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A Protein Powder Composition With Various Flavoring Agents And Taste Potentiator

Abstract: The present disclosure pertains to protein powder composition pack that provide an enhanced perception of an active substance contained therein. Particularly, the protein powder composition pack of the present invention comprise an active substance, plurality of flavoring agents, and a taste potentiator, and wherein the active substance, flavoring agent, and the taste potentiator are packed separately.

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Patent Information

Application #
Filing Date
05 January 2023
Publication Number
28/2024
Publication Type
INA
Invention Field
FOOD
Status
Email
Parent Application

Applicants

GHV Medical Anchor Private Limited
3rd Floor, Capital Cyberscape, Sector 59, Gurugram - 122102, Haryana, India.

Inventors

1. DHUWAN, Ashish
H. No. 3000, Huda Plots, Block G, Sector 57, Sushant Lok 2, Near Hong Kong Market, Gurugram, Haryana - 122003, India.

Specification

DESC:FIELD OF THE INVENTION
[0001] The present disclosure pertains to protein powder compositions that provide an enhanced perception of an active substance contained therein. Particularly, the present disclosure pertains to protein powder compositions, wherein the composition comprises active substance, a flavoring agent, and a taste potentiator, and wherein the taste potentiator may increase the perception of the active substance upon consumption.

BACKGROUND OF THE INVENTION
[0002] The background description includes information that may be useful in understanding the present invention. It is not an admission that any of the information provided herein is prior art or relevant to the presently claimed invention, or that any publication specifically or implicitly referenced is prior art.
[0003] The taste receptor cells located in taste buds primarily on the surface of the tongue and palate in the oral cavity sense five primary categories of taste including sour, salty, sweet, bitter and umami (savory or the taste of glutamate). It is understood that the sour and salty tastes are detected by the passage of ions, hydrogen and sodium, respectively, through the ion channels in taste bud cells thus, triggering a nerve impulse that is sensed in the brain. Sweet, bitter and umami tastes are perceived by physical binding of tastants to G-protein coupled receptors initiating a series of signaling events that trigger a nerve impulse that is sensed in the brain.
[0004] Conventional protein powder compositions available either have neutral flavor or are available only in one type of flavor in a single pack. These conventional protein powder compositions may lead to insensitivity to same taste due to repeated exposure. This may lead to neurotransmitters and taste receptors to ignore and later reject the taste. This may be identified as boredom to the protein powder compositions which is generally recommended to be taken at least once daily.
[0005] There is, therefore, a need in the art to develop a new and improved protein powder composition that allows choice of several flavors. Thus, a different flavor and a taste potentiator available for each time the protein powder composition is consumed, does not allow boredom to a single taste due to the insensitivity that occurs by repeated exposure to the same taste.

OBJECTS OF THE INVENTION
[0006] Primary object of the present disclosure is to provide a composition that overcomes one or more limitations associated with the conventional protein powder compositions/formulations.
[0007] Another object of the present disclosure is to provide a protein powder composition that aids in reducing boredom and insensitivity that occurs by repeated exposure to the same taste and flavor.
[0008] Another object of the present disclosure is to provide a protein powder composition that is easy to prepare and economical.
[0009] Other objects of the present disclosure will be apparent from the description of the invention herein below.

SUMMARY OF THE INVENTION
[00010] Accordingly, the present invention in one aspect provides a protein powder composition comprising an active substance, a flavoring agent, and a taste potentiator.
[00011] The present invention in another aspect provides a protein powder composition pack comprising an active substance mix, plurality of flavoring agents, and a taste potentiator wherein the active substance mix comprises Aspartic acid, threonine, serine, glutamic acid, glycine, Alanine, Valine, Isoleucine, Leucine, Tyrosine, Phenylalanine, Histidine, Lysine, Arginine, Proline, Cystine, Methionine, and Tryptophan.
[00012] In an aspect, the active substance mix comprising Aspartic acid (8-9% w/w), threonine (5-5.5% w/w), serine (4-4.5% w/w), glutamic acid (14-14.5% w/w), glycine (1-2% w/w), Alanine (4-4.5%), Valine (4-5% w/w), Isoleucine (4-5% w/w), Leucine (8-9% w/w), Tyrosine (2-3% w/w), Phenylalanine (2-3% w/w), Histidine (1-2% w/w), Lysine (8-8.5% w/w), Arginine (2-2.5% w/w), Proline (5-5.5% w/w), Cystine (2-2.5% w/w), Methionine (1-2% w/w), and Tryptophan (1-2% w/w).
[00013] In another aspect, the present invention provides the active substance mix comprising Aspartic acid (8.8% w/w), threonine (5.1% w/w), serine (4.2% w/w), glutamic acid (14.1% w/w), glycine (1.5% w/w), Alanine (4.2%), Valine (4.4% w/w), Isoleucine (4.6% w/w), Leucine (8.8% w/w), Tyrosine (2.6% w/w), Phenylalanine (2.7% w/w), Histidine (1.5% w/w), Lysine (8% w/w), Arginine (2.1% w/w), Proline (5.1% w/w), Cystine (2% w/w), Methionine (1.8% w/w), and Tryptophan (1.6% w/w).
[00014] In yet another aspect, the present invention provides a protein powder composition pack comprising plurality of flavoring agents in an amount of 1-2 g per 100 g of the active substance mix, wherein the flavoring agent imparts various flavors such as dates-like flavor, chocolate-like flavor, cinnamon-like flavor, Mango-like flavor, Blueberry-like flavor, Kulfi-like flavor and coffee-like flavor.
[00015] In yet another aspect, the present invention provides a protein powder composition pack comprising a taste potentiator selected from medium chain triglycerides in an amount of 1-2 g per 100 g of the active substance mix.
[00016] Other aspects, advantages, and salient features of the invention will become apparent to those skilled in the art from the following detailed description, which, taken in conjunction with the exemplary embodiments of the invention.

DETAILED DESCRIPTION OF THE INVENTION
[00017] The following is a detailed description of embodiments of the present disclosure. The embodiments are in such detail as to clearly communicate the disclosure. However, the amount of detail offered is not intended to limit the anticipated variations of embodiments; on the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the present disclosure as defined by the appended claims.
[00018] Unless the context requires otherwise, throughout the specification which follow, the word “comprise” and variations thereof, such as, “comprises” and “comprising” are to be construed in an open, inclusive sense that is as “including, but not limited to.”
[00019] Reference throughout this specification to “one embodiment” or “an embodiment” means that a particular feature, structure or characteristic described in connection with the embodiment is included in at least one embodiment. Thus, the appearances of the phrases “in one embodiment” or “in an embodiment” in various places throughout this specification are not necessarily all referring to the same embodiment. Furthermore, the particular features, structures, or characteristics may be combined in any suitable manner in one or more embodiments.
[00020] As used in the description herein and throughout the claims that follow, the meaning of “a,” “an,” and “the” includes plural reference unless the context clearly dictates otherwise. Also, as used in the description herein, the meaning of “in” includes “in” and “on” unless the context clearly dictates otherwise.
[00021] In some embodiments, the numbers expressing quantities of ingredients, properties such as concentration, and so forth, used to describe and claim certain embodiments of the invention are to be understood as being modified in some instances by the term “about.” Accordingly, in some embodiments, the numerical parameters set forth in the written description are approximations that can vary depending upon the desired properties sought to be obtained by a particular embodiment. In some embodiments, the numerical parameters should be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of some embodiments of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as practicable.
[00022] The recitation of ranges of values herein is merely intended to serve as a shorthand method of referring individually to each separate value falling within the range. Unless otherwise indicated herein, each individual value is incorporated into the specification as if it were individually recited herein.
[00023] All methods described herein can be performed in suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided with respect to certain embodiments herein is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention otherwise claimed. No language in the specification should be construed as indicating any non-claimed element essential to the practice of the invention.
[00024] It should also be appreciated that the present invention can be implemented in numerous ways, including as a system, a method or a device. In this specification, these implementations, or any other form that the invention may take, may be referred to as processes. In general, the order of the steps of the disclosed processes may be altered within the scope of the invention.
[00025] The headings and abstract of the invention provided herein are for convenience only and do not interpret the scope or meaning of the embodiments.
[00026] Various terms are used herein. To the extent a term used in a claim is not defined below, it should be given the broadest definition persons in the pertinent art have given that term as reflected in printed publications and issued patents at the time of filing.
[00027] In an embodiment, the present invention provides a dry protein powder composition pack, said pack comprising comprises an active substance mix; a plurality of flavoring agents; and a taste potentiator, wherein, the active substance, the flavoring agents, and the taste potentiator are packed separately.
[00028] In another embodiment, the present invention provides a protein powder composition comprising an active substance mix, a flavoring agent, and a taste potentiator wherein the active substance mix comprises Aspartic acid, threonine, serine, glutamic acid, glycine, Alanine, Valine, Isoleucine, Leucine, Tyrosine, Phenylalanine, Histidine, Lysine, Arginine, Proline, Cystine, Methionine, and Tryptophan.
[00029] In preferred embodiment, the active substance mix comprises a mixture of Aspartic acid (8-9% w/w), threonine (5-5.5% w/w), serine (4-4.5% w/w), glutamic acid (14-14.5% w/w), glycine (1-2% w/w), Alanine (4-4.5% w/w), Valine (4-5% w/w), Isoleucine (4-5% w/w), Leucine (8-9% w/w), Tyrosine (2-3% w/w), Phenylalanine (2-3% w/w), Histidine (1-2% w/w), Lysine (8-8.5% w/w), Arginine (2-2.5% w/w), Proline (5-5.5% w/w), Cystine (2-2.5% w/w), Methionine (1-2% w/w), and Tryptophan (1-2% w/w) based on the total weight of the active substance.
[00030] In most preferred embodiment, the active substance mix comprises a mixture of Aspartic acid (8.8% w/w), threonine (5.1% w/w), serine (4.2% w/w), glutamic acid (14.1% w/w), glycine (1.5% w/w), Alanine (4.2%), Valine (4.4% w/w), Isoleucine (4.6% w/w), Leucine (8.8% w/w), Tyrosine (2.6% w/w), Phenylalanine (2.7% w/w), Histidine (1.5% w/w), Lysine (8% w/w), Arginine (2.1% w/w), Proline (5.1% w/w), Cystine (2% w/w), Methionine (1.8% w/w), and Tryptophan (1.6% w/w) based on the total weight of the active substance.
[00031] In preferred embodiment, the active substance comprises a mixture of Aspartic acid (8-9 g), threonine (5-5.5 g), serine (4-4.5 g), glutamic acid (14-14.5 g), glycine (1-2 g), Alanine (4-4.5 g), Valine (4-5 g), Isoleucine (4-5 g), Leucine (8-9 g), Tyrosine (2-3 g), Phenylalanine (2-3 g), Histidine (1-2 g), Lysine (8-8.5 g), Arginine (2-2.5 g), Proline (5-5.5 g), Cystine (2-2.5 g), Methionine (1-2 g), and Tryptophan (1-2 g) based on 100 g of the active substance.
[00032] In most preferred embodiment, the active substance comprises a mixture of Aspartic acid (8.8 g), threonine (5.1 g), serine (4.2 g), glutamic acid (14.1 g), glycine (1.5 g), Alanine (4.2%), Valine (4.4 g), Isoleucine (4.6 g), Leucine (8.8 g), Tyrosine (2.6 g), Phenylalanine (2.7 g), Histidine (1.5 g), Lysine (8 g), Arginine (2.1 g), Proline (5.1 g), Cystine (2 g), Methionine (1.8 g), and Tryptophan (1.6 g) based on 100 g of the active substance.
[00033] In another embodiment, the present invention provides a protein powder composition comprising an active substance, plurality of flavoring agents, and a taste potentiator wherein the flavoring agent imparts various flavors such as dates-like flavor, chocolate-like flavor, cinnamon-like flavor, Mango-like flavor, Blueberry-like flavor, Kulfi-like flavor and coffee-like flavor.
[00034] In another embodiment, the present invention provides a protein powder composition pack comprising an active substance, a plurality of flavoring agents, and a taste potentiator, fructo-oligosaccharides, stabilizers, common salt, sweeteners, and anti-caking agent.
[00035] In an embodiment, the taste potentiator can be a natural (e.g.) fermented whey protein) or artificial component (e.g. monosodium glutamate, MSG), or any known taste potentiator known in the prior-art. In some embodiments, the taste potentiator is medium chain triglycerides.
[00036] In an embodiment, the flavoring agent includes but not limited to aromatic oils (e.g., caraway, clove, lemon, spearmint, rose, and peppermint); ginger; raspberry; maltol; syrups (e.g., citric acid, sarsaparilla, and cherry); glycerin; cocoa; licorice; vanillin; and ethyl vanillin. Other commonly used flavoring agents are alcohols, esters, ketones, pyrazines, phenolics, and terpenoids. Alcohols may have bitter and medicinal taste, esters are fruity, ketones and pyrazines may taste like caramel, phenolics have a smoky flavor and terpenoids have citrus or pine flavor.
[00037] In an embodiment, the present invention the flavoring agent and the taste potentiator is packaged separately as additives for the active substance. Hence, enabling addition of various different types of flavoring agents and taste potentiators to the same active substance. This allows significant reduction in inventory levels and number of Stock Keeping Units (SKU) that needs to be maintained. This has an advantageous impact on the environment, since the lower inventory leads to lesser amount of product nearing expiry date. Hence, lesser amount of product is wasted.
[00038] In an embodiment, the process of reduced inventory levels and number of Stock Keeping Units (SKU) optimizes cash flow as less inventory is blocked in the overall supply chain.
[00039] In an embodiment, the sweeteners may include but is not limited to sucrose, dextrose, maltose, dextrin, xylose, ribose, glucose, lactose, mannose, galactose, fructose, invert sugar, fructo oligo saccharide syrups, partially hydrolyzed starch, corn syrup solids, isomaltulose, sorbitol, xylitol, erythritol, mannitol, galactitol, maltitol, lactitol, hydrogenated isomaltulose, hydrogenated starch hydrolysates, stevia, dihydrochalcones, monellin, steviosides, rebaudioside A, glycyrrhizin, dihydroflavenol, L-aminodicarboxylic acid aminoalkenoic acid ester amides, saccharin and its soluble salts. However, a person skilled in the art would appreciate that any other sweeteners can be utilized to serve the intended purpose.
[00040] In an embodiment, the medium chain triglycerides may include but is not limited to Caproic acid, Caprylic acid, Capric acid, and Lauric acid, derived from palm kernel oil and coconut oil.
[00041] In an embodiment, the stabilizers may include but is not limited to alginate, agar, carrageen, cellulose and cellulose derivatives, gelatin, guar gum, gum Arabic, locust bean gum, pectin, starch, xanthan gum
[00042] In an embodiment, the present invention provides a method of preparing a protein drink with a desired taste and flavor comprising the steps of:
a. providing the protein powder composition pack as disclosed herein;
b. mixing the active substance mix from the pack in a solvent;
c. selecting a desired flavoring agent, and a taste potentiator from the pack and adding the same to the raw mix to obtain the final mix; and
d. agitating the final mix for about 30 seconds to obtain the protein drink
[00043] In an embodiment, the amount of flavoring agent, and/or taste potentiator is 1-2 g each per 100 mg of the active substance.
[00044] In an embodiment, the present invention provides a method of preparing a protein drink with a desired taste and flavor comprising the steps of:
a. providing the protein powder composition pack as disclosed herein, wherein the active substance in the pack comprises Aspartic acid, threonine, serine, glutamic acid, glycine, Alanine, Valine, Isoleucine, Leucine, Tyrosine, Phenylalanine, Histidine, Lysine, Arginine, Proline, Cystine, Methionine, and Tryptophan;
b. mixing the active substance mix in a solvent to obtain a raw mix;
c. selecting a desired flavoring agent, and a taste potentiator from the pack and adding the same to the raw mix to obtain the final mix; and
d. agitating the final mix for about 20-60 seconds to obtain the protein drink.
[00045] In an embodiment, the present invention provides a method of preparing a protein drink with a desired taste and flavor comprising the steps of:
a) providing the protein powder composition pack as disclosed herein;
b) mixing the active substance mix from the pack in a solvent in a ratio of 1:6 to 1:9 to obtain a raw mix;
c) selecting a desired flavoring agent, and a taste potentiator from the pack and adding the same to the raw mix to obtain the final mix; and
d) agitating the final mix for about 20-60 seconds to obtain the protein drink.
[00046] In an embodiment, the active substance may be mixed in a solvent at a temperature lower than room temperature.
[00047] In an embodiment, the solvent is selected from the group consisting of milk selected from any or a combination of milk from cow, goat, camel or buffalo, whole milk, skimmed milk, fat-free milk, lactose-free milk, butter milk, cashew milk, oat milk, soy milk, rice milk, hemp milk, coconut milk, condensed milk, evaporated milk, and almond milk.
[00048] In an embodiment, the protein powder composition further comprises one or a plurality of excipient(s).
[00049] In an embodiment, the one or a plurality of excipient(s) is selected from any or a combination of a thickening agent, a bulking agent, a lubricant, a solubilizer, a binder, a disintegrant, a chelating agent, a glidant, a coloring agent, a tonicity agent, a sweetening agent, a buffering agent, a preservative, a film former/waterproofing agent, a rheology modifying agent, a fragrance, an emollient, a humectants, an emulsifier, a diluent and a solvent.
[00050] In an embodiment, the thickening agent(s) includes but not limited to, carbopol, carbomer, acrylate copolymer, beeswax, emulsifying cresmer wax, sodium acrylate/sodium acryloyl dimethyl taurate copolymer (0.2-1.2% w/w), and combinations thereof. However, a person skilled in the art would appreciate that any other thickening agent(s) can be utilized to serve the intended purpose.
[00051] In an embodiment, the solubilizer(s) includes but not limited to, cyclodextrins, pH adjusters, salts and buffers, surfactants, fatty acids, phospholipids, metals of fatty acids, and combinations thereof. However, a person skilled in the art would appreciate that any other solubilizer(s) can be utilized to serve the intended purpose.
[00052] In an embodiment, the binder(s) include but not limited to, cellulosic derivatives (such as methylcellulose, carboxymethyl cellulose, hydroxyethyl cellulose, hydroxyethylmethyl cellulose, etc), polyacrylates (such as Carbopol, polycarbophil, etc), Povidone (all grades), Polyox of any molecular weight or grade, irradiated or not, maize starch, povidone, copovidone, corn starch, starch, polyvinylpyrrolidone (PVP), microcrystalline cellulose (Avicel@ -Avicel 101), and combinations thereof. However, a person skilled in the art would appreciate that any other binder(s) can be utilized to serve the intended purpose.
[00053] In an embodiment, the disintegrant(s) includes but not limited to, croscarmellose sodium, crospovidone, sodium starch glyconate, citric acid, calcium carbonate, pregelatinized starch, and combinations thereof. However, a person skilled in the art would appreciate that any other disintegrant(s) can be utilized to serve the intended purpose.
[00054] In an embodiment, the coloring agent(s) includes but not limited to, E102 Tartrazine, E104 Quinoline Yellow, E110 Sunset Yellow FCF, E120 - Cochineal, carminic acid, Carmines, E122 Azorubine (Carmoisine), E123 Amaranth, E124 Ponceau 4R (Cochineal Red A), E127 Erythrosine, E129 Allura Red, E131 Patent Blue, and combinations thereof. However, a person skilled in the art would appreciate that any other coloring agent(s) can be utilized to serve the intended purpose.
[00055] In an embodiment, the preservative(s) includes but not limited to, sodium benzoate, potassium sorbate, phenoxyethanol, p-hydroxybenzoic acid esters, sorbic acid, benzoic acid, propionic acid or salts thereof; Alcohols such as benzyl alcohol, butanol or ethanol, isopropyl alcohol and quaternary ammonium compounds such as benzalkonium chloride, sodium benzoate, and combinations thereof. However, a person skilled in the art would appreciate that any other preservative(s) can be utilized to serve the intended purpose.
[00056] In an embodiment, the emulsifier(s) includes but not limited to, hydrogenated lecithin, C12-16 Alcohols, palmitic acid (e.g., Biophillic™ H) and acetyl alcohol, glyceryl stearate, PEG-75 stearate, ceteth-20, steareth-2 (Emulium® Delta), and combinations thereof. However, a person skilled in the art would appreciate that any other emulsifier (s) can be utilized to serve the intended purpose.
[00057] In an embodiment, the diluent(s) includes but not limited to, microfine cellulose, lactose, starch, pregelatinized starch, calcium carbonate, calcium sulfate, sugar, dextrates, dextrin, dextrose, dibasic calcium phosphate dihydrate, tribasic calcium phosphate, kaolin, magnesium carbonate, magnesium oxide, maltodextrin, mannitol, potassium chloride, powdered cellulose, sodium chloride, sorbitol, talc, and combinations thereof. However, a person skilled in the art would appreciate that any other diluent(s) can be utilized to serve the intended purpose.
[00058] While one or more embodiments of the present disclosure enumerates and describes a list of excipients that may be used in the composition to serve an intended purpose, it should be appreciated that one or more excipient(s) may also serve more than one function, obviating the need of inclusion of separate excipients for the specified purpose. Although several embodiments of the present disclosure names few of the commonly used excipients, any other excipient(s) known to or appreciated by a skilled person can also be used to realize the advantageous compositions of the present disclosure.
[00059] In an embodiment, the present invention the flavoring agent and/or the taste potentiator is separately available in one or several dosage forms. In an embodiment, dosage form is selected from any or a combination of capsule, tablets or caplets; pills; powders such as a sterile packaged powder, a dispensable powder, and an effervescent powder; capsules including both soft or hard gelatin capsules such as HPMC capsules, lozenges, a sachet, a sprinkle, a reconstitutable powder or shake, a troche, granules, liquids such as suspensions, emulsions, semisolids, or gels. In an embodiment, the formulation may be in a solid, a liquid and a semi-solid form. In an embodiment, the solid may be nano-particles or microparticles. However, any or a combination of compositional dosage form(s), as known to or appreciated by a person skilled in the art, can be utilized to serve the intended purpose.
[00060] The present invention provides a substrate with the image transferred thereon which can be suitably used for blister forming of thermoforming for products like medicine, nutraceuticals, food or any other products for human use or any other products required to be packaged to avoid counterfeiting.
[00061] In an embodiment, the composition of the present disclosure can be manufactured by any conventional method such as homogenization method, know to or appreciated by a person skill in the art working in the related industry to serve the intended purpose. In an embodiment, any other method known to or appreciated by a person skilled in the art can be utilized to serve the intended purpose.
[00062] In an embodiment, composition of the present disclosure can be used as a blend in other nutraceutical compositions/formulations. In an embodiment, composition of the present disclosure can be blended with any other compositions or formulations, including but not limited to nutraceutical compositions/formulations. Blending of the other compositions/formulations with the composition of the present disclosure further improves the benefit of the other compositions/formulations.
[00063] The foregoing description of the specific embodiments will so fully reveal the general nature of the embodiments herein that others can, by applying current knowledge, readily modify and/or adapt for various applications such specific embodiments without departing from the generic concept, and, therefore, such adaptations and modifications should and are intended to be comprehended within the meaning and range of equivalents of the disclosed embodiments. It is to be understood that the phraseology or terminology employed herein is for the purpose of description and not of limitation. Therefore, while the embodiments herein have been described in terms of preferred embodiments, those skilled in the art will recognize that the embodiments herein can be practiced with modification within the spirit and scope of the embodiments as described herein.

EXAMPLES
[00064] The present disclosure is further explained in the form of following examples. However, it is to be understood that the foregoing examples are merely illustrative and are not to be taken as limitations upon the scope of the invention. Various changes and modifications to the disclosed embodiments will be apparent to those skilled in the art. Such changes and modifications may be made without departing from the scope of the invention.
[00065] Example 1: Amino acid profile of the Protein powder composition (Table 1):

ADVANTAGES OF THE PRESENT INVENTION
[00066] The present invention provides a composition that overcomes one or more limitations associated with the conventional protein powder compositions/formulations.
[00067] The present invention provides a protein powder composition that aids in reducing boredom and insensitivity that occurs by repeated exposure to the same taste and flavor.
[00068] The present invention provides a protein powder composition that is easy to prepare and economical.
[00069] The present invention provides a protein powder composition that helps maintain low inventory level optimizing cash flow by blocking less inventory in the overall supply chain.
[00070] The present invention provides a packaging for protein powder composition that reduces number of inventory nearing expiry date.
,CLAIMS:1. A dry protein powder composition pack, said pack comprising comprises
an active substance mix, wherein the active substance mix comprises a mixture of Aspartic acid (8-9% w/w), threonine (5-5.5% w/w), serine (4-4.5% w/w), glutamic acid (14-14.5% w/w), glycine (1-2% w/w), Alanine (4-4.5%), Valine (4-5% w/w), Isoleucine (4-5% w/w), Leucine (8-9% w/w), Tyrosine (2-3% w/w), Phenylalanine (2-3% w/w), Histidine (1-2% w/w), Lysine (8-8.5% w/w), Arginine (2-2.5% w/w), Proline (5-5.5% w/w), Cystine (2-2.5% w/w), Methionine (1-2% w/w), and Tryptophan (1-2% w/w) based on the total weight of the active substance;
a flavoring agent, wherein the said flavoring agent is selected from the group consisting of dates-like flavor, chocolate-like flavor, cinnamon-like flavor, Mango-like flavor, Blueberry-like flavor, Kulfi-like flavor and coffee-like flavor;
a taste potentiator comprises medium chain triglycerides; and
optionally, one or more excipients.
wherein, the active substance, flavoring agent, and the taste potentiator are packed separately.
2. The pack as claimed in claim 1, wherein the active substance mix comprises a mixture of Aspartic acid (8.8% w/w), threonine (5.1% w/w), serine (4.2% w/w), glutamic acid (14.1% w/w), glycine (1.5% w/w), Alanine (4.2%), Valine (4.4% w/w), Isoleucine (4.6% w/w), Leucine (8.8% w/w), Tyrosine (2.6% w/w), Phenylalanine (2.7% w/w), Histidine (1.5% w/w), Lysine (8% w/w), Arginine (2.1% w/w), Proline (5.1% w/w), Cystine (2% w/w), Methionine (1.8% w/w), and Tryptophan (1.6% w/w) based on the total weight of the active substance.
3. The pack as claimed in claim 1, wherein the medium chain triglyceride is selected from the group consisting of Caproic acid, Caprylic acid, Capric acid, and Lauric acid, derived from palm kernel oil and coconut oil.
4. The pack as claimed in claim 1, wherein amount of the flavouring agent is 1-2 g per 100 g of the active substance.
5. The pack as claimed in claim 1, wherein amount of the taste potentiator is 1-2 g per 100 g of the active substance.
6. The pack as claimed in claim 1, wherein the excipient is selected from but not limited to a thickening agent, a bulking agent, a lubricant, a solubilizer, a binder, a disintegrant, a chelating agent, a glidant, a coloring agent, a tonicity agent, a sweetening agent, a buffering agent, a preservative, a film former/waterproofing agent, a rheology modifying agent, a fragrance, an emollient, a humectants, an emulsifier, a diluent and a solvent
7. A method of preparing a protein drink with a desired taste and flavor comprising the steps of:
a. providing the pack as claimed in claim 1;
b. mixing the active substance mix as claimed in claims 1 or 2 in a solvent in the ratio of 1:6 to 1:9 to obtain a raw mix;
c. selecting a desired flavoring agent, and a desired taste potentiator from the pack as claimed in claim 1 and adding the same to the raw mix to obtain the final mix; and
d. agitating the final mix for about 20-60 seconds to obtain the protein drink.
8. The method as claimed in claim 7, wherein the solvent is selected from the group consisting of milk or milk products, water, or juice extracted from fruits or vegetables.

Documents

Application Documents

# Name Date
1 202311001172-STATEMENT OF UNDERTAKING (FORM 3) [05-01-2023(online)].pdf 2023-01-05
2 202311001172-PROVISIONAL SPECIFICATION [05-01-2023(online)].pdf 2023-01-05
3 202311001172-POWER OF AUTHORITY [05-01-2023(online)].pdf 2023-01-05
4 202311001172-FORM 1 [05-01-2023(online)].pdf 2023-01-05
5 202311001172-DECLARATION OF INVENTORSHIP (FORM 5) [05-01-2023(online)].pdf 2023-01-05
6 202311001172-ENDORSEMENT BY INVENTORS [04-01-2024(online)].pdf 2024-01-04
7 202311001172-CORRESPONDENCE-OTHERS [04-01-2024(online)].pdf 2024-01-04
8 202311001172-COMPLETE SPECIFICATION [04-01-2024(online)].pdf 2024-01-04