WO2001032037A1 - Compositions et procedes d'enrichissement en calcium de produits laitiers et d'aliments oleagineux - Google Patents
Compositions et procedes d'enrichissement en calcium de produits laitiers et d'aliments oleagineux Download PDFInfo
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- WO2001032037A1 WO2001032037A1 PCT/US2000/030182 US0030182W WO0132037A1 WO 2001032037 A1 WO2001032037 A1 WO 2001032037A1 US 0030182 W US0030182 W US 0030182W WO 0132037 A1 WO0132037 A1 WO 0132037A1
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- calcium
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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
- A23G9/00—Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor
- A23G9/32—Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor characterised by the composition containing organic or inorganic compounds
- A23G9/325—Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor characterised by the composition containing organic or inorganic compounds containing inorganic compounds
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
- A23C19/00—Cheese; Cheese preparations; Making thereof
- A23C19/06—Treating cheese curd after whey separation; Products obtained thereby
- A23C19/068—Particular types of cheese
- A23C19/08—Process cheese preparations; Making thereof, e.g. melting, emulsifying, sterilizing
- A23C19/082—Adding substances to the curd before or during melting; Melting salts
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/12—Fermented milk preparations; Treatment using microorganisms or enzymes
- A23C9/13—Fermented milk preparations; Treatment using microorganisms or enzymes using additives
- A23C9/1307—Milk products or derivatives; Fruit or vegetable juices; Sugars, sugar alcohols, sweeteners; Oligosaccharides; Organic acids or salts thereof or acidifying agents; Flavours, dyes or pigments; Inert or aerosol gases; Carbonation methods
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/12—Fermented milk preparations; Treatment using microorganisms or enzymes
- A23C9/13—Fermented milk preparations; Treatment using microorganisms or enzymes using additives
- A23C9/1322—Inorganic compounds; Minerals, including organic salts thereof, oligo-elements; Amino-acids, peptides, protein-hydrolysates or derivatives; Nucleic acids or derivatives; Yeast extract or autolysate; Vitamins; Antibiotics; Bacteriocins
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/152—Milk preparations; Milk powder or milk powder preparations containing additives
- A23C9/1522—Inorganic additives, e.g. minerals, trace elements; Chlorination or fluoridation of milk; Organic salts or complexes of metals other than natrium or kalium; Calcium enrichment of milk
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/152—Milk preparations; Milk powder or milk powder preparations containing additives
- A23C9/1526—Amino acids; Peptides; Protein hydrolysates; Nucleic acids; Derivatives thereof
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS OR COOKING OILS
- A23D7/00—Edible oil or fat compositions containing an aqueous phase, e.g. margarines
- A23D7/005—Edible oil or fat compositions containing an aqueous phase, e.g. margarines characterised by ingredients other than fatty acid triglycerides
- A23D7/0056—Spread compositions
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS OR COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings or cooking oils
- A23D9/007—Other edible oils or fats, e.g. shortenings or cooking oils characterised by ingredients other than fatty acid triglycerides
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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 OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/16—Inorganic salts, minerals or trace elements
- A23L33/165—Complexes or chelates
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Definitions
- This invention is directed to a composition for calcium fortification of dairy products and oleaginous foods with calcium amino acid chelate complexes and calcium amino acid malic acid chelate complexes.
- the calcium amino acid chelate complexes and calcium amino acid malic acid chelate complexes of the present invention are stable, palatable, and bioavailable.
- calcium is an essential element for formation of bones and teeth in animals, including humans.
- calcium is the most abundant mineral in the body, approximately 99% of the body's calcium is found in the bones and teeth providing an exchangeable pool of calcium. The remaining one percent is widely distributed in cells and body fluids and is responsible for the regulation of a number of metabolic functions such as nerve impulse conduction, muscle fiber contraction, hormone secretion, blood coagulation, normal heart beat, activation of enzymes, and maintenance of cell membranes.
- metabolic functions such as nerve impulse conduction, muscle fiber contraction, hormone secretion, blood coagulation, normal heart beat, activation of enzymes, and maintenance of cell membranes.
- calcium is receiving much attention on the front line of medical science because it has recently been discovered that calcium is one of the most important elements for supporting many life activities.
- Dairy products such as cream, sour cream, milk, cheese, ice cream, and yogurt and oleaginous foods such as margarine, butter, lards, vegetable oil spreads, and vegetable oils are important parts of the human daily diet.
- oleaginous foods such as margarine, butter, lards, vegetable oil spreads, and vegetable oils
- the calcium content found naturally in dairy products and oleaginous foods may be acceptable if consumed at high quantities, there is great public interest in the consumption of calcium fortified dairy products and oleaginous foods that contain a relatively high percentage of stable, palatable and bioavailable calcium. It is common practice to fortify food products with calcium sources, some of which are insoluble and some of which are soluble at or near neutral pH levels.
- an amino acid chelate as "the product resulting from the reaction of a metal ion from a soluble metal salt with amino acids having a mole ratio of one mole of metal to one to three (preferably two) moles of amino acids to form coordinate covalent bonds.
- the average weight of the hydrolyzed amino acids must be approximately 150 and the resulting molecular weight of chelate must not exceed 800.”
- amino acid chelates show enhanced bioavailability as compared to non-chelated minerals. Moreover, it is also known that this increased bioavailability is the result of the active transport of amino acid chelates from the digestive tract and into the blood stream.
- the chelated mineral ions are absorbed through the intestinal lining and into the blood stream, utilizing the amino acids as active transport carriers. More specifically, amino acid chelates are absorbed intact by mucosal cells in the intestines through active transport as is disclosed in U.S. Patent No. 4,863,898.
- inorganic calcium salts are ionic, they cannot make use of this active transport mechanism, thereby limiting absorption. Therefore, ingested inorganic calcium salts are less bioavailable than the corresponding calcium amino acid chelates. This is in part due to the fact that competition of ions for active sites and the resulting suppression of one nutritive mineral element by another are both avoided.
- amino acid chelates can be prepared from metal ions which do not come from soluble salts.
- U.S. Patent Nos. 4,599,152 and 4,830,716 both disclose methods of preparing pure amino acid chelates using metal sources other than soluble metal salts. Additionally, in U.S. Patent No. 5,516,925, methods of preparing amino acid chelates having improved palatability are also disclosed.
- dairy products and oleaginous foods such as cheese, yogurt, ice cream, cream, milk, margarine, oils, etc.
- dairy products and oleaginous foods such as cheese, yogurt, ice cream, cream, milk, margarine, oils, etc.
- fresh skim and whole milk both contain approximately 118 mg of calcium per 100 g of milk.
- milk is advantageously consumed by those persons who may be most in need of an adequate calcium intake including people who are dieting and women who are pregnant or middle aged.
- U.S. Patent 4,784,871 a calcium fortified yogurt is disclosed.
- an acid soluble salt is added to the fruit flavoring prior to combining the flavoring with the yogurt base.
- the preferred calcium salt used is tricalcium phosphate, dicalcium phosphate, and hydrates thereof. Further, the amounts used are visually undetectable.
- U.S. Patent 5,449,523 a calcium fortified yogurt is disclosed. In that patent, the calcium source is added to the yogurt milk base prior to pasteurization without undesirable precipitation.
- the process comprises preparing a yogurt base mix comprised of a fermentable dairy ingredient, a calcium source, a chelating agent, and/or an alkaline agent.
- the chelating and/or alkaline agents are added in amounts to keep the pH of the yogurt base mix above 6.7 prior to pasteurization.
- the preferred chelating agents are alkali metal citrates which have the primary task of moderating the pH level.
- the present invention is drawn to compositions and methods of preparing oleaginous or highly lipid foods emulsified with a calcium amino acid chelate complex or a calcium amino acid malic acid chelate complex. Even when these chelate complexes are incorporated into the various dairy products and oleaginous foods, they are stable and maintain appropriate organoleptic properties, i.e., color, texture, taste, smell, and consistency are acceptable.
- the calcium amino acid chelate complexes of the present invention are prepared by reacting at least one calcium compound, an amino acid ligand, a pH adjuster, and, optionally, a stabilizing/suspending agent in an aqueous environment at a pH from about 6.5 to 9.
- the calcium amino acid chelate complex should have an amino acid ligand to calcium molar ratio of about 1 : 1 and a calcium content from 15 to 22% by weight. Further, the calcium amino acid chelate complex must have a coordinate covalent bond between the ⁇ -amino group of the amino acid ligand and the calcium ion.
- a first embodiment is prepared by reacting calcium carbonate, an amino acid, and phosphoric acid in an aqueous environment producing a calcium amino acid chelate complex having about a 1 : 1 amino acid ligand to metal molar ratio.
- an embodiment may be prepared by reacting calcium oxide, an amino acid, citric acid, and calcium carboxymethylcellulose (CMC) in an aqueous environment producing a calcium amino acid chelate complex having about a 1 : 1 amino acid ligand to metal molar ratio.
- a third embodiment may be prepared by reacting calcium oxide, calcium chloride, calcium carboxymethylcellulose (CMC), an amino acid, and phosphoric acid in an aqueous environment producing a calcium amino acid chelate complex having about a 1 : 1 amino acid ligand to metal molar ratio.
- a fourth embodiment may be prepared by reacting calcium oxide, calcium chloride, an amino acid, and phosphoric acid in an aqueous environment producing a calcium amino acid chelate complex having about a 1 : 1 amino acid ligand to metal molar ratio.
- the calcium amino acid malic acid chelate complexes are prepared by reacting calcium, an amino acid, and malic acid in water.
- the product produced has an amino acid to calcium content molar ratio from about 1 :2 to 1:1.
- malic acid is complexed to the calcium amino acid product at a malic acid to calcium content molar ratio from about 1 :2 to 2: 1. It is believed that the malic acid may complex directly with the calcium and/or form a complex with the calcium amino acid chelate.
- the terms "palatable” and “improved palatability” mean that compositions for calcium fortification of oleaginous or highly lipid foods of this invention are substantially lacking the metallic aftertaste or disagreeable flavor of prior art calcium fortified products to the extent that they have a more pleasant taste to the consuming warm-blooded host, i.e., an animal or human being. This is not to say that these calcium fortified dairy products or oleaginous foods are completely lacking flavor or taste.
- Bioavailable means, for purposes of this invention, that the calcium source is available to the body.
- amino acid chelate means, for purposes of this invention, that the amino acid forms a heterocyclic ring with the metal as the closing member. Typically, a coordinate covalent bonds exist between the metal ion and the ligand at the ⁇ - amino group. However, either ionic bonds, covalent bonds, and/or coordinate covalent bonds may exist between the carboxyl oxygen group and the metal ion.
- Amino acid chelate complex means that as the pH level of the calcium amino acid chelate is lowered, the reaction between the ⁇ -amino group and the calcium remains covalent, but the bond between the carboxyl oxygen and the calcium center becomes more ionic and less covalent.
- amino acid chelate and “amino acid chelate complex” may be used interchangeably, both of which refer to amino acid ligands bonded to metal ions such that a heterocyclic ring is formed with the ⁇ -amino nitrogen being covalently bonded to the metal ion.
- the pH adjuster may act merely to facilitate the reaction or may actually be complexed to the calcium amino acid chelate complex.
- Calcium amino acid malic acid chelate complex is a calcium amino acid chelate complex wherein malic acid, which acts in part as a pH adjuster, is preferably also complexed to the calcium amino acid chelate complex.
- “Stable” means that the fortificant of the present invention will not significantly alter the shelf-life of the oleaginous or highly lipid foods to which the amino acid chelate complex is added.
- “Compatible” refers to the fact that the oleaginous or highly lipid foods fortified with the amino acid chelate complexes of the present invention do not significantly affect the organoleptic properties, i.e., sensory properties of the underlying oleaginous food product. For example, taste, texture and smell of the underlying oleaginous or highly lipid foods are not significantly altered in the presence of the amino acid chelate complexes of the present invention.
- “Dairy products” include, but are not limited to, whole milk, low-fat milk, non-fat milk, flavored milk, cheese, processed cheese, yogurt, frozen yogurt, cream, sour cream, low-fat ice cream, non-fat ice cream, and ice cream.
- Oleaginous food or “highly lipid food” refers to food products containing a majority of oil or fat such as, but not limited to, margarine, butter, lards, vegetable oil spreads, and all kinds of edible plant oil and oil dressings.
- the present invention is directed toward compositions and methods of making and preparing calcium amino acid chelate complexes for fortification of dairy products and oleaginous foods. Additionally, compositions and methods of making calcium amino acid malic acid chelate complexes are also disclosed that can be used to fortify oleaginous foods.
- the calcium amino acid chelate complexes and calcium amino acid malic acid chelate complexes when incorporated in dairy products or oleaginous foods, are bioavailable, palatable, and relatively stable for periods of time comparable to the natural shelf life of the dairy products and oleaginous food products in an unfortified state.
- the fortified dairy products and oleaginous foods may be frozen, refrigerated, or shelf-stored.
- a composition for providing a calcium source for calcium fortification of dairy products and oleaginous foods may be prepared by reacting a calcium compound, an amino acid ligand, and a pH adjuster in an aqueous environment at a pH from about 6.5 to 9.
- the calcium amino acid chelate complex should have an amino acid ligand to calcium molar ratio of about 1 : 1 and a calcium content from about 15 to 22% by weight.
- the calcium amino acid chelate complex must include a coordinate covalent bond between the ⁇ -amino group of the amino acid ligand and the calcium ion.
- the calcium compound may be provided in the form of calcium carbonate, calcium oxide, calcium chloride, or combinations thereof, e.g., calcium oxide/calcium chloride.
- the amino acid ligand may be selected from the group consisting of alanine, arginine, asparagine, aspartic acid, cysteine, cystine, glutamine, glutamic acid, glycine, histidine, hydroxyproline, isoleucine, leucine, lysine, methionine, ornithine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, and valine.
- Other ligands may include dipeptides, tripeptides, and tetrapeptides formed by any combination of the aforementioned amino acids. Glycine is particularly preferred as the chelating ligand.
- the pH adjuster may be phosphoric acid, citric acid, malic acid, lactic acid, and/or acetic acid. Other possible adjusters and/or buffering agents may also be used.
- the pH adjuster may either act merely to adjust the pH of the reaction, or alternatively, may actually complex with the calcium amino acid chelate complexes.
- Calcium carboxymethylcellulose (CaCMC) may optionally be added as a stabilizing/suspending agent.
- a first preferred embodiment is a calcium amino acid chelate complex prepared by reacting calcium carbonate, glycine, and phosphoric acid in an aqueous environment.
- a second preferred embodiment is prepared by reacting calcium oxide, glycine, citric acid, and calcium carboxymethylcellulose (CaCMC) in an aqueous environment.
- CaCMC calcium carboxymethylcellulose
- a third preferred embodiment is a calcium amino acid chelate complex prepared by reacting calcium oxide, calcium chloride, glycine, phosphoric acid, and calcium carboxymethylcellulose (CaCMC) in an aqueous environment.
- a fourth preferred embodiment is prepared by reacting calcium oxide, calcium chloride, glycine, and phosphoric acid in an aqueous environment.
- dairy products and oleaginous foods that may be fortified by one or more embodiments of the present invention.
- Products such as whole milk, low-fat milk, non-fat milk, flavored milk, cheese, processed cheese, yogurt, frozen yogurt, cream, sour cream, low-fat ice cream, non-fat ice cream and ice cream, margarine, butter, lards, and oils are illustrative. It is important to consider that each of these dairy products and oleaginous foods present different challenges in suspending various calcium sources within that product. For example, with milk, there may be more difficulty in suspending the calcium source over long periods of time than would be the case with yogurt or margarine. Therefore, selection of the calcium amino acid chelate complex, pH balance, and/or use of a suspending agent may require some adjustment with respect to each individual product.
- the calcium fortified dairy products and oleaginous foods of the present invention may have suspended therein a calcium amino acid chelate complex ranging from about 0.01 to 5% by weight based upon the weight of the respective dairy product or oleaginous food. However, weight ranges from 0.1 to
- emulsifiers and/or stabilizers may be added as well. Effective suspension and homogenization of the calcium fortified dairy products may be enhanced by the addition of hydrocolloid gums or other emulsifiers such as mono or di-glycerides, lecithin, sodium stearyl lactate, or the citric acid ester of a monoglyceride.
- a method of preparing a calcium amino acid chelate complex having a ligand to metal molar ratio of about 1 : 1 is also disclosed.
- the first step is to admix, in an aqueous environment, the ingredients comprising an amino acid ligand, a calcium compound, a pH adjuster, and, optionally, a stabilizer/suspending agent.
- the ingredients are allowed to react until a pH of from about 6.5 to 9 is reached. Agitation may assist the reaction.
- the reacted ingredients are dried, e.g., spray dried, tray dried, oven dried, drum dried, etc., to form a particulate product.
- the calcium amino acid malic acid chelate complexes can be prepared by reacting calcium, an amino acid, and malic acid in water.
- the product produced has an amino acid to calcium content molar ratio from about 1 :2 to 1 : 1.
- malic acid is complexed to the calcium amino acid product at a malic acid to calcium molar ratio from about 2: 1 to 1 :2.
- Malic acid which is an ⁇ -hydroxy acid, is often used as a buffering agent or a chelating agent and may be represented by Formula 1 below:
- the malic acid may chelate or complex with the amino acid chelate complexes is by bonding with the calcium ion or calcium chelate complex at the ⁇ -hydroxy group and/or at one of the carboxyl oxygen groups. In such an instance, either a six membered ring or, preferably, a five membered ring may be formed. However, this is merely one proposed mechanism of attachment. It is notable that the malic acid may complex directly with the calcium and/or with the calcium amino acid chelate as long as the calcium amino acid chelate complex is comprised of calcium, an amino acid and malic acid in the prescribed ratios.
- the calcium source is preferably calcium oxide.
- other calcium compounds may be used such as calcium hydroxide, calcium carbonate and calcium chloride.
- the amino acid ligand may be selected from the group consisting of alanine, arginine, asparagine, aspartic acid, cysteine, cystine, glutamine, glutamic acid, glycine, histidine, hydroxyproline, isoleucine, leucine, lysine, methionine, ornithine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine and valine, and dipeptides, tripeptides, and tetrapeptides formed by any combination of said amino acids thereof.
- composition of the present invention is prepared by reacting calcium oxide, malic acid, and glycine.
- amino acid ligand to calcium molar ratio is from about 0.85: 1 to 1 : 1.
- malic acid to calcium molar ratio is from about 1 :0.7 to 1 : 1.
- the calcium amino acid malic acid chelate complex may be added to the emulsion process of an oleaginous food product such as margarine, butter, lards and all kinds of edible plant oils, vegetable oil spreads, and oil dressings.
- an emulsifier selected from the group consisting of carrageenans, gum arabic, and guar gum may be used.
- a stabilizer selected from the group consisting of monoglyceride, diglyceride, lecithin, sodium stearyl lactate, citric acid ester of monoglyceride, and combinations thereof may also be added to certain oleaginous foods.
- the heated solution was then filtered and spray dried producing a calcium glycine chelate having a calcium content of 20% by weight.
- the amino acid chelate complex has a ligand to metal molar ratio of about 1 : 1.
- the product obtained was a scentless, white fine powder.
- the particle size of the calcium amino acid chelate complex is preferably within a range of 60- 170 mesh and most preferably about
- the calcium source prepared as described above was stable at 106°F for 12 weeks.
- the calcium amino acid chelate made by the above process can then be added to a dairy product such as cream, sour cream, milk, cheese, ice cream, yogurt, and the like and/or oleaginous foods such as margarine, butter, lards, and oils.
- Example 2 2% Milk fortified with a calcium amino acid chelate complex
- Calcium fortified milk was prepared as follows. The calcium amino acid chelate complex of Example 1 was prepared. Next, to one gallon of low fat milk,
- Example 3 Taste Test of 2% milk fortified with a calcium amino acid chelate complex
- a taste test was conducted by a panel of 20 randomly selected persons. Each panelist was asked to drink Vi glass of milk (4 oz.) prepared as described in Example 2 along with eating a cookie. Each panelist was then asked to rate the taste of the calcium fortified milk. Fifteen out of the twenty stated that the milk was better in taste than expected and four out of the remaining five stated the taste of the milk was acceptable. Seven out of the twenty indicated that, if given a choice, they would substitute the product containing the calcium amino acid chelate complex for their regular milk and nine out of the twenty stated they would buy this product in addition to their regular milk.
- a second embodiment of a calcium amino acid chelate complex was prepared by evenly splitting 2070 pounds of water into two tanks (1035 pounds in each tank). To the first tank, 361 pounds of glycine was added and blended for 15 minutes forming a clear solution. To the second tank, 269 pounds of calcium oxide, 48 pounds of calcium carboxy methyl cellulose (CaCMC) and 5 pounds of a silica based anti-caking agent were added to the water and blended for 15 minutes maintaining the temperature below 140°F to form a milky solution. The contents of both tanks were then combined, blended and held for 30 minutes at 140°F. Once this process was complete, 319 pounds of citric acid was slowly added to the mixture.
- CaCMC calcium carboxy methyl cellulose
- citric acid caused the mixture to heat up, but the temperature was maintained at about 150°F. After about 2/3 of the citric acid was added, the product began to thicken. As such, the addition of the citric acid was done slowly with vigorous agitation and this agitation was maintained throughout the process. Once complete, the product was then spray dried to a particle size of from 100 to 200 mesh. An assay of the product resulted in a white powder having not less than 17.5% calcium and not more than 5% moisture.
- Example 5 Milk fortified with a calcium amino acid chelate complex This model formulation for milk fortified with a calcium amino acid chelate complex as described in Example 4 will provide a product having 600 mg of calcium per 8-fl oz. of milk.
- a calcium amino acid chelate complex fortified milk product was prepared as the milk, milk fat, and milk solids were standardized to prescribed levels. Under good agitation, the dry ingredients were added including the calcium amino acid chelate complex of Example 4. The mixture was pasteurized at 170°F for 30 seconds and homogenized at 2000 psi. Once complete, the product was cooled to from 38 to 40°F. At this point, the product may be packaged, preferably in a container labeled to shake well before using to minimize any variations in calcium content throughout the package.
- Example 6 Preparation of a calcium amino acid chelate complex A third embodiment of a calcium amino acid chelate complex was prepared by evenly splitting 2070 pounds of water into two tanks (1035 pounds in each tank). To the first tank, 359 pounds of glycine was added and blended for 15 minutes forming a clear solution. To the second tank, 239 pounds of calcium oxide, 48 pounds of calcium chloride and 48 pounds of calcium carboxy methyl cellulose (CaCMC) were added to the water and blended for 15 minutes maintaining the temperature below 140°F to form a milky solution. The contents of both tanks were then combined, blended and held for 30 minutes at 140°F. Once this process was complete, 306.5 pounds of phosphoric acid (85%) was slowly added to the mixture.
- CaCMC calcium carboxy methyl cellulose
- Example 7 Milk fortified with a calcium amino acid chelate complex
- This model formulation for milk fortified with a calcium amino acid chelate complex as described in Example 6 will provide a product having 600 mg of calcium per 8-fl oz. of milk.
- a calcium amino acid chelate complex fortified milk product was prepared as the milk, milk fat, and milk solids were standardized to prescribed levels. Under good agitation, the dry ingredients were added including the calcium amino acid chelate complex of Example 6. The mixture was pasteurized at 170°F for 30 seconds and homogenized at 2000 psi. Once complete, the product was cooled to
- Example 8 Yogurt fortified with a calcium amino acid chelate complex
- This model formulation for yogurt fortified with a calcium amino acid chelate complex as described in Example 6 will provide a product having 600 mg of calcium per 8 ounces of yogurt.
- a calcium amino acid chelate complex fortified yogurt product was prepared as the milk, milk fat, and milk solids were standardized to the prescribed levels. Under good agitation, the dry ingredients were added including the calcium amino acid chelate complex of Example 6. The product was pasteurized at 195°F for 3 to 6 minutes and homogenized at 1000 psi. The product was then cooled to 107-112°F, inoculated with the starter culture and held in a tank at from 105 to 108°F until a pH of 4.5 was reached. Next, the product was gently agitated and cooled to 60-65°F, mixed with fruit and flavoring and then packaged in a container. Finally, the yogurt product was cooled to 38- 40°F.
- a fourth embodiment of a calcium amino acid chelate complex was prepared by evenly splitting 2070 pounds of water into two tanks (1035 pounds in each tank). To the first tank, 378 pounds of glycine was added and blended for 15 minutes forming a clear solution. To the second tank, 252 pounds of calcium oxide and 50 pounds of calcium chloride were added to the water and blended for 15 minutes maintaining the temperature below 140°F forming a milky solution. The contents of both tanks were then combined, blended and held for 30 minutes at 140°F. Once this process was complete, 322.6 pounds of phosphoric acid (85%) was slowly added to the mixture. The addition of phosphoric acid caused the mixture to heat up, but the temperature was maintained at about 150°F. After about 2/3 of the phosphoric acid was added, the product began to thicken so the continued addition of the phosphoric acid was done slowly with vigorous agitation. The product was then allowed to react to completion reaching a pH of about 7.5.
- Vigorous agitation was maintained during this process.
- the product was then spray dried to a particle size of from 100 to 200 mesh.
- An assay of the product results in a white powdered calcium amino acid chelate powder having a calcium content of not less than 18%, a moisture content of not more than 5%, and a pH of about 8.
- the product had a clean and non-bitter taste.
- Example 10 80% fat soft margarine fortified with calcium amino acid chelate complexes This model formulation for soft margarine fortified with a calcium amino acid chelate complex as described in Example 9 will provide a product having 200 mg of calcium per ounce margarine.
- a calcium amino acid chelate complex fortified margarine product was prepared by mixing the fat phase ingredients and heating to 122°F. Next, the water phase ingredients were mixed separately and also heated to 122°F. To prepare the emulsion, the water phase was slowly added to the fat phase with high sheer. The emulsion was then run through a scrape surface heat exchanger. The product may then be packaged and tempered at 41°F for 24 to 48 hours.
- Example 1 1 American pasteurized process cheese fortified with a calcium amino acid chelate complex This model formulation for American pasteurized process cheese fortified with a calcium amino acid chelate complex as described in Example 9 will provide a product having 400 mg of calcium per ounce cheese.
- a calcium amino acid chelate complex fortified American pasteurized process cheese was prepared by selecting a blend of mild, medium, sharp chedders and jack cheeses that delivered a desired flavor profile (this may be modified according to taste preference) The cheeses were warmed to room temperature and then ground into fine pieces The ground up cheese pieces were placed into a steam cooker under slow agitation until the cheese was melted throughout Water was added to attain a 40% moisture level Salt, color and the calcium amino acid chelate complex of Example 9 was then added Emulsifying salts were then added to the mixture before the temperature reached 120°F The pH level should remain between 5 6 and 6 However, if the pH level rises above 6 0, small amounts of lactic acid may be added to reduce the pH level The entire batch was cooked until the temperature reached 170°F for about 3 minutes The batch was then poured into a filler where the pH and moisture levels were once again confirmed The product may be filled into desired size packages or formed into slices Finally, the packaged cheese was tempered at room temperature for 4 to 18 hours.
- Example 12 Low-fat frozen yogurt fortified with a calcium amino acid chelate complex This model formulation for low-fat frozen yogurt fortified with a calcium amino acid chelate complex described in Example 9 will provide a product having 400 mg of calcium per 4 fl oz of low-fat frozen yogurt
- a calcium amino acid chelate complex fortified low-fat frozen yogurt was prepared by blending the mix portion with the yogurt portion at a 4: 1 ratio by weight.
- the mix portion was prepared by standardizing the milk, milk fat, and milk solids to the prescribed levels. Under good agitation, dry ingredients including the calcium amino acid chelate of Example 9 were admixed into the milk (excluding the flavoring). This mixture was pasteurized at 190°F for 45 seconds and homogenized at 1,500 psi. The product was then cooled to from 38 to 40°F and held in a blending tank.
- the yogurt portion was prepared by standardizing the milk and milk solids to the prescribed levels where they were pasteurized at 195°F for 3-6 minutes and homogenized at 1000 psi. The product was then cooled to 107-112°F where it was inoculated with the starter culture. The tank was held at 105-108°F until the pH reached 4.6. At this point, the acidic product was gently agitated and cooled to 40-
- Example 13 Ice cream fortified with a calcium amino acid chelate complex
- This model formulation for ice cream fortified with a calcium amino acid chelate complex described in Example 9 will provide a product having 400 mg of calcium per 4 fl oz. of ice cream.
- a calcium amino acid chelate complex fortified ice cream product was prepared by standardizing the milk, milk fat, and milk solids to the prescribed levels. Under good agitation, the dry ingredients including the calcium amino acid chelate complex of Example 9 were added. The product was pasteurized at 180°F for 35 seconds and homogenized at 2200 psi. Next, the pasteurized and homogenized product was cooled to from 38 to 40°F and held in a storage tank for from 4 to 24 hours. The flavor and color were then mixed into the vat containing the product. Once complete, the ice cream product was then sent to the continuous freezer set at 100% overrun.
- Example 14 Preparation of a calcium amino acid malic acid chelate complex
- About 249 parts by weight of calcium oxide was added to 1980 parts by weight of deionized water. The mixture was heated to 140°F and blended for 15 minutes. To this solution was added 228 parts by weight of glycine which was then blended for 60 minutes while maintaining a temperature of 150°F. Next, 518 parts by weight of malic acid was slowly added to the solution and was blended for 15 minutes. The heated solution was filtered and spray dried to produce a calcium glycine malic chelate complex having a content of 17.8% calcium by weight.
- the glycine to calcium molar ratio was about 0.96: 1. Further, the malic acid to calcium molar ratio was about 1 :0.81. When reconstituted in water, the solution had a pH of about 9.
- Example 15 Margarine fortified with a calcium amino acid chelate complex Calcium fortified margarine was prepared by the following process.
- a mixture of the fat phase consisting of partially hydrogenated soybean oil (21.0% by weight), liquid soybean oil (56.5% by weight), lecithin (Actiflo 68UB) (0.20% by weight), emulsifier (Dimodan PVP) (0.20% by weight) and beta carotene (color and vitamin A) (0.004% by weight) was heated to 50°C.
- a mixture of the water phase consisting of water (15.4% by weight), salt (1.20% by weight), non-fat dry milk (1.00% by weight), calcium amino acid chelate prepared as described in
- Example 1 (4.32% by weight), potassium sorbate (0.10% by weight), citric acid (0.05% by weight) and natural or artificial butter flavor (0.02% by weight) was heated to 50°C.
- the water phase was added to the fat phase with high sheer and the emulsion was run through the scrape surface heat exchanger. The product of the emulsion was then packaged and tempered at 5°C for 24-48 hours.
- This 80% soft margarine was fortified at a rate of 200mg calcium per ounce with the calcium amino acid chelate prepared as described in Example 1.
- the calcium fortified margarine prepared as described above was palatable and was stable at refrigerated temperature for up to four months.
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- Inorganic Chemistry (AREA)
- Nutrition Science (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
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Abstract
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU14534/01A AU1453401A (en) | 1999-11-01 | 2000-11-01 | Compositions and methods for calcium fortification of dairy products and oleaginous foods |
| BR0015182-3A BR0015182A (pt) | 1999-11-01 | 2000-11-01 | Composições e métodos para fortificação de cálcio de produtos de leiteria e alimentos oleaginosos |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/430,926 | 1999-11-01 | ||
| US09/431,387 US6294207B1 (en) | 1999-11-01 | 1999-11-01 | Calcium fortification of oleaginous foods |
| US09/430,926 US6299914B1 (en) | 1999-11-01 | 1999-11-01 | Compositions and methods for calcium fortification of dairy products and oleaginous foods |
| US09/431,387 | 1999-11-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2001032037A1 true WO2001032037A1 (fr) | 2001-05-10 |
Family
ID=27028832
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2000/030182 Ceased WO2001032037A1 (fr) | 1999-11-01 | 2000-11-01 | Compositions et procedes d'enrichissement en calcium de produits laitiers et d'aliments oleagineux |
Country Status (3)
| Country | Link |
|---|---|
| AU (1) | AU1453401A (fr) |
| BR (1) | BR0015182A (fr) |
| WO (1) | WO2001032037A1 (fr) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1366664A4 (fr) * | 2001-02-16 | 2004-04-07 | Murakashi Lime Ind | Composition antibacterienne |
| FR2850534A1 (fr) * | 2003-02-03 | 2004-08-06 | Gervais Danone Sa | Yoghourt de structure bimodale et procede de preparation |
| EP1576895A4 (fr) * | 2002-07-31 | 2005-12-14 | Maruo Calcium | Composition d'additif alimentaire et aliment la contenant |
| JP2006509787A (ja) * | 2002-12-05 | 2006-03-23 | エムディー バイオアルファ カンパニー リミテッド | アミノ酸キレートの調製方法 |
| WO2009132950A1 (fr) * | 2008-04-29 | 2009-11-05 | Unilever Nv | Procédé d'élaboration de boisson aqueuse emballée préservée de la chaleur qui renferme des micelles de caséine et des peptides riches en tryptophane, et produits résultants |
| CN105595346A (zh) * | 2015-09-01 | 2016-05-25 | 张伟 | 一种用于补钙的液体制剂及其制备方法 |
| WO2017054109A1 (fr) * | 2015-09-28 | 2017-04-06 | Nestec S.A. | Compositions nutritives synthétiques spécifiques du sexe et systèmes nutritifs les comprenant |
| CN114223907A (zh) * | 2021-12-23 | 2022-03-25 | 湖北省农业科学院农产品加工与核农技术研究所 | 一种小龙虾壳来源的谷氨酸螯合钙片及其制备方法 |
| CN114271336A (zh) * | 2021-12-06 | 2022-04-05 | 临夏燎原乳业产业研究院有限公司 | 一种用于防治骨质疏松的牦牛配方奶粉 |
| CN118511956A (zh) * | 2024-05-13 | 2024-08-20 | 通化康元生物科技有限公司 | 林蛙骨胶原蛋白复合肽固体饮料及其制备方法和应用 |
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| US5504055A (en) * | 1994-03-15 | 1996-04-02 | J.H. Biotech, Inc. | Metal amino acid chelate |
| US5516925A (en) * | 1994-08-23 | 1996-05-14 | Albion International, Inc. | Amino acid chelates having improved palatability |
| GB2299992A (en) * | 1995-04-20 | 1996-10-23 | Willem Jacob Serfontein | Complexes of magnesium and calcium |
| US5700513A (en) * | 1996-01-19 | 1997-12-23 | Abbott Laboratories | Liquid nutritional product containing improved stabilizer composition |
| WO1998014173A1 (fr) * | 1996-10-04 | 1998-04-09 | Natura, Inc. | Compositions comestibles basses calories d'un excipient et d'un ingredient actif et leurs procedes de preparation |
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2000
- 2000-11-01 WO PCT/US2000/030182 patent/WO2001032037A1/fr not_active Ceased
- 2000-11-01 BR BR0015182-3A patent/BR0015182A/pt not_active IP Right Cessation
- 2000-11-01 AU AU14534/01A patent/AU1453401A/en not_active Abandoned
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US5504055A (en) * | 1994-03-15 | 1996-04-02 | J.H. Biotech, Inc. | Metal amino acid chelate |
| US5516925A (en) * | 1994-08-23 | 1996-05-14 | Albion International, Inc. | Amino acid chelates having improved palatability |
| GB2299992A (en) * | 1995-04-20 | 1996-10-23 | Willem Jacob Serfontein | Complexes of magnesium and calcium |
| US5700513A (en) * | 1996-01-19 | 1997-12-23 | Abbott Laboratories | Liquid nutritional product containing improved stabilizer composition |
| WO1998014173A1 (fr) * | 1996-10-04 | 1998-04-09 | Natura, Inc. | Compositions comestibles basses calories d'un excipient et d'un ingredient actif et leurs procedes de preparation |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1366664A4 (fr) * | 2001-02-16 | 2004-04-07 | Murakashi Lime Ind | Composition antibacterienne |
| EP1576895A4 (fr) * | 2002-07-31 | 2005-12-14 | Maruo Calcium | Composition d'additif alimentaire et aliment la contenant |
| JP2006509787A (ja) * | 2002-12-05 | 2006-03-23 | エムディー バイオアルファ カンパニー リミテッド | アミノ酸キレートの調製方法 |
| EP1569943A4 (fr) * | 2002-12-05 | 2007-11-28 | Md Bioalpha Co Ltd | Procede pour la preparation de chelate d'acide amine |
| FR2850534A1 (fr) * | 2003-02-03 | 2004-08-06 | Gervais Danone Sa | Yoghourt de structure bimodale et procede de preparation |
| WO2004068958A1 (fr) * | 2003-02-03 | 2004-08-19 | Compagnie Gervais Danone | Yoghourt de structure bimodale et procede de preparation |
| WO2009132950A1 (fr) * | 2008-04-29 | 2009-11-05 | Unilever Nv | Procédé d'élaboration de boisson aqueuse emballée préservée de la chaleur qui renferme des micelles de caséine et des peptides riches en tryptophane, et produits résultants |
| CN102076221A (zh) * | 2008-04-29 | 2011-05-25 | 帝斯曼知识产权资产管理有限公司 | 制备包含酪蛋白胶束和富含色氨酸的肽的有包装的、热防腐的水性饮品的方法及藉此获得的制品 |
| CN105595346A (zh) * | 2015-09-01 | 2016-05-25 | 张伟 | 一种用于补钙的液体制剂及其制备方法 |
| WO2017054109A1 (fr) * | 2015-09-28 | 2017-04-06 | Nestec S.A. | Compositions nutritives synthétiques spécifiques du sexe et systèmes nutritifs les comprenant |
| CN114271336A (zh) * | 2021-12-06 | 2022-04-05 | 临夏燎原乳业产业研究院有限公司 | 一种用于防治骨质疏松的牦牛配方奶粉 |
| CN114223907A (zh) * | 2021-12-23 | 2022-03-25 | 湖北省农业科学院农产品加工与核农技术研究所 | 一种小龙虾壳来源的谷氨酸螯合钙片及其制备方法 |
| CN114223907B (zh) * | 2021-12-23 | 2023-08-25 | 湖北省农业科学院农产品加工与核农技术研究所 | 一种小龙虾壳来源的谷氨酸螯合钙片及其制备方法 |
| CN118511956A (zh) * | 2024-05-13 | 2024-08-20 | 通化康元生物科技有限公司 | 林蛙骨胶原蛋白复合肽固体饮料及其制备方法和应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| BR0015182A (pt) | 2002-07-16 |
| AU1453401A (en) | 2001-05-14 |
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