386 results about "Carbodiimide" patented technology

The invention discloses a synthesis method of oxyalkyl isourea and application of the oxyalkyl isourea as a free radical alkylation reagent. According to the synthesis method, cheap and rich alcohol compounds and carbodiimide are used as raw materials, oxygen alkyl isourea is synthesized in one step under the mild condition of metal catalysis, the synthesis process is simple and convenient, the yield is high, and hectogram-level large-scale preparation can be achieved. The synthesized oxyalkyl isourea can be used as a free radical alkylation reagent to be applied to a coupling reaction of metal catalysis, so that different alkylate products rich in saturated carbon sequence structures are prepared, and the method has a good application prospect.

The preparation method comprises the following steps: by taking natural chitosan, epsilon-polylysine and polyphenol as raw materials, firstly, respectively preparing polyphenol modified chitosan and carboxyphenylboronic acid modified polylysine through a carbodiimide coupling method, then, mixing single-component solutions of the polyphenol modified chitosan and the carboxyphenylboronic acid modified polylysine, and then, preparing the antibacterial and antioxidant glycopeptide hydrogel based on the polyphenol. And the antibacterial and antioxidant glycopeptide hydrogel is obtained by virtue of the synergistic effect of the phenolic hydroxyl group-boric acid group dynamic bond and the amino group-carboxyl group. The hydrogel disclosed by the invention has broad-spectrum antibacterial property and glucose response oxidation resistance, has self-healing capability and strong wound adhesion, is excellent in biocompatibility and can be naturally degraded; and the process is simple, convenient and controllable, large-scale production is easy to realize, the hydrogel can be used as a wound dressing for treating chronic difficult-to-heal wounds such as diabetes mellitus in a targeting manner, and integrated nursing of antibiosis, antioxidation, wound adhesion and self-repairing is realized.

The invention discloses a functional hydrogel microsphere and a preparation method and application thereof, and relates to the technical field of medicines.The preparation method comprises the steps that a hyaluronic acid methacrylic acid precursor solution and an IL-1beta shRNA adenovirus stock solution are mixed to obtain an Ad-atHAMA precursor solution; preparing the Ad (at) HAMA precursor solution through an oil-in-water micro-fluidic technology to obtain an Ad (at) HAMA microsphere; and sequentially adding the Ad (at) HAMA microspheres, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and N-hydroxysuccinimide into a 2-morpholinoethanesulfonic acid buffer solution, carrying out activating treatment, adding E selectin, and incubating to obtain the functionalized hydrogel microspheres. The functionalized hydrogel microspheres can inhibit a related mechanism of acute spinal cord injury pathological progress and promote neural function repair by targeting adsorption of neutrophil to regulate Nets-triggered innate immune inflammation cascade.

The invention relates to the technical field of batteries, in particular to a low-hydrogen-evolution graphene material for a lead-acid battery and a preparation method thereof.The method comprises the steps that firstly, ethidene diamine is grafted to the surface of graphene oxide through a carbodiimide / active ester method, and aminated graphene is obtained; performing heat treatment in a nitrogen / ammonia gas atmosphere to realize nitrogen doping; compounding with titanium dioxide, and carrying out hydrothermal reaction to form a stable structure; then, sequentially grafting imidazolium silane and perfluorodecyl silane to carry out hydrophobic modification; and finally, stabilization and low-temperature re-nitridation curing are carried out through titanium tetrabutoxide. The graphene material prepared by the method endows the battery with excellent performance, and is low in direct-current internal resistance and high in capacity retention ratio.

The invention provides synthesis of a T-2 toxin antigen and preparation and application of a monoclonal antibody. Relates to the technical field of biotoxin detection. The preparation method of the T-2 toxin antigen comprises the following steps: step 1, synthesizing an immunogen T-2-BSA by adopting a carbodiimide method, dissolving 2mg of T-2 adipic acid with 0.5 mL of dimethylformamide, and recording as a solution A; 5 mg of bovine serum albumin and 3 mg of EDC are dissolved with a 2-morpholine ethanesulfonic acid buffer solution with the pH being 5.5, and the solution is marked as a solution B; step 2, under the condition of stirring, dropwise adding the solution A into the solution B, stirring for 18 hours in a dark place at 4 DEG C, then dialyzing for 3 days by using a phosphate buffer solution, changing the solution once a day, centrifuging the dialysate for 10 minutes at 3,500 r / min, and discarding the precipitate; the adipic acid is coupled with the T-2 toxin through a chemical method, and the unique step enriches the structural characteristics of the hapten, so that the prepared T-2 toxin complete antigen is excellent in immune effect, can efficiently excite immune response of an organism, and shows high specificity and sensitivity.

The invention relates to the technical field of resin composite materials, in particular to a layer-adding adhesive film for an FC-BGA packaging carrier plate, a preparation method of the layer-adding adhesive film and an adhesive-coated copper foil. The layer-adding adhesive film is prepared from the following raw materials in parts by mass: 50 to 60 parts of epoxy resin, 180 to 200 parts of inorganic filler, 30 to 36 parts of curing agent, 4 to 6 parts of modified phenoxy resin, 3 to 5 parts of carbodiimide resin and 0.2 to 0.4 part of 4-dimethylaminopyridine. Modified phenoxy resin and carbodiimide resin are added on the basis of main components such as epoxy resin, inorganic filler and a curing agent, meanwhile, 4-dimethylaminopyridine is used as a curing accelerator, and through the synergistic effect of all the components, the dielectric loss angle tangent of a layer-adding adhesive film can be effectively reduced, the glass-transition temperature of a layer-adding adhesive layer is increased, and the bonding strength of the layer-adding adhesive film is improved. Good flame retardance of the layer-adding adhesive film is ensured, and the layer-adding adhesive film is applied to the adhesive-coated copper foil.

The invention is suitable for the technical field of MCA, and provides an MCA / PA6 flame-retardant composite material and a preparation method thereof. Comprising the following components in parts by weight: 50-60 parts of MCA, 15-20 parts of PA6, 15-25 parts of long glass fiber, 3-8 parts of metal hydroxide, 0.5-1.5 parts of titanium dioxide, 0.3-0.6 part of an antioxidant, 1-2 parts of nano silicon dioxide, 1-3 parts of zinc molybdate, 2-5 parts of aluminum hypophosphite, 1-2 parts of silicone resin, 0.5-1 part of carbodiimide and 5-8 parts of a toughening agent. The MCA / PA6 flame-retardant composite material disclosed by the invention combines the flame-retardant property of MCA and the excellent physical property of PA6, so that the flame-retardant property of the material is remarkably improved, and meanwhile, the original characteristics of light weight, good toughness, chemical resistance, good durability and the like of PA6 are maintained. By adding the long glass fiber, the metal hydroxide, the titanium dioxide, the antioxidant, the nano silicon dioxide, the zinc molybdate, the aluminum hypophosphite, the silicone resin, the carbodiimide, the flexibilizer and other components, the strength, the heat resistance and the flame retardant effect of the composite material are further enhanced.

The present invention relates to a microneedle-based transdermal delivery patch fabricated from a hydrogel composed of polyvinyl alcohol (PVA), arginine-modified chitosan, and a crosslinker. The arginine-modified chitosan is prepared by reacting a chitosan solution with an arginine solution preactivated with N-hydroxy succinimide and 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide at a specific pH. The hydrogel's formulation further comprises a PVA concentration ranging from 10% to 12% (w / v). arginine-modified chitosan and PVA solution are mixed in a 1:2 ratio by volume and are crosslinked using trimethyl orthoformate (TMOF). The patch is further loaded with curcumin, with a concentration of 120μg per patch, demonstrating a 70% release over 48 hours in a controlled manner. This invention represents the first application of PVA crosslinked arginine-modified chitosan hydrogel loaded with curcumin specifically for animal wound healing, providing enhanced wound healing and antibacterial efficacy.

The invention discloses a nano-drug delivery system for treating myocardial fibrosis as well as a preparation method and application of the nano-drug delivery system, and belongs to the technical field of biological medicines. According to the system, ZIF-8 is taken as a core carrier, the loading efficiency of pirfenidone is improved through high specific surface area and adjustable aperture, PCM myocardial targeting peptide is covalently coupled on the surface, and the limitation of tissue selectivity is broken through. Through coordination complexation, pi-pi conjugate accumulation and electrostatic interaction synergy, stable drug loading and microenvironment response release are guaranteed; a one-pot method and a carbodiimide method are adopted to wrap PFD and modify PCM on the surface of ZIF-8 to form a nano-drug delivery system; according to the system, the fibrosis process is intervened through multiple mechanisms, the enrichment degree and the acting time of the medicine at the diseased region are improved, the prepared medicine integrates the carrier structure advantage and the targeting peptide function, efficient medicine carrying, precise delivery and controllable release are achieved, a new scheme is provided for myocardial fibrosis treatment, and the system has wide application prospects.

The invention discloses preparation and application of bacteriophage-loaded sericin microgel, and belongs to the technical field of food preservation. The sericin microgel capable of loading the bacteriophage is prepared from a sericin solution extracted by using 1-ethyl-(3-dimethylaminopropyl) carbodiimide (EDC) in combination with a mechanical shearing method and a high-temperature and high-pressure method. The sericin protein microgel loaded with bacteriophage, which is obtained by soaking the microgel into bacteriophage proliferation liquid after freeze-drying, can significantly improve the storage stability of the bacteriophage and can effectively prolong the shelf life of beef, and the preparation method is green, simple and safe, has a wide application prospect, and is suitable for industrial production. Meanwhile, a new field is opened up for efficient application of the bacteriophage.

The invention discloses a folic acid modified active oxygen response type sodium alginate nano-carrier and application thereof, and the preparation method comprises the following steps: firstly synthesizing-Se-Se-FA: stirring dicyclohexylcarbodiimide, 4-dimethylaminopyridine, dimethyl sulfoxide / pyridine, a double-selenium fragment and folic acid at room temperature for 18-22 hours in an argon environment; and carrying out acetone precipitation, centrifugation, washing, rotary evaporation concentration and freeze-drying. The preparation method comprises the following steps: preparing an ALG-Se-FA carrier, stirring sodium alginate, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and hydroxysuccinimide in a 2-morpholinoethanesulfonic acid buffer solution, adding DMSO, dissolving a double-selenium fragment and a-Se-Se-FA fragment in DMSO and deionized water, adding the dissolved double-selenium fragment and-Se-Se-FA fragment into a system, stirring, dialyzing, and freeze-drying to obtain the product. According to the carrier, a double-selenium bond ROS response unit and folic acid targeting molecules are introduced through covalent bonds, astaxanthin can be efficiently entrapped and protected, and after the carrier is stable in gastrointestinal environment and reaches a colitis disease part, high ROS level can be responded, and intelligent drug slow release is achieved through folic acid receptor targeting.

The invention discloses a low dimer modified isocyanate composition and a preparation method thereof. The content of dimers in the modified isocyanate is reduced to 0.9 wt% or below mainly by controlling the reaction temperature of carbodiimide, the cooling rate after the reaction and the curing temperature. Through the method, the storage time of the modified isocyanate can be prolonged, and the stability of the modified isocyanate product is improved.

This invention discloses a method and sensor for adiponectin detection using a polyaniline and polyacrylic acid-modified wire mesh carbon electrode, relating to the field of adiponectin detection technology. The method involves electrochemically activating the wire mesh carbon electrode, electropolymerizing it to form a polyaniline-polyacrylic acid composite modification layer, immobilizing adiponectin monoclonal antibody after activation with N-hydroxysuccinimide and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, blocking the antibody with bovine serum albumin, and reacting it with a serum sample. The adiponectin concentration is determined based on the peak potential shift and peak current change. This invention simultaneously achieves both conductive transport and antibody immobilization, reduces non-specific adsorption and serum interference, and improves detection sensitivity, repeatability, and quantitative accuracy.

The invention discloses a preparation method of surface-modified degradable polymer microspheres, which comprises the following steps: (1) preparing dry microsphere powder: putting an oil-phase solution and a water-phase solution into emulsifying equipment for mixing and emulsifying to obtain emulsion; carrying out temperature rise and pressure reduction curing on the emulsion to obtain biodegradable microsphere dry powder; (2) dissolving the modification material: dissolving the modification material containing the amino group to obtain a solution containing the modification material; (3) swelling: dispersing the biodegradable microsphere dry powder in a third solvent and stirring to swell the surface structure of the biodegradable microsphere; (4) activation: adding a carbodiimide compound and an N-hydroxyl activator into the swollen biodegradable microsphere solution for activation, so that an O-acyl isourea intermediate is formed on the surface of the microsphere, and a surface-activated microsphere precipitate is obtained; and (5) modification: mixing the microsphere precipitate with a solution containing a modification material, and stirring to obtain the surface-modified degradable polymer microsphere. Compared with the prior art, the hydrogel has good hydrophilicity and biocompatibility.

This invention provides a method for preparing dibenzoyl-p-benzoquinone dioxime using a microchannel reactor. The method includes the following steps: 1,3-dicyclohexylcarbodiimide and a catalyst are mixed uniformly and preheated to obtain a premix; a chloroform solution of p-benzoquinone dioxime, a chloroform solution of benzoic acid, and the premix are simultaneously introduced into the microchannel reactor for reaction; the resulting reaction solution is subjected to vacuum distillation, washing, filtration, and drying to obtain dibenzoyl-p-benzoquinone dioxime. The synthesis method of this invention features high reaction conversion rate, high production efficiency, few side reactions, and high safety. The obtained dibenzoyl-p-benzoquinone dioxime product has stable quality. Furthermore, the organic solvent used can be recovered and reused after vacuum distillation, overcoming the problems of inaccurate temperature control, poor safety, numerous side reactions, and difficult waste treatment in traditional processes. This provides a new approach for the synthesis of dibenzoyl-p-benzoquinone dioxime.

Provided is a method for producing a blow-molded article, whereby it is possible to prevent a wax-derived component from migrating to the surface of the blow-molded article. The method for producing a blow-molded article includes a step of obtaining a blow-molded article by blow-molding a resin mixture containing at least a wax, a polyethylene or polypropylene, and a carbodiimide compound.

To improve the adhesion of the coating film to the resin and the resistance of the coating films to blocking each other. [Solution] The polyurethane aqueous dispersion according to the embodiment comprises a polyurethane resin (A) containing a polyester polyol as a constituent component dispersed in an aqueous dispersion medium, and includes a carbodiimide group-containing compound (B) and a salt (C) of an acid and an alkali metal. The polyurethane resin (A) has carboxyl groups, and the salt (C) is at least one selected from the group consisting of bicarbonates, carbonates, monocarboxylates, dicarboxylates, tricarboxylates, and phosphates, and the salt (C) exists in an ionized state in the aqueous dispersion medium.

The application belongs to the field of metal corrosion protection, and discloses a preparation method of graphene oxide-polyaspartic acid nanomaterial, which comprises the following steps: dispersing nano graphene oxide in a solvent to obtain a nano graphene oxide dispersion; dissolving polyaspartic acid, 4-dimethylaminopyridine and N,N-dicyclohexyl carbodiimide in an organic solvent to obtain a polyaspartic acid mixture; uniformly mixing the nano graphene oxide dispersion and the polyaspartic acid mixture according to a mass ratio of 1:1-1.5 of the nano graphene oxide and the polyaspartic acid, and performing a reaction under the protection of a certain temperature and an inert atmosphere; and after the reaction is completed, performing solid-liquid separation and collecting a solid product, namely, graphene oxide-polyaspartic acid nanomaterial. The corrosion inhibitor of the application can achieve efficient corrosion inhibition effect by adding a small amount of the corrosion inhibitor into water, and the operation is simple and the cost is low.

This polyester resin composition contains a polybutylene terephthalate resin, a recycled polyethylene terephthalate resin, a transesterification inhibitor, a carbodiimide compound, and an elastomer. The amount of terminal hydroxyl groups in the polybutylene terephthalate resin is 30-70 mmol / kg relative to the total amount of the polybutylene terephthalate resin and the recycled polyethylene terephthalate resin. The amount of the carbodiimide compound is 0.2-1.5 mass% relative to the total amount of the polyester resin composition. The amount of the elastomer is 3-15 mass% relative to the total amount of the polyester resin composition.

The invention relates to the technical field of chemical oil-displacing agents for tertiary oil recovery, and particularly discloses a magnetic nano oil-displacing agent and a preparation method thereof. The preparation method comprises the following steps: S1, taking purple phosphorus nanosheets, ferrous sulfate, ferric chloride and ammonia water as raw materials to react to obtain magnetic purple phosphorus nanosheets; s2, reacting the polymer A with ethylenediamine to obtain an aminated polymer A; s3, adding the aminated polymer A or polymer B and 4-dimethylaminopyridine 1, 3-dicyclohexylcarbodiimide into an aqueous solution of the magnetic purple phosphorus nanosheet, so as to obtain a modified magnetic purple phosphorus nanosheet; s4, performing ammonification reaction on the surfactant to obtain an aminated surfactant; and S5, adding an aminated surfactant into the modified magnetic purple phosphorus nanosheet aqueous solution, then adding N-hydroxysuccinimide and 1-ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride, and carrying out a reaction to obtain the magnetic nano oil displacement agent. The oil-displacing agent disclosed by the invention can realize magnetic recovery while realizing a viscosity reduction effect so as to improve the oil recovery rate, and waste of raw materials is avoided.

The invention discloses an ultraviolet-controlled photo-reversible dynamic crosslinking high polymer material with reversible antibacterial, shape deformation and toughening functions, and a preparation method thereof, belonging to the technical field of high polymer materials. Comprising the following steps: step 1) dissolving coumarin-3-formic acid, three-arm PCL (polycaprolactone), dicyclohexylcarbodiimide and 4-dimethylaminopyridine in dry dichloromethane in an inert atmosphere to obtain a reaction mixture; the invention relates to a preparation method of a coumarin-terminated three-arm polycaprolactone cross-linked polymer material.The preparation method comprises the following steps of (1) preparing coumarin-terminated three-arm polycaprolactone, (2) heating a reaction mixture obtained in the step (1) for set time, and filtering and separating an obtained product to obtain coumarin-terminated three-arm polycaprolactone, and (3) cross-linking and curing for set time through 365 nm ultraviolet to obtain a target product cross-linked polymer material.The function is highly integrated and dynamically adjustable, and the limitation that a traditional material is single in function is broken through.

This invention relates to a method for testing the resistance to phenolic yellowing of carbodiimide anti-hydrolysis agent powder and its application. The testing method includes: (1) grinding the sample to be tested and spreading it evenly in a petri dish; (2) placing 2,6-di-tert-butyl-p-cresol in a petri dish of the same size as in step (1); (3) placing the test reagent in a container; (4) placing the petri dish from step (1), the petri dish from step (2), and the container from step (3) into a sealed container for aging; (5) immediately using a colorimeter to detect the yellowing index of the sample after aging in step (4). The method of this invention can accurately detect powdered or crystalline carbodiimide anti-hydrolysis agents, solving the problem that it is currently impossible to accurately detect the phenolic yellowing resistance of powdered samples.

The invention relates to a cellulose-based luminescent material as well as a preparation method and application thereof. Comprising the following steps: dissolving cellulose in ionic liquid to form a cellulose solution; dissolving a phosphor and a stabilizer in a cosolvent to form a phosphor solution; the stabilizer is selected from at least one of N, N '-diisopropyl carbodiimide, N, N'-di-tert-butyl carbodiimide, N, N '-diphenyl carbodiimide and N, N'-dicyclohexylcarbodiimide; uniformly mixing the cellulose solution and the phosphorescent agent solution to form a cellulose-based phosphorescent solution; and immersing the cellulose-based phosphorescent solution into a coagulating bath to obtain the cellulose-based luminescent material. The technical problem to be solved is how to provide a cellulose-based luminescent material which has excellent water resistance, high phosphorescence efficiency and long phosphorescence life and can be applied to the fields of information encryption, underwater rescue, ion detection and the like. Meanwhile, the process is simple and convenient, green and environment-friendly, and the prepared cellulose-based luminescent material is multicolor and adjustable.

The application relates to the technical field of cable material manufacturing, and discloses a light-weight flexible wear-resistant electrical equipment connecting cable, a sheath of the connecting cable being made of raw materials including the following: polyester type thermoplastic polyurethane elastomer, styrene-acrylonitrile copolymer, maleic anhydride grafted polyolefin elastomer, blocked isophorone diisocyanate, wear-resistant premixed solution containing a catalyst, slow-release foaming master batch and functional additives; wherein the wear-resistant premixed solution containing the catalyst contains hydroxyl-terminated polydimethylsiloxane and a bismuth octoate catalyst, the slow-release foaming master batch contains modified azodicarbonamide foaming agent and carrier resin, and the functional additives contain antioxidants and carbodiimide hydrolysis stabilizers. According to the application, the hydroxyl-terminated polydimethylsiloxane containing the catalyst and the blocked isocyanate are introduced into the polyurethane matrix in cooperation through a reaction extrusion process, the isocyanate groups are unblocked at high temperature, and the organic silicon chain segment is chemically bonded with the matrix resin.

Provided is a plug that can maintain a plugged state for a prescribed period even in a fluid or water having a high temperature and a low salt concentration. A plug (5) for temporarily blocking the flow of a fluid in a well, the plug being provided with a resin molded body formed of a polyglycolic acid resin composition containing polyglycolic acid and a cyclic carbodiimide compound, the concentration of carbodiimide groups being 15 eq / t or more, or the plug being composed of the resin molded body.

The present invention relates to a process for dyeing hair keratin fibres comprising: a) the application to the hair keratin fibres of at least one dye composition C comprising at least one colouring agent chosen from direct dyes, oxidation dye precursors and mixtures thereof, and optionally at least one chemical oxidizing agent; and then b) the application of at least one composition T comprising: (1) at least one (poly)carbodiimide compound; (2) at least one polymer comprising at least one reactive group chosen from carboxylic acids; and (3) optionally at least one silicone.

Provided are a resin composition capable of producing a molded article having enhanced durability, and a molded article including the resin composition.SOLUTION: The resin composition contains a semi-aromatic polyamide having a structural unit represented by formula (1), carbon fibers, and a water-soluble carbodiimide. In Formula (1), Ar1 represents a phenylene or naphthylene group, and a plurality of Ar1 contained in the semi-aromatic polyamide may be the same as or different from each other. P is an integer of 4 to 12. [Chemical Formula 1] SELECTED DRAWING: None

The application discloses a manufacturing process of a stamping processing protective film, which comprises the following steps: step one, stirring and mixing zinc oxide, polysebacic acid-decanediol diol and dicyclohexyl carbodiimide at 50-60 DEG C to obtain material A; step two, putting 100 parts of low-density polyethylene with a melt index of 0.5-5 g / 10 min, metallocene linear low-density polyethylene with a melt index of 1.8-2 g / 10 min, oleic acid amide, zinc stearate, stearate and an antioxidant into a mixer, uniformly mixing and then extruding and granulating in a double-screw extruder to obtain material B; step three, putting material A, material B and terpolymer polypropylene into a banbury mixer, discharging after banburying for 10-30 min to obtain a master batch; and step four, blow molding the master batch to obtain a polyethylene base material layer. The protective film improves the elongation at break of the film and also improves the puncture resistance of the protective film.

This application relates to the fields of chemistry and biomedicine, specifically to a tofenamic acid lipid composition, its preparation method, and its application. A tofenamic acid derivative is obtained by reacting a morpholine solution with tofenamic acid, ethyldimethylaminopropylcarbodiimide, and 4-dimethylaminopyridine, followed by purification. The morpholine in the morpholine solution is an N-alkylmorpholine compound. The tofenamic acid derivative is used to prepare tofenamic acid prodrug liposomes via ethanol injection, which are then used in combination with a STING agonist. The synergistic effect of the combined treatment stems from the dual regulation of the tumor immune microenvironment (TME), overcoming the immune escape induced by STING monotherapy. After STING agonist treatment, the intratumoral COX-2 / PGE2 axis is activated, leading to immunosuppression. The combination of tofenamic acid liposomes and a STING agonist inhibits COX-2, thus relieving this negative feedback loop.

The application provides an antitumor compound, an antitumor preparation and a preparation method thereof, and belongs to the technical field of medicines. The method comprises the following steps: (1) dissolving folic acid in water, adding an emulsifier and stirring to mix uniformly, adding a dimethylformamide solution of cholesterol-hemisuccinic acid, dicyclohexyl carbodiimide and 4-dimethylaminopyridine dropwise, stirring to react, dialysis, freeze-drying, and preparing folic acid-cholesterol-hemisuccinic acid; (2) adding an antitumor compound, phospholipid and folic acid-cholesterol-hemisuccinic acid into tetrahydrofuran, rotating to evaporate into a thin film, hydrating, ultrasonicating, filtering through a microporous filter membrane, and obtaining liposomes; and (3) adding the liposomes into a PBS buffer solution, adding N-hydroxysuccinimide and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide, stirring to activate, adding PD-L1 and iRGD, stirring to react, dialysis, freeze-drying, and preparing the antitumor preparation.