Patents
Literature
Hiro is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Hiro

54 results about "Atractylodes japonica" patented technology

Atractylodes japonica (Japanese: オケラ (植物) okera, Eastern ukera, ukira) – Japan, Korea, Manchuria, Inner Mongolia, Primorye Atractylodes koreana – Korean atractylodes [5] – Korea , Liaoning , Shandong

Dried bean curd containing fructus amomi

The invention discloses dried bean curd containing fructus amomi. The dried bean curd comprises the following raw materials in parts by weight: 50-60 parts of yellow beans, 30-40 parts of red beans, 8-10 parts of peanuts, 4-6 parts of dried grapes, 3-4 parts of dried mangoes, 2-3 parts of hawthorn seeds, 2-3 parts of dried sweet potatoes, 1-2 parts of white atractylodes rhizome, 1-2 parts of fructus amomi, 2-3 parts of fresh ginger, 2-6 parts of white sugar, 2-6 parts of salt, 0.5-1 part of monosodium glutamate, a proper amount of mulberries and 0.03-0.05 parts of a bean product de-foaming agent. The dried bean curd provided by the invention is rich in nutrition and good in mouth feel; various powder added before squeezing and a method of utilizing the mulberries as a flavor regulator provide a high healthcare value for the dried bean curd, wherein the mulberries can be used for treating dizziness due to deficiency of liver and kidney and deficiency of blood and essence, soreness of waist, tinnitus, premature graying of hair, insomnia, dreaminess, thirst due to body fluid deficiency, consumptive thirst and constipation due to intestinal dryness, nourishing yin and moisturizing lung; the fructus amomi mainly acts on stomach, kidney and spleen of a human body and can be used for promoting vital energy circulation, regulating flavor, harmonizing stomach and refreshing spleen.
Owner:ANHUI KAILI CEREALS OILS & FOODSTUFFS

Detection method for atractylodes macrocephala koidz medicinal materials

InactiveCN102680631ATrue reflection of qualityEnsure medication safetyComponent separationHplc fingerprintMedicine
The invention discloses a detection method for atractylodes macrocephala koidz medicinal materials. The method adopts HPLC (high performance liquid chromatography) fingerprint spectrum for detection and includes the operation steps of: (1) preparing sample solution; (2) preparing reference solution; and (3) respectively and precisely absorbing the sample solution and the reference solution to inject into a liquid chromatograph so as to elute by taking an acetonitrile-water system as a flowing phase and detect at wavelengths of 248+ / -5nm. After the atractylodes macrocephala koidz medicinal materials are decocted with water, and then the HPLC fingerprint spectrum is applied for detection, so that quality of the atractylodes macrocephala koidz medicinal materials can be reflected more truly. Moreover, chromatographic conditions such as the flowing phase are selected specifically, so that chromatogram baselines are stable and convenient to integrate, resolution of characteristic peaks is good, and similarity among different medicinal materials is high. The detection method for the atractylodes macrocephala koidz medicinal materials can be effectively used for quality control of atractylodes macrocephala koidz and provides a guarantee of medication security of the atractylodes macrocephala koidz medicinal materials.
Owner:CHENGDU UNIV OF TRADITIONAL CHINESE MEDICINE

Propagation method of bighead atractylodes rhizome seedlings and application thereof

InactiveCN105230493AEfficiently provideRapid asexual reproductionCultivating equipmentsPlant tissue cultureBudDominant types
The invention provides a propagation method of bighead atractylodes rhizome seedlings. The method comprises the following steps of: (1) selecting bighead atractylodes rhizome explants, and performing bacteria-free treatment on the explants; (2) performing primary culture on the explants; 3 ) carrying out induction culture on callus tissues; (4) performing propagation culture on the callus tissues; (5) performing tufted bud induction culture on the callus tissues; (6) performing rooting culture on tufty buds; and (7) performing acclimatization and transplanting. According to the method disclosed by the invention, typical single plants of dominant types in variety breeding of bighead atractylodes rhizomes can be quickly propagated, the inheritable characters of the bighead atractylodes rhizomes are stabilized in a tissue culture manner, the number of colonies is increased, and preservation, evaluation and utilization of high-quality intermediate materials in the breeding process are facilitated. The invention further provides the application of the method in planting seedlings of the bighead atractylodes rhizomes in greenhouses. According to the application, the survival rate can be maintained, besides, the propagation quantity can be increased, and the propagation area can be arranged as needed.
Owner:ACAD OF AGRI SCI ENSHI TUJIA MIAOAUTONOMOUS PREFECTURE +1

