US20100285201A1 - Synergistic sweetening compositions - Google Patents
Synergistic sweetening compositions Download PDFInfo
- Publication number
- US20100285201A1 US20100285201A1 US12/810,554 US81055408A US2010285201A1 US 20100285201 A1 US20100285201 A1 US 20100285201A1 US 81055408 A US81055408 A US 81055408A US 2010285201 A1 US2010285201 A1 US 2010285201A1
- Authority
- US
- United States
- Prior art keywords
- stevia
- sucralose
- rebaudioside
- purified
- extract
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 45
- 230000002195 synergetic effect Effects 0.000 title claims description 8
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- 235000019408 sucralose Nutrition 0.000 claims abstract description 54
- 239000004376 Sucralose Substances 0.000 claims abstract description 52
- BAQAVOSOZGMPRM-QBMZZYIRSA-N sucralose Chemical compound O[C@@H]1[C@@H](O)[C@@H](Cl)[C@@H](CO)O[C@@H]1O[C@@]1(CCl)[C@@H](O)[C@H](O)[C@@H](CCl)O1 BAQAVOSOZGMPRM-QBMZZYIRSA-N 0.000 claims abstract description 52
- 239000000284 extract Substances 0.000 claims abstract description 40
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- HELXLJCILKEWJH-UHFFFAOYSA-N entered according to Sigma 01432 Natural products C1CC2C3(C)CCCC(C)(C(=O)OC4C(C(O)C(O)C(CO)O4)O)C3CCC2(C2)CC(=C)C21OC(C1OC2C(C(O)C(O)C(CO)O2)O)OC(CO)C(O)C1OC1OC(CO)C(O)C(O)C1O HELXLJCILKEWJH-UHFFFAOYSA-N 0.000 claims description 11
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- QSRAJVGDWKFOGU-WBXIDTKBSA-N rebaudioside c Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)[C@H](O)[C@@H](CO)O[C@H]1O[C@]1(CC[C@H]2[C@@]3(C)[C@@H]([C@](CCC3)(C)C(=O)O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O)CC3)C(=C)C[C@]23C1 QSRAJVGDWKFOGU-WBXIDTKBSA-N 0.000 claims description 6
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- GSFNWGKBQZDYCL-UHFFFAOYSA-N sodium 2-(3-hydroxy-5-sulfo-1H-indol-2-yl)-3-oxoindole-5-sulfonic acid Chemical compound [Na+].Oc1c([nH]c2ccc(cc12)S(O)(=O)=O)C1=Nc2ccc(cc2C1=O)S(O)(=O)=O GSFNWGKBQZDYCL-UHFFFAOYSA-N 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- QFVOYBUQQBFCRH-VQSWZGCSSA-N steviol Chemical compound C([C@@]1(O)C(=C)C[C@@]2(C1)CC1)C[C@H]2[C@@]2(C)[C@H]1[C@](C)(C(O)=O)CCC2 QFVOYBUQQBFCRH-VQSWZGCSSA-N 0.000 description 1
- 229940032084 steviol Drugs 0.000 description 1
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- 150000008144 steviol glycosides Chemical class 0.000 description 1
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- OHHNJQXIOPOJSC-UHFFFAOYSA-N stevioside Natural products CC1(CCCC2(C)C3(C)CCC4(CC3(CCC12C)CC4=C)OC5OC(CO)C(O)C(O)C5OC6OC(CO)C(O)C(O)C6O)C(=O)OC7OC(CO)C(O)C(O)C7O OHHNJQXIOPOJSC-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BAQAVOSOZGMPRM-UHFFFAOYSA-N sucralose Chemical compound OC1C(O)C(Cl)C(CO)OC1OC1(CCl)C(O)C(O)C(CCl)O1 BAQAVOSOZGMPRM-UHFFFAOYSA-N 0.000 description 1
- 235000012751 sunset yellow FCF Nutrition 0.000 description 1
- 239000004173 sunset yellow FCF Substances 0.000 description 1
- 235000019605 sweet taste sensations Nutrition 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 235000012756 tartrazine Nutrition 0.000 description 1
- 239000004149 tartrazine Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- GMMAPXRGRVJYJY-UHFFFAOYSA-J tetrasodium 4-acetamido-5-hydroxy-6-[[7-sulfonato-4-[(4-sulfonatophenyl)diazenyl]naphthalen-1-yl]diazenyl]naphthalene-1,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].OC1=C2C(NC(=O)C)=CC=C(S([O-])(=O)=O)C2=CC(S([O-])(=O)=O)=C1N=NC(C1=CC(=CC=C11)S([O-])(=O)=O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 GMMAPXRGRVJYJY-UHFFFAOYSA-J 0.000 description 1
- 239000000892 thaumatin Substances 0.000 description 1
- 235000010436 thaumatin Nutrition 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 description 1
- 235000013976 turmeric Nutrition 0.000 description 1
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- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
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- 239000001018 xanthene dye Substances 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
- A23L2/52—Adding ingredients
- A23L2/60—Sweeteners
-
- 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
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
- A23L27/33—Artificial sweetening agents containing sugars or derivatives
- A23L27/36—Terpene glycosides
-
- 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
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
- A23L27/33—Artificial sweetening agents containing sugars or derivatives
- A23L27/37—Halogenated sugars
-
- 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
Abstract
Description
- This application claims the benefit of priority from U.S. Provisional Patent Application No. 61/016,917, filed on Dec. 27, 2007, the content of which is incorporated by reference.
- 1. Field of the Invention
- The present invention relates to sweetening compositions. More particularly, the present invention relates to synergistic sweetening compositions that include sucralose and purified extracts of stevia.
- 2. Related Background Art
- High intensity sweeteners can provide the sweetness of sugar (although often with a slightly different taste), but because they are many times sweeter than sugar, only a small amount is needed to replace the sugar.
- One high intensity sweetener is sucralose (i.e., 4,1′,6′-trichloro-4,1′,6′-trideoxygalactosucrose), which is about 600 times as sweet as sugar. Another is stevia, which has glycosides that are about 100 to about 500 times sweeter than sucrose.
- When two or more components in a system produce a positive or negative effect above or below what is expected or predicted, there is synergy. That is, synergistic combinations of components produce results that are more effective or less effective than the predicted additive result for each component taken separately.
- The present invention is directed to sweetening compositions comprising sucralose and a purified extract of stevia.
- In one embodiment, the sweetening composition comprises sucralose and a purified extract of stevia selected from the group consisting of rebaudioside A, rebaudioside B, rebaudioside C, rebaudioside D, rebaudioside E, dulcoside A, dulcoside B, and combinations thereof.
- In another embodiment, the sweetening composition comprises sucralose and a purified extract of stevia wherein the sweetness contribution ratio of sucralose and the purified stevia extract is about 90:10 to about 10:90, respectively.
- The present invention also includes a method of making a food or beverage product comprising the step of (a) including sucralose and a purified extract of stevia.
- As used herein, the term “high intensity sweetener” means a substance that provides a high sweetness per unit mass compared to a nutritive sweetener and provides little or no nutritive value. Many high intensity sweeteners are known to those skilled in the art and any may be used in the present invention. Examples of high intensity sweeteners useful in the present invention include, for example, aspartame, acesulfame, alitame, brazzein, cyclamic acid, dihydrochalcones, extract of Dioscorophyllum cumminsii, extract of the fruit of Pentadiplandra brazzeana, glycyrrhizin, hernandulcin, monellin, mogroside, neotame, neohesperidin, saccharin, sucralose, extracts of sweet plants, such as stevia, thaumatin, salts, and combinations thereof.
- As used herein, unless otherwise indicated, the term “flavor” means any food-grade material that may be added to the present compositions to provide a desired flavor to a foodstuff. Non-limiting examples of flavors that may be useful in the present invention include, for example, cream, hazelnut, vanilla, chocolate, cinnamon, pecan, lemon, lime, raspberry, peach, mango, vanillin, butter, butterscotch, tea, orange, tangerine, caramel, strawberry, banana, grape, plum, cherry, blueberry, pineapple, elderberry, watermelon, bubblegum, cantaloupe, guava, kiwi, papaya, coconut, mint, spearmint, derivatives, and combinations thereof.
- As used herein, a gram (or other given amount) of Sucrose Equivalent Sweetness (“SES”) means the amount of high intensity sweetener needed to be added to an 8 ounce glass of water in order to provide the same sweetness as an independent 8 ounce glass of water containing one gram (or the other given amount) of sucrose. For example, 1/200 g of aspartame will equal about one gram of SES because aspartame is about 200 times sweeter than sucrose. Similarly, about 1/500 g to about 1/600 g of sucralose will provide one gram of SES because sucralose is about 500 to about 600 times sweeter than sucrose.
- The present invention is directed to a sweetening composition comprising sucralose and a purified extract of stevia.
- In one embodiment, the sucralose and purified extract of stevia are present in a sweetening combination ratio (sucralose:purified extract of stevia) of about 90:10 to about 10:90. Preferably, the sweetening combination ratio is about 80:20 to about 20:80, more preferably, about 70:30 to about 30:70.
- Sucralose, which is also known as 4,1,6′-trideoxy-galactosucrose, is a heat-stable, high-intensity sweetener that may be produced in accordance with the process disclosed in U.K. Patent No. 1,544,167, and U.S. Pat. Nos. 5,136,031 and 5,498,709, which are incorporated by reference herein.
- Stevia is a non-caloric natural sweetener from the plant Stevia rebaudiana bertoni. The plant makes a number of sweet compounds collectively referred to as steviol glycosides, which make stevia 300 times sweeter than sucrose. These glycosides can be extracted from the plant with water and other solvents well known to those skilled in the art. They are heat stable, pH stable, do not ferment, and do not induce a glycemic response.
- Stevioside, sometimes referred to as stevia, (13-[(2-O-β-D-glucopyranosyl)oxy]-kaur-16-en-18-oic acid-4α-β-D-glucopyranosyl ester) and rebaudioside A are exemplary glycosides of the diterpene derivative steviol, extracted and refined from Stevia rebaudiana bertoni (also known as eupatorium rebaudianum bertoni) leaves. These glycosides are high intensity sweeteners, about 100 to about 500 times that of sucrose, but have metallic and bitter notes. They can be used in a wide range of low or reduced calorie food products and beverages.
- Other sweet glycosides can also be extracted from Stevia rebaudiana. These have varying degrees of sweetness. As used herein “stevia extract” or “extracts of stevia” means a sweet glycoside extracted from a stevia plant. Stevia extracts include, for example, rebaudioside A, rebaudioside B, rebaudioside C, rebaudioside D, rebaudioside E, dulcoside A and dulcoside B. These extracts or combinations thereof are suitable for use in the inventive sweetening composition.
- Preferably, the extracts of stevia are purified to select or exclude extract or combinations of extracts. It is desirable that the purity of the extract be about 40-100% pure, preferably about 60-95% pure, and more preferably about 70-90% pure.
- In one preferred embodiment, the extract of stevia is rebaudioside A.
- For example, the synergistic composition may include rebaudioside A ranging from about 40% to about 100%. Preferably, from about 60% to about 95%.
- In an alternative embodiment, the extract of stevia has a low level of rebaudiosides and dulcosides. Preferably, less than about 50% of the stevia extract includes rebaudiosides and dulcosides. More preferably, less than about 40%, even more preferably, less than about 30%, still even more preferably, less than about 20%, still even more preferably, less than about 10%, still even more preferably, less than about 5%, still even more preferably, less than about 2%, and most preferably, less than about 1%.
- For example, the synergistic composition may have low rebaudiosides/dulcosides in a purity ranging from less than about 50%, or preferably, less than about 40%.
- Of the glycosides found in stevia extracts, rebaudioside A is known to have the least aftertaste. This aftertaste described by many as bitter and licorice like, which is present in all current stevia extracts.
- Optionally, a bulking agent may be included. Among those disclosed or used include fructooligosaccharide (FOS) and other fibers, maltodextrins, and erythritol. Erythritol is especially popular as it can mitigate some of the bitter taste.
- Studies performed showed that the combination of sucralose and a purified stevia extract produces a synergistic sweetening composition. That is, the present inventors have found that sweetening blends of sucralose and purified stevia extracts, produce synergistic sweetness results.
- Sucralose and purified extracts of stevia were combined in various blends. In one embodiment, sucralose and stevia RA90 (purified rebaudioside A, 90%) were blended together in the following sweetening ratios (sucralose:stevia RA90): 90:10; 80:20; and 30:70.
- The 90:10 and 80:20 synergy values were determined using bench top estimates for the SEV and 5.13% equisweet to sucrose values for sucralose (526.3 and 0.0095%) and A90 stevia (270 and 0.0211%).
- The 30:70 sucralose:RA90 stevia synergy trials exhibited a higher percentage of synergy (about 27.00%-28.68%) than the 90:10 (about 7.49%-8.43%) or 80:20 (about 9.13%-11.10%) sucralose: RA90 stevia synergy trials.
- The 90:10 ratio of sucralose:low RC and DA stevia exhibited no observed synergy resulting in an approximately equisweet rating to the sucralose control. The 30:70 ratio of sucralose:low RC and DA stevia resulted in about 24.167%-25.160% synergy. Thus, there may be synergy between other ratios of sucralose:low RC and DA stevia.
- Additionally, a variety of ingredients may be included in the sweetening composition of the present invention.
- Suitable “heat-stable, high-intensity sweeteners” include chemical compounds or mixtures of compounds which elicit a sweet taste at least five times sweeter than sucrose, as measured in accordance with the test method described in G.B. Patent No. 1,543,167, which is incorporated by reference herein. Typically such sweeteners are substantially free from degradants after being heated for about one hour at about 40° C. Examples of such suitable sweeteners include, but are not limited to, neotame, saccharin, acesulfame-K, cyclamate, neohesperdine DC, thavmatin, brazzein, aspartame, and mixtures thereof.
- High intensity sweeteners are well known alternatives to nutritive sweeteners. They provide sweetness without the calories and other metabolic impacts of the nutritive sweeteners. In many cases, high intensity sweeteners provide a sweet flavor that is preferred to nutritive sweeteners. Some high intensity sweeteners, such as, aspartame, are nutritive, but are so intense that they still provide negligible calories because very small amounts are required. Other high intensity sweeteners, such as, for example, sucralose, are not absorbed when ingested and are, therefore, non-nutritive sweeteners.
- Often the makers or users of these sweeteners add other components to them to overcome a less pleasant taste, e.g., a bitter taste. For example, cream of tartar may be added to saccharin to offset its bitterness; and 2,4-dihydroxybenzoic acid may be added to sucralose to control lingering sweetness.
- Another optional ingredient in the composition of the present invention is a soluble food ingredient. The soluble food ingredient may be, for example, a fructooligosaccharide (FOS), a digestion resistant maltodextrin (e.g., FiberSol), erythritol, inulin, a sugar polymer, or any combination thereof. Preferably, the soluble food ingredient is a fiber.
- Any coloring agent suitable for use in a food product may be used in the present invention and may include, but not be limited to azo dyes, quinopthalone dyes, triphenylmethane dyes, xanthene dyes, indigoid dyes, iron oxides, iron hydroxides, titanium dioxide, natural dyes, and mixtures thereof. More specifically, suitable colorants include, but are not limited to patent blue V, acid brilliant green BS, red 2G, azorubine, ponceau 4R, amaranth, D&C red 33, D&C red 22, D&C red 26, D&C red 28, D&C yellow 10, FD&C yellow 5, FD&C yellow 6, FD&C red 3, FD&C red 40, FD&C blue 1, FD&C blue 2, FD&C green 3, brilliant black BN, carbon black, iron oxide black, iron oxide red, iron oxide yellow, titanium dioxide, riboflavin, carotenes, antyhocyanines, turmeric, cochineal extract, clorophyllin, canthaxanthin, caramel, betanin, and mixtures thereof.
- Vitamins and minerals may also be present.
- The compositions can contain other components, including flavor, aroma, other nutritional component, binders, and mixtures thereof.
- Synergistic compositions of the present invention can be made by any method known to those skilled in the art that provide homogenous even or homogeneous mixtures of the ingredients. These methods include dry blending, spray drying, agglomeration, wet granulation, compaction, co-crystallization and the like.
- The following examples are provided to further illustrate the compositions and methods of the present invention. These examples are illustrative only and are not intended to limit the scope of the invention in any way.
- The materials used in the Examples include:
- Sucrose Domino granulated sugar
-
-
- Tate & Lyle
RA90 Purified rebaudioside A, 90% - Commercial source
Low R/D Low rebaudioside and dulcoside extract - Commercial source
Water Crystal Rock, purified bottle water, pH 6.3
- Tate & Lyle
- Samples were prepared as follows:
- All sweetener samples were prepared as solutions with purified water (Crystal Rock bottled water at pH 6.3). Sweeteners and combinations were weighed out individually using a four-place scale (0.1 mg scale). The weighed sweetener was deposited into its respective beaker of stirring water one at a time. The solution was allowed to stir for five minutes at ambient temperature to ensure complete dissolution. Then, one drop of blue food coloring was added to each sweetener bulk solution and stirred for two minutes to assure that all sweetener solutions were homogeneous and uniform in appearance.
- Sensory evaluation was performed as follows:
- A 5% solution of sucrose (Domino granulated sugar) was used as the standard control. The concentrations of sucralose and purified rebaudioside, which were equisweet to the standard sucrose control solution, were measured by trained sensory panels using the constant stimulus paired comparison method (Principles of Sensory Evaluation of Food, Academic Press, New York).
- The approximate sucrose equivalency value (SEV) and 5% equisweet to sucrose percentages for sucralose and rebaudioside were determined by bench top evaluation and confirmation with 15 trained panelists by a series of 4-6 concentrations of sweetness intensity for each sweetener so that the mid-concentration was approximately the same sweetness as the sucrose or sucralose SEV control. Coded samples were served at room temperature (20-22° C.) to panelists in pairs according to the methodology for a paired difference test. One pair was the test solution and the other pair was the sucrose control or the constant stimulus. Panelists were instructed to taste the samples in the order provided, rising between samples. Panelists would then circle the number assigned to the sample he or she found to be the sweeter sample. The results were subjected to equisweetness determination by plotting concentration versus percentage of panelists choosing the blend as sweeter than the sucrose control. SEV, the concentration at which 50% of the panelists indicated the test sweetener sample to be sweeter than the control sample was calculated. The resulting SEVs were:
-
Sweetener Intensity SEV %, 5% sucrose Sucrose 1 5 Sucralose 540 0.0093 Rebaudioside A 220 0.0227 Low rebaudioside and 145 0.0345 dulcoside extract - Synergy Determination:
- Synergy was measured by determining the concentration of the sweetener combination having the same level of sweetness as the sucrose control (see table below; see also U.S. Pat. No. 5,380,541).
-
Gram sweetener Sweetener or blend per unit volume Concentration of sweetener A required to A provide the sweetness of the standard control Concentration of sweetener B required to B provide the sweetness of the standard control Concentration of sweeteners in the blend to A′ + B′ provide the sweetness of the standard control Sweetness contribution in blend from A′/A × 100 = A% sweetener A Sweetness contribution in blend from B′/B × 100 = B% sweetener B % Synergy = 100 − (A′ + B′) - A 5% sucrose equivalency value (SEV) sensory test was conducted with a sweetening composition of sucralose and purified rebaudioside A (RA90). The weight ratio of sucralose to RA90 was 90:10.
- Synergy testing results were as follows:
-
Sucralose RA90 concentration, concentration, Number of Test sample g/1000 mL g/1000 mL panelists % Synergy Control, 5% 0.095 0.0 sugar SEV 90:10 C 0.0846 0.0094 30 6.49 90:10 D, 5% 0.0837 0.0093 30 7.49 sugar SEV 90:10 E 0.0828 0.0092 30 8.48 - A 5% SEV sensory test was conducted with a sweetening composition of sucralose and RA90. The weight ratio of sucralose to RA90 was 80:20.
- Synergy testing results were as follows:
-
Sucralose RA90 concentration, concentration, Number of Test sample g/1000 mL g/1000 mL panelists % Synergy Control, 5% 0.095 0.0 sugar SEV 80:20, 5% 0.0776 0.0194 30 9.13 sugar SEV - A 5% SEV sensory test was conducted with a sweetening composition of sucralose and RA90. The weight ratio of sucralose to RA90 was 30:70.
- Synergy testing results were as follows:
-
Sucralose RA90 concentration, concentration, Number of Test sample g/1000 mL g/1000 mL panelists % Synergy Control, 5% 0.095 0.0 sugar SEV 30:70, 5% 0.0347 0.0809 30 27.0 sugar SEV - 5% SEV sensory testing was performed using sweetening compositions of sucralose and low rebaudioside/dulcoside (low RD) blends. The weight ratio of sucralose to low RD is shown in the table below.
- Synergy testing results were as follows:
-
Sucralose Low RD concentration, concentration, Number of Test sample g/1000 mL g/1000 mL panelists % Synergy Control, 5% 0.0923 0.0 sugar SEV 90:10, 5% 0.0899 0.010 30 0.0 sugar SEV 30:70, 5% 0.0427 0.0996 30 25.0 sugar SEV - While the invention has been described above with reference to specific embodiments thereof, it is apparent that many changes, modifications, and variations can be made without departing from the inventive concept disclosed herein. Accordingly, it is intended to embrace all such changes, modifications, and variations that fall within the spirit and broad scope of the appended claims. All patent applications, patents, and other publications cited herein are incorporated by reference in their entirety.
Claims (13)
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- 2008-12-19 CA CA2710629A patent/CA2710629C/en active Active
- 2008-12-19 AU AU2008343039A patent/AU2008343039B2/en not_active Ceased
- 2008-12-19 WO PCT/US2008/087588 patent/WO2009086049A2/en active Application Filing
- 2008-12-19 EP EP08867306.6A patent/EP2230939B1/en active Active
- 2008-12-19 US US12/810,554 patent/US20100285201A1/en not_active Abandoned
- 2008-12-19 NZ NZ586358A patent/NZ586358A/en unknown
-
2017
- 2017-05-26 US US15/606,245 patent/US11311034B2/en active Active
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US9492379B2 (en) * | 2009-06-25 | 2016-11-15 | Chabio & Diostech Co., Ltd. | Quickly soluble oral film dosage containing steviosides as a unpleasant taste masking agent |
US20130039932A1 (en) * | 2009-06-25 | 2013-02-14 | Chabio & Diostech Co., Ltd. | Quickly soluble oral film dosage containing steviosides as a unpleasant taste masking agent |
US20130309389A1 (en) * | 2010-12-13 | 2013-11-21 | Cargill, Incorporated | Glycoside blends |
EP3311677A1 (en) | 2011-02-10 | 2018-04-25 | Purecircle USA | Stevia composition |
EP3915394A1 (en) * | 2011-06-20 | 2021-12-01 | PureCircle USA Inc. | Stevia composition |
WO2012177727A1 (en) | 2011-06-20 | 2012-12-27 | Purecircle Usa Inc. | Stevia composition |
EP2720561A4 (en) * | 2011-06-20 | 2015-04-08 | Purecircle Usa Inc | Stevia composition |
EP3473108A1 (en) * | 2011-06-20 | 2019-04-24 | PureCircle USA Inc. | Stevia composition |
US11737480B2 (en) | 2012-02-15 | 2023-08-29 | Kraft Foods Group Brands Llc | Compositions and methods for inhibiting precipitation of dyes in a beverage |
US10687547B2 (en) | 2012-02-15 | 2020-06-23 | Kraft Foods Group Brands Llc | Compositions and methods for inhibiting precipitation of dyes in a beverage |
US11013248B2 (en) | 2012-05-25 | 2021-05-25 | Kraft Foods Group Brands Llc | Shelf stable, concentrated, liquid flavorings and methods of preparing beverages with the concentrated liquid flavorings |
US20150181919A1 (en) * | 2012-07-09 | 2015-07-02 | Kirin Beverage Company, Limited | Bottled drink containing indigestible dextrin and method for producing the same |
US10568345B2 (en) * | 2012-07-09 | 2020-02-25 | Kirin Beverage Company, Limited | Bottled drink containing indigestible dextrin and method for producing the same |
WO2015126876A1 (en) | 2014-02-18 | 2015-08-27 | Mcneil Nutritionals, Llc. | Process for separation, isolation and characterization of steviol glycosides |
US11306114B2 (en) | 2014-02-18 | 2022-04-19 | Heartland Consumer Products Llc | Process for separation, isolation and characterization of steviol glycosides |
US11399558B2 (en) | 2015-03-03 | 2022-08-02 | Heartland Consumer Products Llc | Rebaudioside-D containing sweetener compositions |
CN109414050A (en) * | 2016-06-30 | 2019-03-01 | 弗门尼舍有限公司 | Food and beverage product through seasoning |
CN110475484A (en) * | 2016-12-01 | 2019-11-19 | 谱赛科美国股份有限公司 | Stevia plant and application thereof |
US11653606B2 (en) | 2016-12-01 | 2023-05-23 | Purecircle Usa Inc. | Stevia plant and uses thereof |
WO2018102648A1 (en) * | 2016-12-01 | 2018-06-07 | Purecircle Usa Inc. | Stevia plant and uses thereof |
US11898184B2 (en) | 2017-09-07 | 2024-02-13 | Sweet Sense Inc. | Low glycemic sugar composition |
Also Published As
Publication number | Publication date |
---|---|
EP2230939A2 (en) | 2010-09-29 |
CA2710629A1 (en) | 2009-07-09 |
CA2710629C (en) | 2016-06-21 |
EP2230939B1 (en) | 2020-04-08 |
WO2009086049A2 (en) | 2009-07-09 |
AU2008343039B2 (en) | 2014-04-24 |
WO2009086049A3 (en) | 2010-01-28 |
US20170258115A1 (en) | 2017-09-14 |
US11311034B2 (en) | 2022-04-26 |
AU2008343039A1 (en) | 2009-07-09 |
NZ586358A (en) | 2013-04-26 |
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