JP2006280276A - Lignan compound-containing milk beverage - Google Patents
Lignan compound-containing milk beverage Download PDFInfo
- Publication number
- JP2006280276A JP2006280276A JP2005104815A JP2005104815A JP2006280276A JP 2006280276 A JP2006280276 A JP 2006280276A JP 2005104815 A JP2005104815 A JP 2005104815A JP 2005104815 A JP2005104815 A JP 2005104815A JP 2006280276 A JP2006280276 A JP 2006280276A
- Authority
- JP
- Japan
- Prior art keywords
- milk
- milk beverage
- oil
- lignan compound
- lignan
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- -1 Lignan compound Chemical class 0.000 title claims abstract description 76
- 229930013686 lignan Natural products 0.000 title claims abstract description 71
- 235000009408 lignans Nutrition 0.000 title claims abstract description 71
- 235000020124 milk-based beverage Nutrition 0.000 title claims abstract description 43
- PEYUIKBAABKQKQ-AFHBHXEDSA-N (+)-sesamin Chemical compound C1=C2OCOC2=CC([C@H]2OC[C@H]3[C@@H]2CO[C@@H]3C2=CC=C3OCOC3=C2)=C1 PEYUIKBAABKQKQ-AFHBHXEDSA-N 0.000 claims description 29
- PEYUIKBAABKQKQ-UHFFFAOYSA-N epiasarinin Natural products C1=C2OCOC2=CC(C2OCC3C2COC3C2=CC=C3OCOC3=C2)=C1 PEYUIKBAABKQKQ-UHFFFAOYSA-N 0.000 claims description 29
- 239000003921 oil Substances 0.000 claims description 24
- VRMHCMWQHAXTOR-CMOCDZPBSA-N sesamin Natural products C1=C2OCOC2=CC([C@@H]2OC[C@@]3(C)[C@H](C=4C=C5OCOC5=CC=4)OC[C@]32C)=C1 VRMHCMWQHAXTOR-CMOCDZPBSA-N 0.000 claims description 23
- 239000003925 fat Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 12
- 235000010469 Glycine max Nutrition 0.000 claims description 5
- 239000003995 emulsifying agent Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 244000068988 Glycine max Species 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 235000019543 dairy drink Nutrition 0.000 claims 1
- 235000013322 soy milk Nutrition 0.000 abstract description 18
- 235000013361 beverage Nutrition 0.000 abstract description 17
- 238000002156 mixing Methods 0.000 abstract description 6
- 239000006185 dispersion Substances 0.000 abstract description 5
- 150000002632 lipids Chemical class 0.000 abstract description 2
- 235000020247 cow milk Nutrition 0.000 abstract 1
- 238000004321 preservation Methods 0.000 abstract 1
- 235000019198 oils Nutrition 0.000 description 22
- 235000019197 fats Nutrition 0.000 description 18
- 239000008159 sesame oil Substances 0.000 description 16
- 235000011803 sesame oil Nutrition 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 239000000284 extract Substances 0.000 description 14
- 235000013336 milk Nutrition 0.000 description 12
- 239000008267 milk Substances 0.000 description 12
- 210000004080 milk Anatomy 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 241000207961 Sesamum Species 0.000 description 8
- 235000003434 Sesamum indicum Nutrition 0.000 description 8
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 8
- 239000000796 flavoring agent Substances 0.000 description 7
- 235000019634 flavors Nutrition 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 235000013861 fat-free Nutrition 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000012488 sample solution Substances 0.000 description 4
- KQRXQIPRDKVZPW-UHFFFAOYSA-N sesaminol Natural products C1=C2OCOC2=CC(C2OCC3C2COC3C2=CC=3OCOC=3C=C2O)=C1 KQRXQIPRDKVZPW-UHFFFAOYSA-N 0.000 description 4
- KQRXQIPRDKVZPW-ISZNXKAUSA-N sesaminol Chemical compound C1=C2OCOC2=CC([C@H]2OC[C@H]3[C@@H]2CO[C@@H]3C2=CC=3OCOC=3C=C2O)=C1 KQRXQIPRDKVZPW-ISZNXKAUSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 244000060011 Cocos nucifera Species 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- 240000007594 Oryza sativa Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 235000014121 butter Nutrition 0.000 description 3
- 235000012000 cholesterol Nutrition 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 235000013402 health food Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 235000020185 raw untreated milk Nutrition 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 230000001953 sensory effect Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 235000019498 Walnut oil Nutrition 0.000 description 2
- 239000008168 almond oil Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 235000020197 coconut milk Nutrition 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 230000035622 drinking Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 230000006870 function Effects 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
- 238000001727 in vivo Methods 0.000 description 2
- 150000005692 lignans Chemical class 0.000 description 2
- 235000004213 low-fat Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229930014626 natural product Natural products 0.000 description 2
- 239000010466 nut oil Substances 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 239000004006 olive oil Substances 0.000 description 2
- 239000003346 palm kernel oil Substances 0.000 description 2
- 235000019865 palm kernel oil Nutrition 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 229940059463 sesame seed extract Drugs 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000000967 suction filtration Methods 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 150000003722 vitamin derivatives Chemical class 0.000 description 2
- 239000008170 walnut oil Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000010497 wheat germ oil Substances 0.000 description 2
- HGXBRUKMWQGOIE-AFHBHXEDSA-N (+)-pinoresinol Chemical compound C1=C(O)C(OC)=CC([C@@H]2[C@@H]3[C@@H]([C@H](OC3)C=3C=C(OC)C(O)=CC=3)CO2)=C1 HGXBRUKMWQGOIE-AFHBHXEDSA-N 0.000 description 1
- 206010001605 Alcohol poisoning Diseases 0.000 description 1
- 244000136475 Aleurites moluccana Species 0.000 description 1
- 235000006667 Aleurites moluccana Nutrition 0.000 description 1
- 235000019489 Almond oil Nutrition 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 235000011437 Amygdalus communis Nutrition 0.000 description 1
- 206010006187 Breast cancer Diseases 0.000 description 1
- 208000026310 Breast neoplasm Diseases 0.000 description 1
- 235000004936 Bromus mango Nutrition 0.000 description 1
- 208000005623 Carcinogenesis Diseases 0.000 description 1
- 206010013911 Dysgeusia Diseases 0.000 description 1
- 208000029951 Laryngeal disease Diseases 0.000 description 1
- 235000018330 Macadamia integrifolia Nutrition 0.000 description 1
- 240000000912 Macadamia tetraphylla Species 0.000 description 1
- 235000003800 Macadamia tetraphylla Nutrition 0.000 description 1
- 240000007228 Mangifera indica Species 0.000 description 1
- 235000014826 Mangifera indica Nutrition 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 240000002834 Paulownia tomentosa Species 0.000 description 1
- 235000009184 Spondias indica Nutrition 0.000 description 1
- 208000007271 Substance Withdrawal Syndrome Diseases 0.000 description 1
- 235000018936 Vitellaria paradoxa Nutrition 0.000 description 1
- 241001135917 Vitellaria paradoxa Species 0.000 description 1
- VBIRCRCPHNUJAS-UHFFFAOYSA-N Xanthoxylol Chemical compound C1=C(O)C(OC)=CC(C2C3C(C(OC3)C=3C=C4OCOC4=CC=3)CO2)=C1 VBIRCRCPHNUJAS-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000000172 allergic effect Effects 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- 239000008163 avocado oil Substances 0.000 description 1
- 235000021302 avocado oil Nutrition 0.000 description 1
- 239000003613 bile acid Substances 0.000 description 1
- 230000008827 biological function Effects 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
- 239000006227 byproduct Substances 0.000 description 1
- 230000036952 cancer formation Effects 0.000 description 1
- 231100000504 carcinogenesis Toxicity 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 150000001982 diacylglycerols Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000008524 evening primrose extract Nutrition 0.000 description 1
- 239000010475 evening primrose oil Substances 0.000 description 1
- 229940089020 evening primrose oil Drugs 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 239000008169 grapeseed oil Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 208000030603 inherited susceptibility to asthma Diseases 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 230000003908 liver function Effects 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 206010025482 malaise Diseases 0.000 description 1
- 150000004667 medium chain fatty acids Chemical class 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 235000021243 milk fat Nutrition 0.000 description 1
- 235000019488 nut oil Nutrition 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- HGXBRUKMWQGOIE-UHFFFAOYSA-N pinoresinol Chemical compound C1=C(O)C(OC)=CC(C2C3C(C(OC3)C=3C=C(OC)C(O)=CC=3)CO2)=C1 HGXBRUKMWQGOIE-UHFFFAOYSA-N 0.000 description 1
- OHOPKHNWLCMLSW-UHFFFAOYSA-N pinoresinol Natural products C1=C(O)C(OC)=CC(C2C3C(C(OC3)C=3C=C(CO)C(O)=CC=3)CO2)=C1 OHOPKHNWLCMLSW-UHFFFAOYSA-N 0.000 description 1
- 235000007221 pinoresinol Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001944 prunus armeniaca kernel oil Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- OJVGWDJIYBTWDS-UHFFFAOYSA-N sesamolinol Chemical compound C1=C(O)C(OC)=CC(OC2C3C(C(OC3)C=3C=C4OCOC4=CC=3)CO2)=C1 OJVGWDJIYBTWDS-UHFFFAOYSA-N 0.000 description 1
- 229940057910 shea butter Drugs 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 239000007901 soft capsule Substances 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- LVUPFEOCDSHRBL-UHFFFAOYSA-N syringaresinol Natural products COc1cccc(OC)c1C2OCC3C2COC3c4c(OC)cccc4OC LVUPFEOCDSHRBL-UHFFFAOYSA-N 0.000 description 1
- KOWMJRJXZMEZLD-UHFFFAOYSA-N syringaresinol Chemical compound COC1=C(O)C(OC)=CC(C2C3C(C(OC3)C=3C=C(OC)C(O)=C(OC)C=3)CO2)=C1 KOWMJRJXZMEZLD-UHFFFAOYSA-N 0.000 description 1
- 239000010913 used oil Substances 0.000 description 1
- BURBOJZOZGMMQF-UHFFFAOYSA-N xanthoxylol Natural products C1=C(O)C(OC)=CC=C1C1C(COC2C=3C=C4OCOC4=CC=3)C2CO1 BURBOJZOZGMMQF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Dairy Products (AREA)
- Beans For Foods Or Fodder (AREA)
Abstract
Description
本発明は、リグナン類化合物を含有する乳飲料に関し、より詳しくはリグナン類化合物を油脂に溶解させた後、該溶解液を乳飲料に添加して製造することを特徴とするリグナン類化合物を含有する乳飲料に関する。 The present invention relates to a dairy beverage containing a lignan compound, and more specifically, after the lignan compound is dissolved in an oil and fat, the lynan compound is produced by adding the solution to the milk beverage. It relates to milk drinks.