Preparation technology and production method for integrated new formulation of bighead atractylodes rhizome and monkshood decoction

The present invention relates to a preparation technology and a production method for an integrated new formulation of a bighead atractylodes rhizome and monkshood decoction, wherein the raw materials of active ingredients comprise: 6 parts by weight of bighead atractylodes rhizome, 10 parts by weight of monkshood, 3 parts by weight of licorice, 4.5 parts by weight of ginger, and 6 parts by weight of Chinese-date. The production process of the integrated new formulation comprises the following steps of: supersonic air-jet crushing, alcohol-water extraction, ultrasonic crushing extraction, water decocting concentration, supersonic spray drying, nanometer grinding, high pressure homogenization, nano particle preparation and the like. According to the invention, the advantages, such as multi-synergism, multi-target, embodied by a nano-carrier coupling technique, are focused to be taken of. After the integrated new formulation of bighead atractylodes rhizome and monkshood decoction is subjected to scale production, the production cost can be greatly reduced, the quality of products is greatly improved and the targeting property, and the sustained and controlled release performance of the medicament are enhanced. The internal and external administration of the integrated new formulation of bighead atractylodes rhizome and monkshood decoction can be realized simultaneously, and the medicament can be separately taken in four time slices according to the midnight-noon ebb-flow and qi and the blood flowing rule of a human body. The integrated new formulation of bighead atractylodes rhizome-monkshood decoction can be further prepared into films and transdermal agents, which are respectively stuck to different parts of a human body according to the midnight-noon ebb-flow and qi and blood flowing rule of the human body, and can be directly absorbed through skin.
Owner:SUZHOU ZHIWEITANG BIOLOGICAL TECH +1

Rhizoma alismatis-largehead atractylodes rhizome tablet quality control method

The invention belongs to the technical field of medicine, and discloses a quality control method for detecting content of butenolide I, butenolide II and 23-acetyl alisol B in a rhizoma alismatis-largehead atractylodes rhizome tablet. The content of one or more components is determined simultaneously or separately by high performance liquid chromatography. C8 and C18 are used as fillers. Isocraticelution or gradient elution is carried out by using 0-100% acetonitrile or methanol as a mobile phase A and 100-0% ultrapure water or glacial acetic acid or a phosphoric acid solution as a mobile phase B. A flow rate is 0.1-2 ml/min, detection wavelength is 203-320 nm, and column temperature is 20-40 DEG C. The method of the invention controls the quality of active components of two medicinal materials in the prescription of the rhizoma alismatis-largehead atractylodes rhizome tablet, and so the quality control of the preparation is more comprehensive, accurate and effective, thereby helpingto ensure the medicine safety and validity. Moreover, the determination method has the advantages of simple operation, accurate result and good precision, stability and reproducibility, is an advancedquality control method and facilitates the standardized production of the medicine.
Owner:TIANJIN INSTITUTE OF PHARMA RESEARCH

Energy-saving and environment-friendly bird repelling device for bighead atractylodes rhizome planting

The invention provides an energy-saving and environment-friendly bird repelling device for atractylodes macrocephala planting. The device comprises a mounting frame, wherein a wind power mechanism is mounted at the top of the mounting frame, a driving assembly matching the wind power mechanism is mounted inside the mounting frame, the driving assembly comprises a vertical shaft, a conical disc and a rotating ring, a transverse shaft is mounted inside the mounting frame and below the conical disc, reflector sets are installed at the end of the transverse shaft, a noise assembly is connected to the bottom of the rotating ring, and a detection assembly is installed on the transverse shaft. The rotating shaft drives the vertical shaft and the rotating ring to rotate in a differential mode through a speed regulating gear set, the conical disc drives a conical sleeve to rotate and deflect up and down, the reflector sets at the two ends of the transverse shaft swing up and down along with rotation of the transverse shaft, then light reflection areas of the reflector sets are enlarged, the reflector sets can horizontally rotate along with a support base, the light bird repelling effect is improved, the transverse shaft moves a pendulum back and forth and hits a noise plate to make noise, a sound bird repelling function is achieved, and the device is simple in structure, low in use cost, capable of saving energy, environmentally friendly and convenient to use.
Owner:佛山市融泽环保科技有限公司

