CN1857706A - Red flavonid and production process of its medicine composition - Google Patents

Red flavonid and production process of its medicine composition Download PDF

Info

Publication number
CN1857706A
CN1857706A CN 200610066025 CN200610066025A CN1857706A CN 1857706 A CN1857706 A CN 1857706A CN 200610066025 CN200610066025 CN 200610066025 CN 200610066025 A CN200610066025 A CN 200610066025A CN 1857706 A CN1857706 A CN 1857706A
Authority
CN
China
Prior art keywords
parts
medicine
herba
duchesneae indicae
water
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN 200610066025
Other languages
Chinese (zh)
Inventor
王跃仁
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
PINGSHAN PHARMACEUTICAL CO Ltd FUZHOU
Original Assignee
PINGSHAN PHARMACEUTICAL CO Ltd FUZHOU
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by PINGSHAN PHARMACEUTICAL CO Ltd FUZHOU filed Critical PINGSHAN PHARMACEUTICAL CO Ltd FUZHOU
Priority to CN 200610066025 priority Critical patent/CN1857706A/en
Publication of CN1857706A publication Critical patent/CN1857706A/en
Pending legal-status Critical Current

Links

Abstract

The present invention relates to the production process of effective Chinese medicine component, and is especially production process of tassel flower herb flavones. The present invention also relates to the production process of one medicine with function of clearing away heat and toxic material, and the medicine may be used in treating common cold, influenza, parotitis, laryngopharyngitis and other diseases. The present invention has simple preparation process, excellent preparation stability, extracts liquid as adhesive and excellent technological result.

Description

Red flavonid and process for producing medicine composition thereof
Technical field
The present invention relates to a kind of Chinese medicine production process of effective component, specifically, relate to the production method of Chinese medicine red flavonid class (Flavones) chemical constituent.The invention still further relates to a kind of medicine production method with antipyretic and antidote functions, described medicine can be used for treating diseases such as flu, influenza, parotitis, pharyngolaryngitis, tonsillitis or tracheitis.The invention belongs to field of medicaments.
Background technology
The feverfew Herba Duchesneae Indicae, it is a kind of plant amedica of a kind of treatment inflammation commonly used, mosquito bite, conjunctivitis, rheumatism, wound etc., contain Pyrrolizidine Alkaloid and flavone compound, and flavone compound is the active component of its antiinflammatory and antioxidation.
Herba Duchesneae Indicae Flavonoid substances content is higher, and Flavonoid substances is the stronger chemical compound of a class physiologically active.Herba Duchesneae Indicae has good heat-clearing and toxic substances removing and antiinflammatory pharmacological action.But the process study of Herba Duchesneae Indicae active component report is less.To the process study of the compound medicine of Herba Duchesneae Indicae also seldom.
Summary of the invention
For development and utilization Chinese medicine Herba Duchesneae Indicae effectively, the invention provides production method and the pharmaceutical composition and the medical applications of Herba Duchesneae Indicae Flavonoid substances.
For this reason, one of purpose of the present invention provides a kind of production method of red flavonid extract.
Two of purpose of the present invention provides a kind of Chinese medicine composition and production method and medical usage that contains Herba Duchesneae Indicae
For realizing purpose of the present invention, the present invention adopts following technical scheme:
A kind of method of extracting red flavonid is characterized in that comprising the step of water as the solvent extraction Herba Duchesneae Indicae.
Wherein, described extraction can be the Chinese medicine extraction method of routine, for example soaks extraction, decocts extraction or diafiltration extraction etc., and the present invention preferably adopts water boiling and extraction.
The present invention also provides a kind of Herba Duchesneae Indicae and other raw material of Chinese medicine are mixed to extract, and calculates 1000 parts of Herba Duchesneae Indicae by weight that is:, 750 parts of Herba Solidaginiss, 63 parts in Rhizoma Zingiberis Recens, 625 parts of Radix Isatidis, mixed back water extracts as solvent, and extracting solution is concentrated into clear paste.
As one of specific embodiments, the invention provides a kind of medicine production method with antipyretic and antidote functions, wherein said medicine calculates by weight, comprise following principal agent composition: 1000 parts of Herba Duchesneae Indicae, 750 parts of Herba Solidaginiss, 63 parts in Rhizoma Zingiberis Recens, 625 parts of Radix Isatidis, 375 parts in Radix Glycyrrhizae, described method comprises the steps:
(1) the mixed back of Herba Duchesneae Indicae, Herba Solidaginis and Rhizoma Zingiberis Recens water is extracted as solvent, extracting solution is condensed into clear paste;
(2) the Radix Isatidis water is extracted as solvent, extracting solution is concentrated in right amount, adds ethanol and precipitates in right amount, leaves standstill after-filtration, is condensed into clear paste behind the filtrate recycling ethanol;
(3) step (1) and the resulting clear paste of step (2) are merged, be condensed into thick paste;
(4) Radix Glycyrrhizae powder is broken into fine powder, and, makes granule Radix Glycyrrhizae fine powder and proper amount of diluting and the resulting thick paste mixing of step (3).
Term of the present invention " clear paste ", " thick paste ", except that special instruction is arranged, promptly refer to Chinese medicine extraction concentrate in term " clear paste " commonly used, " thick paste ".
Above-mentioned ethanol precipitation concentration, the alcohol amount that contains of solution can be 50%~80%, is preferably 60%~70%.
Method of the present invention, during wherein step (4) was granulated, with the water of described thick paste adding 1~2 times (weight), stirring made abundant dissolving as binding agent, makes granule with described binding agent behind Radix Glycyrrhizae fine powder and the diluent mixing.
Can adopt granulating process conventional on the preparation to granulate.As preferred version, granulation of the present invention is after Radix Glycyrrhizae fine powder and diluent are placed airpillow-dry granulator mixing, to granulate as hydrojet with above-mentioned described binding agent.
Above-mentioned resulting granules can further be made suitable preparation.For example,,, mix, carry out tabletting and make tablet with proper amount of lubricating agent with above-mentioned resulting granules as one of preferred version of the present invention.
Diluent of the present invention, it can be pharmaceutically conventional diluent components, for example include but not limited to mannitol (granular or powdery), xylitol, sorbitol, maltose, microcrystalline Cellulose, PROSOLV  SMCC, polymerization sugar (EMDEX ), glucose, lactose, sucrose, dextrin and starch etc., can use separately, also can applied in any combination.
Lubricant of the present invention, it can be pharmaceutically conventional lubricant composition, for example include but not limited to magnesium stearate, calcium stearate, zinc stearate, glyceryl monostearate, Polyethylene Glycol, hydrogenated vegetable oil, sodium stearyl fumarate, polyoxyethylene monostearate, single Laurel sucrose acid ester, sodium laurylsulfate, magnesium laurylsulfate, Stepanol MG and Pulvis Talci etc., can use use also capable of being combined separately.
The medicine that above-mentioned described method prepares has the effect of heat-clearing and toxic substances removing, inflammation-diminishing and cough-controlling, can be used as heat-clearing and toxic substances removing or inflammation-diminishing and cough-controlling medicine, is used for treating diseases such as flu, influenza, parotitis, pharyngolaryngitis, tonsillitis or tracheitis.
The present invention is by the Chinese medicine extraction isolation technics and the Chinese medicine preparation technology of uses advanced, make the modern medicines preparation with what be used for heat-clearing and toxic substances removing and inflammation-diminishing and cough-controlling clinically through proved recipe, kept former composition and the effect that experience side's decoction is arranged, remove crudely and store essence, the pharmaceutical preparation that makes is conveniently taken, preparation stabilization meets medication requirement clinically.And extraction process of the present invention and preparation process are simple, and the technology cost is low, and process stabilizing is suitable for suitability for industrialized production, in the production method particularly of the present invention, find the binding agent that the employing Chinese medicine extract is used as preparation, have obtained beyond thought effect.
The specific embodiment
Following specific embodiment just in order to explain or illustrate the present invention, should not be understood that protection domain of the present invention is construed as limiting.
Embodiment 1
Herba Duchesneae Indicae 540 grams add water an amount of (about 980 grams), and about 1.5 hours of heated and boiled leaches medicinal liquid, and it is an amount of that medicinal residues add water again, and about 1.5 hours of heated and boiled merges filtrate twice, is concentrated into clear paste (relative density was 1.10~1.15 when 50 ℃ of heat were surveyed).
It is an amount of to get above-mentioned clear paste, is dissolved in water, and adds the hydrolysis of dilute sulfuric acid reflux again, puts cold back and uses ethyl acetate extraction, and as test sample, other gets the Quercetin reference substance, after testing, contains the main component of flavonoid in the above-mentioned gained clear paste.
Embodiment 2
10 kilograms of Herba Duchesneae Indicae, 7.5 kilograms of Herba Solidaginiss, 0.63 kilogram in Rhizoma Zingiberis Recens, 6.25 kilograms of Radix Isatidis are got Herba Duchesneae Indicae, Herba Solidaginis and Rhizoma Zingiberis Recens and are placed extractor, decoct with water secondary, and each 1.5 hours, collecting decoction left standstill, and got supernatant concentration and became clear paste.Other gets Radix Isatidis, decocts with water secondary, and each 1.5 hours, collecting decoction filtered, and filtrate is condensed into clear paste (relative density was 1.10~1.15 when 50 ℃ of heat were surveyed), adds ethanol and makes and contain the alcohol amount and reach 60%, and standing over night filters, and is condensed into clear paste behind the filtrate recycling ethanol.Above-mentioned gained clear paste is merged, be condensed into thick paste (relative density was 1.30~1.40 when 80 ℃ of heat were surveyed).
Embodiment 3
With the thick paste of embodiment 2 gained, according to cream: purified water=1: 1.1 (weight ratio) concentration ratio heated and stirred, make abundant dissolving, cross 80 mesh sieves, as binding agent.
Extracting liquorice is 3.75 kilograms in addition, and porphyrize becomes fine powder, crosses 100 mesh sieves.Get 0.45 kilogram in dextrin more in addition.Radix Glycyrrhizae fine powder and dextrin are dropped in the granulator, after fully mixing, are that hydrojet is carried out one-step palletizing and drying was taken out after 30 minutes with the above-mentioned binding agent that makes, and after determination of water is qualified (water content 3-7%), obtain dried granule.
According to doing 5/1000ths of particle weight, add magnesium stearate, behind the mixing, carry out tabletting, make 10000.
Prescription of the present invention is formed, and belongs to clinical experience side, determined curative effect, stable.Preparation process of the present invention is simple, and preparation stability is good, adopts extracting solution as the preparation binding agent, and technology has beyond thought technique effect.
The present invention is described according to preferred embodiment.Should be understood that the description of front and embodiment are just to illustrating the present invention.Under prerequisite without departing from the spirit and scope of the present invention, those skilled in the art can design multiple alternative of the present invention and improvement project, and it all should be understood to be within protection scope of the present invention.

Claims (10)

1, the extracting method of red flavonid is characterized in that comprising the step of water as the solvent extraction Herba Duchesneae Indicae.
2, method according to claim 1, it is characterized in that Herba Duchesneae Indicae is mixed in other medicines and extract, that is: calculate by weight, 1000 parts of Herba Duchesneae Indicae, 750 parts of Herba Solidaginiss, 63 parts in Rhizoma Zingiberis Recens, 625 parts of Radix Isatidis, mixed back water extracts as solvent, and extracting solution is concentrated into clear paste.
3, a kind of medicine production method with antipyretic and antidote functions, wherein said medicine calculates by weight, comprises following principal agent composition: 1000 parts of Herba Duchesneae Indicae, 750 parts of Herba Solidaginiss, 63 parts in Rhizoma Zingiberis Recens, 625 parts of Radix Isatidis, 375 parts in Radix Glycyrrhizae, it comprises the steps:
(1) the mixed back of Herba Duchesneae Indicae, Herba Solidaginis and Rhizoma Zingiberis Recens water is extracted as solvent, extracting solution is condensed into clear paste;
(2) the Radix Isatidis water is extracted as solvent, extracting solution is concentrated in right amount, adds ethanol and precipitates in right amount, leaves standstill after-filtration, is condensed into clear paste behind the filtrate recycling ethanol;
(3) step (1) and the resulting clear paste of step (2) are merged, be condensed into thick paste;
(4) Radix Glycyrrhizae powder is broken into fine powder, and, makes granule Radix Glycyrrhizae fine powder and proper amount of diluting and the resulting thick paste mixing of step (3).
4, the described method of claim 3, wherein in the step (4), with the water of described thick paste adding 1~2 times (weight), stirring makes abundant dissolving as binding agent, makes granule with described binding agent behind Radix Glycyrrhizae fine powder and the diluent mixing.
5, the described method of claim 4, wherein Radix Glycyrrhizae fine powder and diluent are placed airpillow-dry granulator mixing after, granulate as hydrojet with described binding agent.
6, the described method of claim 3-5 also comprises the step of mixing tablet forming behind the particle drying that will make with proper amount of lubricating agent.
7, method according to claim 6, wherein said diluent are dextrin, and described lubricant is a magnesium stearate.
8, a kind of medicine is characterized in that being prepared by the described method of claim 3-7.
9, the described medicine of claim 8 is used to prepare the purposes of heat-clearing and toxic substances removing medicine or inflammation-diminishing and cough-controlling medicine.
10, the described medicine of claim 8 is used to prepare the purposes of disease medicaments such as treatment flu, influenza, parotitis, pharyngolaryngitis, tonsillitis or tracheitis.
CN 200610066025 2006-03-27 2006-03-27 Red flavonid and production process of its medicine composition Pending CN1857706A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200610066025 CN1857706A (en) 2006-03-27 2006-03-27 Red flavonid and production process of its medicine composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200610066025 CN1857706A (en) 2006-03-27 2006-03-27 Red flavonid and production process of its medicine composition

Publications (1)

Publication Number Publication Date
CN1857706A true CN1857706A (en) 2006-11-08

Family

ID=37296694

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 200610066025 Pending CN1857706A (en) 2006-03-27 2006-03-27 Red flavonid and production process of its medicine composition

Country Status (1)

Country Link
CN (1) CN1857706A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101019943B (en) * 2007-03-19 2010-06-30 沈信堂 Tonsillitis treating Chinese medicine
CN102798673A (en) * 2012-07-17 2012-11-28 广西大学 Method for identifying emilia sonchifolia medicinal material
CN108739099A (en) * 2018-04-25 2018-11-06 朱定芳 A kind of implantation methods improving tassel flower yield

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101019943B (en) * 2007-03-19 2010-06-30 沈信堂 Tonsillitis treating Chinese medicine
CN102798673A (en) * 2012-07-17 2012-11-28 广西大学 Method for identifying emilia sonchifolia medicinal material
CN108739099A (en) * 2018-04-25 2018-11-06 朱定芳 A kind of implantation methods improving tassel flower yield

Similar Documents

Publication Publication Date Title
CN102430090B (en) Traditional Tibetan medicine Ruyizhenbao composite preparation and preparation method thereof
CN1723981A (en) Novel use of extractive of Momordica grosvenori as adjuvant drug for preparing medicine
Hossain et al. Hypolipidemic and hepatoprotective effects of different fractions of methanolic extract of Momordica charantia (Linn.) in alloxan induced diabetic rats
CN101538296B (en) Active ingredients of camptosorus sibiricus, and extraction method and use of same
CN101040950A (en) Method of preparing Ynxingchao dropping pills compound
CN1857706A (en) Red flavonid and production process of its medicine composition
CN1927293A (en) Chinese medicine composition for treating skin burn and scald
CN1768772A (en) Compound formulation of breviscapine for treating cardiovascular and cerebrovascular diseases. its preparing process and application
CN1850142A (en) Method for preparing honeysuckle formula granules
CN101214252B (en) Antiviral antibacterial medicinal composition and preparation thereof
CN1823959A (en) Heart vessel free flowing dispersion tablet and its preparation method
JP2021512997A (en) Separated windproof polysaccharides and their uses
CN1070226C (en) Gallnut oil and its extraction process and application in pharmacy
CN1298705A (en) Chinese medicine for treating hepatitis B and its preparing process
CN1314434C (en) Heat-clearing and detoxic medicine and its preparation method
CN1280010A (en) Oral medicine for curing diabetes and its producing method
CN1644203A (en) Oral preparation of red common stone crop polysaccharide and its making method
JP2021512998A (en) Isolated white chili polysaccharide and its uses
CN1475222A (en) Vine leaf extract and its preparation process
CN115364179B (en) Traditional Chinese medicine composition for reducing blood uric acid as well as preparation method and application thereof
CN1456236A (en) Preparation of woman effervescent tablets
CN1824176A (en) Chinese medicinal preparation for anti inflammation and heat resolution and its preparation method
CN1490014A (en) Mangiferin preparation and production thereof
CN100337671C (en) Chinese traditional medicine for treating thrombocytopenia
CN1123683A (en) Series products of radix notoginseng and cortex eucommiae and their productions

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication