JP2021093921A - Powder green tea extraction composition - Google Patents
Powder green tea extraction composition Download PDFInfo
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- JP2021093921A JP2021093921A JP2019225511A JP2019225511A JP2021093921A JP 2021093921 A JP2021093921 A JP 2021093921A JP 2019225511 A JP2019225511 A JP 2019225511A JP 2019225511 A JP2019225511 A JP 2019225511A JP 2021093921 A JP2021093921 A JP 2021093921A
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- 244000269722 Thea sinensis Species 0.000 title claims abstract description 75
- 238000000605 extraction Methods 0.000 title claims abstract description 74
- 239000000203 mixture Substances 0.000 title claims abstract description 67
- 235000009569 green tea Nutrition 0.000 title claims abstract description 63
- BPJYAXCTOHRFDQ-UHFFFAOYSA-L tetracopper;2,4,6-trioxido-1,3,5,2,4,6-trioxatriarsinane;diacetate Chemical compound [Cu+2].[Cu+2].[Cu+2].[Cu+2].CC([O-])=O.CC([O-])=O.[O-][As]1O[As]([O-])O[As]([O-])O1.[O-][As]1O[As]([O-])O[As]([O-])O1 BPJYAXCTOHRFDQ-UHFFFAOYSA-L 0.000 title abstract 3
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 claims abstract description 54
- 235000005487 catechin Nutrition 0.000 claims abstract description 54
- 229920000642 polymer Polymers 0.000 claims abstract description 47
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 45
- 150000001765 catechin Chemical class 0.000 claims description 50
- 235000020688 green tea extract Nutrition 0.000 claims description 45
- 229940094952 green tea extract Drugs 0.000 claims description 45
- 239000003125 aqueous solvent Substances 0.000 claims description 26
- 238000004519 manufacturing process Methods 0.000 claims description 18
- 238000002156 mixing Methods 0.000 claims description 17
- 239000011259 mixed solution Substances 0.000 claims description 16
- 239000007787 solid Substances 0.000 claims description 13
- 238000001035 drying Methods 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 8
- 239000002245 particle Substances 0.000 claims description 8
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 claims description 4
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 claims description 4
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 claims description 4
- 229910001424 calcium ion Inorganic materials 0.000 claims description 4
- 229910001414 potassium ion Inorganic materials 0.000 claims description 4
- 229910001415 sodium ion Inorganic materials 0.000 claims description 4
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 abstract description 4
- 229950001002 cianidanol Drugs 0.000 abstract description 4
- 238000000034 method Methods 0.000 description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 31
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
- 238000003860 storage Methods 0.000 description 16
- 239000002904 solvent Substances 0.000 description 14
- 238000005469 granulation Methods 0.000 description 11
- 230000003179 granulation Effects 0.000 description 11
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
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- 239000000843 powder Substances 0.000 description 8
- 239000002994 raw material Substances 0.000 description 8
- 238000005259 measurement Methods 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
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- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- 241000209507 Camellia Species 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
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- XMOCLSLCDHWDHP-IUODEOHRSA-N epi-Gallocatechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@H]2O)=CC(O)=C(O)C(O)=C1 XMOCLSLCDHWDHP-IUODEOHRSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- LVJJFMLUMNSUFN-UHFFFAOYSA-N gallocatechin gallate Natural products C1=C(O)C=C2OC(C=3C=C(O)C(O)=CC=3)C(O)CC2=C1OC(=O)C1=CC(O)=C(O)C(O)=C1 LVJJFMLUMNSUFN-UHFFFAOYSA-N 0.000 description 2
- 229910017053 inorganic salt Inorganic materials 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 230000001766 physiological effect Effects 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
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- XMOCLSLCDHWDHP-SWLSCSKDSA-N (+)-Epigallocatechin Natural products C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC(O)=C(O)C(O)=C1 XMOCLSLCDHWDHP-SWLSCSKDSA-N 0.000 description 1
- LSHVYAFMTMFKBA-PZJWPPBQSA-N (+)-catechin-3-O-gallate Chemical compound O([C@H]1CC2=C(O)C=C(C=C2O[C@@H]1C=1C=C(O)C(O)=CC=1)O)C(=O)C1=CC(O)=C(O)C(O)=C1 LSHVYAFMTMFKBA-PZJWPPBQSA-N 0.000 description 1
- PFTAWBLQPZVEMU-ZFWWWQNUSA-N (+)-epicatechin Natural products C1([C@@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-ZFWWWQNUSA-N 0.000 description 1
- WMBWREPUVVBILR-GHTZIAJQSA-N (+)-gallocatechin gallate Chemical compound O([C@H]1CC2=C(O)C=C(C=C2O[C@@H]1C=1C=C(O)C(O)=C(O)C=1)O)C(=O)C1=CC(O)=C(O)C(O)=C1 WMBWREPUVVBILR-GHTZIAJQSA-N 0.000 description 1
- WMBWREPUVVBILR-WIYYLYMNSA-N (-)-Epigallocatechin-3-o-gallate Chemical compound O([C@@H]1CC2=C(O)C=C(C=C2O[C@@H]1C=1C=C(O)C(O)=C(O)C=1)O)C(=O)C1=CC(O)=C(O)C(O)=C1 WMBWREPUVVBILR-WIYYLYMNSA-N 0.000 description 1
- PFTAWBLQPZVEMU-UKRRQHHQSA-N (-)-epicatechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-UKRRQHHQSA-N 0.000 description 1
- LSHVYAFMTMFKBA-TZIWHRDSSA-N (-)-epicatechin-3-O-gallate Chemical compound O([C@@H]1CC2=C(O)C=C(C=C2O[C@@H]1C=1C=C(O)C(O)=CC=1)O)C(=O)C1=CC(O)=C(O)C(O)=C1 LSHVYAFMTMFKBA-TZIWHRDSSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- LSHVYAFMTMFKBA-UHFFFAOYSA-N ECG Natural products C=1C=C(O)C(O)=CC=1C1OC2=CC(O)=CC(O)=C2CC1OC(=O)C1=CC(O)=C(O)C(O)=C1 LSHVYAFMTMFKBA-UHFFFAOYSA-N 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- XMOCLSLCDHWDHP-UHFFFAOYSA-N L-Epigallocatechin Natural products OC1CC2=C(O)C=C(O)C=C2OC1C1=CC(O)=C(O)C(O)=C1 XMOCLSLCDHWDHP-UHFFFAOYSA-N 0.000 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 235000006468 Thea sinensis Nutrition 0.000 description 1
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- 230000002378 acidificating effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
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- 238000004220 aggregation Methods 0.000 description 1
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- 150000001298 alcohols Chemical class 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
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- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
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- 238000001479 atomic absorption spectroscopy Methods 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
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- 238000005119 centrifugation Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
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- LPTRNLNOHUVQMS-UHFFFAOYSA-N epicatechin Natural products Cc1cc(O)cc2OC(C(O)Cc12)c1ccc(O)c(O)c1 LPTRNLNOHUVQMS-UHFFFAOYSA-N 0.000 description 1
- 235000012734 epicatechin Nutrition 0.000 description 1
- DZYNKLUGCOSVKS-UHFFFAOYSA-N epigallocatechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3cc(O)c(O)c(O)c3 DZYNKLUGCOSVKS-UHFFFAOYSA-N 0.000 description 1
- 229940030275 epigallocatechin gallate Drugs 0.000 description 1
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- TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 1
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- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- Tea And Coffee (AREA)
Abstract
Description
本発明は、粉末緑茶抽出組成物に関する。 The present invention relates to a powdered green tea extraction composition.
近年、健康志向の高まりから、非重合体カテキン類の生理効果が注目されており、茶飲料等の飲食品の需要が拡大している。非重合体カテキン類による生理効果を十分に発現するには、高濃度の非重合体カテキン類を含む飲食品を継続して摂取することが有利である。そこで、緑茶抽出物を精製して夾雑物を除去し、非重合体カテキン類を高純度化する技術が種々検討されている。例えば、所定濃度の非重合体カテキン類を含有する固体カテキン製剤を、有機溶媒と水の重量比率が一定に制御された溶媒に添加し、これに水を加えることにより有機溶媒と水の重量比率を所定濃度に調整した後、不溶の固形分を除去する方法(特許文献1)、カテキン類組成物を、有機溶媒/水の質量比が一定に制御された混合溶媒に溶解させ、活性炭及び酸性白土又は活性白土と接触させる方法(特許文献2)、緑茶抽出物を、合成吸着剤を充填したカラムに通液して吸着させ、次いで水を通液してカラムを洗浄し、次いで所定濃度のエタノール水溶液をカラムに通液する方法(特許文献3)等が提案されている。 In recent years, due to growing health consciousness, the physiological effects of non-polymerized catechins have been attracting attention, and the demand for foods and drinks such as tea beverages is expanding. In order to fully exhibit the physiological effects of the non-polymer catechins, it is advantageous to continuously ingest foods and drinks containing a high concentration of the non-polymer catechins. Therefore, various techniques for purifying green tea extract to remove impurities and purifying non-polymer catechins have been studied. For example, a solid catechin preparation containing a predetermined concentration of non-polymer catechins is added to a solvent in which the weight ratio of the organic solvent and water is controlled to be constant, and water is added thereto to obtain a weight ratio of the organic solvent and water. (Patent Document 1), a method of removing insoluble solids after adjusting the concentration to a predetermined concentration, the catechin composition is dissolved in a mixed solvent in which the mass ratio of organic solvent / water is controlled to be constant, and activated charcoal and acidic A method of contacting with white clay or active white clay (Patent Document 2), the green tea extract is passed through a column packed with a synthetic adsorbent to be adsorbed, and then water is passed through the column to wash the column, and then a predetermined concentration is obtained. A method of passing an aqueous ethanol solution through a column (Patent Document 3) and the like have been proposed.
一方、粉末飲料の粉体色及び飲用時の水色を改善する技術として、緑茶抽出物、抗酸化物、粉末茶を含有するインスタント緑茶にカリウムを一定量含有させることで、粉体色及び飲用時の水色を鮮やかな緑色に改善できることが報告されている(特許文献4)。しかし、かかる文献に記載された技術は、非重合体カテキン類を高純度化した緑茶抽出物を対象とするものでも、かかる緑茶抽出物自体の外観に着目したものでもない。 On the other hand, as a technique for improving the powder color of powdered beverages and the light blue during drinking, instant green tea containing green tea extract, antioxidants, and powdered tea contains a certain amount of potassium to achieve powder color and drinking. It has been reported that the light blue color of tea can be improved to bright green (Patent Document 4). However, the technique described in such literature does not focus on the green tea extract obtained by purifying non-polymeric catechins, nor on the appearance of the green tea extract itself.
通常、緑茶抽出組成物は、未精製の場合や非重合体カテキン類の純度が比較的低い場合には、粉末化しかつ遮光された条件であれば、長期に亘って保存したとしても、その外観に大きな変化は見られない。ところが、緑茶抽出組成物の精製度を増し非重合体カテキン類の純度を高めるにつれ、粉末化しかつ遮光したとしても、長期に亘って保存すると赤みを帯び、外観が大きく変化しやすいという課題があることを本発明者らは見出した。
したがって、本発明の課題は、高純度の非重合体カテキン類を含み、長期保存したときに色相変化のし難い粉末緑茶抽出組成物及びその製造方法を提供することにある。
Generally, when the green tea extraction composition is unpurified or the purity of the non-polymer catechins is relatively low, the appearance of the green tea extraction composition even if it is stored for a long period of time under the conditions of powdering and shading. No major changes are seen in. However, as the degree of purification of the green tea extraction composition is increased and the purity of the non-polymer catechins is increased, there is a problem that even if the green tea extract composition is powdered and shielded from light, it becomes reddish when stored for a long period of time and its appearance is likely to change significantly. The present inventors have found that.
Therefore, an object of the present invention is to provide a powdered green tea extraction composition containing high-purity non-polymeric catechins and having a hue that does not easily change when stored for a long period of time, and a method for producing the same.
本発明者らは、上記課題に鑑み検討した結果、(A)非重合体カテキン類の含有量を特定量以上とした際に、該(A)非重合体カテキン類に対する(B)金属イオンの質量比[(B)/(A)]を特定値以上に制御することで、非重合体カテキン類を高純度で含有しながらも、長期保存したときの色相変化が抑制された粉末緑茶抽出組成物が得られることを見出した。 As a result of examination in view of the above problems, the present inventors, when the content of (A) non-polymer catechins is set to a specific amount or more, the (B) metal ion with respect to the (A) non-polymer catechins By controlling the mass ratio [(B) / (A)] to a specific value or higher, a powdered green tea extraction composition in which non-polymer catechins are contained with high purity but the hue change during long-term storage is suppressed. I found that I could get things.
すなわち、次の成分(A)及び(B):
(A)非重合体カテキン類、及び
(B)金属イオン
を含有し、
成分(A)の含有量が40質量%以上であり、かつ
成分(A)に対する成分(B)の質量比[(B)/(A)]が0.005以上である、
粉末緑茶抽出組成物を提供するものである。
That is, the following components (A) and (B):
Contains (A) non-polymer catechins and (B) metal ions,
The content of the component (A) is 40% by mass or more, and the mass ratio [(B) / (A)] of the component (B) to the component (A) is 0.005 or more.
It provides a powdered green tea extraction composition.
本発明はまた、(A)非重合体カテキン類の含有量が40質量%以上である緑茶抽出物と、(B)金属イオンとを、成分(A)に対する成分(B)の質量比[(B)/(A)]が0.005以上となるように水系溶媒の存在下に混合した後、当該混合液を乾燥する工程を含む、粉末緑茶抽出組成物の製造方法を提供するものである。 The present invention also comprises (A) a green tea extract having a content of non-polymer catechins of 40% by mass or more and (B) a metal ion in a mass ratio of the component (B) to the component (A) [(). Provided is a method for producing a powdered green tea extraction composition, which comprises a step of mixing in the presence of an aqueous solvent so that B) / (A)] is 0.005 or more, and then drying the mixed solution. ..
本発明によれば、非重合体カテキン類を高純度で含有しながらも、長期保存したときに色相変化のし難い粉末緑茶抽出組成物を提供することができる。 According to the present invention, it is possible to provide a powdered green tea extraction composition which contains non-polymer catechins with high purity but whose hue does not easily change when stored for a long period of time.
〔粉末緑茶抽出組成物〕
本発明の粉末緑茶抽出組成物は、成分(A)として非重合体カテキン類を含有する。ここで、本明細書において「非重合体カテキン類」とは、カテキン、ガロカテキン、エピカテキン及びエピガロカテキン等の非ガレート体と、カテキンガレート、ガロカテキンガレート、エピカテキンガレート及びエピガロカテキンガレート等のガレート体を併せての総称である。本発明においては、上記8種の非重合体カテキン類のうち少なくとも1種を含有すればよい。
[Powdered green tea extraction composition]
The powdered green tea extraction composition of the present invention contains non-polymer catechins as the component (A). Here, the term "non-polymer catechins" as used herein refers to non-gallates such as catechin, gallocatechin, epicatechin and epigallocatechin, and catechin gallate, gallocatechin gallate, epicatechin gallate, epigallocatechin gallate and the like. It is a general term for the catechins of. In the present invention, at least one of the above eight types of non-polymer catechins may be contained.
本発明の粉末緑茶抽出組成物は、成分(A)の含有量が40質量%以上であるが、非重合体カテキン類の強化の観点から、42質量%以上が好ましく、44質量%以上がより好ましく、46質量%以上が更に好ましく、また長期保存したときの色相変化の抑制、生産効率の観点から、95質量%以下が好ましく、90質量%以下がより好ましく、80質量%以下が更に好ましく、70質量%以下がより更に好ましく、60質量%以下がより更に好ましい。かかる成分(A)の含有量の範囲としては、本発明の粉末緑茶抽出組成物中に、好ましくは40〜95質量%であり、より好ましくは42〜90質量%であり、更に好ましくは44〜80質量%であり、更に好ましくは46〜70質量%でありより更に好ましくは46〜60質量%である。成分(A)の含有量は、上記8種の合計量に基づいて定義され、通常知られている測定法のうち測定試料の状況に適した分析法により測定することができる。例えば、液体クロマトグラフィで分析することが可能であり、具体的には、後掲の実施例に記載の方法が挙げられる。また、測定の際には装置の検出域に適合させるため、試料を凍結乾燥したり、装置の分離能に適合させるため試料中の夾雑物を除去したりする等、必要に応じて適宜処理を施してもよい。 The powdered green tea extraction composition of the present invention has a content of the component (A) of 40% by mass or more, but from the viewpoint of strengthening non-polymer catechins, it is preferably 42% by mass or more, more preferably 44% by mass or more. It is more preferably 46% by mass or more, more preferably 95% by mass or less, still more preferably 90% by mass or less, further preferably 80% by mass or less, from the viewpoint of suppressing color change during long-term storage and production efficiency. 70% by mass or less is even more preferable, and 60% by mass or less is even more preferable. The content of the component (A) is preferably 40 to 95% by mass, more preferably 42 to 90% by mass, and further preferably 44 to 44% by mass in the powdered green tea extraction composition of the present invention. It is 80% by mass, more preferably 46 to 70% by mass, and even more preferably 46 to 60% by mass. The content of the component (A) is defined based on the total amount of the above eight types, and can be measured by an analytical method suitable for the situation of the measurement sample among the commonly known measurement methods. For example, it can be analyzed by liquid chromatography, and specific examples thereof include the method described in Examples described later. In addition, at the time of measurement, appropriate treatment is performed as necessary, such as freeze-drying the sample to match the detection range of the device and removing impurities in the sample to match the separability of the device. May be given.
本発明の粉末緑茶抽出組成物は、成分(B)として金属イオンを含有する。
成分(B)としては、食品として許容される金属イオンであれば特に限定されないが、例えば、1価の金属イオン、2価の金属イオン、3価以上の金属イオンを挙げることができる。1価の金属イオンとしては、例えば、ナトリウムイオン、カリウムイオンが挙げられる。また、2価の金属イオンとしては、例えば、カルシウムイオン、マグネシウムイオンを挙げることができる。3価以上の金属イオンとしては、例えば、アルミニウムイオンが挙げられる。成分(B)は、1種又は2種以上含有することができる。
The powdered green tea extraction composition of the present invention contains a metal ion as a component (B).
The component (B) is not particularly limited as long as it is a metal ion acceptable for food, and examples thereof include monovalent metal ions, divalent metal ions, and trivalent or higher metal ions. Examples of the monovalent metal ion include sodium ion and potassium ion. Further, examples of the divalent metal ion include calcium ion and magnesium ion. Examples of trivalent or higher valent metal ions include aluminum ions. The component (B) can be contained alone or in combination of two or more.
中でも、長期保存したときの色相変化の抑制の観点から、1価の金属イオン及び2価の金属イオンから選ばれる1種又は2種以上含むことが好ましく、ナトリウムイオン、カリウムイオン及びカルシウムイオンから選ばれる1種又は2種以上含むことが更に好ましい。 Among them, from the viewpoint of suppressing the change in hue during long-term storage, it is preferable to contain one or more selected from monovalent metal ions and divalent metal ions, and it is selected from sodium ion, potassium ion and calcium ion. It is more preferable to include one type or two or more types.
成分(B)は、原料に由来するものでも、新たに加えたものでもよい。
また、成分(B)は、粉末緑茶抽出組成物を水に溶解したときに金属イオンを生成するものであれば、塩の形態でもよい。塩の形態としては食品として許容されるものであれば特に限定されないが、例えば、無機塩、有機酸塩を挙げることができる。無機塩としては、例えば、塩化物塩、リン酸塩、炭酸塩を挙げることができる。有機酸塩としては、例えば、酢酸、アジピン酸、アスコルビン酸、酪酸、クエン酸、ギ酸、フマル酸、グリコン酸、乳酸、リンゴ酸、シュウ酸、コハク酸、酒石酸等の食用酸塩を挙げることができる。
The component (B) may be derived from a raw material or newly added.
Further, the component (B) may be in the form of a salt as long as it produces metal ions when the powdered green tea extraction composition is dissolved in water. The form of the salt is not particularly limited as long as it is acceptable as a food, and examples thereof include inorganic salts and organic acid salts. Examples of the inorganic salt include chloride salts, phosphates, and carbonates. Examples of the organic acid salt include edible acid salts such as acetic acid, adipic acid, ascorbic acid, butyric acid, citric acid, formic acid, fumaric acid, glycoic acid, lactic acid, malic acid, oxalic acid, succinic acid, and tartrate acid. it can.
本発明の粉末緑茶抽出組成物は、成分(B)の含有量が、長期保存したときの色相変化の抑制の観点から、0.2質量%以上であることが好ましく、1.0質量%以上がより好ましく、2.0質量%以上が更に好ましく、3.0質量%以上がより更に好ましく、4.0質量%以上がより更に好ましく、また長期保存したときの色相変化の抑制、食品への配合のし易さの観点から、14質量%以下が好ましく、12質量%以下がより好ましく、10質量%以下が更に好ましい。かかる成分(B)の含有量の範囲としては、本発明の粉末緑茶抽出組成物中に、好ましくは0.2〜14質量%であり、より好ましくは1.0〜12質量%であり、更に好ましくは2.0〜12質量%であり、より更に好ましくは3.0〜10質量%であり、より更に好ましくは4.0〜10質量%である。なお、成分(B)の含有量は、金属イオンの合計量とする。ここで、本明細書において「成分(B)の含有量」は、原子吸光分析により測定したものであって、具体的には、後掲の実施例に記載の方法により測定することができる。また、測定の際には装置の検出域に適合させるため、試料を凍結乾燥したり、装置の分離能に適合させるため試料中の夾雑物を除去したりする等、必要に応じて適宜処理を施してもよい。 In the powdered green tea extraction composition of the present invention, the content of the component (B) is preferably 0.2% by mass or more, preferably 1.0% by mass or more, from the viewpoint of suppressing the change in hue when stored for a long period of time. Is more preferable, 2.0% by mass or more is further preferable, 3.0% by mass or more is further preferable, 4.0% by mass or more is further preferable, and suppression of color change during long-term storage, and addition to foods. From the viewpoint of ease of blending, 14% by mass or less is preferable, 12% by mass or less is more preferable, and 10% by mass or less is further preferable. The content of the component (B) is preferably 0.2 to 14% by mass, more preferably 1.0 to 12% by mass, and further, in the powdered green tea extraction composition of the present invention. It is preferably 2.0 to 12% by mass, more preferably 3.0 to 10% by mass, and even more preferably 4.0 to 10% by mass. The content of the component (B) is the total amount of metal ions. Here, in the present specification, the "content of the component (B)" is measured by atomic absorption spectroscopy, and can be specifically measured by the method described in Examples described later. In addition, at the time of measurement, appropriate treatment is performed as necessary, such as freeze-drying the sample to match the detection range of the device and removing impurities in the sample to match the separability of the device. May be given.
本発明の粉末緑茶抽出組成物は、成分(A)に対する成分(B)の質量比[(B)/(A)]が0.005以上であるが、長期保存したときの色相変化の抑制の観点から、0.010以上が好ましく、0.02以上がより好ましく、0.04以上が更に好ましく、0.09以上がより更に好ましい。また、かかる質量比[(B)/(A)]は、風味、本発明の効果を享受しやすい点から、0.3以下が好ましく、0.25以下がより好ましく、0.2以下が更に好ましい。かかる質量比[(B)/(A)]の範囲としては、好ましくは0.005〜0.3であり、より好ましくは0.010〜0.3であり、更に好ましくは0.02〜0.3であり、より更に好ましくは0.04〜0.25であり、殊更に好ましくは0.09〜0.2である。 The powdered green tea extraction composition of the present invention has a mass ratio [(B) / (A)] of the component (B) to the component (A) of 0.005 or more, but suppresses the change in hue when stored for a long period of time. From the viewpoint, 0.010 or more is preferable, 0.02 or more is more preferable, 0.04 or more is further preferable, and 0.09 or more is further preferable. Further, the mass ratio [(B) / (A)] is preferably 0.3 or less, more preferably 0.25 or less, and further preferably 0.2 or less, from the viewpoint of easily enjoying the flavor and the effect of the present invention. preferable. The range of the mass ratio [(B) / (A)] is preferably 0.005 to 0.3, more preferably 0.010 to 0.3, and further preferably 0.02 to 0. It is 0.3, more preferably 0.04 to 0.25, and even more preferably 0.09 to 0.2.
また、本発明の粉末緑茶抽出組成物は、長期保存したときの色相変化の抑制、風味、ブロッキング防止の観点から、揮発分が10.0質量%以下であることが好ましく、8.0質量%以下がより好ましく、5質量%以下が更に好ましい。また、生産効率の観点から、揮発分は、0.2質量%以上が好ましく、0.4質量%以上がより好ましく、0.6質量%以上が更に好ましい。かかる揮発分の範囲としては、好ましくは0.2〜10.0質量%であり、より好ましくは0.4〜8.0質量%であり、更に好ましくは0.6〜5.0質量%である。ここで、本明細書において「揮発分」とは、試料を105℃の電気恒温乾燥機で15分間加熱したときの揮発成分の含有割合をいい、加熱前後の試料の質量から、下記式(1)により算出される値をいう。揮発分は、例えば、水と、水以外の揮発性物質とを包含する概念である。 Further, the powdered green tea extraction composition of the present invention preferably has a volatile content of 10.0% by mass or less, preferably 8.0% by mass, from the viewpoint of suppressing hue change during long-term storage, flavor, and preventing blocking. The following is more preferable, and 5% by mass or less is further preferable. From the viewpoint of production efficiency, the volatile content is preferably 0.2% by mass or more, more preferably 0.4% by mass or more, and further preferably 0.6% by mass or more. The range of the volatile content is preferably 0.2 to 10.0% by mass, more preferably 0.4 to 8.0% by mass, and further preferably 0.6 to 5.0% by mass. is there. Here, in the present specification, the "volatile component" refers to the content ratio of the volatile component when the sample is heated in an electric constant temperature dryer at 105 ° C. for 15 minutes, and the following formula (1) is used from the mass of the sample before and after heating. ) Is the value calculated by. Volatiles is a concept that includes, for example, water and volatile substances other than water.
揮発分(質量%)=(P−Q)/P×100 (1) Volatile content (mass%) = (PQ) / P × 100 (1)
〔式中、Pは、加熱前の試料の質量を示し、Qは、加熱後の試料の質量を示す。〕 [In the formula, P indicates the mass of the sample before heating, and Q indicates the mass of the sample after heating. ]
本明細書において「粉末」とは、粒子状形態を意味し、粉末状のみならず、顆粒状も包含する概念である。本発明の粉末緑茶抽出組成物の形態としては、取り扱いのし易さ、溶解性の観点から、粉末状が好ましい。 As used herein, the term "powder" means a particulate form, and is a concept that includes not only a powder form but also a granular form. The powdered green tea extraction composition of the present invention is preferably in the form of powder from the viewpoint of ease of handling and solubility.
本発明の粉末緑茶抽出組成物は、平均粒子径が、溶解時の凝集(継粉)抑制の観点から、1μm以上であることが好ましく、10μm以上がより好ましく、20μm以上更に好ましく、また溶解性の観点から、1000μm以下が好ましく、800μm以下がより好ましく、500μm以下が更に好ましい。かかる平均粒子径の範囲としては、好ましくは1〜1000μmであり、より好ましくは10〜800μmであり、更に好ましくは20〜500μmである。ここで、本明細書において「平均粒子径」とは、レーザー回折・散乱法により測定したものであって、粉末緑茶抽出組成物の粒度分布を個数基準で作成して得られたメディアン径(d50)を平均粒子径としたものである。 The powdered green tea extraction composition of the present invention preferably has an average particle size of 1 μm or more, more preferably 10 μm or more, further preferably 20 μm or more, and solubility, from the viewpoint of suppressing aggregation (sprinkling) during dissolution. From the above viewpoint, 1000 μm or less is preferable, 800 μm or less is more preferable, and 500 μm or less is further preferable. The range of the average particle size is preferably 1 to 1000 μm, more preferably 10 to 800 μm, and further preferably 20 to 500 μm. Here, in the present specification, the "average particle size" is measured by a laser diffraction / scattering method, and the median size (d) obtained by preparing the particle size distribution of the powdered green tea extraction composition on the basis of the number of particles. 50 ) is the average particle size.
本発明の粉末緑茶抽出組成物は、長期保存したときの色相変化が抑制されている。具体的には、37℃/50%RHの雰囲気下で8週間保存した後の粉末緑茶抽出組成物のa*値と、保存開始前(例えば、製造直後)の粉末緑茶抽出組成物のa1 *値との差分の絶対値Δa*(|a*−a1 *|)を、通常6以下、好ましくは5以下、より好ましくは4以下、更に好ましくは3以下、より更に好ましくは2以下、殊更に好ましくは1.5以下とすることができる。 The powdered green tea extraction composition of the present invention suppresses the change in hue when stored for a long period of time. Specifically, the a * value of the powdered green tea extraction composition after storage in an atmosphere of 37 ° C./50% RH for 8 weeks and the a 1 of the powdered green tea extraction composition before the start of storage (for example, immediately after production). The absolute value Δa * (| a * −a 1 * |) of the difference from the * value is usually 6 or less, preferably 5 or less, more preferably 4 or less, still more preferably 3 or less, still more preferably 2 or less. Particularly preferably, it can be 1.5 or less.
なお、37℃/50%RHの雰囲気下で8週間保存という条件は、通常、25℃±2℃/60%RH±5%で約10ヶ月保存したときに相当する。ここで、本明細書において「a*値」とは、色をL*a*b*表色系で表現したときに、色相、彩度を表す座標値であって、赤色方向の彩度を示す座標値である。L*a*b*表色系には、黄色方向の彩度を示す座標値であるb*もあるが、本発明においては、粉末緑茶抽出組成物が色相変化したときに最も顕在化しやすいa*について規定するものである。なお、a*値の測定は、後掲の実施例に記載の「色相変化の測定」にしたがうものとする。 The condition of storage for 8 weeks in an atmosphere of 37 ° C./50% RH usually corresponds to storage at 25 ° C. ± 2 ° C./60% RH ± 5% for about 10 months. Here, in the present specification, the "a * value" is a coordinate value representing hue and saturation when a color is expressed by an L * a * b * color system, and the saturation in the red direction is defined. It is a coordinate value to be shown. The L * a * b * color system also has a coordinate value b * that indicates saturation in the yellow direction, but in the present invention, the powdered green tea extraction composition is most likely to become apparent when the hue changes. * Is specified. The measurement of the a * value shall be in accordance with the "Measurement of hue change" described in the examples below.
〔粉末緑茶抽出組成物の製造方法〕
本発明の粉末緑茶抽出組成物は、上記特性を具備すれば適宜の方法で製造することが可能であり、特に限定されないが、例えば、(a)固形分中の(A)非重合体カテキン類の含有量が40質量%以上である緑茶抽出物と、(B)金属イオンとを、成分(A)に対する成分(B)の質量比[(B)/(A)]が0.005以上となる割合で、水系溶媒の存在下に混合した後、混合液を乾燥する工程を含む方法により製造することができる。ここで、本明細書において「固形分」とは、試料を105℃の電気恒温乾燥機で3時間乾燥して揮発成分を除いた残分をいう。
[Manufacturing method of powdered green tea extract composition]
The powdered green tea extraction composition of the present invention can be produced by an appropriate method as long as it has the above characteristics, and is not particularly limited, but for example, (a) non-polymer catechins in the solid content. The mass ratio of the component (B) to the component (A) [(B) / (A)] of the green tea extract having a content of 40% by mass or more and the metal ion (B) is 0.005 or more. It can be produced by a method including a step of drying the mixed solution after mixing in the presence of an aqueous solvent at a certain ratio. Here, the term "solid content" as used herein refers to a residue obtained by drying a sample in an electric constant temperature dryer at 105 ° C. for 3 hours to remove volatile components.
(a)緑茶抽出物は、原料緑茶抽出物を精製して夾雑物を除去し、固形分中の(A)非重合体カテキン類の含有量を40質量%以上に調整したものである。
原料緑茶抽出物は、通常、緑茶葉から抽出して得られることができる。緑茶葉としては、例えば、Camellia属の茶葉、例えば、C.sinensis.var.sinensis(やぶきた種を含む)、C.sinensis.var.assamica及びそれらの雑種から選択される茶葉(Camellia sinensis)を挙げることができる。具体的には、例えば、煎茶、深蒸し煎茶、焙じ茶、番茶、玉露、かぶせ茶、碾茶、釜入り茶、茎茶、棒茶、芽茶等が挙げられる。なお、茶葉の茶品種及び採取時期は特に限定されず、適宜選択することができる。
The (a) green tea extract is obtained by purifying the raw material green tea extract to remove impurities and adjusting the content of the (A) non-polymer catechins in the solid content to 40% by mass or more.
The raw material green tea extract can usually be obtained by extracting from green tea leaves. Examples of green tea leaves include tea leaves of the genus Camellia, for example, tea leaves selected from C. sinensis.var.sinensis (including Camellia seeds), C.sinensis.var.assamica and their hybrids (Camellia sinensis). Can be mentioned. Specific examples thereof include sencha, deep-steamed sencha, roasted tea, bancha, gyokuro, kabusecha, tencha, potted tea, kukicha, bar tea, and mecha. The tea variety and collection time of the tea leaves are not particularly limited and can be appropriately selected.
抽出方法としては、ニーダー抽出、攪拌抽出(バッチ抽出)、向流抽出(ドリップ抽出)、カラム抽出等の公知の方法を採用することができる。
抽出条件は、抽出方法により適宜選択することが可能であるが、例えば、抽出溶媒として、水系溶媒を使用することができる。ここで、本明細書において「水系溶媒」とは、水を含む溶媒をいい、水系溶媒中の水の含有量は通常1〜100質量%、好ましくは30〜100質量%である。水系溶媒としては、例えば、水、有機溶媒水溶液、炭酸水等が挙げられる。有機溶媒としては、例えば、アルコール、ケトン、エステル等が挙げられ、食品への使用を考慮すると、アルコールが好ましく、エタノールが更に好ましい。中でも、水系溶媒としては、水が好ましい。水としては、例えば、水道水、天然水、蒸留水、イオン交換水等が挙げられる。中でも、味の面から、イオン交換水が好ましい。
As the extraction method, known methods such as kneader extraction, stirring extraction (batch extraction), countercurrent extraction (drip extraction), and column extraction can be adopted.
The extraction conditions can be appropriately selected depending on the extraction method, and for example, an aqueous solvent can be used as the extraction solvent. Here, the "aqueous solvent" as used herein refers to a solvent containing water, and the content of water in the aqueous solvent is usually 1 to 100% by mass, preferably 30 to 100% by mass. Examples of the aqueous solvent include water, an aqueous solution of an organic solvent, carbonated water and the like. Examples of the organic solvent include alcohols, ketones, esters and the like. Considering the use in foods, alcohol is preferable, and ethanol is more preferable. Of these, water is preferable as the aqueous solvent. Examples of water include tap water, natural water, distilled water, ion-exchanged water and the like. Of these, ion-exchanged water is preferable from the viewpoint of taste.
水系溶媒のpH(20℃)は、通常4〜10、好ましくは5〜7である。なお、所望のpHとするために、水系溶媒にpH調整剤を添加してもよい。
水系溶媒の温度は、通常25〜100℃、好ましくは50〜100℃、更に好ましくは80〜99℃である。
抽出倍率及び抽出時間は、抽出方法やスケールにより一様ではないが、例えば、抽出倍率は通常1〜50倍であり、抽出時間は通常5〜60分である。
抽出後、濾過、遠心分離、膜処理等の公知の固液分離手段により、緑茶葉と原料緑茶抽出物とを分離することができる。
The pH (20 ° C.) of the aqueous solvent is usually 4 to 10, preferably 5 to 7. A pH adjuster may be added to the aqueous solvent in order to obtain a desired pH.
The temperature of the aqueous solvent is usually 25 to 100 ° C, preferably 50 to 100 ° C, and more preferably 80 to 99 ° C.
The extraction magnification and the extraction time are not uniform depending on the extraction method and scale, but for example, the extraction magnification is usually 1 to 50 times, and the extraction time is usually 5 to 60 minutes.
After extraction, the green tea leaves and the raw green tea extract can be separated by known solid-liquid separation means such as filtration, centrifugation, and membrane treatment.
また、原料緑茶抽出物として市販品を使用してもよい。例えば、三井農林社製の「ポリフェノン」、伊藤園社製の「テアフラン」、太陽化学社製の「サンフェノン」等が挙げられる。 Further, a commercially available product may be used as the raw material green tea extract. For example, "Polyphenone" manufactured by Mitsui Norin Co., Ltd., "Theafran" manufactured by Ito En Co., Ltd., "Sanphenon" manufactured by Taiyo Kagaku Co., Ltd., and the like can be mentioned.
精製方法としては、固形分中の(A)非重合体カテキン類の含有量が40質量%以上となれば特に限定されないが、風味の観点、本発明の効果を享受しやすい観点から、下記(i)〜(iii)のいずれか一の方法、あるいは二以上の組み合わせを挙げることができる。
(i)原料緑茶抽出物を、水又は有機溶媒水溶液(例えば、エタノール水溶液)に懸濁し、生じた沈殿を除去する方法。
(ii)原料緑茶抽出物を、活性炭、酸性白土及び活性白土から選択される少なくとも1種の吸着剤と接触させる方法。
(iii)原料緑茶抽出物を、合成吸着剤又はイオン交換樹脂と接触させる方法。
The purification method is not particularly limited as long as the content of the (A) non-polymer catechins in the solid content is 40% by mass or more, but from the viewpoint of flavor and the viewpoint of easily enjoying the effects of the present invention, the following ( i) Any one of the methods (iii) to (iii), or a combination of two or more can be mentioned.
(I) A method of suspending a raw material green tea extract in water or an aqueous solution of an organic solvent (for example, an aqueous solution of ethanol) to remove the resulting precipitate.
(Ii) A method in which a raw material green tea extract is brought into contact with at least one adsorbent selected from activated carbon, acid clay and activated clay.
(Iii) A method of contacting a raw material green tea extract with a synthetic adsorbent or an ion exchange resin.
上記(i)の方法については、例えば、特開2004−147508号公報、特開2004−149416号公報等を参照することができる。また、上記(ii)の方法については、例えば、特開2004−222719号公報、特開2005−270094号公報等を参照することができる。更に、上記(iii)の方法については、例えば、特開2004−222592号公報、特開2006−8580号公報、特開2006−160656号公報等を参照することができる。
また、上記(i)〜(iii)の方法においては、原料緑茶抽出物としてタンナーゼ処理したものを使用してもよく、また(i)〜(iii)のいずれか一以上の方法により処理した後、タンナーゼ処理することもできる。ここで、「タンナーゼ処理」とは、緑茶抽出物を、タンナーゼ活性を有する酵素と接触させることをいう。なお、タンナーゼ処理における具体的な操作方法は公知の方法を採用することが可能であり、例えば、特開2004−321105号公報に記載の方法を挙げることができる。
For the method (i) above, for example, JP-A-2004-147508, JP-A-2004-149416 and the like can be referred to. Further, for the method (ii) above, for example, Japanese Patent Application Laid-Open No. 2004-222719, Japanese Patent Application Laid-Open No. 2005-2770094 and the like can be referred to. Further, for the method (iii) above, for example, JP-A-2004-222592, JP-A-2006-8580, JP-A-2006-160656 and the like can be referred to.
Further, in the above methods (i) to (iii), a tannase-treated extract may be used as the raw material green tea extract, or after the treatment by any one or more of the methods (i) to (iii). , Can also be treated with tannase. Here, "tannase treatment" means contacting the green tea extract with an enzyme having tannase activity. As a specific operation method in the tannase treatment, a known method can be adopted, and examples thereof include the method described in JP-A-2004-321105.
このようにして得られた(a)緑茶抽出物は、固形分中の(A)非重合体カテキン類の含有量が40質量%以上であるが、風味の観点、本発明の効果を享受しやすい観点から、固形分中の(A)非重合体カテキン類の含有量が45質量%以上であることが好ましく、50質量%以上がより好ましく、55質量%以上が更に好ましい。なお、固形分中の(A)非重合体カテキン類の含有量の上限値は100質量%であっても構わないが、生産効率の観点から、95質量%以下が好ましく、90質量%以下がより好ましく、85質量%以下が更に好ましい。 The green tea extract thus obtained has a content of (A) non-polymer catechins in the solid content of 40% by mass or more, but enjoys the effects of the present invention from the viewpoint of flavor. From the viewpoint of ease, the content of the (A) non-polymer catechins in the solid content is preferably 45% by mass or more, more preferably 50% by mass or more, still more preferably 55% by mass or more. The upper limit of the content of the (A) non-polymer catechins in the solid content may be 100% by mass, but from the viewpoint of production efficiency, 95% by mass or less is preferable, and 90% by mass or less is preferable. More preferably, 85% by mass or less is further preferable.
(a)緑茶抽出物は、そのままでも、濃縮又は乾燥して使用しても構わない。濃縮方法としては、例えば、常圧にて溶媒の蒸発を行う常圧濃縮法、減圧にて溶媒の蒸発を行う減圧濃縮法、膜分離により溶媒を除去する膜濃縮法等が挙げられる。また、乾燥方法としては、例えば、噴霧乾燥、ドラム乾燥、凍結乾燥等の公知の方法を採用することができる。 (A) The green tea extract may be used as it is, or after being concentrated or dried. Examples of the concentration method include a normal pressure concentration method in which the solvent is evaporated at normal pressure, a vacuum concentration method in which the solvent is evaporated under reduced pressure, and a membrane concentration method in which the solvent is removed by membrane separation. Further, as the drying method, for example, known methods such as spray drying, drum drying, freeze drying and the like can be adopted.
次に、(a)緑茶抽出物と(B)金属イオンとを所定の割合で、水性溶媒の存在下に混合して混合液を調製する。なお、成分(B)は、塩の形態で含有させてもよく、例えば、無機塩、有機酸塩の形態で含有させることができる。塩の具体例は、上記において説明したとおりである。
(a)緑茶抽出物、(B)金属イオンの混合順序は特に限定されず、これらを任意の順序で添加しても、両者を同時に添加してもよく、乾燥前の混合液中に水系溶媒と、(a)緑茶抽出物と、(B)金属イオンとが共存した状態にあればよい。
Next, (a) green tea extract and (B) metal ions are mixed at a predetermined ratio in the presence of an aqueous solvent to prepare a mixed solution. The component (B) may be contained in the form of a salt, for example, an inorganic salt or an organic acid salt. Specific examples of the salt are as described above.
The mixing order of (a) green tea extract and (B) metal ions is not particularly limited, and these may be added in any order or both may be added at the same time, and an aqueous solvent may be added to the mixed solution before drying. It suffices if (a) the green tea extract and (B) the metal ion coexist.
(a)緑茶抽出物と(B)金属イオンは、(A)非重合体カテキン類に対する(B)金属イオンの質量比[(B)/(A)]が0.005以上となる割合で混合するが、かかる質量比[(B)/(A)]は、長期保存したときの色相変化の抑制の観点から、0.010以上が好ましく、0.02以上がより好ましく、0.04以上が更に好ましく、0.09以上がより更に好ましい。また、かかる質量比[(B)/(A)]は、風味、本発明の効果を享受しやすい点から、0.3以下が好ましく、0.25以下がより好ましく、0.2以下が更に好ましい。かかる質量比[(B)/(A)]の範囲としては、好ましくは0.005〜0.3であり、より好ましくは0.010〜0.3であり、更に好ましくは0.02〜0.3であり、より更に好ましくは0.04〜0.25であり、殊更に好ましくは0.09〜0.2である。 (A) Green tea extract and (B) metal ions are mixed at a ratio of (A) mass ratio of (B) metal ions to non-polymer catechins [(B) / (A)] of 0.005 or more. However, the mass ratio [(B) / (A)] is preferably 0.010 or more, more preferably 0.02 or more, and 0.04 or more, from the viewpoint of suppressing color change during long-term storage. More preferably, 0.09 or more is even more preferable. Further, the mass ratio [(B) / (A)] is preferably 0.3 or less, more preferably 0.25 or less, and further preferably 0.2 or less, from the viewpoint of easily enjoying the flavor and the effect of the present invention. preferable. The range of the mass ratio [(B) / (A)] is preferably 0.005 to 0.3, more preferably 0.010 to 0.3, and further preferably 0.02 to 0. It is 0.3, more preferably 0.04 to 0.25, and even more preferably 0.09 to 0.2.
水系溶媒としては、例えば、水、有機溶媒水溶液等を挙げることができる。水及び有機溶媒の具体例としては、前述と同様のものを挙げられる。なお、有機溶媒水溶液は、該有機溶媒水溶液中に水が1質量%以上、好ましくは30質量%以上含まれていればよい。中でも、水系溶媒としては、長期保存したときの色相変化の抑制の観点から、水が好ましく、イオン交換水が更に好ましい。 Examples of the aqueous solvent include water, an aqueous solution of an organic solvent, and the like. Specific examples of the water and the organic solvent include the same as described above. The organic solvent aqueous solution may contain 1% by mass or more, preferably 30% by mass or more of water in the organic solvent aqueous solution. Among them, as the aqueous solvent, water is preferable, and ion-exchanged water is more preferable, from the viewpoint of suppressing hue change during long-term storage.
水系溶媒の使用量は、長期保存したときの色相変化の抑制の観点から、混合液中に(A)非重合体カテキン類を1質量%以上含有するように調整することが好ましく、2.5質量%以上がより好ましく、5質量%以上がより好ましく、7質量%以上が更に好ましく、10質量%以上がより更に好ましく、そして同様の観点から、30質量%以下含有するように調整することが好ましく、25質量%以下がより好ましく、20質量%以下が更に好ましく、15質量%以下がより更に好ましい。かかる混合液中の(A)非重合体カテキン類の含有量の範囲としては、好ましくは1〜30質量%、より好ましくは2.5〜25質量%、更に好ましくは5〜20質量%、より更に好ましくは7〜20質量%、より更に好ましくは10〜15質量%である。 The amount of the aqueous solvent used is preferably adjusted so that the mixed solution contains 1% by mass or more of the (A) non-polymer catechins from the viewpoint of suppressing the change in hue during long-term storage. It is more preferably 5% by mass or more, further preferably 7% by mass or more, further preferably 10% by mass or more, and from the same viewpoint, it may be adjusted to contain 30% by mass or less. Preferably, it is more preferably 25% by mass or less, further preferably 20% by mass or less, still more preferably 15% by mass or less. The range of the content of the (A) non-polymer catechins in the mixed solution is preferably 1 to 30% by mass, more preferably 2.5 to 25% by mass, still more preferably 5 to 20% by mass, and more. It is more preferably 7 to 20% by mass, and even more preferably 10 to 15% by mass.
(a)緑茶抽出物及び(B)金属イオンのいずれにも溶媒が含まれていない場合には、水系溶媒、(a)緑茶抽出物と(B)金属イオンとを混合する際に、水系溶媒の使用量を、混合液中の(A)非重合体カテキン類の含有量が上記範囲内となるように調整すればよい。また、所定量の水系溶媒と、(a)緑茶抽出物と、(B)金属イオンとを混合し、追加の水系溶媒を添加して混合液中の(A)非重合体カテキン類の含有量が上記範囲内となるように調整することもできる。一方、(a)緑茶抽出物及び(B)金属イオンのいずれか1以上に溶媒が含まれている場合には、当該溶媒量を考慮して混合液中の(A)非重合体カテキン類の含有量が上記範囲内となるように水系溶媒の使用量を調整することができる。なお、(a)緑茶抽出物及び(B)金属イオンのいずれか1以上に含まれている溶媒量によって、混合液中の(A)非重合体カテキン類の含有量が上記要件を満たす場合には、その溶媒中に水が含まれていれば、(a)緑茶抽出物と(B)金属イオンとをそのまま混合すればよい。また、(a)緑茶抽出物及び(B)金属イオンのいずれか1以上に含まれている溶媒量によって、混合液中の(A)非重合体カテキン類の含有量が上記要件を満たす場合において、溶媒中に水が含まれていない場合には、その溶媒を濃縮又は除去した後、水系溶媒を添加して混合液中の(A)非重合体カテキン類の含有量が上記範囲内となるように調整することができる。 When neither (a) green tea extract nor (B) metal ion contains a solvent, an aqueous solvent is used. When mixing (a) green tea extract and (B) metal ion, an aqueous solvent is used. The amount of (A) non-polymer catechins in the mixed solution may be adjusted so as to be within the above range. Further, a predetermined amount of an aqueous solvent, (a) green tea extract, and (B) metal ions are mixed, and an additional aqueous solvent is added to add the content of (A) non-polymer catechins in the mixed solution. Can also be adjusted to be within the above range. On the other hand, when any one or more of (a) green tea extract and (B) metal ion contains a solvent, the amount of the solvent is taken into consideration in consideration of the amount of the (A) non-polymer catechins in the mixed solution. The amount of the aqueous solvent used can be adjusted so that the content is within the above range. When the content of (A) non-polymer catechins in the mixed solution satisfies the above requirements depending on the amount of solvent contained in any one or more of (a) green tea extract and (B) metal ion. If water is contained in the solvent, (a) green tea extract and (B) metal ions may be mixed as they are. Further, when the content of (A) non-polymer catechins in the mixed solution satisfies the above requirements depending on the amount of the solvent contained in any one or more of (a) green tea extract and (B) metal ion. If water is not contained in the solvent, the solvent is concentrated or removed, and then an aqueous solvent is added to bring the content of (A) non-polymer catechins in the mixed solution within the above range. Can be adjusted as follows.
混合方法としては、例えば、撹拌、震盪等の適宜の方法を採用することが可能であり、特に限定されない。
混合温度は、長期保存したときの色相変化の抑制の観点から、15℃以上が好ましく、18℃以上がより好ましく、20℃以上が更に好ましく、また風味の観点から、40℃以下が好ましく、35℃以下がより好ましく、30℃以下が更に好ましい。混合温度の範囲としては、好ましくは15〜40℃、より好ましくは18〜35℃、更に好ましくは20〜30℃である。
混合時間は、長期保存したときの色相変化の抑制の観点から、3分以上が好ましく、5分以上がより好ましく、6分以上が更に好ましく、また生産効率の観点から、90分以下が好ましく、60分以下がより好ましく、40分以下が更に好ましい。混合時間の範囲としては、好ましくは3〜90分、より好ましくは5〜60分、更に好ましくは6〜40分である。
As the mixing method, for example, an appropriate method such as stirring or shaking can be adopted, and the mixing method is not particularly limited.
The mixing temperature is preferably 15 ° C. or higher, more preferably 18 ° C. or higher, further preferably 20 ° C. or higher, and preferably 40 ° C. or lower from the viewpoint of flavor, from the viewpoint of suppressing hue change during long-term storage. The temperature is more preferably 30 ° C or lower, and even more preferably 30 ° C or lower. The mixing temperature range is preferably 15 to 40 ° C, more preferably 18 to 35 ° C, and even more preferably 20 to 30 ° C.
The mixing time is preferably 3 minutes or more, more preferably 5 minutes or more, further preferably 6 minutes or more, and preferably 90 minutes or less from the viewpoint of production efficiency, from the viewpoint of suppressing hue change during long-term storage. 60 minutes or less is more preferable, and 40 minutes or less is further preferable. The mixing time range is preferably 3 to 90 minutes, more preferably 5 to 60 minutes, and even more preferably 6 to 40 minutes.
次に、混合液を乾燥する。
乾燥方法としては、公知の方法を採用することができる。例えば、噴霧乾燥、ドラム乾燥、凍結乾燥等が挙げられる。乾燥は、粉末緑茶抽出組成物の揮発分が上記範囲内となるように行い、乾燥時間は適宜選択することができる。
また、公知の造粒法により造粒物としてもよい。造粒方法としては、例えば、噴霧造粒、流動層造粒、圧縮造粒、転動造粒、撹拌造粒、押出造粒、粉末被覆造粒等が挙げられる。なお、造粒条件は、造粒方法により適宜選択することができる。
The mixture is then dried.
As a drying method, a known method can be adopted. For example, spray drying, drum drying, freeze drying and the like can be mentioned. The drying is carried out so that the volatile content of the powdered green tea extraction composition is within the above range, and the drying time can be appropriately selected.
Further, it may be a granulated product by a known granulation method. Examples of the granulation method include spray granulation, fluidized bed granulation, compression granulation, rolling granulation, stirring granulation, extrusion granulation, powder-coated granulation and the like. The granulation conditions can be appropriately selected depending on the granulation method.
上記の実施形態に関し、以下に本発明の好ましい態様を更に開示する。
<1> 次の成分(A)及び(B):
(A)非重合体カテキン類、及び
(B)金属イオン
を含有し、
成分(A)の含有量が40〜95質量%であり、かつ
成分(A)に対する成分(B)の質量比[(B)/(A)]が0.010〜0.3である、粉末緑茶抽出組成物。
With respect to the above embodiments, the preferred embodiments of the present invention will be further disclosed below.
<1> The following components (A) and (B):
Contains (A) non-polymer catechins and (B) metal ions,
A powder having a content of the component (A) of 40 to 95% by mass and a mass ratio of the component (B) to the component (A) [(B) / (A)] of 0.010 to 0.3. Green tea extraction composition.
<2> 次の成分(A)及び(B):
(A)非重合体カテキン類、及び
(B)金属イオン
を含有し、
成分(A)の含有量が40〜95質量%であり、
成分(B)の含有量が1.0〜12質量%であり、かつ
成分(A)に対する成分(B)の質量比[(B)/(A)]が0.005以上である、
粉末緑茶抽出組成物。
<2> The following components (A) and (B):
Contains (A) non-polymer catechins and (B) metal ions,
The content of the component (A) is 40 to 95% by mass, and the content is 40 to 95% by mass.
The content of the component (B) is 1.0 to 12% by mass, and the mass ratio [(B) / (A)] of the component (B) to the component (A) is 0.005 or more.
Powdered green tea extraction composition.
<3> 次の成分(A)及び(B):
(A)非重合体カテキン類、及び
(B)金属イオン
を含有し、
成分(A)の含有量が40質量%以上であり、
成分(B)の含有量が1.0〜12質量%であり、かつ
成分(A)に対する成分(B)の質量比[(B)/(A)]が0.010〜0.3である、粉末緑茶抽出組成物。
<3> The following components (A) and (B):
Contains (A) non-polymer catechins and (B) metal ions,
The content of the component (A) is 40% by mass or more, and the content is 40% by mass or more.
The content of the component (B) is 1.0 to 12% by mass, and the mass ratio [(B) / (A)] of the component (B) to the component (A) is 0.010 to 0.3. , Powdered green tea extraction composition.
<4> 次の成分(A)及び(B):
(A)非重合体カテキン類、及び
(B)金属イオン
を含有し、
成分(A)の含有量が40〜95質量%であり、
成分(B)の含有量が1.0〜12質量%であり、かつ
成分(A)に対する成分(B)の質量比[(B)/(A)]が0.010〜0.3である、粉末緑茶抽出組成物。
<4> The following components (A) and (B):
Contains (A) non-polymer catechins and (B) metal ions,
The content of the component (A) is 40 to 95% by mass, and the content is 40 to 95% by mass.
The content of the component (B) is 1.0 to 12% by mass, and the mass ratio [(B) / (A)] of the component (B) to the component (A) is 0.010 to 0.3. , Powdered green tea extraction composition.
<5> 成分(B)として1価の金属イオン及び2価の金属イオンから選ばれる1種又は2種以上を含む、前記<1>〜<4>のいずれか一に記載の粉末緑茶抽出組成物。
<6> 成分(B)としてナトリウムイオン、カリウムイオン及びカルシウムイオンから選択される1種又は2種以上を含む、前記<1>〜<4>のいずれか一に記載の粉末緑茶抽出組成物。
<7> 揮発分が0.6〜5.0質量%である、前記<1>〜<4>のいずれか一に記載の粉末緑茶抽出組成物。
<8> 平均粒子径が1〜1000μmである、前記<1>〜<4>のいずれか一に記載の粉末緑茶抽出組成物。
<5> The powdered green tea extraction composition according to any one of <1> to <4> above, which comprises one or more selected from monovalent metal ions and divalent metal ions as the component (B). Stuff.
<6> The powdered green tea extraction composition according to any one of <1> to <4> above, which comprises one or more selected from sodium ion, potassium ion and calcium ion as the component (B).
<7> The powdered green tea extraction composition according to any one of <1> to <4>, wherein the volatile content is 0.6 to 5.0% by mass.
<8> The powdered green tea extraction composition according to any one of <1> to <4>, wherein the average particle size is 1 to 1000 μm.
<9> 固形分中の(A)非重合体カテキン類の含有量が40〜95質量%である緑茶抽出物と、(B)金属イオンとを、成分(A)に対する成分(B)の質量比[(B)/(A)]が0.010〜0.3となるように水系溶媒の存在下に混合した後、当該混合液を乾燥する工程を含む、粉末緑茶抽出組成物の製造方法。 <9> The mass of the component (B) with respect to the component (A) of the green tea extract in which the content of the (A) non-polymer catechins in the solid content is 40 to 95% by mass and the (B) metal ion. A method for producing a powdered green tea extraction composition, which comprises a step of mixing in the presence of an aqueous solvent so that the ratio [(B) / (A)] is 0.010 to 0.3, and then drying the mixed solution. ..
<10> 固形分中の(A)非重合体カテキン類の含有量が40〜95質量%である緑茶抽出物と、(B)金属イオン0.2〜14質量%とを、成分(A)に対する成分(B)の質量比[(B)/(A)]が0.005以上となるように水系溶媒の存在下に混合した後、当該混合液を乾燥する工程を含む、粉末緑茶抽出組成物の製造方法。 <10> A green tea extract in which the content of (A) non-polymer catechins in the solid content is 40 to 95% by mass and (B) 0.2 to 14% by mass of metal ions are contained in the component (A). Powdered green tea extraction composition including a step of mixing in the presence of an aqueous solvent so that the mass ratio of the component (B) to (B) / (A)] is 0.005 or more, and then drying the mixed solution. How to make things.
<11> 水系溶媒が、水又は有機溶媒水溶液である、前記<9>又は<10>記載の粉末緑茶抽出組成物の製造方法。
<12> 水系溶媒の使用量が、混合液中に成分(A)が1〜30質量%となる量である、前記<9>又は<10>記載の粉末緑茶抽出組成物の製造方法。
<13> 混合時間が、3〜90分である、前記<9>又は<10>記載の粉末緑茶抽出組成物の製造方法。
<11> The method for producing a powdered green tea extraction composition according to <9> or <10>, wherein the aqueous solvent is water or an aqueous solution of an organic solvent.
<12> The method for producing a powdered green tea extraction composition according to <9> or <10>, wherein the amount of the aqueous solvent used is such that the component (A) is 1 to 30% by mass in the mixed liquid.
<13> The method for producing a powdered green tea extraction composition according to <9> or <10>, wherein the mixing time is 3 to 90 minutes.
1.非重合体カテキン類の分析
純水で溶解希釈した試料を、島津製作所製、高速液体クロマトグラフ(型式SCL−10AVP)を用い、オクタデシル基導入液体クロマトグラフ用パックドカラム(L−カラムTM ODS、4.6mmφ×250mm:財団法人 化学物質評価研究機構製)を装着し、カラム温度35℃でグラジエント法により測定した。移動相A液は酢酸を0.1mol/L含有する蒸留水溶液、B液は酢酸を0.1mol/L含有するアセトニトリル溶液とし、流速は1mL/分、試料注入量は10μL、UV検出器波長は280nmの条件で行った。なお、グラジエント条件は以下の通りである。
1. 1. Analysis of non-polymer catechins A sample dissolved and diluted in pure water was used by a high performance liquid chromatograph (model SCL-10AVP) manufactured by Shimadzu Corporation, and a packed column for an octadecyl group-introduced liquid chromatograph (L-column TM ODS, 4). .6 mmφ × 250 mm: manufactured by Chemical Substance Evaluation and Research Organization) was attached, and the measurement was performed by the gradient method at a column temperature of 35 ° C. The mobile phase A solution is a distilled aqueous solution containing 0.1 mol / L of acetic acid, the B solution is an acetonitrile solution containing 0.1 mol / L of acetic acid, the flow velocity is 1 mL / min, the sample injection amount is 10 μL, and the UV detector wavelength is It was carried out under the condition of 280 nm. The gradient conditions are as follows.
濃度勾配条件(体積%)
時間 A液濃度 B液濃度
0分 97% 3%
5分 97% 3%
37分 80% 20%
43分 80% 20%
43.5分 0% 100%
48.5分 0% 100%
49分 97% 3%
60分 97% 3%
Concentration gradient condition (% by volume)
Time A liquid concentration B liquid concentration 0 minutes 97% 3%
5 minutes 97% 3%
37 minutes 80% 20%
43 minutes 80% 20%
43.5 minutes 0% 100%
48.5 minutes 0% 100%
49 minutes 97% 3%
60 minutes 97% 3%
2.金属イオンの分析
試料2gに10%塩酸5mLを加え、水浴上で蒸発乾固する。さらに10%塩酸5mLを加え、加温した後、全量をメスフラスコに濾過し、水で定容する。1%塩酸を用いて、検量線の範囲内に入るように、適当な濃度に希釈し、20000ppmのストロンチウム液2.5mLを加え、定容したものを試験溶液とする。原子吸光光度計を用いて、試験溶液の吸光度を測定し、あらかじめ作成した検量線から金属の定量を行う。
2. Analysis of metal ions Add 5 mL of 10% hydrochloric acid to 2 g of the sample and evaporate to dryness on a water bath. Further, 5 mL of 10% hydrochloric acid is added and heated, and then the whole volume is filtered into a volumetric flask and the volume is adjusted with water. Dilute to an appropriate concentration with 1% hydrochloric acid so that it is within the range of the calibration curve, add 2.5 mL of 20000 ppm strontium solution, and use the constant volume as the test solution. The absorbance of the test solution is measured using an atomic absorption spectrophotometer, and the metal is quantified from the calibration curve prepared in advance.
・原子吸光光度計:Z−2310(HITACHI製)
・フレーム:空気−アセチレン
・測定波長:589.0nm(ナトリウム)、766.5nm(カリウム)、422.7nm(カルシウム)
-Atomic absorption spectrophotometer: Z-2310 (manufactured by HITACHI)
-Frame: Air-acetylene-Measurement wavelength: 589.0 nm (sodium), 766.5 nm (potassium), 422.7 nm (calcium)
3.色相変化の評価
分光光度計(形式Color Meter ZE-2000、日本電色工業社製)を使用し、粉末試料を30φの円形セルに入れてL*a*b*表色系のa*値を反射測定した。37℃/50%RHの雰囲気下で8週間保存した後の粉末緑茶抽出組成物のa*値と、製造直後の粉末緑茶抽出組成物のa1 *値との差分の絶対値Δa*(|a*−a1 *|)を求めた。
3. 3. Evaluation of hue change Using a spectrophotometer (type Color Meter ZE-2000, manufactured by Nippon Denshoku Kogyo Co., Ltd.), put a powder sample in a 30φ circular cell and set the a * value of the L * a * b * color system. The reflection was measured. Absolute value Δa * (|) of the difference between the a * value of the powdered green tea extract composition after storage in an atmosphere of 37 ° C./50% RH for 8 weeks and the a 1 * value of the powdered green tea extract composition immediately after production. a * −a 1 * |) was obtained.
製造例1
〔緑茶抽出物の製造〕
ケニア産の乾燥緑茶葉3kgを90℃の熱水30Lにて30分間抽出後、濾過し、得られた緑茶抽出液をスプレードライにて乾燥し、粉末状の緑茶抽出物(I)を得た。緑茶抽出物(I)は、(A)非重合体カテキン類の含有量が38.3質量%であった。
92.2質量%のエタノール水溶液800gに、得られた緑茶抽出物(I)200gを投入し、次いで酸性白土(ミズカエース#600、水澤化学社製)を100g、ろ過助剤(ソルカフロック、栗田工業社製)12.6gを添加した。その後、25℃にて6時間撹拌した。次に、プレコート剤を堆積させた2号濾紙にてろ過した。次に、ろ過液をエタノール濃度が60質量%になるように加水した後、遠心分離を行い、上澄み液を回収した。次に、上澄み液を活性炭(SG−K、フタムラ化学製)24gが充填されたカラムに通液し、回収液をトッピングしエタノールを留去することで、緑茶抽出物(II)を得た。得られた緑茶抽出物(II)は、(A)非重合体カテキン類の含有量が14.8質量%であり、固形分中の(A)非重合体カテキン類の含有量が62.5質量%であった。
Manufacturing example 1
[Manufacturing of green tea extract]
3 kg of dried green tea leaves from Kenya were extracted with 30 L of hot water at 90 ° C. for 30 minutes, filtered, and the obtained green tea extract was spray-dried to obtain a powdered green tea extract (I). .. The green tea extract (I) had a content of (A) non-polymer catechins of 38.3% by mass.
200 g of the obtained green tea extract (I) was added to 800 g of a 92.2 mass% ethanol aqueous solution, followed by 100 g of acid clay (Mizuka Ace # 600, manufactured by Mizusawa Industrial Chemicals), and a filtration aid (Solkaflock, Kurita Water Industries, Ltd.). 12.6 g was added. Then, the mixture was stirred at 25 ° C. for 6 hours. Next, it was filtered through No. 2 filter paper on which the precoating agent was deposited. Next, the filtrate was hydrated to an ethanol concentration of 60% by mass, and then centrifuged to recover the supernatant. Next, the supernatant was passed through a column packed with 24 g of activated carbon (SG-K, manufactured by Futamura Chemical Co., Ltd.), topped with the recovered liquid, and ethanol was distilled off to obtain a green tea extract (II). The obtained green tea extract (II) has a content of (A) non-polymer catechins of 14.8% by mass and a content of (A) non-polymer catechins in the solid content of 62.5. It was mass%.
実施例1〜6
緑茶抽出物(II)と、表1に示す金属塩とを、(A)非重合体カテキン類に対する(B)金属イオンの質量比[(B)/(A)]が表1に示す割合となるように混合した後、25℃にて30分間撹拌した。その後、混合液をスプレードライにて、揮発分が表1に示す割合となるまで乾燥し、粉末緑茶抽出組成物を得た。得られた粉末緑茶抽出組成物について分析を行った。また、粉末緑茶抽出組成物2gを用い、色相変化の評価を行った。その結果を表1に示す。
Examples 1-6
The ratio of the green tea extract (II) and the metal salt shown in Table 1 to the mass ratio of (B) metal ion to (A) non-polymer catechins [(B) / (A)] is shown in Table 1. After mixing, the mixture was stirred at 25 ° C. for 30 minutes. Then, the mixed solution was spray-dried until the volatile content became the ratio shown in Table 1 to obtain a powdered green tea extraction composition. The obtained powdered green tea extraction composition was analyzed. Moreover, the hue change was evaluated using 2 g of the powdered green tea extraction composition. The results are shown in Table 1.
比較例1
金属イオンを添加しなかったこと以外は、実施例1と同様の操作により粉末緑茶抽出組成物を得た。得られた粉末緑茶抽出組成物について、実施例1と同様に分析、色相変化の評価を行った。その結果を表1に示す。
Comparative Example 1
A powdered green tea extraction composition was obtained by the same operation as in Example 1 except that no metal ion was added. The obtained powdered green tea extraction composition was analyzed and evaluated for hue change in the same manner as in Example 1. The results are shown in Table 1.
表1から、(A)非重合体カテキン類の含有量を40質量%以上とした際に、(A)非重合体カテキン類に対する(B)金属イオンの質量比[(B)/(A)]を0.005以上に制御することで、長期保存したときの色相変化が抑制された粉末緑茶抽出組成物が得られることがわかる。 From Table 1, when the content of (A) non-polymer catechins is 40% by mass or more, (A) mass ratio of (B) metal ions to non-polymer catechins [(B) / (A)). ] Is controlled to 0.005 or more, it can be seen that a powdered green tea extraction composition in which the hue change during long-term storage is suppressed can be obtained.
Claims (8)
(A)非重合体カテキン類、及び
(B)金属イオン
を含有し、
成分(A)の含有量が40質量%以上であり、かつ
成分(A)に対する成分(B)の質量比[(B)/(A)]が0.005以上である、
粉末緑茶抽出組成物。 The following components (A) and (B):
Contains (A) non-polymer catechins and (B) metal ions,
The content of the component (A) is 40% by mass or more, and the mass ratio [(B) / (A)] of the component (B) to the component (A) is 0.005 or more.
Powdered green tea extraction composition.
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JPH11266841A (en) * | 1998-03-19 | 1999-10-05 | Fukujuen:Kk | Barley-tea bag containing catechin-enriched green tea |
JP2007159541A (en) * | 2005-12-17 | 2007-06-28 | Pharma Foods International Co Ltd | High-concentration solution containing catechins and method for producing the same |
JP2009201384A (en) * | 2008-02-26 | 2009-09-10 | Ito En Ltd | Green tea extract, its use and production method |
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JP2014140354A (en) * | 2012-12-28 | 2014-08-07 | Kao Corp | Process for producing tea extract |
JP2015109829A (en) * | 2013-10-29 | 2015-06-18 | 花王株式会社 | Green tea extract composition |
JP2016208960A (en) * | 2015-04-28 | 2016-12-15 | 花王株式会社 | Green tea extraction composition |
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2019
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JPH09322710A (en) * | 1996-06-03 | 1997-12-16 | Minato Seiyaku Kk | Production of tea extract containing catechins |
JPH11266841A (en) * | 1998-03-19 | 1999-10-05 | Fukujuen:Kk | Barley-tea bag containing catechin-enriched green tea |
JP2007159541A (en) * | 2005-12-17 | 2007-06-28 | Pharma Foods International Co Ltd | High-concentration solution containing catechins and method for producing the same |
JP2009201384A (en) * | 2008-02-26 | 2009-09-10 | Ito En Ltd | Green tea extract, its use and production method |
JP2012115229A (en) * | 2010-12-03 | 2012-06-21 | Kao Corp | Purified tea extract |
JP2014140354A (en) * | 2012-12-28 | 2014-08-07 | Kao Corp | Process for producing tea extract |
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JP2016208960A (en) * | 2015-04-28 | 2016-12-15 | 花王株式会社 | Green tea extraction composition |
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