Hydrogel injection crosslinking device

Abstract

The utility model discloses a hydrogel injection cross-linking device, and relates to the technical field of hydrogel injection cross-linking devices. The hydrogel injection device comprises an injection part, and the injection part is used for providing a storage space for hydrogel and injecting the hydrogel into a human body; the injection part is used for injecting hydrogel, the irradiation part is installed at the bottom of the injection part, the irradiation part is used for promoting crosslinking of polymer chains in the hydrogel, and the irradiation part is installed at the bottom of the injection part in a clamping mode. According to the protection assembly, the sides, close to each other, of the two protection shells in the protection assembly are connected with the injector in a sliding mode, the arc-shaped groove matched with the outer wall of the injector is formed, the two protection shells are fixedly connected through the bolt and the connecting block, and therefore the injector is clamped in the protection shells; the injector is prevented from being damaged by external force collision, friction and the like, the integrity of the injector is protected, and normal storage and injection of hydrogel are ensured.

Description

Technical Field

[0001] The utility model belongs to the technical field of hydrogel injection crosslinking devices, and particularly relates to a hydrogel injection crosslinking device. Background Technique

[0002] As a material with high water content and unique biocompatibility, hydrogel is widely used in the biomedical field, especially in tissue repair, drug delivery, etc. It is often injected into specific parts of the human body through a hydrogel injection crosslinking device, and the treatment purpose is achieved through crosslinking and curing. During the injection process of some existing hydrogel injection crosslinking devices, the syringe is easily affected by external factors. On the one hand, when medical staff operate, the syringe may be damaged due to collision, friction, or accidental dropping of the device; on the other hand, in a complex clinical environment, the syringe may also be scratched by surrounding equipment. These situations may affect the performance of the syringe in storing and injecting hydrogel, resulting in problems such as hydrogel leakage and inaccurate injection dose, which in turn affect the treatment effect and may also increase medical risks. Moreover, some existing hydrogel injection crosslinking devices are not convenient for protecting the syringe. Content of the Utility Model

[0003] The purpose of the utility model is to provide a hydrogel injection crosslinking device. By providing a protection component, specifically, one side of the two protective shells in the protection component that is close to each other is slidably connected to the syringe, and an arc-shaped groove adapted to the outer wall of the syringe is provided. The two protective shells are fixedly connected by bolts and connecting blocks, so that the syringe is clamped inside the protective shell, preventing the syringe from being damaged by external force collision, friction, etc., protecting its integrity, ensuring the normal storage and injection of hydrogel, and solving the problem that some existing hydrogel injection crosslinking devices are not convenient for protecting the syringe.

[0004] To solve the above technical problems, the utility model is realized through the following technical solutions:

[0005] The utility model is a hydrogel injection crosslinking device, including an injection part, the injection part is used to provide a storage space for hydrogel and inject the hydrogel into the human body; and

[0006] An irradiation part, the irradiation part is installed at the bottom of the injection part, and the irradiation part is used to promote the crosslinking of polymer chains in the hydrogel;

[0007] Among them, the irradiation part is installed at the bottom of the injection part by a clamping method.

[0008] Further, the injection part includes a syringe, the syringe is used to store hydrogel; and

[0009] A protection component, the protection component is installed outside the injection part, and the protection component is used to provide protection for the syringe;

[0010] The first card slot is used to connect the syringe and the protection component;

[0011] Among them, the first card slot is adapted to the convex wing on the outer wall of the syringe.

[0012] Furthermore, the irradiation part includes a connection component installed inside the protection component, and the connection component is used to connect the irradiation part and the protection component; and

[0013] an irradiation component installed at the bottom of the connection component, and the irradiation component is used to irradiate light on the hydrogel;

[0014] a rotation component used to provide power for the rotation of the irradiation component;

[0015] Among them, the connection component connects the irradiation component and the rotation component to the bottom of the protection component by means of clamping.

[0016] Furthermore, the protection component includes two protection shells. One side of the two protection shells close to each other is slidably connected to the syringe. Connection blocks are fixedly connected to the left and right sides of the two protection shells, and bolts are respectively threadedly connected between the corresponding two of several connection blocks;

[0017] Among them, arc-shaped grooves adapted to the outer wall of the syringe are opened on one side of the two protection shells close to each other.

[0018] Furthermore, the connection component includes a connection sleeve slidably connected between the two protection shells. The bottom end of the connection sleeve extends to the bottom of the two protection shells. Two clamping blocks are fixedly connected to the outer wall of the connection sleeve. Card slots two are opened on one side of the two protection shells close to each other, and the two clamping blocks are both slidably connected to the corresponding card slots two;

[0019] Among them, the two clamping blocks are both adapted to the corresponding card slots two.

[0020] Furthermore, the irradiation component includes a drive box fixedly connected to the bottom end of the connection sleeve. A rotary sleeve is rotatably connected to the bottom of the drive box, and an ultraviolet lamp is fixedly connected to the outer wall of the rotary sleeve;

[0021] Among them, a notch adapted to the rotary sleeve is opened at the bottom of the drive box, and the rotary sleeve is connected to the inner circular wall surface of the notch opened at the bottom of the drive box through a bearing.

[0022] Furthermore, the rotation component includes a motor installed on the inner top wall of the drive box. The output shaft of the motor is fixedly connected to a rotating shaft through a coupling. A gear is fixedly connected to the bottom end of the rotating shaft. An annular rack is fixedly connected to the outer wall of the rotary sleeve, and the gear meshes with the annular rack;

[0023] Among them, the motor is connected to the inner top wall of the drive box by bolts.

[0024] The utility model has the following beneficial effects:

[0025] 1. By setting the protection component, specifically, the two protection shells in the protection component are slidably connected to the syringe on the side close to each other, and are provided with arc grooves adapted to the outer wall of the syringe. The two protection shells are fixedly connected by bolts and connecting blocks, so that the syringe is clamped inside the protection shell, preventing the syringe from being damaged by external collisions, frictions, etc., protecting its integrity, and ensuring the normal storage and injection of the hydrogel.

[0026] 2. By setting the rotation component, specifically, the motor in the rotation component is installed on the inner top wall of the drive box, and its output shaft drives the rotating shaft to rotate through a coupling, and then the gear rotates, meshes with the annular rack to drive the rotating sleeve to rotate, and the ultraviolet lamp rotates, thereby reducing the irradiation dead angle of the ultraviolet lamp, making the light received by each area of the hydrogel more uniform, avoiding inconsistent crosslinking degree, improving the crosslinking effect and the versatility of the device, and enhancing the quality of treatment or filling.

[0027] Of course, it is not necessary for any product implementing the utility model to achieve all the above advantages simultaneously. BRIEF DESCRIPTION OF THE DRAWINGS

[0028] In order to more clearly illustrate the technical solutions of the embodiments of the present utility model, the drawings required for describing the embodiments will be briefly introduced below. Obviously, the drawings in the following description are only some embodiments of the present utility model, and for those of ordinary skill in the art, other drawings can be obtained based on these drawings without creative efforts.

[0029] Figure 1 is the overall structural schematic diagram of the present utility model;

[0030] Figure 2 is the exploded structural schematic diagram of the present utility model;

[0031] Figure 3 is the left-view sectional structural schematic diagram of the present utility model;

[0032] Figure 4 is the structural schematic diagram of the syringe of the present utility model;

[0033] Figure 5 is the structural schematic diagram of the drive box of the present utility model.

[0034] In the drawings, the list of components represented by each reference numeral is as follows:

[0035] 1. Injection part; 11. Syringe; 12. Protection component; 121. Protection shell; 122. Connecting block; 123. Bolt; 13. First card slot; 2. Irradiation part; 21. Connecting component; 211. Connecting sleeve; 212. Block; 213. Second card slot; 22. Irradiation component; 221. Driving box; 222. Rotating sleeve; 223. Ultraviolet lamp; 23. Rotating component; 231. Motor; 232. Rotating shaft; 233. Gear; 234. Annular rack. Detailed implementation manners

[0036] Next, the technical solutions in the embodiments of the present invention will be clearly and completely described in conjunction with the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only a part of the embodiments of the present invention, rather than all the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative efforts belong to the protection scope of the present invention.

[0037] Please refer to Figures 1-5 As shown, the present invention is a hydrogel injection crosslinking device, including an injection part 1, the injection part 1 is used to provide a storage space for the hydrogel and inject the hydrogel into the human body; and

[0038] An irradiation part 2, the irradiation part 2 is installed at the bottom of the injection part 1, and the irradiation part 2 is used to promote the crosslinking of polymer chains in the hydrogel;

[0039] Among them, the irradiation part 2 is installed at the bottom of the injection part 1 by a clamping method.

[0040] The injection part 1 includes a syringe 11, the syringe 11 is used to store the hydrogel; and

[0041] A protection component 12, the protection component 12 is installed outside the injection part 1, and the protection component 12 is used to provide protection for the syringe 11;

[0042] A first card slot 13, the first card slot 13 is used to connect the syringe 11 and the protection component 12;

[0043] Among them, the first card slot 13 is adapted to the convex wing on the outer wall of the syringe 11.

[0044] The irradiation part 2 includes a connecting component 21, the connecting component 21 is installed inside the protection component 12, and the connecting component 21 is used to connect the irradiation part 2 and the protection component 12; and

[0045] An irradiation component 22, the irradiation component 22 is installed at the bottom of the connecting component 21, and the irradiation component 22 is used to irradiate light on the hydrogel;

[0046] A rotating component 23, the rotating component 23 is used to provide the power for the irradiation component 22 to rotate;

[0047] Among them, the connecting component 21 connects the irradiation component 22 and the rotating component 23 to the bottom of the protection component 12 by means of snap - fitting.

[0048] The protection component 12 includes two protection shells 121. One side of the two protection shells 121 close to each other is slidably connected to the syringe 11. Connecting blocks 122 are fixedly connected to the left and right sides of the two protection shells 121 respectively. Bolts 123 are threadedly connected between the corresponding two of several connecting blocks 122;

[0049] Among them, arc - shaped grooves adapted to the outer wall of the syringe 11 are provided on one side of the two protection shells 121 close to each other.

[0050] The connecting component 21 includes a connecting sleeve 211 slidably connected between the two protection shells 121. The bottom end of the connecting sleeve 211 extends to the bottom of the two protection shells 121. Two clamping blocks 212 are fixedly connected to the outer wall of the connecting sleeve 211. Second clamping grooves 213 are provided on one side of the two protection shells 121 close to each other. The two clamping blocks 212 are slidably connected to the corresponding second clamping grooves 213;

[0051] Among them, the two clamping blocks 212 are adapted to the corresponding second clamping grooves 213.

[0052] The irradiation component 22 includes a driving box 221 fixedly connected to the bottom end of the connecting sleeve 211. A rotating sleeve 222 is rotatably connected to the bottom of the driving box 221. An ultraviolet lamp 223 is fixedly connected to the outer wall of the rotating sleeve 222;

[0053] Among them, the inner wall of the bearing between the rotating sleeve 222 and the driving box 221 is fixedly connected to the rotating sleeve 222, and the outer wall of the bearing is fixedly connected to the inner circular wall surface of the bottom of the driving box 221.

[0054] The rotating component 23 includes a motor 231 installed on the inner top wall of the driving box 221. The output shaft of the motor 231 is fixedly connected to a rotating shaft 232 through a coupling. A gear 233 is fixedly connected to the bottom end of the rotating shaft 232. An annular rack 234 is fixedly connected to the outer wall of the rotating sleeve 222. The gear 233 meshes with the annular rack 234;

[0055] Among them, a notch adapted to the outer wall of the syringe 11 is provided on the top of the driving box 221. The syringe 11 passes through the driving box 221 and the rotating sleeve 222 respectively and is rotatably connected to the notch on the top of the driving box 221 and the rotating sleeve 222.

[0056] A specific application of this embodiment is as follows: When using this device, first, draw the hydrogel through the injection head of the syringe 11, store the hydrogel inside the barrel of the syringe 11, and after completion of the addition, then push out the hydrogel stored in the syringe 11 through the injection head of the syringe 11 and inject it into the part of the human body that needs treatment or filling. The syringe 11 can be protected by the protective shell 121 to prevent the syringe 11 from being damaged by external collisions, friction, etc., protect the integrity of the syringe 11, and ensure its normal functions of storing and injecting the hydrogel. At the same time, the protective shell 121 also provides installation conditions for the irradiation part 2 to be installed on the syringe 11. When injecting the hydrogel, turn on the ultraviolet lamp 223 through an independently set switch, irradiate the hydrogel injected into the human body with light, and prompt the polymer chains in the hydrogel to crosslink, so that the hydrogel is solidified and shaped to achieve the treatment or filling effect. When it is necessary to adjust the irradiation angle of the ultraviolet lamp 223, first start the motor 231. The motor 231 drives the rotation shaft 232 to rotate. When the rotation shaft 232 rotates, it drives the gear 233 to rotate. When the gear 233 rotates, it drives the annular rack 234 and the rotating sleeve 222 to rotate through the gear transmission principle. When the rotating sleeve 222 rotates, it drives the ultraviolet lamp 223 to rotate, thereby adjusting the irradiation angle of the ultraviolet lamp 223, reducing the irradiation dead angle, and making the light received by each area of the hydrogel more uniform, avoiding the situation of inconsistent crosslinking degree caused by insufficient or excessive local irradiation. At the same time, loosen the bolt 123 and remove the bolt 123 from the connecting block 122, then the two protective shells 121 can be separated. After the two protective shells 121 are separated, the syringe 11 and the irradiation part 2 can be disassembled, so as to clean, maintain, and repair the syringe 11 and the irradiation part 2. When assembling the syringe 11 and the irradiation part 2, gradually close the two protective shells 121 to align the connecting blocks 122 on the two protective shells 121. Before the two protective shells 121 are closed, first pass the syringe 11 through the connecting sleeve 211 and the drive box 221, and then place the syringe 11, the connecting sleeve 211, and the drive box 221 between the two protective shells 121, so that the two convex wings on the outer wall of the syringe 11 are respectively located in the first card slots 13 on the side where the two protective shells 121 are close to each other, and at the same time, the two clamping blocks 212 on the outer wall of the connecting sleeve 211 are located in the corresponding second card slots 213. Finally, close the two protective shells 121 and fixedly connect the two protective shells 121 together through the bolt 123 to complete the assembly.

[0057] In the description of this specification, the descriptions referring to the terms "one embodiment", "example", "specific example", etc. mean that the specific features, structures, materials or characteristics described in connection with the embodiment or example are included in at least one embodiment or example of the present utility model. In this specification, the schematic representations of the above terms do not necessarily refer to the same embodiment or example. Moreover, the specific features, structures, materials or characteristics described may be combined in a suitable manner in any one or more embodiments or examples.

[0058] The preferred embodiments of the present utility model disclosed above are only used to help explain the present utility model. The preferred embodiments do not describe all the details in detail, nor do they limit the present utility model to the specific embodiments described. Obviously, many modifications and variations can be made according to the content of this specification. These embodiments are selected and specifically described in this specification in order to better explain the principle and practical application of the present utility model, so that those skilled in the art can well understand and utilize the present utility model. The present utility model is only limited by the claims and their full scope and equivalents.

Claims

1. A hydrogel injection cross-linking device, characterized in that: include: An injection part, which is used to provide a storage space for the hydrogel and inject the hydrogel into the human body; as well as An irradiation part, which is installed at the bottom of the injection part and is used to cause the polymer chains in the hydrogel to cross-link; The irradiation part is mounted on the bottom of the injection part by snapping.

2. A hydrogel injection cross-linking device according to claim 1, characterized in that: The injection part comprises a syringe, and the syringe is used to store the hydrogel; and A protection component, which is installed outside the injection part and is used to provide protection for the syringe; A card slot 1, wherein the card slot 1 is used to connect the syringe and the protection component; The first card slot is matched with the convex wing of the outer wall of the syringe.

3. A hydrogel injection cross-linking device according to claim 2, characterized in that: The irradiation part includes a connection component, the connection component is installed inside the protection component, and the connection component is used to connect the irradiation part with the protection component; as well as An irradiation component, which is installed at the bottom of the connecting component and is used to irradiate light to the hydrogel; A rotating assembly, the rotating assembly being used to provide rotational power to the irradiation assembly; The connecting component connects the irradiating component and the rotating component to the bottom of the protecting component by snapping.

4. A hydrogel injection cross-linking device according to claim 3, characterized in that: The protection assembly comprises two protection shells, the sides of the two protection shells close to each other are slidably connected to the syringe, the left and right sides of the two protection shells are fixedly connected with connection blocks, and bolts are respectively threadedly connected between two corresponding ones of the plurality of connection blocks; Wherein, arc grooves matching with the outer wall of the syringe are provided on the sides of the two protective shells close to each other.

5. A hydrogel injection cross-linking device according to claim 4, characterized in that: The connecting assembly includes a connecting sleeve slidably connected between the two protective shells, the bottom end of the connecting sleeve extends to the bottom of the two protective shells, the outer wall of the connecting sleeve is fixedly connected to two clamping blocks, and the two sides of the two protective shells close to each other are each provided with a second clamping groove, and the two clamping blocks are both slidably connected to the corresponding second clamping groove; Wherein, the two card blocks are both adapted to the corresponding card slots.

6. A hydrogel injection cross-linking device according to claim 5, characterized in that: The irradiation assembly comprises a driving box fixedly connected to the bottom end of the connecting sleeve, the bottom of the driving box is rotatably connected to a rotating sleeve, and the outer wall of the rotating sleeve is fixedly connected to an ultraviolet lamp; The bottom of the driving box is provided with a slot matched with the rotating sleeve, and the rotating sleeve is connected with the inner circular wall of the slot provided at the bottom of the driving box through a bearing.

7. A hydrogel injection cross-linking device according to claim 6, characterized in that: The rotating assembly includes a motor mounted on the top wall of the driving box, the output shaft of the motor is fixedly connected to the rotating shaft through a coupling, the bottom end of the rotating shaft is fixedly connected to a gear, the outer wall of the rotating sleeve is fixedly connected to an annular rack, and the gear is meshed with the annular rack; The motor is connected to the inner top wall of the driving box by bolts.

Images