WO2013096405A1 - Chewing gum products containing [(2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester - Google Patents
Chewing gum products containing [(2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester Download PDFInfo
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- WO2013096405A1 WO2013096405A1 PCT/US2012/070539 US2012070539W WO2013096405A1 WO 2013096405 A1 WO2013096405 A1 WO 2013096405A1 US 2012070539 W US2012070539 W US 2012070539W WO 2013096405 A1 WO2013096405 A1 WO 2013096405A1
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/18—Chewing gum characterised by shape, structure or physical form, e.g. aerated products
- A23G4/20—Composite products, e.g. centre-filled, multi-layer, laminated
-
- 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
- A23L27/20—Synthetic spices, flavouring agents or condiments
-
- 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
- A23L27/20—Synthetic spices, flavouring agents or condiments
- A23L27/205—Heterocyclic compounds
- A23L27/2056—Heterocyclic compounds having at least two different hetero atoms, at least one being a nitrogen atom
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- 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
- A23L27/86—Addition of bitterness inhibitors
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
Definitions
- the present invention relates to chewing gum. More specifically, this invention relates to formulations for chewing gum products containing [(2-isopropyl-5- methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester, from herein called Gly- OiPr. More particularly, the invention relates to producing chewing gum containing [(2- isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester as a physiological cooling agent.
- Peppermint oil is frequently used to create a "cooling" in oral products such as toothpaste, mouthwash, chewing gum, candy and other food products.
- Peppermint oil generally comprises about 45% menthol, about 20% menthone, about 5% menthyl acetate, about 5% eucalyptol and many other constituents.
- Peppermint oil is even used in non-peppermint products, such as spearmint or wintergreen flavored products, in order to create this desired cooling effect. However, peppermint notes are then found in the resulting non- peppermint flavored products.
- Menthol is also known for its physiological cooling effect on the skin and mucous membranes of the mouth. Being a major constituent of peppermint oil, menthol has been used extensively in foods, beverages, dentifrices, mouthwashes, toiletries, lotions and the like. The disadvantages of using menthol, however, are its strong minty odor and the harsh notes it imparts to compositions in which it is found.
- Physiological cooling agents are perceived as cold or cool when contacted with the human body and, in particular, with the mucous membranes of the mouth, nose and throat.
- Several of these compounds have been suggested for use in confectionery products, including chewing gum.
- these physiological cooling agents are less objectionable than menthol, when they are used at high levels to provide desirable refreshing coolness, they also have objectionable flavor characteristics, such as bitterness, biting and sharpness along with off tastes.
- Chewing gum compositions have been invented that provide a high level of refreshing taste with significant breath freshening without objectionable flavor characteristics.
- the invention is a chewing gum composition comprising gum base, flavor, sweetening agent, and about 0.01 % to about 0.4% Gly-OiPr.
- the invention is a chewing gum product comprising a gum composition made from gum base, flavor, and sweetening agent, and wherein the gum product includes about 0.01 % to about 0.4% [(2-isopropyl-5-methyl- cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (Gly-OiPr) by weight of the gum product.
- the invention includes a chewing gum composition which comprises gum base, flavor, at least one sweetening agent selected from the group consisting of sugars, sugar alcohols, and mixtures thereof, and a cooling agent other than Gly-OiPr in a amount to impart cooling to said gum at a level in the range found in typical commercial gum products, the improvement comprising adding about 0.01 % to about 0.4% Gly-OiPr by weight of the total gum composition whereby the cooling and breath freshening are enhanced.
- the invention includes a chewing gum composition
- a chewing gum composition comprising about 5% to about 95% gum base, about 0.1 % to about 10% flavor, about 10% to about 90% sweetening agent selected from the group consisting of sugars, sugar alcohols, and mixtures thereof, and Gly-OiPr present in an amount sufficient to provide the gum with a combination of good cooling properties and breath freshening properties without bitterness.
