CN102771751A - Edible compound stevioside for diabetes patients - Google Patents
Edible compound stevioside for diabetes patients Download PDFInfo
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- CN102771751A CN102771751A CN2012102420747A CN201210242074A CN102771751A CN 102771751 A CN102771751 A CN 102771751A CN 2012102420747 A CN2012102420747 A CN 2012102420747A CN 201210242074 A CN201210242074 A CN 201210242074A CN 102771751 A CN102771751 A CN 102771751A
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Abstract
The invention aims to provide an edible compound sweetener for patients suffering from diabetes and obesity, which has the characteristics of low calorie and good taste, and is a product which is specially prepared for customers suffering from diabetes and obesity. The compound comprises multielement alditol, strong sweetener and functional oligosaccharide. The compound is preferentially prepared from the following raw materials according to parts by weight: 1-60 parts of the multielement alditol, 1-50 parts of the strong sweetener and 1-30 parts of the functional oligosaccharide.
Description
Technical field
The present invention relates to a kind of composite sweetener that is applicable to that diabetes, the obesity patients are taken, particularly relate to the composite composite sweetener of stevioside and sugar alcohol and compound sugar.
Background technology
Diabetes are a kind of chronic diseases, and in the past nearly 15 years, the diabetes number is increased to 3.47 hundred million, and diabetes have become global problem at present, and diabetes have become the 5th cause of death in the world.
Diabetes have main type such as IDDM, type II diabetes and pregnancy pattern diabetes; Cause the reason of diabetes to mainly contain: heredity causes with factor such as acquired environment, and acquired disposition is mainly relevant with bad life, diet such as high sugar, higher fatty acid custom, follows the age that bigger association is also arranged simultaneously; When pancreas has produced not enough insulin or human body and can't effectively utilize the insulin that is produced; Diabetes will occur, hyperglycaemia or blood sugar raise, and is of long duration; Can bring severe impairment to many systems of human body, particularly nerve and vascular system.
Usually the diabetes patient has a sweet tooth, and to this crowd, should eat sugar-free or low sugar diet; Publication number is that the patent application document of CN102273581 discloses a kind of high sugariness compound sweetener; Mix composite forming by stevioside, water-soluble dietary fiber, fructose, amino acid; Owing to added fructose in the prescription, improved the heat of this product, it can only be called the low sugar sweetener.
Publication number is that the patent application document of CN101313743 discloses a kind of compound sweetener; The composition of this compound sweetener contains Aspartame 2-5%, filler 95-98% by weight percentage; Chosen multiple filler such as fructose, lactose, glucose, maltodextrin in order to obtain different tastes, also added a small amount of anticaking agent and prevent that the product caking is convenient to storage; Owing to comprised Aspartame in the effective ingredient, therefore reduced the consumption of sweetener, effectively reduce calorie intake, blood sugar and carious tooth index; Sweetener of the present invention adopts special formula, and inlet can be felt sweet taste rapidly, and kind of a soft and smooth sensation is arranged; Be full of the oral cavity, add in the drink and drink, do not have bad aftertaste; It is long that sweet taste is trapped in time in oral cavity; Better mouthfeel is arranged compared with similar products, but it still containing the sweetener of high heat, is not the sweetener of empty calory truly.
Publication number be the patent application document of CN1042290 disclose sweetener paper sugar particularly stevia rebaudiana extract be novel product with candy purposes; The shortcoming of various illnesss such as the obesity due to no sugar is too much, dental caries moth; Stevia rebaudianum essence, glycerin monostearate, Tween 80, matrimony vine acid, glycine, pigment and spices etc. are melt into solution in water-bath; Put into filter paper bar dipping, take out the back solid dispersion and just condense on the paper, certain with the saliva contact area in mouth; Sweet taste is more stable, at present stevioside of no use and sugar alcohol, the composite public reported of FOS in the prior art.
Summary of the invention
The objective of the invention is to have characteristics low in calories, that mouthfeel is good to diabetes, the edible composite sweetener of the obesity patients, is a product that designs for such crowd specially.
A kind of composition of the present invention comprises multi-sugar alcohol, intense sweetener, functional oligose
Composition of the present invention preferably includes the raw material of following weight parts:
1-60 parts of multi-sugar alcohols, 50 parts of intense sweetener 1-, functional oligose 1-30 part.
20-55 parts of preferred multi-sugar alcohols, intense sweetener 5-25 part, functional oligose 2-15 part.
More preferably 50 parts of multi-sugar alcohols, 20 parts of intense sweeteners, 5 parts of functional oligoses.
Multi-sugar alcohol of the present invention can be a kind of or combination in any in antierythrite, xylitol, sorbierite, sweet mellow wine, maltitol, hydrogenated starch hydrolysate, lactitol, the hydroxyl isomaltulose, preferred antierythrite.
Intense sweetener can be stevioside, Sucralose, the knob a kind of or combination in any in sweet, preferred stevioside.
Functional oligose can be a kind of or combination in any in stachyose, raffinose, isomaltoketose, milk ketose, FOS, xylo-oligosaccharide, inulin, galactooligosaccharide, oligoisomaltose, oligomeric isomaltoketose, oligomeric dragon gallbladder sugar, soyabean oligosaccharides, the chitosan oligomer, preferred FOS.
Preferred stevioside of the present invention and antierythrite and functional oligose are composite.
Antierythrite molecular formula among the present invention: C4H10O4, molecular structural formula is: H2OH-CHOH-CHOH-CH2OH has refrigerant sense; Caloric value is low, is about 1/10th of sucrose caloric value, is not degraded by the human body endoenzyme; Be prone to by little intestinal absorption, can only from blood, drain in the urine through kidney and discharge, not involved in sugar metabolism and change of blood sugar; So be suitable for patients with diabetes mellitus, unlikely fermentation in colon can be avoided digestive discomfort.
Stevioside among the present invention is the smart new type natural sweetener of carrying from catananche's STEVIA REBAUDIANA.It has the characteristics of high sugariness, low heat energy, and its sugariness is 200-300 a times of sucrose, and calorific value is merely 1/300 of sucrose; Through high amount of drug experiment proof; Stevioside has no side effect, and edible safety has certain blood sugar reducing function; Often edible can diabetes-alleviating, illness such as obesity, be the very desirable sweetener of a kind of alternative sucrose; Stevioside glucoside chemical name: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl) oxygen base] kaurene-16-alkene-18-carboxylic acid, β-D-glucopyranosyl ester.
Stevioside glucoside component title
Relative molecular weight: 967.03.
Function compound sugar among the present invention, or claim oligosaccharides is to be connected to form the low polymerization sugar of straight or branched by 2 ~ 10 monose through glycosidic bond, divides functional oligose and ordinary oligosaccharide two big classes; Functional oligose research is now thought and is comprised stachyose, raffinose, isomaltoketose, milk ketose, FOS, xylo-oligosaccharide, galactooligosaccharide, oligoisomaltose, oligomeric isomaltoketose, oligomeric dragon gallbladder sugar, soyabean oligosaccharides, chitosan oligomer etc.
FOS, and molecular formula G-F-Fn (n=1,2,3, wherein G is a fructose for glucose F) be by the ketose of 1-3 fructosyl through the fructosyl be combined in β-1,2 glycosidic bond and the sucrose, the general name of one group of compound sugar such as Nystose and GF4; (low poly lactose, xylo-oligosaccharide, inulin etc.) are to utilize biology enzyme, raw material are hydrolyzed a kind of functional sugar source of purifying then; Because do not have the enzyme of decomposition function compound sugar in the human body, it can not absorbed by human consumption, but directly gets in the large intestine; Preferentially utilized, make Bifidobacterium in enteron aisle, keep certain quantity, thereby suppress the growth of spoilage organisms in the enteron aisle by Bifidobacterium; Reduce the formation of poisonous tunning; And a large amount of human trials is verified, takes in after the compound sugar, can reduce the level of cholesterol in serum.
Inulin is the mixture of one type of natural levulan, levulan be fructose units pass through (2-1) chain connect form and with
GlucoseThe carbohydrate that the unit stops. the average degree of polymerization of levulan is 10-30 in the commercialization inulin usually; Wherein contain a spot of FOS; Can find the existence of inulin in nearly all plant; It is the form of the another kind of energy storage of plant except that starch, is that very good functional food ingredient, the while also is the good raw material of producing products such as FOS, high fructose syrup, crystal diabetin.
The present composition can add auxiliary material and process any one formulation in oral liquid, granule, capsule, tablet, powder, dispersing tablet, the syrup.
The preparation technology that the present composition is prepared into the composite sweetener tablet comprises the following steps:
1, takes by weighing raw material, through the pulverizing of 80-100 order, the granulation of 20-60 order, 65-80 ℃ drying;
2, mixing, 20-60Mpa compressing tablet make.
Composition of the present invention can be made into the sheet or the pulvis sweetener of heart, ellipse, rhombus, is convenient to use in the family.Preparation of compositions of the present invention becomes the product of every weight 0.08-0.1 gram, is equivalent to the white granulated sugar sugariness of 4-5 gram; 100
The water of milliliter adds 2 sweet senses that just are equivalent to 8-10% white granulated sugar solution.
The invention still further relates to the application of composition in preparation composite sweetener product of forming by multi-sugar alcohol, intense sweetener, functional oligose.
The invention still further relates to the application of composition in the composite sweetener of preparation diabetes patient of forming by multi-sugar alcohol, intense sweetener, functional oligose.
The invention still further relates to the application of composition in the edible composite sweetener of preparation the obesity patients of forming by multi-sugar alcohol, intense sweetener, functional oligose.
The invention still further relates to the application of composition in preparation composite sweetener product of forming by antierythrite, stevioside, FOS.
The invention still further relates to the application of composition in the composite sweetener of preparation diabetes patient of forming by antierythrite, stevioside, FOS.
The invention still further relates to the application of composition in the edible composite sweetener of preparation the obesity patients of forming by antierythrite, stevia rebaudianum, FOS.
The sweetener of present composition preparation has slight sweet aftertaste, be applicable to boil mung bean, steamed sweet bun, drink coffee, make dessert, join sweet milk beverage, cook soya-bean milk, the bubble oatmeal, towards fruit juice etc.
The sweetener of present composition preparation has characteristics low in calories, that mouthfeel is good, is applicable to diabetes, the obesity patients, is a composite sweetener product that designs for such crowd specially.
The specific embodiment
Embodiment 1
Take by weighing antierythrite 43 Kg, stevioside 10 Kg, FOS 20 Kg, antierythrite, stevioside, FOS are added in the pulverizer pulverize, cross 80 mesh sieves; 20 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined the V-type blender with the auxiliary material dolomol, mixed 65 ℃ of dryings 30 minutes; Carry out compression molding with 35 stamping machine 20Mpa, regulate pressure and particle weight at 0.1 gram.
Embodiment 2
Take by weighing antierythrite 50Kg, stevioside 7 Kg, inulin 16Kg, antierythrite, stevioside, inulin are added in the pulverizer pulverize, cross 100 mesh sieves; 60 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined the V-type blender with the auxiliary material dolomol, mixed 45 minutes, 80 ℃ of dryings are directly installed with powder packets and are packaged into the finished product of 150 grams.
Embodiment 3
Multi-sugar alcohol 1Kg, intense sweetener 1 Kg, functional oligose 1Kg with pulverizing in multi-sugar alcohol, intense sweetener, the functional oligose adding pulverizer, cross 80 mesh sieves; 20 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined the V-type blender with the auxiliary material dolomol, mixed 65 ℃ of dryings 30 minutes; Carry out compression molding with 35 stamping machine 60Mpa, regulate pressure and particle weight at 0.08 gram.
Embodiment 4
Multi-sugar alcohol 60Kg, intense sweetener 50Kg, functional oligose 30Kg with pulverizing in multi-sugar alcohol, intense sweetener, the functional oligose adding pulverizer, cross 90 mesh sieves; 30 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined the V-type blender with tablet auxiliary material commonly used, mixed 80 ℃ of dryings 35 minutes; Tablet press machine 20Mpa compression molding is processed tablet.
Embodiment 5
Multi-sugar alcohol 20Kg, intense sweetener 5Kg, functional oligose 2 Kg with pulverizing in multi-sugar alcohol, intense sweetener, the functional oligose adding pulverizer, cross 100 mesh sieves; 40 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined blender with tablet auxiliary material commonly used, mixed 70 ℃ of dryings 40 minutes; Tablet press machine 50Mpa compression molding is processed tablet.
Embodiment 6
Multi-sugar alcohol 55Kg, intense sweetener 25 Kg, functional oligose 15 Kg with pulverizing in multi-sugar alcohol, intense sweetener, the functional oligose adding pulverizer, cross 90 mesh sieves; 30 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined blender with tablet auxiliary material commonly used, mixed 80 ℃ of dryings 30 minutes; Tablet press machine 30Mpa compression molding is processed tablet.
Embodiment 7
Multi-sugar alcohol 50Kg, intense sweetener 20 Kg, functional oligose 5Kg with pulverizing in multi-sugar alcohol, intense sweetener, the functional oligose adding pulverizer, cross 80 mesh sieves; 30 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined blender with tablet auxiliary material commonly used, mixed 80 ℃ of dryings 30 minutes; Tablet press machine 60Mpa compression molding is processed tablet.
Embodiment 8
Antierythrite 50 Kg, stevioside 20 Kg, FOS 5 Kg with pulverizing in antierythrite, stevioside, the FOS adding pulverizer, cross 80 mesh sieves; 50 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined the V-type blender with the auxiliary material dolomol, mixed 40 minutes, 70 ℃ of dryings are directly installed with powder packets and are packaged into the finished product of 500 grams.
Embodiment 9
Antierythrite 1 Kg, stevioside 1 Kg, FOS 1 Kg with pulverizing in antierythrite, stevioside, the FOS adding pulverizer, cross 100 mesh sieves; 20 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined the V-type blender with the auxiliary material dolomol, mixed 45 minutes, directly be packaged into finished product with the powder packets installation.
Embodiment 10
Antierythrite 60Kg, stevioside 50Kg, FOS 30Kg with pulverizing in antierythrite, stevioside, the FOS adding pulverizer, cross 100 mesh sieves; 60 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined blender with the auxiliary material dolomol, mixed 45 minutes, directly be packaged into finished product with the powder packets installation.
Embodiment 11
Antierythrite 20Kg, stevioside 5Kg, FOS 2Kg with pulverizing in antierythrite, stevioside, the FOS adding pulverizer, cross 100 mesh sieves; 60 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined blender with the conventional auxiliary material of tablet, mix, process tablet.
Embodiment 12
Antierythrite 55Kg, stevioside 25Kg, FOS 15Kg with pulverizing in antierythrite, stevioside, the FOS adding pulverizer, cross 80 mesh sieves; 50 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined blender with the conventional auxiliary material of tablet, mix, process tablet.
Embodiment 13
Maltitol 60Kg, Sucralose 50Kg, xylo-oligosaccharide 30Kg with pulverizing in maltitol, Sucralose, the xylo-oligosaccharide adding pulverizer, cross 80 mesh sieves; 50 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined blender with the conventional auxiliary material of tablet, mix, process tablet.
Embodiment 14
Maltitol 20Kg, Sucralose 5Kg, xylo-oligosaccharide 2Kg with pulverizing in maltitol, Sucralose, the xylo-oligosaccharide adding pulverizer, cross 80 mesh sieves; Granulation in comminutor adds granule auxiliary material commonly used, mixes, and processes granule by the granule common process.
Embodiment 15
Maltitol 1Kg, Sucralose 1Kg, xylo-oligosaccharide 1Kg with pulverizing in maltitol, Sucralose, the xylo-oligosaccharide adding pulverizer, cross 80 mesh sieves; Be dissolved to 1000L with purified water, stirred 15 minutes, can was sterilized 30 minutes, and was made oral liquid for 105 ℃.
Embodiment 16
Maltitol 55Kg, Sucralose 25Kg, xylo-oligosaccharide 15Kg with pulverizing in maltitol, Sucralose, the xylo-oligosaccharide adding pulverizer, cross 80 mesh sieves; Add conventional auxiliary material and carry out boiling granulating, the gained particle is with the whole grain of 30 mesh sieves, and the can capsule makes capsule.
Embodiment 17
Maltitol 50Kg, Sucralose 20Kg, xylo-oligosaccharide 5Kg with pulverizing in maltitol, Sucralose, the xylo-oligosaccharide adding pulverizer, cross 80 mesh sieves; Process powder.
Embodiment 18
Xylitol 60Kg, Sucralose 50Kg, galactooligosaccharide 30Kg with pulverizing in xylitol, Sucralose, the galactooligosaccharide adding pulverizer, cross 80 mesh sieves; 50 purpose vibratory sieves are crossed in granulation in comminutor then; Use the particle cooling back that makes always auxiliary material with adding syrup, mix, process syrup by the syrup common process.
Embodiment 19
Xylitol 1Kg, Sucralose 1Kg, galactooligosaccharide 1Kg, xylitol, Sucralose, galactooligosaccharide added in the pulverizer pulverize, cross 100 mesh sieves; 60 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined blender with the conventional auxiliary material of tablet, mix, process tablet.
Embodiment 20
Xylitol 20Kg, Sucralose 5Kg, galactooligosaccharide 2Kg with pulverizing in xylitol, Sucralose, the galactooligosaccharide adding pulverizer, cross 80 mesh sieves; 20 purpose vibratory sieves are crossed in granulation in comminutor then, and the particle cooling back that makes is joined the V-type blender with the auxiliary material dolomol; Mixed 30 minutes; 65 ℃ of dryings are carried out compression molding with 35 stamping machine 20Mpa, regulate pressure and particle weight at 0.1 gram.
Embodiment 21
Xylitol 60Kg, Sucralose 50Kg, galactooligosaccharide 30Kg with pulverizing in xylitol, Sucralose, the galactooligosaccharide adding pulverizer, cross 90 mesh sieves; Granulation in comminutor; Cross 60 purpose vibratory sieves then, particle cooling back that makes and the conventional auxiliary material of tablet are mixed together 80 ℃ of dryings; Compression molding is processed tablet.
Embodiment 22
Xylitol 55Kg, Sucralose 25Kg, galactooligosaccharide 15Kg with pulverizing in xylitol, Sucralose, the galactooligosaccharide adding pulverizer, cross 90 mesh sieves; Granulation in comminutor; Cross 50 purpose vibratory sieves then, particle cooling back that makes and the conventional auxiliary material of tablet are mixed together 70 ℃ of dryings; Compression molding is processed tablet.
Embodiment 23
Xylitol 50Kg, Sucralose 20Kg, galactooligosaccharide 5Kg with pulverizing in xylitol, Sucralose, the galactooligosaccharide adding pulverizer, cross 90 mesh sieves; 60 purpose vibratory sieves are crossed in granulation in comminutor then, and the particle cooling back that makes is joined blender with the conventional auxiliary material of tablet; Mix; 65 ℃ of dryings, compression molding is processed tablet.
Embodiment 24
Sorbierite 1Kg, stevioside 1Kg, isomaltoketose 1Kg with pulverizing in sorbierite, stevioside, the isomaltoketose adding pulverizer, cross 90 mesh sieves; 60 purpose vibratory sieves are crossed in granulation in comminutor then, and the particle cooling back that makes is joined blender with the conventional auxiliary material of tablet; Mix; 65 ℃ of dryings are carried out compression molding with tablet press machine 40Mpa, process tablet.
Embodiment 25
Sweet mellow wine 60Kg, stevioside 50Kg, oligomeric isomaltoketose 30Kg with pulverizing in sweet mellow wine, stevioside, the oligomeric isomaltoketose adding pulverizer, cross 100 mesh sieves; 60 purpose vibratory sieves are crossed in granulation in comminutor then, and the particle cooling back that makes is joined blender with the conventional auxiliary material of tablet; Mix; 80 ℃ of dryings, compression molding is processed tablet.
Embodiment 26
Hydroxyl isomaltulose 20Kg, Sucralose 5Kg, oligoisomaltose 2Kg with hydroxyl isomaltulose, Sucralose, oligoisomaltose, add in the pulverizer and pulverize; Cross 100 mesh sieves, 60 purpose vibratory sieves are crossed in granulation in comminutor then; The particle cooling back that makes is joined blender with the conventional auxiliary material of tablet, mix 80 ℃ of dryings; Compression molding is processed tablet.
Embodiment 27
Antierythrite 55 Kg, stevioside 25 Kg, stachyose 15 Kg with pulverizing in antierythrite, stevioside, the stachyose adding pulverizer, cross 90 mesh sieves; 30 purpose vibratory sieves are crossed in granulation in comminutor then, and the particle cooling back that makes is joined blender with the conventional auxiliary material of tablet; Mix; 70 ℃ of dryings, compression molding is processed tablet.
Embodiment 28
Antierythrite 50 Kg, stevioside 20 Kg, soyabean oligosaccharides 5 Kg with pulverizing in antierythrite, stevioside, the soyabean oligosaccharides adding pulverizer, cross 90 mesh sieves; 30 purpose vibratory sieves are crossed in granulation in comminutor then, and the particle cooling back that makes is joined blender with the conventional auxiliary material of tablet; Mix; 70 ℃ of dryings, compression molding is processed tablet.
Embodiment 29
Antierythrite 50 Kg, stevioside 20 Kg, inulin 5 Kg with pulverizing in antierythrite, stevioside, the inulin adding pulverizer, cross 90 mesh sieves; 30 purpose vibratory sieves are crossed in granulation in comminutor then, and the particle cooling back that makes is joined blender with the conventional auxiliary material of tablet; Mix; 80 ℃ of dryings, compression molding is processed tablet.
Claims (11)
1. a composition is characterized in that: comprise multi-sugar alcohol, intense sweetener, functional oligose.
2. composition according to claim 1 is characterized in that comprising the raw material of following weight parts: 1-60 parts of multi-sugar alcohols, 50 parts of intense sweetener 1-, functional oligose 1-30 part.
3. composition according to claim 2 is characterized in that comprising the raw material of following weight parts: 20-55 parts of multi-sugar alcohols, 25 parts of intense sweetener 5-, functional oligose 2-15 part.
4. composition according to claim 3 is characterized in that comprising the raw material of following weight parts: 50 parts of multi-sugar alcohols, 20 parts of intense sweeteners, 5 parts of functional oligoses.
5. composition according to claim 1 is characterized in that: multi-sugar alcohol can be a kind of or combination in any in antierythrite, xylitol, sorbierite, sweet mellow wine, maltitol, hydrogenated starch hydrolysate, lactitol, the hydroxyl isomaltulose; Intense sweetener can be stevioside, Sucralose, the knob a kind of or combination in any in sweet; Functional oligose can be a kind of or combination in any in stachyose, raffinose, isomaltoketose, milk ketose, FOS, xylo-oligosaccharide, inulin, galactooligosaccharide, oligoisomaltose, oligomeric isomaltoketose, oligomeric dragon gallbladder sugar, soyabean oligosaccharides, the chitosan oligomer.
6. composition according to claim 6 is characterized in that: multi-sugar alcohol is that antierythrite, intense sweetener are that stevioside, functional oligose are FOSs.
7. according to the arbitrary described composition of claim 1-6, it is characterized in that: can add auxiliary material and process in oral liquid, granule, capsule, tablet, powder, dispersing tablet, the syrup any one.
8. the preparation technology of tablet according to claim 7 is characterized in that comprising the following steps:
(1), takes by weighing raw material, through the pulverizing of 80-100 order, the granulation of 20-60 order, 65-80 ℃ drying;
(2), mixing, 20-60Mpa compressing tablet make.
9. the application of the arbitrary described composition of claim 1-6 in preparation composite sweetener product.
10. the application of the arbitrary described composition of claim 1-6 in the composite sweetener of preparation diabetes patient.
11. the application of the arbitrary described composition of claim 1-6 in the edible composite sweetener of preparation the obesity patients.
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