Preparation technology and production method of integrative new dosage form of Rhizoma Atractylodis Macrocephalae and Radix aconiti lateralis preparata decoction

The invention relates to a preparation technology and a production method of an integrative new dosage form of a Rhizoma Atractylodis Macrocephalae and Radix aconiti lateralis preparata decoction. The raw materials for the effective components of the decoction comprise 2 parts by weight of licorice, 4 parts by weight of Rhizoma Atractylodis Macrocephalae and 1.5 parts by weight of Radix aconiti lateralis preparata. The production method comprises the production processes of ultrasonic airflow crushing, alcohol-water extraction, supersonic wave crushing extraction, water decoction and concentration, ultrasonic spray drying, nanometer grinding, high-pressure homogenization, nanoparticle preparation and the like. The advantages comprising multiple cooperation, multiple targeting and the like of a nanometer carrier combination technology are utilized in the invention. Great production cost reduction, great product quality improvement, medicine targeting strengthening, and medicine sustained and controlled release property strengthening are realized after the large-scale production. Internal and external administration can be simultaneously carried out, and the decoction can be respectively administrated in four time periods according to the midnight-noon ebb-flow and human qi and blood flow rules. The decoction can also be processed to prepare a film agent and a transdermal agent which are respectively plastered on different positions of a human body according to the midnight-noon ebb-flow and human qi and blood flow rules, and the effective components can be directly absorbed through skins.
Owner:SUZHOU ZHIWEITANG BIOLOGICAL TECH +1

Detection method for atractylodes macrocephala koidz medicinal materials

InactiveCN102680631BTrue reflection of qualityEffective quality controlComponent separationHplc fingerprintMedicine
The invention discloses a detection method for atractylodes macrocephala koidz medicinal materials. The method adopts HPLC (high performance liquid chromatography) fingerprint spectrum for detection and includes the operation steps of: (1) preparing sample solution; (2) preparing reference solution; and (3) respectively and precisely absorbing the sample solution and the reference solution to inject into a liquid chromatograph so as to elute by taking an acetonitrile-water system as a flowing phase and detect at wavelengths of 248+ / -5nm. After the atractylodes macrocephala koidz medicinal materials are decocted with water, and then the HPLC fingerprint spectrum is applied for detection, so that quality of the atractylodes macrocephala koidz medicinal materials can be reflected more truly. Moreover, chromatographic conditions such as the flowing phase are selected specifically, so that chromatogram baselines are stable and convenient to integrate, resolution of characteristic peaks is good, and similarity among different medicinal materials is high. The detection method for the atractylodes macrocephala koidz medicinal materials can be effectively used for quality control of atractylodes macrocephala koidz and provides a guarantee of medication security of the atractylodes macrocephala koidz medicinal materials.
Owner:CHENGDU UNIV OF TRADITIONAL CHINESE MEDICINE

Method for measuring monosaccharide components of rhizoma atractylodis macrocephala polysaccharide

The invention discloses a method for measuring monosaccharide components of rhizoma atractylodis macrocephala polysaccharide. The method comprises the following steps: (1) preparing a rhizoma atractylodis macrocephala polysaccharide hydrolyzed sample; (2) preparing a mixed monosaccharide standard substance; and (3) pre-column derivatization treatment: separately mixing the rhizoma atractylodis macrocephala polysaccharide hydrolyzed sample obtained from step (1) with 0.5 mol / L of a PMP methanol solution and 0.3 mol / L of a NaOH solution, fully shaking, reacting for 30 minutes under the conditionof water bath at the temperature of 70 DEG C, then cooling to the room temperature, adding 0.3 mol / L of hydrochloric acid and neutralizing, adding chloroform and extracting, centrifuging, removing anorganic layer, repeatedly extracting for 2-3 times to obtain water on the upper layer, and filtering with a microfiltration membrane of which the sizes of pores are 0.22 mu m to obtain a rhizoma atractylodis macrocephala polysaccharide derivatization treatment solution and a mixed monosaccharide derivatization treatment solution for subsequent use; and (4) efficient liquid chromatography analysis: determining the monosaccharide components and content of the rhizoma atractylodis macrocephala polysaccharide. The method is high in sensitivity, small in use amount of sample and good in stability;operation is simple; and the monosaccharide components in the rhizoma atractylodis macrocephala polysaccharide are detected at low cost.
Owner:FOSHAN UNIVERSITY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products