CN1706417A - Prepn process and quality control technology of decoction of bupleurum root for regulating Shaoyang - Google Patents
Prepn process and quality control technology of decoction of bupleurum root for regulating Shaoyang Download PDFInfo
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Abstract
The present invention is preparation process and quality control technology of oral decoction liquid of bupleurum root for regulating Shaoyang. The recipe includes seven kinds of Chinese medicinal materials of bupleurum root, skullcap root, pinellia tuber, ginseng, ginger, licorice, etc; and the preparation process includes the steps of: soaking the materials in water and repeated distillation to collect the distillate; decocting the residue and merging decoction; cooling to room temperature, filtering, alcohol precipitation and recovering alcohol; merging the distillate and the concentrated liquid; adding proper amount of preservative, sweetener and water; filtering and sterilizing. The quality control includes the identification and content test of the effect components. The oral decoction liquid is superior to available corresponding decoction with taking inconvenience, lower bioavailability and inaccurate dosage.
Description
Technical field
The invention belongs to a kind of Chinese medicinal preparation method and Quality Control Technology thereof.
Background technology
Herba Sidae Rhombifoliae soup comes from Eastern Han Dynasty's Zhang Zhongjing treatise on Febrile Diseases, form by Radix Bupleuri, Radix Scutellariae, the Rhizoma Pinelliae, Radix Ginseng, Rhizoma Zingiberis Recens, Radix Glycyrrhizae seven flavor Chinese medicines, be first-selected side's medicine of traditional medicine treating SHAO YANG disease by mediation after the appearance, cure mainly alternate attack of chill and fever, feeling of fullness and disecomfort in the chest and hypochondrium, reluctant to speak and eat, vexation and vomiting, bitter taste in the mouth and dry throat, disease such as dizzy.
Mechanism of action by Herba Sidae Rhombifoliae soup carries out systematic study, proved that now we have steroid sample, on-steroidal sample antiinflammatory action, immunological enhancement due to hypophysis one hypothalamic pituitary adrenal axis promotion and activating macrophage and the T lymphocyte, and can directly act on liver, make liver avoid damage and the regeneration of stimulation hepatic tissue, suppress hepatic fibrosis and form.
The Japan and the Herba Sidae Rhombifoliae soup extract powder of the clinical usefulness of Chinese medicine or make granule in Japan owing to determined curative effect, by extensively differential diagnosis of diseases use, discover that simultaneously Herba Sidae Rhombifoliae soup can suppress 70% patient's AIDS reverse transcriptase (RT) activity, suppress the generation of RCE2 and peroxide, duplicating of HIV can also be suppressed indirectly, and the toxicity of AZT can be alleviated.But in China, Herba Sidae Rhombifoliae soup cuts apart with a knife or scissors prescription by the traditional Chinese medical scienceization usually, and medicinal liquid is taken in patient oneself decoction of making up a prescription, and is very inconvenient, influenced the use of Herba Sidae Rhombifoliae soup.In addition, the class Herba Sidae Rhombifoliae soup preparation that is changed into Radix Codonopsis by Radix Ginseng is arranged, as little Radix Bupleuri sheet, little bupleurum particles, but preparation technology all has unreasonable part, does not also have quantitative method of quality control.
Summary of the invention
The purpose of this invention is to provide a kind of preparation method of Herba Sidae Rhombifoliae soup oral liquid, Herba Sidae Rhombifoliae soup is made oral liquid, determined curative effect, taking convenience, quality controllable, benefit extensive patients.This method is on Herba Sidae Rhombifoliae soup is write out a prescription each medicine basic research, and the integrated oral liquid dosage form requires research to form.
The prescription of Herba Sidae Rhombifoliae soup is formed:
Radix Bupleuri 180g Radix Ginseng 90g Radix Scutellariae 135g
Rhizoma Pinelliae (processed with Rhizoma Zingiberis Recens) 135g Rhizoma Zingiberis Recens 135g Radix Glycyrrhizae Preparata 75g
Fructus Jujubae 195g
The preparation method of Herba Sidae Rhombifoliae soup oral liquid, contain Radix Bupleuri, Radix Scutellariae, the Rhizoma Pinelliae, Radix Ginseng, Rhizoma Zingiberis Recens, Radix Glycyrrhizae seven flavor Chinese medicines in its raw material prescription, be characterised in that may further comprise the steps: get each medicine of prescription and add water and flood distill repeatedly in right amount, collect distillate, sealing cold preservation is standby; Medicinal liquid filters; Medicinal residues add water decoct in right amount medicinal liquid, filter; Merge medicinal liquid and concentrate, be chilled to room temperature and filter, precipitate with ethanol, alcohol precipitation concentration 35%～55% filters, filtrate recycling ethanol, concentrated solution and distillate merge, and add an amount of antiseptic and sweeting agent, and mixing adds water move to full dose, filters, sterilization, promptly.
The preparation method of described Herba Sidae Rhombifoliae soup oral liquid is characterized in that each medicine of prescription adds 6～10 times of amount dippings of water 1～2 hour, distills 2～3 times, each 1～2 hour, collects distillate, sealing; Cold preservation is standby; Medicinal liquid filters, and merges; Medicinal residues add an amount of decoction of water 0.5～1 hour again, filter; Merge medicinal liquid, be concentrated into relative density 1.05～1.08 (50 ℃ of heat are surveyed), be chilled to room temperature, filter, precipitate with ethanol, alcohol precipitation concentration 35%, cold preservation 12～24 hours, supernatant is centrifugal, coarse filtration, fine straining, filtrate recycling ethanol concentrated solution and distillate merge, and add 0.2%～1.0% antiseptic and sweeting agent, mixing, adjust pH adds water move to full dose, filters, sterilization, packing, promptly; Antiseptic is a sodium benzoate, and sweeting agent is stevioside or stevioside and Mel; Regulate pH value 0.1mol/L sodium hydroxide or dilute hydrochloric acid.
Alcohol precipitation concentration is defined as 35%～55% through baicalin, saikoside, polysaccharide, the multifactor analysis-by-synthesis of filtering velocity in the technology of the present invention, so both can save a large amount of solvents and man-hour, can avoid the loss of active substance such as Saponin, polysaccharide etc. again.
Pharmacological testing
Studies show that the Herba Sidae Rhombifoliae soup oral liquid the same with former side have antiinflammatory, analgesic, protect the liver and the enhance immunity effect.In addition, Herba Sidae Rhombifoliae soup has stronger inhibitory action to HIV (human immunodeficiency virus), and the infected's lymphocyte, helper T cell and natural killer cell all are significantly increased.
Toxicological test
Medicine of the present invention calculates LD through carrying out acute toxicity testing with Kunming mouse
50＞1320g/Kg, give this product two months continuously, the general state of large and small dosage group rat, body weight gain rate, tip hemogram, serology and hepatic and renal function situation are all similar to matched group, there was no significant difference (P＞0.05), vitals histological examination no abnormality seens such as the heart, liver, spleen, lung, kidney.Above-mentioned animal long term toxicity test result confirms that further this product has the safety same with former side.
Clinical research
420 routine shaoyang disease patients are divided into Herba Sidae Rhombifoliae soup oral liquid test group 300 examples at random, after Herba Sidae Rhombifoliae soup decoction matched group 120 examples are carried out clinical research, the result shows: (1) test group obvious effective rate is 59.33%, total effective rate is 95.67%, the matched group obvious effective rate is 40%, total effective rate is 92.5%, compare total effective rate there was no significant difference ((P＞0.05) for two groups, but the test group obvious effective rate is higher than decoction, there were significant differences (P＜0.05), illustrate that the Herba Sidae Rhombifoliae soup oral liquid has the therapeutic efficiency identical with Herba Sidae Rhombifoliae soup, especially evident in efficacy to flu shaoyang disease type person.(2) this clinical observation 420 routine shaoyang disease patients, the sick kind in the multiple diseases such as being distributed in flu, hypochondriac pain, dizzy, melancholia, gastric abscess, vomiting, stranguria, hysteria, disease disease, no matter the Herba Sidae Rhombifoliae soup oral liquid is described, still miscellaneous diseases caused by endogenous pathogens is seen there is the shaoyang disease person all has wide practical value to exogenous diseases.(3) the Herba Sidae Rhombifoliae soup oral liquid not only to infectious, febrile disease curative effect the best, can reach higher obvious effective rate (72.39%) and total effective rate (98.68%) in the course of treatment; And diseases such as chronic liver and gall diseases, chronic gastritis, psychoneurosis also there is curative effect preferably.
The Herba Sidae Rhombifoliae soup extract powder of medicine of the present invention and Japan and the clinical usefulness of Chinese medicine is carried out effective ingredient relatively, and the result shows both composition basically identicals; Compare with former side's decoction, it is basic identical with decoction that the oral liquid that is made by this technology contains active component (as ether soluble components, Saponin class and flavones ingredient etc.), but amount is higher than the fried liquid of decoction, and have effective ingredient availability height, dosage is accurate, taking convenience, steady quality and be easy to advantages such as control.
More than every result of study show, the Herba Sidae Rhombifoliae soup oral liquid has not only kept former side's effect and the material base that plays a role, and overcome former side's decoction and take shortcomings such as inconvenience, crude drug effective ingredient availability is low, effective dose is inaccurate, suitable tcm clinical practice is promoted the use of.
The specific embodiment:
Example 1:
| Prescription is formed: | |||||
| Radix Bupleuri Rhizoma Pinelliae (processed with Rhizoma Zingiberis Recens) Fructus Jujubae | ??180g ??135g ??195g | Ginseng ginger | ??90g ??135g | The Radix Scutellariae Radix Glycyrrhizae Preparata | ??135g ??75g |
| Make 1000ml | |||||
Method for making:
Get each medicine of prescription that meets a regulation of Chinese Pharmacopoeia current edition, add 8 times of water gaging dippings 1 hour, distillation twice, each 1 hour, collect distillate, sealing, cold preservation is standby; Medicinal liquid filters, and medicinal residues add 4 times of water gagings again and decoct half an hour, filter, and merge medicinal liquid, be concentrated into relative density 1.05～1.08 (50 ℃ of heat are surveyed), be chilled to room temperature, filter precipitate with ethanol, alcohol precipitation concentration 35%, cold preservation 24 hours filters, merge with distillate behind the filtrate recycling ethanol, add 0.3% antiseptic and 0.5% stevioside, mixing, adjust pH is about 5.5, adds water move to full dose, filters, sterilization, packing, promptly.
Herba Sidae Rhombifoliae soup oral liquid character is brownish red or brown liquid, feeble QI perfume (or spice), and the sweet little hardship of distinguishing the flavor of, carry out the quality control of each component by following method:
1.1 differentiate
1.1.1 ginseng effective component ginsenoside
Get [1.3 assay] " Radix Bupleuri " item water elution liquid 150ml down, water-bath is concentrated into 30ml, filters, and uses water saturation n-butanol extraction 3 times, each 10ml.Leave standstill, layering divides and gets n-butyl alcohol liquid, evaporate to dryness; Residue adds methanol 1ml makes dissolving, moves in the 10ml centrifuge tube and waves most methanol in 80 ℃ of water-baths, adds water saturated n-butyl alcohol 0.5ml jolting and makes dissolving, adds 5% sodium hydroxide 1ml of saturated n-butyl alcohol again, shake up, and standing demix, upper strata liquid is as need testing solution; Other gets the Ginsenoside Rb
1, Rg
1, the Re reference substance, add methanol and make the solution that every 1ml contains 1mg, in contrast product solution; Test according to thin layer chromatography (an appendix VI of Chinese Pharmacopoeia version in 2000 B), draw need testing solution 10 μ l, each 5 μ l of reference substance solution put respectively on the efficient lamellae of same silica gel G, are developing solvent with the subnatant of chloroform-methanol-water (65: 35: 10), launch, take out, hot blast drying, spray is with 10% ethanol solution of sulfuric acid, in 110～120 ℃ of heating colour developing in several minutes, inspect under the daylight; In the test sample chromatograph with the corresponding position of reference substance chromatograph on, show the speckle of same color;
1.1.2 Radix Glycyrrhizae active ingredient glycyrrhizin
Get [1.3 assay] " Radix Bupleuri " 5% sodium hydroxide solution of telling down, thin up moves into separatory funnel to 30ml, add dilute hydrochloric acid and regulate pH value to 4～5, add water saturated ethyl acetate extraction 2 times, each 10ml, leave standstill, layering discards the ethyl acetate layer, add water saturated n-butanol extraction 3 times again, each 10ml, standing demix, tell n-butyl alcohol liquid, merge, put evaporate to dryness in the water-bath, residue adds methanol 1ml makes dissolving, as need testing solution; In addition extracting liquorice control medicinal material 1g adds little the boiling of water and extracts 2 times, each 50ml, 30 minutes, filter, filtrate merges, and puts and is concentrated into 15ml in the water-bath, add ethanol 15ml, shake up, left standstill 12 hours, filter, filtrate is put and is flung to ethanol in the water-bath, adds an amount of stirring and dissolving of water and is diluted to 25ml, filters, filtrate moves into separatory funnel, rises from " adding water saturated ethyl acetate extraction 2 times ... " to be equipped with control medicinal material solution with legal system; Test according to thin layer chromatography (an appendix VI of Chinese Pharmacopoeia version in 2000 B), draw each 10 μ l of need testing solution and control medicinal material solution, put respectively on the efficient lamellae of same silica gel G, with chloroform-n-amyl alcohol-methanol-n-butyl alcohol-acetic acid-water (60: 36: 22: 9: 4: 2) is developing solvent, launch, take out, hot blast drying, spray is with 10% ethanol solution of sulfuric acid, it is clear that hot blast is heated to the speckle colour developing, inspects under the daylight, in the test sample chromatograph, with the corresponding position of control medicinal material chromatograph on, show the speckle of same color;
1.2 check
Relative density should be not less than 1.05 (appendix of Chinese Pharmacopoeia version in 2000);
PH value 3.5～6.5 (appendix of Chinese Pharmacopoeia version in 2000);
1.3 assay
The every 1ml of Radix Scutellariae this product contains Radix Scutellariae with baicalin C
21H
18O
8Meter should be no less than 2.5mg;
Accurate this product 1ml that draws adds methanol 1ml, shakes up centrifugal 10 minutes (3000 rev/mins) in back, takes out, and draws supernatant 0.5ml, puts in the 1ml volumetric flask, adds 50% methanol and is diluted to scale as need testing solution.Other gets the baicalin reference substance, adds methanol and makes the solution that every 1ml contains about 1mg, in contrast product solution; Test according to thin layer chromatography (an appendix VI of Chinese Pharmacopoeia version in 2000 B), draw need testing solution 2 μ l, 3 μ l, reference substance solution 2 μ l, 3 μ l, the cross point is on the efficient lamellae of same silica gel G respectively, with n-amyl alcohol-methanol-formic acid-water (7: 2: 1: 1) be developing solvent, launch, exhibition is taken out apart from about 10cm, hot blast drying, 110 ℃ of heating 30 minutes, scan wavelength according to chromatography (57 pages of thin layer chromatography scannings of appendix): λ again
S=280nm, λ
R=207nm measures test sample trap integrated value and reference substance trap integrated value, calculates promptly;
The every 1ml of Radix Bupleuri this product contains Radix Bupleuri with saikoside a (d) C
42H
66O
13Meter should be no less than 0.1mg;
The accurate reference substance solution 20 of drawing of the preparation of reference substance solution, 40,50,60,80,100 μ l, put respectively in the 10ml tool plug test tube, put in 70 ℃ of water-baths and wave most solvent, add 1% paradime thylaminobenzaldehyde alcoholic solution 0.1ml, jump a queue but stay seam, in 70 ℃ of heating in water bath 10 minutes, the flowing water cooling added phosphoric acid 5ml, shake up after jumping a queue, in 70 ℃ of heating in water bath 30 minutes, take out flowing water cooling 10 minutes again, placed 20 minutes, according to spectrophotography (51 pages of appendix of Chinese Pharmacopoeia nineteen ninety version), be blank with the reagent corresponding, measure trap at 540nm wavelength place, with the trap is vertical coordinate, the reference substance micrograms is an abscissa, and the drawing standard curve is obtained regression equation;
The accurate this product 20ml that draws of the preparation of need testing solution, adding distil water 10ml, fully shake up, the accurate again sample 20ml application of sample of drawing dilution (is crossed sieve No. 3 in the polyamide column of having handled well, 12g, φ 2cm) on, treat that sample liquid blots after, add to steam and stay water 150ml eluting, collect eluent for checking Radix Ginseng usefulness; Add methanol 100ml eluting again, collect meoh eluate, reclaim methanol to doing, residue adds water saturated n-butyl alcohol in 80 ℃ of water-baths, heating for dissolving 6 times, 2ml for the first time, each thereafter 1ml, filter, merge n-butyl alcohol liquid to separatory funnel, add 5% saturated sodium hydroxide 10ml of n-butyl alcohol, shaking by swirling is even, standing demix, tell the alkali liquor layer, standby, the reuse pipet sucks n-butyl alcohol liquid in the 10ml volumetric flask, the n-butyl alcohol washing container 3 times that adds saturation water, each 1ml, washing liquid is incorporated measuring bottle into, adds n-butyl alcohol to scale, shake up, promptly;
Algoscopy is according to thin layer chromatography (57 pages of appendix of Chinese Pharmacopoeia nineteen ninety version) test, and the accurate need testing solution 200 μ l that draw are at silica gel G F
254Carry out the strip point sample on the lamellae, with chloroform-n-amyl alcohol-methanol-n-butyl alcohol-acetic acid-water (60: 36: 22: 9: 4: 2) is developing solvent, launch, chromatography cylinder presaturation exhibition in 30 minutes is apart from about 10cm, take out, hot blast drying is put 110 ℃ of heating again and was taken out in 40 minutes, observe dark-coloured band down at uviol lamp (254nm), scrape two blanking bars getting about 0.5 place of Rf value, put in the 10ml centrifuge tube, scrape simultaneously to get and put in another centrifuge tube as blank with the blank silica GF254 of test sample streak blanking bar homalographic, in 70 ℃ of water-baths methanol thorough washing 4 times, for the first time, each 2ml for the second time, the 3rd, the 4th each 1ml, centrifugal (3000r/min) 10min, draw supernatant, filter, the methanol washing liquid is incorporated in the 10ml tool plug test tube, and methanol is flung in 70 ℃ of water-baths, under the sighting target directrix curve preparation: rise from " adding 1% paradime thylaminobenzaldehyde ethanol liquid 0.1ml ... ", with the method operation, measure trap at 540nm wavelength place, obtain the weight (μ g) of saikoside in the test sample according to regression equation, calculate, promptly.
Example 2:
| Prescription is formed: | |||||
| Radix Bupleuri Rhizoma Pinelliae (processed with Rhizoma Zingiberis Recens) Fructus Jujubae | ??180g ??135g ??195g | Ginseng ginger | ?90g ?135g | The Radix Scutellariae Radix Glycyrrhizae Preparata | 135g 75g |
| Make 1000ml | |||||
Method for making:
Get each medicine of prescription that meets a regulation of Chinese Pharmacopoeia current edition, add 8 times of water gaging dippings 1 hour, distillation twice, each 1 hour, collect distillate, sealing, cold preservation is standby; Medicinal liquid filters, and medicinal residues add 4 times of water gagings again and decoct half an hour, filter, and merge medicinal liquid, be concentrated into relative density 1.05～1.08 (50 ℃ of heat are surveyed), be chilled to room temperature, filter precipitate with ethanol, alcohol precipitation concentration 45%, cold preservation 24 hours filters, merge with distillate behind the filtrate recycling ethanol, add 0.3% antiseptic and 1% sweeting agent, mixing, adjust pH is about 5.5, adds water move to full dose, filters, sterilization, packing, promptly.
Example 3:
| Prescription is formed: | |||||
| Radix Bupleuri | ??180g | Radix Ginseng | ??90g | Radix Scutellariae | ??135g |
| The Rhizoma Pinelliae (processed with Rhizoma Zingiberis Recens) Fructus Jujubae | ??135g ??195g | Rhizoma Zingiberis Recens | 135g | Radix Glycyrrhizae Preparata | 150g |
| Make 1000ml | |||||
Method for making:
Get each medicine of prescription that meets a regulation of Chinese Pharmacopoeia current edition, add 8 times of water gaging dippings 1 hour, distillation twice, each 1 hour, collect distillate, sealing, cold preservation is standby; Medicinal liquid filters, and medicinal residues add 4 times of water gagings again and decoct half an hour, filter, and merge medicinal liquid, be concentrated into relative density 1.05～1.08 (50 ℃ of heat are surveyed), be chilled to room temperature, filter precipitate with ethanol, alcohol precipitation concentration 55%, cold preservation 24 hours filters, merge with distillate behind the filtrate recycling ethanol, add 0.3% antiseptic and 0.5% stevioside, mixing, adjust pH is about 5.5, adds water move to full dose, filters, sterilization, packing, promptly.
[function with cure mainly] be traditional Chinese medical science disease 1.: heat-clearing and toxic substances removing, dispersing the stagnated liver-QI for regulating the stomach.Be used for alternate attack of chill and fever, feeling of fullness and disecomfort in the chest and hypochondrium, vexation and vomiting, bitter taste in the mouth and dry throat, dizzy disease such as grade.2. modern medicine: treatment upper respiratory tract infection, bronchitis, bronchial asthma, pertussis, infantile asthma, hepatitis, hepatitis interstitialis chronica, cholecystitis, gastritis, gastric ulcer, duodenal ulcer, nephritis, atrophic nephritis (nephrosclerosis), otitis media, parotitis, skin infection, measles, lochiopyra, mastitis, rhinitis, neurosis etc.The auxiliary treatment that also is used for anti-AIDS disease.
[usage and consumption] is oral, a 20ml, 3 times on the one; Or follow the doctor's advice.Suitable one after each meal, the time spent shakes up.
[storage] is airtight, puts shady and cool dry place and preserves.
Claims (3)
1, the preparation method of Herba Sidae Rhombifoliae soup oral liquid, contain Radix Bupleuri, Radix Scutellariae, the Rhizoma Pinelliae, Radix Ginseng, Rhizoma Zingiberis Recens, Radix Glycyrrhizae seven flavor Chinese medicines in its raw material prescription, it is characterized in that may further comprise the steps: get each medicine of prescription and add water and flood distill repeatedly in right amount, collect distillate, sealing cold preservation is standby; Medicinal liquid filters; Medicinal residues add water decoct in right amount medicinal liquid, filter; Merge medicinal liquid and concentrate, be chilled to room temperature and filter, precipitate with ethanol, alcohol precipitation concentration 35%～55% filters, filtrate recycling ethanol, concentrated solution and distillate merge, and add an amount of antiseptic and sweeting agent, and mixing adds water move to full dose, filters, sterilization, promptly.
2, the preparation method of Herba Sidae Rhombifoliae soup oral liquid as claimed in claim 1 is characterized in that each medicine of prescription adds 6～10 times of amount dippings of water 1～2 hour, distills 2～3 times, each 1～2 hour, collects distillate, sealing; Cold preservation is standby; Medicinal liquid filters, and merges; Medicinal residues add an amount of decoction of water 0.5～1 hour again, filter; Merge medicinal liquid, be concentrated into relative density 1.05～1.08 (50 ℃ of heat are surveyed), be chilled to room temperature, filter, precipitate with ethanol, alcohol precipitation concentration 35%, cold preservation 12～24 hours, supernatant is centrifugal, coarse filtration, fine straining, filtrate recycling ethanol concentrated solution and distillate merge, and add 0.2%～1.0% antiseptic and sweeting agent, mixing, adjust pH adds water move to full dose, filters, sterilization, packing, promptly; Antiseptic is a sodium benzoate, and sweeting agent is stevioside or stevioside and Mel; Regulate pH value 0.1mol/L sodium hydroxide or dilute hydrochloric acid.
3, Herba Sidae Rhombifoliae soup oral liquid Quality Control Technology according to claim 1 is characterized in that regulation this product character is brownish red or brown liquid, feeble QI perfume (or spice), and the sweet little hardship of distinguishing the flavor of, carry out the quality control of each component by following method:
1.1 differentiate
1.1.1 ginseng effective component ginsenoside
Get [3.3 assay] " Radix Bupleuri " item water elution liquid 150ml down, water-bath is concentrated into 30ml, filters, and uses water saturation n-butanol extraction 3 times, each 10ml.Leave standstill, layering divides and gets n-butyl alcohol liquid, evaporate to dryness; Residue adds methanol 1ml makes dissolving, moves in the 10ml centrifuge tube and waves most methanol in 80 ℃ of water-baths, adds water saturated n-butyl alcohol 0.5ml jolting and makes dissolving, adds 5% sodium hydroxide 1ml of saturated n-butyl alcohol again, shake up, and standing demix, upper strata liquid is as need testing solution; Other gets the Ginsenoside Rb
1, Rg
1, the Re reference substance, add methanol and make the solution that every 1ml contains 1mg, in contrast product solution; Test according to thin layer chromatography (appendix VIB of Chinese Pharmacopoeia version in 2000), draw need testing solution 10 μ l, each 5 μ l of reference substance solution put respectively on the efficient lamellae of same silica gel G, are developing solvent with the subnatant of chloroform-methanol-water (65: 35: 10), launch, take out, hot blast drying, spray is with 10% ethanol solution of sulfuric acid, in 110～120 ℃ of heating colour developing in several minutes, inspect under the daylight; In the test sample chromatograph with the corresponding position of reference substance chromatograph on, show the speckle of same color;
1.1.2 Radix Glycyrrhizae active ingredient glycyrrhizin
Get [3.3 assay] " Radix Bupleuri " 5% sodium hydroxide solution of telling down, thin up moves into separatory funnel to 30ml, add dilute hydrochloric acid and regulate pH value to 4～5, add water saturated ethyl acetate extraction 2 times, each 10ml, leave standstill, layering discards the ethyl acetate layer, add water saturated n-butanol extraction 3 times again, each 10ml, standing demix, tell n-butyl alcohol liquid, merge, put evaporate to dryness in the water-bath, residue adds methanol 1ml makes dissolving, as need testing solution; In addition extracting liquorice control medicinal material 1g adds little the boiling of water and extracts 2 times, each 50ml, 30 minutes, filter, filtrate merges, and puts and is concentrated into 15ml in the water-bath, add ethanol 15ml, shake up, left standstill 12 hours, filter, filtrate is put and is flung to ethanol in the water-bath, adds an amount of stirring and dissolving of water and is diluted to 25ml, filters, filtrate moves into separatory funnel, rises from " adding water saturated ethyl acetate extraction 2 times ... " to be equipped with control medicinal material solution with legal system; Test according to thin layer chromatography (appendix VIB of Chinese Pharmacopoeia version in 2000), draw each 10 μ l of need testing solution and control medicinal material solution, put respectively on the efficient lamellae of same silica gel G, with chloroform-n-amyl alcohol-methanol-n-butyl alcohol-acetic acid-water (60: 36: 22: 9: 4: 2) is developing solvent, launch, take out, hot blast drying, spray is with 10% ethanol solution of sulfuric acid, it is clear that hot blast is heated to the speckle colour developing, inspects under the daylight, in the test sample chromatograph, with the corresponding position of control medicinal material chromatograph on, show the speckle of same color;
1.2 check
Relative density should be not less than 1.05 (appendix of Chinese Pharmacopoeia version in 2000);
PH value 3.5～6.5 (appendix of Chinese Pharmacopoeia version in 2000);
1.3 assay
The every 1ml of Radix Scutellariae this product contains Radix Scutellariae with baicalin C
21H
18O
8Meter should be no less than 2.5mg;
Accurate this product 1ml that draws adds methanol 1ml, shakes up centrifugal 10 minutes (3000 rev/mins) in back, takes out, and draws supernatant 0.5ml, puts in the 1ml volumetric flask, adds 50% methanol and is diluted to scale as need testing solution.Other gets the baicalin reference substance, adds methanol and makes the solution that every 1ml contains about 1mg, in contrast product solution; Test according to thin layer chromatography (appendix VIB of Chinese Pharmacopoeia version in 2000), draw need testing solution 2 μ l, 3 μ l, reference substance solution 2 μ l, 3 μ l, the cross point is on the efficient lamellae of same silica gel G respectively, with n-amyl alcohol-methanol-formic acid-water (7: 2: 1: 1) be developing solvent, launch, exhibition is taken out apart from about 10cm, hot blast drying, 110 ℃ of heating 30 minutes, scan wavelength according to chromatography (57 pages of thin layer chromatography scannings of appendix): λ again
S=280nm, λ
R=207nm measures test sample trap integrated value and reference substance trap integrated value, calculates promptly;
The every 1ml of Radix Bupleuri this product contains Radix Bupleuri with saikoside a (d) C
42H
66O
13Meter should be no less than 0.1mg;
The accurate reference substance solution 20 of drawing of the preparation of reference substance solution, 40,50,60,80,100 μ l, put respectively in the 10ml tool plug test tube, put in 70 ℃ of water-baths and wave most solvent, add 1% paradime thylaminobenzaldehyde alcoholic solution 0.1ml, jump a queue but stay seam, in 70 ℃ of heating in water bath 10 minutes, the flowing water cooling added phosphoric acid 5ml, shake up after jumping a queue, in 70 ℃ of heating in water bath 30 minutes, take out flowing water cooling 10 minutes again, placed 20 minutes, according to spectrophotography (51 pages of appendix of Chinese Pharmacopoeia nineteen ninety version), be blank with the reagent corresponding, measure trap at 540nm wavelength place, with the trap is vertical coordinate, the reference substance micrograms is an abscissa, and the drawing standard curve is obtained regression equation;
The accurate this product 20ml that draws of the preparation of need testing solution, adding distil water 10ml, fully shake up, the accurate again sample 20ml application of sample of drawing dilution (is crossed sieve No. 3 in the polyamide column of having handled well, 12g, φ 2cm) on, treat that sample liquid blots after, add to steam and stay water 150ml eluting, collect eluent for checking Radix Ginseng usefulness; Add methanol 100ml eluting again, collect meoh eluate, reclaim methanol to doing, residue adds water saturated n-butyl alcohol in 80 ℃ of water-baths, heating for dissolving 6 times, 2ml for the first time, each thereafter 1ml, filter, merge n-butyl alcohol liquid to separatory funnel, add 5% saturated sodium hydroxide 10ml of n-butyl alcohol, shaking by swirling is even, standing demix, tell the alkali liquor layer, standby, the reuse pipet sucks n-butyl alcohol liquid in the 10ml volumetric flask, the n-butyl alcohol washing container 3 times that adds saturation water, each 1ml, washing liquid is incorporated measuring bottle into, adds n-butyl alcohol to scale, shake up, promptly;
Algoscopy is according to thin layer chromatography (57 pages of appendix of Chinese Pharmacopoeia nineteen ninety version) test, and the accurate need testing solution 200 μ l that draw are at silica gel G F
254Carry out the strip point sample on the lamellae, with chloroform-n-amyl alcohol-methanol-n-butyl alcohol-acetic acid-water (60: 36: 22: 9: 4: 2) is developing solvent, launch, chromatography cylinder presaturation exhibition in 30 minutes is apart from about 10cm, take out, hot blast drying is put 110 ℃ of heating again and was taken out in 40 minutes, observe dark-coloured band down at uviol lamp (254nm), scrape two blanking bars getting about 0.5 place of Rf value, put in the 10ml centrifuge tube, scrape simultaneously to get and put in another centrifuge tube as blank with the blank silica GF254 of test sample streak blanking bar homalographic, in 70 ℃ of water-baths methanol thorough washing 4 times, for the first time, each 2ml for the second time, the 3rd, the 4th each 1ml, centrifugal (3000r/min) 10min, draw supernatant, filter, the methanol washing liquid is incorporated in the 10ml tool plug test tube, and methanol is flung in 70 ℃ of water-baths, under the sighting target directrix curve preparation: rise from " adding 1% paradime thylaminobenzaldehyde ethanol liquid 0.1ml ... ", with the method operation, measure trap at 540nm wavelength place, obtain the weight (μ g) of saikoside in the test sample according to regression equation, calculate, promptly.
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102349993A (en) * | 2011-10-18 | 2012-02-15 | 广州白云山光华制药股份有限公司 | Bupleurum tenue granules and preparation method thereof |
| CN102824493A (en) * | 2012-09-08 | 2012-12-19 | 河北科星药业有限公司 | Bupleurum tenue oral liquid for veterinary use and preparation method thereof |
| CN105866319A (en) * | 2016-04-20 | 2016-08-17 | 广西壮族自治区梧州食品药品检验所 | Method for qualitatively identifying baicalin in Qinghouliyan granules by thin-layer chromatography |
| CN110187047A (en) * | 2019-06-13 | 2019-08-30 | 兰州市肺科医院 | A kind of detection method for syndrome of yin deficiency of lung and kidney Chinese medicine composition |
| CN113281449A (en) * | 2021-04-21 | 2021-08-20 | 广东志道医药科技有限公司 | Thin-layer identification method of bupleurum tenue preparation |
| CN114225001A (en) * | 2021-12-31 | 2022-03-25 | 北京橘井健康科技集团有限公司 | Preparation method of improved bupleuri decoction |
| CN114432415A (en) * | 2020-11-03 | 2022-05-06 | 四川新绿色药业科技发展有限公司 | Preparation process and quality control method of Inula and Haematitum decoction formula granules |
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- 2004-06-05 CN CNB2004100412205A patent/CN100522138C/en not_active Expired - Fee Related
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102349993A (en) * | 2011-10-18 | 2012-02-15 | 广州白云山光华制药股份有限公司 | Bupleurum tenue granules and preparation method thereof |
| CN102824493A (en) * | 2012-09-08 | 2012-12-19 | 河北科星药业有限公司 | Bupleurum tenue oral liquid for veterinary use and preparation method thereof |
| CN105866319A (en) * | 2016-04-20 | 2016-08-17 | 广西壮族自治区梧州食品药品检验所 | Method for qualitatively identifying baicalin in Qinghouliyan granules by thin-layer chromatography |
| CN110187047A (en) * | 2019-06-13 | 2019-08-30 | 兰州市肺科医院 | A kind of detection method for syndrome of yin deficiency of lung and kidney Chinese medicine composition |
| CN110187047B (en) * | 2019-06-13 | 2021-07-23 | 兰州市肺科医院 | Detection method of traditional Chinese medicine composition for lung-kidney yin deficiency syndrome |
| CN114432415A (en) * | 2020-11-03 | 2022-05-06 | 四川新绿色药业科技发展有限公司 | Preparation process and quality control method of Inula and Haematitum decoction formula granules |
| CN113281449A (en) * | 2021-04-21 | 2021-08-20 | 广东志道医药科技有限公司 | Thin-layer identification method of bupleurum tenue preparation |
| CN113281449B (en) * | 2021-04-21 | 2022-04-08 | 广东志道医药科技有限公司 | Thin-layer identification method of bupleurum tenue preparation |
| CN114225001A (en) * | 2021-12-31 | 2022-03-25 | 北京橘井健康科技集团有限公司 | Preparation method of improved bupleuri decoction |
| CN114225001B (en) * | 2021-12-31 | 2024-04-19 | 北京橘井健康科技集团有限公司 | Preparation method of improved major bupleurum decoction |
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|---|---|
| CN100522138C (en) | 2009-08-05 |
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