KR20210131039A - Composition of Nutrient Delivery System for Improving Brain Function - Google Patents
Composition of Nutrient Delivery System for Improving Brain Function Download PDFInfo
- Publication number
- KR20210131039A KR20210131039A KR1020200049340A KR20200049340A KR20210131039A KR 20210131039 A KR20210131039 A KR 20210131039A KR 1020200049340 A KR1020200049340 A KR 1020200049340A KR 20200049340 A KR20200049340 A KR 20200049340A KR 20210131039 A KR20210131039 A KR 20210131039A
- Authority
- KR
- South Korea
- Prior art keywords
- sialic acid
- brain function
- nest
- delivery system
- swallow
- Prior art date
Links
- 230000003925 brain function Effects 0.000 title claims abstract description 55
- 235000015097 nutrients Nutrition 0.000 title claims abstract description 36
- 239000000203 mixture Substances 0.000 title claims abstract description 27
- SQVRNKJHWKZAKO-UHFFFAOYSA-N beta-N-Acetyl-D-neuraminic acid Natural products CC(=O)NC1C(O)CC(O)(C(O)=O)OC1C(O)C(O)CO SQVRNKJHWKZAKO-UHFFFAOYSA-N 0.000 claims abstract description 78
- SQVRNKJHWKZAKO-OQPLDHBCSA-N sialic acid Chemical compound CC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(O)=O)OC1[C@H](O)[C@H](O)CO SQVRNKJHWKZAKO-OQPLDHBCSA-N 0.000 claims abstract description 77
- 239000000284 extract Substances 0.000 claims abstract description 46
- 239000011324 bead Substances 0.000 claims abstract description 15
- 239000000126 substance Substances 0.000 claims abstract description 14
- 239000002105 nanoparticle Substances 0.000 claims abstract description 13
- 238000010521 absorption reaction Methods 0.000 claims abstract description 12
- 238000005516 engineering process Methods 0.000 claims abstract description 10
- 239000004480 active ingredient Substances 0.000 claims abstract description 9
- 238000000746 purification Methods 0.000 claims abstract description 7
- 238000000926 separation method Methods 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 240000004371 Panax ginseng Species 0.000 claims description 6
- 235000008434 ginseng Nutrition 0.000 claims description 6
- 229920006113 non-polar polymer Polymers 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 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 3
- TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 claims description 3
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 claims description 3
- 235000011299 Brassica oleracea var botrytis Nutrition 0.000 claims description 3
- 235000017647 Brassica oleracea var italica Nutrition 0.000 claims description 3
- 240000003259 Brassica oleracea var. botrytis Species 0.000 claims description 3
- 241000195649 Chlorella <Chlorellales> Species 0.000 claims description 3
- 244000163122 Curcuma domestica Species 0.000 claims description 3
- 235000003392 Curcuma domestica Nutrition 0.000 claims description 3
- SBJKKFFYIZUCET-JLAZNSOCSA-N Dehydro-L-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(=O)C1=O SBJKKFFYIZUCET-JLAZNSOCSA-N 0.000 claims description 3
- 240000001008 Dimocarpus longan Species 0.000 claims description 3
- 235000000235 Euphoria longan Nutrition 0.000 claims description 3
- 240000008397 Ganoderma lucidum Species 0.000 claims description 3
- 235000001637 Ganoderma lucidum Nutrition 0.000 claims description 3
- 239000009429 Ginkgo biloba extract Substances 0.000 claims description 3
- ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 claims description 3
- 244000230712 Narcissus tazetta Species 0.000 claims description 3
- 235000002789 Panax ginseng Nutrition 0.000 claims description 3
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 claims description 3
- 235000003140 Panax quinquefolius Nutrition 0.000 claims description 3
- 241000241413 Propolis Species 0.000 claims description 3
- 235000021329 brown rice Nutrition 0.000 claims description 3
- SUHOQUVVVLNYQR-MRVPVSSYSA-N choline alfoscerate Chemical compound C[N+](C)(C)CCOP([O-])(=O)OC[C@H](O)CO SUHOQUVVVLNYQR-MRVPVSSYSA-N 0.000 claims description 3
- 235000003373 curcuma longa Nutrition 0.000 claims description 3
- PEYUIKBAABKQKQ-UHFFFAOYSA-N epiasarinin Natural products C1=C2OCOC2=CC(C2OCC3C2COC3C2=CC=C3OCOC3=C2)=C1 PEYUIKBAABKQKQ-UHFFFAOYSA-N 0.000 claims description 3
- 235000013372 meat Nutrition 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 229940069949 propolis Drugs 0.000 claims description 3
- 229940109850 royal jelly Drugs 0.000 claims description 3
- 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 3
- 229940083466 soybean lecithin Drugs 0.000 claims description 3
- 235000013976 turmeric Nutrition 0.000 claims description 3
- 239000000052 vinegar Substances 0.000 claims description 3
- 235000021419 vinegar Nutrition 0.000 claims description 3
- 241001105098 Angelica keiskei Species 0.000 claims description 2
- 229940124447 delivery agent Drugs 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 18
- 238000001727 in vivo Methods 0.000 abstract description 3
- 210000004556 brain Anatomy 0.000 abstract description 2
- 238000012360 testing method Methods 0.000 description 58
- 241001465754 Metazoa Species 0.000 description 20
- 244000000626 Daucus carota Species 0.000 description 13
- 235000005770 birds nest Nutrition 0.000 description 13
- 235000005765 wild carrot Nutrition 0.000 description 13
- 239000000243 solution Substances 0.000 description 11
- 239000003814 drug Substances 0.000 description 10
- 235000013305 food Nutrition 0.000 description 10
- 239000000902 placebo Substances 0.000 description 9
- 229940068196 placebo Drugs 0.000 description 9
- 229940079593 drug Drugs 0.000 description 8
- 238000009472 formulation Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 7
- 235000015872 dietary supplement Nutrition 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 230000005978 brain dysfunction Effects 0.000 description 5
- 230000006872 improvement Effects 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 208000024891 symptom Diseases 0.000 description 5
- 235000013311 vegetables Nutrition 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 206010012289 Dementia Diseases 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 239000003613 bile acid Substances 0.000 description 4
- 239000002775 capsule Substances 0.000 description 4
- 208000026106 cerebrovascular disease Diseases 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 230000006735 deficit Effects 0.000 description 4
- 210000001320 hippocampus Anatomy 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- -1 that is Substances 0.000 description 4
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 description 3
- 102000013455 Amyloid beta-Peptides Human genes 0.000 description 3
- 108010090849 Amyloid beta-Peptides Proteins 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 230000005856 abnormality Effects 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 230000007850 degeneration Effects 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 230000037406 food intake Effects 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 210000000056 organ Anatomy 0.000 description 3
- 238000000053 physical method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 210000001519 tissue Anatomy 0.000 description 3
- 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 description 2
- CERZMXAJYMMUDR-QBTAGHCHSA-N 5-amino-3,5-dideoxy-D-glycero-D-galacto-non-2-ulopyranosonic acid Chemical class N[C@@H]1[C@@H](O)CC(O)(C(O)=O)O[C@H]1[C@H](O)[C@H](O)CO CERZMXAJYMMUDR-QBTAGHCHSA-N 0.000 description 2
- 208000000044 Amnesia Diseases 0.000 description 2
- 108010053652 Butyrylcholinesterase Proteins 0.000 description 2
- 206010008111 Cerebral haemorrhage Diseases 0.000 description 2
- 102100032404 Cholinesterase Human genes 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- WZUVPPKBWHMQCE-UHFFFAOYSA-N Haematoxylin Chemical compound C12=CC(O)=C(O)C=C2CC2(O)C1C1=CC=C(O)C(O)=C1OC2 WZUVPPKBWHMQCE-UHFFFAOYSA-N 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 208000027530 Meniere disease Diseases 0.000 description 2
- 241000699666 Mus <mouse, genus> Species 0.000 description 2
- SQVRNKJHWKZAKO-PFQGKNLYSA-N N-acetyl-beta-neuraminic acid Chemical compound CC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(O)=O)O[C@H]1[C@H](O)[C@H](O)CO SQVRNKJHWKZAKO-PFQGKNLYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 208000006011 Stroke Diseases 0.000 description 2
- 208000032851 Subarachnoid Hemorrhage Diseases 0.000 description 2
- WBWWGRHZICKQGZ-UHFFFAOYSA-N Taurocholic acid Natural products OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(=O)NCCS(O)(=O)=O)C)C1(C)C(O)C2 WBWWGRHZICKQGZ-UHFFFAOYSA-N 0.000 description 2
- 244000299461 Theobroma cacao Species 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000007815 allergy Effects 0.000 description 2
- 238000000540 analysis of variance Methods 0.000 description 2
- 230000036772 blood pressure Effects 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 206010008118 cerebral infarction Diseases 0.000 description 2
- 208000013677 cerebrovascular dementia Diseases 0.000 description 2
- 230000004456 color vision Effects 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- ADEBPBSSDYVVLD-UHFFFAOYSA-N donepezil Chemical compound O=C1C=2C=C(OC)C(OC)=CC=2CC1CC(CC1)CCN1CC1=CC=CC=C1 ADEBPBSSDYVVLD-UHFFFAOYSA-N 0.000 description 2
- 230000007717 exclusion Effects 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 235000013402 health food Nutrition 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- 239000000787 lecithin Substances 0.000 description 2
- 235000010445 lecithin Nutrition 0.000 description 2
- 229940067606 lecithin Drugs 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 206010027175 memory impairment Diseases 0.000 description 2
- 239000000693 micelle Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 210000002569 neuron Anatomy 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 208000027765 speech disease Diseases 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- WBWWGRHZICKQGZ-GIHLXUJPSA-N taurocholic acid Chemical compound C([C@@H]1C[C@H]2O)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@@H]([C@@H](CCC(=O)NCCS(O)(=O)=O)C)[C@@]2(C)[C@H](O)C1 WBWWGRHZICKQGZ-GIHLXUJPSA-N 0.000 description 2
- PKYCWFICOKSIHZ-UHFFFAOYSA-N 1-(3,7-dihydroxyphenoxazin-10-yl)ethanone Chemical compound OC1=CC=C2N(C(=O)C)C3=CC=C(O)C=C3OC2=C1 PKYCWFICOKSIHZ-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- MIDXCONKKJTLDX-UHFFFAOYSA-N 3,5-dimethylcyclopentane-1,2-dione Chemical compound CC1CC(C)C(=O)C1=O MIDXCONKKJTLDX-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 229920001817 Agar Polymers 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
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 208000024827 Alzheimer disease Diseases 0.000 description 1
- 208000031091 Amnestic disease Diseases 0.000 description 1
- 244000061520 Angelica archangelica Species 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 241000271566 Aves Species 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 208000014644 Brain disease Diseases 0.000 description 1
