Effective use of tea flowers

Abstract

To provide a novel form of utilization of tea flowers, which has a high utilization efficiency of saponin compounds contained in the tea flowers and has a reduced caffeine content. [Solution] Powder of tea flowers. The average particle size can be 1 to 200 μm, the maximum particle size can be 2 to 1000 μm, and the powder can be passed through a sieve with a mesh size of any one of No. 18 to No. 200.

Description

[Technical field]

[0001] The present invention relates to a form for effectively utilizing tea flowers, which are useful as medicines and foods. [Background technology]

[0002] Tea (Camellia sinensis) of the Theaceae family, Camellia genus, is originally a tropical or subtropical perennial plant, but is an evergreen tree that grows wild or is cultivated widely in Asia, including India, Sri Lanka, Indonesia, China, and Japan. In particular, it is cultivated in large quantities in Fujian Province, China, as a raw material for green tea and other products.

[0003] Traditionally, tea leaves have been processed into green tea, oolong tea, black tea, etc. by unfermenting, semi-fermenting, or fermenting, and these are then extracted with hot water and widely enjoyed as a beverage. Extracts from tea leaves (hereafter sometimes simply referred to as "tea") have a variety of pharmacological activities, and have long been known to have awakening, diuretic, antipyretic, sedative, digestive, and energy-boosting effects. In China, the oldest herbal book (specialized pharmaceutical book), the Shennong Bencaojing (late Han period), lists tea leaves as a superior medicine under the name "Kina" (bitter cai), and many other herbal books, such as the Chajing (around 761, written by Lu Yu), also list various medicinal effects. In Japan, the medicinal effects are also recorded in the Kissa Yojoki (Record of Drinking Tea for Health) (established in 1211, written by Eisai) and Honcho Shokan (published in 1697, written by Hitomi Hisada). In recent years, it has been reported that polyphenols such as catechins contained in tea leaves have various functionalities, such as an active oxygen scavenging effect. In addition, the present inventors have reported that tea leaves contain small amounts of saponin compounds foliatheasaponins I to V, which have anti-inflammatory effects (degranulation inhibitory effects) (Non-Patent Documents 1, 2, Patent Document 1, etc.). In addition, the present inventors have isolated and determined the structures of 29 types of saponin components, theasaponins, contained in tea seeds, and have revealed sweetness suppression effects, gastroprotection effects, gastric emptying inhibitory effects, and small intestinal motility enhancement effects (Non-Patent Document 3, etc.).

[0004] In addition, hot water extracts of tea flowers (hereinafter sometimes referred to as "cha-bana") have been drunk since ancient times, and well-known varieties include Botebotecha and Hanabancha from Shimane Prefecture. The present inventors have reported that tea flower extracts contain floratheasaponins, saponin compounds with anti-allergic effects (Non-Patent Document 4, etc.). The present inventors have also reported that tea flower extracts contain chakasaponins as well as floratheasaponins, saponin compounds with neutral fat absorption inhibitory effects, sugar absorption inhibitory effects, gastric mucosa protective effects, anti-allergic effects, gastric emptying function inhibitory effects, intestinal motility enhancement effects, pancreatic lipase activity inhibitory effects, and gastric cancer cell proliferation inhibitory effects (Non-Patent Documents 5-10, etc., Patent Documents 2-6).

[0005] Tea flowers contain saponin compounds that are useful for treating diabetes, hyperlipidemia, obesity, inflammation, allergies, etc., and are therefore extremely useful as a health food ingredient. Conventionally, tea flower extracts have been used industrially as a health food ingredient. As a method for obtaining tea flower extract, Patent Documents 2 to 6 report a method of extraction using a solvent such as aqueous ethanol, aqueous methanol, aqueous butanol, or aqueous ethyl acetate. However, the methods of Patent Documents 2 to 6 all require a multi-step process. In addition, the methods of Patent Documents 2 to 6 aim to isolate saponin compounds from the extract by combining various types of chromatography and determine their structures, so they use ethanol, methanol, butanol, or ethyl acetate as solvents. However, ethanol is expensive and therefore not suitable for industrial use as an extraction solvent, and methanol, butanol, and ethyl acetate are not suitable for food production. Therefore, in practice, hot water extracts obtained by heating and extracting tea flowers multiple times with water, combining and concentrating the extracts, and drying them are used as health food ingredients. However, the production of hot water extracts, like the use of other solvents, requires multiple steps of operation, which is a hassle. In addition, the yield of tea flower hot water extracts is only about 20% by mass of the raw tea flowers.

[0006] On the other hand, tea, which contains tea flowers, contains a relatively large amount of caffeine. Caffeine, when taken in excess, can cause dizziness, increased heart rate, and stimulant effects, and even small amounts can cause insomnia. Today, from the perspective of ensuring the quality of sleep, there are quite a few people who prefer decaffeinated beverages, including decaffeinated beverages. Decaffeinated beverages are also recommended for infants and children to avoid these effects. Since supplements are taken daily for health purposes, it is desirable to keep the caffeine content as low as possible. [Prior art documents] [Patent documents]

[0007] [Patent Document 1] Patent No. 3441488 [Patent Document 2] Patent No. 4771713 [Patent Document 3] Patent No. 514949 [Patent Document 4] Patent No. 5341382 [Patent Document 5] Patent No. 5275678 [Patent Document 6] Patent No. 5620660 [Non-patent literature]

[0008] [Non-Patent Document 1] Yuko Teisaka et al., Pharmaceutical Journal, 116, 238-243 (1996) [Non-Patent Document 2] Toshio Morikawa et al., Chem. Pharm. Bull., 55(2), 293-298(2007) [Non-Patent Document 3] Masayuki Yoshikawa et al., Chem. Pharm. Bull., 55(1), 57-63(2007) [Non-Patent Document 4] Masayuki Yoshikawa et al., Chem. Pharm. Bull., 55(4) 598-605(2007) [Non-Patent Document 5] Masayuki Yoshikawa et al., J. Nat. Prod., 68(9), 1360-1365(2005) [Non-Patent Document 6] Toshio Morikawa et al., J. Nat. Med., 66, 608-613 (2012) [Non-Patent Document 7] Toshio Morikawa et al., Natural Product Communications, 8(11), 1553-1557(2013) [Non-Patent Document 8] Masayuki Yoshikawa et al., Chemistry & Biodiversty, 6, 903-915(2009) [Non-Patent Document 9] Makoto Hamao et al., Bioorg. Med. Chem., 19, 6033-6041 (2011) [Non-Patent Document 10] Masayuki Yoshikawa et al., YAKUGAKU ZASSHI, 128(1), 141-151(2008) Summary of the Invention [Problem to be solved by the invention]

[0009] An object of the present invention is to provide a novel form of utilization of tea flowers which provides good utilization efficiency of the tea flowers themselves and the saponin compounds contained therein, and has a reduced caffeine content. [Means for solving the problem]

[0010] The present inventors have conducted extensive research to solve the above problems and have obtained the following findings. (1) When comparing the amounts of compounds contained in the same amount of tea flower powder and tea flower hot water extract, tea flower powder contains the same amount of saponin compounds as the tea flower hot water extract. On the other hand, the caffeine content of tea flower powder is less than that of the hot water extract, about one-quarter. (2) When orally administered to olive oil-loaded mice, tea flower powder had a stronger and longer-lasting inhibitory effect on the increase in blood triglycerides than a hot water extract. (3) When orally administered to mice, tea flower powder was more effective at inhibiting the movement of stomach contents to the intestines (inhibitory effect on gastric emptying) than a hot water extract.

[0011] The present invention has been completed based on the above findings, and provides the following [1] to

[11] . [1] Tea flower powder. [2] The powder according to [1], having an average particle size of 1 to 200 μm. [3] The powder according to [1] or [2], having a maximum particle size of 2 to 1000 μm. [4] The powder according to any one of [1] to [3], which has passed through a sieve having a mesh size of any one of No. 18 to No. 200. [5] The powder according to any one of [1] to [4], having a total saponin content of 1 to 20 mass% based on the total amount of tea flower powder. [6] The powder according to any one of [1] to [5], wherein the total content of chakasaponin I, chakasaponin II, and chakasaponin III is 1 to 20 mass% based on the total amount of tea flower powder. [7] The powder according to any one of [1] to [6], wherein the caffeine content is 2 mass% or less based on the total amount of the tea flower powder. [8] The powder according to any one of [1] to [7], which is used for suppressing neutral fat levels, suppressing gastric emptying function, suppressing sugar absorption, suppressing an increase in blood glucose level, protecting the gastric mucosa, suppressing or alleviating allergies, promoting intestinal motility, inhibiting pancreatic lipase activity, suppressing obesity or metabolic syndrome, or for dieting. [9] A method for producing tea flower powder, comprising the steps of pulverizing tea flowers or a dried product thereof and adjusting the particle size of the pulverized product.

[10] A food composition containing tea flower powder.

[11] The food composition according to

[10] , comprising 1 to 99 mass% of tea flower powder based on the total amount of the composition. Effect of the Invention

[0012] Tea flower powder contains the same amount of saponin compounds, which have favorable medicinal properties as a diet ingredient, as the same amount of tea flower hot water extract. Tea flower hot water extract can only be obtained at about 20% from tea flowers, while tea flower powder can be obtained at a yield of over 80% from tea flowers. For this reason, the utilization efficiency of saponin is about four times better when using tea flower powder as it is.

[0013] When comparing the diet effects of tea flower powder and tea flower hot water extract, tea flower powder is superior. More specifically, when the same amount of tea flower powder and tea flower hot water extract are ingested, tea flower powder suppresses the rise in blood triglyceride levels more effectively and for a longer period of time than tea flower hot water extract. In addition, tea flower powder is stronger than tea flower hot water extract in suppressing the movement of stomach contents to the intestinal tract (inhibiting gastric emptying function). Considering that the various medicinal effects of tea flower ingredients are due to the same group of saponin compounds, it is predicted that tea flower powder will have stronger and longer-lasting effects than tea flower extract, not only in terms of the triglyceride level suppression effect and gastric emptying function suppression effect, but also in terms of other effects of tea flowers (sugar absorption suppression effect, gastric mucosa protection effect, anti-allergic effect, intestinal motility enhancement effect, pancreatic lipase activity inhibition effect, etc.). Thus, the extraction effect of saponin compounds using hot water is low, while the saponin compounds contained in the powder are effectively utilized by digestive enzymes, so using the powdered tea flowers as is is more efficient. On the other hand, the content of caffeine, which has a strong stimulating effect, is about one-quarter of that of the same amount of hot water extract of tea flowers, which significantly reduces the stimulating effect of caffeine.

[0014] As described above, the hot water extraction method that has been widely used for tea flowers has a low extraction efficiency for the active ingredient saponin compound and no concentration effect was observed, but caffeine was concentrated and the content was high. It is not practical to consume tea flowers in their raw form, as with tea leaves, and even if consumed, it is difficult to obtain medicinal effects such as neutral fat level suppression and gastric emptying function suppression. In other words, tea flowers in their raw form are hardly usable as functional foods, so tea flower hot water extracts have traditionally been used as materials for functional foods. However, tea flower powder can be obtained from tea flowers in a yield four times higher than that of hot water extracts, contains the same amount of saponin compounds as hot water extracts, and has the same or greater effects, such as long-lasting effects. Nevertheless, tea flower powder is highly valuable as a material for functional foods, etc., in that it contains less caffeine than tea flower hot water extracts.

[0015] Furthermore, when the same amount of tea flower powder and tea flower hot water extract are ingested, tea flower powder suppresses the rise in blood triglyceride levels more effectively and for a longer period of time than tea flower hot water extract. Tea flower powder also has a stronger inhibitory effect on the movement of stomach contents to the intestinal tract (inhibitory effect on gastric emptying function) than tea flower hot water extract. Considering that the various medicinal effects of tea flower ingredients are due to the same group of saponin compounds, it is thought that tea flower powder is stronger and longer-lasting than tea flower extract, not only in terms of its inhibitory effect on triglyceride levels and inhibitory effect on gastric emptying function, but also in terms of other effects of tea flowers (sugar absorption inhibitory effect, gastric mucosa protective effect, anti-allergic effect, intestinal motility enhancement effect, pancreatic lipase activity inhibitory effect, etc.).

[0016] Tea flower powder does not require an extraction operation and can be easily produced by simply grinding tea flowers, but is a useful form that allows the effective ingredients of tea flowers to be efficiently utilized while reducing the caffeine content, and is extremely valuable industrially as a diet material, etc. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0017] The tea flower powder (particularly the fine powder) of the present invention will now be described in detail. The tea flowers used in the present invention refer to the flower parts of tea (Camellia sinensis) belonging to the genus Camellia of the family Theaceae, i.e., so-called flowers, flower buds, buds, etc., including pistils, stamens, petals, calyx, bracts, rachis, pedicels, etc. Parts of flower parts such as petals also fall under the category of tea flowers in the present invention. Tea is broadly divided into Chinese species (Camellia sinensis L. var. sinensis) and Assam species (Camellia sinensis L. var. assamica), and in the present invention, tea includes both of these.

[0018] The average particle size of the tea flower powder can be 1 μm or more, 5 μm or more, 10 μm or more, or 15 μm or more. Within this range, the waste of tea flowers due to the discharge of cotton-like material during the grinding operation can be suppressed. Furthermore, the average particle size of the tea flower powder can be 200 μm or less, 100 μm or less, 70 μm or less, 50 μm or less, 40 μm or less, 30 μm or less, or 25 μm or less. Within this range, the effect of the present invention can be obtained. In other words, within the above range, the material will have a strong and sustained medicinal effect when taken orally. In the present invention, the average particle size is a value measured by a laser diffraction / scattering method using a particle size distribution measuring device.

[0019] Maximum particle size of tea flower powder (D 100 ) can be 2 μm or more, 5 μm or more, 10 μm or more, 50 μm or more, 70 μm or more, or 100 μm or more. Within this range, the waste of tea flowers due to the discharge of cotton-like material during the grinding operation can be suppressed. In addition, the maximum particle size of the tea flower powder can be 1000 μm or less, 700 μm or less, 500 μm or less, 400 μm or less, 300 μm or less, 200 μm or less, 170 μm or less, or 150 μm or less. Within this range, the effect of the present invention can be obtained. In other words, within the above range, the material will have a strong and sustained medicinal effect when taken orally. In the present invention, the maximum particle size is a value measured by a laser diffraction / scattering method using a particle size distribution measuring device.

[0020] The tea flower powder can be one that has passed through a sieve with a mesh size of any one of 18 to 200. In particular, it can be a coarse powder that has passed through a sieve with a mesh size of 18 (850 μm), a medium powder that has passed through a sieve with a mesh size of 50 (300 μm), a fine powder that has passed through a sieve with a mesh size of 100 (150 μm), or a fine powder that has passed through a sieve with a mesh size of 200 (75 μm). Of these, fine powder that has passed through a sieve with a mesh size of 200 is preferred. Any powder that has passed through a sieve with the above mesh size may be used, but if necessary, a powder that has passed through the sieve with the above mesh size and not through a sieve with a mesh size of 635 (20 μm), or a powder that has passed through the sieve with the above mesh size and not through a sieve with a mesh size of 75 μm, may be used. 100 It is sufficient to make the powder so that the particle size is 2 μm or more. The effects of the present invention can be obtained within the above ranges. That is, within the above ranges, the material provides strong and sustained medicinal effects when orally ingested.

[0021] Tea flowers can be used as they are or dried. The pulverization can be carried out using a medium crusher (roll crusher, cutter mill, autogenous crusher, stamp mill, stone mill, crusher, ring mill, etc.) capable of pulverizing to a size of several mm to several hundred μm, a fine crusher (roller mill, jet mill, impact mill (hammer mill, pin mill, etc.), rotary mill, vibration mill, planetary mill, etc.) capable of pulverizing to a size of several μm, or an ultrafine crusher (attritor, bead mill, etc.) capable of pulverizing to a size of several μm or less. The crusher and the pulverization method can be selected according to the size of the fine powder. If necessary, the powder may be dried after grinding.

[0022] The caffeine content of the tea flower powder may be 2% by mass or less, 1.5% by mass or less, 1% by mass or less, 0.8% by mass or less, 0.7% by mass or less, or 0.6% by mass or less, and may be 0.05% by mass or more, 0.1% by mass or more, 0.2% by mass or more, 0.3% by mass or more, or 0.4% by mass or more, based on the total amount of the tea flower powder.

[0023] The total saponin content of the tea flower powder may be 1% by mass or more, 3% by mass or more, 5% by mass or more, or 6% by mass or more, and may be 20% by mass or less, 15% by mass or less, or 10% by mass or less, based on the total amount of the tea flower powder. In addition, the total content of chakasaponins I, II, and III in the tea flower powder may be 1 mass% or more, 3 mass% or more, or 5 mass% or more, and may be 20 mass% or less, 15 mass% or less, or 10 mass% or less, relative to the total amount of the tea flower powder.

[0024] The moisture content of the tea flower powder can be 0.1 mass% or more, 1 mass% or more, or 3 mass% or more, and can be 20 mass% or less, 10 mass% or less, 7 mass% or less, or 6 mass% or less, relative to the total amount of the tea flower powder.

[0025] The tea flower powder can be used as it is. It can also be mixed with general foods such as confectionery, bread, noodles, cooked grains, seasonings, processed meat products, pastes, and beverages to make food compositions. It can also be formulated with additives to make supplement food compositions. Examples of additives include sweeteners, colorants, preservatives, thickening stabilizers, antioxidants, acidulants, emulsifiers, flavorings, excipients, binders, disintegrants, and lubricants. Examples of the dosage form of the preparation include powders, granules, capsules (hard capsules, soft capsules), tablets, and jellies. The tea flower powder of the present invention does not include those that are suspended in water or hot water and consumed. When blended or formulated into general foods, those that are suspended in water are also excluded. In addition, it is preferable that the tea flower powder is consumed in a dry state.

[0026] The content of tea flower powder in a food composition containing tea flower powder can be 1 mass% or more, 5 mass% or more, 10 mass% or more, 25 mass% or more, 50 mass% or more, 70 mass% or more, 80 mass% or more, or 90 mass% or more, and can be 99 mass% or less, 95 mass% or less, 90 mass% or less, 80 mass% or less, or 50 mass% or less, relative to the total amount of the food composition. Within this range, tea flower powder is contained in an amount that is easy to eat, enough to fully exert its pharmacological effects. Tea flower hot water extracts tend to clump if left to stand, so a relatively large amount of additives such as excipients must be added, but tea flower powder maintains a smooth state even when left to stand, so additives can be omitted, or relatively small amounts can be used. With the recent trend toward health consciousness, supplements containing many additives are not popular, so the fact that fewer additives are required is also a major advantage of tea flower powder.

[0027] The tea flower powder of the present invention can be used to suppress neutral fat levels, suppress gastric emptying, suppress sugar absorption, suppress blood sugar level rise, protect gastric mucosa, suppress or alleviate allergies, enhance intestinal motility, and inhibit pancreatic lipase activity.Furthermore, based on these effects, it can be used to suppress obesity and metabolic syndrome, i.e., for dieting. The daily intake of tea flower powder can be 1 mg or more, 10 mg or more, or 50 mg or more, and can be 1000 mg or less, 500 mg or less, or 300 mg or less. If it is within this range, the medicinal effect of tea flower powder is fully exerted. In the case of a food composition containing tea flower powder, the daily intake of tea flower powder can be taken so that it is within this range.

[0028] The tea flower powder of the present invention can be produced by a method including a step of pulverizing tea flowers or dried tea flowers and a step of adjusting the particle size. The particle size can be adjusted, for example, by using a sieve. The type of pulverizer and the properties of the obtained powder (particle size, component content, etc.) are as described for the tea flower powder of the present invention. EXAMPLES

[0029] The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these.

[0030] (1) Manufacturing of tea flower powder 20 kg of floral parts (the so-called flowers including the pistil, stamens, petals, calyx, bracts, rachis, pedicel, etc.; harvested in 2022) of tea (Camellia sinensis) from Fujian Province, China were sterilized with superheated steam for a few seconds using an air flow sterilizer (KPU, Okawara Seisakusho Co., Ltd.) and then dried. The sterilized and dried tea flowers were pulverized using an impact pulverizer (ACM Pulverizer (registered trademark), Hosokawa Micron Corporation) to obtain 16 kg of fine powder with an average particle size of 21.15 μm and a maximum particle size of 124.5 μm.

[0031] (2) Manufacturing of hot water extract of tea flowers 80 kg of the flower parts of tea (Camellia sinensis) from Fujian Province, China, used in "(1) Manufacturing of tea flower powder", was placed in a quadruple extraction apparatus and treated with 1950 L of hot water at 95°C for 60 minutes, after which the extract was collected by solid-liquid separation. The solid matter (extraction residue) was placed again in the quadruple extraction apparatus and treated with 1650 L of hot water at 95°C for 60 minutes, after which the liquid was collected by solid-liquid separation and combined with the first extract. The obtained extract was concentrated using a vacuum concentrator at 50°C or less, and the degree of vacuum was changed from 21.3 kPa to 2.7 kPa to obtain 800 L of a concentrated liquid with Brix 35. The concentrated liquid was stored in a refrigerator and cooled to 5°C or less, then processed in an ultra-high speed centrifuge to remove solid impurities, and the supernatant was sterilized at 125±5°C for 120 seconds using a concentrated liquid sterilizer. The liquid was further adjusted to Brix 30±2 with clean water, and 800 L of adjusted liquid was obtained. The adjusted liquid was dried using a spray dryer at an inlet temperature of 135°C, an outlet temperature of 85°C, and an atomizer rotation speed of 18,500 rpm to obtain 14 kg of tea flower hot water extract. The yield of the extract was 17.5%.

[0032] (3) Quantitative Analysis of Tea Flower Saponin Compounds The experiment was carried out according to Non-Patent Documents 6 and 7. (3-1) Preparation of sample solution Preparation of a sample solution of tea flower powder Approximately 1.0 g of the tea flower fine powder obtained in "(1) Production of tea flower fine powder" was precisely weighed and placed in an eggplant-shaped flask, 50 mL of methanol was added, and the mixture was heated to reflux in a water bath at 80°C for 30 minutes and filtered through filter paper. An additional 50 mL of methanol was added to the residue and the same procedure was repeated. The filtrates were combined and concentrated to dryness under reduced pressure. Methanol and water (volume ratio, 1:1) were added to the resulting residue and ultrasonically irradiated for 5 minutes (ultrasonic cleaner AS ONE cleaner, AS ONE Corporation, model ASU-10M, output 500W). The resulting solution was made up to exactly 20 mL and filtered through a membrane filter with a pore size of 0.45 μm to prepare the sample solution. According to the research of the present inventor, it has been found that the saponin compounds can be most efficiently extracted from tea flowers by using a mixture of methanol and water in a volume ratio of 1:1 as the extraction solution. Therefore, the amount of saponin extracted with a mixture of methanol and water in a volume ratio of 1:1 is regarded as the amount of saponin compounds in the tea flower fine powder.

[0033] Preparation of sample solution of hot water extract of tea flowers In addition, about 500 mg of the tea flower hot water extract obtained in the section "(2) Production of tea flower hot water extract" was precisely measured and placed in an eggplant-shaped flask, 50 mL of methanol was added, and the mixture was heated to reflux for 30 minutes and filtered through filter paper. An additional 50 mL of methanol was added to the residue and the same procedure was carried out. The filtrates were combined and concentrated to dryness using an evaporator under reduced pressure. 3 mL of a mixture of methanol and water (1:1) was added to the resulting residue, which was then thoroughly stirred and ultrasonicated for 5 minutes using an ultrasonic cleaner. The solution was transferred to a 20 mL measuring flask using a Pasteur pipette. Further, 3 mL of methanol and water (volume ratio, 1:1) was added to the residue, and the operation of stirring and ultrasonic cleaning was repeated twice. Methanol was added to the resulting solution to make exactly 10 mL, and the solution was filtered through a membrane filter with a pore size of 0.45 μm (0.45 μm) to prepare the sample solution.

[0034] (3-2) Quantification Chakasaponins I, II, and III, which were isolated and purified from the flowers of tea (Camellia sinensis) produced in Fujian Province, China, by the methods described in Non-Patent Document 7 and Patent Document 5, were dissolved in methanol to prepare standard solutions of three concentrations. The concentrations of the standard solutions were 0.5 mg / mL, 0.25 mg / mL, and 0.025 mg / mL for chakasaponin I, 1.0 mg / mL, 0.5 mg / mL, and 0.05 mg / mL for chakasaponin II, and 0.3 mg / mL, 0.15 mg / mL, and 0.015 mg / mL for chakasaponin III.

[0035] 20 μL of each sample solution and standard solution were accurately measured and subjected to liquid chromatography under the following conditions. The amount of each saponin compound in the sample solution was quantified by applying the results to a calibration curve created from the area value of the standard solution. <Liquid chromatography conditions> Detector: Ultraviolet spectrophotometer (measurement wavelength: 230 nm) Column: A stainless steel tube with an inner diameter of 4.6 mm and a length of 25 cm packed with octadecylsilylated silica gel for liquid chromatography with an average particle size of 5 μm. Column temperature: constant temperature around 40℃ Mobile phase: Methanol / 0.01 mol / L sodium phosphate buffer (pH 2.3) (Note 1) mixture (volume ratio 65:35) Flow rate: 1.0ml / min Analysis time: 60 minutes (Note 2) (Note 1) Dissolve 1.55 g of sodium dihydrogen phosphate dihydrate in 1000 mL of water and adjust the pH to 2.3 using diluted phosphoric acid (1 → 10). (Note 2) Since many peaks of impurity components were detected even after 60 minutes, when performing consecutive analyses, the column was washed with methanol for 15 minutes, and then the mobile phase was passed through for 15 minutes before performing the analysis again.

[0036] Tea flowers contain 10 types of floratheasaponins A to J and 6 types of chakasaponins I to VI as saponin components (Non-Patent Documents 6, 7, 10). Of these, chakasaponins I, II, and III are the main components that exhibit useful medicinal effects. The contents of chakasaponins I, II, and III were calculated by applying them to a calibration curve created from the area values ​​of each standard solution. In addition, the total peak area of ​​the 16 types of tea flower saponins was roughly estimated from the liquid chromatographic peak areas of the 10 types of floratheasaponins A to J and the 6 types of chakasaponins I to VI (peak positions are described in Non-Patent Documents 6, 7, and 10) and the measured content of chakasaponin II, and the total tea flower saponin content was calculated by fitting this to the calibration curve for chakasaponin II.

[0037] The content (mass %) of total tea flower saponins, including chakasaponins and floratheasaponins, in the tea flower fine powder or dried tea flower extract is shown in Table 1. [Table 1] The tea flower powder contained the same amount of saponin compounds as the hot water extract of tea flowers. Saponin components such as chakasaponins are the main medicinal components of tea flowers. Considering that only about 20% by mass of tea flower hot water extract can be obtained from tea flowers, it can be seen that the utilization efficiency of tea flowers is extremely high when using tea flower powder.

[0038] (4) Quantitative determination of caffeine The experiment was carried out according to Non-Patent Document 10. (4-1) Preparation of sample solution Approximately 0.5 g of the test sample (tea flower fine powder obtained in section "(1) Production of tea flower fine powder" or tea flower hot water extract obtained in section "(2) Production of tea flower hot water extract") was precisely weighed and placed in an eggplant flask, 70 mL of purified water was added, and the mixture was heated to reflux in a mantle heater for 60 minutes and filtered through filter paper. 20 mL of purified water was added to the residue to wash once, and the filtrate was combined, purified water was added to make exactly 100 mL, and the mixture was filtered through a membrane filter (0.45 μm) to prepare the sample solution.

[0039] (4-2) Quantification 10 mg of anhydrous caffeine was precisely weighed and placed in a measuring flask, and water was added to make exactly 100 mL. 8 mL of this solution was precisely weighed and water was added to make exactly 20 mL to make the standard solution. 5 μL of the sample solution and the standard solution were precisely weighed and measured by liquid chromatography under the following conditions to determine the total caffeine peak area AT of each sample solution and the caffeine area AS of the standard solution. <Liquid chromatography conditions> Detector: Ultraviolet spectrophotometer (measurement wavelength: 270 nm) Column: A stainless steel tube having an inner diameter of 6 mm and a length of 15 cm is packed with 5 μm octadecylsilylated silica gel for liquid chromatography. Column temperature: constant temperature around 40℃ Mobile phase: 2% acetic acid / methanol (80:20) Flow rate: Adjust so that the caffeine retention time is approximately 10 minutes. The amount of caffeine contained in the test sample was calculated using the following formula, and the caffeine concentration in the tea flower fine powder or tea flower hot water extract was also calculated. Amount of caffeine (mg) = WS × (AT / AS) WS: Measured amount of caffeine (mg) The caffeine concentration of the tea flower fine powder was 0.49% by mass, and the caffeine concentration of the tea flower hot water extract was 2.07% by mass. The caffeine concentration of the tea flower fine powder was 0.24 times that of the tea flower hot water extract.

[0040] (5) Measurement of moisture content 2 g of the test sample (obtained in section "(1) Production of tea flower fine powder") was placed in a weighing bottle whose mass had been measured in advance, its mass was accurately measured, and it was dried at 105°C for 5 hours. It was allowed to cool in a desiccator (containing silica gel) and then its mass was accurately measured. The percentage of the mass loss due to drying (loss on drying) relative to the mass of the tea flower fine powder before drying was taken as the moisture content (%) of the tea flower fine powder. The moisture content was 5.45% by mass.

[0041] (6) Functional evaluation (6-1) Suppression of increase in blood triglyceride levels The experiment was carried out according to Non-Patent Document 5 and Patent Document 2. The test sample (the tea flower fine powder or tea flower hot water extract measured above) was suspended in a 5 (w / v)% gum arabic powder aqueous solution and given orally at a dose of 1g / kg body weight to ddY male mice (6 weeks old). The dose of the test sample was 1000mg / kg body weight. The 5 w / v% gum arabic powder aqueous solution is viscous. Thirty minutes later, 5 mL / kg body weight of olive oil was orally administered to the mice. Two and four hours after the oral administration of the test sample, approximately 0.1 mL of blood was collected from the orbital vein under ether anesthesia. The collected blood was mixed with 5 units / tube of sodium heparin, and the serum triglyceride concentration obtained by centrifugation was measured using a Wako Triglyceride E Test. Serum triglyceride concentrations were also measured in the same manner for normal mice that were not administered olive oil or the test sample, and for control mice that were administered olive oil, but not the test sample, and only 5 (w / v)% aqueous solution of powdered gum arabic.

[0042] Serum triglyceride concentrations (mg / dL) are shown in Table 2. [Table 2] The hot water extract of tea flowers strongly inhibited the rise in triglyceride concentration after 2 hours, but after 4 hours the triglyceride concentration became extremely high. In contrast, the fine powder of tea flowers stably inhibited the rise in triglyceride concentration up to 4 hours. The AUC of the fine powder of tea flowers was lower than that of the hot water extract of tea flowers, and the fine powder of tea flowers showed an overall stronger effect of inhibiting the rise in blood lipids.

[0043] (6-2) Suppressing gastric emptying ability The experiment was carried out according to Non-Patent Document 9 and Patent Document 4. Male ddY mice (6 weeks old, weighing approximately 30g) purchased from Kiwa Laboratory Animal Research Institute were acclimated for one week and then fasted for 20 hours. A 5 w / v% gum arabic powder solution was dispersed with the test sample (the tea flower fine powder or tea flower hot water extract as measured above) and the mice were orally administered 10mL / kg body weight by force. The dose of the test sample was 500mg / kg body weight. The 5 w / v% gum arabic powder solution is viscous. Thirty minutes after administration of the samples, 1.5% CMC-Na aqueous solution containing 0.05% phenol red was orally administered at a dose of 0.3 mL / mouse. Thirty minutes after administration of the CMC-Na aqueous solution, the mice were euthanized by cervical dislocation, and the stomach was excised by laparotomy. The excised stomach was homogenized in 0.1 M NaOH (10 mL). The mixture was left at room temperature for 1 hour, and 0.5 mL of 20% trichloroacetic acid (Nacalai Tesque) was added to 5 mL of the supernatant, stirred to remove proteins, and then centrifuged (3000 rpm, 20 minutes, room temperature). 2 mL of the supernatant was added to 0.5 M NaOH (2 mL), placed on a plate, and the OD value was measured using a microplate reader (main wavelength 600 nm, reference wavelength 670 nm). This OD value indicates the amount of CMC-Na remaining in the stomach. The OD value was also measured in the same manner for control mice that were administered the CMC-Na aqueous solution but not the test sample. Because the tea flower fine powder and the tea flower hot water extract were tested separately, a control group was set up for each. Gastric emptying (GE%) was calculated using the following formula: GE(%)=[1-(amount of phenol red remaining in stomach) / (amount of phenol red administered)]×100

[0044] Gastric emptying (%) is shown in Table 3. [Table 3] The ratio of gastric emptying to the control was lower for the tea flower powder than for the tea flower hot water extract, indicating a stronger inhibitory effect on gastric emptying. Tea flower powder inhibits gastric emptying, prolonging the feeling of fullness and suppressing appetite, and therefore preventing obesity caused by overeating. [Industrial Applicability]

[0045] The tea flower powder of the present invention can be produced more easily than conventional tea flower extracts, has good tea flower utilization efficiency, and has a strong preferable pharmacological activity while suppressing the caffeine content, so it has a very high commercial value as a diet material.

Claims

1. A powder of tea flowers having an average particle size of 10-100 μm and a maximum particle size of 10-500 μm, which is used for oral intake.

2. 2. The powder according to claim 1, which passes through any sieve from No. 18 to No. 200 mesh.

3. The powder according to claim 1 or 2, wherein the total content of chakasaponin I, chakasaponin II, and chakasaponin III is 1 to 20 mass% based on the total amount of tea flower powder.

4. The method for producing tea flower powder for oral ingestion includes the steps of pulverizing tea flowers or a dried product thereof and adjusting the particle size of the pulverized product to have an average particle size of 10 to 100 μm and a maximum particle size of 10 to 500 μm.

Images