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43 results about "Palmatine hydrochloride" patented technology

Palmatine hydrochloride is a hydrochloride salt of palmatine which is a protoberberine alkaloid, it can induce remarkable cell apoptosis, has potential in photodynamic therapy on colon adenocarcinoma.

Total alkaloids extraction of corydalis, its preparation method, medicine composition containing the total alkaloids extraction and application thereof

InactiveCN101054377AEfficient preparation methodIn line with the proportion of natural occurrencePowder deliveryAlkaloids chemistryHarmineFreeze-drying
The present invention discloses a Rhizoma Corydalis Decumbentis total alkaloids extract, its preparation method, pharmaceutical composition containing same. The total alkaloids mainly comprise : macleyine, tetrahydropalmatine, bicucalline, palmatine hydrochloride, 'xiawuning' alkaloid, corydaline harmine, other alkaloid and extract. The preparation method is : using Rhizoma Corydalis Decumbentis as material, adding right amount of polar solvent for leaching, merging the leachate, carrying out large pore adsorption resin chromatography, eluting impurity with diluted acid and alkaline aqueous solution orderly, eluting using polar organic solvent, collecting elution liquor, eliminating impurity further by alumina column adsorption, Collecting after-column liquid, concentrating liquor to obtain the Rhizoma Corydalis Decumbentis total alkaloids extract. The present invention also discloses a pharmaceutical composition containing the total alkaloids extract and uses of the pharmaceutical composition in preparing tablet, capsule, soft capsule, suppository, granula, transdermal absorption agent, drop pills, oral disintegrating agent, slow release agent, freeze-drying powder injection etc.
Owner:SHANGHAI INST OF PHARMA IND

Method for extracting total alkaloid of common fibraurea stems, separate fibriuretinin and jatrorrhizine

The invention provides a total alkaloid of common fibraurea stems, which contains palmatine hydrochloride with the weight percentage content over 60 percent and jatrorrhizine hydrochloride with the weight percentage content more than 10 percent. The invention also provides a method for preparing the total alkaloid of common fibraurea stems, fibriuretinin and jatrorrhizine. The method can be adopted to prepare the total alkaloid of common fibraurea stems and to extract separate fibriuretinin and jatrorrhizine, wherein if dry products are calculated on the basis of anhydrous palmatine hydrochloride (C21H22O4N.HCl), the fibriuretinin has the weight percentage content higher than 98.0 percent and is high in purity. The extraction-separation method enables the transfer rate of the palmatine hydrochloride to be up to over 26 percent and is 1.7 times higher than the prior conventional process (about 15 percent). The extraction process also maintains the jatrorrhizine while raising the transfer rate of the palmatine hydrochloride serving as a main component of the fibriuretinin, thereby greatly improving the resource utilization rate of medicinal materials. The process adopts a resin purification method, is simple and feasible in process flow, capable of regenerating and repeatedly utilizing resin and reducing environmental pollution caused by lye compared with the conventional salting-out method.
Owner:CHENGDU UNIV OF TRADITIONAL CHINESE MEDICINE

Total alkaloid of stephania delavayi and preparation and application thereof

The invention discloses a total alkaloid of Stephania delavayi Diels, the content of which is measured by tetrahydropalmatine. Tetrahydropalmatine occupies 55-95 percent of the total alkaloid extract of Stephania delavayi Diels, wherein the weight percentage of tetrahydropalmatine contained is no less than 2 percent, while the weight percentage of palmatine hydrochloride contained is no less than 0.8 percent. The invention also discloses a preparation method of the total alkaloid of Stephania delavayi Diels, which relates to the steps as follows: adding the Stephania delavayi Diels meal into ethanol for diacolation or reflux to acquire alcohol extract, decompressing and recycling the ethanol and concentrating into a condensed ointment for dissolving and filtrating with acid to acquire a filtrate, passing the filtrate through a macroporous resin column or a strong acid cation exchange resin column for adsorption, washing with water to remove the impurities and extracting with a eluent, collecting the eluent and decompressing and recycling the extract and then concentrating and drying, thus acquiring the total alkaloid of Stephania delavayi Diels; the steps can also be decompressing a percolating liquid to recycle the ethanol, concentrating, dissolving with acid and then filtrating, adjusting the pH value of the filtrate with weak base to produce deposition, filtrating the deposition to acquire a filter residue, adding ethanol into the filter residue to resolve and decompress, recycle the ethanol and then drying, thus acquiring the total alkaloid. The results of a pharmacological study on the acquired total alkaloid show that the total alkaloid of Stephania delavayi Diels has good effect on spasmolysis, pain relieving, antiphlogosis and antibiosis, blood activating and so on, and can combine with the acceptable components in pharmacy to prepare various sustained release or controlled release formulation or other formulations.
Owner:GUANGZHOU BOJI MEDICINE SERVICES

Microbial secondary metabolite palmatine hydrochloride and application thereof

The invention relates to a microbial secondary metabolite palmatine hydrochloride and application thereof and belongs to the technical field of biological pesticides. The secondary metabolite is prepared by the following steps: (a), producing a strain of L.antibioticus YFY02 with the collection number of CGMCC NO.2403; (b) culturing the strain YFY02 for two days by utilizing a KB culture medium, performing enlarged culture by adopting a conventional fermentation method, extracting the fermentation liquor by using ethyl acetate, and performing rotary evaporation, thereby obtaining a crude metabolite extract; (c) by utilizing liquid chromatography, Sephadex LH-20 gel column chromatography, mass spectrometry, nuclear magnetic resonance and other spectroscopic techniques, and separating, purifying and identifying the crude extract of the secondary metabolite; and (d) identifying to obtain the effective secondary metabolite palmatine hydrochloride. The invention also discloses application of the microbial secondary metabolite palmatine hydrochloride in the preparation of agents for preventing and controlling bacterial blight of rice, bacterial leaf streak and plasmodiophora brassicae woronin. The microbial secondary metabolite disclosed by the invention has the advantages of environment friendliness, low cost and excellent effects of preventing and controlling the rice bacterial diseases and plasmodiophora brassicae woronin.
Owner:YUNNAN AGRICULTURAL UNIVERSITY

Detection method for drug capable of treating fever in children

The invention discloses a detection method for a drug capable of treating fever in children. The detection method comprises the following steps of 1) weighing a palmatine hydrochloride reference substance, a berberine hydrochloride reference substance, a liquiritin reference substance and an ammonium glycyrrhetate reference substance, preparing a mixed solution of the reference substances with an alcohol solvent, smashing Linghuang Bao'er pills, mixing the smashed Linghuang Bao'er pills with the alcohol aqueous solution to obtain a test sample solution; 2) measuring the mixed solution of the reference substances with different concentrations, detecting through HPLC to obtain the peak area respectively, making a standard curve to obtain the standard curve of the mixed solution of the reference substances; and 3) detecting the test sample solution through HPLC to obtain the peak area of the test sample solution, and comparing with the standard curve to obtain the content of palmatine hydrochloride, berberine hydrochloride, liquiritin and ammonium glycyrrhetate in the test sample solution. The detection method overcomes one-sidedness that the quality of a drug is determined only by measuring one component, is comprehensive and reliable, and has the advantages of high accuracy, high precision, stability, and relatively good repeatability.
Owner:GUANGZHOU BAIYUNSHAN JINGXIUTANG PHARM CO LTD

Establishment method for variable-wavelength fingerprint spectrum of Chinese pulsatilla root decoction granules and standard fingerprint spectrum thereof

The invention discloses an establishment method for a variable-wavelength fingerprint spectrum of Chinese pulsatilla root decoction granules. The method comprises the following steps of (1) preparing reference substance solutions: preparing reference substance solutions of berberine hydrochloride, palmatine hydrochloride, coptisine, jatrorrhizine hydrochloride, aesculin, aesculetin and pulchinenoside anemoside B4 respectively; (2) preparing a test sample solution: weighing the Chinese pulsatilla root decoction granules, extracting the Chinese pulsatilla root decoction granules and filtering an extracted solution by using a microporous membrane to obtain the test sample solution; (3) obtaining the fingerprint spectrum by determining with high performance liquid chromatography, wherein chromatographic conditions are as follows: octadecylsilane chemically bonded silica is used as a filler by a chromatographic column; gradient elution is adopted; variable wavelengths are detected by ultraviolet light wavelengths; and (4) evaluating similarity: evaluating the fingerprint spectrum of the test sample by "Similarity Evaluation System for Chromatographic Fingerprint of Traditional Chinese medicine (Edition 2004A)". The method is simple, stable, high in precision and good in repeatability, and can identify the authenticity and merits of products accurately.
Owner:DIHON PHARMA GROUP +1

Quality control method of powerful dysentery relieving soluble powder preparation

InactiveCN106841499AOptimize the effect of identificationEnsure controllabilityComponent separationBerberine hydrochlorideControllability
The invention provides a quality control method of a powerful dysentery relieving soluble powder preparation, and belongs to the field of the detection of medicines. The quality control method comprises the following steps of a first step, preparing the preparation; a second step, using berberine hydrochloride and palmatine hydrochloride as reference substances, and identifying whether ten great meritorious components are contained in powerful dysentery relieving soluble powder or not by thin layer chromatography; a third step, using cortex ilicis rotundae as a reference medicinal material and syringoside as a reference substance, and identifying whether a component of the cortex ilicis rotundae is contained in the powerful dysentery relieving soluble powder or not by the thin layer chromatography; a fourth step, using matrine and sophoridine as reference substances, and identifying whether a component of radix sophorae flavescentis is contained in the powerful dysentery relieving soluble powder or not by the thin layer chromatography; a fifth step, using the syringoside as the reference substance, and measuring the content of the cortex ilicis rotundae in a powerful dysentery relieving soluble powder formula by high performance liquid chromatography. The quality control method has the beneficial effects that an established quality standard control method has characteristics of high accuracy, good repeatability and the like. Meanwhile, the controllability of a quality standard of a preparation can be guaranteed; the inner quality and the curative effect of a product are guaranteed; the quality control method has guidance significance for clinical medication.
Owner:QINGDAO BAIHUIZHIYE BIOTECH

Total alkaloid of stephania delavayi and preparation and application thereof

The invention discloses a total alkaloid of Stephania delavayi Diels, the content of which is measured by tetrahydropalmatine. Tetrahydropalmatine occupies 55-95 percent of the total alkaloid extract of Stephania delavayi Diels, wherein the weight percentage of tetrahydropalmatine contained is no less than 2 percent, while the weight percentage of palmatine hydrochloride contained is no less than0.8 percent. The invention also discloses a preparation method of the total alkaloid of Stephania delavayi Diels, which relates to the steps as follows: adding the Stephania delavayi Diels meal into ethanol for diacolation or reflux to acquire alcohol extract, decompressing and recycling the ethanol and concentrating into a condensed ointment for dissolving and filtrating with acid to acquire a filtrate, passing the filtrate through a macroporous resin column or a strong acid cation exchange resin column for adsorption, washing with water to remove the impurities and extracting with an eluent, collecting the eluent and decompressing and recycling the extract and then concentrating and drying, thus acquiring the total alkaloid of Stephania delavayi Diels; the steps can also be decompressing a percolating liquid to recycle the ethanol, concentrating, dissolving with acid and then filtrating, adjusting the pH value of the filtrate with weak base to produce deposition, filtrating the deposition to acquire a filter residue, adding ethanol into the filter residue to resolve and decompress, recycle the ethanol and then drying, thus acquiring the total alkaloid. The results of a pharmacological study on the acquired total alkaloid show that the total alkaloid of Stephania delavayi Diels has good effect on spasmolysis, pain relieving, antiphlogosis and antibiosis, blood activating and so on, and can combine with the acceptable components in pharmacy to prepare various sustained release or controlled release formulation or other formulations.
Owner:GUANGZHOU BOJI MEDICINE SERVICES

Pharmaceutical formulation for treating gastric ulcer and preparation method of pharmaceutical formulation

The invention discloses a pharmaceutical formulation for treating gastric ulcer and a preparation method of the pharmaceutical formulation. The pharmaceutical formulation comprises main materials of 4 parts of radix tinosporae and 1 part of Chinese olive, and comprises agents of ethanol, methanol, a standard substance of palmatine hydrochloride, and a standard substance of gallic acid. The preparation method comprises: extraction of active ingredients of radix tinosporae and Chinese olive, measurement of the content of the active ingredients of radix tinosporae and Chinese olive, preparation of a solution of a reference substance, exploration of a linear relation, and preparation of a test solution. In comparison with a medicine for treating related diseases in the prior art, the pharmaceutical formulation is relatively pure, is accurate in curative effect and short in course of treatment, and has no toxic or side effect. In comparison with the prior art, the preparation method takes 70% of ethanol as an extraction solvent, has no toxic effect on the body, is low in cost, and is suitable for industrial mass production. The main anti-ulcer component of palmatine hydrochloride in radix tinosporae is subjected to optimization of an extraction process and quantitative analysis through high performance liquid chromatography. The pharmaceutical formulation and the preparation method provide a theoretical reference for promoting development and utilization of radix tinosporae, and have promotion and application value.
Owner:SICHUAN AGRI UNIV
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