97results about How to "Avoid secondary surgery" patented technology

The invention relates to a tissue sealant and a preparation method and application thereof. The sealant mainly comprises hydrophilic raw material, nucleophilic raw material, a marker and physiological thinner, wherein the hydrophilic raw material mainly refers to the derivatives of polyethylene glycol and the nucleophilic raw material mainly refers to polyamino acid. The preparation method includes: physically mixing the hydrophilic raw material, the nucleophilic raw material, the marker and the physiological thinner through a mixing tool, and performing covalent cross-linking to form hydrogel. The tissue sealant has the advantages that the sealant mainly used for sealing small wounds after eye surgery is good in tissue cohesive force and film-forming property, good in biocompatibility, capable of promoting epithelization healing and preventing seepage leakage, simple in preparation method, capable of being quantified to form a stable production line, and good in clinical application value.

The invention provides an artificial dental abutment, an artificial dental multi-part implanting system and an implanting method. A crown connection section and an implant connection section are respectively arranged at two ends of the artificial dent abutment, wherein the included angle of the axis of the crown connection section and the axis of the implant connection section is 10-30 degrees. The artificial dental abutment can adapt to various oral implanting conditions and angles. An artificially implanted tooth has a harmonious and beautiful repairing effect with surrounding tissues and remained dentition by adopting the abutment. The invention discloses an artificial dental multi-part implanting system comprising the artificial dental abutment, wherein the implant is a multi-part and nonsubmerged technology combined implant, is high in stability and strength, and can adapt to various oral implanting conditions and angles, can be used for effectively reducing the local stress, shortening the healing time and reducing the hurt of patients.

The invention discloses an easily-removing implant device and a screwing-out tool thereof. The easily-removing implant device comprises an implant, a base station and a central bolt; the easily-removing implant device is characterized in that the implant comprises a gum-penetrating neck part and a head part, wherein a thread is formed on the outer surface of the head part, at least two spiral self-tapping grooves are also formed in the outer surface of the head part, a connecting hole coaxial with the implant is formed in the implant, the connecting hole comprises a tapered hole, an anti-rotation hole, an implant taking-out section and a blind threaded hole, which are sequentially connected coaxially, the base station comprises a dental crown connecting section and an implant connecting section, the implant connecting section comprises a conical table and an anti-rotation column, a stepped hole matched with the central bolt is formed in the base station, and the central bolt penetrates through the stepped hole to be connected with the blind threaded hole, so that the base station and the implant are fixed integrally. According to the easily-removing implant device, the implant taking-out section with a reverse thread is additionally arranged in the implant, the problem that a part of the implant, which is remained in dentale due to fracture of the implant, is difficult to take out is solved, and the easily-removing implant device has the advantages of simple structure, strong practicability, and the like.

The invention discloses a degradable iron, zinc and magnesium-based gradient composite material based on biological bone healing. A zinc layer and an iron layer are sequentially arranged on the surface of a magnesium matrix, and the thickness or the diameter of the magnesium matrix is 30-90% of bone dimension in the repaired part. The thicknesses of the zinc and iron layers are respectively determined according to the corrosion rates of zinc and iron in an in vitro simulated body fluid. According to the composite material, rigid fixation in early stage is realized to promote bone healing, the composite material is gradually degraded, use of the material with lower rigidity is transited to dynamic fixation, and finally, the material is fully absorbed in vivo to prevent from being taken out in the second operation. Rapid degradation in the non-mechanical bearing later stage is realized, and growth by differentiation of bone cells and ingrowth of blood vessels on the surface of material are induced by hoping to combine the advantages that iron in higher rigidity in the early stage realizes rigid fixation and zinc in lower rigidity in the middle stage realizes dynamic fixation by means of quicker corrosion rate of magnesium. Finally, the composite material is fully absorbed, so as to realize the bone repairing purpose. The composite material disclosed by the invention is applicable to gradient structure designs of internal fixing materials after fracture with change demands on mechanical property with the passage of time.

The invention provides a 3D printing PCL / beta-TCP composite material and a preparation method, application and a printing method thereof. The 3D printing PCL / beta-TCP composite material is mainly prepared from, by weight, beta-tricalcium phosphate 40-95% and polycaprolactone 5-60%, wherein the mass percentage sum of the two raw materials is 100% or below. After the composite material is implanted, bone tissue regeneration can be promoted, and the material has a good bone repair effect. In addition, the PCL / beta-TCP composite material further has good biodegradable properties, the negative impact of a long-term implant can be reduced, secondary operation is avoided, and the material can be well applied to 3D printing.

