35 results about "Hypertrophic scar" patented technology

The scar removing cream is prepared from the following raw materials in percentage by weight: 30 to 80 percent of silica gel component, 5 to 30 percent of solvent, 0.1 to 10 percent of emulsifying agent, 1 to 5 percent of thickening agent, 0.01 to 10 percent of extract / synergistic component, 0.1 to 20 percent of medicament component, 1 to 50 percent of moisturizing component, 0.01 to 0.1 percent of growth factor, 0.1 to 2 percent of other component, 0.01 to 0.5 percent of preservative and 0.1 to 2 percent of pH (Potential of Hydrogen) regulator. The traditional Chinese medicine composition has the effects of improving skin repair, whitening and diminishing inflammation, accelerates skin elasticity recovery and reduces scars.

The embodiment of the invention provides a self-powered microneedle patch for repairing hypertrophic scars as well as a preparation method and application of the self-powered microneedle patch. The self-powered microneedle patch comprises: a friction nano-generator for generating a current; the conductive drug-loaded microneedle patch is connected with the friction nano-generator, and the friction nano-generator is connected with the conductive drug-loaded microneedle patch; the conductive drug-loaded microneedle patch comprises a conductive microneedle patch body and a crosslinked gelatin-crosslinked hyaluronic acid microneedle bearing Sb4. The surface of the conductive micro-needle patch is provided with a metal coating, and the conductive micro-needle patch is used for mediating current generated by the friction nano-generator and applying percutaneous electrical stimulation; the cross-linked gelatin-cross-linked hyaluronic acid microneedle is coated at the tip of the conductive microneedle patch. According to the self-powered microneedle patch provided by the embodiment of the invention, myofibroblasts of hypertrophic scars are transdifferentiated into adipocytes by providing percutaneous electrochemical stimulation, inflammatory factor release is inhibited, and a tissue microenvironment is remodeled, so that the hypertrophic scars are reversed, and skin repair and tissue regeneration are realized.

Some embodiments are directed to a skin treatment system that contains a laser generating device. A hydrogel patch may include a region, at a first side of the hydrogel patch, to be in contact with a person's skin. The region may contain an adsorbing medium (e.g., carbon black or any other substance that would have a similar effect) that, when receiving a laser beam from the laser generating device, results in Extracorporeal Shock Wave Therapy (“ESWT”) being applied to the person's skin to treat a dermatologic condition such as an epidermal or dermal tissue structure irregularity, cellulite, a stretch mark, a scar, scar-tissue, a hypertrophic scar, an acne scar, etc.

The invention discloses double-network hydrogel based on chlorogenic acid as well as a preparation method and application of the double-network hydrogel, and belongs to the technical field of wound dressings. A first network of the double-network hydrogel based on the chlorogenic acid is formed by coordination of the chlorogenic acid and Zn < 2 + >, and CA and Zn < 2 + > can be quickly released in inflammation and proliferation stages, so that the effects of resisting bacteria, resisting oxidation, diminishing inflammation and generating blood vessels are achieved; the second network is formed by covalent crosslinking of heparin grafted gelatin and genipin, crosslinking of gelatin and genipin can enhance the mechanical strength, heparin is grafted into gelatin, bFGF can be stably added, the release time of bFGF at a wound part can be prolonged, and bFGF is slowly released in proliferation and remodeling stages, so that scars are prevented from being formed; in-vivo studies of MRSA infected diabetic mouse models and rabbit ear hyperplastic scar models show that the dual-network hydrogel can significantly promote healing of scar-free wounds. The programmed release function of the CZGF hydrogel plays a key role in accelerating chronic wound healing and preventing scar formation.

A microneedle loaded with at least curcumin, exosomes, and an acellular matrix. Curcumin is incorporated into the exosomes to form functionalized exosomes (Cur@EV), which serve as the primary active ingredient for the repair of hypertrophic scars. Cur@EV has been shown to exhibit a high affinity for hypertrophic scar fibroblasts, while more efficient delivery of curcumin to HSFs has demonstrated enhanced anti-HSF cell proliferation activity and significant anti-fibrosis effects, potentially meeting clinical needs for the repair of hypertrophic scars.

The present specification discloses a method, system, and apparatus for inhibiting collagen production in fibroblasts using an alternating electric field. In one aspect, the present invention can effectively regulate ECM homeostasis by inhibiting the production of type I procollagen and increasing MMP-1 expression using a low-frequency and low-intensity alternating electric field, thereby effectively regulating (inhibiting) collagen production in fibroblasts. In another aspect, it has the advantage of being applicable not only to the treatment of fibroproliferative skin diseases such as hypertrophic scars and keloids, but also to the prevention and treatment of general surgical wounds that occur after surgery.

The invention discloses an application of an activator combined by one or more genes / proteins in preparation of drugs for treating hypertrophic scars, and belongs to the technical field of biological medicines. In order to solve the problem that when retinoic acid cream is used for preparing hypertrophic scars, a specific mode and an action target of a retinoic acid signal channel for regulating and controlling fibroblasts are not disclosed yet, the action target and a regulation and control mechanism of ATRA for regulating and controlling fibroblast activation and glucose metabolism remodeling are explored through in-vivo and in-vitro experiments; and on the basis of a Cre-loxP system, the function of the target gene is verified. Researches in the invention show that ATRA promotes transcription of HIC1 and inhibits transcription and expression of TGF-beta1 by activating RAR alpha on one hand, and ATRA promotes transcription of HIC1 and inhibits transcription and expression of TGF-beta1 on the other hand; on the other hand, the transcription of PCK1 and PCK2 is promoted, so that the proliferation and abnormal activation of HSFs are reduced, and the occurrence and development processes of hypertrophic scars are finally inhibited. The conclusion provides a sufficient theoretical basis for inhibiting hypertrophic scar formation by ATRA.

The invention discloses a bionic hybrid carrier for actively targeting hypertrophic scars as well as a preparation method and application of the bionic hybrid carrier. According to the preparation method, materials such as scar fibroblast cell membrane protein, a cation carrier and siRNA are adopted, hybridization of a cell membrane and the cation carrier is achieved through an ultrasonic co-extrusion technology, and the carrier is endowed with immune escape and homologous targeting capacity; high-efficiency loading of TGF-beta1 siRNA is realized by utilizing electrostatic self-assembly, so that a bionic transdermal delivery system with an active targeting characteristic is constructed. The bionic hybrid carrier not only provides an innovative thought for root therapy of hypertrophic scars, but also opens up a new way for gene intervention of other skin fibrosis and inflammation related diseases, and has important clinical transformation value.

The invention discloses an adjustable post-burn hypertrophic scar treatment device, relates to the technical field of medical instruments, and provides the following scheme that the adjustable post-burn hypertrophic scar treatment device comprises a bed body, an arch bridge is slidably connected to the bed body, a fixing cylinder is connected to the arch bridge, a fixing shell is rotatably connected to the bottom end of the fixing cylinder, and a fixed air bag is embedded into the bottom end of the fixing shell; the bottom end of the fixing shell is sleeved with a rubber sleeve, the fixing barrel is connected with mesh cloth, a fixing block is installed at the bottom end in the air bag, and the bottom end of the fixing block is slidably connected with a plurality of knocking columns. The air bag is moved to the position above the scar through the arch bridge, the expanded air bag extrudes the scar, in the process of pressurizing the scar, the air bag extrudes the rubber sleeve and the screen cloth to make the rubber sleeve and the screen cloth tightly abut against the surface of the scar and drive the air bag and the rubber sleeve to rotate, and absorption of the scar to liquid medicine is promoted through pressurization and rotating friction of the rubber sleeve; and the knocking column continuously strikes the rubber sleeve, so that the scar softening is promoted.

The application discloses a kind of active targeting hyperplastic scar's biomimetic hybrid delivery vehicle and its preparation method and application.The application uses scar fibroblast membrane protein, cationic delivery vehicle and siRNA and other materials, realizes the hybridization of cell membrane and cationic delivery vehicle by ultrasonic co-extrusion technology, and gives the immune escape and homologous targeting ability of carrier;Efficient loading of TGF-β1 siRNA is realized by using electrostatic self-assembly, so as to construct a biomimetic transdermal delivery system with active targeting characteristics.The biomimetic hybrid delivery vehicle not only provides an innovative approach for the root cause treatment of hyperplastic scar, but also opens up a new way for gene intervention of other skin fibrosis and inflammation-related diseases, and has important clinical translation value.

The application belongs to the field of new use of drugs, and more particularly relates to application of 3-Deazaadenosine in preparation of a therapeutic drug for treating hypertrophic scars. 3-Deazaadenosine is an S-adenosylhomocysteine hydrolase inhibitor, and has antiviral, anti-inflammatory and other activities. Experiments show that the compound can significantly reduce the modification level of m6A in fibroblasts in hypertrophic scar tissue, inhibit the proliferation and migration of fibroblasts, promote the apoptosis of fibroblasts, and also can reduce the expression levels of Collagen I, Collagen III and alpha-SMA in fibroblasts. Therefore, the compound can be used for preparing a drug for relieving or treating hypertrophic scars, and has important clinical application value.

The present invention discloses a supramolecular anti-hypertrophic scar material and its preparation and application, which relates to the technical field of nano-diagnostic and therapeutic materials. The material comprises amphiphilic vesicles formed by the assembly of water-soluble supramolecular macrocycles and hydrophobic Chinese herbal molecules through host-guest interactions, wherein the inner and outer layers of the vesicles are both supramolecular macrocycles, and the hydrophobic Chinese herbal molecules are located between the inner and outer layers of the vesicles; the interior of the amphiphilic vesicles is loaded with enriched metal nanoclusters. The present invention assembles hydrophilic supramolecular macrocycles and active ingredient hydrophobic Chinese herbal molecules into vesicles through supramolecular host-guest interactions, and then loads functional component metal nanoclusters, thereby constructing a high-performance supramolecular material for the treatment of hypertrophic scars based on the ferroptosis-apoptosis synergistic mechanism.

The invention provides multi-effect composite scar repair gel as well as a preparation method and application thereof, and belongs to the technical field of biological medicines. The invention develops a multi-effect composite scar repair gel with barrier protection, anti-inflammatory regeneration and long-acting permeation by integrating a silicone base material, traditional Chinese medicine active ingredients and an ionic liquid permeation promotion technology. Wherein the high-viscosity polydimethylsiloxane is used for reducing skin tension; the low-viscosity polydimethylsiloxane improves the skin comfort level; the traditional Chinese medicine extract inhibits fibroblast proliferation and promotes microcirculation; the Ectoin-allantoin microcapsule is capable of realizing 72-hour slow-release anti-inflammatory repair; the BPC157 polypeptide can promote angiogenesis and accelerate wound healing; the transdermal rate of the active ingredients is increased by more than 3 times by the arginine-malic acid ionic liquid; the zinc hyaluronate can synergistically moisturize and regulate the inflammation microenvironment. Through cooperation of multiple mechanisms, the effects of barrier protection, anti-inflammatory regeneration and long-acting permeation are achieved, and the anti-inflammatory and long-acting anti-inflammatory ointment is suitable for repairing hypertrophic scars, acne scars and postoperative incisions.

The invention relates to the field of traditional Chinese medicine, in particular to a traditional Chinese medicine composition, a pharmaceutical preparation and a preparation method and application thereof, and the traditional Chinese medicine composition comprises the following components in parts by weight: 0.15-0.3 part of blumea balsamifera, 0.15-0.3 part of borneol, 1-3 parts of juncus effuses, 6-10 parts of eucommia ulmoides, 6-10 parts of kelp, 0.1-0.5 part of wormwood essential oil, 4-5 parts of myrrh, 6-10 parts of eclipta, 9-15 parts of muskmelon seed and 4.5-6 parts of gallnut. The traditional Chinese medicine composition provided by the invention can reverse hypertrophic scar key imbalance signal channels and inhibit scar cell proliferation and migration, is high in safety and reliability, and can effectively inhibit scar hyperplasia and improve color, softness and thickness of pathological scars.

The invention relates to the technical field of drugs for treating hypertrophic scars, in particular to application of triglycosyl ceramide in treatment of hypertrophic scars. Based on a newly found molecular regulation mechanism, the heterogeneity of skin fibroblasts is regulated in a targeted manner, so that pathological fibrosis and scar formation in a burn wound healing process are effectively inhibited. The invention provides a strategy for accurately intervening the transdifferentiation of fibroblasts to myofibroblasts and promoting the fibrosis direction. In the prior art, an effective target spot aiming at a fibroblast heterogeneity key regulation and control node on a burn wound surface is lacked. The invention discloses a new'HEXB-Gb3-FGF2 'regulation axis, and develops a treatment method for specifically targeting a key product triglycosyl ceramide of glycosphingolipid metabolism.

