WO2006018992A1 - 高級脂肪族化合物を含有する水性混合体 - Google Patents
高級脂肪族化合物を含有する水性混合体 Download PDFInfo
- Publication number
- WO2006018992A1 WO2006018992A1 PCT/JP2005/014429 JP2005014429W WO2006018992A1 WO 2006018992 A1 WO2006018992 A1 WO 2006018992A1 JP 2005014429 W JP2005014429 W JP 2005014429W WO 2006018992 A1 WO2006018992 A1 WO 2006018992A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- mixture
- compound
- higher aliphatic
- water
- surfactant
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 318
- 150000007824 aliphatic compounds Chemical class 0.000 title claims abstract description 88
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 101
- -1 polyol compound Chemical class 0.000 claims abstract description 87
- 235000020669 docosahexaenoic acid Nutrition 0.000 claims abstract description 66
- 150000001875 compounds Chemical class 0.000 claims abstract description 62
- 230000005484 gravity Effects 0.000 claims abstract description 55
- 239000004094 surface-active agent Substances 0.000 claims abstract description 50
- 239000007864 aqueous solution Substances 0.000 claims abstract description 48
- 239000007788 liquid Substances 0.000 claims abstract description 43
- 229920005862 polyol Polymers 0.000 claims abstract description 30
- 150000002148 esters Chemical class 0.000 claims abstract description 22
- 238000000034 method Methods 0.000 claims abstract description 21
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 15
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 8
- GZJLLYHBALOKEX-UHFFFAOYSA-N 6-Ketone, O18-Me-Ussuriedine Natural products CC=CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O GZJLLYHBALOKEX-UHFFFAOYSA-N 0.000 claims abstract description 6
- KAUVQQXNCKESLC-UHFFFAOYSA-N docosahexaenoic acid (DHA) Natural products COC(=O)C(C)NOCC1=CC=CC=C1 KAUVQQXNCKESLC-UHFFFAOYSA-N 0.000 claims abstract description 6
- MBMBGCFOFBJSGT-KUBAVDMBSA-N docosahexaenoic acid Natural products CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 claims description 118
- 229940126062 Compound A Drugs 0.000 claims description 73
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims description 73
- 238000003756 stirring Methods 0.000 claims description 72
- 229940090949 docosahexaenoic acid Drugs 0.000 claims description 60
- 235000020673 eicosapentaenoic acid Nutrition 0.000 claims description 59
- 229960005135 eicosapentaenoic acid Drugs 0.000 claims description 59
- JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 claims description 59
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 claims description 57
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 49
- 235000021323 fish oil Nutrition 0.000 claims description 48
- 238000002156 mixing Methods 0.000 claims description 43
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 38
- 229930195729 fatty acid Natural products 0.000 claims description 38
- 239000000194 fatty acid Substances 0.000 claims description 38
- 235000013305 food Nutrition 0.000 claims description 31
- 235000011187 glycerol Nutrition 0.000 claims description 29
- 235000021056 liquid food Nutrition 0.000 claims description 25
- 239000000845 maltitol Substances 0.000 claims description 25
- 235000010449 maltitol Nutrition 0.000 claims description 25
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 claims description 25
- 229940035436 maltitol Drugs 0.000 claims description 25
- 238000004519 manufacturing process Methods 0.000 claims description 25
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 22
- 239000000654 additive Substances 0.000 claims description 20
- 240000007594 Oryza sativa Species 0.000 claims description 18
- 235000007164 Oryza sativa Nutrition 0.000 claims description 18
- 230000000996 additive effect Effects 0.000 claims description 18
- 235000009566 rice Nutrition 0.000 claims description 18
- 239000003651 drinking water Substances 0.000 claims description 17
- 235000020188 drinking water Nutrition 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 13
- 125000004185 ester group Chemical group 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 12
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims description 11
- 150000004665 fatty acids Chemical class 0.000 claims description 11
- 239000000787 lecithin Substances 0.000 claims description 11
- 235000010445 lecithin Nutrition 0.000 claims description 11
- 229940067606 lecithin Drugs 0.000 claims description 11
- 230000001954 sterilising effect Effects 0.000 claims description 11
- 238000004659 sterilization and disinfection Methods 0.000 claims description 11
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 9
- 239000002994 raw material Substances 0.000 claims description 8
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 7
- 235000005487 catechin Nutrition 0.000 claims description 7
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 claims description 7
- 229950001002 cianidanol Drugs 0.000 claims description 7
- 238000010411 cooking Methods 0.000 claims description 7
- 229920000223 polyglycerol Polymers 0.000 claims description 6
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 5
- 239000002563 ionic surfactant Substances 0.000 claims description 5
- 239000000600 sorbitol Substances 0.000 claims description 5
- 239000002736 nonionic surfactant Substances 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 238000001694 spray drying Methods 0.000 claims description 4
- 239000010775 animal oil Substances 0.000 claims description 3
- 235000013361 beverage Nutrition 0.000 claims description 3
- 150000005846 sugar alcohols Chemical class 0.000 claims description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 3
- 239000008158 vegetable oil Substances 0.000 claims description 3
- 229920003169 water-soluble polymer Polymers 0.000 claims description 3
- 238000001291 vacuum drying Methods 0.000 claims description 2
- DVSZKTAMJJTWFG-SKCDLICFSA-N (2e,4e,6e,8e,10e,12e)-docosa-2,4,6,8,10,12-hexaenoic acid Chemical compound CCCCCCCCC\C=C\C=C\C=C\C=C\C=C\C=C\C(O)=O DVSZKTAMJJTWFG-SKCDLICFSA-N 0.000 abstract description 4
- 238000013019 agitation Methods 0.000 abstract description 3
- 206010001497 Agitation Diseases 0.000 abstract 1
- 239000012736 aqueous medium Substances 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 23
- 235000019198 oils Nutrition 0.000 description 23
- 239000003995 emulsifying agent Substances 0.000 description 22
- 239000006185 dispersion Substances 0.000 description 18
- 235000013336 milk Nutrition 0.000 description 15
- 239000008267 milk Substances 0.000 description 15
- 210000004080 milk Anatomy 0.000 description 15
- 239000000243 solution Substances 0.000 description 12
- 239000000839 emulsion Substances 0.000 description 11
- 235000013618 yogurt Nutrition 0.000 description 9
- 239000002253 acid Substances 0.000 description 7
- 230000004075 alteration Effects 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 208000000474 Poliomyelitis Diseases 0.000 description 6
- 239000003963 antioxidant agent Substances 0.000 description 6
- 239000010419 fine particle Substances 0.000 description 6
- 235000013373 food additive Nutrition 0.000 description 6
- 239000002778 food additive Substances 0.000 description 6
- 150000003077 polyols Chemical class 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 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 description 5
- 244000294411 Mirabilis expansa Species 0.000 description 5
- 235000015429 Mirabilis expansa Nutrition 0.000 description 5
- 230000009471 action Effects 0.000 description 5
- 235000006708 antioxidants Nutrition 0.000 description 5
- 235000013527 bean curd Nutrition 0.000 description 5
- 235000015110 jellies Nutrition 0.000 description 5
- 239000008274 jelly Substances 0.000 description 5
- 235000013536 miso Nutrition 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 235000019640 taste Nutrition 0.000 description 5
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 4
- HDTRYLNUVZCQOY-WSWWMNSNSA-N Trehalose Natural products O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-WSWWMNSNSA-N 0.000 description 4
- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 4
