CN108142948A - One kind loosens sleeping composition and preparation method thereof and preparation - Google Patents
One kind loosens sleeping composition and preparation method thereof and preparation Download PDFInfo
- Publication number
- CN108142948A CN108142948A CN201810252532.2A CN201810252532A CN108142948A CN 108142948 A CN108142948 A CN 108142948A CN 201810252532 A CN201810252532 A CN 201810252532A CN 108142948 A CN108142948 A CN 108142948A
- Authority
- CN
- China
- Prior art keywords
- preparation
- parts
- sleeping
- crude extract
- composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 41
- 238000002360 preparation method Methods 0.000 title claims abstract description 38
- 238000000855 fermentation Methods 0.000 claims abstract description 18
- 230000004151 fermentation Effects 0.000 claims abstract description 18
- 238000000605 extraction Methods 0.000 claims abstract description 9
- 238000001802 infusion Methods 0.000 claims abstract description 8
- 230000002829 reductive effect Effects 0.000 claims abstract description 8
- 239000000287 crude extract Substances 0.000 claims description 44
- 239000002904 solvent Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 12
- 244000197580 Poria cocos Species 0.000 claims description 9
- 235000008599 Poria cocos Nutrition 0.000 claims description 9
- 241000186660 Lactobacillus Species 0.000 claims description 8
- 241000234435 Lilium Species 0.000 claims description 8
- 229940039696 lactobacillus Drugs 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 8
- 244000144730 Amygdalus persica Species 0.000 claims description 7
- 244000111489 Gardenia augusta Species 0.000 claims description 7
- 235000018958 Gardenia augusta Nutrition 0.000 claims description 7
- 229920002774 Maltodextrin Polymers 0.000 claims description 7
- 235000006040 Prunus persica var persica Nutrition 0.000 claims description 7
- 241000194017 Streptococcus Species 0.000 claims description 7
- 235000019813 microcrystalline cellulose Nutrition 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 6
- 239000005913 Maltodextrin Substances 0.000 claims description 3
- 229920000168 Microcrystalline cellulose Polymers 0.000 claims description 3
- 239000002054 inoculum Substances 0.000 claims description 3
- 229940035034 maltodextrin Drugs 0.000 claims description 3
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- 241000894006 Bacteria Species 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 12
- 239000004615 ingredient Substances 0.000 abstract description 6
- 239000003814 drug Substances 0.000 abstract description 5
- 231100000331 toxic Toxicity 0.000 abstract 1
- 230000002588 toxic effect Effects 0.000 abstract 1
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 23
- 230000007958 sleep Effects 0.000 description 14
- 210000004556 brain Anatomy 0.000 description 13
- 229960003692 gamma aminobutyric acid Drugs 0.000 description 13
- 239000000284 extract Substances 0.000 description 11
- 229960003495 thiamine Drugs 0.000 description 10
- 239000011721 thiamine Substances 0.000 description 10
- 244000269722 Thea sinensis Species 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- OGNSCSPNOLGXSM-UHFFFAOYSA-N (+/-)-DABA Natural products NCCC(N)C(O)=O OGNSCSPNOLGXSM-UHFFFAOYSA-N 0.000 description 7
- 235000013616 tea Nutrition 0.000 description 7
- 238000001514 detection method Methods 0.000 description 5
- 210000004185 liver Anatomy 0.000 description 5
- 239000008108 microcrystalline cellulose Substances 0.000 description 5
- 229940016286 microcrystalline cellulose Drugs 0.000 description 5
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 4
- 241001269238 Data Species 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 235000013305 food Nutrition 0.000 description 4
- 230000036541 health Effects 0.000 description 4
- 108091022930 Glutamate decarboxylase Proteins 0.000 description 3
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 3
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 210000004369 blood Anatomy 0.000 description 3
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical class CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 3
- PXEDJBXQKAGXNJ-QTNFYWBSSA-L disodium L-glutamate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](N)CCC([O-])=O PXEDJBXQKAGXNJ-QTNFYWBSSA-L 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 235000013923 monosodium glutamate Nutrition 0.000 description 3
- 210000005036 nerve Anatomy 0.000 description 3
- 230000001624 sedative effect Effects 0.000 description 3
- 239000009396 suanzaoren Substances 0.000 description 3
- 102000008214 Glutamate decarboxylase Human genes 0.000 description 2
- DATAGRPVKZEWHA-YFKPBYRVSA-N N(5)-ethyl-L-glutamine Chemical compound CCNC(=O)CC[C@H]([NH3+])C([O-])=O DATAGRPVKZEWHA-YFKPBYRVSA-N 0.000 description 2
- 206010041349 Somnolence Diseases 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 229940024606 amino acid Drugs 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000001147 anti-toxic effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 230000035622 drinking Effects 0.000 description 2
- 235000013922 glutamic acid Nutrition 0.000 description 2
- 239000004220 glutamic acid Substances 0.000 description 2
- 210000003734 kidney Anatomy 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000000932 sedative agent Substances 0.000 description 2
- 230000003860 sleep quality Effects 0.000 description 2
- 210000000952 spleen Anatomy 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 208000011580 syndromic disease Diseases 0.000 description 2
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 2
- HBZVNWNSRNTWPS-UHFFFAOYSA-N 6-amino-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C(O)C2=CC(N)=CC=C21 HBZVNWNSRNTWPS-UHFFFAOYSA-N 0.000 description 1
- 206010008190 Cerebrovascular accident Diseases 0.000 description 1
- 206010013786 Dry skin Diseases 0.000 description 1
- 206010013789 Dry throat Diseases 0.000 description 1
- 206010013980 Dyssomnias Diseases 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 102000018997 Growth Hormone Human genes 0.000 description 1
- 108010051696 Growth Hormone Proteins 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- 206010058359 Hypogonadism Diseases 0.000 description 1
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 1
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
- 208000019255 Menstrual disease Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 206010033557 Palpitations Diseases 0.000 description 1
- 208000001431 Psychomotor Agitation Diseases 0.000 description 1
- 206010038743 Restlessness Diseases 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 229930013930 alkaloid Natural products 0.000 description 1
- -1 amides compound Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 230000008344 brain blood flow Effects 0.000 description 1
- 229960001948 caffeine Drugs 0.000 description 1
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 1
- 230000001914 calming effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 208000029078 coronary artery disease Diseases 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- 208000002173 dizziness Diseases 0.000 description 1
- 230000005059 dormancy Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000037336 dry skin Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000005713 exacerbation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 235000009569 green tea Nutrition 0.000 description 1
- 230000005283 ground state Effects 0.000 description 1
- 239000000122 growth hormone Substances 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 235000001497 healthy food Nutrition 0.000 description 1
- 235000008216 herbs Nutrition 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 206010022437 insomnia Diseases 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 230000033001 locomotion Effects 0.000 description 1
- KBPHJBAIARWVSC-RGZFRNHPSA-N lutein Chemical compound C([C@H](O)CC=1C)C(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\[C@H]1C(C)=C[C@H](O)CC1(C)C KBPHJBAIARWVSC-RGZFRNHPSA-N 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 230000036651 mood Effects 0.000 description 1
- 210000002569 neuron Anatomy 0.000 description 1
- 239000002858 neurotransmitter agent Substances 0.000 description 1
- 206010029410 night sweats Diseases 0.000 description 1
- 230000036565 night sweats Effects 0.000 description 1
- 238000010606 normalization Methods 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000013558 reference substance Substances 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 230000033764 rhythmic process Effects 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 229940073490 sodium glutamate Drugs 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229940026510 theanine Drugs 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000002936 tranquilizing effect Effects 0.000 description 1
- 230000001228 trophic effect Effects 0.000 description 1
- 230000002618 waking effect Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/065—Microorganisms
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/11—Lactobacillus
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/21—Streptococcus, lactococcus
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Mycology (AREA)
- Botany (AREA)
- Microbiology (AREA)
- Medicines Containing Plant Substances (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
The invention discloses a kind of preparation methods for loosening sleeping composition, are by carrying out subcritical abstraction and fermentation operation to tealeaves, carrying out infusion extraction, then be evaporated under reduced pressure and be spray-dried respectively to traditional Chinese medicine ingredients such as spina date seeds, obtain loosening sleeping composition.The preparation method is safe, controllability is strong, and the obtained sleeping composition that loosens substantially has no toxic side effect, and has effects that preferably to loosen, sleeping.
Description
Technical field
The invention belongs to healthy food fields, and in particular to one kind loosens sleeping composition and preparation method thereof and preparation.
Background technology
With the quickening of modern life rhythm, the exacerbation of life and work pressure, social insomniac is increasing now, loses
Dormancy has become a kind of potential threat for health.2017 Chinese sleep quality reports --- based on Huawei's sport health big data
It has been shown that, Chinese generally face sleeping problems, and 67% user's sound sleep is insufficient, also have sleep is too short, fall asleep too late, dreaminess, night it is easy
It wakes up, situation irregular, that sleep-respiratory quality is bad of working and resting.Due to being chronically at dyssomnia state, it be easy to cause immune work(
Can decline, is digestive function and hypogona dism, decrease of memory, short-tempered, also easily induce hypertension, coronary heart disease, apoplexy,
The problems such as diseases such as diabetes, women is then also easy to produce dry skin, menstrual disorder.The traditional Chinese medical science thinks that the etiology and pathogenesis of insomnia is defended for battalion
It becomes estranged, imbalance of yin and yang, sick position and the heart, liver, courage, spleen, stomach, kidney are in close relations.
Brain wave can be used for the sleep relaxation state of appraiser.Human brain launches frequency in 0.5-3Hz under the state of sleeping soundly
δ waves, θ wave of the frequency in 4-7Hz is launched under doze state, launches the α waves of 8-13Hz under ground state waking to loosen,
Launch the β waves of 14Hz under the excitedly state that wakes.When α wave brain wave quantity increases, show that people is in " loosening " state.
When people, which are in, regains consciousness, thinks deeply or take active action state, brains will send out β E.E.Gs.Research confirms that L-thiamine can promote
Brain surface α waves generate, θ wave number amounts when human body being made to generate happy, pleasant feeling, but not being caused in sleep state
Increase.L-thiamine is taken, can allow people's " brains is very awake ", " mood becomes stable ", " be easy to generate inspiration ".Absorb GABA
When, there is the phenomenon that apparent increase of α waves but significantly suppressed β waves, so taking GABA, the calm brain of meeting reduces pressure, stresses
It is calm.
Suanzaoren decoction is documented in《Synopsis Golden Chamber》, complete is just spina date seed 30g, Radix Glycyrrhizae 3g, rhizoma anemarrhenae 9g, Poria cocos 6g, Rhizoma Chuanxiong 6g,
With nourishing blood and tranquilization, the effect of clearing heat and relieving fidgetness.Main ingredient:Spina date seed, nourishing the liver blood, tranquilizing mind;Adjuvant:Rhizoma Chuanxiong raises liver blood, pungent to dissipate
It is soothing the liver;Adjutant:Poria cocos, rhizoma anemarrhenae, tonifying spleen calming heart, nourishing Yin and clearing heat.Make medicine:Radix Glycyrrhizae, coordinating the drug actions of a prescription.Curing mainly consumptive disease with restlessness must not sleep,
Palpitation and night sweat is had a dizzy spell, dry throat.The party has long edible history, and wherein Rhizoma Chuanxiong and rhizoma anemarrhenae is unusable in commonly
In food.
Chinese patent CN201410501131 discloses a kind of antitoxic heart-soothing and sedative, the health products for helping sleep, which provides one
Kind antitoxic heart-soothing and sedative, the health products for helping sleep, have the advantages that pure plant or extract combination form, without any toxicity and side effects, together
When to calm the nerves and assisting sleep have preferable effect.But the research of no extracting method is had no, also without animal or human experimentation work(
It can evaluation.
After tealeaves is generally considered with sedative action, but part drinking person takes tealeaves, easily causes and have difficulty in going to sleep, is spiritual
Phenomena such as excited, reason may be with the ingredient partly calmed the nerves while also with alkaloids such as caffeines to nerve in tealeaves
There is the ingredient of stimulation.Chinese patent CN201510230130 is disclosed extracts biology from low-grade tea and tea making leftover bits and pieces
The method of active material, the method which extracts bioactive substance from low-grade tea and tea making leftover bits and pieces, including following
Step:1)Caffeine is extracted from raw material;2)Extract tea polyphenols;3)Extract tea polysaccharide;4)Extract mono- amino fourth of theanine and γ
Acid;5)Extract extract and extract remainder protein feed;6)Extract separation obtains high-purity lutein ester and chlorophyll.The present invention
Method is at low cost, environmentally protective, is suitble to large-scale production.But extraction of substance type is more, and L-thiamine and γ-aminobutyric acid carry
It takes rate low, and yield cannot be controlled.It is used in extraction process to poisonous and harmful reagent, is not suitable for field of food.
Invention content
It is high, safe one of the objects of the present invention is to provide a kind of controllability for overcome the deficiencies in the prior art
The preparation method for loosening sleeping composition.
An object of the present invention is achieved through the following technical solutions:
A kind of preparation method for loosening sleeping composition, includes the following steps:
1)Using solid-liquid ratio as 1:(5-10)PH=7 water for solvent, subcritical abstraction operation and fermentation operation are carried out to tealeaves,
Obtain the first crude extract;Fermenting microbe is one or more in galactococcus, streptococcus and lactobacillus;Wherein, subcritical abstraction
Process conditions be:Pressure is 0.6-0.8MPa, temperature is 45-55 DEG C;The process conditions of fermentation are:The inoculum concentration of strain is 1-
5%, 32 DEG C -37 DEG C of fermentation temperature;
2)Take 30 parts of spina date seed, 2.5-3.5 parts of Radix Glycyrrhizae, 8-10 parts of lily, 4-8 parts of Poria cocos, 4-8 parts of peach kernel, 4-8 parts of cape jasmine, with
Solid-liquid ratio is 1:(5-10)PH=7 water be solvent infusion extraction, obtain the second crude extract;
3)First crude extract and the second crude extract respectively at 80-90 DEG C are evaporated under reduced pressure, are spray-dried, with(1-10): 3
Ratio mixing, obtain loosening sleeping composition;The technological parameter being wherein spray-dried is:100-120 DEG C of inlet air temperature, outlet air
70-80 DEG C of temperature.
Further, step 1)In, fermentation operation is carried out again after first carrying out subcritical abstraction operation.
Further, step 1)In, subcritical abstraction operation is carried out after first being fermented again.
Further, step 1)In, the sodium glutamate for adding in tealeaves weight 5-20wt% ferments.
Further, step 1)In, strain is pressed by galactococcus, streptococcus and lactobacillus(1-2):(1-2):10 weight ratio
Composition.
The second object of the present invention is to provide that above-mentioned preparation method obtains loosens sleeping composition.
The third object of the present invention is to provide a kind of preparation for loosening sleeping composition.
The third object of the present invention adopts the following technical scheme that realization:
One kind loosens sleeping preparation, is made including following components by weight:4-8 parts above-mentioned to loosen sleeping composition, 1-3
Part maltodextrin and 1-3 parts of microcrystalline celluloses.
Compared with prior art, the beneficial effects of the present invention are:
1)Sleeping preparation provided by the invention is to loosen sleeping ingredient, i.e. L-thiamine and gamma-amino in selective extraction tealeaves
Butyric acid also known as 4-Aminobutanoicacid with reference to integration of drinking and medicinal herbs, loosen and determine the traditional Chinese medicine ingredients of gas, can effectively improve the sleep matter of user
Amount;Experiencing experiment display through human body, there is good sleeping to loosen effect;
2)The present invention makes by using fermentation and the mode of subcritical abstraction in active ingredient and the suanzaoren decoction side in tealeaves
The mutually auxiliary phase separation of active ingredient improves the effect of this loosens sleeping composition and acts on;
3)The controllability of the preparation method provided by the invention for loosening sleeping composition is higher, can be by controlling zymotechnique and Asia
The sequencing and design parameter of critical extraction process controls the relative amount of L-thiamine and γ-aminobutyric acid, so as to
Selectively stress sleeping or loosen effect.
Specific embodiment
In the following, with reference to specific embodiment, the present invention is described further, it should be noted that is do not collided
Under the premise of, new embodiment can be formed between various embodiments described below or between each technical characteristic in any combination.
The present invention provides a kind of preparation method for loosening sleeping composition, includes the following steps:
1)Using solid-liquid ratio as 1:(5-10)PH=7 water for solvent, subcritical abstraction operation and fermentation operation are carried out to tealeaves,
Obtain the first crude extract;Fermenting microbe is one or more in galactococcus, streptococcus and lactobacillus;Wherein, subcritical abstraction
Process conditions be:Pressure is 0.6-0.8MPa, temperature is 45-55 DEG C;The process conditions of fermentation are:The inoculum concentration of strain is 1-
5%, 32 DEG C -37 DEG C of fermentation temperature;
2)Take 30 parts of spina date seed, 2.5-3.5 parts of Radix Glycyrrhizae, 8-10 parts of lily, 4-8 parts of Poria cocos, 4-8 parts of peach kernel, 4-8 parts of cape jasmine, with
Solid-liquid ratio is 1:(5-10)PH=7 water be solvent infusion extraction, obtain the second crude extract;
3)First crude extract and the second crude extract respectively at 80-90 DEG C are evaporated under reduced pressure, are spray-dried, with(1-10):3
Ratio mixes, and obtains loosening sleeping composition;The technological parameter being wherein spray-dried is:100-120 DEG C of inlet air temperature, goes out wind-warm syndrome
70-80 DEG C of degree.
The preparation method extracts tealeaves by using fermentation and the matched mode of subcritical abstraction mode, can effectively improve
The extraction efficiency of L-thiamine and γ-aminobutyric acid, and reduce the precipitation of the ingredients such as the theophylline for being unfavorable for loosening, so as to make
User, which experiences, to be loosened, is pleasant;The preparation method passes through to improving《Synopsis Golden Chamber》In suanzaoren decoction formula, select medicine food same
The component in source substitutes the component that can not apply ordinary food and adds in lily, can make consumer more on the basis of loosening,
Heat-clearing is except dry etc., so as to play the role of improving sleep quality.
L-thiamine belongs to amides compound, is the primary amino acid in tealeaves, typically constitutes from 50 % of free amino acid
More than, the 1 %-2 % of content in stem tea, content can be more than 2 % in certain green tea.Leucine carrier can be passed through in 30min
Movement system reaches cerebral tissue, will not accumulate in vivo.
γ-aminobutyric acid also known as 4-Aminobutanoicacid (4-Aminobutanoic acid, 4-AB, abbreviation GABA) and γ-ammonia
Butyric acid is widely present in nature, by glutamic acid (Glutamic acid, Glu) through glutamate decarboxylase(Glutamate
Decarboxylase, EC4.1.1.15, abbreviation GAD or GDC)Catalysis, is the weight in mammalian central nervous system
The inhibitory neurotransmitter wanted.With important physiological function, the physiological activity reported, which has, to be adjusted blood pressure, promotes spiritual peace
Fixed, promotion brain blood flow promotes brain vigor, trophic nerve cell, increases growth hormone secretion, strong liver profit kidney, pre- preventing obesity, rush
Into alcohol metabolism(It sobers up), improve the multiple efficacies such as climacteric syndrome.
Embodiment 1:
A kind of preparation method for loosening sleeping composition, includes the following steps:
1)Using the water of 0.7L pH=7 as solvent, subcritical abstraction operation is carried out to 100g tealeaves;The process conditions of subcritical abstraction
For:Pressure is 0.7MPa, temperature is 50 DEG C;
The fermenting microbe of 1wt% is added in the extracting solution that subcritical abstraction is obtained, in 36 DEG C of fermentations for 24 hours;First is obtained slightly to carry
Liquid;Fermenting microbe presses 1 by galactococcus, streptococcus and lactobacillus:1:8 weight ratio composition;
2)Take spina date seed 30g, 3 g of Radix Glycyrrhizae, 9 g of lily, 6 g of Poria cocos, 6 g of peach kernel, 6 g of cape jasmine, using the water of 0.42L pH=7 as
10h is extracted in solvent infusion, obtains the second crude extract;
3)First crude extract and the second crude extract are evaporated under reduced pressure and are spray-dried respectively at 85 DEG C, wherein the first crude extract
Weight is 7.8g after drying, and weight is 6.2g after the drying of the second crude extract;First crude extract dried object and the second crude extract dried object with
3:1 ratio mixing, obtains loosening sleeping composition;The technological parameter being wherein spray-dried is:110 DEG C of inlet air temperature, outlet air
75 DEG C of temperature.
Embodiment 2:
A kind of preparation method for loosening sleeping composition, includes the following steps:
1)Using the water of 0.7L pH=7 as solvent, 10g sodium glutamates are added in, to the strain of access 5% in 100g tealeaves, in 36 DEG C of hairs
Ferment 60h, obtains zymotic fluid;Wherein strain presses 1 by galactococcus, streptococcus and lactobacillus:1:8 weight ratio composition;
To zymotic fluid pressure is 0.7MPa, temperature is 50 DEG C of subcritical abstraction 10h, the first crude extract is obtained;
2)Spina date seed 30g, 3 g of Radix Glycyrrhizae, 9 g of lily, 6 g of Poria cocos, 6 g of peach kernel, 6 g of cape jasmine are taken, with the water of 0.42L pH=neutrality
10h is extracted for solvent infusion, obtains the second crude extract;
3)First crude extract and the second crude extract are evaporated under reduced pressure and are spray-dried respectively at 85 DEG C, wherein the first crude extract
Weight is 8.1g after drying, and weight is 6.3g after the drying of the second crude extract;First crude extract dried object and the second crude extract dried object with
1:3 ratio mixing, obtains loosening sleeping composition;The technological parameter being wherein spray-dried is:110 DEG C of inlet air temperature, outlet air
75 DEG C of temperature.
Embodiment 3:
A kind of preparation method for loosening sleeping composition, includes the following steps:
1)Using the water of 0.7L pH=7 as solvent, subcritical abstraction operation is carried out to 100g tealeaves;The process conditions of subcritical abstraction
For:Pressure is 0.6MPa, temperature is 55 DEG C;
The fermenting microbe of 1wt% is added in the extracting solution that subcritical abstraction is obtained, in 35 DEG C of fermentations for 24 hours;First is obtained slightly to carry
Liquid;Fermenting microbe is lactobacillus;
2)Spina date seed 30g, 3 g of Radix Glycyrrhizae, 9 g of lily, 6 g of Poria cocos, 6 g of peach kernel, 6 g of cape jasmine are taken, with the water of 0.42L pH=neutrality
10h is extracted for solvent infusion, obtains the second crude extract;
3)First crude extract and the second crude extract are evaporated under reduced pressure and are spray-dried respectively at 85 DEG C, wherein the first crude extract
Weight is 7.2g after drying, and weight is 6.2g after the drying of the second crude extract;First crude extract dried object and the second crude extract dried object with
2:1 ratio mixing, obtains loosening sleeping composition;The technological parameter being wherein spray-dried is:110 DEG C of inlet air temperature, outlet air
75 DEG C of temperature.
Embodiment 4:
A kind of preparation method for loosening sleeping composition, includes the following steps:
1)Using the water of 0.7L pH=7 as solvent, 10g sodium glutamates are added in, to accessing the lactobacillus of 5wt% in 100g tealeaves, in 35
DEG C fermentation 55h, obtain zymotic fluid;
To zymotic fluid pressure is 0.7MPa, temperature is 50 DEG C of subcritical abstraction 10h, the first crude extract is obtained;
2)Spina date seed 30g, 3 g of Radix Glycyrrhizae, 9 g of lily, 6 g of Poria cocos, 6 g of peach kernel, 6 g of cape jasmine are taken, with the water of 0.42L pH=neutrality
10h is extracted for solvent infusion, obtains the second crude extract;
3)First crude extract and the second crude extract are evaporated under reduced pressure and are spray-dried respectively at 85 DEG C, wherein the first crude extract
Weight is 8.0g after drying, and weight is 6.3g after the drying of the second crude extract;First crude extract dried object and the second crude extract dried object with
1:3 ratio mixing, obtains loosening sleeping composition;The technological parameter being wherein spray-dried is:110 DEG C of inlet air temperature, outlet air
75 DEG C of temperature.
Embodiment 5:
A kind of preparation for loosening sleeping composition, by the gained of 6g embodiments 1 to loosen sleeping composition, 2g maltodextrins and 2g micro-
Crystalline cellulose mixes, and tabletting is made.
Embodiment 6:
A kind of preparation for loosening sleeping composition, by the gained of 6g embodiments 2 to loosen sleeping composition, 2g maltodextrins and 2g micro-
Crystalline cellulose mixes, and tabletting is made.
Embodiment 7:
A kind of preparation for loosening sleeping composition, by the gained of 6g embodiments 3 to loosen sleeping composition, 2g maltodextrins and 2g micro-
Crystalline cellulose mixes, and tabletting is made.
Embodiment 8:
A kind of preparation for loosening sleeping composition, by the gained of 6g embodiments 4 to loosen sleeping composition, 2g maltodextrins and 2g micro-
Crystalline cellulose mixes, and tabletting is made.
Performance detection and effect assessment
1. analysis of effective component
To in embodiment 1-4, L-thiamine and γ-aminobutyric acid in the first crude extract are tested by area normalization method using HPLC
Content, the results are shown in table below:
Analysis of effective component in 1 first crude extract of table
Embodiment 1 | Embodiment 2 | Embodiment 3 | Embodiment 4 | |
L-thiamine (g/L) | 10.2 | 6.5 | 9.6 | 6.2 |
γ-aminobutyric acid (g/L) | 5.0 | 11.9 | 5.1 | 11.7 |
By table 1 it is found that fermenting again after first carrying out subcritical abstraction, the concentration of L-thiamine is relatively high, and first carries out
Subcritical abstraction is carried out after fermentation again, the content of γ-aminobutyric acid is relatively high.
2. relaxation effect detects
To the preparation that embodiment 5-8 is obtained, using double-blind study, 1 is pressed with maltodextrin and microcrystalline cellulose:1 weight ratio tabletting
Product after rest state 30min, uses wet electrode as reference substance, oral test-meal(Ag/AgCl)Monitoring test person's brain wave
Situation and the performance state of record volunteer.
5 groups of brain wave detection datas of embodiment show that α waves and β wave number amounts significantly increase, and the ratio of α waves and β waves is
0.9:1, apparent δ waves and θ waves are not monitored.Volunteer is visited in observation and inquiry, and volunteer, which experiences, to be loosened, is pleasant, illustrates to implement
The preparation of example 5, which has, significantly loosens effect;
6 groups of brain wave detection datas of embodiment show that the quantity of α waves, δ waves and θ waves significantly increases, and α waves/β waves are 1.4:1, β wave
It is suppressed.Volunteer is visited in observation and inquiry, and volunteer has sleepy sense, quickly enters sleep state, illustrates the preparation tool of embodiment 6
There is apparent function for assisting sleep.
7 groups of brain wave detection datas of embodiment show that α waves and β wave number amounts significantly increase, and the ratio of α waves and β waves is
0.8:1, apparent δ waves and θ waves are not monitored.Volunteer is visited in observation and inquiry, and volunteer, which experiences, to be loosened, is pleasant, illustrates to implement
The preparation of example 7, which has, significantly loosens effect;
8 groups of brain wave detection datas of embodiment show that the quantity of α waves, δ waves and θ waves significantly increases, and α waves/β waves are 1.5:1, β wave
It is suppressed.Volunteer is visited in observation and inquiry, and volunteer has sleepy sense, quickly enters sleep state, illustrates the preparation tool of embodiment 8
There is apparent function for assisting sleep.
The above embodiment is only the preferred embodiment of the present invention, it is impossible to the scope of protection of the invention is limited with this,
The variation and replacement for any unsubstantiality that those skilled in the art is done on the basis of the present invention belong to institute of the present invention
Claimed range.
Claims (7)
1. a kind of preparation method for loosening sleeping composition, which is characterized in that include the following steps:
1)Using solid-liquid ratio as 1:(5-10)PH=7 water for solvent, subcritical abstraction operation and fermentation operation are carried out to tealeaves,
Obtain the first crude extract;Fermenting microbe is one or more in galactococcus, streptococcus and lactobacillus;Wherein, subcritical abstraction
Process conditions be:Pressure is 0.6-0.8MPa, temperature is 45-55 DEG C;The process conditions of fermentation are:The inoculum concentration of strain is 1-
5%, 32 DEG C -37 DEG C of fermentation temperature;
2)Take 30 parts of spina date seed, 2.5-3.5 parts of Radix Glycyrrhizae, 8-10 parts of lily, 4-8 parts of Poria cocos, 4-8 parts of peach kernel, 4-8 parts of cape jasmine, with
Solid-liquid ratio is 1:(5-10)PH=7 water be solvent infusion extraction, obtain the second crude extract;
3)First crude extract and the second crude extract respectively at 80-90 DEG C are evaporated under reduced pressure, are spray-dried, with(1-10): 3
Ratio mixing, obtain loosening sleeping composition;The technological parameter being wherein spray-dried is:100-120 DEG C of inlet air temperature, outlet air
70-80 DEG C of temperature.
2. preparation method as described in claim 1, which is characterized in that step 1)In, after first progress subcritical abstraction operation again
Carry out fermentation operation.
3. preparation method as described in claim 1, which is characterized in that step 1)In, it is carried out again after first being fermented subcritical
Extracting operation.
4. preparation method as claimed in claim 3, which is characterized in that step 1)In, the paddy ammonia of addition tealeaves weight 5-20wt%
Sour sodium ferments.
5. preparation method as described in claim 1, which is characterized in that step 1)In, strain is by galactococcus, streptococcus and newborn bar
Bacterium is pressed(1-2):(1-2):10 weight ratio composition.
It is 6. a kind of as what claim 1-4 any one of them preparation methods obtained loosens sleeping composition.
7. a kind of preparation for loosening sleeping composition, which is characterized in that be made including following components by weight:4-8 parts
Loosen sleeping composition, 1-3 portion maltodextrin and 1-3 parts of microcrystalline celluloses described in claim 6.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810252532.2A CN108142948A (en) | 2018-03-26 | 2018-03-26 | One kind loosens sleeping composition and preparation method thereof and preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810252532.2A CN108142948A (en) | 2018-03-26 | 2018-03-26 | One kind loosens sleeping composition and preparation method thereof and preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
CN108142948A true CN108142948A (en) | 2018-06-12 |
Family
ID=62456307
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810252532.2A Pending CN108142948A (en) | 2018-03-26 | 2018-03-26 | One kind loosens sleeping composition and preparation method thereof and preparation |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN108142948A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102488826A (en) * | 2011-12-14 | 2012-06-13 | 哈药集团中药二厂 | Method for preparing freeze-dried oral preparation of spina date seed decoction |
CN105077477A (en) * | 2015-08-12 | 2015-11-25 | 北京晚安科技有限责任公司 | Sleeping-aid beverage |
CN107197966A (en) * | 2017-05-18 | 2017-09-26 | 华南农业大学 | A kind of method of microorganism ferment making GABA tea |
-
2018
- 2018-03-26 CN CN201810252532.2A patent/CN108142948A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102488826A (en) * | 2011-12-14 | 2012-06-13 | 哈药集团中药二厂 | Method for preparing freeze-dried oral preparation of spina date seed decoction |
CN105077477A (en) * | 2015-08-12 | 2015-11-25 | 北京晚安科技有限责任公司 | Sleeping-aid beverage |
CN107197966A (en) * | 2017-05-18 | 2017-09-26 | 华南农业大学 | A kind of method of microorganism ferment making GABA tea |
Non-Patent Citations (2)
Title |
---|
宁侠: "《周绍华脑病临证经验实录》", 30 September 2016, 中国医药科技出版社 * |
崔山风: "《保健食品制剂技术》", 31 July 2010, 中国医药科技出版社 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN107594272A (en) | A kind of warm the womb menstruation regulating, the health drink for nourishing beauty treatment and preparation method thereof | |
CN103271273A (en) | Health food for treating alopecia and preparation method thereof | |
CN112869162A (en) | Composition with functions of resisting fatigue and improving sleep and preparation method thereof | |
CN100500014C (en) | Health-care tea | |
CN107319086A (en) | A kind of matrimony vine spun gold emperor chrysanthemum pressed candy and preparation method thereof | |
CN105707598A (en) | Plant drink for dispelling alcohol effects and preparation method thereof | |
CN110710678A (en) | Marine polypeptide donkey-hide gelatin paste capable of nourishing liver and kidney, nourishing blood and soothing nerves and preparation method thereof | |
CN105168057A (en) | Figwort root body wash | |
CN110810693A (en) | A beverage composition containing Ampelopsis grossedentata and its preparation method | |
CN106692356A (en) | Spina-date-seed-containing solid beverage and preparation method thereof | |
CN109700019A (en) | It is a kind of to improve the tree peony ferment slept and its production method | |
CN103444935B (en) | Noon tea bag for preserving health in autumn | |
CN108485816A (en) | A kind of extracting method of turmeric essential oil | |
CN108142948A (en) | One kind loosens sleeping composition and preparation method thereof and preparation | |
CN105724696A (en) | Refreshing mangosteen tea | |
CN103800422A (en) | Preparation of eucommia health-care compound electuary and product thereof | |
JP7170357B2 (en) | External agent for hair growth | |
CN107259024A (en) | A kind of medicine-food two-purpose ganoderma lucidum ginseng tea and preparation method thereof | |
CN107712724A (en) | A kind of method of ginkgo powder detoxification | |
CN104222400A (en) | Pu'er tea cream with functions of dispelling alcohol effect, protecting liver, nourishing heart and tranquilizing mind and processing method thereof | |
CN105496934A (en) | Cactus mask for treating acne and preparation method | |
CN107432467B (en) | Effervescent tablet and preparation method thereof | |
CN110964618A (en) | Anti-fatigue health wine and preparation method thereof | |
CN110711245A (en) | Active polysaccharide compound botanical drug for improving immunity and resisting fatigue and preparation method thereof | |
CN110437008A (en) | A kind of pure Chinese medicine Biological water soluble fertilizer and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination |