CN103816281A - Traditional Chinese medicine composition for preventing and treating wind-heat common cold - Google Patents

Traditional Chinese medicine composition for preventing and treating wind-heat common cold Download PDF

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CN103816281A
CN103816281A CN201410082674.0A CN201410082674A CN103816281A CN 103816281 A CN103816281 A CN 103816281A CN 201410082674 A CN201410082674 A CN 201410082674A CN 103816281 A CN103816281 A CN 103816281A
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radix
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medicine
volatile oil
flos lonicerae
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CN103816281B (en
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兰太进
刘元
张颖
宋志钊
文志云
李星宇
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Guangxi Institute Of Chinese Medicine & Pharmaceutical Science
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Guangxi Institute Of Chinese Medicine & Pharmaceutical Science
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Abstract

The invention provides a traditional Chinese medicine composition for preventing and treating wind-heat common cold. The traditional Chinese medicine composition is prepared from the main raw materials of narrowleaf screwtree root and picria fel-terrae lour, other traditional Chinese medicines such as indigowoad root and honeysuckle can be added according to state of an illness, wherein the used honeysuckle refers to volatile oil extracted from the honeysuckle. A large number of experiments in vitro and animal experiments before clinical application, and clinical experiment prove that the traditional Chinese medicine composition provided by the invention has obvious effects on treating fever, cough, pain and the like, which are caused by wind-heat common cold.

Description

The Chinese medicine composition of a kind of prevention and treatment anemopyretic cold
Technical field:
The invention belongs to the field of Chinese medicines, relate to the Chinese medicine composition of a kind of prevention and treatment anemopyretic cold.
Background technology:
Flu is the common exogenous diseases that being invaded by exogenous pathogen causes.Due to four o'clock six gas differences, and human quality's difference, wind and cold, wind heat and heat-damp in summer accompanied symptoms had therefore clinical.As anemopyretic cold, because wind heat is violated table, the heat stagnation flesh natural fibre line of meat, defends table discord, therefore see fever of the body, micro evil wind is cold, sweating is not smooth; Wind-heat troubling, distending pain in the head; Stifling the cleaning the street of heresy of wind heat, thus laryngopharynx swelling and pain, parched throat, thirst with desire to drink, turbid nasal discharge; Wind-heat invading the lung, impairment of purifying function of the lung, cough, expectoration sticky or Huang, tongue tip side of red, thin white fur of tongue or micro-Huang, floating and rapid pulse are that wind heat is invaded levying of defending in lung.This disease is attacked due to human body mainly due to wind-heat evil toxin, therefore its treatment is worked as take dispelling wind to relieve the exterior syndrome, heat-clearing and toxic substances removing as the rule for the treatment of.
Anemopyretic cold is the common high morbidity in the subtropical zones such as Guangxi.Although have the proved recipe much with better clinical effectiveness, as application number: CN200810073696.5) adopt " Folium Eucalypti Robustae and Flos Ilicis Asprellae " in prescription; In patent " a kind of Chinese medicinal tablet for the treatment of anemopyretic cold, upper respiratory tract infection or capsule and preparation method thereof, application number: CN201110456838.8 " prescription, adopt " Flos Ilicis Asprellae, Herba lygodii, Radix achyranthis asperae (Herba Achyranthis Asperae) and Merremia umbellata subsp. orientalis "; In patent " a kind of Chinese medicine preparation application number of Rhizoma Et Radix Baphicacanthis Cusiae: CN201310191571.3 " prescription, adopt " Rhizoma Et Radix Baphicacanthis Cusiae " etc.But have no the medicine that adopts Guangxi conventional crude drugs Radix Helicteris and Radix Picriae felterrae to carry out prescription and adopt modern technology of preparing to be prepared from.
Summary of the invention:
The Chinese medicine that the object of the present invention is to provide a kind of prevention and treatment anemopyretic cold, has dispelling wind to relieve the exterior syndrome, heat-clearing and toxic substances removing, dredging microcirculation, and cure rate is high.
Technical scheme of the present invention is such:
Treat a Chinese medicine composition for anemopyretic cold, the raw material of preparing described compositions comprises Radix Helicteris and Radix Picriae felterrae, and the amount ratio of the two is: 6~8 parts of Radix Helicteriss, and 5~7 parts of Radix Picriae felterrae, described part is weight portion.
The drug matching that can catch a cold with conventional treatment in above-mentioned composition, in optimization formula of the present invention, also comprises Radix Isatidis and/or Flos Lonicerae, the medicinal residues after volatile oil and extraction that Flos Lonicerae used refers to extract with Flos Lonicerae;
The preparation method of described Flos Lonicerae volatile oil and form can adopt this area routine techniques method, such as Flos Lonicerae is extracted after volatile oil, make according to a conventional method inclusion agent, then for the preparation of this pharmaceutical preparation.
The parts by weight proportioning of each raw material is: 6~8 parts of Radix Helicteriss, 5~7 parts of Radix Picriae felterrae, 5~7 parts and 5~7 portions Flos Loniceraes of Radix Isatidis.
In above-mentioned formula, can also add Radix Platycodonis and/or Radix Glycyrrhizae, consumption is 1.6~2.4 parts of Radix Platycodoniss, 1.6~2.4 parts, Radix Glycyrrhizae.
A kind of preferred parts by weight proportioning is: 2 parts, 7 parts of Radix Helicteriss, 7 parts of Radix Picriae felterrae, 6 parts of Flos Loniceraes, 6 parts of Radix Isatidis, 2 parts of Radix Platycodoniss and Radix Glycyrrhizae.
The monarch drug that plays main work in we is Radix Helicteris and Radix Picriae felterrae; Ministerial drug Flos Lonicerae, Radix Isatidis; Adjuvant drug Radix Platycodonis, Radix Glycyrrhizae;
Radix Helicteris, the micro-hardship of acrid in the mouth, cool in nature, there are relieving the exterior syndrome with drugs of pungent in flavor and cool in nature, heat-clearing and toxic substances removing, reducing swelling and alleviating pain function.
Radix Picriae felterrae, bitter in the mouth, cold in nature, there are heat-clearing and toxic substances removing, reducing swelling and alleviating pain function.
Although this two tastes medicine of Radix Helicteris and Radix Picriae felterrae is all found that there is separately the effect to flu, has no the effect of two medicine compatibilities in prior art.
Inventor's discovery, the compatibility of two medicines, has synergism for heat-clearing and toxic substances removing, reducing swelling and alleviating pain.
Flos Lonicerae, bitter in the mouth, cold in nature, heat-clearing and toxic substances removing, and have the merit of light a surname's evacuation, be anemopyretic cold common medicine; Radix Isatidis, bitter in the mouth, cold in nature, heat-clearing and toxic substances removing, for affection due to external wind and heat, heating, laryngopharynx swelling and pain etc.Upper two medicines are strengthened monarch drug dispelling wind to relieve the exterior syndrome, heat-clearing toxin-expelling functions, are ministerial drug in side.
Radix Platycodonis, bitter in the mouth is pungent, and property is flat, opens lung qi dispersing gas, expelling phlegm for arresting cough; Radix Glycyrrhizae nourishing the lung to arrest cough, relieving spasm to stop pain, upper two medicines share lung qi dispersing eliminating phlegm and stopping cough, are adjuvant drug in side.
The raw material of Chinese medicine medicine pharmacological property of the above Chinese medicine composition:
1, Radix Helicteris is dry root or the Herb of Sterculiaceae plant Radix Helicteris Helicteres angustifolia L..Property hardship, cold.Function heat-clearing and toxic substances removing, for the high heat of catching a cold, tonsillitis, pharyngolaryngitis, parotitis, skin eczema.
2, Radix Picriae felterrae is the dry herb of goatweed Picria fel-terrae Lour..Property hardship, cold.Function heat-clearing and toxic substances removing, reducing swelling and alleviating pain.For cold anemopyretic, laryngopharynx swelling and pain, mumps, gastric heat stomachache, dysentery, furuncle and phyma, venom.
3, Flos Lonicerae is the dry flower of caprifoliaceae plant Radix Ophiopogonis Lonicera japonica Thunb. or the flower that band is just opened.Property sweet, cold.Function heat-clearing and toxic substances removing, wind-heat dissipating.For carbuncle furuncle, sore throat, erysipelas, toxic-heat and blood stasis, anemopyretic cold, pestilence heating.
4, the dry root of Baphicacanthus cusia root system cruciferae isatis Isatis indigotica Fort..Property hardship, cold.Function heat-clearing and toxic substances removing, removing heat from blood sore-throat relieving.For maculae caused by violent heat pathogen, crimson tongue is dark violet, mumps, sore throat, scarlet fever, major part pestilence, erysipelas, carbuncle.
5, Radix Platycodonis is the dry root of Campanulaceae Radix Platycodonis Platycodon grandiflorum (Jacq.) A.DC..Property hardship, pungent, flat.Function lung qi dispersing, sore-throat relieving, eliminate the phlegm, evacuation of pus.For cough with copious phlegm, uncomfortable in chest not smooth, pharyngalgia, hoarseness, lung abscess vomiting pus, skin infection difficulty in discharging of pus.
6, Radix Glycyrrhizae is the dry root and rhizome of glycyrrhizic legume Glycyrrhiza uralensis Fisch., Glycyrrhiza inflata Bat. Glycyrrhiza inflata Bat. or Glycyrrhiza glabra L. Glycyrrhiza glabra L..Property sweet, flat.Function invigorating the spleen and replenishing QI, heat-clearing and toxic substances removing, expelling phlegm for arresting cough, relieving spasm to stop pain, coordinating the actions of various ingredients in a prescription.For weakness of the spleen and stomach, fatigue and weakness, shortness of breath and palpitation, cough with copious phlegm, gastral cavity abdomen, the anxious pain of extremity contraction, carbuncle sore tumefacting virus, cushion toxicity, strong.
The above raw material of Chinese medicine can mix with pharmaceutically acceptable adjuvant, makes various oral formulations, such as powder, capsule, tablet, electuary etc.
In one embodiment of the present invention, preparation method is:
1) prepare Flos Lonicerae volatile oil inclusion complex
Extract the method for volatile oil by routine and extract after Flos Lonicerae volatile oil, add inclusion material to be prepared into inclusion complex, the remaining Flos Lonicerae medicinal residues of institute give over to lower step and use.
2) other medical material is cut off respectively, pulverize, merge with Flos Lonicerae medicinal residues, decoct with water secondary, concentrated add ethanol and stir evenly, hold over night, filters, and reclaims ethanol, is concentrated into after thick paste, adds auxiliary materials and mixing, dry,
3) by 2) add 1 in gained medicated powder) the Flos Lonicerae volatile oil inclusion complex of gained;
4) add pharmaceutic adjuvant, after mix homogeneously, obtain powder.
Gained powder can be directly medicinal, also can make various preparations with it again.
In said method, described inclusion material comprises the cyclodextrin derivative such as alpha-cyclodextrin, beta-schardinger dextrin-, gamma-cyclodextrin and 2,6 dimethyl-cyclodextrin.Described excipient substance comprises medicinal filler and lubricant, and wherein filler comprises starch, modified starch, dextrin, calcium hydrogen phosphate and other medicinal filler adjuvants, and lubricant comprises Polyethylene Glycol, calcium stearate, Pulvis Talci and other medicinal lubricants.
Advantage of the present invention and good effect:
This Chinese medicine composition is made according to theory of Chinese medical science and clinical practice experience, has good therapeutic effect for symptoms such as anemopyretic cold and the heating causing, cough and laryngopharynx swelling and pain.Carry out multinomial pharmacodynamic experiment with medicine of the present invention:
One, preclinical pharmacodynamics of San experiment
Show to have certain antibacterial, antitussive, diaphoresis, antipyretic, antiinflammatory, analgesia, immunoregulation effect, experimental result is as follows:
(1) In Vitro Bacteriostasis
Result shows, capsule of the present invention all has bacteriostasis in various degree to bacterial strains such as staphylococcus aureus (20771), staphylococcus aureus (18153), staphylococcus epidermidis (20289), α-hemolytic streptococcus (181818), streptococcus pneumoniae (B) 31002.
(2) mice is coughed to the impact of reaction
Result shows, medicine of the present invention can extend mouse cough incubation period to some extent, reduces mouse cough number of times.
(3) impact on normal rat sweat secretion
Result shows, normal rat paw portion sweat secretion is had to obvious facilitation.
(4) refrigeration function to rat
Result shows, to the exothermic reaction of 2,4-DNP pyrogenicity rat, all have inhibitory action in various degree.
(5) impact on mice ear
Result shows that Oleum Tiglii induced mice ear swelling is had to obvious inhibitory action.
(6) on the leukocytic impact in rat thoracic cavity
Result shows, can obviously suppress rat thoracic cavity leukoplania due to 1% carrageenin, but pleural effusion is not had to obvious inhibitory action.
(7) analgesic activity to mice
Result shows, can obviously suppress acetic acid induced mice writhing response, has obvious analgesic activity.
(8) impact on mouse immunity
Result shows, immunocompromised mice carbon powder is cleaned up to index K value remarkable increasing action, and the potentiation that this medicine has the immunity of immunocompromised mice is described.
But staphylococcus aureus infecting mouse is tested and is shown, medicine of the present invention does not have significant protective effect to staphylococcus aureus infecting mouse.Specific experiment data refer to embodiment.
Two, clinical pharmacodynamic experiment
Result shows, this traditional Chinese medicine composition for treating anemopyretic cold is rapid-action, and curative effect is high, safe and reliable, has good clinical efficacy, and anemopyretic cold total effective rate reaches 95.3%(and refers to embodiment).
The specific embodiment:
Below in conjunction with embodiment, the present invention is described in further detail, listed embodiment is only the present invention is described and is never limited to the present invention.
Embodiment 1 prevents and treats the Chinese medicine powder of anemopyretic cold
Raw material: Radix Helicteris 3.5kg, Radix Picriae felterrae 3.0kg, Flos Lonicerae 3.0kg, Radix Isatidis 3.0kg, Radix Platycodonis 1.0kg, Radix Glycyrrhizae 1.0kg
Preparation method:
1) prepare Flos Lonicerae volatile oil inclusion complex
A collects volatile oil
Adopt volatile oil catcher to carry out the collection of volatile oil, extracting honeysuckle 2.4kg, the 4-10 that adds water doubly measures, and each 3-5h, extracts 1 time, collects and obtains volatile oil 2ml, yield 0.083%.
B prepares beta-cyclo dextrin included compound
Volatile oil and beta-schardinger dextrin-are mixed and made into inclusion complex in 0.8-1.2:8 (ml/g) ratio: by beta-schardinger dextrin-8g add water 100ml make dissolve, measure volatile oil 0.8-1.2ml and a small amount of dehydrated alcohol dilution, under constantly stirring, be slowly added drop-wise in beta-schardinger dextrin-solution, in 45~50 ℃ of constant temperature, continue to stir after 3 hours, in 5~10 ℃, place 24 hours, filter, in 40 ℃ of cold drying, pulverize, sieve, obtain inclusion complex.
The inclusion complex of preparation is respectively according to two appendix XD of Chinese Pharmacopoeia version in 2005 as stated above, and in determination of volatile oil method mensuration inclusion complex, volatile oil content and inclusion complex recovery rate are calculated average inclusion 92.3%, and average recovery rate is 91.1%.Extract after volatile oil, the remaining Flos Lonicerae medicinal residues of institute give over to lower step and use.
2) other medical material is cut off respectively, pulverize, merge with Flos Lonicerae medicinal residues, decoct with water secondary, amount of water is 5~12 times of medical material amount for the first time, soaks 0.5~1h, heated and boiled 1~3h; Amount of water is 5~12 times of medical material amount for the second time, boils 1~3h; Filter, merging filtrate, is concentrated into the clear paste that density is 1.10~1.20g/ml, add ethanol, reach 50~90%(percent by volume to ethanol content in total amount) time, stir evenly, hold over night, filter, decompression heating recovery ethanol, is concentrated into thick paste, add starch 0~1.5kg, mix, dry, pulverize and sieve 80~100 orders;
3) by 2) add 1 in gained medicated powder) the Flos Lonicerae volatile oil inclusion complex of gained;
4) add modified starch 0~1.5kg, after mix homogeneously, obtain powder.
The Chinese medicine powder of embodiment 2~4 preventions and treatment anemopyretic cold
Preparation method is with embodiment 1, and only material composition is different with consumption.
Embodiment 5 prevents and treats the Chinese medicine capsules of anemopyretic cold
Ingredient and consumption be with embodiment 1, in preparation method, 1), 2), 3) step is with embodiment 1;
Step 4) adds starch and the each 0~1.5kg of Pulvis Talci, encapsulated and get final product every capsules 5g after mix homogeneously.
The Chinese medicine capsules of embodiment 6~8 preventions and treatment anemopyretic cold
Preparation method is with embodiment 5, and only material composition is different with consumption.
Embodiment 9 prevents and treats the Chinese medicinal tablet of anemopyretic cold
Ingredient and consumption be with embodiment 1, in preparation method, 1), 2), 3) step is with embodiment 1;
Step 4): add starch 0~1.5kg, after mix homogeneously, granulate, dry, tablet machine film-making, every weight is 0.5g.
The Chinese medicinal tablet of embodiment 10~11 preventions and treatment anemopyretic cold
Preparation method is with embodiment 9, and only material composition is different with consumption.
The amount ratio of each embodiment Raw is in table 1
The amount ratio of the each embodiment Raw of table 1.
Figure BDA0000474257470000061
Preclinical pharmacodynamics of San experiment
(1) In Vitro Bacteriostasis
Adopt plate doubling dilution, the Experimental agents having diluted (capsule of embodiment 5-8) is added respectively in the sterilising medium that is cooled to 55 ℃ of left and right, mix, make the medicine flat board of variable concentrations.Experimental bacteria suspension (the bacterial concentrations 10 such as depletion Staphylococcus aureus, α-hemolytic streptococcus, streptococcus pneumoniae 5cFU/ml), draw respectively and plant in the pastille flat board of variable concentrations, cultivate 18h, observed and recorded minimal inhibitory concentration (MIC) for 37 ℃.
The results are shown in Table 2.
Table 2. In Vitro Bacteriostasis
Figure BDA0000474257470000062
Figure BDA0000474257470000071
Result shows, capsule of the present invention all has bacteriostasis in various degree to trial bacterial strain.
Below in experiment, Experimental agents used is embodiment 6 capsules.
(2) mice ammonia mist is caused to the impact of coughing reaction
50 of mices, female, hero half and half, body weight 20 ± 2g, is divided into 5 groups at random, 10 every group.Wherein organize ig respectively and give capsule of the present invention 6.0,3.0,1.5/kg for 3; 1 group ig gives intensified loquet capsule 3.0/kg; Yu 1 group be blank group, give equivalent distilled water.Be administered once every day, 3d continuously, and 1h after last medicine, every Mus constant-pressure atomization ammonia 15s, observes the incubation period of mouse cough, and records mouse cough number of times in 2min.The results are shown in Table 3.
Table 3. capsule of the present invention causes on mice ammonia mist the impact of coughing reaction
Figure BDA0000474257470000072
Figure BDA0000474257470000073
T check, with relatively * P<0.05**P<0.01***PLEssT.LTssT. LT0.001 of matched group
Result shows, 6.0,3.0,1.5/kg of capsule of the present invention all has and extends to some extent mouse cough incubation period, reduces mouse cough number of times.
(3) impact on normal rat paw sweat secretion (colouring)
Get 50 of rats, male and female half and half, body weight 160 ± 40g, is divided into 5 groups at random, 10 every group.Wherein organize ig respectively and give capsule of the present invention 6.0,3.0,1.5/kg for 3; 1 group ig gives Ephedrae Decoction 1g/kg; Yu 1 group be blank, ig is to equal-volume distilled water.After administration, rat is inserted respectively in rat fixator, face upward position fixing, expose two hind legs, dip dehydrated alcohol gently by sufficient sole of the foot portion dirt scrub with cotton swab, then wipe gently dry with dry cotton swab, after administration, 15min coats and field-Gao Yuan Shi reagent A liquid in rat paw portion skin, after fully dry, the very thin B liquid of coating of 30min after administration, observes and records the Chinese and count after 30min, 1 integral and calculating pressed in a Chinese, the difference of comparative control group and medicine group.The results are shown in Table 4.
The impact of table 4. capsule of the present invention on normal rat paw sweat secretion
Figure BDA0000474257470000074
Figure BDA0000474257470000081
T check, with relatively * * P<0.01 of matched group
Result shows, 6.0,3.0,1.5/kg of capsule of the present invention all has obvious facilitation to normal rat paw portion sweat secretion.
(4) refrigeration function to 2,4-DNP pyrogenicity rat
Rat body weight 250 ± 40g, female, male half and half, before experiment, water 16h is can't help in fasting, and the same day was measured rat temperature 2 times in experiment, chose body temperature and changed 50 of rats that are no more than 0.3 ℃, was divided into 4 groups, 10 every group.Wherein organize ig respectively and give capsule of the present invention 6.0,3.0,1.5/kg for 3; 1 group of ig is to aspirin 0.3g/kg; Yu 1 group be blank, ig is to equivalent distilled water.30min subcutaneous accurate injection 2 in each Mus back after medicine, 2, 4-dinitrophenol solution 20mg/kg, after pyrogenicity, each group of 45min is administered once again, after pyrogenicity respectively at 0.5,1,2,3,4,5h measures rat temperature 1 time, survey altogether 6 times, calculate each group of rat temperature changing value.The results are shown in Table 5.
The refrigeration function of table 5. capsule of the present invention to 2,4-DNP pyrogenicity rat
Figure BDA0000474257470000082
T check, with relatively * P<0.05**P<0.01***PLEssT.LTssT. LT0.001 of matched group
Result shows, the exothermic reaction of 6.0,3.0,1.5/kg of capsule of the present invention to 2,4-DNP pyrogenicity rat, all has inhibitory action in various degree.
(5) impact on Oleum Tiglii induced mice ear swelling
50 of mices, female, hero half and half, body weight 20 ± 2g, is divided into 5 groups at random, 10 every group.Wherein organize ig respectively and give capsule of the present invention 6.0,3.0,1.5/kg for 3; 1 group ig gives dexamethasone tablet 2.5/kg; Yu 1 group be blank, ig is to equivalent distilled water.30min after medicine, the left ear of each Mus causes inflammation with 2% Oleum Tiglii mixture 0.05ml/ ear, and auris dextra compares.Cause scorching rear 30min and be administered once again, after 4h, mice is broken to cervical vertebra and put to death, cut two ears, lay garden auricle at coating position respectively with diameter 9mm card punch, take mice left and right ear weight with analytical balance, using its difference as inflammatory swelling degree, and calculate swelling inhibition percentage.The results are shown in Table 6.
The impact of table 6. capsule of the present invention on the swelling of Oleum Tiglii induced mice auricular concha
Figure BDA0000474257470000092
T check, with relatively * * * P<0.001*P<0.05 of matched group
Result shows, 6.0/kg of capsule of the present invention has obvious inhibitory action to Oleum Tiglii induced mice ear swelling.
(6) impact on rat thoracic cavity leukoplania
Get 50 of rats, male and female half and half, body weight 210~240g, is divided into 5 groups by body weight, 10 every group.Wherein 3 groups of ig give capsule of the present invention 6.0,3.0,1.5/kg; 1 group of positive matched group, ig gives dexamethasone tablet 2.5/kg, remaining 1 group be blank group, ig waits capacity distilled water.Administration every day 1 time, 10d continuously, 1h after last administration only causes inflammation from right side intrapleural injection 1% carrageenin 0.2ml/ under ether light anaesthesia, puts to death rat after 5h, opens thoracic cavity, with suction pipe sucking-off pleural effusion, records transudate volume and counts total white blood cells.The results are shown in Table 7.
The impact of table 7. capsule of the present invention on rat thoracic cavity leukoplania
Figure BDA0000474257470000093
Figure BDA0000474257470000094
T check, with relatively * P<0.05**P<0.01 of matched group
Result shows, 6.0,3.0,1.5/kg of capsule of the present invention all can obviously suppress rat thoracic cavity leukoplania due to 1% carrageenin, but pleural effusion is not had to obvious inhibitory action.
(7) impact of Dichlorodiphenyl Acetate induced mice writhing response
50 of mices, female, hero half and half, body weight 20 ± 2g, is divided into 5 groups at random, 10 every group.Wherein organize ig respectively and give capsule of the present invention 6.0,3.0,1.5/kg for 3; 1 group ig gives aspirin 0.3g/kg; Yu 1 group be blank, ig is to equivalent distilled water.30min after administration, each Mus respectively lumbar injection 0.6% glacial acetic acid 0.2ml/ only, is observed the writhing response number of times occurring in the rear 20min of injection.The results are shown in Table 8.
The impact of table 8. capsule Dichlorodiphenyl Acetate of the present invention induced mice writhing response
Figure BDA0000474257470000101
Figure BDA0000474257470000102
T check, with relatively * P<0.05**P<0.01***PLEssT.LTssT. LT0.001 of matched group
Result shows, 6.0,3.0,1.5/kg of capsule of the present invention all can obviously suppress acetic acid induced mice writhing response, has obvious analgesic activity.
(8) on impact that in immunocompromised Mice Body, carbon granule is cleaned up function
Get 60 of mices, male and female half and half, body weight 18~22g, is evenly divided into 6 groups by body weight, 10 every group.Wherein 3 groups of ig give capsule of the present invention 6.0,3.0,1.5/kg; 2 groups is blank group and model group, and ig waits capacity distilled water; Yu 1 group of positive matched group, ig gives SHENQI PIAN 0.75g/kg.Administration every day 1 time, successive administration 7d.In 6d ig administration simultaneously, except blank group, all the other 5 groups of mices respectively subcutaneous injection prednisolone acetate 25mg/kg are made immunodeficiency models, after 24h (not 1h after time administration), the india ink 0.1ml/10g body weight of mouse tail vein injection 10%, 2min and the 7min eye socket venous plexus 20 μ l that take a blood sample after injection, be dissolved in 2ml0.1%Na2CO3 solution, put 722 type spectrophotometers and measure trap in 680nm place, and cut open and get liver, spleen and weigh and calculate its organ coefficient, calculate that carbon powder is cleaned up index K and index α is cleaned up in correction.The results are shown in Table 9.
Table 9. capsule of the present invention is cleaned up the impact of ability on mice carbon granule
Figure BDA0000474257470000111
T check, with matched group comparison Δ Δp<0.01 Δ Δ Δp<0.001; Compare * P<0.05 with prednisolone acetate (model group)
Result shows, 6.0,3.0,1.5/kg of capsule of the present invention cleans up index K value to immunocompromised mice carbon powder remarkable increasing action, and the potentiation that this medicine has the immunity of immunocompromised mice is described.
(9) protective effect of mouse experiment antibacterial being infected
80 of mices, female, hero half and half, body weight 20 ± 2g, is divided into 4 groups at random, 20 every group.Wherein organize oral cavity respectively and give capsule of the present invention 21.6,5.4/kg for 2; 1 group ig gives acetyl Luo Xuan mycin 1g/kg; Yu 1 group be blank, ig is to equal-volume distilled water.Be administered once every day, continuously 3d.Staphylococcus aureus is inoculated in 2ml nutrient broth, cultivate 8h for 37 ℃, get 0.1ml transferred species in 10ml nutrient broth, cultivate 18h for 37 ℃, for experiment original bacteria liquid, original bacteria liquid is suitably diluted with physiological saline solution, be finally diluted to infection animal 100% minimum lethal dose (MLD) with 5% high activity dried yeast liquid.1h after last medicine, the bacteria suspension 0.5ml of definite MLD (1 × 105CFU/ml) in every mouse peritoneal of injection prerun, 2h administration 1 time again after microbiological contamination, Continuous Observation 7d, records each group of dead mouse situation.The results are shown in Table 10.
The vivo bacteria corrosion action of table 10. capsule of the present invention to staphylococcus aureus infecting mouse
Figure BDA0000474257470000112
X 2check, with matched group comparison, * * P<0.01
Result shows, 21.6,5.4/kg of capsule of the present invention does not have significant protective effect to staphylococcus aureus infecting mouse.
Clinical pharmacodynamic experiment
(1) case selection standard:
Disease is shown in heating micro evil wind, and antiperspirant is let out not smooth, distending pain in the head, and cough, expectorant is sticky or yellow, parched throat, laryngopharynx swelling and pain, nasal obstruction, stream turbid nasal discharge, thirst with desire to drink, tongue tip side of red, thin lingual fur or micro-Huang, floating and rapid pulse person.
(2) Therapeutic Method:
Embodiment 1 medicated powder for oral administration, 3 times on the one 7th is a course for the treatment of, after the course for the treatment of, optionally appends treatment.Viewing duration requires the medicine without other treatment primary disease.
(3) effect criterion:
1, effective: anemopyretic cold relevant symptoms disappears, sign and lab testing are without extremely.
2, take a turn for the better: anemopyretic cold relevant symptoms, sign and lab testing are improved.
3, invalid: anemopyretic cold relevant symptoms, sign and lab testing are all without improving.
(4) result:
My Out-patient Department portion treats total case load 85 people altogether, wherein: effective 75 people, take a turn for the better 6 people, invalid 4 people, total effective rate 95.3%.Above results suggest this Chinese medicine composition anemopyretic cold is had to good clinical efficacy.
(5) model case:
Case 1
Revive certain, man, 7 years old.In February, 2002, main suit was because upper sense causes heating 4d, used quiet of penicillin, and after each transfusion, body temperature can be down to normally, cross body temperature after 2~3h and start again to raise, with afternoon, night for very, 38.5 ℃~40.0 ℃ of body temperature, nasal obstruction, watery nasal discharge, cough, pharyngalgia, red tongue, yellow fur, floating and tense pulse.Lab testing: leukocyte 11.0 × l0 9/ L, neutrophilic granulocyte 0.72%.Chest X-rays: two lung marking strengthen.Give the Drug therapy in the present embodiment 1, after medication 2d, heating stops, and after 5d, fully recovers.
Song, man, 27 years old, in June, 2002 recurrent cough of main suit 5d, heating 2d, once Oral Acetyl Spiramycin sheet 2d treatment, symptom is without improvement.39.6 ℃ of body temperature, pharyngeal congestion, antiadoncus, leukocyte 13.0 × 10 9/ L, neutrophilic granulocyte 0.82%.Give the Drug therapy in the present embodiment 1, after medication 1d, heating stops, and after 7d, fully recovers.
Huang, female, 25 years old, 3d was medical on August 30th, 2003 for patient's heating, cough companion malaise.There is heating, cough in main suit's 3d cause, has a little mucoid expectorant after suffering from cold, headache, and pharyngalgia discomfort, general fatigue is unable, and loss of appetite is felt sick.After private clinic treatment, (use the medicines such as KUAIKE, cefradine, SHUANGHUANLIAN, ampicillin).The state of an illness still increases the weight of gradually.Have a medical check-up: 38.5 ℃ of body temperature.110 beats/min, pulse.Breathe 21 beats/min.Sanity, listlessness.Swallow red.Two pulmonary respiration sounds are low, audible and dry moist rale.Leukocyte 15.0 × 10 9/ L, neutrophilic granulocyte 0.86%.Rabat shows bottom right pulmonary infection.Give the Drug therapy in the present embodiment 1, after medication 3d, heating stops, and after 12d, fully recovers.

Claims (10)

1. the application of the effective ingredient of Radix Helicteris and Radix Picriae felterrae composition in the medicine of preparation prevention and treatment anemopyretic cold, the weight portion proportioning of two survival doses is 6~8 parts of Radix Helicteriss, 5~7 parts of Radix Picriae felterrae.
2. application according to claim 1, prepares in the raw material of described medicine and also comprises 5~7 parts of Radix Isatidis and/or the volatile oil made from 5~7 portions of Flos Loniceraes.
3. application according to claim 1 and 2, prepares in the raw material of described medicine and also comprises Radix Platycodonis and/or Radix Glycyrrhizae, and consumption is 1.6~2.4 parts of Radix Platycodoniss, 1.6~2.4 parts, Radix Glycyrrhizae.
4. application according to claim 3, the weight ratio of preparing the raw material of described medicine is: 2 parts, 7 parts of Radix Helicteriss, 7 parts of Radix Picriae felterrae, 6 parts of Flos Loniceraes, 6 parts of Radix Isatidis, 2 parts of Radix Platycodoniss and Radix Glycyrrhizae; Described Flos Lonicerae is that Flos Lonicerae volatile oil inclusion complex and Flos Lonicerae are extracted the medicinal residues after volatile oil.
5. a medicine for prevention and treatment anemopyretic cold, is characterized in that containing Radix Helicteris and Radix Picriae felterrae, and the weight portion proportioning of two survival doses is 6~8 parts of Radix Helicteriss, 5~7 parts of Radix Picriae felterrae.
6. medicine according to claim 5, prepares in the raw material of described medicine and also comprises 5~7 parts of Radix Isatidis and/or the volatile oil made from 5~7 portions of Flos Loniceraes.
7. according to the medicine described in claim 5 or 6, to prepare in the raw material of described medicine and also comprise Radix Platycodonis and/or Radix Glycyrrhizae, consumption is 1.6~2.4 parts of Radix Platycodoniss, 1.6~2.4 parts, Radix Glycyrrhizae.
8. according to the medicine described in claim 6 or 7, described volatile oil is Flos Lonicerae volatile oil inclusion complex, and in described raw material, also comprises the medicinal residues after Flos Lonicerae extraction volatile oil.
9. medicine according to claim 8, the inclusion material of described Flos Lonicerae volatile oil inclusion complex is selected from alpha-cyclodextrin, beta-schardinger dextrin-, gamma-cyclodextrin or 2,6 dimethyl-cyclodextrin.
10. according to arbitrary described medicine in claim 5~9, be oral agents, be selected from powder, capsule, tablet or electuary.
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