- 239000000796 flavoring agent Substances 0.000 description 4
- 235000019634 flavors Nutrition 0.000 description 4
- 235000015220 hamburgers Nutrition 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 235000013824 polyphenols Nutrition 0.000 description 4
- 238000005057 refrigeration Methods 0.000 description 4
- 235000013322 soy milk Nutrition 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- 241000251468 Actinopterygii Species 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 244000269722 Thea sinensis Species 0.000 description 3
- 239000008272 agar Substances 0.000 description 3
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000002537 cosmetic Substances 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- 235000019197 fats Nutrition 0.000 description 3
- 235000019688 fish Nutrition 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000004006 olive oil Substances 0.000 description 3
- 235000008390 olive oil Nutrition 0.000 description 3
- WQEPLUUGTLDZJY-UHFFFAOYSA-N pentadecanoic acid Chemical compound CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 150000008442 polyphenolic compounds Chemical class 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000008107 starch Substances 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
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000019484 Rapeseed oil Nutrition 0.000 description 2
- 241001125048 Sardina Species 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- 240000001417 Vigna umbellata Species 0.000 description 2
- 235000011453 Vigna umbellata Nutrition 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 150000004965 peroxy acids Chemical class 0.000 description 2
- 230000001766 physiological effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 235000019512 sardine Nutrition 0.000 description 2
- 235000003441 saturated fatty acids Nutrition 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 235000015067 sauces Nutrition 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- PFTAWBLQPZVEMU-ZFWWWQNUSA-N (+)-epicatechin Chemical compound 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-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
- LGQKSQQRKHFMLI-SJYYZXOBSA-N (2s,3r,4s,5r)-2-[(3r,4r,5r,6r)-4,5,6-trihydroxyoxan-3-yl]oxyoxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)CO[C@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)OC1 LGQKSQQRKHFMLI-SJYYZXOBSA-N 0.000 description 1
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- LGQKSQQRKHFMLI-UHFFFAOYSA-N 4-O-beta-D-xylopyranosyl-beta-D-xylopyranose Natural products OC1C(O)C(O)COC1OC1C(O)C(O)C(O)OC1 LGQKSQQRKHFMLI-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 201000004569 Blindness Diseases 0.000 description 1
- 206010006187 Breast cancer Diseases 0.000 description 1
- 208000026310 Breast neoplasm Diseases 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 206010009944 Colon cancer Diseases 0.000 description 1
- 208000001333 Colorectal Neoplasms Diseases 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 description 1
- SQNRKWHRVIAKLP-UHFFFAOYSA-N D-xylobiose Natural products O=CC(O)C(O)C(CO)OC1OCC(O)C(O)C1O SQNRKWHRVIAKLP-UHFFFAOYSA-N 0.000 description 1
- 206010012289 Dementia Diseases 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 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
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 241000237502 Ostreidae Species 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000004347 Perilla Nutrition 0.000 description 1
- 244000124853 Perilla frutescens Species 0.000 description 1
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 1
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241000269851 Sarda sarda Species 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000003266 anti-allergic effect Effects 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 230000002205 anti-dementic effect Effects 0.000 description 1
- 230000003178 anti-diabetic effect Effects 0.000 description 1
- 230000002785 anti-thrombosis Effects 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- 235000021342 arachidonic acid Nutrition 0.000 description 1
- 229940114079 arachidonic acid Drugs 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 150000001765 catechin Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000015071 dressings Nutrition 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000011194 food seasoning agent Nutrition 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
- 150000002314 glycerols Chemical class 0.000 description 1
- 238000009775 high-speed stirring Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 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
- 229960000367 inositol Drugs 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 201000005202 lung cancer Diseases 0.000 description 1
- 208000020816 lung neoplasm Diseases 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 229960001855 mannitol Drugs 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 230000006993 memory improvement Effects 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 235000020124 milk-based beverage Nutrition 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 235000020636 oyster Nutrition 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 150000004804 polysaccharides Chemical class 0.000 description 1
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229920006395 saturated elastomer Polymers 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
- 235000014102 seafood Nutrition 0.000 description 1
- 235000020374 simple syrup Nutrition 0.000 description 1
- 235000021055 solid food Nutrition 0.000 description 1
- 235000013555 soy sauce Nutrition 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 230000004393 visual impairment Effects 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 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
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/52—Adding ingredients
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/152—Milk preparations; Milk powder or milk powder preparations containing additives
- A23C9/1528—Fatty acids; Mono- or diglycerides; Petroleum jelly; Paraffine; Phospholipids; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/115—Fatty acids or derivatives thereof; Fats or oils
- A23L33/12—Fatty acids or derivatives thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Definitions
- Aqueous mixture containing higher aliphatic compounds Aqueous mixture containing higher aliphatic compounds
- the present invention relates to an aqueous mixture containing a higher aliphatic compound, a method for producing the same, and a food or drink containing the higher aliphatic compound.
- DHA docosahexaenoic acid
- EPA eicosapentaenoic acid
- memory enhancement effect 'vision loss suppression effect' anticancer effect especially colorectal cancer, breast cancer, lung cancer
- blood lipid lowering action especially blood lipid lowering action
- antithrombotic action especially antithrombotic action
- antiallergic action-anti-inflammatory action 'antidiabetic action'
- Research results that have anti-dementia effects have been announced and are attracting attention.
- DHA and EPA are abundant in oil extracted from seafood oysters, and attempts have been made to add them to general foods such as bread, confectionery, tofu and miso.
- a public researcher has recently announced that average Japanese people can expect the effect of taking 300 mg or more of DHA per day.
- an aqueous liquid food containing DHA or EPA By adding (dispersing or emulsifying) DHA, EPA or an ester thereof to an aqueous liquid food such as milk, soy milk or yogurt, an aqueous liquid food containing DHA or EPA can be obtained.
- an aqueous liquid food containing DHA or EPA can be obtained.
- DHA, EPA, or its ester is added to the aqueous liquid food and simply dispersed, DHA, EPA, or its ester is an oily substance. It will surface. Therefore, it was very difficult to obtain a product because of the dispersion stability in which DHA, EPA or its ester was uniformly dispersed in an aqueous liquid food!
- higher aliphatic compounds such as higher fatty acids and higher fatty acid esters are oily liquids having a specific gravity of 1 or less, and thus are long in aqueous liquid media such as water, milk, soy milk, and yogurt. It is very difficult to disperse (emulsify) stably over time. Therefore, there is a strong demand for the emergence of a technique for stably dispersing higher aliphatic compounds in an aqueous liquid medium over a long period of time!
- a special emulsifier (decaglycerin monoester) is used.
- a method using stearate and Z or decaglycerin monooleate is shown.
- the mixture M is formed by stirring and mixing the compound A into a mixture of the aqueous solution of the compound P and the aqueous solution of the surfactant S at a rotational speed of 6000 rpm or less.
- Mixture M according to (1) characterized in that it exists.
- the mixture M is formed by stirring and mixing the aqueous solution of the compound A, the compound P, and the aqueous solution of the surfactant S at a rotational speed of 6000 rpm or less. Mixture M according to (1).
- the unsaturated fatty acid ester strength The mixture M according to (8), which is an ester of docosahexaenoic acid (DHA) and Z or eicosapentaenoic acid (EPA).
- DHA docosahexaenoic acid
- EPA eicosapentaenoic acid
- the compound A consists of vegetable oil and Z or animal oil, described in (1) Listed mixture M,
- the mixture A according to (1) which comprises a fish oil containing docosahexaenoic acid ester and Z or eicosapentaenoic acid ester.
- the mixture M is formed by stirring and mixing the compound A and the aqueous solution of the compound P at a rotational speed of 6000 rpm or less. Mixture M.
- the mixture M is formed by stirring and mixing the compound A and the aqueous solution of the compound P under conditions of a rotation speed of 6000 rpm or less. A mixture of M.
- a method for producing an aqueous mixture M containing a higher aliphatic compound comprising: (i) At least one higher aliphatic compound A (having a specific gravity of 1 or less) having 12 or more carbon atoms having an alkyl group or a carboxyl group, (ii) having no higher aliphatic group! /, Polyol compound P ( The specific gravity is greater than 1) and an aqueous solution of surfactant S. The mixture is stirred at room temperature to 75 ° C and under a speed of 6000 rpm or less. Method.
- a method for producing an aqueous mixture M containing a higher aliphatic compound comprising: (i) at least one higher aliphatic compound A having 12 or more carbon atoms having an ester group or a carboxyl group (its specific gravity is 1 or less) and (ii) no higher aliphatic group! /, An aqueous solution of polyol compound P (its specific gravity is greater than 1) and (iii) an aqueous solution of surfactant S.
- the mixture M described in (1), (20) or (26) or a liquid medium containing the mixture M is spray-dried or vacuum-dried in the presence or absence of a water-soluble polymer substance.
- a food or drink containing a higher aliphatic compound comprising the mixture M or (38) described in (1), (20) or (26).
- the additive according to (1), (20) or (26), or the additive according to (38) is stirred with respect to raw water Mixing, and
- a method for producing drinking water containing a higher aliphatic compound, comprising a step of stirring and mixing a polyglycerin surfactant with the raw water.
- the mixture M or the additive according to (1), (20) or (26) is stirred and mixed with the liquid raw material And a step of stirring and mixing a polyglycerin surfactant with the liquid raw material.
- Additives used in rice cooking (i) an aqueous solution of at least one higher aliphatic compound A having an ester group or a carboxyl group and having 12 or more carbon atoms (having a specific gravity of 1 or less) and (ii) ) An additive for cooking rice, comprising a mixture M formed by stirring and mixing an aqueous solution of a higher fatty acid ester of polyglycerol (having a specific gravity greater than 1) under a stirring speed of 6000 rpm or less.
- an aqueous mixture M containing a higher aliphatic compound is provided.
- an advantageous method for producing the mixture M is provided. Furthermore, according to the present invention, a water-dispersible and highly powdered food additive containing a higher aliphatic compound is provided. Furthermore, according to the present invention, a food and drink containing the mixture M and an advantageous production method thereof are provided. Furthermore, according to the present invention, a solid or semi-solid food containing the mixture M is provided.
- the higher aliphatic compound A in the present invention has a carboxyl group (-COOH) or an ester group (COOR, R: alcohol residue).
- the carbon number (RC) is 12 or more, and the upper limit is not particularly limited.
- the higher aliphatic compound mentioned in the present specification means such a compound.
- the higher aliphatic compound A used in the present invention may be a saturated aliphatic compound, It may be an unsaturated aliphatic compound or a mixture thereof.
- the higher aliphatic compound A may be a mixture of at least two higher aliphatic compounds.
- such mixtures include a mixture of at least two higher fatty acid esters, a mixture of at least two higher fatty acids, a mixture of higher fatty acid esters and higher fatty acids, a higher saturated fatty acid ester and a higher unsaturated fatty acid ester. And a mixture of at least two higher unsaturated fatty acid esters.
- the melting point thereof is preferably 90 ° C or lower, more preferably 50 ° C or lower, and further preferably 0 ° C or lower.
- the higher aliphatic compound A or a mixture thereof is preferably a liquid, a paste or a semi-solid at room temperature.
- a higher aliphatic compound having a lower melting point than that of the compound is mixed and the melting point is lowered to the required temperature. It can be preferably used as a single mixture.
- the higher aliphatic compound A used in the present invention include, for example, oleic acid, elaidic acid, linoleic acid, linolenic acid, arachidonic acid, docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA) and the like.
- oleic acid elaidic acid
- linoleic acid linolenic acid
- arachidonic acid docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA) and the like.
- DHA docosahexaenoic acid
- EPA eicosapentaenoic acid
- esters of these fatty acids are exemplified.
- esters examples include alkyl esters having 1 to 6, preferably 1 to 3 carbon atoms such as methyl ester, ethyl ester, and propyl ester, and glycerin such as glycerin monoester, diester, and triester (triglyceride). Esters are included.
- the higher aliphatic compound A used in the present invention can be fats and oils (fatty acid tridalide) such as vegetable oil and animal oil.
- fats and oils include fish oil (tuna oil, sardine oil, etc.), olive oil, soybean oil, rapeseed oil, castor oil, corn oil, amani oil, beef tallow, cottonseed oil, coconut oil, menhadin oil, perilla Oil, castor oil, bevana oil, hydrogenated oil, drill oil and the like.
- Polyol compound P used in the present invention has at least 2, preferably 3 or more, more preferably 5 or more hydroxyl groups in the molecule, and the upper limit of the number of hydroxyl groups is Special It is not constrained by.
- Polio-Louis compound P includes various sugar compounds (for example, monosaccharides).
- Oligosaccharides (trehalose, sucrose, lactose, maltose, xylobiose sugar), polysaccharides, sugar alcohols, etc.) and various glycerin compounds.
- Specific examples include, for example, dariserine, polyglycerin, glucose, D-darcosamine, funoleritose, ribose, xylose, maltose, reducing sugar syrup, sugarcane, starch sugar, alginic acid, chitosan, sorbitol (sorbit) , Mannitol, maltitol, xylitol, inositol and the like.
- these Polio-Louis compounds can be preferably used in the form of a mixture.
- examples include sorbitol Z glycerin mixture, maltitol / polyglycerin mixture, glycerin Z glucose mixture, maltitol Z glycerin mixture, maltitol z glucose mixture and the like.
- polyglycerol is preferred.
- the degree of polymerization is 2 or more, preferably 5 or more, more preferably 8 or more, and the upper limit is not particularly limited, but is usually about 20.
- polyglycerin having a polymerization degree of 8 to 15 can be advantageously used.
- This polyglycerin is a polyol having a high binding force by mixing polydaricerin into the polyol compound P (l) having a strong binding force to the higher aliphatic compound A and a weak binding force. P (l) mixture can be obtained.
- the polyol P (l) includes sugar compounds such as dalco monosucrose, sorbitol, maltitol and the like.
- the amount of polyglycerin mixed in the total polyol compound P is 5% by weight or more, preferably 15% by weight or more, more preferably 20% by weight or more.
- the upper limit is not particularly limited, but is usually about 50 to 90% by weight.
- the polyol compound P is used as an aqueous solution.
- the water content is 50% by weight or less, preferably 40% by weight or less, more preferably 30% by weight or less.
- the content of the polyol compound P is 50% by weight or more, and the upper limit is the saturation concentration.
- the polyol compound P integrally associates (bonds) with the higher aliphatic compound A, acts as a specific gravity regulator of the compound, surrounds the compound A, and protects the compound A from oxidation. It acts as an agent.
- the specific gravity of the polyol compound aqueous solution is the kind of the polyol compound P. And its concentration.
- the at least one higher aliphatic compound A is formed in a mixture M with an aqueous solution of the polyol compound P.
- the higher aliphatic compound or a mixture thereof is brought to normal temperature of the polyol-based compound P and stirred and mixed under heating.
- the stirring and mixing temperature is a temperature at which the higher aliphatic compound A or a mixture thereof exhibits a liquid or paste suitable for stirring, and is usually 50 to 70%.
- the higher aliphatic compound A and the polyol compound P are integrally bonded (associated) and behave like a single molecule.
- the bond in this case is thought to be due to a hydrogen bond.
- the water present in the mixture M behaves like combined water and structured water.
- the higher aliphatic compound A and the polyoligomeric compound P are integrally bonded, so that when the mixture M is poured into water, the higher aliphatic compound A is substantially on the water surface. Can be confirmed by not surfacing.
- hydrophilic substances can be contained as required.
- Such substances include antioxidants, surfactants (emulsifiers), pH adjusters, viscosity adjusters and the like.
- tocopherols, polyphenols (such as power textile compounds), palmitoyl-ascorbic acid, and the like can be preferably used as the anti-oxidation agent.
- a specific example of a force-tin compound is tea catechin.
- the mixing ratio of the higher aliphatic compound A and the aqueous solution of the polyol-based compound P may be such that the mixture M of both can stably exist in water.
- the aqueous polyol compound solution contains 0.5 to 5 parts by weight of the polyol compound P, preferably 1 part by weight of the higher aliphatic compound, preferably! ⁇ -4 parts by weight, more preferably 1.5-3 parts by weight.
- Polio-Louis compound P to high aliphatic compound A to weight ratio [P] Z [A] is 0.5-5, preferably! ⁇ ⁇ 4, more preferably in the range of 1.5-3.
- M (hereinafter also referred to as M (I)), which is composed of a higher aliphatic compound A and a polyol compound P and a hydropower and does not contain a surfactant S
- the compound A and the compound Stir and mix with an aqueous solution of P.
- the stirring and mixing device has a rotational speed of 6000 rpm or more.
- a low speed stirring and mixing apparatus is preferably used at a lower speed of 2000 rpm or lower, more preferably 10OOrpm or lower, particularly preferably 500 rpm. It is not preferable to use a high-speed stirring mixing device that applies high shear stress such as a homogenizer to a mixture with a high concentration of Compound A.
- the higher aliphatic compound A is prone to alteration due to heat, shear stress, oxidation reaction, etc. of unsaturated fatty acids such as DHA and EPA and their esters, etc.
- a high-speed agitation mixer is used.
- the unsaturated compound is altered by the high shear stress and frictional heat generated by the high-speed agitation, and the unsaturated compound is in strong contact with the dissolved oxygen in the atmosphere (air). Also occurs.
- the liquid unsaturated compound is converted into fine particles having a high surface area, so that the deterioration due to oxidation is further increased. As a result, an unpleasant odor due to alteration of the unsaturated compound is generated.
- the stirring and mixing temperature is preferably lower, but is generally from room temperature to 75 ° C, preferably from 50 to 70 ° C, more preferably from 40 to 65 ° C.
- the stirring and mixing in the present invention is preferably carried out so as to gradually increase the stirring speed continuously or intermittently.
- this stirring and mixing is preferably performed as follows. For example, stirring is started at a stirring speed of 500 rpm or less, stirring is performed under these conditions for a predetermined time (0.3 to 5 minutes, preferably 0.5 to 2 minutes), and then continuously or intermittently at a predetermined stirring speed (800 to The stirring speed is increased to 6000 rpm, and stirring is performed for a predetermined time (0.5 to 5 minutes, preferably 0.8 to 3 minutes) under this stirring condition.
- the mixture M (I) obtained as described above contains an oily higher aliphatic compound A, but has good retention in water (retention property). When put into water, it will be held in the form of oily liquid spheres at the bottom of the water without floating and separating on the water surface. When stirred, the mixture M (I) becomes fine particles and is dispersed in water. However, when stirring is stopped, the mixture M (I) settles again at the bottom of the water. In this case, when a surfactant is present in the water into which the mixture M is charged, the mixture M can be dispersed in the water in the form of fine particles.
- the specific gravity of the mixture M (I) is 1.01 or more, preferably 1.02 or more, preferably 1.05 or more, and the upper limit is about 2.0.
- the mixture M (I) When the mixture M (I) is put into water, it is held as an oily liquid bulb at the bottom of the water. It is. Therefore, when this mixture M (I) is contained in a solid or semi-solid food containing water, the mixture is stably held in the food without being floated and separated on the surface. . Therefore, contact with the atmosphere is prevented, and alteration due to oxidation of the mixture M (I) is effectively prevented.
- the mixture M (I) is preferably used as a liquid held in water at a concentration of 20% by weight or more, preferably 30% by weight or more.
- the upper limit of the concentration of the mixture M (I) is usually about 45% by weight.
- M (II) a mixture M (hereinafter also referred to as M (II)) composed of a higher aliphatic compound A, a polyolene compound P, a surfactant S, and water is shown.
- any surfactant can be used as long as it does not hinder the formation of the mixture M (II).
- Such surfactant S includes ionic surfactants, nonionic surfactants and amphoteric surfactants.
- the ionic surfactant includes an anionic surfactant and a cationic surfactant.
- the surfactant may be edible, for example, propylene glycol fatty acid ester, glycerin fatty acid ester, polyglycene fatty acid ester, sorbitan fatty acid ester. Sucrose fatty acid ester, lecithin and the like.
- a polydaricene surfactant which is a nonionic surfactant can be preferably used. This compound has 1 to 3 higher aliphatic groups having 12 to 24 carbon atoms, preferably 16 to 20 carbon atoms, to polydalysene having a degree of polymerization of 2 to 20, preferably 5 to 15. It is what I entered.
- this polydaricene surfactant is preferably used as a mixture with lecithin which is an ionic surfactant.
- the weight ratio [L] Z [E] of lecithin L and polyglycene fatty acid ester E is 0.1 to 0.9, preferably 0.2 to 0.8, more preferably 0.4 to 0.6.
- Surfactant S is usually used as an aqueous solution.
- the concentration of surfactant S is 5 to 20% by weight, preferably 8 to 15% by weight.
- the ratio of the Polio-Iri compound ⁇ as an aqueous solution is 0.5 to 5 parts by weight, preferably 1 to 3 parts by weight, per 1 part by weight of the higher aliphatic compound A. The ratio is preferably 1.5 to 2 parts by weight.
- the proportion of surfactant S is 0.5 to 15% by weight, preferably 1 to 10% by weight, based on the higher aliphatic compound.
- the water content is 25 to 50% by weight, preferably 30 to 45% by weight, based on the polyol compound P.
- the specific gravity of this mixture ⁇ ( ⁇ ) is 1.01 or more, preferably 1.02 or more, and its upper limit is about 2.0.
- the mixture ⁇ ⁇ ⁇ ( ⁇ ) is preferably used as a dispersion (emulsion) in which the mixture is dispersed at a concentration of 20% by weight or more.
- the upper limit of the concentration of the mixture (II) is usually about 45% by weight.
- the specific gravity of the mixture ⁇ (II) is greater than the specific gravity of water, so that the mixture ⁇ (II) is always present in the water and the outside air (air ) Is cut off. As a result, deterioration of the mixture ⁇ ( ⁇ ) due to acid ⁇ is effectively prevented.
- This mixture (II) is excellent in water dispersibility and emulsified particle forming property. When this mixture is put into water and stirred, it is dispersed as fine particles in water. This state is maintained for a long time even if the stirring is stopped.
- the mixture ⁇ (II) is contained in the form of emulsified particles by adding it to an aqueous liquid medium.
- An aqueous composition can be obtained.
- the mixture M (I) and the mixture M (II) may contain a hydrophilic substance. Such substances include antioxidants, pH regulators, viscosity modifiers and the like.
- the polyphenolate compound is used in an amount of 5 to 50% by weight, preferably 10 to 25% by weight, based on the higher aliphatic compound A.
- the mixtures M (I) and ⁇ ( ⁇ ) containing such a polyphenol compound are obtained by effectively preventing acidity of the higher aliphatic compound.
- a polyglycerin surfactant is used as the polio complex compound ⁇ , thereby exhibiting an action equivalent to that of the mixture ( ⁇ ) ⁇ (III) can be obtained.
- the polyglycerin surfactant since the polyglycerin surfactant has a large number of hydroxyl groups, it also acts as a polyol-based compound in the present invention.
- various aqueous compositions containing the higher aliphatic compound ⁇ in a dispersed state by mixing the mixture ⁇ (II) or ⁇ (III) in various aqueous liquid media with stirring can be obtained.
- the stirring and mixing device in this case include various conventional devices such as a normal stirring mixer, a homogenizer, and a homomixer.
- aqueous liquid medium to which the mixture M is added is optionally added to conventional auxiliary components such as surfactants, antioxidants, deodorants, fragrances, colorants, vitamins, pH adjusters, and the like. An appropriate amount can be added.
- the stirring and mixing temperature should be a temperature at which the mixture M exhibits a liquid paste state so that the mixture M can be easily dispersed.
- the “dispersion” naturally includes “emulsification”.
- a dispersion in which the higher aliphatic compound A is dispersed in an aqueous liquid medium is obtained.
- the higher aliphatic compound A is integrally bonded with the polyol compound having a specific gravity greater than 1, so that the higher aliphatic compound A is Floating separation is prevented and the dispersion stability is very good.
- the specific gravity [M] of the mixture M and water The ratio [M] Z [W] of the specific liquid medium W to the specific gravity [W] is 1.0 to 2.0, preferably 1.01 to L5, more preferably 1.02 to L2. Particularly preferably, it should be adjusted to the range of 1.05 to L15.
- the aqueous liquid medium in the present invention is various liquid compositions containing water or containing water.
- Such products include various aqueous compositions such as drinking water, aqueous liquid foods, aqueous liquid cosmetics, and aqueous liquid pharmaceuticals.
- the aqueous liquid food contains water and contains various nutrients and foods.
- Such products include milk, soy milk, yogurt, soy sauce, sauce, various juices, tea, lactic acid bacteria drinking water, lactic acid fermented drinking water and the like.
- the specific gravity of these aqueous liquid foods is usually 1.01 or more.
- the higher aliphatic compound A dispersed therein can be, for example, DHA, EPA, or an ester thereof (glycerol ester, ethyl ester, etc.).
- the higher aliphatic compound A it is particularly preferable to use fish oil (eg, tuna oil, bonito oil, sardine oil) containing DHA or EPA.
- DHA and EPA have a variety of excellent physiological activities, and taking these substances daily together with foods that are regularly consumed is very favorable for human health.
- DHA and Z or EPA contained therein is at least 5% by weight, preferably 10% by weight or more, and usually 10 to 40% by weight based on the total fatty acid contained in fish oil. The amount is about%.
- the aqueous liquid medium is an aqueous liquid food
- the DHA and / or EPA component content is appropriately selected according to the type of the liquid food. Usually 0.1 to 30% by weight, preferably Is 0.2 to 10% by weight.
- Drinking water or aqueous liquid food containing the mixture M (III) is usually subjected to a heat sterilization treatment.
- a heat sterilization treatment it was observed that a small amount of oil (a compound A) floats on the surface of the liquid.
- This floating oil component reduces the commercial value of the product, so it is highly desirable to prevent the oil component from floating.
- this floating separation of the oil is caused by the polyglycerin-based interface for drinking water or aqueous liquid food containing the mixture M. It has been discovered that it can be prevented by adding an activator.
- the method for producing drinking water including the heat sterilization step, the step of stirring and mixing the mixture M or the powdered additive with the raw water, and the raw water
- a method for producing a drinking water containing a higher aliphatic compound comprising a step of stirring and mixing a polyglycerin surfactant.
- the step of stirring and mixing the mixture M or the powdered additive with the liquid raw material, and the liquid raw material with polyglycerol there is provided a method for producing an aqueous liquid food containing a high-grade aliphatic compound, comprising a step of stirring and mixing a system surfactant.
- a strong stirring type homogenizer or homomixer can be used in addition to a normal low-speed stirrer.
- the stirring and mixing temperature is 50 to 75 ° C, preferably 55 to 65 ° C.
- the polyglycerin surfactant is used as an aqueous solution, and its concentration is about 2 to 15% by weight.
- the amount of addition is about 0.2 to 10% by weight, preferably about 0.5 to 5% by weight, with respect to drinking water or aqueous liquid food.
- the heating temperature is usually 80 to 140 ° C.
- aqueous composition of the present invention by using an aqueous liquid cosmetic or an aqueous liquid medicine (for example, an aqueous lotion type cosmetic or medicine) as the aqueous liquid medium, higher fats such as DHA and NPA are used. Products containing group compounds can be obtained.
- an aqueous liquid cosmetic or an aqueous liquid medicine for example, an aqueous lotion type cosmetic or medicine
- a mixture M containing the compound A is provided as an additive for adding the higher aliphatic compound A to water (drinking water) and various foods.
- a mixture containing a higher unsaturated aliphatic compound such as DHA and / or its ester or EPA and / or its ester is preferably used.
- the mixture M (I), M (II), or M (III) is contained in a predetermined food or drink, or a raw material thereof, whereby a food or drink containing the higher aliphatic compound A is contained. You can get goods.
- Mixture M (I) has the property of settling in water, so it is a solid, semi-solid containing water. It can be advantageously used as a body food additive.
- an additive used in cooking rice to make cooked rice is provided.
- the additive is (i) a carbon atom having 12 or more carbon atoms having an ester group or a carboxyl group.
- one higher aliphatic compound A (whose specific gravity is less than 1)
- an aqueous solution of a higher fatty acid ester of polyglycerol (whose specific gravity is greater than 1) are stirred and mixed at a stirring speed of 6000 rpm or less.
- the mixture M formed as follows.
- Cooked rice obtained using this additive is one in which the higher aliphatic compound A is dispersed with good uniformity.
- the oil does not disperse from the mixture during cooking.
- the mixture M (I), M (II) or M (III) or an aqueous liquid medium containing the mixture is sprayed in the presence or absence of a water-soluble polymer substance.
- Powdered food additives formed by dry or vacuum drying are provided.
- various edible substances such as starch, protein, dextrin and the like are preferably used as the polymer substance.
- the spray drying method is a conventionally well-known method, and a general spray drying method can be preferably used in the present invention.
- the ratio of the polymer substance is 1 to 30% by weight, preferably 2 to 20% by weight in the total powder.
- Emulsifier liquid E (i) Emulsifier (1) “Sunsoft Q-18SW” (a paste containing 40% decaglycerin fatty acid ester) 5%,
- This mixture Ml is suitable as a food additive for miso, tofu, rice, sauce, dressing and the like.
- this mixture M2 When 5 g of this mixture M2 is put into 100 ml of water, the mixture M2 becomes an oily liquid ball and sinks, and even if it is dispersed by stirring, it will sink again to the bottom and will not float up.
- This product is suitable as an additive for solid foods such as tofu, red bean paste, jam and miso.
- This mixture has a specific gravity of 1.18 and contains an emulsifier, so when it is put into water, it will sink to the bottom, but it gently disperses from the bottom to the whole water due to the action of the emulsifier.
- water has a lower specific gravity, so the dispersion of the mixture occurs in the middle of the water, and the mixture does not float on the surface.
- Example 5 Fish oil A (50 ° C): 6g, maltitol MAL (50 ° C): 9g and emulsifier aqueous solution E: lg (60 ° C) are stirred and mixed (400rpm) and cooled to 7 ° C by rapid refrigeration. A white emulsified mixture M5: 17 g was obtained. The specific gravity of this mixture M5 is 1.26, and the DHA'EPA content in lg is 99 mg. When this mixture M5 was warmed to room temperature and added to 980 g of water, the mixture M5 was settled on the bottom of the water gently by the action of the emulsifier. In this case, the mixture M5 does not float on the surface of the water. This phenomenon indicates that fish oil was stabilized in water, and a dispersion with excellent antioxidant, storage stability and dispersion stability was obtained.
- DHA'EPA-containing mixture M5 obtained in Example 5 15 g of normal temperature milk (sterilized at 120 ° CZ for 2 seconds) 490 g, water 490 g, trehalose 4 g and milk flavor (23051M, Nippon Fragrance Chemicals) lg Then, the mixture was stirred with a mixer (400 rpm) to obtain a white drink containing lOOOOg DHA'EPA.
- Purified fish oil A 3 g and maltitol MAL: 5 g were stirred and mixed at room temperature to obtain DHA'EPA-containing mixture M7: 8 g.
- the characteristic of this mixture is that it sinks into an oily liquid ball when placed in water, and even if stirred, it will sink to the bottom after stirring and will not float.
- Fish oil A 6 g and maltitol MAL: 8 g were stirred at room temperature with a mixer (400 rpm) to obtain a mixture M8: 14 g. This was gently agitated into 500 g (80 ° C.) of a paste-like aqueous solution of raw material powder for agar jelly (manufactured by Kitahara Sangyo Co., Ltd.) and then cooled in a refrigerator for about 1 hour. In this way, agar jelly with a DHA'EPA content of 336 mg in lOOg was produced. Fish oil does not come out on the surface, it's clear! Compared with normal jelly, it was completely indistinguishable, and the smell and taste of fish oil was not felt. Fish oil A: When only 6g was added, the fish oil floated on the surface and a smell was generated, and an edible jelly could not be produced.
- DHA'EPA-containing mixture M5 obtained in Example 5 30 g of catechin (Polyphenone 70A, manufactured by Mitsui Norin Co., Ltd.) at a room temperature of 15 ° C. Contains DHA, EPA, catechin Mixture M10: 33.5 g was obtained.
- Example 6 an experiment was conducted in the same manner except that commercial soymilk was diluted with water and adjusted to a specific gravity of about 1.02, instead of milk.
- Example 3 instead of glycerin, sorbite liquid (D-sorbit 54%, reduced starch sugar product 16%, water 30%, “Sorpert”, manufactured by Ueno Pharmaceutical Co., Ltd.) and glycerin ( The experiment was carried out in the same manner except that a glycerin mixing ratio of 50% by weight was used. Also in this case, an emulsion (mixture M12) having good dispersion stability was obtained. The emulsified liquid also felt unpleasant odor.
- sorbite liquid D-sorbit 54%, reduced starch sugar product 16%, water 30%, “Sorpert”, manufactured by Ueno Pharmaceutical Co., Ltd.
- Example 2 an experiment was conducted in the same manner except that a mixed oil of soybean oil and rapeseed oil was used instead of fish oil A. Also in this case, a mixture Ml 3 in which the mixed oil and maltitol MAL were combined was obtained.
- Example 15 The contents of the two beakers were then transferred to a 200 ml beaker and the entire contents (temperature about 53 ° C.) were stirred using a mixer at a rotational speed of 400 rpm for 3 minutes to form a mixture M14. [0059]
- Example 15 The contents of the two beakers were then transferred to a 200 ml beaker and the entire contents (temperature about 53 ° C.) were stirred using a mixer at a rotational speed of 400 rpm for 3 minutes to form a mixture M14.
- Example 4 an experiment was conducted in the same manner except that olive oil was used instead of fish oil A. Also in this case, a mixture M15 in which olive oil and maltitol MAL were combined was obtained. This mixture M15 also showed the same behavior as the mixture M4 of Example 4.
- Example 3 fish oil A was added to the mixture of maltitol MAL and milky lotion aqueous solution E, which had been formed in advance, and a homomixer (rotation speed: 10,000 times for Z minutes) was used. The experiment was conducted in the same manner except that the stirring temperature was 90 ° C. and stirring and mixing was performed.
- Oleic acid (specific gravity 0.890, purity 88.9%): 5 g, glycerin G: 10 g, and water: 2 g were stirred and mixed with a mixer (rotation speed: 400 rpm) to obtain a mixture M16. It was confirmed that when this was put into water, it settled in the water and an oleic acid / glycerin mixture was formed.
- Example 17 an experiment was performed in the same manner except that an aqueous solution of a surfactant (alkyl ether sulfate Na) was used instead of the emulsifier solution (2), to obtain a mixture M18.
- a surfactant alkyl ether sulfate Na
- a mixture M19 was obtained in the same manner as in Example 17 except that maltitol MAL was used instead of glycerin G. This mixture M19 also showed the same behavior as the mixture M17.
- Emulsifier solution A 7.3 g
- Catechin C H 0.4 g
- Vitamin E _ 0.2 g ⁇ _
- Emulsifier (1) 8 g
- Emulsifier (2) 2 g
- Emulsifier (1) 12g
- Maltitol MAL mixture 32.5 g in a beaker and stir as follows with a hand mixer. The mixture was stirred for 30 seconds at a rotational speed of 400 rpm, then stirred for 30 seconds at a rotational speed of 1200 rpm, and then stirred for 60 seconds at a rotational speed of 2000 rpm to obtain 32.5 g of a maltitol MAL mixed solution (60 ° C).
- this emulsion was stored at 10 ° C for 60 days and analyzed, and as a result, it showed a good appearance without causing alteration with an acid value (AV) of 0.84 and a peroxy acid value (POV) of 1.75 meqZkg. .
- this DHA-containing milk was heated to 60 ° C in a microwave oven, and the changes in taste were compared. It was evaluated that there was no fishy odor and the taste resembled that of commercially available milk.
- DHA mixture M20 obtained in Example 20: 28.6 g was added to 1000 ml (60 ° C.) of milk to obtain 1000 ml of milk containing 308 mg DHA ⁇ EPA in 100 ml as described in Example 20.
- Using this milk we made a trial of power spicy sea yogurt, which resulted in DHA'EPA 308 mg yogurt in 100 g yogurt.
- Example 20 32.5 g of the maltitol MAL mixed solution (60 ° C) and 21.5 g of fish oil A: (60 ° C) shown in Example 20 are placed in a beaker and stirred and mixed by the method of Example 20. A mixture M22 with a DHA'EPA content of 3 OOmg in 2.72g was obtained.
- maltitol wraps fish oil in a stable manner in the hamburger, and the medium force of the hamburger does not come out on the surface. it is conceivable that.
- Fish oil A 10 g and emulsifier solution B: 5 g were stirred at room temperature for 30 seconds with a mixer (rotation speed 400 rpm) to obtain a mixture M23 containing 1.6 mg of DHA'EPA 300 mg. 11.9g of this mixture is 370g of rice In addition to 370 g of water, gently stirred. This was cooked in an electric rice cooker. Cooking rice hot water 720g of rice with a fishy smell was cooked. When subjected to a panel test, the fishy odor was not felt at all, and it was indistinguishable from commercial rice. The rice balls were frozen for 10 days, warmed in a dens range, and tasted.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Mycology (AREA)
- Biophysics (AREA)
- Fats And Perfumes (AREA)
- Non-Alcoholic Beverages (AREA)
Abstract
Description
Claims
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004-231300 | 2004-08-06 | ||
JP2004231300 | 2004-08-06 | ||
JP2005084999 | 2005-03-23 | ||
JP2005-084999 | 2005-03-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006018992A1 true WO2006018992A1 (ja) | 2006-02-23 |
Family
ID=35907382
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/014429 WO2006018992A1 (ja) | 2004-08-06 | 2005-08-05 | 高級脂肪族化合物を含有する水性混合体 |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2006018992A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019146207A1 (ja) * | 2018-01-25 | 2019-08-01 | 不二製油グループ本社株式会社 | 高度不飽和脂肪酸を含有する豆乳飲料 |
JP2020168091A (ja) * | 2019-04-01 | 2020-10-15 | 東芝ホームテクノ株式会社 | 炊飯器 |
Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62250941A (ja) * | 1986-04-23 | 1987-10-31 | Taiyo Kagaku Co Ltd | 可溶化液の製造法 |
JPS63226244A (ja) * | 1987-03-16 | 1988-09-20 | Wakoudou Kk | 合成乳 |
JPH04248955A (ja) * | 1991-01-30 | 1992-09-04 | Kanebo Ltd | 組合わせ菓子 |
JPH06228245A (ja) * | 1993-02-02 | 1994-08-16 | Mitsubishi Rayon Co Ltd | 車輛モール用樹脂および車輛モール用構造体 |
JPH07147899A (ja) * | 1993-11-29 | 1995-06-13 | Nippon Oil & Fats Co Ltd | 油脂含有水溶性組成物 |
JPH07227227A (ja) * | 1993-12-20 | 1995-08-29 | Sanei Gen F F I Inc | 安定な乳化組成物及びそれを含有する食品 |
JPH10316551A (ja) * | 1997-05-20 | 1998-12-02 | Noevir Co Ltd | 液状洗浄料 |
JPH10316552A (ja) * | 1997-05-20 | 1998-12-02 | Noevir Co Ltd | 液状洗浄料 |
JPH10316553A (ja) * | 1997-05-20 | 1998-12-02 | Noevir Co Ltd | 液状洗浄料 |
JP2000270791A (ja) * | 1999-03-26 | 2000-10-03 | Taiyo Kagaku Co Ltd | 澱粉複合体形成用乳化剤製剤 |
JP2002370931A (ja) * | 2001-06-19 | 2002-12-24 | Shiseido Co Ltd | 油状組成物 |
WO2003066025A1 (en) * | 2002-02-01 | 2003-08-14 | Micelle Products, Inc. | Clear micellized formulations of beta-carotene for treating leukoplakia |
JP2004083874A (ja) * | 2002-06-28 | 2004-03-18 | Taiyo Kagaku Co Ltd | 水中油滴型乳化組成物 |
JP2005036206A (ja) * | 2003-06-26 | 2005-02-10 | Mitsubishi Chemicals Corp | ポリグリセリン脂肪酸エステル及びこれを含有する乳化または可溶化組成物 |
JP2005143424A (ja) * | 2003-11-18 | 2005-06-09 | Takasago Internatl Corp | 低アルコール飲料用の乳化ないし可溶化剤、これを含有する乳化ないし可溶化製剤および低アルコール飲料 |
-
2005
- 2005-08-05 WO PCT/JP2005/014429 patent/WO2006018992A1/ja active Application Filing
Patent Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62250941A (ja) * | 1986-04-23 | 1987-10-31 | Taiyo Kagaku Co Ltd | 可溶化液の製造法 |
JPS63226244A (ja) * | 1987-03-16 | 1988-09-20 | Wakoudou Kk | 合成乳 |
JPH04248955A (ja) * | 1991-01-30 | 1992-09-04 | Kanebo Ltd | 組合わせ菓子 |
JPH06228245A (ja) * | 1993-02-02 | 1994-08-16 | Mitsubishi Rayon Co Ltd | 車輛モール用樹脂および車輛モール用構造体 |
JPH07147899A (ja) * | 1993-11-29 | 1995-06-13 | Nippon Oil & Fats Co Ltd | 油脂含有水溶性組成物 |
JPH07227227A (ja) * | 1993-12-20 | 1995-08-29 | Sanei Gen F F I Inc | 安定な乳化組成物及びそれを含有する食品 |
JPH10316551A (ja) * | 1997-05-20 | 1998-12-02 | Noevir Co Ltd | 液状洗浄料 |
JPH10316552A (ja) * | 1997-05-20 | 1998-12-02 | Noevir Co Ltd | 液状洗浄料 |
JPH10316553A (ja) * | 1997-05-20 | 1998-12-02 | Noevir Co Ltd | 液状洗浄料 |
JP2000270791A (ja) * | 1999-03-26 | 2000-10-03 | Taiyo Kagaku Co Ltd | 澱粉複合体形成用乳化剤製剤 |
JP2002370931A (ja) * | 2001-06-19 | 2002-12-24 | Shiseido Co Ltd | 油状組成物 |
WO2003066025A1 (en) * | 2002-02-01 | 2003-08-14 | Micelle Products, Inc. | Clear micellized formulations of beta-carotene for treating leukoplakia |
JP2004083874A (ja) * | 2002-06-28 | 2004-03-18 | Taiyo Kagaku Co Ltd | 水中油滴型乳化組成物 |
JP2005036206A (ja) * | 2003-06-26 | 2005-02-10 | Mitsubishi Chemicals Corp | ポリグリセリン脂肪酸エステル及びこれを含有する乳化または可溶化組成物 |
JP2005143424A (ja) * | 2003-11-18 | 2005-06-09 | Takasago Internatl Corp | 低アルコール飲料用の乳化ないし可溶化剤、これを含有する乳化ないし可溶化製剤および低アルコール飲料 |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019146207A1 (ja) * | 2018-01-25 | 2019-08-01 | 不二製油グループ本社株式会社 | 高度不飽和脂肪酸を含有する豆乳飲料 |
JPWO2019146207A1 (ja) * | 2018-01-25 | 2020-04-02 | 不二製油株式会社 | 高度不飽和脂肪酸を含有する豆乳飲料 |
JP2020168091A (ja) * | 2019-04-01 | 2020-10-15 | 東芝ホームテクノ株式会社 | 炊飯器 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4417039B2 (ja) | 水中油滴型乳化組成物 | |
JP3414530B2 (ja) | 安定な乳化組成物及びそれを含有する食品 | |
JP3941073B2 (ja) | 油脂組成物及びそれを含む食品 | |
JP6715930B2 (ja) | ゲル状食品組成物及びこれを用いた食品 | |
JP4044354B2 (ja) | 耐アルコール性、耐酸性、耐塩性を有する組成物および用途 | |
WO2005104865A1 (ja) | 油脂組成物 | |
JP2019004877A (ja) | 乳化組成物及び飲料 | |
JPH07305088A (ja) | 粉末油脂組成物 | |
JP3452713B2 (ja) | 乳化又は粉末機能性物質の製造方法 | |
EP1275309A1 (en) | Sterol fatty acid ester composition and foods containing the same | |
JP5211854B2 (ja) | 飲料用油脂組成物およびこれを含有する飲料 | |
JP3596059B2 (ja) | 高度不飽和脂肪酸含有油脂乳化組成物 | |
JP2005185234A (ja) | 多価不飽和脂肪酸成分含有発酵乳製品及びその製造方法 | |
JP2009284859A (ja) | 飲食品の甘味増強剤および甘味増強方法 | |
JP4670008B2 (ja) | 高級脂肪族化合物を含有する炊飯用添加剤 | |
JPH06169735A (ja) | 栄養飲料組成物 | |
JP4457568B2 (ja) | 酸性乳化食品 | |
WO2006018992A1 (ja) | 高級脂肪族化合物を含有する水性混合体 | |
JP4396334B2 (ja) | 起泡性水中油型乳化物 | |
JP2004248593A (ja) | 魚油乳化組成物及び該魚油乳化組成物を配合した乳関連飲料 | |
JP4766557B2 (ja) | 食品用添加剤及びそれを含有する食品、並びに該食品の製造方法 | |
JP3419351B2 (ja) | フレーバー組成物およびそれを含有する安定な透明飲料 | |
JPH08259943A (ja) | 乳化油脂用酸化安定剤 | |
JP3422338B2 (ja) | 高度不飽和脂肪酸含有粉末飲料 | |
JP3762276B2 (ja) | 乳化食品 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU LV MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
DPE1 | Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |