351 results about "Nano emulsion" patented technology

The invention discloses a PHA / PVA nano-scale paper-based barrier emulsion as well as a preparation method and application thereof. The water-based emulsion comprises PHA particles with the average particle size ranging from 100 nanometers to 300 nanometers and PVA, the PHA and the PVA are blended according to a specific proportion, and the PVA serves as a main film forming component and a barrier property contribution component and is blended with the PHA to form the nano-emulsion. The preparation method comprises the following steps: mixing PHA particles with an initial average particle size of 1-100 microns with a PVA aqueous solution, and carrying out high-pressure homogenization and other nanocrystallization means to obtain the nano-emulsion. The emulsion can be coated on the surfaces of paper-based materials such as paper and paperboards, and a barrier coating is formed after the emulsion is dried. The obtained emulsion is small in particle size, good in stability and good in leveling property, a uniform and compact barrier film is easily formed on a paper base, the film has excellent water vapor, oxygen and grease barrier performance, and the material is bio-based, biodegradable and environmentally friendly.

The present invention discloses a PHA / PVA nanoscale paper-based barrier emulsion, and its preparation method and application. The aqueous emulsion comprises PHA particles with an average particle size of 100 nanometers to 300 nanometers and PVA, wherein PHA and PVA are blended in a specific ratio, and PVA is blended with PHA as the main film-forming component and barrier performance contributing component to form the nanoemulsion. The preparation method comprises mixing PHA particles with an initial average particle size of 1 micron to 100 microns with a PVA aqueous solution, and processing the nanoemulsion by nano-processing means such as high-pressure homogenization. The emulsion can be applied to paper-based materials, such as paper and cardboard surfaces, and forms a barrier coating after drying. The emulsion obtained by the present invention has small particle size, good stability, good leveling properties, and is easy to form a uniform and dense barrier film on the paper base. The film has excellent water vapor, oxygen and grease barrier properties, and the material is bio-based, biodegradable, and environmentally friendly.

The invention discloses a high-stability endotoxin-free PHA nano-emulsion and a preparation method thereof, and belongs to the technical field of biodegradable high polymer material compositions and processing thereof. The nano-emulsion is characterized in that the endotoxin content is not higher than 0.10 EU / g, the median particle size d50 is 100-200 nm, and the PDI is not higher than 0.15, and the nano-emulsion is stable in long-term storage. The preparation method is a continuous solvent-free process and comprises the steps of melt extrusion, high-pressure thermal emulsification and deep endotoxin removal. By adopting the specific pH-insensitive cationic polymer emulsifier and the crystallization inhibitor, the chemical contradiction that an efficient alkaline purification process is incompatible with a nano-emulsion stable system is solved, physical aging is inhibited, and an unexpected technical effect is obtained. The invention also discloses an O / W type cream containing the nano emulsion.

The invention discloses a cationic core-shell PHA nano-emulsion reinforcing agent as well as preparation and application thereof, and belongs to the technical field of papermaking chemicals. The problems that a traditional wet strength agent is poor in environmental protection property and difficult to recycle, and a conventional bio-based material needs high-temperature curing and is high in energy consumption are solved. According to the reinforcing agent, low-MFFT bio-based polyhydroxyalkanoate is used as a core, and a positive ion shell layer with strong positive charges is wrapped outside the core. The method has the core advantages that extra high-temperature curing is not needed, the film can be efficiently formed under the conventional 105 DEG C drying condition, and the energy consumption is remarkably reduced; meanwhile, high dry and wet strength and water resistance are achieved, the treated paper has excellent re-pulping recycling suitability, and the industrial pain point that traditional wet strength paper is difficult to recycle is solved.

The present invention relates to pro-nano-emulsion compositions comprising at least one type of Omega 3 fatty acid capable of converting to nano-emulsion composition having average droplet size of below Ip, typically below 0.5p, and use thereof, particularly as dietary supplement, for preferential delivery of the Omega 3 fatty acid to heart and / or liver tissue of a subject consuming the composition, thereby maintaining normal cardiovascular / hepatic function and / or improving cardiovascular / hepatic disease or disorders.

The invention relates to the technical field of pharmaceutical preparations, in particular to a multiple nano emulsion adjuvant and a preparation method thereof. The multiple nano emulsion adjuvant is prepared from 2.73 to 6.37 g of an oil phase matrix based on 100 g of a raw material system, 0.10 to 0.25 g of a sterol compound; 0.212 to 0.424 g of a nonionic surfactant; 0.00050 to 0.00200 g of a triterpenoid saponin type active adjuvant; 0.010 to 0.020 g of an anionic polymer modifier; 0.005 to 0.015 g of a cationic polymer modifier; 70-90 g of a buffer solution; the total mass of the raw materials is 100 g. The nano emulsion adjuvant prepared by the invention can be stored for 6 months at 2-8 DEG C under a low sterol condition, the particle size change does not exceed + 5%, no crystallization or layering is generated, and the stability of the active adjuvant is remarkably improved.

The invention discloses a preparation process of a pure plant essential oil disinfectant, and relates to the technical field of disinfectants. The problems that plant essential oil is poor in solubility in a water phase, low in stability and the like are solved. The method specifically comprises the following steps: preparing raw materials; preparing a nano emulsion; preparing a solvent and mixing; constructing a natural stable system to obtain a primary product; filtering and sterilizing; and carrying out sterile filling on the disinfectant finished product. The invention provides a pure plant essential oil disinfectant prepared by dissolving type 1 and 8 melaleuca alternifolia essential oil in water, efficient dispersion is realized through a nano-emulsification and natural stabilization technology so as to form a stable aqueous solution, an amphiphilic structure of soapbark saponin is utilized, aglycone and essential oil terpene form a supramolecular compound, and the stable aqueous solution can be used for sterilizing the melaleuca alternifolia essential oil and the melaleuca alternifolia essential oil and the melaleuca alternifolia essential oil. The technical problems of poor dissolvability and low stability of plant essential oil in a water phase are solved, and the plant essential oil has broad-spectrum antibacterial and antiviral characteristics and can meet the disinfection requirements in multiple fields such as medical treatment, object surface treatment, home furnishing and personal care.

The utility model discloses an ultrasonic microreactor which is formed by directly attaching an ultrasonic transducer and a microreactor, the ultrasonic microreactor is formed by connecting a plurality of fluid microchannel reaction layers in series; the fluid micro-channel reaction layer is formed by alternately connecting a plurality of thin channels and thick channels; a reaction layer turbulent flow chip is arranged in the middle of the thick channel; under the synergistic effect of ultrasound and the microreactor, the ultrasonic microreactor has higher energy density and more accurate sound field and flow field regulation and control capability, and can solve the problems that channels are easy to block and the like, so that nano-emulsion with uniform particle size can be continuously prepared, and the efficiency of an emulsification process and the quality of an emulsion product are improved.

The invention belongs to the technical field of plant extraction and cosmetics, and particularly relates to camellia composition nano-emulsion with anti-aging and repairing effects on fatigue skin as well as a preparation method and application of the camellia composition nano-emulsion. The camellia flower extract, the camellia leaf extract, the camellia seed oil, the camellia seed extract and the PEG-40 hydrogenated castor oil are used as raw materials and are compounded according to a certain dosage to prepare the nano-emulsion, and the nano-emulsion has multiple effects of moisturizing, tightening, removing acnes and the like; the skin care product solves the problems that a conventional skin care product is not remarkable enough in fatigue muscle improvement effect, not quick enough in effect and insufficient in pertinence, and the skin is restored to be tender, moisturized and bright.

The invention discloses a slow-release antibacterial and antioxidant composite preservative film and a preparation method thereof. The slow-release antibacterial and antioxidant composite preservative film is prepared from a chitosan matrix and Chuzhou chrysanthemum essential oil nano-emulsion loaded in the chitosan matrix, the Chuzhou chrysanthemum essential oil nano-emulsion comprises Chuzhou chrysanthemum essential oil, a surfactant and a cosurfactant, and the average particle size of the Chuzhou chrysanthemum essential oil nano-emulsion is smaller than 200 nm; the composite preservative film has the function of slowly releasing the Chuzhou chrysanthemum essential oil and shows antibacterial and antioxidant activity; the preparation method comprises the following steps: firstly preparing Chuzhou chrysanthemum essential oil into a nano-emulsion by adopting a nano-encapsulation method through a high-pressure homogenization method to form the Chuzhou chrysanthemum essential oil nano-emulsion, then embedding the Chuzhou chrysanthemum essential oil nano-emulsion into chitosan to prepare an active chitosan composite film, and finally applying the antibacterial coating material to food preservation. The antibacterial coating film not only can effectively inhibit pathogenic microorganism infection in berry storage and logistics transportation in a wider spectrum, but also can regulate physiological metabolism of picked berries, delay the senescence process and reduce loss of internal moisture.

A preparation method of plant compound essential oil comprises the following steps: preparing mixed powder from dried lemon slices, mint and litsea coreana, carrying out carbon dioxide supercritical extraction, and collecting an extract; the preparation method comprises the following steps: dropwise adding a carboxymethyl-beta-cyclodextrin solution into a mixture of eugenol and thymol, carrying out ultrasonic treatment to obtain an ultrasonic mixed solution, standing, centrifuging, collecting supernate, and drying to obtain a white powdery inclusion compound; and adding lecithin, Tween 80, disodium pyrophosphate and deionized water into the extract, heating and stirring, continuing to add the inclusion compound, homogenizing to obtain a nano-emulsion, adding gelatin and propylene glycol, heating and preserving heat, and cooling to obtain the plant composite essential oil. The compound essential oil disclosed by the invention has antibacterial and antioxidant effects, and has relatively strong antibacterial ability on botrytis cinerea and penicillium germs, and the DPPH free radical scavenging rate is greater than or equal to 90%. According to the invention, the active ingredients of the essential oil are wrapped by carboxymethyl-beta-cyclodextrin and synergistically embedded by lipidosome through a nano-embedding technology to realize slow release, so that the antioxidant and antibacterial properties are effectively prolonged.

The invention discloses a preparation process of a moxidectin pouring solution. The preparation process comprises the following steps: S1, respectively preparing a moxidectin initial solution and a thickener premixed solution; s2, the moxidectin initial solution and the thickener premixed solution are stirred and mixed uniformly at the temperature of 25-35 DEG C to form a mixture A, the stirring speed is 150-250 rpm, and the mixing time is 10-20 min; s3, adding auxiliary materials into the mixture A, and uniformly mixing to form a mixture B; s4, supplementing the second solvent into the mixture B to the total amount, uniformly mixing, and filtering to obtain a moxidectin pouring solution; the method comprises the following steps: dissolving a moxidectin raw material in a first solvent to obtain a moxidectin initial solution, and synthesizing the moxidectin raw material by using biological catalysis; the first solvent is a nano-emulsion formed after homogenization. According to the preparation method, the solubility of the medicament, the stability of the preparation and the transdermal drug delivery efficiency are improved by improving the solvent system and controlling the process in the preparation process of the moxidectin pouring solution.

They are prepared by a high energy method (e.g. by sonication) from: an oily solution of edible oils (e.g. high-oleic sunflower oil) as solvent, with melatonin (e.g. 100 μM) and edible fat-soluble antioxidant agents (e.g. 100 μM α-tocopherol), and an aqueous solution of edible water-soluble stabilizing agents (e.g. dextrin 1% w / v). These formulations, applied externally (e.g. by spraying) are useful for preharvest application and / or postharvest preservation of fruits or vegetables, particularly of stone fruits, and specifically of sweet cherries. In two varieties of sweet cherries and two varieties of plums, preservations with the formulations are significantly better than those reached with aqueous solutions of melatonin, or with a commercial formulation, or in the absence of treatment.

The invention provides a preparation method of candies containing a sodium alginate-whey protein composite wall material. The preparation method comprises the following steps: dissolving sodium alginate and whey protein, and then adding active ingredients and the like to prepare a nano-emulsion; performing spray drying to obtain microcapsule powder; after the candy matrix is boiled, microcapsule powder and nano silicon dioxide aerogel are mixed in stages; and finally, carrying out surface coating and ultraviolet curing. The method mainly achieves the following breakthroughs: firstly, a triple protection system is formed, and the problem of survival of probiotics is solved; 2, synergistic release of flavor and functional components is realized; and thirdly, the adaptability problem of the composite wall material is solved, the stability is improved, and the moisture demand contradiction is solved.

The invention discloses a long-acting cool and refreshing lingering paste based on compound matrix slow release and a preparation method thereof, and belongs to the technical field of cosmetics. The ointment body comprises 20-24 parts of beewax, 35-40 parts of a substance with an HLB (Hydrophile-Lipophile Balance) value of 12-15, 28-35 parts of a freshener and 5-7 parts of a plant extract composition. The plant extract is embedded into the matrix in the form of nano emulsion by combining staged temperature control with a nano emulsion technology. The invention has the following effects: by regulating and controlling the proportion of the beewax and the esters with high HLB (Hydrophile Lipophile Balance) value, a honeycomb porous structure is formed, and the body temperature triggered slow release of high-concentration cooling components is realized; through a low-temperature gradient process, staged temperature control (melting-> 40 DEG C emulsification) is combined with a nano-emulsification technology, and the activity of volatile components is retained (the retention rate gt is 98%). The product provided by the invention has the advantages that the cooling feeling lasts for 4-6 hours, the irritation is obviously lower than that of similar products, and the product is suitable for non-face resident type cooling and refreshing nursing for adults.

The invention discloses a multilevel liver targeting drug delivery system based on ionizable amino lipid and a preparation method thereof, the system comprises the following components: target modified ionizable amino lipid, ionizable amino lipid, auxiliary lipid and structural lipid in a molar ratio of (10-30): (30-60): (5-40): (15-55), according to the system, nano lipid particles exist in a water-in-oil-in-water nano emulsion form; wherein the ionizable ammonia lipid is a compound with a structure as shown in a formula (I). The system is suitable for delivering nucleic acid, protein and other active pharmaceutical ingredients to the liver so as to improve the accuracy and treatment effect of drug delivery and reduce the side effects of non-target organs.

The invention relates to a reverse osmosis membrane and a preparation method and application thereof.The preparation method of the reverse osmosis membrane comprises the following steps that oil, a surfactant and water are mixed to prepare an oil-in-water type nano-emulsion, the surfactant comprises a nonionic surfactant, the average particle size of the oil-in-water type nano-emulsion is 80-200 nm, and the polydispersity index is smaller than or equal to 0.3; an aqueous solution of inorganic metal salt and an oil-in-water type nano-emulsion are sequentially placed on the same surface of a supporting film, dendrites are formed through heat treatment, and the mass ratio of the inorganic metal salt to the oil-in-water type nano-emulsion is 1: 50-1: 30; and preparing a polyamide separation layer on the surface of the support membrane on which the dendrites are distributed through reverse interfacial polymerization to obtain the reverse osmosis membrane. When the reverse osmosis membrane prepared by the preparation method is applied to water treatment, high desalination rate can be maintained, and meanwhile, high water flux is achieved.

The invention belongs to the technical field of medicines, and relates to a metformin hydrochloride-loaded PLGA (poly (lactic-co-glycolic acid)) nanoparticle material as well as a preparation method and application thereof. The preparation method comprises the following steps: carrying out first shear emulsification on a metformin hydrochloride aqueous solution and an organic solution containing a first emulsifier and PLGA (poly (lactic-co-glycolic acid)) to obtain a water-in-oil primary emulsion; carrying out second shear emulsification on the primary emulsion and an aqueous solution containing a second emulsifier to obtain a water-in-oil-in-water type crude emulsion; homogenizing and emulsifying the crude emulsion to obtain a W1 / O / W2 nano-emulsion; and removing the organic solvent from the nano-emulsion, centrifuging and drying to obtain the nano-emulsion. The preparation method disclosed by the invention not only has relatively high reproducibility for preparing the nano-particles, but also obviously reduces the average size of the obtained nano-particles, improves the bioavailability of the medicine, and simultaneously keeps the uniform dispersity and high biocompatibility of the nano-particles.

The invention discloses a self-emulsifying adjuvant of a vaccine and a preparation method of the self-emulsifying adjuvant, and relates to the technical field of vaccine adjuvants. The adjuvant comprises an oil phase, an emulsifier and a freeze-drying protective agent, the oil phase comprises squalene and tocopherol, the emulsifier comprises polysorbate and a polyoxyethylene-polyoxypropylene block copolymer, and the freeze-drying protective agent comprises sugar and sugar alcohol. The preparation method comprises the following steps: emulsifying an oil phase and a water phase to form a nano-emulsion, and then freeze-drying to obtain freeze-dried powder. The adjuvant has the advantages of small particle size, uniform distribution, high stability, rapid reconstruction and the like, and can effectively maintain active components and improve the immune effect of vaccines.

The invention relates to a paper pulp-based hydroxyethyl cellulose antibacterial composite film as well as a preparation method and application thereof. The preparation method comprises the following steps: (1) preparing paper pulp-based hydroxyethyl cellulose; (2) preparing a peppermint essential oil nano-emulsion; and (3) preparing the paper pulp-based hydroxyethyl cellulose antibacterial composite film. The average thickness of the paper pulp based hydroxyethyl cellulose antibacterial composite film provided by the invention is 0.205 + / -0.017 mm, and the density is 0.59 + / -0.05 g / cm < 3 >. Hydroxyl in paper pulp base HEC and carboxyl and hydroxyl of SA form a multiple hydrogen bond network; pO is used as a hydrophobic plasticizer and generates interfacial tension with a hydrophilic SA / HEC matrix, and tiny liquid drops or agglomerates are easily formed in the film forming process; ca < 2 + > and carboxylate radicals in SA form ionic bonds through electrostatic interaction to generate a calcium alginate gel network, so that the tensile strength of the paper pulp-based hydroxyethyl cellulose antibacterial composite film reaches 6.1 MPa, the water vapor permeability is 5.32 * 10 <-10 > g.m <-1 >. S <-1 >. Pa <-1 >, and the paper pulp-based hydroxyethyl cellulose antibacterial composite film has a remarkable inhibition effect on growth of penicillium oxalicum.

The invention discloses a nanometer emulsion based on a citrus extract and a preparation method of the nanometer emulsion. The nano-emulsion takes citrus pectin as a main chain, gallic acid, ascorbic acid-phosphate and oleic acid are sequentially grafted, the oleic acid is lipophilic, the rest is hydrophilic, and the amphiphilic pectin can form the whitening nano-emulsion which can be stably stored for a long time. The natural citrus extract is used for replacing traditional synthetic components, has the anti-oxidation, whitening and anti-inflammatory effects, can reduce the skin sensitivity risk, and conforms to the green beauty makeup trend; meanwhile, the oil phase is anchored by a hydrophobic block, steric hindrance is formed by a hydrophilic block, the stability of the emulsion is remarkably improved, and the shelf life is prolonged to 24 months; phenolic acid and ascorbic acid contained in the traditional Chinese medicine composition can effectively scavenge free radicals, inhibit tyrosinase activity, reduce melanogenesis and reduce release of a proinflammatory factor IL-6; the composition is low in cost, environment-friendly, suitable for the fields of cosmetics and medicines and wide in market prospect.

The invention provides a rare ginsenoside high-internal-phase Pickering emulsion microcapsule, a preparation method thereof and application of the rare ginsenoside high-internal-phase Pickering emulsion microcapsule in the aspects of uric acid reduction and kidney protection, and the preparation method comprises the following steps: (1) mixing a pectin aqueous solution and a tannic acid aqueous solution, adjusting the pH value, and stirring to obtain pectin-tannic acid composite sol, namely a water phase; (2) adding rare ginsenoside into the oil, and stirring to fully dissolve the rare ginsenoside to obtain an oil phase; (3) mixing the water phase and the oil phase, stirring, standing and carrying out ultrasonic treatment to obtain a crude emulsion; (4) emulsifying and homogenizing the crude emulsion to obtain crude emulsion; (5) carrying out high-pressure homogenization on the crude emulsion, so as to obtain a rare ginsenoside high-internal-phase Pickering emulsion; and (6) drying the rare ginsenoside high internal phase Pickering emulsion, so as to obtain the rare ginsenoside high internal phase Pickering emulsion microcapsule. The invention solves the problems of low safety, poor stability and low bioavailability of the traditional nano-emulsion, and belongs to the technical field of functional foods.

The invention relates to the technical field of functional drinks, in particular to a polypeptide synergistically strengthened cubilose collagen composite drink with a breast enlarging function and a preparation method of the polypeptide synergistically strengthened cubilose collagen composite drink. The drink contains fish collagen tripeptide, elastin peptide, cubilose peptide, pueraria mirifica isoflavone, red clover isoflavone and saffron crocus extract. A lipidosome delivery system is adopted to entrap polypeptide to form a nano-scale compound, nano-emulsion entraps phytoestrogen, and berry polyphenol and lipidosome-polypeptide form a stable ternary compound. Through the multi-way synergistic effect that phytoestrogen activates a mammary gland estrogen receptor, polypeptide promotes connective tissue collagen synthesis and cubilose peptide activates a growth factor signal, mammary gland development is remarkably promoted, the breast enlarging effect is achieved, the bioavailability reaches 85% or above, and the retention rate of active ingredients stored at normal temperature for 24 months is larger than 90%.

The invention belongs to the field of chemical reaction equipment, and discloses a triple enhanced flow field structure for enhancing a micro-flow field reaction process, which comprises a channel shell and a flow field structure arranged in a channel, the channel shell comprises a mixing channel, an outlet and at least two inlet channels, all the channels are circular through holes, and the flow field structure is arranged in the mixing channel. The flow field structure is formed by sequentially and alternately arranging and combining first flow field structures and second flow field structures, at least two reaction fluids enter the mixing channel through the inlet channel to be mixed, and the mixed fluid flows out through the outlet. The invention provides a safe, efficient and easy-to-amplify micro-flow field chemical reactor, and provides a universal solution for industrial processes such as nano-emulsion preparation, heterogeneous catalytic reaction, drug-loaded microsphere preparation and the like.

The invention discloses a layered volatilization sleep-aiding essential oil product based on lavender essential oil and sandalwood essential oil and a preparation method of the layered volatilization sleep-aiding essential oil product. The preparation method comprises the following steps: mixing a high-volatility essential oil component and a low-volatility essential oil component with a natural emulsifier according to a specific ratio, carrying out an ultrasonic emulsification technology to obtain a nano-emulsion, and drying the nano-emulsion to prepare the microcapsule essential oil particles. According to the invention, different volatile components are coated by a specific emulsification method to reduce the volatilization loss and improve the stability, and layered slow release with synchronous starting and controllable speed is realized by utilizing the difference between high and low volatility; wherein the high-volatility component is quickly released in the early stage to provide an instant tranquilizing and allaying excitement effect, and the low-volatility component is slowly released in the later stage to provide a continuous sleep aiding effect. The layered volatile sleep-aiding essential oil product based on the lavender essential oil and the sandalwood essential oil provided by the invention is good in stability, has the advantages of rapid effect taking, lasting controlled release, uniform volatilization, good skin compatibility and the like, and can be used for preparing more sleep-aiding and nerve-soothing products.

The present disclosure relates to nanoemulsions of 5-amino-[4-(4-chlorobenzoyl)-3,5-dichlorobenzyl]-1,2,3-triazole-4-carboxamide (carboxy-amido-triazole or CAI), methods of preparing thereof, and their use in the treatment of inflammatory optic neuropathies.

The invention relates to the technical field of food processing, and particularly discloses a preparation method of medium-chain fatty acid oil powder capable of promoting weight loss, which comprises the following steps: S1, preparing a nano-emulsion: mixing medium-chain triglyceride (MCT) oil, sodium caseinate and citrus pectin with esterification degree of 20-35% according to a mass ratio of (6-8): (1.2-1.8): (0.6-0.8), adjusting the solid content to 25 + / -3% (w / w), and uniformly stirring to obtain the nano-emulsion; shearing and emulsifying for 8 minutes at a high speed of 12000 rpm at 55 + / -2 DEG C to obtain a crude emulsion; s2, high-pressure homogenization: homogenizing the crude emulsion in the step S1 under the pressure of 80MPa for three times for circulation to obtain a nano-emulsion with the particle size of 150 + / -30nm; s3, preparing a flavor masking system: mixing beta-cyclodextrin and menthol according to a mass ratio of 12: 1, and stirring at 45 DEG C for 2.5 h to enable the entrapment rate of menthol to be greater than or equal to 93% so as to obtain an entrapment product; by adopting a preparation method combining a nano emulsion technology and freeze drying, the particle size of the medium-chain fatty acid oil powder is remarkably reduced, so that the dispersity and the dissolution rate of the medium-chain fatty acid oil powder in water are greatly improved.

The invention discloses ailanthus altissima extract nano-emulsion and a preparation method and application thereof, the nano-emulsion comprises ailanthus altissima extract, holly essential oil, an emulsifier and water, and the ailanthus altissima extract is ailanthus altissima bark extract; the preparation method comprises the following steps: uniformly mixing the ailanthus altissima extract, the holly essential oil and the emulsifier as an oil phase, dropwise adding water into the oil phase while stirring, and continuously stirring after dropwise adding to obtain the uniform ailanthus altissima extract nano-emulsion. Compared with the ailanthus altissima extract, the ailanthus altissima nano-emulsion has the advantages that the insecticidal effect is obviously improved, the obvious insecticidal effect on various pests is achieved, the plant source pesticide is good in environmental compatibility, diversified in biological activity, safe to higher animals and natural enemies and not prone to generating drug resistance to pests.

The present application relates to a kind of nanodroplet system based on interface crosslinking curcumin and its preparation method, by the crosslinking complexation between gallic acid ester, metal ion, curcumin to construct nanodroplet system.Gallic acid ester is polyphenol compound, contains a large number of phenolic hydroxyl in structure, has strong chelating metal ability, can be complexed with most of trivalent metal ions and divalent excessive metal ions, called metal phenolic network;Metal ions such as copper, iron and other metal ions form complex by electrostatic interaction with the beta diketone group in the structure of curcumin.Therefore, the nanodroplet system constructed by the present application can maintain the chemical stability and light stability of curcumin, and has wide prospect for improving the current food field curcumin low solubility, poor stability and other problems.

The subject matter of the present invention is a perfusion fluid in the form of an oil-in-water PFC nanoemulsion, methods of producing this perfusion fluid, and its use in particular for organ perfusion and as a blood substitute preparation.