- 206010048962 Brain oedema Diseases 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000397426 Centroberyx lineatus Species 0.000 description 1
- 206010008132 Cerebral thrombosis Diseases 0.000 description 1
- 102000003914 Cholinesterases Human genes 0.000 description 1
- 108090000322 Cholinesterases Proteins 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 208000022540 Consciousness disease Diseases 0.000 description 1
- 241000938605 Crocodylia Species 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- 208000027534 Emotional disease Diseases 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 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 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 235000001287 Guettarda speciosa Nutrition 0.000 description 1
- 241000167880 Hirundinidae Species 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 201000001429 Intracranial Thrombosis Diseases 0.000 description 1
- 229930194542 Keto Natural products 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
- 241000124008 Mammalia Species 0.000 description 1
- 208000026139 Memory disease Diseases 0.000 description 1
- 208000016285 Movement disease Diseases 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 208000001431 Psychomotor Agitation Diseases 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 206010038743 Restlessness Diseases 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 238000000692 Student's t-test Methods 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 description 1
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 description 1
- RXRFEELZASHOLV-JAJWTYFOSA-N [(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] acetate Chemical compound CC(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O RXRFEELZASHOLV-JAJWTYFOSA-N 0.000 description 1
- 210000000683 abdominal cavity Anatomy 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 239000003655 absorption accelerator Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 210000000577 adipose tissue Anatomy 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000006986 amnesia Effects 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 229940005524 anti-dementia drug Drugs 0.000 description 1
- 201000007201 aphasia Diseases 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 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
- 238000003149 assay kit Methods 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 230000003542 behavioural effect Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 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
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 230000008344 brain blood flow Effects 0.000 description 1
- 230000004641 brain development Effects 0.000 description 1
- 208000006752 brain edema Diseases 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 235000001046 cacaotero Nutrition 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000013736 caramel Nutrition 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 235000015218 chewing gum Nutrition 0.000 description 1
- 229940112822 chewing gum Drugs 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 229940048961 cholinesterase Drugs 0.000 description 1
- 230000004087 circulation Effects 0.000 description 1
- 230000006999 cognitive decline Effects 0.000 description 1
- 208000010877 cognitive disease Diseases 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 210000001947 dentate gyrus Anatomy 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 235000013325 dietary fiber Nutrition 0.000 description 1
- 210000002249 digestive system Anatomy 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229960003530 donepezil Drugs 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- YQGOJNYOYNNSMM-UHFFFAOYSA-N eosin Chemical compound [Na+].OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 YQGOJNYOYNNSMM-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 235000013376 functional food Nutrition 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000007903 gelatin capsule Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000010562 histological examination Methods 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000015255 meat loaf Nutrition 0.000 description 1
- 230000006984 memory degeneration Effects 0.000 description 1
- 208000023060 memory loss Diseases 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000003068 molecular probe Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 230000001144 postural effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 210000002763 pyramidal cell Anatomy 0.000 description 1
- 238000011552 rat model Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 235000021067 refined food Nutrition 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000012679 serum free medium Substances 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000007901 soft capsule Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000012030 stroop test Methods 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical group S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 238000012353 t test Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 235000021404 traditional food Nutrition 0.000 description 1
- 230000037317 transdermal delivery Effects 0.000 description 1
- 230000004304 visual acuity Effects 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/56—Materials from animals other than mammals
- A61K35/57—Birds; Materials from birds, e.g. eggs, feathers, egg white, egg yolk or endothelium corneum gigeriae galli
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- 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
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- 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
- A23L33/125—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives containing carbohydrate syrups; containing sugars; containing sugar alcohols; containing starch hydrolysates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7012—Compounds having a free or esterified carboxyl group attached, directly or through a carbon chain, to a carbon atom of the saccharide radical, e.g. glucuronic acid, neuraminic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
- A61K9/1075—Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
-
- 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
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/322—Foods, ingredients or supplements having a functional effect on health having an effect on the health of the nervous system or on mental function
-
- 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
- A23V2250/00—Food ingredients
- A23V2250/20—Natural extracts
- A23V2250/204—Animal extracts
Abstract
Description
본 발명은 뇌기능을 개선하기 위해 사용되는 영양전달체 조성물에 관한 것으로, 좀 더 상세하게는 제비집에서 추출된 시알산 추출물을 유효성분으로 포함하는 뇌기능 개선용 영양전달체 조성물에 관한 것이다. The present invention relates to a nutrient delivery system composition used to improve brain function, and more particularly, to a nutrient delivery system composition for improving brain function comprising a sialic acid extract extracted from swallow's nest as an active ingredient.
우리나라는 급격한 고령화 사회를 맞고 있으며, 그 때문에 뇌혈관 장해 또는 치매의 증가가 예상되고 있다. 이들 뇌질환의 예방 또는 치료를 위해 뇌순환, 대사개선약 또는 항치매약 등의 뇌기능 개선성을 가진 의약의 연구, 개발이 진행되고 있다.Korea is facing a rapidly aging society, and therefore, an increase in cerebrovascular disorders or dementia is expected. For the prevention or treatment of these brain diseases, research and development of drugs having brain function improvement properties such as cerebral circulation, metabolism improving drugs, or anti-dementia drugs are in progress.
최근, 학습능력, 기억력 등의 뇌 기능을 높이는 물질의 탐색이 다방면에 걸쳐 연구되고 있다. 또한, 예방의 관점에서 식생활 등을 통해 섭취할 수 있는 뇌기능을 개선하는 물질도 필요하다.Recently, the search for substances that enhance brain functions such as learning ability and memory have been studied in various fields. In addition, from the viewpoint of prevention, substances that improve brain function that can be ingested through diet and the like are also required.
제비집은 바다제비가 분비한 타액과 깃털 등으로 만든 둥지, 즉 제비집으로 중국 명나라 시기부터 먹어오던 전통식품이다. 제비집에는 시알산(sialic acid)이 함유되어 있으며 시알산은 cholinesterase(AChE), butyrylcholinesterase(BuChE)의 저해제(inhibitor)로 작용하여 알츠하이머 치매의 치료에 유효한 것으로 규명되었다. 제비집이 고급 중국 요리점 및 중식당 등과 온라인 유통 및 홈쇼핑 등을 통해 알려지면서 여러 가지 가공식품 및 식재료로서 관심과 소비가 급격히 증가하고 있으나 대부분 단순 건조물 및 가공품이 대부분이어서 기능성 원료로서 제비집 추출액을 제조함에 있어서 이들 기능성 물질 즉, 뇌기능 개선용 물질을 효율적으로 추출하는 추출법에 대한 개발이 절실히 필요하고, 이러한 추출법으로 추출된 뇌기능 개선용 물질을 포함한 조성물의 개발이 절실히 요구되고 있다.Swallow's nest is a nest made of saliva and feathers secreted by sea swallows. It is a traditional food that has been eaten since the Ming Dynasty in China. Swallow's nest contains sialic acid, which has been found to be effective in the treatment of Alzheimer's dementia by acting as an inhibitor of cholinesterase (AChE) and butyrylcholinesterase (BuChE). As swallowtail's nest is known through online distribution and home shopping at high-end Chinese restaurants and Chinese restaurants, interest and consumption as various processed foods and ingredients are rapidly increasing, but most of them are simple dried products and processed products. There is an urgent need for development of an extraction method for efficiently extracting functional substances, that is, substances for improving brain function, and development of a composition including substances for improving brain functions extracted by this extraction method is urgently required.
본 발명은 종래의 문제점을 해결하기 위해 안출된 것으로서, The present invention has been devised to solve the problems of the prior art,
본 발명의 목적은 ABT(Affinity Beads Technology) 기반의 시알산 분리 정제 방법으로 제비집에 함유되어 있는 뇌기능 개선 물질인 시알산을 효율적으로 추출하고, 상기 방법으로 추출된 시알산 추출물을 유효성분으로 포함하는 뇌기능 개선용 영양전달체 조성물을 제공하는 데 있다.An object of the present invention is to efficiently extract sialic acid, a brain function improving substance contained in swallow's nest, by a method for separating and purifying sialic acid based on ABT (Affinity Beads Technology), and including the sialic acid extract extracted by the above method as an active ingredient To provide a nutrient delivery system composition for improving brain function.
본 발명의 또 다른 목적은 제비집으로부터 추출된 시알산 추출물에 마이셀 나노 입자의 영양전달체를 부가하여 시알산 추출물의 체내흡수율을 높임으로써 뇌기능 개선효과를 증대시키는 뇌기능 개선용 영양전달체 조성물을 제공하는 데 있다.Another object of the present invention is to provide a nutrient carrier composition for improving brain function that increases the brain function improvement effect by adding a nutrient carrier of micellar nanoparticles to a sialic acid extract extracted from swallow's nest to increase the absorption rate of the sialic acid extract in the body. there is
상기와 같은 목적을 달성하기 위해 제공되는 본 발명의 일실시 예에 따른 뇌기능 개선용 영양전달체 조성물은 제비집의 시알산추출물을 유효성분으로 포함하는 것을 특징으로 한다.The nutrient delivery system composition for improving brain function according to an embodiment of the present invention, which is provided to achieve the above object, is characterized in that it contains the sialic acid extract of swallow's nest as an active ingredient.
여기서, 상기 시알산추출물은 제비집을 물, 알칼리 이온수 또는 유기용매로 이루어진 군으로부터 선택된 1종 이상의 용매를 투입하여 추출하는 단계; 상기 추출된 용매에 비극성 고분자 비드를 투입하여 시알산(sialic acid)를 흡착하는 단계; 상기 시알산이 흡착된 비극성 고분자 비드를 분리하고 이에 탈착제를 투입하여 시알산을 탈착하는 단계; 상기 탈착된 시알산을 고형화하는 단계;를 포함하는 ABT(Affinity Beads Technology) 기반의 시알산 분리정제 방법으로 추출되는 것을 특징으로 한다.Here, the step of extracting the sialic acid extract by adding one or more solvents selected from the group consisting of water, alkaline ionized water or an organic solvent to the swallow's nest; adsorbing sialic acid by adding non-polar polymer beads to the extracted solvent; separating the non-polar polymer beads to which the sialic acid is adsorbed and desorbing the sialic acid by adding a desorbent thereto; It is characterized in that the extraction is performed by an ABT (Affinity Beads Technology)-based sialic acid separation and purification method comprising a; solidifying the desorbed sialic acid.
그리고, 상기 제비집의 시알산 추출물에는 체내흡수율을 높이는 영양전달체가 더 포함되는 것을 특징으로 하며, 상기 영양전달체는 마이셀 나노입자인 것을 특징으로 한다.And, the sialic acid extract of the swallow's nest is characterized in that it further comprises a nutrient delivery system that increases the absorption rate in the body, and the nutrient delivery system is characterized in that the micelle nanoparticles.
또한, 상기 제비집의 시알산 추출물에는 뇌기능 개선 물질인 알파-지피씨, 대두레시틴, DHA, 포스파티딜세린, 브로컬리, 참당귀, 수선화, 용안육, 단삼, 맥문동, 천마, 은행나무잎 엑기스, 로얄제리, 영지, 고려인삼, 클로렐라, 현미흑초, 프로폴리스, 세사민, 우콘 중 선택되는 어느 하나 또는 둘 이상의 것이 더 포함되는 것을 특징으로 한다. In addition, the sialic acid extract of the swallow's nest contains brain function improving substances alpha-GPC, soybean lecithin, DHA, phosphatidylserine, broccoli, Angelica keiskei, daffodils, longan meat, ginseng, maekmundong, cheonma, ginkgo leaf extract, royal jelly, Reishi, Korean ginseng, chlorella, brown rice black vinegar, propolis, sesamin, characterized in that any one or two or more selected from turmeric is further included.
본 발명의 실시 예에 따르면, ABT(Affinity Beads Technology) 기반의 시알산 분리 정제 방법으로 제비집에 함유되어 있는 뇌기능 개선 물질인 시알산을 효율적으로 추출하고, 상기 방법으로 추출된 시알산 추출물을 유효성분으로 포함함으로써 뇌기능을 개선시키는 효과가 있다.According to an embodiment of the present invention, sialic acid, a brain function improving substance contained in swallow's nest, is efficiently extracted by ABT (Affinity Beads Technology)-based sialic acid separation and purification method, and the sialic acid extract extracted by the above method is effective By including it as an ingredient, it has the effect of improving brain function.
또한, 제비집으로부터 추출된 시알산 추출물에 마이셀 나노 입자의 영양전달체를 부가하여 시알산 추출물의 체내흡수율을 높임으로써 뇌기능 개선효과를 증대시키는 효과가 있다. In addition, the nutrient delivery system of micellar nanoparticles is added to the sialic acid extract extracted from the swallow's nest to increase the absorption rate of the sialic acid extract in the body, thereby increasing the brain function improvement effect.
도 1은 본 발명의 일실시예에 따른 뇌기능 개선용 영양전달체 조성물에서 ABT(Affinity Beads Technology) 기반의 시알산 분리 정제 방법을 도시한 공정도.
도 2는 본 발명의 일실시예에 따른 뇌기능 개선용 영양전달체 조성물에서 담즙산 및 시알산을 포함하는 속효성 마이셀 나노입자를 설명하기 위한 개념도.
도 3은 본 발명의 일실시예에 따른 뇌기능 개선용 영양전달체 조성물에서 AChE 활성에 대한 제비집 추출물과 시알산의 효능을 비교한 그래프.
도 4는 본 발명의 일실시예에 따른 뇌기능 개선용 영양전달체 조성물에서 헤마부위의 신경세포의 퇴화정도를 관찰하기 위해 아밀로이드 베타 단백질을 뇌실 내 처리한 군과 아무것도 처리하지 않은 군의 세포 퇴화 비교 이미지.1 is a process diagram illustrating a method for separating and purifying sialic acid based on ABT (Affinity Beads Technology) in a nutrient delivery system composition for improving brain function according to an embodiment of the present invention.
2 is a conceptual diagram for explaining fast-acting micellar nanoparticles containing bile acid and sialic acid in the nutrient delivery system composition for improving brain function according to an embodiment of the present invention.
3 is a graph comparing the efficacy of bird's nest extract and sialic acid on AChE activity in the nutrient delivery system composition for improving brain function according to an embodiment of the present invention.
Figure 4 is a comparison of cell degeneration of the group treated with amyloid beta protein in the ventricle and the group not treated with anything in order to observe the degree of degeneration of neurons in the hema region in the nutrient delivery system composition for improving brain function according to an embodiment of the present invention; image.
이하의 본 발명에 대한 상세한 설명들은 본 발명이 실시될 수 있는 실시 예이고 해당 실시 예에 대한 예시로써 도시된 첨부 도면을 참조한다. 이들 실시 예는 당업자가 본 발명을 실시하기에 충분하도록 상세히 설명된다. 본 발명의 다양한 실시 예는 서로 다르지만 상호 배타적일 필요는 없음이 이해되어야 한다. 예를 들어, 여기에 기재되어 있는 특정 형상, 구조 및 특성은 일실시 예에 관련하여 본 발명의 사상 및 범위를 벗어나지 않으면서 다른 실시 예로 구현될 수 있다. 또한 각각의 기재된 실시 예 내의 개별 구성요소의 위치 또는 배치는 본 발명의 사상 및 범위를 벗어나지 않으면서 변경될 수 있음이 이해되어야 한다.DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The following detailed description of the present invention is an embodiment in which the present invention may be practiced, and reference is made to the accompanying drawings shown by way of example for the embodiment. These embodiments are described in sufficient detail to enable those skilled in the art to practice the present invention. It should be understood that various embodiments of the present invention are different but need not be mutually exclusive. For example, certain shapes, structures, and characteristics described herein may be implemented in other embodiments without departing from the spirit and scope of the invention with respect to one embodiment. It should also be understood that the position or arrangement of individual components in each described embodiment may be changed without departing from the spirit and scope of the present invention.
따라서 후술되는 상세한 설명은 한정적인 의미로서 취하려는 것이 아니며, 본 발명의 범위는 적절하게 설명된다면 그 청구항들이 주장하는 것과 균등한 모든 범위와 더불어 첨부된 청구항에 의해서만 한정된다. 도면에서 유사한 참조부호는 여러 측면에 걸쳐서 동일하거나 유사한 기능을 지칭한다.Accordingly, the detailed description set forth below is not intended to be taken in a limiting sense, and the scope of the present invention, if properly described, is limited only by the appended claims, along with all scopes equivalent to those claimed by the claims. Like reference numerals in the drawings refer to the same or similar functions throughout the various aspects.
본 발명에서 사용되는 용어는 본 발명에서의 기능을 고려하면서 가능한 현재 널리 사용되는 일반적인 용어들을 선택하였으나, 이는 당 분야에 종사하는 기술자의 의도 또는 판례, 새로운 기술의 출현 등에 따라 달라질 수 있다. 또한 특정한 경우는 출원인이 임의로 선정한 용어도 있으며, 이 경우 해당되는 발명의 설명 부분에서 상세히 그 의미를 기재할 것이다. 따라서 본 발명에서 사용되는 용어는 단순한 용어의 명칭이 아닌, 그 용어가 가지는 의미와 본 발명의 전반에 걸친 내용을 토대로 정의되어야 한다.The terms used in the present invention have been selected as currently widely used general terms as possible while considering the functions in the present invention, but these may vary depending on the intention or precedent of a person skilled in the art, the emergence of new technology, and the like. In addition, in specific cases, there are also terms arbitrarily selected by the applicant, and in this case, the meaning will be described in detail in the description of the corresponding invention. Therefore, the term used in the present invention should be defined based on the meaning of the term and the overall content of the present invention, rather than the name of a simple term.
발명의 전체에서 어떤 부분이 어떤 구성요소를 "포함"한다고 할 때, 이는 특별히 반대되는 기재가 없는 한, 다른 구성요소를 제외하는 것이 아니라 다른 구성요소를 더 포함할 수 있음을 의미한다. 또한 명세서에 기재된 "…부", "…모듈" 등의 용어는 적어도 하나의 기능이나 동작을 처리하는 단위를 의미하며, 이는 하드웨어 또는 소프트웨어로 구현되거나 하드웨어와 소프트웨어의 결합으로 구현될 수 있다.In the whole of the invention, when a part "includes" a certain element, it means that other elements may be further included, rather than excluding other elements, unless otherwise stated. Also, terms such as “…unit” and “…module” described in the specification mean a unit that processes at least one function or operation, which may be implemented as hardware or software, or a combination of hardware and software.
본 발명의 일실시 예에 따른 뇌기능 개선용 영양전달체 조성물은 제비집에 함유되어 있는 시알산 추출물을 유효성분으로 한다.The nutrient delivery system composition for improving brain function according to an embodiment of the present invention uses sialic acid extract contained in swallow's nest as an active ingredient.
여기서, 제비집은 제비집 자체 또는 제비집의 작은 조각 또는 제비집을 건조하여 분말화한 것 또는 제비집 추출액 또는 제비집 농축액 또는 제비집 액기스 분말 또는 이들의 현탁액 등이 원료로 사용될 수 있다. Here, the nest itself or a small piece of the nest, dried and powdered, or a bird's nest extract or a bird's nest concentrate or a bird's nest extract powder or a suspension thereof, etc. may be used as a raw material.
이러한 제비집에 함유되어 있는 성분들은 시알산 유도체, 예를 들어 뉴라민산의 N-아실체와 그 유도체, N-아세틸뉴라민산(Neu5Ac)과 N-글리콜뉴라민산(Neu5Gc), 그리고 히드록실기가 아세틸기, 황산기, 인산기 등으로 변형된 유도체 등이 있다. The components contained in this bird's nest include sialic acid derivatives, such as N-acyl and its derivatives of neuraminic acid, N-acetylneuraminic acid (Neu5Ac) and N-glycolneuraminic acid (Neu5Gc), and hydroxylamide. There are derivatives in which the actual group is modified with an acetyl group, a sulfuric acid group, a phosphoric acid group, or the like.
그리고, 제비집에 함유되는 시알산은 하기의 일반식으로 표시되는 뉴라민산 골격을 갖는다.And, the sialic acid contained in the swallow's nest has a neuraminic acid skeleton represented by the following general formula.
[화학식 1][Formula 1]
이러한 제비집에 함유되어 있는 뇌기능 개선 물질인 시알산은 ABT(Affinity Beads Technology) 기반의 시알산 분리정제 방법으로 추출된다.Sialic acid, a brain function improving substance contained in the swallow's nest, is extracted by ABT (Affinity Beads Technology)-based sialic acid separation and purification method.
도 1에 도시된 바와 같이 ABT(Affinity Beads Technology) 기반의 시알산 분리정제 방법은 먼저, 제비집을 물, 알칼리 이온수 또는 유기용매로 이루어진 군으로부터 선택된 1종 이상의 용매를 투입하여 추출한다. As shown in FIG. 1, in the ABT (Affinity Beads Technology)-based sialic acid separation and purification method, first, swallow's nest is extracted by adding one or more solvents selected from the group consisting of water, alkaline ionized water, or an organic solvent.
그리고, 추출된 용매에 비극성 고분자 비드를 투입하여 시알산(sialic acid)를 흡착한다. Then, non-polar polymer beads are added to the extracted solvent to adsorb sialic acid.
이어, 시알산이 흡착된 비극성 고분자 비드를 분리한 후, 이에 탈착제를 투입하여 시알산을 탈착한다. Then, after separating the non-polar polymer beads to which the sialic acid is adsorbed, a desorbent is added thereto to desorb the sialic acid.
그리고, 탈착된 시알산을 고형화 한다. Then, the desorbed sialic acid is solidified.
이때, 시알산을 대량으로 함유한 제비집 추출물을 얻고 싶은 경우에는 칼럼으로서 SEPHADEXLH-20(Amersham pharmacia Biotech AB사 제조 : Cat17-0090-01)을 이용하는 것이 바람직하다.At this time, if it is desired to obtain a bird's nest extract containing a large amount of sialic acid, it is preferable to use SEPHADEXLH-20 (manufactured by Amersham pharmacia Biotech AB: Cat17-0090-01) as a column.
이렇게 하여 얻어진 추출액의 HPLC(고속액체 크로마토그래피)에 의한 크로마토그램을 표준품의 시알산 크로마토그램과 비교한 바, 추출액에는 시알산 유도체가 함유되어 있는 것이 확인되었다.The chromatogram of the thus-obtained extract by HPLC (high-performance liquid chromatography) was compared with the sialic acid chromatogram of the standard product, and it was confirmed that the extract contained a sialic acid derivative.
이에 더하여, 제비집의 시알산 추출물에는 체내흡수율을 높이는 영양전달체가 포함될 수 있다. In addition, the sialic acid extract of swallow's nest may contain a nutrient carrier that increases the absorption rate in the body.
영양전달체는(Nutrient Delivery System)는 식품업계에서 사용하는 용어이며, 시알산과 같은 영양물질을 효과적으로 필요한 장기로 전달해주는 시스템이다. 비슷한 예로는 제약업계에서는 약물전달체(Drug Delivery System), 화장품업계에서는 피부전달체(Transdermal Delivery System)로 특정 약물이나 화장품 소재를 체내에 흡수 및 전달해 주는 전달 시스템이 있다.Nutrient Delivery System is a term used in the food industry, and it is a system that effectively delivers nutrients such as sialic acid to necessary organs. Similar examples include a drug delivery system in the pharmaceutical industry and a transdermal delivery system in the cosmetic industry, which is a delivery system that absorbs and delivers a specific drug or cosmetic material into the body.
이처럼 영양전달체는 대부분의 영양물질이 체내에 흡수되어 특정의 장기조직이나 세포로 용이하게 전달되지 않아 장기에 그 효능을 최대한 전달하기 어렵다는 것을 고려하여 영양물질의 체내 흡수율을 높이는 역할을 한다. As such, the nutrient delivery system plays a role in increasing the absorption rate of nutrients in the body, considering that most nutrients are absorbed into the body and are not easily delivered to specific organ tissues or cells, making it difficult to deliver their efficacy to the organs as much as possible.
도 2에 도시된 바와 같이, 영양전달체는 담즙산을 이용 시 체내 흡수율 및 효능이 우수한 속효성 마이셀 나노 입자이다. 여기서, 담즙산과 시알산은 도 2에 도시된 바와 같이 연결되어 존재한다. 그리고, 마이셀 나노입자는 100 내지 200 nm의 크기를 가지며, 바람직하게는 110 내지 190 nm의 크기를 갖고, 더욱 바람직하게는 120 내지 180 nm의 크기를 갖는다. 상기의 크기를 가지는 영양전달체인 마이셀 나노 입자는 체내 조직 투과 및 흡수가 용이하여 시알산의 체내 흡수율을 높인다. 이로 인하여 시알산의 효능인 뇌기능 개선 효과를 증대시킨다. As shown in FIG. 2 , the nutrient carrier is a fast-acting micelle nanoparticle having excellent absorption rate and efficacy in the body when bile acid is used. Here, the bile acid and the sialic acid are connected as shown in FIG. 2 . And, the micellar nanoparticles have a size of 100 to 200 nm, preferably have a size of 110 to 190 nm, more preferably have a size of 120 to 180 nm. The micellar nanoparticles, which are nutrient carriers having the above size, facilitate penetration and absorption of tissues in the body, thereby increasing the absorption rate of sialic acid in the body. Due to this, the effect of improving brain function, which is the efficacy of sialic acid, is increased.
또한, 영양전달체인 마이셀 나노 입자는 계면활성제로 리조레시틴을 포함함으로써 높은 조직 투과 및 흡수율을 갖게 된다.In addition, micellar nanoparticles, which are nutrient carriers, have high tissue permeation and absorption rates by including lyzolecithin as a surfactant.
이에 더하여, 제비집의 시알산 추출물에는 뇌기능 개선 물질인 알파-지피씨, 대두레시틴, DHA, 포스파티딜세린, 브로컬리, 참당귀, 수선화, 용안육, 단삼, 맥문동, 천마, 은행나무잎 엑기스, 로얄제리, 영지, 고려인삼, 클로렐라, 현미흑초, 프로폴리스, 세사민, 우콘 중 선택되는 어느 하나 또는 둘 이상의 것이 더 포함될 수 있다.In addition, the sialic acid extract of swallow's nest contains brain function improving substances such as alpha-GPC, soybean lecithin, DHA, phosphatidylserine, broccoli, angelica, daffodil, longan meat, ginseng, maekmundong, cheonma, ginkgo leaf extract, royal jelly, Reishi, Korean ginseng, chlorella, brown rice black vinegar, propolis, sesamin, any one or two or more selected from turmeric may be further included.
또한, 시알산의 효과를 손상시키지 않은 범위 내에서 부형제, 감미료, 산미료, 증점제, 향료, 색소, 유화제, 및 기타 의약품이나 식품 등으로 일반에 이용되고 있는 첨가제나 소재를 포함할 수도 있다.In addition, excipients, sweeteners, acidulants, thickeners, fragrances, colorants, emulsifiers, and other additives or materials commonly used in pharmaceuticals or foods, etc. may be included within the range that does not impair the effect of sialic acid.
[실시예 1][Example 1]
이하, 제조예, 제제예, 시험예 등을 들어 본 발명을 더욱 상세히 구체적으로 설명하는데, 본 발명은 이들에 한정되는 것이 아니다. 특히, 여기서는 본 발명의 제비집을 발효와 비발효로 나누지 않고 실시예를 나타내고 있는데, 제비집을 발효하여 사용할 수도 있다.Hereinafter, the present invention will be described in more detail with reference to Preparation Examples, Formulation Examples, Test Examples, and the like, but the present invention is not limited thereto. In particular, although examples are shown here without dividing the swallow's nest of the present invention into fermented and non-fermented, fermented swallow's nest may also be used.
사용한 제비집은 네스투랄(Nastural Ltd, Thailand)사가 제조한 제왕의 아침(The King's Morning)이라는 상품명으로 판매되고 있는 제비집 엑기스로 만들었다. 이 제비집 엑기스는 표 1에 나타내는 바와 같은 시알산을 갖고 있었다. 또한, 유용성분은 콜라겐, 시알산, 폴리페놀, 칼슘, 철분, 식이섬유이었으며 결합당은 갈락토스와 아라비노스 뿐이었다. 사용한 제비집은 아세틸계 42.5%, 케토계 27.5%로 아세틸계의 시알산이 많이 포함되어 있었다.The swallow's nest used was made from swallow's nest extract sold under the trade name The King's Morning manufactured by Natural Ltd, Thailand. This swallow's nest extract had sialic acid as shown in Table 1. In addition, the useful ingredients were collagen, sialic acid, polyphenol, calcium, iron, and dietary fiber, and the binding sugars were only galactose and arabinose. The swallow's nest used was 42.5% acetyl and 27.5% keto, which contained a lot of acetyl sialic acid.
1. 제비집 추출물과 시알산 추출액의 제조 및 영양전달체 제조(제조예 1)1. Preparation of bird's nest extract and sialic acid extract and preparation of nutrient delivery system (Preparation Example 1)
제비집을 정제수와 함께 분쇄하고 추출하여 얻어진 제비집 추출물을 Sep-Pac Plus C18 Cartridge 칼럼(Waters사 제조)에 흡착시키고, 멸균수로 세척한 후, 1% HCI-메탄올 용액으로 용출시킴으로써 제비집 중의 시알산 추출액을 분리했다. 이렇게 하여 얻어진 시알산 추출액을 온도 37℃에서 증발기에 의해 농축한 후, pH를 7.0으로 조정하고, DMSO(디메틸술폭시드)에 용해시키고, 이어 건조시켜 제비집 추출물과 시알산 추출액을 얻었다. 또한, 시알산을 대량으로 함유한 제비집 추출물을 얻고 싶은 경우에는 칼럼으로서 SEPHADEXLH-20(Amersham pharmacia Biotech AB사 제품: Cat17-0090-01)을 이용한 ABT공법으로 제조할 수도 있다. The bird's nest extract obtained by pulverizing the nest with purified water and extracting it was adsorbed on a Sep-Pac Plus C18 Cartridge column (manufactured by Waters), washed with sterile water, and eluted with 1% HCI-methanol solution to extract sialic acid in the nest. has been separated The sialic acid extract thus obtained was concentrated by an evaporator at a temperature of 37°C, the pH was adjusted to 7.0, dissolved in DMSO (dimethyl sulfoxide), and then dried to obtain a bird's nest extract and a sialic acid extract. In addition, if it is desired to obtain a bird's nest extract containing a large amount of sialic acid, it may be prepared by the ABT method using SEPHADEXLH-20 (Amersham pharmacia Biotech AB, Cat17-0090-01) as a column.
영양전달체 즉, 마이셀 나노입자는 타우로콜산(taurocholic aicd) 5.78g을 25 ml 메탄올 (메탄올 85 : 물 15의 부피비)에 혼합하여 430mM의 타우로콜산 용액을 만들었다. 상기 타우로콜산 용액 2.25mL에 레시틴 용액 1.8mL(클로로폼에 100 mg/mL로 용해된 레시틴 용액)를 첨가하여 1차 용액을 제조하였다. 제조된 상기 1차 용액을 테플론 캡을 가진 유리 튜브에 넣고 55℃ water bath에서 5시간 동안 온열 처리 하였다. 그리고 끈적거리고 걸쭉해져 누르스름해질 때까지 상기 1차 용액을 질소 가스를 이용하여 증발시켰다. 증발된 잔여물을 2시간 동안 -70 ℃에서 냉동시키고 튜브를 열어 9시간 이상 감압 하에서 동결건조 시키고, 다시 PBS에서 용해시켜 4시간 동안 56℃에서 온열처리 하였다. 온열처리가 완료된 후 용액을 무혈청 배지에서 1:10으로 희석시키고(부피 기준) 0.45um 필터를 이용하여 여과하여 시알산-담즙산 콘쥬게이트된 마이셀 나노 입자를 제조하였다 A nutrient carrier, that is, micellar nanoparticles, 5.78 g of taurocholic aicd was mixed with 25 ml methanol (methanol 85: water 15 volume ratio) to make a 430 mM taurocholic acid solution. A first solution was prepared by adding 1.8 mL of a lecithin solution (a lecithin solution dissolved in chloroform at 100 mg/mL in chloroform) to 2.25 mL of the taurocholic acid solution. The prepared primary solution was placed in a glass tube with a Teflon cap and heated in a 55° C. water bath for 5 hours. Then, the first solution was evaporated using nitrogen gas until it became sticky and thick and yellowish. The evaporated residue was frozen at -70°C for 2 hours, opened the tube, and lyophilized under reduced pressure for more than 9 hours, then dissolved in PBS and heated at 56°C for 4 hours. After the heat treatment was completed, the solution was diluted 1:10 in serum-free medium (by volume) and filtered using a 0.45um filter to prepare sialic acid-bile acid conjugated micellar nanoparticles.
2. 시험식의 제조2. Preparation of test formula
이하의 처방에 기초하여 관용적인 방법에 따라 배합성분을 연질 캅셀(OVAL No.6) 속에 채워 시험식으로 제제예 1 및 플라시보식을 제조했다.Formulation Example 1 and a placebo formula were prepared as test formulas by filling the compounding ingredients into a soft capsule (OVAL No. 6) according to a conventional method based on the following prescription.
캅셀의 피막은 젤라틴 분말, 글리세린, 이산화티타늄, 및 카라멜 색소로 이루어진다.The capsule shell is made of gelatin powder, glycerin, titanium dioxide, and caramel pigment.
3. 피험자3. Subject
시험실시 전에 생활습관 앙케이트 조사를 한 50~70세 남녀에서, 이하의 제외 기준에 해당하지 않는 자를 피험자로 했다.Subjects were those who did not meet the following exclusion criteria among men and women aged 50 to 70 who had conducted a lifestyle questionnaire survey before the test.
제외기준 :Exclusion criteria:
a) 이미 제비집을 상용하고 있는 자a) A person who is already using swallow's nest
b) 제비집을 주성분으로 하는 의약품 또는 건강보조식품을 상용하고 있는 자b) A person who regularly uses drugs or health supplements containing swallow's nest as a main ingredient
c) 뇌기능 또는 혈액 순환에 영향을 주는 의약품 또는 건강보조식품을 섭취하고 있는 자c) Those who are taking medicines or health supplements that affect brain function or blood circulation
d) 당뇨병, 또는 뇌기능, 혈액 순환, 소화기, 췌장, 간장 혹은 신장 등에 심각한 질환을 갖고 있는 자d) Those with diabetes or serious diseases such as brain function, blood circulation, digestive system, pancreas, liver or kidney
e) 본 시험 개시 시 다른 임상시험에 참가중인 자e) Those who are participating in another clinical trial at the start of this trial
f) 특정 알레르기(제비집을 포함)가 있는 자f) Persons with certain allergies (including swallow's nest)
g) 생활습관 앙케이트 조사의 결과에서, 피험자로서 부적합하다고 판단된 자(예를 들어, 피험식 조성중인 성분에서 알레르기를 일으킨 적인 있는 자, 극단적인 음주경향이 있는 자 등)g) A person judged unsuitable as a test subject from the results of the lifestyle questionnaire survey (for example, a person who has ever caused an allergy to an ingredient in the test formula, a person with an extreme tendency to drink, etc.)
h) 색각 이상 또는 색각 장해가 있는 자h) Persons with color vision abnormality or color vision impairment
i) 기타, 시험담당 의사가 부적합하다고 판단한 자i) Others, those judged by the examination doctor to be inappropriate
4. 시험 스케줄4. Exam Schedule
시험은 이중맹검 평행군 간 비교로 수행했다.The trial was performed as a double-blind, parallel-group comparison.
우선, 상기 피험자를 시험기간 첫날(시험 첫째날)에 내원시켜 문진, 신체계측, 및 뇌기능 검사 1 및 2를 했다.First, the subject was brought to the hospital on the first day of the test period (the first day of the test), and questionnaires, physical measurements, and brain function tests 1 and 2 were performed.
이어 이들 피험자를 시험군 및 플라시보군의 2군에, 각각 30명씩을 무작위로 분할하여, 시험식의 섭취를 개시시켰다.Then, these subjects were randomly divided into two groups of a test group and a placebo group, 30 each, and ingestion of the test food was started.
시험군의 피험자에게는 제제예 1을, 플라시보군의 피험자에게는 플라시보식을, 각각 매일 1회, 2캅셀, 12주간 섭취하게 했다. 또한, 섭식 중에는 피험자에게 일지도 쓰게 했다.The subjects in the test group were given Formulation Example 1, and the subjects in the placebo group were given a placebo meal, respectively, once daily, 2 capsules, for 12 weeks. In addition, subjects were asked to keep a journal while feeding.
섭식을 개시하고 나서 4주 후(시험 28일째), 8주후(시험 56일째), 및 12주후(시험 84일째)에 문진, 신체계측, 및 뇌기능 검사 2를 각각 수행했다.After the start of feeding, the questionnaire, physical measurement, and brain function test 2 were performed 4 weeks (test day 28), 8 weeks (test day 56), and 12 weeks (test day 84), respectively.
5. 검사항목5. Inspection items
본 시험에서는 문진, 신체계측, 및 뇌기능 검사를 했다. 각 검사 방법은 이하와 같았다. 또, 각 검사에서 얻어진 값은 평균값 ㅁ 표준오차로 나타냈다.In this test, questionnaires, physical measurements, and brain function tests were performed. Each inspection method was as follows. In addition, the values obtained in each test were expressed as the average value ㅁ standard error.
a) 문진a) Paperweight
자각증상 및 타각 증상의 유무를 문진했다.The presence or absence of subjective symptoms and subjective symptoms was asked.
b) 신체계측b) body measurements
신장, 체중, 체지방, 혈압, 맥박수, 및 시력을 측정했다.Height, weight, body fat, blood pressure, pulse rate, and visual acuity were measured.
c) 뇌기능 검사c) brain function test
뇌기능 검사로서, 이하와 같은 뇌기능 검사 1 및 2를 했다. 검사는 공복 상태에서 했다. 또, 끽연자에 대해서는 검사를 마칠 때까지는 금연시켰다.As a brain function test, the following brain function tests 1 and 2 were performed. The test was done on an empty stomach. Also, smokers were banned from smoking until the test was completed.
