WO2001028357A2 - Sugar substitutes - Google Patents
Sugar substitutes Download PDFInfo
- Publication number
- WO2001028357A2 WO2001028357A2 PCT/US2000/028557 US0028557W WO0128357A2 WO 2001028357 A2 WO2001028357 A2 WO 2001028357A2 US 0028557 W US0028557 W US 0028557W WO 0128357 A2 WO0128357 A2 WO 0128357A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- sweetener
- sucrose
- sweeteners
- food product
- 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.)
- Ceased
Links
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/60—Salad dressings; Mayonnaise; Ketchup
-
- A—HUMAN NECESSITIES
- A21—BAKING; EDIBLE DOUGHS
- A21D—TREATMENT OF FLOUR OR DOUGH FOR BAKING, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS
- A21D13/00—Finished or partly finished bakery products
- A21D13/80—Pastry not otherwise provided for elsewhere, e.g. cakes, biscuits or cookies
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- 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
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- 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 OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- 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
- A23L27/38—L-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
Definitions
- This invention relates to compositions and methods for making ingestible sugar substitutes, and more particularly, relates to sugar substitutes having unique and desirable properties.
- Sugar is one of the leading additives in prepared foods. Sugar not only acts as a sweetener, but it plays many additional roles in processed foods. Sugar may act as a texturizing or tenderizing agent in baked goods such as cakes and cookies. Because sugar possesses the ability to bind water, it can aid in retarding spoilage of products such as jams and syrups. Sugars can provide a variety of desired textures to candies, from crystalline, as in fudge, to non-crystalline, as in caramels. Sugars are also useful for enhancing flavors and preserving cured meats, as well as providing food for fermenting microorganisms in the preparation of breads, pickles, and alcoholic beverages. Of great importance, is the use of sugar to provide bulk in recipes.
- “Sugar” is a broad term for carbohydrates that vary in degree of sweetness.
- Carbohydrates, or saccharides are polyhydroxy aldehydes or ketones, most having the general empirical formula (CH O) n .
- Families of carbohydrates are distinguished by the number of carbon atoms in the basic molecule, and the stereochemical configuration of the hydrogen and oxygen atoms within the molecule.
- Carbohydrates are classified into three main groups: monosaccharides, disaccharides, and polysaccharides.
- Glucose (dextrose), fructose (levulose) and galactose are examples of hexoses, one form of monosaccharide.
- Disaccharides are made up of combinations of two monosaccharides and include sucrose (table sugar), maltose and lactose.
- Polysaccharides are also known as complex carbohydrates and are made up of multiple monosaccharides. They may be linear or branched. Examples include starches, fiber and glycogen.
- Sugar alcohols are hydrogenation products of sugars and are also used as sweeteners in prepared foods. Common sugar alcohols include sorbitol, mannitol, lactitol and xylitol.
- Insulin dependent diabetes mellitus is a chronic condition resulting from the absolute or relative absence of the endocrine hormone insulin. Under these conditions, the body is unable to maintain normal control of carbohydrate metabolism.
- the traditional treatment for patients with diabetes has included prohibition of dietary sucrose. Dietary sugar is also the major factor leading to dental caries.
- Dental caries is a pathological process of localized destruction of tooth tissues by microorganisms, which can be greatly reduced by elimination of sucrose.
- Another condition, obesity is known to increase the risk of developing diabetes mellitus and hypertension and can lead to mortality.
- Gallbladder disease, degenerative joint disease and atherosclerosis have also been linked to obesity.
- High glycemic sugars are also associated with problems in immune function. Cancer cells thrive on high glycemic sugars, which can also disrupt the Krebs Cycle and suppress antibody function. High glycemic sugars are also associated with the depletion of B-vitamins and the neurotransmitter dopamine. Because of the conditions associated with traditional carbohydrate sweeteners, manufacturers have routinely begun to experiment with the use of many different kinds of alternate sweeteners in prepared foods. A number of intense, non-caloric sweeteners have begun to replace the traditional carbohydrate sweeteners. Examples of those having already received regulatory approval in the United States include, saccharin, aspartame and acesulfame potassium. Each compound has particular drawbacks.
- Aspartame is currently the most widely used, however, it is often unstable under conditions of prolonged heat and may break down to diketopiperazine. Saccharin has been widely studied and has been found to be a carcinogen in animals and a potential carcinogen in humans. Acesulfame potassium has been approved only for specific limited uses. Other intense sweeteners are also being investigated for potential use as sugar substitutes. Among those are cyclamate, alitame, and neotame. As a class, intense sweeteners routinely have inferior flavor, such as bitter, metallic and persistent sensations. Many of them are acid or heat labile, or are otherwise unstable.
- the sweetener could be formulated for use in recipes calling for sucrose while requiring little or no adaptation.
- the ideal sweetener should be similar in sweetness to sucrose, with an untainted taste, and without delayed onset or persistence of sweetness.
- the ideal sweetener would have properties similar to those of sucrose, including the ability, among other things, to caramelize, tenderize, preserve, viscosity, brown and remain stable when heated.
- sweeteners of the present invention may be used directly in place of sucrose in existing recipes with few, if any, alterations.
- the sweeteners are non- or low-caloric and non-cariogenic. They provide exceptionally improved taste and consistency results.
- compositions provide for a sweetening component that imparts certain reactive functions and characteristics that are possessed by the traditional carbohydrate sweeteners, but not by the intense sweeteners. Those characteristics include, but are not limited to, preservative effects, stabilization, use as a carrier, acceptable mouth feel, and Maillard (browning) reaction. Other characteristics include use in bulking, thickening, viscosifying, caramelizing and caking. Also included, are the important characteristics of intensity, duration and quality of sweetness.
- compositions employ particular combinations of an intense sweetener and a traditional bulk sweetener chosen such that the resulting sweetener may be used as a direct substitute for sucrose, having an indistinguishable taste as well as possessing the same reactive properties, thereby enabling direct substitution into existing recipes calling for sucrose.
- Lo Han Kuo (also known as Luo Han Guo, or rakanka) is the fruit from the plant Momordica grosvenori (also known as Thladiantha grosvenori, Siraitia grosvenorii, or Cucurbitaceae fruit), native to southern China. The fruits have traditionally been used by the Chinese in household remedies for colds, sore throats, stomach problems, and the like. Used by itself, Lo Han Kuo can possess a licorice-like aftertaste, similar to that of stevioside, although much more mild. Lo Han Kuo (HerbaSway, Wallingford, CT) is naturally derived and is several hundred times sweeter than sucrose. It has been determined to contain a trite ⁇ enoid moiety and several glucose units.
- the dried Lo Han Kuo fruit may be used whole, as extracts, or in powdered or block form.
- Lo Han Kuo is most preferred because of its superior flavor and because it is naturally derived
- other trite ⁇ ene derivatives from plants may be employed.
- Examplary plants include, but are not limited to S. africana, S. borneensis, S. siamensis, S. sikkimensis, S. silomaradjae, and S. taiwaniana.
- Licorice derivatives from Glycyrrhiza glabra, G. hersuta, and G.uralensi may also be useful, as is hernandulcin, a sesquite ⁇ ene derived from
- Compounds containing dite ⁇ ene glycosides may also be used as the intense sweetener. Such compounds may be derived, for example, from the leaves ofStevia rebaudiana, and include steviolbioside, stevioside, rebaudioside (types A, B, C, D, and E), and dulcoside. Other dite ⁇ ene glycosides include steviolmonoside and ruboside, for example.
- Additional compounds which may be inco ⁇ orated into the compositions of the present invention include, but are not limited to proteins such as thaumatin derived from the fruit of Thaumatococcus daniellii, monellin derived from the fruit of Dioscoreophyllum cumminsii, brazzein derived from Peneadiplandra brazzeana, mabinlin derived from Capparis masaikai, as well as other plant extracts such as kiwi (Trutina Dulcem). Other high intensity sweeteners may also be employed. Most preferred for superior taste are sucralose (Johnson & Johnson, New Brunswick, NJ) and neotame (Monsanto, St. Louis, MO).
- the amount of the high intensity sweetener will vary depending upon the relative sweetness that it possesses. Based upon the values known for each compound, any person having ordinary skill in the art could easily make adjustments so that the resulting composition is nearly identical in taste to sucrose. Naturally derived sweeteners are most preferred.
- Bulk sweeteners useful for the present invention include carbohydrates, such as mono-, di- and polysaccharides. Most preferred is rhamnose (Maypro Industries, Purchase, NY) because it is non-caloric. However, trehalose (Hayashibara U.S.A., Inc., Amarillo, TX) is also preferred because it can be used in proportions that allow for direct substitution of the final product for sugar. These carbohydrates possess exceptionally clean taste, heat stability, and ability to directly replace sugar in recipes without reformulation.
- Other carbohydrates include, but are not limited to inulin, maltose, glucose, galactose, mannose, fructose, dextrose, neosugar and sugar alcohols, including, for example, erythritol, mannitol, sorbitol and xylitol.
- the carbohydrates may be either naturally or synthetically derived. However, not all of the carbohydrates possess the range of reactive qualities found in sucrose, rhamnose, and trehalose. The appropriate amounts of the bulking agents will result in a final composition that may be used exactly as sucrose would be used. Any person having ordinary skill in the art can easily determine the appropriate amounts.
- sweeteners that may be used instead of, or in addition to, the aforementioned high intensity sweeteners include nitroanilines, trihalogenated benzamides, amino acids, dipeptides (ie., aspartame), dihydrochalcones, flavonoids, isocoumarins (ie., amacha, phyllodulcin), sulfamates (ie., sodium cyclamate), oximes, saccharins, acesulfames, urea derivatives (ie., dulcin), sesquite ⁇ enes (ie., hernadulcin), and steroid saponins.
- the appropriate amounts of each particular compound can be determined according to the desired sweetness properties of the remaining ingredients used for the resulting composition. These values may easily be determined by any person having ordinary skill in the art.
- the sweeteners of the invention may be used in edible products intended to be consumed and digested, as well as in products such as chewing gums, chewing compositions, smoking compositions, and oral hygiene compositions, which may or may not be swallowed.
- the edible product may be a food (including a pet or avian food), a beverage or a pharmaceutical product.
- the products may or may not have a nutritional value.
- Chewing gums may include, but are not limited to chicle or substitutes therefore, jetulong, guttakay rubber, or other natural or synthetic resins or waxes.
- Chewing compositions may include, but are not limited to chewing tobacco, smokeless tobacco, snuff, and other compositions which are generally masticated and periodically expectorated.
- Smoking compositions may include, but are not limited to all types of cigarette, cigar and pipe tobacco, including tobacco substitutes.
- Oral hygiene compositions may include, but are not limited to mouthwashes, mouth rinses, toothpastes, tooth whiteners and bleaches, tooth polishes, dentifrices, mouth sprays and mouth refreshers.
- Food materials may include, but are not limited to confections, candies, icings, puddings, custards, baked goods, batters, frozen foods, cereals, vegetables, fruits, spices, condiments, soups, stews, sauces, cocoa products, chocolate products, animal feed and the like.
- Beverages may include, but are not limited to coffees, teas, herbal teas, carbonated and non-carbonated types, dairy products, fruit drinks, beers, lagers, pilsners, ales, stouts, wines, champagnes and the like.
- Pharmaceutical products may include, but are not limited to solids, gases and liquids including cough syrups, cough drops, medicinal sprays, vitamins, lozenges, herbal remedies and the like.
- additives may be useful and will be apparent to any person having average skill within the art. These may include, for example, flavorings, colorings, natural and/or artificial preservatives, vitamins, minerals and excipients such as corn starch, silica, or oils, for example.
- VTP vinegar toner powder
- VTP is su ⁇ risingly useful for mitigating the slightly bitter taste associated with the carbohydrates that are less sweet than sucrose. It also helps to eliminate the slight licorice aftertaste associated with some of the intense sweeteners. Finally, it helps to merge the flavor of the two types of sweetener and make the resulting composition very similar to sucrose.
- masking compounds exist, such as miraculin, curculin, artichoke extract, apple extract, kiwi extract and blue agava , that are not used as sweeteners per se, but used similarly to vinegar toner powder in order to alter the perceived taste of certain foods so that they seem sweeter or less bitter.
- Miraculin is the fruit of the shrub Synsepalum dulcificum.
- Curculin is derived from Curculigo latifolia.
- Blue agava is extracted from the plant Agave Tequilana weber and is routinely used in the production of tequila beverages.
- the masking agents may optionally be included with the high intensity sweetener and bulking agent combination as needed. For example, compositions prepared with neotame or sucralose may require little to none of the masking agent as compared to those compositions prepared with Lo Han Kuo.
- compositions of the present invention may be used in place of sucrose in recipes. Additionally, the composition may be placed in a blender in order to produce powdered sugar. If the bulk sweetener is more crystalline than the intense sweetener, it can be treated in a blender before combining such that the two sweeteners are similar in texture, which prevents settling and separation after blending.
- the compositions may also be prepared as a liquid and may include optional preservatives.
- a substitute for sucrose was prepared as follows:
- a substitute for sucrose was prepared as follows:
- a substitute for sucrose was prepared as follows:
- a substitute for sucrose was prepared as follows:
- the butter was cut into V2 inch pieces.
- all base ingredients were processed until the mixture began to form small lumps.
- the mixture was sprinkled into a 13"x9"x2" baking pan and was pressed evenly onto the bottom with a metal spatula.
- the pan was placed in the center of the oven and baked at 350°F for about 20 minutes, during which time the topping was prepared as follows.
- the eggs and sugar were combined in a bowl and whisked until mixed well.
- the lemon juice, zest and flour were added.
- This mixture was poured over the hot base when it was done baking.
- the pan was returned to the oven, with the oven temperature reduced to 300°F, and baked in the middle of the oven until set (about 30 minutes). After baking, the pan was cooled completely and the remaining finale of substitute sugar was sprinkled on top of the baked lemon bars.
- the butter, sugar substitute and cornstarch were placed in a mixing bowl and whipped with a wire whisk until blended. Then the egg yolks were added and whisked until blended, but not beaten. The chocolate mixture was added and also blended.
- the batter was poured into the prepared pan, and was shaken slightly to settle the batter.
- the pan was placed in the center of the oven and baked at 350°F for 15 minutes.
- the oven heat was turned off and the oven door was left slightly open so as to allow the cake to cool for 10 minutes. 6.
- the cake was then removed from the oven and placed on a wire rack to cool.
- Cornmeal waffles were prepared as follows:
- Poppy Seed Dressing was prepared as follows: l cup sugar substitute as prepared in Example 2 V ⁇ TBS dry Dijon mustard
- a date shake was prepared as follows:
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Seasonings (AREA)
Abstract
Description
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU10889/01A AU1088901A (en) | 1999-10-15 | 2000-10-13 | Sugar substitutes |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41845299A | 1999-10-15 | 1999-10-15 | |
| US41912399A | 1999-10-15 | 1999-10-15 | |
| US09/418,452 | 1999-10-15 | ||
| US09/419,123 | 1999-10-15 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2001028357A2 true WO2001028357A2 (en) | 2001-04-26 |
| WO2001028357A3 WO2001028357A3 (en) | 2002-01-24 |
Family
ID=27024140
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2000/028557 Ceased WO2001028357A2 (en) | 1999-10-15 | 2000-10-13 | Sugar substitutes |
Country Status (2)
| Country | Link |
|---|---|
| AU (1) | AU1088901A (en) |
| WO (1) | WO2001028357A2 (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002087359A1 (en) * | 2001-04-27 | 2002-11-07 | Pepsico, Inc. | Use of erythritol and d-tagatose in diet or reduced-calorie beverages and food products |
| WO2002087358A1 (en) | 2001-05-01 | 2002-11-07 | Pepsico, Inc. | Use of erythritol and d-tagatose in zero- or low-calorie beverages and food products |
| WO2006128493A1 (en) * | 2005-05-27 | 2006-12-07 | Südzucker Aktiengesellschaft Mannheim/Ochsenfurt | Isomaltulose as an aftertaste-reducing agent |
| WO2007061898A1 (en) | 2005-11-23 | 2007-05-31 | The Coca-Cola Company | Baked goods comprising high-potency sweetener |
| WO2007061797A3 (en) * | 2005-11-23 | 2007-07-12 | Coca Cola Co | Condiments with high-potency sweetener |
| WO2007061753A3 (en) * | 2005-11-23 | 2008-01-10 | Coca Cola Co | High-potency sweetener composition with glucosamine and compositions sweetened therewith |
| WO2007061872A3 (en) * | 2005-11-23 | 2008-02-21 | Coca Cola Co | High potency sweetener composition with saponin and compositions sweetened therewith |
| WO2007061907A3 (en) * | 2005-11-23 | 2008-03-06 | Coca Cola Co | High-potency sweetener composition for treatment and/or prevention of autoimmune disorders and compositions sweetened therewith |
| EP1791442A4 (en) * | 2004-07-30 | 2008-05-07 | Pharmed Medicare Pty Ltd | Reduced calorie sweetener composition |
| WO2007081442A3 (en) * | 2005-11-23 | 2008-05-08 | Coca Cola Co | Synthetic sweetener compositions with improved temporal profile and/or flavor profile, methods for their formulation, and uses |
| CN101312653A (en) * | 2005-11-23 | 2008-11-26 | 可口可乐公司 | Baked food containing high-potency sweetener |
| EP1835818A4 (en) * | 2004-12-09 | 2009-01-07 | Eurark Llc | PRODUCT AND METHOD FOR ORAL ADMINISTRATION OF UTILITY |
| CN102018016A (en) * | 2010-12-27 | 2011-04-20 | 暨南大学 | Cake containing neotame and preparation method thereof |
| AU2007221796B2 (en) * | 2006-10-03 | 2012-08-09 | Pepsico, Inc. | Use of erythritol and d-tagatose in diet or reduced-calorie beverages and food products |
| US8465786B2 (en) | 2001-04-20 | 2013-06-18 | The Coca-Cola Company | Non caloric frozen carbonated beverage |
| US8993027B2 (en) | 2005-11-23 | 2015-03-31 | The Coca-Cola Company | Natural high-potency tabletop sweetener compositions with improved temporal and/or flavor profile, methods for their formulation, and uses |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3898323A (en) * | 1970-04-15 | 1975-08-05 | Mirlin Corp | Taste modifying composition |
| US5433965A (en) * | 1993-02-16 | 1995-07-18 | The Procter & Gamble Company | Beverage compositions and sweetening compositions which contain juice derived from botanical subfamily Cucurbitaceae |
| DE4416429A1 (en) * | 1994-05-10 | 1995-11-16 | Hoechst Ag | Sweetener with an improved sucrose-like taste and process for its production and use |
| AU3968697A (en) * | 1996-07-26 | 1998-02-20 | Kristine A. Bateman | Dietetic one-to-one sugar substitute composition for table top, baking and cooking applications |
| US6103240A (en) * | 1999-02-05 | 2000-08-15 | Zhou; James H. | Herbal sweetening and preservative composition comprising licorice extract and mogrosides obtained from plants belonging to cucurbitaceae and/or momordica |
-
2000
- 2000-10-13 WO PCT/US2000/028557 patent/WO2001028357A2/en not_active Ceased
- 2000-10-13 AU AU10889/01A patent/AU1088901A/en not_active Abandoned
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8465786B2 (en) | 2001-04-20 | 2013-06-18 | The Coca-Cola Company | Non caloric frozen carbonated beverage |
| WO2002087359A1 (en) * | 2001-04-27 | 2002-11-07 | Pepsico, Inc. | Use of erythritol and d-tagatose in diet or reduced-calorie beverages and food products |
| WO2002087358A1 (en) | 2001-05-01 | 2002-11-07 | Pepsico, Inc. | Use of erythritol and d-tagatose in zero- or low-calorie beverages and food products |
| EP1791442A4 (en) * | 2004-07-30 | 2008-05-07 | Pharmed Medicare Pty Ltd | Reduced calorie sweetener composition |
| EP1835818A4 (en) * | 2004-12-09 | 2009-01-07 | Eurark Llc | PRODUCT AND METHOD FOR ORAL ADMINISTRATION OF UTILITY |
| WO2006128493A1 (en) * | 2005-05-27 | 2006-12-07 | Südzucker Aktiengesellschaft Mannheim/Ochsenfurt | Isomaltulose as an aftertaste-reducing agent |
| CN101312653A (en) * | 2005-11-23 | 2008-11-26 | 可口可乐公司 | Baked food containing high-potency sweetener |
| WO2007061898A1 (en) | 2005-11-23 | 2007-05-31 | The Coca-Cola Company | Baked goods comprising high-potency sweetener |
| WO2007061872A3 (en) * | 2005-11-23 | 2008-02-21 | Coca Cola Co | High potency sweetener composition with saponin and compositions sweetened therewith |
| WO2007081442A3 (en) * | 2005-11-23 | 2008-05-08 | Coca Cola Co | Synthetic sweetener compositions with improved temporal profile and/or flavor profile, methods for their formulation, and uses |
| WO2007061753A3 (en) * | 2005-11-23 | 2008-01-10 | Coca Cola Co | High-potency sweetener composition with glucosamine and compositions sweetened therewith |
| WO2007061797A3 (en) * | 2005-11-23 | 2007-07-12 | Coca Cola Co | Condiments with high-potency sweetener |
| US8993027B2 (en) | 2005-11-23 | 2015-03-31 | The Coca-Cola Company | Natural high-potency tabletop sweetener compositions with improved temporal and/or flavor profile, methods for their formulation, and uses |
| US8956677B2 (en) | 2005-11-23 | 2015-02-17 | The Coca-Cola Company | High-potency sweetener composition with glucosamine and compositions sweetened therewith |
| US8940351B2 (en) | 2005-11-23 | 2015-01-27 | The Coca-Cola Company | Baked goods comprising high-potency sweetener |
| CN101312653B (en) * | 2005-11-23 | 2013-04-24 | 可口可乐公司 | Baked goods with high-potency sweeteners |
| WO2007061907A3 (en) * | 2005-11-23 | 2008-03-06 | Coca Cola Co | High-potency sweetener composition for treatment and/or prevention of autoimmune disorders and compositions sweetened therewith |
| CN103210971A (en) * | 2005-11-23 | 2013-07-24 | 可口可乐公司 | Baked goods comprising high-potency sweetener |
| EP2644040A1 (en) * | 2005-11-23 | 2013-10-02 | The Coca-Cola Company | Condiments with rebaudioside A and erythritol |
| AU2007221796B2 (en) * | 2006-10-03 | 2012-08-09 | Pepsico, Inc. | Use of erythritol and d-tagatose in diet or reduced-calorie beverages and food products |
| CN102018016B (en) * | 2010-12-27 | 2013-01-02 | 暨南大学 | Cake containing neotame and preparation method thereof |
| CN102018016A (en) * | 2010-12-27 | 2011-04-20 | 暨南大学 | Cake containing neotame and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| AU1088901A (en) | 2001-04-30 |
| WO2001028357A3 (en) | 2002-01-24 |
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