589 results about "Supermolecule" patented technology

The invention provides a hydroxytyrosol supramolecular compound and a preparation method and application thereof, and belongs to the technical field of cosmetics and biological medicine, the supramolecular compound comprises the following chemical components by mass: 0.01-10% of hydroxytyrosol, 2-45% of an amino acid compound, 2-20% of alpha hydroxy acid, 2-30% of urea, and 15-92% of water. The supramolecular compound can promote transdermal delivery of hydroxytyrosol and maintain the biological activity of hydroxytyrosol, shows high biocompatibility, and can be applied to product development in the antibacterial field, the regeneration field and the anti-aging field.

The invention provides an enzyme response type supramolecular PDRN-mini ECM liposome and a preparation method and application thereof.The enzyme response type supramolecular PDRN-mini ECM liposome comprises phospholipid, a membrane stabilizer, a supramolecular compound and an emulsifier, a water phase formed by the supramolecular compound and the emulsifier serves as an inner core, and the supramolecular compound is formed by PDRN and mini ECM through intermolecular acting force; the mini ECM is formed by self-assembly of collagen peptide, elastin and hyaluronic acid. The supramolecular PDRN-mini ECM liposome with uniform particle size and good stability is obtained through a microfluidic technology, the process is simple, the controllability is high, and amplification is easy.

The invention relates to the technical field of cosmetic functional raw material preparation methods, in particular to a plant extract and an extraction method and application thereof. The invention provides a plant extraction method, which comprises the following steps: adding a glycol ether or polyhydric alcohol solvent containing 5-7 carbon atoms into a product containing phenolic acid compound components and lignan compound components, carrying out homogeneous reaction, carrying out heating extraction, and collecting the extract. By adopting a supramolecular technology, phenolic acid compound components can form a supramolecular solvent with glycol ether or polyol solvents containing 5-7 carbon atoms, and the supramolecular solvent is further combined with lignan compound components to form a supramolecular structure, so that the stability of an extracting solution is remarkably enhanced, the specific enrichment of the lignan compound components is realized, and the specific enrichment of the lignan compound components is realized. The problems that an existing extraction technology is poor in stability, poor in formula applicability, not prominent in effect and the like are successfully solved.

The application provides a preparation method of a self-coiled structure molybdenum disulfide / nitrogen-doped porous carbon composite material, a product and application, high-content nitrogen-doped porous carbon material is synthesized by inducing dicyandiamide molecules to undergo a supramolecular self-assembly process, and on this basis, a hydrothermal reaction is carried out to coat molybdenum sulfide sheet layer material on the surface, and finally, a self-heating coiling treatment is carried out to form a carbon-based electrocatalyst of the self-coiled structure molybdenum disulfide / nitrogen-doped porous carbon. Compared with a high specific surface area carbon-based catalyst, high doping concentration of nitrogen atoms can provide more electron-rich properties to facilitate the adsorption of substances, and the self-coiled carbon-based material can exhibit very excellent electrochemical performance, especially in the aspect of electrochemical hydrogen production. The preparation method is simple in operation, low in preparation cost and suitable for large-scale production.

The invention discloses a simple preparation method of a barium-based metal organic framework (Ba-H2Sip) and proton conduction application of the barium-based metal organic framework (Ba-H2Sip), belongs to the field of functional material synthesis and energy application, and is characterized in that functional differentiation design of a 5-sulfoisophthalic acid ligand: a sulfonic group forms a two-dimensional layered structure by chelating Ba < 2 + >; the carboxyl groups are differentiated into'anchoring carboxyl groups' for constructing a three-dimensional supramolecular skeleton and'proton supply carboxyl groups' for providing a proton source, and the design is reported for the first time in Ba-based MOFs; according to the present invention, the large-scale preparation can be achieved by stirring the low-cost raw material in 1 mol / L hydrochloric acid at the room temperature, the yield exceeds 70%, the product can resist 8 M acid and pH = 13 alkali liquid, the conductivity at 90 DEG C / 90% humidity can achieve 1.39 * 10 <-2 > Scm <-1 >, the high-temperature process is not required, the raw material is low in cost and easy to obtain, and the feasible scheme is provided for the high-efficiency proton conductor industrialization.

