CN1270817C - Pollen sac deaeration embedding method - Google Patents
Pollen sac deaeration embedding method Download PDFInfo
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- CN1270817C CN1270817C CNB021111103A CN02111110A CN1270817C CN 1270817 C CN1270817 C CN 1270817C CN B021111103 A CNB021111103 A CN B021111103A CN 02111110 A CN02111110 A CN 02111110A CN 1270817 C CN1270817 C CN 1270817C
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- pollen
- sac
- deaeration
- embedding method
- bag
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- Y02A40/948—
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- Cosmetics (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Jellies, Jams, And Syrups (AREA)
Abstract
The present invention relates to a pollen sac deaeration embedding method which uses a pollen sac as a wall material. Firstly, a pollen slag is pretreated, and then a sac core material to be embedded is filled in the pollen sac by passing through the germ pore of the pollen under the action of negative pressure; subsequently, the germ pore is sealed by a sealing agent to form a microcapsule of 10 to 200 mu m, wherein the sealing agent is a natural polymer material, such as chitosan, or a resinous material. According to the character of the sac core material, the pollen sac deaeration embedding method can be concretely divided into three methods for preparing microcapsules. The present invention has the advantages that a wall material combined by pollen slags, chitosan or resin is embedded with fat-soluble nutritive substances and water-soluble nutritive substances to be made into a microcapsule, and the microcapsule masks the unpleasant smell of the embedded substances and can prevent the oxygenizing deterioration of the embedded substances, so that the physical property of the embedded substances is stabilized, the embedded substances have higher biological activity and longer shelf life, and the shelf life of a commodity is prolonged.
Description
Technical field
The present invention relates to a kind of preparation method of microcapsules, mainly is a kind of pollen sac deaeration embedding method.
Background technology
Microcapsules technology is a kind of technology that solid or liquid coating is made the formation fine particle with filmogen.The fine particle that obtains is microcapsules, and general appearance is spherical, and size is at the 5-500 mu m range.Generally, capsule is exactly " pocket ", and microcapsules are exactly " small pocket ".The material that wraps in microcapsules inside is called the capsule heart.The capsule heart can be a solid, also can be liquid or gas.The coating film that the microcapsules outside is formed by filmogen is called the wall material.The wall material is normally formed by macromolecular material natural or that synthesize, also may be inorganic compound.When the advantage of microcapsules technology was to form microcapsules, the capsule heart was isolated with external environment by coating, and its character can be retained with having no effect, and under proper condition, the capsule heart can be discharged again when the capsule material is destroyed.This brings many facilities to use.Behind liquid formation microcapsules, become pressed powder, this all brings great convenience for its use, transportation, storage.
The material that can use of preparation microcapsules is a lot, as natural macromolecular material or organic synthesis material.The maximum characteristics of these materials are to have certain film forming, and more stable at normal temperatures.Commonly used have a starch based: maltodextrin, cyclodextrine, converted starch etc.; Water-soluble glue class: gelatin, Arabic gum, agar, algin etc.; Synthesized polymer material: polyamide, polyisoprene, polyethylene, epoxy resin etc.
The determining and should consider of microcapsule preparation method in actual production according to combined factors such as physicochemical property, product quality requirement and the equipment of encapsulated heart material, costs, the purpose that reaches not only economy but also meet the demands.The cyst material of selecting for use must meet the national health requirement, does not react with the core material that is wrapped.The method that the feed addictive microencapsulation adopts is mainly spray drying process, complex coacervation, beta-schardinger dextrin-investment.
Summary of the invention
Technical problem to be solved by this invention provides a kind of biologically active that stability is high, maintenance is higher that can make core material, and the lower pollen sac deaeration embedding method of financial cost.
The technical solution adopted for the present invention to solve the technical problems.This pollen sac deaeration embedding method adopts pollen bag as the wall material, and after described pollen bag was meant and produces pollen extract, discarded pollen slag was mainly the pollen shell of hollow, i.e. the pollen bag that germinal aperature is open and content has disengaged.The pollen slag is carried out preliminary treatment, with the pollen slag behind the extraction pollen extract, wash with water again and remove residual sugar, anhydrate so that 3000rpm is centrifugal with centrifuge, dry or put baking oven low temperature with daylight, temperature is controlled at below 70 ℃, can keep active material such as flavonoids useful in the pollen slag to biology, oven dry will prevent to go mouldy and damage by worms after doing, and can carry out the 5-8kGy radiation treatment.Core material with want embedding is entered in the pollen bag by the germinal aperature of pollen under suction function then, and core material is the solution or the composite bacteria liquid of oily liquids or soluble solids; After then adopting sealing compound that germinal aperature is sealed, finally make microcapsules.
The technical solution adopted for the present invention to solve the technical problems can also be further perfect.Described sealing compound is natural macromolecular material such as shitosan, its deacetylation>90%, and ash content<8%, mercury<0.3mg/kg is dissolved in shitosan in 2% the acetum, is made into the chitosan-acetic acid solution of 1-1.5%.The deacetylation of shitosan is big more, is soluble in diluted acid more, and the consumption of shitosan liquid is the 10-15% of the capsule heart and wall material total amount, and the embedding effect is better.Described sealing compound also can adopt resinous material, and as polymethacrylates, in 95% ethanol, state reaches capacity with resin dissolves.The use amount of resin ethanolic solution is the 10-15% of the capsule heart and wall material total amount during embedding.
1), core material is oily liquids (fish oil), adds vitamin E or other antioxidants of fish oil amount 1-3% in refining fish oil, fully mixing proterties according to core material can be specially following three kinds of microcapsule preparation methods:; The fish oil capsule heart is added in the pollen slag that the degassing is handled, fish oil is entered in the pollen bag through pollen germination pore under suction function, after the inflation, again with the fish oil outside the beta-schardinger dextrin-absorption pollen bag of 5-10%, close the germinal aperature of pollen bag at last with the shitosan fluid-tight, after the low temperature drying, promptly make the fish oil powdery product of microencapsulation.2), core material is soluble solids solution (complex enzyme for feed), and complex enzyme is dissolved in water, reaches saturation state; The complex enzyme saturated solution is added in the pollen slag that the degassing is handled, the enzyme saturated solution is entered in the pollen bag through pollen germination pore under suction function, after the inflation, dry under low temperature (under 40 ℃) or freezing conditions; Close the germinal aperature of pollen bag again with the alcohol resin fluid-tight, after the low temperature drying, promptly make the complex enzyme powdery product of microencapsulation.3), core material is compound lactobacillus bacterium liquid, will make 10 by cultivation and fermentation
9-10
10The bacterium liquid of individual/ml adds in the pollen slag that the degassing is handled, and bacterium liquid is entered in the pollen bag through pollen germination pore under suction function, after the inflation, and freeze drying; Promptly make the compound lactobacillus powdery product of microencapsulation.
The effect that the present invention is useful is: carry out the fat-soluble and water-soluble nutrient substance of embedding by the wall material of pollen slag, shitosan or resin combination and make micro-capsule, this kind micro-capsule has been covered by the unhappy smell of embedding substance, can prevent by the oxidation deterioration of embedding substance, make by the embedding substance stable in properties and have higher biologically active, have the long shelf-life, prolonged the shelf life of commodity.
The specific embodiment
Below in conjunction with embodiment the present invention is further described.This pollen sac deaeration embedding method, adopt pollen bag as the wall material, at first the pollen slag is carried out preliminary treatment, core material with want embedding is entered in the pollen bag by the germinal aperature of pollen under suction function then, after then adopting sealing compound that germinal aperature is sealed, promptly become the microcapsules of 10~200 μ m.After described pollen bag was meant and produces pollen extract, discarded pollen slag was mainly the pollen shell of hollow, and promptly germinal aperature is open, the pollen bag that content has disengaged.Described sealing compound is natural macromolecular material such as shitosan, its deacetylation>90%, and ash content<8%, mercury<0.3mg/kg is dissolved in shitosan in 2% the acetum, is made into the chitosan-acetic acid solution of 1-1.5%.The deacetylation of shitosan is big more, is soluble in diluted acid more, and the consumption of shitosan liquid is the 10-15% of the capsule heart and wall material total amount, and the embedding effect is better.Described sealing compound also can adopt resinous material, and as polymethacrylates, in 95% ethanol, state reaches capacity with resin dissolves.The use amount of resin ethanolic solution is the 10-15% of the capsule heart and wall material total amount during embedding; In the process of preparation micro-capsule, being controlled at vacuum in the degassing condition is 0.05-0.08Mpa; The proportioning of the capsule heart and wall material is capsule heart 20-30%, wall material 70-80%; The beta-schardinger dextrin-consumption is the 5-10% of the capsule heart and wall material total amount.Described pollen slag carries out preliminary treatment, be with the pollen slag behind the extraction pollen extract, wash with water again and remove residual sugar, anhydrate so that 3000rpm is centrifugal with centrifuge, dry or put baking oven low temperature with daylight, temperature is controlled at below 70 ℃, can keep active material such as flavonoids useful to biology in the pollen slag, oven dry.To prevent to go mouldy and damage by worms after doing, can carry out the 5-8kGy radiation treatment.
Embodiment 1: core material is oily liquids (fish oil), adds vitamin E or other antioxidants of fish oil amount 1-3% in refining fish oil, fully mixing; The fish oil capsule heart is added in the pollen slag that the degassing is handled, fish oil is entered in the pollen bag through pollen germination pore under suction function, after the inflation, again with the fish oil outside the beta-schardinger dextrin-absorption pollen bag of 5-10%, close the germinal aperature of pollen bag at last with the shitosan fluid-tight, after the low temperature drying, promptly make the fish oil powdery product of microencapsulation.
Embodiment 2: core material is soluble solids solution (complex enzyme for feed), and complex enzyme is dissolved in water, reaches saturation state; The complex enzyme saturated solution is added in the pollen slag that the degassing is handled, the enzyme saturated solution is entered in the pollen bag through pollen germination pore under suction function, dry under low temperature (under 40 ℃) or freezing conditions; Close the germinal aperature of pollen bag again with the alcohol resin fluid-tight, after the low temperature drying, promptly make the complex enzyme powdery product of microencapsulation.
Embodiment 3: core material is a compound lactobacillus liquid, and it is made 10 by cultivation and fermentation
9-10
10The bacterium liquid of individual/ml adds in the pollen slag that the degassing is handled, and makes bacterium liquid enter in the pollen bag freeze drying through pollen germination pore under suction function; Promptly make the compound lactobacillus powdery product of microencapsulation.
Claims (7)
1, a kind of pollen sac deaeration embedding method is characterized in that:
1), adopt pollen bag as the wall material, after described pollen bag was meant and produces pollen extract, discarded pollen slag was mainly the pollen shell of hollow, i.e. the pollen bag that germinal aperature is open and content has disengaged;
2), the pollen slag is carried out preliminary treatment, extract the pollen slag behind the pollen extract, wash with water and remove residual sugar, carry out centrifugal anhydrating with centrifuge, temperature is controlled at below 70 ℃, dries or put the baking oven low temperature drying with daylight;
3), the core material of want embedding is entered in the pollen bag by the germinal aperature of pollen under suction function, core material is the solution or the composite bacteria liquid of oily liquids or soluble solids; After then adopting sealing compound that germinal aperature is sealed, finally make microcapsules.
2, pollen sac deaeration embedding method according to claim 1 is characterized in that: described sealing compound is natural macromolecular material or resinous material.
3, pollen sac deaeration embedding method according to claim 2, it is characterized in that: described sealing compound is a shitosan, its deacetylation>90%, ash content<8%, mercury<0.3mg/kg, shitosan is dissolved in 2% the acetum, is made into the chitosan-acetic acid solution of 1-1.5%, the consumption of shitosan liquid is the 10-15% of the capsule heart and wall material total amount.
4, pollen sac deaeration embedding method according to claim 2 is characterized in that: described resin adopts polymethacrylates, and in 95% ethanol, state reaches capacity with resin dissolves; The use amount of resin ethanolic solution is the 10-15% of the capsule heart and wall material total amount during embedding.
5, pollen sac deaeration embedding method according to claim 1 is characterized in that: core material is a fish oil, adds vitamin E or other antioxidants of fish oil amount 1-3% in refining fish oil, fully mixing; The fish oil capsule heart is added in the pollen slag that the degassing is handled, fish oil is entered in the pollen bag through pollen germination pore under suction function, after the inflation, again with the fish oil outside the beta-schardinger dextrin-absorption pollen bag of Sq, close the germinal aperature of pollen bag at last with the shitosan fluid-tight, after the low temperature drying, make the fish oil powdery product of microencapsulation.
6, pollen sac deaeration embedding method according to claim 1 is characterized in that: core material is a complex enzyme for feed solution, and complex enzyme is dissolved in water, reaches saturation state; The complex enzyme saturated solution is added in the pollen slag that the degassing is handled, the enzyme saturated solution is entered in the pollen bag through pollen germination pore under suction function, after the inflation, dry under low temperature or freezing conditions; Close the germinal aperature of pollen bag again with the alcohol resin fluid-tight, after the low temperature drying, make the complex enzyme powdery product of microencapsulation.
7, pollen sac deaeration embedding method according to claim 1 is characterized in that: core material is a compound lactobacillus bacterium liquid, will make 10 by cultivation and fermentation
9-10
10The bacterium liquid of individual/ml adds in the pollen slag that the degassing is handled, and bacterium liquid is entered in the pollen bag through pollen germination pore under suction function, and after the inflation, the compound lactobacillus powdery product of microencapsulation are made in freeze drying.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CNB021111103A CN1270817C (en) | 2002-03-21 | 2002-03-21 | Pollen sac deaeration embedding method |
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CNB021111103A CN1270817C (en) | 2002-03-21 | 2002-03-21 | Pollen sac deaeration embedding method |
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CN1380134A CN1380134A (en) | 2002-11-20 |
CN1270817C true CN1270817C (en) | 2006-08-23 |
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CNB021111103A Expired - Fee Related CN1270817C (en) | 2002-03-21 | 2002-03-21 | Pollen sac deaeration embedding method |
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Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2009147973A1 (en) * | 2008-06-02 | 2009-12-10 | 国立大学法人新潟大学 | Microcapsules, method of producing the microcapsules and food and drink containing the microcapsules |
CN101518552B (en) * | 2009-04-10 | 2012-01-04 | 南京师范大学 | Pine pollen and cyclodextrin composition, method for preparing same, use of same in preparation of health-care products for resisting fatigue and improving immunity of organisms |
US9993019B2 (en) * | 2010-03-26 | 2018-06-12 | Philip Morris Usa Inc. | Method for making particle of a hydrophobic additive and a polysaccharide coating and tobacco products containing particle of a hydrophobic additive and a polysaccharide coating |
CN102240531B (en) * | 2011-03-21 | 2013-07-10 | 徐涵 | Plant cell microspheres and use thereof |
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