CN106334044A - Medicament capable of improving central nervous system inflammation - Google Patents

Medicament capable of improving central nervous system inflammation Download PDF

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Publication number
CN106334044A
CN106334044A CN201610668034.7A CN201610668034A CN106334044A CN 106334044 A CN106334044 A CN 106334044A CN 201610668034 A CN201610668034 A CN 201610668034A CN 106334044 A CN106334044 A CN 106334044A
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parts
extract
freeze
nervous system
central nervous
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胡明军
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No 1 Hospital of Xian
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/88Liliopsida (monocotyledons)
    • A61K36/888Araceae (Arum family), e.g. caladium, calla lily or skunk cabbage
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    • A61K36/32Burseraceae (Frankincense family)
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    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/35Caprifoliaceae (Honeysuckle family)
    • A61K36/355Lonicera (honeysuckle)
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    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/63Oleaceae (Olive family), e.g. jasmine, lilac or ash tree
    • A61K36/634Forsythia
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    • A61K2236/30Extraction of the material
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    • A61K2236/333Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones using mixed solvents, e.g. 70% EtOH
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    • A61K2236/50Methods involving additional extraction steps
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K2236/55Liquid-liquid separation; Phase separation

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Abstract

The invention discloses a medicament capable of improving central nervous system inflammation, wherein the medicament is prepared from the following raw materials in parts by weight: 20-30 parts of a nostoc commune powder, 25-35 parts of a pine needles baking powder, 15-25 parts of a honeysuckle extract, 6-18 parts of a radix isatidis extract, 6-18 parts of a fructus forsythiae extract, 13-17 parts of a raw mung bean freeze-dried powder, 23-37 parts of cranberry, 26-38 parts of olive leaves, 25-35 parts of a celery seed freeze-dried powder, and 27-33 parts of konjac flour. Through a special process, the pine needle baking powder, the honeysuckle extract, the radix isatidis extract, the fructus forsythiae extract, the raw mung bean freeze-dried powder and the celery seed powder are obtained and are combined together with the cranberry, the olive leaves, the konjac powder and the like according to the optimal ratio, so epidemic cerebrospinal meningitis can be effectively prevented, the body resistance is increased, and no drug resistance is generated.

