60results about How to "Acceptable" patented technology

The invention discloses a nano-emulsion medicine for treating foot rot. The grain diameter of the nano-emulsion is in a range of 1-100 nanometers and the nano-emulsion is composed of the following raw materials: 0.1-10.0% of pine tar, 0.1-6.0% of cinnamyl aldehyde, 0.1-6.0% of carvacrol, 0.1-5.0% of camphor oil, 0.01-0.1% of clobetasol propionate, 18.0-35.0% of surfactant, 0-7.0% of co-surfactant and residual amount of distilled water; and the sum of the mass percentages of the components is 100%. The nano-emulsion disclosed by the invention has the functions of dissolving cutin, relieving itching, diminishing inflammation, restraining, partially disinfecting and resisting corrosion, accelerating absorption and the like, and is mainly used for treating animal foot rot. According to the nano-emulsion medicine for treating the foot rot, the solubility of the medicine is increased, the medicinal stability and the biological utilization rate are improved, the dosage of the medicine is reduced, the skin transmission rate is higher than that of common preparations including a medicinal extract and the like, and the cost is low, so that the nano-emulsion medicine has a wide market prospect in a veterinary medicine field.

The invention discloses ampelopsis grossedentata selenium-enriched functional drink and a preparation method thereof and relates to natural health functional drink added with no preservative. The ampelopsis grossedentata selenium-enriched functional drink is prepared from the following components in percentage by weight: 10-80% of ampelopsis grossedentata extracting solution, 1-20% of cordyceps militaris extracting solution, 0.01-0.05% of vitamin C, 0.2-0.8% of beta-cyclodextrin, 0.01-0.05% of flavoured enzyme, (1-5)*10<-4>% of plant organic selenium and the balance of water. The prepared drink has the health effects of resisting to oxidation, protecting liver, helping digestion and improving immunity and can meet market diversification demand of drink.

The invention provides a highland barley cake which is prepared from highland barley powder, wheat flour, eggs, white sugar, butter, edible salt and lemon juice. The highland barley cake comprises preparation steps as follows: heating and melting the butter and then pouring into mixed flour of the highland barley powder and the wheat flour, stirring to obtain hot butter paste, adding the eggs, the salt and the lemon juice into the hot butter paste, stirring uniformly and then adding the white sugar, placing the stirred cake paste into an oven, baking and then discharging the cake from the oven, and cooling to obtain the highland barley cake. The highland barley cake provided by the invention is suitable for health needs of modern people, a healthy food is supplied to the people, and the food can be divided into two varieties of a sugary food and a sugar-free food to adapt to more people, especially diabetic patient to eat, and the sugar-free food adopts maltitol, xylitol and bifidus factor to replace the white sugar in the prescription.

The invention relates to a method for preparing composite flavor oil powder grease. The method comprises the following steps: (1) increasing the temperature of animal grease to 140-150 degrees centigrade; (2) adding spices to grease; stirring a mixture until the mixture is pale brown; (3) adding natural seasoning sauce; stirring the mixture evenly so as to acquire composite flavor oil; and (4) processing microcapsule embedding to the composite flavor oil so as to acquire the composite flavor oil powder grease, wherein the weight proportion of the animal grease: the spices: the natural seasoning sauce is 25-60: 12-23.1: 5-25. According to the invention, the method draws the traditional diet essence and simulates novel technical specialties such as family kitchen conditioning, comprehensive thermal reaction, microencapsulation and the like; animal grease deodorization treatment can be processed by the spices so as to acquire special aroma; and powder grease with special flavor is developed.

The invention relates to ginseng polysaccharide yoghurt, ginseng saponin yoghurt and a preparation method thereof, and belongs to the technical field of health-care food. The formula of the ginseng polysaccharide yoghurt comprises pure milk, ginseng polysaccharide and high-quality white sugar. The formula of the ginseng saponin yoghurt comprises pure milk, ginseng saponin and high-quality white sugar. The preparation method comprises the following steps of: 1, extracting ginseng polysaccharide or ginseng saponin; and 2, preparing yoghurt. The yoghurt has specific flavor of ginseng, light coffee color, harmony and cheerful color, flavor and taste and high acceptability, and is sweet, sour and delicious. The ginseng polysaccharide yoghurt and the ginseng saponin yoghurt comprise ginseng polysaccharide or ginseng saponin, has the health-care function of the common yoghurt, can enhance immunity, reduce blood sugar, delay senility, resist tumor and the like, and is nutritional and health-care beverage.

Formulations of azole antifungals such as itraconazole and particularly formulations, co-formulations and compositions of itraconazole with one or more oligomeric and / or polymeric excipients are disclosed. Methods for preparation of the formulations, co-formulations and compositions include co-precipitating the two materials from a common solvent or solvent mixture using a compressed (typically supercritical or near-critical) fluid anti-solvent as in the GAS (Gas Anti-Solvent) precipitation method. The formulations, co-formulations, compositions, methods of making and methods of delivering, are useful as pharmaceutical compositions and in medical treatment by virtue of their at least parity, preferably improved or enhanced solubility or dissolution characteristics, resulting in at least parity, preferably improved or enhanced bioavailability and / or pharmacokinetics.

A lubricant composition comprises: (A) a non-silicone base stock oil; and (B) a silicone oil. The Viscosity Index of the lubricant composition, as measured in accordance with ASTM D 2270-10e1, is greater than that of the non-silicone lubricant base stock oil (A) by at least 10% and is shear stable according to DIN 51350-6.

The invention discloses a user identity recognition method based on hand exercise. Identity recognition is achieved by means of hand exercise characteristics of users. The method comprises an off-line stage and an on-line stage. In the off-line stage, hand exercise tracks of all the users to be recognized are recorded through a depth camera, then the tracks are segmented, space-time parameters are extracted from the segmented tracks to be used as characteristic information, and finally the characteristic data are trained by means of a machine learning method to obtain a user identity recognition model. In the on-line stage, the hand exercise tracks of the users are collected similarly, and segmentation and characteristic extraction are carried out on the tracks. Then, on-line recognition is carried out on the tracks through the user identity recognition model obtained in the off-line stage. According to the user identity recognition method, with the help of the depth camera, identity recognition is achieved by means of hand exercise behaviors of the users, physiological characteristics and behavioral characteristics of the users are combined, and the user identity recognition method has the advantages of being capable of being carried with the users, universal, noninvasive, receptible and the like.

The invention relates to specific Antibody-Drug-Conjugates (ADCs) with KSP inhibitors and anti-CD 123-antibodies, to the use of these conjugates for the treatment and / or prophylaxis of diseases and to the use of these conjugates for preparing medicaments for treatment and / or prevention of diseases, in particular hyperproliferative and / or angiogenic disorders such as, for example, cancer diseases. Such treatments can be carried out as monotherapy or else in combination with other medicaments or further therapeutic measures.

Hybrid intra-cell / inter-cell remote unit antenna bonding in multiple-input, multiple-output (MIMO) distributed antenna systems (DASs), and related components, systems, and methods. The MIMO DASs are capable of supporting distributed MIMO communications with client devices. To provide enhanced MIMO coverage areas, hybrid intra-cell / inter-cell remote unit antenna bonding is employed. For example, if a client device has acceptable MIMO communications signal quality with MIMO antennas within a single remote unit, intra-cell bonding of the MIMO antennas can be employed to provide MIMO coverage for MIMO communications, which may avoid power imbalance issues that would result with inter-cell bonded MIMO antennas. However, if a client device has acceptable MIMO communications signal quality with MIMO antennas in a separate, neighboring remote unit(s), inter-cell bonding of the MIMO antennas can be employed to provide MIMO coverage for MIMO communications.

Hybrid intra-cell / inter-cell remote unit antenna bonding in multiple-input, multiple-output (MIMO) distributed antenna systems (DASs), and related components, systems, and methods. The MIMO DASs are capable of supporting distributed MIMO communications with client devices. To provide enhanced MIMO coverage areas, hybrid intra-cell / inter-cell remote unit antenna bonding is employed. For example, if a client device has acceptable MIMO communications signal quality with MIMO antennas within a single remote unit, intra-cell bonding of the MIMO antennas can be employed to provide MIMO coverage for MIMO communications, which may avoid power imbalance issues that would result with inter-cell bonded MIMO antennas. However, if a client device has acceptable MIMO communications signal quality with MIMO antennas in a separate, neighboring remote unit(s), inter-cell bonding of the MIMO antennas can be employed to provide MIMO coverage for MIMO communications.

The invention provides a modular joint for a lower limb rehabilitation training exoskeleton, and relates to an exoskeleton robot. The modular joint includes a transmission and limiting mechanism, thetransmission and limiting mechanism includes a cover plate, a driving motor, a bracket, a bottom plate, a transmission assembly and an output connecting rod, the cover plate and the bottom plate are connected together in a buckled mode, and the driving motor, the bracket, the transmission assembly and the output connecting rod are arranged between the cover plate and the bottom plate; the drivingmotor is mounted on the bracket, the bracket is mounted on the bottom plate, the driving motor drives the transmission assembly, one end of the output connecting rod is connected with the transmissionassembly, the other end of the output connecting rod extends out of the cover plate and the bottom plate, and the transmission assembly drives the output connecting rod to rotate; and an arc-shaped slide rail and a vertical slide rail are mounted on the inner side of the bottom plate, and a first limiting stop dog and a second limiting stop dog can be slidably mounted on the arc-shaped slide railand the vertical slide rail correspondingly. According to the modular joint, the structure is compact, length adjustment is flexible, the adaptability is good, the modular joint is suitable for patients to accept, and targeted training can be achieved.

The invention provides a sea -flavor potato full-powder low-sugar biscuit, and the raw materials, in quality portion, comprise 30-50 portions of potato full-powder, 10-20 portions of wheat weak gluten flour, 5-10 portions of cream, 3-6 portions of milk powder, 2-4 portions of protein liquid, 5-10 portions of seafood meat emulsion, 1-3 portions of salt, 0.2-1 portion of sodium bicarbonate, 0.2-0.5 portion of ammonium bicarbonate, 10-15 portions of edible oil, 10-15 portions of alga juice, and 30-50 portions of water. The invention also provides a method for preparing the sea -flavor potato full-powder low-sugar biscuit, and the method comprises the steps of modulating a mixed liquor, modulating a dough, making biscuit blanks, and baking the biscuits. According to the invention, the biscuit takes the potato full-powder as the main raw material and has no cane sugar, therefore, the glycemic index is low and the biscuit is suitable for the diabetes; the prepared biscuit has an obvious sea flavor, which covers the special flavor of the potato, therefore, the biscuit can be easily accepted by the consumers; the biscuit has a higher protein content and a higher nutrition value.

The invention belongs to the technical field of microorganisms, and particularly relates to debaryomyces hansenii with good fermentation performance and an aroma production function and a screening method thereof. The strain is named as Debaryomyces hansenii SH4, which is preserved in the China General Microbiological Culture Collection Center on May 12, 2021, and the preservation number of the Debaryomyces hansenii SH4 is CGMCC No.22507. After the debaryomyces hansenii SH4 is inoculated into a fermented sausage simulation system and fermented for 12 days, the contents of aldehydes, acids, alcohols and esters are obviously higher than those of an uninoculated control group (P is greater than 0.05). The fat taste of the simulation system is reduced, the fermentation taste, the wine fragrance, the fruit fragrance and the flower fragrance are increased, and good quality as an aroma production leavening agent is shown. The debaryomyces hansenii provided by the invention is applied to the air-dried sausages and has important significance in improving the fragrance of products and increasing the strength and complexity of the fragrance.

The invention relates to specific Antibody-Drug-Conjugates (ADCs) with KSP inhibitors and anti-CD123-antibodies, to the use of these conjugates for the treatment and / or prophylaxis of diseases and to the use of these conjugates for preparing medicaments for treatment and / or prevention of diseases, in particular hyperproliferative and / or angiogenic disorders such as, for example, cancer diseases. Such treatments can be carried out as monotherapy or else in combination with other medicaments or further therapeutic measures.

A preparation method of a refuse derived fuel comprises the following steps of: providing fiber sludge, adding a mixed material containing microbial flora, a bulking agent and a microbial fermentation promoter which are mixed according to a predetermined proportion, uniformly mixing, and carrying out fermentation on the uniformly-mixed materials and fiber sludge for a period of time so as to form the solid refuse fuel.

The invention belongs to the technical field of vehicle test, and particularly relates to a heart rate change-based vehicle sound quality evaluation method. The method comprises steps: 1, a vehicle sound quality evaluator is selected; 2, in-vehicle audio data of a to-be-evaluated vehicle under a to-be-evaluated working condition are collected as to-be-evaluated samples; 3, the heart rate data L1 of the evaluator when the in-vehicle audio data A0 are played back are collected, and an average period T1 and a heart rate R peak mean value H1 are recorded; 4, the heart rate data L2 of the evaluatorwhen the in-vehicle audio data A0 are not played back are collected, and an average period T2 and a heart rate R peak mean value H2 are recorded; and 5, the weight omega1 of the average period and the weight omega2 of the heart rate R peak mean value are calculated, and a vehicle sound quality quantitative index is further acquired to judge the vehicle sound quality. The operation is simple, theused instrument is cheap, the shortcomings of inaccurate and unreasonable data caused by the evaluator in the subjective evaluation due to the personal emotion are overcome, and the acceptability andthe practicality are strong.

The invention relates to specific Antibody-Drug-Conjugates (ADCs) with KSP inhibitors and anti-CD 123-antibodies, to the use of these conjugates for the treatment and / or prophylaxis of diseases and to the use of these conjugates for preparing medicaments for treatment and / or prevention of diseases, in particular hyperproliferative and / or angiogenic disorders such as, for example, cancer diseases. Such treatments can be carried out as monotherapy or else in combination with other medicaments or further therapeutic measures.

The invention relates to the technical field of sweet almond oil deep processing, in particular to a sweet almond oil soft capsule and a preparation method thereof. The sweet almond oil is gained by squeezing sweet almonds of common apricots, has rich nutrient constituents, contains nutrient elements such as 94.7% of unsaturated fatty acid, vitamin C, oleic acid, linoleic acid, a-linolenic acid, selenium, carotene, and the like, and has very high health care value. In past, consumers directly eat the sweet almond oil as a health care product, some people are not suitable for the greasy taste in the mouth, and the carrying is not convenient. In the invention, the sweet almond oil is packaged in a capsule shell prepared by gelatin, glycerol and purified water as raw materials, is prepared into soft capsules, is convenient to carry, is convenient to eat, and is more popular in consumers.

The invention provides oil-in-water drilling fluid taking biodiesel as a dispersion phase as well as a preparation method and application thereof. The oil-in-water drilling fluid comprises 40-70 parts by volume of water and 30-60 parts by volume of biodiesel, wherein the total volume of water and biodiesel is 100%; the oil-in-water drilling fluid further comprises the following components: bentonite with the mass-to-volume ratio (g / mL) of 1%-6%, sodium carbonate with the mass-to-volume ratio of 0.05%-0.3%, sodium hydroxide with the mass-to-volume ratio of 0.02%-0.05%, a main emulsifier with the mass-to-volume ratio of 2%-5%, an auxiliary emulsifier with the mass-to-volume ratio of 0.2%-1%, a shale inhibitor with the mass-to-volume ratio of 0.5%-5% and a filtrate reducer with the mass-to-volume ratio of 0.5%-5%. The oil-in-water drilling fluid provided by the invention has the characteristics of being low in cost, non-toxic, non-fluorescent, low in density, adjustable, good in rheological property, low in filter loss, excellent in lubricating property and high in upper temperature resistance limit, and further has advantages of being excellent in antifouling property, shale inhibition property, reservoir protection property and environment acceptability.

The invention relates to a device for measuring the walking gait characteristic of a human body. The device comprises a highly stable microwave signal source, a continuous wave transmitter, a circulator, a transceiving antenna, an amplifying, mixing and receiving channel, a signal processor and a parallel data processing and display terminal, wherein the output of the highly stable microwave signal source provide a stable signal for the continuous wave transmitter; the continuous wave transmitter is connected with the circulator, transmits a microwave signal to the transceiving antenna and transmits the microwave signal through the antenna; the transceiving antenna receives a reflection echo from a target and transmits the reflection echo to the amplifying, mixing and receiving channel through the circulator; the output of the amplifying, mixing and receiving channel is transmitted to the signal processor; the signal processor converts an analog signal into a digital signal and performs digital filtering and time frequency processing; and the processed digital signal is connected with the data processing and display terminal. The device can realize gait identification, extracts the gait characteristic of a pedestrian a certain distance away, and has non-compulsivity and acceptability.

The invention discloses a refreshing vegetable beverage and a production method of the refreshing vegetable beverage. The refreshing vegetable beverage is prepared from water extract of a mixed material of seven vegetables such as rhodiola rosea, seed of Chinese dodder, roasted malt, chrysanthemum, folium mori, red dates and mint and a proper amount of cane sugar. The production method of the refreshing vegetable beverage comprises the steps of: according to ratios, firstly placing the raw materials of the seven vegetables into a container, adding water and boiling for 3 times, with the first additive quantity of water being not more than a half of the total volume of the container and the second and the third additive quantity of water being respectively not more than a quarter of the total volume of the container, merging filtrate, adding the cane sugar with the quantity in a formula, adjusting the total quantity by using purified water, chilling, sterilizing and then filling. The refreshing vegetable beverage provided by the invention has a refreshing efficacy, and is simple in production method and low in cost.

The invention discloses a medicine composition curing gynaecological mass diseases such as fibroids and a preparation method and application of the medicine composition. The medicine composition mainly comprises the following raw materials: glabrous greenbrier rhizome, lightyellow sophora roots, cortex phellodendri, zedoray rhizome, rhizoma sparganic, roots of red-rooted salvia, red peony roots, szechwan chinaberry fruits, rhizoma corydalis, rhizoma corydalis, chinese angelica, Gorgon fruits and Chinese yams, extraction and purification are carried out through a certain technique, and auxiliary materials and components which are acceptable in the pharmacy are added to prepare the medicine composition. According to the preparation method, volatile components are extracted in a supercritical mode and prepared into micro-capsules to avoid loss of the volatile components, the preservation time limit of the product is promoted, and the stimulus effect on gastrointestinal tracts is reduced. The method is extensive in medicinal herbs resources and free of toxic, strong and tabooed medicines, all the effective components contribute to synergistic effects, the effective substances are clear, the quality safety is controllable, the curative effect is definite, and the medicine composition can be accepted well and is a new effective medicine curing the gynaecological mass diseases such as the fibroids.

The invention discloses a preparation method of modified remediation plant biochar for cadmium-contaminated soil remediation. The preparation method comprises the following steps: (1) harvesting remediation plants containing a certain concentration of heavy metals, washing, drying, crushing and screening to obtain biomass raw materials; (2) putting the biomass into a tubular furnace in a nitrogenatmosphere for high-temperature carbonization, keeping the pyrolysis temperature at 400-700 DEG C and the retention time at 1-2 hours, cooling to room temperature, and grinding to obtain remediation plant biochar with different pyrolysis temperatures; (3) taking a certain mass of repair plant biochar, flatly laying the repair plant biochar in a glass ware of about 2 mm, and irradiating the repairplant biochar under a 250 W ultraviolet lamp for 8-24 h; and (4) taking out the culture dish after the irradiation is finished to obtain the modified repair plant biochar. The remediation plant biochar prepared by the method is low in toxic leaching amount, has environmental acceptability, and is simple in preparation method, the modified biochar effectively inhibits the effectiveness and mobilityof heavy metals in soil, and dual values of safe disposal and resource reutilization of hazardous wastes are realized.

The invention relates to an external application medicine for treating phlebitis caused by intravenous infusion. The medicine is characterized by comprising the following components in percentage by weight: 12-16 percent of rhubarb, 12-16 percent of gypsum, 12-16 percent of sanguisorba officinalis, 8-12 percent of myrrh, 12-16 percent of catechu, 4-7 percent of borneol, 12-16 percent of gypsum rubrum, and 12-16 percent of cortex phellodendri, 100 percent in total; the components are ground into fine powder, screened through a 80-mesh screen and uniformly mixed; and the mixture is put in a clean box for later use. The using method of the external application medicine for treating phlebitis caused by intravenous infusion is characterized by comprising the following steps: adding a proper amount of sesame oil into the medicinal powder, and uniformly mixing to prepare paste according to the size of an affected area when the medicine is used; uniformly applying medicine to a range which is slightly larger than the area of phlebitis, the thickness of the applied medicine is about 1mm; and coating the medicine with a plastic wrap for 30-60 minutes each time, and 1-2 times everyday. The external application medicine has the effects of clearing heat and removing toxicity, activating blood circulation to remove stasis, relieving pain, diminishing swelling and the like, is scientific and reasonable in prescription, simple in production process, exact and remarkable in curative effect, low in cost and convenient to use, can be easily accepted by patients, and does not have toxic or side effect.

The invention relates to the technical field of bioactive components, in particular to a preparation method of fishy-smell-free low-molecular-weight oyster peptide. The preparation method comprises the following steps: S1, dispersing fresh shell-free oyster powder serving as a raw material into an acetic acid-sodium acetate buffer solution with the pH value of 6.5-7.5 to prepare an oyster powder solution with the mass concentration of 5-8%, and adding sucrose fatty acid ester; S2, adding a compound enzyme into the oyster powder solution for enzymolysis, and adding pullulan after enzymolysis is finished to prepare oyster enzymatic hydrolysate; S3, performing enzyme deactivation operation on the oyster enzymatic hydrolysate, adjusting the pH value of the oyster enzymatic hydrolysate to be 5.5-6.0, carrying out centrifuging, and taking supernatant; dialyzing the supernatant by using a regenerated cellulose dialysis bag, and carrying out concentrating and drying to obtain the oyster peptide. The oyster peptide prepared by the method does not have fishy smell or peculiar smell, is extremely easily accepted by customers, and has a better anti-allergic effect; and the hydrolysis degree of protein in the oyster enzymatic hydrolysate can reach 42% or above, and the recovery rate can reach 90% or above.

The invention relates to the fields of educational technology and studies in mathematical sciences, in particular to a Goldbach conjecture proving coordinate plane demonstrator, aiming to solve the technical problems that no instruments and models are provided for school teaching of Goldbach conjecture, proving of the Goldbach conjecture cannot be solved in the prior art and the like. The Goldbach conjecture proving coordinate plane demonstrator comprises a coordinate plane grid board (1), a coordinate-plane integrated circuit board (2), an odd-prime base addition equation number vertical-coordinate board (3), an odd-prime base addition equation prism bottom slot board (4), a one-equation proving boundary (5), a maximum-equation proving boundary (6), a double-base theorem proving boundary (7), a moving contact connection switch (8) and bases (9). Stable Goldbach spaces are below the double-base theorem proving boundary (7) and the maximum-equation proving boundary (6), a seamless fluctuation Goldbach space is below the one-equation proving boundary (5), and ranges, methods and natural laws for proving the Goldbach conjecture to be true are demonstrated and decided.

The invention provides an immunity-enhancing ginseng polysaccharide oral liquid, prepared from, by weight, 200-400 parts of ginseng polysaccharides, 40-90 parts of arginine, 20-70 parts of taurine, 1-4 parts of acesulfame-K, 1-3 parts of lysine, 1-3 parts of nicotinamide, 1-4 parts of potassium sorbate, 1-2 parts of vitamin B6, 1-2 parts of vitamin B12, and 200-300 parts of purified water. The invention also provides a preparation method of the ginseng polysaccharide oral liquid. The prepared ginseng polysaccharide oral liquid has unique aroma of ginseng, is fresh and cool in taste, is sour and sweet, has coordinated and pleasing color, aroma and taste, is highly acceptable, and has the effects of enhancing immunity, resisting tumors, fighting thrombus, improving body intestinal micro-ecological balance, lowering blood glucose, lowering cholesterol, delaying senility, resisting fatigue and the other effects.

The invention discloses a Chinese medicament for treating cholecystitis, which is prepared from the following raw materials (by weight portion): Chinese yam 30-50 weight parts, iron ocher 20-30 weight parts, asparagus root 15-40 weight parts, ophiopogon root 10-30 weight parts, pinellia tuber 15-20 weight parts, bamboo shavings 5-15 weight parts, germinated barley 5-20 weight parts, oriental wormwood 5-9 weight parts, dipsacus root 5-15 weight parts, chicken's gizzard-membrane 5-15 weight parts, gentian root 5-15 weight parts and dry fodder 5-15 weight parts.