner cavity.

8. The protein delivery device for scar repair according to claim 7, characterized in that: The disinfection mechanism includes a housing, at least one heating tube, and at least one ultraviolet disinfection lamp; the disinfection cavity is located inside the housing; the heating tube is connected to the inside of the housing, and the heating direction of the heating tube is directed towards the housing; the ultraviolet disinfection lamp is connected to the inside of the housing, and the light direction of the ultraviolet disinfection lamp is directed towards the housing.

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