JP2005304323A - Method for preventing generation of odd smell component in vitamin b1-containing or its derivative-containing acidic beverage composition - Google Patents
Method for preventing generation of odd smell component in vitamin b1-containing or its derivative-containing acidic beverage composition Download PDFInfo
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- JP2005304323A JP2005304323A JP2004122647A JP2004122647A JP2005304323A JP 2005304323 A JP2005304323 A JP 2005304323A JP 2004122647 A JP2004122647 A JP 2004122647A JP 2004122647 A JP2004122647 A JP 2004122647A JP 2005304323 A JP2005304323 A JP 2005304323A
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- vitamin
- derivative
- tea extract
- generation
- beverage composition
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- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 title claims abstract description 45
- 239000000203 mixture Substances 0.000 title claims abstract description 32
- 238000000034 method Methods 0.000 title claims abstract description 17
- 230000002378 acidificating effect Effects 0.000 title claims abstract description 16
- 235000013361 beverage Nutrition 0.000 title abstract description 7
- 229930003451 Vitamin B1 Natural products 0.000 claims abstract description 40
- 229960003495 thiamine Drugs 0.000 claims abstract description 40
- 235000010374 vitamin B1 Nutrition 0.000 claims abstract description 40
- 239000011691 vitamin B1 Substances 0.000 claims abstract description 40
- 239000000284 extract Substances 0.000 claims abstract description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000002798 polar solvent Substances 0.000 claims abstract description 7
- 241001122767 Theaceae Species 0.000 claims abstract 4
- 239000000796 flavoring agent Substances 0.000 claims description 22
- 230000035622 drinking Effects 0.000 claims description 14
- RUYNUXHHUVUINQ-UHFFFAOYSA-N 2-Methyl-3-furanthiol Chemical compound CC=1OC=CC=1S RUYNUXHHUVUINQ-UHFFFAOYSA-N 0.000 claims description 12
- 238000000605 extraction Methods 0.000 claims description 10
- 150000004347 all-trans-retinol derivatives Chemical class 0.000 claims description 9
- 238000000354 decomposition reaction Methods 0.000 claims description 5
- 244000269722 Thea sinensis Species 0.000 description 37
- 235000013616 tea Nutrition 0.000 description 24
- 229940088594 vitamin Drugs 0.000 description 16
- 229930003231 vitamin Natural products 0.000 description 16
- 235000013343 vitamin Nutrition 0.000 description 15
- 239000011782 vitamin Substances 0.000 description 15
- 150000003722 vitamin derivatives Chemical class 0.000 description 15
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 235000006468 Thea sinensis Nutrition 0.000 description 11
- 235000020688 green tea extract Nutrition 0.000 description 11
- 235000020279 black tea Nutrition 0.000 description 10
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 238000003860 storage Methods 0.000 description 9
- 229940094952 green tea extract Drugs 0.000 description 8
- 229940074391 gallic acid Drugs 0.000 description 7
- 235000004515 gallic acid Nutrition 0.000 description 7
- CWVRJTMFETXNAD-FWCWNIRPSA-N 3-O-Caffeoylquinic acid Natural products O[C@H]1[C@@H](O)C[C@@](O)(C(O)=O)C[C@H]1OC(=O)\C=C\C1=CC=C(O)C(O)=C1 CWVRJTMFETXNAD-FWCWNIRPSA-N 0.000 description 6
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 6
- PZIRUHCJZBGLDY-UHFFFAOYSA-N Caffeoylquinic acid Natural products CC(CCC(=O)C(C)C1C(=O)CC2C3CC(O)C4CC(O)CCC4(C)C3CCC12C)C(=O)O PZIRUHCJZBGLDY-UHFFFAOYSA-N 0.000 description 6
- CWVRJTMFETXNAD-KLZCAUPSSA-N Neochlorogenin-saeure Natural products O[C@H]1C[C@@](O)(C[C@@H](OC(=O)C=Cc2ccc(O)c(O)c2)[C@@H]1O)C(=O)O CWVRJTMFETXNAD-KLZCAUPSSA-N 0.000 description 6
- 229940074393 chlorogenic acid Drugs 0.000 description 6
- CWVRJTMFETXNAD-JUHZACGLSA-N chlorogenic acid Chemical compound O[C@@H]1[C@H](O)C[C@@](O)(C(O)=O)C[C@H]1OC(=O)\C=C\C1=CC=C(O)C(O)=C1 CWVRJTMFETXNAD-JUHZACGLSA-N 0.000 description 6
- FFQSDFBBSXGVKF-KHSQJDLVSA-N chlorogenic acid Natural products O[C@@H]1C[C@](O)(C[C@@H](CC(=O)C=Cc2ccc(O)c(O)c2)[C@@H]1O)C(=O)O FFQSDFBBSXGVKF-KHSQJDLVSA-N 0.000 description 6
- 235000001368 chlorogenic acid Nutrition 0.000 description 6
- BMRSEYFENKXDIS-KLZCAUPSSA-N cis-3-O-p-coumaroylquinic acid Natural products O[C@H]1C[C@@](O)(C[C@@H](OC(=O)C=Cc2ccc(O)cc2)[C@@H]1O)C(=O)O BMRSEYFENKXDIS-KLZCAUPSSA-N 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 235000013305 food Nutrition 0.000 description 4
- 235000016709 nutrition Nutrition 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 235000019225 fermented tea Nutrition 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000002523 gelfiltration Methods 0.000 description 3
- 235000009569 green tea Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 235000011496 sports drink Nutrition 0.000 description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 229930003268 Vitamin C Natural products 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000015897 energy drink Nutrition 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- FVTCRASFADXXNN-SCRDCRAPSA-N flavin mononucleotide Chemical compound OP(=O)(O)OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O FVTCRASFADXXNN-SCRDCRAPSA-N 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 235000021552 granulated sugar Nutrition 0.000 description 2
- 239000002198 insoluble material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229960003512 nicotinic acid Drugs 0.000 description 2
- 235000001968 nicotinic acid Nutrition 0.000 description 2
- 239000011664 nicotinic acid Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000008213 purified water Substances 0.000 description 2
- ZUFQODAHGAHPFQ-UHFFFAOYSA-N pyridoxine hydrochloride Chemical compound Cl.CC1=NC=C(CO)C(CO)=C1O ZUFQODAHGAHPFQ-UHFFFAOYSA-N 0.000 description 2
- 229950001574 riboflavin phosphate Drugs 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 2
- UIERGBJEBXXIGO-UHFFFAOYSA-N thiamine mononitrate Chemical compound [O-][N+]([O-])=O.CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N UIERGBJEBXXIGO-UHFFFAOYSA-N 0.000 description 2
- 150000003544 thiamines Chemical class 0.000 description 2
- 235000019154 vitamin C Nutrition 0.000 description 2
- 239000011718 vitamin C Substances 0.000 description 2
- 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
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- STJLLECREIYBCK-UHFFFAOYSA-M 2-[3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-methyl-1,3-thiazol-3-ium-5-yl]ethanol;5-sulfonaphthalene-1-sulfonate Chemical compound CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1S([O-])(=O)=O STJLLECREIYBCK-UHFFFAOYSA-M 0.000 description 1
- 241000209507 Camellia Species 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 description 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- 229930003779 Vitamin B12 Natural products 0.000 description 1
- 229930003471 Vitamin B2 Natural products 0.000 description 1
- LXNHXLLTXMVWPM-UHFFFAOYSA-N Vitamin B6 Natural products CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- DDEDPQYNISJXLF-XTMYEIJHSA-N [(z)-4-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-3-benzoylsulfanylpent-3-enyl] benzoate;hydrochloride Chemical compound Cl.C=1C=CC=CC=1C(=O)OCC\C(SC(=O)C=1C=CC=CC=1)=C(/C)N(C=O)CC1=CN=C(C)N=C1N DDEDPQYNISJXLF-XTMYEIJHSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 229960001948 caffeine Drugs 0.000 description 1
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 1
- FAPWYRCQGJNNSJ-UBKPKTQASA-L calcium D-pantothenic acid Chemical compound [Ca+2].OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O.OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O FAPWYRCQGJNNSJ-UBKPKTQASA-L 0.000 description 1
- 229960002079 calcium pantothenate Drugs 0.000 description 1
- PHIQHXFUZVPYII-UHFFFAOYSA-N carnitine Chemical compound C[N+](C)(C)CC(O)CC([O-])=O PHIQHXFUZVPYII-UHFFFAOYSA-N 0.000 description 1
- 229960000678 carnitine chloride Drugs 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- AGVAZMGAQJOSFJ-WZHZPDAFSA-M cobalt(2+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+2].N#[C-].[N-]([C@@H]1[C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP(O)(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O AGVAZMGAQJOSFJ-WZHZPDAFSA-M 0.000 description 1
- 239000005515 coenzyme Substances 0.000 description 1
- 235000018597 common camellia Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 231100000676 disease causative agent Toxicity 0.000 description 1
- PXEDJBXQKAGXNJ-QTNFYWBSSA-L disodium L-glutamate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](N)CCC([O-])=O PXEDJBXQKAGXNJ-QTNFYWBSSA-L 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 235000019152 folic acid Nutrition 0.000 description 1
- 239000011724 folic acid Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 229960000367 inositol Drugs 0.000 description 1
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 230000003340 mental effect Effects 0.000 description 1
- 229960003966 nicotinamide Drugs 0.000 description 1
- 235000005152 nicotinamide Nutrition 0.000 description 1
- 239000011570 nicotinamide Substances 0.000 description 1
- 235000020333 oolong tea Nutrition 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- -1 polyphenol compound Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- RADKZDMFGJYCBB-UHFFFAOYSA-N pyridoxal hydrochloride Natural products CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 description 1
- 235000019171 pyridoxine hydrochloride Nutrition 0.000 description 1
- 239000011764 pyridoxine hydrochloride Substances 0.000 description 1
- 229960004172 pyridoxine hydrochloride Drugs 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 235000019190 thiamine hydrochloride Nutrition 0.000 description 1
- 239000011747 thiamine hydrochloride Substances 0.000 description 1
- 229960000344 thiamine hydrochloride Drugs 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000019163 vitamin B12 Nutrition 0.000 description 1
- 239000011715 vitamin B12 Substances 0.000 description 1
- 235000019164 vitamin B2 Nutrition 0.000 description 1
- 239000011716 vitamin B2 Substances 0.000 description 1
- 235000019158 vitamin B6 Nutrition 0.000 description 1
- 239000011726 vitamin B6 Substances 0.000 description 1
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 229940011671 vitamin b6 Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Tea And Coffee (AREA)
- Non-Alcoholic Beverages (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
本発明は、ビタミンB1またはその誘導体を含有する飲食品又は医薬品等の飲用組成物の保存中に発生する不快な異臭成分の発生を防止する方法に関する。 The present invention relates to a method for preventing the generation of unpleasant off-flavor components that occur during storage of drinking compositions such as foods and drinks or pharmaceuticals containing vitamin B1 or a derivative thereof.
ビタミンB1は糖代謝酵素の補酵素として働き、疲労回復、精神安定などの効果があるとされ、従来から栄養食品に利用されている。また、ビタミンB1は酸性領域において比較的安定な水溶性ビタミンであることから、栄養ドリンクやスポーツドリンク等の酸性飲用組成物に使用されることが多い。しかし、ビタミンB1を上記酸性飲用組成物に配合する場合、保存中にビタミン臭と言われる異臭が発生し商品的な価値を減ずるという欠点がある。 Vitamin B1 works as a coenzyme for sugar-metabolizing enzymes and is said to have effects such as fatigue recovery and mental stability, and has been used for nutritional foods. Moreover, since vitamin B1 is a water-soluble vitamin that is relatively stable in the acidic region, it is often used in acidic drinking compositions such as nutritional drinks and sports drinks. However, when vitamin B1 is blended in the acidic drinking composition, there is a drawback that an off-flavor called a vitamin odor occurs during storage, reducing the commercial value.
このビタミン臭の原因はビタミンB1の分解により生成する2−メチル−3−フランチオール等の各種の揮発性含硫化合物であることが知られている (非特許文献1)。これら含硫化合物の中でも特に2−メチル−3−フランチオールの匂いの閾値は極めて低く、ごく少量発生するだけでも異臭の原因となる。
従って、ビタミンB1を配合した酸性飲用組成物を保存する場合、ビタミンB1含量が低くても保存期間中の異臭の発生は避けられない。
The cause of this vitamin odor is known to be various volatile sulfur-containing compounds such as 2-methyl-3-furanthiol produced by the decomposition of vitamin B1 (Non-patent Document 1). Among these sulfur-containing compounds, 2-methyl-3-furanthiol has a particularly low odor threshold, and even a very small amount of odor can cause off-flavors.
Therefore, when an acidic drinking composition containing vitamin B1 is stored, the generation of a bad odor during the storage period is inevitable even if the vitamin B1 content is low.
従来からドリンク剤等のビタミンB1を配合した酸性飲料における異臭の発生を防止する方法が提案されている。例えば、没食子酸等の多価フェノール化合物を添加する方法(特許文献1)、ビタミンB1とアスコルビン酸を特定の割合で配合する方法(特許文献2)などが提案されている。しかしながら、上記方法では、ビタミンB1由来の異臭成分に対する抑制効果は十分でなく更なる技術の向上が望まれていた。 Conventionally, methods for preventing the generation of off-flavors in acidic beverages containing vitamin B1 such as drinks have been proposed. For example, a method of adding a polyphenol compound such as gallic acid (Patent Document 1), a method of blending vitamin B1 and ascorbic acid at a specific ratio (Patent Document 2), and the like have been proposed. However, in the above method, the inhibitory effect on the off-flavor component derived from vitamin B1 is not sufficient, and further technical improvement has been desired.
本発明が解決しようとする問題は、ビタミンB1またはその誘導体を含有する酸性飲用組成物は、保存中にビタミンB1由来の異臭成分が発生し、商品価値を減ずるという問題である。 The problem to be solved by the present invention is that an acidic drinking composition containing vitamin B1 or a derivative thereof generates a malodorous component derived from vitamin B1 during storage, thereby reducing the commercial value.
本発明者らは上記従来技術の問題点を解決すべく鋭意研究した結果、ビタミンB1またはその誘導体を含有する酸性飲用組成物に茶抽出物を添加することによりビタミンB1の分解に起因する異臭成分の発生が顕著に抑制されることを見出し、本発明を完成させるにいたった。すなわち、本発明はビタミンB1またはその誘導体含有酸性飲用組成物の製造に当たり、茶抽出物を含有させることを特徴とするビタミンB1由来の異臭成分の発生を防止する方法である。また、前記異臭成分がビタミンB1の分解によって発生する2−メチル−3−フランチオールである異臭成分の発生を防止する方法である。この茶抽出物は、水、極性溶媒またはこれらの混合物で抽出して得られる。 As a result of diligent research to solve the above-mentioned problems of the prior art, the present inventors have found that an off-flavor component resulting from the decomposition of vitamin B1 by adding a tea extract to an acidic drinking composition containing vitamin B1 or a derivative thereof. As a result, the inventors have found that the occurrence of this is remarkably suppressed, and completed the present invention. That is, the present invention is a method for preventing the generation of off-flavor components derived from vitamin B1, characterized by containing a tea extract in the production of an acidic drinking composition containing vitamin B1 or a derivative thereof. Moreover, it is the method of preventing generation | occurrence | production of the off-flavor component whose said off-flavor component is 2-methyl-3-furanthiol generated by decomposition | disassembly of vitamin B1. This tea extract is obtained by extraction with water, a polar solvent or a mixture thereof.
本発明のビタミンB1由来の異臭成分の発生を防止する方法により、栄養ドリンク等のビタミンB1またはその誘導体含有飲用組成物の保存中に発生する不快なビタミン臭の発生が抑制され、風味良好な飲用組成物を提供することができる。 The method for preventing the generation of off-flavor components derived from vitamin B1 of the present invention suppresses the generation of unpleasant vitamin odor that occurs during storage of vitamin B1 or a derivative-containing drinking composition such as an energy drink, and has a good flavor. A composition can be provided.
本発明に使用する茶抽出物は、ツバキ科の植物であるCamellia
Sinensisの葉より製造される茶葉を溶媒抽出することにより製造できる。原料の茶葉は特に限定されるものではなく、不発酵茶である緑茶、半発酵茶である烏龍茶、発酵茶である紅茶などが挙げられる。それらの中で、不発酵茶である緑茶又は発酵茶である紅茶を用いるのが好ましい。
The tea extract used in the present invention is Camellia, a plant of the camelliaceae family.
It can be produced by solvent extraction of tea leaves produced from the leaves of Sinussis. The raw tea leaves are not particularly limited, and examples include green tea that is non-fermented tea, oolong tea that is semi-fermented tea, and black tea that is fermented tea. Among them, it is preferable to use green tea that is unfermented tea or black tea that is fermented tea.
本発明の抽出処理に使用する溶媒は、水又は極性溶媒であり、極性溶媒は含水物であっても良い。極性溶媒としてはアルコール、アセトン、酢酸エチル等があげられ、これらの混合物であっても良い。特に水又はエタノール、或いはこれらの混合物が望ましい。溶媒の量は任意に選択できるが、一般には上記茶葉1重量部に対し溶媒量2〜100重量部を使用する。 The solvent used for the extraction treatment of the present invention is water or a polar solvent, and the polar solvent may be a hydrate. Examples of the polar solvent include alcohol, acetone, ethyl acetate and the like, and a mixture thereof may be used. In particular, water or ethanol or a mixture thereof is desirable. Although the quantity of a solvent can be selected arbitrarily, generally 2-100 weight part of solvent amounts are used with respect to 1 weight part of said tea leaves.
抽出方法は特に限定されるものではなく、例えば、茶葉又は粉砕した茶葉を溶媒中に入れ、浸漬又は加熱還流することによって茶抽出物を得ることができる。ついで、溶媒に不溶な固形物を除去して抽出液を得るが、固形物除去方法としては遠心分離、濾過、圧搾等の固液分離手段を用いることができる。 The extraction method is not particularly limited. For example, a tea extract can be obtained by placing tea leaves or crushed tea leaves in a solvent and immersing or heating to reflux. Next, the solid solution insoluble in the solvent is removed to obtain an extract. As the solid material removal method, solid-liquid separation means such as centrifugation, filtration, and pressing can be used.
得られた茶抽出液は、そのままビタミンB1またはその誘導体含有酸性飲用組成物に配合して、ビタミンB1由来の異臭成分発生を防止するために使用することができるが、さらに、脱色、脱臭等の精製処理をすることができる。精製処理には活性炭や多孔性のスチレン−ジビニルベンゼン共重合体からなる合成樹脂吸着剤、親水性ビニルポリマーを基材とするゲル濾過用充填剤などが使用できる。精製用の合成樹脂吸着剤としては例えば三菱化学株式会社製「ダイヤイオンHP−20(商品名)」やオルガノ株式会社製「アンバーライトXAD−2(商品名)」などが使用できる。また、ゲル濾過用充填剤としては東ソー株式会社製「トヨパールHW−40(商品名)」などが使用できる。 The obtained tea extract can be used as it is by mixing it with an acidic drinking composition containing vitamin B1 or a derivative thereof to prevent the generation of off-flavor components derived from vitamin B1. Purification process can be performed. For the purification treatment, activated carbon, a synthetic resin adsorbent made of porous styrene-divinylbenzene copolymer, a gel filtration filler based on a hydrophilic vinyl polymer, or the like can be used. As the synthetic resin adsorbent for purification, for example, “Diaion HP-20 (trade name)” manufactured by Mitsubishi Chemical Corporation or “Amberlite XAD-2 (trade name)” manufactured by Organo Corporation can be used. As a filler for gel filtration, “Toyopearl HW-40 (trade name)” manufactured by Tosoh Corporation can be used.
このようにして得られた茶抽出物は、液剤として使用することができるが、凍結乾燥又は加熱乾燥などの処理を行い固形物にすることも可能である。また、賦形剤(デキストリン等)を添加し噴霧乾燥により粉末状にすることも可能であり、用途に応じて種々の剤形を採用することができる。 The tea extract thus obtained can be used as a liquid agent, but it can also be made into a solid by performing a treatment such as freeze drying or heat drying. Moreover, it is also possible to add excipients (dextrin etc.) and to make it into a powder form by spray drying, and various dosage forms can be employ | adopted according to a use.
また、市販の茶抽出物を使用することもでき、例としては緑茶抽出物である東京フードテクノ(株)「ポリフェノン」、伊藤園(株)「テアフラン」、太陽化学(株)「サンフェノン」などが挙げられる。これらをさらに再精製したものを用いてもよい。 Commercial tea extracts can also be used, such as Tokyo Food Techno Co., Ltd. “Polyphenone”, ITO EN Co., Ltd. “Theafranc”, Taiyo Kagaku Co., Ltd. “Sunphenon”, etc., which are green tea extracts. Can be mentioned. You may use what refine | purified these further.
本発明のビタミンB1由来の異臭成分の発生を防止する方法は、上記で得られた茶抽出物をビタミンB1またはその誘導体含有酸性飲用組成物に適宜添加することで実現できる。本発明が適用できるビタミンB1誘導体としては、チアミン塩酸塩、チアミン硝酸塩、ジベンゾイルチアミン塩酸塩、チアミンナフタレン−1,5−ジスルホン酸塩、ビスベンチアミンおよびそれらの誘導体などがあげられるがこれらに限定されるものではない。また、これらのビタミンB1誘導体は1種または2種以上を混合して使用することもできる。本発明が適用できるビタミンB1またはその誘導体含有酸性飲用組成物は、通常0.1〜100ppmの範囲でビタミンB1塩類を含有し、クエン酸等の添加によりpH2.5〜4.0に調整されている。例としては栄養ドリンク剤、ビタミン飲料、ゼリー飲料、スポーツドリンク等をあげることができるが、これらに限定されるものではない。ビタミンB1またはその誘導体含有酸性飲用組成物に対する茶抽出物の添加量は、茶抽出物の固形成分として1〜500ppmの範囲が適当である。商品に茶抽出物自身の香味が影響を及ぼさない範囲内で添加するという観点からは1〜200ppmが好ましく、特に1〜100ppmが好ましい。
以下に実施例を挙げて本発明を具体的に説明するが、本発明は実施例の記載に限定されるものではない。
The method for preventing the occurrence of off-flavor components derived from vitamin B1 of the present invention can be realized by appropriately adding the tea extract obtained above to an acidic drinking composition containing vitamin B1 or a derivative thereof. Examples of the vitamin B1 derivative to which the present invention can be applied include thiamine hydrochloride, thiamine nitrate, dibenzoylthiamine hydrochloride, thiamine naphthalene-1,5-disulfonate, bisbenchamine, and derivatives thereof. Is not to be done. Moreover, these vitamin B1 derivatives can also be used 1 type or in mixture of 2 or more types. Vitamin B1 or its derivative-containing acidic drinking composition to which the present invention can be applied usually contains vitamin B1 salts in the range of 0.1 to 100 ppm, and is adjusted to pH 2.5 to 4.0 by addition of citric acid or the like. Yes. Examples include nutritional drinks, vitamin drinks, jelly drinks, sports drinks, and the like, but are not limited thereto. The amount of the tea extract added to the vitamin B1 or its derivative-containing acidic drinking composition is suitably in the range of 1 to 500 ppm as a solid component of the tea extract. From the viewpoint of adding to the product within a range where the flavor of the tea extract itself does not affect, 1 to 200 ppm is preferable, and 1 to 100 ppm is particularly preferable.
EXAMPLES The present invention will be specifically described below with reference to examples, but the present invention is not limited to the description of the examples.
〔抽出例1〕
紅茶抽出物の調製
紅茶葉50gに、50質量%エタノール水溶液500gを加え1時間加熱還流して抽出した。不溶物を濾過により除去した後、濾液を減圧濃縮、凍結乾燥し褐色の紅茶抽出物15.1gを得た。
[Extraction Example 1]
Preparation of Black Tea Extract To 50 g of black tea leaves, 500 g of a 50% by mass aqueous ethanol solution was added and extracted by heating under reflux for 1 hour. The insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure and lyophilized to obtain 15.1 g of a brown tea extract.
〔抽出例2〕
緑茶抽出物の調製
緑茶葉50gに、50質量%エタノール水溶液500gを加え1時間加熱還流して抽出した。不溶物を濾過により除去した後、濾液を50gまで減圧で濃縮した。この濃縮液に水150gを加え、ゲル濾過用充てん剤(トヨパールHW−40C)100mlに吸着させた。15質量%エタノール水溶液200mlを用いて洗浄後、80質量%エタノール水溶液200mlで溶出した。溶出液を減圧濃縮後、凍結乾燥し赤褐色の緑茶抽出物5.6gを得た
[Extraction Example 2]
Preparation of Green Tea Extract To 50 g of green tea leaves, 500 g of a 50% by mass aqueous ethanol solution was added and extracted by heating under reflux for 1 hour. The insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure to 50 g. 150 g of water was added to this concentrated solution and adsorbed on 100 ml of a gel filtration filler (Toyopearl HW-40C). After washing with 200 ml of 15% by mass aqueous ethanol solution, elution was performed with 200 ml of 80% by mass aqueous ethanol solution. The eluate was concentrated under reduced pressure and lyophilized to obtain 5.6 g of a reddish brown green tea extract.
ビタミンB1由来の異臭成分の発生抑制効果の評価
ビタミンB1由来の異臭成分の発生に対する茶抽出物の抑制効果を、異臭の原因物質とされる2−メチル−3−フランチオールの生成量を測定することにより評価した。
Evaluation of the generation inhibitory effect of off-flavor components derived from vitamin B1 The amount of 2-methyl-3-furanthiol produced as a causative agent of off-flavors is measured by the suppression effect of tea extract on the generation of off-flavor components derived from vitamin B1. It was evaluated by.
〔試験例1〕
1/10Mクエン酸−1/5Mリン酸水素二ナトリウムで調整したpH3.0の緩衝溶液にビタミンB1塩酸塩を濃度が10ppmになるように添加してビタミンB1含有酸性水溶液を調製した。この溶液に抽出例1で得られた紅茶抽出物、及び抽出例2で得られた緑茶抽出物を濃度が30ppmになるよう添加した液を各々調製した。また茶抽出物無添加の溶液を対照液とした。各溶液をガラス瓶に充填して70℃にて10分間殺菌した後、恒温槽内で40℃にて14日間保存した。保存期間中、各溶液をサンプリングしてジクロロメタンで抽出した後、ガスクロマトグラフィー質量分析法によりを2−メチル−3−フランチオールの生成量を定量した。保存期間中の2−メチル−3−フランチオールの生成量の変化を図1に示す。
[Test Example 1]
Vitamin B1 hydrochloride was added to a pH 3.0 buffer solution adjusted with 1 / 10M citric acid-1 / 5M disodium hydrogen phosphate so as to have a concentration of 10 ppm to prepare an aqueous solution containing vitamin B1. Liquids were prepared by adding the black tea extract obtained in Extraction Example 1 and the green tea extract obtained in Extraction Example 2 to a concentration of 30 ppm. A solution without the tea extract was used as a control solution. Each solution was filled in a glass bottle and sterilized at 70 ° C. for 10 minutes, and then stored in a thermostatic chamber at 40 ° C. for 14 days. During the storage period, each solution was sampled and extracted with dichloromethane, and then the amount of 2-methyl-3-furanthiol produced was quantified by gas chromatography mass spectrometry. The change in the amount of 2-methyl-3-furanthiol produced during the storage period is shown in FIG.
〔試験例2〕
茶抽出物の代わりにクロロゲン酸、及び特開平5−155756号公報開示の没食子酸を用い試験例1と同様の試験を行った。
[Test Example 2]
A test similar to Test Example 1 was conducted using chlorogenic acid and gallic acid disclosed in JP-A-5-155756 instead of the tea extract.
試験例1および試験例2における、40℃で7日間保存時の2−メチル−3−フランチオールの生成量を表1に示す。 Table 1 shows the amount of 2-methyl-3-furanthiol produced in Test Example 1 and Test Example 2 when stored at 40 ° C for 7 days.
〔表1〕
添加剤 2−メチル−3−フランチオールの生成量(ppb)
対照(無添加) 1.04
紅茶抽出物 0.28
緑茶抽出物 0.39
没食子酸 0.65
クロロゲン酸 1.05
[Table 1]
Additive Amount of 2-methyl-3-furanthiol produced (ppb)
Control (no addition) 1.04
Black tea extract 0.28
Green tea extract 0.39
Gallic acid 0.65
Chlorogenic acid 1.05
図1から明らかなように紅茶及び緑茶抽出物はビタミンB1の分解によって発生する2−メチル−3−フランチオールの生成を顕著に抑制していることがわかる。また表1から明らかなように紅茶及び緑茶抽出物の2−メチル−3−フランチオール生成に対する抑制効果は多価フェノール成分であるクロロゲン酸及び没食子酸よりも優れていることがわかる。 As is clear from FIG. 1, it can be seen that the black tea and green tea extracts remarkably suppress the production of 2-methyl-3-furanthiol generated by the decomposition of vitamin B1. Moreover, it turns out that the inhibitory effect with respect to 2-methyl-3-furanthiol production | generation of black tea and a green tea extract is superior to chlorogenic acid and gallic acid which are polyhydric phenol components evidently from Table 1.
〔処方例1〕
飲料用ビタミンミックスの組成(製品0.5g当たりの含有量):
ビタミンA 1667IU
ビタミンB1 0.5mg
ビタミンB2 0.57mg
ビタミンB6 0.67mg
ビタミンB12 2μg
ナイアシン 6.67mg
葉酸 0.14mg
ビタミンC 20mg
ビタミンD 3 133IU
ビタミンE 6.71mg
[Prescription Example 1]
Composition of vitamin mix for beverages (content per 0.5 g of product):
Vitamin A 1667 IU
Vitamin B1 0.5mg
Vitamin B2 0.57mg
Vitamin B6 0.67mg
Vitamin B12 2μg
Niacin 6.67mg
Folic acid 0.14mg
Vitamin C 20mg
Vitamin D 3 133 IU
Vitamin E 6.71mg
〔試験例3〕
ビタミン飲料における効果
処方例1に示す成分組成の飲料用ビタミンミックス(理研ビタミン株式会社製)の0.02質量%水溶液に、抽出例1で調製した紅茶抽出物及び抽出例2で調製した緑茶抽出物、また比較例としてクロロゲン酸及び没食子酸を濃度が30ppmになるよう添加した液を各々調製した。また無添加の飲料用ビタミンミックス水溶液を対照液とした。各溶液をガラス瓶に充填して70℃にて10分間殺菌した後、恒温槽内で40℃にて7日間保存した。各溶液について、訓練されたパネラー6名によりビタミン臭を評価項目として官能評価を行った。評価点はビタミン臭を強く感じたものを7点、ビタミン臭を全く感じなかったものを1点とした。評価結果の平均値を表2に示した。
[Test Example 3]
Effects in vitamin drinks Extracted from tea extract prepared in Extraction Example 1 and green tea extract prepared in Extraction Example 2 into a 0.02% by weight aqueous solution of the vitamin mix for beverages (made by Riken Vitamin Co., Ltd.) having the composition shown in Formulation Example 1. As a comparative example, chlorogenic acid and gallic acid were added to give a concentration of 30 ppm. An additive-free vitamin mix solution for beverages was used as a control solution. Each solution was filled in a glass bottle and sterilized at 70 ° C. for 10 minutes, and then stored in a thermostatic bath at 40 ° C. for 7 days. Each solution was subjected to sensory evaluation using 6 trained panelists using vitamin odor as an evaluation item. The evaluation score was 7 points for those who felt a strong vitamin odor, and 1 point for those who did not feel any vitamin odor. The average value of the evaluation results is shown in Table 2.
〔表2〕
添加剤 評価点数
対照(無添加) 7.0
紅茶抽出物 1.5
緑茶抽出物 2.5
没食子酸 4.0
クロロゲン酸 6.5
[Table 2]
Additives Evaluation score Control (no addition) 7.0
Black tea extract 1.5
Green tea extract 2.5
Gallic acid 4.0
Chlorogenic acid 6.5
表2の結果より紅茶及び緑茶抽出物は、ビタミン飲料の保存後に発生するビタミン臭を効果的に抑制し、その効果は多価フェノール成分であるクロロゲン酸及び没食子酸よりも優れていることがわかる。 From the results in Table 2, it can be seen that the black tea and green tea extracts effectively suppress the vitamin odor generated after storage of vitamin beverages, and the effect is superior to chlorogenic acid and gallic acid which are polyhydric phenol components. .
〔実施例1〕
以下に示す処方によりビタミンB1含有栄養ドリンクを作成した。
グラニュー糖 150 (g)
クエン酸 2
ビタミンB1硝酸塩 0.05
リン酸リボフラビンナトリウム 0.05
塩酸ピリドキシン 0.05
ニコチン酸アミド 0.2
タウリン 10
イノシトール 0.5
無水カフェイン 0.5
塩化カルニチン 1
安息香酸ナトリウム 0.5
香料 1
紅茶抽出物 0.03
炭酸水 600
精製水 234.12
合計 1000
[Example 1]
A vitamin B1-containing nutritional drink was prepared according to the following formulation.
Granulated sugar 150 (g)
Citric acid 2
Vitamin B1 nitrate 0.05
Riboflavin sodium phosphate 0.05
Pyridoxine hydrochloride 0.05
Nicotinamide 0.2
Taurine 10
Inositol 0.5
Anhydrous caffeine 0.5
Carnitine chloride 1
Sodium benzoate 0.5
Fragrance 1
Black tea extract 0.03
Carbonated water 600
Purified water 234.12
Total 1000
以下に示す処方によりビタミンB1含有スポーツドリンクを作成した
レモン果汁 5 (g)
グラニュー糖 100
クエン酸 2
食塩 0.62
塩化カリウム 0.37
ビタミンC 1.2
ビタミンB1塩酸塩 0.0025
リン酸リボフラビンナトリウム 0.001
ナイアシン 0.02
パントテン酸カルシウム 0.001
L−グルタミン酸ナトリウム 0.05
香料 1
緑茶抽出物 0.03
精製水 889.7055
合計 1000
Lemon juice with a vitamin B1-containing sports drink prepared according to the prescription shown below 5 (g)
Granulated sugar 100
Citric acid 2
Salt 0.62
Potassium chloride 0.37
Vitamin C 1.2
Vitamin B1 hydrochloride 0.0025
Riboflavin sodium phosphate 0.001
Niacin 0.02
Calcium pantothenate 0.001
Sodium L-glutamate 0.05
Fragrance 1
Green tea extract 0.03
Purified water 889.77055
Total 1000
本発明のビタミンB1由来の異臭成分の発生を防止する方法により、保存中に発生する不快なビタミン臭の発生を抑制することができ、栄養ドリンク等のビタミンB1またはその誘導体含有飲用組成物に適用すれば優れた効果が発揮できる。 By the method for preventing the generation of off-flavor components derived from vitamin B1 of the present invention, the generation of unpleasant vitamin odor occurring during storage can be suppressed, and it is applied to vitamin B1 or a derivative-containing drinking composition such as an energy drink If it does, the outstanding effect can be demonstrated.
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JP2007143427A (en) * | 2005-11-24 | 2007-06-14 | Sankai Kasei Kk | Refreshing drink |
JP2007159572A (en) * | 2005-11-21 | 2007-06-28 | Riken Vitamin Co Ltd | Vitamin e-containing drinking composition |
JP2010143894A (en) * | 2008-12-22 | 2010-07-01 | Ss Pharmaceut Co Ltd | Oral solution medicine of reduced unpleasant taste and unpleasant odor |
JP2011167144A (en) * | 2010-02-19 | 2011-09-01 | Ito En Ltd | Vitamin b1-containing drink and method for producing the same, and method for controlling unpleasant smell of vitamin b1-containing drink |
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JP2010143894A (en) * | 2008-12-22 | 2010-07-01 | Ss Pharmaceut Co Ltd | Oral solution medicine of reduced unpleasant taste and unpleasant odor |
JP2011167144A (en) * | 2010-02-19 | 2011-09-01 | Ito En Ltd | Vitamin b1-containing drink and method for producing the same, and method for controlling unpleasant smell of vitamin b1-containing drink |
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