The invention relates to the technical field of nuclear waste treatment, in particular to a cucurbituril-based supramolecular organic framework material as well as a preparation method and application thereof. A construction unit of the supramolecular organic framework material is constructed by taking cucurbit [8] uril (CB8) as a subject and terephthalyl viologen ligand 1, 1 ''-(1, 4-phenylene) bis ([4, 4 '-bipyridyl]-1-onium) salt (PBV. 2X) as an object through the bonding effect of the subject and the object; in the molecular structure of the supramolecular organic framework material, the construction units are staggered and stacked in parallel in the space, and NO3 <-> is located at the gap of the adjacent CB8. The supramolecular organic framework material disclosed by the invention has high structural stability and cationic framework characteristics, and a rigid framework and a pyridine conjugated system of CB8 endow the material with excellent chemical / irradiation stability, so that the material shows ultrahigh removal rate on ReO4 <-> / TcO4 <-> in extreme environments (strong acid, strong alkali and high irradiation).

The invention relates to a poly (deoxyribonucleotide) self-assembled supramolecular nanoparticle composition, a preparation method and application thereof and cosmetics, the poly (deoxyribonucleotide) self-assembled supramolecular nanoparticle composition comprises PDRN and mussel protein, and the mass ratio of the PDRN to the mussel protein is 1: (0.05-10). The PDRN-mussel protein self-assembled supramolecular nano-particles have the beneficial effects that the PDRN-mussel protein self-assembled supramolecular nano-particles are prepared by utilizing the inherent charge properties of PDRN and mussel protein, so that the microscopic sizes of the PDRN and mussel protein are compressed, the transdermal absorption of the PDRN and mussel protein is greatly improved by utilizing the properties of the nano-particles, and a synergistic repairing effect is shown.

The invention discloses a non-noble metal ORR catalyst and a preparation method thereof, and belongs to the technical field of electro-catalysis. The method comprises the following steps: (1) adding 5, 10, 15, 20-tetra (4-cyanophenyl) porphyrin and nickel salt into an organic solvent, and synthesizing a supramolecular crystal precursor UPC-S7 through solvothermal reaction; (2) carbonizing the supramolecular crystal precursor UPC-S7 in an inert atmosphere to obtain a Ni-coated NC material; (3) oxidizing the Ni-coated NC material in an oxygen-containing atmosphere to obtain a Ni / NiO-coated NC material; and (4) sequentially soaking and etching the Ni / NiO-coated NC material by using a nitric acid solution and an ammonia water solution, and then washing and drying to obtain the non-noble metal ORR catalyst. The prepared catalyst does not contain precious metal such as platinum, the raw material cost is remarkably reduced on the basis of ensuring the ORR activity and stability of the catalyst, and a new scheme is provided for solving the cost bottleneck of a fuel cell.

The invention relates to the technical field of aquatic product preservation, and discloses a natural eutectic solvent for maintaining the quality of frozen penaeus vannamei boone and application, the natural eutectic solvent is composed of choline chloride, sorbitol and water, the molar ratio of choline chloride to sorbitol is (1-5): (1-5), and the mass of water is 15-25% of the total mass of choline chloride and sorbitol. The invention also provides an application of the solvent, and the application comprises the following steps: soaking the penaeus vannamei meat in the solvent, and then freezing and storing the penaeus vannamei meat. A supramolecular network system is constructed through hydrogen-bond interaction between choline chloride and sorbitol, growth of ice crystals in the freezing storage process is inhibited, a protein structure is stabilized, and loss of unfrozen juice is reduced, so that the quality of the penaeus vannamei, such as texture, color and flavor, is maintained. The natural deep-eutectic solvent is natural and safe in component, low in heat, simple to prepare and convenient to apply, the application limitation of a traditional anti-freezing agent is solved, and the natural deep-eutectic solvent has a good industrial prospect.

The invention relates to the technical field of microelectronic devices, in particular to a single-molecule memristor-rectifier device based on supramolecular assembly and a preparation method thereof. According to the preparation method, the guest molecule B is covalently connected with the tail end of the graphene electrode pair, so that stable and tight interface bonding between the supramolecular functional molecule and the electrode can be ensured; and then soaking the graphene electrode pair connected with the guest molecule B in a solution containing the host molecule A and the guest molecule C to form a supramolecular functional molecule between the graphene electrode pair. The guest molecule C in the supramolecular functional molecule has intrinsic oxidation-reduction activity, and the molecular structure of the guest molecule C can generate a reversible electron gain and loss process, so that controllable and reversible adjustment of charge distribution in the molecule is realized. Under the action of an electric field, through the reversible oxidation-reduction reaction of the guest molecule C, significant changes of intramolecular charge distribution and electron transmission characteristics are triggered, and finally reliable switching of high and low resistance states of the device is achieved.

Provided herein are peptide amphiphiles (PAs) comprising a bioactive peptide, nanofibers displaying the bioactive PAs, and methods of use thereof. The disclosed peptide amphiphiles comprise a hydrophobic tail, a structural peptide segment, a charged peptide segment, and a bioactive IKVAV peptide. The disclosed PAs may be used in cell culture methods and in methods of treating central nervous system injury.

An organometallic compound is provided which includes a central metal atom; and organic ligands capable of forming polydentate bonds to the central metal atom. Related methods and articles having a metal carbide coating are also provided.

The application discloses oligomerization degree carbon nitride nanosheet containing partial supramolecular chains and a preparation method and application of photocatalytic decomposition of water to simultaneously produce hydrogen and oxygen, and the preparation method comprises the following steps: adding melamine and cyanuric acid into a solvent, stirring after ultrasonic treatment, and drying to obtain supramolecular precursor powder; and calcining the supramolecular precursor powder to obtain oligomerization degree carbon nitride containing partial supramolecular chains. The application retains partial supramolecular oxygen-containing structures to optimize adsorption and dissociation of oligomerization degree carbon nitride nanosheet and water molecules at a reaction liquid interface, realizes high H and OH enrichment of a local environment, and promotes performance improvement of photocatalytic complete decomposition of water.

The invention relates to the technical field of papermaking and food packaging materials, in particular to a preparation method of full-degradable plastic-substituted high-strength food packaging paper. Preparing a fiber layer by taking plant fiber as a base material; the preparation method comprises the following steps: grafting a methyl methacrylate-butyl acrylate block copolymer on nano-cellulose through an atom transfer radical polymerization technology to prepare enhanced nano-cellulose; dialdehyde starch rich in aldehyde groups and chitosan are subjected to a Schiff base reaction to form a dynamic cross-linked network, polylactic acid microspheres modified by beta-cyclodextrin are introduced to serve as supramolecular enhancement units, and functional coating liquid is prepared; and finally, coating the functional coating liquid on the fiber layer, and drying, cross-linking and curing to obtain a finished product. Through cooperation of chemical grafting, dynamic covalent bonds and supramolecular action, the packaging paper is endowed with extremely high strength and toughness and excellent oil and moisture resistance and heat sealability, meanwhile, it is ensured that the packaging paper can be completely biodegraded in the natural environment, and functional replacement of traditional plastic packaging is successfully achieved.

The invention discloses a fluorescent probe for detecting spermine and spermidine in a water sample and urine as well as a preparation method and application of the fluorescent probe, and relates to the technical field of supramolecular fluorescent probes, and the fluorescent probe is formed by reacting 14-membered cucurbit urils (tQ [14]) and a compound (E)-1-(4-boron benzyl)-4-(4-hydroxyl styryl) quinoline-1-ammonium bromide according to a molar ratio of 1: 1. The novel fluorescent probe provided by the invention can specifically detect spermine and spermidine in a water sample and urine, and the preparation method of the fluorescent probe is simple and easy to implement; the method for detecting spermine and spermidine in a water sample and urine by using the fluorescent probe has the advantages of high sensitivity, high selectivity, low cost, simple sample treatment, convenient operation, rapid determination and the like.

The invention discloses an ellagic acid-copper metal organic framework nano material, a preparation method thereof and application of the nano material as an anti-tumor drug carrier. According to the nano material, natural polyphenol ellagic acid is used as an organic ligand, copper ions are used as a metal center, and a three-dimensional supramolecular frame structure is formed through coordination. The preparation method comprises the following steps: mixing an N-methyl pyrrolidone solution of ellagic acid with a methanol solution of copper sulfate, and stirring and reacting at room temperature to efficiently synthesize the copper sulfate. The nano material has excellent antibacterial activity and efficient anti-tumor drug loading capacity, has the intelligent drug release characteristic of dual response of pH and glutathione, and can accurately release drugs in a tumor microenvironment. The nano material provided by the invention can be used as an anti-tumor drug carrier, synchronously realizes anti-tumor and antibacterial dual effects, effectively prevents and treats bacterial infection complications in tumor treatment, and provides a new material for developing a new strategy for tumor synergistic treatment.

The invention discloses a 4-BrPA / beta-CD supramolecular photosensitizer as well as a preparation method and application thereof, and belongs to the field of biomedical materials. According to the method, beta-cyclodextrin is used as a subject, 4-bromophthalic anhydride is used as an object, and the water-soluble photosensitizer is constructed through a chemically modified supramolecular assembly strategy. The preparation method comprises the following specific steps: reacting beta-cyclodextrin with paratoluensulfonyl chloride to obtain mono-(6-O-paratoluensulfonyl)-beta-cyclodextrin; then carrying out a reaction with ethidene diamine to obtain mono-(6-ethidene diamine-6-deoxy)-beta-cyclodextrin; then reacting with 4-bromophthalic anhydride in N, N-dimethylformamide, and precipitating and purifying through ethyl acetate to obtain a crude product; and finally, carrying out ultrasonic treatment, centrifugal separation and freeze drying to obtain a pure product. The prepared 4-BrPA / beta-CD supramolecular photosensitizer is excellent in water solubility, has at least 7 excitation centers in a visible light region of 400-520 nm, correspondingly generates at least 7 emission centers in a range of 500-780 nm, has a maximum excitation wavelength of about 460 + / -10 nm and a maximum emission wavelength of about 620 + / -10 nm, has an extremely wide visible light response characteristic, and can be used for antibacterial photodynamic therapy.

This invention provides an organic ferroelectric eutectic material, its preparation method, and its applications, relating to the field of ferroelectric materials technology. The organic ferroelectric eutectic material constructs a crystal system with "rigid constraint and flexible adaptation coexisting, dipole order and controllable polarization synchronously" through "molecular selection-supramolecular assembly-crystal structure regulation," achieving a synergistic effect of high Curie temperature, strong polarization characteristics, and excellent flexibility. The preparation method of the organic ferroelectric eutectic material utilizes a simplified "solvent dissolution-solvent evaporation" process, leveraging the mediating effect of the solvent to promote the supramolecular self-assembly of donor and acceptor molecules. This achieves the preparation of an organic ferroelectric eutectic material possessing both high Curie temperature, strong polarization characteristics, and excellent flexibility. The preparation method has multiple advantages, including "stable process, low cost, and suitability for large-area processing," making it a simple, efficient, and universally applicable preparation method suitable for large-scale industrial production.

The invention discloses deep-eutectic solvent supramolecular gel, a preparation method thereof and application of the deep-eutectic solvent supramolecular gel in DNA room-temperature storage, and belongs to the technical field of biological material storage. The deep-eutectic solvent supramolecular gel for embedding DNA provided by the invention comprises a deep-eutectic solvent matrix, a supramolecular gel agent and a DNA-positive salt compound water phase, the DNA-electropositive salt compound water phase is an upper phase solution obtained by mixing a DNA water solution with a hydrophilic polymer and electropositive salt and then carrying out phase separation. The deep-eutectic solvent supramolecular gel provided by the invention can effectively encapsulate DNA, can resist high temperature, enzymolysis, free radicals, microorganisms and the like erosion, and is beneficial to realizing long-term stable storage of the DNA at room temperature.

The invention discloses a high-thermal-conductivity self-adhesion thermal interface material and a preparation method thereof, and is characterized in that polylipoic acid (polyTA) formed by high-temperature ring opening polymerization of lipoic acid (LA) is used as a dynamic reversible polymer matrix, the dynamic reversible polymer matrix has the characteristics of recoverability, self-healing and adhesion due to the inherent dynamic property of disulfide bonds, a spherical thermal conductive filler is modified by a polyphenol compound, and the high-thermal-conductivity self-adhesion thermal interface material is prepared. Polyhydroxy functional groups are given, the surface energy is reduced, meanwhile, certain viscosity is achieved, polyethylene glycol diacrylate is added to serve as a stabilizer, ferric iron salt is evenly stirred and mixed, the reaction time is controlled, and a stable cross-linked network system is constructed. Hydroxyl groups on the surface of the polyphenol-decorated heat-conducting filler and carboxyl groups in polylipoic acid are subjected to esterification reaction, and meanwhile, Fe < 3 + > and the carboxyl groups in the polylipoic acid form supramolecular coordination, so that uniform dispersion and stable bonding of the filler in a matrix are realized, the interface thermal resistance is remarkably reduced, and a continuous heat-conducting passage is formed. The preparation method of the thermal interface material is simple in process, and the thermal interface material has high thermal conductivity and self-adhesion, has soft elasticity and is suitable for various application fields needing efficient thermal conduction and interface thermal management.

A process for preparing a supramolecular carrier photosensitizer for photodynamic therapy and a formulation thereof is disclosed for prevention, treatment, anti-inflammatory and sterilization of oral dental diseases. Supramolecular carrier consists of refined lignin, glucomannan, cysteine, and sodium benzoate at a mass ratio of 0.1-1.0%: 0.5-3%: 0.1-0.5%: 0.05%, and the balance of water. Aqueous solutions of refined lignin, glucomannan, cysteine and sodium benzoate are prepared, and a pH value of combined solution is adjusted to 6.5, so that dissolved alkali lignin is precipitated to form an efficient and stable three-dimensional polymer network skeleton, and rich hydrogen bonds are facilitated to be formed between the same molecules and different molecules of lignin and glucomannan, thereby forming a supramolecular carrier formulation loaded with the photosensitizer. It ensures long-term storage stability of physicochemical traits of formulation, which is conducive to rapidly promoting application of PDT in anti-inflammatory and sterilization treatment of oral dental diseases.

The invention discloses a dissipative elastomer as well as a preparation method and application thereof, and belongs to the technical field of high polymer materials. The dissipative elastomer is prepared by taking an acrylate monomer as a raw material, adding a lithium salt and a photoinitiator, mixing and stirring to form a transparent precursor solution, injecting the transparent precursor solution into a mold, and initiating an in-situ free radical polymerization reaction through ultraviolet irradiation, the lithium salt is introduced to construct multiple supramolecular effects, and a polymer network is induced to form a supramolecular-nano domain synergistic structure, so that the elastomer has excellent damping dissipation capability, self-adaptability and mechanical strength, the highest breaking strength of the elastomer can reach 4.5 MPa, the maximum toughness of the elastomer can reach 26.8 MJ / m < 3 >, and the modulus of the elastomer is matched with that of biological tissues (0.1 MPa-10 MPa); the dissipative elastomer can effectively bear dynamic load and low-frequency interference, has wide application prospects in the fields of flexible sensing, wearable medical equipment and the like, and is simple and controllable in preparation process, low in raw material cost and suitable for large-scale production.

The invention relates to the technical field of gelators and functional cosmetics, in particular to a porphyrin core-based gelator, preparation thereof and application of the porphyrin core-based gelator in preparation of products for removing skin glycated toxins. The gel factor provided by the invention is a C2 symmetric chiral gel factor: L-Por-Phe. A central core (porphyrin ring) of the gelator provides strong hydrophobic acting force and pi-pi stacking driving force, is not only a driving core for supramolecular self-assembly, but also is a key site for adsorbing aromatic AGEs toxins; a natural chiral source and an additional benzene ring side group are introduced into a side chain, the hydrophilic-hydrophobic balance of molecules is adjusted, and a supramolecular assembly is induced to form a single chiral spiral nanofiber; the connecting arms provide intermolecular hydrogen bonds to stabilize the three-dimensional network structure of the hydrogel; the terminal group endows the molecule with pH responsiveness, so that the gel can maintain a stable gel state in a skin physiological pH environment, and has good moisture retention.

The invention provides macroporous silicon dioxide with the surface covalently expressed by single-layer branched polyethyleneimine and a preparation method of the macroporous silicon dioxide. The preparation method comprises the following steps: mixing and stirring branched polyethyleneimine and an aqueous solution of a water-soluble anionic surfactant to obtain a supramolecular micelle system; the preparation method comprises the following steps: mixing tetraethoxysiloxane, glycidoxypropyltrimethoxysilane and an optional organic solvent to form a siloxane solution; dropwise adding a siloxane solution into the supramolecular micelle system under stirring to obtain a concentrated emulsion; and incubating the concentrated emulsion at normal temperature, crushing, washing and drying in vacuum. According to the synthesis of surface polyaminated silicon dioxide, due to the use of a small amount of glycidoxypropyltrimethoxysilane, branched polyethyleneimine can form a small amount of covalent bonds with silicon dioxide so as to be fixed on the pore surface, and meanwhile, a large amount of active amino hydrogen of polyethyleneimine can be retained; the hydrolysis rate of the siloxane can be adjusted by the polarity of the organic solvent.

The invention discloses a circularly polarized light-emitting supramolecular self-assembly crystalline material as well as a preparation method and application of the circularly polarized light-emitting supramolecular self-assembly crystalline material. The supramolecular assembly crystalline material comprises a three-dimensional structure, and the three-dimensional structure is connected through a hydrogen bond formed between a hydrogen atom in a chiral secondary structure unit and an oxygen atom in a sulfonic acid group of 4, 4 '-bis (2-sulfostyryl) biphenyl disodium CBS. The crystalline material disclosed by the invention shows excellent chiral optical properties, good solvent stability and a remarkable luminous asymmetric factor; the circularly polarized light-emitting film material prepared from the material can effectively realize transmission and amplification of crystal optical performance.

The application discloses a supramolecular lotus leaf peptide-narcotic alkaloid Pickering emulsion as well as a preparation method and application thereof. The water phase of the supramolecular lotus leaf peptide-narcotic alkaloid Pickering emulsion is a purified lotus leaf peptide aqueous solution, and the oil phase is camellia seed oil loaded with narcotic alkaloids. The camellia seed oil not only serves as a fat-soluble carrier to improve the solubility of the narcotic alkaloids, but also has nursing effects due to the unsaturated fatty acids, vitamin E and phytosterols contained therein. The supramolecular assembly technology is used to mediate the lotus leaf peptide and the narcotic alkaloids to form high-performance emulsified particles, to replace synthetic surfactants to stabilize the Pickering emulsion, and to construct a natural emulsion system with high emulsification efficiency, high stability and high performance, so that the performance and the nursing effect of the emulsion are optimized.

This invention belongs to the field of biomaterial preparation technology, specifically disclosing a self-assembled supramolecular peptide nanozyme material, its preparation method, and its application. The preparation method includes the following steps: S1, dissolving β-alanyl-L-histidine in ultrapure water and stirring until homogeneous to obtain solution A; S2, dissolving heme chloride in dimethyl sulfoxide and stirring until homogeneous to obtain solution B; S3, mixing solution A and solution B until homogeneous, adjusting the pH, heating in a water bath, incubating at room temperature, centrifuging, discarding the precipitate, and retaining the supernatant; S4, lyophilizing and grinding the supernatant obtained in S3 to obtain the self-assembled supramolecular peptide nanozyme material. This invention discloses a self-assembled supramolecular peptide nanozyme material, its preparation method, and its application. This supramolecular peptide nanozyme, when applied to food quality and safety testing, can achieve visual and sensitive colorimetric detection of biogenic amines in spoiled food.

The invention relates to a method for specifically detecting tetrahydrocannabinol and hydride thereof by utilizing bridged beta-cyclodextrin, and belongs to the technical field of analysis and detection of supramolecular materials. The method comprises the following steps: firstly, combining 1, 6-hexamethylenediamine bridged bis-beta-cyclodextrin with an indicator to form a supramolecular probe; in a buffer system with a pH value of 9-11, tetrahydrocannabinol or a hydride thereof specifically competes to be combined with a cavity and displaces an indicator by utilizing a synergistic inclusion effect of a bridging subject and dissociation difference of guest molecules, so that the system is subjected to fluorescence quenching or color change, and a structural analogue cannabidiol does not generate obvious interference. The method solves the problems that the sensitivity is low and cannabidiol cannot be effectively distinguished in the prior art through cooperation of specific main body construction and environment regulation, has the advantages of being rapid in detection, high in specificity, high in accuracy and the like, and is suitable for environment monitoring and field screening.

the present invention provides a method for producing a protein having a supramolecular structure in which a bioactive substance is encapsulated, comprising: (I) bringing a subunit of a protein, which forms a supramolecular structure, a bioactive substance, and a solution for forming the protein having the supramolecular structure from the subunit into contact with one another in a flow micro mixer.