WO2017003522A1 - Animal feed composition and method of making same - Google Patents
Animal feed composition and method of making same Download PDFInfo
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- WO2017003522A1 WO2017003522A1 PCT/US2016/016147 US2016016147W WO2017003522A1 WO 2017003522 A1 WO2017003522 A1 WO 2017003522A1 US 2016016147 W US2016016147 W US 2016016147W WO 2017003522 A1 WO2017003522 A1 WO 2017003522A1
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- fatty acid
- acid composition
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/158—Fatty acids; Fats; Products containing oils or fats
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/105—Aliphatic or alicyclic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/142—Amino acids; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/174—Vitamins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/195—Antibiotics
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/20—Inorganic substances, e.g. oligoelements
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K40/00—Shaping or working-up of animal feeding-stuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K50/00—Feeding-stuffs specially adapted for particular animals
- A23K50/10—Feeding-stuffs specially adapted for particular animals for ruminants
Definitions
- a fatty acid composition for animal feed comprises a fatty acid component and a surfactant component.
- the fatty acid composition melts at not less than about 40°C.
- the fatty acid component has an Iodine Value not greater than about 45.
- the fatty acid composition is in free flowing solid form. In some embodiments, the fatty acid composition is formed as prilled solid beads or solid flakes.
- the solid bead containing the fatty acid composition may have an outer layer and an inner core.
- the percentage of the surfactant component in the outer layer may be substantially similar to the percentage of the surfactant component in the inner core. In some embodiments, the percentage of the surfactant component in the outer layer may be higher than the percentage of the surfactant component in the inner core. In some embodiments, the percentage of the surfactant component in the outer layer may be less than the percentage of the surfactant component in the inner core. In some embodiments, the surfactant component in the outer layer may differ from the surfactant component in the inner core. In some embodiments, the fatty acid component in the outer layer may differ from the fatty acid component in the inner core.
- the fatty acid composition melts at not less than about 50°C, about 60°C, about 65°C, or about 70°C.
- the fatty acid composition has a moisture level of not greater than about 2% by weight. In some embodiments, the fatty acid composition has a moisture level of not greater than about 0.1% by weight, or about 0.01% by weight.
- the fatty acid composition has a particle size not greater than 10mm. In some embodiments, the fatty acid composition has a particle size from about ⁇ ⁇ to about 10mm. In some embodiments, the fatty acid composition has a particle size from about ⁇ to about 2mm. In some embodiments, the fatty acid composition has an average particle size of about 0.5mm, about 1mm, or about 2mm. In some embodiments, the fatty acid has a mean particle size of about 0.5mm, about 1mm, or about 2mm. In some embodiments, the fatty acid composition has a particle size not greater than 5 mm.
- a weight/weight ratio of the surfactant component to the fatty acid component is about 1 : 100 to about 1 : 1. In some embodiments, a weight/weight ratio of the surfactant component to the fatty acid component is about 1 :20 to about 1 : 1. In some embodiments, a weight/weight ratio of the surfactant component to the fatty acid component is about 1 : 10 to about 1 :2. In some embodiments, a weight/weight ratio of the surfactant component to the fatty acid component is about 1 : 10 to about 1 :3.
- the fatty acid composition comprises no more than 20% by weight of the surfactant component. In some embodiments, the fatty acid composition comprises no more than 5%, 10%, 15%, or 25% by weight of the surfactant component. In some embodiments, the fatty acid composition comprises from about 0.01% to about 30% by weight of the surfactant component. In some embodiments, the fatty acid composition further comprises a nutritional agent or a carrier. In some embodiments, the carrier comprises a porous carrier material. In some embodiments, the porous carrier material comprises protein, grain, roughage, or metal-organic framework.
- the nutritional agent comprises an antioxidant, a bioactive agent, a flavoring agent, a colorant, a glucogenic precursor, a vitamin, a mineral, an amino acid, a trace element, or derivatives thereof.
- the antioxidant comprises ethoxyquin (l,2-dihydro-6- ethoxy-2,2,4-trimethylquinoline), BHA (butylated hydroxyanisole), BHT (butylated hydroxytoluene), ascorbic acid, ascorbyl palmitate, benzoic acid, calcium ascorbate, calcium propionate, calcium sorbate, citrate acid, dilauryl thiodipropionate, distearyl thiodipropionate, erythorbic acid, formic acid, methylparaben, potassium bisulphite, potassium metabisulphite, potassium sorbate, propionic acid, propyl gallate, propyl paraben, resin guaiae, sodium ascorbate, sodium benzoate, sodium bisulphite, sodium metabisulphite, sodium nitrite, sodium propionate, sodium sorbate, sodium sulphite, sorbic acid, stannous chloride, sulphur dioxide,
- the bioactive agent comprises a prebiotic agent, a probiotic agent, or an antimicrobial agent.
- the prebiotic agent comprises fructo-oligosaccahrides, inulin, galacto-oligosaccahride, mannan-oligosaccahride, a yeast, a component of a yeast, a yeast extract, or a combination thereof.
- the probiotic agent comprises lactic acid-producing bacteria, live yeast cells, yeast culture, enzymes, protease, amylase, or a combination thereof.
- the antimicrobial agent comprises monensin, bambermycin, lasalocid, salinomycin, a sesquiterpene, a terpene, an alkaloid, an essential oil, or their derivative thereof.
- the glucogenic precursor comprises glycerol, propylene glycol, propanediol, polyol, calcium or sodium propionate, or a derivative thereof.
- the vitamin comprises biotin, vitamin A, vitamin C, vitamin D, vitamin E, vitamin H, vitamin K, vitamin , vitamin B2, vitamin B3, vitamin
- vitamin B5 vitamin Bg, vitamin B7, vitamin B9, vitamin B ⁇ 2, or vitamin Bp, or a derivative thereof.
- the mineral comprises a derivative of calcium, sodium, magnesium, phosphorous, potassium, manganese, zinc, selenium, copper, iodine, iron, cobalt, or molybdenum.
- the mineral comprises an amino acid chelated or glycinated mineral or selenium yeast.
- the mineral comprises an organic mineral derivative.
- the amino acid is carnitine, histidine, alanine, isoleucine, arginine, leucine, asparagine, lysine, aspartic acid, methionine, cysteine, phenylalanine, glutamic acid, threonine, glutamine, tryptophan, glycine, valine, ornithine, proline, selenocysteine, selenomethionine, serine, tyrosine, or derivatives thereof.
- the surfactant component may include a non-ionic emulsifier or an ionic emulsifier.
- the surfactant component comprises an emulsifier having a hydrophilic-lipophilic balance value of about 5 to about 25.
- the surfactant component comprises an emulsifier having a hydrophilic-lipophilic balance value of from about 10 to about 20.
- the surfactant component comprises an emulsifier having a hydrophilic-lipophilic balance value of about 5, about 8, about 15 or about 18.
- the surfactant component comprises esters or salts of long chain fatty acid.
- the surfactant component comprises lecithin, soy lecithin, cephalin, castor oil ethoxylate, sorbitan mono-, di-, or tri-oleate, tallow ethoxylate, lauric acid, polyethylene glycol, or derivatives thereof.
- the surfactant component comprises calcium stearoyl dilaciate, polyglycerol ester, glycerol ester, sorbitan ester, polysorbitan ester, polyethylene glycol ester, sugar ester, mono-, di- or triglyceride, acetylated mono-, di- or triglyceride, acetylated monoglyceride, lactylated monoglyceride, phospholipid, or derivatives thereof.
- the surfactant component comprises polyoxyethylene stearate, polysorbate, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monooleate, polyoxyethylene sorbitan monopalmitate, polyoxyethylene sorbitan monostearate, polyoxyethylene sorbitan tristearate, ammonium phosphatides, sodium or potassium or calcium salts of fatty acids, magnesium salts of fatty acids, mono- and diglycerides of fatty acids, acetic acid esters of mono- and diglycerides of fatty acids, lactic acid esters of mono- and diglycerides of fatty acids, citric acid esters of mono- and diglycerides of fatty acids, mono- and diacetyl tartaric acid esters of mono- and diglycerides of fatty acids, acetic acid esters of mono- and diglycerides of fatty acids, tartaric acid esters of mono- and diglycerides of fatty acids, sucrose esters of fatty acids sucroglycerides,
- the surfactant component comprises a surfactant derived from oleic acid. In some embodiments, the surfactant component comprises a non-ionic oleate ester derived surfactant. In some embodiments, the surfactant component comprises an ionic oleic acid derived surfactant.
- the surfactant component comprises sodium oleate, potassium oleate, calcium oleate, ammonium oleate, sorbitan oleate, sorbitan mono-, di- or trioleate, polycorbitan oleate, polysorbitan mono-, di- or trioleate, glyceryl oleate, methyl oleate, ethyl oleate, PEG oleate, triethanolamine oleate (TEA oleate), polysorbitan oleate, or a combination thereof.
- the fatty acid component may have a melting point not less than about 45°C. In some embodiments, the fatty acid component melts at not less than about 50°C, about 60°C, about 65°C, or about 70°C.
- the fatty acid component comprises free fatty acid, salt or ester of fatty acid, fatty acid ester, mono-, di-, or triglyceride, or a combination thereof. In some embodiments, the fatty acid component comprises by weight, at least, about 70%, 75%, 80%, 85%, 90%, 95%, 98% or 99% of free fatty acid.
- the fatty acid component comprises a rumen stable fatty acid. In some embodiments, the fatty acid component comprises by weight, at least, about 70%, 75%, 80%, 85%, 90%, 95%, 98% or 99% of rumen stable fatty acid. In some embodiments, the fatty acid component comprises, by weight, at least about 70%, 75%, 80%, 85%, 90%, 95%, 98% or 99% of saturated fatty acid. In some embodiments, the saturated fatty acid may be free fatty acid. In some embodiments, the saturated fatty acid may be in ester form.
- the fatty acid component comprises by weight, at least, about 70%, 80%, 85%, 90%, 95%, 98%, or 99% of a palmitic acid compound by weight.
- the palmitic acid compound comprises free palmitic acid, palmitate mono-, di-, or triglyceride, one or more salts of palmitic acid.
- the salt of palmitic acid comprises sodium palmitate, calcium palmitate, magnesium palmitate, ammonium palmitate, zinc palmitate, aluminum palmitate, copper palmitate, iron palmitate, chromium palmitate, selenium palmitate, or a combination thereof.
- the fatty acid component comprises by weight, at least, about 70%, 80%, 85%, 90%, 95%, 98% or 99% of free palmitic acid by weight.
- the fatty acid component comprises a stearic acid compound.
- the stearic acid compound comprises free stearic acid, stearate mono-, di- or triglyceride, sodium stearate, calcium stearate, magnesium stearate, or ammonium stearate.
- the fatty acid component consists essentially of a palmitic acid compound and a stearic acid compound. In some embodiments, the fatty acid component consists essentially of free palmitic acid and free stearic acid having a weight/weight ratio from about 10: 1 to about 1 : 10. In some embodiments, the weight/weight ratio is from about 6:4 to about 4:6. In some embodiments, the weight/weight ratio is from about 8:2 to about 2:8.
- the fatty acid component comprises an oleic acid compound.
- the oleic acid compound comprises free oleic acid, an oleic acid ester, mono-, di-, or triglyceride of oleic acid, a high oleic content oil, or a combination thereof.
- the fatty acid component comprises from about 1% to about 50% by weight of the oleic acid compound.
- the high oleic content oil may have an oleic content not less than 40% by weight. In some embodiments, the high oleic content oil may have an oleic content not less than about 50%, about 60%, about 70%, or about 80% by weight.
- the fatty acid component comprises oil.
- the oil may be vegetable oil, plant oil, or animal oil.
- the fatty acid component comprises from about 1% to about 50% by weight of the oil.
- the fatty acid component comprises olive oil, pecan oil, canola oil, peanut oil, macadamia oil, sunflower oil, corn oil, cottonseed oil, flaxseed oil, palm oil, soybean oil, grape seed oil, sea buckthorn oil, chicken fat, turkey fat, lard, or a combination thereof. In some embodiments, the fatty acid component comprises from about 1%) to about 40% by weight of canola oil. In some embodiments, the fatty acid component comprises free palmitic acid and canola oil at a weight/weight ratio from about 50: 1 to about 1 : 1. In some embodiments, the fatty acid component has a moisture level no greater than about 2%, about 1%, about 0.5%, or about 0.1% by weight.
- the fatty acid component comprises unsaponifiable matter no greater than about 45%, about 25%, about 15%, or about 2% by weight.
- the fatty acid component has an Iodine Value not greater than about 45, about 30, about 25, about 15, about 5, about 1, or about 0.5. In some embodiments, the fatty acid component has an Iodine Value from about 5 to about 15. In some embodiments, the fatty acid component has an Iodine Value from about 10 to about 30.
- the disclosure provides a fatty acid composition for animal feed consists essentially of a fatty acid component and a surfactant component, wherein the fatty acid composition melts at not less than 40°C, and wherein the fatty acid component has an Iodine Value not greater than 45.
- the disclosure provides a fatty acid composition for ruminant feed consists of a fatty acid component and a surfactant component, wherein the fatty acid composition melts at not less than 50°C, and wherein the fatty acid component has an Iodine Value not greater than 30.
- the disclosure provides a fatty acid composition for ruminant feed comprises about 70% to about 99.99% by weight of a fatty acid component, about 0.01% to about 30% by weight of a surfactant component, wherein the fatty acid composition melts at not less than 50°C, and wherein the fatty acid component has an Iodine Value not greater than 30.
- the fatty acid composition can ,have no more than about 2% by weight water.
- the fatty acid composition melts at not less than 40°C.
- the disclosure provides methods for making a fatty acid composition for animal feed.
- the method includes combining a fatty acid component with a surfactant component to provide a fatty acid composition and forming the fatty acid composition into solid beads.
- the method further comprises heating the fatty acid composition into liquid form before forming the fatty acid composition into solid beads.
- the fatty acid component and the surfactant component are combined in liquid form.
- forming the fatty acid composition into solid beads comprises prilling the fatty acid composition into solid beads.
- the FIGURE is a flow diagram of an illustrative method of preparing a fatty acid composition including a fatty acid component and a surfactant component.
- percents are weight percents and ratios are weight/weight ratios.
- An "animal” may be any house based or farm based animal.
- An example animal may be an animal raised for meat or for milk.
- a “ruminant” is generally a suborder of mammal with a multiple chamber stomach that gives the animal the ability to digest cellulose-based food by softening it within a first chamber (rumen) of the stomach and to regurgitate the semi-digested mass to be chewed again by the ruminant for digestion in one or more other chambers of the stomach.
- ruminants include, but are not limited to, lactating animals such as cattle, goats and sheep.
- Cattle may include dairy cows, which are generally animals of the species Bos taurus. The milk produced by ruminants is widely used in a variety of dairy-based products.
- the present disclosure generally relates to fatty acid compositions, animal feed mixtures, ruminant feed mixtures, the dietary compositions made therefrom, and to the methods for making the dietary compositions that can be fed to animal.
- the dietary compositions may be configured to improve various aspects of animal production including, for example, animal growth, animal reproduction or milk production. For instance, some embodiments provide that the dietary compositions may increase the amount of milk production, increase the milk fat content or yield, increase the milk protein content or yield, or all three.
- Specific compositions described herein may include animal feed mixtures, ruminant feed mixtures, supplements, or the like.
- the dietary compositions may include liquids, solids or combinations thereof, such as dry particles, pellets, liquid suspensions, emulsions, slurries, pastes, gels, or the like.
- the fat in the feed is modified by the rumen to provide a milk fat profile that is different from the profile of fat in the feed.
- Fats that are not inert in the rumen may decrease feed intake and rumen digestibility of the feed material.
- Milk composition and fat quality may be influenced by the ruminant's diet.
- oil feeding the feeding of vegetable oils, for example
- the milk protein concentration may decrease, the milk fat concentration may decrease, and the proportion of trans fatty acids may increase.
- a typical fatty acid composition of milk fat may contain more than about 70% by weight saturated fatty acids and a total amount of trans fatty acids may be from about 3%> to about 10%) by weight. When vegetable oil is added into the feed, the proportion of trans fatty acids may rise to more than about 10%> by weight.
- Fatty acid hydrogenation can be decreased, for example, by protecting fats with formaldehyde-treated casein.
- Another alternative is to feed the ruminant fatty acid calcium salts whereby hydrogenation in the rumen can be decreased.
- fatty acid salts typically have a pungent taste that may result in decreased feed intake by the ruminant.
- the salts may also disturb certain processes for forming the feed into pellets.
- a fatty acid component, described herein, may allow for the transfer of a fatty acid from the feed via the digestive tract into the blood circulation of a ruminant. This may improve the milk fat, the energy efficiency of milk production and the utilization of energy by the ruminant, which positively impact the milk production and the milk protein.
- the dietary composition may be configured to enhance fat synthesis in the mammary gland by bringing milk fat components to the cell such that energy consumed in the fat synthesis in the mammary gland is reduced.
- glucose may be used more efficiently for lactose production causing increased milk production.
- the milk protein content may increase because there is no need to produce glucose from amino acids.
- the ruminant may not lose weight at the beginning of the lactation period, thereby improving the fertility of the ruminant.
- a surfactant component may enhance rumen function when digested by a ruminant.
- the surfactant component may increase the emulsification of ruminal liquid, the growth rate of rumen microbes, the number of ruminal microorganisms, the activity of enzymes secreted by ruminal microbes, or fermentation of cellulosic materials, which may lead to increased digestibility of roughages or crude fibers in rumen and increases feed efficiency.
- the ruminal microbes may include without limitation microbial protease and cellulase.
- the cellulosic materials may include without limitation fibers, silage, and roughages.
- the surfactant component may also change the contents and proportion of volatile fatty acids and enhance the feed efficiency and performance by improving the rumen fermentation characteristics. Additionally or alternatively, the surfactant component, described herein, may improve the digestibility of the fatty acid component or a subcomponent thereof when an animal consumes the fatty acid composition. For example, the surfactant component or any part thereof may aid in the micelle formation of the fatty acid component in the animal's digestive tract, enhance the emulsification process, and/or facilitate the digestion and/or absorption of the fatty acid component.
- the FIGURE depicts a schematic illustration of an example method of making fatty acid compositions for an animal feed.
- One embodiment of the method employed for making solid beads of a fatty acid composition is referred to as "prilling.”
- Prilling also called “spray chilling,” “spray cooling,” or “spray congealing,” generally refers to a process of spraying droplets through nozzles and allowing droplets to congeal in mid-air as they fall from the top of a prilling tower toward a collection surface. Air may be circulated upward through the tower to aid in congealing the droplets into a solid.
- the size and shape of the droplets may be affected by the height of the tower, the nozzle size, and the nozzle shape.
- larger sized droplets may require a higher tower than smaller sized droplets.
- the droplets tend to congeal without agglomerating, and the surface tension of the liquid droplets results in a generally rounded bead surface.
- the beads may be round or oval shaped.
- a fatty acid component herein described, is heated to a temperature sufficient to melt the fatty acid component using a heater, block 12.
- the temperature of the fatty acid component leaving the heater can be at or slightly above the melt temperature of the fatty acid component.
- a temperature at or slightly above the melt temperature requires less tower height for the process of congealing.
- a surfactant component, block 14 can be introduced with the fatty acid component to be heated and melted simultaneously with the fatty acid component.
- the surfactant component can be combined with the fatty acid component after the heater, provided that the introduction of the surfactant component does not cause the fatty acid component to congeal or otherwise solidify prematurely.
- liquid surfactant components may be used.
- the liquid comprising the fatty acid component and surfactant component can be pumped via a pump, block 12. Then, the liquid is distributed through a droplet- producing device at the top of the prilling tower, block 16. As the droplets fall in the tower, the droplets will congeal and solidify into beads by the time they reach the bottom of the tower.
- the resulting solid prilled beads are a fatty acid composition having a fatty acid component and a surfactant component, block 18.
- the particles may be manufactured with an encapsulation process producing solid beads having at least an outer layer and an inner core.
- the particles may be manufactured with encapsulation prilling process in which the core material and the shell material are sprayed from different nozzles.
- the particles may be manufactured with curtain coating encapsulation process.
- Other example processes may include, without limitation, extrusion, co- extrusion, pan coating, fluidized bed, and coacervation.
- the solid bead may have a homogeneous composition. In some embodiments, the solid bead may have a layered structure. In some embodiments, the compositions in different layers may differ. In some embodiments, the difference in the layers may be in chemical compositions. In some embodiments, the difference in the layers may be in the concentrations.
- the bead may have an outer layer and an inner core.
- the percentage of the surfactant component in the outer layer may be substantially similar to the percentage of the surfactant component in the inner core. In some embodiments, the percentage of the surfactant component in the outer layer may be higher than the percentage of the surfactant component in the inner core. In some embodiments, the percentage of the surfactant component in the outer layer may be less than the percentage of the surfactant component in the inner core. In some embodiments, the surfactant component in the outer layer may differ from the surfactant component in the inner core.
- the outer layer may contain a first surfactant and the inner core may contain a second surfactant, and the first surfactant and the second surfactant may be different.
- the surfactants in the outer layer and inner core may have the same chemical compositions but with different concentrations.
- the fatty acid component in the outer layer may differ from the fatty acid component in the inner core.
- the difference may be in the chemical composition.
- the difference may be in the concentration.
- the outer layer may have lower percentage of the fatty acid component than the inner core.
- the outer layer may contain a first fatty acid and the inner core may have a second fatty acid; and the first fatty acid differs from the second fatty acid.
- the method includes combining a fatty acid component with a surfactant component to provide a fatty acid composition and forming the fatty acid composition into solid beads. In some embodiments, the method further comprises heating the fatty acid composition into liquid form before forming the fatty acid composition into solid beads. In some embodiments, the fatty acid component and the surfactant component are combined in liquid form. In some embodiments, forming the fatty acid composition into solid beads comprises prilling the fatty acid composition into solid beads.
- the fatty acid composition includes a fatty acid component and a surfactant component. In some embodiments, the fatty acid composition melts at not less than 40°C. In some embodiments, the fatty acid component has an Iodine Value not greater than 45. In some embodiments, the fatty acid composition can consist essentially of a fatty acid component and a surfactant component, wherein the fatty acid composition melts at not less than 40°C; and the fatty acid component has an Iodine Value not greater than 45.
- the fatty acid composition can consist of a fatty acid component and a surfactant component, wherein, the fatty acid composition melts at not less than 50°C; and the fatty acid component has an Iodine Value not greater than 30.
- the fatty acid composition can comprise about 70% to about 99.99% by weight of a fatty acid component; about 0.01% to about 30%) by weight of a surfactant component.
- the fatty acid composition melts at not less than 50°C, and wherein the fatty acid component has an Iodine Value not greater than 30.
- the fatty acid composition can have no more than about 2% by weight water. In some embodiments, the fatty acid composition melts at not less than 40°C.
- the fatty acid compositions of a fatty acid component and a surfactant component can be used in the making of an animal feed mixture.
- the fatty acid composition is in a free flowing solid form.
- the fatty acid composition is formed as prilled solid beads.
- the fatty acid composition is formed as solid flakes.
- the fatty acid composition melts at not less than about 50°C, about 60°C, about 65°C, or about 70°C. In some embodiments, the fatty acid composition has a moisture level of not greater than about 2%, about 1%, about 0.5% or about 0.1%) by weight. In some embodiments, the fatty acid composition has a moisture level of not greater than about 0.1%>, or about 0.01%> by weight.
- the fatty acid composition includes particles having a particle size not greater than 10mm. In some embodiments, the fatty acid composition includes particles having a particle size from about ⁇ ⁇ to about 10mm. In some embodiments, the fatty acid composition includes particles having a particle size from about ⁇ to about 2mm. In some embodiments, the fatty acid composition includes particles having a particle size of about 0.1mm, about 0.5mm, about 1mm, or about 2mm. In some embodiments, the fatty acid composition includes particles having an average particle size of about 0.1mm, about 0.5mm, about 1mm or about 2mm. In some embodiments, the fatty acid composition includes particles having a mean particle size of about 0.1mm, about 0.5mm, about 1mm or about 2mm. In some embodiments, the fatty acid composition has a particle size not greater than 5mm.
- the fatty acid composition may have a weight/weight ratio of the surfactant component to the fatty acid component of about 1 : 100 to about 1 : 1, or about 1 :20 to about 1 : 1, or about 1 : 10 to about 1 :2, or about 1 : 10 to about 1 :3.
- the fatty acid composition can comprise no more than 25%, 20%, 15%, 10%, 8%, 5% or 2% by weight of the surfactant component. In some embodiments, the fatty acid composition can comprise from about 0.01%> to about 30%> by weight of the surfactant component.
- the fatty acid composition can further comprise a nutritional agent or a carrier, such as a porous carrier material.
- a nutritional agent or a carrier, such as a porous carrier material.
- the nutritional agent can be added to the fatty acid component before, during, or after the heating process.
- the porous carrier material can include protein, grain, roughage, or a metal-organic framework.
- the nutritional agent can comprise an antioxidant, a bioactive agent, a flavoring agent, a colorant, a glucogenic precursor, a vitamin, a mineral, an amino acid, a trace element, or derivatives thereof.
- the antioxidant to be added to the fatty acid composition can include ethoxyquin (l,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline), BHA (butylated hydroxyanisole), BHT (butylated hydroxytoluene), ascorbic acid, ascorbyl palmitate, benzoic acid, calcium ascorbate, calcium propionate, calcium sorbate, citrate acid, dilauryl thiodipropionate, distearyl thiodipropionate, erythorbic acid, formic acid, methylparaben, potassium bisulphite, potassium metabi sulphite, potassium sorbate, propionic acid, propyl gallate, propyl paraben, resin guaiae, sodium ascorbate, sodium benzoate, sodium bisulphite, sodium metabi sulphite, sodium nitrite, sodium propionate, sodium sorbate, sodium sulphite, sorbic acid,
- the bioactive agent can include a prebiotic agent, a probiotic agent, an antimicrobial agent or combinations thereof.
- Prebiotic agents may include fructo-oligosaccahrides, inulin, galacto-oligosaccahride, mannan-oligosaccahride, a yeast, a component of a yeast, a yeast extract, or a combination thereof.
- Probiotic agents may include, without limitation, lactic acid-producing bacteria, live yeast cells, yeast culture, enzymes such as protease and amylase, or a combination thereof.
- Antimicrobial agents may include, without limitation, monensin, bambermycin, lasalocid, salinomycin, a sesquiterpene, a terpene, an alkaloid, an essential oil, or their derivatives.
- the glucogenic precursor can include glycerol, propylene glycol, propanediol, polyol, calcium or sodium propionate, or a derivative thereof.
- vitamins can include biotin, vitamin A, vitamin C, vitamin D, vitamin E, vitamin H, vitamin K, vitamin , vitamin B2, vitamin B3, vitamin B5, vitamin Bg, vitamin B7, vitamin B9, vitamin B12, vitamin B p , or a derivative thereof.
- minerals can include derivatives of calcium, sodium, magnesium, phosphorous, potassium, manganese, zinc, selenium, copper, iodine, iron, cobalt, or molybdenum.
- the mineral is an amino acid chelated or glycinated mineral or selenium yeast.
- the mineral is an organic mineral derivative.
- Amino acids may be an essential, non-essential, common, uncommon, synthetic or natural amino acid.
- amino acids can include carnitine, histidine, alanine, isoleucine, arginine, leucine, asparagine, lysine, aspartic acid, methionine, cysteine, phenylalanine, glutamic acid, threonine, glutamine, tryptophan, glycine, valine, ornithine, proline, selenocysteine, selenomethionine, serine, tyrosine, or derivatives thereof.
- the flavoring agent can be any natural or synthetic flavoring agent.
- the flavoring agent comprises a fruit extract, a fruit flavor, an essential oil, or a combination thereof.
- the flavoring agent comprises ethyl methylphenylglycidate, isoamyl acetate, isoamyl acetate limonene, malic acid, allyl hexanoate, ethyl propionate, cinnamic aldehyde, acetophenone, an essential oil, or a combination thereof.
- the coloring agent can be any natural or synthetic coloring agent.
- the coloring agent comprises a food coloring, a fruit extract, a plant extract, or an essential oil.
- the coloring agent comprise curcumin, turmeric, anthocyanin, phycocyanin, lutein, lycopene, capsanathin, annatto, beta- carotenen, paprika oleoresin, carmine, cochineal, carminic acid, beta-apo-8' carotenol, methyl ester of beta-apo-8' carotenoic acid, canthaxanthin, chlorophyll, riboflavin, lactoflavin, caramel, saffron, betanine, curcumene, crocin, lucin, flavonoid, flavanone, quinone, antioxidant, or a combination thereof.
- the coloring agent comprises carrot oil, cohineal extract, beet juice or extract, red cabbage juice or extract, graph juice or extract, graph color extract, grape skin extract, paprika, paprika oleoresin, turmeric oleoresin, vegetable juice, fruit juice, cotton seed flour, .
- the coloring agent comprises FD&C blue no. 1 or 2, FD&C green no. 3, FD&C red no. 3 or 40, FD&C yellow no. 5 or 6, Orange B, or citrus red no. 2.
- the coloring agent comprises titanium dioxide or iron oxide.
- the surfactant component can include a non-ionic or an ionic emulsifier.
- the emulsifier can have a hydrophilic-lipophilic balance (HLB) value of about 5 to about 25.
- the emulsifier can have a hydrophilic-lipophilic balance (HLB) value of about 10 to about 20.
- the emulsifier can have a hydrophilic-lipophilic balance (HLB) value of about 1, 2, 3, 4, 5, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20.
- the emulsifier can have a hydrophilic-lipophilic balance (HLB) value of not greater than about 20.
- the HLB value provides an indication of the degree to which a surfactant component is hydrophilic or lipophilic.
- HLB values can be determined formulaically by assigning values to certain regions of the surfactant molecule.
- the HLB value can be determined by one of several well-known methods, including, for example, Griffin's method.
- the emulsifier may be an ester or salt of a long chain fatty acid.
- the long chain fatty acid may be any saturated or unsaturated fatty acid having from about 4 to about 30 carbons.
- the example long chain fatty acid may include C16:0, C18:0, C18: l, C18:2, C28:3, C20:0, C20: 1,C20:2, C20:3, C20:4, C20:5, C22:0, C22:4, or any combination thereof.
- the surfactant component can include lecithin, soy lecithin, cephalin, castor oil ethoxylate, sorbitan mono-, di-, or tri-oleate, polysorbitan mono-, di-, or tri-oleate, tallow ethoxylate, lauric acid, polyethylene glycol, or derivatives thereof.
- the surfactant component can include calcium stearoyl dilaciate, polyglycerol ester, glycerol ester, sorbitan ester, polysorbitan ester, polyethylene glycol ester, sugar ester, mono-, di-, or triglyceride, phospholipids, acetylated monoglyceride, lactylated monoglyceride, or derivatives thereof.
- the surfactant component can include polyoxyethylene stearate, polysorbate, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monooleate, polyoxyethylene sorbitan monopalmitate, polyoxyethylene sorbitan monostearate, polyoxyethylene sorbitan tristearate, ammonium phosphatides, sodium or potassium or calcium salts of fatty acids, magnesium salts of fatty acids, mono- and diglycerides of fatty acids, acetic acid esters of mono- and diglycerides of fatty acids, lactic acid esters of mono- and diglycerides of fatty acids, citric acid esters of mono- and diglycerides of fatty acids, mono- and diacetyl tartaric acid esters of mono- and diglycerides of fatty acids, acetic acid esters of mono- and diglycerides of fatty acids, tartaric acid esters of mono- and diglycerides of fatty acids, sucrose esters of fatty acids sucroglycerides
- the surfactant component comprises a surfactant derived from oleic acid.
- the surfactant derived from oleic acid may be a non-ionic oleate ester derived surfactant or an ionic oleic acid derived surfactant.
- the surfactant component comprises sodium oleate, potassium oleate, calcium oleate, ammonium oleate, sorbitan oleate, sorbitan mono-, di- or trioleate, polycorbitan oleate, polysorbitan mono-, di- or trioleate, glyceryl oleate, methyl oleate, ethyl oleate, PEG oleate, triethanolamine oleate (TEA oleate), polysorbitan oleate, or a combination thereof.
- the fatty acid component may have a melting point not less than about 45°C. In some embodiments, the fatty acid component melts at not less than about 50°C, about 60°C, about 65°C, or about 70°C. In some embodiments, the fatty acid component has a melting point from about 50°C to about 70°C.
- the fatty acid component may include free fatty acid, salt or ester of fatty acid, fatty acid ester, mono-, di-, or triglyceride, or a combination thereof.
- the fatty acid component may include at least about 70%, 75%, 80%, 85%, 90%, 95%, 98%, or 99% by weight of free fatty acid.
- the fatty acid component can include a rumen stable fatty acid.
- fatty acid component include at least about 70%, 75%, 80%,
- the fatty acid component comprises at least about 70%, 75%, 80%, 85%,
- the saturated fatty acid may be free fatty acid. In some embodiments, the saturated fatty acid may be in ester form.
- the fatty acid component includes at least about 70%, 80%,
- the palmitic acid compound is not limited by this disclosure, and may include one or more of a conjugated palmitic acid, unconjugated palmitic acid, free palmitic acid, palmitate mono-, di- or triglyceride, one or more salts of palmitic acid, or a palmitic acid derivative.
- the salt of palmitic acid comprises sodium palmitate, calcium palmitate, magnesium palmitate, ammonium palmitate, zinc palmitate, aluminum palmitate, copper palmitate, iron palmitate, chromium palmitate, selenium palmitate or a combination thereof.
- Palmitic acid also known as hexadecanoic acid, has a molecular formula of ⁇ 3 ⁇ 4( ⁇ 3 ⁇ 4) ⁇ 4 ⁇ 02 ⁇ .
- Non-limiting examples of palmitic acid derivatives include palmitic acid esters, palmitic acid amides, palmitic acid salts, palmitic acid carbonates, palmitic acid carbamates, palmitic acid imides, and palmitic acid anhydrides.
- the fatty acid component comprises at least about 70%, 80%, 85%, 90%, 95%, 98% or 99% of free palmitic acid by weight.
- the palmitic acid compound can include free palmitic acid, palmitate mono-, di-, or triglyceride, or one or more salts of palmitic acid.
- the salt of palmitic acid can include sodium palmitate, calcium palmitate, magnesium palmitate, ammonium palmitate, zinc palmitate, aluminum palmitate, copper palmitate, iron palmitate, chromium palmitate, selenium palmitate, or a combination thereof.
- the fatty acid component includes at least 90% or at least 95% of free palmitic acid by weight.
- the fatty acid component includes a stearic acid compound.
- the stearic acid compound can include free stearic acid, stearate mono-, di- or triglyceride, sodium stearate, calcium stearate, magnesium stearate, ammonium stearate, conjugated stearic acid, unconjugated stearic acid, and stearic acid derivatives.
- Stearic acid also known as octadecanoic acid, has a molecular formula of CH3(CH 2 )i6 0 2 H.
- stearic acid derivatives may include stearic acid esters, stearic acid amides, stearic acid salts, stearic acid carbonates, stearic acid carbamates, stearic acid imides, and stearic acid anhydrides.
- the fatty acid component can consist essentially of a palmitic acid compound and a stearic acid compound. In some embodiments, the fatty acid component can include a palmitic acid compound and a stearic acid compound. In some embodiments, the fatty acid component can consist essentially of free palmitic acid and free stearic acid having a weight/weight ratio from about 10: 1 to about 1 : 10, a ratio from about 6:4 to about 4:6, or a ratio from about 8:2 to about 2:8.
- the fatty acid component comprises an oleic acid compound.
- the oleic acid compound comprises free oleic acid, an oleic acid ester, mono-, di- or triglyceride of oleic acid, a high oleic oil, or a combination thereof.
- the fatty acid component comprises from about 1% to about 50% by weight of the oleic acid compound.
- the high oleic content oil may have an oleic content not less than 40% by weight.
- the high oleic content oil may have an oleic content not less than about 50%), about 60%), about 70%>, or about 80%> by weight.
- the fatty acid component comprises from about 1%> to about 50%> by weight of the high oleic oil.
- the fatty acid component comprises from about 1%> to about 50%> by weight of the oleic acid compound.
- the fatty acid component comprises oil.
- the oil may be plant based or animal based.
- the oil may be vegetable oil, plant oil, or animal oil.
- the fatty acid component may include not less than about 30%>, 35%>, 40%), 50%), 60%) or 70%> by weight of the oil.
- the fatty acid component comprises from about 1%> to about 50%> by weight of the oil.
- the fatty acid component comprises olive oil, pecan oil, canola oil, peanut oil, macadamia oil, sunflower oil, corn oil, cottonseed oil, flaxseed oil, algal oil, palm oil, soybean oil, grape seed oil, sea buckthorn oil, chicken fat, turkey fat, lard, or a combination thereof.
- the fatty acid component comprises from about 1% to about 50% by weight of oil.
- the fatty acid component comprises from about 1% to about 40% by weight of canola oil.
- the fatty acid component comprises free palmitic acid and canola oil at a weight/weight ratio from about 50: 1 to about 1 : 1.
- the fatty acid component may include a fatty acid salt, a fatty acid ester, a fatty acid amide, a fatty acid anhydride, or a fatty acid alcohol.
- the fatty acid component may include one or more free fatty acids and/or glycolipids.
- a fatty acid salt may be any acid addition salt, including, but not limited to, halogenic acid salts such as, for example, hydrobromic, hydrochloric, hydrofluoric, and hydroiodic acid salt; an inorganic acid salt such as, for example, nitric, perchloric, sulfuric, and phosphoric acid salt; an organic acid salt such as, for example, sulfonic acid salts (methanesulfonic, trifluoromethane sulfonic, ethanesulfonic, benzenesulfonic, or p-toluenesulfonic), acetic, malic, fumaric, succinic, citric, benzoic, gluconic, lactic, mandelic, mucic, pamoic, pantothenic, oxalic, and maleic acid salts; and an amino acid salt such as aspartic or glutamic acid salt.
- halogenic acid salts such as, for example, hydrobromic, hydrochlor
- the acid addition salt may be a mono- or di-acid addition salt, such as a di-hydrohalogenic, di-sulfuric, di-phosphoric, or di-organic acid salt.
- the acid addition salt is used as an achiral reagent which is not selected on the basis of any expected or known preference for interaction with or precipitation of a specific optical isomer of the products of this disclosure.
- a fatty acid ester includes, for example, a fatty acid ester in a form of RCOOR'.
- R may be any saturated or unsaturated alkyl group including, without limitation, CIO, C12, C14, C16, C18, C20, and C24.
- R may be any group having from about 1 to about 1000 carbon atoms and with or without hetero atoms. In some embodiments, R may have from about 1 to about 20, from about 3 to about 10, and from about 5 to about 15 carbon atoms.
- the hetero atoms may include, without limitation, N, O, S, P, Se, halogen, Si, and B.
- R may be a C ⁇ alkyl, such as methyl, ethyl or t-butyl; a C ⁇ galkoxyC ⁇ g alkyl; a heterocyclyl, such as tetrahydrofuranyl; a Cg ⁇ Q aryloxyC ⁇ galkyl, such as benzyloxy methyl (BOM); a silyl, such as trimethylsilyl, t-butyldimethylsilyl and t-butyldiphenylsilyl; a cinnamyl; an allyl; a C ⁇ galkyl which is mono-, di- or tri substituted by halogen, silyl, cyano or C ⁇ aryl, wherein the aryl ring is unsubstituted or substituted by one, two or three, residues selected from the group consisting of C ⁇ alkyl, C ⁇ alkoxy, halogen, nitro, cyano and CF 3 ; or a
- a fatty acid amide may generally include amides of fatty acids where the fatty acid is bonded to an amide group.
- the fatty acid amide may have a formula of RCO R'R".
- R may be any saturated or unsaturated alkyl group including, without limitation, CIO, C12, C14, C16, C18, C20, and C24.
- R and R" may be any group having from about 1 to about 1000 carbon atoms and with or without hetero atoms.
- R may have from about 1 to about 20, from about 3 to about 10, and from about 5 to about 15 carbon atoms.
- the hetero atoms may include, without limitation, N, O, S, P, Se, halogen, Si, and B.
- R and R" each may be an alkyl, an alkenyl, an alkynyl, an aryl, an aralkyl, a cycloalkyl, a halogenated alkyl, or a heterocycloalkyl group.
- a fatty acid anhydride may generally refer to a compound which results from the condensation of a fatty acid with a carboxylic acid.
- carboxylic acids that may be used to form a fatty acid anhydride include acetic acid, propionic acid, benzoic acid, and the like.
- a fatty acid alcohol refers to a fatty acid having straight or branched, saturated, radical groups with 3-30 carbon atoms, and one or more hydroxy groups.
- the alkyl portion of the alcohol component can be propyl, butyl, pentyl, hexyl, iso-propyl, iso-butyl, sec-butyl, tert-butyl, or the like.
- One of skill in the art may appreciate that other alcohol groups may also useful in the present disclosure.
- the fatty acid component can have a moisture level of not greater than about 2%, about 1%, about 0.5% or about 0.1% by weight.
- the fatty acid component can include unsaponifiable matter no greater than about 45%, about 25%, about 15%, or about 2% by weight.
- the fatty acid component can have an Iodine Value not greater than about 45, about 30, about 25, about 20, about 15, about 10, about 5, about 1 or about 0.5. In some embodiments, the fatty acid component has an Iodine Value from about 5 to about 15. In some embodiments, the fatty acid component has an Iodine Value from about 10 to about 30.
- the Iodine Value is also sometimes referred to in the literature as the Iodine Number.
- the Iodine Value provides a measure of the unsaturation of a chemical material. Accordingly, the fatty acid component may include some unsaturated fatty acid compounds.
- the Iodine Value is a measure of iodine absorbed in a given amount of time by the fatty acid component.
- the Iodine Value can represent the number of grams of iodine consumed by 100 grams of the fatty acid component. The lower the Iodine Value is, the lower the degree of unsaturation.
- a well- known method of determining the Iodine Value is the Wijs Method. However, the disclosure is not limited to using any one specific method of determining the Iodine Value. It is also possible that other methods of determining the degree of unsaturation may not involve the use of iodine or another halogen. It is therefore intended herein that the "Iodine Value" gives a representation of the degree of unsaturation by whatever method, and is not to be construed as limited solely to the iodine method.
- compositions, methods, and devices are described in terms of “comprising” various components or steps (interpreted as meaning “including, but not limited to”), the compositions, methods, and devices can also “consist essentially of or “consist of the various components and steps, and such terminology should be interpreted as defining essentially closed-member groups. It will be further understood by those within the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases “at least one” and “one or more” to introduce claim recitations.
- a range includes each individual member.
- a group having 1-3 cells refers to groups having 1, 2, or 3 cells.
- a group having 1-5 cells refers to groups having 1, 2, 3, 4, or 5 cells, and so forth.
- Palmitic acid and emulsifier mixture compositions as shown in TABLE 1.
- a round-bottomed flask fitted with a magnetic stir bar was charged with palmitic acid and polysorbate 80 emulsifier (oleate).
- the mixture was heated on an oil bath to 80°C with vigorous stirring and maintained at 80°C for 30 minutes with vigorous stirring. After 30 minutes, the heat was turned off, stirring continued, and the mixture was allowed to cool to room temperature. A uniform solid was formed even before reaching room temperature and the flask was maintained at room temperature for 24hrs. The solid mass formed was crushed using a spatula and transferred to a vial. Melting points of the mixtures of Palmitic acid with polysorbate 80 were determined using a melting point apparatus.
- Palmitic acid (950 g) and polysorbate 80 (50 g) was charged into a three liter beaker and was slowly heated in an oil bath to 80°C over a period of 4-5 hrs until a uniform clear liquid was formed.
- the contents were maintained at 80°C for 30 minutes with vigorous stirring. The heating was stopped and the contents were allowed to come to room temperature over a period of 24 hrs.
- the solid mass was cut into chunks with a knife and crushed to small pieces with a hammer and finally crushed into a fine powder using a blender.
- the result mixture has a melting point 69-70 °C.
- a mixture of palmitic acid and stearic acid (6/4 w/w) (950 g) and polysorbate 80 (50 g) was charged into a three liter beaker and was slowly heated in an oil bath to 80°C over a period of 4-5 hrs until a uniform clear liquid was formed.
- the contents were maintained at 80°C for 30 minutes with vigorous stirring. The heating was stopped and the contents were allowed to come to room temperature over a period of 24 hrs.
- the solid mass was cut into chunks with a knife and crushed to small pieces with a hammer and finally crushed into a fine powder using a blender.
- the mixture has a melting point 57-58 °C.
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| CN201680010185.1A CN107249348A (zh) | 2015-02-02 | 2016-02-02 | 动物饲料组合物及其制备方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| FR3043890B1 (fr) * | 2015-11-25 | 2020-05-08 | Pancosma Sa | Procede d'amelioration des performances zootechniques d'un ruminant |
| CN106343180B (zh) * | 2016-08-31 | 2020-09-01 | 贵州大学 | 一种用于提高黑山羊体重的饲料及其制备方法 |
| CN108029873A (zh) * | 2017-12-28 | 2018-05-15 | 长沙善道新材料科技有限公司 | 一种反刍动物饲料添加剂 |
| EP3823461A1 (en) * | 2018-07-17 | 2021-05-26 | Nutreco IP Assets B.V. | Methods to increase milk yield and yield of milk constituents in lactating ruminants |
| CN112955158A (zh) | 2018-09-05 | 2021-06-11 | 康肾医药有限公司 | 含铁组合物及其用途 |
| CN109258936A (zh) * | 2018-11-26 | 2019-01-25 | 上海牧高生物科技有限公司 | 奶牛饲料添加剂及其制备方法以及奶牛复合预混料 |
| CN109463553A (zh) * | 2018-12-24 | 2019-03-15 | 上海牧高生物科技有限公司 | 哺乳母猪复合预混料及制备方法、复合饲料以及饲喂方法 |
| MY205508A (en) * | 2019-04-19 | 2024-10-23 | Delstasia Sdn Bhd | Method for pelleting animal feed in hot weather conditions |
| CN110050885A (zh) * | 2019-05-15 | 2019-07-26 | 北京波尔莱特饲料有限公司 | 一种发酵纤维饲料及其制备方法和应用方法 |
| US20230301957A1 (en) * | 2020-04-02 | 2023-09-28 | Singao (Xuzhou) Biotech Co., Ltd | Polyglycerol fatty acid ester composition and application thereof |
| CA3201057A1 (en) | 2020-12-08 | 2022-06-16 | Mark Christopher LAY | Improvements to devices and methods for delivery of substances to animals |
| WO2022217031A1 (en) * | 2021-04-08 | 2022-10-13 | Eastman Chemical Company | Methods of using formaldehyde-free antimicrobial compositions in animal by-product compositions |
| CN115251238A (zh) * | 2021-04-29 | 2022-11-01 | 内蒙古伊利实业集团股份有限公司 | 饲料添加组合物及其应用和饲料 |
| CN114702687B (zh) * | 2022-04-20 | 2023-12-26 | 宁夏京成天宝科技有限公司 | 一种环糊精mof颗粒抗生素替代剂的制备方法及其应用 |
| CN115486497B (zh) * | 2022-11-15 | 2023-05-02 | 北京挑战农业科技有限公司 | 一种反刍动物用酵母培养物及其制备方法与应用 |
| KR102802617B1 (ko) * | 2024-08-16 | 2025-05-07 | 영주한우타운 주식회사 농업회사법인 | 햄프 부산물을 활용한 기능성 축산 사료 조성물 및 이의 제조 방법 |
Citations (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2881074A (en) * | 1955-07-29 | 1959-04-07 | Armour & Co | Growth promotant substances |
| US3468667A (en) * | 1965-03-19 | 1969-09-23 | Armour Ind Chem Co | Coated dust free phosphate feed supplement |
| US4599234A (en) * | 1983-10-07 | 1986-07-08 | Amer M Samir | Synergistic diet comprising selenium based compounds |
| US4826694A (en) * | 1985-10-14 | 1989-05-02 | Balfour Manufacturing Company | Ruminant feedstuffs, their production and apparatus for use therein |
| US5215768A (en) * | 1992-03-20 | 1993-06-01 | Church & Dwight Co., Inc. | Deodorized fatty acid salt feed supplement |
| US5456927A (en) * | 1991-12-04 | 1995-10-10 | Church & Dwight Co., Inc. | Ruminant feed supplement product |
| US5585134A (en) * | 1993-06-29 | 1996-12-17 | Volac, Inc. | Production of rumen-bypass fatty acid salt and protein dietary supplement |
| US5601860A (en) * | 1990-11-30 | 1997-02-11 | American Home Products Corporation | Corandomized fat compositions for infant formulas |
| US6204291B1 (en) * | 1998-06-26 | 2001-03-20 | The Iams Company | Process for promoting weight loss in overweight dogs |
| CA2335745A1 (en) * | 2001-02-13 | 2002-08-13 | Her Majesty In Right Of Canada As Represented By The Minister Of Fisheries And Oceans | Process for preparing nutritionally upgraded canola products |
| US20030180352A1 (en) * | 1999-11-23 | 2003-09-25 | Patel Mahesh V. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
| US6939864B1 (en) * | 2001-07-09 | 2005-09-06 | Purdue Research Foundation | Animal feed compositions and methods of using the same |
| CA2578903A1 (en) * | 2004-08-31 | 2006-03-09 | Akzo Nobel N.V. | Method for pigment solubilisation, a pigment composition and its use |
| US20090285931A1 (en) * | 2008-02-04 | 2009-11-19 | Shelby Nancy J | Feed supplement for animals for reducing methane production |
| WO2009148521A1 (en) * | 2008-06-03 | 2009-12-10 | Nestec S.A. | Palatability enhancers and methods for enhancing palatability |
| WO2011060084A1 (en) * | 2009-11-10 | 2011-05-19 | MyCell Holdings Limited | Stabilized formulations of fatty acids |
| US20130323362A1 (en) * | 2010-12-06 | 2013-12-05 | Degama Berrier Ltd. | Composition and method for improving stability and extending shelf life of probiotic bacteria and food products thereof |
| US20140154392A1 (en) * | 2010-05-21 | 2014-06-05 | H R D Corporation | Process for upgrading low value renewable oils |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2958900A (en) * | 1955-06-23 | 1960-11-08 | Edgar N Meakin | Pellet mill die assembly |
| US3130054A (en) * | 1960-03-14 | 1964-04-21 | Grace W R & Co | Method of producing a food supplement |
| WO1980001351A1 (en) * | 1978-12-26 | 1980-07-10 | Brewer Co Ltd | Ruminant feeds from bagasse |
| JPH02295438A (ja) * | 1989-05-09 | 1990-12-06 | Toyo Jozo Co Ltd | 泌乳用飼料ペレット及びそれを用いる方法 |
| US5093128A (en) * | 1989-07-18 | 1992-03-03 | Draguesku Oliver J | Rumen and other stomach chamber bypass nutrients and methods of fabrication |
| GB9101462D0 (en) * | 1991-01-23 | 1991-03-06 | Unilever Plc | Edible spread |
| CA2140298C (en) * | 1994-01-14 | 1998-12-08 | Thomas L. Meade | Rumen by-pass feed supplement |
| JPH07289172A (ja) * | 1994-04-20 | 1995-11-07 | Ajinomoto Co Inc | 反すう動物用飼料添加物 |
| JPH09299038A (ja) * | 1996-05-16 | 1997-11-25 | Nof Corp | 飼料組成物の製造方法 |
| JPH1014500A (ja) * | 1996-07-04 | 1998-01-20 | Nof Corp | 飼料組成物の製造方法 |
| JPH10215787A (ja) * | 1997-02-10 | 1998-08-18 | Sagami Chem Res Center | オレイン酸強化動物性食品の生産方法及びオレイン酸強化動物性食品 |
| JP4017227B2 (ja) * | 1998-01-20 | 2007-12-05 | 白石カルシウム株式会社 | ペレット状脂肪酸含有混合飼料造粒品及びその製造方法 |
| EP1405570A1 (en) * | 1998-03-04 | 2004-04-07 | Ajinomoto Co., Inc. | Process for producing ruminant feed additive composition |
| US6242013B1 (en) * | 1999-07-27 | 2001-06-05 | Land O'lakes, Inc. | Method and composition for enhancing oleic acid content of milk produced by ruminants |
| CA2357265C (en) * | 2001-04-24 | 2004-04-13 | University Of British Columbia | Improved additive for livestock feeds |
| JP4378089B2 (ja) * | 2003-02-24 | 2009-12-02 | 日本曹達株式会社 | ルーメンバイパス製剤の製造方法 |
| FR2879074B1 (fr) * | 2004-12-15 | 2007-08-03 | Adisseo France Sas Soc Par Act | Granules de principe actif hydrophile |
| CN100405923C (zh) * | 2005-05-17 | 2008-07-30 | 内蒙古多源新技术研究开发中心 | 反刍动物的过瘤胃保护性氨基酸营养添加剂及生产方法 |
| CN101133777A (zh) * | 2006-09-01 | 2008-03-05 | 内蒙古多源新技术研究开发中心 | 反刍动物过瘤胃维生素营养填加剂及生产方法 |
| US10092533B2 (en) * | 2010-10-18 | 2018-10-09 | H. J. Baker & Bro., Llc | Granular feed supplement |
| US20130196034A1 (en) * | 2012-01-31 | 2013-08-01 | Raisio Plc. | Animal feed and a process for its preparation |
| CA2861193C (en) * | 2012-01-31 | 2020-06-09 | Benemilk Ltd. | Ruminant feed enhancing energy metabolism in milk production |
| DE102012021545A1 (de) * | 2012-10-29 | 2014-04-30 | ETH Zürich | Fettsystem, z.B. Lebensmittel-Fettsystem, Kosmetik-Fettsystem, Pharma-Fettsystem und Produkt zur Verwendung für fetthaltige Lebensmittel, Kosmetika oder Pharmaka |
| CA2925105C (en) * | 2013-10-15 | 2021-02-09 | Benemilk Oy | Protein-containing dietary compositions and methods for their preparation and use |
| EP3057579A4 (en) * | 2013-10-15 | 2017-07-26 | Benemilk Oy | Carbohydrate-containing dietary compositions and methods for their preparation and use |
| WO2015116232A1 (en) * | 2014-02-03 | 2015-08-06 | Benemilk Oy | Dietary compositions for ruminants and methods of making the same |
| CN104222667A (zh) * | 2014-09-26 | 2014-12-24 | 广州市优百特饲料科技有限公司 | 一种反刍动物过瘤胃稳定均衡脂肪粉及其制备方法 |
| EP3011839A1 (en) * | 2014-10-22 | 2016-04-27 | Fernando Cantini | A food composition for ruminant animals |
| WO2016126234A1 (en) * | 2015-02-02 | 2016-08-11 | Benemilk Us Ltd. | Method for making animal feed |
| CN107708430A (zh) * | 2015-03-25 | 2018-02-16 | 拜内梅尔克公司 | 氨基酸动物饲料组合物 |
-
2016
- 2016-02-02 JP JP2017540563A patent/JP2018510618A/ja active Pending
- 2016-02-02 CN CN201680010185.1A patent/CN107249348A/zh active Pending
- 2016-02-02 WO PCT/US2016/016147 patent/WO2017003522A1/en not_active Ceased
- 2016-02-02 EP EP16818369.7A patent/EP3316701A4/en not_active Withdrawn
- 2016-02-02 JP JP2017540565A patent/JP2018503389A/ja active Pending
- 2016-02-02 WO PCT/US2016/016134 patent/WO2016126683A1/en not_active Ceased
- 2016-02-02 US US15/547,790 patent/US20180020696A1/en not_active Abandoned
- 2016-02-02 US US15/547,784 patent/US20180014557A1/en not_active Abandoned
- 2016-02-02 CN CN201680010488.3A patent/CN107205437A/zh active Pending
- 2016-02-02 EP EP16747099.6A patent/EP3253228A4/en not_active Withdrawn
Patent Citations (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2881074A (en) * | 1955-07-29 | 1959-04-07 | Armour & Co | Growth promotant substances |
| US3468667A (en) * | 1965-03-19 | 1969-09-23 | Armour Ind Chem Co | Coated dust free phosphate feed supplement |
| US4599234A (en) * | 1983-10-07 | 1986-07-08 | Amer M Samir | Synergistic diet comprising selenium based compounds |
| US4826694A (en) * | 1985-10-14 | 1989-05-02 | Balfour Manufacturing Company | Ruminant feedstuffs, their production and apparatus for use therein |
| US5601860A (en) * | 1990-11-30 | 1997-02-11 | American Home Products Corporation | Corandomized fat compositions for infant formulas |
| US5456927A (en) * | 1991-12-04 | 1995-10-10 | Church & Dwight Co., Inc. | Ruminant feed supplement product |
| US5215768A (en) * | 1992-03-20 | 1993-06-01 | Church & Dwight Co., Inc. | Deodorized fatty acid salt feed supplement |
| US5585134A (en) * | 1993-06-29 | 1996-12-17 | Volac, Inc. | Production of rumen-bypass fatty acid salt and protein dietary supplement |
| US6204291B1 (en) * | 1998-06-26 | 2001-03-20 | The Iams Company | Process for promoting weight loss in overweight dogs |
| US20030180352A1 (en) * | 1999-11-23 | 2003-09-25 | Patel Mahesh V. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
| CA2335745A1 (en) * | 2001-02-13 | 2002-08-13 | Her Majesty In Right Of Canada As Represented By The Minister Of Fisheries And Oceans | Process for preparing nutritionally upgraded canola products |
| US6939864B1 (en) * | 2001-07-09 | 2005-09-06 | Purdue Research Foundation | Animal feed compositions and methods of using the same |
| CA2578903A1 (en) * | 2004-08-31 | 2006-03-09 | Akzo Nobel N.V. | Method for pigment solubilisation, a pigment composition and its use |
| US20090285931A1 (en) * | 2008-02-04 | 2009-11-19 | Shelby Nancy J | Feed supplement for animals for reducing methane production |
| WO2009148521A1 (en) * | 2008-06-03 | 2009-12-10 | Nestec S.A. | Palatability enhancers and methods for enhancing palatability |
| WO2011060084A1 (en) * | 2009-11-10 | 2011-05-19 | MyCell Holdings Limited | Stabilized formulations of fatty acids |
| US20140154392A1 (en) * | 2010-05-21 | 2014-06-05 | H R D Corporation | Process for upgrading low value renewable oils |
| US20130323362A1 (en) * | 2010-12-06 | 2013-12-05 | Degama Berrier Ltd. | Composition and method for improving stability and extending shelf life of probiotic bacteria and food products thereof |
Non-Patent Citations (1)
| Title |
|---|
| See also references of EP3316701A4 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN107205437A (zh) | 2017-09-26 |
| US20180014557A1 (en) | 2018-01-18 |
| EP3316701A1 (en) | 2018-05-09 |
| CN107249348A (zh) | 2017-10-13 |
| EP3253228A1 (en) | 2017-12-13 |
| WO2017003522A8 (en) | 2017-08-24 |
| EP3316701A4 (en) | 2019-04-10 |
| JP2018510618A (ja) | 2018-04-19 |
| EP3253228A4 (en) | 2018-11-14 |
| US20180020696A1 (en) | 2018-01-25 |
| WO2016126683A1 (en) | 2016-08-11 |
| JP2018503389A (ja) | 2018-02-08 |
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