뇌기능 검사 1 : 개정 하세가와식 간이지능평가 스케일(HDS-R)로 검사했다.Brain function test 1: The test was conducted using the revised Hasegawa Simple Intelligence Assessment Scale (HDS-R).
뇌기능 검사 2 : 단어의 상기시험 및 스트로프 테스트(Stroop test)로 검사했다. 각 시험 모두 이하와 같이 수행했다.Brain function test 2: It was tested by the recall test of words and the Stroop test. Each test was performed as follows.
(1) 단어의 상기 시험(1) Recall test of words
"당신이 알고 있는 동물 이름을 되도록 많이 말해 주십시오"라고 피험자에게 알려주고, 첫번째 동물 이름이 거론되고나서 60초 이내에 열거할 수 있는 동물의 이름을 기재했다. 중복된 것은 제외하고 열거된 동물 이름의 수를 기록하고, 상기수로 했다."Tell me as many animal names as you know" was said to the subject, followed by listing the names of animals that could be enumerated within 60 seconds of the first animal name being mentioned. The number of animal names listed, excluding duplicates, was recorded and counted as the number.
첫번째 동물이 좀처럼 생각나지 않을 때에는, "예를 들어, 개가 동물 이름인데요, 그 밖에는 어떤 것이 있습니까?"라고 피험자를 유도했다. 이 유도 후에도 생각나지 않고 30초가 경과했다면, 검사를 중지하고 상기수를 0으로 했다.When the first animal could hardly be remembered, the subject was induced by saying, "For example, dog is the name of an animal, what else is there?" If 30 seconds had elapsed without recalling even after this induction, the test was stopped and the above count was set to zero.
동물은 포유류에 한정되지 않고 파충류, 조류, 어류 등의 명칭도 상기수에 더했다.Animals are not limited to mammals, and names of reptiles, birds, fish, etc. are also added to the above number.
마찬가지로 야채 및 "아"로 시작되는 말에 대해서도 각각 열거시키고, 이들의 상기수도 기록했다.Similarly, vegetables and words beginning with "ah" were listed respectively, and their recalls were recorded.
또한, 이들 동물, 야채 및 "아"로 시작되는 말 각각의 상기수를 총계하고, 이것을 총상기수로 했다.In addition, the said number of each of these animals, a vegetable, and a horse beginning with "ah" was totaled, and this was made into the total number.
(2) 스트로프 테스트 :(2) Stroke test:
"적" "청" "흑"의 3종류의 색의 70문자가 무작위로 쓰여져 있는 문자를 읽는 시험(단계 1),A test in which 70 characters of three colors of “red”, “blue” and “black” are randomly written (step 1),
"적" "청" "흑"의 3종류의 색 70개를 읽는 시험(단계 2), 및 "적" "청" "흑"으로 기입된 70문자를 "적" "청" "흑"의 3종류로 무작위로 색분류하고, 그 문자를 읽는 시험(단계 3) 및 그 색을 읽는 시험(단계 4)의 총 4종류의 시험을 실시하고, 읽는데 필요한 초수를 기록했다.Examination of reading 70 colors of 3 types of "red", "blue" and "black" (step 2), and 70 characters written in "red", "blue" and "black" of "red", "blue" and "black" The colors were randomly classified into three types, and a total of four tests, a test for reading the character (step 3) and a test for reading the color (step 4), were performed, and the number of seconds required for reading was recorded.
a) 일지a) journal
시험식의 섭취상황, 자각증상, 및 다른 의약품의 복용상황을 피험자에게 기재하게 했다.The subjects were asked to describe the intake status of the test food, subjective symptoms, and the status of taking other medicines.
6. 시험 결과6. Test results
a) 피험자의 배경a) the background of the subject
플라시보군 및 시험군에서, 각각 25명 및 25명의 피험자(계50명)가 시험에 참가했는데, 탈락, 중지한 자가 없었다. 시험에 참가한 피험자의 배경을 표 3에 나타냈다. 연령, 성별, 및 HDS-R에 의한 점수에서 군 사이에 불균형은 보이지 않았다In the placebo group and the test group, 25 and 25 subjects (50 total), respectively, participated in the trial, but no one dropped out or stopped. Table 3 shows the background of the subjects who participated in the test. There was no disparity between groups in scores by age, sex, and HDS-R.
(P>0.05). 또한, 통계분석은 분산분석(ANOVA)으로 했다.(P>0.05). In addition, statistical analysis was carried out by analysis of variance (ANOVA).
값 : 평균값 ± 표준오차 Value: mean ± standard error
b) 유효성b) validity
시험 첫째날, 28일째. 56일째, 및 84일째의 피험자의 뇌기능 검사 2의 측정값에서 제제예 1의 뇌기능에 대한 유효성을 평가했다.The first day of the exam, the 28th. The effectiveness on brain function of Formulation Example 1 was evaluated from the measured values of the brain function test 2 of the subjects on the 56th day and the 84th day.
통계 해석은 동일군 내에서 시험 첫날과, 시험 28일째, 56일째, 및 84일째를 비교하는 경우에는 군내의 대응하는 t검사에 의해 검정했다. 유의 수준은 양측 5%로 했다.Statistical interpretation was tested by the corresponding within-group t-test when comparing the first day of the test and the 28th, 56th, and 84th days of the test within the same group. The significance level was set to 5% on both sides.
c) 뇌기능 검사c) brain function test
(1) 단어의 상기 시험(1) Recall test of words
시험군에서는 동물, 야채, 및 "아"로 시작되는 말의 상기수 및 총상기수가 섭취전보다 증가했는데(표 4), 플라시보군에서는 증가가 나타나지 않았다.In the test group, the counts and total counts of animals, vegetables, and horses beginning with "ah" were increased compared to before ingestion (Table 4), but no increase was seen in the placebo group.
(2) 스트로프 테스트(2) strobe test
시험군에서는 단계 1∼4의 각 단계에서 읽는데 필요로 한 초수가 감소했는데(표 5), 플라시보군에서는 감소가 나타나지 않았다.In the test group, the number of seconds required to read each step of steps 1 to 4 decreased (Table 5), but no decrease was seen in the placebo group.
이상과 같이, 플라시보군에서는 효과는 명확히 인정할 수 없으며, 제제예 1의 뇌기능 개선 효과는 분명했다.As described above, the effect was not clearly recognized in the placebo group, and the brain function improvement effect of Formulation Example 1 was clear.
단위 : 개Unit: dog
값 : 평균값 ± 표준오차Value: mean ± standard error
단위 : 초Unit: Seconds
값 : 평균값 ± 표준오차Value: mean ± standard error
단계 1 : 문자를 읽는데 필요한 초수, 단계 2 : 색을 읽는데 필요한 초수, 단계 3 : 색칠된 글자를 읽는데 필요한 초수, 단계 4 : 색칠된 글자색을 읽는데 필요한 초수를 각각 나타낸다.Step 1: The number of seconds required to read the character, Step 2: The number of seconds required to read the color, Step 3: The number of seconds required to read the colored text, Step 4: The number of seconds required to read the colored text.
d) 안전성d) safety
체중, 혈압 및 맥박에 이상은 없었다. 일지에도 특별히 이상을 나타내는 소견은 없었다. 또, 본 시험기간 중에 시험식과 관련된 유해 사항은 볼 수 없었다.There were no abnormalities in body weight, blood pressure and pulse. There were no abnormal findings in the diary. In addition, no harmful matters related to the test formula were observed during this test period.
이상에서, 제제에 1은 안전성이 있다라고 할 수 있었다.From the above, it can be said that the formulation is safe with a value of 1.
[실시예 2][Example 2]
1. AChE 활성에 대한 제비집 추출물과 시알산의 효능 비교1. Comparison of Efficacy of Bird's Nest Extract and Sialic Acid on AChE Activity
제비집 추출물과 시알산을 이용하여 AChE 활성에 대한 비교 실험을 다음과 같이 진행하였다. 실험동물로 5주령의 수컷 ICR 마우스(Orient Bio, 대한민국)를 구입하여 일주일의 적응기간을 유지하였다. 생체 내 AChE 활성 억제 효과를 비교하기 위하여 대조군(Donepezil 1.0mg/kg) 및 시알산(200mg/kg)과 제비집 추출물(50 mg/kg)을 각각의 마우스(각 군당 3마리)에 1회 경구 투여하였다. 각각의 물질을 투여한 후 6시간째에 해마를 분리한 후 1 M 인산 완충용액(pH 8.0)을 이용하여 균질화 한 후 균질액을 획득하였다. 획득한 균질액은 Amplex red assay kit(Molecular probe, USA)를 이용하여 생체 내 AChE 활성을 측정하였다. 그 결과, 제비집 추출물의 경우 AChE 활성 억제 효과가 미미한 반면에 시알산의 경우 약 71.5%의 AChE 활성 억제효과를 관찰하였다(도 3참조).A comparative experiment on AChE activity was conducted using the swallow's nest extract and sialic acid as follows. As an experimental animal, a 5-week-old male ICR mouse (Orient Bio, Korea) was purchased and an adaptation period of one week was maintained. In order to compare the effect of inhibiting AChE activity in vivo, a control group (Donepezil 1.0mg/kg) and sialic acid (200mg/kg) and bird's nest extract (50mg/kg) were orally administered to each mouse (3 mice in each group) once. did. Six hours after administration of each substance, the hippocampus was isolated and homogenized using 1 M phosphate buffer (pH 8.0) to obtain a homogenate. The obtained homogenate was measured for AChE activity in vivo using Amplex red assay kit (Molecular probe, USA). As a result, in the case of the bird's nest extract, the inhibitory effect on AChE activity was insignificant, whereas in the case of sialic acid, about 71.5% of the inhibitory effect on AChE activity was observed (see FIG. 3 ).
2. 아밀로이드 베타 단백질 유도 치매 래트 모델에서 해마 부위의 조직학적 검사2. Histological examination of hippocampus in amyloid beta protein-induced dementia rat model
행동학적 검사가 끝난 래트는 다이에틸 에스터로 마취한 뒤 복강을 열어 심장을 통하여 염수로 관류 하였다. 이후 뇌를 적출하여 10% 중성의 완충용 포르말린에 고정시킨 뒤 헤마톡실린&에오신 염색을 통해 해마 부위의 신경 세포의 퇴화 정도를 관찰하였다. 그 결과, 아밀로이드 베타 단백질을 뇌실 내 처리한 군을 보면 아무것도 처리하지 않은 군에 비하여 해마의 치상회(dentate gyrus) 부위의 기억과 관련된 피라미드 세포(pyramidal cell)의 퇴화가 관찰되었다. 시알산을 200 mg/kg 농도로 4주간 투여한 군에서는 그 손상 정도가 약하게 나타났다(도 4참조). After the behavioral examination was completed, the rats were anesthetized with diethyl ester, and the abdominal cavity was opened and perfused with saline through the heart. Then, the brain was extracted and fixed in 10% neutral buffered formalin, and the degree of degeneration of the nerve cells in the hippocampus was observed through hematoxylin & eosin staining. As a result, in the group treated with amyloid beta protein in the ventricle, deterioration of pyramidal cells related to memory in the dentate gyrus of the hippocampus was observed compared to the group not treated with anything. In the group administered with sialic acid at a concentration of 200 mg/kg for 4 weeks, the degree of damage was weak (see FIG. 4 ).
이와 같이 본 발명은 뇌기능 장해의 예방 및 치료에 유용하다. 여기서, 뇌기능 장해는 뇌혈관성 치매, 알츠하이머형 치매 및 양자의 혼합형 등의 치매증; 건망증 또는 기억상실 등의 기억력 저하 ; 인지력 저하 ; 학습능력 저하 ; 메니에르증 및 지주막하출혈(수막 졸증), 뇌출혈, 뇌혈전, 뇌경색, 및 뇌부종 등의 뇌혈관 장해의 후유증(휴유증으로 인한 의식장해, 운동장해 및 언어장해, 구음장해, 실어증, 감정장해, 사고장해, 감각장해, 기억장해, 및 자세이상) 등을 들 수 있다.As described above, the present invention is useful for the prevention and treatment of brain dysfunction. Here, the brain dysfunction includes dementia such as cerebrovascular dementia, Alzheimer's type dementia, and a mixture of both; memory loss, such as forgetfulness or amnesia; cognitive decline; poor learning ability; Meniere's disease and subarachnoid hemorrhage (meningoencephalopathy), cerebral hemorrhage, cerebral thrombosis, cerebral infarction, and sequelae of cerebrovascular disorders such as cerebral edema (impairment of consciousness, movement and speech disorders due to restlessness, speech disorders, aphasia, emotional disorders, accidents) impairment, sensory impairment, memory impairment, and postural abnormality) and the like.
또한, 본 발명은 알츠하이머형 치매; 메니에르증; 및 지주막하출혈, 뇌출혈 및 뇌경색의 후유증의 예방 및 치료에 유용하다.In addition, the present invention is Alzheimer's type dementia; Meniere's disease; and subarachnoid hemorrhage, cerebral hemorrhage and sequelae of cerebral infarction.
또한, 본 발명은 뇌기능 장해의 예방 및 치료라는 목적으로 사용할 뿐 아니라, 건강한 사람의 학습능력, 기억력 또는 반사반응능력 등의 뇌기능을 더욱 향상시키는 것을 목적으로 사용할 수도 있다.In addition, the present invention can be used not only for the purpose of preventing and treating brain dysfunction, but also for the purpose of further improving brain functions such as learning ability, memory or reflex response ability of a healthy person.
또한, 본 발명은 식품 또는 동물용 사료로, 예를 들어, 건강식품, 기능성 식품, 건강보조식품, 특정 보건용 식품, 미용식품, 또는 영양보조식품(서플리먼트)으로서 사용할 수 있다. 이들 식품 및 동물용 사료는 예를 들어, 차 및 쥬스 등의 음료수 ; 및 아이스크림, 젤리, 엿, 쵸콜렛, 및 츄잉껌 등의 형태일 수도 있다. 또한, 액제, 분말제, 과립제, 캅셀제, 또는 정제의 형태일 수도 있다. 여기서, 동물용 사료의 동물에는 애완동물 축산동물 또는 동물원 등에서 사육되고 있는 동물을 포함하는, 부종의 예방 또는 치료를 필요로 하는 모든 동물이 포함된다.In addition, the present invention can be used as a food or animal feed, for example, as a health food, a functional food, a health supplement, a food for specific health use, a beauty food, or a nutritional supplement (supplement). These foodstuffs and animal feeds include, for example, beverages such as tea and juice; and ice cream, jelly, candy, chocolate, and chewing gum. In addition, it may be in the form of a liquid, powder, granule, capsule, or tablet. Here, the animal feed for animals includes all animals that require the prevention or treatment of edema, including pet livestock animals or animals raised in zoos, etc.
또한, 본 발명은 의약품 또는 의약부외품으로서 사용할 수 있다. 이들 의약품 또는 의약부외품은 예를 들어, 산제, 정제, 코팅정, 당의정, 경질 혹은 연질 젤라틴 캅셀제, 액제, 유제, 또는 현탁제의 형태로 경구에 투여할 수 있는데, 예를 들어, 좌제의 형태로 직장으로, 예를 들어, 주사제 또는 윤액(輪液)의 형태로 ; 예를 들어, 연고, 크림제, 겔제, 또는 액제의 형태로 국소적 또는 경피로 비경구적으로 투여할 수도 있다. 바람직한 것은 경구투여다. In addition, the present invention can be used as a pharmaceutical or quasi-drug. These pharmaceuticals or quasi-drugs can be administered orally in the form of, for example, powder, tablet, coated tablet, dragee, hard or soft gelatin capsule, solution, emulsion, or suspension, for example, in the form of a suppository. rectally, for example, in the form of an injection or lubricating fluid; For example, it may be administered parenterally or topically in the form of an ointment, cream, gel, or solution. Preferred is oral administration.
또한, 본 발명은 정제의 형태로 이용하는 경우에, 약학적 또는 식품학적으로 인용된 다양한 담체를 이용할 수 있고, 유당, 포도당 등의 부형제, 물, 에탄올 등의 결합제, 한천말, 건조전분 등의 붕해제, 스테아린, 카카오버터 등의 붕괴억제제, 카오린, 벤토나이트 등의 흡착제, 라우릴황산나트륨 등의 흡수촉진제, 글리세린, 전분 등의 보습제, 붕산말, 폴리에틸렌글리콜 등의 활택제 등을 예시할 수 있다.In addition, when the present invention is used in the form of a tablet, various carriers cited in pharmaceutical or food science can be used, and excipients such as lactose and glucose, binders such as water and ethanol, and boron such as agar powder and dry starch Disintegration inhibitors such as release, stearin and cacao butter, adsorbents such as kaolin and bentonite, absorption accelerators such as sodium lauryl sulfate, humectants such as glycerin and starch, lubricating agents such as boric acid malt and polyethylene glycol, and the like can be exemplified.
또한, 본 발명의 섭취량은 특별히 제한되지 않지만, 제형, 및 사용자 혹은 환자 등의 섭취자 또는 섭취동물의 연령, 체중 및 증상에 따라 적절히 선택할 수 있다. 예를 들어, 유효성분량으로 1일당 섭취자 또는 섭취동물의 체중 1kg에 대해 시알산량으로 0.3∼5mg, 바람직하게는 0.35∼3mg, 더욱 바람직하게는 0.35∼1.5mg을 경구 섭취하는 것이 뛰어난 뇌기능 개선효과를 얻을 수 있으므로 바람직하다. 또한. 섭취기간은 섭취자 또는 섭취동물의 연령, 증상에 따라 임의로 정할 수 있다.In addition, the intake amount of the present invention is not particularly limited, but may be appropriately selected according to the dosage form and the age, weight, and symptoms of the ingester or the ingested animal such as the user or patient. For example, excellent brain function improvement by oral intake of 0.3 to 5 mg, preferably 0.35 to 3 mg, more preferably 0.35 to 1.5 mg of sialic acid per 1 kg of body weight of the ingestor or ingested animal per day as an active ingredient It is preferable because the effect can be obtained. In addition. The ingestion period can be arbitrarily determined according to the age and symptoms of the ingestor or animal.
이와 같이 본 발명은 ABT(Affinity Beads Technology) 기반의 시알산 분리 정제 방법으로 제비집에 함유되어 있는 뇌기능 개선 물질인 시알산을 효율적으로 추출하고, 상기 방법으로 추출된 시알산 추출물을 유효성분으로 포함함으로써 뇌기능의 개선은 물론 뇌기능 장해의 예방 및 치료에 유용하다. 또한, 제비집으로부터 추출된 시알산 추출물에 마이셀 나노 입자의 영양전달체를 부가하여 시알산 추출물의 체내흡수율을 높임으로써 뇌기능의 개선 효과 및 뇌기능 장해의 예방, 치료효과를 증대시킨다. 또한, 장기 복용하더라도 부작용 등의 걱정이 적고, 안전성이 높다. 그리고, 의약품, 혹은 건강식품, 건강보조식품, 특정 보건용 식품, 또는 영양보조식품 등의 식품으로서 이용할 수 있다.As described above, the present invention efficiently extracts sialic acid, a brain function improving substance contained in swallow's nest, by using ABT (Affinity Beads Technology)-based sialic acid separation and purification method, and includes the sialic acid extract extracted by the above method as an active ingredient By doing so, it is useful not only to improve brain function, but also to prevent and treat brain dysfunction. In addition, the nutrient delivery system of micellar nanoparticles is added to the sialic acid extract extracted from the swallow's nest to increase the absorption rate of the sialic acid extract into the body, thereby improving brain function and preventing and treating brain dysfunction. In addition, even if it is taken for a long time, there is little worry about side effects and the like, and the safety is high. And, it can be used as food, such as a pharmaceutical or health food, a health supplement, a food for specific health use, or a nutritional supplement.
이상에서 본 발명의 바람직한 실시 예에 대하여 설명하였으나, 본 발명은 상술한 특정의 실시 예에 한정되지 아니한다. 즉, 본 발명이 속하는 기술 분야에서 통상의 지식을 가지는 자라면 첨부된 특허청구범위의 사상 및 범주를 일탈함이 없이 본 발명에 대한 다수의 변경 및 수정이 가능하며, 그러한 모든 적절한 변경 및 수정은 균등물들로 본 발명의 범위에 속하는 것으로 간주 되어야 할 것이다.Although preferred embodiments of the present invention have been described above, the present invention is not limited to the specific embodiments described above. That is, a person of ordinary skill in the art to which the present invention pertains can make numerous changes and modifications to the present invention without departing from the spirit and scope of the appended claims, and all such appropriate changes and modifications are Equivalents are to be considered as falling within the scope of the present invention.
Claims (5)
상기 시알산추출물은 제비집을 물, 알칼리 이온수 또는 유기용매로 이루어진 군으로부터 선택된 1종 이상의 용매를 투입하여 추출하는 단계; 상기 추출된 용매에 비극성 고분자 비드를 투입하여 시알산(sialic acid)를 흡착하는 단계; 상기 시알산이 흡착된 비극성 고분자 비드를 분리하고 이에 탈착제를 투입하여 시알산을 탈착하는 단계; 상기 탈착된 시알산을 고형화하는 단계;를 포함하는 ABT(Affinity Beads Technology) 기반의 시알산 분리정제 방법으로 추출되는 것을 특징으로 하는 뇌기능 개선용 영양전달체 조성물. The method of claim 1,
The step of extracting the sialic acid extract by adding one or more solvents selected from the group consisting of water, alkaline ionized water, or an organic solvent to the swallow's nest; adsorbing sialic acid by adding non-polar polymer beads to the extracted solvent; separating the non-polar polymer beads to which the sialic acid is adsorbed and desorbing the sialic acid by adding a desorbent thereto; A nutrient delivery system composition for improving brain function, characterized in that it is extracted by an ABT (Affinity Beads Technology)-based sialic acid separation and purification method comprising a step of solidifying the desorbed sialic acid.
상기 제비집의 시알산 추출물에는 체내흡수율을 높이는 영양전달체가 더 포함되는 것을 특징으로 하는 뇌기능 개선용 영양전달체 조성물. The method of claim 1,
A nutrient delivery system composition for improving brain function, characterized in that the sialic acid extract of the swallow's nest further includes a nutrient delivery agent that increases absorption into the body.
상기 영양전달체는 마이셀 나노입자인 것을 특징으로 하는 뇌기능 개선용 영양전달체 조성물. 4. The method of claim 3,
The nutrient delivery system is a nutrient delivery system composition for improving brain function, characterized in that the micellar nanoparticles.
상기 제비집의 시알산 추출물에는 뇌기능 개선 물질인 알파-지피씨, 대두레시틴, DHA, 포스파티딜세린, 브로컬리, 참당귀, 수선화, 용안육, 단삼, 맥문동, 천마, 은행나무잎 엑기스, 로얄제리, 영지, 고려인삼, 클로렐라, 현미흑초, 프로폴리스, 세사민, 우콘 중 선택되는 어느 하나 또는 둘 이상의 것이 더 포함되는 것을 특징으로 하는 뇌기능 개선용 영양전달체 조성물.The method of claim 1,
The sialic acid extract of the swallow's nest includes brain function improving substances alpha-GPC, soybean lecithin, DHA, phosphatidylserine, broccoli, Angelica keiskei, daffodils, longan meat, ginseng, maekmundong, cheonma, ginkgo leaf extract, royal jelly, reishi, Korean ginseng, chlorella, brown rice black vinegar, propolis, sesamin, nutrient delivery system composition for improving brain function, characterized in that it further comprises any one or two or more selected from turmeric.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020200049340A KR102439576B1 (en) | 2020-04-23 | 2020-04-23 | Composition of Nutrient Delivery System for Improving Brain Function |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020200049340A KR102439576B1 (en) | 2020-04-23 | 2020-04-23 | Composition of Nutrient Delivery System for Improving Brain Function |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20210131039A true KR20210131039A (en) | 2021-11-02 |
KR102439576B1 KR102439576B1 (en) | 2022-09-02 |
Family
ID=78476544
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020200049340A KR102439576B1 (en) | 2020-04-23 | 2020-04-23 | Composition of Nutrient Delivery System for Improving Brain Function |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR102439576B1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114878705A (en) * | 2022-04-20 | 2022-08-09 | 中轻食品检验认证有限公司 | Method for measuring sialic acid stable carbon isotope ratio in cubilose product |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100569089B1 (en) | 2002-07-20 | 2006-04-10 | 주식회사 엘컴사이언스 | Composition having brain function and congnition enhancing activity |
CN102532208A (en) * | 2012-01-06 | 2012-07-04 | 南京工业大学 | Method for continuously separating sialic acid |
KR20160007708A (en) | 2014-06-24 | 2016-01-21 | 월드그린영농조합법인 | Composition comprising rice bran extracts for improving brain function |
CN108003202A (en) * | 2017-11-28 | 2018-05-08 | 广西佛斯肽生物科技有限公司 | A kind of method that Sialic acid is extracted from bird's nest |
-
2020
- 2020-04-23 KR KR1020200049340A patent/KR102439576B1/en active IP Right Grant
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100569089B1 (en) | 2002-07-20 | 2006-04-10 | 주식회사 엘컴사이언스 | Composition having brain function and congnition enhancing activity |
CN102532208A (en) * | 2012-01-06 | 2012-07-04 | 南京工业大学 | Method for continuously separating sialic acid |
KR20160007708A (en) | 2014-06-24 | 2016-01-21 | 월드그린영농조합법인 | Composition comprising rice bran extracts for improving brain function |
CN108003202A (en) * | 2017-11-28 | 2018-05-08 | 广西佛斯肽生物科技有限公司 | A kind of method that Sialic acid is extracted from bird's nest |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114878705A (en) * | 2022-04-20 | 2022-08-09 | 中轻食品检验认证有限公司 | Method for measuring sialic acid stable carbon isotope ratio in cubilose product |
CN114878705B (en) * | 2022-04-20 | 2023-10-27 | 中轻食品检验认证有限公司 | Method for determining sialic acid stable carbon isotope ratio in bird's nest product |
Also Published As
Publication number | Publication date |
---|---|
KR102439576B1 (en) | 2022-09-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2008501012A (en) | Compositions for treating neurodegenerative disorders and methods of use thereof | |
EP3173089A1 (en) | Brain function improving agent, and prophylactic or therapeutic agent for cognitive dysfunction | |
AU2016353600A1 (en) | Method for treating mucositis | |
JP2003261456A (en) | Brain aging-preventing agent | |
KR101789424B1 (en) | Medicinal-Herb Composition Comprising Chinese matrimony vine Proving Insomniac and the Method of Making the Same | |
JP2009500446A (en) | Pharmaceutical composition having an effect of preventing and treating liver diseases, comprising an extract of keyonomi | |
JP5071618B2 (en) | Exocrine gland dysfunction improving agent and foods | |
KR102439576B1 (en) | Composition of Nutrient Delivery System for Improving Brain Function | |
WO2005074961A1 (en) | Body fat-controlling agent | |
JP2007145825A (en) | Composition for brain function improvement | |
JP2014148479A (en) | Anti-obesity composition containing complex of gallate type catechin with protein, and caffeine | |
EP3725320A1 (en) | Composition comprising agathobaculum sp. strain as effective ingredient for prevention, alleviation, or treatment of autism spectrum disorder | |
US9737583B2 (en) | Composition for prevention or treatment of acute renal failure including herbal extract or fraction thereof as active ingredient | |
WO2005094858A1 (en) | Antidiabetic composition | |
JP2014139160A (en) | Cerebral function-reforming agent and cerebral function-reforming food | |
JP6782381B1 (en) | Food composition for improving brain function, brain function improving agent, food composition for increasing brain-derived neurotrophic factor, food composition for suppressing stress hormone secretion, brain-derived neurotrophic factor increasing agent and stress hormone secretion inhibitor | |
KR20150107938A (en) | Composition for Improving Memory and Cognitive Function Comprising Psyllium husk | |
KR101241455B1 (en) | Bean curd having hypotensive effect | |
CN109153693B (en) | Safe and stable plasmalogen, preparation thereof, and method for determining non-diseased state of cognitive disorder | |
WO2019131444A1 (en) | Cognitive function improvement agent | |
JPH07135923A (en) | Composition for functional food | |
TWI745609B (en) | Composition for promoting antioxidative activity | |
KR102634302B1 (en) | Composition for preventing or treating cognitive impairment comprising extract of iris lactea | |
WO2021225343A1 (en) | Composition for preventing or treating cognitive disorder, comprising iris lactea extract | |
WO2021085496A1 (en) | Composition, antioxidant agent, antisaccharification agent, neurite outgrowth promoter, and cognitive function improver |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
E902 | Notification of reason for refusal | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant |