CN112402484A - Preparation method of liquorice particles and liquorice particles prepared by same - Google Patents
Preparation method of liquorice particles and liquorice particles prepared by same Download PDFInfo
- Publication number
- CN112402484A CN112402484A CN202011345508.7A CN202011345508A CN112402484A CN 112402484 A CN112402484 A CN 112402484A CN 202011345508 A CN202011345508 A CN 202011345508A CN 112402484 A CN112402484 A CN 112402484A
- Authority
- CN
- China
- Prior art keywords
- licorice
- decoction
- liquorice
- granules
- particles
- 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
Links
- 235000006200 Glycyrrhiza glabra Nutrition 0.000 title claims abstract description 182
- 244000303040 Glycyrrhiza glabra Species 0.000 title claims abstract description 70
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 title claims abstract description 63
- 239000002245 particle Substances 0.000 title claims abstract description 62
- 235000011477 liquorice Nutrition 0.000 title claims abstract description 56
- 238000002360 preparation method Methods 0.000 title claims abstract description 21
- 235000001453 Glycyrrhiza echinata Nutrition 0.000 claims abstract description 114
- 235000017382 Glycyrrhiza lepidota Nutrition 0.000 claims abstract description 114
- 229940010454 licorice Drugs 0.000 claims abstract description 114
- 241000202807 Glycyrrhiza Species 0.000 claims abstract description 112
- 239000008187 granular material Substances 0.000 claims abstract description 99
- 238000002156 mixing Methods 0.000 claims abstract description 34
- 239000012530 fluid Substances 0.000 claims abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000000706 filtrate Substances 0.000 claims abstract description 15
- 239000000945 filler Substances 0.000 claims abstract description 12
- 239000000314 lubricant Substances 0.000 claims abstract description 10
- 239000000843 powder Substances 0.000 claims description 39
- 229920002774 Maltodextrin Polymers 0.000 claims description 26
- 239000005913 Maltodextrin Substances 0.000 claims description 26
- 229940035034 maltodextrin Drugs 0.000 claims description 26
- 238000007873 sieving Methods 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 19
- 238000001035 drying Methods 0.000 claims description 18
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical group [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 10
- 235000019359 magnesium stearate Nutrition 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000003814 drug Substances 0.000 abstract description 30
- 239000000047 product Substances 0.000 abstract description 10
- 230000000694 effects Effects 0.000 abstract description 3
- 229940126680 traditional chinese medicines Drugs 0.000 abstract description 2
- 238000011049 filling Methods 0.000 description 48
- 238000007789 sealing Methods 0.000 description 36
- 238000000605 extraction Methods 0.000 description 26
- 239000000463 material Substances 0.000 description 20
- 238000001914 filtration Methods 0.000 description 18
- 239000007788 liquid Substances 0.000 description 18
- 239000003651 drinking water Substances 0.000 description 17
- 235000020188 drinking water Nutrition 0.000 description 17
- 235000017443 Hedysarum boreale Nutrition 0.000 description 12
- 235000007858 Hedysarum occidentale Nutrition 0.000 description 12
- 239000011362 coarse particle Substances 0.000 description 12
- 239000010419 fine particle Substances 0.000 description 12
- 239000001947 glycyrrhiza glabra rhizome/root Substances 0.000 description 12
- 238000010438 heat treatment Methods 0.000 description 12
- 238000012856 packing Methods 0.000 description 12
- 238000003860 storage Methods 0.000 description 12
- 238000005303 weighing Methods 0.000 description 12
- 239000001649 glycyrrhiza glabra l. absolute Substances 0.000 description 9
- 229940051810 licorice root extract Drugs 0.000 description 9
- 235000020725 licorice root extract Nutrition 0.000 description 9
- LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 description 7
- 229960004949 glycyrrhizic acid Drugs 0.000 description 7
- UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 description 7
- 235000019410 glycyrrhizin Nutrition 0.000 description 7
- VTAJIXDZFCRWBR-UHFFFAOYSA-N Licoricesaponin B2 Natural products C1C(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2)C(O)=O)C)(C)CC2)(C)C2C(C)(C)CC1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O VTAJIXDZFCRWBR-UHFFFAOYSA-N 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 6
- 230000009286 beneficial effect Effects 0.000 description 6
- 238000005429 filling process Methods 0.000 description 6
- 239000001685 glycyrrhizic acid Substances 0.000 description 6
- 238000005469 granulation Methods 0.000 description 6
- 230000003179 granulation Effects 0.000 description 6
- 238000004806 packaging method and process Methods 0.000 description 6
- 238000005086 pumping Methods 0.000 description 6
- 238000005070 sampling Methods 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 229910001220 stainless steel Inorganic materials 0.000 description 6
- 239000010935 stainless steel Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000006228 supernatant Substances 0.000 description 6
- KSDSYIXRWHRPMN-UHFFFAOYSA-N 4'-O-beta-D-Galactopyranoside-6''-p-Coumaroylprunin-4',5,7-Trihydroxyflavanone Natural products OC1C(O)C(O)C(CO)OC1OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2)C=C1 KSDSYIXRWHRPMN-UHFFFAOYSA-N 0.000 description 5
- DEMKZLAVQYISIA-ONJCETCRSA-N Liquiritin Natural products O([C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1)c1ccc([C@@H]2Oc3c(C(=O)C2)ccc(O)c3)cc1 DEMKZLAVQYISIA-ONJCETCRSA-N 0.000 description 5
- DEMKZLAVQYISIA-UHFFFAOYSA-N Liquirtin Natural products OC1C(O)C(O)C(CO)OC1OC1=CC=C(C2OC3=CC(O)=CC=C3C(=O)C2)C=C1 DEMKZLAVQYISIA-UHFFFAOYSA-N 0.000 description 5
- 238000007908 dry granulation Methods 0.000 description 5
- DEMKZLAVQYISIA-ZRWXNEIDSA-N liquiritin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC=C([C@H]2OC3=CC(O)=CC=C3C(=O)C2)C=C1 DEMKZLAVQYISIA-ZRWXNEIDSA-N 0.000 description 5
- GSZUGBAEBARHAW-UHFFFAOYSA-N sophoraflavone B Natural products OC1C(O)C(O)C(CO)OC1OC1=CC=C(C=2OC3=CC(O)=CC=C3C(=O)C=2)C=C1 GSZUGBAEBARHAW-UHFFFAOYSA-N 0.000 description 5
- 229940079593 drug Drugs 0.000 description 4
- 238000011194 good manufacturing practice Methods 0.000 description 4
- 206010011224 Cough Diseases 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 206010062717 Increased upper airway secretion Diseases 0.000 description 2
- 208000002193 Pain Diseases 0.000 description 2
- 208000005392 Spasm Diseases 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 230000035622 drinking Effects 0.000 description 2
- 208000026435 phlegm Diseases 0.000 description 2
- 210000000952 spleen Anatomy 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 206010007247 Carbuncle Diseases 0.000 description 1
- 208000030453 Drug-Related Side Effects and Adverse reaction Diseases 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 240000008917 Glycyrrhiza uralensis Species 0.000 description 1
- 235000000554 Glycyrrhiza uralensis Nutrition 0.000 description 1
- 239000004378 Glycyrrhizin Substances 0.000 description 1
- 206010033557 Palpitations Diseases 0.000 description 1
- 206010070863 Toxicity to various agents Diseases 0.000 description 1
- 230000003187 abdominal effect Effects 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 206010003549 asthenia Diseases 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 235000019633 pungent taste Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 235000019605 sweet taste sensations Nutrition 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/48—Fabaceae or Leguminosae (Pea or Legume family); Caesalpiniaceae; Mimosaceae; Papilionaceae
- A61K36/484—Glycyrrhiza (licorice)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/30—Extraction of the material
- A61K2236/33—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones
- A61K2236/331—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones using water, e.g. cold water, infusion, tea, steam distillation or decoction
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/30—Extraction of the material
- A61K2236/39—Complex extraction schemes, e.g. fractionation or repeated extraction steps
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/50—Methods involving additional extraction steps
- A61K2236/51—Concentration or drying of the extract, e.g. Lyophilisation, freeze-drying or spray-drying
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Alternative & Traditional Medicine (AREA)
- Botany (AREA)
- Medical Informatics (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
The invention provides a preparation method of liquorice particles and the liquorice particles prepared by the same, and relates to the technical field of traditional Chinese medicines. The preparation method of the licorice granules comprises the following steps: concentrating the decoction filtrate of Glycyrrhrizae radix to relative density of 1.05-1.20, and collecting fluid extract; mixing the filler and the clear paste according to a ratio of 2.5-3.0: 1, adding a lubricant, and granulating to obtain the licorice granules; the weight ratio of the liquorice to water during decoction is 1: 14-15, the temperature during decoction is 90-100 ℃, the decoction time is 3-4 h, and the weight percentage of the lubricant in the liquorice particles is 0.5-1.0%; the concentration temperature is 65-85 ℃. The invention has the advantages that the finally prepared liquorice granules have better curative effect, uniform granules, uniform product quality, high yield, high content of effective components, and accord with GMP standard and traditional Chinese medicine theory and principle.
Description
Technical Field
The invention relates to the technical field of traditional Chinese medicines, and particularly relates to a preparation method of liquorice particles and the liquorice particles prepared by the same.
Background
The licorice is a common traditional Chinese medicine, and the Chinese pharmacopoeia collects the dry roots and rhizomes of licorice (Glycyrrhiza uralensis Fisch.) which is a leguminous plant. Collecting Glycyrrhrizae radix in spring and autumn, removing fibrous root, and sun drying to obtain decoction pieces. Licorice root, radix Glycyrrhizae is slightly fragrant, sweet in flavor, sweet in nature, cool, thin, soft and soft. Has the effects of moistening lung for arresting cough, invigorating spleen and replenishing qi, clearing away heat and toxic materials, eliminating phlegm and arresting cough, relieving spasm and pain, and harmonizing the drugs. Can be used for treating weakness of spleen and stomach, asthenia, palpitation, short breath, cough, excessive phlegm, abdominal and limb spasm, pain, carbuncle, suppurative sore, and relieving drug toxicity and pungency. At present, liquorice on the market mostly takes liquorice decoction pieces as main materials, and during use, the liquorice is decocted at present after decoction pieces are used, but with the continuous acceleration of the pace of modern life, the traditional medication mode needs a large amount of decoction time, is inconvenient to carry, has large drinking amount, and cannot meet the pace of modern life.
Disclosure of Invention
The invention aims to provide a preparation method of licorice granules, and the licorice granules prepared by the preparation method have uniform size, stable product quality, high yield and high content of effective components, meet GMP (good manufacturing practice) standards and meet the traditional Chinese medicine medication theory and principle.
The invention also aims to provide the liquorice particles prepared by the preparation method, which not only saves the decoction time of medicinal materials, but also keeps the property of the original medicinal materials, is convenient to carry, can be eaten at any time and is more suitable for the fast-paced life of contemporary people.
The technical problem to be solved by the invention is realized by adopting the following technical scheme.
On one hand, the embodiment of the application provides a preparation method of licorice granules, which comprises the following steps: concentrating the decoction filtrate of Glycyrrhrizae radix to relative density of 1.05-1.20, and collecting fluid extract; mixing the filler and the clear paste according to a ratio of 2.5-3.0: 1, adding a lubricant, and granulating to obtain the licorice granules; the weight ratio of the liquorice to water during decoction is 1: 14-15, the temperature during decoction is 90-100 ℃, the decoction time is 3-4 h, and the weight percentage of the lubricant in the liquorice particles is 0.5-1.0%; the concentration temperature is 65-85 ℃.
In another aspect, the present application provides a licorice granule prepared by the aforementioned method.
Compared with the prior art, the embodiment of the invention has at least the following advantages or beneficial effects:
according to the preparation method of the liquorice particles, the beneficial ingredients in the liquorice are fully reserved through a specific extraction and concentration process, and the concentrated clear paste is dried and granulated by using a drying and spraying method, so that the finally prepared liquorice particles are better in curative effect, uniform in particle, uniform in product quality, high in yield and high in effective ingredient, meet GMP (good manufacturing practice) standards, and meet the traditional Chinese medicine medication theory and principle. Compared with the traditional Chinese medicine decoction, the liquorice particles prepared by the preparation method of the liquorice particles provided by the invention not only save the decoction time of medicinal materials, but also keep the property of the original medicinal materials, are convenient to carry and can be eaten at any time, and the drinking amount is small, so that the liquorice particles are more suitable for the fast-paced life of contemporary people.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings needed to be used in the embodiments will be briefly described below, it should be understood that the following drawings only illustrate some embodiments of the present invention and therefore should not be considered as limiting the scope, and for those skilled in the art, other related drawings can be obtained according to the drawings without inventive efforts.
FIG. 1 is a flow chart of a method for preparing licorice granules provided in embodiments 1 to 6 of the present invention.
Detailed Description
In order to make the objects, technical solutions and advantages of the embodiments of the present invention clearer, the technical solutions in the embodiments of the present invention will be clearly and completely described below. The examples, in which specific conditions are not specified, were conducted under conventional conditions or conditions recommended by the manufacturer. The reagents or instruments used are not indicated by the manufacturer, and are all conventional products available commercially.
It should be noted that the embodiments and features of the embodiments in the present application may be combined with each other without conflict. The present invention will be described in detail below with reference to specific examples.
On one hand, the embodiment of the application provides a preparation method of licorice granules, which comprises the following steps: concentrating the decoction filtrate of Glycyrrhrizae radix to relative density of 1.05-1.20, and collecting fluid extract; mixing the filler and the clear paste according to a ratio of 2.5-3.0: 1, adding a lubricant, and granulating to obtain the licorice granules; the weight ratio of the liquorice to water during decoction is 1: 14-15, the temperature during decoction is 90-100 ℃, the decoction time is 3-4 h, and the weight percentage of the lubricant in the liquorice particles is 0.5-1.0%; the concentration temperature is 65-85 ℃.
In some embodiments, the decoction comprises two times of decoction, wherein the weight ratio of the liquorice to water in the first decoction is 1: 8-8.5, and the decoction time is 2-2.5 hours; wherein the weight ratio of the liquorice to the water in the second decoction is 1: 6-6.5, and the decoction time is 1-1.5 h.
In some embodiments of the present invention, in the preparation method of the licorice granule, the filler is maltodextrin.
In some embodiments of the present invention, in the above method for preparing licorice granules, the lubricant is magnesium stearate.
In some embodiments of the method for preparing licorice granules provided by the present invention, the filtrate is left to stand for more than 3 hours and then concentrated.
In some embodiments, in the preparation method of the licorice granules, the weight ratio of licorice to water in the first decoction is 1: 8; the weight ratio of the liquorice to the water during the second decoction is 1: 6.
In some embodiments provided by the invention, the step of mixing the filler and the clear paste comprises the step of mixing the filler and the clear paste for 20-30 min and then drying to obtain dry paste powder, wherein the drying temperature is 175-185 ℃.
In some embodiments of the preparation method of the licorice granules provided by the invention, the equipment used for drying is a drying sprayer, the air outlet temperature of the drying sprayer is 85-95 ℃, and the negative pressure in a tower of the drying sprayer is-8 to-12 Pa.
In some embodiments provided by the invention, the preparation method of the licorice granules further comprises the following steps, the mesh number of the concentrated licorice granules is 180-200 meshes, the mesh number of the concentrated licorice granules obtained by mixing the filler and the clear paste is 80-100 meshes, and the mesh number of the dry paste powder is 80-100 meshes.
In another aspect, the present application provides a licorice granule prepared by the method for preparing a licorice granule described above.
The features and properties of the present invention are described in further detail below with reference to examples.
Example 1
The objective of this embodiment is to provide a licorice granule, the flow is shown in fig. 1, wherein the shaded square blocks represent the clean zone, i.e. the aseptic zone, and the unshaded square blocks represent the general working zone, comprising the following steps:
1.1 extraction and concentration:
carefully selecting impurity-free and high-quality liquorice pieces, accurately weighing 6000g of liquorice pieces, putting into an extraction tank, adding drinking water into the extraction tank, decocting twice, keeping the temperature of the water at 90-100 ℃ and decocting for 2 hours, wherein the mass of the drinking water added for the first time is 8 times of that of the liquorice pieces, heating the water in the extraction tank to boiling, and filtering the liquid medicine after the first decoction is finished to leave dregs of a decoction.
Adding drinking water 6 times the weight of the licorice decoction pieces into the dregs of a decoction, heating to boil, decocting for 1 hour, filtering out the liquid medicine of the second time after the second time of decoction is finished, combining the liquid medicine with the filtrate obtained by the first time of decoction, pumping the combined filtrate into a liquid medicine storage tank, and standing for more than 3-3.5 hours; filtering out supernatant obtained by standing, transferring into a vacuum concentration tank, operating according to the operating specification of the vacuum concentrator, opening a steam valve, vacuum concentrating to obtain fluid extract with relative density of 1.05-1.20 and temperature of 85 ℃, passing through a 180-mesh and 200-mesh sieve while hot to obtain Glycyrrhrizae radix fluid extract, and temporarily storing in a fluid extract storage tank.
1.2, preparing materials:
accurately weighing maltodextrin and licorice clear paste, wherein the mass ratio of the maltodextrin to the licorice clear paste is 2.5: 1, standby.
1.3 mixing:
gradually adding Glycyrrhrizae radix fluid extract and maltodextrin into spray dryer according to small amount, setting temperature at 180 deg.C, controlling air inlet temperature at 175 deg.C, air outlet temperature at 85 deg.C, and negative pressure at-8 Pa, mixing Glycyrrhrizae radix fluid extract and maltodextrin, stirring, collecting Glycyrrhrizae radix dry extract powder at regular time, pulverizing Glycyrrhrizae radix dry extract powder, sieving with 80 mesh sieve, adding appropriate amount of 0.5% magnesium stearate, placing in mixing tank, and mixing for 20-40 min.
1.4 dry granulation:
granulating dry licorice powder by using a dry granulator, sieving the dry licorice powder by 80-100 meshes, pouring the dry licorice powder onto the dry granulator, sieving coarse particles and fine particles by using 20-40 mesh sieves respectively, adding the coarse particles and the fine particles into the granulator again for granulation, and finally obtaining the licorice granules with the particle size of 20-40 meshes, uniform particle color, and the particle size of the granules which can not pass through the sum of a No. one sieve (10 meshes) and a No. five sieve (80 meshes) and can not exceed 15%, and warehousing after the examination is qualified.
1.5 particle:
and (4) inspecting the licorice granules obtained in the step (1.4), wherein the licorice granules are required to meet relevant regulations of quality standards of licorice formula granules, and the moisture, the granularity and the dissolubility are required to meet the regulations.
1.6, subpackaging:
and (4) subpackaging the licorice granules obtained in the step (1.4), taking a stainless steel measuring cup of a corresponding model according to the filling specification, and checking whether the measuring cup has a groove, a curled edge, a unfilled corner and abrasion. The filling is firstly carried out before filling, the filling amount difference of each measuring cup is checked, the filling amount is adjusted according to the weight of each bag, the operation is carried out according to the operation regulations of 'granule filling SOP' and granule subpackaging post, and the machine is started up formally (the production speed is 60-80 bags/min; the temperature of a longitudinal sealing roller is 100-210 ℃ and the temperature of a transverse sealing roller is 120-220 ℃) after meeting the requirements. The average bag weight was checked every 20 minutes after start-up. In the filling process, the filling amount difference and the sealing performance are controlled, and the sampling result is recorded, so that the filling amount of each bag is ensured to be in a control range. The bagged particles are put into a special container. Each bag contains 0.5g of raw medicinal materials, which is equivalent to 3 g. According to the standard operation rules of the outer packing posts, in the packing procedure, a small box is packed, a large box is packed, an anti-counterfeiting trademark is pasted, a batch number is covered, and an outer box is packed; placing a product certificate in the outer box, sealing with sealing tape, bundling firmly, sealing, and packaging into corrugated paper box.
Example 2
The objective of this embodiment is to provide a licorice granule, the flow is shown in fig. 1, wherein the shaded square blocks represent the clean zone, i.e. the aseptic zone, and the unshaded square blocks represent the general working zone, comprising the following steps:
1.1 extraction and concentration:
carefully selecting impurity-free and high-quality liquorice pieces, accurately weighing 6000g of liquorice pieces, putting into an extraction tank, adding drinking water into the extraction tank, decocting twice, keeping the temperature of the water at 90-100 ℃ and decocting for 2.5 hours, wherein the mass of the drinking water added for the first time is 8.4 times of that of the liquorice pieces, heating the water in the extraction tank to boil, and filtering the liquid medicine after the first decoction is finished to leave dregs.
Adding drinking water 6.2 times the weight of Glycyrrhrizae radix decoction pieces into the residue, heating to boil, decocting for 1 hr, filtering the second decoction, mixing with the first decoction, pumping the mixed filtrate into a medicinal liquid storage tank, standing for 3-3.5 hr or more; filtering out supernatant obtained by standing, transferring into a vacuum concentration tank, operating according to the operating specification of the vacuum concentrator, opening a steam valve, vacuum concentrating to obtain fluid extract with relative density of 1.05-1.20 and temperature of 70 ℃, passing through a 180-mesh and 200-mesh sieve while hot to obtain Glycyrrhrizae radix fluid extract, and temporarily storing in a fluid extract storage tank.
1.2, preparing materials:
accurately weighing maltodextrin and licorice clear paste, wherein the mass ratio of the maltodextrin to the licorice clear paste is 2.6: 1, standby.
1.3 mixing:
gradually adding the licorice root clear paste and maltodextrin into a traditional Chinese medicine clear paste spray dryer according to a small amount of times, setting the temperature at 180 ℃, controlling the air inlet temperature at 175-185 ℃, the air outlet temperature at 85-95 ℃, and setting the negative pressure in a tower at-8 to-12 Pa, fully mixing the licorice root clear paste and the maltodextrin, stirring, crushing the licorice root dry paste powder, sieving by a sieve of 80-100 meshes, adding a proper amount of 0.5 percent magnesium stearate, placing the mixture in a mixing tank, and mixing for 20-40 minutes.
1.4 dry granulation:
granulating dry licorice powder by using a dry granulator, sieving the dry licorice powder by 80-100 meshes, pouring the dry licorice powder onto the dry granulator, sieving coarse particles and fine particles by using 20-40 mesh sieves respectively, adding the coarse particles and the fine particles into the granulator again for granulation, and finally obtaining the licorice granules with the particle size of 20-40 meshes, uniform particle color, and the particle size of the granules which can not pass through the sum of a No. one sieve (10 meshes) and a No. five sieve (80 meshes) and can not exceed 15%, and warehousing after the examination is qualified.
1.5 particle:
and (4) inspecting the licorice granules obtained in the step (1.4), wherein the licorice granules are required to meet relevant regulations of quality standards of licorice formula granules, and the moisture, the granularity and the dissolubility are required to meet the regulations.
1.6, subpackaging:
and (4) subpackaging the licorice granules obtained in the step (1.4), taking a stainless steel measuring cup of a corresponding model according to the filling specification, and checking whether the measuring cup has a groove, a curled edge, a unfilled corner and abrasion. The filling is firstly carried out before filling, the filling amount difference of each measuring cup is checked, the filling amount is adjusted according to the weight of each bag, the operation is carried out according to the operation regulations of 'granule filling SOP' and granule subpackaging post, and the machine is started up formally (the production speed is 60-80 bags/min; the temperature of a longitudinal sealing roller is 100-210 ℃ and the temperature of a transverse sealing roller is 120-220 ℃) after meeting the requirements. The average bag weight was checked every 20 minutes after start-up. In the filling process, the filling amount difference and the sealing performance are controlled, and the sampling result is recorded, so that the filling amount of each bag is ensured to be in a control range. The bagged particles are put into a special container. Each bag contains 0.5g of raw medicinal materials, which is equivalent to 3 g. According to the standard operation rules of the outer packing posts, in the packing procedure, a small box is packed, a large box is packed, an anti-counterfeiting trademark is pasted, a batch number is covered, and an outer box is packed; placing a product certificate in the outer box, sealing with sealing tape, bundling firmly, sealing, and packaging into corrugated paper box.
Example 3
The objective of this embodiment is to provide a licorice granule, the flow is shown in fig. 1, wherein the shaded square blocks represent the clean zone, i.e. the aseptic zone, and the unshaded square blocks represent the general working zone, comprising the following steps:
1.1 extraction and concentration:
carefully selecting impurity-free and high-quality liquorice pieces, accurately weighing 6000g of liquorice pieces, putting into an extraction tank, adding drinking water into the extraction tank, decocting twice, keeping the temperature of the water at 90-100 ℃ and decocting for 2 hours, wherein the mass of the drinking water added for the first time is 8.2 times of that of the liquorice pieces, heating the water in the extraction tank to boil, and filtering the liquid medicine after the first decoction is finished to leave dregs of a decoction.
Adding drinking water 6.3 times the weight of the liquorice decoction pieces into the dregs of a decoction, heating to boil, decocting for 1 hour, filtering out the liquid medicine of the second time after the second time of decoction is finished, combining the liquid medicine with the filtrate obtained by the first time of decoction, pumping the combined filtrate into a liquid medicine storage tank, and standing for more than 3-3.5 hours; filtering out supernatant obtained by standing, transferring into a vacuum concentration tank, operating according to the operating specification of the vacuum concentrator, opening a steam valve, vacuum concentrating to obtain fluid extract with relative density of 1.08-1.20 and temperature of 80 ℃, passing through a 180-mesh and 200-mesh sieve while hot to obtain Glycyrrhrizae radix fluid extract, and temporarily storing in a fluid extract storage tank.
1.2, preparing materials:
accurately weighing maltodextrin and licorice clear paste, wherein the mass ratio of the maltodextrin to the licorice clear paste is 2.7: 1, standby.
1.3 Total mix (paste powder):
gradually adding the licorice root clear paste and maltodextrin into a traditional Chinese medicine clear paste spray dryer according to a small amount of times, setting the temperature at 180 ℃, controlling the air inlet temperature at 175-185 ℃, the air outlet temperature at 85-95 ℃, and setting the negative pressure in a tower at-8 to-12 Pa, fully mixing the licorice root clear paste and maltodextrin, stirring, collecting dry licorice root extract powder at regular time, crushing the dry licorice root extract powder, sieving by a sieve of 80-100 meshes, adding a proper amount of 0.5 percent of magnesium stearate, placing the mixture in a mixing tank, and mixing for 20-40 minutes.
1.4 dry granulation:
granulating dry licorice powder by using a dry granulator, sieving the dry licorice powder by 80-100 meshes, pouring the dry licorice powder onto the dry granulator, sieving coarse particles and fine particles by using 20-40 mesh sieves respectively, adding the coarse particles and the fine particles into the granulator again for granulation, and finally obtaining the licorice granules with the particle size of 20-40 meshes, uniform particle color, and the particle size of the granules which can not pass through the sum of a No. one sieve (10 meshes) and a No. five sieve (80 meshes) and can not exceed 15%, and warehousing after the examination is qualified.
1.5 particle:
and (4) inspecting the licorice granules obtained in the step (1.4), wherein the licorice granules are required to meet relevant regulations of quality standards of licorice formula granules, and the moisture, the granularity and the dissolubility are required to meet the regulations.
1.6, subpackaging:
and (4) subpackaging the licorice granules obtained in the step (1.4), taking a stainless steel measuring cup of a corresponding model according to the filling specification, and checking whether the measuring cup has a groove, a curled edge, a unfilled corner and abrasion. The filling is firstly carried out before filling, the filling amount difference of each measuring cup is checked, the filling amount is adjusted according to the weight of each bag, the operation is carried out according to the operation regulations of 'granule filling SOP' and granule subpackaging post, and the machine is started up formally (the production speed is 60-80 bags/min; the temperature of a longitudinal sealing roller is 100-210 ℃ and the temperature of a transverse sealing roller is 120-220 ℃) after meeting the requirements. The average bag weight was checked every 20 minutes after start-up. In the filling process, the filling amount difference and the sealing performance are controlled, and the sampling result is recorded, so that the filling amount of each bag is ensured to be in a control range. The bagged particles are put into a special container. Each bag contains 0.5g of raw medicinal materials, which is equivalent to 3 g. According to the standard operation rules of the outer packing posts, in the packing procedure, a small box is packed, a large box is packed, an anti-counterfeiting trademark is pasted, a batch number is covered, and an outer box is packed; placing a product certificate in the outer box, sealing with sealing tape, bundling firmly, sealing, and packaging into corrugated paper box.
Example 4
The objective of this embodiment is to provide a licorice granule, the flow is shown in fig. 1, wherein the shaded square blocks represent the clean zone, i.e. the aseptic zone, and the unshaded square blocks represent the general working zone, comprising the following steps:
1.1 extraction and concentration:
carefully selecting impurity-free and high-quality liquorice pieces, accurately weighing 6000g of liquorice pieces, putting into an extraction tank, adding drinking water into the extraction tank, decocting twice, keeping the temperature of the water at 90-100 ℃ and decocting for 2.5 hours, wherein the mass of the drinking water added for the first time is 8.3 times of that of the liquorice pieces, heating the water in the extraction tank to boil, and filtering the liquid medicine after the first decoction is finished to leave dregs.
Adding drinking water 6.5 times the weight of Glycyrrhrizae radix decoction pieces into the residue, heating to boil, decocting for 1 hr, filtering the second decoction, mixing with the first decoction, pumping the mixed filtrate into a medicinal liquid storage tank, standing for 3-3.5 hr or more; filtering out supernatant obtained by standing, transferring into a vacuum concentration tank, operating according to the operating specification of the vacuum concentrator, opening a steam valve, vacuum concentrating to obtain fluid extract with relative density of 1.08-1.20 and temperature of 60 ℃, passing through a 180-mesh and 200-mesh sieve while hot to obtain Glycyrrhrizae radix fluid extract, and temporarily storing in a fluid extract storage tank.
1.2, preparing materials:
accurately weighing maltodextrin and licorice clear paste, wherein the mass ratio of the maltodextrin to the licorice clear paste is 2.8: 1, standby.
1.3 Total mix (paste powder):
gradually adding the licorice root clear paste and maltodextrin into a traditional Chinese medicine clear paste spray dryer according to a small amount of times, setting the temperature at 180 ℃, controlling the air inlet temperature at 175-185 ℃, the air outlet temperature at 85-95 ℃, and setting the negative pressure in a tower at-8 to-12 Pa, fully mixing the licorice root clear paste and maltodextrin, stirring, collecting dry licorice root extract powder at regular time, crushing the dry licorice root extract powder, sieving by a sieve of 80-100 meshes, adding a proper amount of 0.5 percent of magnesium stearate, placing the mixture in a mixing tank, and mixing for 20-40 minutes.
1.4 granulating:
granulating dry licorice powder by using a dry granulator, sieving the dry licorice powder by 80-100 meshes, pouring the dry licorice powder onto the dry granulator, sieving coarse particles and fine particles by using 20-40 mesh sieves respectively, adding the coarse particles and the fine particles into the granulator again for granulation, and finally obtaining the licorice granules with the particle size of 20-40 meshes, uniform particle color, and the particle size of the granules which can not pass through the sum of a No. one sieve (10 meshes) and a No. five sieve (80 meshes) and can not exceed 15%, and warehousing after the examination is qualified.
1.5 particle:
and (4) inspecting the licorice granules obtained in the step (1.4), wherein the licorice granules are required to meet relevant regulations of quality standards of licorice formula granules, and the moisture, the granularity and the dissolubility are required to meet the regulations.
1.6, subpackaging:
and (4) subpackaging the licorice granules obtained in the step (1.4), taking a stainless steel measuring cup of a corresponding model according to the filling specification, and checking whether the measuring cup has a groove, a curled edge, a unfilled corner and abrasion. The filling is firstly carried out before filling, the filling amount difference of each measuring cup is checked, the filling amount is adjusted according to the weight of each bag, the operation is carried out according to the operation regulations of 'granule filling SOP' and granule subpackaging post, and the machine is started up formally (the production speed is 60-80 bags/min; the temperature of a longitudinal sealing roller is 100-210 ℃ and the temperature of a transverse sealing roller is 120-220 ℃) after meeting the requirements. The average bag weight was checked every 20 minutes after start-up. In the filling process, the filling amount difference and the sealing performance are controlled, and the sampling result is recorded, so that the filling amount of each bag is ensured to be in a control range. The bagged particles are put into a special container. Each bag contains 0.5g of raw medicinal materials, which is equivalent to 3 g. According to the standard operation rules of the outer packing posts, in the packing procedure, a small box is packed, a large box is packed, an anti-counterfeiting trademark is pasted, a batch number is covered, and an outer box is packed; placing a product certificate in the outer box, sealing with sealing tape, bundling firmly, sealing, and packaging into corrugated paper box.
Example 5
The objective of this embodiment is to provide a licorice granule, the flow is shown in fig. 1, wherein the shaded square blocks represent the clean zone, i.e. the aseptic zone, and the unshaded square blocks represent the general working zone, comprising the following steps:
1.1 extraction and concentration:
carefully selecting impurity-free and high-quality liquorice pieces, accurately weighing 6000g of liquorice pieces, putting into an extraction tank, adding drinking water into the extraction tank, decocting twice, keeping the temperature of the water at 90-100 ℃ and decocting for 2 hours, wherein the mass of the drinking water added for the first time is 8.2 times of that of the liquorice pieces, heating the water in the extraction tank to boil, and filtering the liquid medicine after the first decoction is finished to leave dregs of a decoction.
Adding drinking water 6.4 times the weight of the liquorice decoction pieces into the dregs of a decoction, heating to boil, decocting for 1 hour, filtering out the liquid medicine of the second time after the second time of decoction is finished, combining the liquid medicine with the filtrate obtained by the first time of decoction, pumping the combined filtrate into a liquid medicine storage tank, and standing for more than 3-3.5 hours; filtering out supernatant obtained by standing, transferring into a vacuum concentration tank, operating according to the operating specification of the vacuum concentrator, opening a steam valve, vacuum concentrating to obtain fluid extract with relative density of 1.08-1.20 and temperature of 80 ℃, passing through a 180-mesh and 200-mesh sieve while hot to obtain Glycyrrhrizae radix fluid extract, and temporarily storing in a fluid extract storage tank.
1.2, preparing materials:
accurately weighing maltodextrin and licorice clear paste, wherein the mass ratio of the maltodextrin to the licorice clear paste is 2.9: 1, standby.
1.3 Total mix (paste powder):
gradually adding the licorice root clear paste and maltodextrin into a traditional Chinese medicine clear paste spray dryer according to a small amount of times, setting the temperature at 180 ℃, controlling the air inlet temperature at 175-185 ℃, the air outlet temperature at 85-95 ℃, and setting the negative pressure in a tower at-8 to-12 Pa, fully mixing the licorice root clear paste and maltodextrin, stirring, collecting dry licorice root extract powder at regular time, crushing the dry licorice root extract powder, sieving by a sieve of 80-100 meshes, adding a proper amount of 0.5 percent of magnesium stearate, placing the mixture in a mixing tank, and mixing for 20-40 minutes.
1.4 dry granulation:
granulating dry licorice powder by using a dry granulator, sieving the dry licorice powder by 80-100 meshes, pouring the dry licorice powder onto the dry granulator, sieving coarse particles and fine particles by using 20-40 mesh sieves respectively, adding the coarse particles and the fine particles into the granulator again for granulation, finally obtaining particles with the particle size of 20-40 meshes, wherein the particles are uniform in color and luster, checking the particle size of the particles, and determining the particles to be the licorice particles after the particles are qualified by checking, wherein the particles cannot pass through the sum of the first sieve and the fifth sieve and cannot exceed 15%.
1.5 particle:
and (4) inspecting the licorice granules obtained in the step (1.4), wherein the licorice granules are required to meet relevant regulations of quality standards of licorice formula granules, and the moisture, the granularity and the dissolubility are required to meet the regulations.
1.6, subpackaging:
and (4) subpackaging the licorice granules obtained in the step (1.4), taking a stainless steel measuring cup of a corresponding model according to the filling specification, and checking whether the measuring cup has a groove, a curled edge, a unfilled corner and abrasion. The filling is firstly carried out before filling, the filling amount difference of each measuring cup is checked, the filling amount is adjusted according to the weight of each bag, the operation is carried out according to the operation regulations of 'granule filling SOP' and granule subpackaging post, and the machine is started up formally (the production speed is 60-80 bags/min; the temperature of a longitudinal sealing roller is 100-210 ℃ and the temperature of a transverse sealing roller is 120-220 ℃) after meeting the requirements. The average bag weight was checked every 20 minutes after start-up. In the filling process, the filling amount difference and the sealing performance are controlled, and the sampling result is recorded, so that the filling amount of each bag is ensured to be in a control range. The bagged particles are put into a special container. Each bag contains 0.5g of raw medicinal materials, which is equivalent to 3 g. According to the standard operation rules of the outer packing posts, in the packing procedure, a small box is packed, a large box is packed, an anti-counterfeiting trademark is pasted, a batch number is covered, and an outer box is packed; placing a product certificate in the outer box, sealing with sealing tape, bundling firmly, sealing, and packaging into corrugated paper box.
Example 6
The objective of this embodiment is to provide a licorice granule, the flow is shown in fig. 1, wherein the shaded square blocks represent the clean zone, i.e. the aseptic zone, and the unshaded square blocks represent the general working zone, comprising the following steps:
1.1 extraction and concentration:
carefully selecting impurity-free and high-quality liquorice pieces, accurately weighing 6000g of liquorice pieces, putting into an extraction tank, adding drinking water into the extraction tank, decocting twice, keeping the temperature of the water at 90-100 ℃ and decocting for 2.5 hours, heating the water in the extraction tank to boil, and filtering the liquid medicine after the first decoction to leave dregs.
Adding drinking water 6.5 times the weight of Glycyrrhrizae radix decoction pieces into the residue, heating to boil, decocting for 1 hr, filtering the second decoction, mixing with the first decoction, pumping the mixed filtrate into a medicinal liquid storage tank, standing for 3-3.5 hr or more; filtering out supernatant obtained by standing, transferring into a vacuum concentration tank, operating according to the operating specification of the vacuum concentrator, opening a steam valve, vacuum concentrating to obtain fluid extract with relative density of 1.08-1.20 and temperature of 70 ℃, passing through a 180-mesh and 200-mesh sieve while hot to obtain Glycyrrhrizae radix fluid extract, and temporarily storing in a fluid extract storage tank.
1.2, preparing materials:
accurately weighing maltodextrin and licorice clear paste, wherein the mass ratio of the maltodextrin to the licorice clear paste is 2.7: 1, standby.
1.3 Total mix (paste powder):
gradually adding the licorice root clear paste and maltodextrin into a traditional Chinese medicine clear paste spray dryer according to a small amount of times, setting the temperature at 180 ℃, controlling the air inlet temperature at 175-185 ℃, the air outlet temperature at 85-95 ℃, and setting the negative pressure in a tower at-8 to-12 Pa, fully mixing the licorice root clear paste and maltodextrin, stirring, collecting dry licorice root extract powder at regular time, crushing the dry licorice root extract powder, sieving the crushed dry licorice root extract powder by a sieve of 80-100 meshes, and placing the powder in a mixing tank for mixing for 20-30 minutes.
1.4 dry granulation:
granulating dry licorice powder by using a dry granulator, sieving the dry licorice powder by 80-100 meshes, pouring the dry licorice powder onto the dry granulator, sieving coarse particles and fine particles by using 20-40 mesh sieves respectively, adding the coarse particles and the fine particles into the granulator again for granulation, and finally obtaining the licorice granules with the particle size of 20-40 meshes, uniform particle color, and the particle size of the granules which can not pass through the sum of a No. one sieve (10 meshes) and a No. five sieve (80 meshes) and can not exceed 15%, and warehousing after the examination is qualified.
1.5 particle:
and (4) inspecting the licorice granules obtained in the step (1.4), wherein the licorice granules are required to meet relevant regulations of quality standards of licorice formula granules, and the moisture, the granularity and the dissolubility are required to meet the regulations.
1.6, subpackaging:
and (4) subpackaging the licorice granules obtained in the step (1.4), taking a stainless steel measuring cup of a corresponding model according to the filling specification, and checking whether the measuring cup has a groove, a curled edge, a unfilled corner and abrasion. The filling is firstly carried out before filling, the filling amount difference of each measuring cup is checked, the filling amount is adjusted according to the weight of each bag, the operation is carried out according to the operation regulations of 'granule filling SOP' and granule subpackaging post, and the machine is started up formally (the production speed is 60-80 bags/min; the temperature of a longitudinal sealing roller is 100-210 ℃ and the temperature of a transverse sealing roller is 120-220 ℃) after meeting the requirements. The average bag weight was checked every 20 minutes after start-up. In the filling process, the filling amount difference and the sealing performance are controlled, and the sampling result is recorded, so that the filling amount of each bag is ensured to be in a control range. The bagged particles are put into a special container. Each bag contains 0.5g of raw medicinal materials, which is equivalent to 3 g. According to the standard operation rules of the outer packing posts, in the packing procedure, a small box is packed, a large box is packed, an anti-counterfeiting trademark is pasted, a batch number is covered, and an outer box is packed; placing a product certificate in the outer box, sealing with sealing tape, bundling firmly, sealing, and packaging into corrugated paper box.
The drying temperatures in examples 1 to 6 were set at 180 ℃ and the temperatures were set at 175 to 185 ℃, preferably 180 ℃. In the preliminary test, 3g, 5g and 8g of liquorice formula granules with drying temperatures of 175 ℃, 180 ℃ and 185 ℃ respectively are taken, the moisture content of the granules is measured by a moisture measuring instrument, and the moisture content condition of the granules is recorded. The test results are shown in Table 1, which shows that the water content of the granules is 5-6% at a drying temperature of 180 ℃, the fluctuation is minimal, and the licorice formulation granules can be well stored. The drying temperature was thus determined to be 180 ℃.
TABLE 1 moisture content fluctuation of the granulate
Performing sensory identification on the licorice granules provided in the embodiments 1 to 6, wherein the licorice granules are light brown yellow granules with uniform color and size; slightly fragrant smell and sweet taste. Liquid chromatography detection shows that the licorice particles provided by the embodiment of the invention contain a large amount of beneficial components such as glycyrrhizic acid and liquiritin, wherein the glycyrrhizic acid is between 2.60% and 2.69%, and the liquiritin is between 1.80% and 1.93%, compared with the glycyrrhizic acid content of 2.32% to 2.38% and the liquiritin content of 1.81% to 1.87% in the original decoction piece decoction, the liquiritin component contained in the licorice particles is equivalent to the liquiritin beneficial component in the original decoction piece, and the glycyrrhizic acid component is slightly higher than the glycyrrhizic acid content in the original decoction piece, which is shown in table 2 specifically.
TABLE 2 comparison of glycyrrhizic acid and glycyrrhizin in Licorice decoction pieces and Licorice granule
In summary, according to the preparation method of licorice granules provided by the embodiment of the present invention, through specific extraction and concentration processes, beneficial ingredients in licorice are fully retained, raw materials are more uniformly mixed by a high-speed mixing granulator, and then the concentrated fluid extract is dried and granulated by using a dry spraying method, so that unqualified granules with wide granules are greatly reduced, and the yield is improved. Compared with the traditional Chinese medicine decoction, the liquorice particles prepared by the preparation method of the liquorice particles provided by the invention not only save the decoction time of medicinal materials, but also keep the property of the original medicinal materials, are convenient to carry and can be eaten at any time, and the dosage of a large amount of beneficial components is smaller, so that the liquorice particles are more suitable for the fast-paced life of modern people.
The embodiments described above are some, but not all embodiments of the invention. The detailed description of the embodiments of the present invention is not intended to limit the scope of the invention as claimed, but is merely representative of selected embodiments of the invention. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Claims (10)
1. The preparation method of the liquorice particles is characterized by comprising the following steps: concentrating the decoction filtrate of Glycyrrhrizae radix to relative density of 1.05-1.20, and collecting fluid extract; mixing the filler and the clear paste according to a ratio of 2.5-3.0: 1, adding a lubricant, and granulating to obtain the licorice granules; the weight ratio of the liquorice to water during decoction is 1: 14-15, the temperature during decoction is 90-100 ℃, the decoction time is 3-4 h, and the weight percentage of the lubricant in the liquorice particles is 0.5-1.0%; the concentration temperature is 65-85 ℃.
2. The preparation method of licorice granules according to claim 1, wherein the decoction comprises two times of decoction, wherein the weight ratio of licorice to water in the first time of decoction is 1: 8-8.5, and the decoction time is 2-2.5 hours; wherein the weight ratio of the liquorice to the water in the second decoction is 1: 6-6.5, and the decoction time is 1-1.5 h.
3. The method for preparing licorice granules according to claim 1 or 2, wherein the filler is maltodextrin.
4. The method for preparing licorice granules according to claim 1 or 2, wherein the lubricant is magnesium stearate.
5. The method for preparing licorice particles according to claim 1 or 2, wherein the filtrate is concentrated after standing for 3 hours or more.
6. The method for preparing licorice granules according to claim 2, wherein the weight ratio of licorice to water in the first decoction is 1: 8; the weight ratio of the liquorice to the water during the second decoction is 1: 6.
7. The preparation method of the licorice granule according to claim 1 or 2, wherein the mixing of the filler and the fluid extract comprises the step of mixing the filler and the fluid extract for 20-30 min and then drying the mixture to obtain dry paste powder, wherein the drying temperature is 175-185 ℃.
8. The method for preparing licorice granules according to claim 7, wherein the equipment used for drying is a drying sprayer, the air outlet temperature of the drying sprayer is 85-95 ℃, and the negative pressure in the tower of the drying sprayer is-8 to-12 Pa.
9. The method for preparing licorice granules according to claim 7, further comprising the step of sieving the concentrated licorice granules to 180 to 200 meshes, sieving the concentrated licorice granules to 80 to 100 meshes after mixing the filler and the fluid extract, and sieving the dry extract powder to 80 to 100 meshes.
10. A licorice granule produced by the method for producing a licorice granule according to any one of claims 1 to 9.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011345508.7A CN112402484A (en) | 2020-11-25 | 2020-11-25 | Preparation method of liquorice particles and liquorice particles prepared by same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011345508.7A CN112402484A (en) | 2020-11-25 | 2020-11-25 | Preparation method of liquorice particles and liquorice particles prepared by same |
Publications (1)
Publication Number | Publication Date |
---|---|
CN112402484A true CN112402484A (en) | 2021-02-26 |
Family
ID=74843568
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202011345508.7A Pending CN112402484A (en) | 2020-11-25 | 2020-11-25 | Preparation method of liquorice particles and liquorice particles prepared by same |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN112402484A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113332248A (en) * | 2021-06-02 | 2021-09-03 | 祈蒙股份有限公司 | Kaempferia galanga composition particles and preparation process thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104280360A (en) * | 2014-09-26 | 2015-01-14 | 广东一方制药有限公司 | Preparation and quality control method of liquorice formula granules |
CN105412212A (en) * | 2015-12-04 | 2016-03-23 | 安徽腾博中药饮片有限公司 | Preparation method of licorice formula granules |
CN105998165A (en) * | 2016-07-20 | 2016-10-12 | 四川康而好动物药业有限公司 | Preparation method of licorice granules |
CN109568383A (en) * | 2018-08-14 | 2019-04-05 | 广东方制药有限公司 | A kind of preparation method of Radix Glycyrrhizae or honey-fried licorice root dispensing granule |
-
2020
- 2020-11-25 CN CN202011345508.7A patent/CN112402484A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104280360A (en) * | 2014-09-26 | 2015-01-14 | 广东一方制药有限公司 | Preparation and quality control method of liquorice formula granules |
CN105412212A (en) * | 2015-12-04 | 2016-03-23 | 安徽腾博中药饮片有限公司 | Preparation method of licorice formula granules |
CN105998165A (en) * | 2016-07-20 | 2016-10-12 | 四川康而好动物药业有限公司 | Preparation method of licorice granules |
CN109568383A (en) * | 2018-08-14 | 2019-04-05 | 广东方制药有限公司 | A kind of preparation method of Radix Glycyrrhizae or honey-fried licorice root dispensing granule |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113332248A (en) * | 2021-06-02 | 2021-09-03 | 祈蒙股份有限公司 | Kaempferia galanga composition particles and preparation process thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1788783A (en) | Granule containing ginseng ,Siberian cocklebur ,lagehead atractylodes and its preparation method | |
CN107712533A (en) | A kind of Traditional Chinese Herb micro-crystal powder | |
CN107875393A (en) | A kind of lozenge flavouring and preparation method thereof | |
CN114600989A (en) | Instant tea composition and preparation method thereof | |
CN106578089A (en) | Ginger, milk and tea electuary and making method thereof | |
CN112402484A (en) | Preparation method of liquorice particles and liquorice particles prepared by same | |
CN1742870A (en) | Kuntai tablet preparation and preparation thereof | |
CN105796924A (en) | Officinal Dendrobium Stem granules and preparation method thereof | |
CN111346206A (en) | Perilla frutescens, ginger and ginseng tea and preparation method thereof | |
CN103356815B (en) | Forming method of granules for regulating qi and reducing phlegm | |
CN105343723B (en) | A kind of preparation method of the remote cough-relieving micro-capsule of tangerine | |
CN101317983A (en) | Method for preparing capsule for nourishing Yin and suppressing Yang, discharging fire and pacifying the mind | |
CN101317951A (en) | Method for preparing capsule for reinforcing body fluid and nourish the blood, clearing hot, tonifying heart and pacifying the mind | |
CN100490868C (en) | Preparing method of coated Tongshu tablet | |
WO2020119255A1 (en) | Dioscorea alata formula granules and preparation method therefor | |
CN109528825A (en) | A kind of salvia bowleyana Dunn granule and preparation method thereof with activating microcirculation and removing stasis medicinal and menstruction regulating and pain relieving | |
CN109985159A (en) | A kind of infantile lung heat cough and asthma oral gel of fruity and preparation method thereof | |
CN103798462A (en) | Health-care tea for nourishing heart and soothing nerves | |
CN106511667A (en) | Pills capable of promoting dispersing function of lungs | |
CN115919988B (en) | Preparation method of thrombolytic and vein relaxing tablet | |
CN107890519A (en) | A kind of dendrobium candidum soft capsule and preparation method thereof | |
CN1070575A (en) | The processing method of American ginseng fruit tea | |
CN115779033A (en) | Qi-tonifying and nerve-soothing tablet and preparation method thereof | |
CN116650601A (en) | Preparation method of concentrated tuberculosis pill | |
CN114304332A (en) | Sperm-nourishing and refreshing goldthread root tea and preparation process thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20210226 |