WO2008147798A2 - Edible composition comprising a slowly digestible or digestion resistant oligosaccharide composition - Google Patents
Edible composition comprising a slowly digestible or digestion resistant oligosaccharide composition Download PDFInfo
- Publication number
- WO2008147798A2 WO2008147798A2 PCT/US2008/064321 US2008064321W WO2008147798A2 WO 2008147798 A2 WO2008147798 A2 WO 2008147798A2 US 2008064321 W US2008064321 W US 2008064321W WO 2008147798 A2 WO2008147798 A2 WO 2008147798A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- oligosaccharides
- soluble fiber
- starch
- sweetener
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 230
- 229920001542 oligosaccharide Polymers 0.000 title claims abstract description 51
- 150000002482 oligosaccharides Chemical class 0.000 title claims abstract description 51
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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
- A23L7/00—Cereal-derived products; Malt products; Preparation or treatment thereof
-
- 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
- A23L9/00—Puddings; Cream substitutes; Preparation or treatment thereof
- A23L9/10—Puddings; Dry powder puddings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/716—Glucans
- A61K31/718—Starch or degraded starch, e.g. amylose, amylopectin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/716—Glucans
- A61K31/719—Pullulans
-
- 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
- a variety of carbohydrates are used in food products, such as various sugars and starches. Many of these carbohydrates are digested in the human stomach and small intestine. Dietary fiber in food products, in contrast, is generally not digested in the stomach or small intestine, but is potentially fermentable by microorganisms in the large intestine.
- Englyst assay is an in vitro enzyme test that can be used to estimate the amounts of a carbohydrate ingredient that are rapidly digestible, slowly digestible or resistant to digestion. European Journal of Clinical Nutrition (1992) Volume 46 (Suppl. 2), pages S33-S50.
- the bloodstream of the consumer When rapidly digestible carbohydrates are consumed, the bloodstream of the consumer typically displays a peak glycemic response within a short time frame, usually 15 to 45 minutes after the food is eaten. The peak is frequently followed by a hypoglycemic "overshoot" through the action of insulin released by the pancreas. Hypoglycemia is commonly associated with feelings of hunger. When hunger is followed by consumption of rapidly digestible carbohydrates, a vicious cycle of eating, followed shortly thereafter by feelings of hunger can ensue.
- One aspect of the invention is an edible composition that comprises a soluble fiber composition that is derived from starch and that comprises oligosaccharides that are digestion resistant, oligosaccharides that are slowly digestible, or a combination thereof.
- the edible composition also comprises at least one material selected from fructose, sorbitol, pullulan, a non-nutritive high-intensity sweetener, and combinations of any two or more thereof.
- Another aspect of the invention is a food product that comprises the above-described edible composition.
- the edible composition can be used a replacement for other sweeteners, such as sucrose, in the food product.
- Another aspect of the invention is a method of decreasing the glycemic response of a mammal to a food product. This method comprises replacing a nutritive sweetener in the ingredients of the food product with the above-described edible composition.
- Figure 1 is a graph of the change in blood glucose concentration over time in dogs fed 10 DE maltodextrin or compositions according to the present invention, which are labeled as Blend 1, Blend 2, Blend 3, and Blend 4.
- the edible composition comprises a soluble fiber composition that is made from starch and that comprises oligosaccharides that are digestion resistant, oligosaccharides that are slowly digestible, or a combination thereof.
- the edible composition also comprises fructose.
- the fractions of the soluble fiber composition that are digestion resistant or slowly digestible can be determined by the Englyst assay.
- oligosaccharides and “saccharide oligomers” are used herein to refer to saccharides comprising at least two saccharide units, for example saccharides having a degree of polymerization (“DP") of about 2-30. For example, a disaccharide has a DP of 2.
- the composition comprises a major amount of soluble fiber composition on a dry solids basis.
- the percentage of soluble fiber composition that is present in the edible composition is greater than or equal to the percentage of any other ingredient.
- the soluble fiber composition can be derived from a variety of starch sources, such as cereal grains, potato, or tapioca.
- the soluble fiber composition can be made from any of a variety of cereal grains, such as corn, wheat, rice, and combinations thereof.
- SCF soluble corn fiber
- the starch source is not a genetically modified organism (GMO).
- GMO genetically modified organism
- the starch source can be non-GMO corn.
- the soluble fiber composition can also contain substances that are not soluble fiber.
- soluble fiber will make up the majority of the soluble fiber composition on a dry solids basis.
- SCF can, at least in some embodiments, be classified as a corn syrup or maltodextrin, it does not have the regulatory limitations imposed in poly dextrose in the U.S.
- the soluble fiber composition is produced by a process that comprises: producing an aqueous composition that comprises at least one oligosaccharide and at least one monosaccharide by saccharification of starch derived from the cereal grain; fractionating the aqueous composition by a method comprising at least one of membrane filtering and sequential simulated moving bed chromatography to form a monosaccharide-rich stream and a digestion resistant oligosaccharide-rich stream; and recovering the oligosaccharide-rich stream.
- the oligosaccharide-rich stream comprises a minor amount of dextrose and fructose
- the process further comprises contacting the oligosaccharide-rich stream with an isomerization enzyme such that at least some of the dextrose is converted to fructose, thereby producing an isomerized oligosaccharide-rich stream.
- the oligosaccharide-rich stream comprises a minor amount of monosaccharides, and wherein the process further comprises hydrogenating the oligosaccharide-rich stream to convert at least some of the monosaccharides therein to alcohols, thereby producing a hydrogenated oligosaccharide-rich stream.
- the process further comprises contacting the oligosaccharide-rich stream with a glucosidase enzyme such that at least some of any residual monosaccharides present in the stream are covalently bonded to oligosaccharides or other monosaccharides. Additional details and information regarding this embodiment are found in U.S. patent application 11/083,347, filed on March 17, 2005, and published as US-2006-0210696- Al, which is incorporated herein by reference.
- the soluble fiber composition is produced by a process comprising: heating an aqueous feed composition that comprises at least one monosaccharide or linear saccharide oligomer derived from the cereal grain, and that has a solids concentration of at least about 70% by weight, to a temperature of at least about 4O 0 C; and contacting the feed composition with at least one catalyst that accelerates the rate of cleavage or formation of glucosyl bonds for a time sufficient to cause formation of non-linear saccharide oligomers, wherein a product composition is produced that contains a higher concentration of non- linear saccharide oligomers than linear saccharide oligomers.
- the catalyst is an enzyme that accelerates the rate of cleavage or formation of glucosyl bonds.
- a glucoamylase enzyme composition is one suitable example.
- the catalyst is an acid. Suitable acids include hydrochloric acid, sulfuric acid, phosphoric acid, and combinations thereof.
- the catalyst used in the process comprises a combination of acid and enzyme. The acid and enzyme can be used sequentially in any order (e.g., acid followed by enzyme, or enzyme followed by acid).
- the feed composition has a solids concentration of about 70 - 99% and is maintained at a temperature of about 70 - 18O 0 C during the contacting with the acid.
- the product composition comprises non-linear saccharide oligomers having a degree of polymerization of at least three in a concentration of at least about 50% by weight on a dry solids basis. Additional details and information regarding this embodiment are found in U.S. patent applications 11/339,306, filed on January 25, 2006, 11/532,219, filed on September 15, 2006, and 11/610,639, filed on December 14, 2006, each of which is incorporated herein by reference.
- the soluble fiber composition can be used in any of several different physical forms, such as a syrup or concentrated syrup solids.
- the soluble fiber composition is in particulate form.
- the particulates can be held together by a binder, such as a binder composition that comprises a major amount of maltodextrin.
- An agglomeration of particulates can have advantages in terms of rate of dissolution and dispersion. This can be useful in applications where more rapid dissolution and lower shear rates of mixing are important, such as table top sugar replacement, table top fiber supplementation, and on-the- go dry powder drink mix products.
- the edible composition can also comprise additional nutritive or non- nutritive saccharides and/or polysaccharides.
- the edible composition comprises sorbitol, pullulan, or a combination thereof. Sorbitol delivers about 60% of the sweetness of sugar to foods, but at a significant reduction in caloric content (2.6 vs. 4.0 kcal/g, Livesay) and with a negligible glycemic response.
- Pullulan gum is a slowly digestible carbohydrate that gives about a 50% relative glycemic response in humans compared to rapidly digestible carbohydrate, but may deliver similar caloric content as sugar to foods.
- the edible composition comprises about 50-99% soluble fiber composition, 0-50% fructose, 0-33% pullulan, and 0-33% sorbitol, provided that the concentration of at least one of fructose, pullulan, or sorbitol is at least 1%. (All of these percentages are by weight.)
- the edible composition comprises about 60-80% soluble fiber composition, 1-20% fructose, 0-20% pullulan, and 0-20% sorbitol.
- the edible composition comprises about 65-75% soluble fiber composition, 5-15% fructose, 5-15% pullulan, and 5-15% sorbitol.
- the concentration of that ingredient can be about 0.001 - 0.5%.
- the edible composition optionally can also contain resistant starch or other fiber sources.
- non-nutritive high-intensity sweetener In order to make the edible composition suitable for use as a sweetener composition in food, in many cases it will be desirable for it also to include a non-nutritive high-intensity sweetener. Suitable examples of such non-nutritive high-intensity sweeteners include, but are not limited to sucralose, acesulfame potassium, aspartame, and combinations thereof.
- the edible composition can be used in food products. It should be understood that the terms "food” and “food product” are used in a broad sense herein to include a variety of substances that can be ingested by humans, such as beverages and medicinal capsules or tablets. Suitable food products in which the edible composition can be used include, but are not limited to baked foods, breakfast cereal, dairy products, confections, jams and jellies, beverages, fillings, extruded and sheeted snacks, gelatin desserts, snack bars, cheese and cheese sauces, edible and water-soluble films, soups, syrups, sauces, dressings, creamers, icings, frostings, glazes, pet food, tortillas, meat and fish, dried fruit, infant and toddler food, and batters and breadings.
- Another aspect of the invention is a method of decreasing the glycemic response of a mammal to a food product.
- the method involves replacing a nutritive sweetener in the ingredients of the food product with the above-described edible composition.
- the edible composition can be used for total or partial replacement of nutritive sweeteners such as sucrose, high fructose corn syrup (HFCS), fructose, dextrose, regular corn syrup, or corn syrup solids in food products.
- HFCS high fructose corn syrup
- the inclusion of the edible composition in food products can provide a number of benefits, such as lower glycemic response, lower glycemic index, and lower glycemic load than a similar food product in which a conventional carbohydrate is used. Further, because at least some of the oligosaccharides are either only digested very slowly or are not digested at all in the human stomach or small intestine, the caloric content of the food product can be reduced.
- the edible composition can be added to food products as a source of soluble fiber without having a negative impact on flavor, mouth feel, or texture.
- Soluble fiber in food can have several beneficial effects, such as reducing cholesterol, attenuating blood glucose, and maintaining gastrointestinal health.
- the edible composition is particularly useful in foods in which nutritive sweetener systems and other similar carbohydrates are included at 2 to 3 grams (or more) per serving.
- Food products that contain the edible composition can be used to help control the blood glucose concentration in mammals, such as humans, that suffer from diabetes.
- the slowly digestible and/or digestion resistant components in the food product can cause a more moderate relative glycemic response in the bloodstream, which can be beneficial for diabetes patients.
- Control in this context should be understood as a relative term; i.e., the glycemic response can be improved relative to that occurring when the same mammal consumes a similar food product that does not contain such digestion-resistant and/or slowly digestible components, although the glycemic response may not necessarily be equivalent to what would be observed in a mammal that does not suffer from diabetes.
- Table 1 shows the relative sweetness, relative glycemic response (RGR), caloric content, and dietary fiber content of the ingredients sucralose, fructose, sucrose, sorbitol, Soluble Corn Fiber (SCF), and pullulan.
- SCF Soluble Corn Fiber
- Relative sweetness is a sensory measurement in which table sugar (sucrose) is defined as having a relative sweetness of one.
- Sucralose is assumed to have a negligible glycemic response and caloric content at typical usage levels.
- sucralose, fructose, sucrose and sorbitol are excluded from contributing to dietary fiber by definition.
- Monosaccharides and disaccharides e.g., sucralose, fructose, and sucrose
- SCF was assigned a relative sweetness of 0.1 due to its monosaccharide content of about 10-15% and is estimated to possess energy content of about 2 kcal/gram based on results of in vivo TME measurements.
- a "good source of dietary fiber" claim on a product label can be achieved by delivering 3 g of dietary fiber per serving. For SCF, inclusion of 4 grams per serving will deliver 3 grams of dietary fiber based upon its analyzed fiber content of 75%.
- “Sustained energy” is used herein to include not only the energy derived from fully digestible carbohydrate, but also to include the energy derived from short chain fatty acids (SCFA) formed as metabolic products through fermentation by the microbiota of the large intestine.
- SCFA short chain fatty acids
- An average value of about 2 kcal/gram has been proposed for the caloric content (energy value) of the SCFA formed by fermentation of the dietary fibers (Livesay).
- fully digestible carbohydrate implies absorption of hydrolyzed monosaccharide by the small intestine, resulting in the typical carbohydrate caloric content of about 4 kcal/gram.
- rapidly digestible carbohydrate typically leads to a peak glycemic response that occurs within a short time frame, usually 15 to 45 minutes.
- hypoglycemic overshoot The peak is frequently followed by a hypoglycemic "overshoot" through the action of insulin released by the pancreas.
- Hypoglycemia is commonly associated with feelings of hunger.
- hunger is followed by rapidly digestible carbohydrate consumption, then a vicious cycle of eating, followed shortly thereafter by feelings of hunger can ensue.
- a more slowly digestible carbohydrate leads to a more gradually increasing blood sugar response, followed by a slowly decreasing plateau that avoids the hypoglycemic overshoot, thus avoiding the vicious cycle of consumption followed by hunger as described above.
- the edible composition provides a sustained energy carbohydrate that has not only the characteristic of slowly digestible carbohydrate (gradually increasing glycemic response followed by slowly decreasing plateau), but also has a digestion resistant fraction that passes into the large intestine and becomes a fermentation substrate for the microbiota residing there. Fermentation releases short chain fatty acids (SCFA) that are absorbed by the host and serve as an energy source themselves. In fact, butyrate is a preferred energy source for the host cells lining the colon, thus promoting healthy cell function and resistance to disease and cancer.
- SCFA short chain fatty acids
- compositions described in this patent are capable of delivering digestion resistant carbohydrate to the large bowel, and that they are capable of being transformed into SCFA (capable of delivering sustained energy) after fermentation by organisms inoculated from fresh fecal material.
- SCFA sustained energy
- the edible composition can be used to replace traditional sugar sweeteners and provide sustained energy and dietary fiber to nearly any food item, while simultaneously controlling sweetness at reduced calories and glycemic load.
- Fructose and optionally sorbitol
- the soluble fiber added by SCF and SCF/pullulan blends is soluble, with good flavor and low color and therefore is highly versatile in food systems.
- SCF/pullulan blends can provide fiber benefits over either ingredient alone with respect to dietary tolerance and prebiotic effect.
- the composition comprises a starch-derived soluble fiber composition that is made from cereal grain and that comprises oligosaccharides that are digestion resistant, oligosaccharides that are slowly digestible, or a combination thereof.
- the composition also comprises a non-nutritive high-intensity sweetener (e.g., sucralose), and is in a package that is adapted to be opened by a consumer.
- the packaged sweetener composition further comprises at least one material selected from fructose, pullulan, sorbitol, and combinations of two or more thereof, and can optionally also comprise maltodextrin.
- the starch-derived soluble fiber composition comprises about 70- 99% by weight of the packaged sweetener composition.
- compositions that contain agglomerated soluble corn fiber can have greatly improved dispersibility and dissolution rate compared to SCF by itself.
- An aqueous solution of, for example, 10 DE maltodextrin can be used to bind raw SCF particles together in an agglomeration process. This results in a product with lower bulk density (e.g., in some embodiments, 0.1-0.85 g per cubic centimeter, or in some other embodiments, 0.45-0.65 g per cubic centimeter).
- the enhanced dispersibility and dissolution rate of the agglomerated product can be valuable especially in applications where shorter times and lower shear rates of mixing are critical, such as table top sugar replacement, table top fiber supplementation, and on-the-go dry powder drink mix products.
- a corn syrup composition that comprises a starch-derived soluble fiber composition (as described above), fructose, and a non-nutritive high-intensity sweetener (e.g., sucralose).
- the composition comprises about 35-50% by weight fructose and about 35-50% by weight of the soluble fiber composition on a dry solids basis.
- This corn syrup composition can be blended with conventional high fructose corn syrup to produce a sweetener composition that has a lower caloric content than HFCS by itself.
- Another embodiment of the invention relates to an edible calcium supplement that comprises a starch-derived soluble fiber composition (as described above) and at least one calcium compound.
- the calcium compound can be a calcium salt, such as calcium citrate, calcium carbonate, or a combination thereof.
- a calcium supplement containing SCF could enhance calcium absorption due to the pH lowering effect of SCF fermentation, rendering the supplement more effective.
- a diet beverage that comprises a starch-derived soluble fiber composition (as described above) pullulan, a non-nutritive high- intensity sweetener (e.g., sucralose), and at least one flavor.
- the beverage comprises about 3-7% by weight of the starch-derived soluble fiber composition and about 0.1-3% by weight pullulan.
- This diet beverage can help overcome taste problems observed with previous diet beverages.
- many diet beverages do not taste the same as their full sugar counterparts.
- the sensory experience associated with consumption of a diet vs. a full sugar beverage is multifaceted, but two of the major sensory differences can be classified in terms of "sweetness” and "mouthfeel.”
- Diet beverages derive their sweetness through inclusion of high intensity sweeteners (HIS) such as sucralose, aspartame and acesulfame potassium.
- HIS high intensity sweeteners
- a very low concentration of HIS typically in the range of 0.02% to 0.06% by weight, is used in diet beverages to replace the sugar or high fructose corn syrup that is used (at about 10% by weight) in a full calorie beverage.
- soluble corn fiber This combination not only adds viscosity and mouthfeel back to the diet beverage, but also moves the sensory experience of sweet and tart flavors much closer to that found in a full sugar beverage.
- Example 1 Canine Glycemic Response Testing Protocol
- Experimental design A series of 5 x 5 Latin square designs were used in which dogs were subjected to three separate 3 hr meal tolerance tests. Tolerance tests were spaced 3 to 4 days apart. After 15 hr of food deprivation, dogs will consume their allotted treatment.
- Phosphate Buffer I 0.1M, pH 6.0 - Dissolve 2.1 g of sodium phosphate dibasic, anhydrous, and 11.76 g of sodium phosphate monobasic, monohydrate in a 1 liter volumetric flask. Bring up to volume with distilled water. Check by pH measurement. This solution will keep for up to 48 hrs if kept refrigerated.
- Hydrochloric Acid 0.2N - Place 16.7 ml HCl in a 1 liter volumetric flask. Bring up to volume with dd water.
- HChPepsin Solution - Place 1 g pepsin (Sigma P-7000) in a 100 ml volumetric flask. Dissolve in 50 ml distilled water. Add 10 ml HCl. Bring up to volume with distilled water. Prepare fresh on day of use.
- Chloramphenicol Solution Place 0.5 g chloramphenicol (Sigma C-0378) in a 100 ml volumetric flask. Bring up to volume with 95% ethanol. 5.
- Sodium Hydroxide Solution, 0.6N Place 24 g NaOH in a 1 liter volumetric flask.
- Pancreatin Solution Place 5 g porcine pancreatin (Sigma P- 1750) in a 100 ml volumetric flask. Bring up to volume with phosphate buffer II. Prepare fresh on day of use.
- Riboflavin Solution In a 100 ml volumetric flask, place 0.001 g riboflavin and 0.13 g HEPES. Bring up to volume with dd water. Store in the refrigerator. Stable.
- Hemin Solution In a 100 ml volumetric flask, place 0.05 g hemin and 0.04 g sodium hydroxide. Bring up to volume with dd water. Store in the refrigerator. Stable.
- Short Chain Fatty Acid Mix - Mix together equal volumes of n- valerate, isovalerate, isobutyrate, and DL-2-methylbutyrate. 16. Resazurin Solution 0.1% - Place 0.1 g resazurin in a 100 ml volumetric flask.
- Mineral Solution No. 2 In a 500 ml volumetric flask, dissolve successively 6 g sodium chloride, 6 g ammonium sulfate, 3 g potassium phosphate monobasic anhydrous, 0.6 g calcium chloride dihydrate, 1.23 g magnesium sulfate heptahydrate, and 1O g sodium citrate dihydrate. Bring up to volume with dd water. Store in the refrigerator. Stable. 20.
- Sodium Bicarbonate Solution Place 91 g sodium bicarbonate in a 1 liter volumetric flask. Bring up to volume with dd water. Store at room temperature. Stable.
- Stopper tubes Mix gently. Incubate at 39 0 C for 18 hours. Mix on a regular basis.
- Example 3 Drink Dry Mix with Fiber
- a dry drink mix was prepared with the following ingredients (proportions listed on a weight basis):
- the product was prepared as follows: Dry blend using controlled atmosphere, low humidity. Add 4.98 g per 100 ml of water. Mix until dissolved.
- a soft drink mix was prepared with the following ingredients:
- the product was prepared as follows: Dissolve the carbohydrate blend into water. Add the preservative and completely dissolve. Add acid. Then dissolve caffeine and add flavors. This makes a concentrate. Use the concentrate at a 5:1 throw in a finished beverage.
- Example 5 Rehydration Drink A drink mix was prepared with the following ingredients:
- the product was prepared as follows: Dry blend using controlled atmosphere, low humidity. Add 5.48 g per 100 ml of water mix until dissolved.
- a beverage mix was prepared with the following ingredients:
- the product was prepared as follows: Dissolve dry ingredients into water. Pasteurize at 19O 0 F for 30 seconds. Hot fill into bottles. Cool.
- a pudding mix was prepared with the following ingredients: MiraSperse 2000 37.275
- Titanium dioxide 1.225
- the product was prepared as follows: Dry blend using controlled atmosphere, low humidity. Add 52.26 g in two cups of milk. Mix on high speed for 2 minutes. Let sit 5 minutes before eating.
- a cookie mix was prepared with the following ingredients: Shortening 18.22 Sugar 11.72
- the product was prepared as follows: Stir together shortening, sugar, CHO blend, and salt in Kitchenaid mixer. Scrape sides, stir on speed 2 for 2 minutes. Add flavor, water, color, sucralose, Isosweet, resistant starch, and whey. Scrape down bowl and stir on speed 1 for 1 minute. Scrape down bowl and mix on speed 2 for 2 minutes. Scrape down bowl and add rest of ingredients except chips. Stir on speed 1 for one minute, scrape bowl after 30 seconds. Shape 48 g into 1.5" cookie cutter and cut ⁇ 12 g cookies with a wire cutter. Bake at 425 0 F on Vi sheet pan with a single parchment for 6:45 minutes. Let cool on pan.
- a mix was prepared with the following ingredients: 3A c CHO blend 1 (replaces standard sugar 1 :1)
- the product was prepared as follows: Cream sugars and butter. Add 2 eggs and 1 t vanilla. Mix well. Add 2 1 A c flour, 1 t baking soda, and 1 t salt. Blend well. Add 12 oz of chocolate chips, scoop onto cookie sheet, and bake at 375 0 F for 7-10 minutes.
- TSRl Table Sugar Replacement Version 1
- a table top sugar replacer mix was prepared with the following ingredients: Core M-60 8.3 grams Soluble Corn Fiber 491.7 grams
- Core M-60 is 10% sucralose by weight on 10 DE maltodextrin. Sucralose is 600 times sweeter than table sugar by weight. The SCF gives 3 grams of dietary fiber per 4 g teaspoonful. This blended ingredient gives the same sweetness but half the calories as table sugar by weight.
- a table top sugar replacer mix was prepared with the following ingredients: Sucralose 0.83 grams Soluble Corn Fiber 499.17 grams
- Example 12 High Fructose Corn Syrup Fiber (HFCSF 42, 71%ds, recipe for 645 g batch)
- a mix was prepared as follows: Prepare 395 grams of a 67.2% by weight solution of TSR2 in water (from Example 11 above). Blend in 250 grams of a 77% by weight solution of fructose (Krystar® Liquid) and thoroughly mix the two solutions. This gives a syrup product with 71% dry solids content, 42% fructose on a dry solids basis and 43.5% fiber on a dry solids basis. This syrup also provides 29% fewer calories than an equal quantity of a standard High Fructose Corn Syrup (HFCS) such as ISOSWEET 100® (Tate & LyIe).
- HFCS High Fructose Corn Syrup
- This material could be blended with an HFCS with similar dry solids and fructose concentration (ISOSWEET 100®) in order to adjust fiber level and calorie reduction to fit the needs of nearly any food product or beverage any application.
- Example 13 High Fructose Corn Syrup Fiber (HFCSF 42, 80%ds, recipe for 573 g batch)
- a mix was prepared as follows:
- a mix was prepared as follows:
- This material could be blended with an HFCS with similar dry solids and fructose concentration (ISOSWEET 5500®) in order to adjust fiber level and calorie reduction to fit the needs of nearly any food product or beverage any application.
- Soluble Corn Fiber was agglomerated using a Glatt ProCell 5 fluid bed agglomerator in top spray mode, with the GF batch insert.
- a 25% StarDri 10 (10 DE maltodextrin) solution was used as the binding solution.
- Four hundred and fifty grams of the SCF were placed into the fluid bed and agglomerated with 200 g of the maltodextrin solution.
- the process was run with the following parameters: product temperature of 53 0 C, air volume of 70m /hr, atomization air at 1.5 bar, spray rate at about 8 g/min. After 200 g of the solution was sprayed, the pump and heater were shut off and the product was dried for 1 minute.
- the finished product was then discharged from the chamber and sieved through a 10 mesh screen to remove large particles. This results in a product with lower bulk density (0.2 to 0.5 grams per cubic centimeter) compared to the raw SCF ( ⁇ 0.8 g/cc).
- the SCF can be sieved through a 60 mesh prior to agglomeration.
- the product that goes through the screen can then be used to charge the bed. Using a finer starting product improves dispersibility of the final product.
- Example 16 Agglomerated Soluble Corn Fiber with Sucralose Soluble Corn Fiber (SCF) was agglomerated using a Glatt ProCell 5 in top spray mode, with the GF insert. A 25% StarDri 10 (10 DE maltodextrin) solution was used as the binding solution. A small amount of sucralose is added to the binder to add sweetness to the final product.
- SCF Sucralose Soluble Corn Fiber
- the SCF can be sieved through a 60 mesh prior to agglomeration.
- the product that goes through the screen can then be used to charge the bed.
- Using a finer starting product improves dispersibility of the final product.
- Example 17 Caramel Chew With Calcium Citrate
- a chewable caramel-flavored calcium supplement was prepared with the following ingredients:
- Soluble Corn Fiber 55 (syrup containing 72% dry solids)
- the product was prepared as follows: Place sugar, non-fat dry milk and water in a cooking kettle. Stir until lump free. Add soluble corn fiber syrup. Cook to just above the boiling temperature (-216 0 F). Add butter with stirring. Cook until -236 0 F. Add salt, calcium and flavor. Pour onto oiled slab. Allow to cool and cut to desired shape in pieces weighing 5-6 grams each. Wrap.
- a chewable caramel-flavored calcium supplement was prepared with the following ingredients:
- Soluble Corn Fiber 55 (syrup containing 72% dry solids)
- Calcium carbonate 40 The product was prepared as follows: Place sugar, non-fat dry milk and water in a cooking kettle. Stir until lump free. Add soluble corn fiber syrup. Cook to just above the boiling temperature (-216 0 F). Add butter with stirring. Cook until -236 0 F. Add salt, calcium and flavor. Pour onto oiled slab. Allow to cool and cut to desired shape in pieces weighing 5-6 grams each. Wrap.
- a two piece serving of either one of these chewable caramel flavored calcium supplements (Examples 17 and 18) provides 1 gram of calcium and 2 grams of dietary fiber at a total caloric intake of about 30 calories.
- a control diet cola beverage was made by dissolving the following ingredients in water at the specified concentrations, followed by carbonation:
- a diet cola beverage was made using a blend of pullulan and SCF by dissolving the following ingredients in water at the specified concentrations, followed by carbonation:
- the two diet beverages were then tested by a trained sensory panel using coded sample identifiers.
- the panel found that the beverage that contained SCF and pullulan imparted both enhanced flavor and mouthfeel compared to the control diet cola.
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- Proteomics, Peptides & Aminoacids (AREA)
- Birds (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Fodder In General (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN200880017057A CN101677603A (en) | 2007-05-23 | 2008-05-21 | The edible composition that comprises the oligosaccharides composition of slowly digestible or digestion resistant |
JP2010509513A JP2010527613A (en) | 2007-05-23 | 2008-05-21 | Edible composition comprising a slowly digestible or digestion resistant oligosaccharide composition |
BRPI0810953-2A2A BRPI0810953A2 (en) | 2007-05-23 | 2008-05-21 | EDIBLE COMPOSITION, FOOD PRODUCT, METHOD FOR REDUCING THE GLYCEMIC RESPONSE OF A MAMMAL TO A FOOD PRODUCT, SWEET COMPOSITION PACKED FOR SINGLE PORTION, MAKING SYRUP COMPOSITION, ADDICTIVE ADDICTION COMPOSITION . |
EP08756021A EP2154992A2 (en) | 2007-05-23 | 2008-05-21 | Edible composition comprising a slowly digestible or digestion resistant oligosaccharide composition |
MX2009011696A MX2009011696A (en) | 2007-05-23 | 2008-05-21 | Edible composition comprising a slowly digestible or digestion resistant oligosaccharide composition. |
CA002684902A CA2684902A1 (en) | 2007-05-23 | 2008-05-21 | Edible composition comprising a slowly digestible or digestion resistant oligosaccharide composition |
AU2008256938A AU2008256938B2 (en) | 2007-05-23 | 2008-05-21 | Edible composition comprising a slowly digestible or digestion resistant oligosaccharide composition |
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US93974407P | 2007-05-23 | 2007-05-23 | |
US60/939,744 | 2007-05-23 | ||
US93994107P | 2007-05-24 | 2007-05-24 | |
US60/939,941 | 2007-05-24 | ||
US94780407P | 2007-07-03 | 2007-07-03 | |
US60/947,804 | 2007-07-03 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008147798A2 true WO2008147798A2 (en) | 2008-12-04 |
WO2008147798A3 WO2008147798A3 (en) | 2009-07-30 |
Family
ID=39739688
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2008/064321 WO2008147798A2 (en) | 2007-05-23 | 2008-05-21 | Edible composition comprising a slowly digestible or digestion resistant oligosaccharide composition |
Country Status (10)
Country | Link |
---|---|
US (1) | US20080292766A1 (en) |
EP (1) | EP2154992A2 (en) |
JP (1) | JP2010527613A (en) |
KR (1) | KR20100021997A (en) |
CN (1) | CN101677603A (en) |
AU (1) | AU2008256938B2 (en) |
BR (1) | BRPI0810953A2 (en) |
CA (1) | CA2684902A1 (en) |
MX (1) | MX2009011696A (en) |
WO (1) | WO2008147798A2 (en) |
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CN103110044A (en) * | 2012-11-29 | 2013-05-22 | 哈尔滨贵迪软件有限公司 | Red jujube stuffing with good water-retaining property |
CN103783353A (en) * | 2012-11-29 | 2014-05-14 | 哈尔滨贵迪软件有限公司 | High-water-retention chocolate stuffing |
CN103783364A (en) * | 2012-11-30 | 2014-05-14 | 哈尔滨贵迪软件有限公司 | Coconut filling with good water-retaining property |
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US20130167837A1 (en) | 2011-12-30 | 2013-07-04 | Renmatix, Inc. | Compositions comprising c5 and c6 monosaccharides |
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JP6453897B2 (en) | 2014-09-22 | 2019-01-16 | 日本食品化工株式会社 | Slowly digestive sustained energy supplement |
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US20160235098A1 (en) * | 2014-11-21 | 2016-08-18 | LFS Products, LLC | Naturally sweet fibrous blends and fibrous saccharide blends |
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- 2008-05-21 CN CN200880017057A patent/CN101677603A/en active Pending
- 2008-05-21 CA CA002684902A patent/CA2684902A1/en not_active Abandoned
- 2008-05-21 WO PCT/US2008/064321 patent/WO2008147798A2/en active Application Filing
- 2008-05-21 EP EP08756021A patent/EP2154992A2/en not_active Withdrawn
- 2008-05-21 JP JP2010509513A patent/JP2010527613A/en active Pending
- 2008-05-21 KR KR1020097022620A patent/KR20100021997A/en not_active Application Discontinuation
- 2008-05-21 US US12/124,364 patent/US20080292766A1/en not_active Abandoned
- 2008-05-21 AU AU2008256938A patent/AU2008256938B2/en not_active Ceased
- 2008-05-21 MX MX2009011696A patent/MX2009011696A/en not_active Application Discontinuation
- 2008-05-21 BR BRPI0810953-2A2A patent/BRPI0810953A2/en not_active IP Right Cessation
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103110044A (en) * | 2012-11-29 | 2013-05-22 | 哈尔滨贵迪软件有限公司 | Red jujube stuffing with good water-retaining property |
CN103783353A (en) * | 2012-11-29 | 2014-05-14 | 哈尔滨贵迪软件有限公司 | High-water-retention chocolate stuffing |
CN103110047A (en) * | 2012-11-30 | 2013-05-22 | 哈尔滨贵迪软件有限公司 | Hawthorn stuffing with good water-retaining property |
CN103783364A (en) * | 2012-11-30 | 2014-05-14 | 哈尔滨贵迪软件有限公司 | Coconut filling with good water-retaining property |
Also Published As
Publication number | Publication date |
---|---|
CA2684902A1 (en) | 2008-12-04 |
AU2008256938B2 (en) | 2013-02-28 |
KR20100021997A (en) | 2010-02-26 |
AU2008256938A1 (en) | 2008-12-04 |
JP2010527613A (en) | 2010-08-19 |
CN101677603A (en) | 2010-03-24 |
BRPI0810953A2 (en) | 2014-10-14 |
MX2009011696A (en) | 2009-11-10 |
EP2154992A2 (en) | 2010-02-24 |
US20080292766A1 (en) | 2008-11-27 |
WO2008147798A3 (en) | 2009-07-30 |
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