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CN111358891A - Immune activation spray and preparation method thereof - Google Patents

Immune activation spray and preparation method thereof Download PDF

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Publication number
CN111358891A
CN111358891A CN202010242232.3A CN202010242232A CN111358891A CN 111358891 A CN111358891 A CN 111358891A CN 202010242232 A CN202010242232 A CN 202010242232A CN 111358891 A CN111358891 A CN 111358891A
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leaching
rhizoma polygonati
yeast
rhizoma
water
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孙宁
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    • AHUMAN NECESSITIES
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    • A61K36/06Fungi, e.g. yeasts
    • A61K36/062Ascomycota
    • A61K36/064Saccharomycetales, e.g. baker's yeast
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Abstract

The invention belongs to the technical field of medicine spray processing, and discloses an immune activation spray and a preparation method thereof. The spray for activating immunity comprises rhizoma Polygonati, oleum herba Pogostemonis, Atractylodis rhizoma, Borneolum Syntheticum, yeast and related emulsifier, cosolvent, and antiseptic. The dosage of each raw material is as follows according to the parts by weight: 25-35 parts of rhizoma polygonati; 0.05 to 0.1 portion of patchouli oil; 15-25 parts of bighead atractylodes rhizome; 0.01-0.06 part of borneol; 3-7 parts of yeast; proper amount of related emulsifier, cosolvent, preservative, etc. The immune activation spray provided by the invention is prepared by combining Chinese herbal medicines and yeast compounds, can give full play to multiple ways and multiple targets of medicines, comprehensively exerts the prevention and intervention of the Chinese herbal medicines, improves the immunity of the organism and improves the disease resistance of the organism.

Description

Immune activation spray and preparation method thereof
Technical Field
The invention belongs to the technical field of medicine spray processing, and relates to an immune activation spray and a preparation method thereof.
Background
Infectious diseases caused by viruses are a serious threat to human life and health. Statistically, more than 80% of infectious diseases are caused by viruses. Viral diseases have been implicated in various areas of clinical medicine and many non-infectious diseases have been found to be associated with viral infections, some of which are still associated with certain neoplastic and autoimmune diseases. Thus, viruses and diseases caused by the viruses are hot spots of much subject attention. The most common of viral infections are those caused by respiratory and enteric viruses. Respiratory viruses are a large group of viruses which can invade the respiratory tract and cause local lesions of the respiratory tract or only take the respiratory tract as an invasion portal, and firstly proliferate in the mucosal epithelial cells of the respiratory tract to cause respiratory tract and systemic infection, thereby causing lesions of the respiratory tract and related tissues and organs. Respiratory viruses are the major pathogens responsible for acute respiratory infections. Since the 90 s in the 20 th century, researchers found many new antiviral drugs, and the number of antiviral drugs currently used in clinic exceeds more than 20, but the exact curative effect is still greatly controversial. The research on the antiviral drug has important practical significance, and the research on finding the antiviral drug with high efficiency, safety and less side effects is imperative. The universality of diseases caused by viruses, particularly respiratory viruses, and the severity of damages caused by the diseases are always research hotspots, although western antiviral medicines are effective in treating the diseases, the toxic and side effects are large, drug resistance is easy to generate after long-term administration, and virus strains can also be changed into new drug-resistant strains due to variation, so that the clinical application of the existing western antiviral medicines and the research and development of new western antiviral medicines face huge challenges, and the vaccine can only temporarily and unstably treat the high-variability viruses, so that the search for traditional Chinese medicines with remarkable curative effect, small toxic and side effects and wide antiviral spectrum is still the research focus of the inventor.
The immune system is an important defense line against pathogen infection, the attack is actually the result of struggle between the pathogen and the human immunity, and the pathogen breaks the defense line of the immune system to cause rapid propagation of virus or bacteria, thus causing the occurrence of diseases. The immune function of the organism can be promoted and regulated as soon as possible, the anti-infection capability of the organism can be enhanced, and the anti-infection health-care tea has important significance for preventing and controlling diseases.
The traditional Chinese medicine is a natural medicine with a long use history for human beings, and contains various effective components capable of enhancing the immune function of organisms. The traditional Chinese medicine has the advantages of rich resources, small toxic and side effects, insignificant drug resistance, various performances and the like, contains various active ingredients for enhancing the immune function of organisms, and can be combined into various compounds according to the needs, so that the traditional Chinese medicine has wide and selective clinical application.
In recent years, researches on antiviral effects of plant polysaccharides have been receiving more and more attention. Polysaccharides are important biological information macromolecules and widely exist in animals, plants and microorganisms. At present, the regulation and control effect of polysaccharide on the body immune system is generally accepted by academia. The polysaccharide as an immunomodulator has the advantages of good curative effect, low toxicity and the like, and can act on an immune system through a plurality of ways, such as stimulating the differentiation and proliferation of various immunocompetent cells of an organism; promoting expression of various receptor molecules; inducing the production of cytokines such as Interleukin (IL), Tumor Necrosis Factor (TNF) and Interferon (IFN); promoting antibody formation; activation of complement system activation pathways, and the like. Modern molecular immunology studies have found that modulating the immune response of the body by ingestion of natural active substances is the most promising immunoadjuvant for replacement and adjuvant antibiotic therapy. Polysaccharide is one of important active ingredients in traditional Chinese medicines, at present, polysaccharide preparations such as astragalus polysaccharide injection, ginseng polysaccharide injection, pachyman oral liquid and the like are widely applied to clinic, but no polysaccharide spray is clinically available, and particularly no traditional Chinese medicine polysaccharide and zymosan compound spray is available.
Therefore, there is a need to develop a polysaccharide immune activation spray and a preparation method thereof, which are used for activating and improving the immunity of the organism and preventing and treating virus infection.
Disclosure of Invention
In order to overcome the defects of the prior art, the invention provides an immune activation spraying agent and a preparation method thereof. Compared with the injection, the immune activation spray provided by the invention has the characteristics of convenient administration, wide antiviral spectrum, small toxic and side effects, remarkable curative effect, rich medicine sources and low price.
The above purpose of the invention is realized by the following technical scheme:
an immunity activating spray comprises rhizoma Polygonati, oleum herba Pogostemonis, Atractylodis rhizoma, Borneolum Syntheticum, yeast and related emulsifier, cosolvent, and antiseptic.
The dosage of each raw material is as follows according to the parts by weight: 25-35 parts of rhizoma polygonati; 0.05 to 0.1 portion of patchouli oil; 15-25 parts of bighead atractylodes rhizome; 0.01-0.06 part of borneol; 3-7 parts of yeast; 0.5 to 1.2 portions of related emulsifier, 0.4 to 1.0 portion of cosolvent and 0.05 to 0.3 portion of preservative.
The emulsifier is polysorbate 80; the cosolvent is ethanol; the preservative is potassium sorbate.
The preparation method of the immune activation spraying agent comprises the following steps:
1) cleaning rhizoma Polygonati decoction pieces, adding water, extracting, and filtering to obtain rhizoma Polygonati extract;
2) cleaning Atractylodis rhizoma decoction pieces, adding water, extracting, and filtering to obtain Atractylodis rhizoma extract;
3) mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, centrifuging, and concentrating to obtain rhizoma Polygonati and Atractylodis rhizoma concentrated solution;
4) adding cosolvent into Borneolum Syntheticum to obtain Borneolum Syntheticum solution;
5) adding emulsifier into oleum herba Pogostemonis to obtain oleum Pogostemonis emulsion;
6) preparing yeast suspension for later use;
7) dissolving the preservative to obtain a preservative solution for later use;
8) mixing rhizoma Polygonati and Atractylodis rhizoma concentrated solution, Borneolum Syntheticum solution, herba Agastaches oil emulsion, yeast suspension, and antiseptic solution, metering volume, sterilizing, and packaging to obtain the spray.
Further, the yeast is saccharomyces cerevisiae.
Further, the preparation process of the yeast suspension comprises the following steps:
a) cleaning rhizoma Polygonati decoction pieces, adding water, extracting, and filtering to obtain rhizoma Polygonati extract; the leaching conditions were: the material-water ratio of the rhizoma polygonati decoction pieces to water is 1: 100-120, soaking for 4-6 hours, leaching for 2 times with hot water at 98-100 ℃ for 1-2 hours each time, and filtering with 200 meshes to obtain sealwort leaching liquor.
b) Cleaning Atractylodis rhizoma decoction pieces, adding water, extracting, and filtering to obtain Atractylodis rhizoma extract; the leaching conditions were: the material-water ratio of the atractylodes macrocephala decoction pieces to water is 1: 100-120, soaking for 4-6 hours, leaching for 2 times with hot water at 98-100 ℃ for 1-2 hours each time, and filtering with 200 meshes to obtain a bighead atractylodes rhizome leaching solution;
c) mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, concentrating, adding glucose to dissolve, diluting to constant volume to obtain yeast culture solution, sterilizing, cooling, inoculating yeast, fermenting and amplifying to obtain yeast fermentation liquid;
d) and (3) carrying out centrifugal concentration on the yeast fermentation liquor to obtain yeast (wet weight), wherein the weight ratio of the yeast to the liquid is 1: 1 in the presence of a yeast suspension.
The yeast culture solution comprises the following raw materials in parts by weight: 0.5-2 parts of rhizoma polygonati decoction pieces; 0.5-1 part of bighead atractylodes rhizome decoction pieces; 1-5 parts of glucose; 95-99 parts of water.
In the step 1) of the preparation method of the immune activation spraying agent, the leaching conditions are as follows: the material-water ratio of the rhizoma polygonati decoction pieces to water is 1: 10-20, soaking for 4-6 hours, leaching for 2 times with hot water at 98-100 ℃ for 1-2 hours each time, and filtering with 200 meshes to obtain sealwort leaching liquor.
In step 2) of the preparation method of the immune activation spraying agent, the leaching conditions are as follows: the material-water ratio of the atractylodes macrocephala decoction pieces to water is 1: 10-15, soaking for 4-6 hours, leaching for 2 times with hot water at 98-100 ℃ for 1-2 hours each time, and filtering with 200 meshes to obtain a white atractylodes rhizome leaching liquor.
In step 3) of the preparation method of the immune activation spraying agent, the method comprises the following steps: mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, centrifuging at 12000 and 16000rpm tube or butterfly type, and concentrating the obtained liquid under reduced pressure.
Compared with the prior art, the invention has the beneficial effects that:
the immune activation spray provided by the invention can be sprayed to oral cavity and nasal cavity, is used for oral cavity and nasal cavity administration, can prevent the medicine from being degraded in gastrointestinal tract or due to liver metabolism, can promote the quick absorption of the medicine, improves the bioavailability, and plays a localized and directional local effect. Compared with an injection, the immune activation spraying agent provided by the invention has the characteristic of convenient administration.
The immune activation spray provided by the invention is prepared by compounding and combining rhizoma polygonati, bighead atractylodes rhizome, yeast, borneol and patchouli oil, accords with the theory of traditional Chinese medicine and modern pharmacology, and is mainly used for preventing viral respiratory tract infection. Different structure-activity relationships of various active polysaccharides such as polygonatum polysaccharides, atractylodes polysaccharides, zymosan and the like are combined and utilized, the anti-inflammatory and antiviral effects of patchouli oil are assisted, the mucosal absorption is promoted through the transdermal promoting effect of borneol, the respiratory tract mucosal immunoreaction is activated through multiple ways, the immunity of the organism is comprehensively and comprehensively improved, and the purpose of preventing viruses from infecting respiratory tracts is achieved.
The immune activation spray provided by the invention can act on respiratory tract mucous membrane, stimulate local mucous membrane immunity to generate secretory IgA, enhance the function of the pharyngeal mucous membrane immunity of organisms for resisting virus, and inhibit virus adsorption and invasion, thereby achieving the effects of prevention and treatment, achieving the purpose of preventing diseases before first and preventing diseases after recovery, and having important significance for preventing respiratory tract virus infection.
The immune activation spray provided by the invention is prepared by combining Chinese herbal medicines and yeast compounds, can give full play to multiple ways and multiple targets of medicines, comprehensively exerts the prevention and intervention of the Chinese herbal medicines, improves the immunity of the organism and improves the disease resistance of the organism.
The immune activation spraying agent provided by the invention has the advantages of abundant medicinal sources, simple and quick preparation method, contribution to batch production, low cost and certain social and economic values.
Polygonatum sibiricum (Polygonatum sibiricum), a perennial herbal plant of Liliaceae, which is widely used in traditional Chinese medicine clinical medicine since ancient times, has been 2000 years ago to date. Modern researches show that rhizoma polygonati contains various chemical components such as polysaccharide, oligosaccharide, flavone, steroid saponin, alkaloid, lignan, amino acid, inorganic elements, volatile oil and the like. The rhizoma Polygonati polysaccharide is the main active ingredient of rhizoma Polygonati, and has the pharmacological effects of regulating immunity, resisting bacteria and virus, diminishing inflammation, resisting aging, reducing blood sugar, reducing blood lipid, resisting atherosclerosis, and treating diabetes.
Atractylodis rhizoma belongs to perennial herb of Compositae and Atractylodes. In recent years, research shows that: the rhizoma Atractylodis Macrocephalae contains abundant polysaccharides, saponins, volatile oils, amino acids, and other effective components, which can act on digestive system, immune system, urinary system, etc. Wherein, the Atractylodes macrocephala Polysaccharide (PAM) is one of the main bioactive components of the Atractylodes macrocephala, is commonly used as an immunomodulator of an organism, has the functions of resisting oxidation, resisting aging, reducing blood sugar, resisting tumor, acting on myocardial cells and the like, and is clinically used for treating diseases such as hepatitis, tumor and the like. The atractylodes macrocephala polysaccharide can coordinate and play a role in regulating immunity of an organism through three levels of regulating immune organs, immune cells and immune molecules, not only acts on specific immunity of the organism, but also acts on non-specific immunity of the organism, and plays a role in regulating immunity of normal and abnormal organisms.
The β -glucan has the most basic function of immunoregulation, and the β -glucan can stimulate the innate immune system so as to achieve the purpose of greatly improving the capability of resisting bacteria, fungi, viruses and the like through in vivo and in vitro experimental researches, β -glucan can stimulate the differentiation and activation of T lymphocytes by activating T cells, macrophages and natural killer cells, influence and activate the change of pathway complements and finally achieve the effect of enhancing the cellular and humoral immunity of organisms, β -glucan in the yeast cell wall can act on receptors on the surface of immune cells so as to activate immune related signal transduction pathways, promote the immune cells to release downstream signal molecules and induce the organisms to generate nonspecific and specific immune response.
Borneol is a traditional Chinese medicine, also called borneol and 2-borneol, and modern research shows that the borneol belongs to a small molecular fat-soluble monoterpene substance and has pharmacological activities of promoting medicine absorption, protecting cardiovascular and cerebrovascular vessels, protecting central nerves, resisting bacteria, diminishing inflammation, easing pain, resisting fertility and the like. Borneol transdermal promotion mainly changes the lipid molecular arrangement of the stratum corneum of the skin to increase fluidity. The borneol reaching a certain concentration can promote the nasal cavity absorption, oral mucosa absorption and intestinal section absorption of the medicine. The barrier action of the oral mucosa is the most important influencing factor of the oral mucosa drug delivery system, and can block the drugs from entering the blood circulation of a human body through the oral mucosa. The application of the penetration enhancer borneol can promote the medicine to penetrate through oral mucosa and has small irritation to the mucosa.
Patchouli oil (Patchouli oil) is volatile oil extracted from Patchouli by a steam distillation method, and the main active ingredients of the Patchouli oil are Patchouli alcohol, Patchouli, α -guaiene, delta-guaiene, α -Patchouli, β -Patchouli, Patchouli ketone, tularenone and the like.
Detailed Description
The invention is described in more detail below with reference to specific examples, without limiting the scope of the invention. Unless otherwise specified, the experimental methods adopted by the invention are all conventional methods, and experimental equipment, materials, reagents and the like used in the experimental method can be obtained from commercial sources.
Example 1
An immunity activating spray comprises rhizoma Polygonati, oleum herba Pogostemonis, Atractylodis rhizoma, Borneolum Syntheticum, yeast and related emulsifier, cosolvent, and antiseptic.
The dosage of each raw material is as follows according to the parts by weight: 25 parts of rhizoma polygonati; 0.05 part of patchouli oil; 15 parts of bighead atractylodes rhizome; 0.01 part of borneol; 3 parts of yeast; proper amount of related emulsifier, cosolvent, preservative, etc.
The preparation method of the immune activation spraying agent comprises the following steps:
1) cleaning rhizoma Polygonati decoction pieces, adding water, extracting, and filtering to obtain rhizoma Polygonati extract;
2) cleaning Atractylodis rhizoma decoction pieces, adding water, extracting, and filtering to obtain Atractylodis rhizoma extract;
3) mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, centrifuging, and concentrating to obtain rhizoma Polygonati and Atractylodis rhizoma concentrated solution;
4) adding cosolvent into Borneolum Syntheticum to obtain Borneolum Syntheticum solution;
5) adding emulsifier into oleum herba Pogostemonis to obtain oleum Pogostemonis emulsion;
6) preparing yeast suspension for later use;
7) dissolving the preservative to obtain a preservative solution for later use;
8) mixing rhizoma Polygonati and Atractylodis rhizoma concentrated solution, Borneolum Syntheticum solution, herba Agastaches oil emulsion, yeast suspension, and antiseptic solution, metering volume, sterilizing, and packaging to obtain the spray.
Further, the yeast is saccharomyces cerevisiae.
Further, the preparation process of the yeast suspension comprises the following steps:
a) cleaning rhizoma Polygonati decoction pieces, adding water, extracting, and filtering to obtain rhizoma Polygonati extract; the leaching conditions were: the material-water ratio of the rhizoma polygonati decoction pieces to water is 1: 100, soaking for 4 hours, leaching for 2 times with hot water at 98 ℃ for 1 hour each time, and filtering with 200 meshes to obtain rhizoma polygonati leaching liquor.
b) Cleaning Atractylodis rhizoma decoction pieces, adding water, extracting, and filtering to obtain Atractylodis rhizoma extract; the leaching conditions were: the material-water ratio of the atractylodes macrocephala decoction pieces to water is 1: 100, soaking for 4 hours, leaching for 2 times with hot water at 98 ℃ for 1 hour each time, and filtering with 200 meshes to obtain a white atractylodes rhizome leaching liquor;
c) mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, concentrating, adding glucose to dissolve, diluting to constant volume to obtain yeast culture solution, sterilizing, cooling, inoculating yeast, fermenting and amplifying to obtain yeast fermentation liquid;
d) and (3) carrying out centrifugal concentration on the yeast fermentation liquor to obtain yeast (wet weight), wherein the weight ratio of the yeast to the liquid is 1: 1 in the presence of a yeast suspension.
The yeast culture solution comprises the following raw materials in parts by weight: 0.5 part of sealwort decoction pieces; 0.5 part of bighead atractylodes rhizome decoction pieces; 1 part of glucose; and 95 parts of water.
In the step 1) of the preparation method of the immune activation spraying agent, the leaching conditions are as follows: the material-water ratio of the rhizoma polygonati decoction pieces to water is 1: 10, soaking for 4 hours, leaching for 2 times with hot water at 98 ℃ for 1 hour each time, and filtering with 200 meshes to obtain rhizoma polygonati leaching liquor.
In step 2) of the preparation method of the immune activation spraying agent, the leaching conditions are as follows: the material-water ratio of the atractylodes macrocephala decoction pieces to water is 1: 10, soaking for 4 hours, leaching for 2 times with hot water at 98 ℃ for 1 hour each time, and filtering with 200 meshes to obtain a white atractylodes rhizome leaching liquor.
In step 3) of the preparation method of the immune activation spraying agent, the method comprises the following steps: mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, centrifuging at 16000rpm, centrifuging to obtain liquid, and concentrating under reduced pressure.
Example 2
An immunity activating spray comprises rhizoma Polygonati, oleum herba Pogostemonis, Atractylodis rhizoma, Borneolum Syntheticum, yeast and related emulsifier, cosolvent, and antiseptic.
The dosage of each raw material is as follows according to the parts by weight: 35 parts of rhizoma polygonati; 0.1 part of patchouli oil; 25 parts of bighead atractylodes rhizome; 0.06 part of borneol; 7 parts of yeast; proper amount of related emulsifier, cosolvent, preservative, etc.
The preparation method of the immune activation spraying agent comprises the following steps:
1) cleaning rhizoma Polygonati decoction pieces, adding water, extracting, and filtering to obtain rhizoma Polygonati extract;
2) cleaning Atractylodis rhizoma decoction pieces, adding water, extracting, and filtering to obtain Atractylodis rhizoma extract;
3) mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, centrifuging, and concentrating to obtain rhizoma Polygonati and Atractylodis rhizoma concentrated solution;
4) adding cosolvent into Borneolum Syntheticum to obtain Borneolum Syntheticum solution;
5) adding emulsifier into oleum herba Pogostemonis to obtain oleum Pogostemonis emulsion;
6) preparing yeast suspension for later use;
7) dissolving the preservative to obtain a preservative solution for later use;
8) mixing rhizoma Polygonati and Atractylodis rhizoma concentrated solution, Borneolum Syntheticum solution, herba Agastaches oil emulsion, yeast suspension, and antiseptic solution, metering volume, sterilizing, and packaging to obtain the spray.
Further, the yeast is saccharomyces cerevisiae.
Further, the preparation process of the yeast suspension comprises the following steps:
a) cleaning rhizoma Polygonati decoction pieces, adding water, extracting, and filtering to obtain rhizoma Polygonati extract; the leaching conditions were: the material-water ratio of the rhizoma polygonati decoction pieces to water is 1: 120, soaking for 6 hours, leaching for 2 times with hot water at 100 ℃ for 2 hours each time, and filtering with 200 meshes to obtain rhizoma polygonati leaching liquor.
b) Cleaning Atractylodis rhizoma decoction pieces, adding water, extracting, and filtering to obtain Atractylodis rhizoma extract; the leaching conditions were: the material-water ratio of the atractylodes macrocephala decoction pieces to water is 1: 120, soaking for 6 hours, leaching for 2 times with hot water at 100 ℃ for 2 hours each time, and filtering with 200 meshes to obtain a white atractylodes rhizome leaching liquor;
c) mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, concentrating, adding glucose to dissolve, diluting to constant volume to obtain yeast culture solution, sterilizing, cooling, inoculating yeast, fermenting and amplifying to obtain yeast fermentation liquid;
d) and (3) carrying out centrifugal concentration on the yeast fermentation liquor to obtain yeast (wet weight), wherein the weight ratio of the yeast to the liquid is 1: 1 in the presence of a yeast suspension.
The yeast culture solution comprises the following raw materials in parts by weight: 2 parts of rhizoma polygonati decoction pieces; 1 part of bighead atractylodes rhizome decoction pieces; 5 parts of glucose; and 99 parts of water.
In the step 1) of the preparation method of the immune activation spraying agent, the leaching conditions are as follows: the material-water ratio of the rhizoma polygonati decoction pieces to water is 1: 20, soaking for 6 hours, leaching for 2 times with hot water at 100 ℃ for 2 hours each time, and filtering with 200 meshes to obtain rhizoma polygonati leaching liquor.
In step 2) of the preparation method of the immune activation spraying agent, the leaching conditions are as follows: the material-water ratio of the atractylodes macrocephala decoction pieces to water is 1: 15, soaking for 6 hours, leaching for 2 times with hot water at 100 ℃ for 2 hours each time, and filtering with 200 meshes to obtain the rhizoma atractylodis macrocephalae leaching liquor.
In step 3) of the preparation method of the immune activation spraying agent, the method comprises the following steps: mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, centrifuging at 12000rpm, centrifuging to obtain liquid, and concentrating under reduced pressure.
Example 3
An immunity activating spray comprises rhizoma Polygonati, oleum herba Pogostemonis, Atractylodis rhizoma, Borneolum Syntheticum, yeast and related emulsifier, cosolvent, and antiseptic.
The dosage of each raw material is as follows according to the parts by weight: 30 parts of rhizoma polygonati; 0.08 part of patchouli oil; 20 parts of bighead atractylodes rhizome; 0.03 part of borneol; 5 parts of yeast; proper amount of related emulsifier, cosolvent, preservative, etc.
The preparation method of the immune activation spraying agent comprises the following steps:
1) cleaning rhizoma Polygonati decoction pieces, adding water, extracting, and filtering to obtain rhizoma Polygonati extract;
2) cleaning Atractylodis rhizoma decoction pieces, adding water, extracting, and filtering to obtain Atractylodis rhizoma extract;
3) mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, centrifuging, and concentrating to obtain rhizoma Polygonati and Atractylodis rhizoma concentrated solution;
4) adding cosolvent into Borneolum Syntheticum to obtain Borneolum Syntheticum solution;
5) adding emulsifier into oleum herba Pogostemonis to obtain oleum Pogostemonis emulsion;
6) preparing yeast suspension for later use;
7) dissolving the preservative to obtain a preservative solution for later use;
8) mixing rhizoma Polygonati and Atractylodis rhizoma concentrated solution, Borneolum Syntheticum solution, herba Agastaches oil emulsion, yeast suspension, and antiseptic solution, metering volume, sterilizing, and packaging to obtain the spray.
Further, the yeast is saccharomyces cerevisiae.
Further, the preparation process of the yeast suspension comprises the following steps:
a) cleaning rhizoma Polygonati decoction pieces, adding water, extracting, and filtering to obtain rhizoma Polygonati extract; the leaching conditions were: the material-water ratio of the rhizoma polygonati decoction pieces to water is 1: 150, soaking for 5 hours, leaching for 2 times with hot water at 100 ℃ for 1.5 hours each time, and filtering with 200 meshes to obtain rhizoma polygonati leaching liquor.
b) Cleaning Atractylodis rhizoma decoction pieces, adding water, extracting, and filtering to obtain Atractylodis rhizoma extract; the leaching conditions were: the material-water ratio of the atractylodes macrocephala decoction pieces to water is 1: 110, soaking for 5 hours, leaching for 2 times with hot water at 100 ℃ for 1.5 hours each time, and filtering with 200 meshes to obtain a white atractylodes rhizome leaching liquor;
c) mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, concentrating, adding glucose to dissolve, diluting to constant volume to obtain yeast culture solution, sterilizing, cooling, inoculating yeast, fermenting and amplifying to obtain yeast fermentation liquid;
d) and (3) carrying out centrifugal concentration on the yeast fermentation liquor to obtain yeast (wet weight), wherein the weight ratio of the yeast to the liquid is 1: 1 in the presence of a yeast suspension.
The yeast culture solution comprises the following raw materials in parts by weight: 1 part of rhizoma polygonati decoction pieces; 0.8 part of bighead atractylodes rhizome decoction pieces; 3 parts of glucose; and 96 parts of water.
In the step 1) of the preparation method of the immune activation spraying agent, the leaching conditions are as follows: the material-water ratio of the rhizoma polygonati decoction pieces to water is 1: 15, soaking for 5 hours, leaching for 2 times with hot water at 100 ℃ for 1.5 hours each time, and filtering with 200 meshes to obtain rhizoma polygonati leaching liquor.
In step 2) of the preparation method of the immune activation spraying agent, the leaching conditions are as follows: the material-water ratio of the atractylodes macrocephala decoction pieces to water is 1: 12, soaking for 5 hours, leaching for 2 times with hot water at 100 ℃ for 1.5 hours each time, and filtering with 200 meshes to obtain the rhizoma atractylodis macrocephalae leaching liquor.
In step 3) of the preparation method of the immune activation spraying agent, the method comprises the following steps: mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, centrifuging at 12000rpm, centrifuging to obtain liquid, and concentrating under reduced pressure.
The rhizoma polygonati leaching liquor, the rhizoma atractylodis macrocephalae leaching liquor and the yeast suspension prepared in the embodiment all contain the active ingredient polysaccharide.
The embodiments described above are merely preferred embodiments of the invention, rather than all possible embodiments of the invention. Any obvious modifications to the above would be obvious to those of ordinary skill in the art, but would not bring the invention so modified beyond the spirit and scope of the present invention.

Claims (8)

1. An immune activation spray is characterized by comprising rhizoma polygonati, patchouli oil, bighead atractylodes rhizome, borneol, yeast and related emulsifying agents, cosolvents and preservatives.
2. The immune activation spray as claimed in claim 1, wherein the dosage of each raw material is as follows by weight: 25-35 parts of rhizoma polygonati; 0.05 to 0.1 portion of patchouli oil; 15-25 parts of bighead atractylodes rhizome; 0.01-0.06 part of borneol; 3-7 parts of yeast.
3. The method for preparing an immune-activating spray according to claim 1 or 2, which comprises the steps of:
1) cleaning rhizoma Polygonati decoction pieces, adding water, extracting, and filtering to obtain rhizoma Polygonati extract;
2) cleaning Atractylodis rhizoma decoction pieces, adding water, extracting, and filtering to obtain Atractylodis rhizoma extract;
3) mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, centrifuging, and concentrating to obtain rhizoma Polygonati and Atractylodis rhizoma concentrated solution;
4) adding cosolvent into Borneolum Syntheticum to obtain Borneolum Syntheticum solution;
5) adding emulsifier into oleum herba Pogostemonis to obtain oleum Pogostemonis emulsion;
6) preparing yeast suspension for later use;
7) dissolving the preservative to obtain a preservative solution for later use;
8) mixing rhizoma Polygonati and Atractylodis rhizoma concentrated solution, Borneolum Syntheticum solution, herba Agastaches oil emulsion, yeast suspension, and antiseptic solution, metering volume, sterilizing, and packaging to obtain the spray.
4. The method of preparing an immune-activating spray according to claim 3, wherein the yeast is Saccharomyces cerevisiae.
5. The method of preparing an immune-activating spray according to claim 3, wherein the yeast suspension is prepared by the steps of:
a) cleaning rhizoma Polygonati decoction pieces, adding water, extracting, and filtering to obtain rhizoma Polygonati extract; the leaching conditions were: the material-water ratio of the rhizoma polygonati decoction pieces to water is 1: 100-120, soaking for 4-6 hours, leaching for 2 times with hot water at 98-100 ℃ for 1-2 hours each time, and filtering with 200 meshes to obtain rhizoma polygonati leaching liquor;
b) cleaning Atractylodis rhizoma decoction pieces, adding water, extracting, and filtering to obtain Atractylodis rhizoma extract; the leaching conditions were: the material-water ratio of the atractylodes macrocephala decoction pieces to water is 1: 100-120, soaking for 4-6 hours, leaching for 2 times with hot water at 98-100 ℃ for 1-2 hours each time, and filtering with 200 meshes to obtain a bighead atractylodes rhizome leaching solution;
c) mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, concentrating, adding glucose to dissolve, diluting to desired volume, sterilizing, cooling, inoculating yeast, fermenting and amplifying to obtain yeast fermentation liquid;
d) and (3) carrying out centrifugal concentration on the yeast fermentation liquor to obtain yeast and liquid with the weight ratio of 1: 1 in the presence of a yeast suspension.
6. The method for preparing an immune-activating spray according to claim 3, wherein the leaching conditions in step 1) are as follows: the material-water ratio of the rhizoma polygonati decoction pieces to water is 1: 10-20, soaking for 4-6 hours, leaching for 2 times with hot water at 98-100 ℃ for 1-2 hours each time, and filtering with 200 meshes to obtain sealwort leaching liquor.
7. The method for preparing an immune-activating spray according to claim 3, wherein the leaching conditions in step 2) are as follows:
the material-water ratio of the atractylodes macrocephala decoction pieces to water is 1: 10-15, soaking for 4-6 hours, leaching for 2 times with hot water at 98-100 ℃ for 1-2 hours each time, and filtering with 200 meshes to obtain a white atractylodes rhizome leaching liquor.
8. The method for preparing an immune-activating spray according to claim 3, wherein the step 3) comprises the steps of:
mixing rhizoma Polygonati leaching solution and Atractylodis rhizoma leaching solution, and centrifuging at 12000 and 16000 rpm.
CN202010242232.3A 2020-03-31 2020-03-31 Immune activation spray and preparation method thereof Pending CN111358891A (en)

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Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110123946A (en) * 2019-05-21 2019-08-16 四川农业大学 A kind of process using saccharomyces cerevisiae solid state fermentation rhizoma polygonati

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110123946A (en) * 2019-05-21 2019-08-16 四川农业大学 A kind of process using saccharomyces cerevisiae solid state fermentation rhizoma polygonati

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Application publication date: 20200703