Absorbable surgical suture
By designing absorbable surgical sutures including suture body and reinforcement components, the problem of existing sutures being easily pulled out when too much force is applied is solved, significantly improving the strength and tensile performance of the suture, thereby improving the efficiency of surgical operations.
Patent Information
- Application Number
- CN202510250025.5
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-03-04
- Publication Date
- 2025-05-30
- Estimated Expiration
- Not applicable · inactive patent
AI Technical Summary
The existing absorbable surgical sutures are easily pulled off when they are too strong, which extends the suture time of surgical operations, reduces the efficiency of surgical operations, and even affects the patient's surgical treatment effect.
An absorbable surgical suture including a suture body and a reinforcement assembly was designed. The suture body consists of an outer layer, an inner layer and a support, and the reinforcement components include bone chains, melting plates and dissolving elements, through which the overall strength and tensile properties of the suture are enhanced.
Through enhanced components and multi-layer settings, the overall strength of the suture is significantly enhanced, reducing the risk of pulling off the suture when stressed, thereby improving the efficiency and accuracy of the surgical procedure.
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Figure CN120052991A_ABST
Abstract
Description
Technical Field
[0001] The present invention relates to the technical field of absorbable surgical sutures, and particularly to an absorbable surgical suture. Background Art
[0002] The absorbable surgical suture is made of glycolide, lactide, cyclopropane carbonate and lactide, and is suitable for the suture and ligation of general soft tissues, but cannot be used in nerve surgery, cardiovascular surgery, etc. It can be completely degraded or absorbed by tissues in the body, has a small reaction with body tissues, and does not require suture removal after suture, solving the problem of the pain brought to patients by secondary surgery after using non-absorbable surgical sutures.
[0003] Currently, when surgical operators use absorbable surgical sutures to suture tissues, when they apply too much force, it is easy to cause the absorbable surgical suture to break, prolonging the suture time of surgical operations, reducing the efficiency of surgical operations, and even affecting the surgical treatment effect of patients. Summary of the Invention
[0004] The purpose of this part is to outline some aspects of the embodiments of the present invention and briefly introduce some preferred embodiments. Some simplifications or omissions may be made in this part, as well as in the abstract and title of the present application, to avoid obscuring the purpose of this part, the abstract and the title, and such simplifications or omissions shall not be used to limit the scope of the present invention.
[0005] In view of the problems existing in the above-mentioned existing absorbable surgical sutures, the present invention is proposed.
[0006] Therefore, the purpose of the present invention is to provide an absorbable surgical suture.
[0007] To solve the above technical problems, the present invention provides the following technical solution: an absorbable surgical suture, comprising a suture body, including an outer layer, an inner layer disposed within the outer layer, and a support member disposed between the inner layer and the outer layer; and a reinforcement assembly, including a bone chain disposed within the inner layer, a melting plate disposed on the bone chain, and a dissolving member disposed on the melting plate.
[0008] As a preferred embodiment of the absorbable surgical suture of the present invention, wherein: the dissolving member includes a melting groove opened on the melting plate, a decomposition plate disposed within the melting groove, and a plurality of through holes disposed on the decomposition plate, and the melting plates are hinged to each other.
[0009] As a preferred embodiment of the absorbable surgical suture of the present invention, wherein: the supporting member further includes a bracket provided at the lower end of the connecting cylinder and a protection member provided in the bracket. The bracket includes a plurality of connecting bar frames connected to the connecting cylinder and gaskets provided at the lower ends of the plurality of connecting bar frames. The protection member is restricted by the space surrounded by the gasket and the connecting bar frame after installation.
[0010] As a preferred embodiment of the absorbable surgical suture of the present invention, wherein: a protection layer is provided between the inner layer and the outer layer. The protection layer includes a plurality of connected connecting ring bodies and flexible bands provided between the connecting ring bodies.
[0011] As a preferred embodiment of the absorbable surgical suture of the present invention, wherein: the connecting ring body includes a first bending edge, a second bending edge connected to the first bending edge, and an arc end connecting the first bending edge and the second bending edge. The arc end includes a first arc edge and a second arc edge, and the connection between the first arc edge and the second arc edge is bent towards the directions of the first bending edge and the second bending edge.
[0012] As a preferred embodiment of the absorbable surgical suture of the present invention, wherein: the support member includes a strut layer provided between the inner layer and the outer layer and a plurality of retention grooves provided in the strut layer. The connecting bar frame is provided in the retention groove.
[0013] As a preferred embodiment of the absorbable surgical suture of the present invention, wherein: a recessed groove is provided at the upper end of the connecting cylinder. A first flanging and a second flanging are provided on the recessed groove. The first flanging and the second flanging are arranged annularly, and the first flanging and the second flanging are arranged closely. The width ratio of the second flanging to the width of the first flanging is 1:1.8 - 1:2. A bent flanging is provided on the upper surface of the first flanging.
[0014] As a preferred embodiment of the absorbable surgical suture of the present invention, wherein: after the second flanging is bent by the impact of blood, it is blocked by the bent flanging and guided by the bent flanging to further bend to form a bent space.
[0015] As a preferred embodiment of the absorbable surgical suture of the present invention, wherein: after the first flanging is bent, it surrounds and wraps the outside of the protection member. The first flanging and the second flanging are made of flexible materials.
[0016] As a preferred embodiment of the absorbable surgical suture of the present invention, wherein: the outer layer includes a thick skin and a plurality of bending points provided on the thick skin.
[0017] The beneficial effects of the present invention: Furthermore, by using the strengthening components and the multi-layer setting, the overall strength of the suture is enhanced.
[0018] And in the initial state, the first flanging and the second flanging are in a bent state. When the second flanging is bent, the second flanging cooperates with the bent flanging, and after being guided by the bent flanging, it bends back to form a blood storage space. At this time, the blood will first be blocked by the first flanging. After the first flanging fails to block, the water flow breaks through the first flanging, and the water flow enters the blood storage space through the water permeable holes. Due to the structural design of the water permeable holes, the amount of water flowing out of the water storage space is less than the amount of water entering the water storage space, causing the water flow to accumulate in the water storage space, which exactly corresponds to the connection between the first bending edge and the second bending edge, thereby increasing the blood pressure here and further enhancing the dissolution effect. BRIEF DESCRIPTION OF THE DRAWINGS
[0019] In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the following will briefly introduce the drawings required for the description of the embodiments. Obviously, the following drawings are only some embodiments of the present invention. For those of ordinary skill in the art, without creative efforts, other drawings can also be obtained based on these drawings. Among them:
[0020] Figure 1 is a schematic diagram of the overall structure of the absorbable surgical suture of the present invention.
[0021] Figure 2 is an exploded schematic diagram of the internal structure of the absorbable surgical suture of the present invention.
[0022] Figure 3 is a front view schematic diagram of the end of the absorbable surgical suture of the present invention.
[0023] Figure 4 is a cross-sectional view schematic diagram of the protective layer of the absorbable surgical suture of the present invention.
[0024] Figure 5 is a schematic diagram of the dissolution body of the absorbable surgical suture of the present invention.
[0025] Figure 6 is a schematic diagram of the supporting component of the absorbable surgical suture of the present invention.
[0026] Figure 7 is a cross-sectional view schematic diagram of the supporting component of the absorbable surgical suture of the present invention.
[0027] Figure 8 of the absorbable surgical suture of the present invention Figure 7 is an enlarged schematic diagram of part A. DETAILED DESCRIPTION OF THE EMBODIMENTS
[0028] In order to make the above objects, features, and advantages of the present invention more obvious and understandable, the following will make a detailed description of the specific embodiments of the present invention with reference to the drawings in the specification.
[0029] In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present invention. However, the present invention may be practiced in other ways different from those described herein. Those skilled in the art can make similar generalizations without departing from the spirit of the present invention. Therefore, the present invention is not limited by the specific embodiments disclosed below.
[0030] Secondly, the so-called "one embodiment" or "embodiment" herein refers to a specific feature, structure, or characteristic that may be included in at least one implementation manner of the present invention. The phrase "in one embodiment" appearing in different places in this specification does not necessarily refer to the same embodiment, nor is it an individual or alternative embodiment that is mutually exclusive with other embodiments.
[0031] Thirdly, the present invention is described in detail in conjunction with schematic diagrams. When detailing the embodiments of the present invention, for ease of explanation, the cross-sectional views showing the device structure are enlarged locally in a non-general proportion, and the schematic diagrams are only examples and should not limit the scope of protection of the present invention herein. In addition, in actual production, three-dimensional spatial dimensions of length, width, and depth should be included.
[0032] Embodiment 1
[0033] Referring to Figures 1-8 , the present invention discloses an absorbable surgical suture, including a suture body 100. In this embodiment, the suture body 100 includes an outer layer 101, an inner layer 102 disposed within the outer layer 101, and a support member 103 disposed between the inner layer 102 and the outer layer 101. The designs of the outer layer 101, the inner layer 102, and the support member 103 enable the entire suture to have a certain strength, and also have a certain tensile property as a whole. Moreover, during subsequent melting and absorption, it also ensures that the melting speed is not very fast.
[0034] Furthermore, the present invention further includes a reinforcement assembly 200. The reinforcement assembly 200 is mainly used for support and can increase the main strength of the entire suture. In this embodiment, the reinforcement assembly 200 includes a bone chain 201 disposed within the inner layer 102, a melting plate 202 disposed on the bone chain 201, and a dissolving member 203 disposed on the melting plate 202. A plurality of melting plates 202 are connected together by the bone chain 201 and form a line along the length of the suture. A number of such lines are provided and are evenly laid on the outer side of the inner layer 102.
[0035] In this embodiment, when the dissolving member 203 is dissolving, it can pour more blood into the suture, thereby playing a certain role in accelerating the dissolution of the inner layer 102 of the suture. The dissolving member 203 includes a melting groove 203a formed in the melting plate 202, a decomposition plate 203b disposed in the melting groove 203a, and a plurality of through holes 203c disposed on the decomposition plate 203b. The melting plate 202 is hinged to the melting plate 202. There are a plurality of through holes 203c. Five large-sized through holes 203c are provided on each decomposition plate 203b, and four small-sized through holes 203c are provided near each large through hole 203c. The through holes 203c can better penetrate the blood downward.
[0036] In this embodiment, the support member 103 includes a pillar layer 103a disposed between the inner layer 102 and the outer layer 101, and a plurality of retention grooves 103b formed in the pillar layer 103a.
[0037] In this embodiment, the supporting member 300 includes a bracket 301 disposed in the outer layer 101 and a protection member 302 disposed in the bracket 301. The bracket 301 includes a plurality of connecting bar frames 303 connected to the connecting cylinder. In this embodiment, there are 8 connecting bar frames 303, which are arranged in a ring shape, and the connecting bar frames 303 are disposed in the retention grooves 103b.
[0038] A gasket 304 is fixedly connected to the lower ends of the plurality of connecting bar frames 303. The gasket 304 is circular in shape, with the inner edge retracting inward and the outer edge extending outward. The gasket 304 and the connecting bar frame 303 form a cylindrical-like bearing space, and a protection member 302 is disposed in the formed bearing space.
[0039] In this embodiment, the protection member 302 has openings at both ends and is in the shape of a hollow long cylindrical. The outer diameter of the blood is smaller than the inner diameter of the connecting cylinder, the outer diameter of the blood is smaller than the outer diameter of the gasket 304, and larger than the inner diameter of the gasket 304, ensuring that the bottom of the blood is supported by the gasket 304.
[0040] Further, a protective layer 400 is provided between the inner layer 102 and the outer layer 101. The protective layer 400 includes a plurality of connected connecting ring bodies 401 and flexible bands 402 disposed between the connecting ring bodies 401.
[0041] In this embodiment, the connecting ring body 401 includes a first bent edge 401a, a second bent edge 401b connected to the first bent edge 401a, and an arc end connecting the first bent edge 401a and the second bent edge 401b. The arc end includes a first arc edge 401c and a second arc edge 401d. The connection point of the first arc edge 401c and the second arc edge 401d bends towards the directions of the first bent edge 401a and the second bent edge 401b. Thus, the connecting ring body 401 forms a shape similar to a heart. And the connection point of the first bent edge 401a and the second bent edge 401b is the thinnest part of the entire connecting ring body 401. When the blood dissolves, it will dissolve this part first and then enter the interior of the connecting ring body 401 from here, thereby expanding the entire connecting ring body 401 outwards.
[0042] A recessed groove 403 is provided on the inner wall of the connecting cylinder. The recessed groove 403 is circumferentially provided inside the connecting cylinder and recesses towards the inside of the connecting cylinder wall. And a first flanging 404 and a second flanging 405 are provided on the recessed groove 403, and the first flanging 404 and the second flanging 405 are arranged in a ring shape.
[0043] Furthermore, there is a certain height difference between the first flanging 404 and the second flanging 405. The shapes of the first flanging 404 and the second flanging 405 are both annular without external force. When blood enters the connecting cylinder, the blood will stir the first flanging 404 and the second flanging 405.
[0044] Preferably, the width ratio of the second flanging 405 to the width of the first flanging 404 is 1:1.8 - 1:2. Thus, when the blood is inserted, the flipping area of the first flanging 404 is larger than that of the second flanging 405, so that the first flanging 404 has a larger relative area in contact with the blood.
[0045] Furthermore, a bent flanging 406 is provided on the upper surface of the first flanging 404. The bent flanging 406 faces upwards. When the second flanging 405 is bent by the inserted blood, it will be blocked by the bent flanging 406 and guided by the bent flanging 406 to bend further, thus forming a bent space, so that the blood accumulates here. And this place exactly corresponds to the connection point of the first bent edge 401a and the second bent edge 401b. Thus, the blood pressure here increases, further enhancing the dissolution effect.
[0046] Preferably, a number of water-permeable holes are provided on the bent flanging 406. In this embodiment, the outer layer 101 includes a thick skin and a number of bending points provided on the thick skin.
[0047] Operation process: In the initial state, the first flanging 404 and the second flanging 405 are in a bent state. When the second flanging 405 is bent, the second flanging 405 cooperates with the bent flanging 406, and after being guided by the bent flanging 406, it bends back to form a blood storage space. At this time, the blood will be blocked by the first flanging 404 first. After the first flanging 404 fails to block, the water flow breaks through the first flanging 404, and the water flow enters the blood storage space through the water permeable holes. Due to the structural design of the water permeable holes, the amount of water flowing out of the water storage space is less than the amount of water entering the water storage space, so that the water flow accumulates in the water storage space, and this place exactly corresponds to the connection between the first bent edge 401a and the second bent edge 401b, thereby increasing the pressure of the blood here and further enhancing the dissolution effect.
[0048] Importantly, it should be noted that the construction and arrangement of the present application shown in multiple different exemplary embodiments are merely illustrative. Although only a few embodiments are described in detail in this disclosure, those who refer to this disclosure should easily understand that many modifications are possible on the premise of substantially not deviating from the novel teachings and advantages of the subject matter described in this application (for example, the dimensions, scales, structures, shapes and proportions of various components, and parameter values (such as temperature, pressure, etc.), installation arrangements, use of materials, changes in color, orientation, etc.). For example, an element shown as integrally formed may be composed of multiple parts or elements, the position of the element may be inverted or otherwise changed, and the nature, number or position of discrete elements may be changed or altered. Therefore, all such modifications are intended to be included within the scope of the present invention. The order or sequence of any process or method steps may be changed or reordered according to alternative embodiments. In the claims, any "means plus function" clause is intended to cover the structure that performs the recited function described herein, and not only structural equivalents but also equivalent structures. Other substitutions, modifications, changes and omissions may be made in the design, operating conditions and arrangement of the exemplary embodiments without departing from the scope of the present invention. Therefore, the present invention is not limited to a specific embodiment, but extends to various modifications that still fall within the scope of the appended claims.
[0049] In addition, in order to provide a concise description of the exemplary embodiments, not all features of the actual embodiments may be described (i.e., those features that are not relevant to the currently considered best mode of implementing the present invention, or those features that are not relevant to the implementation of the present invention).
[0050] It should be understood that, during the development of any actual implementation, such as in any engineering or design project, a large number of specific implementation decisions can be made. Such development efforts may be complex and time-consuming, but for those of ordinary skill in the art who benefit from this disclosure, without undue experimentation, such development efforts will be routine work in design, manufacturing, and production.
[0051] It should be noted that the above embodiments are only used to illustrate the technical solutions of the present invention and not to limit them. Although the present invention has been described in detail with reference to the preferred embodiments, those of ordinary skill in the art should understand that the technical solutions of the present invention can be modified or equivalently replaced without departing from the spirit and scope of the technical solutions of the present invention, and they should all be covered within the scope of the claims of the present invention.
Claims
1. An absorbable surgical suture, characterized in that: include, A suture body (100) comprises an outer layer (101), an inner layer (102) disposed inside the outer layer (101), a supporting component (300) disposed inside the outer layer (101), and a supporting member (103) disposed between the inner layer (102) and the outer layer (101); and, The reinforcing assembly (200) comprises a bone chain (201) arranged in an inner layer (102), a melting plate (202) arranged on the bone chain (201), and a dissolving member (203) arranged on the melting plate (202).
2. The absorbable surgical suture according to claim 1, characterized in that: The dissolving part (203) comprises a melting groove (203a) provided on the melting plate (202), a decomposition plate (203b) arranged in the melting groove (203a), and a plurality of through holes (203c) arranged on the decomposition plate (203b), and the melting plate (202) is hinged to the melting plate (202).
3. The absorbable surgical suture according to claim 1, characterized in that: The supporting component (300) further comprises a bracket (301) arranged in the outer layer (101) and a protective member (302) arranged in the bracket (301); the bracket (301) comprises a plurality of connecting bars (303) connected to the connecting tube and a plurality of gaskets (304) connected to the lower ends of the connecting bars (303); after installation, the protective member (302) is restricted by the space enclosed by the gaskets (304) and the connecting bars (303).
4. The pipeline disinfection device according to claim 1, characterized in that: A protective layer (400) is provided between the inner layer (102) and the outer layer (101), and the protective layer (400) comprises a plurality of connected connecting ring bodies (401) and a flexible belt (402) provided between the connecting ring bodies (401).
5. The pipeline disinfection device according to claim 1, characterized in that: The connecting ring body (401) comprises a first bending edge (401a), a second bending edge (401b) connected to the first bending edge (401a), and an arc end connecting the first bending edge (401a) and the second bending edge (401b), wherein the arc end comprises a first curved edge (401c) and a second curved edge (401d), and the portion where the first curved edge (401c) and the second curved edge (401d) are connected is bent in the direction of the first curved edge (401a) and the second curved edge (401b).
6. The pipeline disinfection device according to claim 1, characterized in that: The support member (103) comprises a support layer (103a) arranged between the inner layer (102) and the outer layer (101) and a plurality of retention grooves (103b) opened in the support layer (103a), and the connecting frame (303) is arranged in the retention grooves (103b).
7. The pipeline disinfection device according to claim 6, characterized in that: A recessed groove (403) is provided at the upper end of the connecting tube, and a first flange (404) and a second flange (405) are provided on the recessed groove (403). The first flange (404) and the second flange (405) are arranged in a ring shape, and the first flange (404) and the second flange (405) are arranged close to each other. The ratio of the width of the second flange (405) to the width of the first flange (404) is 1:1.8-1:2, and a bent flange (406) is provided on the upper surface of the first flange (404).
8. The pipeline disinfection device according to claim 6 or 7, characterized in that: After being bent by the impact of blood, the second flange (405) is blocked by the bending flange (406) and guided by the bending flange (406) to be further bent to form a bending space.
9. The absorbable surgical suture according to claim 7, characterized in that: The first flange (404) is bent to surround and wrap around the outside of the protective component (302), and the first flange (404) and the second flange (405) are made of flexible material.
10. The absorbable surgical suture according to claim 1, characterized in that: The outer layer (101) comprises a thick skin and a plurality of bending points arranged on the thick skin.