CN102294003A - Preparation method of ease pill - Google Patents

Preparation method of ease pill Download PDF

Info

Publication number
CN102294003A
CN102294003A CN 201110247776 CN201110247776A CN102294003A CN 102294003 A CN102294003 A CN 102294003A CN 201110247776 CN201110247776 CN 201110247776 CN 201110247776 A CN201110247776 A CN 201110247776A CN 102294003 A CN102294003 A CN 102294003A
Authority
CN
China
Prior art keywords
gained
filter pressing
pressing
membrane filter
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.)
Granted
Application number
CN 201110247776
Other languages
Chinese (zh)
Other versions
CN102294003B (en
Inventor
冯天炯
胡黎明
顾维菊
程地英
刘小均
余佳文
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.)
TAIJI GROUP CHONGQING FULING PHARMACEUTICAL FACTORY CO Ltd
Original Assignee
TAIJI GROUP CHONGQING FULING PHARMACEUTICAL FACTORY CO Ltd
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 TAIJI GROUP CHONGQING FULING PHARMACEUTICAL FACTORY CO Ltd filed Critical TAIJI GROUP CHONGQING FULING PHARMACEUTICAL FACTORY CO Ltd
Priority to CN 201110247776 priority Critical patent/CN102294003B/en
Publication of CN102294003A publication Critical patent/CN102294003A/en
Application granted granted Critical
Publication of CN102294003B publication Critical patent/CN102294003B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Medicines Containing Plant Substances (AREA)

Abstract

The invention discloses a preparation method of an ease pill (condensed pill). According to the preparation method disclosed by the invention, effective components in medicinal materials in a prescription are extracted by adopting a diaphragm filter press circulation, extraction and separation integrated technology, thus the process flow can be simplified, the production period is greatly shortened, the energy consumption is reduced, environmental protection and utilization of waste residue are facilitated, and the recovery rate of the effective components can be greatly improved.

Description

The preparation method of ease pill
Technical field
The invention belongs to pharmaceutical field, relate to a kind of preparation method of Chinese medicine preparation.
Background technology
The Sanitation Ministry medicine standard WS3-B-2220-96 record: ease pill (concentrated pill) has soothing liver and strengthening spleen, the effect of nourishing blood for regulating menstruation, be used for that gloomy due to the stagnation of liver-QI with deficiency of the spleen do not relax, distending pain in the chest and hypochondrium, have a dizzy spell, loss of appetite, menoxenia.Its prescription is Radix Bupleuri 100g, Radix Angelicae Sinensis 100g, Radix Paeoniae Alba 100g, Rhizoma Atractylodis Macrocephalae (parched) 100g, Poria 100g, Herba Menthae 20g, Rhizoma Zingiberis Recens 100g, Radix Glycyrrhizae Preparata 80g.Its preparation method is that Radix Bupleuri, Radix Angelicae Sinensis 50g, Herba Menthae, Rhizoma Zingiberis Recens are extracted volatile oil; The medicinal residues and the Rhizoma Atractylodis Macrocephalae, Poria decoct with water secondary, and each 2 hours, collecting decoction filtered, and filtrate is condensed into the thick paste that relative density is 1.35-1.40; The Radix Paeoniae Alba and residue Radix Angelicae Sinensis powder are broken into fine powder; The about 20g of extracting liquorice is ground into fine powder, and the residue Radix Glycyrrhizae is made extractum; With above-mentioned cream, powder and volatile oil and an amount of mixing of maltose, pill, drying, polishing, promptly.Adopt decocting method to extract the effective ingredient of medical material in the said method, exist extraction time long, extract that temperature height, energy consumption height, thermal sensitivity composition easily lose, shortcomings such as the effective ingredient response rate is low, post processing trouble.
Summary of the invention
In view of this; the object of the present invention is to provide a kind of method of utilizing membrane filter pressing circulation extraction separation integrated technique to prepare ease pill (concentrated pill); not only can simplify technological process; significantly shorten the production cycle; energy efficient; be beneficial to environmental conservation and waste residue utilization, and can greatly improve the response rate of effective ingredient.
For achieving the above object, the invention provides following technical scheme:
The preparation method of ease pill, make by following raw materials by weight proportions: 80 parts of 100 parts of Radix Bupleuri, 100 parts of Radix Angelicae Sinensis, 100 parts of the Radix Paeoniae Albas, 100 parts of Rhizoma Atractylodis Macrocephalae (parched)s, 100 parts in Poria, 20 parts of Herba Menthaes, 100 parts in Rhizoma Zingiberis Recens and Radix Glycyrrhizae Preparatas, preparation method may further comprise the steps:
A. the extraction of Radix Bupleuri, Herba Menthae, Rhizoma Zingiberis Recens and Radix Angelicae Sinensis
A1. the Radix Angelicae Sinensis with Radix Bupleuri, Herba Menthae, Rhizoma Zingiberis Recens and proportional quantity 1/2nd mixes, and is ground into coarse powder, and is standby;
A2. the medicated powder with step a1 gained extracts volatile oil with steam distillation, and the aqueous solution after medicinal residues and the distillation is standby;
A3. in the medicinal residues of step a2 gained, add water, be heated with stirring to 60-90 ℃, slip is pumped into diaphragm filter press carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, will be preheated to 60-90 ℃ water again and pump into diaphragm filter press and carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, start the squeezing program of diaphragm filter press, collect pressed liquor; Aqueous solution after the distillation of twice pressing filtering liquid, pressed liquor and step a2 gained is merged, be designated as extracting solution A;
B. the extraction of the Rhizoma Atractylodis Macrocephalae, Poria and Radix Glycyrrhizae
B1. the Radix Glycyrrhizae with the Rhizoma Atractylodis Macrocephalae, Poria and proportional quantity 3/4ths mixes, and is ground into coarse powder, and is standby;
B2. the extracting solution A and the water that add step a3 gained in material-compound tank are heated to 50-90 ℃ and insulation; Three-way valve is switched to the material-compound tank position, water in the material-compound tank is pumped into diaphragm filter press, when pressing filtering liquid passes back into material-compound tank, the medicated powder that under stirring condition, in material-compound tank, adds step b1 gained, finish, under 50-90 ℃ condition, carry out the membrane filter pressing circulation first time and extract, afterwards three-way valve is switched to the filtrate tank position and carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, again three-way valve is switched to the material-compound tank position, in material-compound tank, add entry, under 50-90 ℃ condition, carry out the membrane filter pressing circulation second time and extract, afterwards three-way valve is switched to the filtrate tank position and carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, start the squeezing program of diaphragm filter press, collect pressed liquor; Merge twice pressing filtering liquid and pressed liquor, be designated as extracting solution B;
C. preparation
C1. the Radix Angelicae Sinensis of the Radix Paeoniae Alba, proportional quantity 1/2nd and the Radix Glycyrrhizae of proportional quantity 1/4th are mixed, be ground into fine powder, standby;
C2. the extracting solution with step b2 gained is condensed into the thick paste that relative density is 1.35-1.40, and is standby;
C3. with the thick paste of step c2 gained, the medicated powder of step c1 gained, the volatile oil and the maltose mixing of step a2 gained, pill, drying, polishing promptly gets ease pill.
Preferably, described step a3 adds earlier to be equivalent to step a1 gained medicated powder weight 2-4 water doubly in medicinal residues, is heated with stirring to 75-85 ℃, insulated and stirred 5-15 minute, with slip pump into diaphragm filter press carry out the membrane filter pressing To be equivalent to step a1 gained medicated powder weight 1-3 75-85 ℃ the water of being preheated to doubly again and pump into diaphragm filter press, with slip pump into diaphragm filter press carry out the membrane filter pressing
Described step b2 adds earlier the extracting solution A of step a3 gained and adds 6-9 that the water ad pond om is equivalent to step b1 gained medicated powder weight doubly, carries out membrane filter pressing circulation extraction first time under 55-65 ℃ condition, and extraction time is 30-50 minute; Add and be equivalent to step b1 gained medicated powder weight 3-5 water doubly, carry out the membrane filter pressing circulation second time and extract under 55-65 ℃ condition, extraction time is 10-30 minute.
Preferred, described step a3 adds earlier the water that is equivalent to 3 times of step a1 gained medicated powder weight in medicinal residues, be heated with stirring to 80 ℃, insulated and stirred 10 minutes, with slip pump into diaphragm filter press carry out the membrane filter pressing To be equivalent to again 2 times of step a1 gained medicated powder weight be preheated to 80 ℃ water pump into diaphragm filter press carry out the membrane filter pressing
Described step b2 adds earlier the extracting solution A of step a3 gained and adds the water ad pond om to be equivalent to 7.5 times of step b1 gained medicated powder weight, carries out membrane filter pressing circulation extraction first time under 65 ℃ condition, and extraction time is 40 minutes; Add the water that is equivalent to 3.5 times of step b1 gained medicated powder weight again, carry out the membrane filter pressing circulation second time and extract under 65 ℃ condition, extraction time is 20 minutes.
Membrane filter pressing circulation extraction separation integrated technique of the present invention, be that the discharging opening of material-compound tank is communicated with the charging aperture of diaphragm filter press by pump (as membrane pump etc.), the liquid outlet of diaphragm filter press is communicated with the import of the charging aperture and the filtrate tank of material-compound tank respectively with three-way valve.When three-way valve switches to the material-compound tank position, the liquid outlet of diaphragm filter press is communicated with the charging aperture of material-compound tank, constitute membrane filter pressing circulation extraction system, slip in the material-compound tank is pumped to diaphragm filter press to carry out the pressing filtering liquid that membrane filter pressing comes out from diaphragm filter press and passes back into (medicated powder then is deposited on the filter cloth surface of each filter pressing chamber of diaphragm filter press equably) the material-compound tank, be re-used as and extract solvent and be pumped to diaphragm filter press and carry out membrane filter pressing and constantly circulate, thereby the membrane filter pressing circulation that realizes medical material is extracted; When three-way valve switches to the filtrate tank position, the liquid outlet of diaphragm filter press is communicated with the import of filtrate tank, constitute the membrane filter pressing solid-liquid separation system, after the membrane filter pressing circulation extraction of medical material finishes, to send into the filtrate tank storage from pressing filtering liquid and pressed liquor that diaphragm filter press comes out, thereby herbal extract is well separated with medicinal residues.
About extracting the problem of material, usually pulverizing medicinal materials is become coarse powder as extracting material, the soft medical material (as Radix Rehmanniae Preparata, Fructus Jujubae etc.) that difficulty is ground into coarse powder can add the water that 2-4 doubly measures and be ground into slip as extracting material with feed grinder or tissue mashing machine.
About the problem of charging sequence, when the medical material fibre-bearing more after a little while, can be in material-compound tank directly add medicated powder and extract solvent, under stirring condition, carry out the membrane filter pressing circulation and extract; When the medical material fibre rich, then should adopt the outer circulation method of feeding in raw material, to stop that medicated powder stops up in material-compound tank discharging opening and feeding pipe and phenomenon that the stock circulation is obstructed.The reinforced method of so-called outer circulation is will extract required whole solvents earlier first to add in the material-compound tank, three-way valve is switched to the material-compound tank position, solvent is pumped into diaphragm filter press, (can observe) when passing back into material-compound tank when observing pressing filtering liquid (this moment is actual to be solvent) from the manhole of material-compound tank, under stirring condition, progressively drop into medicated powder again, the gained feed liquid is pumped to diaphragm filter press thereupon carries out the membrane filter pressing pressing filtering liquid and passes back in the material-compound tank and circulate, and medicated powder then is deposited on the filter cloth surface of each filter pressing chamber of diaphragm filter press equably.
About extracting the problem of temperature, when being solvent with water, extract temperature and can be controlled at 50-90 ℃, according to polarized light microscopy method measurement result and in conjunction with bibliographical information, starch gelatinization temperature in the plant tissue mostly is 70-71 ℃, for fear of occurring because of starch gelatinization blocks cell inclusion (mostly being effective ingredient) stripping or stops up phenomenons such as filter cloth, the medical material of rich in starch is carried out water when carrying, extract temperature and should be controlled at below 70 ℃, preferred 55-65 ℃.And when adopting organic solvent extraction, the boiling point height of looking organic solvent can not heat (promptly at room temperature extracting) or suitably heating.
About the problem of extraction time and extraction time, can require according to the response rate of index components and economy requirement suitable adjustment extraction time and extraction time.For the extraction of general medicinal material coarse powder, but selective extraction 2 times extracted 30-40 minute for the 1st time, extracted 10-20 minute for the 2nd time; Higher for price of medicinal material, require the higher kind of the index components response rate, extraction time can suitably increase, as extracts 4 times, extracts the 2-4 time extraction 10-20 minute 40-60 minute the 1st time; Also last 1 time extracting solution can be carried out recycled as the solvent of extraction first of next group material.When serving as when extracting solvent with alcohol-water mixed solution, carry out membrane filter pressing and wash and squeeze medicinal residues thoroughly in the extraction back available water that finishes, after gained pressing filtering liquid and pressed liquor are measured pure content, can be used as the next group material and extract preparing solvent liquid and carry out recycled.Carry out membrane filter pressing when washing thoroughly at water, also can close two liquid valves that are in low level in four jiaos of liquid valves of diaphragm filter press, water is fully soaked overflow the top filtering layer, to strengthen washing effect.
Need to extract earlier volatile oil about part medical material in the compound preparation prescription, medicinal residues merge the problem of carrying out decocting with other medical material again, reach a few hours owing to extract the process of volatile oil with the water azeotropic, during the water soluble ingredient of medical material fully is soluble in the aqueous phase in the process of extracting volatile oil, so generally do not need with medicinal residues and other medical material merging carrying out decocting, and save follow-up concentrated energy consumption simultaneously for the response rate that guarantees effective ingredient, can be after extracting volatile oil, the water of doubly measuring with 2-4 is heated to the 60-90 ℃ of saturating wash slag of membrane filter pressing, wash 1-2 time thoroughly, aqueous solution after saturating washing liquid of gained and the distillation merges, as the extraction solvent of water first of other medical material.
About the problem of diaphragm filter press, filter cloth should be selected polypropylene multifilament filter cloth for use, and its Air permenbility selection principle is: less (as 3-10L/m with the appropriate to the occasion Air permenbility of selecting for use of organic solvent extraction 2.s) filter cloth is big (as 50-1200L/m with the appropriate to the occasion Air permenbility of selecting for use of water extraction 2.s) filter cloth.Membrane filter plate should select polypropylene etc. to meet the plastic material of medicinal requirements.The feed liquid pipeline should be selected the plastic conduit of 304 above rustless steels or non-PVC for use.
Beneficial effect of the present invention is: (1) has improved the response rate of effective ingredient: the present invention adopts the membrane filter pressing circulating extraction method to substitute the effective ingredient that decocting method extracts the prescription medical material, this method system adopts the pressure-driven of 0.5-0.6Mpa, circulation is extracted and is piled up in hundreds of the powder beds on the eluting face, effect with pressurized column chromatography or pressurization percolation, extraction efficiency significantly improves, the extraction temperature reduces, the loss of thermal sensitivity composition reduces, the response rate of index components significantly increases, for example, the Rhizoma Atractylodis Macrocephalae, the content that the content of glycyrrhizic acid improves about 23%, 60% ethanol-soluble extractives in Poria and the Radix Glycyrrhizae extract improves about 18%; And the filter cloth aperture of adopting because of diaphragm filter press is far below being used for the isolating filter screen of medicinal residues and decocting liquid aperture at present, and gained extracting solution clarity is good, and naked eyes visible particle thing can not enter in the finished product, has also correspondingly improved the content of active ingredient in the finished product.(2) simplified technological process, shortened the production cycle: the present invention will have the Rhizoma Atractylodis Macrocephalae in the method now, Poria decocts with water and prepare Radix Glycyrrhizae fluidextract separately is revised as the Rhizoma Atractylodis Macrocephalae, Poria, Radix Glycyrrhizae mixed and carries out the membrane filter pressing circulation and extract, prepare Radix Glycyrrhizae extractum no longer separately, simplified technological process greatly; Simultaneously, extract the medical material of same weight, adopt decocting method to need 4 hours usually, and adopt the membrane filter pressing circulating extraction method to be no more than 1.5 hours, extraction time shortens more than 60%; And the inventive method has realized the integrated of circulation extraction and solid-liquid separation, does not have the worry of the existing follow-up solid-liquid separation of decocting method.(3) energy savings: with 1m 3Water is heated to 55-65 ℃ from 20 ℃ and needs raw coal 18.4-21.7kg, needs raw coal 37.6kg and be heated to 98 ℃, and 42-51% on year-on-year basis lowers consumption; The extraction time of prescription medical material foreshortened to 1.5 hours by 4 hours, and the extraction energy consumption is reduced greatly.(4) be beneficial to environmental conservation and waste residue utilization: the medicinal residues after membrane filter pressing circulation extraction separation integrated technique is handled are the nearly powdered form block of doing; water content is few; not only be convenient to transhipment; can not pollute to environment; and be convenient to later use; as insert in the coal dust burning with reduce the coal consumption, biofermentation is made feedstuff, dry distilling is made as the charcoal piece and makes heating or domestic fuel etc.(5) require Radix Bupleuri in the existing method, Herba Menthae, Rhizoma Zingiberis Recens and Radix Angelicae Sinensis extract the medicinal residues and the Rhizoma Atractylodis Macrocephalae behind the volatile oil, Poria decocts with water, reach a few hours owing to extract the process of volatile oil with the water azeotropic, Radix Bupleuri, Herba Menthae, during the water soluble ingredient of Rhizoma Zingiberis Recens and Radix Angelicae Sinensis fully is soluble in the aqueous phase in the process of extracting volatile oil, so the inventive method no longer will be extracted the medicinal residues and the Rhizoma Atractylodis Macrocephalae behind the volatile oil, Poria is fried in shallow oil altogether, and only with hot water medicinal residues are washed thoroughly, aqueous solution after saturating washing liquid and the distillation merges, as the Rhizoma Atractylodis Macrocephalae, the solvent of extraction first of Poria is applied mechanically, and extracts solvent load to save, reduce follow-up concentrated energy consumption.
Description of drawings
Fig. 1 is the preferred corollary apparatus figure of membrane filter pressing circulation extraction separation integrated technique.
The specific embodiment
In order to make the purpose, technical solutions and advantages of the present invention clearer, the preferred embodiments of the present invention are described in detail below in conjunction with accompanying drawing.
The preferred corollary apparatus figure of membrane filter pressing circulation extraction separation integrated technique as shown in Figure 1, the discharging opening of material-compound tank is communicated with the charging aperture of diaphragm filter press by membrane pump, the liquid outlet of diaphragm filter press is communicated with the import of the charging aperture and the filtrate tank of material-compound tank respectively with three-way valve, when three-way valve switches to the material-compound tank position, the liquid outlet of diaphragm filter press is communicated with the charging aperture of material-compound tank, the pressing filtering liquid that comes out from diaphragm filter press passes back into material-compound tank, constitutes membrane filter pressing circulation extraction system; When three-way valve switched to the filtrate tank position, the liquid outlet of diaphragm filter press was communicated with the import of filtrate tank, and the pressing filtering liquid that comes out from diaphragm filter press enters the filtrate tank storage, constitutes the membrane filter pressing solid-liquid separation system.
Embodiment 1
Prescription: Radix Bupleuri 5kg, Radix Angelicae Sinensis 5kg, Radix Paeoniae Alba 5kg, Rhizoma Atractylodis Macrocephalae (parched) 5kg, Poria 5kg, Herba Menthae 1kg, Rhizoma Zingiberis Recens 5kg, Radix Glycyrrhizae Preparata 4kg
Preparation method may further comprise the steps:
A. the extraction of Radix Bupleuri, Herba Menthae, Rhizoma Zingiberis Recens and Radix Angelicae Sinensis
A1. the Radix Angelicae Sinensis with Radix Bupleuri, Herba Menthae, Rhizoma Zingiberis Recens and the recipe quantity 1/2nd of recipe quantity mixes, and is ground into coarse powder, and is standby;
A2. step a1 gained medicated powder is put in the multi-function extractor, extracted volatile oil with straight-through steam distillation method, the aqueous solution after distillation device is in addition collected, and is standby;
A3. add the water that is equivalent to 3 times of step a1 gained medicated powder weight in the multi-function extractor that extracts medicinal residues behind the volatile oil is housed, is heated with stirring to 80 ℃, insulated and stirred 10 minutes pumps into diaphragm filter press with slip and (adopts 80 ± 10 L/m 2.s polypropylene multifilament filter cloth) carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, in multi-function extractor, add 80 ℃ the water of being preheated to be equivalent to 2 times of step a1 gained medicated powder weight again, pump into diaphragm filter press and carry out membrane filter pressing, collect pressing filtering liquid; Start the squeezing program of diaphragm filter press, collect pressed liquor, last release is opened plate, slag dumping; Aqueous solution after the distillation of pressing filtering liquid, pressed liquor and step a2 gained is merged, be designated as extracting solution A;
B. the extraction of the Rhizoma Atractylodis Macrocephalae, Poria and Radix Glycyrrhizae
B1. the Radix Glycyrrhizae with the Rhizoma Atractylodis Macrocephalae, Poria and the recipe quantity 3/4ths of recipe quantity mixes, and is ground into coarse powder, and is standby;
B2. in material-compound tank, add the extracting solution A of step a3 gained and add the water ad pond om and be equivalent to 7.5 times of step b1 gained medicated powder weight, be heated to 65 ℃ and insulation; Three-way valve is switched to the material-compound tank position, open agitator, membrane pump and the diaphragm filter press of material-compound tank, the water in the material-compound tank is pumped into diaphragm filter press (adopt 80 ± 10 L/m 2.s polypropylene multifilament filter cloth), when pressing filtering liquid passes back into material-compound tank, in material-compound tank, at the uniform velocity add step b1 gained medicated powder, finish, 65 ℃ of membrane filter pressing circulations were extracted 40 minutes, afterwards three-way valve were switched to the filtrate tank position and carried out membrane filter pressing, collected pressing filtering liquid; After filter pressing finishes, again three-way valve is switched to the material-compound tank position, in material-compound tank, add 65 ℃ the water of being preheated to be equivalent to 3.5 times of step b1 gained medicated powder weight, the circulation of insulation membrane filter pressing was extracted 20 minutes, afterwards three-way valve is switched to the filtrate tank position and carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, start the squeezing program of diaphragm filter press, collect pressed liquor, last release is opened plate, slag dumping; Merge twice pressing filtering liquid and pressed liquor, be designated as extracting solution B;
C. preparation
C1. the Radix Paeoniae Alba of recipe quantity, the Radix Angelicae Sinensis of recipe quantity 1/2nd and the Radix Glycyrrhizae of recipe quantity 1/4th are mixed, be ground into fine powder, standby;
C2. the extracting solution with step b2 gained is condensed into the thick paste that relative density is 1.35-1.40, and is standby;
C3. with the thick paste of step c2 gained, the medicated powder of step c1 gained, the volatile oil and the maltose mixing of step a2 gained, pill, drying, polishing promptly gets ease pill (concentrated pill).
Embodiment 2
Prescription: Radix Bupleuri 5kg, Radix Angelicae Sinensis 5kg, Radix Paeoniae Alba 5kg, Rhizoma Atractylodis Macrocephalae (parched) 5kg, Poria 5kg, Herba Menthae 1kg, Rhizoma Zingiberis Recens 5kg, Radix Glycyrrhizae Preparata 4kg
Preparation method may further comprise the steps:
A. the extraction of Radix Bupleuri, Herba Menthae, Rhizoma Zingiberis Recens and Radix Angelicae Sinensis
A1. the Radix Angelicae Sinensis with Radix Bupleuri, Herba Menthae, Rhizoma Zingiberis Recens and the recipe quantity 1/2nd of recipe quantity mixes, and is ground into coarse powder, and is standby;
A2. step a1 gained medicated powder is put in the multi-function extractor, extracted volatile oil with straight-through steam distillation method, the aqueous solution after distillation device is in addition collected, and is standby;
A3. add the water that is equivalent to 2 times of step a1 gained medicated powder weight in the multi-function extractor that extracts medicinal residues behind the volatile oil is housed, is heated with stirring to 75 ℃, insulated and stirred 15 minutes pumps into diaphragm filter press with slip and (adopts 80 ± 10 L/m 2.s polypropylene multifilament filter cloth) carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, in multi-function extractor, add 75 ℃ the water of being preheated to be equivalent to 1 times of step a1 gained medicated powder weight again, pump into diaphragm filter press and carry out membrane filter pressing, collect pressing filtering liquid; Start the squeezing program of diaphragm filter press, collect pressed liquor, last release is opened plate, slag dumping; Aqueous solution after the distillation of pressing filtering liquid, pressed liquor and step a2 gained is merged, be designated as extracting solution A;
B. the extraction of the Rhizoma Atractylodis Macrocephalae, Poria and Radix Glycyrrhizae
B1. the Radix Glycyrrhizae with the Rhizoma Atractylodis Macrocephalae, Poria and the recipe quantity 3/4ths of recipe quantity mixes, and is ground into coarse powder, and is standby;
B2. in material-compound tank, add the extracting solution A of step a3 gained and add the water ad pond om and be equivalent to 6 times of step b1 gained medicated powder weight, be heated to 55 ℃ and insulation; Three-way valve is switched to the material-compound tank position, open agitator, membrane pump and the diaphragm filter press of material-compound tank, the water in the material-compound tank is pumped into diaphragm filter press (adopt 80 ± 10 L/m 2.s polypropylene multifilament filter cloth), when pressing filtering liquid passes back into material-compound tank, in material-compound tank, at the uniform velocity add step b1 gained medicated powder, finish, 55 ℃ of membrane filter pressing circulations were extracted 50 minutes, afterwards three-way valve were switched to the filtrate tank position and carried out membrane filter pressing, collected pressing filtering liquid; After filter pressing finishes, three-way valve is switched to the material-compound tank position again, add 55 ℃ the water of being preheated to be equivalent to 3 times of step b1 gained medicated powder weight in material-compound tank, the circulation of insulation membrane filter pressing was extracted 30 minutes, afterwards three-way valve is switched to the filtrate tank position and carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, start the squeezing program of diaphragm filter press, collect pressed liquor, last release is opened plate, slag dumping; Merge twice pressing filtering liquid and pressed liquor, be designated as extracting solution B;
C. preparation
C1. the Radix Paeoniae Alba of recipe quantity, the Radix Angelicae Sinensis of recipe quantity 1/2nd and the Radix Glycyrrhizae of recipe quantity 1/4th are mixed, be ground into fine powder, standby;
C2. the extracting solution with step b2 gained is condensed into the thick paste that relative density is 1.35-1.40, and is standby;
C3. with the thick paste of step c2 gained, the medicated powder of step c1 gained, the volatile oil and the maltose mixing of step a2 gained, pill, drying, polishing promptly gets ease pill (concentrated pill).
Embodiment 3
Prescription: Radix Bupleuri 5kg, Radix Angelicae Sinensis 5kg, Radix Paeoniae Alba 5kg, Rhizoma Atractylodis Macrocephalae (parched) 5kg, Poria 5kg, Herba Menthae 1kg, Rhizoma Zingiberis Recens 5kg, Radix Glycyrrhizae Preparata 4kg
Preparation method may further comprise the steps:
A. the extraction of Radix Bupleuri, Herba Menthae, Rhizoma Zingiberis Recens and Radix Angelicae Sinensis
A1. the Radix Angelicae Sinensis with Radix Bupleuri, Herba Menthae, Rhizoma Zingiberis Recens and the recipe quantity 1/2nd of recipe quantity mixes, and is ground into coarse powder, and is standby;
A2. step a1 gained medicated powder is put in the multi-function extractor, extracted volatile oil with straight-through steam distillation method, the aqueous solution after distillation device is in addition collected, and is standby;
A3. add the water that is equivalent to 4 times of step a1 gained medicated powder weight in the multi-function extractor that extracts medicinal residues behind the volatile oil is housed, is heated with stirring to 85 ℃, insulated and stirred 5 minutes pumps into diaphragm filter press with slip and (adopts 80 ± 10 L/m 2.s polypropylene multifilament filter cloth) carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, in multi-function extractor, add 85 ℃ the water of being preheated to be equivalent to 3 times of step a1 gained medicated powder weight again, pump into diaphragm filter press and carry out membrane filter pressing, collect pressing filtering liquid; Start the squeezing program of diaphragm filter press, collect pressed liquor, last release is opened plate, slag dumping; Aqueous solution after the distillation of pressing filtering liquid, pressed liquor and step a2 gained is merged, be designated as extracting solution A;
B. the extraction of the Rhizoma Atractylodis Macrocephalae, Poria and Radix Glycyrrhizae
B1. the Radix Glycyrrhizae with the Rhizoma Atractylodis Macrocephalae, Poria and the recipe quantity 3/4ths of recipe quantity mixes, and is ground into coarse powder, and is standby;
B2. in material-compound tank, add the extracting solution A of step a3 gained and add the water ad pond om and be equivalent to 9 times of step b1 gained medicated powder weight, be heated to 60 ℃ and insulation; Three-way valve is switched to the material-compound tank position, open agitator, membrane pump and the diaphragm filter press of material-compound tank, the water in the material-compound tank is pumped into diaphragm filter press (adopt 80 ± 10 L/m 2.s polypropylene multifilament filter cloth), when pressing filtering liquid passes back into material-compound tank, in material-compound tank, at the uniform velocity add step b1 gained medicated powder, finish, 60 ℃ of membrane filter pressing circulations were extracted 30 minutes, afterwards three-way valve were switched to the filtrate tank position and carried out membrane filter pressing, collected pressing filtering liquid; After filter pressing finishes, three-way valve is switched to the material-compound tank position again, add 60 ℃ the water of being preheated to be equivalent to 5 times of step b1 gained medicated powder weight in material-compound tank, the circulation of insulation membrane filter pressing was extracted 10 minutes, afterwards three-way valve is switched to the filtrate tank position and carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, start the squeezing program of diaphragm filter press, collect pressed liquor, last release is opened plate, slag dumping; Merge twice pressing filtering liquid and pressed liquor, be designated as extracting solution B;
C. preparation
C1. the Radix Paeoniae Alba of recipe quantity, the Radix Angelicae Sinensis of recipe quantity 1/2nd and the Radix Glycyrrhizae of recipe quantity 1/4th are mixed, be ground into fine powder, standby;
C2. the extracting solution with step b2 gained is condensed into the thick paste that relative density is 1.35-1.40, and is standby;
C3. with the thick paste of step c2 gained, the medicated powder of step c1 gained, the volatile oil and the maltose mixing of step a2 gained, pill, drying, polishing promptly gets ease pill (concentrated pill).
Employing is with a collection of medicinal raw material, adopt described method of embodiment 1-3 and existing method (the Sanitation Ministry medicine standard WS3-B-2220-96 records method) to compare experiment respectively, and products obtained therefrom carried out quality inspection, the result shows: the product that adopts the described method of embodiment 1-3 to make all meets the requirement of quality standard, and the response rate of index components is higher.Wherein, the cost-effectiveness of embodiment 1 described method is than best, and the content that the content of glycyrrhizic acid improves about 23%, 60% ethanol-soluble extractives in the gained Rhizoma Atractylodis Macrocephalae, Poria and the Radix Glycyrrhizae extract improves about 18%.
Explanation is at last, above embodiment is only unrestricted in order to technical scheme of the present invention to be described, although by invention has been described with reference to the preferred embodiments of the present invention, but those of ordinary skill in the art is to be understood that, can make various changes to it in the form and details, and the spirit and scope of the present invention that do not depart from appended claims and limited.

Claims (3)

1. the preparation method of ease pill, make by following raw materials by weight proportions: 80 parts of 100 parts of Radix Bupleuri, 100 parts of Radix Angelicae Sinensis, 100 parts of the Radix Paeoniae Albas, 100 parts of Rhizoma Atractylodis Macrocephalae (parched)s, 100 parts in Poria, 20 parts of Herba Menthaes, 100 parts in Rhizoma Zingiberis Recens and Radix Glycyrrhizae Preparatas, it is characterized in that preparation method may further comprise the steps:
A. the extraction of Radix Bupleuri, Herba Menthae, Rhizoma Zingiberis Recens and Radix Angelicae Sinensis
A1. the Radix Angelicae Sinensis with Radix Bupleuri, Herba Menthae, Rhizoma Zingiberis Recens and proportional quantity 1/2nd mixes, and is ground into coarse powder, and is standby;
A2. the medicated powder with step a1 gained extracts volatile oil with steam distillation, and the aqueous solution after medicinal residues and the distillation is standby;
A3. in the medicinal residues of step a2 gained, add water, be heated with stirring to 60-90 ℃, slip is pumped into diaphragm filter press carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, will be preheated to 60-90 ℃ water again and pump into diaphragm filter press and carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, start the squeezing program of diaphragm filter press, collect pressed liquor; Aqueous solution after the distillation of twice pressing filtering liquid, pressed liquor and step a2 gained is merged, be designated as extracting solution A;
B. the extraction of the Rhizoma Atractylodis Macrocephalae, Poria and Radix Glycyrrhizae
B1. the Radix Glycyrrhizae with the Rhizoma Atractylodis Macrocephalae, Poria and proportional quantity 3/4ths mixes, and is ground into coarse powder, and is standby;
B2. the extracting solution A and the water that add step a3 gained in material-compound tank are heated to 50-90 ℃ and insulation; Three-way valve is switched to the material-compound tank position, water in the material-compound tank is pumped into diaphragm filter press, when pressing filtering liquid passes back into material-compound tank, the medicated powder that under stirring condition, in material-compound tank, adds step b1 gained, finish, under 50-90 ℃ condition, carry out the membrane filter pressing circulation first time and extract, afterwards three-way valve is switched to the filtrate tank position and carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, again three-way valve is switched to the material-compound tank position, in material-compound tank, add entry, under 50-90 ℃ condition, carry out the membrane filter pressing circulation second time and extract, afterwards three-way valve is switched to the filtrate tank position and carry out membrane filter pressing, collect pressing filtering liquid; After filter pressing finishes, start the squeezing program of diaphragm filter press, collect pressed liquor; Merge twice pressing filtering liquid and pressed liquor, be designated as extracting solution B;
C. preparation
C1. the Radix Angelicae Sinensis of the Radix Paeoniae Alba, proportional quantity 1/2nd and the Radix Glycyrrhizae of proportional quantity 1/4th are mixed, be ground into fine powder, standby;
C2. the extracting solution with step b2 gained is condensed into the thick paste that relative density is 1.35-1.40, and is standby;
C3. with the thick paste of step c2 gained, the medicated powder of step c1 gained, the volatile oil and the maltose mixing of step a2 gained, pill, drying, polishing promptly gets ease pill.
2. the preparation method of ease pill according to claim 1, it is characterized in that described step a3 adds earlier to be equivalent to step a1 gained medicated powder weight 2-4 water doubly, is heated with stirring to 75-85 ℃ in medicinal residues, insulated and stirred 5-15 minute, slip is pumped into diaphragm filter press carry out membrane filter pressing To be equivalent to step a1 gained medicated powder weight 1-3 75-85 ℃ the water of being preheated to doubly again and pump into diaphragm filter press, with slip pump into diaphragm filter press carry out the membrane filter pressing
Described step b2 adds earlier the extracting solution A of step a3 gained and adds 6-9 that the water ad pond om is equivalent to step b1 gained medicated powder weight doubly, carries out membrane filter pressing circulation extraction first time under 55-65 ℃ condition, and extraction time is 30-50 minute; Add and be equivalent to step b1 gained medicated powder weight 3-5 water doubly, carry out the membrane filter pressing circulation second time and extract under 55-65 ℃ condition, extraction time is 10-30 minute.
3. the preparation method of ease pill according to claim 2, it is characterized in that described step a3 adds the water that is equivalent to 3 times of step a1 gained medicated powder weight earlier in medicinal residues, be heated with stirring to 80 ℃, insulated and stirred 10 minutes pumps into diaphragm filter press with slip and carries out membrane filter pressing To be equivalent to again 2 times of step a1 gained medicated powder weight be preheated to 80 ℃ water pump into diaphragm filter press carry out the membrane filter pressing
Described step b2 adds earlier the extracting solution A of step a3 gained and adds the water ad pond om to be equivalent to 7.5 times of step b1 gained medicated powder weight, carries out membrane filter pressing circulation extraction first time under 65 ℃ condition, and extraction time is 40 minutes; Add the water that is equivalent to 3.5 times of step b1 gained medicated powder weight again, carry out the membrane filter pressing circulation second time and extract under 65 ℃ condition, extraction time is 20 minutes.
CN 201110247776 2011-08-26 2011-08-26 Preparation method of ease pill Active CN102294003B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201110247776 CN102294003B (en) 2011-08-26 2011-08-26 Preparation method of ease pill

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201110247776 CN102294003B (en) 2011-08-26 2011-08-26 Preparation method of ease pill

Publications (2)

Publication Number Publication Date
CN102294003A true CN102294003A (en) 2011-12-28
CN102294003B CN102294003B (en) 2013-04-17

Family

ID=45354836

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201110247776 Active CN102294003B (en) 2011-08-26 2011-08-26 Preparation method of ease pill

Country Status (1)

Country Link
CN (1) CN102294003B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102908600A (en) * 2012-11-05 2013-02-06 太极集团重庆中药二厂有限公司 Preparation method for ease pills
CN103142722A (en) * 2013-03-13 2013-06-12 辛秀芳 Traditional Chinese medicine composition for treating liver qi depression type irregular menstruation
CN105853986A (en) * 2016-06-06 2016-08-17 李晓维 Traditional Chinese medicine composition for treating hyperplasia of mammary glands
CN107998356A (en) * 2017-12-28 2018-05-08 湖州品创孵化器有限公司 A kind of ease pill and its preparation process

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1733020A (en) * 2005-07-29 2006-02-15 王衡新 Chinese medicinal preparation for soothing liver, strengthening spleen, nourishing blood and normalizing menstruation and its preparation process

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1733020A (en) * 2005-07-29 2006-02-15 王衡新 Chinese medicinal preparation for soothing liver, strengthening spleen, nourishing blood and normalizing menstruation and its preparation process

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
《2008年成渝药学学术年会论文集》 20081231 陈彪等 隔膜压滤工艺在甘草流浸膏生产上的应用研究 第117-118页 1-3 , *
《中华人民共和国卫生部药品标准中药成方制剂第十一册》 19961231 中华人民共和国卫生部药典委员会编 逍遥丸(浓缩丸) 第164页 1-3 , *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102908600A (en) * 2012-11-05 2013-02-06 太极集团重庆中药二厂有限公司 Preparation method for ease pills
CN102908600B (en) * 2012-11-05 2014-06-25 太极集团重庆中药二厂有限公司 Preparation method for ease pills
CN103142722A (en) * 2013-03-13 2013-06-12 辛秀芳 Traditional Chinese medicine composition for treating liver qi depression type irregular menstruation
CN105853986A (en) * 2016-06-06 2016-08-17 李晓维 Traditional Chinese medicine composition for treating hyperplasia of mammary glands
CN107998356A (en) * 2017-12-28 2018-05-08 湖州品创孵化器有限公司 A kind of ease pill and its preparation process

Also Published As

Publication number Publication date
CN102294003B (en) 2013-04-17

Similar Documents

Publication Publication Date Title
CN102294003B (en) Preparation method of ease pill
CN102293896B (en) Preparation method of tablet for tonifying kidney and controlling asthma
CN102258659A (en) Method for preparing ageratum oral liquid
CN102302709B (en) Preparation method for medicament for treating pediatric disease
CN102247477B (en) Method for preparing bezoar soft capsules
CN102247555B (en) Method for preparing granule for clearing heat of cold
CN102247436B (en) Preparation method of Qingxuanpian
CN102293973B (en) Preparation method of cough-relieving tablets
CN102319358B (en) Preparation method of kidney-tonifying and life-prolonging capsule
CN102293897B (en) Preparation method of Liuweidihuang pills
CN102247588B (en) Preparation method of pill for tonifying middle-Jiao and Qi
CN102293925B (en) Preparation method of Jiangzhiling tablets
CN102293812B (en) Preparation method of stranguria-treating and calculus-removing particles
CN102247582B (en) Preparation method of liquid for internally eliminating breast nodules
CN102247469B (en) Preparation method for acute bronchitis syrup
CN102293898B (en) Preparation method of rhizoma dioscoreae nipponicae bone spur tablet
CN102293873B (en) Preparation method of Bazheng mixture
CN102247476B (en) Method for preparing nine immortal extract
CN102319307B (en) Preparation method of Baoxin tablet
CN102319311B (en) Preparation method of tincture of oranges
CN102247522B (en) Preparation method for fritillaria cirrhosa fluid extract and fritillary and loquat particle
CN102293826B (en) Preparation method of traditional Chinese medicine composition for treating infection of upper respiratory tract
CN102293884B (en) Preparation method of anti-diarrheal medicinal composition
CN102302546B (en) Method for preparing motherwort herb paste
CN102247525B (en) Method for preparing pulse activating decoction

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant