975 results about "Dopamine" patented technology

The invention relates to the technical field of medical dressings, in particular to a perianal drug dressing of a multi-layer flow guide composite fabric and a preparation method and application of the perianal drug dressing of the multi-layer flow guide composite fabric. The perianal drug dressing is of a four-layer structure, a wet tissue adhesion layer is made of polydopamine modified chitosan / oxidized hyaluronic acid hydrogel, and wet-state adhesion is achieved; the drug sustained-release layer is used for dispersing mesoporous silica loaded with ciprofloxacin hydrochloride / defensin and chitosan microspheres loaded with epidermal growth factors / lonicera japonica into a polycaprolactone fiber membrane to achieve synergistic antibacterial and healing promotion; the directional flow guide layer is of a gradient wettability sandwich structure with a bionic micro-channel, and one-way rapid drainage can be achieved; the high-absorption outer layer is carboxymethyl cellulose / sodium polyacrylate composite sponge, liquid is locked efficiently, the wound surface is kept dry and comfortable, the clinical problem in perianal infection wound treatment can be effectively solved, and the treatment effect and the patient comfort are remarkably improved.

The invention discloses a hydrogel wound dressing with a synergistic healing promoting function as well as a preparation method and application thereof. The preparation method comprises the following steps: 1, dissolving oxidized methacrylated hyaluronic acid and dopamine in deionized water to obtain a solution A; the preparation method comprises the following steps: dissolving N-isopropylacrylamide, a photoinitiator 2-hydroxy-2-methyl-1-(4-(2-hydroxyethoxy) phenyl)-1-acetone and a cross-linking agent N, N '-methylene bisacrylamide in deionized water to obtain a solution B; 2, mixing the solution A and the solution B to obtain a pre-gel solution; or dissolving polyphenylboronic acid ester nanoparticles or polyphenylboronic acid ester-kaempferol with deionized water to obtain a solution C, and mixing the solution C with the solution A and the solution B to obtain a pre-gel solution; and 3, injecting the pre-gel liquid into a mold, and illuminating to obtain the hydrogel wound dressing loaded with the nanoparticles. The hydrogel disclosed by the invention can be used for effectively solving various problems in a wound healing process and promoting rapid and high-quality healing of a wound.

The invention relates to the technical field of membrane separation, in particular to a composite forward osmosis membrane based on mussel bionic interface enhancement and a preparation method thereof. The preparation method comprises the following steps: immersing a base material in a dopamine hydrochloride solution for oscillation reaction to obtain a modified base material; the surface of the modified base material is coated with a membrane casting solution in a blade coating mode, then phase inversion is carried out, the residual solvent is removed, then airing is carried out, and the composite forward osmosis membrane based on mussel bionic interface enhancement is obtained. By introducing the mussel bionic polydopamine intermediate layer, the long-standing technical contradictions of poor interfacial compatibility and weak binding force between the hydrophobic substrate and the hydrophilic separation layer are ingeniously solved, and the internal concentration polarization effect is remarkably inhibited. The prepared composite membrane has the advantages of high water flux, low salt reverse flux, stable structure and the like, and has wide application prospects in the fields of water treatment and substance separation.

The invention discloses a Parkinson's disease animal model, a construction method and application, and relates to the field of animal genetic engineering and disease model construction. According to the model, seven mutation sites related to the human familial Parkinson's disease are introduced behind an initiation codon of a fourth exon of an endogenous SNCA gene, and the mutation sites are A18T, A29S, A30P, E46K, H50Q, G51D and A53T and have genotypes related to the human familial Parkinson's disease. The pig model shows nigra dopaminergic neuron reduction and cortical neuron reduction in the newborn period, and the core pathological process of the human Parkinson's disease can be systematically reproduced. The model can be widely applied to Parkinson's disease pathogenesis research, drug screening and cell therapy effect evaluation, and has important scientific research and preclinical application values.

The invention relates to the technical field of water treatment filter materials, in particular to an intelligent clean gradient composite water purification filter element and a preparation method thereof. The filter element adopts an integrated design of'natural gradient base material + ZIF-67 function enhancement + fluorescence-ultrasonic intelligent regeneration ': modified vegetable sponge is used as a porous support layer, a silica gel / ZIF-67 composite gradient layer is constructed on the porous support layer to realize adsorption and antibacterial dual functions, and dopamine-aluminum ions are used for composite surface modification to enhance hydrophilicity and interlayer binding force; a matched automatic system senses pollution in real time through the fluorescence monitoring module and triggers the ultrasonic regeneration module to complete self-cleaning, and the flux recovery rate is larger than or equal to 97.5%; the interception rate of the filtering element to anabaena under the operation pressure of 0.1-0.3 MPa is larger than or equal to 99.2%, the filtering flux is increased by 6-8 times compared with that of a commercial element, the filtering element can tolerate complex water quality in the coexistence of drugs and personal care products, natural vegetable sponge serves as a base material, and the filtering element has the advantages of biocompatibility and low cost and is suitable for drinking water purification and eutrophication water body treatment.

The invention provides a cation exchange membrane chromatography medium and a preparation method and application thereof, the cation exchange membrane chromatography medium comprises a homo-porous membrane, polydopamine is loaded on two side surfaces and in a pore structure of the homo-porous membrane, and a cation exchange functional ligand is grafted on the polydopamine; a homogeneous pore membrane is selected as a matrix membrane, polydopamine is loaded on the surface and in an internal pore structure of the homogeneous pore membrane, and then a cation exchange functional ligand is further grafted, so that the surface of a chromatography medium of the obtained cation exchange membrane has relatively strong negative charges, and biomolecules with positive charges can be effectively adsorbed, thereby being separated from biomolecules with negative charges; meanwhile, the membrane is relatively low in transmembrane pressure and relatively high in separation degree, also has the characteristics of high permeability and high selectivity, and is suitable for being applied to separation and purification of biological drug macromolecules.

The invention is applicable to the technical field of hydrogel, and provides dynamic cross-linked hydrogel and a preparation method and application thereof, and the preparation method comprises the following steps: cross-linking oxidized dextran and carboxymethyl chitosan containing phenylboronic acid modification groups; glucanase is added before the hydrogel is formed, and calcium peroxide nanoparticles coated with polydopamine are introduced; wherein the mass concentration of the oxidized dextran is 2-10% w / v, the mass concentration of the carboxymethyl chitosan containing the phenylboronic acid modified group is 2% w / v, the concentration of the glucanase is 10-100 U, and the concentration of the calcium peroxide nanoparticles coated with the polydopamine is 0.1-1% w / v. The hydrogel disclosed by the invention shows good cell compatibility, angiogenesis promoting capability and bioactivity for promoting dental pulp regeneration in multiple in-vitro and in-vivo experiments, is suitable for tissue engineering fields such as dental pulp injury repair and the like, and effectively solves the technical problem that conventional hydrogel is insufficient in cell survival support in three-dimensional culture and the like.

The invention discloses a polydopamine modified metatitanic acid type lithium ion sieve and a preparation method thereof, and belongs to the technical field of lithium ion sieves, the preparation method comprises the following steps: grinding and uniformly mixing lithium acetate dihydrate and titanium dioxide in an organic solvent, and calcining the mixture at 650-800 DEG C for 3-5 hours to prepare a Li2TiO3 precursor; the preparation method comprises the following steps: putting dopamine hydrochloride, aminated crown ether and a Li2TiO3 precursor into a tris (hydroxymethyl) aminomethane solution with the pH value of 8-9, carrying out a constant-temperature oscillation reaction, carrying out suction filtration, and drying at low temperature, so as to obtain the polydopamine modified metatitanic acid type lithium ion sieve. According to the lithium ion sieve, the adsorption effect on lithium ions can be improved, the lithium extraction efficiency is improved, and the problem of low adsorption capacity of a lithium ion sieve in the prior art is solved.

The invention discloses an ultrasonic activation type piezoelectric gel dressing and a preparation method and application thereof.The surface of a system is an antibacterial hydrogel layer, the antibacterial hydrogel layer is composed of polyethyleneimine (PEI) and polyvinyl alcohol (PVA) cross-linked hydrogel, and ultrasound and current can be transmitted to a deep area; bT-dNO piezoelectric nanoparticles are packaged inside, and BT-dNO is prepared by coating a nitric oxide (NO) donor on the surface of piezoelectric barium titanate (BT) subjected to hydroxylation and dopamine modification. Under the stimulation of low intensity focused ultrasound (LIFU), the donor can release NO as required, and the BT nanoparticles can generate reactive oxygen species (ROS) and output piezoelectric current. The dressing system has an effective combined repair effect, excellent biocompatibility and good anti-inflammatory ability.

The invention discloses a covalent organic framework material based on a boric acid structure, a preparation method of the covalent organic framework material and application of the covalent organic framework material in dopamine detection, and relates to a covalent organic framework material and a preparation method and application of the covalent organic framework material. The technical problems that an existing dopamine recognition method is high in detection limit and harsh in recognition environment are solved. The periodic structure fragment of the covalent organic framework material based on the boric acid structure is shown in the specification. The 2-(4-boric acid phenyl)-5, 10-dinitro-1H-phenanthro [9, 10-d] imidazole diamine and 4, 4 ', 4', 4 ''-(pyrene-1, 3, 6, 8-tetrayl) tetrabenzaldehyde are subjected to a reaction to obtain the 2-(4-boric acid phenyl)-5, 10-dinitro-1H-phenanthro [9, 10-d] imidazole diamine derivative. The covalent organic framework material based on the boric acid structure is used for detecting dopamine, has relatively high selectivity and anti-interference capability, and is not interfered by amino acid in the environment. And the covalent organic framework material based on the boric acid structure can be embedded in the hydrogel, so that the hydrogel is convenient to carry. The method can be applied to detection of dopamine in environment and biological systems.

The invention belongs to the technical field of water treatment, and particularly relates to a preparation method and application of a PDA / CS composite adsorbent loaded with a bimetallic system, and the preparation method comprises the following steps: 1) dissolving dopamine in a Tris buffer solution to prepare a dopamine prepolymer solution; then adding FeCl3, and carrying out constant-temperature water bath; centrifuging the obtained black suspension, performing suction filtration, washing, collecting a filter cake, and performing freeze drying to obtain PDA microspheres; 2) dispersing PDA microspheres in deionized water, and carrying out ultrasonic treatment until the PDA microspheres are uniformly dispersed; 3) dissolving chitosan in an acetic acid solution, and adding CuCl2 to prepare a mixed solution; the suspension obtained in the step 2 is dropwise added into a mixed solution for constant-temperature water bath, the pH of the mixed solution is adjusted through a NaOH solution, glutaraldehyde is added for constant-temperature water bath after constant-temperature water bath, and 4, the obtained suspension is subjected to centrifugation, suction filtration, washing, filter cake collection and freeze drying.

The invention discloses a preparation method of a nuclear magnetic resonance imaging contrast agent based on surface hepatocyte targeting molecule modification ferroferric oxide nanoparticles, which comprises the following steps: synthesizing ferroferric oxide nanoparticles (Fe3O4 NPs) by a thermal decomposition method, and connecting the Fe3O4 NPs with a ligand dopamine-PEG2000-EOB carrying hepatocyte targeting molecules by a ligand exchange method to obtain the nuclear magnetic resonance imaging contrast agent. The nanoparticles Fe3O4-EOB-PEG capable of carrying out selective T2 nuclear magnetic resonance imaging on the hepatocytes are formed. The method is simple and easy to operate, the controllability of the preparation process is high, the biocompatibility of the obtained product is good, T2 signals of hepatocytes can be remarkably improved, the good early diagnosis effect on liver tumors is achieved, and wide application prospects are achieved.

The present application relates to a kind of phosphine oxy group covalent modification composite adsorption material and its preparation method and purposes, the preparation method includes the following steps: (1) mixing dopamine hydrochloride, phosphine-containing substrate, tris-hydroxymethyl aminomethane hydrochloride and sodium hydroxide in solvent, to obtain mixed solution;(2) the mixed solution obtained in step (1) and solid phase material are mixed, then oscillation reaction is carried out, to obtain solid-liquid mixture;(3) the solid-liquid mixture obtained in step (2) is carried out solid-liquid separation, and the solid phase part obtained is sequentially washed and dried, to obtain phosphine oxy group covalent modification composite adsorption material.The phosphine oxy group covalent modification composite adsorption material provided by the present application has excellent adsorption selectivity and material stability, and can be used for the high-selectivity separation and recovery of rare metals indium and gallium.

The invention belongs to the technical field of biological materials, and discloses a PEEK bone implant material of a piezoelectric catalysis biological heterojunction and a preparation method of the PEEK bone implant material, the material comprises a PEEK bone implant loaded with the biological heterojunction, the biological heterojunction is composed of BiVOO and a chalcogenide calcium compound in a molar ratio of 1-3, and the chalcogenide calcium compound is calcium sulfide, calcium selenide or calcium telluride; during preparation, the BiVO / CaX biological heterojunction is firstly prepared by a hydrothermal method or an in-situ composite method, then PEEK is sequentially subjected to acetone, ethanol and deionized water cleaning, sulfuric acid ultrasonic treatment for 5-10 minutes and dopamine modification, the biological heterojunction is in contact with the modified PEEK at 4 DEG C for 12 hours to complete loading, and improvement means can be introduced into part of schemes. The material has the acoustic catalytic antibacterial function and the bone repair promoting function, the antibacterial effect can be regulated and controlled through ultrasound, the process is simple, and the reaction condition is mild; the multi-drug-resistant bacterial infection can be dealt with, and the heterojunction loading stability and the material cell compatibility are improved.

The invention discloses a method for detecting aflatoxin B1 in coffee based on colorimetric and photo-thermal dual modes of MXene (at) Pt nano-enzyme, which comprises the following steps: etching Ti3AlC2 by using LiF and HCl to obtain MXene, synthesizing platinum nano-particle modified MXene nano-enzyme (MXene (at) Pt) by using dopamine carbon dots and sodium borohydride as reducing agents and adopting an in-situ reduction technology, and detecting aflatoxin B1 in coffee by using the MXene (at) Pt nano-enzyme (MXene (at) Pt nano-enzyme (MXene (at) Pt nano-enzyme (MXene (at) Pt nano-enzyme (MXene (at) Pt). The MXene (at) Pt shows near-infrared light stimulation enhanced peroxidase-like activity and photo-thermal performance and can catalyze blue deepening and temperature rising of a substrate 3, 3 ', 5, 5'-tetramethyl benzidine (TMB), when aflatoxin B1 exists, POD-like activity of MXene (at) Pt nano-enzyme is inhibited, and colorimetric and temperature signals are reduced; a method for detecting the AFB1 by the colorimetric temperature dual-mode sensor is established, and the method has the characteristics of high sensitivity, strong specificity, simplicity and rapidness in operation and the like.

The invention relates to a reverse osmosis membrane and a preparation method thereof, and the preparation method comprises the following steps: immersing a polysulfone-based membrane into a dopamine-containing mixed solution, and carrying out constant-temperature oscillation to form a dopamine pretreatment layer so as to obtain a modified base membrane; dissolving rosmarinic acid ester modified m-phenylenediamine, piperazine, a surfactant, an auxiliary agent and a pH regulator in water, and stirring for dissolving to obtain a water phase solution; dissolving an acyl chloride monomer in an organic solvent, stirring and dissolving, then adding the modified titanium dioxide, and carrying out ultrasonic dispersion to obtain an oil phase solution; immersing the modified base membrane into the water phase solution, taking out the modified base membrane, immersing the modified base membrane into the oil phase solution, taking out the modified base membrane and drying the modified base membrane to obtain a pre-compounded reverse osmosis membrane; and carrying out post-treatment on the pre-compounded reverse osmosis membrane to obtain the reverse osmosis membrane. Under the condition that the water yield is guaranteed, the reverse osmosis membrane disclosed by the invention has a high desalination rate and the oxidation resistance of the reverse osmosis membrane is improved for a long time.

A preparation method of a high-activity nitrogen-doped carbon-loaded CoRu nano-alloy is used for enhancing pH universal hydrogen evolution, and is characterized by comprising the following steps: dissolving dopamine hydrochloride in an aqueous solution containing H2O2 and CuSO4. 5H2O, and magnetically stirring to form a uniform mixture; and pre-wetting carbon cloth with ethanol, immersing the pre-wetted carbon cloth in the dopamine solution for 10 minutes, taking out the pre-wetted carbon cloth, washing the pre-wetted carbon cloth with deionized water for three times, and carrying out vacuum drying to obtain the polydopamine modified carbon cloth marked as PDA / CC. And immersing the obtained PDA / CC into 20 mL of aqueous solution containing Co (NO3) 2.6 H2O and RuCl3 for 6 hours to realize metal ion adsorption. And washing and drying a sample, and calcining the sample in a tubular furnace at 700 DEG C in an N atmosphere for 2 hours to obtain the self-supporting nitrogen-doped porous carbon-loaded CoRu alloy material which is recorded as CoxRu (at) CN / CC. Through a synthesis strategy based on active ion capture and in-situ carbon thermal reduction, and through construction of a nitrogen-doped carbon cobalt ruthenium alloy nanostructure and a strong metal-carrier synergistic effect, efficient hydrogen overflow and establishment of stable active sites are realized; therefore, the performance bottleneck that high activity and high stability of a traditional electrocatalyst in a wide pH range are difficult to cooperate is broken through.

The invention provides a seawater soaking wound hydrogel dressing and a preparation method thereof, a drug-loaded nano system 4OI (at) ZIF-8 (at) PAD with a core-shell structure is constructed, an anti-inflammatory drug 4-octyl itaconic acid and zinc ions are jointly encapsulated in a ZIF-8 framework, and a polydopamine coating is wrapped, so that synergistic loading and controllable release of the drug and metal ions are realized. According to the dressing, dopamine modified hyaluronic acid is used as a matrix, a temperature-sensitive material and an enzyme catalysis cross-linking system are combined, stable gel can be rapidly formed in situ within 5 seconds, and the dressing has excellent tissue adhesion performance (the adhesion strength reaches 6.7 kPa). Experiments prove that the hydrogel dressing has the characteristics of broad-spectrum antibiosis, inflammation regulation and control and long-acting release. Animal experiments prove that the healing rate of seawater soaking wounds treated by the dressing on the twelfth day is as high as 95.7% and is remarkably superior to that of a commercial silver ion gel control group, scars are less after healing, and an efficient, safe and easy-to-implement scheme is provided for marine environment wound nursing.

The invention provides a preparation method of a polydopamine modified material, the polydopamine modified material and application of the polydopamine modified material, and relates to the technical field of material modification. The preparation method of the polydopamine modified material comprises the following steps: mixing a buffer solution, a dopamine monomer, a metal source and an oxidizing agent to obtain a mixed solution; a substrate material is placed in the mixed solution, stirring treatment is conducted, and a polydopamine-metal precursor is obtained; and carrying out activating treatment on the polydopamine-metal precursor under a constant flow to obtain the polydopamine modified material. According to the preparation method of the polydopamine modified material, a thin film is formed on the surface of a substrate material through the characteristics of polydopamine, so that a metal source is attached more uniformly, the content of the metal source is remarkably increased, the high-activity polydopamine modified material is obtained, the problem that the risk of secondary pollution is caused due to the fact that metal is prone to overflow is solved, and the service life of the polydopamine modified material is prolonged. And the service life of the polydopamine modified material is remarkably prolonged.

The invention belongs to the technical field of microorganisms, and particularly discloses lactobacillus plantarum CX1-3-2 capable of producing gamma-aminobutyric acid and improving sleep and application of the lactobacillus plantarum CX1-3-2. The preservation number of the lactobacillus plantarum CX1-3-2 strain is CGMCC (China General Microbiological Culture Collection Center) No. 34340. The lactobacillus plantarum CX1-3-2 can achieve the effect of improving sleep by improving the levels of GABA and 5-HT in brain tissues and reducing the levels of glutamic acid Glu, dopamine DA and noradrenaline NE; the scavenging rate of DPPH free radicals of the strain reaches 96.4%, the scavenging rate of ABTS free radicals of the strain reaches 78.3%, and the strain has an excellent anti-oxidation effect; the diameters of inhibition zones of the strain on staphylococcus aureus, bacillus cereus, escherichia coli and pseudomonas fluorescens are all larger than 17 mm, and the strain has an excellent antibacterial effect.

The invention provides a pharmaceutical composition containing polypeptide and application of the pharmaceutical composition to preparation of a medicine for preventing and treating Parkinson's disease, and belongs to the technical field of polypeptide and biology. The amino acid sequence of the polypeptide is PCVLYDLREKM, the damage of 6-OHDA induced BZ555 nematode dopaminergic neurons can be obviously relieved, mouse dyskinesia caused by a Parkinson's disease model can be obviously improved, the spontaneous standing frequency can be improved, the movement speed in an open field can be increased, and meanwhile the IL-1beta and IL-18 levels caused by the mouse Parkinson's disease model can be reduced; the polypeptide provided by the invention can significantly reduce MAO-B level while significantly increasing DA level in nigra of brain tissues of rats with Parkinson's disease, which prompts that the polypeptide provided by the invention has a significant therapeutic effect on Parkinson's disease, and has a wide market prospect in many fields such as health food and medicine.

The invention discloses modified cellulose nanofiber reinforced bi-crosslinking immunoregulation hydrogel as well as a preparation method and application thereof, and belongs to the technical field of biological materials and biomedical engineering. Oxidized sodium alginate and dopamine grafted gelatin are adopted to prepare a main body of the composite hydrogel, aldehyde groups on the oxidized sodium alginate and amino groups on the gelatin can form Schiff base bonds, and borax, the oxidized sodium alginate and vicinal diol structures on modified cellulose nanofibers can form boric acid ester bonds. The double-crosslinking structure enhances the mechanical property of the hydrogel. The borate bond and the Schiff base bond are both dynamic chemical bonds and can respond to pH change, so that the hydrogel is endowed with self-healing performance and pH-responsive drug release ability, the hydrogel can quickly release liposome with an anti-inflammatory function in an acidic inflammatory environment in the early stage of cartilage injury, and the hydrogel recovers to an original state after fracture caused by joint movement. And the overall stability of the hydrogel is ensured by the double-crosslinking structure.

The invention provides multifunctional bionic hydrogel as well as preparation and application thereof in traumatic brain injury treatment, and belongs to the field of biomedical materials. The preparation method comprises the following steps: combining polydopamine modified hemoglobin nanoparticles with curcumin-based carbon quantum dots with anti-inflammatory activity, and embedding into bionic hyaluronic acid-collagen double-network hydrogel, so as to prepare the multifunctional bionic hydrogel. The hydrogel can effectively relieve neuron hypoxia, reduce apoptosis, promote the polarity of microglial cells to be converted into anti-inflammatory phenotype, and significantly down-regulate the expression of S100A8, thereby inhibiting pathological neural immune crosstalk. In a traumatic brain injury model, hydrogel implantation improves the pathological microenvironment, enhances endogenous nerve regeneration, and ultimately results in significant neurological function and cognitive recovery. The multifunctional bionic hydrogel prepared by the invention has a good application prospect in preparation of materials for preventing and / or treating traumatic brain injury.

The present application relates to the technical field of targeted cargo delivery, and more particularly to a drug loading and delivery method and a cell carrying method of core-shell mesoporous micro-nanorobot. The drug loading and delivery method is realized based on the drug loading capacity of the mesoporous structure, the magnetism of the iron oxide core and the photothermal effect of the polydopamine shell. The core-shell mesoporous micro-nanorobot can adsorb and load drugs through the capillary force and electrostatic force generated by the mesoporous structure; then the movement of the core-shell mesoporous micro-nanorobot is driven by an external magnetic field; when the core-shell mesoporous micro-nanorobot approaches the target area, the pore structure is irradiated by near-infrared light, the temperature of the pore structure is increased and the thermal vibration is accompanied, the drugs in the mesoporous structure are effectively released to the target area, and the drug delivery effect is achieved. At the same time of drug loading and delivery, the core-shell mesoporous micro-nanorobot has a carrying capacity after clustering under the magnetic field, and carries cells through two methods of eddy current carrying and contact adhesion. The targeted cargo delivery of targeted drugs and cells and other cargos can be realized by the micro-nanorobot.

The invention discloses a near-infrared two-region photosensitive molecule, a preparation method of the near-infrared two-region photosensitive molecule and application of the near-infrared two-region photosensitive molecule in preparation of suture lines, belongs to the technical field of medical materials, and synthesizes an aggregation-induced emission organic photosensitizer molecule T-TBT-P for near-infrared two-region emission. The AIE nano aggregate carrying positive charges is formed by self-assembly of hydrophilic and hydrophobic groups of the molecule in water; preparing a polydopamine nano coating on the surface of the suture line by using a dopamine oxidation auto-polymerization method, so that the surface of the suture line carries negative charges and has super-hydrophilicity; finally, the T-TBT-P nano aggregate is loaded on the surface of the suture line through the electrostatic adsorption effect, finally, the diagnosis and treatment integrated suture line is prepared, and the diagnosis and treatment integrated suture line has good antibacterial, subcutaneous tracing and tissue adhesion resisting performance and has good application prospects.

The invention belongs to the field of biomedical materials, and discloses a preparation method and application of a mesoporous polydopamine nano preparation loaded with ultra-small nano enzyme. The nano preparation takes mesoporous polydopamine nanoparticles as a carrier skeleton and is combined with ultra-small nano enzyme through an in-situ reaction: the mesoporous polydopamine nanoparticles can efficiently carry drugs and accurately deliver the drugs to inflammatory tissues such as psoriasis, gout, colitis and the like by virtue of a modified targeting ligand by virtue of high specific surface area, biocompatibility and modifiability; the ultra-small nano enzyme has catalytic activity of catalase and the like, and can remove active oxygen and relieve oxidative stress. The two components are combined to achieve a synergistic effect, so that the catalytic efficiency of the enzyme is improved by virtue of the characteristics of the carrier, the high activity of the enzyme under different conditions is maintained by virtue of the stability of the carrier, and the platform can synchronously realize targeted delivery, enzymatic treatment and drug controlled release, and has a wide application prospect in the fields of inflammatory disease intervention and wound repair. And an efficient, accurate and low-toxicity universal treatment strategy is provided for chronic inflammatory diseases.

The invention discloses a periodontal local drug delivery system with antioxidant, anti-inflammatory and antibacterial synergistic effects and a preparation method of the periodontal local drug delivery system, and belongs to the technical field of pharmaceutical preparations. The preparation method comprises the following steps: firstly, preparing an organic phase from DSPC, cholesterol, SA and resveratrol, and preparing a cationic liposome by taking PBS as a water phase; then preparing a water phase from AlgMA and LAP, taking a surfactant solution as an oil phase, and preparing polydopamine hydrogel microspheres through PDA surface modification; and finally, carrying out physical adsorption loading. Through the synergistic effect of the resveratrol, the cationic liposome and the polydopamine, a periodontitis pathological chain is comprehensively intervened, synergistic treatment is achieved, excellent antibacterial performance, anti-inflammatory effect and antioxidant effect are achieved, the retention rate of the medicine is increased, and the problems that traditional treatment medicine cannot achieve antibacterial, inflammation regulation and oxidative stress synergistic treatment at the same time, and the treatment effect is poor are solved. The residence time of the medicine in the periodontal pocket is short, and frequent administration is needed.

The invention discloses a polydopamine-tea polyphenol coated copper manganese oxide composite nano-enzyme as well as a preparation method and application thereof, and belongs to the technical field of biomedical materials. According to the invention, a DA-Cu (II)-EGCG (epigallocatechin gallate) complex is formed by virtue of chelation of main components of dopamine and tea polyphenol, namely epigallocatechin gallate, and copper ions; potassium permanganate is introduced for oxidative polymerization to obtain the polydopamine-tea polyphenol / copper manganese oxide organic-inorganic hybrid nano composite material, the nano composite material is monodisperse nano particles, the average particle size is about 80 nm, the nano composite material shows excellent nano enzyme catalytic activity, active oxygen free radicals can be effectively removed, and the nano composite material can be used for preparing nano-enzyme. The material has good photo-thermal conversion performance under near-infrared light, and shows excellent photo-thermal and photodynamic synergistic antibacterial effects. The preparation method disclosed by the invention is simple, mild, environment-friendly, low in cost and convenient for batch production.

The invention discloses a cephalotaxus hainanensis Ch2OGD1 gene and application thereof, and belongs to the technical field of gene engineering. The Ch2OGD1 gene is used for coding a 2-oxoglutaric acid dependent dioxygenase (2OGD) type Pictet-Spengler enzyme, and the Pictet-Spengler enzyme is used for coding a Pictet-Spengler enzyme. Through a tobacco transient expression system and in-vitro enzyme activity determination, the Ch2OGD1 is proved to be capable of specifically catalyzing the condensation of dopamine and 4-hydroxyphenylpropanal to generate 1-phenethyl isoquinoline. The invention provides a directional preparation method of 1-phenethyl isoquinoline based on the Ch2OGD1 gene, provides a key enzyme element for biosynthesis of a cephalotaxine alkaloid precursor compound, and provides a technical basis for expanding the application of the gene in plant genetic engineering. And a potential technical path is provided for relieving the problem of resource shortage of cephalotaxine alkaloids.

The invention provides a glass nanopore probe based on an aptamer and application of the glass nanopore probe in dopamine detection, and belongs to the technical field of electrochemical sensing and scanning probe microscopy. The sensor comprises: a glass nanopore probe, the inner wall of which is modified with a gold layer; a cDNA (complementary deoxyribonucleic acid) single chain is fixed on the gold layer through a gold-sulfur bond; a part of the sequence of the dopamine aptamer is hybridized and combined with the cDNA single chain; wherein the combination of the dopamine and the dopamine aptamer causes the change of an ion current rectification signal of the glass nanopore probe, so that the detection of the dopamine is realized based on the change of the ion current rectification signal of the glass nanopore probe. The invention provides a valuable scheme for developing an aptamer nanopore scanning electrochemical sensor for single cell analysis and researching neurotransmitter-related diseases.