リグナン類化合物は、種々の用途での使用が知られている。例えば、USP4427694には、セサミンがアルコール中毒やアルコールや喫煙の禁断症状の緩和に有効であること、また特開平2−138120号公報には、セサミノールやエピセサミノールが気管支喘息等のアレルギー症の治療・予防に有効であることが開示されている。本出願人らによっても、リグナン類化合物の用途が種々開発されており、現在までに血中コレステロール低下(特許3001589号)、Δ5 −不飽和化酵素阻害(特許3070611号)、肝機能改善(特許3075358号)、コレステロール降下(特許3075360号)、悪酔防止(特許3124062号)、コレステロール及び胆汁酸の代謝阻害、コレステロール低下(特許3283274号)、発癌抑制(特願平2−281839号)、乳癌抑制(特願平3−200757号)や、過酸化脂質生成抑制(特願平3−212295号)、活性酸素除去(特願平5−14884号)の効果が確認されている。このような優れた生体内機能を有するリグナン類化合物について、本出願人らは、ソフトカプセル剤の健康食品「セサミンE」、「セサミンEプラス」等を販売している。 Lignans compounds are known for use in various applications. For example, US Pat. No. 4,427,694 discloses that sesamin is effective in alleviating alcohol poisoning and withdrawal symptoms of alcohol and smoking, and JP-A-2-138120 discloses that sesaminol and episesaminol are allergic to bronchial asthma. It is disclosed that it is effective for treatment and prevention. Various uses of lignan compounds have also been developed by the present applicants. To date, blood cholesterol lowering (Patent No. 3001589), Δ 5 -desaturase inhibition (Patent No. 3070611), liver function improvement ( Patent 3075358), cholesterol lowering (patent 3075360), prevention of sickness (patent 3124062), metabolism inhibition of cholesterol and bile acids, cholesterol lowering (patent 3283274), carcinogenesis suppression (Japanese Patent Application No. 2-281839), breast cancer The effects of inhibition (Japanese Patent Application No. 3-200757), lipid peroxide production inhibition (Japanese Patent Application No. 3-212295), and removal of active oxygen (Japanese Patent Application No. 5-14884) have been confirmed. With regard to lignan compounds having such excellent in vivo functions, the present applicants sell soft capsule health foods “Sesamin E”, “Sesamin E Plus” and the like.
一方、高齢者や咽頭、喉頭に疾患を持つ人にとっては、錠剤やカプセル剤の服用が困難であるという問題が指摘されている。優れた生体内機能を有するリグナン類化合物について、上記のとおりカプセル剤の健康食品は開発されているが、高齢者等を含めた誰もが容易に摂取しうる飲料の形態で服用しうるリグナン類化合物の飲食品の開発も望まれていた。しかし、リグナン類化合物を飲料に配合した場合、リグナン類化合物の難溶性の性質から、保存中に沈殿を生じるという問題があった。分散安定性を付与する目的で、乳化剤を添加すると沈殿は防止できるが、添加した乳化剤により官能的に好ましくない風味を呈するという問題があった。
本発明の課題は、リグナン類化合物を容易に十分量摂取することができる実用的な飲料を提供するである。とりわけ、保存安定性を有し、官能的に優れた、リグナン類化合物を含有する乳飲料を提供することである。 An object of the present invention is to provide a practical beverage capable of easily taking a sufficient amount of a lignan compound. In particular, it is to provide a milk beverage containing a lignan compound having storage stability and excellent sensory properties.
本発明者らは、上記課題を解決するために鋭意検討を行った結果、牛乳、豆乳等の乳飲料は乳化食品であり、脂質との相性が良く、これらの乳飲料に油脂を添加しても分離しにくく混ざりやすいということを見出した。そこで、難溶性のリグナン類化合物を油脂に溶解した後に乳飲料に混合すると、分散安定性が良好で、官能的にも良好なリグナン類化合物含有飲料が得られることを見出し、本発明を完成するに至った。 As a result of intensive studies to solve the above-mentioned problems, the present inventors have found that milk beverages such as milk and soy milk are emulsified foods, have good compatibility with lipids, and fats and oils are added to these milk beverages. Also found that it is difficult to separate and mix easily. Thus, when a poorly soluble lignan compound is dissolved in an oil and fat and then mixed with a milk beverage, it is found that a lignan compound-containing beverage with good dispersion stability and good sensory properties can be obtained, and the present invention is completed. It came to.
すなわち、本発明は、油脂に溶解したリグナン類化合物を含有する乳飲料である。 That is, this invention is a milk drink containing the lignan compound melt | dissolved in fats and oils.
本発明のリグナン類化合物を含有する乳飲料は、優れたリグナン類化合物の分散安定性を有する。リグナン類化合物を高濃度で配合することができるので、例えば、リグナン類化合物がセサミンである場合、1日の摂取量の目安である10mgを一回量の飲料(約30〜2000ml)から摂取することもできる。 The milk beverage containing the lignan compound of the present invention has excellent dispersion stability of the lignan compound. Since a lignan compound can be blended at a high concentration, for example, when the lignan compound is sesamin, 10 mg, which is a standard of daily intake, is taken from a single dose (about 30 to 2000 ml). You can also.
また、本発明の乳飲料は、リグナン類化合物独特の風味が乳成分によってマスキングされているため官能的に好ましい風味を呈するものであり、嗜好飲料としても日常的に容易に摂取できるものである。 Moreover, since the flavor peculiar to a lignan compound is masked by the milk component, the milk beverage of this invention exhibits a sensory preferable flavor, and can be easily ingested as a favorite beverage on a daily basis.
リグナン類化合物
本発明で使用するリグナン類化合物としては、セサミン、セサミノール、エピセサミン、エピセサミノール、セサモリン、2−(3,4−メチレンジオキシフェニル)−6−(3−メトキシ−4−ヒドロキシフェニル)−3,7−ジオキサビシクロ[3,3,0]オクタン、2,6−ビス−(3−メトキシ−4−ヒドロキシフェニル)−3,7−ジオキサビシクロ[3,3,0]オクタン、または2−(3,4−メチレンジオキシフェニル)−6−(3−メトキシ−4−ヒドロキシフェノキシ)−3,7−ジオキサビシクロ[3,3,0]オクタン等を挙げることができ、これらを単独で、または混合して使用することができる。
Lignan compounds The lignan compounds used in the present invention include sesamin, sesaminol, episesamin, episesaminol, sesamoline, 2- (3,4-methylenedioxyphenyl) -6- (3-methoxy-4-hydroxy Phenyl) -3,7-dioxabicyclo [3,3,0] octane, 2,6-bis- (3-methoxy-4-hydroxyphenyl) -3,7-dioxabicyclo [3,3,0] And octane or 2- (3,4-methylenedioxyphenyl) -6- (3-methoxy-4-hydroxyphenoxy) -3,7-dioxabicyclo [3,3,0] octane. These can be used alone or in admixture.
