Patent Application
20230381262
The present application claims priority to Korean Patent Application No. 10-2022-0066326, filed May 30, 2022, the entire contents of which are hereby incorporated by reference.
The disclosure relates to a composition for reducing the absorption of microplastics.
In general, microplastics refer to synthetic polymer compounds with a size of 5 mm or less, and are classified into primary microplastics and secondary microplastics based on origin. Primary microplastics refer to plastic particles produced for an intended purpose, resin pellets, scrubs in facial wash or toothpaste, industrial abrasives, or the like. Secondary microplastics refer to micronized plastic fragments that are decomposed or pulverized into small sizes in the process of using plastic products or due to corrosion by ultraviolet rays or various collisions of discarded plastic waste. These microplastics are not filtered out in a sewage treatment plant and flow into the sea through streams and rivers.
Microplastics can adsorb, transport, and release not only toxic persistent organic pollutants such as polychlorinated biphenyls(PCBs), dioxins, and dichloro-diphenyl-trichloroethane(DDT), but also endocrine disruptors such as phthalates and bisphenols. Thus, microplastics are also called deadly bites of grain, which have serious adverse effects on rivers, marine environments and various ecosystems. After continuously accumulated in the body of an organism along the food chain, the microplastics are finally consumed by humans in the form of food, and the microplastics can also be included in tap water (drinking water) that has gone through a purification process. Through this process, when a large amount of microplastics is accumulated in the body as microplastics are consumed for a long time, the microplastics become a factor of carcinogenesis or cause health damage by environmental hormone.
In one aspect, the disclosure is to provide a composition for reducing the absorption of microplastics in the body.
In one aspect, the disclosure provides a composition for reducing absorption of microplastics into the body, comprising a green tea extract as an active ingredient.
In an exemplary embodiment, the green tea extract may be an extract of water, an organic solvent, or a mixed solvent thereof.
In an exemplary embodiment, the green tea extract may comprise 30 to 45% by weight of catechin based on a total weight of the green tea extract.
In an exemplary embodiment, the green tea extract may be administered at a dosage of 1 to 200 mg/kg/day.
In one exemplary embodiment, the composition may aggregate the microplastics.
In one exemplary embodiment, the composition may inhibit inflammation caused by absorption of the microplastics.
In one exemplary embodiment, the composition may inhibit oxidative stress in a cell caused by the microplastics.
In one exemplary embodiment, the composition may prevent, alleviate or treat lipid metabolism disorder in a cell caused by the microplastics.
In one exemplary embodiment, the composition may be administered orally.
In one exemplary embodiment, the composition may be a food composition.
In an exemplary embodiment, the composition may be a pharmaceutical composition.
In one aspect, the composition according to the disclosure has an excellent effect of reducing the absorption of microplastics into the body without side effects.
In one aspect, the composition according to the disclosure can inhibit inflammation caused by the microplastic absorption.
Although the terms used in the specification are selected from generally known and used terms mile considering functions of the disclosure, they may vary according to intention or customs of those skilled in the art or emergence of new technology. In certain cases, some of the terms may have been selected by the applicant at his or her discretion, and in such cases the detailed meanings thereof will be described in relevant parts of the description herein. Thus, the terms used in this specification may be interpreted based on the substantial meanings of the terms and the whole content of this specification rather than their simple names or meanings.
Not only technical or scientific terms but also all terms used herein shall have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs, unless otherwise defined. Terms that are generally understood may be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and may not be interpreted in an idealized or overly formal sense unless expressly so defined herein.
Numerical ranges include the numbers defined in the disclosure. All maximum numerical limitations defined in this specification include all lower numerical limitations, as if such limitations were expressly written. All minimum numerical limitations defined in this specification include all higher numerical limitations as if such higher numerical limitations were expressly written. All numerical limitations defined in this specification include all preferred numerical ranges within their broader numerical ranges as if such narrower numerical limitations were expressly written.
As used in the specification, the terms “comprising,” “having,” and “containing” are inclusive or open-ended and do not exclude features or method steps that are not further mentioned. The term “or a combination thereof” as used herein refers to all permutations and combinations of the plurality of items listed prior to the term. For example, “A, B, C, or combinations thereof” is intended to include at least one of: A, B, C, AB, AC, BC, or ABC and, if order is important in a particular context, also BA, CA, CB, CBA, BCA, ACE, BAC, or CAB. Continuing with this example, expressly included are combinations that contain repeats of one or more item or term, such as BB, AAA, MB, BBC, AAABCCCC, CBBAAA, CABABB, and so forth.
The skilled artisan will understand that typically there is no limit on the number of items or terms in any combination, unless otherwise apparent from the context.
Hereinafter, exemplary embodiments of the disclosure are described in detail.
In one aspect, the disclosure provides a composition for reducing absorption of microplastics into the body, comprising a green tea extract as an active ingredient.
In the specification, “green tea” refers to tea (Camellia sinensis), which is an evergreen shrub belonging to the tea family, and can be used without limitation on its type and cultivation days, and the tea may include one or more selected from the group consisting of leaves, flowers, stems, fruits, and roots of tea tree. In addition, in the specification, green tea may be used without limitation in its parts (leaves, flowers, stems, fruits, roots, etc.), and for example, tea leaves may be used.
In the specification, “green tea extract” includes an extract extracted from Camellia sinensis, which belongs to the tea family, regardless of the extraction method, extraction solvent, extracted ingredient, or form of extract, an extract extracted from tea leaves inoculated with Bacillus subtilis spp. and fermented, an extract extracted from naturally fermented tea leaves, or the like, and includes a fraction obtained by fractionating the extracted extract with a specific solvent. The tea may include one or more selected from the group consisting of leaves, flowers, stems, fruits, and roots, and may preferably be leaves. Further, the form of extract may be preferably in a powder form. The extraction or fractionation may be performed using water, an organic solvent, or a mixed solvent thereof. The organic solvent may be an alcohol, isopropanol, acetone, hexane, ethyl acetate, carbon dioxide, or a mixed solvent of two or more thereof, but is not limited thereto, and an active ingredient of green tea may′ be extracted or fractionated at room temperature or by heating under the condition that the active ingredient is not destroyed or is minimized. The alcohol may be a C1 to C6 alcohol. The number or method of extraction or fractionation is not particularly limited, and for example, it is possible to use a method such as cold precipitation extraction, Ultrasonic extraction, reflux cooling extraction, and hot-water extraction, and preferably, the active ingredient may be extracted or fractionated by cold precipitation or heating and filtered, and then the filtrate may be concentrated under reduced pressure to obtain the green tea extract.
In the specification, the “active ingredient” refers to an ingredient that alone exhibits the desired activity or that can exhibit the activity in combination with a carrier having no activity by itself.
In the specification, the “microplastics” refer to synthetic high-molecular compounds with a diameter of 5 mm or less that are intentionally manufactured or micronized by fragmenting existing plastic products.
In one embodiment, the green tea extract may be an extract of water, an organic solvent, or a mixed solvent thereof. The water may include distilled water or purified water, and the organic solvent may include one or more selected from the group consisting of alcohol, isopropanol, acetone hexane, ethyl acetate, and carbon dioxide, but is not limited thereto. The alcohol may be a C1-C6 alcohol.
In one embodiment, the green tea extract may include 30 to 45% by weight of catechin based on the total weight of the green tea extract. For example, the green tea extract may include 30% by weight or more, 30.5% by weight or more, 31% by weight or more, 31.5% by weight or more, 32% by weight or more, 32.5% by weight or more, 33% by weight or more, 33.5% by weight or more, 34% by weight or more, 34.5% by weight or more, 35% by weight or more, 45% by weight or less, 44.5% by weight or less, 44% by weight or less, 43.5% by weight or less, 43% by weight or less, 42.5% by weight or less, 42% by weight or less, 41.5% by weight or less, 41% by weight or less, 40.5% by weight or less, or 40% by weight or less of catechin based on the total weight of the green tea extract, but is not limited thereto.
In one embodiment, the composition may include 0.1 to 70% by weight of green tea extract based on the total weight of the composition. If the content is less than 0.1% by weight, the effect of reducing the absorption of microplastics may be insignificant, and if the content is greater than 70% by weight, the efficacy of reducing the absorption of microplastics may be reduced. For example, the composition may include 0.1% by weight or more, 0.2% by weight or more, 0.3% by weight or more, 0.4% by weight or more, 0.5% by weight or more, 0.6% by weight or more, 0.7% by weight or more, 0.8% by weight or more, 0.9% by weight or more, 1% by weight or more, 2% by weight or more, 3% by weight or more, 4% by weight or more, 5% by weight or more, 6% by weight or more, 7% by weight or more, 8% by weight or more, 9% by weight or more, 10% by weight or more, 11% by weight or more, 12% by weight or more, 13% by weight or more, 14% by weight or more, 15% by weight or more, 16% by weight or more, 17% by weight or more, 18% by weight or more, 19% by weight or more, 20% by weight or more, 21% by weight or more, 22% by weight or more, 23% by weight or more, 24% by weight or more, 25% by weight or more, 26% by weight or more, 27% by weight or more, 28% by weight or more, 29% by weight or more, 30% by weight or more, 70% by weight or less, 69.9% by weight or less, 69.8% by weight or less, 69.7% by weight or less, 69.5% by weight or less, 69% by weight or less, 68.5% by weight or less, 68% by weight or less, 67.5% by weight or less, 67% by weight or less, 66.5% by weight or less, 66% by weight or less, 65.5% by weight or less, 65% by weight or less, 64.5% by weight or less, 64% by weight or less, 63.5% by weight or less, 63% by weight or less, 62.5% by weight or less, 62% by weight or less, 61.5% by weight or less, 61% by weight or less, 60.5% by weight or less, 60% by weight or less, 59% by weight or less, 58% by weight or less, 57% by weight or less, 56% by weight or less, 55% by weight or less, 54% by weight or less, 53% by weight or less, 52% by weight or less, 51% by weight or less, 50% by weight or less, 49% by weight or less, 48% by weight or less, 47% by weight or less, 46% by weight or less, 45% by weight or less, 44% by weight or less, 43% by weight or less, 42% by weight or less, 41% by weight or less, 40% by weight or less, 39% by weight or less, 38% by weight or less, 37% by weight or less, 36% by weight or less, 35% by weight or less, 34% by weight or less, 33% by weight or less, 32% by weight or less, 31% by weight or less, 30% by weight or less, 29% by weight or less, 28% by weight or less, 27% by weight or less, 26% by weight or less, 25% by weight or less, 24% by weight or less, 23% by weight or less, 22% by weight or less, 21% by weight or less, 20% by weight or less, 19% by weight or less, 18% by weight or less, 17% by weight or less, 16% by weight or less, 15% by weight or less, 14% by weight or less, 13% by weight or less, 12% by weight or less, 11% by weight or less, or 10% by weight or less of the green tea extract, based on the total weight of the composition, but is not limited thereto.
In one embodiment, the green tea extract may be administered at a dosage of 1 to 200 mg/kg/day. If the dosage of the green tea extract is less than 1 mg/kg/day, the effect of reducing the absorption of microplastics may be insignificant, and if the dosage exceeds 200 mg/kg/day, the efficiency of reducing the absorption of microplastics may be reduced. Particularly, the dosage of the green tea extract may be 1 mg/kg/day or more, 1.1 mg/kg/day or more, 1.2 mg/kg/day or more, 1.3 mg/kg/day or more, 1.4 mg/kg/day or more, 1.5 mg/kg/day or more, 1.6 mg/kg/day or more, 1.7 mg/kg/day or more, 1.8 mg/kg/day or more, 1.9 mg/kg/day or more, 2 mg/kg/day or more, 2.5 mg/kg/day or more, 3 mg/kg/day or more, 4 mg/kg/day or more, 5 mg/kg/day or more, 6 mg/kg/day or more, 7 mg/kg/day or more, 8 mg/kg/day or more, 9 mg/kg/day or more, 10 mg/kg/day or more, 11 mg/kg/day or more, 12 mg/kg/day or more, 13 mg/kg/day or more, 14 mg/kg/day or more, 15 mg/kg/day or more, 16 mg/kg/day or more, 17 mg/kg/day or more, 18 mg/kg/day or more, 19 mg/kg/day or more, 20 mg/kg/day or more, 21 mg/kg/day or more, 22 mg/kg/day or more, 23 mg/kg/day or more, 24 mg/kg/day or more, 25 mg/kg/day or more, 26 mg/kg/day or more, 27 mg/kg/day or more, 28 mg/kg/day or more, 29 mg/kg/day or more, 30 mg/kg/day or more, 31 mg/kg/day or more, 32 mg/kg/day or more, 33 mg/kg/day or more, 34 mg/kg/day or more, 35 mg/kg/day or more, 36 mg/kg/day or more, 37 mg/kg/day or more, 38 mg/kg/day or more, 39 mg/kg/day or more, 40 mg/kg/day or more, 41 mg/kg/day or more, 42 mg/kg/day or more, 43 mg/kg/day or more, 44 mg/kg/day or more, 45 mg/kg/day or more, 46 mg/kg/day or more, 47 mg/kg/day or more, 48 mg/kg/day or more, 49 mg/kg/day or more, 50 mg/kg/day or more, 200 mg/kg/day or less, 199 mg/kg/day or less, 198 mg/kg/day or less, 197 mg/kg/day or less, 196 mg/kg/day or less, 195 mg/kg/day or less, 194 mg/kg/day or less, 193 mg/kg/day or less, 192 mg/kg/day or less, 191 mg/kg/day or less, 190 mg/kg/day or less, 189 mg/kg/day or less, 188 mg/kg/day or less, 187 mg/kg/day or less, 186 mg/kg/day or less, 185 mg/kg/day or less, 184 mg/kg/day or less, 183 mg/kg/day or less, 182 mg/kg/day or less, 181 mg/kg/day or less, 180 mg/kg/day or less, 179 mg/kg/day or less, 178 mg/kg/day or less, 177 mg/kg/day or less, 176 mg/kg/day or less, 175 mg/kg/day or less, 174 mg/kg/day or less, 173 mg/kg/day or less, 172 mg/kg/day or less, 171 mg/kg/day or less, 170 mg/kg/day or less, 169 mg/kg/day or less, 168 mg/kg/day or less, 167 mg/kg/day or less, 166 mg/kg/day or less, 165 mg/kg/day or less, 164 mg/kg/day or less, 163 mg/kg/day or less, 162 mg/kg/day or less, 161 mg/kg/day or less, 160 mg/kg/day or less, 159 mg/kg/day or less, 158 mg/kg/day or less, 157 mg/kg/day or less, 156 mg/kg/day or less, 155 mg/kg/day or less, 154 mg/kg/day or less, 153 mg/kg/day or less, 152 mg/kg/day or less, 151 mg/kg/day or less, or 150 mg/kg/day or less, but is not limited thereto.
In one embodiment, the microplastic may be, for example, a plastic such as polystyrene, polypropylene, polyethylene, poly amide(PA), acrylonitrile-butadiene-styrene(ABS), polytetrafluoroethylene(PTFE), cellulose acetate(CA), polycarbonate(PC), polymethyl methacrylate(PMMA), polyvinyl chloride(PVC), polyethylene terephthalate(PET), acrylic, melamine resin, polyurethane(PU), but is not limited thereto.
In one embodiment, the composition may aggregate microplastics. As the size of a material increases, penetration of microplastics through cells or periplasmic space becomes difficult. The composition may reduce the absorption of microplastics into the body by aggregating the ingested microplastics, making it difficult for the microplastics to pass through cells or periplasmic space, and excreting them out of the body through excretion.
In one exemplary embodiment, the composition may inhibit inflammation caused by absorption of the microplastics.
In one exemplary embodiment, the composition may inhibit oxidative stress in a cell caused by the microplastics.
In one exemplary embodiment, the composition may prevent, alleviate or treat lipid metabolism disorder in a cell caused by the microplastics.
In one exemplary embodiment, the composition may be administered orally, but is not limited thereto.
In one embodiment, the composition may be a food composition. The formulation of the food composition is not particular limited, but may be made in, for example, tablets, granules, pills, powders, solutions such as drinks, caramels, gels, bars, tea bags, or the like. In the food composition of the respective formulations, in addition to the active ingredient, ingredients typically used in the pertinent field can be suitably selected and blended by a person skilled in the art without any difficulty, depending on the formulation or purpose of use, and when this composition is applied together with other raw material, a synergistic; effect would be generated.
The food composition according to one embodiment may include several nutritional supplements, vitamins, minerals (electrolyte), flavoring agents such as synthetic flavoring agents and natural flavoring agents, colorants and enhancers (cheese, chocolate, etc.), pectic acids and salts thereof, alginic acids and salts thereof, organic acids, protective colloid thickeners, pH regulators, stabilizers, preservatives, glycerin, alcohol, carbonation used for carbonated beverages, and the like in addition, the food compositions according to one embodiment may include natural fruit juices and fruit pulps for the preparation of fruit juice drink and vegetable drink. Such ingredients may be used independently or in combination. The ratio of such additives is not important, but the additives are generally comprised in an amount ranging from 0 to about 50 parts by weight per the 100 parts by weight of the composition according to one embodiment.
In one embodiment, the composition may be a pharmaceutical composition. The pharmaceutical composition may be administered orally, parenterally, rectally, topically, transdermally, intravenously, intramuscularly, intraperitoneally, subcutaneously, or the like. The formulation for the oral administration may be tablets, pills, soft and hard capsules, granules, powders, fine granules, solutions, emulsifying agents or pellets, but is not limited thereto. The formulation for the parenteral administration may be solutions, suspensions, liquids, gels, injections, drops, suppository, patches or sprays, but is not limited thereto. The formulations can be easily prepared according to a commonly employed method in the pertinent field, and may further comprise surfactants, excipients, hydrating agent, emulsifiers, suspensions, salts and/or buffers for osmotic pressure control, colorants, spices, stabilizers, antimicrobial agents, preservatives, or other commercial auxiliaries.
In one aspect, the disclosure provides a use of a green tea extract for preparing a composition for reducing the absorption of microplastics in the body.
In one aspect, the disclosure provides a method for reducing the absorption of microplastics into the body, comprising administering to a subject in need thereof a composition comprising an effective amount of a green tea extract.
In one aspect, the disclosure provides a use of a green tea extract for reducing the absorption of microplastics in the body.
Hereinafter, the disclosure will be explained in more detail with reference to examples. These examples are only for illustrating the disclosure, and it will be apparent to those skilled in the art that the scope of the disclosure is not to be construed as being limited by these examples.
After drying green tea leaves (Camellia sinensis, Jeju O'Sulloc Farm), 50% (v/v) alcohol in an amount equivalent to 20 times the weight of the dried green tea leaves was added to the dried green tea leaves, extracted at 60° C. for 2 hours, and freeze-dried to prepare a green tea extract. The content of catechin in the green tea extract thus prepared was measured using high performance liquid chromatography(HPLC), and the results were shown in Table 1 below.
After drying green tea leaves (Camellia sinensis, Jeju O'Sulloc Farm), distilled water in an amount equivalent to 20 times the weight of the dried green tea leaves was added to the dried green tea leaves, extracted at 60° C. for 2 hours, and freeze-dried to prepare a green tea extract.
A coffee extract was prepared by adding 50% (v/v) alcohol in an amount of equivalent to times the weight of the beans to dry coffee beans, extracting the mixture at 60° C. for 2 hours, and freeze-drying the extracted mixture.
The microplastics are known to induce oxidative stress in cells. Since oxidative stress is closely related to a chronic inflammatory response, microplastics(MP) were treated in RAW 264.7 (ATCC) macrophage cell line to determine whether the microplastics can induce the chronic inflammatory responses in cells. The treated microplastics were polystyrene-based microparticles (Sigma Aldrich) with diameters of 10 μm, 1 μm, and 0.1 respectively, the macrophage cell line was treated with each microplastic at concentrations of 100 μg/ml and 500 μg/ml for 6 to 72 hours. As a positive control for the inducement of the inflammatory response, 10 ng/ml of lipopolysaccharide (LPS; Sigma Aldrich), which was a component of the cell wall of Gram-negative bacteria and induced an acute inflammatory response, was used. At each time point (6 hours, 24 hours, 48 hours, 72 hours after the treatment of microplastic), RNAs were extracted from the cells using the MiniBEST Universal RNA Extraction kit (Takara Bio Inc.), and cDNAs were synthesized using a RevertAid 1st strand cDNA Synthesis kit (Thermo Fisher Scientific). The expression of genes related to the inflammatory response was determined with qPCR primers custom-made by Bioneer using a CFX96 thermocycler (Bio-Rad) and the results were shown in
As shown in the results in
Oxidative stress induces an inflammatory response and at the same time damages each tissue within the cell, causing cell metabolism disorder. Hepatocytes (HepG2; ATCC) were treated with the microplastics(MP) to examine whether the inflammatory response and oxidative stress caused by the microplastics change energy metabolism in cells. The treated microplastics were polystyrene-based microparticles (Sigma Aldrich) with diameters of 10 μm, 1 μm, and 0.1 μm, and the hepatocytes were treated with each microplastic at concentrations of 100 μg/ml and 500 μg/ml for 24 hours. As a positive control, oleic acid(OA) was used. Then, the expression of genes related to the inflammatory response and the degree of oxidative stress were measured in the same manner as in Experimental Example 1, and were shown in
As shown in
Accordingly, the expression of genes related to lipid metabolism was additionally measured in the microplastic-treated hepatocytes, and the results were shown in
As shown in
In order to determine whether the green tea extract induces the aggregation of the microplastics, the green tea extract of Example 1 was mixed with the microplastics(MP) at different concentrations (10 ug/ml, 50 ug/ml, 100 ug/ml) in PBS. The microplastics used were polystyrene-based microparticles with a diameter of 10 μm (Sigma Aldrich), and the concentrations of the microplastics were 100 ppm and 500 ppm. After mixing the green tea extract and the microplastics, the mixture was placed in a shaker for 2 hours to induce aggregation and observed under an EVOS M5000 microscope (Thermo Fisher Scientific), and the result was shown in
As shown in
Each of Examples 1 and 2 and Comparative Example 1 was mixed with the microplastics by concentration (10 ug/ml, 50 ug/ml), and the degree of aggregation was observed and shown in
As shown in
In order to examine whether the microplastic aggregation by the green tea extract affected the absorption of the microplastics in the body, a permeation experiment was conducted using CaCo2 (ATCC) enterocytes, which were mainly used for unidirectional material transport experiments. Specifically, CaCo2 cells were laid inside a transwell (Corning) and the medium was treated with the microplastics (diameter: 10 μm Sigma Aldrich) and the green tea extract of Example 1 by concentration (10, 50, 100 ug/ml). Afterwards, the amount of microplastic that mitigated down the transwell through CaCo2 was observed and shown in
As shown in
In Experimental Example 1, it was confirmed that the microplastics continuously induced inflammatory reactions in cells and increased oxidative stress. In order to determine whether the green tea extract could alleviate abnormalities in cells caused by the microplastics, macrophages were pretreated with the green tea extract of Example 1, and then the microplastics were treated in the same manner as in Experimental Example 1 to measure the degree of the expressions of genes related to the inflammatory response and the degree of oxidative stress, and the results were shown in
As shown in
In addition, after the pretreatment of the green tea extract of Example 1 to hepatocytes, the microplastics were treated in the same manner as in Experimental Example 2 to measure the expression of genes related to the inflammatory response in hepatocytes (
As shown in
Tables were prepared by mixing 100 mg of the green tea extract (Example 1) according to examples of the disclosure, 400 mg of lactose, 400 mg of corn starch, and 2 mg of magnesium stearate, and then tableting the mixture according to a commonly employed method for preparing tablets. The specific composition was shown in Table 2 below.
Capsules were prepared by mixing 150 mg of the green tea extract (Example 1) according to examples of the disclosure, 220 mg of soybean oil, 2 mg of palm oil, 8 mg of hydrogenated vegetable oil, 4 mg of yellow wax, and 6 mg of lecithin and filling the mixture in one capsule according to a commonly employed method for preparing capsules. The specific composition was shown in Table 3 below.
Granules were prepared by mixing 80 mg of the green tea extract (Example 1) according to examples of the disclosure, 250 mg of anhydrous crystalline glucose and 550 mg of starch, forming the mixture into granules using a fluidized bed granulator, and then filling them into a pouch.
A powder was prepared by mixing 200 mg of the green tea extract (Example 1) according to an embodiment of the disclosure, 500 mg of lactose, and 500 mg of cornstarch and filling the mixture in an airtight pouch.
According to the composition shown in Table 4 below, health functional foods were prepared in a commonly employed manner.
A drink was prepared by mixing 100 mg of the green tea extract (Example 1) according to an embodiment of the disclosure, 1000 mg of citric acid, 15 g of oligosaccharide, and 1 g of taurine, adding 190 ml of purified water and filling 200 ml in each bottle. After filling the mixture in the bottle, the bottle was sterilized for 4 to 5 seconds at 130° C. to prepare ale drink.
The disclosure is further illustrated by the following embodiments, which do not limit the scope of the claims.
Embodiment 1. A method for reducing absorption of a microplastic in a body, comprising administering a composition comprising an effective amount of a green tea extract to a subject in need thereof.
Embodiment 2. The method of Embodiment 1, wherein the green tea extract is an extract of water, an organic solvent, or a mixed solvent thereof.
Embodiment 3. The method of Embodiment 1 or 2, wherein the green tea extract comprises 30 to 45% by weight of catechin based on a total weight of the green tea extract.
Embodiment 4. The method of any one of Embodiments 1 to 3 wherein the green tea extract is administered at a dosage of 1 to 200 mg/kg/day.
Embodiment 5. The method of any one of Embodiments 1 to 4, wherein the subject is in need of aggregating the microplastics.
Embodiment 6. The method of any one of Embodiments 1 to 5, wherein the subject is in need of inhibiting inflammation caused by absorption of the microplastics.
Embodiment 7. The method of any one of Embodiment 1 to 6, wherein the subject is in need of inhibiting oxidative stress in a cell caused by the microplastics.
Embodiment 8. The method of any one of Embodiments 1 to 7, wherein the subject is in need of preventing, alleviating or treating lipid metabolism disorder in a cell caused by the microplastics.
Embodiment 9. The method of any one of Embodiments 1 to 8, wherein the composition is administered orally.
Embodiment 10. The method of any one of Embodiments 1 to 9, wherein the composition is a food composition.
Embodiment 11. The method of any one of Embodiments 1 to 9, wherein the composition is a pharmaceutical composition.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2022-0066326 | May 2022 | KR | national |
