CN105832752A - Pharmaceutical composition for clinical nursing of upper respiratory infection - Google Patents

Pharmaceutical composition for clinical nursing of upper respiratory infection Download PDF

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Publication number
CN105832752A
CN105832752A CN201610218810.3A CN201610218810A CN105832752A CN 105832752 A CN105832752 A CN 105832752A CN 201610218810 A CN201610218810 A CN 201610218810A CN 105832752 A CN105832752 A CN 105832752A
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parts
pharmaceutical composition
acid
upper respiratory
respiratory tract
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王金霞
王夕花
高伟荣
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7028Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
    • A61K31/7034Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/045Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
    • A61K31/05Phenols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/12Ketones
    • A61K31/122Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/192Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid 
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
    • A61K31/198Alpha-aminoacids, e.g. alanine, edetic acids [EDTA]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/235Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365Lactones
    • A61K31/366Lactones having six-membered rings, e.g. delta-lactones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365Lactones
    • A61K31/375Ascorbic acid, i.e. vitamin C; Salts thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/401Proline; Derivatives thereof, e.g. captopril
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/56Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7028Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7048Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/06Tripeptides

Abstract

The invention discloses a pharmaceutical composition for clinical nursing of upper respiratory infection. The pharmaceutical composition mainly consists of the following components in parts by weight: 0.1-0.6 parts of syringin, 0.2-0.5 parts of calanolide E, 0.1-0.4 parts of aurantio-obtusin, 0.5-0.8 parts of protocatechuic acid, 0.6-0.8 parts of sialbin, 0.2-0.6 parts of ursolic acid, 0.1-0.5 parts of bergenin, 0.1-0.7 parts of butyl gallate, 0.2-0.3parts of robinin, 0.4-1.2 parts of columbin, 0.3-0.5 parts of thymol, 0.2-0.4 parts of glutathione, 0.6-0.8 parts of phytosterol, 0.9-1.5 parts of vitamin V and 0.8-2.3 parts of compound amino acid. The pharmaceutical composition disclosed by the invention is capable of resisting bacteria, diminishing inflammation, resisting viruses, clearing away heat and toxic materials, relieving exterior syndrome and relieving cough and boosting body immunity, and the pharmaceutical composition is capable of effectively improving various adverse symptoms in patients with the upper respiratory infection; and the pharmaceutical composition is significant in effect, mild in overall prescription and free from obvious side effects.

Description

A kind of pharmaceutical composition of clinical care upper respiratory tract infection
Technical field
The present invention relates to Respiratory Medicine nursing practical technique field, be specifically related in a kind of clinical care breathe The pharmaceutical composition that road infects.
Background technology
Upper respiratory tract infection great majority are caused by virus, including rhinovirus, coronavirus, adenovirus, Influenza and parainfluenza virus, respiratory syncytial virus, echovirus, Coxsackie virus etc..Separately have 20%~ The upper sense of 30% is caused by antibacterial, and antibacterial infects and is often secondary to after virus infects, with Hemolytic streptococcus for Common, it is secondly hemophilus influenza, streptococcus pneumoniae, staphylococcus etc., is occasionally gram-negative bacteria. These disease four seasons, any age all can fall ill, by containing the virulent spittle, droplet, or the apparatus through polluting Propagate.Often when Abwehrkraft des Koepers reduces, as caught cold, fatigue, the situation such as drench with rain, former existed or The virus invaded by the external world, or/and antibacterial, mushrooms out breeding, causes infecting.This disease prognosis bona, has certainly Sex-limited ,-as 5-7 days recovery from illness.Chang Jifa bronchitis, pneumonia, nasal sinusitis, a few peoples can complicated with acute Myocarditis, nephritis, rheumatic fever etc..
Cause the extraneous factor of this disease, the various reasons causing whole body or respiratory tract local defense function to reduce, As suffered from cold, drenching with rain, abrupt change of climate, fatigue etc. can make former that be present in upper respiratory tract or invade from the external world The virus or the antibacterial that enter breed rapidly, thus induce primary disease.Old germling is weak, immunologic hypofunction or suffer from slow The patient susceptible of property respiratory tract disease.
Existing medicine is mainly antiviral drug, and curative effect is inconspicuous, poor prognosis, the most also can give Patient brings side effect, increases patient suffering.
Summary of the invention
Present invention solves the technical problem that and be to provide-the pharmaceutical composition of kind of clinical care upper respiratory tract infection, effect Fruit is notable, is effectively improved patients symptomatic, alleviates patient suffering.
The technical scheme is that, the pharmaceutical composition of a kind of clinical care upper respiratory tract infection, by weight Component meter, mainly consists of the following composition: Syringa oblata Lindl. phenolic glycoside 0.1-0.6 part, poon element E 0.2-0.5 Part, aurantio-obtusin 0.1-0.4 part, protocatechuic acid 0.5-0.8 part, Sinapine glucosinalbate. 0.6-0.8 part, Bears Fruit acid 0.2-0.6 part, Bergeninum 0.1-0.5 part, butyl gallate 0.1-0.7 part, acaciin 0.2-0.3 part, fibralactone 0.4-1.2 part, thymol 0.3-0.5 part, glutathion 0.2-0.4 Part, plant sterol 0.6-0.8 part, vitamin C 0.9-1.5 part, aminoacids complex 0.8-2.3 part.
Optimum ratio is: Syringa oblata Lindl. phenolic glycoside 0.35 part, poon element E 0.35 part, aurantio-obtusin 0.25 part, Protocatechuic acid 0.65 part, Sinapine glucosinalbate. 0.7 part, ursolic acid 0.4 part, Bergeninum 0.3 part, Galla Turcica (Galla Helepensis) Acid butyl ester 0.4 part, acaciin 0.25 part, fibralactone 0.8 part, thymol 0.4 part, glutathion 0.3 part, plant sterol 0.7 part, vitamin C 1.2 parts, aminoacids complex 1.55 parts.
The extraction preparation method of described Sinapine glucosinalbate. is: take the sodium chloride that Semen Sinapis Albae mass fraction is 3-6% molten Immersion is steeped 20-30 minute, and taking-up is dried, and is ground into coarse powder, is placed in 160-220 DEG C of process 2-5 in baking box Minute, take out, cooling, be again placed in baking box 150-180 DEG C and process 4-6 minute, take out, cooling, By the pure water reflux, extract, twice of 6 times amount, 1.3 hours for the first time, 0.5 hour for the second time, merge back into Flow liquid, filters, is centrifuged 8-10 minute with the rotating speed of centrifuge 800-1200r/min, takes supernatant, concentrates Crystallization, obtains Sinapine glucosinalbate..
The extraction preparation method of described fibralactone is: takes Caulis Fibraureae and is ground into coarse powder, by 5 times amount mass concentrations It is the alcohol reflux twice of 90%, 1.5 hours for the first time, 1.0 hours for the second time, merges back into flow liquid, Filter, reclaim ethanol and be concentrated into every lml medical material Han 1.5g, stand crystallization, leaching crystal;Crystal Add the ethanol that mass concentration is 90% (in terms of crystal weight) of l8-20 times amount, stirring and dissolving, heating Reflux 4O minute, filter, filtrate recycling ethanol, stand 10 hours, filtering for crystallizing, drying under reduced pressure, powder It is broken into fine powder, i.e. obtains fibralactone.
Further, described aminoacids complex is by Radix Asparagi aminoacid, glutamic acid, alanine, proline The mixture of composition.
The preparation method of the pharmaceutical composition of described a kind of clinical care upper respiratory tract infection is:
(1) get the raw materials ready: weigh Syringa oblata Lindl. phenolic glycoside, poon element E, aurantio-obtusin, former catechu by described proportioning Acid, Sinapine glucosinalbate., ursolic acid, Bergeninum, butyl gallate, acaciin, fibralactone, in hundred Fragrant phenol, glutathion, plant sterol, vitamin C, aminoacids complex;
(2) by Syringa oblata Lindl. phenolic glycoside, poon element E, aurantio-obtusin, protocatechuic acid, Sinapine glucosinalbate., Folium Vaccinii vitis-idaeae Acid, Bergeninum, acaciin, thymol, glutathion, plant sterol, vitamin C, compound ammonia Base acid is ground into the nano powder of 200-500 nanometer, mixing, adds butyl gallate and fibralactone, I.e. obtain described pharmaceutical composition.
Further, described compositions is prepared as corresponding oral formulations according to pharmacy conventional manner technique.
Further, described oral formulations includes: tablet, granule, capsule.
The invention has the beneficial effects as follows: the pharmaceutical composition of the present invention can antibacterial, antiinflammatory, antiviral, clearly Thermal detoxification, cough-relieving of inducing sweat, improves patient's resistance, is effectively improved the various bad of upper respiratory tract infection patient Symptom, effect is notable, and integral formula is gentle, non-evident effect.
Detailed description of the invention
Embodiment 1:
The pharmaceutical composition of a kind of clinical care upper respiratory tract infection, by weight component meter, mainly by following One-tenth is grouped into: Syringa oblata Lindl. phenolic glycoside 0.1 part, poon element E 0.2 part, aurantio-obtusin 0.1 part, former catechu Acid 0.5 part, Sinapine glucosinalbate. 0.6 part, ursolic acid 0.2 part, Bergeninum 0.1 part, butyl gallate 0.1 part, acaciin 0.2 part, fibralactone 0.4 part, thymol 0.3 part, glutathion 0.2 part, Plant sterol 0.6 part, vitamin C 0.9 part, aminoacids complex 0.8 part.
The extraction preparation method of described Sinapine glucosinalbate. is: take the sodium chloride solution that Semen Sinapis Albae mass fraction is 3% Soaking 20 minutes, taking-up is dried, and is ground into coarse powder, is placed in baking box 160 DEG C and processes 2 minutes, takes out, Cooling, is again placed in baking box 150 DEG C and processes 4 minutes, take out, cooling, return with the pure water of 6 times amount Stream extraction twice, 1.3 hours for the first time, 0.5 hour for the second time, merges back into flow liquid, filters, with centrifugal The rotating speed of machine 800r/min is centrifuged 8 minutes, takes supernatant, condensing crystallizing, obtains Sinapine glucosinalbate..
The extraction preparation method of described fibralactone is: carry with the alcohol reflux that 5 times amount mass concentrations are 90% Take twice, 1.5 hours for the first time, 1.0 hours for the second time, merge back into flow liquid, filter, reclaim ethanol dense It is reduced to every lml medical material Han 1.5g, stands crystallization, leaching crystal;Crystal adds the quality of l8 times amount Concentration is the ethanol (in terms of crystal weight) of 90%, and stirring and dissolving is heated to reflux 4O minute, filters, filter Liquid reclaims ethanol, stands 10 hours, filtering for crystallizing, and drying under reduced pressure is ground into fine powder, i.e. obtains in Caulis Fibraureae Ester.
The mixing that described aminoacids complex is made up of Radix Asparagi aminoacid, glutamic acid, alanine, proline Thing, the mass ratio between four is 3:2:1:1.
This pharmaceutical composition is prepared as tablet, and preparation method is:
(1) get the raw materials ready: weigh Syringa oblata Lindl. phenolic glycoside, poon element E, aurantio-obtusin, former catechu by described proportioning Acid, Sinapine glucosinalbate., ursolic acid, Bergeninum, butyl gallate, acaciin, fibralactone, in hundred Fragrant phenol, glutathion, plant sterol, vitamin C, aminoacids complex;
(2) by Syringa oblata Lindl. phenolic glycoside, poon element E, aurantio-obtusin, protocatechuic acid, Sinapine glucosinalbate., Folium Vaccinii vitis-idaeae Acid, Bergeninum, acaciin, thymol, glutathion, plant sterol, vitamin C, compound ammonia Base acid is ground into the nano powder of 200 nanometers, mixing, adds butyl gallate and fibralactone, to obtain final product To described pharmaceutical composition, add filler, bonding disintegrating agent, granulate, tabletting, be prepared as tablet.
Embodiment 2:
The pharmaceutical composition of a kind of clinical care upper respiratory tract infection, by weight component meter, mainly by following One-tenth is grouped into: Syringa oblata Lindl. phenolic glycoside 0.35 part, poon element E 0.35 part, aurantio-obtusin 0.25 part, former youngster Boheic acid 0.65 part, Sinapine glucosinalbate. 0.7 part, ursolic acid 0.4 part, Bergeninum 0.3 part, gallic acid fourth Ester 0.4 part, acaciin 0.25 part, fibralactone 0.8 part, thymol 0.4 part, glutathion 0.3 Part, plant sterol 0.7 part, vitamin C 1.2 parts, aminoacids complex 1.55 parts.
The extraction preparation method of described Sinapine glucosinalbate. is: take the sodium chloride that Semen Sinapis Albae mass fraction is 4.5% molten Immersion is steeped 25 minutes, and taking-up is dried, and is ground into coarse powder, is placed in baking box 190 DEG C and processes 3.5 minutes, takes Go out, cooling, be again placed in baking box 165 DEG C and process 5 minutes, take out, cooling, pure by 6 times amount Water reflux, extract, twice, 1.3 hours for the first time, 0.5 hour for the second time, merges back into flow liquid, filters, and uses The rotating speed of centrifuge 1000r/min is centrifuged 9 minutes, takes supernatant, condensing crystallizing, obtains Sinapine glucosinalbate..
The extraction preparation method of described fibralactone is: carry with the alcohol reflux that 5 times amount mass concentrations are 90% Take twice, 1.5 hours for the first time, 1.0 hours for the second time, merge back into flow liquid, filter, reclaim ethanol dense It is reduced to every lml medical material Han 1.5g, stands crystallization, leaching crystal;Crystal adds the quality of 19 times amount Concentration is the ethanol (in terms of crystal weight) of 90%, and stirring and dissolving is heated to reflux 4O minute, filters, filter Liquid reclaims ethanol, stands 10 hours, filtering for crystallizing, and drying under reduced pressure is ground into fine powder, i.e. obtains in Caulis Fibraureae Ester.
The mixing that described aminoacids complex is made up of Radix Asparagi aminoacid, glutamic acid, alanine, proline Thing, the mass ratio between four is 3:2:1:1.
This pharmaceutical composition is prepared as granule, and preparation method is:
(1) get the raw materials ready: weigh Syringa oblata Lindl. phenolic glycoside, poon element E, aurantio-obtusin, former catechu by described proportioning Acid, Sinapine glucosinalbate., ursolic acid, Bergeninum, butyl gallate, acaciin, fibralactone, in hundred Fragrant phenol, glutathion, plant sterol, vitamin C, aminoacids complex;
(2) by Syringa oblata Lindl. phenolic glycoside, poon element E, aurantio-obtusin, protocatechuic acid, Sinapine glucosinalbate., Folium Vaccinii vitis-idaeae Acid, Bergeninum, acaciin, thymol, glutathion, plant sterol, vitamin C, compound ammonia Base acid is ground into the nano powder of 350 nanometers, mixing, adds butyl gallate and fibralactone, to obtain final product To described pharmaceutical composition, add filler, binding agent, correctives are prepared as granule.
Embodiment 3:
The pharmaceutical composition of a kind of clinical care upper respiratory tract infection, by weight component meter, mainly by following One-tenth is grouped into: Syringa oblata Lindl. phenolic glycoside 0.6 part, poon element E 0.5 part, aurantio-obtusin 0.4 part, former catechu Acid 0.8 part, Sinapine glucosinalbate. 0.8 part, ursolic acid 0.6 part, Bergeninum 0.5 part, butyl gallate 0.7 part, acaciin 0.3 part, fibralactone 1.2 parts, thymol 0.5 part, glutathion 0.4 part, Plant sterol 0.8 part, vitamin C 1.5 parts, aminoacids complex 2.3 parts.
The extraction preparation method of described Sinapine glucosinalbate. is: take the sodium chloride solution that Semen Sinapis Albae mass fraction is 6% Soaking 30 minutes, taking-up is dried, and is ground into coarse powder, is placed in baking box 220 DEG C and processes 5 minutes, takes out, Cooling, is again placed in baking box 180 DEG C and processes 6 minutes, take out, cooling, return with the pure water of 6 times amount Stream extraction twice, 1.3 hours for the first time, 0.5 hour for the second time, merges back into flow liquid, filters, with centrifugal The rotating speed of machine 1200r/min is centrifuged 8-10 minute, takes supernatant, condensing crystallizing, obtains Sinapine glucosinalbate..
The extraction preparation method of described fibralactone is: carry with the alcohol reflux that 5 times amount mass concentrations are 90% Take twice, 1.5 hours for the first time, 1.0 hours for the second time, merge back into flow liquid, filter, reclaim ethanol dense It is reduced to every lml medical material Han 1.5g, stands crystallization, leaching crystal;Crystal adds the quality of 20 times amount Concentration is the ethanol (in terms of crystal weight) of 90%, and stirring and dissolving is heated to reflux 4O minute, filters, filter Liquid reclaims ethanol, stands 10 hours, filtering for crystallizing, and drying under reduced pressure is ground into fine powder, i.e. obtains in Caulis Fibraureae Ester.
The mixing that described aminoacids complex is made up of Radix Asparagi aminoacid, glutamic acid, alanine, proline Thing, the mass ratio between four is 3:2:1:1.
This pharmaceutical composition is prepared as capsule, and preparation method is:
(1) get the raw materials ready: weigh Syringa oblata Lindl. phenolic glycoside, poon element E, aurantio-obtusin, former catechu by described proportioning Acid, Sinapine glucosinalbate., ursolic acid, Bergeninum, butyl gallate, acaciin, fibralactone, in hundred Fragrant phenol, glutathion, plant sterol, vitamin C, aminoacids complex;
(2) by Syringa oblata Lindl. phenolic glycoside, poon element E, aurantio-obtusin, protocatechuic acid, Sinapine glucosinalbate., Folium Vaccinii vitis-idaeae Acid, Bergeninum, acaciin, thymol, glutathion, plant sterol, vitamin C, compound ammonia Base acid is ground into the nano powder of 500 nanometers, mixing, adds butyl gallate and fibralactone, to obtain final product To described pharmaceutical composition, add filler, binding agent, lubricant, wetting agent, be prepared as capsule.
Model case:
1, so-and-so is revived, female, 28 years old, pharyngeal discomfort, it is dried, and cough, rhinorrhea occurs, with head The symptom of pain heating, upon examination it is found that its submandibular lymph nodes enlargement, and throat is the most congested, is diagnosed as breathing Road infects, and uses the tablet of the embodiment of the present invention 1 preparation to treat, oral, three times a day, every time 0.5-1g, after 1 day, throat lymphadenectasis diminishes, and after 2 days, cough alleviates, and headache alleviates, and body temperature is extensive Multiple normal, after 4 days, all ill symptomses all disappear, on inspection for recovery from illness.Follow up a case by regular visits to after 3 months, have no multiple Send out.
2, road so-and-so, man, 21 years old, have sore throat, hoarseness, heating, headache, limbs are aching and limp weary Power, upon examination it is found that its submandibular lymph nodes enlargement, and throat is the most congested, is diagnosed as upper respiratory tract infection, makes Treat with the granule of the embodiment of the present invention 2 preparation, oral, three times a day, and each 0.5-1g, 1 In the future, temperature recovery is normal, and headache alleviates, and after 2 days, has sore throat and alleviates, headache relief, limbs acid Soft weak being also eased, after 3 days, headache disappears, and throat is without significant discomfort sense, and remaining symptom is the most complete Disappear, on inspection for recovery from illness.
3, Lee so-and-so, female, 39 years old, early discovery oneself throat discomfort, develop into the most again dry pain of itching, And it being attended by sneeze and nasal obstruction, loss of appetite, fever and headache, submandibular lymph nodes enlargement has tenderness sense, through inspection Looking into its submandibular lymph nodes enlargement of discovery, throat is the most congested, in being diagnosed as upper respiratory tract infection, uses this The capsule of bright embodiment 3 preparation is treated, oral, every day 2 times, each 0.5-1g, after 2 days, All ill symptomses are all eased, and after 5 days, all ill symptomses all disappear, and patient feels good, warp Check as recovery from illness.
Last it is noted that above example is only in order to illustrate technical scheme, rather than right It limits;Although the present invention being described in detail with reference to previous embodiment, the ordinary skill of this area Personnel are it is understood that the technical scheme described in previous embodiment still can be modified by it or right Wherein portion of techniques feature carries out equivalent;And these amendments or replacement, do not make appropriate technical solution Essence depart from embodiment of the present invention technical scheme spirit and scope.

Claims (6)

1. the pharmaceutical composition of a clinical care upper respiratory tract infection, it is characterised in that component meter by weight, Mainly consist of the following composition: Syringa oblata Lindl. phenolic glycoside 0.1-0.6 part, poon element E 0.2-0.5 part, orange Obtusin 0.1-0.4 part, protocatechuic acid 0.5-0.8 part, Sinapine glucosinalbate. 0.6-0.8 part, ursolic acid 0.2- 0.6 part, Bergeninum 0.1-0.5 part, butyl gallate 0.1-0.7 part, acaciin 0.2-0.3 part, Fibralactone 0.4-1.2 part, thymol 0.3-0.5 part, glutathion 0.2-0.4 part, plant sterol 0.6-0.8 part, vitamin C 0.9-1.5 part, aminoacids complex 0.8-2.3 part.
The pharmaceutical composition of a kind of clinical care upper respiratory tract infection the most as claimed in claim 1, its feature It is, it is characterised in that component meter by weight, mainly consists of the following composition: Syringa oblata Lindl. phenolic glycoside 0.35 Part, poon element E 0.35 part, aurantio-obtusin 0.25 part, protocatechuic acid 0.65 part, Sinapine glucosinalbate. 0.7 Part, ursolic acid 0.4 part, Bergeninum 0.3 part, butyl gallate 0.4 part, acaciin 0.25 part, Fibralactone 0.8 part, thymol 0.4 part, glutathion 0.3 part, plant sterol 0.7 part, dimension are raw Element C 1.2 parts, aminoacids complex 1.55 parts.
The pharmaceutical composition of a kind of clinical care upper respiratory tract infection the most as claimed in claim 1 or 2, its Being characterised by, described aminoacids complex is made up of Radix Asparagi aminoacid, glutamic acid, alanine, proline Mixture.
4. the pharmaceutical composition of a kind of clinical care upper respiratory tract infection as described in claims 1 to 3, its Being characterised by, preparation method is:
(1) get the raw materials ready: weigh Syringa oblata Lindl. phenolic glycoside, poon element E, aurantio-obtusin, former catechu by described proportioning Acid, Sinapine glucosinalbate., ursolic acid, Bergeninum, butyl gallate, acaciin, fibralactone, in hundred Fragrant phenol, glutathion, plant sterol, vitamin C, aminoacids complex.
(2) by Syringa oblata Lindl. phenolic glycoside, poon element E, aurantio-obtusin, protocatechuic acid, Sinapine glucosinalbate., Folium Vaccinii vitis-idaeae Acid, Bergeninum, acaciin, thymol, glutathion, plant sterol, vitamin C, compound ammonia Base acid is ground into the nano powder of 200-500 nanometer, mixing, adds butyl gallate and fibralactone, I.e. obtain described pharmaceutical composition.
The preparation side of the pharmaceutical composition of a kind of clinical care upper respiratory tract infection the most as claimed in claim 4 Method, it is characterised in that described compositions is prepared as corresponding oral formulations according to pharmacy conventional manner technique.
The preparation side of the pharmaceutical composition of a kind of clinical care upper respiratory tract infection the most as claimed in claim 4 Method, it is characterised in that described oral formulations includes: tablet, granule, capsule.
CN201610218810.3A 2016-04-08 2016-04-08 Pharmaceutical composition for clinical nursing of upper respiratory infection Pending CN105832752A (en)

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