本発明の飲料に添加するリグナン類化合物およびリグナン類化合物を主成分とする抽出物を得る方法として次の手順で行うことができる。まず、リグナン類化合物を主成分とする抽出物を胡麻油から得るには、胡麻油とは実質的に非混和性であり、かつリグナン類化合物を抽出・溶解することができる種々の有機溶剤を用いて抽出・濃縮することで得られる。このような有機溶剤として、例えばアセトン、メチルエチルケトン、ジエチルケトン、メタノール、エタノール等を挙げることができる。リグナン類化合物を主成分とする抽出物を得るには、例えば胡麻油と上記の溶剤のいずれかとを均一に混同した後、低温において静置し、遠心分離等の定法に従って相分離を行い、溶剤画分から溶剤を蒸発除去することにより得られる。さらに具体的には、胡麻油を2〜10倍、好ましくは6〜8倍容量のアセトンに溶かし、−80℃で一晩放置する。その結果、油成分が沈殿となり、濾過により得た濾液から有機溶剤を留去して、リグナン類化合物を主成分とする抽出物が得られる。あるいは、胡麻油を熱メタノールまたは熱エタノールで混合した後、室温において静置し、溶剤画分から溶剤を蒸発除去することにより得られる、さらに具体的には、胡麻油を2〜10倍、好ましくは5〜7倍容量の熱メタノール(50℃以上)または熱エタノール(50℃以上)で混合し激しく抽出する。室温に静置あるいは遠心分離等の定法に従って相分離を行い、溶剤画分から溶剤を留去して、リグナン類化合物を主成分とする抽出物が得られる。また、超臨界ガス抽出も利用できる。この抽出物より、各々のリグナン類化合物を得るためには、抽出物をカラムクロマトグラフィー、高速液体クロマトグラフィー、再結晶、蒸留、液々交流分配クロマトグラフィー等の定法に従って処理することにより目的とする化合物を単離すればよい。さらに具体的には、逆相カラム、溶離液にメタノール/水(60:40)を使って、上記抽出物を高速液体クロマトグラフィーで分取し、溶媒を留去した後、得られた結晶をエタノールで再結晶化することで、セサミン、エピセサミン、セサミノール、エピセサミノール等の各リグナン類化合物が得られる。用いる胡麻油は精製品でもよく、また胡麻油の製造過程で脱色工程前のいずれの粗製品でもよく、さらに、胡麻種子あるいは胡麻粕(脱脂胡麻種子、残油分8〜10%)であってもよい。この場合、胡麻種子あるいは胡麻粕を必要により破砕した後、任意の溶剤、例えば胡麻油からの抽出について前記した溶剤を用いて定法により抽出することができる。抽出残渣を分離した後、抽出液から蒸発等により溶剤を留去することにより抽出物が得られる。このように精製された胡麻種子抽出物、胡麻粕抽出物あるいは粗製品の胡麻油抽出物からは、セサミン、エピセサミン、セサミノール、エピセサミノール以外に、セサモリン、2−(3,4−メチレンジオキシフェニル)−6−(3−メトキシ−4−ヒドロキシフェニル)−3,7−ジオキサビシクロ[3,3,0]オクタン、2,6−ビス−(3−メトキシ−4−ヒドロキシフェニル)−3,7−ジオキサビシクロ[3,3,0]オクタン、または2−(3,4−メチレンジオキシフェニル)−6−(3−メトキシ−4−ヒドロキシフェノキシ)−3,7−ジオキサビシクロ[3,3,0]オクタンの各リグナン類化合物が同様の手法で得られる。 The lignan compound added to the beverage of the present invention and a method for obtaining an extract containing the lignan compound as a main component can be performed by the following procedure. First, in order to obtain an extract based on lignan compounds from sesame oil, various organic solvents that are substantially immiscible with sesame oil and that can extract and dissolve lignan compounds are used. Obtained by extraction and concentration. Examples of such an organic solvent include acetone, methyl ethyl ketone, diethyl ketone, methanol, ethanol and the like. In order to obtain an extract containing a lignan compound as a main component, for example, sesame oil and any of the above-mentioned solvents are uniformly mixed, and then allowed to stand at a low temperature and subjected to phase separation according to a conventional method such as centrifugation, It is obtained by evaporating and removing the solvent from the components. More specifically, sesame oil is dissolved in 2 to 10 times, preferably 6 to 8 times the volume of acetone, and left overnight at -80 ° C. As a result, the oil component becomes a precipitate, and the organic solvent is distilled off from the filtrate obtained by filtration to obtain an extract containing a lignan compound as a main component. Alternatively, sesame oil is obtained by mixing sesame oil with hot methanol or hot ethanol, and then allowing to stand at room temperature and evaporating and removing the solvent from the solvent fraction. More specifically, sesame oil is 2 to 10 times, preferably 5 to 5 times. Mix vigorously with 7 volumes of hot methanol (over 50 ° C) or hot ethanol (over 50 ° C). Phase separation is performed according to a conventional method such as standing at room temperature or centrifugation, and the solvent is distilled off from the solvent fraction to obtain an extract containing a lignan compound as a main component. Supercritical gas extraction can also be used. In order to obtain each lignan compound from this extract, the objective is to treat the extract according to a conventional method such as column chromatography, high performance liquid chromatography, recrystallization, distillation, liquid-liquid exchange chromatography, etc. What is necessary is just to isolate a compound. More specifically, the extract was separated by high performance liquid chromatography using a reverse phase column and methanol / water (60:40) as an eluent, and the solvent was distilled off. By recrystallization from ethanol, lignan compounds such as sesamin, episesamin, sesaminol, episesaminol and the like are obtained. The sesame oil used may be a refined product, or any crude product before the decolorization step in the process of producing sesame oil, and may be sesame seeds or sesame seeds (defatted sesame seeds, residual oil content 8 to 10%). In this case, the sesame seeds or sesame seeds can be crushed as necessary, and then extracted by a conventional method using any solvent, for example, the solvent described above for extraction from sesame oil. After separating the extraction residue, the extract is obtained by evaporating the solvent from the extract by evaporation or the like. In addition to sesamin, episesamin, sesaminol, and episesaminol, sesamorin, 2- (3,4-methylenedioxy) is obtained from the sesame seed extract, sesame seed extract, or crude sesame oil extract thus purified. Phenyl) -6- (3-methoxy-4-hydroxyphenyl) -3,7-dioxabicyclo [3,3,0] octane, 2,6-bis- (3-methoxy-4-hydroxyphenyl) -3 , 7-dioxabicyclo [3,3,0] octane, or 2- (3,4-methylenedioxyphenyl) -6- (3-methoxy-4-hydroxyphenoxy) -3,7-dioxabicyclo [ Each lignan compound of 3,3,0] octane is obtained in the same manner.
なお、細辛から得られるセサミンも胡麻種子および胡麻油より得られるセサミンと同等の効果を有し、これら光学活性体もリグナン類化合物に含まれる。さらに、胡麻油製造過程の副産物からもリグナン類化合物を得ることができる。なお、リグナン類化合物の精製法および抽出物を得る方法はこれに限られるものではない。さらに、上記リグナン類化合物およびリグナン類化合物を主成分とする抽出物は胡麻油、胡麻粕、および胡麻種子から得たものに限定したわけではなく、リグナン類化合物を含む天然物自体も使用することができる。このような天然物としては、例えば、五加皮、桐木、白果樹皮、ヒハツ、細辛等を挙げることができる。 In addition, sesamin obtained from fine spice has the same effect as sesamin obtained from sesame seeds and sesame oil, and these optically active substances are also included in the lignan compounds. Furthermore, lignan compounds can also be obtained from byproducts of the sesame oil production process. In addition, the purification method of a lignan compound and the method of obtaining an extract are not restricted to this. Furthermore, the above lignan compounds and extracts based on lignan compounds are not limited to those obtained from sesame oil, sesame seeds, and sesame seeds, and natural products containing lignan compounds themselves can also be used. it can. Examples of such natural products include pentagonal bark, paulownia tree, white fruit bark, hihatsu, and spicy.
また、合成によりリグナン類化合物を得る方法としては、以下のものがあげられる。例えば、セサミン、エピセサミンについては、Berozaらの方法(J. Am. Chem. Soc., 78, 1242(1956) )で合成できる他、ピノレシノールはFreundenbergらの方法(Chem. Ber., 86, 1157(1953))によって、シリンガレシノールはFreundenbergらの方法(Chem. Ber., 88, 16(1955))によって合成することができる。 Examples of methods for obtaining lignan compounds by synthesis include the following. For example, sesamin and episesamin can be synthesized by the method of Beroza et al. (J. Am. Chem. Soc., 78, 1242 (1956)), and pinoresinol can be synthesized by the method of Freundenberg et al. (Chem. Ber., 86, 1157 ( 1953)), syringaresinol can be synthesized by the method of Freundenberg et al. (Chem. Ber., 88, 16 (1955)).
さらに、リグナン類化合物は、配糖体の形で使用することもできる上、これらを単独で、または適宜組み合わせて飲料の成分とすることもできる。
油脂
リグナン類化合物の溶剤となる油脂は、リグナン類化合物を溶解しうるものであれば何ら制限されるものではなく、例えば、アーモンドオイル(スイートアーモンドオイル)、アプリコットカーネルオイル、アボガドオイル、月見草オイル、ウィートジャームオイル(小麦胚芽油)、ウォールナッツオイル(クルミオイル)、オリーブオイル、キャスターオイル(ひまし油)、ククイナッツオイル、グレープシードオイル、ココアバター、ココナッツオイル、米油、セサミオイル(ごま油)、パーム核油、パームオイル、ホホバオイル、マカダミアナッツオイル、シアバター、マンゴーバター等挙げることができ、上記オリーブ油等に含まれるジアシルグリセロールを主成分とする油脂やパーム核油等に含まれる中鎖脂肪酸トリグリセリドを主成分とする油脂等を用いることもできるが、中でも常温で液体のものが使用の容易さから好ましく、また飽和脂肪酸を多く有する油脂が酸化安定性に優れることから好ましい。
Furthermore, the lignan compounds can be used in the form of glycosides, and these can be used alone or in appropriate combination as a beverage component.
The fats and oils used as the solvent for the fat and oil lignan compounds are not limited as long as they can dissolve the lignan compounds. For example, almond oil (sweet almond oil), apricot kernel oil, avocado oil, evening primrose oil, Wheat germ oil (wheat germ oil), walnut oil (walnut oil), olive oil, castor oil (castor oil), kukui nut oil, grape seed oil, cocoa butter, coconut oil, rice oil, sesame oil (sesame oil), palm kernel Oil, palm oil, jojoba oil, macadamia nut oil, shea butter, mango butter, etc. Medium chain fatty acid triglycerides contained in oils and palm kernel oils mainly composed of diacylglycerol contained in the above olive oils etc. It can also be used oil mainly composed of, preferably from the preferred ease of those liquid used among others normal temperature and fats having many saturated fatty acid has excellent oxidation stability.
さらに、本発明で使用する油脂として、炭素数8〜12の中鎖脂肪酸トリグリセリド(MCT)を好適に例示できる。リグナン類化合物は、溶剤にMCTを用いると溶解度が上がるので、リグナン類化合物を高濃度に配合できる、もしくは配合する油脂量を少量に抑えることができるという利点がある。また、MCTは他の油脂と比較して、粘性が低いことから、飲料に配合した場合に油脂特有の粘り気が少なく飲みやすいという利点も有する。 Furthermore, as oils and fats used by this invention, a C8-C12 medium chain fatty acid triglyceride (MCT) can be illustrated suitably. Since the solubility of lignan compounds increases when MCT is used as a solvent, there is an advantage that the lignan compounds can be blended at a high concentration or the amount of fats and oils to be blended can be suppressed to a small amount. In addition, since MCT has a lower viscosity than other fats and oils, it has an advantage that it is easy to drink when it is blended in a beverage with less stickiness specific to fats and oils.
乳飲料
本発明は、油脂に溶解したリグナン類化合物を含有する乳飲料である。本発明でいう乳飲料とは、牛乳、大豆、ココナッツ等由来の乳を原料として得られる飲料であって、乳成分を主原料として含有するものであれば特に限定されることはない。前記主原料となる乳原料としては、脱脂粉乳、全脂粉乳、部分脱脂粉乳、脱脂乳、濃縮乳、バター、クリームなど生乳由来のもの、大豆パウダー、豆乳、粉末豆乳、脱脂大豆粉末など大豆由来のもの、ココナッツミルク、ココナッツパウダーなどココナッツ由来のもの等を例示できるが、乳原料として使用可能な原料であれば特に限定されることはない。乳飲料が乾燥状態または濃縮状態であるときは、飲用時と同程度の水分に戻してから、本発明の飲料の製造に使用する。
Milk beverage The present invention is a milk beverage containing a lignan compound dissolved in an oil or fat. The milk beverage as used in the present invention is a beverage obtained using milk derived from milk, soybean, coconut or the like as a raw material, and is not particularly limited as long as it contains a milk component as a main raw material. Examples of the milk material that is the main ingredient include non-fat dry milk, full-fat dry milk, partially non-fat dry milk, non-fat milk, concentrated milk, butter, cream-derived raw milk, soy powder, soy milk, powdered soy milk, non-fat soy powder, etc. Coconut milk, coconut milk, coconut powder and the like derived from coconut, but not limited as long as it can be used as a milk raw material. When the milk beverage is in a dry or concentrated state, it is used to produce the beverage of the present invention after returning to the same level of water as when drinking.
本発明のリグナン類化合物含有乳飲料は、まず粉末状のリグナン類化合物を油脂に溶解させた後、該溶解液を乳飲料と混合することにより調製する。リグナン類化合物の油脂への溶解は、常温で行っても加温下で行っても良いが、加温下で攪拌することにより十分に溶解させることができる。配合(重量)比は、リグナン類が溶解しうる割合であれば特に制限されず、リグナン類化合物および油脂の種類により異なるが、通常、リグナン類化合物:油脂=1:15〜100程度である。 The lignan compound-containing milk beverage of the present invention is prepared by first dissolving a powdered lignan compound in an oil and fat and then mixing the solution with the milk beverage. The lignan compound can be dissolved in the oil or fat at room temperature or under heating, but can be sufficiently dissolved by stirring under heating. The blending (weight) ratio is not particularly limited as long as the lignans can be dissolved, and usually varies depending on the types of lignan compounds and fats and oils, but is usually about lignan compounds: fats = 1: 15 to 100.
リグナン類化合物が溶解した油脂(溶解液)の乳飲料への添加は、公知の方法を用いて行うことができる。例えば、ホモミキサー(T.K.ホモミキサー)を用いた場合には、7500rpmで10分間程度の攪拌を行う。混合温度は、特に制限されず、工程に合わせて常温でまたは加温下で行えばよいが、リグナン類化合物が溶解した油脂が液状であることが混合の容易さから好ましい。添加量は特に制限されないが、乳飲料中の総脂質量が、生乳の乳脂肪分3.6〜4.2%程度と等しくなるように調整すると、官能的にコク味があり、油っぽくない好ましい乳飲料を得る。従って、リグナン類化合物の添加量を高めるためには、原料の乳飲料には脂肪分量が低いものを用いることが好ましい。なお、溶解液を乳飲料に添加する際は、定法により乳化剤等を用いて分散安定性を向上させても良いが、本発明の飲料の特徴は、分散剤を全くもしくは僅かしか使用しなくてもリグナン類化合物の含有量を高めることができることである。 Addition of fats and oils (dissolved solution) in which a lignan compound is dissolved to a milk beverage can be performed using a known method. For example, when a homomixer (TK homomixer) is used, stirring is performed at 7500 rpm for about 10 minutes. The mixing temperature is not particularly limited, and may be performed at normal temperature or under heating according to the process, but it is preferable from the viewpoint of easy mixing that the oil and fat in which the lignan compound is dissolved is liquid. The amount added is not particularly limited, but if the total fat content in the milk drink is adjusted to be equal to about 3.6 to 4.2% of milk fat content of raw milk, it is sensually rich and oily. Get no preferred milk drink. Therefore, in order to increase the amount of lignan compound added, it is preferable to use a raw milk beverage having a low fat content. In addition, when adding the dissolution liquid to the milk beverage, the dispersion stability may be improved by using an emulsifier or the like by a conventional method, but the feature of the beverage of the present invention is that the dispersant is used at all or only slightly. In addition, the content of the lignan compound can be increased.
乳飲料中のリグナン類化合物濃度は特に制限されないが、通常、0.01〜20重量%、好ましくは0.1〜10重量%となるように調製する。この量は、乳飲料100ml当たり、リグナン類化合物0.1〜10mgに相当し、日常的飲用により、リグナン類化合物の優れた生体機能の発揮が期待できる。 The concentration of the lignan compound in the milk beverage is not particularly limited, but is usually 0.01 to 20% by weight, preferably 0.1 to 10% by weight. This amount corresponds to 0.1 to 10 mg of lignan compound per 100 ml of milk drink, and the excellent biological functions of the lignan compound can be expected by daily drinking.
