CA2185345C - Stable preservation method of powdered soft drink preparation and powdered soft drink preparation - Google Patents
Stable preservation method of powdered soft drink preparation and powdered soft drink preparation Download PDFInfo
- Publication number
- CA2185345C CA2185345C CA002185345A CA2185345A CA2185345C CA 2185345 C CA2185345 C CA 2185345C CA 002185345 A CA002185345 A CA 002185345A CA 2185345 A CA2185345 A CA 2185345A CA 2185345 C CA2185345 C CA 2185345C
- Authority
- CA
- Canada
- Prior art keywords
- soft drink
- powdered soft
- drink preparation
- weight
- carbohydrate
- 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.)
- Expired - Lifetime
Links
- 238000002360 preparation method Methods 0.000 title claims abstract description 100
- 235000014214 soft drink Nutrition 0.000 title claims abstract description 51
- 238000000034 method Methods 0.000 title claims abstract description 23
- 238000004321 preservation Methods 0.000 title claims abstract description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 43
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000000292 calcium oxide Substances 0.000 claims abstract description 21
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 21
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 21
- 150000001720 carbohydrates Chemical class 0.000 claims abstract description 20
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 14
- 239000000843 powder Substances 0.000 claims abstract description 7
- 230000000087 stabilizing effect Effects 0.000 claims description 11
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 9
- 239000011575 calcium Substances 0.000 claims description 9
- 229910052791 calcium Inorganic materials 0.000 claims description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 9
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 6
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 6
- 150000007524 organic acids Chemical group 0.000 claims description 6
- 150000002772 monosaccharides Chemical class 0.000 claims description 4
- 229930014626 natural product Natural products 0.000 claims description 4
- 239000003381 stabilizer Substances 0.000 claims description 4
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 3
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 claims description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 3
- 229930091371 Fructose Natural products 0.000 claims description 3
- 239000005715 Fructose Substances 0.000 claims description 3
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 3
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 claims description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 3
- 229930006000 Sucrose Natural products 0.000 claims description 3
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 3
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 3
- 235000010323 ascorbic acid Nutrition 0.000 claims description 3
- 239000011668 ascorbic acid Substances 0.000 claims description 3
- 229960005070 ascorbic acid Drugs 0.000 claims description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 3
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 claims description 3
- 235000015165 citric acid Nutrition 0.000 claims description 3
- 239000001530 fumaric acid Substances 0.000 claims description 3
- 235000011087 fumaric acid Nutrition 0.000 claims description 3
- 239000008103 glucose Substances 0.000 claims description 3
- 239000004310 lactic acid Substances 0.000 claims description 3
- 235000014655 lactic acid Nutrition 0.000 claims description 3
- 239000001630 malic acid Substances 0.000 claims description 3
- 235000011090 malic acid Nutrition 0.000 claims description 3
- 239000002245 particle Substances 0.000 claims description 3
- 239000005720 sucrose Substances 0.000 claims description 3
- 235000002906 tartaric acid Nutrition 0.000 claims description 3
- 239000011975 tartaric acid Substances 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- 150000004676 glycans Chemical class 0.000 claims 2
- 229920001282 polysaccharide Polymers 0.000 claims 2
- 239000005017 polysaccharide Substances 0.000 claims 2
- 235000019640 taste Nutrition 0.000 abstract description 17
- 230000015271 coagulation Effects 0.000 abstract description 10
- 238000005345 coagulation Methods 0.000 abstract description 10
- 238000002845 discoloration Methods 0.000 abstract description 8
- 238000004519 manufacturing process Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 239000000796 flavoring agent Substances 0.000 description 11
- 235000019634 flavors Nutrition 0.000 description 11
- 229960001866 silicon dioxide Drugs 0.000 description 11
- 235000014633 carbohydrates Nutrition 0.000 description 9
- 230000006866 deterioration Effects 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- 241000282320 Panthera leo Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000002274 desiccant Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 230000009967 tasteless effect Effects 0.000 description 2
- 101150110592 CTS1 gene Proteins 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 description 1
- 229930064664 L-arginine Natural products 0.000 description 1
- 235000014852 L-arginine Nutrition 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- LKDRXBCSQODPBY-ZXXMMSQZSA-N alpha-D-fructopyranose Chemical compound OC[C@]1(O)OC[C@@H](O)[C@@H](O)[C@@H]1O LKDRXBCSQODPBY-ZXXMMSQZSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 235000019658 bitter taste Nutrition 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- -1 disintegrators Substances 0.000 description 1
- 210000003278 egg shell Anatomy 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000000050 nutritive effect Effects 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 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
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/385—Concentrates of non-alcoholic beverages
- A23L2/39—Dry compositions
-
- 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
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/42—Preservation of non-alcoholic beverages
- A23L2/44—Preservation of non-alcoholic beverages by adding preservatives
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Non-Alcoholic Beverages (AREA)
Abstract
The present invention provides a stable preservation method of a powdered so ft drink preparation, which comprises adding 0.2 to 1.0 % by weight of a calcium oxide and 0.02 to 2.0 % by weight of a particul ate silicon dioxide in the powdered soft drink preparati on containing a carbohydrate and a sour agent as a main component. The powdered soft drink preparation of the present invention maintai ns the original powder state, color and taste, which are obtained immediately a fter the production, for a long period of time without c ausing comparatively rapid coagulation of powders, discoloration and change in tast e at the time of preservation.
Description
2~~5~4~
DESCRIPTION
STABLE PRESERVATION METHOD OF POWDERED SOFT DRINK PREPARATION
AND POWDERED SOFT DRINK PREPARATION
TECHNICAL FIELD
The present invention relates to a stable preservation method of a powdered soft drink preparation, and a powdered soft drink preparation.
BACKGROUND ART
A powdered soft drink preparation normally contain a carbohydrate and a sour agent as a main component, and is prepared by additionally adding a subraw material such as fruit juice. It is necessary that the powdered soft drink preparation maintains the dried state as much as possible because of it's high moisture absorption. That is, the soft drink preparation causes deterioration such as coagulation, browning, discoloration in the presence of water, which results in deterioration of the quality.
In addition, this preparation always contain about 1 $ of water derived from the raw material even if water is severely controlled. When the component causing the reaction between water and the above main component is present in the subraw material, for example, when a basic nutritive component is present, the neutralization reaction proceeds with time.
When amino acid is added, the browning due to Mailard reaction arises. Therefore, there is a drawback in both cases that it ~~.~~~45 W O 96!22704 PCT/JP96100109 becomes very difficult to maintain the preparation stably.
Furthermore, even if the pr,~~~aration is reserved in an enclosed container, it is diffit to avoid deterioration . ., of quality arid change of taste with time, which are caused by the above-described water of about 1 $, water adhered on raw materials,, water to be formed by the neutralization reaction between the added components. Therefore, it is essential for the preparation to use a desiccant at gresent. Thus, it is requested to develop a novel method for preventing deterioration due to water for a long period of time-to maintain the quality.
DISCLOSURE OF THE INVENTION
A main object of the present invention is to solve a drawback such as deterioration caused in the presence of water, which is admitted in a conventional powdered soft drink preparation, thereby providing a powdered soft drink having an excellent preservation stability for a long period of time.
The present inventors have intensively studied so as to accomplish the, above object. As a result, it has been found that a powdered soft drink preparation having an excellent preservation stability can be obtained when a predetermined amount of a calcium oxide and a particulate silicon dioxide are added in a conventional powdered soft drink preparation.
That is,--according to the present invention, there W096I22704 ~, .;~ "1 ~r,7 ~ !~ ~r° PCTIJP96100109 is provided a stable preservation method of a powdered soft ' drink preparation, which comprises adding 0.2 to 1.D $ by weight of a calcium oxide and D_02 to 2.D ~ by weight of a particulate silicon dioxide in the powdered soft drink preparation containing a carbohydrate and a sour agent as a main component. There is also provided a powdered soft drink preparation thus obtained and having an improved reservation stability.
According to the method of the present invention, it is considered that the calcium oxide to be added reacts chemically with water derived from the raw material in the preparation to remove water. Thereby, a water content in the preparation is reduced to stabilize the preparation. As a result, the preparation exhibits a high preservation stabilization effectfor a sufficiently long period of time without using no desiccant. On the other hand, it is considered that the particulate silicon dioxide serves as a so-called coating agent-which coats the surfaces of the raw material powders to reduce the opportunity of direct contacting between powders having a high reactivity, thereby improving physical properties and stability of the preparation.
According to the method of the present invention, there can be obtained a powdered soft drink preparation having a high preservation stability which has never been accomplished, heretofore. That is, regarding the preparation of the present invention, the commercial value such as flavor is not deteriorated, and drawbacks such as coagulation and browning are prevented. Furthermore, the above-mentioned components to be added have safety guaranteed in the field of the food industry. At the same time, they are tasteless and odorless and, therefore, there is not any fear of exerting a harmful influence on the taste of the soft drink preparation itself.
In another aspect, the present invention provides a method for stabilizing and preserving a powdered soft drink preparation, comprising adding 0.2 to 0.5 ~ by weight of a calcium oxide and 0.03 to 1.0 $ by weight of a particulate silicon dioxide to a powdered soft drink preparation containing a carbohydrate and a sour agent as a main component, each amount being based on the total amount of the preparation.
In another aspect, the present invention provides a powdered soft drink preparation, comprising a carbohydrate and a sour agent as a main component, wherein 0.2 to 0.5 o by weight of a calcium oxide and 0.03 to 1.0 % by weight of a particulate silicon dioxide are added as a preservation stabilizer.
REST MODE FOR CARRYING OUT THE INVENTION
The calcium oxide to be added in the powdered soft -4a-drink preparation is contained in an amount of not less than 0.2 % by weight, thereby exhibiting the desired stabilization effect of the preparation. Even if the large amount of the calcium oxide is added, the stabilization effect is not improved in proportion to the amount, and the taste, flavor, solubility, etc. of the preparation are likely to be deteriorated. Therefore, it is preferred to use the calcium oxide in an amount of not more than 1.0 ~ by weight.
Particularly preferred amount is selected within a range of 0.2 to 0.5 o by weight.
Regarding the silicon dioxide, the desired effect can be exhibited by adding in an amount within a range of 0.02 to 2.0 $ by weight, and it is preferred to use it in an amount within a range of 0.03 to 1.0 ~ by weight.
t...
WO 96J22704 ~ J ~ ~ PCTIJP96100109 _5_ The calcium oxide is not specifically limited, but those synthesized chemically and those obtained by calcining shells or egg shells derived from natural products can be advantageously used-in the present invention. Among them, the chemically synthesized calcium oxide and shell-calcined calcium derived from natural products are particularly preferred from the viewpoint of organoleptic properties such as taste of the resulting preparation.
The particulate silicon dioxide is not also specifically limited and various ones which are known to public can be used. Among them, those having a three-dimensional amorphous structure like silica gel is-normally preferred. Further, as-the particulate silicon dioxide, those having an average particle size of not more than 15 um, which are defined as a food additive at present, are used.
The powdered soft drink preparation to be stabilized by adding the above two specific components according to the present invention may be the same composition as that of a most popular one containing, as a main component, a carbohydrate and an organic acid as a sour agent. The amount of the main component to be added can be decided within a normal range according to the shape, use and purpose of using of the preparation. It s preferred that the amount of the.
carbohydrate in order to obtain good organoleptic properties is selected within a range of about 65 to 95 ~ by weight in 2~.~~3~5 W0 96122704 ~ , ~ ' , PCT/JP96100109 the powdered preparation. After the carbohydrate was dissolved in water, the amount is selected within a range of about 4 to 12 % by weight.
Examples of the above carbohydrate are one or more of normal carbohydrates, which can be selected-from monosaccharides such as glucose and fructose; disaccharides such as sucrose and maltose; polysaccharides-such as oligosaccharide. The effect of the present invention is enhanced, when using monosaccharides (e. g. fructose) which have high moisture absorption and high reactivity.
The sour agent to be used as another main component may be various organic acids which are normally used. Typical examples include citric acid, tartaric acid, fumaric acid, malic acid, lactic acid and ascorbic acid. They may be used alone or in combination.
Optional components such as various vitamins, amino acids and minerals can be appropriately added in the powdered soft drink preparation of the present invention according to the purpose of using. In addition to them, there can be appropriately added binders, excipients, disintegrators, lubricants, thickeners, surfactants, osmotic pressure adjustors, electrolytes, sweeteners, flavors,-pigments, pH
adjustors and the like.
The powdered soft drink preparation of the present invention can be prepared-according to the same manner as in y . r~ . ~ ..:
..",.. ,-. ~ ~. y; ~' !,.
WO 96/12704 ~,I ~ ~ 3 4 5 pCTIJP96100109 the normal powdered soft'drink preparation except for adding a predetermined amount of the above two components. The time of the addition of the above essential two components is not specifically limited and it may be any time in the desired preparation step of the preparation.
Thus, the desired powdered soft drink preparation whose preservation stability has been improved can be obtained.
FIELD OF INDUSTRIAL APPLICABILITY
According to the method of the present invention, a preservation stability of a powdered soft drink preparation is remarkably improved. As a result, regarding the preparation of the present invention, the commercial value such as flavor is not deteriorated, and drawbacks such as the coagulation and browning are prevented. Components to be added as preservative stabilizers have safety guaranteed in the field of the food industry. At the same time, they are tasteless and odorless and, therefore, there is not any fear of exerting a harmful influence on the taste of the soft drink preparation 2D itself.
EXAMPLES
In order to explain the present invention in detail, Preparation Examples of ahe preparation of the present invention will be described below. Then, Stability Test carried out with respect to the resulting preparation will be 2~~~~~ i .
WO 96!22704 a ..' . PCTIJP96I00109 ~, , , ~,, ,...
_g_ described. In the respective Examples, "percentages" are by weight unless otherwise stated.
Rxam2?~ ~ ~ 0 q -The respective components described in Table 1 were weighed and mixed to prepare powdered soft drink preparations.
These are dissolved in 1 liter of water to be-served as a drink.
~~O 9G1~~70a PCTlJP9610U109 _g_ i ~ ~ I
', p . . .
"~'1t ~ p~OL')rJ w L~.
; fv i j "", I V: c~7 f'~ (I~N
-: p ~ ~f ':
v i I p ra ~ r~ Ln r L?
I .~ Ln ca i c ~
I I V; ,~7 t''7 tn N
V ~~ tf I
I
1 ~ ILrJC'7~L~p C5 L
t t~ ~ I
. o :
1 !fl (''") U~ N
C'~ N i I . O o I
t~ p I f; O ('~ rJ Lr7 ~ I O L'7 O ~ I
rJ
;J ff. ~ f ~ G: N
.-~ p .-i ~
f4 I In . .
L'1 ,7 l ~ ~] ("7 to L'7 r Lr7 -l L ~
; r r, ~ .. . . . , .
. . . I
I U; f'~ C7 fJ~N
o O -~ U,' j I
x I:.i~' J 1 f0 ,~~ t'~ Iv L~y I I L'"1 L~. I
O rJ
U ~ J , . . ;~~
O
U: f~ fh !f N
N UJ
O O
,,..I . .
I
CTS 1 I t0 p C'7 f~ L
O O L'7 ;,~ ;
<J
p .
.-i f~ f'~ ,"~ UJ N
.-1 p .-, UJ
a ro N t I fJ O f'~ t~ L~
C L'7 .-i ' 4~7 f~
p . . . . . . , . I
U' ~~ ~7 !I~N
O O -~ U1 I
" ~ I 1 Iv p C' i ,""..L7 p L"7 L7 'v.7 I
~
. N O . . .
~
I U7 t''') U, N
f~ N !n ' I
O O L~
i x i -.; ~ I
n ~ I 4 .- . I
v ,..~ ~
~
;~U I ~.
c~ i r r ~~ .~
.-', _~ ~ I ...
.,.~ I
C%
J C~ i~ J
o\o !l:t~ . .~. ..:
(~
.,.
C .-.r n >
~J :.~U ~ ..., i ~ .~ ~
e~ a~ r :~, ~ - U ~ ..
V~ : w ~~ c~
I '- !n --itO O -i I :.r C' I,~ ;..:
~
c o~ ~ Ua.=-~c~o o .-;
..
d U ~ a cn ~ .-~ > r U :-' 'p -.~ i .
~ c~~ r~ c~ cU r~ :~
~ t~ ,; :: ~
r 0 j -a Lr~~ I I ~ ...p ~ ~ ~
U I U :~U~ .-. r '..:.,:-l.:.. : ;n C., ~ I
.... ' v:
WO 96122704 PC?/JP96/00109 p rod ~ or. ~ ~~'~Y-~ '~
The prepay anon o~' the prese.~. t invention obtained according to the fol'_owing Preparation Example T_ and the Following control preparations were subjected to a comparison.
test.
~rP~a,-ate; o., ~-x~mp~ ( =ormul a tion ) r uc rose g3 ~
Sour agent suitable amount L-arginine 3.3 ~
L - a J c O r b i c a C i d 2 . J o Powdered ~rui t juice 2.0 ~
Sodium chloride suitable amount Shell-calcined calcium 0.25 $
Par ticula to sil icon dioxide 0. 0~
15 P 1 avor and piymen t sui table amoun t Total 100 ~ ( total amount. 62. ~ g ) (1) Control preparation (containing no she'_~-calcined ca_cium): preparation obtained according to the same manner as tha t descr ibed in Pr epar a Lion Example A excep t io= addi.~.c 20 no shell-ca-c~~ned calcium i Con t_ ,._ pr od~,:ct _ _ pr epar a tio:~ ob rained accer ding tc t..~.
same ma::ner as tha ~ desc=ibed i.~. Preparatic~. Examp~ a .~ el:ce~
;c; adcinc no shell-cal cined calcium and oar t_cula to s~.l_~....
..~.~.7~:~ua Cc~. tr ~ ~~ _ r od::c t 2 : pr epar a Lion ob-a;ned accc_ ~v~=
WO 96/22704 ~ ~ ~ PCTIJP96/00109 same manner as that described in Preparation Example A except ~ for adding no particulate silicon dioxide The above respective preparations were prepared by mixing with hands and packed separately in a bag made of an aluminum laminated film,'respectively. The bag was preserved in a constant temperature room and the preservation stability thereof was tested.
The followings were selected as the test item.
1. Coagulation of preparation 2. Degree of discoloration of preparation 3. Change in organoleptic property (taste) in dissolution of preparation The results were as follows.
1. Coagulation of preparation The preparation of Preparation Example A (product of the present invention) and control preparation (containing no shell-calcined calcium, controls 1 and 2) were allowed to stand in a constant temperature room at 50 °C to visually observe the state of the respective samples after 2, 3 and 4 weeks, respectively.
As a result, the product of the present invention caused no coagulation even after standing at 50 °C for 4 weeks and was superior in powder fluidity. To the contrary, in all control preparations, the coagulation state became serious by adding no shell-calcinedcalcium and/or particulate silicon ~~85345 dioxide. After standing~fbr'3 weeks, the preparations were coagulated tightly arid.showed a sheet-like state (regarding the control product 2, the mass was sometimes broken because the degree of. the coagulation is slightly-low) and it could npt be easily returned to thepowder state. Furthermore, the solubility of the respective control preparations in water became inferior, in comparison with the preparation of the present-invention after standing under the same condition.
2. Degree of discoloration of preparation The respective preparation samples whose coagulation state was judged according to the above item 1 were visually observed and the change in color with time of-the respective samples was examined using a color difference meter.- Further, the value after a predetermined time has been passed was judged by NBS unit (DE: color difference) and Lab, using the value before the beginning of the test as a standard. The explanation of the value of the NBS unit and indication of visual sense ("Matter with respect to Color", published by Nihon Denshoku Kogyo) as well as evaluation of Lab are as follows.
(NBS unit) (Visual sense) 0 to 0.5 faintly 0.5 to-1.5 slightly 1_5 to 3_D _ in the degree capable of perceiving WO 96122704 ~ ~ ~ ~ ~ PCTIJP96100109 3.0 to 6.0 in the degree of being remarkable 6.0 to 12.0 greatly 12.0 or more drastically Lab L: The larger the value of L, the higher the brightness is.
a: It shows a degree of red at the (+) side, and a degree of green at the (-) side.
b: It shows a degree of yellow at the (+) side, and a degree of blue at the (-) side.
The test results of the preparation of the Preparation Example A (product of the present invention) and control product 1 are shown in Tables 2 and 3.
WO 96122704 ~ ~ g 5 ~ 4 ~
Y.
U
a o N
O ~ .-aN
~1 C
O
U
+~
C
U
O
Ti O
C
S~
N
a>
G
N r1 c0 O ~
.2 M (~ O
r-t C N 'cNIn C
.G 0 N
H ~
m N
ua m am a +~
a.
m _ r~ v~ u~ ~n W Y Y S
w OJ N O
Z
~.
G
N
O N Ch C~
E
+~
~
~ a-~a~ a~
t C
+p ~.~
U ~n ~n ~n ,. "
PCTlJP96I00109 ' ~r ,~ ~ m o~ m n o R
m n m a~ o r1 ~-IN
a, N In c0 CO
ro N N V~
O cm n m m ~ o a o~ o o ,-i m m c~
+~
U ~ m vo 7 t~ O~ N tn b A
0 ~ m rt ,1 H
a 4 a~ O O N
ro O O ~ O
ro H +.~
ro N m o, m ~ N N V~
a CL o~ o, m m N
a ro c ro.
t -ZO U .O W u1 UI UJ
ro o x x x w a ro ro ro o .- ai a~ a~ m ~ 3 3 3 O
O c i~ N m C
+.~ N
;~ C
~ t +t.~ ~ k~ a~
-.Oi U ~ ~ O o U ~
3 . !
A
218~~4~
W0 96122704 PCTlJP96100109 As is apparent from the above tables, the discoloration was hardly observed in the product ofthe present-invention, in comparison with the control product 1_ That is, regarding the product of the present-invention, the brightness hardly changed and a stable color tone was. shown even after preservation at 5D °C for 4 weeks. To the contrary, regarding the control product 1, the brightness was decreased with time during preserving at 50 °C and the degree of red and yellow was increased. This means that the fact that browning proceeds with time is showed clearly with the numerical value.
Actually, regarding the product of the present invention, little discoloration was admitted by visual observation even after preservation at 5D °C for 4 weeks. To the contrary, regarding the control product 1, a remarkable discoloration has already been admitted after-2 weeks.
Further, regarding the control preparation containing no shell-calcined calcium and the control product 2, a remarkable discoloration which is almost the same as that-of the above control product 1 was admitted. Among them, the control product 2 tends to cause a weak degree of browning.
3. Change in organoleptic property (taste) in dissolution of preparation A standard sample which was preserved in a dark place at 4°C after preparation, and samples which were _ ~ WO 96122704 ~ ~ ~ PCTIJP96/00109 =17-obtained by preserving the standard samples at 37°C or 50°C
' for a predetermined time were used. The change in taste of each sample due to preservation was evaluated by asking three panelists to try each drink which was prepared by dissolving 62.5 g of each sample in 1 liter of cold water. Evaluation was carried out on the basis of the following five-level marks in comparison of the standard sample by the organoleptic test.
DESCRIPTION
STABLE PRESERVATION METHOD OF POWDERED SOFT DRINK PREPARATION
AND POWDERED SOFT DRINK PREPARATION
TECHNICAL FIELD
The present invention relates to a stable preservation method of a powdered soft drink preparation, and a powdered soft drink preparation.
BACKGROUND ART
A powdered soft drink preparation normally contain a carbohydrate and a sour agent as a main component, and is prepared by additionally adding a subraw material such as fruit juice. It is necessary that the powdered soft drink preparation maintains the dried state as much as possible because of it's high moisture absorption. That is, the soft drink preparation causes deterioration such as coagulation, browning, discoloration in the presence of water, which results in deterioration of the quality.
In addition, this preparation always contain about 1 $ of water derived from the raw material even if water is severely controlled. When the component causing the reaction between water and the above main component is present in the subraw material, for example, when a basic nutritive component is present, the neutralization reaction proceeds with time.
When amino acid is added, the browning due to Mailard reaction arises. Therefore, there is a drawback in both cases that it ~~.~~~45 W O 96!22704 PCT/JP96100109 becomes very difficult to maintain the preparation stably.
Furthermore, even if the pr,~~~aration is reserved in an enclosed container, it is diffit to avoid deterioration . ., of quality arid change of taste with time, which are caused by the above-described water of about 1 $, water adhered on raw materials,, water to be formed by the neutralization reaction between the added components. Therefore, it is essential for the preparation to use a desiccant at gresent. Thus, it is requested to develop a novel method for preventing deterioration due to water for a long period of time-to maintain the quality.
DISCLOSURE OF THE INVENTION
A main object of the present invention is to solve a drawback such as deterioration caused in the presence of water, which is admitted in a conventional powdered soft drink preparation, thereby providing a powdered soft drink having an excellent preservation stability for a long period of time.
The present inventors have intensively studied so as to accomplish the, above object. As a result, it has been found that a powdered soft drink preparation having an excellent preservation stability can be obtained when a predetermined amount of a calcium oxide and a particulate silicon dioxide are added in a conventional powdered soft drink preparation.
That is,--according to the present invention, there W096I22704 ~, .;~ "1 ~r,7 ~ !~ ~r° PCTIJP96100109 is provided a stable preservation method of a powdered soft ' drink preparation, which comprises adding 0.2 to 1.D $ by weight of a calcium oxide and D_02 to 2.D ~ by weight of a particulate silicon dioxide in the powdered soft drink preparation containing a carbohydrate and a sour agent as a main component. There is also provided a powdered soft drink preparation thus obtained and having an improved reservation stability.
According to the method of the present invention, it is considered that the calcium oxide to be added reacts chemically with water derived from the raw material in the preparation to remove water. Thereby, a water content in the preparation is reduced to stabilize the preparation. As a result, the preparation exhibits a high preservation stabilization effectfor a sufficiently long period of time without using no desiccant. On the other hand, it is considered that the particulate silicon dioxide serves as a so-called coating agent-which coats the surfaces of the raw material powders to reduce the opportunity of direct contacting between powders having a high reactivity, thereby improving physical properties and stability of the preparation.
According to the method of the present invention, there can be obtained a powdered soft drink preparation having a high preservation stability which has never been accomplished, heretofore. That is, regarding the preparation of the present invention, the commercial value such as flavor is not deteriorated, and drawbacks such as coagulation and browning are prevented. Furthermore, the above-mentioned components to be added have safety guaranteed in the field of the food industry. At the same time, they are tasteless and odorless and, therefore, there is not any fear of exerting a harmful influence on the taste of the soft drink preparation itself.
In another aspect, the present invention provides a method for stabilizing and preserving a powdered soft drink preparation, comprising adding 0.2 to 0.5 ~ by weight of a calcium oxide and 0.03 to 1.0 $ by weight of a particulate silicon dioxide to a powdered soft drink preparation containing a carbohydrate and a sour agent as a main component, each amount being based on the total amount of the preparation.
In another aspect, the present invention provides a powdered soft drink preparation, comprising a carbohydrate and a sour agent as a main component, wherein 0.2 to 0.5 o by weight of a calcium oxide and 0.03 to 1.0 % by weight of a particulate silicon dioxide are added as a preservation stabilizer.
REST MODE FOR CARRYING OUT THE INVENTION
The calcium oxide to be added in the powdered soft -4a-drink preparation is contained in an amount of not less than 0.2 % by weight, thereby exhibiting the desired stabilization effect of the preparation. Even if the large amount of the calcium oxide is added, the stabilization effect is not improved in proportion to the amount, and the taste, flavor, solubility, etc. of the preparation are likely to be deteriorated. Therefore, it is preferred to use the calcium oxide in an amount of not more than 1.0 ~ by weight.
Particularly preferred amount is selected within a range of 0.2 to 0.5 o by weight.
Regarding the silicon dioxide, the desired effect can be exhibited by adding in an amount within a range of 0.02 to 2.0 $ by weight, and it is preferred to use it in an amount within a range of 0.03 to 1.0 ~ by weight.
t...
WO 96J22704 ~ J ~ ~ PCTIJP96100109 _5_ The calcium oxide is not specifically limited, but those synthesized chemically and those obtained by calcining shells or egg shells derived from natural products can be advantageously used-in the present invention. Among them, the chemically synthesized calcium oxide and shell-calcined calcium derived from natural products are particularly preferred from the viewpoint of organoleptic properties such as taste of the resulting preparation.
The particulate silicon dioxide is not also specifically limited and various ones which are known to public can be used. Among them, those having a three-dimensional amorphous structure like silica gel is-normally preferred. Further, as-the particulate silicon dioxide, those having an average particle size of not more than 15 um, which are defined as a food additive at present, are used.
The powdered soft drink preparation to be stabilized by adding the above two specific components according to the present invention may be the same composition as that of a most popular one containing, as a main component, a carbohydrate and an organic acid as a sour agent. The amount of the main component to be added can be decided within a normal range according to the shape, use and purpose of using of the preparation. It s preferred that the amount of the.
carbohydrate in order to obtain good organoleptic properties is selected within a range of about 65 to 95 ~ by weight in 2~.~~3~5 W0 96122704 ~ , ~ ' , PCT/JP96100109 the powdered preparation. After the carbohydrate was dissolved in water, the amount is selected within a range of about 4 to 12 % by weight.
Examples of the above carbohydrate are one or more of normal carbohydrates, which can be selected-from monosaccharides such as glucose and fructose; disaccharides such as sucrose and maltose; polysaccharides-such as oligosaccharide. The effect of the present invention is enhanced, when using monosaccharides (e. g. fructose) which have high moisture absorption and high reactivity.
The sour agent to be used as another main component may be various organic acids which are normally used. Typical examples include citric acid, tartaric acid, fumaric acid, malic acid, lactic acid and ascorbic acid. They may be used alone or in combination.
Optional components such as various vitamins, amino acids and minerals can be appropriately added in the powdered soft drink preparation of the present invention according to the purpose of using. In addition to them, there can be appropriately added binders, excipients, disintegrators, lubricants, thickeners, surfactants, osmotic pressure adjustors, electrolytes, sweeteners, flavors,-pigments, pH
adjustors and the like.
The powdered soft drink preparation of the present invention can be prepared-according to the same manner as in y . r~ . ~ ..:
..",.. ,-. ~ ~. y; ~' !,.
WO 96/12704 ~,I ~ ~ 3 4 5 pCTIJP96100109 the normal powdered soft'drink preparation except for adding a predetermined amount of the above two components. The time of the addition of the above essential two components is not specifically limited and it may be any time in the desired preparation step of the preparation.
Thus, the desired powdered soft drink preparation whose preservation stability has been improved can be obtained.
FIELD OF INDUSTRIAL APPLICABILITY
According to the method of the present invention, a preservation stability of a powdered soft drink preparation is remarkably improved. As a result, regarding the preparation of the present invention, the commercial value such as flavor is not deteriorated, and drawbacks such as the coagulation and browning are prevented. Components to be added as preservative stabilizers have safety guaranteed in the field of the food industry. At the same time, they are tasteless and odorless and, therefore, there is not any fear of exerting a harmful influence on the taste of the soft drink preparation 2D itself.
EXAMPLES
In order to explain the present invention in detail, Preparation Examples of ahe preparation of the present invention will be described below. Then, Stability Test carried out with respect to the resulting preparation will be 2~~~~~ i .
WO 96!22704 a ..' . PCTIJP96I00109 ~, , , ~,, ,...
_g_ described. In the respective Examples, "percentages" are by weight unless otherwise stated.
Rxam2?~ ~ ~ 0 q -The respective components described in Table 1 were weighed and mixed to prepare powdered soft drink preparations.
These are dissolved in 1 liter of water to be-served as a drink.
~~O 9G1~~70a PCTlJP9610U109 _g_ i ~ ~ I
', p . . .
"~'1t ~ p~OL')rJ w L~.
; fv i j "", I V: c~7 f'~ (I~N
-: p ~ ~f ':
v i I p ra ~ r~ Ln r L?
I .~ Ln ca i c ~
I I V; ,~7 t''7 tn N
V ~~ tf I
I
1 ~ ILrJC'7~L~p C5 L
t t~ ~ I
. o :
1 !fl (''") U~ N
C'~ N i I . O o I
t~ p I f; O ('~ rJ Lr7 ~ I O L'7 O ~ I
rJ
;J ff. ~ f ~ G: N
.-~ p .-i ~
f4 I In . .
L'1 ,7 l ~ ~] ("7 to L'7 r Lr7 -l L ~
; r r, ~ .. . . . , .
. . . I
I U; f'~ C7 fJ~N
o O -~ U,' j I
x I:.i~' J 1 f0 ,~~ t'~ Iv L~y I I L'"1 L~. I
O rJ
U ~ J , . . ;~~
O
U: f~ fh !f N
N UJ
O O
,,..I . .
I
CTS 1 I t0 p C'7 f~ L
O O L'7 ;,~ ;
<J
p .
.-i f~ f'~ ,"~ UJ N
.-1 p .-, UJ
a ro N t I fJ O f'~ t~ L~
C L'7 .-i ' 4~7 f~
p . . . . . . , . I
U' ~~ ~7 !I~N
O O -~ U1 I
" ~ I 1 Iv p C' i ,""..L7 p L"7 L7 'v.7 I
~
. N O . . .
~
I U7 t''') U, N
f~ N !n ' I
O O L~
i x i -.; ~ I
n ~ I 4 .- . I
v ,..~ ~
~
;~U I ~.
c~ i r r ~~ .~
.-', _~ ~ I ...
.,.~ I
C%
J C~ i~ J
o\o !l:t~ . .~. ..:
(~
.,.
C .-.r n >
~J :.~U ~ ..., i ~ .~ ~
e~ a~ r :~, ~ - U ~ ..
V~ : w ~~ c~
I '- !n --itO O -i I :.r C' I,~ ;..:
~
c o~ ~ Ua.=-~c~o o .-;
..
d U ~ a cn ~ .-~ > r U :-' 'p -.~ i .
~ c~~ r~ c~ cU r~ :~
~ t~ ,; :: ~
r 0 j -a Lr~~ I I ~ ...p ~ ~ ~
U I U :~U~ .-. r '..:.,:-l.:.. : ;n C., ~ I
.... ' v:
WO 96122704 PC?/JP96/00109 p rod ~ or. ~ ~~'~Y-~ '~
The prepay anon o~' the prese.~. t invention obtained according to the fol'_owing Preparation Example T_ and the Following control preparations were subjected to a comparison.
test.
~rP~a,-ate; o., ~-x~mp~ ( =ormul a tion ) r uc rose g3 ~
Sour agent suitable amount L-arginine 3.3 ~
L - a J c O r b i c a C i d 2 . J o Powdered ~rui t juice 2.0 ~
Sodium chloride suitable amount Shell-calcined calcium 0.25 $
Par ticula to sil icon dioxide 0. 0~
15 P 1 avor and piymen t sui table amoun t Total 100 ~ ( total amount. 62. ~ g ) (1) Control preparation (containing no she'_~-calcined ca_cium): preparation obtained according to the same manner as tha t descr ibed in Pr epar a Lion Example A excep t io= addi.~.c 20 no shell-ca-c~~ned calcium i Con t_ ,._ pr od~,:ct _ _ pr epar a tio:~ ob rained accer ding tc t..~.
same ma::ner as tha ~ desc=ibed i.~. Preparatic~. Examp~ a .~ el:ce~
;c; adcinc no shell-cal cined calcium and oar t_cula to s~.l_~....
..~.~.7~:~ua Cc~. tr ~ ~~ _ r od::c t 2 : pr epar a Lion ob-a;ned accc_ ~v~=
WO 96/22704 ~ ~ ~ PCTIJP96/00109 same manner as that described in Preparation Example A except ~ for adding no particulate silicon dioxide The above respective preparations were prepared by mixing with hands and packed separately in a bag made of an aluminum laminated film,'respectively. The bag was preserved in a constant temperature room and the preservation stability thereof was tested.
The followings were selected as the test item.
1. Coagulation of preparation 2. Degree of discoloration of preparation 3. Change in organoleptic property (taste) in dissolution of preparation The results were as follows.
1. Coagulation of preparation The preparation of Preparation Example A (product of the present invention) and control preparation (containing no shell-calcined calcium, controls 1 and 2) were allowed to stand in a constant temperature room at 50 °C to visually observe the state of the respective samples after 2, 3 and 4 weeks, respectively.
As a result, the product of the present invention caused no coagulation even after standing at 50 °C for 4 weeks and was superior in powder fluidity. To the contrary, in all control preparations, the coagulation state became serious by adding no shell-calcinedcalcium and/or particulate silicon ~~85345 dioxide. After standing~fbr'3 weeks, the preparations were coagulated tightly arid.showed a sheet-like state (regarding the control product 2, the mass was sometimes broken because the degree of. the coagulation is slightly-low) and it could npt be easily returned to thepowder state. Furthermore, the solubility of the respective control preparations in water became inferior, in comparison with the preparation of the present-invention after standing under the same condition.
2. Degree of discoloration of preparation The respective preparation samples whose coagulation state was judged according to the above item 1 were visually observed and the change in color with time of-the respective samples was examined using a color difference meter.- Further, the value after a predetermined time has been passed was judged by NBS unit (DE: color difference) and Lab, using the value before the beginning of the test as a standard. The explanation of the value of the NBS unit and indication of visual sense ("Matter with respect to Color", published by Nihon Denshoku Kogyo) as well as evaluation of Lab are as follows.
(NBS unit) (Visual sense) 0 to 0.5 faintly 0.5 to-1.5 slightly 1_5 to 3_D _ in the degree capable of perceiving WO 96122704 ~ ~ ~ ~ ~ PCTIJP96100109 3.0 to 6.0 in the degree of being remarkable 6.0 to 12.0 greatly 12.0 or more drastically Lab L: The larger the value of L, the higher the brightness is.
a: It shows a degree of red at the (+) side, and a degree of green at the (-) side.
b: It shows a degree of yellow at the (+) side, and a degree of blue at the (-) side.
The test results of the preparation of the Preparation Example A (product of the present invention) and control product 1 are shown in Tables 2 and 3.
WO 96122704 ~ ~ g 5 ~ 4 ~
Y.
U
a o N
O ~ .-aN
~1 C
O
U
+~
C
U
O
Ti O
C
S~
N
a>
G
N r1 c0 O ~
.2 M (~ O
r-t C N 'cNIn C
.G 0 N
H ~
m N
ua m am a +~
a.
m _ r~ v~ u~ ~n W Y Y S
w OJ N O
Z
~.
G
N
O N Ch C~
E
+~
~
~ a-~a~ a~
t C
+p ~.~
U ~n ~n ~n ,. "
PCTlJP96I00109 ' ~r ,~ ~ m o~ m n o R
m n m a~ o r1 ~-IN
a, N In c0 CO
ro N N V~
O cm n m m ~ o a o~ o o ,-i m m c~
+~
U ~ m vo 7 t~ O~ N tn b A
0 ~ m rt ,1 H
a 4 a~ O O N
ro O O ~ O
ro H +.~
ro N m o, m ~ N N V~
a CL o~ o, m m N
a ro c ro.
t -ZO U .O W u1 UI UJ
ro o x x x w a ro ro ro o .- ai a~ a~ m ~ 3 3 3 O
O c i~ N m C
+.~ N
;~ C
~ t +t.~ ~ k~ a~
-.Oi U ~ ~ O o U ~
3 . !
A
218~~4~
W0 96122704 PCTlJP96100109 As is apparent from the above tables, the discoloration was hardly observed in the product ofthe present-invention, in comparison with the control product 1_ That is, regarding the product of the present-invention, the brightness hardly changed and a stable color tone was. shown even after preservation at 5D °C for 4 weeks. To the contrary, regarding the control product 1, the brightness was decreased with time during preserving at 50 °C and the degree of red and yellow was increased. This means that the fact that browning proceeds with time is showed clearly with the numerical value.
Actually, regarding the product of the present invention, little discoloration was admitted by visual observation even after preservation at 5D °C for 4 weeks. To the contrary, regarding the control product 1, a remarkable discoloration has already been admitted after-2 weeks.
Further, regarding the control preparation containing no shell-calcined calcium and the control product 2, a remarkable discoloration which is almost the same as that-of the above control product 1 was admitted. Among them, the control product 2 tends to cause a weak degree of browning.
3. Change in organoleptic property (taste) in dissolution of preparation A standard sample which was preserved in a dark place at 4°C after preparation, and samples which were _ ~ WO 96122704 ~ ~ ~ PCTIJP96/00109 =17-obtained by preserving the standard samples at 37°C or 50°C
' for a predetermined time were used. The change in taste of each sample due to preservation was evaluated by asking three panelists to try each drink which was prepared by dissolving 62.5 g of each sample in 1 liter of cold water. Evaluation was carried out on the basis of the following five-level marks in comparison of the standard sample by the organoleptic test.
5 Marks: Not changed.
4 Marks: The flavor became faint, slightly, but the total unity of the taste was not changed.
3 Marks: The flavor became faint and the pleasant taste was disappeared.
2.Marks: The change in flavor and taste were clearly admitted and the nasty smell was also admitted.
I Mark: The flavor becomes inferior, drastically, and the nasty taste and smell (e. g. bitter taste, burnt smell, etc.) were admitted.
The results of the product of the present invention and control 1 are, shown in the following Table 4.
WO 96122704 ~ ~ ~ ~ ' ' PCTIJP96/00109 U
ro ~ x x x x n, a a a a a m m m m m a E E E E E
a N r1 .1 C'~N
+~
C
O
U
~, _ +~
C
U
O
C~
ro~
oC
ao a>
.r c N X Y
a . x ~' G
~ C
.R 0 E E E E E
m N
E ~ ~ c~7r7 cn V~
tC
H
ua ro o, a~
a~
x H
+~
GL
~
N
C
~ m ..
m x x x w N 0 41 c c a v 3 E
C
N
0 N f~7V' r1 N
E
,i TI
ro 2~ 2-~a~ ~' k~
.C
C
+~
~ 0 0 U3 ~
WO 96122704 ~ ~ ~ ~ '~ ~ ~ PCT/JP96100109 As is apparent from Table 4, regarding the product.
of the present invention, the change in taste did not become a problem, substantially, even after preservation at 50 °C for 2 weeks (37 °~, 2 months). To the contrary, regarding the control-.1, the taste has already changed after preservation at 37 °C for one month.. After-preservation at 5a °C for 2 weeks, an clear change in taste was admitted and an initial pleasant flavor was disappeared organoleptically. Therefore, a main flavor was replaced by a burnt smell by which the browning is accompanied, which results in flavor which is far different from that of a normal soft drink.
Further, regar=ding the control preparation containing no shell-calcined calcium and control 2, a clear change in taste could be observed, similar to the above control product 1.
4 Marks: The flavor became faint, slightly, but the total unity of the taste was not changed.
3 Marks: The flavor became faint and the pleasant taste was disappeared.
2.Marks: The change in flavor and taste were clearly admitted and the nasty smell was also admitted.
I Mark: The flavor becomes inferior, drastically, and the nasty taste and smell (e. g. bitter taste, burnt smell, etc.) were admitted.
The results of the product of the present invention and control 1 are, shown in the following Table 4.
WO 96122704 ~ ~ ~ ~ ' ' PCTIJP96/00109 U
ro ~ x x x x n, a a a a a m m m m m a E E E E E
a N r1 .1 C'~N
+~
C
O
U
~, _ +~
C
U
O
C~
ro~
oC
ao a>
.r c N X Y
a . x ~' G
~ C
.R 0 E E E E E
m N
E ~ ~ c~7r7 cn V~
tC
H
ua ro o, a~
a~
x H
+~
GL
~
N
C
~ m ..
m x x x w N 0 41 c c a v 3 E
C
N
0 N f~7V' r1 N
E
,i TI
ro 2~ 2-~a~ ~' k~
.C
C
+~
~ 0 0 U3 ~
WO 96122704 ~ ~ ~ ~ '~ ~ ~ PCT/JP96100109 As is apparent from Table 4, regarding the product.
of the present invention, the change in taste did not become a problem, substantially, even after preservation at 50 °C for 2 weeks (37 °~, 2 months). To the contrary, regarding the control-.1, the taste has already changed after preservation at 37 °C for one month.. After-preservation at 5a °C for 2 weeks, an clear change in taste was admitted and an initial pleasant flavor was disappeared organoleptically. Therefore, a main flavor was replaced by a burnt smell by which the browning is accompanied, which results in flavor which is far different from that of a normal soft drink.
Further, regar=ding the control preparation containing no shell-calcined calcium and control 2, a clear change in taste could be observed, similar to the above control product 1.
Claims (22)
1. A method for stabilizing and preserving a powdered soft drink preparation, which comprises adding 0.2 to 1.0% by weight of a calcium oxide and 0.02 to 2.0% by weight of a particulate silicon dioxide in the powdered soft drink preparation containing a carbohydrate and a sour agent as a main component, each amount being based on the total amount of the preparation.
2. The method according to claim 1, wherein the calcium oxide is selected from a chemically synthesized calcium oxide and a shell-calcined calcium derived from a natural product.
3. The method according to claim 1, wherein the particulate silicon dioxide has a three-dimensional amorphous structure.
4. The method according to claim 1, wherein an average particle size of the particulate silicon dioxide is not more than 15 µm.
5. A stabilized powdered soft drink preparation, comprising a carbohydrate and a sour agent as a main component, wherein 0.2 to 1.0% by weight of a calcium oxide and 0.02 to 2.0% by weight of a particulate silicon dioxide are added as a preservation stabilizer.
6. The powdered soft drink preparation according to claim 5, wherein the carbohydrate is added in a proportion of 65 to 95% by weight, based on the total amount of the powder.
7. A method for stabilizing and preserving a powdered soft drink preparation, comprising adding 0.2 to 0.5% by weight of a calcium oxide and 0.03 to 1.0% by weight of a particulate silicon dioxide to a powdered soft drink preparation containing a carbohydrate and a sour agent as a main component, each amount being based on the total amount of the preparation.
8. The method for stabilizing and preserving a powdered soft drink preparation according to claim 7, wherein the calcium oxide is selected from the group consisting of a chemically synthesized calcium oxide and a shell-calcined calcium derived from a natural product.
9. The method for stabilizing and preserving a powdered soft drink preparation according to claim 7, wherein the particulate silicon dioxide has a three-dimensional amorphous structure.
10. The method for stabilizing and preserving a powdered soft drink preparation according to claim 7, wherein an average particle size of the particulate silicon dioxide is not more than 15 µm.
11. The method for stabilizing and preserving a powdered soft drink preparation according to claim 7, wherein the carbohydrate is selected from the group consisting of monosaccharide and polysaccharide.
12. The method for stabilizing and preserving a powdered soft drink preparation according to claim 7, wherein the carbohydrate is selected from the group consisting of glucose, fructose, sucrose and maltose.
13. The method for stabilizing and preserving a powdered soft drink preparation according to claim 7, wherein the sour agent is an organic acid.
14. The method for stabilizing and preserving a powdered soft drink preparation as claimed in claim 13, wherein the organic acid is selected from the group consisting of citric acid, tartaric acid, fumaric acid, malic acid, lactic acid and ascorbic acid.
15. The method for stabilizing and preserving a powdered soft drink preparation according to claim 7, wherein the amount of calcium oxide added is 0.25% by weight and the amount of particulate silicon dioxide is 0.05% by weight.
16. A powdered soft drink preparation, comprising a carbohydrate and a sour agent as a main component, wherein 0.2 to 0.5% by weight of a calcium oxide and 0.03 to 1.0% by weight of a particulate silicon dioxide are added as a preservation stabilizer.
17. The powdered soft drink preparation according to claim 16, wherein the carbohydrate is added in a proportion of 65 to 95% by weight, based on the total amount of the powder.
18. The powdered soft drink preparation according to claim 16, wherein the carbohydrate is selected from the group consisting of monosaccharide and polysaccharide.
19. The powdered soft drink preparation according to claim 16, wherein the carbohydrate is selected from the group consisting of glucose, fructose, sucrose and maltose.
20. The powdered soft drink preparation according to claim 16, wherein the sour agent is an organic acid.
21. The powdered soft drink preparation according to claim 20, wherein the organic acid is selected from the group consisting of citric acid, tartaric acid, fumaric acid, malic acid, lactic acid and ascorbic acid.
22. The powdered soft drink preparation according to claim 16, wherein the amount of calcium oxide added is 0.25%
by weight and the amount of particulate silicon dioxide added is 0.05% by weight.
by weight and the amount of particulate silicon dioxide added is 0.05% by weight.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP02880495A JP3598389B2 (en) | 1995-01-24 | 1995-01-24 | Method for stable storage of powdered soft drink formulation and powdered soft drink formulation |
JP7/28804 | 1995-01-24 | ||
PCT/JP1996/000109 WO1996022704A1 (en) | 1995-01-24 | 1996-01-22 | Stable preservation method of powdered soft drink preparation and powdered soft drink preparation |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2185345A1 CA2185345A1 (en) | 1996-08-01 |
CA2185345C true CA2185345C (en) | 2006-10-03 |
Family
ID=37101736
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002185345A Expired - Lifetime CA2185345C (en) | 1995-01-24 | 1996-01-22 | Stable preservation method of powdered soft drink preparation and powdered soft drink preparation |
Country Status (1)
Country | Link |
---|---|
CA (1) | CA2185345C (en) |
-
1996
- 1996-01-22 CA CA002185345A patent/CA2185345C/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
CA2185345A1 (en) | 1996-08-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3082091A (en) | Effervescing composition in particle form | |
EP0751718B1 (en) | Stable preservation method of powdered soft drink preparation and powdered soft drink preparation | |
US5288510A (en) | Palatable low salt substitutes | |
CA1053965A (en) | Fortified gelatin dessert powder and process | |
US4716046A (en) | Pulverulent water-soluble nonhygroscopic composition for preparing beverages with a lasting effervescence and method for preparing the same | |
JP2688098B2 (en) | Method for treating lactoferrin-containing liquid | |
CA1287252C (en) | Pulverulent water-soluble non-hygroscopic composition for preparing beverages having a lasting effervescence and method for preparing same | |
CA2185345C (en) | Stable preservation method of powdered soft drink preparation and powdered soft drink preparation | |
US20080138425A1 (en) | Method for the Preparation of a Stable Lactate Metal Salt in Powder Form and Stable Metal Lactate Salt | |
JP2004033083A (en) | Method for producing dried green vegetable or dried herb and dried green vegetable and dried herb obtained by the method | |
AU691717C (en) | Stable preservation method of powdered soft drink preparation and powdered soft drink preparation | |
WO1995018546A1 (en) | Palatable low salt substitutes | |
US4339451A (en) | Flavor stabilized beet colorant composition | |
JP7228887B2 (en) | Quality Preserving Agent for Boiled Green Vegetables and Quality Preserving Method | |
EP3692806A1 (en) | A colored beverage having a neutral ph | |
US5888568A (en) | Limitation of browning | |
WO1996039048A1 (en) | Dry mix texture modified beverage using gellan gum | |
JP2019208504A (en) | Quality keeping agent for chlorophyll-containing food | |
JP2004180614A (en) | Freshness-retaining agent | |
JP3386722B2 (en) | Chlorophyll decomposition inhibitor, chlorophyll-containing food containing the chlorophyll decomposition inhibitor, and method for preventing fading of chlorophyll-containing food | |
JP3506134B2 (en) | Egg spread | |
JPS6258974A (en) | Preservative composition for food | |
JP7351515B2 (en) | Powder quality preservation agent and quality preservation method | |
JPH01132344A (en) | Food and drink | |
EP0785728A1 (en) | Palatable low salt substitutes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKEX | Expiry |
Effective date: 20160122 |