Hard lozenge made with dietary fiber, including human milk oligoosaccharides

Abstract

Disclosed are compositions of dietary fiber and nonnutritive bulk sweeteners and/or nonnutritive high-intensity sweeteners and/or flavors in a hard, amorphous structure that can be administered to humans and dissolves slowly in the mouth and supports gastrointestinal tract health.

Claims

1. A composition comprising: a nondigestible fructooligosaccharide, a nondigestible glucose polymer, a human milk oligosaccharide, and a nonnutritive bulk sweetener in a hard, amorphous structure with a water content less than 6 wt%; wherein said nondigestible fructooligosaccharides, said nondigestible glucose polymers, and said human milk oligosaccharides account for 70 to 79 wt% on a dry matter basis; and sucrose, glucose, and fructose account for less than 5 wt% on a dry matter basis.

2. A composition as in claim 1 wherein said nondigestible fructooligosaccharides contribute 15 to 50 wt% and preferably 33 wt% of the dietary fiber, said nondigestible glucose polymers contribute 15 to 50 wt% and preferably 33 wt% of the dietary fiber, and said human milk oligosaccharides contribute 15 to 50 wt% and preferably 33 wt% of the dietary fiber.

3. A composition as in claim 1 wherein said nondigestible fructooligosaccharides comprise 1-kestose, nystose, and β-fructofuranosylnystose, said nondigestible glucose polymer is resistant maltodextrin, said nonnutritive bulk sweetener is D-allulose, and said human milk oligosaccharides are selected from a group including 2′-fucosyllactose, 3-fucosyllactose, lacto-N-tetraose, lacto-N-neotetraose, 3′-siallylactose, and 6′-siallylactose.

4. A composition comprising: a 1-kestose, nystose, and β-fructofuranosylnystose, a resistant maltodextrin, D-allulose, and a human milk oligosaccharide selected from a group including 2′-fucosyllactose, 3-fucosyllactose, lacto-N-tetraose, lacto-N-neotetraose, 3′-siallylactose, and 6′-siallylactose in a hard, amorphous structure with a water content of less than 6 wt%; wherein said 1-kestose, nystose, and β-fructofuranosylnystose, said resistant maltodextrin, and said human milk oligosaccharides account for 70 to 79 wt% on a dry matter basis; and sucrose, glucose, and fructose account for less than 5 wt% on a dry matter basis.

5. A composition as in claim 4 wherein said 1-kestose, nystose, and β-fructofuranosylnystose contribute 15 to 50 wt% and preferably 33 wt% of the dietary fiber, said resistant maltodextrin contributes 15 to 50 wt% and preferably 33 wt% of the dietary fiber, and said human milk oligosaccharide selected from a group including 2′-fucosyllactose, 3-fucosyllactose, lacto-N-tetraose, lacto-N-neotetraose, 3′-siallylactose, and 6′-siallylactose contributes 15 to 50 wt% and preferably 33 wt% of the dietary fiber.

6. A composition comprising: a 1-kestose, nystose, and β-fructofuranosylnystose, a resistant maltodextrin, D-allulose, and 2′-fucosyllactose in a hard, amorphous structure with a water content less than 6 wt%; wherein said 1-kestose, nystose, and β-fructofuranosylnystose, said resistant maltodextrin, and said 2′-fucosyllactose account for 70 to 79 wt% on a dry matter basis; and sucrose, glucose, and fructose account for less than 5 wt% on a dry matter basis.

7. A composition as in claim 6 wherein said 1-kestose, nystose, and β-fructofuranosylnystose contribute 15 to 50 wt% and preferably 33 wt% of the dietary fiber, said resistant maltodextrin contributes 15 to 50 wt% and preferably 33 wt% of the dietary fiber, and 2′-fucosyllactose contributes 15 to 50 wt% and preferably 33 wt% of the dietary fiber.

8. A method of delivering dietary fiber, comprising: by combining nondigestible fructooligosaccharides, nondigestible glucose polymers, human milk oligosaccharides, and a nonnutritive bulk sweetener in a hard, amorphous structure with a water content of less than 6 wt% that dissolves in the mouth; wherein said nondigestible fructooligosaccharides, said nondigestible glucose polymers, and said human milk oligosaccharides account for 70 to 79 wt% on a dry matter basis; and sucrose, glucose, and fructose account for less than 5 wt% on a dry matter basis.

9. A method as in claim 8 wherein said nondigestible fructooligosaccharides contribute 15 to 50 wt% and preferably 33 wt% of the dietary fiber, said nondigestible glucose polymers contribute 15 to 50 wt% and preferably 33 wt% of the dietary fiber, and said human milk oligosaccharides contribute 15 to 50 wt% and preferably 33 wt% of the dietary fiber.

10. A method as in claim 8 wherein said nondigestible fructooligosaccharide comprises 1-kestose, nystose, and β-fructofuranosylnystose, said nondigestible glucose polymer is resistant maltodextrin, said nonnutritive bulk sweetener is D-allulose, and said human milk oligosaccharides are selected from a group including 2′-fucosyllactose, 3-fucosyllactose, lacto-N-tetraose, lacto-N-neotetraose, 3′-siallylactose and 6′-siallylactose.

11. A method of delivering dietary fiber, comprising: a 1-kestose, nystose, and β-fructofuranosylnystose, a resistant maltodextrin, D-allulose, and a human milk oligosaccharide selected from a group including 2′-fucosyllactose, 3-fucosyllactose, lacto-N-tetraose, lacto-N-neotetraose, 3′-siallylactose, and 6′-siallylactose in a hard, amorphous structure with a water content of less than 6 wt%; wherein said 1-kestose, nystose, and β-fructofuranosylnystose, said resistant maltodextrin, and said human milk oligosaccharides account for 70 to 79 wt% on a dry matter basis; and sucrose, glucose, and fructose account for less than 5 wt% on a dry matter basis.

12. A method as in claim 11 wherein said 1-kestose, nystose, and β-fructofuranosylnystose contribute 15 to 50 wt% and preferably 33 wt% of the dietary fiber, said resistant maltodextrin contributes 15 to 50 wt% and preferably 33 wt% of the dietary fiber, and said human milk oligosaccharide selected from a group including 2′-fucosyllactose, 3-fucosyllactose, lacto-N-tetraose, lacto-N-neotetraose, 3′-siallylactose, and 6′-siallylactose contributes 15 to 50 wt% and preferably 33 wt% of the dietary fiber.

13. A method of delivering dietary fiber, comprising: a 1-kestose, nystose, and β-fructofuranosylnystose, a resistant maltodextrin, D-allulose, and 2′-fucosyllactose in a hard, amorphous structure with a water content less than 6 wt%; wherein said 1-kestose, nystose, and β-fructofuranosylnystose, said resistant maltodextrin, and said 2′-fucosyllactose account for 70 to 79 wt% on a dry matter basis; and sucrose, glucose, and fructose account for less than 5 wt% on a dry matter basis.

14. A composition as in claim 13 wherein said 1-kestose, nystose, and β-fructofuranosylnystose contribute 15 to 50 wt% and preferably 33 wt% of the dietary fiber, said resistant maltodextrin contributes 15 to 50 wt% and preferably 33 wt% of the dietary fiber, and 2′-fucosyllactose contributes 15 to 50 wt% and preferably 33 wt% of the dietary fiber.

15. A method of delivering human milk oligosaccharides in a hard amorphous structure.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0006] A hard lozenge comprised of a blend of dietary fibers and a nonnutritive bulk sweetener and/or nonnutritive high-intensity sweeteners and/or flavorings is discussed herein. The present disclosure is considered to exemplify the invention and is not intended to limit the invention to the specific embodiments illustrated by the figures and descriptions below. The term “dietary fiber” as used herein, unless otherwise specified, refers to the edible parts of plants or analogous carbohydrates that are resistant to digestion and absorption in the human small intestine, with complete or partial fermentation in the large intestine. The term “human milk oligosaccharide” as used herein, unless otherwise specified, refers to oligosaccharides identified in human milk that are not digested by the endogenous enzymes of the digestive tract but fermented by microorganisms inhabiting the large bowel. The term “nondigestible” as used herein, unless otherwise specified, refers to material not being digested and absorbed in the human small intestine. The term “lozenge” as used herein, unless otherwise specified, refers to a hard structure that dissolves slowly in the mouth. The term “amorphous” as used herein, unless otherwise specified, refers to a state of material where the molecules have a random arrangement. The term “glucose polymer” as used herein, unless otherwise specified, refers to large molecules composed of greater than five glucose molecules. The term “fructooligosaccharides” as used herein, unless otherwise specified, refers to a linear chain of fructose molecules, linked by beta (2-1) bonds ranging from 2 to 5 units and often terminate in glucose. The term “nonnutritive” as used herein, unless otherwise specified, refers to not providing nourishment by delivering little to no calories to the diet. The term “sweetener” as used herein, unless otherwise specified, is a substance that impacts sweetness. The term “flavoring” as used herein, unless otherwise specified, refers to a substance that provides flavor. The term “nonnutritive bulk sweetener” as used herein, unless otherwise specified, refers to an ingredient that does not provide nourishment by delivering little to no calories to the diet but provides bulk and sweetness to food comparable to that provided by sucrose and fructose. The term “nonnutritive high-intensity sweeteners” as used herein, unless otherwise specified, refers to an ingredient that does not provide nourishment by delivering little to no calories to the diet and provides essentially no bulk to food due to having a sweetness level greater than 100 times that of sucrose.

[0007] For the purpose of this invention, the sources of dietary fiber will include nondigestible fructooligosaccharides, nondigestible glucose polymers, and human milk oligosaccharides. An example of a nondigestible fructooligosaccharide is short-chain fructooligosaccharides. Short-chain fructooligosaccharides are composed of GF2 (1-kestose), GF3 (nystose), and GF4 (β-fructofuranosylnystose) with G representing glucose and F representing fructose. The degree of polymerization ranges from 3 - 5 monosaccharides with a molecular weight distribution of 500 -830 Da. An example of a commercial source of fructooligosaccharides composed of GF2, GF3, and GF4 is Nutraflora P-95 (Ingredion Corporation, Westchester, Illinois). On a dry matter basis, Nutraflora P-95 is composed of 30 - 42% GF2, 45 - 57% GF3, and 5 - 15% GF4 (www.ingredion.com). According to specifications provided by Ingredion, Nutraflora scFOS P-95 is a powder with a maximum water content of 5%, a maximum sugar content (sucrose, glucose, fructose) of 5%, and a minimum of 95% short-chain fructooligosaccharides on a dry matter basis. Short-chain fructooligosaccharides cannot be digested by the endogenous enzymes of the human gastrointestinal tract and are considered a source of dietary fiber. An example of nondigestible glucose polymers includes resistant maltodextrins. Resistant maltodextrins are produced from starch with a process involving heat and/or acid and/or enzymes that form linkages that cannot be cleaved by mammalian enzymes in the gastrointestinal tract. An example of a resistant maltodextrin is Fibersol-2 (ADM/Matsutani, LLC, Decatur, Illinois). On a dry matter basis, soluble fiber content is 90% minimum. Fibersol-2 contains a maximum of 2% sugars (glucose, fructose, sucrose) on a dry matter basis. Fibersol-2 has a degree of esterification of less than 20 and an average molecular weight of 2,000 Da (Ohkuma, K.; Wakabayashi, S. Fibersol-2: a soluble, nondigestible, starch derived dietary fibre. Advanced Dietary Fibre Technology. 2017, 509-522.) For the purpose of this invention, the nonnutritive bulk sweetener will include the rare sugar D-allulose (Tate & Lyle, London, UK). D-allulose, also known as D-psicose, is a C-3 epimer of fructose that has about two-thirds the sweetness of sucrose but minimal caloric content (0.4 kcal/g). About 70% of D-allulose is absorbed in the small intestine within one hour but is excreted intact in the urine within 24 hours, while the other 30% is transported to the large intestine, where it is not fermented and thus excreted intact within 48 hours. An example of a human milk oligosaccharide is 2′-fucosyllactose (2′-FL) with a commercial source available from DSM (Heerlen, Netherlands). The hard lozenge comprising dietary fiber will desirably include a nonnutritive high-intensity sweetener to provide the product with appealing sweetness. Examples of useful nonnutritive high-intensity sweeteners include stevia extract and monk fruit extract. The hard lozenge comprising dietary fiber will also desirably include a flavoring and/or coloring to provide the product with an appealing appearance and an acceptable taste for oral consumption. Examples of useful flavorings include peppermint, ginger, strawberry, mint, watermelon, cherry, lemon, orange, apple, grape, and raspberry.

[0008] The process to make the hard dietary fiber lozenge is similar to the process for making hard candy. In the process of making hard candy, sugar (sucrose), corn syrup, and water are combined and heated until reaching a temperature of approximately 300° F. (Hartel, R. Hard Candy: from hard crack to the glass transition. The Manufacturing Confectioner. 2012, 92, 70-80.) Reduced temperatures (e.g., 280° F.) are possible if a vacuum cooker is used. Once removed from heat and cooled the syrup hardens forming a hard, amorphous structure with a moisture content less than 5% that is referred to as hard glass candy. In the current invention, short-chain fructooligosaccharides, human milk oligosaccharides, and D-allulose replace sucrose and resistant maltodextrin replaces corn syrup.

[0009] The following examples illustrate specific embodiments and/or features of the present disclosure. The examples are given solely for the purpose of illustration and are not to be construed as limitations of the present disclosure, as many variations thereof are possible without departing from the spirit and scope of the disclosure.

Example1

[0010] Hard lozenges were prepared using Nutraflora P-95, Fibersol-2, 2′-fucosyllactose, D-allulose, and water. One hundred and ten grams of Nutraflora P-95, 116 grams of Fibersol-2, 111 grams of 2′-fucosyllactose, 79 grams of D-allulose, and 151 milliliters of water were combined and heated to 300° F. The resulting syrup was removed from the heat source. The syrup was allowed to cool and formed into hard lozenges. Nutraflora P-95, Fibersol-2, and 2′-fucosyllactose each provide about 33% of the dietary fiber to the final product. A sample was subjected to X-ray diffraction (XRD) to determine the crystallinity of the hard lozenge by H&M Analytical Services, Inc., 18C Hornerstown Rd, Cream Ridge, NJ 08514. The lozenge was ground to a fine powder with a mortar and pestle. The powder was backloaded into a standard sample cup and put into a Panalytical X′Pert Pro diffractometer using Cu radiation at 45 KV/40mA. The scan was run over the 20 range of 6° to 80° with a step size of 0.0167° and an accumulated counting time of 250 seconds per step. Based on the pattern collected, no crystalline peaks were noted, and the sample was 100% amorphous. An amorphous structure indicates that a hard glass candy structure was obtained. Free sugars (fructose, glucose, lactose, maltose, sucrose) were also measured in the sample using a modification of AOAC method 982.14 to determine if the Nutraflora P-95, Fibersol-2 or 2′-fucosyllactose were degraded during processing. Based on ingredient specifications for sugar content of Nutraflora P-95, Fibersol-2, and 2′-fucosyllactose the hard lozenge may contain up to 5% by weight total sugars. Analysis of the sample showed that it contained 1.82% total sugars indicating that the primary ingredients, Nutraflora P-95, Fibersol-2, and 2′-fucosyllactose were not degraded during thermal processing. Moisture content of the sample using the Karl Fischer method (AOCS Ca 2e-84) was found to be 5.75%. Sugar and moisture analyses were performed by Eurofins Scientific Inc., 2200 Rittenhouse Street, Suite 50, Des Moines, IA 50321.

Example 2

[0011] Hard lozenges were prepared using Nutraflora P-95, Fibersol 2, 2′-fucosyllactose, D-allulose, water, peppermint oil (www.LorAnnOils.com), and stevia extract (Shandong Haigen Biotechnology). One hundred and ten grams of Nutraflora P-95, 116 grams of Fibersol-2, 111 grams of 2′-fucosyllactose, 79 grams of D-allulose, and 151 grams of water were combined and heated to 300° F. The syrup was removed from the heat and one gram stevia extract, and 1.2 milliliters of peppermint oil were added. After mixing, the syrup was allowed to cool and formed into hard lozenges. Nutraflora P-95, Fibersol-2, and 2′-fucosyllactose each provide about 33% of the dietary fiber to the final product. Free sugars (fructose, glucose, lactose, maltose, sucrose) were also measured in the peppermint flavored sample using a modification of AOAC method 982.14 to determine if the Nutraflora P-95, Fibersol-2 or 2′-fucosyllactose were degraded during processing. Based on ingredient specifications for sugar content of Nutraflora P-95, Fibersol-2, and 2′-fucosyllactose, the hard lozenge may contain up to 5% by weight total sugars. Analysis of the sample showed that it contained 2.28% total sugars indicating that the primary ingredients, Nutraflora P-95, Fibersol-2, and 2′-fucosyllactose, were not degraded during thermal processing. Moisture content of the sample using the Karl Fischer method (AOCS Ca 2e-84) was found to be 4.07%. Sugar and moisture analyses were performed by Eurofins Scientific Inc., 2200 Rittenhouse Street, Suite 50, Des Moines, IA 50321.