The invention belongs to the field of biological regenerative medicine and relates to an absorbable transmitting tissue regeneration membrane based on a magnesium alloy and a preparation method thereof. The absorbable transmitting tissue regeneration membrane solves the problem that the existing absorbable transmitting tissue regeneration membrane has poor space maintaining ability, has a poor acid production and bone induction capacity in degradation and needs second operation for tissue regeneration membrane removal. The absorbable transmitting tissue regeneration membrane can be processed into a compact membrane, an asymmetric membrane or a porous membrane. Through fluorine conversion, calcium and phosphorus deposition, phosphating and magnetron sputtering, the surface is modified and the modified transmitting tissue regeneration membrane has good biocompatibility. Through degradation of released ions, the inhibition of inflammation and induction of bone tissue regeneration are realized and the clinical needs of transmitting tissue regeneration and repair are satisfied.

The invention provides a degradable conducting wire. The degradable conducting wire comprises a substrate and a protective part. The substrate and the protective part are formed by adopting absorbableor degradable materials, wherein the protective part is used for encapsulating the degradable conducting wire. The invention also provides a preparation method of the degradable conducting wire. Thedegradable conducting wire and the preparation method thereof disclosed by the invention have the advantages of simple preparation process, wide raw material sources, low economic cost, stable performance and capability of being used for large-scale batch production; by means of the degradable conducting wire, the problems that conducting wires of electronic devices at the current stage cannot bedegraded and the like are effectively solved.

A bone injury repair fixation instrument and a method of manufacturing same. A crosslinked biodegradable polymer material is adopted for the instrument. The polymer material is a homopolymer of monomers, a copolymer of multiple monomers or a blend of 2 or 3 kinds of the homopolymer and copolymer, and has a three-dimensional crosslinked network structure. The instrument comprises a bone nail, a bone screw, a bone plate or a fixing support, and has great mechanical performance, structural stability, controllable degradation speed, and excellent biocompatibility.

The invention discloses a flexible intramedullary nail, which pertains to the technical field of orthopedic medical devices and aims at providing a flexible intramedullary nail which can spare secondary operation, eliminate stress shielding, promote fracture healing and has the advantages of simple structure, practicality and low cost. The technical proposal of the invention is that a nail pole of the intramedullary nail consists of a proximal-end nail body, a distal-end nail body and a spring body, wherein, the proximal-end nail body and the distal-end nail body are positioned at both ends of the nail pole respectively and a proximal-end fixed screw hole and a distal-end fixed screw hole are arranged on the two ends; the spring body is arranged in the middle of the nail pole and both ends of the spring body are tightly connected with the proximal-end nail body and the distal-end nail body respectively; the length and quantity of the spring body can be adjusted according to the characteristics of a long bone and the diameter of the spring body can be 2mm to 6mm and can be adjusted according to the requirements of fracture fixing. The flexible intramedullary nail has simple structure and innovative design, resolves the problems of eliminating stress shielding, promoting fracture healing, avoiding secondary operation, and the like after the intrameduallary nail is put in the body, and also has the advantages of simple structure, practicality and low cost.

A degradable high-molecular material used for preparing the lacrimale suppositary to treat xerophthalmia is prepared from lactic acid, alcoholic acid and / or caprolactone through copolycondensating reaction or from lactide, glycollide and / or caprolactone through open-ring polymerizing. Its vitrification temp is 32 + / - 1 deg.C. It can be degradated into CO2 and H2O.

The invention relates to a degradable intestinal tract complete flow transporting stent. The degradable intestinal tract complete flow transporting stent comprises an intestinal tract fixing part 1, wherein the intestinal tract fixing part 1 comprises a circular tube 11 for forming intestinal cut crawling matching sections on two sides; loudspeaker-shaped openings 12 which are gradually extended are respectively connected to two ends of the circular tube 11; and convex rings 13 for binding the intestine breaking end are respectively arranged adjacent to the corresponding loudspeaker-shaped openings 12, of the circular tube 11. The degradable intestinal tract complete flow transporting stent is characterized in that a separating diaphragm 2 for separating a hollow inner cavity is arranged in a hollow inner cavity in the circular tube 11; and the intestinal tract fixing part 1 and the separating diaphragm 2 are manufactured by degradable materials having biocompatibility. The degradableintestinal tract complete flow transporting stent disclosed by the invention cooperates with a drainage tube for usage, so that intestinal tract complete flow transporting can be realized, a secondarysurgery of stoma return is not needed, the infection risk is not generated, and the degradable intestinal tract complete flow transporting stent can be developed in X-ray examination or CT examination.

The nickel-titanium memory alloy product miniature vertebral body opening device includes a handle and two claws, the rear ends of two claws and front end of the handle are fixed together, and the front end of two claws is separated into V-shaped form, the centre of the handle is equipped with an axial through hole. It has its matched conveying device including conveying bar and handle, and the front end of the conveying bar is equipped with a projection which can be inserted into the above-mentioned central hole of the handle of the miniature vertebral body opening device.

The invention belongs to the technical field of intelligent materials, nanocomposite functional materials and biomedical materials and discloses a photothermal drive type shape memory multiscale porenanocomposite biological scaffold and a preparation method thereof. The method comprises the following steps: (1) performing hydrophobic modification on graphene oxide by low molecular weight carboxyl-terminated polylactic acid to obtain hydrophobic modified graphene oxide; (2) adding the hydrophobic modified graphene oxide, a biodegradable shape polymer and a rheological agent to an organic solvent to form an oil phase; adding water to the oil phase, performing mixing and emulsification to obtain a water-in-oil type viscous pickering emulsion; and (3) obtaining a 3D porous emulsion scaffold by extrusion type 3D printing with the water-in-oil type viscous pickering emulsion, and performing drying to obtain the composite biological scaffold. The scaffold consists of multiscale pores and hasthe porosity of 65%-95%; and the scaffold has good shape memory performance under two stimulations of heating and near infrared light irradiation and has good application prospects in the tissue engineering field.

The invention discloses a biodegradable lacrimal duct embolus and a preparation method thereof. The lacrimal duct embolus is prepared by using one or more of a lactide / caprolactone copolymer, a glycolide / caprolactone copolymer, a lactide / dioxane ketone copolymer and a lactide / trimethylene carbonate copolymer as raw materials through the following steps of sequentially carrying out melt extrusion,hot stretching and cold cutting on the raw materials in an inert gas atmosphere. The biodegradable lacrimal duct embolus is used for treating dry eye syndromes; in the process of operation, a part ofthe lacrimal duct embolus is implanted into a lacrimal duct, and the rest of the lacrimal duct embolus can automatically be shrunk into the lacrimal duct, therefore, in the process of operation, a patient feels no pain, the diameter of the lacrimal duct of the patient is not required to be measured before operation, and the lacrimal duct embolus in one product specification can be suitable for the lacrimal ducts in different sizes; in the process of preparing the biodegradable lacrimal duct embolus, the embolus can load anti-inflammatory agents, antibiotics and antiproliferative drugs so as to avoid the generation of complications such as inflammations, wrapping and the like; and in addition, the lacrimal duct embolus is good in biocompatibility and can be completely biodegraded in the lacrimal duct, and the final products of the embolus are non-toxic water and carbon dioxide, thereby avoiding secondary surgery of the patient.

The invention relates to the fields of bioengineering and biomedicine, in particular to a 3D printing material, a neural restoration catheter and a preparation method of the neural restoration catheter. The novel 3D printing material is provided by the invention, substances capable of reducing ultraviolet light transmittance are added into conventional raw materials for biomaterial printing, and thus the 3D printing material can be used for high-precision printing is obtained. Through the material, high-precision biomaterials such as the neural restoration catheter can be prepared by 3D printing equipment.

A polyether-ether-ketone artificial spine intervertebral disc comprises an upper end plate, a lower end plate and a nucleus pulposus prosthesis arranged between the upper end plate and the lower end plate. The nucleus pulposus prosthesis is made of medical stainless steel or vitallium or biological ceramic and the upper end plate and the lower end plate are made of polyether-ether-ketone. The upper surface of the upper end plate and the lower surface of the lower end plate are respectively provided with a coarse surface and each coarse surface is formed according to the physical machining methods such as carving conducted by a carving machine and emery spraying. The upper end plate and the lower end plate are fixed to the spine in a fused mode, the nucleus pulposus prosthesis is placed between the upper end plate and the lower end plate and is also called a rotary center, three-dimensional rotary movement is achieved among the nucleus pulposus prosthesis, the upper end plate and the lower end plate, and therefore the function of motion of the normal spine intervertebral disc of a person can be provided. The upper end plate and the lower end plate which are made of the polyether-ether-ketone are good in biocompatibility and self-lubrication and quite resistant to abrasion. The nucleus pulposus prosthesis is good in mechanical performance and high in strength. The polyether-ether-ketone artificial spine intervertebral disc has the advantages of being simple in structure, good in biocompatibility, durable, and wide in adaptation disease range.

