19 results about "Acide Nicotinique" patented technology

The invention relates to a functional drinking water preparation method based on a pH response type microcapsule slow release system, and belongs to the technical field of drinking water processing. The functional drinking water is prepared from the following materials: 50-65 parts of base water, 3-6 parts of hydrolyzed protein peptide melt, 5-12 parts of transparent gel, 5-10 parts of a mixture of vitamin C and acerola cherry powder, 1-3 parts of a zinc lactate aqueous solution and 6-12 parts of nicotinic acid microcapsule liquid. By adding natural plant extracts and trace elements and supplementing by oral administration, the health-care beverage can endogenously improve physical quality, promote blood circulation, increase the oxidation resistance of the body of a drinker, and contribute to improving the body vitality and enhancing the immunity; the functional drinking water prepared by the invention is suitable for long-term storage, inhibits the growth of microorganisms, and maximally retains the biological activity of the microorganisms.

The application provides a full-value pet can for maintaining bone health and a preparation method, which comprises the following raw materials in mass parts: chicken breast meat 15-20 parts, chicken skeleton 3-7 parts, chicken heart 2-6 parts, beef 1-5 parts, beef liver 2-5 parts, tuna 5-10 parts, starch 9-14 parts, vegetables 17-23 parts, EPA 3-7 parts, vitamin K1-3 parts, folic acid 1-2 parts, nicotinic acid 0.5-1 part, mineral 2-6 parts, plant fermentation extract 5-9 parts, plant enzymolysis extract 3-6 parts and water 50-60 parts. The full-value pet can can provide full-value nutrition for pet cats, is beneficial to maintaining the bone health of the pet cats, prolongs the can storage time, inhibits the breeding of bacteria on the bottle opening and in the bottle after the can is opened, and improves the edible safety and storage time after the can is opened.

The invention belongs to the technical field of cosmetics, and discloses a vitamin E emulsion and a preparation method thereof, the vitamin E emulsion comprises the following components by mass: 0.5-2 wt% of vitamin E and derivatives thereof, 10-20 wt% of a stabilizer, 10-20 wt% of a humectant, 3-6 wt% of an emulsifier, 0.3-1 wt% of a thickener, 0.5-1 wt% of a preservative, and the balance of water; wherein the vitamin E and the derivative thereof comprise at least one of vitamin E, tocopheryl acetate, tocopheryl linoleate, tocopheryl nicotinate and tocopheryl phosphate; the stabilizer comprises at least one of petrolatum, polydimethylsiloxane, hydrogenated polyisobutene, caprylic / capric triglyceride and butyrospermum parkii butter. Through the components, the antioxidant activity of vitamin E in the storage and skin retention process of the vitamin E milk can be effectively maintained.

The invention relates to a composition with an emotion conditioning function as well as a preparation method and application thereof, and belongs to the technical field of functional foods. The composition comprises core components: calcium 6S-5-methyltetrahydrofolate, N-acetylneuraminic acid, spirulina maxima powder and betaine, and further comprises synergistic components such as vitamin B6, vitamin B12, a zinc source, a selenium source and vitamin B1, vitamin B2, nicotinic acid and pantothenic acid. The composition is designed on the basis of an intestine-brain linkage mechanism, and the brain-intestine axis function is systematically adjusted through multi-target cooperation of intestinal barrier repair, neurotransmitter efficient synthesis, neural network structure support and the like. Experiments show that the composition can effectively improve anxiety, depression and other emotional states, provides a synergistic and safe nutrition intervention scheme for related people, and has a definite application prospect in the fields of emotional health functional foods and brain-intestine axis targeted special diet foods.

The invention relates to the technical field of functional foods, and particularly discloses a dietary therapy composition for promoting repair of cranial nerve damaged cells and a preparation method. The composition is prepared from the following raw materials in parts by weight: artichoke peptide, taurine, phosphatidylserine, natural nicotinic acid, guarana extract, collagen peptide, acerola cherry fruit powder, inulin, yak bone marrow powder, vitamin B family, sialic acid and sucralose. The preparation method comprises the following steps: S1, pretreating the raw materials; s2, performing nano crushing; s3, low-temperature drying; s4, embedding the inulin; and S5, mixing and forming. The artichoke peptide and the phosphatidylserine are synergistically matched, and a compound component with liver and brain axis functions is taken into consideration, so that a multi-target synergistic effect is achieved, the requirements of cell repair and neural development are synchronously met, and compared with single-component supplement or neglect of the influence of liver detoxification on brain repair in the prior art, the brain repair effect is greatly improved. The problems of low repairing efficiency and insufficient component utilization rate are solved.

The invention discloses a corn softening method based on composite biochemical synergistic treatment, and relates to the technical field of food processing, and the method comprises the following steps: raw material pretreatment: soaking corn kernels in cold water at 10-15 DEG C for 10-14 hours, and carrying out salting-out treatment according to the proportion that 0.4-0.6 kg of edible salt is added into 100 kg of corn; the biological-chemical synergistic treatment comprises the following steps: a) compound alkali treatment: adding edible sodium carbonate accounting for 0.4-0.6% of the dry weight of the corn, adding food-grade baking soda accounting for 0.3-0.7% of the dry weight of the corn, mixing, and maintaining the pH value at 8.5-9.2 for 1-2 hours; b) compound enzyme treatment: 0.002%-0.005% of cellulase, 0.001%-0.003% of hemicellulase and 0.0005%-0.0015% of lignin peroxidase are synchronously added; and nicotinic acid release: carrying out alkali treatment on 0.5 jin / 100 jin of corn to destroy combined nicotinic acid, and further releasing vitamin B groups by combining microbial fermentation pine fungus spores and coprinus comatus enzyme to improve the biological accessibility.

The application discloses a kind of serum-free epidermal melanocyte culture medium and its application, method includes by dissolving adenine, hepatocyte growth factor (HGF), glutamine, retinoic acid, vitamin E, nicotinic acid, sodium selenite, sodium hyaluronate and recombination human type XVII collagen are configured into initial culture medium;Preparation of melanocyte stimulating hormone, endothelin-3, transferrin, triiodothyronine, cholesterol, neuroregulin 1 (NRG1), 3-isobutyl-1-methyl purine (IBMX), dibutyryl cyclic adenosine monophosphate (db-cAMP), cholera toxin, hydrocortisone and recombination human insulin mother liquor;Step three: according to culture and concentration, a certain amount of mother liquor of step two is added to initial culture medium.The culture medium can effectively promote human epidermal melanocyte proliferation, melanin accumulation and help to promote human umbilical cord mesenchymal stem cells into human epidermal melanocyte, provide key advantage for obtaining functional melanocyte with high activity and therapeutic potential.

The invention relates to a composition and a preparation method of a reproduction nursing external preparation with effects of inhibiting bacteria, relieving and improving male functions. The invention discloses an external preparation for male reproduction nursing. The plant essential oil comprises natural plant extracts (clove, herba epimedii, ginseng, dendrobium officinale, tribulus terrestris, radix sophorae flavescentis, fructus cnidii, saw palmetto fruit and aloe vera), nutritional ingredients (arginine, hydrolyzed collagen zinc, nicotinic acid, tocopherol, biotin and B-group vitamin yeast polypeptide) and compound essential oil (tea tree oil, jasmine flower oil, iris oil, cananga odorata flower oil and sandalwood oil). The composition can be prepared into spray, cream, lotion and other dosage forms. The preparation improves erectile function, enhances microcirculation, relieves pressure, improves sexual desire and realizes precise adjustment of male function and protection of gonad axis through mechanisms of inhibiting bacteria, diminishing inflammation, improving testosterone concentration, enhancing nitric oxide synthase activity, promoting vasodilatation, blocking neural signals, delaying ejaculation and the like.

The invention relates to the technical field of drinks, in particular to a drink capable of reducing blood sugar and blood fat and a preparation method. Comprising opuntia ficus-indica, a potato extract, a white kidney bean extract, a yeast extract, purified water, mulberry leaf polypeptide, bitter gourd peptide, marine fish oligopeptide, double-petal red rose pollen, Guanshania cerasus pollen, acerola cherry juice powder, inulin, moringa oleifera leaf powder, turmeric powder, saffron crocus powder, roxburgh rose juice powder, natto powder, earthworm protein powder, black tea powder, nicotinic acid and stevioside. Sodium carboxymethyl cellulose and potassium sorbate. The drink for reducing blood sugar and blood fat selects opuntia ficus-indica, the potato extract, the white kidney bean extract and the yeast extract as main materials and has the effects of promoting intestinal tract movement, enhancing immunity, improving digestion, promoting metabolism, providing nutrition and resisting oxidation, and various kinds of powder are supplemented, so that the prepared drink is good in curative effect and free of toxic and side effects. The tea is suitable for long-term drinking by patients with hyperglycemia and hyperlipidemia to inhibit hyperglycemia and hyperlipidemia and reduce complications.

The invention provides a method of promoting weight management in a mammal comprising administering to the mammal a composition comprising at least one weight loss agent and at least one mitochondrial enhancer. The weight loss agent can be selected from the group consisting of psyllium, guar gum, capsaicin, chitosan, caffeine, gamboge, mume, capsaicin, yohimbine, butterfly pea, glucomannan, African mango, guarana, pyruvate, carnitine, beta-glucan, fucoxanthin, raspberry ketone, white kidney bean, kola nut, chromium, ginseng, psyllium, St. John's wort, dandelion, hydroxycitric acid, conjugated linoleic acid, green tea, black tea, coffee bean extract, forskolin, and bitter orange. The mitochondrial enhancer can be selected from the group consisting of beetroot extract, nitrate, idebenone, nicotinamide riboside, elamipretide, vitamin C, vitamin D, vitamin E, thiamine, riboflavin, magnesium, calcium, phosphate, phospholipid, creatine, pyruvate, coenzyme Q10, NADH, niacin, L-carnitine, dichloroacetate, curcumin, schisandrin, and resveratrol. Compositions for weight management are also provided.

The invention discloses a culture method for ginseng adventitious root in-vitro propagation. The method comprises the following steps: inoculating disinfected ginseng adventitious roots to a culture medium containing ammonium nitrate, potassium nitrate, monopotassium phosphate, calcium chloride dehydrate, magnesium sulfate heptahydrate, EDTA-disodium, ferrous sulfate, potassium iodide, sodium molybdate dehydrate, zinc sulfate heptahydrate, cobalt chloride hexahydrate, copper sulfate pentahydrate, boric acid, manganese sulfate tetrahydrate, glycine, inositol, nicotinic acid, vitamin B6, vitamin B1 and glutamine; the method comprises the following steps: carrying out suspension culture on a ginseng adventitious root liquid culture medium containing casein hydrolysate, IBA and cane sugar for 7 days, adding jasmonic acid and gibberellin, and culturing for 30-40 days to obtain proliferated ginseng adventitious roots. The method is beneficial to rapid growth of ginseng tissue culture adventitious roots and efficient synthesis of ginsenoside, and an effective way is provided for directional production of ginsenoside in a cell factory.

Provided herein are compositions comprising nicotinic acid, a vitamin B3-related nicotinamide adenine dinucleotide precursor, or a combination thereof for use as a medicament, a food supplement, or the like. These compositions are provided to treat and prevent the progression of pituitary intermediate dysfunction (PPID) in non-human animals, such as equine animals.

The lip plumper composition described in this patent introduces a novel chemical blend of hydrating, plumping, and nourishing ingredients designed to enhance lip volume while maintaining long-term lip health. The product is formulated using a combination of Botanisil PDH-151, Botanessential Olive S-EHO, Botanol HSO, Vitamin E Nicotinate, and Benzyl Nicotinate, with additional stabilizers such as Aerosil R 974 and a flavor component. The lip and skin treatment composition described in this patent utilizes a two-phase emulsion system to deliver multi-functional cosmetic benefits, including hydration, firmness, and anti-aging effects. The formula combines an oil-based Phase 1, containing Emulsil WO 3155, Euxyl PE 9010, and Vitamin E Acetate, with a water-based Phase 2, containing Water, Propandiol, Sodium Nitrate, Caffeine, Algacktiv Collage, and Botanecuetical.

The invention discloses a dairy cow feeding method capable of reducing and controlling saturated fatty acid in raw milk in a targeted manner, and the preparation method comprises the following steps: (1) preparing a mixed ration which comprises a basic ration and an additive; the additives comprise a ponkan peel-bo-chrysanthemum-boxthorn leaf compound extract, linseed oil, lysine and nicotinic acid; (2) feeding the dairy cows with mixed daily ration every day by adopting a feeding method of free feeding and water drinking; the temperature of the cowshed is controlled to be 10-16 DEG C, a good ventilation environment is kept, and bed bedding is replaced regularly; and (3) starting to add conjugated linoleic acid into the mixed ration after 6-8 days after delivery. When the method is used for feeding the dairy cows, the content of saturated fatty acid in raw milk can be remarkably reduced, and the core is that the rumen function is optimized through regulation and control of daily ration.

The application discloses a detection method of B vitamins, wherein the detection method comprises the following steps: preparation of a control sample solution: B vitamin control samples are respectively dissolved to obtain the control sample solution; preparation of a sample solution: a sample solution containing B vitamins is diluted to obtain the sample solution; determination: high performance liquid chromatography is used to determine the content of B vitamins in the sample solution containing B vitamins. The method has good repeatability, high accuracy, high stability, good separation effect and high separation degree for detecting VB1, riboflavin, nicotinamide, pantothenic acid, vitamin B6, biotin, folic acid, vitamin B12, nicotinic acid and pterin, and can be simultaneously used for common detection of multiple B vitamins in a hyaluronic acid complex solution, thereby providing a good means for research and development and quality evaluation of the hyaluronic acid complex solution.

Disclosed are compositions and methods for increasing NAD+ in a subject (e.g., in a human subject) for treatment of skin conditions selected from the group consisting of contact dermatitis, irritant contact dermatitis, or for treatment of diseases or disorders associated with cell death, neuronal dysfunction, or muscular cell death or dysfunction selected from Parkinson's disease; Alzheimer's disease; multiple sclerosis.

The application provides a feed additive and application thereof. The feed additive comprises the following components in parts by weight: 20-30 parts of flaxseed, 10-20 parts of perilla seed, 1-2 parts of choline, 0.05-0.15 parts of vitamin E, 0.1-0.2 parts of zinc sulfate, 0.01-0.05 parts of nicotinic acid and 48-68 parts of wheat bran. The feed additive and the feed containing the feed additive provided by the application are used for 6-13 month old non-pregnant cows, the mammary gland development of the cows in puberty is intervened, the growth of the mammary gland fat pad in the period is promoted, the growth and development of the lactiferous duct in the gestation period are provided with a material basis, the number of the lactiferous duct and the acinus is increased, and thus the initial number of the mammary epithelial cells in the lactation period is increased, and the peak milk yield of the cows after delivery is improved.

The invention discloses an external preparation suitable for people with weakness of spleen and stomach and a preparation method thereof, the external preparation comprises a traditional Chinese medicine extract composite component, and the external preparation is prepared from the following raw materials in parts by weight: maguey leaf extract; a salvia miltiorrhiza root extract; a polygonum multiflorum root extract; a ginseng root extract; an angelica root extract; a zanthoxylum fruit extract; an astragalus membranaceus root extract; an abrus herb extract; a microcos paniculata extract; and striga asiatica extract. A microbial fermentation product comprising a Thermus thermophilus fermentation product; and Leuconostoc / radish root fermentation filtrate. The transdermal enhancer comprises a ginger extract, methyl nicotinate and a pepper extract. And the auxiliary materials comprise cyclopentasiloxane, squalane, inulin, and disteardimonium hectorite. Chinese herbal medicines are combined with a modern microbial fermentation technology, and based on a percutaneous delivery system, sub-health symptoms such as unsmooth defecation, abdominal distension, abdominal cold, abdominal fat accumulation, edema and poor complexion of people with weakness of the spleen and the stomach are improved.

The application discloses a preparation method of inositol nicotinate tablets and belongs to the technical field of pharmaceutical preparations. The method comprises the following steps: dispersing inositol nicotinate in mixed oil to prepare an oil phase, mixing and emulsifying the oil phase with a water phase, spray drying the drug emulsion powder, and coating the drug emulsion powder with modified chitosan and then directly compressing the drug emulsion powder with excipients. The inositol nicotinate is uniformly dispersed in the mixed oil, so that the drug content uniformity is maintained in the subsequent process, the solid particles are adsorbed on the surface of the drug-containing oil droplets through the emulsification technology, and the drug components are protected. The coating components are reasonably designed, the drug is released at a fixed point, the anti-pressing capacity is endowed, and the drug can be directly compressed. The drug particles after coating are mixed with excipients and then directly compressed, so that the process is simplified, and the coating structure of the drug particles is protected. The inositol nicotinate tablets prepared by the method have stable drug dissolution, good taste and small stimulation to gastric mucosa.