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696 results about "Xanthonoid" patented technology

A xanthonoid is a chemical natural phenolic compound formed from the xanthone backbone. Many members of the Clusiaceae contain xanthonoids. Xanthonoid biosynthesis in cell cultures of Hypericum androsaemum involves the presence of a benzophenone synthase condensing a molecule of benzoyl-CoA with three malonyl-CoA yielding to 2,4,6-trihydroxybenzophenone. This intermediate is subsequently converted by a benzophenone 3′-hydroxylase, a cytochrome P450 monooxygenase, leading to the formation of 2,3′,4,6-tetrahydroxybenzophenone.

Flavonoide esters and their use notably in cosmetics

The invention relates to a flavonoid ester. This flavonoid ester results from the reaction product of at least one flavonoid selected from the group consisting of a flavonoid with a ketone group in the 4-position, a salt, ester or ether of such a flavonoid, and a C-heteroside and / or O-heteroside derivative of such a flavonoid, with the proviso that this flavonoid contains at least one free alcohol group, with an organic monoacid having from 3 to 30 carbon atoms. These flavonoid esters constitute useful active principles for the manufacture of cosmetic, dermopharmaceutical, pharmaceutical, dietetic or agri-foodstuff compositions.
Owner:BASF BEAUTY CARE SOLUTIONS FRANCE SAS

Compositions of flavonoids and flavonoid-containing extracts and the treatment of diseases

In this invention, we describe a group of flavonoids and flavonoid-containing extracts that have pharmaceutical properties which are useful in the medicinal therapy of fibrotic diseases for the treatment or reparation and prevention of fibrotic lesional tissues. Representative flavonoids and flavonoid-containing extracts have the active compositions of the below formula. Those compositions can be extracted and purified from the botanicals, including Scutellaria baicalensis Georgi, Scutellaria scordifolia Fisch,Oroxylum indicum(L.) Vent, Plantago major L. The compositions of the invention are novel as an anti-fibrotic drugs, as agents for treating fibrosis.
Owner:SHANGHAI COMMAN PHARMA

Nakedflower beautyberry extract as well as preparation method, preparation and application thereof

The invention relates to a nakedflower beautyberry extract as well as a preparation method, a preparation and an application thereof. The nakedflower beautyberry extract is an extract which is extracted from nakedflower beautyberry leaves and contains a nakedflower beautyberry total flavonoid compound and a tannide class compound. The extract is obtained by the steps of extracting the nakedflower beautyberry leaves by water, diluted alcohol or diluted ketone and carrying out macroporous adsorptive resin column chromatography purification on an extracting solution after being concentrated. The nakedflower beautyberry extract has high purity and has the functions of bacteriostasis, hemostasis, pain relieving and convergence.
Owner:HAINAN JIUZHITANG PHARMACY

Compositions and methods for treatment of diabetes

Flavonoids, especially luteolin, are shown to be effective against insulin dependent (Type I) and insulin independent (Type II) diabetes mellitus. It is demonstrated that luteolin works in mammals by binding and blocking the Kv1.3 potassium channel of T-cell and Beta cells. Antidiabetic and anti-autoimmune compounds can be selected by measuring their ability to bind to and block the Kv1.3 channel.
Owner:ZIEGLER RANDY

Application of extracting agent and deep-eutectic solvent in determining of effective ingredients in traditional Chinese medicine

The invention relates to the technical field of preparation of extracting agents and deep-eutectic solvents, and relates to application of an extracting agent and a deep-eutectic solvent in determining of effective ingredients in traditional Chinese medicine, in particular to application in determining of flavonoid ingredient in radix scutellariae, and application of an extracting agent and a deep-eutectic solvent in determining of effective ingredients of baicalin, baicalein, wogonoside, wogonin and scutellarin in radix scutellariae. The application is characterized in that the radix scutellariae is used as the raw material, the deep-eutectic solvent, especially choline deep-eutectic solvent, is used as the extracting agent, the water is used as a thinner for reducing the system viscosity, and the flavonoid compound is forcibly extracted under the ultrasonic condition. An extracting method has the advantages that the extracting efficiency of the flavonoid ingredient is higher, the extracting conditions are moderate, and the operation is simple and convenient. The extracting agent has the characteristics of no burning explosion and volatizing, small loss, low energy consumption andthe like. The extracting method is also suitable for extracting the flavonoid-containing traditional Chinese medicines, such as radix astragali seu hedysari, liquorice root, radix puerariae and radixsophorae flavescentis.
Owner:SHENYANG PHARMA UNIVERSITY

Skin care composition containing dehydroacetic acid and skin care actives

InactiveUS20050214332A1Uneven texturePreventing, retarding, and/or treating uneven skin textureCosmetic preparationsToilet preparationsDehydroacetic acidHydroxyproline
Skin care compositions containing dehydroacetic acid, its isomers, salts, and derivatives thereof; at least two skin care actives selected from sugar amines, vitamin B3 compounds, phytosterols, salicylic acid compounds, hexamidines, dialkanoyl hydroxyproline compounds, flavonoids, n-acyl amino acid compounds, and their derivatives, and combinations thereof; and a dermatologically acceptable carrier for the dehydroacetic acid and the skin care actives. The invention further relates to methods for regulating the condition of mammalian keratinous tissue wherein the methods each comprise the step of topically applying to the keratinous tissue of a mammal needing such treatment, a safe and effective amount of the skin care composition of the invention.
Owner:THE PROCTER & GAMBLE COMPANY

Extraction separation purification and identification of flavonoid monomers in oriental blueberry melanin

This is a method for flavonoid monomer's extraction, separation, purification and structural identification, belonging to flavonoid field. In this invention, the original source blueburry leaves turn to be blueburry leaves melanin solution after ethanol extraction. Then, macroreticular resinous adsorbent is used for crude separation of flavonoid in melanin solution, polyamide and HW-40 for flavonoid monomer's pufification, high efficiency liquid chromatography-mass spectrum and NMRR for structural identification. Finally, we obtain 7 kinds of flavonoid monomer, named A B C D E F and G. Exact structural identification help to determine B C D E and F is quercetin, chrysin, versulin, Kacmpferol and digitoflavone respectively, and their relative contents are 37.51%,2.26%,9.57%,1.72% and 15.16%.
Owner:JIANGNAN UNIV

Buckwheat malt seedling dish and production method thereof

The invention discloses a buckwheat sprout seedling dish and a preparation method thereof, belonging to the field of foods. The preparation method of the buckwheat sprout seedling dish comprises the steps of seed selection, sterilization, seed soaking, sowing, sprouting, harvesting and the like, and the water content of the obtained buckwheat sprout seedling dish is 80% to 90%. In the invention, the buckwheat sprout seedling dish made by buckwheat after sprouting has the savory taste of buckwheat sprouts and is rich in flavonoid compounds, such as rutin and the like, and 18 kinds of amino acids necessary to a human body simultaneously, the mineral content of the buckwheat sprout seedling dish is higher than that of common buckwheat kernels, the activity of nutritional ingredients is reinforced, and the nutritional ingredients are easy for the human body to absorb; by eating the buckwheat sprout seedling dish frequently, the immunity of the human body can be enhanced, and the health of the human body is strengthened.
Owner:SHANGHAI INST OF TECH

Method for separating flavone compound from hericium erinaceus by applying high-speed countercurrent chromatography

The invention discloses a method for separating a flavone compound from hericium erinaceus by applying a high-speed countercurrent chromatography. The method comprises the following steps: 1) subjecting hericium erinaceus fermented mycelia to extraction by adopting high-purity ethanol, then carrying out filtration, carrying out pressure-reducing concentration so as to recover ethanol, and carrying out extraction with petroleum ether and ethyl acetate so as to obtain a crude extract; 2) mixing chloroform, dichloromethane, methanol and water according to a volume ratio of 4: 2: 3: 2 so as to obtain a mixed solution used as a two-phase solvent system, and carrying out standing and stratifying, wherein the upper phase is used as a stationary phase, and the lower phase is used as a mobile phase; and 3) carrying out separation through the high-speed countercurrent chromatography so as to obtain the flavone compound. The method is simple and convenient, has good reproducibility, can be used for large-scale preparation of compounds, and lays a material foundation for further research on activity.
Owner:ZHEJIANG UNIV OF TECH

Method for extraction and separation of xanthophyll and flavones in marigold

The invention relates to a method for extraction and separation of xanthophyll and flavones in marigold, and belongs to the technical field of extraction of the xanthophyll and flavonoids compounds. According to the method, marigold petal powder is added into an isopropanol-potassium hydroxide two-aqueous-phase system for one-step extraction to separate an upper phase and a lower phase, and a final product is prepared by dealkalization, filtration and evaporation. The method greatly simplifies the process of extraction and separation of the xanthophyll and the flavones, and overcomes the defects of large use amount of organic solvents, high material consumption and high energy consumption. The extraction rate of the xanthophyll in the upper phase reaches 86.73%, and the xanthophyll ester saponification rate reaches 93.98%, and the extraction rate of the flavonoids compounds in the lower phase reaches 78.31%. The method is easy to operate, and green, can realize simultaneous xanthophyll saponification and extraction, and can be used for effective separation of the flavonoids compounds.
Owner:JIANGSU UNIV

Alpha-L-rhamnosidase and preparing method and applications thereof

ActiveCN104762281AThe optimum reaction temperature is highImprove thermal stabilityHydrolasesFermentationNaringinXanthonoid
Alpha-L-rhamnosidase and a preparing method and applications thereof are disclosed. The amino acid sequence of the alpha-L-rhamnosidase is shown as SEQ ID NO.1. The recombinase is high in optimum temperature, good in thermal stability, and capable of efficiently expressing target protein under preferred conditions, so that the recombinase has wide applications in the fields of selective hydrolysis of rutoside, hesperidin, naringin, prunin, saikoside and other flavonoid compounds connecting alpha-rhamnoside or rhamnose in terpene fragrance precursor compounds, and the like.
Owner:NANJING FORESTRY UNIV

Method for extracting propolis by simulative biological fluid bed supercritical CO2 fluid

The invention provides a method for extracting propolis by simulative biological fluid bed supercritical CO2 fluid, which comprises that: bran (or rice bran and the like) taken as biomembrane carrier and original gum particles after physical treatment simulate a fluid bed in an extraction kettle to perform gridded filling, the supercritical CO2 fluid is used for extraction, and the lowest speed of a granular bed converting from a stationary state to fluidization is regulated by regulating temperature, pressure and flow rate of the fluid in the extraction process so as to reach the critical fluidization state; therefore, high-quality and high-yield propolis extract is obtained through a cyclic process of fluidization diffusion, dissolution and separation between granules and the fluid. The method improves the yield of the propolis extract, reduces the cost, and extracts nearly all terpene compounds and 40 to 50 percent of flavonoid compounds in the propolis at the same time; and products do not have organic solvent.
Owner:JIANGSU JIANGDAYUAN ECOLOGICAL BIOLOGICAL TECH

Extraction, purification and conversion of flavonoids from plant biomass

A process for preparing a rutin-enriched composition from plant biomass comprises extraction with an aqueous solution, and precipitation. An enzyme preparation, such as naringinase, is used for the transformation of rutin to higher value compositions containing increased proportions of isoquercitrin and quercetin.
Owner:HER MAJESTY THE QUEEN & RIGHT OF CANADA

Preparation of Flavonoid Compounds

Disclosed is an improved method for preparing the isoflavonoid compound (+ / −)-equol, the method comprising reducing an organic diester of the isoflavone daidzein under hydrogen-transfer conditions using palladium hydroxide catalyst.
Owner:YASOO HEALTH

Extract of smilax glabra saponins and flavonoid and preparation method thereof

The invention discloses an extract of smilax glabra saponins and flavonoid and a preparation method thereof. The preparation method comprises the steps of (1) smilax glabra medical materials are dried in vacuum, crushed and hydrolyzed by enzyme; and (2) smilax glabra saponins and flavonoid compound are extracted with ethanol under the auxiliary function of ultrasonic in inverse flow and condensed; the condensed compound is degreased with petroleum ether and extracted with chloroform and ethyl acetate; after the solvent is recovered, the solvent is dried in vacuum to obtain the extract of smilax glabra saponins and flavonoid which contains 30-80 percent of flavonoid compound. The obtained smilax glabra saponins extract contains 20-70 percent of saponins compound. The method utilizes composite plant extracting enzyme to pretreat the smilax glabra medical materials and extract the smilax glabra saponins and flavonoid compound with ultrasonic auxiliary extract technology, has high utilization degree of the medical materials and high yield of product, consumes low energy and is convenient to operate. The extract of smilax glabra saponins and flavonoid is widely applied to the field of medical materials, midbody and health-care food and has wide market foreground.
Owner:湖南湘泉药业股份有限公司

Method for deep eutectic solvent extraction and macroporous resin separation and purification of burdock leaf total flavonoids

The invention belongs to the technical field of biological extraction and particularly relates to a method for deep eutectic solvent extraction and macroporous resin separation and purification of burdock leaf total flavonoids. The extraction solvent in the method consists of the deep eutectic solvent with water content of 0 to 50 percent, wherein the deep eutectic solvent is prepared by reactingcholine chloride with one of ethylene glycol, glycerol, triethanolamine, levulinic acid and malonic acid. The deep eutectic solvent has unique physicochemical properties of greenness, no pollution, low vapor pressure, no toxicity, biodegradability, good solubility and the like; in addition, the deep eutectic solvent has a good extraction effect on flavonoid compounds. According to the method disclosed by the invention, by adopting the method for ultrasonic assisted green novel deep eutectic solvent extraction and the macroporous resin separation and purification of the burdock leaf total flavonoids, the deep eutectic solvent extracting solution can be directly used for separation and purification of macroporous resin. The method has the characteristics of simple operation, low cost, greenness and environment friendliness, and provides a novel idea for extraction, separation and enrichment of burdock leaves.
Owner:LINYI UNIVERSITY

Compositions for protection against superficial vasodilator flush syndrome, and methods of use

Compositions for protection against SVFS induced by niacin, a carcinoid, mesenteric traction, serotonin, post-menopause, alcohol, monosodium glutamate, mastocytosis, atopic dermatitis, food-allergy or food intolerance, and mast cell activation syndrome, or against individual symptoms of SVFS, superficial vasodilation, feeling of warmth, itching (pruritus) and hives, comprising a flavonoid compound of the structure 2-phenyl-4H-1-benzopyran or 2-phenyl-4-keto-1-benzopyran or glycosides thereof, or chalconoid compounds, with appropriate substitutions of their hydroxyl groups to render them water soluble or in combination with a pshospholipid or cyclodextrin to render them to have higher oral absorption, administered alone or together with an anti-superficial vasodilation dose of one or more of, olive kernel oil, a serotonin inhibitor, a prostaglandin inhibitor, willow bark extract. A composition for treating cardiovascular disease with niacin, but without eliciting the SVFS effects of niacin, has also been invented.
Owner:THETA BIOMEDICAL CONSULTING & DEVMENT

Anti-ageing yoghourt containing flavonoid compounds and production method for same

ActiveCN103181414AImprove the level ofExpand anti-aging functionalityMilk preparationPre treatmentBitter taste
The invention provides a yoghourt containing flavonoid compounds and a production method for the same. The production method comprises the following steps of: pre-treating the flavonoid compounds; adding the pre-treated flavonoid compounds in milk, or adequately dissolving the pre-treated flavonoid compounds and milk powder in water, and preparing fermentation substrate solution; and producing the yoghourt after homogenizing and sterilizing. According to the production method disclosed by the invention, the flavonoid compounds are added in the yoghourt after a special pre-treatment process, so that the product has a certain anti-ageing function because of containing the flavonoid compounds; moreover, the influences of the colour and bitter taste of the natural flavonoid compounds on the yoghourt are furthest eliminated and reduced, so that the quality of the product is ensured; further, via the addition of the flavonoid compounds, a fermentation process can also be promoted.
Owner:INNER MONGOLIA YILI INDUSTRIAL GROUP CO LTD

Alpha-L-rhamnosidase Rha1 as well as expressed gene and application of alpha-L-rhamnosidase Rha1

The invention relates to alpha-L-rhamnosidase Rha1 as well as an expressed gene and an application of the alpha-L-rhamnosidase Rha1. An amino acid sequence is shown in SEQIDNO.2, a nucleotide sequence of the gene coding alpha-L-rhamnosidase Rha1 is shown in SEQIDNO.1. 1.5g / L of rutin is hydrolyzed for 20min by the alpha-L-rhamnosidase Rha1 under the conditions that the dosage of enzyme is 13U / ml, pH value is 6.5 and the temperature is 35 DEG C, and the hydrolyzing efficiency is more than 98%. Flavonoids compounds, such as rutin, aringin and the like can biologically catalyzed and converted by alpha-L-rhamnosidase Rha1 at a low temperature, and the energy consumption is greatly reduced.
Owner:NANJING FORESTRY UNIV

Method for preparing onion functional components by using double-stage extraction based on subcritical water and solvent method

The invention relates to a method for preparing onion functional components by using double-stage extraction based on a subcritical water and solvent method, belonging to the technical field of food refine and deep processing. The invention mainly aims at a series of problems about low survival ratio and more destroys of active components, caused by extracting onion oil by using the traditional constant pressure steam distillation method, solvent residue caused by extracting onion oil by using an organic solvent extraction method, high cost of supercritical extraction, difficult large-scale industrialization production and the like. In the method, with the onions or processed by-products (onionskins, leftovers and the like) thereof as raw materials, and onion oil and flavonoid compounds are respectively prepared through a low-frequency industrial microwave pre-drying wall-broken technology and subcritical water extraction and ethanol-water solvent two-stage extraction technologies so that the quality of the product and the comprehensive utilization ratio of resources are effectively improved. Therefore, the invention meets the development direction of food nutrition, security and health in China and also opens up a new method for effective utilization of onions.
Owner:JIANGNAN UNIV

Preparation method of choline eutectic solvent and application of choline eutectic solvent in extraction of flavonoid compounds

The invention discloses a preparation method of a choline eutectic solvent and application of the choline eutectic solvent in extraction of flavonoid compounds. The preparation process of the cholineeutectic solvent is as follows: taking proper amounts of choline chloride or choline hydroxide for uniformly mixing with a proper amount of an organic acid according to a ratio (mole number) of 1:1-1:10; putting a uniformly mixed reactant into a flat-bottomed flask with a proper size, and then adding a proper amount of water to initiate a reaction; and putting a magnetic stirrer at the temperature of 25-50 DEG C, putting the flat-bottomed flask on a magnetic stirrer, performing stirring for 1-24h at a proper rotating speed, after reactants in the bottle become transparent and uniform viscousliquid, transferring the liquid in the bottle into a rotary evaporator, and performing spin-drying on excessive moisture to obtain a viscous transparent liquid, namely a DES solvent finished product.The flavonoid compound extracted by the method has the characteristics of high purity, high extraction rate and simple and convenient process, the extraction time is shortened, the traditional solventis changed into an environment-friendly DES solvent which is easy to decompose, and the flavonoid compound is a real green chemical.
Owner:中科萱嘉医养(珠海)健康科技有限公司

Pharmaceutical composition having alpha-glucosidase inhibition activity, and applications thereof

The invention relates to a pharmaceutical composition having alpha-glucosidase inhibition activity, wherein the pharmaceutical composition comprises a flavone compound and an alpha-glucosidase inhibitor, the flavone compound is at least one selected from a monomer such as baicalein, quercetin, luteolin, baicalein-7-O-glucoside and catechin, an organic salt of the monomer, and an inorganic salt of the monomer, and the alpha-glucosidase inhibitor is at least one selected from a monomer such as acarbose, voglibose and miglitol, an organic salt of the monomer, and an inorganic salt of the monomer. According to the present invention, the pharmaceutical composition can effectively reduce postprandial blood glucose, can inhibit the activity of alpha-glucosidase adopting starch, maltose and sucrose as substrates, and less uses the alpha-glucosidase inhibitor, such that the efficacy can be improved, the side effect of the alpha-glucosidase inhibitor can be effectively reduced, and hypoglycemia and other problems easily caused by drug combination are effectively solved.
Owner:上海皋鱼医药科技有限公司

Synthesis of isoflavone compound through Stille crossed coupling reaction

The invention belongs to heterocyclic compound technical field, concretely relating to a heterocyclic compound in which unhydrogenated six-member heterocyclic ring containing an only ring hetero atom of an oxygen atom fuses with other phenyl rings. The invention provides a synthetic method of an isoflavone compound. The method comprises the steps of adding a reactant (substituted) 3-iodine chromone and tetraarylated tin into a solvent for a chemical reaction, and using column chromatography and recrystallization methods to purify the above resultant to obtain the pure compound of the present invention. By using the method, medicinal isoflavone such as daidzein, genistein, Ipriflavone, puerarin, formononetin and the like is prepared, and a new technical route of industrialization production of the above medicaments is established. Simultaneously, a series of novel isoflavone compounds with potential physiological activity are prepared.
Owner:SHAANXI NORMAL UNIV

Preparation method of enzymatic grafting based antioxidant silk fibroin membrane

ActiveCN103819707AEnzyme catalytic efficiency is highLess enzyme preparationTyrosinaseGrafting
The invention discloses a preparation method of an enzymatic grafting based antioxidant silk fibroin membrane, and belongs to the biological technical field of textiles. With the help of tyrosinase, antioxidant flavonoids compounds are grafted onto silk fibroin surface after catalytic oxidation; and by crosslinking of tyrosine and the flavonoids compounds in the enzymatic silk fibroin, the antioxidant properties of the silk fibroin membrane is enhanced. The specific processes include silk fibroin solution preparation, silk fibroin membrane preparation, grafting of the flavonoids compounds on the enzymatic silk fibroin and after treatment of the modified silk fibroin membrane. The silk fibroin membrane prepared by the preparation method has improved antioxidant and antimicrobial properties, and the membrane material mechanical properties also are improved. Compared with a silk fibroin membrane modification method based on chemical crosslinking, the enzymatic modification method is low in energy consumption, high in efficiency, less in pollution and in favour of environmental protection.
Owner:广东资恩解码基因检测科技有限公司

Drug for treating purine metabolic disorder disease

The invention relates to a drug for treating purine metabolic disorder disease, provides a flavonoids compound represented by the formula (I) and a modified derivative thereof, and a use in inhibition of xanthine oxidase activity and promotion of uric acid excretion function, wherein R1, R2 and R3 independently represent -H or monosaccharide residues, and R4 represents -H or -OH. In particular, the drug is used for treating purine metabolic disorder disease, and can be used for treating hyperuricemia and related diseases and reducing a individual serum UA level; the drug is used for treating hyperuricemia; the drug is used for treating the related diseases, such as for treating gouty arthritis and arthrophlogosis caused by hyperuricemia, and for treating chronic interstitial nephritis, kidney stones and the like caused by hyperuricemia. The drug has the advantages of natural chemical structure, safety, low toxicity, rapid curative effect and fewer side effects. (I).
Owner:广东世信药业有限公司

Application of flavonoid

The invention relates to an application of a flavonoid compound, the flavonoid compound is 3, 3', 4', 5, 7-pentahydroxyflavone dihydrate, the ELISA and protein fluorescence quenching experiments provethat the compound can effectively inhibit interaction of PD-1 / PD-L1 proteins, and has a strong affinity for PD-L1 protein. Cell clone number formation and ELISA detection of IL-2 secretion assay prove that the compound can effectively enhance the tumor killing activity of T lymphocyte Jurkat cells against MDA-MB-231 and NCI-H460 tumor cells as well as the expression level of IL-2, and then reverse T cellular immunosuppression. The research results of the application provide a drug for tumor immunotherapy targeting the PD-1 / PD-L1 immunological test site.
Owner:TIANJIN UNIVERSITY OF SCIENCE AND TECHNOLOGY

Gene sequence related to flavone composite in radix scutellariae and application thereof

The invention discloses a gene related to flavone composite in radix scutellariae. The gene includes one or several in flavone synthetase gene with a sequence shown in SEQ ID No.1, flavone 6-site hydroxylase gene with a sequence shown in SEQ ID No.3 and flavone 8-site hydroxylase gene with a sequence shown in SEQ ID No.5. The invention further provides primer composite for amplifying the gene, protein encoded by the gene, a recombinant vector, host cell or transgenic cell line containing the gene and application thereof. The protein encoded by the gene disclosed by the invention can participate in synthesizing baicalein and wogonin and catalyzing synthesis and hydroxylation reaction of flavone matters of the similar structures, can provide very good basis for producing effective active matters, provides theoretical basis for producing baicalein, wogonin and aglycone of the baicalein and the wogonin in a large scale and establishes solid basis for industrially producing other related flavonoid compound.
Owner:SHANGHAI CHENSHAN BOTANICAL GARDEN

Preparation method of aloe herbal tea compound health beverage and product thereof

ActiveCN103609802AMake up for the disadvantages of damaging the spleen and stomachEnhance beautyTea substituesBiotechnologySterculia scaphigera
The invention relates to an aloe herbal tea compound health beverage and a preparation method thereof. The preparation method comprises the following steps of: by taking aloe, mesona blume, plumeria rubra, chrysanthemum, hawthorn, honeysuckle, boat-fruited scaphium seed, liquorice, lotus leaf, mint and the like as materials, preparing aloe juice through pulping and enzymolysis, preparing herbal tea juice by hot water extraction, compounding the aloe juice with the herbal tea juice, adding pure water and white granulated sugar, uniformly mixing, filtering, sterilizing, filling and cooling to prepare the aloe herbal tea compound health beverage. The product is unique in flavor, harmonious and soft in taste, pure in mouthfeel, and clear and bright in color, contains beneficial factors such as flavonoid compounds, maslinic acid, various active polysaccharides and aloin, effectively overcomes the defect that spleen and stomach are damaged by drinking the conventional herbal tea for a long time, further has the effects of maintaining beauty and keeping young, clearing away the lung-heat and relieving sore-throat, promoting digestion to eliminate stagnation, refreshing, decreasing blood pressure, assimilating cholesterol and the like on the health basis of clearing away heat and toxic materials, relieving a cough and moistening throat, clearing damp and promoting secretion of saliva or body fluid, and relieving summer heat and decreasing internal heat, and has stronger health function.
Owner:JIANGSU ACAD OF AGRI SCI
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