Description

A kind of have the medicament improving inflammation of the central nervous system
Technical field
The present invention relates to a kind of field of traditional Chinese is and in particular to a kind of have the medicine improving inflammation of the central nervous system Agent.
Background technology
Epidemic meningitis is the abbreviation of meningococal meningitis, and it is the purulent inflammation being caused by diplococcus meningitidis, has Stronger infectiousness.Winter-spring season is the epidemic peak phase, and less than 15 years old children easily suffer from this disease, and the baby of two years old about is ill Rate is higher.When there is epidemic meningitis, it is the infection of the upper respiratory tract phase at the PD initial stage, infant occurs some similar colds Symptom such as pharyngalgia, nasal obstruction, runny nose, cough and slight heating etc..
Content of the invention
The present invention there is provided a kind of medicament having and improving inflammation of the central nervous system, can be with effectively preventing stream Brain, and do not develop immunity to drugs.
For achieving the above object, the technical scheme that the present invention takes is:
A kind of have the medicament improving inflammation of the central nervous system, is prepared from by the raw material of following weight portion:
Nostoc powder 20-30 part, pine needle yeast powder 25-35 part, Honegsukle flower P.E 15-25 part, isatis root extract 6- 18 parts, forsythia suspense extraction 6-18 part, raw mung bean freeze-dried powder 13-17 part, Cranberry 23-37 part, olive leaf 26-38 part, celery seed Freeze-dried powder 25-35 part, konjaku flour 27-33 part.
Wherein, described Honegsukle flower P.E prepares gained by following steps:
S11, the aqueous solution of Honegsukle flower P.E is first passed through composite polrvinyl chloride milipore filter and carry out UF membrane, collect and pass through Liquid, then extract is concentrated into the 11% of original volume with the NF membrane of molecular cut off 250, collect concentrate;
S12, by the concentrate obtaining with the flow velocity of 2-6bv/h pass through macroporous resin column, after Dynamic Adsorption saturation, spend from Sub- water is colourless to efflux with the above-mentioned macroporous resin column of flow velocity drip washing of 3-11bv/h, then is 30%-110%'s with volume fraction Organic solvent is eluted with the flow velocity of 7-13bv/h, collects organic solvent eluent until no chlorogenic acid flows out, finally will receive Collection gained eluent reduced pressure concentration, obtains medicinal extract;
S13, will after medicinal extract water dissolves with the flow velocity of 1-5bv/h pass through polyamide column, after Dynamic Adsorption saturation, use 3- 8bv deionized water is with the above-mentioned polyamide column of flow velocity drip washing of 1-10bv/h, then is the organic molten of 20%-100% with volume fraction The agent aqueous solution is eluted with the flow velocity of 5-10bv/h, collects organic solvent eluent until no chlorogenic acid flows out, is spray-dried, Obtain Honegsukle flower P.E.
Wherein, described pine needle yeast powder prepares gained by following steps:
By fresh pine needle after ultramicro grinding, according to the ratio microbe inoculation leavening of inoculum concentration 1.5-1.7%, protect Hold temperature 25-35 DEG C, after fermentation 48-54 hour, high-temperature inactivation, low temperature drying, obtain pine needle yeast powder.
Wherein, described microbe leaven is by Bacillus acidi lactici, bacillus licheniformis, Corynebacterium glutamicum in mass ratio 3: 2: 1 mixing gained.
Wherein, described isatis root extract prepares gained by following steps:
The Radix Isatidis being dried is placed in 90% methyl alcohol or the ethanol solution that flash extracter adds 6 times of volumes, processes 1-3 and divide Clock, after separation of solid and liquid, reclaims methyl alcohol or ethanol solution, concentrates so that extract is in paste, then with water-saturated n-butanol to carrying Take thing to extract 4 times, after recycling design, drying concentrated in vacuo for extract obtains isatis root extract.
Wherein, described forsythia suspense extraction prepares gained by following steps:
The capsule of weeping forsythia being dried is placed in steam-explosion jar, being first passed through nitrogen to steam explosion pressure inside the tank is 0.7-1.3mpa, at explosion Reason 8-25min;Then being passed through rapidly steam to steam explosion pressure inside the tank is 1.3-1.7mpa, Steam explosion treatment 0.5-2.5min, Filter, the dregs of a decoction are to add water refluxing extraction 2 time at 1: 10 in mass ratio, each refluxing extraction 1 hour, No. 3 extracts of merging are concentrated into Relative density 1.10-1.20 (room temperature), is spray-dried concentrate, obtains forsythia suspense extraction.
Wherein, described raw mung bean freeze-dried powder prepares gained by following steps:
By raw mung bean after ultramicro grinding, carry out pre-freeze distillation process, pre-freezing temperature is 20 DEG C, pre-freeze time 6h;Rising China processes separate explosion and processes, and sublimation temperature is -9.5 DEG C, and vacuum is 260pa, sublimation time 210min.
Wherein, described celery seed freeze-dried powder prepares gained by following steps:
It is placed in steam explosion in steam-explosion jar after celery seed is cleaned to process three times, freeze-drying obtains celery seed freeze-dried powder;Wherein, Onepull processes and keeps pressure to be 0.6-0.9mpa, temperature 65-95 degree Celsius, time 7-23min, and second explosion treatment is protected Holding pressure is 0.9-1.1mpa, temperature 95-115 degree Celsius, time 0.8-1.2min, and it is 3- that third time explosion treatment keeps pressure 5mpa, temperature 70-90 degree Celsius, time 0.8-2.8min.
Wherein, described nostoc powder is nostoc through ultramicro grinding gained;Described konjaku flour is for konjaku through ultramicro grinding institute ?.
The method have the advantages that
By special technique, obtain pine needle yeast powder, Honegsukle flower P.E, isatis root extract, forsythia suspense extraction, Raw mung bean freeze-dried powder and celery seed freeze-dried powder, and these raw materials are pressed optimal proportion and the combination such as Cranberry, olive leaf, konjaku flour Together, the resistance of human body with effectively preventing epidemic meningitis, can be increased, and do not develop immunity to drugs.
Specific embodiment
In order that objects and advantages of the present invention become more apparent, with reference to embodiments the present invention is carried out further Describe in detail.It should be appreciated that specific embodiment described herein, only in order to explain the present invention, is not used to limit this Bright.
In following examples, the Honegsukle flower P.E that used prepares gained by following steps:
S11, the aqueous solution of Honegsukle flower P.E is first passed through composite polrvinyl chloride milipore filter and carry out UF membrane, collect and pass through Liquid, then extract is concentrated into the 11% of original volume with the NF membrane of molecular cut off 250, collect concentrate;
S12, by the concentrate obtaining with the flow velocity of 2-6bv/h pass through macroporous resin column, after Dynamic Adsorption saturation, spend from Sub- water is colourless to efflux with the above-mentioned macroporous resin column of flow velocity drip washing of 3-11bv/h, then is 30%-110%'s with volume fraction Organic solvent is eluted with the flow velocity of 7-13bv/h, collects organic solvent eluent until no chlorogenic acid flows out, finally will receive Collection gained eluent reduced pressure concentration, obtains medicinal extract;
S13, will after medicinal extract water dissolves with the flow velocity of 1-5bv/h pass through polyamide column, after Dynamic Adsorption saturation, use 3- 8bv deionized water is with the above-mentioned polyamide column of flow velocity drip washing of 1-10bv/h, then is the organic molten of 20%-100% with volume fraction The agent aqueous solution is eluted with the flow velocity of 5-10bv/h, collects organic solvent eluent until no chlorogenic acid flows out, is spray-dried, Obtain Honegsukle flower P.E.
The pine needle yeast powder being used prepares gained by following steps:
By fresh pine needle after ultramicro grinding, according to the ratio microbe inoculation leavening of inoculum concentration 1.5-1.7%, protect Hold temperature 25-35 DEG C, after fermentation 48-54 hour, high-temperature inactivation, low temperature drying, obtain pine needle yeast powder.Wherein, described microorganism Leavening mixes gained by Bacillus acidi lactici, bacillus licheniformis, Corynebacterium glutamicum in mass ratio 3: 2: 1.
The isatis root extract being used prepares gained by following steps:
The Radix Isatidis being dried is placed in 90% methyl alcohol or the ethanol solution that flash extracter adds 6 times of volumes, processes 1-3 and divide Clock, after separation of solid and liquid, reclaims methyl alcohol or ethanol solution, concentrates so that extract is in paste, then with water-saturated n-butanol to carrying Take thing to extract 4 times, after recycling design, drying concentrated in vacuo for extract obtains isatis root extract.
The forsythia suspense extraction being used prepares gained by following steps:
The capsule of weeping forsythia being dried is placed in steam-explosion jar, being first passed through nitrogen to steam explosion pressure inside the tank is 0.7-1.3mpa, at explosion Reason 8-25min;Then being passed through rapidly steam to steam explosion pressure inside the tank is 1.3-1.7mpa, Steam explosion treatment 0.5-2.5min, Filter, the dregs of a decoction are to add water refluxing extraction 2 time at 1: 10 in mass ratio, each refluxing extraction 1 hour, No. 3 extracts of merging are concentrated into Relative density 1.10-1.20 (room temperature), is spray-dried concentrate, obtains forsythia suspense extraction.
The raw mung bean freeze-dried powder being used prepares gained by following steps:
By raw mung bean after ultramicro grinding, carry out pre-freeze distillation process, pre-freezing temperature is 20 DEG C, pre-freeze time 6h;Rising China processes separate explosion and processes, and sublimation temperature is -9.5 DEG C, and vacuum is 260pa, sublimation time 210min.
The celery seed freeze-dried powder being used prepares gained by following steps:
It is placed in steam explosion in steam-explosion jar after celery seed is cleaned to process three times, freeze-drying obtains celery seed freeze-dried powder;Wherein, Onepull processes and keeps pressure to be 0.6-0.9mpa, temperature 65-95 degree Celsius, time 7-23min, and second explosion treatment is protected Holding pressure is 0.9-1.1mpa, temperature 95-115 degree Celsius, time 0.8-1.2min, and it is 3- that third time explosion treatment keeps pressure 5mpa, temperature 70-90 degree Celsius, time 0.8-2.8min.
The nostoc powder being used is nostoc through ultramicro grinding gained;The konjaku flour being used is konjaku through ultramicro grinding Gained.
Embodiment 1
A kind of have the medicament improving inflammation of the central nervous system, is prepared from by the raw material of following weight portion:
20 parts of nostoc powder, 25 parts of pine needle yeast powder, 15 parts of Honegsukle flower P.E, 6 parts of isatis root extract, the capsule of weeping forsythia extract 6 parts of thing, 13 parts of raw mung bean freeze-dried powder, 23 parts of Cranberry, 26 parts of olive leaf, 25 parts of celery seed freeze-dried powder, 27 parts of konjaku flour.
Embodiment 2
A kind of have the medicament improving inflammation of the central nervous system, is prepared from by the raw material of following weight portion:
30 parts of nostoc powder, 35 parts of pine needle yeast powder, 25 parts of Honegsukle flower P.E, 18 parts of isatis root extract, the capsule of weeping forsythia carry Take 18 parts of thing, 17 parts of raw mung bean freeze-dried powder, 37 parts of Cranberry, 38 parts of olive leaf, 35 parts of celery seed freeze-dried powder, 33 parts of konjaku flour.
Embodiment 3
A kind of have the medicament improving inflammation of the central nervous system, is prepared from by the raw material of following weight portion:
25 parts of nostoc powder, 30 parts of pine needle yeast powder, 20 parts of Honegsukle flower P.E, 12 parts of isatis root extract, the capsule of weeping forsythia carry Take 12 parts of thing, 15 parts of raw mung bean freeze-dried powder, 30 parts of Cranberry, 32 parts of olive leaf, 30 parts of celery seed freeze-dried powder, 30 parts of konjaku flour.
The above is only the preferred embodiment of the present invention it is noted that ordinary skill people for the art For member, under the premise without departing from the principles of the invention, some improvements and modifications can also be made, these improvements and modifications also should It is considered as protection scope of the present invention.

Claims (9)

1. a kind of there is the medicament improving inflammation of the central nervous system it is characterised in that by following weight portion raw material prepare and Become:
Nostoc powder 20-30 part, pine needle yeast powder 25-35 part, Honegsukle flower P.E 15-25 part, isatis root extract 6-18 part, Forsythia suspense extraction 6-18 part, raw mung bean freeze-dried powder 13-17 part, Cranberry 23-37 part, olive leaf 26-38 part, celery seed freeze-dried powder 25-35 part, konjaku flour 27-33 part.
2. a kind of as claimed in claim 1 have the medicament improving inflammation of the central nervous system it is characterised in that described gold and silver Flower extract prepares gained by following steps:
S11, the aqueous solution of Honegsukle flower P.E is first passed through composite polrvinyl chloride milipore filter and carries out UF membrane, collect permeate, Extract is concentrated into the 11% of original volume with the NF membrane of molecular cut off 250 again, collects concentrate;
S12, by the concentrate obtaining with the flow velocity of 2-6bv/h pass through macroporous resin column, after Dynamic Adsorption saturation, deionized water Colourless to efflux with the above-mentioned macroporous resin column of flow velocity drip washing of 3-11bv/h, then be the organic of 30%-110% with volume fraction Solvent is eluted with the flow velocity of 7-13bv/h, collects organic solvent eluent until no chlorogenic acid flows out, finally will collect institute Obtain eluent reduced pressure concentration, obtain medicinal extract;
S13, will after medicinal extract water dissolves with the flow velocity of 1-5bv/h pass through polyamide column, after Dynamic Adsorption saturation, gone with 3-8bv Ionized water is with the above-mentioned polyamide column of flow velocity drip washing of 1-10bv/h, then the organic solvent being 20%-100% with volume fraction is water-soluble Liquid is eluted with the flow velocity of 5-10bv/h, collects organic solvent eluent until no chlorogenic acid flows out, is spray-dried, obtains gold and silver Flower extract.
3. a kind of as claimed in claim 1 have the medicament improving inflammation of the central nervous system it is characterised in that described pine needle Yeast powder prepares gained by following steps:
By fresh pine needle after ultramicro grinding, according to the ratio microbe inoculation leavening of inoculum concentration 1.5-1.7%, keep temperature 25-35 DEG C of degree, after fermentation 48-54 hour, high-temperature inactivation, low temperature drying, obtain pine needle yeast powder.
4. a kind of as claimed in claim 3 have the medicament improving inflammation of the central nervous system it is characterised in that described micro- life Thing leavening mixes gained by Bacillus acidi lactici, bacillus licheniformis, Corynebacterium glutamicum in mass ratio 3: 2: 1.
5. a kind of as claimed in claim 1 have the medicament improving inflammation of the central nervous system it is characterised in that described plate is blue Root extract prepares gained by following steps:
The Radix Isatidis being dried is placed in 90% methyl alcohol or the ethanol solution that flash extracter adds 6 times of volumes, processes 1-3 minute, After separation of solid and liquid, reclaim methyl alcohol or ethanol solution, concentrate so that extract is in paste, then with water-saturated n-butanol to extraction Thing extracts 4 times, after recycling design, drying concentrated in vacuo for extract obtains isatis root extract.
6. a kind of as claimed in claim 1 have the medicament improving inflammation of the central nervous system it is characterised in that the described capsule of weeping forsythia Extract prepares gained by following steps:
The capsule of weeping forsythia being dried is placed in steam-explosion jar, being first passed through nitrogen to steam explosion pressure inside the tank is 0.7-1.3mpa, explosion treatment 8- 25min;Then being passed through rapidly steam to steam explosion pressure inside the tank is 1.3-1.7mpa, Steam explosion treatment 0.5-2.5min, filters, The dregs of a decoction add water refluxing extraction 2 times for 1: 10 in mass ratio, and each refluxing extraction 1 hour merges No. 3 extracts, is concentrated into relatively Density 1.10-1.20 (room temperature), is spray-dried concentrate, obtains forsythia suspense extraction.
7. a kind of as claimed in claim 1 have the medicament improving inflammation of the central nervous system it is characterised in that described life is green Beans freeze-dried powder prepares gained by following steps:
By raw mung bean after ultramicro grinding, carry out pre-freeze distillation process, pre-freezing temperature is 20 DEG C, pre-freeze time 6h;At distillation Reason separate explosion is processed, and sublimation temperature is -9.5 DEG C, and vacuum is 260pa, sublimation time 210min.
8. a kind of as claimed in claim 1 have the medicament improving inflammation of the central nervous system it is characterised in that described celery Seed freeze-dried powder prepares gained by following steps:
It is placed in steam explosion in steam-explosion jar after celery seed is cleaned to process three times, freeze-drying obtains celery seed freeze-dried powder;Wherein, for the first time It is 0.6-0.9mpa, temperature 65-95 degree Celsius, time 7-23min that explosion treatment keeps pressure, and second explosion treatment keeps pressure Power is 0.9-1.1mpa, temperature 95-115 degree Celsius, time 0.8-1.2min, and it is 3- that third time explosion treatment keeps pressure 5mpa, temperature 70-90 degree Celsius, time 0.8-2.8min.
9. a kind of as claimed in claim 1 have the medicament improving inflammation of the central nervous system it is characterised in that described Ge Xian Ground rice is nostoc through ultramicro grinding gained;Described konjaku flour is konjaku through ultramicro grinding gained.
CN201610668034.7A 2016-08-16 2016-08-16 Medicament capable of improving central nervous system inflammation Pending CN106334044A (en)

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