なお、乳飲料の中で豆乳は健康食品として注目を集めており、本発明で特に好ましく使用できる。豆乳として、無調整豆乳と調整豆乳とが市販されている。前者は大豆からおから成分を除去したものであり、脂肪分が低くコク味に欠けるものであるが、後者は無調整豆乳に米油等を添加して風味調整を行っているものである。したがって、リグナン類化合物を米油等に予め溶解しておけば、従来の調整豆乳と同様の製造方法で簡便に本発明のリグナン類化合物含有乳飲料を製造することができる。その他の乳飲料においても、添加されるクリームやバター等に予めリグナン類化合物を溶解しておくことで、従来の乳飲料と同様の製造方法で本発明のリグナン類化合物含有乳飲料を得ることができる。 In the milk beverage, soy milk is attracting attention as a health food and can be particularly preferably used in the present invention. As the soy milk, unadjusted soy milk and adjusted soy milk are commercially available. The former is obtained by removing the ingredients from soybeans and has a low fat content and lacks the rich taste, while the latter is prepared by adding rice oil or the like to unadjusted soymilk to adjust the flavor. Therefore, if the lignan compound is dissolved in rice oil or the like in advance, the lignan compound-containing milk beverage of the present invention can be easily produced by the same production method as in conventional prepared soymilk. Also in other milk beverages, the lignan compound-containing milk beverage of the present invention can be obtained by the same production method as conventional milk beverages by dissolving the lignan compounds in the cream or butter to be added in advance. it can.
以下、実施例に沿ってさらに説明するが、本発明は実施例に限定されるものではない。
セサミン入り豆乳飲料中の安定性評価
1.実験材料
乳飲料として市販の調整豆乳、油脂としてMCT;理研ビタミン製のアクターM-1(C8、C10、C12中鎖脂肪酸が56:42:2であるトリグリセリド)を用いた。リグナン類化合物として、セサミン粉末(セサミン:エピセサミン=51.1:48.2であるもの)を用いた。
Hereinafter, although it further demonstrates along an Example, this invention is not limited to an Example.
Evaluation of stability in soymilk drink containing sesamin Experimental Materials Commercially-adjusted soy milk was used as a milk beverage, MCT as an oil and fat; Actor M-1 manufactured by Riken Vitamin (a triglyceride in which C8, C10, and C12 medium chain fatty acids are 56: 42: 2). As the lignan compound, sesamin powder (sesamin: episesamin = 51.1: 48.2) was used.
2.実験方法
セサミン粉末108mgを120℃に加熱したMCT2gに溶解させた溶液を調製した。この溶液を40mlの豆乳に添加し、十分に撹拌し、試料溶液(P)とした。一方、比較対照としてMCTに溶解させずに粉末のまま豆乳に添加した試料溶液(Q)を調製した。PおよびQをNo.5Aのろ紙を用いて吸引ろ過を行い、ろ液の一部(1ml)を別の試験管に取り、4mlのクロロホルムにてセサミンを抽出した。クロロホルム層500μlを2倍希釈し、0.45μmのフィルターを通した後、HPLCにてセサミン含量を分析した。HPLCの分析条件は、カラム;Inertsil ODS-3 (4.6×150mm、GL Sciences Inc.)、移動相;70%メタノール、注入量;20μl、流速;1ml/min、カラム温度:40℃、検出:UV280nmにて行った。
2. Experimental Method A solution was prepared by dissolving 108 mg of sesamin powder in 2 g of MCT heated to 120 ° C. This solution was added to 40 ml of soy milk and stirred well to obtain a sample solution (P). On the other hand, a sample solution (Q) that was added to soy milk as a powder without being dissolved in MCT was prepared as a comparative control. P and Q were subjected to suction filtration using No. 5A filter paper. A part (1 ml) of the filtrate was taken in another test tube, and sesamin was extracted with 4 ml of chloroform. After diluting 500 μl of the chloroform layer twice and passing through a 0.45 μm filter, the sesamin content was analyzed by HPLC. HPLC analysis conditions were as follows: column; Inertsil ODS-3 (4.6 × 150 mm, GL Sciences Inc.), mobile phase; 70% methanol, injection volume: 20 μl, flow rate: 1 ml / min, column temperature: 40 ° C., detection: UV280 nm I went there.
3.結果
試料溶液(P)および(Q)を吸引ろ過した後のろ液からのセサミンの回収率はそれぞれ73.3%、0.43%となり、試料溶液(Q)はセサミンが粉のまま凝集し、豆乳中で均一に混ざっていないが、試料溶液(P)はセサミンがほぼ均一に混合されていることが判明した。
3. Results The recovery rates of sesamin from the filtrate after suction filtration of the sample solutions (P) and (Q) were 73.3% and 0.43%, respectively. Although not uniformly mixed, it was found that the sample solution (P) was almost uniformly mixed with sesamin.
セサミン入り豆乳の香味評価
1.実験方法
セサミン入り豆乳の香味評価試験を9人のパネラーを用いて実施した。評価した飲料は、市販の豆乳40mlにセサミン108mgを2gのMCT(アクターM-1、理研ビタミン製)に溶解させた後に添加した飲料(P)とセサミン108mgを粉末のまま40mlの豆乳に添加した飲料(Q)である。評価は次に示すアンケートによって行った。PとQを比較して(1) ざらつきを感じる、(2) 口当たりがまろやかである、(3) 飲みやすい、(4) 後味が残る、(5) どちらを好むかといった5つのポイントについて評価した。
Evaluation of flavor of soymilk containing sesamin Experimental method A flavor evaluation test of sesamin-containing soymilk was conducted using nine panelists. Beverages evaluated were prepared by dissolving 108 mg of sesamin in 2 g of MCT (Actor M-1, manufactured by Riken Vitamin) in 40 ml of commercially available soy milk and adding 108 mg of sesamin in powder form to 40 ml of soymilk Beverage (Q). Evaluation was performed by the following questionnaire. Comparing P and Q, we evaluated five points: (1) feeling rough, (2) mellow, (3) easy to drink, (4) aftertaste, (5) which one you prefer. .
