CN1626146A - Icy seven drop pills and preparation method - Google Patents
Icy seven drop pills and preparation method Download PDFInfo
- Publication number
- CN1626146A CN1626146A CN 200310107305 CN200310107305A CN1626146A CN 1626146 A CN1626146 A CN 1626146A CN 200310107305 CN200310107305 CN 200310107305 CN 200310107305 A CN200310107305 A CN 200310107305A CN 1626146 A CN1626146 A CN 1626146A
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- China
- Prior art keywords
- drop pill
- adjuvant
- starch
- xylitol
- ethanol
- 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.)
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Abstract
A medicine 'Bingqi dripping pill' for treating coronary heart diseaseand angina pectoris is disclosed. Its advantages are high safety and lower toxic by-effect.
Description
Technical field
The present invention relates to field of medicaments, particularly, relating to Chinese medicine is medicine of the treatment cardiovascular and cerebrovascular disease made of raw material and preparation method thereof.
Background technology
Cardiovascular and cerebrovascular disease is to cause human first dead sick the kind, and along with the raising of social life level and the aging of population, the research of cardiovascular and cerebrovascular diseases medicament becomes the focus of drug development.Coronary heart disease is the abbreviation of coronary heart disease, is a kind of sickness rate height, the mortality rate height, and human healthy disease in serious harm, thereby b referred to as " the first human killer ".Angina pectoris is a coronary insufficiency, cardiac muscle is rapid, of short duration ischemia and the caused clinical syndrome of anoxia, usually occur in fatigue, heavy meal, catch cold and when excited, vexed pain, squeezing pain or constriction that the right occurrence scope of metosteon is not clear, patient is conscious to have palpitation, suffocates, sometimes with dying sensation.Ischemia apoplexy (cerebral infarction) all is important opportunitys of its prevention and treatment at acute attack stage and in apoplexy early stage and convalescent period.Hypertension is the modal cardiovascular disease in the world, also is one of maximum epidemic diseases, often causes the complication of internal organs such as the heart, brain, kidney, and human beings'health in serious harm.Show that according to national statistics the existing hyperpietic of China has reached 100,000,000, annual newly-increased more than 3,000,000.Therefore treat and prevent above-mentioned disease to have important effect, these diseases of treatment by Chinese herbs have long history, also are the focuses of recent researches.
Radix Notoginseng belongs to hemostasis class Chinese medicine.Chinese medicine thinks that it has the hemostasis of becoming silted up of loosing, and the function of subduing swelling and relieving pain is not only stopped blooding but also invigorate blood circulation.The existing anastalsis of modern pharmacological research proof Radix Notoginseng has blood coagulation resisting function again.Anastalsis comprises and shortens clotting time, platelet increasing quantity and make it occur stretch pseudopodium, assemble, take off phenomenon such as granule, can also reduce capillary permeability.What show blood coagulation resisting function is part composition in the Radix Notoginseng: the total soap formula of Radix Notoginseng, Radix Notoginseng panoxadiol type soap summation triol type soap formula, they all can suppress the gathering of people and rabbit platelet.The total soap formula of Radix Notoginseng can promote vascular endothelial cell secretory tissue type plasminogen (t-N), stops the formation of thrombosis.
Borneolum Syntheticum is the processing crystallization product of the outstanding brain balsam of Dipterocarpaceae plant.The hot hardship of loosing of Borneolum Syntheticum is let out, and fragrance is walked string, can lead to all keys, and the stagnated fire of loosing has similar merit of shielding the fragrant refreshment of having one's ideas straightened out.Modern pharmacological research proof Borneolum Syntheticum has the effect that resists myocardial ischemia, and coronary flow is obviously increased; In addition, Borneolum Syntheticum can also increase the permeability of blood brain barrier, strengthens medicine and strides the barrier ability.
The BINGQI PIAN of being made up of above-mentioned two flavor Chinese medicines has activating blood circulation to dissipate blood stasis, analgesic function; Its clinical indication is coronary heart disease, angina pectoris.Icing seven drop pill is the drop pills that develop on this basis, and curative effect is better than BINGQI PIAN.Its characteristics are onset rapidly (sublingual administration), nine its be applicable to anginal acute attack, oral in addition effective too.
The synthetic chemical substance that modern medicine is commonly used has spreaded all over each corner of human lives, chemical synthetic drug becomes the main flow of medicine, yet, appearance along with multiple difficult serious symptom miscellaneous diseases, western medical treatment presents imperfect, the human lives and the healthy reality and the up-to-date successes achieved in research have all proposed query to this situation, particularly along with the continuous appearance of chemical drugs toxic and side effects, the change of spectrum of disease and conversion of medical, make modern medicine be subjected to unprecedented challenge, and people also place hope in the application and development of traditional medicine on gradually.Advocate back to nature, pay attention to plant amedica use, hanker after traditional remedies, the trend of advocating natural drug forms, making full use of natural materials is human best selections.
At present, in the world, natural drug all has certain market, along with people increasing and the aging of population to the health requirements level of understanding, sub-health stateization, people thirst for back to nature more, the problem of utilize the high Drug therapy of pure natural degree, preventing some chemical synthetic drugs cann't be solved, so the background that exceeds its original traditional national culture has been expanded in the application of natural plant.From natural drug, seek the little and inexpensive medicine of side effect and become the target that countries in the world pharmaceutical manufacturer is chased.The European Community has carried out unified legislation to medical herbs, state medical herbs status such as Canada and Australia have legalized, U.S. government has also drafted the plant amedica management method, the compound recipe mix preparation that begins to accept natural drug is as curative, and these provide good international environment for Chinese medicine enters international medical market as curative.On the other hand, along with the quickening of global economic integration progress, particularly China becomes a full member of WTO, and Chinese Medicine market incorporates the breadth and depth of international medical big market and will further aggravate.Face the enormous impact of Asian countries's traditional medicine product such as the keen competition of powerful transnational medical group and Japan, Korea S, India, Thailand and European countries' plant amedica such as Germany, France, numerous products that China's Chinese medicine produces are owing to still can not meet the standard of international medical market and requirement and being kept outside of the door.
Expansion and human back to nature requirement along with the market global range, use the low medicine of toxic and side effects, especially pure natural medical more and more becomes people's first-selection, dropping pill formulation be a kind of have efficient, quick-acting new medicine preparations, it has overcome the shortcoming and deficiency of Chinese medicine preparation in the past, but present dropping pill formulation generally faces following problem: 1, drop pill adjuvant pure natural degree is not high: at present, drop pill substrate adjuvant mostly is synthetic, natural degree is lower, the searching of new alternative substrate adjuvant, the searching of the alternative substrate adjuvant that particularly natural degree is high and preparation technology thereof determine, it is again very difficult thing, because the required preparation condition of at present common possible natural substrates adjuvant succedaneum is very harsh, it all is to influence the key that drop pill prepares molding that adjuvant temperature and drop pill thereof drip the system condition.The too high then viscosity of adjuvant melt temperature is low, and poor plasticity is though the adjuvant melt temperature is crossed lowplastcity by force, but drop pill has shortcomings such as easily sticking ball, distortion, therefore, seek pure natural degree height, and the adjuvant that is suitable for substituting existing drop pill substrate is a very job of hardships.2, the drop pill outlet encounters problems: along with expanding economy, more and more internationalize in market, China is also just making great efforts to adapt to this trend, present Chinese medicine dripping pills preparation as health food, successful export to many countries, but also face many problems at present, because different countries is different to the approval of the selected adjuvant of Chinese medicine dropping pill formulation, especially industrial flourishing Europe, more strict to food adjuvant and medical auxiliary materials, and as the selected chemosynthesis adjuvant (as Polyethylene Glycol) of the dropping pill formulation of health food outlet not in the catalogue of some national food additive, it is very unfavorable that this moves towards the international market to the Chinese medicine dropping pill formulation, becomes the stumbling-block that Chinese medicine enters the international market, therefore, seek the new of one or more, can be particularly important, also very urgent for the substrate adjuvant that the international market is accepted.3, the shortcoming of mouthfeel and onset speed: the mouthfeel of Chinese medicine and preparation thereof is relatively poor to be the big characteristics of one, people when taking some drugs to the frightened of disagreeable taste that medicine had even be better than fear far away to disease, What is more, some patients are because can not overcome the poor taste of medicine or abnormal smells from the patient and abandon the treatment of medicine, though can improve mouthfeel as medicine being made capsule or sugar coated tablet, reducing stimulates, but disintegration rate prolongs, be unfavorable for the rapid onset of medicine, to some disease, particularly need the disease of the rapid onset of medicine inapplicable.4, the preparation process difficulty of drop pill suitability for industrialized production: in the replacement process of dropping pill formulation adjuvant, determining of the preparation process of its suitability for industrialized production is very difficult something, as the ratio of the melt temperature of substrate adjuvant, the proportioning of dripping system temperature, adjuvant and medicine, dropper bore, condensing agent etc. all are the factors that influence drop pill, therefore, the replacement of substrate and to be suitable for suitability for industrialized production be a job consuming time, as to expend substantial contribution.
In order to change drop pill substrate adjuvant for a long time based on the situation of chemosynthesis adjuvant, it is low to solve the pure natural degree that present drop pill substrate faced, and can not satisfy more and more that people require back to nature, take low toxicity, the problem of the pure natural medical that has no side effect; Also can solve some problems that Chinese medicine preparation, particularly dropping pill formulation are run in exit procedure, strengthen the competitiveness of international market; The present invention has invented the pure Chinese medicine dripping pills preparation that a kind of toxic and side effects is low, evident in efficacy, moderate, adapt to industrialized great production by a large amount of tests and the research of preparation process.
Summary of the invention
The medicine that the purpose of this invention is to provide a kind of treatment cardiovascular and cerebrovascular disease with new type natural substrate adjuvant preparation.
Another object of the present invention provides a kind of preparation method for the treatment of the pharmaceutical preparation of cardiovascular and cerebrovascular disease.
The present invention is the new pharmacological action that the qi-blood relationship theory learned according to Chinese traditional medicine and modern medicine are found various institutes of Chinese materia medica, according to the principle of " symptomatic treatment in acute condition, radical treatment in chronic case ", set upright based on reinforcing, " lead to " and just must not hinder, " benefit " must not be detained, treating both the principal and secondary aspects of a disease.The medicine of producing according to this method has late result again, and finally reaches the healing purpose the existing short term effect of the treatment of coronary heart disease, and generation without any side effects.The selected substrate adjuvant of the present invention is resulting by a large amount of tests, it is little to have molecular weight, soluble in water, and molten diffusing speed is faster, pure natural degree height, toxic and side effects is low, and can reduce the medicine irritation abnormal smells from the patient, has the oral cavity of improvement acid-base value during the buccal of oral cavity, improve the characteristics of oral cavity smell, the used substrate adjuvant of the present invention is the agent of food sedan-chair flavor, takes that mouthfeel is good, the acceptant characteristics of patient, is the direction of following substrate adjuvant development.
The consumption of drug component of the present invention and the selection of adjuvant thereof also grope to sum up to draw through the inventor in a large number, each amounts of components all has curative effect preferably in following ranges: 150～600 parts of Radix Notoginseng, 1.5～50 parts of Borneolum Syntheticums, appropriate amount of auxiliary materials is made, wherein adjuvant comprises filler and plasticity substrate, said filler is selected from the natural adjuvant of following one or more plant origins: erythritol, sorbitol, fructose, D-ribonic acid-gamma lactone, arabitol, trehalose, D-ribose, low melting-point agarose, Lac, xylitol, Raffinose, glucose, malic acid, citric acid, isomalt, lactose, maltose etc., and they contain the water of crystallization chemical compound; Said plasticity substrate is selected from the natural adjuvant of following one or more plant origins: starch and derivant thereof, cellulose and derivant thereof, arabic gum, dextran, chitin, sesbania gum, carrageenan, Ficus elastica, Furcellaran, tragakanta, carrageenin, tamarind gum, pectin, xanthan gum, alginic acid and salt thereof, dextrin, cyclodextrin, agar, lactose; Described starch and derivant thereof such as pregelatinized Starch, modified starch, hydroxypropyl starch, carboxymethyl starch, described cellulose and derivant thereof such as methylcellulose, microcrystalline Cellulose, sodium carboxymethyl cellulose, hydroxypropyl emthylcellulose, cross-linking sodium carboxymethyl cellulose, hydroxyethylmethyl-cellulose, hydroxyethyl-cellulose, hydroxypropyl cellulose; Be chosen as 260～450 parts of the Radix Notoginseng, 2～10 parts of Borneolum Syntheticums, appropriate amount of auxiliary materials of preferred drug component consumption of the present invention and adjuvant thereof are made, filler adjuvant wherein is selected from following one or more the natural adjuvant of plant origin: sorbitol, xylitol, lactose, maltose, and they contain the water of crystallization chemical compound; Plasticity substrate wherein is selected from following one or more the natural adjuvant of plant origin: pregelatinized Starch, carboxymethyl starch, methylcellulose, sodium carboxymethyl cellulose, hydroxypropyl emthylcellulose, arabic gum, alginic acid, dextrin, cyclodextrin, agar, lactose; Be chosen as 260～450 parts of the Radix Notoginseng, 2～10 parts of Borneolum Syntheticums, appropriate amount of auxiliary materials of best drug component consumption of the present invention and adjuvant thereof are made, and filler adjuvant wherein is selected from following one or more the natural adjuvant of plant origin: xylitol, lactose; Plasticity substrate wherein is selected from following one or more the natural adjuvant of plant origin: starch, arabic gum.
Can also contain chemosynthesis adjuvant and animal origin adjuvant in the above-mentioned dressing, wherein filler comprises phenylglycol, hexadecanol, octadecanol, sodium stearate, tristerin, tripalmitin, carbamide, polyoxyethylene monostearate, polyoxyethylene alkyl ether; Wherein plasticity substrate comprises polyvinylpyrrolidone, crospolyvinylpyrrolidone, carbomer, polyvinyl alcohol, acrylic resin, poloxamer, gelatin.
In screening to above adjuvant, we find: plant colloid such as carrageenan, the tragakanta, pectin, agar, arabic gum, Ficus elastica, tamarind gum, locust bean gum, Pseudobulbus Bletillae (Rhizoma Bletillae) glue, guar gum, Konjac glucomannan, it is big that plant colloids such as POLY-karaya have viscosity, mobile poor, characteristics such as do not solidify after the condensation, and arabic gum has high dense low sticking character, can be mixed with the aqueous solution of 50% concentration and still have flowability, this is one of not available characteristics of other hydrophilic colloid, arabic gum has at high temperature, under the low concentration, can ooze, but not condensation, at low temperature, under the high concentration, be difficult for oozing, but characteristics such as energy condensation.Polysaccharide such as polysaccharide such as starch and derivant thereof (as gelling starch, carboxymethyl starch etc.), cellulose derivative (as methylcellulose, sodium carboxymethyl cellulose, hydroxypropyl emthylcellulose etc.), alginic acid, dextrin, cyclodextrin, lactose, in screening, find alginic acid have viscosity big, be the fruit jelly sample, dextrin has the colloid sample, characteristics such as lactose coagulability difference; And starch and derivant thereof are materials commonly used in the medical science adjuvant, thus in polysaccharide preferred starch and derivant thereof.Polyhydric alcohol such as sorbitol (88～102 ℃), xylitol (88～94.5 ℃), lactose (70～80 ℃), mannitol (166～169 ℃), maltose alcohol (135～140 ℃), isomalt polyhydric alcohol such as (98～103 ℃) screen, and find that it has following characteristics as drop pill substrate: sorbitol, lactose, isomalt are mobile poor; Mannitol, maltose alcohol fusing point are too high; The xylitol coagulability is poor slightly.After Preliminary screening, preferred xylitol, lactose, sorbitol in the selection of polyhydric alcohol, the best is an xylitol.Xylitol has following characteristics as drop pill substrate: in the time of 91 ℃, molten condition has appearred in xylitol, but not fusion fully, cooling rapidly, it separates out crystallization very soon, xylitol mixes the back good fluidity with extractum at certain proportion, can drip and can condensation, but be condensed into Powdered thing, loosely organized, the toughness extreme difference, that pinches is promptly broken.Organic acid and salt, alkali such as citric acid (100 ℃), sorbic acid (133 ℃), succinic acid (181～189 ℃), sodium acetate organic acid such as (58 ℃) and salt, alkali, its as drop pill substrate have fusing point too high, with Chinese medical concrete can't mixing etc. shortcoming.
Because of above single adjuvant existing shortcoming in as the drop pill preparation process, particularly we by above-mentioned Preliminary screening after, determine two kinds of adjuvants are used and screen: mainly be that above various adjuvants are carried out combined sorting, final determine following several: the plant colloid cooperates with the plant colloid, the cooperating of polyhydric alcohol and polyhydric alcohol, polyhydric alcohol and plant colloidally cooperate, the cooperating of the cooperating of xylitol and arabic gum, lactose and arabic gum, based on the composite auxiliary material of xylitol.Find preferred the cooperation to be xylitol, lactose and the compound use of other adjuvant, this kind combination has following characteristics: make up with mannitol: can drip not condensation; Make up with sorbic acid: both do not dissolve each other; Make up with lactose: can drip the energy condensation, but frangible; Make up with pomelo-pectin, tragakanta, sodium alginate: viscosity is big, can't drip; Make up with arabic gum: can drip, coagulability is poor slightly; Make up with dextrin: can drip, coagulability is poor slightly; Make up with starch: can drip, coagulability is also better.Determine that at last best of breed is that xylitol cooperates with arabic gum with starch, xylitol with starch, lactose.
At xylitol and starch, lactose and starch, in the research of xylitol and arabic gum combination, xylitol and starch Application of composite being prepared some required in the process of drop pill factors investigated, mainly is to the xylitol type, condensed fluid, condensate temperature influences the drop pill mouldability, xylitol and starch proportion influence mouldability, temperature is to the influence of drop pill mouldability, the extractum amount influences the drop pill mouldability, mixing time influences the drop pill mouldability, the dropper bore is to the influence of drop pill particle diameter, the formulation optimization of drop pill, the Preliminary Determination of drop pill, dissolve scattered time limit is investigated.Find that the solid xylitol has three types of powder, granular and crystallinity, and the easiest fusion of powder xylitol, again can fine dissolving be dispersed in the mixed liquor that starch, extractum forms, good fluidity, drippage is easy, and granular and crystalline xyhose alcohol is difficult for fusion, solubility property is also slightly poor, the mix flow that they and starch, extractum form is relatively poor, viscosity is very big, almost cannot drip, and therefore drips first-selected powder xylitol in the system process at drop pill.
At ratio of adjuvant molding is found in the sex research, in the combination of xylitol and starch, lactose and starch, xylitol and arabic gum, low melting point substrate adjuvant is 1: 0～1: 1.5 with the ratio of the weight of plasticity substrate adjuvant, be preferably 1: 0.1～1: 0.9, the best is 1: 0.1～1: 0.5.Low melting point substrate adjuvant of being formed within this scope and plasticity substrate adjuvant, the drug matrices fused solution all can ooze, and can condensation.Specific to each combination, xylitol is preferably 1: 0.2 with the ratio of the weight of starch～1: 0.3, and lactose is preferably 1: 0.2 with the ratio of the weight of starch～1: 0.3, and the ratio of the weight of xylitol and arabic gum is preferably 1: 0.2～and 1: 0.4.Find that in the research of temperature temperature is big especially to the influence of drop pill mouldability to the influence of drop pill mouldability, when temperature is too low, owing to the too big effect that oozes that influences drop pill of viscosity of substrate, when temperature is too high, not condensation of drop pill.Find that mixing time can have influence on the mouldability of drop pill in mixing time in to the sex research of drop pill molding, mixing time is too short, and mobile poor, influence oozes, and mixing time is oversize, influences the condensation of drop pill.Dripping under the system temperature, mixing time in 1～120 minute all can, suitable mixing time was at 10～30 minutes.Consider that mixing time can not be too short in the suitability for industrialized production, adopt the method that low temperature stirs for a long time, high temperature drips system.Find that in the research of dropper bore to the influence of drop pill particle diameter the dropper bore influences the size of drop pill and the flowability of fusion substrate, the system effect is dripped in influence.Drop pill diminishes and diminishes along with bore, but after 1.4 millimeters, along with the bore change of size that diminishes is not obvious, but the matrix flow reduction, system is dripped in influence.
So in the preparation method of preparation, medicine mixes mixing time with the substrate adjuvant be 10～30 minutes; The mixed heating and melting temperature of medicine and substrate adjuvant is 45～115 ℃, dripping the system temperature is 45～95 ℃, and liquid coolant is liquid paraffin, methyl-silicone oil or vegetable oil (Oleum Glycines, Semen Ricini wet goods), and the temperature of liquid coolant is-20～25 ℃, dropper mouth internal diameter is 1.0～4.0 millimeters; Preferred heating and melting temperature is 60～85 ℃, and dripping a system temperature is 60～85 ℃, and condensing agent is liquid paraffin, methyl-silicone oil, and the condensing agent temperature is 0～18 ℃, and the dropper bore is 1.1～3.5 millimeters, and the difference of dropper mouth external diameter and internal diameter is less for well; Best heating and melting temperature is that to make temperature be that 64 ℃, dropper bore are that 1.2～2.5 millimeters, condensing agent are 0 ℃ methyl-silicone oil to 64 ℃, droplet.
The substrate adjuvant of the best of the present invention is xylitol and starch, and xylitol is 1: 0.2～1: 0.3 with the ratio of the weight of starch; Or be lactose and starch, lactose is 1: 0.2～1: 0.3 with the ratio of the weight of starch; Or be xylitol and arabic gum, the ratio of the weight of xylitol and arabic gum is 1: 0.2～1: 0.4.
Xylitol is a kind of natural plant sweetening agent, approve through World Health Organization (WHO), xylitol is a kind of safest sweeting agent, countries in the world are extensive use of in fields such as food and oral-cavity articles, xylitol enters the help that need not insulin in the cell, when sugar utilizes obstacle, can not cause blood sugar increasing yet, can improve diabetics symptom, have the ketoplastic effect of powerful inhibition, can promote the generation of liver glycogen, directly infiltrate the Developmental and Metabolic Disorder that tissue is participated in metabolism, can be corrected protein, fat and steroid; Xylose is the internal metabolism intermediate product, and body has higher toleration to it.Clinical practice proves: the highest oral dosis tolerata can reach 220g every day, and intravenous drip every day can reach 100g.The oral 25700mg/Kg of median lethal dose(LD 50) (LD50) mice, quiet notes 6400mg/Kg, the quiet notes of rat 6200mg/Kg.
Medicine mesostroma adjuvant of the present invention and amount of drug are than can being the scope that allows on the galenic pharmacy, medicine described here can be that crude drug also can be the effective ingredient extract, in order to adapt to industrialized great production, the ratio range of mesostroma adjuvant of the present invention and medicine refers to the weight proportion of adjuvant and extract drugs extractum, and the substrate adjuvant is 1: 0.1～1: 1 with the ratio of the weight of drug extract; Preferred substrate adjuvant is 1: 0.1～1: 0.6 with the ratio of the weight of extract drugs extractum; Best substrate adjuvant is 1: 0.2～1: 0.4 with the ratio of the extraction extractum weight of medicine.
Medicine of the present invention can adopt the preparation of Chinese medicine preparation conventional method.The preparation of effective ingredient of the present invention can be adopted following method: water extraction, decoction and alcohol sedimentation technique, extraction, infusion process, percolation, reflux extraction, continuous backflow extraction method, macroreticular resin absorbing method preparation.For example, these crude drug pulverize mix homogeneously can be made powder takes after mixing it with water; Also can be with these medicines decocting together, the condensed water decocting liquid is made oral liquid then; But, preferably adopt following technology to extract, but this can not limit protection scope of the present invention to raw material in order to make each crude drug of this medicine better bring into play drug effect.
The preparation method of medicine of the present invention is as follows:
(a): get 150～600 parts of Radix Notoginseng, 1.5～50 parts of Borneolum Syntheticums are standby;
(b): get Radix Notoginseng and decoct with water 1～5 time, collecting decoction filters, filtrate concentrates, and adds 0.5～5 times of amount 80～99% ethanol, leaves standstill 12～36 hours, filter, reclaim ethanol, filtrate is concentrated under 30～80 ℃ of conditions, relative density is 1.05～1.45 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the appropriate amount of auxiliary materials, fully mix heating and melting, stir, insulation is 1.0～4.0 millimeters at 45～95 ℃ of temperature following system, dropper bore, splash in-20～25 ℃ liquid paraffin, methyl-silicone oil or the vegetable oil, make drop pill, promptly.
Preferred manufacturing procedure is as follows:
(a): get 260～450 parts of Radix Notoginseng, 2～10 parts of Borneolum Syntheticums are standby;
(b): get Radix Notoginseng and decoct with water 2～4 times, collecting decoction filters, filtrate concentrates, and adds 1～3 times of amount 90～97% ethanol, leaves standstill 18～30 hours, filter, reclaim ethanol, filtrate is concentrated under 50～75 ℃ of conditions, relative density is 1.20～1.40 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the appropriate amount of auxiliary materials, fully mix, mixture stirs at 50～115 ℃ of heating and meltings, and mixing time is 10～30 minutes, insulation, at 60～85 ℃ of temperature following system, dropper bore is 1.1～3.5 millimeters, splashes in 0～18 ℃ the liquid paraffin, methyl-silicone oil back packing to be dried, make drop pill, promptly.
Best preparation method is as follows:
(a): get 330 parts of Radix Notoginseng, 3.3 parts of Borneolum Syntheticums are standby;
(b): get Radix Notoginseng and decoct with water three times, collecting decoction filters, and filtrate concentrates, and adds 2 times of amount 95% ethanol, leaves standstill 24 hours, filter, and recovery ethanol, filtrate is concentrated under 55～60 ℃ of conditions, relative density is 1.33～1.35 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the adjuvant, fully mix, mixture stirs at 64 ℃ of heating and meltings, mixing time is 10～30 minutes, insulation is 1.2～2.5 millimeters at 64 ℃ of temperature following system, dropper bore, splashes in 0 ℃ the methyl-silicone oil, liquid coolant is use up and wiped to the drop pill drop that forms, back packing to be dried is made drop pill, promptly.
The best preparation method of medicine of the present invention is:
(a): get 330 parts of Radix Notoginseng, 3.3 parts of Borneolum Syntheticums are standby;
(b): get Radix Notoginseng and decoct with water three times, collecting decoction filters, and filtrate concentrates, and adds 2 times of amount 95% ethanol, leaves standstill 24 hours, filter, and recovery ethanol, filtrate is concentrated under 55～60 ℃ of conditions, relative density is 1.33～1.35 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); The ratio that (1) (2) are added weight is 1: 0.2～1: 0.3 xylitol and starch mixture; Or the ratio of weight is 1: 0.2～1: 0.3 lactose and starch mixture; Or the ratio of weight is in 1: 0.2～1: 0.4 xylitol and the arabic gum mixture, fully mix, mixture stirs at 64 ℃ of heating and meltings, mixing time is 10～30 minutes, insulation is 1.2～2.5 millimeters at 64 ℃ of temperature following system, dropper bore, splashes in 0 ℃ the methyl-silicone oil, liquid coolant is use up and wiped to the drop pill drop that forms, back packing to be dried is made drop pill, promptly.
More than form when producing and to increase or to reduce according to corresponding ratio, as large-scale production can be unit with kilogram or with the ton, small-scale production can be unit with the gram also, and weight can increase or reduce, but the crude drug material weight proportion constant rate between each composition.
More than each single medicinal material, especially adjuvant drug, messenger drug or adjuvant drug and messenger drug in forming, can be replaced by suitable Chinese medicine individually or simultaneously with the identical property of medicine, effect, it is constant to replace back Chinese medicine preparation and drug effect thereof.
Medicine of the present invention can be determined usage and dosage according to patient's situation in use, but every day 1-3 time, and every day, each crude drug consumption was as the criterion with the state-promulgated pharmacopoeia dosage, was no more than the pharmacopeia ormal weight.
The drop pill that the present invention is prepared, conventional drop pill advantage is simple as preparing except having, steady quality, can make liquid medicine solidification, convenient drug administration, and efficient, quick-acting, its biggest advantage is:
1, the selected adjuvant pure natural of the present invention degree height: the substrate adjuvant that employed substrate adjuvant derives from natural plants or originates based on natural plants among the present invention, selected substrate adjuvant is xylitol and starch or lactose and starch or xylitol and arabic gum, this substrate adjuvant has pure natural degree height, toxic and side effects is low, mouthfeel is good, dissolve scattered time limit is short, rapid-action, it is a kind of new medium adjuvant, can be used for substituting present chemosynthesis substrate adjuvant, the drop pill made from this kind adjuvant, it is low to solve the pure natural degree that present drop pill substrate faced, and more and more can not satisfy people and require back to nature, take low toxicity, the problem of the pure natural medical that has no side effect.
2, some problems in the outlet of solution Chinese medicine: medicine of the present invention also can solve Chinese medicine preparation, some problems of in exit procedure, being run into of dropping pill formulation particularly, solve because different countries, especially the European countries of industry prosperity are to the difference identification of the selected adjuvant of Chinese medicine dropping pill formulation, overcome as the selected adjuvant Polyethylene Glycol of the dropping pill formulation of the health food outlet defective in some national food additive catalogue not, improve the Chinese medicine dripping pills preparation and move towards the international market, strengthen the competitiveness of international market.
3, solve the relatively poor problem of drop pill taste and further improve drug effect speed (dissolve scattered time limit): the medicinal dropping ball made from this kind substrate adjuvant of the present invention, can improve Chinese medicine preparation, the particularly present not good shortcoming of dropping pill formulation taste, improve mouthfeel, more easy for patients to accept, and the drop pill that adopts the selected adjuvant of medicine of the present invention to make has shorter dissolve scattered time limit, making drug effect faster, is the medicine that coronary heart disease, angina pectoris, myocardial ischemia are treated in a kind of onset faster.
4, higher safety and solve some problems in the drop pill storage process: the selected substrate of the present invention is not only additive, nutrient commonly used in the food industry, and can do medicinal, but do not see that it uses as the drug matrices adjuvant, therefore, with regard to substrate, be perfectly safe, have no side effect, a large amount of evidences, the drop pill that this adjuvant is made can reduce effective ingredient separating out in storage process, the sticking ball of drop pill, easy shortcomings such as moisture absorption deliquescing, but the big production of suitability for industrialized.
Medicine of the present invention confirms through a large amount of tests, has treatment angina pectoris, hypertension, alleviates the radical pair cardiac vascular endothelial cell injury, alleviates the radical pair myocardial cell injury, anti-angiogenic permeability, that vascular permeability strengthens microcirculation disturbance, hepatic disease, diabetes and complication thereof is all effective in cure.
In order to understand the present invention better, dissolve scattered time limit, weight differential, drop pill soft durometer, the drop pill with ice seven drop pill glues test explanation advantages of the present invention such as ball below.
Test example 1: dissolve scattered time limit, weight differential contrast experiment's example of icing seven drop pill
In vitro tests
The present invention be that ice seven drop pill that adjuvant is made compare with the Polyethylene Glycol, by measuring dissolve scattered time limit, investigate its good releasing effect; By measuring indexs such as the ball method of double differences is different, whether ripe, whether be fit to suitability for industrialized production if investigating its preparation technology.
1. test medication: the new substrate of the present invention is iced seven drop pill (newly), is ice seven drop pill (old) that adjuvant is made with the Polyethylene Glycol.
2. method and result:
Dissolve scattered time limit: by " method is measured under this item of Chinese pharmacopoeia; The ball method of double differences is different: by " method is measured under this item of Chinese pharmacopoeia.Result of the test sees Table 1.
Ice seven drop pill (newly) that three batches in table 1 is made with the new medium adjuvant with the polyethylene glycol 6000 be ice seven drop pill (old) dissolve scattered time limit made of adjuvant, weight differential relatively
| 0 month | January | February | March | June | December | 18 months | ||
| 1 batch | Criterion | The result | ||||||
| Weight differential (± 15%) | All in 10% | All in 10% | All in 10% | All in 10% | All in 10% | All in 10% | All in 10% | |
| Dissolve scattered time limit (newly) (30 minutes) (old) | ??1′55″ ????4′28″ | ??1′55″ ????4′29″ | ??1′56″ ????4′31″ | ??1′58″ ????4′34″ | ??1′59″ ????4′39″ | ??2′1″ ????4′32″ | ??2′3″ ????4′35″ | |
| 2 batches | Weight differential (± 15%) | All in 10% | All in 10% | All in 10% | All in 10% | All in 10% | All in 10% | All in 10% |
| Dissolve scattered time limit (newly) (30 minutes) (old) | ??1′53″ ????4′29″ | ??1′55″ ????4′31″ | ??1′55″ ????4′31″ | ??2′56″ ????4′35″ | ??1′58″ ????4′32″ | ??2′2″ ????4′34″ | ??2′2″ ????4′36″ | |
| 3 batches | Weight differential (± 15%) | All in 10% | All in 10% | All in 10% | All in 10% | All in 10% | All in 10% | All in 10% |
| Dissolve scattered time limit (newly) (30 minutes) (old) | ??1′55″ ????4′30″ | ??1′56″ ????4′31″ | ??1′57″ ????4′33″ | ??1′57″ ????4′38″ | ??1′59″ ????4′36″ | ??2′2″ ????4′30″ | ??2′3″ ????4′35″ |
Test data shows, the dissolve scattered time limit that new substrate is iced seven drop pill is lacking of ice seven drop pill made of adjuvant with the Polyethylene Glycol, and new and old substrate drop pill weight differential all is controlled in the pharmacopeia prescribed limit.Result of the test explanation, the molten diffusing speed of ice seven drop pill made from novel adjuvant is faster, is more conducive to medicine and plays a role in the shortest time, and the ice seven drop pill weight differentials that new and old substrate is made all are controlled in the pharmacopeia prescribed limit, but suitability for industrialized production.
Test example 2: the present invention with the polyethylene glycol 6000 be the sticking ball comparative observation of ice seven drop pill soft durometer, drop pill that adjuvant is made
1. reagent: the new substrate of the present invention is iced seven drop pill (newly), is ice seven drop pill (old) that adjuvant is made with the Polyethylene Glycol.
2. method and result: three batches of the things of getting it filled are loaded in the porcelain vase respectively, and use the bottle stopper good seal.Putting it into the bottom has in the exsiccator of saturated Nacl (humidity 75%) solution, exsiccator is put into 40 ℃ of drying baker of constant temperature again, and timing sampling is observed situations such as drop pill soft durometer, the sticking ball of drop pill, the results are shown in Table 2.1, table 2.2.
Three batches in table 2.1 is that the ice seven drop pill reserved sample observings that adjuvant is made compare with the polyethylene glycol 6000
| 0 month | January | February | March | June | December | 18 months | ||
| 1 batch | Criterion | The result | ||||||
| Sticking ball | Not sticking | Not sticking | Not sticking | Not sticking | Not sticking | Sticking slightly | Sticking slightly | |
| Soft durometer | Firmly | Firmly | Firmly | Firmly | Firmly | Harder | Harder | |
| 2 batches | Sticking ball | Not sticking | Not sticking | Not sticking | Not sticking | Not sticking | Not sticking | Sticking slightly |
| Soft durometer | Firmly | Firmly | Firmly | Firmly | Firmly | Harder | Harder | |
| 3 batches | Sticking ball | Not sticking | Not sticking | Not sticking | Not sticking | Not sticking | Sticking slightly | Sticking slightly |
| Soft durometer | Firmly | Firmly | Firmly | Firmly | Firmly | Harder | Harder | |
Table 2.2: three batches of ice seven drop pill made from the new medium adjuvant (newly) with the polyethylene glycol 6000 be ice seven drop pill (old) character observation made of adjuvant relatively
| 0 month | January | February | March | June | December | 18 months | ||
| Criterion | The result | |||||||
| 1 batch | Sticking ball | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) slightly | Sticking (old) glues (newly) slightly slightly | Sticking (old) be sticking (newly) slightly |
| Soft durometer | (old) hard (newly) firmly | (old) hard (newly) firmly | (old) hard (newly) firmly | (old) hard (newly) firmly | Hard (old) hard (newly) | Hard slightly (old) hard (newly) | Hard slightly (old) be hard (newly) slightly | |
| 2 batches | Sticking ball | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) slightly | Sticking (old) glues (newly) slightly slightly |
| Soft durometer | (old) hard (newly) firmly | (old) hard (newly) firmly | (old) hard (newly) firmly | (old) hard (newly) firmly | Hard (old) hard (newly) | Hard slightly (old) hard (newly) | Hard slightly (old) be hard (newly) slightly | |
| 3 batches | Sticking ball | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) | Sticking (old) do not glue (newly) slightly | Sticking (old) do not glue (newly) slightly | Sticking (old) be sticking (newly) slightly |
| Soft durometer | (old) hard (newly) firmly | (old) hard (newly) firmly | (old) hard (newly) firmly | (old) hard (newly) firmly | (old) hard (newly) firmly | Hard slightly (old) hard (newly) | Hard slightly (old) be hard (newly) slightly |
Table 2.1,2.2 test data show, new substrate is iced seven drop pill soft durometer and changed and with the Polyethylene Glycol be the similar, strong slightly of ice seven drop pill made of adjuvant; The sticking ball variation of the drop pill of new substrate drop pill, firmness change and be the similar of ice seven drop pill made of adjuvant with the Polyethylene Glycol.The sticking ball of ice seven drop pill that presentation of results, new and old substrate adjuvant are made changes, firmness change is similar, and the alternative present chemosynthesis adjuvant of this natural substrates adjuvant is described, but suitability for industrialized production.
The specific embodiment
Embodiment 1:
(a): get Radix Notoginseng 330g, Borneolum Syntheticum 3.3g, xylitol 12g, xanthan gum 3g are standby;
(b): get Radix Notoginseng and decoct with water 5 times, collecting decoction filters, and filtrate concentrates, and adds 2 times of amount 90% ethanol, leaves standstill 20 hours, filter, and recovery ethanol, filtrate is concentrated under 50 ℃ of conditions, relative density is 1.15～1.25 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the xylitol and starch mixture of water-bath thawing, stir, insulation is 1.30～4.0 millimeters at 55～75 ℃ of temperature following system, dropper bore, drips system with the speed of 30～60 of per minutes, splash in the methyl-silicone oil, make 1000, after the shaping, ball is taken out, wipe away dried drop pill surface with absorbent paper, promptly.
Embodiment 2:
(a): get Radix Notoginseng 20g, Borneolum Syntheticum 1.5g, lactose 83g, starch 17g are standby;
(b): get Radix Notoginseng and decoct with water 2 times, collecting decoction filters, and filtrate concentrates, and adds 4 times of amount 85～95% ethanol, leaves standstill 36 hours, filter, and recovery ethanol, filtrate is concentrated under 70～80 ℃ of conditions, relative density is 1.10～1.25 clear paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the mixture of lactose that water-bath melts and starch, stir, insulation is 1.10～3.0 millimeters at 65～95 ℃ of temperature following system, dropper bore, drips system with the speed of 20～50 of per minutes, splash in the vegetable oil, make 1000 drop pill, after the shaping, ball is taken out, wipe away dried drop pill surface with absorbent paper, promptly.
Embodiment 3:
(a): get Radix Notoginseng 15g, Borneolum Syntheticum 0.8g, xylitol 37.5g, arabic gum 12.5g are standby;
(b): get Radix Notoginseng and decoct with water 3 times, collecting decoction filters, and filtrate concentrates, and adds 4 times of amount 85～90% ethanol, leaves standstill 18 hours, filter, and recovery ethanol, filtrate is concentrated under 40～50 ℃ of conditions, relative density is 1.05～1.15 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the mixture of xylitol and arabic gum, fully mix, mixture is at 50～95 ℃ of heating and meltings, stir, mixing time is 10～30 minutes, insulation, at 60～85 ℃ of temperature following system, dropper bore is 1.1～3.5 millimeters, speed with 50～60 of per minutes is dripped system, splashes in the methyl-silicone oil, makes 1000 drop pill, after the shaping, ball is taken out, wipe away dried drop pill surface with absorbent paper, promptly.
Embodiment 4
(a): get Radix Notoginseng 14g, Borneolum Syntheticum 1.2g, xylitol 30.7, arabic gum 8.3g is standby;
(b): get Radix Notoginseng and decoct with water 3 times, collecting decoction filters, and filtrate concentrates, and adds 3 times of amount 95% ethanol, leaves standstill 24 hours, filter, and recovery ethanol, filtrate is concentrated under 50～75 ℃ of conditions, relative density is 1.20～1.30 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the mixture of xylitol and arabic gum, fully mix, mixture is at 50～115 ℃ of heating and meltings, stir, mixing time is 10～30 minutes, insulation, at 60～85 ℃ of temperature following system, dropper bore is 1.1～3.5 millimeters, drips system with the speed of 20～60 of per minutes, splashes in 0～18 ℃ the liquid paraffin, back packing to be dried, make 1000 drop pill, after the shaping, ball is taken out, inhale the liquid Paraffin that goes to the ball surface with absorbent paper, promptly.
Embodiment 5
(a): Radix Notoginseng 20g, Borneolum Syntheticum 1.0g, xylitol 36g, pregelatinized Starch 4g are standby;
(b): get Radix Notoginseng and decoct with water 2～4 times, collecting decoction filters, filtrate concentrates, and adds 1～3 times of amount 90～97% ethanol, leaves standstill 18～30 hours, filter, reclaim ethanol, filtrate is concentrated under 50～75 ℃ of conditions, relative density is 1.20～1.40 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the xylitol and pregelatinized Starch mixture of water-bath thawing, fully mix, mixture stirs at 80～95 ℃ of heating and meltings, mixing time is 10～30 minutes, insulation is 1.2～2.5 millimeters at 60～65 ℃ of temperature following system, dropper bore, drips system with the speed of 40～60 of per minutes, splash in 0～18 ℃ the methyl-silicone oil, make 1000 drop pill, back packing to be dried, promptly.
Embodiment 6
(a): get Radix Notoginseng 17.6g, Borneolum Syntheticum 1g, sorbitol 15.5, starch 4.5g is standby;
(b): get Radix Notoginseng and decoct with water 3 times, collecting decoction filters, and filtrate concentrates, and adds 2 times of amount 95% ethanol, leaves standstill 24 hours, filter, and recovery ethanol, filtrate is concentrated under 60 ℃ of conditions, relative density is 1.20～1.40 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in sorbitol and the starch mixture, stir evenly, mixture is at 50～75 ℃ of heating and meltings, stir, mixing time is 10～30 minutes, insulation, at 60～65 ℃ of temperature following system, dropper bore is 1.1～3.5 millimeters, speed with 60～80 of per minutes is dripped system, splashes in 0～18 ℃ the liquid paraffin, makes 1000 drop pill, after the shaping, ball is taken out, inhale the liquid Paraffin that goes to the ball surface with absorbent paper, promptly.
Embodiment 7
(a): get Radix Notoginseng 17.6g, Borneolum Syntheticum 1g, xylitol 14.6g, carrageenan 5.4g are standby;
(b): get Radix Notoginseng and decoct with water three times, collecting decoction filters, and filtrate concentrates, and adds 2 times of amount 95% ethanol, leaves standstill 24 hours, filter, and recovery ethanol, filtrate is concentrated under 55～60 ℃ of conditions, relative density is 1.33～1.35 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in xylitol and the carrageenan mixture, stir evenly, mixture is at 80～115 ℃ of heating and meltings, stir, mixing time is 10～30 minutes, insulation, 70 ± 2 ℃ following system, drip system with the speed of 60～80 of per minutes, the dropper bore is 1.1～3.5 millimeters, splash in 0～18 ℃ the liquid vegetable oil, make 1000 drop pill, after the shaping, ball is taken out, inhale the liquid Paraffin that goes to the ball surface with absorbent paper, promptly.
Embodiment 8
(a): get Radix Notoginseng 17.6g, Borneolum Syntheticum 1g, lactose 16g, starch 4g are standby;
(b): get Radix Notoginseng and decoct with water three times, collecting decoction filters, and filtrate concentrates, and adds 2 times of amount 95% ethanol, leaves standstill 24 hours, filter, and recovery ethanol, filtrate is concentrated under 55～60 ℃ of conditions, relative density is 1.33～1.35 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the mixture of lactose and starch, mixture stirs at 64 ℃ of heating and meltings, mixing time is 10～30 minutes, insulation is 1.2～2.5 millimeters at 64 ℃ of temperature following system, dropper bore, drips system with the speed of 20～60 of per minutes, splash in 0 ℃ the methyl-silicone oil, make 1000 drop pill, liquid coolant is use up and wiped to the drop pill drop that forms, back packing to be dried, make 1000 drop pill, promptly
Embodiment 9
(a): get Radix Notoginseng 17.6g, Borneolum Syntheticum 1g, xylitol 14g, arabic gum 6g are standby;
(b): get Radix Notoginseng and decoct with water three times, collecting decoction filters, and filtrate concentrates, and adds 2 times of amount 95% ethanol, leaves standstill 24 hours, filter, and recovery ethanol, filtrate is concentrated under 55～60 ℃ of conditions, relative density is 1.33～1.35 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the mixture of xylitol and arabic gum, mixture stirs at 64 ℃ of heating and meltings, mixing time is 10～30 minutes, insulation, in following system of 64 ℃ of temperature, the dropper bore is 1.2～2.5 millimeters, speed with 20～40 of per minutes is dripped system, splash in 10 ℃ the methyl-silicone oil, to the greatest extent and wipe liquid coolant, back packing to be dried the drop pill drop that forms, make 1000 drop pill, promptly.
Embodiment 10
(a): get Radix Notoginseng 8.03g, Borneolum Syntheticum 0.46g, xylitol 12g, arabic gum 8g are standby;
(b): the pseudo-ginseng of the coarse pulverization of learning from else's experience adds 5 times of water gagings to extraction pot, decocts 2 hours, filters, and filtering residue carries out the second time and extracts, and adds 4 times of water gagings, decocts 1 hour, filters, and filtering residue discards, merging filtrate; Filtrate decompression is concentrated into medicine liquid volume (L) and medical material weight (Kg) than being 1: 0.9～1.1, slowly adds 95% ethanol, makes medicinal liquid contain determining alcohol 69～71%, leaves standstill 12 hours; Get the supernatant of medicinal liquid behind the precipitate with ethanol, filter, filtrate recycling ethanol, the simmer down to relative density is 1.32～1.40 extractum;
(c): get above-mentioned extractum and Borneolum Syntheticum, evenly mixed with the mixture of xylitol and arabic gum, mixture stirs at 64 ℃ of heating and meltings, mixing time is 10～30 minutes, insulation is 1.2～2.5 millimeters at 64 ℃ of temperature following system, dropper bore, splashes in 0 ℃ the methyl-silicone oil, liquid coolant is use up and wiped to the drop pill drop that forms, back packing to be dried is made drop pill, promptly.
Embodiment 11
(a): get Radix Notoginseng 6.38g, Borneolum Syntheticum 0.34g, lactose 11g, arabic gum 9g are standby;
(b): get Radix Notoginseng and decoct with water three times, collecting decoction filters, and filtrate concentrates, and adds 2 times of amount 95% ethanol, leaves standstill 24 hours, filter, and recovery ethanol, filtrate is concentrated under 55～60 ℃ of conditions, relative density is 1.33～1.35 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); In the lactose that (1) (2) are added and the mixture of arabic gum, mixture stirs at 75 ℃ of heating and meltings, mixing time is 10～30 minutes, insulation, in following system of 70 ℃ of temperature, the dropper bore is 1.2～2.5 millimeters, speed with 30～80 of per minutes is dripped system, splash in 0 ℃ the methyl-silicone oil, to the greatest extent and wipe liquid coolant, back packing to be dried the drop pill drop that forms, make 1000 drop pill, promptly.
Embodiment 12
(a): get Radix Notoginseng 8.03g, Borneolum Syntheticum 0.46g, lactose 15g, carboxymethyl starch 3g, arabic gum 2g is standby;
(b): the pseudo-ginseng of the coarse pulverization of learning from else's experience adds 5 times of water gagings to extraction pot, decocts 2 hours, filters, and filtering residue carries out the second time and extracts, and adds 4 times of water gagings, decocts 1 hour, filters, and filtering residue discards, merging filtrate; Filtrate decompression is concentrated into medicine liquid volume (L) and medical material weight (Kg) than being 1: 0.9～1.1, slowly adds 95% ethanol, makes medicinal liquid contain determining alcohol 69～71%, leaves standstill 12 hours; Get the supernatant of medicinal liquid behind the precipitate with ethanol, filter, filtrate recycling ethanol, the simmer down to relative density is 1.32～1.40 extractum.
(c): get above-mentioned extractum and Borneolum Syntheticum, with the ratio of weight be the mixture of 1: 0.2～1: 0.4 lactose, carboxymethyl starch and arabic gum, fully mix, mixture is at 80～95 ℃ of heating and meltings, stir, mixing time is 10～30 minutes, and insulation is 1.21～2.5 millimeters at 60～85 ℃ of temperature following system, dropper bore, splash in 0～18 ℃ the vegetable oil, back packing to be dried is made drop pill, promptly.
Embodiment 13:
(a): get the extractum 7g for preparing by embodiment 8 methods, Borneolum Syntheticum 0.1g, xylitol 18.5g, starch 1.5g are standby;
(b): with xylitol and starch mix homogeneously, add above-mentioned extractum and Borneolum Syntheticum, mixture is at 75 ℃ of heating and meltings, stir, mixing time is 10～30 minutes, and insulation is 1.2～2.5 millimeters at 60～70 ℃ of temperature following system, dropper bore, splash in 0 ℃ the methyl-silicone oil, speed with 50～60 of per minutes is dripped system, splashes in the methyl-silicone oil, makes 1000, after the shaping, ball is taken out, liquid coolant is use up and wiped to the drop pill drop that forms, back packing to be dried, make 1000 drop pill, promptly.
Embodiment 13:
(a): it is standby to get Radix Notoginseng extractum 6.5g, the Borneolum Syntheticum 1.2g, xylitol 16.5g, the arabic gum 3.5g that obtain by embodiment 3 methods;
(b) xylitol is mixed with arabic gum, mixture adds above-mentioned extractum, Borneolum Syntheticum at 55～85 ℃ of heating and meltings, stir, mixing time is 10～30 minutes, insulation, in following system of 60～75 ℃ of temperature, the dropper bore is 1.2～2.5 millimeters, drips system with the speed of 60～80 of per minutes, splashes in 0 ℃ the vegetable oil, make 1000 drop pill, liquid coolant is use up and wiped to the drop pill drop that forms, back packing to be dried, promptly.
Embodiment 14:
(a): it is standby to get Radix Notoginseng extractum 12.5g, the Borneolum Syntheticum 3.2g, lactose 20g, the arabic gum 3.5g that obtain by embodiment 1 method;
(b) lactose is mixed with arabic gum, mixture adds above-mentioned extractum, Borneolum Syntheticum at 55～85 ℃ of heating and meltings, stir, mixing time is 10～30 minutes, insulation, in following system of 60～75 ℃ of temperature, the dropper bore is 1.2～2.5 millimeters, drips system with the speed of 30～50 of per minutes, splashes in 5～10 ℃ the vegetable oil, make 1000 drop pill, liquid coolant is use up and wiped to the drop pill drop that forms, back packing to be dried, promptly.
Embodiment 15
(a): it is standby to get Radix Notoginseng extractum 5.5g, the Borneolum Syntheticum 0.5g, xylitol 16.5g, the starch 3.5g that obtain by embodiment 7 methods;
(b) xylitol is mixed with starch, mixture adds above-mentioned extractum, Borneolum Syntheticum at 60～85 ℃ of heating and meltings, stir, mixing time is 10～30 minutes, insulation, in following system of 60～85 ℃ of temperature, the dropper bore is 1.2～2.5 millimeters, drips system with the speed of 20～60 of per minutes, splashes in 5～15 ℃ the liquid paraffin, make 1000 drop pill, liquid coolant is use up and wiped to the drop pill drop that forms, back packing to be dried, promptly.
Embodiment 16
(a): it is standby to get Radix Notoginseng extractum 4.65g, the Borneolum Syntheticum 0.85g, xylitol 15.5g, the arabic gum 4.5g that obtain by embodiment 4 methods;
(b) xylitol is mixed with arabic gum, mixture adds above-mentioned extractum, Borneolum Syntheticum at 65～85 ℃ of heating and meltings, stir, mixing time is 10～20 minutes, insulation, in following system of 60～65 ℃ of temperature, the dropper bore is 1.21～2.5 millimeters, drips system with the speed of 20～40 of per minutes, splashes in-10～15 ℃ the vegetable oil, make 1000 drop pill, liquid coolant is use up and wiped to the drop pill drop that forms, back packing to be dried, promptly.
Claims (13)
1, a kind of ice seven drop pill, it is characterized in that it is to be made by 150～600 parts of Radix Notoginseng, 1.5～50 parts of Borneolum Syntheticums, appropriate amount of auxiliary materials, wherein adjuvant comprises filler and plasticity substrate, said filler is selected from the natural adjuvant of following one or more plant origins: erythritol, sorbitol, fructose, D-ribonic acid-gamma lactone, arabitol, trehalose, D-ribose, low melting-point agarose, Lac, xylitol, Raffinose, glucose, malic acid, citric acid, isomalt, lactose, maltose etc., and they contain the water of crystallization chemical compound; Said plasticity substrate is selected from the natural adjuvant of following one or more plant origins: starch and derivant thereof, cellulose and derivant thereof, arabic gum, dextran, chitin, sesbania gum, carrageenan, Ficus elastica, Furcellaran, tragakanta, carrageenin, tamarind gum, pectin, xanthan gum, alginic acid and salt thereof, dextrin, cyclodextrin, agar, lactose; Described starch and derivant thereof such as pregelatinized Starch, modified starch, hydroxypropyl starch, carboxymethyl starch, described cellulose and derivant thereof such as methylcellulose, microcrystalline Cellulose, sodium carboxymethyl cellulose, hydroxypropyl emthylcellulose, cross-linking sodium carboxymethyl cellulose, hydroxyethylmethyl-cellulose, hydroxyethyl-cellulose, hydroxypropyl cellulose.
2, ice seven drop pill as claimed in claim 1, it is characterized in that it is to be made by 260～450 parts of Radix Notoginseng, 2～10 parts of Borneolum Syntheticums, appropriate amount of auxiliary materials, filler adjuvant wherein is selected from following one or more the natural adjuvant of plant origin: sorbitol, xylitol, lactose, maltose, and they contain the water of crystallization chemical compound; Plasticity substrate wherein is selected from the natural adjuvant of following one or more plant origins: pregelatinized Starch, carboxymethyl starch, methylcellulose, sodium carboxymethyl cellulose, hydroxypropyl emthylcellulose, arabic gum, alginic acid, dextrin, cyclodextrin, agar, lactose.
3, ice seven drop pill as claimed in claim 2 is characterized in that it is to be made by 330 parts of Radix Notoginseng, 3.3 parts of Borneolum Syntheticums, appropriate amount of auxiliary materials, and filler adjuvant wherein is selected from following one or more the natural adjuvant of plant origin: xylitol, lactose; Plasticity substrate wherein is selected from the natural adjuvant of following one or more plant origins: starch, arabic gum.
4, as claim 1,2 or 3 described ice seven drop pill, it is characterized in that it can also contain chemosynthesis adjuvant and animal origin adjuvant in above-mentioned dressing, wherein filler comprises phenylglycol, hexadecanol, octadecanol, sodium stearate, tristerin, tripalmitin, carbamide, polyoxyethylene monostearate, polyoxyethylene alkyl ether; Wherein plasticity substrate comprises polyvinylpyrrolidone, crospolyvinylpyrrolidone, carbomer, polyvinyl alcohol, acrylic resin, poloxamer, gelatin.
5, ice seven drop pill as claimed in claim 3 is characterized in that described adjuvant is xylitol and starch, and xylitol is 1: 0.2～1: 0.3 with the ratio of the weight of starch.
6, ice seven drop pill as claimed in claim 3 is characterized in that described adjuvant is lactose and starch, and lactose is 1: 0.2～1: 0.3 with the ratio of the weight of starch.
7, ice seven drop pill as claimed in claim 3 is characterized in that described adjuvant is xylitol and arabic gum, and the ratio of the weight of xylitol and arabic gum is 1: 0.2～1: 0.4.
8,, it is characterized in that the adjuvant and the ratio of the weight of extract drugs extractum are 1: 0.1～1: 1 as claim 1,2 or 3 described ice seven drop pill.
9,, it is characterized in that the adjuvant and the ratio of the weight of extract drugs extractum are 1: 0.1～1: 0.6 as claim 1,2 or 3 described ice seven drop pill.
10,, it is characterized in that the adjuvant and the ratio of the weight of extract drugs extractum are 1: 0.2～1: 0.4 as claim 1,2 or 3 described ice seven drop pill.
11, the preparation method of claim 1,2 or 3 described ice seven drop pill is characterized in that this method comprises the steps:
(a): get 150～600 parts of Radix Notoginseng, 1.5～50 parts of Borneolum Syntheticums are standby;
(b):. get Radix Notoginseng and decoct with water 1～5 time, collecting decoction filters, filtrate concentrates, and adds 0.5～5 times of amount 80～99% ethanol, leaves standstill 12～36 hours, filter, reclaim ethanol, filtrate is concentrated under 30～80 ℃ of conditions, relative density is 1.05～1.45 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the appropriate amount of auxiliary materials, fully mix heating and melting, stir, insulation is 1.0～4.0 millimeters at 45～95 ℃ of temperature following system, dropper bore, splash in-20～25 ℃ liquid paraffin, methyl-silicone oil or the vegetable oil, make drop pill, promptly.
12, the preparation method of ice seven drop pill as claimed in claim 11 is characterized in that this method comprises the steps:
(a): get 260～450 parts of Radix Notoginseng, 2～10 parts of Borneolum Syntheticums are standby;
(b):. get Radix Notoginseng and decoct with water 2～4 times, collecting decoction filters, filtrate concentrates, and adds 1～3 times of amount 90～97% ethanol, leaves standstill 18～30 hours, filter, reclaim ethanol, filtrate is concentrated under 50～75 ℃ of conditions, relative density is 1.20～1.40 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the appropriate amount of auxiliary materials, fully mix, mixture stirs at 50～115 ℃ of heating and meltings, and mixing time is 10～30 minutes, insulation, at 60～85 ℃ of temperature following system, dropper bore is 1.1～3.5 millimeters, splashes in 0～18 ℃ the liquid paraffin, methyl-silicone oil back packing to be dried, make drop pill, promptly.
13, the preparation method of ice seven drop pill as claimed in claim 11 is characterized in that this method comprises the steps:
(a): get 330 parts of Radix Notoginseng, 3.3 parts of Borneolum Syntheticums are standby;
(b): get Radix Notoginseng and decoct with water three times, collecting decoction filters, and filtrate concentrates, and adds 2 times of amount 95% ethanol, leaves standstill 24 hours, filter, and recovery ethanol, filtrate is concentrated under 55～60 ℃ of conditions, relative density is 1.33～1.35 thick paste (1);
(c): get Borneolum Syntheticum and be dissolved in the adequate amount of ethanol, get solution (2); (1) (2) are added in the adjuvant, fully mix, mixture stirs at 64 ℃ of heating and meltings, mixing time is 10～30 minutes, insulation is 1.2～2.5 millimeters at 64 ℃ of temperature following system, dropper bore, splashes in 0 ℃ the methyl-silicone oil, liquid coolant is use up and wiped to the drop pill drop that forms, back packing to be dried is made drop pill, promptly.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2003101073054A CN100512825C (en) | 2003-12-11 | 2003-12-11 | Icy seven drop pills and its preparation method |
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| Application Number | Priority Date | Filing Date | Title |
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| CNB2003101073054A CN100512825C (en) | 2003-12-11 | 2003-12-11 | Icy seven drop pills and its preparation method |
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| CN1626146A true CN1626146A (en) | 2005-06-15 |
| CN100512825C CN100512825C (en) | 2009-07-15 |
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Granted publication date: 20090715 Termination date: 20191211 |