- Gly-OiPr at levels of about 0.01 % to about 0.4% has been surprisingly found to provide a gum composition and gum products that have high levels of refreshing taste with considerable cooling and breath freshening but without unwanted flavor characteristics as compared to even ethyl ester of N-[[5-methyl-2-(1 - methylethyl)-cyclohexyl] carbonyl] glycine (WS-5), which Gly-OiPr is an analogue of WS-5.
- the Gly-OiPr physiological cooling agent may be used in combination with other physiological cooling agents, and it may be treated to control its release and enhance its shelf life stability.
- the Gly-OiPr physiological cooling agent may be added as part of a cooling flavor composition, or used in a chewing gum coating. Additional features and advantages of the disclosed embodiments are described in, and will be apparent from, the following Detailed Description and the attached drawings.
- Figure 1 is a graphical illustration of the average cooling intensity at each minute interval, during 20 minutes of chewing, of a chewing gum of the present invention compared to chewing gum composition containing WS-5.
- Figure 2 is a graphical illustration of the average bitterness intensity of solutions with Gly-OiPr compared to solutions with WS-5 at different concentrations.
- chewing gum refers to chewing gum, bubble gum and the like.
- breath freshening discussed herein is consumer perceived breath freshening, rather than objectively measured breath freshening.
- Physiological cooling agents encompass any number of physiological cooling agents.
- the term "physiological cooling agent” does not include traditional flavor-derivatives such as menthol or menthone.
- Preferred physiological cooling agents do not have a perceptible flavor of their own, but simply provide a cooling effect.
- Gly-OiPr refers to [(2-isopropyl-5-methyl-cyclohexanecarbonyl)- amino]-acetic acid isopropyl ester.
- isomers of Gly-OiPr that may be used in the present invention and one example is [((1 R,2S,5R)-2-isopropyl-5-methyl- cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester.
- Gly-OiPr has a structure illustrat low:
- compositions obtained as Gly-OiPr may not be pure [(2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester, but may contain small percentages of impurities that are byproducts of manufacture.
- the Gly-OiPr used in the gum compositions of the present invention will have a purity of at least 96% Gly-OiPr.
- Gly-OiPr means 100% pure [(2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester. If an impure mixture is used, usage levels may need to be adjusted to take the purity level into account.
- physiological cooling agents that may be used along with Gly-OiPr in chewing gums of the present invention include:
- acyclic carboxamides e.g., N,2,3-trimethyl-2-isopropyl butanamide (WS-23, FEMA 3804)
- physiological cooling agents that are presently preferred to be included with the Gly-OiPr are menthyl succinate; menthyl lactate; 3-1- menthoxypropane-1 ,2-diol; N-substituted p-menthane carboxamides; acyclic
- the concentration of physiological cooling agent will depend on the intensity of the physiological cooling agent (for example, WS-5 has a higher cooling effect than WS-3 and WS-23 at the same concentration levels) and the desired cooling effect.
- the additional physiological cooling agent when used, will preferably be present at about 0.01 % to about 0.5% of the chewing gum product, preferably with no one of the additional physiological cooling agents comprising more that about 0.4% of the gum product.
- the level of the other physiological cooling agents may be between about 0.05% and about 0.4%, or even between about 0.1 % and about 0.3% of the chewing gum product.
- the present invention contemplates that optionally sensates like warming agents and/or tingling agents may also be included in the chewing gum.
- Warming agents provide to the user a sensation of warmth and tingling agents provide to the user a sensation of tingling. Examples of warming and tingling agents can be found in U.S. Patent No. 6,890,567, which is incorporated herein by reference.
- the present invention contemplates that Gly-OiPr and optional additional physiological cooling agents may be added to the flavor used to make the chewing gum.
- the flavor and cooling agents may be added separately anywhere within the manufacturing process for making a chewing gum.
- physiological cooling agents including Gly-OiPr may be encapsulated to modify their release rate from chewing gum.
- the physiological cooling agents or sweeteners may be fully or partially encapsulated with water-soluble or water-insoluble materials.
- Encapsulation materials include acrylic polymers and copolymers, carboxyvinyl polymer, polyamides, polystyrene, polyvinyl acetate, polyvinyl acetate phthalate, polyvinyl pyrrolidone, waxes, shellac, zein, agar, alginates, a wide variety of cellulose derivatives like ethyl cellulose and hydroxypropyl methyl cellulose, dextrin, gelatin, modified starches, acacia, maltodextrin, gum arabic, guar gums, locust bean gum, carrageenan, and mixtures thereof.
- physiological cooling agents may also be adsorbed onto an inert or water-insoluble material such as silicas, silicates, pharmasorb clay, sponge-like beads or microbeads, amorphous carbonates and hydroxides, including aluminum and calcium lakes.
- the cooling agents including Gly-OiPr may be modified in a multiple step process comprising any of the techniques noted.
- flavors include any flavor which is of food acceptable quality commonly known in the art such as essential oils, synthetic flavors or mixtures thereof.
- flavors include, but are not limited to, oils derived from plants and fruits such as citrus oils, fruit essences, peppermint oil, spearmint oil, eucalyptus, other mint oils, clove oil, oil of wintergreen, cinnamic aldehyde, anise, spice flavors, and the like.
- Flavors that are very strong, such as menthol flavors are also contemplated in this invention.
- Preferred flavors include cooling flavors such as peppermint, eucalyptus, menthol, wintergreen and fruity-mint; non-cooling flavors such as spearmint and cinnamon; and combinations thereof.
- the chewing gum products will include menthol, and may include about 0.01 % to about 2.0% menthol, preferably less than 0.5%.
- the flavor may be added to the chewing gum formula in an amount such that it will contain from about 0.1 % to about 10% flavor, preferably from about 0.2% to about 4.0% flavor, and most preferably about 0.5% to about 2% flavor.
- Physiological cooling agents in a liquid form may be added directly to a chewing gum formulation in its liquid form or may be combined with flavors or with other solvents such as alcohol, glycerin, propylene glycol, flavor solvents, emulsifiers, or vegetable oils.
- Physiological cooling agents in crystalline or powder form may also be added directly to a chewing gum formulation in its powder form or may be combined with other powdered bulking agents such as sugars, polyols, and other types of powdered ingredients.
- physiological cooling agents may be emulsified in flavor/water compositions or oil/water compositions. Most importantly, because of the low level of usage, the physiological cooling agents need to be evenly dispersed throughout the chewing gum composition.
- liquid physiological cooling agents may be combined and readily added directly to a gum or confectionery formulation.
- crystalline or powder physiological cooling agents as well as menthol may be dissolved in other liquid physiological cooling agents and the combinations readily added directly to a gum or confectionery formulation. It is also known that some crystalline or powder physiological cooling agents as well as menthol may be dissolved in other liquid physiological cooling agents and the combinations readily added directly to a gum or confectionery formulation. It is also known that some crystalline or powder physiological cooling agents as well as menthol may be dissolved in other liquid physiological cooling agents and the combinations readily added directly to a gum or confectionery formulation. It is also known that some crystalline or powder physiological cooling agents as well as menthol may be dissolved in other liquid physiological cooling agents and the combinations readily added directly to a gum or confectionery formulation. It is also known that some crystalline or powder physiological cooling agents as well as menthol may be dissolved in other liquid physiological cooling agents and the combinations readily added directly to a gum or confectionery formulation. It is also known that some crystalline or powder physiological cooling agents as well as ment
- physiological cooling agents as well as menthol may be combined to form eutectic mixtures which have a lower melting point than the individual crystalline cooling agents themselves.
- mixtures of some crystalline physiological cooling agents can be melted, blended together, and remain liquid at or near room temperature and can then be added directly to a chewing gum or confectionery formulation.
- physiological cooling agents such as menthyl lactate, menthyl succinate, p-menthane carboxamides like WS-3, acyclic carboxamides like WS-23, can be melted together and used readily in liquid form in product formulations.
- the Gly-OiPr may be used in sugarless gum formulations and may also be used in a sugar chewing gum.
- the Gly-OiPr may be used in either regular chewing gum or bubble gum.
- the Gly-OiPr may also be used in a low-moisture gum.
- a chewing gum composition typically contain a chewable gum base portion which is essentially free of water and is water-insoluble, a water-soluble bulk portion and flavors which are typically water insoluble.
- the water- soluble portion dissipates with a portion of the flavor over a period of time during chewing.
- the gum base portion is retained in the mouth throughout the chew.
- the insoluble gum base generally comprises elastomers, elastomer solvents, plasticizers, waxes, emulsifiers and inorganic fillers.
- Plastic polymers such as polyvinyl acetate, which behave somewhat as plasticizers, are also often included.
- Other plastic polymers that may be used include polyvinyl laureate, polyvinyl alcohol and polyvinyl pyrrolidone.
- Elastomers may include polyisobutylene, butyl rubber, (isobutylene-isoprene copolymer) and styrene butadiene rubber, as well as natural latexes such as chicle.
- Elastomer solvents are often resins such as terpene resins and rosin esters.
- Plasticizers sometimes called softeners, are typically fats and oils, including tallow, hydrogenated and partially hydrogenated vegetable oils, and cocoa butter. Commonly employed waxes include paraffin, microcrystalline and natural waxes such as beeswax and carnauba. Microcrystalline waxes, especially those with a high degree of crystallinity, may be considered bodying agents or textural modifiers.
- the insoluble gum base constitutes between about 5% to about 95% by weight of the gum. More preferably the insoluble gum base comprises between 10% and 50% by weight of the gum and most preferably about 20% to 35% by weight of the gum.
- the gum base typically also includes a filler component.
- the filler component may be calcium carbonate, magnesium carbonate, talc, dicalcium phosphate or the like.
- the filler may constitute between about 5% and about 60% by weight of the gum base.
- Preferably the filler comprises about 5% to 50% by weight of the gum base.
- Gum bases typically also contain softeners including glycerol monostearate and glycerol triacetate. Gum bases may also contain optional ingredients such as antioxidants, colors, and emulsifiers. The present invention contemplates employing any commercially acceptable gum base.
- the water-soluble portion of the chewing gum may further comprise softeners, sweeteners, flavors, fillers, physiological cooling agents and combinations thereof.
- the sweeteners often fulfill the role of bulking agents in the gum.
- the bulking agents typically comprise about 5% to about 95% of the gum composition.
- Softeners are added to the chewing gum in order to optimize the chewability and mouth feel of the gum.
- Softeners also known in the art as plasticizers or plasticizing agents, generally constitute between about 0.5% to about 15% of the chewing gum.
- Softeners contemplated by the present invention include glycerin, lecithin and combinations thereof.
- aqueous sweetener solutions such as those containing sorbitol, hydrogenated starch hydrolysate, corn syrup and combinations thereof may be used as softeners and binding agents in gum.
- the Gly-OiPr and optional additional physiological cooling agents of the present invention may be used in sugarless gum formulations.
- formulations containing sugar are also within the scope of the invention.
- Sugar sweeteners generally include saccharide-containing components commonly known in the chewing gum art which comprise, but are not limited to, sucrose, dextrose, maltose, dextrin, dried invert sugar, fructose, galactose, corn syrup solids and the like, alone or in any combination.
- the Gly-OiPr and optional additional physiological cooling agents of the present invention can also be used in combination with sugarless sweeteners.
- sugarless sweeteners include components with sweetening characteristics but which are devoid of the commonly known sugars and comprise, but are not limited to, sugar alcohols such as sorbitol, hydrogenated isomaltulose, mannitol, xylitol, lactitol, erythritol, hydrogenated starch hydrolysate, maltitol and the like alone or in any combination
- sugar alcohols such as sorbitol, hydrogenated isomaltulose, mannitol, xylitol, lactitol, erythritol, hydrogenated starch hydrolysate, maltitol and the like alone or in any combination
- free or encapsulated high-intensity sweeteners may be used in the chewing gum composition, or may be used in a coating applied to centers made from those gum compositions.
- High-intensity sweeteners preferably aspartame, may be used at levels from about 0.01 % to about 3.0%.
- Encapsulated aspartame is a high intensity
- the chewing gum composition will preferable comprise about 0.5% to about 90% sweetening agents. Most typically the sweetening agents will comprises at least one bulk sweetener and at least one high-intensity sweetener.
- Optional ingredients such as colors, emulsifiers and pharmaceutical agents may also be added as separate components of the chewing gum composition, or added as part of the gum base.
- Aqueous syrups such as corn syrup and hydrogenated corn syrup may be used, particularly if their moisture content is reduced. This can preferably be done by coevaporating the aqueous syrup with a plasticizer, such as glycerin or propylene glycol, to a moisture content of less than 10%.
- a plasticizer such as glycerin or propylene glycol
- Preferred compositions include hydrogenated starch hydrolysate solids and glycerin.
- a preferred method of manufacturing chewing gum according to the present invention is by sequentially adding the various chewing gum ingredients to any commercially available mixer known in the art. After the ingredients have been thoroughly mixed, the gum is discharged from the mixer and shaped into the desired form such as by rolling into sheets and cutting into sticks, extruding into chunks, or casting into pellets.
- the ingredients are mixed by first melting the gum base and adding it to the running mixer.
- the base may also be melted in the mixer itself.
- Color or emulsifiers may also be added at this time, along with syrup and a portion of the bulking agent. Further portions of the bulking agent may then be added to the mixer.
- a flavoring agent is typically added with the final portion of the bulking agent.
- the Gly- OiPr physiological cooling agent may be mixed with the flavor composition of the present invention and preferably added as part of the flavor addition. If the Gly-OiPr is encapsulated to modify its release rate, it will preferably be added after the final portion of bulking agent and flavor has been added. The entire mixing procedure typically takes from five to twenty minutes, but longer mixing times may sometime be required.
- the chewing gum composition can be coated.
- the coating is initially present as a liquid syrup which contains from about 30% to about 80% or 85% sugars or sugar alcohols, and from about 15% or 20% to about 70% of a solvent such as water.
- the coating process is carried out in conventional panning equipment. Gum center tablets to be coated are placed into the panning equipment to form a moving mass.
- the material or syrup which will eventually form the coating is applied or distributed over the gum center tablets. Flavors may be added before, during and after applying the syrup to the gum centers. Once the coating has dried to form a hard surface, additional syrup additions can be made to produce a plurality of coatings or multiple layers of coating.
- the Gly-OiPr may be added in the coating from about 0.01 % to about 0.4% by weight of the coating or from about 0.05% to about 0.3% or from about 0.07% to about 0.2% of the coating.
- syrup is added to the gum center tablets at a temperature range of from about 100 °F to about 240 °F.
- the syrup is added to the gum center tablets at a temperature range of from about 100 °F to about 240 °F.
- the syrup is added to the gum center tablets at a temperature range of from about 100 °F to about 240 °F.
- the syrup is added to the gum center tablets at a temperature range of from about 100 °F to about 240 °F.
- the syrup is added to the gum center tablets at a temperature range of from about 100 °F to about 240 °F.
- the temperature is from about 140°F to about 200 °F.
- the syrup is from about 140°F to about 200 °F.
- the syrup may be mixed with, sprayed upon, poured over, or added to the gum center tablets in any way known to those skilled in the art.
- a soft coating is formed by adding a powder coating after a liquid coating.
- the powder coating may include natural carbohydrate gum hydrolysates, maltodextrin, gelatin, cellulose derivatives, starches, modified starches, sugars, sugar alcohols, natural carbohydrate gums and fillers like talc and calcium carbonate.
- Each component of the coating on the gum center may be applied in a single layer or in a plurality of layers.
- a plurality of layers is obtained by applying single coats, allowing the layers to dry, and then repeating the process.
- the amount of solids added by each coating step depends chiefly on the concentration of the coating syrup. Any number of coats may be applied to the gum center tablet. Preferably, no more than about 75 coats are applied to the gum center. More preferably, less than about 60 coats are applied and most preferably, about 30 to about 60 coats are applied.
- the present invention contemplates applying an amount of syrup sufficient to yield a coated chewing gum product containing about 10% to about 65% coating.
- the final product will contain from about 20% to about 50% coating.
- a plurality of premeasured aliquots of coating syrup may be applied to the gum center. It is contemplated, however, that the volume of aliquots of syrup applied to the gum center may vary throughout the coating procedure.
- a preferred drying medium comprises air.
- forced drying air contacts the wet syrup coating in a temperature range of from about 70 °F to about 1 10°F. More preferably, the drying air is in the temperature range of from about 80 °F to about 100°F.
- the invention also contemplates that the drying air possesses a relative humidity of less than about 15 percent. Preferably, the relative humidity of the drying air is less than about 8 percent.
- the drying air may be passed over and admixed with the syrup coated gum centers in any way commonly known in the art. Preferably, the drying air is blown over and around the syrup coated gum center. If a flavor is applied after a syrup coating has been dried, the present invention contemplates drying the flavor with or without the use of a drying medium.
- the peppermint oil used in Comparative Examples A and Example 1 naturally contain menthol (from 40% to 50%), menthone (from 20% to 25%), and eucalyptol (from 6% to 7%).
- Figure 1 shows the plotted graph of the scores in Table 2. Comparative Example A contains 0.1 % of WS-5 in the chewing gum and Example 1 contains 0.1 % of Gly-OiPr. Even though the chewing gum formulations are the same between
- Example 1 with Gly-OiPr surprisingly sustained a higher level of cooling intensity for the rest of the 20 minute chew as compared to the chewing gum composition with WS-5. Based on this test, the composition with Gly-OiPr was able to sustain a higher level of cooling with the same amount of material compared to WS-5. Therefore, Gly-OiPr has an advantage over WS-5 in that it is possible to achieve the same level of cooling without putting in as much material which can have cost advantages and decreased bitterness as well.
- Table 3 and Figure 2 show test results of a trained sensory panel of five to six panelists where the panelists were asked to rate the bitterness intensity of solutions prepared with different concentrations of WS-5 and Gly-OiPr.
- Chewing gum products including Gly-OiPr may be made that have components other than a single chewing gum composition.
- the level of Gly-OiPr should be based on the weight of the product, rather than just the composition.
- a chewing gum composition with 0.4% Gly-OiPr in the composition could be formed into a pellet and then coated. If the coating comprises 25% of the total product weight, then the Gly-OiPr would comprise 0.32% of the chewing gum product.
- the Gly-OiPr may be in other parts of the product besides or in addition to the chewing gum composition.
- Gly-OiPr may be included in the centerfill of a liquid center chewing gum product, or a multilayer gum product could be made with Gly-OiPr in the compositions used to make one or more of the layers.
- the gum product comprises about 0.01 % to about 0.4% Gly-OiPr by weight of the gum product.
- the Gly-OiPr comprises about 0.05% to 0.3% by weight of the gum product.
- the product comprises about 0.07% to 0.2% Gly-OiPr by weight of the gum product.
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Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201280063888.2A CN104159580A (en) | 2011-12-21 | 2012-12-19 | Chewing gum products containing [ (2 - isopropyl - 5-methyl-cyclohexanecarbon yl) - amino] - acetic acid isopropyl ester |
BR112014014872-4A BR112014014872B1 (en) | 2011-12-21 | 2012-12-19 | CHEWING GUM COMPOSITIONS CONTAINING [(2-ISOPROPYL-5-METHYL-CYCLOHEXANECARBONYL)-AMINO]ACETIC ACID ISOPROPYL ESTER |
CA2859501A CA2859501C (en) | 2011-12-21 | 2012-12-19 | Chewing gum products containing [(2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester |
PL12860213.3T PL2793877T5 (en) | 2011-12-21 | 2012-12-19 | Chewing gum products containing [(2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester |
MX2014007498A MX357068B (en) | 2011-12-21 | 2012-12-19 | Chewing gum products containing [(2-isopropyl-5-methyl-cyclohexan ecarbonyl)-amino]-acetic acid isopropyl ester. |
EP12860213.3A EP2793877B2 (en) | 2011-12-21 | 2012-12-19 | Chewing gum products containing [(2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester |
AU2012321090A AU2012321090B8 (en) | 2011-12-21 | 2012-12-19 | Chewing gum products containing [ (2 - isopropyl - 5-methyl-cyclohexanecarbon yl) - amino] - acetic acid isopropyl ester |
US14/367,255 US20150272161A1 (en) | 2011-12-21 | 2012-12-19 | Chewing gum products containing (r)-2-[((1r,2s,5r)-2-isopropyl-5-methylclohexanecarbonyl)-amino]-acetic acid isopropyl ester |
RU2014126486A RU2627839C2 (en) | 2011-12-21 | 2012-12-19 | Chewing gum and its composition (versions) |
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US201161578714P | 2011-12-21 | 2011-12-21 | |
US61/578,714 | 2011-12-21 | ||
US201261605256P | 2012-03-01 | 2012-03-01 | |
US61/605,256 | 2012-03-01 |
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WO2013096405A1 true WO2013096405A1 (en) | 2013-06-27 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/US2012/070539 WO2013096405A1 (en) | 2011-12-21 | 2012-12-19 | Chewing gum products containing [(2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester |
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Country | Link |
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US (1) | US20150272161A1 (en) |
EP (1) | EP2793877B2 (en) |
CN (1) | CN104159580A (en) |
BR (1) | BR112014014872B1 (en) |
CA (1) | CA2859501C (en) |
MX (1) | MX357068B (en) |
PL (1) | PL2793877T5 (en) |
RU (1) | RU2627839C2 (en) |
WO (1) | WO2013096405A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017004437A1 (en) * | 2015-06-30 | 2017-01-05 | Wm. Wrigley Jr. Company | Long-lasting cooling formulations |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102019204936A1 (en) * | 2019-04-05 | 2020-10-08 | Südzucker AG | Process for the production of a confectionery product having a sugar-free coating coating |
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- 2012-12-19 PL PL12860213.3T patent/PL2793877T5/en unknown
- 2012-12-19 CN CN201280063888.2A patent/CN104159580A/en active Pending
- 2012-12-19 BR BR112014014872-4A patent/BR112014014872B1/en active IP Right Grant
- 2012-12-19 EP EP12860213.3A patent/EP2793877B2/en active Active
- 2012-12-19 WO PCT/US2012/070539 patent/WO2013096405A1/en active Application Filing
- 2012-12-19 MX MX2014007498A patent/MX357068B/en active IP Right Grant
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Also Published As
Publication number | Publication date |
---|---|
CA2859501C (en) | 2017-01-10 |
EP2793877B2 (en) | 2022-05-04 |
CN104159580A (en) | 2014-11-19 |
US20150272161A1 (en) | 2015-10-01 |
EP2793877B1 (en) | 2018-08-15 |
PL2793877T5 (en) | 2022-08-16 |
RU2627839C2 (en) | 2017-08-14 |
EP2793877A1 (en) | 2014-10-29 |
RU2014126486A (en) | 2016-02-10 |
CA2859501A1 (en) | 2013-06-27 |
MX2014007498A (en) | 2014-07-30 |
BR112014014872A2 (en) | 2017-06-13 |
PL2793877T3 (en) | 2019-03-29 |
BR112014014872B1 (en) | 2022-11-16 |
MX357068B (en) | 2018-06-25 |
EP2793877A4 (en) | 2015-10-28 |
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