CN103372071B - A kind of pharmaceutical composition for the treatment of of insomnia patients - Google Patents

A kind of pharmaceutical composition for the treatment of of insomnia patients Download PDF

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CN103372071B
CN103372071B CN201210124241.8A CN201210124241A CN103372071B CN 103372071 B CN103372071 B CN 103372071B CN 201210124241 A CN201210124241 A CN 201210124241A CN 103372071 B CN103372071 B CN 103372071B
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insomnia
pharmaceutical composition
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medicine
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CN103372071A (en
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吕姗珊
周年华
谯志文
唐桂英
高燕妮
陈晓雪
高武翔
陈成
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CHONGQING HILAN PHARMACEUTICAL Co Ltd
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CHONGQING HILAN PHARMACEUTICAL Co Ltd
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Abstract

The present invention relates to a kind of pharmaceutical composition for the treatment of of insomnia patients, that the present invention selects is invaluable, spina date seed, polygala root, mother-of-pearl, wilsonii, the fruit of Chinese magnoliavine, Ligusticum wallichii are raw material, is prepared into any conventional oral formulations according to the conventional preparation method of modern preparation process technology. Chinese medicine composition of the present invention has effect of the flat liver of heat-clearing, mental-tranquilization, can improve insomnia and dreamful sleep, forgetful, dysphoria, the micro-hardship of dry, dizzy, the palpitation of having a headache, unconsciously sweat and tire. To stagnant heat in the liver and gall, the insomnia determined curative effect due to having no peace of mind, effect is remarkable.

Description

A kind of pharmaceutical composition for the treatment of of insomnia patients
[technical field]
The present invention relates to a kind of pharmaceutical composition taking vegetable Chinese herbal medicine as raw material, specifically a kind of medicine for the treatment of of insomnia patientsComposition.
[background technology]
Sleep-disorder has now become a kind of epidemic disease. Insomnia is modal sleep-disorder problem, in recent years, and the incidence of disease of insomniaBe the situation rising year by year, become one of modern popular disease. WHO data shows that the whole world exceedes 30% adult and is subject to insomnia tiredDisturb, the insomnia incidence of the U.S. is up to 32%~50%, Britain 10%~14%, Japan 20%, France 30%. Sleep according to ChinaThe up-to-date sleep investigation result that research association announces, China adult insomnia illness rate is up to 57%, higher than the insomnia of developed countriesIncidence, and insomniac's quantity is in continuous increase, and only the domestic market of hypnotic sedative agent in 2010 has exceeded 8,000,000,000 yuan.
The harm of insomnia is apparent, from short-term effect, does not have enough sleep and causes unable, mood One's spirits are drooping, tired outShakiness, absent minded; Long-term insomnia easily causes anxiety disorder, occurs hidrosis, palpitaition simultaneously, is short of breath, trembles, chestThere is constriction in portion, and four limbs do not have the symptoms such as power numbness.
The calm class chemical drug short term efficacy that is used for having a sleepless night is remarkable, but long-term use can cause side effect and withdrawal reaction.
Insomnia is divided into type of hyperactivity of fire caused by deficiency of YIN, type of deficiency of both the heart and spleen, flaring heart fire, type of phlegm-heat attacking internally, type of deficiency of heart-QI and gallbladder-QI by the traditional Chinese medical science, largeAmount bibliographical information has been affirmed the curative effect for the treatment of by Chinese herbs insomnia, as added taste for the guipi decoction of type of deficiency of both the heart and spleen and for type of hyperactivity of fire caused by deficiency of YINTianwang Buxin Dan; The side of calming the nerves of Liu Rongdong etc. (amber end, cortex albiziae, Polygonum multiflower knotweed, the fruit of Chinese magnoliavine, spina date seed, the seed of Oriental arborvitae,Mother-of-pearl, raw dens draconis, raw oyster, wilsonii, Fructus Corni, fushen); Application number is 200810228564.5 the anti-mistake of oneIn the medicine and preparation method thereof of sleeping, disclosing having of preparing taking the red sage root, corydalis tuber, spina date seed, the fruit of Chinese magnoliavine as bulk drug nourishes heartThe anti-insomnia medicine of calming the nerves; Application number is 201012552167.0, the pharmaceutical composition that denomination of invention is a kind for the treatment of of insomnia patients andIn the application of its preparation method, announced formed by red ginseng, the vine of multiflower knotweed, spina date seed, corydalis tuber, cortex albiziae, Radix Glycyrrhizae for godThrough weak, dizzy insomnia, deficiency of blood dreaminess there is nourishing heart, the pharmaceutical composition of the effect of calming the nerves; Application number is 201110073643.2,Denomination of invention is in a kind of medicine for the treatment of of insomnia patients, to disclose with spina date seed, the seed of Oriental arborvitae, mother-of-pearl, Polygonum multiflower knotweed, yncaria stem with hooks, closeWhat joyous flower, fushen, polygala root, keel, the fruit of Chinese magnoliavine, the dried rhizome of rehmannia, Poria cocos, Rhizoma Dioscoreae, astragalus root, Radix Glycyrrhizae were bulk drug has benefitThe peaceful heart of kidney, the intelligence development of calming the nerves, arresting convulsion improving eyesight, tonifying spleen nourishing the stomach, the flat liver of heat-clearing, the pharmaceutical composition of beneficial gas bowl spares; Application number is200910244915.6, in the Chinese medicine composition that denomination of invention is a kind of Cure for insomnia, disclose with yncaria stem with hooks, Radix Angelicae Sinensis, the dried rhizome of rehmannia, whitePrepared by the bulk drugs such as Chinese herbaceous peony, stir-baked SEMEN ZIZIPHI SPINOSAE, the seed of Oriental arborvitae, Radix Achyranthis Bidentatae, chrysanthemum, river rhizoma Gastrodiae have to nourish blood nourishes heart, calming the liver to stop the wind effectPharmaceutical composition.
In summary it can be seen, traditional Chinese medicine in treating insomnia medicine is more, but prescription complexity, active ingredient is indefinite, dose is large, riseThe shortcomings such as the effect time is slow, curative effect time is short, therefore develop have that rapid-action, curative effect time is long, in the sleeping peacefully of determined curative effectMedical instrument is significant.
[summary of the invention]
Object of the present invention is just to work out the pure Chinese medicinal preparation for the treatment of of insomnia patients, overcomes the deficiency of above-mentioned all kinds, and providesOne,, containing hormone, is not had no side effect containing chemical components by pure Chinese medicine, treating both the exterior and interior, determined curative effect, the long energy of curative effect timeReach the medicine of the treatment of insomnia patients of effect of the flat liver of better heat-clearing, mental-tranquilization. This pharmaceutical composition can be for patient in additionNeed to be prepared into different dosage form, be convenient to take, easy to carry.
The pharmaceutical composition for the treatment of of insomnia patients of the present invention, comprises that the bulk drug of following weight parts is made:
Invaluable 3-10 part spina date seed (stir-fry) 10-50 part polygala root (system) 3-10 part
Mother-of-pearl 10-40 part fruit of Chinese magnoliavine 3-10 part Ligusticum wallichii 3-10 part
Wilsonii 10-40 part.
More preferably, the bulk drug that comprises following weight parts is made:
Invaluable 5-8 part spina date seed (stir-fry) 15-40 part polygala root (system) 5-8 part
Mother-of-pearl 15-25 part fruit of Chinese magnoliavine 5-8 part Ligusticum wallichii 5-8 part
Wilsonii 15-25 part.
Best, the bulk drug that comprises following weight parts is made:
8 parts of 25 parts of polygala roots of invaluable 6 parts of spina date seeds (stir-fry) (system)
6 parts of 5 parts of Ligusticum wallichiis of 20 portions of fruit ofs Chinese magnoliavine of mother-of-pearl
20 parts of wilsoniis.
The pharmaceutical composition for the treatment of of insomnia patients of the present invention can be prepared as any formulation of the prior art, be prepared into tablet,Capsule, granule, pill, oral liquid are best.
Preparation method:
A) Concha Margaritifera powder is broken into fine powder, for subsequent use;
B) get invaluable, wilsonii, the fruit of Chinese magnoliavine adds 5~10 times of amounts of its total amount, 5~8 times of amount 60% alcohol extracts two jointlyInferior, extract 0.5~1.5 hour at every turn, filter, merging filtrate, is concentrated into 60 DEG C of liquid extracts of surveying relative density 1.10~1.20;
C) get polygala root (system), spina date seed, Ligusticum wallichii, jointly add the common decoction twice of 6~10 times of water gagings of its total amount, for the first time2 hours, 1.5 hours for the second time, to filter after merging twice decocting liquid, filtrate is reduced to 60 DEG C to survey relative densities is 1.10~1.20Medicinal extract;
D) medicinal extract that powder step being made in a) and step b), c) obtain merges, and stirs evenly.
Add auxiliary material or the agent of flavouring granulation, capsule, tablet, pill or oral liquid.
The bulk drug that the present invention adopts:
Spina date seed have tranquilizing soporific, analgesia, anticonvulsion, strengthen the effects such as immunologic function. Also have obviously with multiple hypnotic sedative agentSynergy.
Invaluable: different name, kerr treebine root and stem (" conventional Chinese herbal medicine color atlas "), stone qin potato, mountain tortoise (" Guangxi Chinese herbal medicine "),Ground tortoise (Nanchuan " conventional Chinese herbal medicine handbook "), (" mountain of papers Chinese herbal medicine ") do not allowed on ground. Property hardship, cold. Sweet, micro-hardship, temperature. ReturnWarp: return liver, stomach warp. Loose stasis of blood hemostasis, detumescence ding-tong. There is analgesia, hypnosis and sedation.
The fruit of Chinese magnoliavine not only has stable effect to central nervous system, and also has anticonvulsant action. Extend the length of one's sleep, reduce certainlyMain activity, has extensive central inhibitory action.
Mother-of-pearl, taste is sweet, salty, cold in nature, returns liver, the heart channel of Hang-Shaoyin. Useful the moon, calming the liver, arresting convulsion hemostasia effect.
Wilsonii, hides micro-hardship, pungent, warm in nature, returns spleen, kidney, the heart channel of Hang-Shaoyin. There are replenishing kidney, strengthening waist, benefiting qi for tranquillization, effect promoting blood circulation and removing obstruction in channels.
Polygala root, bitter, pungent, slightly warm in nature, the thoughts of returning home, kidney, lung channel. Have the intelligence development of calming the nerves, the effect of eliminating the phlegm, subside a swelling.
Ligusticum wallichii, taste is pungent, warm in nature, returns liver, courage, pericardium channel. There are blood-activating and qi-promoting, wind-expelling pain-stopping effect.
The present invention has effect of the flat liver of heat-clearing, mental-tranquilization. Be used for the treatment of stagnant heat in the liver and gall, the insomnia due to having no peace of mind, rightInsomnia and dreamful sleep, forgetful, dysphoria, the micro-hardship of dry, dizzy, the palpitation of having a headache, unconsciously sweat and tire is effective in cure.
Further illustrate below the drug action of the pharmaceutical composition for the treatment of of insomnia patients of the present invention by pharmacodynamics test.
According to " study of tcm new drug guide ", the pharmacodynamics of composition of the present invention comprises the following aspects: observed different agentPharmaceutical composition in amount situation is by testing spontaneous activity in mice and outstanding tail, and it is frightened that strychnine, pentylenetetrazol and isoniazid cause mouseThe test of fainting, mice sleep dosage and sub-threshold dose yellow Jackets Synergism Testing, the impact of mouse hot-plate analgesia test.
1. the impact of dead time when medicine of the present invention is on spontaneous activity in mice and tail suspension
Experimental technique: 60 of mouse, male and female dual-purpose, is divided into 5 groups, 10 every group. The other gavage of drug component 4,2,1g/kg,Control group gives equivalent distilled water, positive controls gavage estazolam sheet 2.4mg/kg. Gavage after administration 30min, by mouseBe placed in spontaneous activity in mice instrument, first adapt to 1min, then measure spontaneous activity in mice number of times in 5min. Measure complete, by littleMouse afterbody is fixed on an iron, upside down apart from desktop 5cm, records the dead time of mouse in 5min. Result is united with SPSSMeter software carries out t inspection, in table 1.
The impact of table 1 medicine of the present invention on normal spontaneous activity in mice
Note: with control group comparison,**P<0.01。
Result shows, the high, medium and low dosage group of medicine of the present invention can significantly reduce the Assay of spontaneous activity (P < 0.01) of mouse,The dead time (P < 0.01) that high, the middle dosage group of medicine of the present invention can significantly increase mouse while hanging by the feet, represent that medicine of the present invention hasCertain sedation.
2. medicine of the present invention causes the impact of convulsions mouse on strychnine
Experimental technique: 50 of mouse, male and female dual-purpose, is divided into 5 groups, 10 every group. Drug component do not gavage administration 4,2,1g/kg, control group gives isometric(al) distilled water, positive controls gavage estazolam sheet 4.8mg/kg. After administration 30min, everyMouse lumbar injection strychnine 1.8mg/kg, records the indexs such as mice convulsion incubation period, death time, dead animal number. Result is usedThe t of SPSS10.0 statistical software inspection, in table 2.
The impact of table 2 medicine of the present invention on strychnine convulsions mouse
Note:*For comparing P < 0.05 with control group,**For comparing P < 0.01 with control group.
Result shows, high, the middle dosage group of medicine of the present invention can cause mice convulsion time of occurrence by significant prolongation strychnine, of the present inventionHigh dose group can cause mouse diing time (P < 0.05) by significant prolongation strychnine, but strychnine is caused to not obviously protection of dead mouse,Show that medicine of the present invention has certain antagonism to strychnine induced mice convulsions.
3. the impact of medicine pentetrazole convulsions mouse of the present invention
Experimental technique: 50 of mouse, male and female dual-purpose, is divided into 5 groups, 10 every group. The other gavage of drug component 4,2,1g/kg,Control group gives isometric(al) distilled water, positive controls gavage estazolam sheet 4.8mg/kg. Administration 30min, every mouse abdominal cavity notePenetrate pentylenetetrazol 100mg/kg, record the indexs such as mice convulsion incubation period, death time, dead animal number. Result is united with SPSSMeter software carries out t inspection, in table 3.
The impact of table 3 medicine pentetrazole of the present invention convulsions mouse
Note:**For comparing P < 0.01 with control group.
Result shows, the high, medium and low dosage group of medicine of the present invention can necessarily extend pentylenetetrazol and cause the time of occurrence of mice convulsion and deadDie the time, but there was no significant difference (P > 0.05). High, the middle dosage group of medicine of the present invention can significantly reduce pentylenetetrazol and cause mice convulsionDeath toll (P < 0.01). Disclose medicine pentetrazole induced mice convulsions of the present invention and have certain antagonism.
4. medicine of the present invention causes the impact of convulsions mouse on isoniazid
Experimental technique: 50 of mouse, male and female half and half, are divided into 5 groups, 10 every group. The other gavage of drug component 4,2,1g/kg,Control group gives isometric(al) distilled water, positive controls gavage estazolam sheet 4.8mg/kg. Administration 30min, every mouse abdominal cavity notePenetrate isoniazid 30mg/kg, record the indexs such as mice convulsion incubation period, dead animal number. Result is carried out t with SPSS statistical softwareInspection, in table 4.
The impact of table 4 medicine of the present invention on isoniazid convulsions mouse
Note:*For comparing P < 0.05 with control group,**For comparing P < 0.01 with control group.
Result shows, high, the middle dosage group of medicine of the present invention can significant prolongation isoniazid causes the time of occurrence (P < 0.01) of mice convulsion,But isoniazid is caused to the dead unprotect effect of mice convulsion (P > 0.05). Represent that medicine of the present invention has isoniazid induced mice convulsionsCertain antagonism.
5. the impact of medicine of the present invention on sleep dosage yellow Jackets mouse
Experimental technique: 50 of mouse, male and female half and half, are divided into 5 groups, 10 every group. The other gavage of drug component 4,2,1g/kg,Control group gives isometric(al) distilled water, positive controls gavage estazolam sheet 2.4mg/kg. Administration 30min, every mouse abdominal cavity notePenetrate yellow Jackets 40mg/kg, record the indexs such as mouse dropping asleep latency, the length of one's sleep. Result is carried out with SPSS statistical softwareT inspection, in table 5.
The impact of table 5 medicine of the present invention on sleep dosage yellow Jackets mouse
Note:*For comparing P < 0.05 with control group,**For comparing P < 0.01 with control group.
Result shows, the high, medium and low dosage group of medicine of the present invention can significantly shorten sleep dosage pentobarbital sodium in mice while falling asleepBetween (P < 0.01), and the significant prolongation length of one's sleep (P < 0.05). Disclose medicine of the present invention to sleep dosage pentobarbital sodium in miceSleep has certain synergy.
6. the impact of medicine of the present invention on sub-threshold dose yellow Jackets mouse
Experimental technique: 50 of mouse, male and female half and half, are divided into 5 groups, 10 every group. The other gavage of drug component 4,2,1g/kg,Control group gives isometric(al) distilled water, positive controls gavage estazolam sheet 2.4mg/kg. Administration 30min, every mouse abdominal cavity notePenetrate yellow Jackets 30mg/kg, record the mouse indexs such as number of animals of falling asleep. Result is carried out t inspection and card with SPSS statistical softwareSide's inspection, in table 6.
The impact of table 6 medicine of the present invention on sub-threshold dose yellow Jackets mouse
Note:*For comparing P < 0.05 with control group,**For comparing P < 0.01 with control group.
Result shows, medicine of the present invention is high, medium and low can significantly increase the sub-threshold dose yellow Jackets mouse number of animals of falling asleep(P < 0.01). Prompting, medicine of the present invention has certain synergy to hypnosis of pentobarbital sodium of subthreshold dose.
7. the impact of medicine of the present invention on mouse hot plate induced pain
Experimental technique: through prerun, get pain threshold 50 of female mices in 10~30s, be divided into 5 groups, 10 every group. MedicineThing group is gavage 4,2,1g/kg respectively, and control group gives isometric(al) distilled water, positive controls gavage estazolam sheet 2.4mg/kg.Administration 30min, is placed in mouse respectively in 50 ± 1 DEG C of hot-plate instruments, records mouse and licks the metapedes time as pain threshold (in 60s notLick and be recorded as 60s). Result is carried out t inspection with SPSS statistical software, in table 7.
The impact of table 7 medicine of the present invention on mouse hot plate induced pain
Note:*For comparing P < 0.05 with control group.
Result shows, the pain threshold (P < 0.05) that high, the middle dosage group of medicine of the present invention can significant prolongation mouse hot plate. Prompting, thisInvention medicine has certain analgesic activity to hot plate induced pain mouse.
To sum up test explanation, medicine of the present invention, by the inhibitory action to central nervous system, has significant sedative-hypnotic effect.
Drug extract of the present invention, is prepared by embodiment 4, and Chongqing Hil'an Pharmaceutical Co., Ltd provides, lot number 110201.
Proterties: brown medicinal extract. Content: every g medicinal extract is containing crude drug in whole 11.06g. With distilled water diluting to desired concn.
The mouse using in this experiment is Kunming mouse, body weight 18~22g, and Chongqing Institute of Chinese Medicine animal housing provides.
Estazolam sheet, Anhui Bang Ning pharmaceutical Co. Ltd produces, specification 1mg, lot number 100214.
Strychnine, Shanghai reagent two factories, specification 5g, lot number 080622.
Pentylenetetrazol, is provided lot number 064K0686 by sigma company of the U.S..
Isoniazid, Chengdu Jin Hua pharmaceutcal corporation, Ltd, specification 0.1g, lot number 100904.
[detailed description of the invention]
Below in conjunction with embodiment, the pharmaceutical composition for the treatment of of insomnia patients of the present invention is described in further detail.
Embodiment 1
A) get 35 parts of mother-of-pearls and be ground into fine powder, for subsequent use;
B) get 9 parts of invaluable 9 parts, 35 parts of wilsoniis, the fruit of Chinese magnoliavine and jointly add 9 times of amounts of its total amount, 7 times of amount 60% ethanolExtract secondary, extract 1 hour at every turn, filter, merging filtrate, is concentrated into 60 DEG C of liquid extracts of surveying relative density 1.15;
C) get 9 parts of polygala roots (system), 40 parts of spina date seeds, 9 parts of Ligusticum wallichiis, jointly add the common decoction two of 9 times of water gagings of its total amountInferior, 2 hours for the first time, 1.5 hours for the second time, to filter after merging twice decocting liquid, filtrate is reduced to 60 DEG C, and to survey relative densities be 1.10Medicinal extract;
D) medicinal extract that fine powder step being made in a) and step b), c) obtain merges, and stirs evenly.
Embodiment 2
A) get 15 parts of mother-of-pearls and be ground into fine powder, for subsequent use;
B) get invaluable 8 parts, 25 parts of wilsoniis, 8 parts, the fruit of Chinese magnoliavine, jointly add 8 times of amounts of its total amount, 7 times of amount 60% secondAlcohol extracting secondary extracts 1.5 o'clock at every turn, filters, and merging filtrate, is concentrated into 60 DEG C of liquid extracts of surveying relative density 1.15;
C) get 8 parts of polygala roots (system), 15 parts of spina date seeds, 5 parts of Ligusticum wallichiis, jointly add the common decoction two of 8 times of water gagings of its total amountInferior, 2 hours for the first time, 1.5 hours for the second time, to filter after merging twice decocting liquid, filtrate is reduced to 60 DEG C, and to survey relative densities be 1.15Medicinal extract;
D) medicinal extract that fine powder step being made in a) and step b), c) obtain merges, and stirs evenly.
Embodiment 3
A) get 25 parts of mother-of-pearls and be ground into fine powder, for subsequent use;
B) get 5 parts of invaluable 5 parts, 15 parts of wilsoniis, the fruit of Chinese magnoliavine and jointly add 7 times of amounts of its total amount, 6 times of amount 60% ethanolExtract secondary, extract 1 hour at every turn, filter, merging filtrate, is concentrated into 60 DEG C of liquid extracts of surveying relative density 1.20;
C) get 5 parts of polygala roots (system), 40 parts of spina date seeds, 8 parts of Ligusticum wallichiis, jointly add the common decoction two of 7 times of water gagings of its total amountInferior, 2 hours for the first time, 1.5 hours for the second time, to filter after merging twice decocting liquid, filtrate is reduced to 60 DEG C, and to survey relative densities be 1.20Medicinal extract;
D) medicinal extract that fine powder step being made in a) and step b), c) obtain merges, and stirs evenly.
Embodiment 4
A) get 20 parts of mother-of-pearls and be ground into fine powder, for subsequent use;
B) get invaluable 6 parts, 20 parts of wilsoniis, 5 parts, the fruit of Chinese magnoliavine, jointly add 8 times of amounts of its total amount, 6 times of amount 60% secondAlcohol extracting secondary extracts 1 hour at every turn, filters, and merging filtrate, is concentrated into 60 DEG C of liquid extracts of surveying relative density 1.15;
C) get 8 parts of polygala roots (system), 25 parts of spina date seeds, 6 parts of Ligusticum wallichiis, jointly add the common decoction two of 8 times of water gagings of its total amountInferior, 2 hours for the first time, 1.5 hours for the second time, to filter after merging twice decocting liquid, filtrate is reduced to 60 DEG C, and to survey relative densities be 1.15Medicinal extract;
D) medicinal extract that fine powder step being made in a) and step b), c) obtain merges, and stirs evenly.
Embodiment 5
A) get 30 parts of mother-of-pearls and be ground into fine powder, for subsequent use;
B) get invaluable 6 parts, 25 parts of wilsoniis, the fruit of Chinese magnoliavine and jointly add 6 times of amounts of its total amount, 7 times of amount 60% alcohol extractsSecondary extracts 0.5 hour at every turn, filter, merging filtrate, be concentrated into 60 DEG C survey relative densities 1.10~liquid extract;
C) get 7 parts of polygala roots (system), 30 parts of spina date seeds, 7 parts of Ligusticum wallichiis, jointly add the common decoction two of 6 times of water gagings of its total amountInferior, 2 hours for the first time, 1.5 hours for the second time, to filter after merging twice decocting liquid, filtrate is reduced to 60 DEG C, and to survey relative densities be 1.10Medicinal extract;
D) medicinal extract that fine powder step being made in a) and step b), c) obtain merges, and stirs evenly.
Embodiment 6
A) get 23 parts of mother-of-pearls and be ground into fine powder, for subsequent use;
B) get 5 parts of invaluable 8,22 parts of wilsoniis, the fruit of Chinese magnoliavine and jointly add 7 times of amounts of its total amount, 6 times of amount 60% alcohol extractsSecondary extracts 1 o'clock at every turn, filters, and merging filtrate, is concentrated into 60 DEG C of liquid extracts of surveying relative density 1.15;
C) get 9 parts of polygala roots (system), 25 parts of spina date seeds, Ligusticum wallichii, jointly add the common decoction twice of 8 times of water gagings of its total amount,2 hours for the first time, 1.5 hours for the second time, to filter after merging twice decocting liquid, filtrate is reduced to 60 DEG C to survey relative densities is 1.15Medicinal extract;
D) medicinal extract that fine powder step being made in a) and step b), c) obtain merges, and stirs evenly.
Embodiment 7 prepares tablet
By steps d in arbitrary embodiment in embodiment 1~embodiment 6) in the medicinal extract that makes, add 5% starch of its total amount,Mix, granulation is compressing tablet afterwards, makes the tablet of 0.5g/ sheet.
Embodiment 8 prepares capsule
By steps d in arbitrary embodiment in embodiment 1~embodiment 7) in make 3% the starch that adds its total amount in medicinal extract,Mix, after granulation, dry, pulverize, filled capsules, makes the capsule of 0.5g/ grain.
Embodiment 9 prepares granule
By steps d in arbitrary embodiment in embodiment 1~embodiment 6) in make and in medicinal extract, add its total amount 50% dextrin and 20%Sucrose, granulates, dry, dresses up the granule of 10g/ bag.
Embodiment 10 prepares pill
Using steps d in arbitrary embodiment in embodiment 1~embodiment 6) in make the refined honey that adds its total amount 80% in medicinal extract asAdhesive and 20% starch, mix, and pill is dry, makes honeyed bolus.
Embodiment 11 prepares oral liquid
By steps d in arbitrary embodiment in embodiment 1~embodiment 6) in make medicinal extract and add water to 60 DEG C of relative densities and be 1.05~1.10, mix, pour in oral stable medicinal polythene bottle with high density, obtain oral liquid.

Claims (6)

1. a pharmaceutical composition for Cure for insomnia, is characterized in that being prepared from by the bulk drug of following weight parts:
Invaluable 3-10 part spina date seed 10-50 part polygala root 3-10 part
Mother-of-pearl 10-40 part fruit of Chinese magnoliavine 3-10 part Ligusticum wallichii 3-10 part
Wilsonii 10-40 part.
2. the pharmaceutical composition of a kind of Cure for insomnia as claimed in claim 1, is characterized in that the more excellent proportioning of described bulk drug is:
Invaluable 5-8 part spina date seed 15-40 part polygala root 5-8 part
Mother-of-pearl 15-25 part fruit of Chinese magnoliavine 5-8 part Ligusticum wallichii 5-8 part
Wilsonii 15-25 part.
3. the pharmaceutical composition of a kind of Cure for insomnia as claimed in claim 1, is characterized in that the best proportioning of described bulk drug is:
8 parts of 25 parts of polygala roots of invaluable 6 parts of spina date seeds
6 parts of 5 parts of Ligusticum wallichiis of 20 portions of fruit ofs Chinese magnoliavine of mother-of-pearl
20 parts of wilsoniis.
4. the pharmaceutical composition of the Cure for insomnia as described in as arbitrary in claim 1~3, is characterized in that described composition is prepared as any formulation of the prior art.
5. the pharmaceutical composition of Cure for insomnia as claimed in claim 4, is characterized in that described composition is prepared as any existing pharmaceutical dosage form in tablet, capsule, granule, pill, oral liquid.
6. the pharmaceutical composition as described in arbitrary as described in claim 1~5 is in the application of preparing in medicament for treating insomnia.
CN201210124241.8A 2012-04-25 2012-04-25 A kind of pharmaceutical composition for the treatment of of insomnia patients Active CN103372071B (en)

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