2.評価結果
下表1に示すように試験飲料(P)の方が(Q)よりも香味が優れていることが判明した。
なお、下表に示した数字はパネラー(9人)のうち、各項目においてPまたはQを選んだ人数を表す。
2. Evaluation Results As shown in Table 1 below, it was found that the test beverage (P) had a better flavor than (Q).
The numbers shown in the table below indicate the number of panelists (9 people) who selected P or Q for each item.
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005104815A JP4473765B2 (en) | 2005-03-31 | 2005-03-31 | Milk beverage containing lignan compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005104815A JP4473765B2 (en) | 2005-03-31 | 2005-03-31 | Milk beverage containing lignan compounds |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2006280276A true JP2006280276A (en) | 2006-10-19 |
JP4473765B2 JP4473765B2 (en) | 2010-06-02 |
Family
ID=37402822
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2005104815A Active JP4473765B2 (en) | 2005-03-31 | 2005-03-31 | Milk beverage containing lignan compounds |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4473765B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007114013A1 (en) * | 2006-03-31 | 2007-10-11 | Suntory Limited | Composition containing lignan compound |
US7943663B2 (en) | 2005-09-30 | 2011-05-17 | Suntory Holdings Limited | Process and an apparatus for producing episesamin-rich compositions |
WO2015072570A1 (en) * | 2013-11-15 | 2015-05-21 | 日清オイリオグループ株式会社 | Improved soy milk and method for producing same |
CZ308418B6 (en) * | 2015-06-23 | 2020-08-12 | Mendelova Univerzita V Brně, Zahradnická Fakulta,Ústav Posklizňové Technologie Zahradnických Produktů | Beer or beer-based beverage containing lignans and method of producing it |
-
2005
- 2005-03-31 JP JP2005104815A patent/JP4473765B2/en active Active
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7943663B2 (en) | 2005-09-30 | 2011-05-17 | Suntory Holdings Limited | Process and an apparatus for producing episesamin-rich compositions |
WO2007114013A1 (en) * | 2006-03-31 | 2007-10-11 | Suntory Limited | Composition containing lignan compound |
US9408803B2 (en) | 2006-03-31 | 2016-08-09 | Suntory Holdings Limited | Compositions containing lignan-class compounds |
WO2015072570A1 (en) * | 2013-11-15 | 2015-05-21 | 日清オイリオグループ株式会社 | Improved soy milk and method for producing same |
JP5764270B1 (en) * | 2013-11-15 | 2015-08-19 | 日清オイリオグループ株式会社 | Improved soymilk and method for producing the same |
US9833007B2 (en) | 2013-11-15 | 2017-12-05 | The Nisshin Oillio Group, Ltd. | Soy milk and method for producing same |
CZ308418B6 (en) * | 2015-06-23 | 2020-08-12 | Mendelova Univerzita V Brně, Zahradnická Fakulta,Ústav Posklizňové Technologie Zahradnických Produktů | Beer or beer-based beverage containing lignans and method of producing it |
Also Published As
Publication number | Publication date |
---|---|
JP4473765B2 (en) | 2010-06-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5096138B2 (en) | Oil-in-water emulsion containing lignan compounds and composition containing the same | |
JP4829963B2 (en) | Lignan compounds containing O / W / O type emulsion and composition containing the same | |
JP2022533838A (en) | Nanoemulsion composition containing bioactive ingredients | |
US7214394B2 (en) | Policosanol compositions, extraction from novel sources, and uses thereof | |
AU2005320579B2 (en) | Sesamin/episesamin compositions | |
JP3283274B2 (en) | New composition | |
JP2009263257A (en) | Agent for preventing and/or improving fatty liver | |
JP4473765B2 (en) | Milk beverage containing lignan compounds | |
JPH08268887A (en) | Preventing or improving agent for hypertension or medical symptom caused thereby | |
JP4644135B2 (en) | Coenzyme Q10-containing composition | |
JP5666760B2 (en) | Composition containing lignan compounds | |
TWI434858B (en) | Compositions containing xylan compounds | |
KR100732727B1 (en) | Pharmaceutical compositions for hypercholesterolemia treatment | |
US20140235715A1 (en) | Taste masking formulations of fatty acids | |
JP5995700B2 (en) | Process for producing polymethoxyflavones | |
JP2011001348A (en) | Formulation for prevention or alleviation of alcohol drunkenness or hangover | |
JP7504609B2 (en) | Composition containing lignan compounds dissolved in clove oil, and method for increasing solubility of sesamin | |
JP2007246429A (en) | Lipase inhibitor, and food and drink | |
JP2010095477A (en) | Lipase inhibitor | |
JP7239135B2 (en) | α-Glucosidase activity inhibitor and blood sugar elevation inhibitor | |
JP2010241792A (en) | Lipase inhibitor, and food and drink | |
KR20020085507A (en) | Preparation of 3,4-dicaffeoylquinic acid and use thereof as anti-cholesterol agent | |
JPH0558898A (en) | Agent for treating and preventing hyperlipidemia |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20080227 |
|
A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A712 Effective date: 20090422 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20090616 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20090706 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20090904 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20091111 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100107 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100112 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20100225 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20100305 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130312 Year of fee payment: 3 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 4473765 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130312 Year of fee payment: 3 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20140312 Year of fee payment: 4 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |