CN101829162A - Pharmaceutical composition for treating allergic rhinitis and preparation method thereof - Google Patents
Pharmaceutical composition for treating allergic rhinitis and preparation method thereof Download PDFInfo
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- CN101829162A CN101829162A CN201010182489A CN201010182489A CN101829162A CN 101829162 A CN101829162 A CN 101829162A CN 201010182489 A CN201010182489 A CN 201010182489A CN 201010182489 A CN201010182489 A CN 201010182489A CN 101829162 A CN101829162 A CN 101829162A
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- 201000010105 allergic rhinitis Diseases 0.000 title claims abstract description 42
- 206010039085 Rhinitis allergic Diseases 0.000 title claims abstract description 41
- 238000002360 preparation method Methods 0.000 title claims abstract description 29
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 24
- 239000003814 drug Substances 0.000 claims abstract description 21
- 241000238675 Periplaneta americana Species 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 13
- 238000002156 mixing Methods 0.000 claims abstract description 8
- 239000000203 mixture Substances 0.000 claims abstract description 5
- 239000000284 extract Substances 0.000 claims description 56
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 44
- 239000000706 filtrate Substances 0.000 claims description 40
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 36
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 36
- 238000001914 filtration Methods 0.000 claims description 23
- 239000007788 liquid Substances 0.000 claims description 22
- 239000002674 ointment Substances 0.000 claims description 22
- 239000000843 powder Substances 0.000 claims description 19
- 238000003756 stirring Methods 0.000 claims description 16
- 238000000605 extraction Methods 0.000 claims description 13
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- SSISHJJTAXXQAX-ZETCQYMHSA-N L-ergothioneine Chemical compound C[N+](C)(C)[C@H](C([O-])=O)CC1=CNC(=S)N1 SSISHJJTAXXQAX-ZETCQYMHSA-N 0.000 description 1
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- 208000036284 Rhinitis seasonal Diseases 0.000 description 1
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- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
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- Medicines Containing Plant Substances (AREA)
Abstract
The invention discloses a pharmaceutical composition for treating allergic rhinitis, mainly comprising mixtures with effective components prepared from 1-2 parts by weight of periplaneta Americana extractive and 4-18 parts by weight of ephedra. The method for preparing the pharmaceutical composition for treating allergic rhinitis comprises the following steps of: extracting the periplaneta Americana extractive and the effective components of the ephedra, and mixing to prepare the medicine. The preparation method of the invention is simple, gives full play to the periplaneta Americana extractive, and effectively improves the healing effect of allergic rhinitis; and the pharmaceutical composition is a new medicament worth of promoting, is convenient to use and has little toxic and side-effect.
Description
Technical field
The present invention relates to medical technical field, be specifically related to pharmaceutical composition of a kind of treatment of allergic rhinitis and preparation method thereof.
Background technology
It is documented that periplaneta americana is the insecticide of volume maximum in the Blattidae, originates in South America, periplaneta americana is traditional Chinese crude drug, is used as medicine its property plug salty in the mouth with dry and bright adult, poisonous, acid is arranged, functions such as dissipating blood stasis, removing food stagnancy, detoxifcation, diuretic, detumescence are arranged; Curing mainly infantile malnutrition, tonsillitis, health enclosed mass, carbuncle skin ulcer swells and ache and Scolopendra, venom etc.
Along with science and technology constantly develops, after years of research and found that in recent years the periplaneta americana epidermis contains sclerotin and chitin, elements such as bromine, zinc, nickel, violent, potassium, calcium, titanium, chlorine, sulfur, silicon, aluminum, magnesium; Muscle hydrolysis 13 seed amino acids; Its alcohol extract has the obvious suppression effect to cancerous cell, and cardiovascular disease is had tangible curative effect.In addition, health storage vitamin B
1, B
2, nicotinic acid and ascorbic acid etc., lymph contain trehalose, trehalase, glycoprotein, inositol, protocatechuic acid Fructus Vitis viniferae glycoside etc.All contain ergothioneine, 1-methyl-2-pyridinium carboxylate, trigonelline, glycine, betanin, anus alkali, trimethylamine, adenine etc.Clinical main application has: treat infantile malnutrition, control the carbuncle pyogenic infections from tumour or sore, control the Scolopendra wound, control innominate toxic swelling, control the worm venom.But also have periplaneta americana and medical herbs compatibility auxiliary treatment colon cancer.American-cockroach-extract can be controlled hepatitis B, and extract A T-2 preparation can cure mainly primary hepatocarcinoma, cardiovascular disease etc.
Notification number is CN 100525781C, name is called " American-cockroach-extract; contain pharmaceutical composition of this extract and preparation method thereof " and publication number is CN1943600A, it is two with the American-cockroach-extract relevant patent documentations of applicant in application in 2006 that name is called " pharmaceutical composition and the new purposes thereof that contain periplaneta americana and ethanol extraction thereof ", it discloses the preparation method and the part medical usage of American-cockroach-extract, in recent years, along with the further research to American-cockroach-extract, American-cockroach-extract has obtained further development in purposes pharmaceutically.
Allergic rhinitis is allergic rhinitis (allergic rhintis) again, is the allergic disease of nasal membrane, and can causes multiple complications.Sickness rate has rising to warm up in recent years.Allergic rhinitis is morbidity easily in the winter time generally, and the branch of long-term property, seasonality is arranged.Seasonal allergic rhinitis then is the outbreak in season, how in spring, morbidity in autumn.Classical symptom is that nasal obstruction, rhinocnesmus, headache, paroxysmal sneeze are shown effect continuously, a large amount of water sample nasal mucus and olfactory disorder etc.Badly influence patient's the quality of life so that the health status of whole machine body, also have influence on patient's doings and physical work.For example the allergic rhinitis outbreak time is difficult to the work of concentrating one's energy, if attend a meeting or in other public arenas outbreaks, also can bring embarrassed sensation to the people.The expert points out that allergic rhinitis should be treated as early as possible, otherwise can cause allergic asthma.
The allergic rhinitis common method of treatment has: 1, avoid therapy; 2, pharmacotherapy; 3, intranasal spray; 4, nasal injection method; 5, electricity burns or cryotherapy; 6, laser therapy; 7, hyposensitization; 8, hands art; 9, traditional Chinese medical science intranasal point medicine method.
At present, doctor trained in Western medicine is many to the many employings of the treatment of allergic rhinitis with antihistamine drug for oral administration, the interim inhibition of corticosteroids medicine, as oral western medicine, oral hormone, externally used solution lotion, Emulsion, mud cream, oil preparation, ointment, Emulsion, liniment, tincture and plaster etc.The corticosteroids medicine is used in long-time or heavy dose of external, can addiction cause drug dependence, and modal is that sb.'s illness took a favorable turn after the medication, in case after the drug withdrawal, the agents area primary affection increases the weight of.After again with hormone, above-mentioned sb.'s illness took a favorable turn or disappearance; As drug withdrawal again, knock-on property is sent out again, and than more serious in the past.
In sum, existing medicine still has unsatisfactory part for treatment of allergic rhinitis.For this reason, the invention provides a kind of new pharmaceutical composition that is used for the treatment of allergic rhinitis.
Summary of the invention
The objective of the invention is to: overcome above-mentioned deficiency of the prior art, a kind of pharmaceutical composition and preparation method thereof of treatment of allergic rhinitis of effective raising cure rate is provided.
Purpose of the present invention is achieved through the following technical solutions: a kind of pharmaceutical composition of treatment of allergic rhinitis is provided, it is characterized in that: the main component of described pharmaceutical composition and mass parts thereof are such as shown in down: 1~2 part of American-cockroach-extract; 4~18 parts in Herba Ephedrae.
The proportioning of one of preferred version of the pharmaceutical composition of above-mentioned treatment of allergic rhinitis is: 1 part of American-cockroach-extract; 8 parts in Herba Ephedrae.
Two proportioning of the preferred version of the pharmaceutical composition of above-mentioned treatment of allergic rhinitis is: 2 parts of American-cockroach-extracts; 15 parts in Herba Ephedrae.
The preparation of drug combination method of above-mentioned treatment of allergic rhinitis may further comprise the steps:
1., the preparation of American-cockroach-extract:
A, coarse crushing: exsiccant periplaneta americana is pulverized, make the periplaneta americana coarse powder;
B, immersion: will add the water of 3~5 times of amounts in the coarse powder among the step a, soak and made the coarse powder mixed liquor in 0.5~2 hour, soaking temperature is 70 ℃~78 ℃, and the coarse powder mixed liquor adopts the method that decocts to carry out three times and extracts, and makes extracting solution;
C, three extractions: the coarse powder mixed liquor is carried out the first time extract, extraction time is 7~9 hours; Carry out the second time then behind the water that adds 2~4 times of amounts of surplus liquid in the surplus liquid after extracting for the first time and extract, extraction time is 5~7 hours; Extract for the third time behind the water that adds 2~4 times of amounts of surplus liquid in the surplus liquid after extracting for the second time at last, extraction time is 3~5 hours;
D, filtration for the first time: the extracting solution that three times are extracted among the step c is merged mixing, filter then and make one-level filtrate;
E, concentrated for the first time: relative density was 1.05~1.25 one-level concentrated solution when the one-level filtrate in the steps d was concentrated into 70 ℃~90 ℃;
F, alcoholization are handled: add the ethanol that concentration is 93%w/w~97%w/w in the one-level concentrated solution that makes in step e gradually, and fully stir, making it contain the alcohol amount reaches till 45%~55%, under 70 ℃~90 ℃ temperature conditions, be incubated 20~40 minutes, left standstill then 10~14 hours, and made solution of alcoholized;
G, filtration for the second time: the solution of alcoholized among the step f is discarded the upper strata oils and fats, and lower floor's medicinal liquid filters and makes secondary filtrate;
H, the second time concentrate: after the secondary filtrate in the step g was carried out the ethanol recycling, relative density was 1.20~1.25 secondary concentrated solution when being concentrated into 70 ℃~90 ℃;
I, unguentum preparation: the unguentum that the secondary concentrated solution among the step h is concentrated into moisture≤25%~35% under condition of normal pressure;
J, extract preparation: according to unguentum: the ratio of purified water: glycerol=1000g: 800ml~1200ml: 4ml~6ml adds purified water and glycerol in unguentum, stir, through plate-and-frame filtration, after filtrate is boiled 30 minutes, be chilled to room temperature, promptly get American-cockroach-extract, standby;
2., Herba Ephedrae is decocted with water twice, 2~4 hours for the first time, 1~3 hour for the second time, decocting liquid filtered filtrate merging, and sheet frame filters, and is concentrated into an amount of, standby;
3., with step 1. with step in 2. prepared two kinds of extracts mix and stir, through plate-and-frame filtration, after filtrate is boiled 2~40 minutes, again through the autoclave sterilization postcooling to room temperature, promptly get patent medicine.
Amount of water is 4 times of amounts in above-mentioned steps b, and soak time is 1 hour, and soaking temperature is 74 ℃.
At the autoclave sterilization of above-mentioned steps described in 3. is to carry out sterilization under 115 ℃~127 ℃ of temperature, pressure are the condition of 0.05Mpa~0.15Mpa, and sterilization time is 25~35 minutes.
In sum, the preparation of drug combination method that is used for the treatment of allergic rhinitis provided by the present invention is simple, and given full play to the effect of American-cockroach-extract, effectively improved curative effect to allergic rhinitis, and easy to use, toxic and side effects is little, is a kind of new medicine that is worthy to be popularized.
The specific embodiment
Below in conjunction with embodiment the specific embodiment of the present invention is described in further detail:
The main component of the pharmaceutical composition of treatment of allergic rhinitis provided by the present invention and mass parts ratio thereof are: 1~2 part of American-cockroach-extract; 4~18 parts in Herba Ephedrae.
The proportioning of one of preferred version of the pharmaceutical composition of above-mentioned treatment of allergic rhinitis is: 1 part of American-cockroach-extract; 8 parts in Herba Ephedrae.
Two proportioning of the preferred version of the pharmaceutical composition of above-mentioned treatment of allergic rhinitis is: 2 parts of American-cockroach-extracts; 15 parts in Herba Ephedrae.
The preparation of drug combination method of above-mentioned treatment of allergic rhinitis may further comprise the steps:
1., the preparation of American-cockroach-extract:
A, coarse crushing: exsiccant periplaneta americana is pulverized, make the periplaneta americana coarse powder;
B, immersion: will add the water of 3~5 times of amounts in the coarse powder among the step a, soak and made the coarse powder mixed liquor in 0.5~2 hour, soaking temperature is 70 ℃~78 ℃, and the coarse powder mixed liquor adopts the method that decocts to carry out three times and extracts, and makes extracting solution;
C, three extractions: the coarse powder mixed liquor is carried out the first time extract, extraction time is 7~9 hours; Carry out the second time then behind the water that adds 2~4 times of amounts of surplus liquid in the surplus liquid after extracting for the first time and extract, extraction time is 5~7 hours; Extract for the third time behind the water that adds 2~4 times of amounts of surplus liquid in the surplus liquid after extracting for the second time at last, extraction time is 3~5 hours;
D, filtration for the first time: the extracting solution that three times are extracted among the step c is merged mixing, filter then and make one-level filtrate;
E, concentrated for the first time: relative density was 1.05~1.25 one-level concentrated solution when the one-level filtrate in the steps d was concentrated into 70 ℃~90 ℃;
F, alcoholization are handled: add the ethanol that concentration is 93%w/w~97%w/w in the one-level concentrated solution that makes in step e gradually, and fully stir, making it contain the alcohol amount reaches till 45%~55%, under 70 ℃~90 ℃ temperature conditions, be incubated 20~40 minutes, left standstill then 10~14 hours, and made solution of alcoholized;
G, filtration for the second time: the solution of alcoholized among the step f is discarded the upper strata oils and fats, and lower floor's medicinal liquid filters and makes secondary filtrate;
H, the second time concentrate: after the secondary filtrate in the step g was carried out the ethanol recycling, relative density was 1.20~1.25 secondary concentrated solution when being concentrated into 70 ℃~90 ℃;
I, unguentum preparation: the unguentum that the secondary concentrated solution among the step h is concentrated into moisture≤25%~35% under condition of normal pressure;
J, extract preparation: according to unguentum: the ratio of purified water: glycerol=1000g: 800ml~1200ml: 4ml~6ml adds purified water and glycerol in unguentum, stir, through plate-and-frame filtration, after filtrate is boiled 30 minutes, be chilled to room temperature, promptly get American-cockroach-extract, standby;
2., Herba Ephedrae is decocted with water twice, 2~4 hours for the first time, 1~3 hour for the second time, decocting liquid filtered filtrate merging, and sheet frame filters, and is concentrated into an amount of, standby;
3., with step 1. with step in 2. prepared two kinds of extracts mix and stir, through plate-and-frame filtration, after filtrate is boiled 2~40 minutes, again through the autoclave sterilization postcooling to room temperature, promptly get patent medicine.
Amount of water is 4 times of amounts in above-mentioned steps b, and soak time is 1 hour, and soaking temperature is 74 ℃.
At the autoclave sterilization of above-mentioned steps described in 3. is to carry out sterilization under 115 ℃~127 ℃ of temperature, pressure are the condition of 0.05Mpa~0.15Mpa, and sterilization time is 25~35 minutes.
Embodiment 1:
The prescription that is adopted is: 1 part of American-cockroach-extract; 8 parts in Herba Ephedrae.
Preparation method is: with exsiccant periplaneta americana coarse crushing, every 100Kg coarse powder adds 300Kg water, soaks after 0.5 hour, and temperature is extracted three times about 70 ℃, 7 hours for the first time; For the second time add water 200Kg, extracted 5 hours; Add water 200Kg for the third time, extracted 3 hours.Merge three times extracting solution, filter, when filtrate was concentrated into relative density and is 1.05 (70 ℃), adding concentration was the ethanol of 93%w/w, make that to become to contain alcohol amount be 45%, 70 ℃ of insulated and stirred 20 minutes left standstill 10 hours, discarded the upper strata oils and fats, lower floor's medical filtration, filtrate recycling ethanol, being evaporated to relative density is 1.20 (70 ℃), normal pressure is concentrated into the cream of moisture≤25%; Herba Ephedrae is decocted with water twice, and 2 hours for the first time, 1 hour for the second time, decocting liquid filtered filtrate merging, and sheet frame filters, and is concentrated into an amount of, standby; To stir after above-mentioned two kinds of extracts mixing, through plate-and-frame filtration, after filtrate was boiled 20 minutes, again through 115 ℃, pressure was 0.05Mpa, sterilized 25 minutes, was chilled to room temperature, promptly.
Embodiment 2:
The prescription that is adopted is: 2 parts of American-cockroach-extracts; 15 parts in Herba Ephedrae.
Preparation method is: with exsiccant periplaneta americana coarse crushing, every 100Kg coarse powder adds 500Kg water, soaks after 2 hours, and temperature is extracted three times about 78 ℃, 9 hours for the first time; For the second time add water 400Kg, extracted 7 hours; Add water 400Kg for the third time, extracted 5 hours.Merge three times extracting solution, filter, when filtrate was concentrated into relative density and is 1.25 (90 ℃), adding concentration was the ethanol of 97%w/w, make that to become to contain alcohol amount be 55%, 90 ℃ of insulated and stirred 40 minutes left standstill 14 hours, discarded the upper strata oils and fats, lower floor's medical filtration, filtrate recycling ethanol, being evaporated to relative density is 1.25 (90 ℃), normal pressure is concentrated into the unguentum of moisture≤35%; According to unguentum: the ratio of purified water: glycerol=1000g: 1200ml: 6ml adds purified water and glycerol in unguentum, stir, and through plate-and-frame filtration, filtrate is chilled to room temperature after boiling 30 minutes, promptly gets American-cockroach-extract, and is standby; Herba Ephedrae is decocted with water twice, and 4 hours for the first time, 3 hours for the second time, decocting liquid filtered filtrate merging, and sheet frame filters, and is concentrated into an amount of, standby; To stir after above-mentioned two kinds of extracts mixing, through plate-and-frame filtration, after filtrate was boiled 40 minutes, again through 127 ℃, pressure was 0.15Mpa, sterilized 35 minutes, was chilled to room temperature, promptly.
Embodiment 3:
The prescription that is adopted is: 1 part of American-cockroach-extract; 18 parts in Herba Ephedrae.
Preparation method is: with exsiccant periplaneta americana coarse crushing, every 100Kg coarse powder adds 400Kg water, soaks after 1 hour, and temperature is extracted three times about 74 ℃, 8 hours for the first time; For the second time add water 300Kg, extracted 6 hours; Add water 300Kg for the third time, extracted 4 hours.Merge three times extracting solution, filter, when filtrate was concentrated into relative density and is 1.15 (80 ℃), adding concentration was the ethanol of 95%w/w, make that to become to contain alcohol amount be 50%, 80 ℃ of insulated and stirred 30 minutes left standstill 12 hours, discarded the upper strata oils and fats, lower floor's medical filtration, filtrate recycling ethanol, being evaporated to relative density is 1.25 (80 ℃), normal pressure is concentrated into the unguentum of moisture≤30%; According to unguentum: the ratio of purified water: glycerol=1000g: 1000ml: 5ml adds purified water and glycerol in unguentum, stir, and through plate-and-frame filtration, filtrate is chilled to room temperature after boiling 30 minutes, promptly gets American-cockroach-extract, and is standby; Herba Ephedrae is decocted with water twice, and 3 hours for the first time, 2 hours for the second time, decocting liquid filtered filtrate merging, and sheet frame filters, and is concentrated into an amount of, standby; To stir after above-mentioned two kinds of extracts mixing, through plate-and-frame filtration, after filtrate was boiled 35 minutes, again through 121 ℃, pressure was 0.1Mpa, sterilized 30 minutes, was chilled to room temperature, promptly.
Embodiment 4:
The prescription that is adopted is: 2 parts of American-cockroach-extracts; 13 parts in Herba Ephedrae.
Preparation method is: with exsiccant periplaneta americana coarse crushing, every 100Kg coarse powder adds 380Kg water, soaks after 0.8 hour, and temperature is extracted three times about 74 ℃, 7.5 hours for the first time; For the second time add water 280Kg, extracted 5 hours; Add water 280Kg for the third time, extracted 3 hours.Merge three times extracting solution, filter, when filtrate was concentrated into relative density and is 1.2 (80 ℃), adding concentration was the ethanol of 95%w/w, make that to become to contain alcohol amount be 50%, 80 ℃ of insulated and stirred 30 minutes left standstill 11 hours, discarded the upper strata oils and fats, lower floor's medical filtration, filtrate recycling ethanol, being evaporated to relative density is 1.20 (80 ℃), normal pressure is concentrated into the unguentum of moisture≤30%; According to unguentum: the ratio of purified water: glycerol=1000g: 1100ml: 6ml adds purified water and glycerol in unguentum, stir, and through plate-and-frame filtration, filtrate is chilled to room temperature after boiling 30 minutes, promptly gets American-cockroach-extract, and is standby; Herba Ephedrae is decocted with water twice, and 2 hours for the first time, 2 hours for the second time, decocting liquid filtered filtrate merging, and sheet frame filters, and is concentrated into an amount of, standby; To stir after above-mentioned two kinds of extracts mixing, through plate-and-frame filtration, after filtrate was boiled 30 minutes, again through 121 ℃, pressure was 0.1Mpa, sterilized 30 minutes, was chilled to room temperature, promptly.
The pharmaceutical composition of treatment of allergic rhinitis provided by the present invention can be made various ways such as tablet, suppository, capsule, is beneficial to satisfy different patients' medication custom.
The clinical testing data of allergic rhinitis cure rate:
One, patient's classified data:
Allergic Rhinitis 99 examples meet diagnostic criteria.Be divided into treatment group and matched group at random, 52 examples are organized in treatment, male's 28 examples, women's 24 examples, 16~40 years old age; Matched group 47 examples, male's 24 examples, women's 23 examples, 16~40 years old age.Two groups of patient ages, sex and courses of disease are learned processing by statistics, and difference does not have the significance meaning, has comparability.
Two, Therapeutic Method:
The treatment group: get tablet according to drug prepared of the present invention, oral, once two, twice on the one.
Matched group: chlorphenamine, oral, once two, twice on the one.
Three, curative effect comparative result:
Table 1 is depicted as two groups of curative effects relatively, and wherein 52 examples are organized in treatment, cure 48 examples, and cure rate is 92.31%, and total effective rate is 100%; Matched group 47 examples are cured 35 examples, and cure rate is 74.47%, and total effective rate is 95.75%.Table 2 is depicted as two groups of 7 days curative effects relatively, treats in 7 days, and treatment group cure rate is 78.85%, and the matched group cure rate is 51.06%.This shows that treatment group curative effect obviously is better than matched group.(n number of delegates in table 1 and the table 2)
Table 1
Table 2
Group | ??n | 7 days healing patient numbers | 7 days cure rates (%) |
The treatment group | ??52 | ??41 | ?78.85 |
Matched group | ??47 | ??24 | ?51.06 |
Four, conclusion (of pressure testing):
The generation of allergic rhinitis is relevant with multiple factor, and common have infection, immunity or the like.Chlorphenamine is a kind of medicine that is usually used in the allergic rhinitis treatment, and certain curative effect is arranged.Periplaneta americana is a kind of insecticide, be commonly called as Blatta seu periplaneta, body contains the various active composition, its extract main component is polyalcohols and peptide class active substance, confirms effect with enhance immunity through pharmacological research, but does not have antibacterial action, the medicine that American-cockroach-extract and Herba Ephedrae are made not only can infection, simultaneously can promote the quick rehabilitation of allergic rhinitis, improve the allergic rhinitis cure rate, shorten the allergic rhinitis healing time.Comparing data shows that the curative effect that this medicine is used for the treatment of allergic rhinitis obviously is better than medicine chlorphenamine commonly used.
Though in conjunction with specific embodiments the specific embodiment of the present invention has been done to describe in detail, should not be construed as is limitation of the invention.In the protection domain that claims limited, various modifications that those skilled in the art can make without creative work or distortion still belong to the protection domain of this patent.
Claims (6)
1. the pharmaceutical composition of a treatment of allergic rhinitis is characterized in that: the main component of described pharmaceutical composition and mass parts thereof are such as shown in down:
1~2 part of American-cockroach-extract;
4~18 parts in Herba Ephedrae.
2. the pharmaceutical composition of treatment of allergic rhinitis according to claim 1 is characterized in that: the main component of described pharmaceutical composition and mass parts thereof are such as shown in down:
1 part of American-cockroach-extract;
8 parts in Herba Ephedrae.
3. the pharmaceutical composition of treatment of allergic rhinitis according to claim 1 is characterized in that: the main component of described pharmaceutical composition and mass parts thereof are such as shown in down:
2 parts of American-cockroach-extracts;
15 parts in Herba Ephedrae.
4. the preparation of drug combination method of a claim 1,2 or 3 described treatment of allergic rhinitis, it is characterized in that: described preparation method may further comprise the steps:
1., the preparation of American-cockroach-extract:
A, coarse crushing: exsiccant periplaneta americana is pulverized, make the periplaneta americana coarse powder;
B, immersion: will add the water of 3~5 times of amounts in the coarse powder among the step a, soak and made the coarse powder mixed liquor in 0.5~2 hour, soaking temperature is 70 ℃~78 ℃, and the coarse powder mixed liquor adopts the method that decocts to carry out three times and extracts, and makes extracting solution;
C, three extractions: the coarse powder mixed liquor is carried out the first time extract, extraction time is 7~9 hours; Carry out the second time then behind the water that adds 2~4 times of amounts of surplus liquid in the surplus liquid after extracting for the first time and extract, extraction time is 5~7 hours; Extract for the third time behind the water that adds 2~4 times of amounts of surplus liquid in the surplus liquid after extracting for the second time at last, extraction time is 3~5 hours;
D, filtration for the first time: the extracting solution that three times are extracted among the step c is merged mixing, filter then and make one-level filtrate;
E, concentrated for the first time: relative density was 1.05~1.25 one-level concentrated solution when the one-level filtrate in the steps d was concentrated into 70 ℃~90 ℃;
F, alcoholization are handled: add the ethanol that concentration is 93%w/w~97%w/w in the one-level concentrated solution that makes in step e gradually, and fully stir, making it contain the alcohol amount reaches till 45%~55%, under 70 ℃~90 ℃ temperature conditions, be incubated 20~40 minutes, left standstill then 10~14 hours, and made solution of alcoholized;
G, filtration for the second time: the solution of alcoholized among the step f is discarded the upper strata oils and fats, and lower floor's medicinal liquid filters and makes secondary filtrate;
H, the second time concentrate: after the secondary filtrate in the step g was carried out the ethanol recycling, relative density was 1.20~1.25 secondary concentrated solution when being concentrated into 70 ℃~90 ℃;
I, unguentum preparation: the unguentum that the secondary concentrated solution among the step h is concentrated into moisture≤25%~35% under condition of normal pressure;
J, extract preparation: according to unguentum: the ratio of purified water: glycerol=1000g: 800ml~1200ml: 4ml~6ml adds purified water and glycerol in unguentum, stir, through plate-and-frame filtration, after filtrate is boiled 30 minutes, be chilled to room temperature, promptly get American-cockroach-extract, standby;
2., Herba Ephedrae is decocted with water twice, 2~4 hours for the first time, 1~3 hour for the second time, decocting liquid filtered filtrate merging, and sheet frame filters, and is concentrated into an amount of, standby;
3., with step 1. with step in 2. prepared two kinds of extracts mix and stir, through plate-and-frame filtration, after filtrate is boiled 20~40 minutes, again through the autoclave sterilization postcooling to room temperature, promptly get patent medicine.
5. the preparation of drug combination method of treatment of allergic rhinitis according to claim 4, it is characterized in that: amount of water is 4 times of amounts among the described step b, and soak time is 1 hour, and soaking temperature is 74 ℃.
6. the preparation of drug combination method of treatment of allergic rhinitis according to claim 4, it is characterized in that: described step 3. in autoclave sterilization be under 115 ℃~127 ℃ of temperature, pressure are the condition of 0.05Mpa~0.15Mpa, to carry out sterilization, sterilization time is 25~35 minutes.
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CN104721234A (en) * | 2013-12-20 | 2015-06-24 | 舒梅 | Periplaneta Americana extract product ion-activated in-situ gel and preparation method thereof |
CN107638429A (en) * | 2017-04-08 | 2018-01-30 | 昆明赛诺制药股份有限公司 | A kind of medicine for treating rhinitis and preparation method thereof |
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CN1939345A (en) * | 2006-09-30 | 2007-04-04 | 耿福能 | American falx extract, medicinal composition containing it and its making method |
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CN1939345A (en) * | 2006-09-30 | 2007-04-04 | 耿福能 | American falx extract, medicinal composition containing it and its making method |
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---|
《中外医疗》 20091231 祝庆海 麻黄附子细辛汤配合洗鼻法治疗过敏性鼻炎的体会 109-110 1-6 , 第24期 2 * |
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CN104721234A (en) * | 2013-12-20 | 2015-06-24 | 舒梅 | Periplaneta Americana extract product ion-activated in-situ gel and preparation method thereof |
CN107638429A (en) * | 2017-04-08 | 2018-01-30 | 昆明赛诺制药股份有限公司 | A kind of medicine for treating rhinitis and preparation method thereof |
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