The invention discloses an anastomotic fistula protective flusher and solves the problems that patients need to go through secondary operation, the medical cost is high, rectum bruise is caused easily, the wear comport is poor and operation is inconvenient in existing anastomotic fistula treatment method and devices. The flusher comprises a protective flushing stopper adopting a hollow structure and is characterized in that a middle contraction part is arranged between an upper arc body and a lower discharge end of the protective flushing stopper, and a drainage inlet and a flushing part are arranged above the upper arc body; a drainage joint is arranged at a drainage outlet of the lower discharge end and connected with a drainage liquid collecting bag through a drainage hose; an injectionport of the lower discharge end is connected with a liquid inlet of the washing part through an injection inlet pipe; an inflating port of the lower discharge end is connected with a closed air bag through an air delivery pipe. The flusher is reasonable in design and compact in structure, capable of avoiding secondary operation, facilitating transfer of excrement, reducing anastomotic stoma tension, helping fistula healing and performing postoperative disinfection on anastomotic stoma.

The invention provides a filter device which comprises a filter component, a restraining component and a support component, wherein the filter component, the restraining component and the support component all are made of a biodegradable material; the restraining component is used for restraining the filter component; the support component is connected with the filter component and arranged coaxially with the filter component; and the time of completing degradation by the restraining component is shorter than that by the support component. The filter device is implanted in vivo through a minimally invasive surgery; and various components are made of the biodegradable material and can be automatically degraded in vivo until the components disappear in vivo after works are completed, so that the problems of vena cave obstruction and long-term immunological rejection due to the fact that a permanent filter device exists in vivo for a long period of time are solved, and the problems that a second operation is caused by a temporary filter device and a filter cannot be taken out are also solved.

The invention discloses a 3D (three-dimensional) printing degradable trachea outer stent for treating tracheostenosis and a manufacturing method thereof. The 3D printing degradable trachea outer stent comprises an outer stent main body and a bellmouth formed in the end part of the outer stent main body, wherein the inside of the outer stent main body is a passage used for bronchus narrow position passing; a notch for connecting a passage is formed in the side wall of the outer stent main body in the axial direction; a plurality of annular bulges are formed in the outer stent main body in the peripheral direction; a suture needle hole penetrating through the passage is formed between the adjacent annular bulges; the trachea outer stent is prepared from degradable materials through 3D printing. The trachea outer stent can be used for expanding the narrow trachea; the re-compression of the peripheral tissues can be prevented; in addition, the stent naturally degrades along with the time; the injury of secondary operation is avoided; the novel thought and the effective treatment measure can be provided for tracheobronchial stenosis caused by various reasons.

The invention relates to a monitoring bougie and a monitoring device. The monitoring bougie comprises a monitoring probe, a connector and a first storage module, wherein the monitoring probe is used for acquiring a collection signal; one end of the connector is connected with the monitoring probe through a lead wire, and the other end of the connector is provided with a first connection opening connected with the monitoring device in a detachable manner; the first storage module is used for storing an ID and a preset threshold value of the monitoring bougie. By the arrangement of the first storage module on the monitoring bougie, various types of data can be backed up, and independency of the monitoring bougie and the monitoring device can be realized; when being pulled out of the monitoring device, the monitoring bougie can be connected with other monitoring devices; the monitoring device can continuously carry out monitoring work by identifying information (the ID of the monitoring bougie) recorded on a storage chip of the monitoring bougie.

The invention discloses a repair system applied in a craniocerebral operation. The system is characterized by comprising movable repair patches, wherein the repair patches are overlaid to form a movable topological structure; the movable topological structure can expand with increased intracranial pressures and can retract with decreased intracranial pressures; and a topological system is composed through arrangement of the multiple repair patches, and the system can expand or retract with intracranial pressure changes. The repair system can be reset after an intracranial pressure of a patient returns to normal after the operation and can finally become consistent with the form of a skeletal flap of the patient removed during the operation. Through application of the repair system, traumas and economic burdens caused to the patient by a second-time operation in a traditional treatment scheme can be avoided; and possible infection and complications such as epilepsy caused by the second-time operation to the patient can be avoided.

The invention discloses an oral implant device for avoiding secondary surgery, comprising an implant, a screw, an implanting receiving area bone plate and a threaded cover part; the outside of the implant is provided with a thread, the lower end of the implant is provided with the nut that is in threaded connection, the bottom of the implant is fixedly connected to the implanting receiving area bone plate, a threaded hole is arranged at the center of the bottom of the implant, and the threaded cover part is in threaded connection to the threaded hole. The secondary injury is effectively avoided, wound treatment time is shortened, and pain of a patient is relieved.

The invention discloses a synthesis method and application of a low-temperature-melting drug sustained-release medical polymer material. The material is modified on the basis of a polycaprolactone polymer with good biocompatibility, and remains in a molten state for a sufficient time after being heated to body temperature. In addition, the material is biodegradable in vivo and degradation productsare harmless. The material can be used for wound filling under body temperature, medicine carrying and slow release, low-temperature medical coating, and the like, is simple and feasible to operate and remarkable in effect, and has wide medical application prospects.

The invention relates to the technical field of medical apparatuses, in particular to a spine dynamic growth rod, which comprises at least one connecting rod, one conical elastic clamping sleeve, one sleeve cylinder and one cover plate. When one connecting rod is used, a conical hole is formed in one end of the sleeve cylinder, a circular hole is formed in the other end of the sleeve cylinder, the connecting rod is arranged in the sleeve cylinder in a clearance fit way through the conical elastic clamping sleeve, and the sleeve cylinder is connected with a cover plate; when two connecting rods are used, conical holes are formed in the two ends of each sleeve cylinder, a circular hole is formed in the middle part of each sleeve cylinder, the two connecting rods are symmetrically arranged, the symmetrical end surfaces are respectively provided with a limiting block, the two connecting rods are respectively arranged in the sleeve cylinders in the clearance fit way through the corresponding conical elastic clamping sleeve, and the two ends of each sleeve cylinder are connected with the corresponding cover plate by threads. The spine dynamic growth rod has the advantages that by utilizing the simple conical structure, the dynamic growth rod grows along with the growth of a patient, so the pain of the patient caused by secondary operation and multiple operations because of growth is avoided; by selecting a one-way growth mode and a two-way growth mode, the operation time of the doctor is effectively shortened, and the foreign body sensation of the patient in the use process is effectively reduced.

The invention discloses a magnetic peritoneal drainage tube device. The magnetic peritoneal drainage tube device comprises a drainage tube, an inner core arranged in the drainage tube and a magnetic controller arranged in vitro, wherein the inner core is magnetic, and the magnetic inner core enables the head end of the drainage tube to change the drainage position in vivo under the action of the magnetic controller; the magnetic inner core is provided with an air bag at the head end in vivo and is provided with an air extractor at the tail end in vitro, and the air extractor is communicated with an air guide tube arranged in the magnetic inner core. The magnetic peritoneal drainage tube device is simple in structure, can be used for accurately adjusting the head end of the drainage tube according to the specific drainage position after the drainage tube enters a body, and provides reliable guarantee for smooth drainage.

The invention discloses a minorcaliber tissue engineering artificial vessel. The excised extract cell umbilical vessel is taken as a bracket, the gap part of the bracket is filled with smooth muscle cells and mechanocyte; the endothelial progenitor cells or mesenchymal stem cells are planted in the surface of the inner wall of the excised extract cell umbilical vessel. The minorcaliber tissue engineering artificial vessel has good biocompatibility and has the abilities of inducing, supporting and maintaining cell functions, thus reducing the reciprocal infection of virus among seeds. The artificial vessel produced by the invention overcomes the problem that the supply of autologous vessel plantation is limited and the failure problem of the synthesized implants for formation of thrombosisand / or endometrial hyperplasia, thus improving the long transplantation patency that the minorcaliber tissue engineering artificial vessel is planted into human body, leading the sufferers to avoid asecondary operation. The raw materials of the artificial vessel are obtained easily, the preparation method is simple, and cost is low, thus being accepted by the sufferers and having vast social benefit and economic benefit.

The invention relates to the technical field of a cut-off apparatus, in particular to a cut-off apparatus used for intestinal tract therapy. The cut-off apparatus comprises a fixing piece and a drainage tube; the fixing piece is used for fixing the drainage tube into an intestinal tract; the drainage tube is used for draining digestion substances in the intestinal tract; the fixing piece is made of a combination of an elastic intestinal tract-friendly material and a dissolving material; in actual use, the fixing piece can be automatically sucked on the inner wall of the intestinal tract; and after surgery is done, the apparatus can be mostly dissolved and separated. The cut-off apparatus aims to realize that secondary surgery is not needed after a large intestine is treated surgically; after large intestine surgery of a patient is done, the drainage tube in the apparatus dissolves and separates in the intestinal tract, and the fixing piece for the drainage tube automatically falls off;and secondary surgery for reduction of a neostomy intestinal tube is not needed for fear that the treatment risk of the patient is increased, and meanwhile, the treatment cost is increased. The apparatus is easy to use, simple to operate and suitable for being popularized.

The invention relates to a negative-pressure double-sleeve drainage tube which comprises an outer sleeve and an inner dredging sleeve. The negative-pressure double-sleeve drainage tube is characterized in that a plurality of convex strips are evenly distributed on the inner side wall of an inner section of an outer sleeve body in the circumferential direction, holes are formed in the centers of the convex strips, the holes of the convex strips converge with and are communicated with a channel formed in the outer end side wall of the outer sleeve body, a circle of groove is formed in the inner wall of an outer section of the outer sleeve body in the circumferential direction, and an opening, corresponding to the channel, is formed in the groove and is communicated with the channel. After the technical scheme is adopted, it is ensured that the in-cavity position of the outer sleeve is not moved, various blockages such as blood clots, tissue fragments and mixed proteins are simply and effectively cleared, smooth drainage is easily restored, passive drainage is safely and efficiently changed into initiative drainage, a best drainage effect is achieved and is the priority among priorities of conservative treatment means, and accordingly possible second operation is avoided.

The invention discloses a medical internal fracture fixation needle and a medical fracture fixation tool. The medical internal fracture fixation needle is made of biodegradable magnesium or magnesiumalloy materials, and comprises a needle head, a needle body and a needle tail, wherein the needle head is conical so that an internal fixation needle can be inserted into a bone hole; the needle bodyis cylindrical, and a clamping structure is arranged on the needle body, and is used for achieving locking of the needle body after the internal fixation needle is inserted into the bone hole; multiple tail vane structures arranged at intervals are arranged on the surface of the needle tail, the ends, away from the needle tail, of the tail vane structures are pointed, so that the tail vane structures are inserted into the bone hole to achieve the anchoring effect, and a sliding groove for achieving the guiding effect is formed between every two tail vane structures. By means of the medical internal fracture fixation needle and the medical fracture fixation tool, the discomfort of a patient in the application process is reduced while a fixation operation can be conveniently carried out on the patient, and a second operation is avoided; as a degradation product of magnesium and magnesium alloy is alkalescency, stem cells can be better differentiated into osteoblast, generation of new bones is facilitated, and fracture healing is promoted.

The invention discloses a biodegradable ultra-fine grain Zn-Li alloy material as well as a preparation method and application thereof. The mechanical property of the biodegradable ultra-fine grain Zn-Li alloy material is improved through adding of the Li element and multi-pass deformation processing. The strengthening effect of the Li element on the zinc alloy is most obvious mainly depending on the pinning effect of the intermediate phase LiZn4. The multi-pass deformation processing is mainly performed through the grain refinement effect. The zinc alloy in the invention can be naturally degraded in the human body, meanwhile, the degradation rate is controllable, the zinc alloy can naturally disappear from the human body after the medical effect is achieved, and a secondary operation is avoided. Besides, zinc is one of trace elements necessary for the human body, and degradation products of zinc are harmless to the human body. The Zn-Li intermediate alloy is added into the zinc alloy, and the structure of the alloy can be further optimized by regulating and controlling the content of the Li element, so that the comprehensive mechanical property and the biocompatibility of the zinc alloy are improved, and the corrosion rate of the zinc alloy can be properly regulated and controlled.