This invention discloses a combination of biomarkers, a kit, and their applications for detecting hypertrophic scars (HTS). The biomarker combination includes a core biomarker and / or auxiliary biomarker 1 and / or auxiliary biomarker 2; the core biomarker is ABCC9 and CSPG4, auxiliary biomarker 1 is RGS5 and ACTA2, and auxiliary biomarker 2 is PDGFRB and TRPC6. This invention also provides a kit containing the above biomarker combination detection reagents and a drug screening method. This invention reveals for the first time that pathological pericytes are the core fibrotic cells in HTS, breaking through the traditional understanding that fibroblasts are the dominant cells. By targeting and inhibiting the abnormal activation, proliferation, and transdifferentiation of pericytes into myofibroblasts, the generation of myofibroblasts and matrix deposition are curbed at the source, providing a new strategy for precision treatment of HTS. Compared with traditional therapies, this approach has higher specificity and can achieve early molecular warning and quantitative detection of trace tissues for HTS, effectively overcoming the lag and subjectivity of clinical morphological diagnosis.

The application belongs to the technical field of biological medicine, and discloses soluble microneedles for treating hyperplastic scars, and a preparation method and application thereof. The hyaluronic acid is modified to obtain sulfonated hyaluronic acid, which is blended with natural penetration enhancer dextro-borneol having anti-inflammatory activity, rotary evaporated and freeze-dried to obtain a sulfonated hyaluronic acid-dextro-borneol solid dispersion, and then the solid dispersion is loaded into the microneedles to obtain the soluble microneedles having the function of treating hyperplastic scars. The method improves the bioavailability and biocompatibility of dextro-borneol, and the dextro-borneol is loaded into the microneedles, so that the anti-inflammatory and migration inhibition of fibroblasts of the solid dispersion can be maximized, and the microneedles and dextro-borneol can penetrate the dense scar tissue to achieve the purpose of deep drug delivery under the double penetration of the microneedles and dextro-borneol. The application provides a safe and efficient novel transdermal drug delivery system for treating hyperplastic scars, and has a wide clinical application prospect and market value.

The invention discloses a double-drug-loading soluble microneedle patch with a hypertrophic scar improving function as well as a preparation method and application of the double-drug-loading soluble microneedle patch, and belongs to the technical field of medical cosmetology. The microneedle patch comprises a substrate and a needle body arranged on the surface of the substrate, wherein the needle body is mainly prepared from a cyclodextrin inclusion compound, colchicine and a microneedle framework material; the cyclodextrin inclusion compound is prepared from an insoluble drug shikonin and beta-cyclodextrin, and the microneedle framework material is prepared from sodium hyaluronate and polyvinylpyrrolidone. The double-drug-loading soluble microneedle patch has good mechanical strength and can accurately penetrate through scar skin to form a drug delivery channel. Compared with a traditional transdermal patch, the soluble microneedle has the advantages that the transdermal permeation efficiency of the medicine is greatly improved, and compared with traditional injection administration, the soluble microneedle reduces long-term irritation to the skin, reduces the risk of adverse reactions such as infection and bleeding and has a very good application prospect.

The present invention relates to the technical field of medical dressings, and discloses a scar repair gel containing recombinant mussel mucin and a preparation method thereof. The scar repair gel comprises the following components in percentage by mass: 0.01-0.2% recombinant mussel mucin, 0.4-0.8% thickener, 6-15% compound emulsifier, 1-2% pH adjuster, 20-40% silicone, 0.1-0.3% preservative and the balance of water, wherein the silicone comprises polydimethylsiloxane, polydimethylsiloxane crosslinker and decamethylcyclopentasiloxane. The scar repair gel containing recombinant mussel mucin has good film-forming properties, forms a moisturizing barrier on the surface of the wound, can inhibit the formation of hypertrophic scars, reduce itching during wound healing, reduce the production and deposition of melanin, effectively improve the patient's comfort during use and the stability of the mussel mucin and silicone gel system.

The invention discloses a control method of a microneedle patch for treating hypertrophic scars and related equipment. The method is used for being connected with a controller of the microneedle patch for treating hypertrophic scars. The microneedle patch for treating hypertrophic scars comprises a plurality of heating units and a plurality of microneedles, each microneedle contains a medicine wrapped by a thermal response material, and the heating units are in one-to-one correspondence with the microneedles; according to the method, a first image containing a hypertrophic scar area and a second image formed by pasting a hypertrophic scar treatment microneedle patch on the hypertrophic scar area can be obtained; drawing a target contour of the hypertrophic scar area in the second image based on the first image; determining a target heating unit corresponding to the target contour; and heating each target microneedle by using each target heating unit. Therefore, according to the application, the corresponding microneedle can be accurately positioned and heated according to the specific forms of different hypertrophic scars, so that the customization of the drug release shape is realized, and the problem that the fixed-shape drug release of the traditional microneedle patch is difficult to adapt to different scars is solved.

The invention discloses a pharmaceutical composition for treating hypertrophic scars and / or keloids. The pharmaceutical composition is prepared from the following raw materials in parts by weight: 15-25 parts of gallnut, 15-25 parts of smoked plum, 15-25 parts of senecio scandens, 15-25 parts of fructus cnidii, 10-20 parts of radix angelicae, 10-20 parts of cortex lycii radicis, 170-230 parts of vinegar and 170-230 parts of honey. The composition disclosed by the invention has the effects of detoxifying, diminishing swelling, astringing dampness and relieving itching. The traditional Chinese medicine composition has obvious effects on hypertrophic scars and keloids formed after trauma, operation, burns and scalds, acne, folliculitis and other inflammations, and itching and pain caused by the hypertrophic scars and keloids.

This application relates to the field of diagnostic reagents, specifically to a scar diagnostic reagent and its application. This application is the first to discover CD3+ in the peripheral blood of keloid patients. + CD8 + The study revealed a significant decrease in cytotoxic T cells, highlighting for the first time the crucial role of the immune microenvironment in the pathogenesis of keloids. Furthermore, it was the first time that sHLA-E expression was significantly different in normal individuals compared to patients with hypertrophic scars and keloids. Using sHLA-E as a diagnostic marker can differentiate between hypertrophic scars and keloids, which are traditionally considered pathological scars, and can also be used to assess the effectiveness of keloid treatment.

The invention relates to the technical field of biological medicine manufacturing, in particular to a traditional Chinese medicine compound gel containing bioactive organic components and capable of synergistically repairing hypertrophic scars based on four-season qi and a preparation method of the traditional Chinese medicine compound gel. The compound gel is formed by mixing a bottle A base matrix and a bottle B four-season additive according to the ratio of 9: 1, the base substrate of the bottle A contains various bioactive organic components such as a salvia miltiorrhiza extract, asiatic acid, bioactive hirudin, perilla oil and the like; according to the four-season additive in the bottle B, corresponding traditional Chinese medicine extracts are selected according to seasons, the preparation method adopts a biotechnology process including supercritical COextraction, a biocompatibility nanometer co-grinding technology and other modern biotechnologies, the transdermal absorption rate of mineral components is remarkably increased, the anti-fibrosis effect is enhanced through a hirudin-perilla oil soluble synergistic system, and the anti-fibrosis effect is improved. The four-season differentiated formula realizes accurate repair of preventing wind evil in spring, clearing blood heat in summer, moistening dryness injury in autumn and dredging collaterals in winter.

The invention provides a pharmaceutical composition for treating hypertrophic scars and application, and belongs to the technical field of traditional Chinese medicine, the pharmaceutical composition is obtained by screening traditional Chinese medicine centella asiatica and rheum officinale through an immobilized Notch1 receptor chromatography model, and the pharmaceutical composition is added into optimized blank ointment to prepare an anti-hypertrophic scar external cream preparation. A hypertrophic scar animal model is copied to evaluate the drug effect of the traditional Chinese medicine composition, and it is found that the screened traditional Chinese medicine composition has a good hypertrophic scar resisting effect.

The invention provides a construction method and application of an artificial scar-like organ based on a micro-fluidic chip, the artificial scar-like organ is constructed based on the micro-fluidic chip with multiple channels, the tissue microenvironment can be accurately controlled through a micro-fluidic technology, and the tissue microenvironment can be accurately controlled. And epidermis, dermis and vein endothelial cells from a human body can be subjected to differential culture through design of different channels, so that a humanized scar tissue model which is more simulated compared with a traditional method is constructed. The device has the advantages of being small in size, good in visibility, derived from a human body and capable of being stored for a long time. Therefore, the model can be prepared on a large scale for scar drug treatment effect research, and experimental materials and research bases can be provided for treatment prescriptions of pathological hypertrophic scars caused by wounds and burns.

The invention relates to the technical field of deep learning, in particular to an orthopaedic surgery postoperative scar recovery dynamic evaluation system based on deep learning, and the system comprises the steps: obtaining gray images of a dermoscope at different sampling moments, and dividing the gray images to obtain a scar region and a capillary region around the scar; determining a recovery state index according to the area change of the microvessel texture distribution characteristic scar region in the microvessel region; when the hypertrophic scar appears, determining the area and the gray scale of the hypertrophic scar in the scar region, and determining the hyperplasia degree of the hypertrophic scar according to the area characteristic and the gray scale characteristic; and adjusting the recovery state index according to the hyperplasia degrees in the images with different gray levels to obtain a recovery evaluation coefficient, and determining a recovery evaluation result according to the recovery evaluation coefficients at different sampling moments. According to the invention, timely evaluation can be carried out in combination with the overall recovery state and the hyperplasia condition of the pathological scar area, and the accuracy and reliability of the evaluation result of scar recovery are effectively improved.

The application discloses a traditional Chinese medicine for treating scars, which comprises the following components in terms of weight: white chrysanthemum 10-15 parts, canty caterpillar fungus 8-12 parts, clove 20-30 parts, peach kernel 4-8 parts, soapberry 3-5 parts, dandelion 20-40 parts, schizonepeta 6-8 parts, salvia miltiorrhiza 8-12 parts, rhubarb 3-5 parts and licorice 6-10 parts. The application can obviously improve superficial scars and hypertrophic scars within one month, soften scar tissues, promote epithelialization of scar tissues and normalization of skin gland tissue secretion, disperse local melanocyte aggregation, and increase skin gloss and skin elasticity.

This invention provides a FAP-targeted engineered exosome for treating hypertrophic scars, its preparation method, and its application, belonging to the field of biopharmaceutical manufacturing technology. After co-incubation with an ferroptosis inducer, the FAP-targeting small molecule ligand SUC-Lys(Ac)-PEG3-UAMC1110 is covalently linked to the exosome membrane surface using an EDC / NH-mediated amide bond coupling strategy to obtain engineered exosomes. These engineered exosomes are then used to prepare microneedle patches. The microneedle patches allow the engineered exosomes to accumulate at the scar site and preferentially enter FAP-highly expressed scar fibroblasts, inhibiting their abnormal proliferation, migration, and pro-fibrotic phenotype, reducing collagen deposition, and promoting hypertrophic scar tissue remodeling. This invention combines the advantages of strong targeting, low off-target toxicity, minimally invasive drug delivery, sustained local retention, and stable efficacy, making it suitable for preparing drugs to treat or improve hypertrophic scars, and possessing good clinical translational potential.

The invention discloses a microneedle system for treating hypertrophic scars and a preparation method, application and medicine of the microneedle system, and belongs to the technical field of medical treatment. According to the technical scheme, the microneedle system for treating the hypertrophic scars comprises a needle body and a load; the load is a mixture of collagenase and 5-fluorouracil, and the mass ratio of the collagenase to the 5-fluorouracil is 1: (4-6); on one hand, the collagenase in the application can break a scar collagen barrier and increase the permeability of medicine tissues, and on the other hand, the collagenase can perform enzymolysis on excessively deposited collagenous fibers; 5-fluorouracil in the micro-needle system has a deep effect to inhibit abnormal proliferation of fibroblasts, so that the micro-needle system synergistically inhibits and clears scars from a plurality of channels, and synergistic interaction is realized.

The invention discloses a mouse skin wound traction device which comprises a first stretching part and a second stretching part which are symmetrically arranged with a mouse skin wound as a symmetry axis, the first stretching part and the second stretching part compress a spring through a nut to enable the wound stretching part to obtain traction force on the wound, and the first stretching part and the second stretching part are connected to the two sides of the wound through a stud and a placement plate. And the wound is pulled. The invention further discloses a using method of the device. According to the invention, dynamic adjustable traction can be realized; the 3D printing technology is adopted to replace part of original parts, the weight of the device is greatly reduced, the comfort of a mouse after the device is installed is improved, and even pressure is applied to the two sides at the same time to pull a wound, so that hypertrophic scars can be formed more easily.