NUTRITIONAL SUPPLEMENTS

Abstract

The present invention provides nutritional supplements comprising alginate, preferably in combination with pectin, which will form hydrogels in the stomach when exposed to the low pH of the gastric juice. The formation of a hydrogel will lead to delayed release of sugars and other active ingredients in the stomach. The nutritional supplements can comprise high concentrations of sugars and complex carbohydrates without causing unwanted gastrointestinal symptoms.

Claims

1. (canceled)

2. A liquid nutritional supplement comprising; a) 0.1 to 2.0 wt % alginate b) 0.1 to 1.5 wt % pectin, and c) 35 to 80 wt % active ingredients, where the active ingredients are selected from one or more of the ingredients consisting of sugars, complex carbohydrates, electrolytes, and amino acids.

3. (canceled)

4. A liquid nutritional supplement comprising; a) 0.1 to 3.5 wt % alginate, and b) 35 to 80 wt % active ingredients, where the active ingredients are selected from one or more of the ingredients consisting of sugars, complex carbohydrates, electrolytes, and amino acids.

5. The liquid nutritional supplement according to claim 4, wherein the alginate content is 0.1 to 2.0 wt %.

6. The liquid nutritional supplement according to claim 2, wherein the alginate content is 0.3 to 0.7 wt %.

7. The liquid nutritional supplement according to claim 2, wherein the alginate is high-guluronate (high-G) alginate.

8. The liquid nutritional supplement according to claim 2, wherein the pectin content is 0.2 to 1.0 wt %.

9. The liquid nutritional supplement according to claim 8, wherein the pectin content is 0.2 to 0.6 wt %.

10. The liquid nutritional supplement according to claim 9, wherein the pectin content is 0.3 to 0.5 wt %.

11. The liquid nutritional supplement according to claim 2, wherein the pectin is high-ester/high-methylated (HE/HM) pectin.

12. The liquid nutritional supplement according to claim 2, wherein the content of active ingredients is 40 to 80 wt %.

13. The liquid nutritional supplement according to claim 12, wherein the content of active ingredients is 50 to 80 wt %.

14. The liquid nutritional supplement according to claim 13, wherein the content of active ingredients is 50 to 75 wt %.

15. The liquid nutritional supplement according to claim 2, wherein the sugar content is 35 to 75 wt %.

16. The liquid nutritional supplement according to claim 2, wherein the sugar content is 50 to 65 wt %.

17. The liquid nutritional supplement according to claim 2, wherein the sugars comprise at least one or more of glucose, fructose, sucrose and isomaltose.

18. The liquid nutritional supplement according to claim 2, wherein the complex carbohydrates comprise at least one or more of starch, maltodextrin, glucose syrup and fructose syrup.

19. The liquid nutritional supplement according to claim 2, wherein the electrolytes comprise at least one or more of chloride, phosphate and citrate salts of sodium, potassium, zinc and magnesium.

20. The liquid nutritional supplement according to claim 2, comprising a) 0.3 to 0.7 wt % alginate, b) 0.3 to 0.5 wt % pectin, and c) 50 to 75 wt % active ingredients, consisting of 0 to 35 wt % fructose, 0 to 35 wt % glucose, 0 to 70 wt % sucrose, 0 to 35 wt % maltodextrin, and 0 to 1 wt % sodium chloride.

Description

LEGEND TO THE FIGURE

[0096] FIG. 1. Release of carbohydrates from a formulation after gelling in simulated gastric fluid (SGF). BRIX concentrations measured in SGX at different time point after 0.5-21 min given as percentage of BRIX concentrations measured after-24 h.

DETAILED DESCRIPTION OF THE INVENTION

[0097] Upon digestion the liquid nutritional supplements comprising pectin and alginate will form a gel in the stomach when exposed to the low pH of gastric juice. The gel formation will lead to slow release of sugars in the stomach (FIG. 1), avoiding unwanted gastrointestinal symptoms.

Pectin

[0098] Pectin, also known as pectic polysaccharides, is rich in galacturonic acid. Several distinct polysaccharides have been identified and characterised within the pectic group. Homogalacturonans are linear chains of -(1-4)-linked D-galacturonic acid. Rhamnogalacturonan I pectins (RG-I) contain a backbone of the repeating disaccharide: .fwdarw.4)--D-galacturonic acid-(1,2)--L-rhamnose-(1.fwdarw.. From many of the rhamnose residues, sidechains of various neutral sugars branch off. The neutral sugars are mainly D-galactose, L-arabinose and D-xylose, with the types and proportions of neutral sugars varying with the origin of pectin. Another structural type of pectin is rhamnogalacturonan II (RG-II), which is a less frequent, complex, highly branched polysaccharide. Rhamnogalacturonan II can be classified within the group of substituted galacturonans since the rhamnogalacturonan II backbone is made exclusively of D-galacturonic acid units.

[0099] Isolated pectin has a molecular weight of typically 60-150,000 g/mol, varying with origin and extraction conditions.

[0100] The carboxyl group of the homogalacturonan is, in nature, highly esterified with methyl groups (typically 70%). The proportion between methylated and non-methylated carboxyl groups, or the degree of methylation (DM) depends among other aspects on maturity of the plant. Once the homogalacturonan is extracted from the plant, the DM is routinely varied, either increased via dispersion in methanol under acid conditions or decreased via acid, alkali or enzymic treatment. The ratio of esterified to non-esterified galacturonic acid determines the gelation behavior of pectin. Pectin with a high degree of methyl esters (>50%) are denoted high methoxy pectin (HM pectin) or high ester pectin (HE pectin) and those with low methoxy content (<50%) as low methoxy pectin (LM pectin) or low ester pectin (LE pectin).

[0101] The non-esterified galacturonic acid units can be either free acids (carboxyl groups) or salts with sodium, potassium, or calcium. The salts of partially esterified pectins are called pectinates, if the degree of esterification is below 5 percent the salts are called pectates, the insoluble acid form, pectic acid. All forms of pectin, including HM-pectin, LM-pectin, and amidated LM-pectin, can be used according to the invention. The preferred pectin is HM-pectin.

Alginates

[0102] Alginate, also called algin or alginic acid, is an anionic polysaccharide distributed widely in the cell walls of brown algae. Alginate acid is a linear copolymer with homopolymeric blocks of (1-4)-linked -D-mannuronate (M) and its C-5 epimer -L-guluronate (G) residues, respectively, covalently linked together in different sequences or blocks. The monomers can appear in homopolymeric blocks of consecutive G-residues (G-blocks), consecutive M-residues (M-blocks) or alternating M and G-residues (MG-blocks). All forms of alginate, including high-G alginate and high-M alginate, can be used according to the invention. The preferred alginate is high-G alginate. The counter ion can e.g. be sodium (sodium-alginate), potassium (potassium-alginate), ammonium (ammonium alginate) or other suitable cations, or mixtures thereof.

Sugars

[0103] Sugars that can be used according to invention, but not limited to, are monosaccharides like glucose, fructose, galactose, disaccharides like lactose, maltose, sucrose, lactulose, trehalose, cellobiose.

Complex Carbohydrates

[0104] Complex carbohydrates that can be used according to the invention, but not limited to, are components of starch like amylose and amylopectin, maltodextrin, glucose syrup and fructose syrup.

EXAMPLES

Material and Methods

[0105] Maltodextrin (35 g), fructose (25 g), sodium alginate (0.105 g), Pectin (0.07 g), and NaCl (1.1 g) were mixed with water (total weight 100 g) in a closed vial by magnetic stirring for 2 h. Release tests were carried out by pouring 15 ml of a mixture into 40 ml of simulated gastric fluid (SGF) in a 60-ml cylindrical container (inner diameter 26 mm, length 120 mm) which was slowly rotated (16 rpm). Samples (0.20 ml) of the SGF were taken at 0.5, 1, 2, 3, 6, 9, 12, 15, 18 and 21 min and after 24 h. Optical density and corresponding BRIX-concentration was measured by an ATAGO PAL-3 refractometer.

Results

[0106] The formulation formed a gel in contact with SGF. Carbohydrates were slowly released from the gel (FIG. 1). BRIX concentrations measured after 21 min were 65% of BRIX concentration measured after 24 h (FIG. 1).