JP7579733B2 - Semi-solid nutritional composition - Google Patents
Semi-solid nutritional composition Download PDFInfo
- Publication number
- JP7579733B2 JP7579733B2 JP2021056975A JP2021056975A JP7579733B2 JP 7579733 B2 JP7579733 B2 JP 7579733B2 JP 2021056975 A JP2021056975 A JP 2021056975A JP 2021056975 A JP2021056975 A JP 2021056975A JP 7579733 B2 JP7579733 B2 JP 7579733B2
- Authority
- JP
- Japan
- Prior art keywords
- semi
- nutritional composition
- solid nutritional
- viscosity
- mass
- 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.)
- Active
Links
- 239000000203 mixture Substances 0.000 title claims description 166
- 235000016709 nutrition Nutrition 0.000 title claims description 160
- 239000007787 solid Substances 0.000 title claims description 141
- 229920001817 Agar Polymers 0.000 claims description 38
- 239000008272 agar Substances 0.000 claims description 34
- 235000013325 dietary fiber Nutrition 0.000 claims description 34
- 229920001277 pectin Polymers 0.000 claims description 32
- 239000001814 pectin Substances 0.000 claims description 32
- 235000010987 pectin Nutrition 0.000 claims description 32
- 230000003204 osmotic effect Effects 0.000 claims description 29
- 229920001353 Dextrin Polymers 0.000 claims description 19
- 239000004375 Dextrin Substances 0.000 claims description 19
- 235000019425 dextrin Nutrition 0.000 claims description 19
- 150000001720 carbohydrates Chemical class 0.000 claims description 16
- 235000014633 carbohydrates Nutrition 0.000 claims description 16
- 235000015110 jellies Nutrition 0.000 claims description 13
- 239000008274 jelly Substances 0.000 claims description 13
- 235000018102 proteins Nutrition 0.000 claims description 13
- 102000004169 proteins and genes Human genes 0.000 claims description 13
- 108090000623 proteins and genes Proteins 0.000 claims description 13
- 230000032050 esterification Effects 0.000 claims description 12
- 238000005886 esterification reaction Methods 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 12
- 150000002632 lipids Chemical class 0.000 claims description 9
- 229960004203 carnitine Drugs 0.000 claims description 7
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 claims description 3
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 claims description 3
- 229960001231 choline Drugs 0.000 claims description 3
- 229960000367 inositol Drugs 0.000 claims description 3
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 claims description 3
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 claims description 3
- PHIQHXFUZVPYII-ZCFIWIBFSA-O (R)-carnitinium Chemical compound C[N+](C)(C)C[C@H](O)CC(O)=O PHIQHXFUZVPYII-ZCFIWIBFSA-O 0.000 claims 1
- 235000010419 agar Nutrition 0.000 description 32
- 238000000034 method Methods 0.000 description 23
- 239000000839 emulsion Substances 0.000 description 21
- 238000005345 coagulation Methods 0.000 description 20
- 230000015271 coagulation Effects 0.000 description 20
- 238000002360 preparation method Methods 0.000 description 20
- 239000000243 solution Substances 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 230000035764 nutrition Effects 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 9
- PHIQHXFUZVPYII-ZCFIWIBFSA-N (R)-carnitine Chemical compound C[N+](C)(C)C[C@H](O)CC([O-])=O PHIQHXFUZVPYII-ZCFIWIBFSA-N 0.000 description 8
- 108010046377 Whey Proteins Proteins 0.000 description 8
- 102000007544 Whey Proteins Human genes 0.000 description 8
- 230000001954 sterilising effect Effects 0.000 description 8
- -1 etc.) Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 238000004659 sterilization and disinfection Methods 0.000 description 7
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 6
- 206010012735 Diarrhoea Diseases 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 235000013305 food Nutrition 0.000 description 6
- 235000013373 food additive Nutrition 0.000 description 6
- 239000002778 food additive Substances 0.000 description 6
- 239000000499 gel Substances 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 6
- 235000015097 nutrients Nutrition 0.000 description 6
- 210000002784 stomach Anatomy 0.000 description 6
- 235000021119 whey protein Nutrition 0.000 description 6
- 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 5
- 235000010724 Wisteria floribunda Nutrition 0.000 description 5
- 239000013256 coordination polymer Substances 0.000 description 5
- 208000021302 gastroesophageal reflux disease Diseases 0.000 description 5
- 239000008103 glucose Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 229940088594 vitamin Drugs 0.000 description 5
- 229930003231 vitamin Natural products 0.000 description 5
- 235000013343 vitamin Nutrition 0.000 description 5
- 239000011782 vitamin Substances 0.000 description 5
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 4
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 239000008280 blood Substances 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 3
- 229920000936 Agarose Polymers 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 3
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 3
- 229920002774 Maltodextrin Polymers 0.000 description 3
- 239000005913 Maltodextrin Substances 0.000 description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 3
- 206010035669 Pneumonia aspiration Diseases 0.000 description 3
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 3
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 3
- 108010073771 Soybean Proteins Proteins 0.000 description 3
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 3
- 229930003471 Vitamin B2 Natural products 0.000 description 3
- 229930003268 Vitamin C Natural products 0.000 description 3
- 229930003448 Vitamin K Natural products 0.000 description 3
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 3
- 235000001014 amino acid Nutrition 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 201000009807 aspiration pneumonia Diseases 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 206010012601 diabetes mellitus Diseases 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 210000001035 gastrointestinal tract Anatomy 0.000 description 3
- 238000012812 general test Methods 0.000 description 3
- 230000000968 intestinal effect Effects 0.000 description 3
- NPFOYSMITVOQOS-UHFFFAOYSA-K iron(III) citrate Chemical compound [Fe+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NPFOYSMITVOQOS-UHFFFAOYSA-K 0.000 description 3
- 239000004310 lactic acid Substances 0.000 description 3
- 235000014655 lactic acid Nutrition 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229940035034 maltodextrin Drugs 0.000 description 3
- 235000013336 milk Nutrition 0.000 description 3
- 239000008267 milk Substances 0.000 description 3
- 210000004080 milk Anatomy 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 239000011733 molybdenum Substances 0.000 description 3
- SHUZOJHMOBOZST-UHFFFAOYSA-N phylloquinone Natural products CC(C)CCCCC(C)CCC(C)CCCC(=CCC1=C(C)C(=O)c2ccccc2C1=O)C SHUZOJHMOBOZST-UHFFFAOYSA-N 0.000 description 3
- 108090000765 processed proteins & peptides Proteins 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 229960002477 riboflavin Drugs 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000011669 selenium Substances 0.000 description 3
- 229910052711 selenium Inorganic materials 0.000 description 3
- 239000011573 trace mineral Substances 0.000 description 3
- 235000013619 trace mineral Nutrition 0.000 description 3
- 235000019155 vitamin A Nutrition 0.000 description 3
- 239000011719 vitamin A Substances 0.000 description 3
- 235000019164 vitamin B2 Nutrition 0.000 description 3
- 239000011716 vitamin B2 Substances 0.000 description 3
- 235000019154 vitamin C Nutrition 0.000 description 3
- 239000011718 vitamin C Substances 0.000 description 3
- 235000019168 vitamin K Nutrition 0.000 description 3
- 239000011712 vitamin K Substances 0.000 description 3
- 150000003721 vitamin K derivatives Chemical class 0.000 description 3
- 229940045997 vitamin a Drugs 0.000 description 3
- 229940046010 vitamin k Drugs 0.000 description 3
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N 2,3,4,5-tetrahydroxypentanal Chemical compound OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical compound [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 229920002907 Guar gum Polymers 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 2
- 235000004347 Perilla Nutrition 0.000 description 2
- 244000124853 Perilla frutescens Species 0.000 description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
- 235000011613 Pinus brutia Nutrition 0.000 description 2
- 241000018646 Pinus brutia Species 0.000 description 2
- DLRVVLDZNNYCBX-UHFFFAOYSA-N Polydextrose Polymers OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(O)O1 DLRVVLDZNNYCBX-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Chemical compound OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 2
- 229930003779 Vitamin B12 Natural products 0.000 description 2
- LXNHXLLTXMVWPM-UHFFFAOYSA-N Vitamin B6 Natural products CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 description 2
- 229930003316 Vitamin D Natural products 0.000 description 2
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 2
- 229930003427 Vitamin E Natural products 0.000 description 2
- 239000005862 Whey Substances 0.000 description 2
- WHMDKBIGKVEYHS-IYEMJOQQSA-L Zinc gluconate Chemical compound [Zn+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O WHMDKBIGKVEYHS-IYEMJOQQSA-L 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 2
- 235000021120 animal protein Nutrition 0.000 description 2
- 229960002685 biotin Drugs 0.000 description 2
- 235000020958 biotin Nutrition 0.000 description 2
- 239000011616 biotin Substances 0.000 description 2
- 210000001124 body fluid Anatomy 0.000 description 2
- 239000010839 body fluid Substances 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229960005069 calcium Drugs 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 235000001465 calcium Nutrition 0.000 description 2
- 239000004227 calcium gluconate Substances 0.000 description 2
- 235000013927 calcium gluconate Nutrition 0.000 description 2
- 229960004494 calcium gluconate Drugs 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- NEEHYRZPVYRGPP-UHFFFAOYSA-L calcium;2,3,4,5,6-pentahydroxyhexanoate Chemical compound [Ca+2].OCC(O)C(O)C(O)C(O)C([O-])=O.OCC(O)C(O)C(O)C(O)C([O-])=O NEEHYRZPVYRGPP-UHFFFAOYSA-L 0.000 description 2
- 230000001055 chewing effect Effects 0.000 description 2
- 235000015165 citric acid Nutrition 0.000 description 2
- AGVAZMGAQJOSFJ-WZHZPDAFSA-M cobalt(2+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+2].N#[C-].[N-]([C@@H]1[C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP(O)(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O AGVAZMGAQJOSFJ-WZHZPDAFSA-M 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229940108925 copper gluconate Drugs 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 239000011640 ferrous citrate Substances 0.000 description 2
- 235000019850 ferrous citrate Nutrition 0.000 description 2
- 235000021323 fish oil Nutrition 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 229960000304 folic acid Drugs 0.000 description 2
- 235000019152 folic acid Nutrition 0.000 description 2
- 239000011724 folic acid Substances 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 2
- 239000000665 guar gum Substances 0.000 description 2
- 235000010417 guar gum Nutrition 0.000 description 2
- 229960002154 guar gum Drugs 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- 235000011147 magnesium chloride Nutrition 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 235000011090 malic acid Nutrition 0.000 description 2
- 239000001630 malic acid Substances 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000005486 organic electrolyte Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000011112 polyethylene naphthalate Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- RADKZDMFGJYCBB-UHFFFAOYSA-N pyridoxal hydrochloride Natural products CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 description 2
- ZUFQODAHGAHPFQ-UHFFFAOYSA-N pyridoxine hydrochloride Chemical compound Cl.CC1=NC=C(CO)C(CO)=C1O ZUFQODAHGAHPFQ-UHFFFAOYSA-N 0.000 description 2
- 210000002027 skeletal muscle Anatomy 0.000 description 2
- 229940001941 soy protein Drugs 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 230000009747 swallowing Effects 0.000 description 2
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 235000019163 vitamin B12 Nutrition 0.000 description 2
- 239000011715 vitamin B12 Substances 0.000 description 2
- 235000019158 vitamin B6 Nutrition 0.000 description 2
- 239000011726 vitamin B6 Substances 0.000 description 2
- 235000019166 vitamin D Nutrition 0.000 description 2
- 239000011710 vitamin D Substances 0.000 description 2
- 150000003710 vitamin D derivatives Chemical class 0.000 description 2
- 235000019165 vitamin E Nutrition 0.000 description 2
- 229940046009 vitamin E Drugs 0.000 description 2
- 239000011709 vitamin E Substances 0.000 description 2
- 229940011671 vitamin b6 Drugs 0.000 description 2
- 229940046008 vitamin d Drugs 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- 239000000230 xanthan gum Substances 0.000 description 2
- 235000010493 xanthan gum Nutrition 0.000 description 2
- 229940082509 xanthan gum Drugs 0.000 description 2
- 239000011670 zinc gluconate Substances 0.000 description 2
- 235000011478 zinc gluconate Nutrition 0.000 description 2
- 229960000306 zinc gluconate Drugs 0.000 description 2
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000512259 Ascophyllum nodosum Species 0.000 description 1
- 235000016068 Berberis vulgaris Nutrition 0.000 description 1
- 241000335053 Beta vulgaris Species 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 239000001736 Calcium glycerylphosphate Substances 0.000 description 1
- 206010058892 Carnitine deficiency Diseases 0.000 description 1
- 108010076119 Caseins Proteins 0.000 description 1
- 102000011632 Caseins Human genes 0.000 description 1
- GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 description 1
- 244000089742 Citrus aurantifolia Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 208000019505 Deglutition disease Diseases 0.000 description 1
- 229920002245 Dextrose equivalent Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- DKKCQDROTDCQOR-UHFFFAOYSA-L Ferrous lactate Chemical compound [Fe+2].CC(O)C([O-])=O.CC(O)C([O-])=O DKKCQDROTDCQOR-UHFFFAOYSA-L 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- 241000206581 Gracilaria Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920001202 Inulin Polymers 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 208000002720 Malnutrition Diseases 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 108010011756 Milk Proteins Proteins 0.000 description 1
- 229920000715 Mucilage Polymers 0.000 description 1
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 108010064851 Plant Proteins Proteins 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920001100 Polydextrose Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 208000004210 Pressure Ulcer Diseases 0.000 description 1
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical group CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 241000206572 Rhodophyta Species 0.000 description 1
- 235000019774 Rice Bran oil Nutrition 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 229930003451 Vitamin B1 Natural products 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- DFPAKSUCGFBDDF-ZQBYOMGUSA-N [14c]-nicotinamide Chemical compound N[14C](=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-ZQBYOMGUSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 229940023476 agar Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000013527 bean curd Nutrition 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- FAPWYRCQGJNNSJ-UBKPKTQASA-L calcium D-pantothenic acid Chemical compound [Ca+2].OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O.OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O FAPWYRCQGJNNSJ-UBKPKTQASA-L 0.000 description 1
- YYRMJZQKEFZXMX-UHFFFAOYSA-L calcium bis(dihydrogenphosphate) Chemical compound [Ca+2].OP(O)([O-])=O.OP(O)([O-])=O YYRMJZQKEFZXMX-UHFFFAOYSA-L 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229960003563 calcium carbonate Drugs 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 229960002713 calcium chloride Drugs 0.000 description 1
- 235000011148 calcium chloride Nutrition 0.000 description 1
- FNAQSUUGMSOBHW-UHFFFAOYSA-H calcium citrate Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O FNAQSUUGMSOBHW-UHFFFAOYSA-H 0.000 description 1
- 239000001354 calcium citrate Substances 0.000 description 1
- 229960004256 calcium citrate Drugs 0.000 description 1
- 229940062672 calcium dihydrogen phosphate Drugs 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 229940095618 calcium glycerophosphate Drugs 0.000 description 1
- UHHRFSOMMCWGSO-UHFFFAOYSA-L calcium glycerophosphate Chemical compound [Ca+2].OCC(CO)OP([O-])([O-])=O UHHRFSOMMCWGSO-UHFFFAOYSA-L 0.000 description 1
- 235000019299 calcium glycerylphosphate Nutrition 0.000 description 1
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 229940095643 calcium hydroxide Drugs 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 description 1
- 239000001527 calcium lactate Substances 0.000 description 1
- 235000011086 calcium lactate Nutrition 0.000 description 1
- 229960002401 calcium lactate Drugs 0.000 description 1
- 229960002079 calcium pantothenate Drugs 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 229940078456 calcium stearate Drugs 0.000 description 1
- OEUVSBXAMBLPES-UHFFFAOYSA-L calcium stearoyl-2-lactylate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C([O-])=O.CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C([O-])=O OEUVSBXAMBLPES-UHFFFAOYSA-L 0.000 description 1
- 229940095672 calcium sulfate Drugs 0.000 description 1
- 235000011132 calcium sulphate Nutrition 0.000 description 1
- VEJCUEBBRSCJRP-UHFFFAOYSA-L calcium;hydron;phosphonato phosphate Chemical compound [Ca+2].OP(O)(=O)OP([O-])([O-])=O VEJCUEBBRSCJRP-UHFFFAOYSA-L 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 208000026106 cerebrovascular disease Diseases 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- 229960000355 copper sulfate Drugs 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 150000001982 diacylglycerols Chemical class 0.000 description 1
- 235000019700 dicalcium phosphate Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000004715 ethylene vinyl alcohol Substances 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000011706 ferric diphosphate Substances 0.000 description 1
- 235000007144 ferric diphosphate Nutrition 0.000 description 1
- CADNYOZXMIKYPR-UHFFFAOYSA-B ferric pyrophosphate Chemical compound [Fe+3].[Fe+3].[Fe+3].[Fe+3].[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O CADNYOZXMIKYPR-UHFFFAOYSA-B 0.000 description 1
- 229940036404 ferric pyrophosphate Drugs 0.000 description 1
- 239000004222 ferrous gluconate Substances 0.000 description 1
- 235000013924 ferrous gluconate Nutrition 0.000 description 1
- 229960001645 ferrous gluconate Drugs 0.000 description 1
- 239000004225 ferrous lactate Substances 0.000 description 1
- 235000013925 ferrous lactate Nutrition 0.000 description 1
- 229940037907 ferrous lactate Drugs 0.000 description 1
- 229960001781 ferrous sulfate Drugs 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 230000007661 gastrointestinal function Effects 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 201000001421 hyperglycemia Diseases 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 description 1
- 229940029339 inulin Drugs 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- VRIVJOXICYMTAG-IYEMJOQQSA-L iron(ii) gluconate Chemical compound [Fe+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O VRIVJOXICYMTAG-IYEMJOQQSA-L 0.000 description 1
- 210000002429 large intestine Anatomy 0.000 description 1
- 235000021374 legumes Nutrition 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021056 liquid food Nutrition 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 1
- 229910000400 magnesium phosphate tribasic Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 230000001071 malnutrition Effects 0.000 description 1
- 235000000824 malnutrition Nutrition 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 150000004667 medium chain fatty acids Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 235000021243 milk fat Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 235000019691 monocalcium phosphate Nutrition 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 208000018360 neuromuscular disease Diseases 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 230000000474 nursing effect Effects 0.000 description 1
- 208000015380 nutritional deficiency disease Diseases 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 238000001139 pH measurement Methods 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
- 239000011713 pantothenic acid Substances 0.000 description 1
- 229940055726 pantothenic acid Drugs 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 208000000689 peptic esophagitis Diseases 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 235000021118 plant-derived protein Nutrition 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 239000001259 polydextrose Substances 0.000 description 1
- 235000013856 polydextrose Nutrition 0.000 description 1
- 229940035035 polydextrose Drugs 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 150000004804 polysaccharides Chemical class 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 230000002980 postoperative effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000008165 rice bran oil Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 235000014102 seafood Nutrition 0.000 description 1
- 229940091258 selenium supplement Drugs 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 208000016505 systemic primary carnitine deficiency disease Diseases 0.000 description 1
- JHYAVWJELFKHLM-UHFFFAOYSA-H tetrasodium;2-hydroxypropane-1,2,3-tricarboxylate;iron(2+) Chemical compound [Na+].[Na+].[Na+].[Na+].[Fe+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O JHYAVWJELFKHLM-UHFFFAOYSA-H 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 229960003495 thiamine Drugs 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 235000013337 tricalcium citrate Nutrition 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 235000015870 tripotassium citrate Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 235000010374 vitamin B1 Nutrition 0.000 description 1
- 239000011691 vitamin B1 Substances 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Description
本発明は、半固形栄養組成物に関する。 The present invention relates to a semi-solid nutritional composition.
経腸栄養法は、消化管を経由する生理的な栄養投与経路であり、高カロリー輸液法の問題点を解決できるため、咀嚼・嚥下機能の著しい低下や意識障害などによって、食物の経口摂取が困難な患者向けの重要な栄養投与法である。 Enteral nutrition is a physiological route of nutrition via the digestive tract and can solve the problems associated with high-calorie infusion. It is therefore an important method of nutrition for patients who have difficulty taking food orally due to a marked decline in chewing and swallowing function or impaired consciousness.
経管栄養法には、胃瘻経管栄養投与法や経鼻経管栄養法などがある。 Tube feeding methods include gastrostomy tube feeding and nasogastric tube feeding.
胃瘻経管栄養投与法においては、下記(1)~(3)の点から経腸栄養組成物に粘度や保形性を付与する手法が検討されている。(1)液体の経腸栄養組成物を胃に急速に投与することにより胃食道逆流が生じ、誤嚥性肺炎が発症することを防ぐ。(2)液体の経腸栄養組成物を胃に急速に投与することにより胃から腸に一気に経腸栄養組成物が落下し(ダンピング)、糖質が急速に吸収されて高血糖となったり、下痢の症状を引き起こすことを防止する。(3)液状の経腸栄養組成物は(2)に記載の症状を防止するために、患者に同一体位で長時間投与する必要があったが、経腸栄養組成物に粘度や保形性を付与した場合、短時間で投与が可能になる。結果として、褥瘡を防止したり、患者の負担を軽減し、患者のQOLの向上に貢献できる。 In the gastrostomy tube feeding method, a method of imparting viscosity and shape retention to the enteral nutrition composition has been considered from the viewpoints of (1) to (3) below. (1) Rapid administration of a liquid enteral nutrition composition to the stomach prevents gastroesophageal reflux and the development of aspiration pneumonia. (2) Rapid administration of a liquid enteral nutrition composition to the stomach prevents the enteral nutrition composition from dropping from the stomach to the intestines all at once (dumping), causing rapid absorption of carbohydrates and resulting in hyperglycemia and diarrhea. (3) In order to prevent the symptoms described in (2), liquid enteral nutrition compositions have had to be administered to patients in the same position for a long period of time, but if the enteral nutrition composition is given viscosity and shape retention, it can be administered in a short period of time. As a result, it is possible to prevent bedsores, reduce the burden on patients, and contribute to improving their QOL.
経腸栄養組成物に粘度を付与する方法としては、従来種々の方法が検討されてきた。例えば、特許文献1では、経腸栄養組成物に寒天を添加する方法が開示されている。また、寒天、キサンタンガム及びカラギーナンを含むゲル状流動食(特許文献2)、タンパク質の等電点ゲルとペクチン、キサンタンガムなどのゲル化剤ゲルとの複合ゲルからなる嚥下障害者に適したゲル状組成物(特許文献3)などが開示されている。 Various methods have been studied to impart viscosity to enteral nutrition compositions. For example, Patent Document 1 discloses a method of adding agar to an enteral nutrition composition. In addition, a gel-like liquid food containing agar, xanthan gum, and carrageenan (Patent Document 2) and a gel-like composition suitable for people with swallowing disorders, consisting of a composite gel of a protein isoelectric gel and a gelling agent gel such as pectin or xanthan gum (Patent Document 3) have been disclosed.
しかしながら、従来の経腸栄養組成物は、ある種の疾患の患者、乳幼児、高齢者、要介護者等を様々な状態を一括して、標準となる熱量及び栄養成分の濃度になるように配合されているのが現状である。この場合、ある栄養成分が不足の場合は追加投与は可能であるが、過剰の場合は抜き出すことはできない。このため、過剰に投与される栄養成分、特に三大栄養素であるたんぱく質、脂質、糖質で合併症を引き起こす可能性がある。経管栄養療法を受ける患者は、年齢、性別、病歴、病勢等は様々であるが、一般的に高齢者が多い。高齢者は、生理機能が低下しており、各臓器の予備能力も低下している。その中でも、特に耐糖能が低下している。通常の糖質であれば、血糖値が高くなる場合がある。この状態が長期間続くと、糖尿病に罹患している場合は病状を悪化したり、罹患していない場合は糖尿病を合併する可能性がある。加えて、経腸栄養組成物の浸透圧は高いものが多くなり、下痢の原因となっている可能性もある。 However, conventional enteral nutritional compositions are currently formulated to provide standard calorie and nutritional component concentrations for various conditions, including patients with certain diseases, infants, the elderly, and those requiring care. In this case, if a certain nutrient is insufficient, it can be administered in addition, but if it is in excess, it cannot be extracted. For this reason, excessive administration of nutrients, especially the three major nutrients, protein, lipid, and carbohydrate, may cause complications. Patients undergoing tube feeding therapy vary in age, sex, medical history, and disease severity, but are generally elderly. Elderly people have reduced physiological functions and reduced reserve capacity of each organ. Among these, glucose tolerance is particularly reduced. With normal carbohydrates, blood glucose levels may increase. If this condition continues for a long period of time, it may worsen the condition in those with diabetes, or cause diabetes in those without diabetes. In addition, many enteral nutritional compositions have high osmotic pressure, which may cause diarrhea.
また、食物繊維は、便の体積を増やす材料となるとともに、大腸内の環境を改善する腸内細菌に利用され、これらの菌を増殖させる。食物繊維を栄養組成物への配合を考えた場合、通常は高分子であるため、栄養組成物の粘度を上昇させ、PEGカテーテルから栄養組成物を胃内へ投与する際の注入抵抗が高いため、栄養組成物を押し出す際に大きな力が必要となり、医療従事者や介護者等の身体的負担が大きい場合があった。 Dietary fiber also serves as a material to increase the volume of stool, and is utilized by intestinal bacteria that improve the environment in the large intestine, promoting the proliferation of these bacteria. When dietary fiber is added to a nutritional composition, it is usually a polymer, which increases the viscosity of the nutritional composition and increases the resistance to injection when the nutritional composition is administered into the stomach from a PEG catheter. This requires a large force to push out the nutritional composition, which can place a large physical burden on medical professionals and caregivers.
さらに、ビタミン様物質であるカルニチンは骨格筋などの組織中に分布し、血中にプールされている量は1%にも満たない。したがって、骨格筋量が少ない高齢者では、体内カルニチンプールも少ないため、カルニチン欠乏症に陥りやすい。 Furthermore, carnitine, a vitamin-like substance, is distributed in tissues such as skeletal muscles, and the amount pooled in the blood is less than 1%. Therefore, elderly people with low skeletal muscle mass have a low carnitine pool in the body and are prone to carnitine deficiency.
上記課題は以下の本発明により解決される。
(1)たんぱく源、脂質、糖質及び食物繊維を含有し、熱量が1.0~2.5kcal/g、25℃における粘度が15,000~30,000mPa・s、浸透圧が400~500mOsm/Lの半固形栄養組成物であって、前記糖質としてDEが15~25である遅消化性デキストリンを10~25質量%、前記食物繊維として重量平均分子量が1,000~25,000、かつ5質量%溶液の粘度が10mPa・s以下である食物繊維を1~5質量%を含有する半固形栄養組成物。
(2)ゼリー強度が10~50g/cm2の寒天及びエステル化度が50~75%のペクチンを含み、前記ゼリー強度10~50g/cm2の寒天の配合量が前記半固形栄養組成物の全量に対して0.1~0.7質量%、前記エステル化度が50~75%のペクチンの配合量が前記半固形栄養組成物の全量に対して0.3~1質量%である上記(1)に記載の半固形栄養組成物。
(3)pHが3.0~4.5である上記(1)または(2)に記載の半固形栄養組成物。
(4)カルニチンを含む(1)ないし(3)のいずれか1項に記載の半固形栄養組成物。
(5)(1)ないし(4)のいずれか1項に記載の半固形栄養組成物と、前記半固形栄養組成物を充填した容器とを有することを特徴とする包装体。
The above problems are solved by the present invention described below.
(1) A semi-solid nutritional composition comprising a protein source, lipids, carbohydrates and dietary fiber, and having a calorific value of 1.0 to 2.5 kcal/g, a viscosity at 25°C of 15,000 to 30,000 mPa·s and an osmotic pressure of 400 to 500 mOsm/L, wherein the carbohydrate is 10 to 25% by mass of slowly digestible dextrin having a DE of 15 to 25, and the dietary fiber is 1 to 5% by mass of dietary fiber having a weight average molecular weight of 1,000 to 25,000 and a viscosity of a 5% by mass solution of 10 mPa·s or less.
(2) The semi-solid nutritional composition according to (1) above, comprising agar having a jelly strength of 10 to 50 g/ cm2 and pectin having an esterification degree of 50 to 75%, wherein the amount of the agar having a jelly strength of 10 to 50 g/ cm2 is 0.1 to 0.7 mass% relative to the total amount of the semi-solid nutritional composition, and the amount of the pectin having an esterification degree of 50 to 75% is 0.3 to 1 mass% relative to the total amount of the semi-solid nutritional composition.
(3) The semi-solid nutritional composition according to (1) or (2) above, having a pH of 3.0 to 4.5.
(4) A semi-solid nutritional composition according to any one of (1) to (3), which contains carnitine.
(5) A package comprising the semi-solid nutritional composition according to any one of (1) to (4) and a container filled with the semi-solid nutritional composition.
本発明の半固形栄養組成物は、たんぱく質、脂質、糖質及び食物繊維を含有し、かつ適度な粘度を有するため、投与された患者が胃食道逆流を起こすことなく、確実に安心かつ容易に栄養を摂取することが可能となる。また、糖質としてDEが15~25である遅消化性デキストリンを10~25質量%配合していることで、血糖値が高くなることを抑え、さらに重量平均分子量が1,000~25,000、かつ5質量%溶液の粘度が10mPa・s以下である食物繊維を1~5質量%胃内へ投与する際の注入抵抗が高くなることを抑えつつ、浸透圧を適切な範囲に保つことができる。 The semi-solid nutritional composition of the present invention contains proteins, lipids, carbohydrates, and dietary fiber, and has a suitable viscosity, allowing patients to ingest nutrients reliably, safely, and easily without experiencing gastroesophageal reflux. In addition, the incorporation of 10-25% by mass of slowly digestible dextrin with a DE of 15-25 as carbohydrate prevents blood glucose levels from increasing, and further prevents injection resistance from increasing when 1-5% by mass of dietary fiber with a weight-average molecular weight of 1,000-25,000 and a viscosity of a 5% by mass solution of 10 mPa·s or less is administered into the stomach, while maintaining the osmotic pressure within an appropriate range.
以下、本発明の半固形栄養組成物を詳細に説明する。 The semi-solid nutritional composition of the present invention is described in detail below.
本発明の半固形栄養組成物の熱量は、1~2.5kcal/g以下、好ましくは1~2kcal/gである。熱量が1kcal/gより少ないと、濃度が薄いため、投与する量が多くなり、好ましくない。熱量が2.5kcal/gを超えると、水分不足となり、患者等が脱水状態となる可能性があるため、好ましくない。 The calorific value of the semi-solid nutritional composition of the present invention is 1 to 2.5 kcal/g or less, preferably 1 to 2 kcal/g. If the calorific value is less than 1 kcal/g, the concentration will be low and a large amount will have to be administered, which is not preferable. If the calorific value exceeds 2.5 kcal/g, the patient may become dehydrated due to a lack of water, which is not preferable.
本発明の半固形栄養組成物は、25℃における粘度が15,000~30,000mPa・s、好ましくは17,500~25,000mPa・sである。半固形栄養組成物の粘度が15,000mPa・sより小さいと、胃食道逆流や誤嚥性肺炎等が生じるため、好ましくない。一方、半固形栄養組成物の粘度が30,000mPa・sを越えるとと、半固形栄養組成物をPEGカテーテルから投与する際の注入抵抗が高くなるため、好ましくない。 The semi-solid nutritional composition of the present invention has a viscosity at 25°C of 15,000 to 30,000 mPa·s, preferably 17,500 to 25,000 mPa·s. If the viscosity of the semi-solid nutritional composition is less than 15,000 mPa·s, gastroesophageal reflux, aspiration pneumonia, etc. may occur, which is undesirable. On the other hand, if the viscosity of the semi-solid nutritional composition exceeds 30,000 mPa·s, the injection resistance increases when the semi-solid nutritional composition is administered through a PEG catheter, which is undesirable.
本発明の半固形栄養組成物に示される「半固形」とは、15,000~30,000mPa・sの粘度を有することである。本明細書において、粘度は、第8版食品添加物公定書「B.一般試験法、28.粘度測定法 第2法 回転粘度計法」に記載された方法に準じて測定される。例えば、B形回転粘度計DV-II+Pro(Brookfield社)、RB80L(東機産業株式会社)等を用いて測定した値をいう。 The term "semi-solid" as used in the semi-solid nutritional composition of the present invention means that the composition has a viscosity of 15,000 to 30,000 mPa·s. In this specification, the viscosity is measured according to the method described in the 8th Edition of the Official Standards of Food Additives, "B. General Test Methods, 28. Viscosity Measurement Method, Method 2, Rotational Viscometer Method." For example, the viscosity refers to values measured using a B-type rotational viscometer DV-II+Pro (Brookfield), RB80L (Toki Sangyo Co., Ltd.), etc.
本発明の半固形栄養組成物の浸透圧は、400~500mOsm/L、好ましくは420~480mOsm/Lである。半固形栄養組成物の浸透圧が400mOsm/Lより小さいと、水分が体内に急速に流入し、浮腫を起こす可能性があるため、好ましくない。一方、半固形栄養組成物の浸透圧が500mOsm/Lを越えると、消化管内に入った物質が吸収されにくく、体液浸出で腸内溶液が増加して下痢を生じるため、好ましくない。 The osmotic pressure of the semi-solid nutritional composition of the present invention is 400 to 500 mOsm/L, preferably 420 to 480 mOsm/L. If the osmotic pressure of the semi-solid nutritional composition is less than 400 mOsm/L, water will flow into the body too quickly, which may cause edema, and this is not preferred. On the other hand, if the osmotic pressure of the semi-solid nutritional composition exceeds 500 mOsm/L, substances that enter the digestive tract are not easily absorbed, and the amount of intestinal fluid increases due to exudation of body fluids, causing diarrhea, which is also not preferred.
本発明の半固形栄養組成物は、糖質として、遅消化性デキストリンを用いる。「遅消化性デキストリン」とは、通常のマルトデキストリンと比較して摂取後の血糖値の上昇が低いデキストリンのことである。具体的には、α-1,6結合からなる分岐構造の多い高分岐デキストリンが好ましい。市販品としては、HBD-20(松谷化学工業株式会社)等がある。 The semi-solid nutritional composition of the present invention uses slowly digestible dextrin as the carbohydrate. "Slowly digestible dextrin" refers to dextrin that causes a lower rise in blood glucose level after ingestion compared to regular maltodextrin. Specifically, highly branched dextrin with many branched structures consisting of α-1,6 bonds is preferred. Commercially available products include HBD-20 (Matsutani Chemical Industry Co., Ltd.).
本発明の半固形栄養組成物はの糖質のDEとは、Dextrose Equivalentの略称で、デキストリンの加水分解の程度を意味し、式:DE=直接還元糖(グルコース換算)/固形分×100で表される。 The DE of the carbohydrates in the semi-solid nutritional composition of the present invention is an abbreviation for Dextrose Equivalent, and refers to the degree of hydrolysis of dextrin, and is expressed by the formula: DE = direct reducing sugar (glucose equivalent) / solid content x 100.
糖質のDEを求める方法は、当該技術分野における慣用技術ならびに知識がそのまま、もしくは適宜変更を加えた形で適用され、代表的にはソモジ法が挙げられる。 The method for determining the DE of carbohydrates is to use conventional techniques and knowledge in the relevant technical field, either directly or with appropriate modifications, and a representative example is the Somogyi method.
本発明の半固形栄養組成物において、遅消化性デキストリンの含有量は、半固形栄養組成物の全量に対して10~25質量%、好ましくは12~24質量%である。遅消化性デキストリンの配合量が10質量%より少ないと、糖質としての熱量が不足するため、好ましくない。一方、半固形栄養組成物の粘度が25質量%を越えるとと、糖質としての熱量が過剰となるため、好ましくない。 In the semi-solid nutritional composition of the present invention, the content of slowly digestible dextrin is 10 to 25% by mass, preferably 12 to 24% by mass, based on the total amount of the semi-solid nutritional composition. If the amount of slowly digestible dextrin is less than 10% by mass, the calorific value as carbohydrates will be insufficient, which is not preferred. On the other hand, if the viscosity of the semi-solid nutritional composition exceeds 25% by mass, the calorific value as carbohydrates will be excessive, which is not preferred.
本発明の半固形栄養組成物は、食物繊維として、重量平均分子量が1,000~25,000、好ましくは1,000~23,000であるものを用いる。重量平均分子量が1,000より小さいと、半固形栄養組成物の浸透圧が上昇し、消化管内に入った物質が吸収されにくく、体液浸出で腸内溶液が増加して下痢を生じるため、好ましくない。重量平均分子量が25,000より大きいと、半固形栄養組成物の粘度が上昇し、半固形栄養組成物をPEGカテーテルから投与する際の注入抵抗が高くなるため、好ましくない。 The semi-solid nutritional composition of the present invention uses dietary fiber with a weight-average molecular weight of 1,000 to 25,000, preferably 1,000 to 23,000. If the weight-average molecular weight is less than 1,000, the osmotic pressure of the semi-solid nutritional composition increases, making it difficult for substances that enter the digestive tract to be absorbed, and causing diarrhea due to an increase in intestinal fluid caused by exudation of body fluids, which is undesirable. If the weight-average molecular weight is more than 25,000, the viscosity of the semi-solid nutritional composition increases, which is undesirable because it increases the injection resistance when the semi-solid nutritional composition is administered through a PEG catheter.
また、本発明の半固形栄養組成物の食物繊維としては、上記の重量平均分子量を有し、かつ5質量%溶液の粘度が10mPa・s以下、好ましくは5mPa・s以下である。5質量%溶液の粘度が10mPa・sを超えると、半固形栄養組成物の粘度が上昇し、半固形栄養組成物をPEGカテーテルから投与する際の注入抵抗が高くなるため、好ましくない。 The dietary fiber in the semi-solid nutritional composition of the present invention has the above weight-average molecular weight and a viscosity of a 5% by mass solution of 10 mPa·s or less, preferably 5 mPa·s or less. If the viscosity of the 5% by mass solution exceeds 10 mPa·s, the viscosity of the semi-solid nutritional composition increases, and the injection resistance increases when the semi-solid nutritional composition is administered through a PEG catheter, which is not preferable.
本発明の半固形栄養組成物に使用する食物繊維の配合量は、半固形栄養組成物の全量に対して1~5質量%であり、好ましくは1~4質量%である。食物繊維の配合量が1質量%より少ないと、半固形栄養組成物の粘度が低下するため、好ましくない。食物繊維の配合量が5質量%を超えると、半固形栄養組成物の粘度が上昇して、半固形栄養組成物をPEGカテーテルから投与する際の注入抵抗が高くなるため、好ましくない。 The amount of dietary fiber used in the semi-solid nutritional composition of the present invention is 1 to 5% by mass, preferably 1 to 4% by mass, based on the total amount of the semi-solid nutritional composition. If the amount of dietary fiber is less than 1% by mass, the viscosity of the semi-solid nutritional composition decreases, which is not preferred. If the amount of dietary fiber is more than 5% by mass, the viscosity of the semi-solid nutritional composition increases, which is not preferred, as the injection resistance increases when the semi-solid nutritional composition is administered through a PEG catheter.
本発明の半固形栄養組成物においては、ゼリー強度が10~50g/cm2の寒天及びエステル化度が50~75%のペクチンによって、その粘度が調整されることが好ましい。 In the semi-solid nutritional composition of the present invention, the viscosity is preferably adjusted by agar having a jelly strength of 10-50 g/ cm2 and pectin having an esterification degree of 50-75%.
本発明の半固形栄養組成物に示される「ゼリー強度」とは、寒天1.5%水溶液を20℃で15時間放置し、凝固させたゲルの固さを測定し、寒天ゲルの表面積1cm2あたり20秒間耐える最大重量(g)のことである。ゲルの固さは、通常に使用されるレオメーター等で測定できる。 The "jelly strength" shown for the semi-solid nutritional composition of the present invention is the maximum weight (g) that the agar gel can withstand for 20 seconds per cm2 of surface area when a 1.5% aqueous agar solution is left at 20°C for 15 hours and the hardness of the solidified gel is measured. The hardness of the gel can be measured using a commonly used rheometer or the like.
本発明の半固形栄養組成物に使用する寒天は、特に制限されず、従来の方法によって製造されるものが使用できる。一般的に、寒天は、テングサ、オゴノリ等の紅藻類の粘液質を凍結・乾燥したものであり、アガロースやアガロペクチン等の多糖類を主成分として含む。前記アガロースやアガロペクチンは、ガラクトース及び3,6-アンデヒドロガラクトースが交互に重合した構造を有する。寒天は、アガロースやアガロペクチンの重合度や分子量、寒天中の硫酸基及びピルビン酸基の配合量等によって性状が異なる場合があるが、本発明の半固形栄養組成物においては、特に制限されず、いずれのものを用いてもよい。 The agar used in the semi-solid nutritional composition of the present invention is not particularly limited, and agar produced by a conventional method can be used. In general, agar is prepared by freezing and drying the mucilage of red algae such as Agareae and Gracilaria, and contains polysaccharides such as agarose and agaropectin as main components. The agarose and agaropectin have a structure in which galactose and 3,6-andehydrogalactose are polymerized alternately. The properties of agar may differ depending on the degree of polymerization and molecular weight of the agarose or agaropectin, the amount of sulfate groups and pyruvic acid groups in the agar, etc., but there is no particular limit to the agar used in the semi-solid nutritional composition of the present invention, and any agar may be used.
本発明の半固形栄養組成物に使用する寒天のゼリー強度は、10~50g/cm2のものが好ましい。寒天のゼリー強度が10g/cm2より低いと、分子量分布が小さい範囲にある寒天であり、ゲル化力が非常に抑えられているため、半固形栄養組成物の粘度が低下し、PEGカテーテルを急速に流れ、PEGカテーテル周辺から栄養組成物が漏出したり、患者が下痢を起こす可能性があるため、好ましくない。寒天のゼリー強度が50g/cm2を超えると、分子量分布が大きい範囲にある寒天であり、ゲル化力が非常に強いため、半固形栄養組成物の粘度が上昇し、PEGカテーテルから栄養組成物を投与する場合、PEGカテーテルを通過するのに長時間要し、好ましくない。 The jelly strength of the agar used in the semi-solid nutritional composition of the present invention is preferably 10 to 50 g/ cm2 . If the jelly strength of the agar is less than 10 g/ cm2 , the agar has a narrow molecular weight distribution and a very suppressed gelling power, which reduces the viscosity of the semi-solid nutritional composition and causes it to flow rapidly through the PEG catheter, leading to leakage of the nutritional composition from around the PEG catheter and the patient suffering from diarrhea, which is not preferred. If the jelly strength of the agar is more than 50 g/ cm2 , the agar has a wide molecular weight distribution and a very strong gelling power, which increases the viscosity of the semi-solid nutritional composition, which is not preferred because it takes a long time to pass through the PEG catheter when the nutritional composition is administered through the PEG catheter.
本発明の半固形栄養組成物に使用する寒天の配合量は、半固形栄養組成物の全量に対して0.1~0.7質量%であり、好ましくは0.1~0.5質量%である。寒天の配合量が0.1質量%より少ないと、半固形栄養組成物の固形分が分散されずに沈澱し、PEGカテーテルの閉塞を起こす可能性があるため、好ましくない。寒天の配合量が0.5質量%を超えると、半固形栄養組成物の粘度が上昇し、PEGカテーテルから半固形栄養組成物を投与する場合、PEGカテーテルを通過するのに長時間要し、好ましくない。 The amount of agar used in the semi-solid nutritional composition of the present invention is 0.1 to 0.7% by mass, preferably 0.1 to 0.5% by mass, based on the total amount of the semi-solid nutritional composition. If the amount of agar is less than 0.1% by mass, the solid content of the semi-solid nutritional composition will not disperse and will precipitate, which may cause blockage of the PEG catheter, and is therefore undesirable. If the amount of agar is more than 0.5% by mass, the viscosity of the semi-solid nutritional composition will increase, and when the semi-solid nutritional composition is administered through a PEG catheter, it will take a long time to pass through the PEG catheter, which is undesirable.
本発明の半固形栄養組成物に使用することのできる寒天として、具体的には、ウルトラ寒天UX-30(伊那食品工業株式会社、ゼリー強度:30g/cm2)などがあげられる。 Specific examples of agar that can be used in the semi-solid nutritional composition of the present invention include Ultra Agar UX-30 (Ina Food Industry Co., Ltd., jelly strength: 30 g/cm 2 ).
本発明の半固形栄養組成物に使用するペクチンは、原材料は広く植物組織中に存在するが、主にライム、レモン、オレンジなどの柑橘類の皮、リンゴの絞りかす、ビートのパルプから抽出したものが使用できる。また、通常市販されているものを用いることもできる。 The raw material for the pectin used in the semi-solid nutritional composition of the present invention is widely present in plant tissues, but it is mainly extracted from the peels of citrus fruits such as limes, lemons, and oranges, apple pomace, and beet pulp. Commercially available products can also be used.
本発明の半固形栄養組成物に使用するペクチンのエステル化度は、50~75%、好ましくは68~75%の高メトキシルペクチンであることが好ましい。エステル化度が50%より低い低メトキシルペクチンでは、半固形栄養組成物がゲル化するため、好ましくない。 The degree of esterification of the pectin used in the semi-solid nutritional composition of the present invention is preferably 50-75%, more preferably 68-75%, high methoxyl pectin. Low methoxyl pectin with a degree of esterification of less than 50% is not preferred because it causes the semi-solid nutritional composition to gel.
本発明の半固形栄養組成物に使用するペクチンの配合量は、半固形栄養組成物の全量に対して0.3~1質量%であり、好ましくは0.3~0.8質量%である。ペクチンの配合量が0.3質量%より少ないと、半固形栄養組成物の固形分が分散されずに沈澱し、PEGカテーテルの閉塞を起こす可能性があるため、好ましくない。ペクチンの配合量が1質量%を超えると、半固形栄養組成物の粘度が上昇し、PEGカテーテルから半固形栄養組成物を投与する場合、PEGカテーテルを通過するのに長時間要し、好ましくない。 The amount of pectin used in the semi-solid nutritional composition of the present invention is 0.3 to 1% by mass, preferably 0.3 to 0.8% by mass, based on the total amount of the semi-solid nutritional composition. If the amount of pectin is less than 0.3% by mass, the solid content of the semi-solid nutritional composition will not disperse and will precipitate, which may cause blockage of the PEG catheter, and is therefore undesirable. If the amount of pectin is more than 1% by mass, the viscosity of the semi-solid nutritional composition will increase, and when the semi-solid nutritional composition is administered through a PEG catheter, it will take a long time to pass through the PEG catheter, which is undesirable.
本発明の半固形栄養組成物に使用することのできる具体的なペクチンとしては、具体的に、GENUペクチンYM-150-LJ、GENUペクチンYM-115-LJ、GENUペクチンJM-115-H-J、GENUペクチンJM-150-J、GENUペクチンJMJ-J(CP Kelco社)、UNIPECTINE AYD 30T、UNIPECTINE AYD 358、UNIPECTINE AYD 380B(ユニテックフーズ株式会社)が挙げられる。 Specific examples of pectins that can be used in the semi-solid nutritional composition of the present invention include GENU Pectin YM-150-LJ, GENU Pectin YM-115-LJ, GENU Pectin JM-115-H-J, GENU Pectin JM-150-J, GENU Pectin JMJ-J (CP Kelco), UNIPECTINE AYD 30T, UNIPECTINE AYD 358, and UNIPECTINE AYD 380B (Unitech Foods Co., Ltd.).
本発明の半固形栄養組成物のpHは、3.0~4.5であり、好ましくは3.5~4.0である。pHが3.0より低いと、酸性が強くなり、清涼感が得られないため、好ましくない。pHが4.5を超えると、栄養組成物使用時のPEGカテーテル内の細菌の増殖を抑制しづらくなるため、好ましくない。 The pH of the semi-solid nutritional composition of the present invention is 3.0 to 4.5, preferably 3.5 to 4.0. If the pH is lower than 3.0, it is undesirable because it becomes too acidic and does not provide a refreshing feeling. If the pH is higher than 4.5, it is undesirable because it becomes difficult to inhibit the growth of bacteria in the PEG catheter when the nutritional composition is used.
本発明の半固形栄養組成物のpHは、pH調整剤や酸味料等の添加量を適宜設定することで調節することができる。なお、本明細書において、pHは、第8版食品添加物公定書「B.一般試験法、31.pH測定法」に記載された方法に準じて測定された値である。 The pH of the semi-solid nutritional composition of the present invention can be adjusted by appropriately setting the amount of pH adjuster, acidulant, etc. added. In this specification, the pH is a value measured in accordance with the method described in "B. General Test Methods, 31. pH Measurement Method" of the 8th Edition of the Japanese Standards for Food Additives.
本発明の半固形栄養物に使用するビタミン様物質は、体内においてビタミンと似た重要な働きをするが、体内で合成でき、欠乏症が起こらないため、ビタミンと区別されている物質のことである。具体的には、カルニチン、イノシトール、コリンなどが挙げられ、これら1種類、あるいは複数を組み合わせて配合するのが好ましい。 The vitamin-like substances used in the semi-solid nutritional product of the present invention are substances that perform important functions similar to those of vitamins in the body, but are distinguished from vitamins because they can be synthesized in the body and do not cause deficiencies. Specific examples include carnitine, inositol, and choline, and it is preferable to use one or a combination of these.
本発明のビタミン様物質の配合量は、半固形栄養組成物100g中、次の範囲が適当である。カルニチンは、好ましくは10~1000mg、より好ましくは20~1000mgである。イノシトールは、好ましくは10~1000mg、より好ましくは20~1000mgである。コリンは、好ましくは10~1000mg、より好ましくは20~1000mgである。 The amounts of the vitamin-like substances of the present invention are preferably within the following ranges per 100 g of the semi-solid nutritional composition. Carnitine is preferably 10 to 1000 mg, more preferably 20 to 1000 mg. Inositol is preferably 10 to 1000 mg, more preferably 20 to 1000 mg. Choline is preferably 10 to 1000 mg, more preferably 20 to 1000 mg.
本発明の半固形栄養組成物に使用するたんぱく源は、従来より栄養組成物で利用されている公知のたんぱく質、ペプチド及びアミノ酸のいずれも使用できる。 The protein source used in the semi-solid nutritional composition of the present invention can be any of the known proteins, peptides, and amino acids that have been used in nutritional compositions in the past.
たんぱく質としては、植物性たんぱく質及び動物性たんぱく質が使用できる。 Vegetable and animal proteins can be used as proteins.
動物性たんぱく質としては、卵、肉類、魚介類、牛乳等に含まれるたんぱく質が挙げられる。植物性たんぱく質としては、米等の穀類、大豆、豆腐等の豆類等に含まれるたんぱく質が挙げられる。 Examples of animal proteins include proteins found in eggs, meat, seafood, milk, etc. Examples of plant proteins include proteins found in grains such as rice, soybeans, tofu, and other legumes.
これらのうち、牛乳(乳清)を原料とするホエイたんぱく質、牛乳に含まれるカゼインたんぱく質、大豆たんぱく質を用いることが好ましく、ホエイたんぱく質を用いることがより好ましい。当該ホエイたんぱく質としては、ホエイプロテインコンセントレート(WPC)、ホエイプロテインアイソレート(WPI)、加水分解ホエイペプチド(WPH)等が挙げられる。WPCやWPI、大豆たんぱく等は市販されているものを用いてもよく、市販品としては、WPC392(Fonterra社製)、WPC80(Fonterra社製)、WPC7009(Fonterra社製)、WPC164(Fonterra社製)、WPC162(Fonterra社製)、WPC132(Fonterra社製)、WPC472(Fonterra社製)、WPI8855(Fonterra社製)、WPI8899(Fonterra社製)、WPI895(Fonterra社製)、プロリーナ900(不二製油株式会社製)、ニューフジプロ3000(不二製油株式会社製)、ニューフジプロ1700N(不二製油株式会社製)等が挙げられる。 Of these, it is preferable to use whey protein made from milk (whey), casein protein contained in milk, and soy protein, and it is more preferable to use whey protein. Examples of whey protein include whey protein concentrate (WPC), whey protein isolate (WPI), and hydrolyzed whey peptide (WPH). Commercially available WPC, WPI, soybean protein, etc. may be used. Examples of commercially available products include WPC392 (Fonterra), WPC80 (Fonterra), WPC7009 (Fonterra), WPC164 (Fonterra), WPC162 (Fonterra), WPC132 (Fonterra), WPC472 (Fonterra), WPI8855 (Fonterra), WPI8899 (Fonterra), WPI895 (Fonterra), Prolina 900 (Fuji Oil Co., Ltd.), New Fujipro 3000 (Fuji Oil Co., Ltd.), and New Fujipro 1700N (Fuji Oil Co., Ltd.).
上述のたんぱく質、アミノ酸またはペプチドは、単独で用いても、2種以上を混合して用いてもよい。 The above-mentioned proteins, amino acids, or peptides may be used alone or in combination of two or more.
本発明の半固形栄養組成物中のたんぱく源の配合量は、適用する対象者によって適宜調節されうるが、半固形栄養組成物全量に対して3~15質量%であることが好ましい。 The amount of protein source in the semi-solid nutritional composition of the present invention can be adjusted as appropriate depending on the subject to which it is applied, but is preferably 3 to 15% by mass based on the total amount of the semi-solid nutritional composition.
本発明の半固形栄養組成物に配合する脂質は、従来より栄養組成物で利用されてきている公知の各種のもののいずれも使用できる。例えば、アマニ油、エゴマ油、オリーブ油、ごま油、米ぬか油、サフラワー油、シソ油、大豆油、とうもろこし油、ナタネ油、胚芽油、パーム油、パーム核油、ひまわり油、綿実油、やし油、落花生油等の植物性油脂、魚油、乳脂等の動物性油脂、中鎖脂肪酸、高度不飽和脂肪酸などが挙げられる。これらは1種用いてもよいし、2種以上を組み合わせてもよい。また、その他にDHA、EPA、ジアシルグリセロールなどの加工製剤も添加することができる。 The lipids to be incorporated in the semi-solid nutritional composition of the present invention may be any of the various known lipids that have been used in nutritional compositions. Examples include vegetable fats and oils such as linseed oil, perilla oil, olive oil, sesame oil, rice bran oil, safflower oil, perilla oil, soybean oil, corn oil, rapeseed oil, germ oil, palm oil, palm kernel oil, sunflower oil, cottonseed oil, coconut oil, and peanut oil; animal fats and oils such as fish oil and milk fat; medium-chain fatty acids; and highly unsaturated fatty acids. These may be used alone or in combination of two or more. In addition, processed preparations such as DHA, EPA, and diacylglycerol may also be added.
本発明の半固形栄養組成物中の脂質の配合量は、適用する対象者によって適宜調節されうるが、半固形栄養組成物全量に対して1~8質量%であることが好ましい。 The amount of lipids in the semi-solid nutritional composition of the present invention can be adjusted as appropriate depending on the subject to which it is applied, but is preferably 1 to 8% by mass based on the total amount of the semi-solid nutritional composition.
本発明の半固形栄養組成物には、ビタミンを配合することができ、具体的には、ビタミンB1、ビタミンB2、ビタミンB6、ビタミンB12、ナイアシン、パントテン酸、葉酸、ビオチン、ビタミンC、ビタミンA、ビタミンD、ビタミンE、ビタミンKなどが挙げられ、これら複数をできる限り組み合わせて配合するのが好ましい。また、ビタミンとして、ビタミン誘導体を使用してもよい。 The semi-solid nutritional composition of the present invention can contain vitamins, specifically vitamin B1, vitamin B2, vitamin B6, vitamin B12, niacin, pantothenic acid, folic acid, biotin, vitamin C, vitamin A, vitamin D, vitamin E, vitamin K, etc., and it is preferable to use a combination of multiple of these as much as possible. Vitamin derivatives may also be used as vitamins.
本発明の半固形栄養組成物には、ミネラルを配合することができ、具体的には、ナトリウム、カリウム、カルシウム、マグネシウム、リン、鉄、銅、亜鉛、マンガン、セレン、ヨウ素、クロム及びモリブデンなどが挙げられ、これら複数をできる限り組み合わせて配合するのが好ましい。これらは、無機電解質成分として配合されていても良いし、有機電解質成分、として配合されていてもよい。無機電解質成分としては、例えば、塩化物、硫酸化物、炭酸化物、リン酸化物などのアルカリ金属またはアルカリ土類金属の塩類が挙げられる。また、有機電解質成分としては、有機酸、例えばクエン酸、乳酸、アミノ酸(例えば、グルタミン酸、アスパラギン酸など)、アルギン酸、リンゴ酸またはグルコン酸と、無機塩基、例えばアルカリ金属またはアルカリ土類金属との塩類が挙げられる。例えば、塩化カルシウム、クエン酸カルシウム、グリセロリン酸カルシウム、グルコン酸カルシウム、水酸化カルシウム、ステアリン酸カルシウム、ステアロイル乳酸カルシウム、炭酸カルシウム、乳酸カルシウム、ピロリン酸二水素カルシウム、硫酸カルシウム、リン酸三カルシウム、リン酸一水素カルシウム、リン酸二水素カルシウム、未焼成カルシウム、塩化マグネシウム、ステアリン酸マグネシウム、炭酸マグネシウム、硫酸マグネシウム、リン酸三マグネシウム、塩化第二鉄、クエン酸第一鉄ナトリウム、クエン酸鉄、クエン酸鉄アンモニウム、グルコン酸第一鉄、乳酸鉄、ピロリン酸第二鉄、硫酸第一鉄、グルコン酸亜鉛、硫酸亜鉛、グルコン酸銅、硫酸銅などが挙げられる。また、ヨウ素、セレン、クロム、モリブデン、マンガンなどは、高濃度の微量元素化合物を含有する培地内で培養して得られる微量元素蓄積性を有する微生物由来の微量元素含有微生物菌体を用いても良い。 The semi-solid nutritional composition of the present invention can contain minerals, specifically sodium, potassium, calcium, magnesium, phosphorus, iron, copper, zinc, manganese, selenium, iodine, chromium and molybdenum, and it is preferable to combine a plurality of these as much as possible. These may be contained as inorganic electrolyte components or organic electrolyte components. Examples of inorganic electrolyte components include salts of alkali metals or alkaline earth metals such as chlorides, sulfates, carbonates and phosphates. Examples of organic electrolyte components include salts of organic acids such as citric acid, lactic acid, amino acids (e.g., glutamic acid, aspartic acid, etc.), alginic acid, malic acid or gluconic acid with inorganic bases such as alkali metals or alkaline earth metals. Examples of such elements include calcium chloride, calcium citrate, calcium glycerophosphate, calcium gluconate, calcium hydroxide, calcium stearate, calcium stearoyl lactate, calcium carbonate, calcium lactate, calcium dihydrogen pyrophosphate, calcium sulfate, tricalcium phosphate, calcium monohydrogen phosphate, calcium dihydrogen phosphate, uncalcined calcium, magnesium chloride, magnesium stearate, magnesium carbonate, magnesium sulfate, trimagnesium phosphate, ferric chloride, sodium ferrous citrate, ferrous citrate, ammonium ferrous citrate, ferrous gluconate, ferrous lactate, ferric pyrophosphate, ferrous sulfate, zinc gluconate, zinc sulfate, copper gluconate, copper sulfate, etc. In addition, for iodine, selenium, chromium, molybdenum, manganese, etc., trace element-containing microbial cells derived from microorganisms having the ability to accumulate trace elements and obtained by culturing them in a medium containing a high concentration of a trace element compound may be used.
本発明の半固形栄養組成物には、食品の加工もしくは保存の目的で、食品添加物を配合することができる。食品添加物としては、保存料、防かび剤、酸化防止剤、着色料、甘味料、pH調整剤、酸味剤、乳化剤、香料等が挙げられる。 Food additives can be added to the semi-solid nutritional composition of the present invention for the purpose of food processing or preservation. Food additives include preservatives, fungicides, antioxidants, colorants, sweeteners, pH adjusters, acidulants, emulsifiers, flavors, etc.
半固形栄養組成物中の食品添加物の配合量は、適用する対象者等によって適宜調節されうる。 The amount of food additives in the semi-solid nutritional composition can be adjusted as appropriate depending on the recipient, etc.
本発明の半固形栄養組成物には、ゼリー強度が10~50g/cm2の寒天及びエステル化度が50~75%のペクチン以外の増粘剤を配合することができる。半固形栄養組成物中の増粘剤の配合量は、粘度等を考慮して適宜調節されうる。 The semi-solid nutritional composition of the present invention may contain a thickener other than agar having a jelly strength of 10 to 50 g/ cm2 and pectin having an esterification degree of 50 to 75%. The amount of thickener in the semi-solid nutritional composition may be appropriately adjusted taking into consideration the viscosity, etc.
本明細書において、粘度は、第8版食品添加物公定書「B.一般試験法、28.粘度測定法 第2法 回転粘度計法」に記載された方法に準じて測定される。例えば、B型回転粘度計DV-II+Pro(Brookfield社)、RB80L(東機産業株式会社)などを用いて測定した値をいう。 In this specification, viscosity is measured according to the method described in the 8th Edition of the Food Additives Standards, "B. General Test Methods, 28. Viscosity Measurement Method, Method 2, Rotational Viscometer Method." For example, it refers to values measured using a B-type rotational viscometer DV-II+Pro (Brookfield) or RB80L (Toki Sangyo Co., Ltd.).
なお、熱量は、糖質、脂質、たんぱく源、及び食物繊維等の添加量を適宜設定することで調節することができる。なお、本明細書において、「熱量」とは、Atwaterのエネルギー換算係数を参考にして算出された値である。具体的には、熱量=(4kcal×糖質含量)+(9kcal×脂質含量)+(4kcal×たんぱく質含量)+(2kcal×食物繊維含量)として計算し、試料g当たりのkcalとして示す。 The calorie content can be adjusted by appropriately setting the amount of carbohydrates, lipids, protein sources, dietary fiber, etc. added. In this specification, "calorie content" is a value calculated with reference to Atwater's energy conversion coefficient. Specifically, calorie content is calculated as (4 kcal x carbohydrate content) + (9 kcal x lipid content) + (4 kcal x protein content) + (2 kcal x dietary fiber content) and is expressed as kcal per gram of sample.
本発明の半固形栄養組成物は、公知の方法によって製造することができる。例えば、加温した水に栄養素、寒天、ペクチン、及びその他所望とする成分を添加し、撹拌することにより製造することができる。また、加温した水に寒天を溶解した溶液と、水にペクチンを溶解した溶液とを準備し、栄養素及びその他所望とする成分をいずれかに添加して、2つの溶液を混合、撹拌することで製造することができる。 The semi-solid nutritional composition of the present invention can be produced by known methods. For example, it can be produced by adding nutrients, agar, pectin, and other desired ingredients to heated water and stirring. It can also be produced by preparing a solution of agar dissolved in heated water and a solution of pectin dissolved in water, adding nutrients and other desired ingredients to one of them, and mixing and stirring the two solutions.
得られた半固形栄養組成物は、例えば、連続殺菌した後に容器に充填して、製品化することができる。当該連続殺菌の方法としては、特に制限されないが、超高温短時間(UHT)殺菌、熱水殺菌、バッチ式殺菌、及びこれらの組み合わせが挙げられる。前記殺菌は、短時間で行うことが好ましい。短時間で殺菌を行うことにより、半固形栄養組成物に含まれる成分の劣化を抑制することができる。 The obtained semi-solid nutritional composition can be commercialized, for example, by continuously sterilizing it and then filling it into a container. The method of continuous sterilization is not particularly limited, but includes ultra-high temperature short time (UHT) sterilization, hot water sterilization, batch sterilization, and combinations thereof. The sterilization is preferably performed for a short time. By performing sterilization for a short time, deterioration of the components contained in the semi-solid nutritional composition can be suppressed.
半固形栄養組成物を充填する容器としては、特に限定されず、公知の容器が用いられうる。当該容器としては、テトラパック(登録商標)、カート缶、ガラス容器、金属缶、アルミパウチ、プラスチック容器等が挙げられる。これらのうち、プラスチック容器を用いることが好ましい。 The container into which the semi-solid nutritional composition is filled is not particularly limited, and any known container may be used. Examples of such containers include Tetra Pak (registered trademark), cart cans, glass containers, metal cans, aluminum pouches, and plastic containers. Of these, it is preferable to use a plastic container.
前記プラスチック容器の原料としては、ポリエチレン(PE)、ポリプロピレン(PP)、ポリ塩化ビニル(PVC)、ポリ酢酸ビニル(PVAc)、ポリカーボネート(PC)、ポリブチレンテレフタレート(PBT)、ポリエチレンテレフタレート(PET)、ポリエチレンナフタレート(PEN)、エチレン-酢酸ビニル共重合体(EVA)、エチレン-α-オレフィン共重合体、ポリフルオロカーボン、ポリイミド等を用いることが好ましい。 The raw materials for the plastic containers are preferably polyethylene (PE), polypropylene (PP), polyvinyl chloride (PVC), polyvinyl acetate (PVAc), polycarbonate (PC), polybutylene terephthalate (PBT), polyethylene terephthalate (PET), polyethylene naphthalate (PEN), ethylene-vinyl acetate copolymer (EVA), ethylene-α-olefin copolymer, polyfluorocarbon, polyimide, etc.
前記プラスチック容器には、さらにポリエチレンテレフタレート(PET)、ポリエチレンナフタレート(PEN)、エチレン-ビニルアルコール共重合体(EVOH)、ポリ塩化ビニリデン(PVDC)、ポリアクリロニトリル、ポリビニルアルコール、ポリアミド、ポリエステル等を含むガスバリア性樹脂層;アルミ箔、アルミ蒸着フィルム、酸化ケイ素皮膜、酸化アルミ被膜等のガスバリア性無機層を適宜組み合わせて用いてもよい。当該ガスバリア層を設けることによって、酸素や水蒸気等による半固形栄養組成物の劣化を防止しうる。 The plastic container may further include a gas barrier resin layer containing polyethylene terephthalate (PET), polyethylene naphthalate (PEN), ethylene-vinyl alcohol copolymer (EVOH), polyvinylidene chloride (PVDC), polyacrylonitrile, polyvinyl alcohol, polyamide, polyester, etc.; or a gas barrier inorganic layer such as aluminum foil, aluminum vapor deposition film, silicon oxide film, aluminum oxide film, etc. The provision of such a gas barrier layer can prevent deterioration of the semi-solid nutritional composition due to oxygen, water vapor, etc.
また、前記容器はさらに遮光されていてもよい。当該遮光によって、例えば、半固形栄養組成物に配合されうるビタミンA、ビタミンB2、ビタミンC、ビタミンK等の光による劣化が抑制されうる。 The container may further be light-shielded. This light-shielding can suppress the deterioration of vitamin A, vitamin B2, vitamin C, vitamin K, etc., which may be incorporated into the semi-solid nutritional composition, due to light.
上述の容器は市販されているものを用いてもよく、例えば、ソフトパウチ(株式会社フジシール)、ボトルドパウチ(凸版印刷株式会社)、スパウチ(大日本印刷株式会社)、チアーパック(株式会社細川洋行)等が用いられうる。 The above-mentioned containers may be commercially available, for example, a soft pouch (Fuji Seal Co., Ltd.), a bottled pouch (Toppan Printing Co., Ltd.), a spout (Dai Nippon Printing Co., Ltd.), a Cheer Pack (Hosokawa Yoko Co., Ltd.), etc.
本発明の半固形栄養組成物は、適切な粘度に調整され且つ必要な栄養源をバランスよく配合されているため、加齢に伴い胃が縮小した高齢者、脳血管障害、神経筋障害などにより嚥下・咀嚼能力が低下した患者、意識障害などにより経口摂取が困難である患者、術後の患者等の胃腸管機能の治療用、低栄養状態の治療用、逆流性食道炎予防・治療用、誤嚥性肺炎予防・治療用に適している。投与では下痢や胃食道逆流の恐れがあることから長時間投与を余儀なくされているが、本発明の半固形栄養組成物の使用により、短時間且つ容易に注入することができ、患者のQOL向上及び介護・看護現場における作業効率性上昇に非常に役立つことが期待される。 The semi-solid nutritional composition of the present invention has an appropriate viscosity and contains a well-balanced blend of necessary nutritional sources, making it suitable for treating gastrointestinal function in elderly people whose stomachs have shrunk with age, patients whose swallowing and chewing abilities have decreased due to cerebrovascular disorders, neuromuscular disorders, etc., patients who have difficulty with oral intake due to impaired consciousness, and postoperative patients, as well as for treating malnutrition, preventing and treating reflux esophagitis, and preventing and treating aspiration pneumonia. Administration of the composition is unavoidable over a long period of time due to the risk of diarrhea and gastroesophageal reflux, but the semi-solid nutritional composition of the present invention can be easily injected in a short period of time, and is expected to be extremely useful in improving the quality of life of patients and increasing the work efficiency in nursing and care settings.
以下、実施例を挙げて本発明を具体的に説明するが、本発明はこれらに限定されるものではない。 The present invention will be specifically explained below with reference to examples, but the present invention is not limited to these.
(実施例1)
以下に4000g仕込み時の調合方法を記す。各原料の配合量は、表1に示す通りである。5Lのステンレスビーカーに調合水700gを計量し、湯浴にて80℃以上に加温した。次いで、寒天(ゼリー強度30g/cm2、ウルトラ即溶性寒天UX-30、伊那食品工業株式会社、配合量0.3質量%)、ペクチン(エステル化度70%、GENUペクチンJM-150-J、CP Kelco社、配合量0.55質量%)を加え、十分に溶解させた後に65℃まで冷却し、乳清たんぱく(アラセン392、Fonterra社)、大豆たんぱく(プロリーナ800、不二製油株式会社)、デキストリン(遅消化性デキストリン、DE20、HBD-20、松谷化学工業株式会社、配合量19質量%)、食物繊維(重量平均分子量20,000、5質量%溶液の粘度4mPa・s、グアーガム分解物、サンファイバーR、太陽化学株式会社、配合量2質量%)を添加した。当該溶液に植物混合油、魚油、グリセリン脂肪酸エステルを70℃で混合した分散液を混合した。さらに、ビタミンとしてビタミンA、ビタミンD、ビタミンE、ビタミンK、ビタミンB1塩酸塩、ビタミンB2、ニコチン酸アミド、ビタミンB6、ビタミンB12、葉酸、パントテン酸カルシウム、ビオチン、ビタミンC、カルニチン、ミネラルとして精製塩、乳酸ナトリウム、リン酸二水素ナトリウム、グルコン酸カルシウム、塩化マグネシウム、クエン酸三カリウム、塩化カリウム、クエン酸鉄、グルコン酸亜鉛、グルコン酸銅、セレン酵母、モリブデン酵母、クロム酵母、マンガン酵母、昆布抽出物、乳酸、酸味料として乳酸、リンゴ酸、クエン酸、香料を適宜添加して攪拌した。全量が4000gとなるまで水を添加し、均一な状態となるまで溶解分散させた。得られた溶液は、均質化し、1個当たり500gとなるように口栓付きのアルミパウチに充填後、90℃で10分間の殺菌処理を行った。前記殺菌処理の後、冷却することで、半固形栄養組成物を製造した。
Example 1
The method of blending when preparing 4000 g is described below. The blending amounts of each raw material are as shown in Table 1. 700 g of blending water was weighed into a 5 L stainless steel beaker and heated to 80° C. or higher in a water bath. Next, agar (jelly strength 30 g/ cm2 , Ultra Instant Dissolve Agar UX-30, Ina Food Industry Co., Ltd., blend amount 0.3% by mass), pectin (degree of esterification 70%, GENU Pectin JM-150-J, CP Kelco, blend amount 0.55% by mass), and after sufficient dissolution, cooled to 65°C, whey protein (Aracene 392, Fonterra), soy protein (Prolina 800, Fuji Oil Co., Ltd.), dextrin (slowly digestible dextrin, DE20, HBD-20, Matsutani Chemical Industry Co., Ltd., blend amount 19% by mass), and dietary fiber (weight average molecular weight 20,000, viscosity of 5% by mass solution 4 mPa·s, guar gum hydrolyzate, Sunfiber R, Taiyo Kagaku Co., Ltd., blend amount 2% by mass) were added. The solution was mixed with a dispersion of mixed vegetable oil, fish oil, and glycerin fatty acid ester at 70°C. Furthermore, vitamin A, vitamin D, vitamin E, vitamin K, vitamin B1 hydrochloride, vitamin B2, nicotinamide, vitamin B6, vitamin B12, folic acid, calcium pantothenate, biotin, vitamin C, and carnitine as vitamins, refined salt as minerals, sodium lactate, sodium dihydrogen phosphate, calcium gluconate, magnesium chloride, tripotassium citrate, potassium chloride, iron citrate, zinc gluconate, copper gluconate, selenium yeast, molybdenum yeast, chromium yeast, manganese yeast, kelp extract, lactic acid, lactic acid, malic acid, citric acid, and flavoring as acidulants were appropriately added and stirred. Water was added until the total amount was 4000g, and the mixture was dissolved and dispersed until it became uniform. The obtained solution was homogenized and filled into aluminum pouches with stoppers so that each pouch was 500g, and then sterilized at 90°C for 10 minutes. After the sterilization treatment, the mixture was cooled to produce a semi-solid nutritional composition.
得られた半固形栄養組成物について性状を観察し、各種物性を評価した。評価方法は以下の通りである。
(1)pH:半固形栄養組成物を25℃で24時静置後、pH測定器METTLER TOLEDO MP220(METTLER TOLEDO社)を用いてpHを測定した。
(2)粘度:半固形栄養組成物を25℃で24時静置後、B型回転粘度計(メーカー:BROOKFIELD、型式:DV-II+Pro、測定条件:回転速度6rpm、測定時間1分、ローターNo.64)を用いて測定した。
(3)浸透圧:半固形栄養組成物を25℃のRO水を用いて希釈した溶液を氷点降下式浸透圧計3D3(アドバンス社)で測定した。
(4)乳化安定性:半固形栄養組成物を25℃で24時静置後、油層と水層の分離状況を目視で確認し、以下の評価によって評価した:
◎:油層と水層の分離が見られない
〇:油層と水層の僅かな分離が見られる
△:油層と水層の分離が散見される
×:油層と水層の明らかな分離が見られる。
(5)凝集性:半固形栄養組成物を25℃で24時静置後、凝集物の状況を目視で確認し、以下の評価によって評価した:
◎:凝集物が見られない
○:細かな凝集物が見られるが、分散している
△:大きな凝集物が見られるが、分散している
×:大きな凝集物が沈殿している。
The properties of the obtained semi-solid nutritional composition were observed, and various physical properties were evaluated according to the following methods.
(1) pH: After the semi-solid nutritional composition was allowed to stand at 25° C. for 24 hours, the pH was measured using a pH meter METTLER TOLEDO MP220 (METTLER TOLEDO).
(2) Viscosity: The semi-solid nutritional composition was allowed to stand at 25° C. for 24 hours, and then the viscosity was measured using a B-type rotational viscometer (manufacturer: BROOKFIELD, model: DV-II+Pro, measurement conditions: rotation speed 6 rpm, measurement time 1 minute, rotor No. 64).
(3) Osmotic pressure: A solution obtained by diluting the semi-solid nutritional composition with RO water at 25° C. was measured using a freezing point depression osmometer 3D3 (Advance Corporation).
(4) Emulsion stability: After leaving the semi-solid nutritional composition at 25° C. for 24 hours, the separation state of the oil layer and the aqueous layer was visually confirmed and evaluated according to the following criteria:
◎: No separation between the oil layer and the water layer is observed. ◯: Slight separation between the oil layer and the water layer is observed. △: Separation between the oil layer and the water layer is occasionally observed. ×: Clear separation between the oil layer and the water layer is observed.
(5) Cohesiveness: After the semi-solid nutritional composition was allowed to stand at 25° C. for 24 hours, the state of the aggregates was visually observed and evaluated according to the following criteria:
⊚: no agglomerates are observed; ◯: fine agglomerates are observed but are dispersed; Δ: large agglomerates are observed but are dispersed; ×: large agglomerates have settled.
得られた半固形栄養組成物の熱量は1.5kcal/g、粘度は26,000mPa・s、浸透圧は463mOsm/L、pHは3.85、乳化安定性は「◎」、凝集性は「◎」であった。結果を表2に示す。 The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the viscosity was 26,000 mPa·s, the osmotic pressure was 463 mOsm/L, the pH was 3.85, the emulsion stability was "◎", and the coagulation property was "◎". The results are shown in Table 2.
(実施例2)
実施例1において、デキストリンの配合量を12質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.2kcal/g、粘度は23,500mPa・s、浸透圧は445mOsm/L、pHは3.87、乳化安定性は「◎」、凝集性は「◎」であった。結果を表2に示す。
Example 2
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the amount of dextrin was changed to 12% by mass. The calorific value of the obtained semi-solid nutritional composition was 1.2 kcal/g, the viscosity was 23,500 mPa·s, the osmotic pressure was 445 mOsm/L, the pH was 3.87, the emulsion stability was "◎", and the coagulation property was "◎". The results are shown in Table 2.
(実施例3)
実施例1において、デキストリンの配合量を23質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.7kcal/g、粘度は28,000mPa・s、浸透圧は480mOsm/L、pHは3.86、乳化安定性は「◎」、凝集性は「◎」であった。結果を表2に示す。
Example 3
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the blending amount of dextrin was changed to 23% by mass. The calorific value of the obtained semi-solid nutritional composition was 1.7 kcal/g, the viscosity was 28,000 mPa·s, the osmotic pressure was 480 mOsm/L, the pH was 3.86, the emulsion stability was "◎", and the coagulation property was "◎". The results are shown in Table 2.
(実施例4)
実施例1において、食物繊維の重量平均分子量を2,000、食物繊維の5質量%溶液の粘度を3mPa・s、食物繊維の種類を難消化デキストリン(パインファイバーC、松谷化学工業株式会社)に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、粘度は24,800mPa・s、浸透圧は484mOsm/L、pHは3.86、乳化安定性は「◎」、凝集性は「◎」であった。結果を表2に示す。
Example 4
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the weight average molecular weight of the dietary fiber was changed to 2,000, the viscosity of a 5% by mass solution of the dietary fiber was changed to 3 mPa·s, and the type of dietary fiber was changed to indigestible dextrin (Pine Fiber C, Matsutani Chemical Industry Co., Ltd.). The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the viscosity was 24,800 mPa·s, the osmotic pressure was 484 mOsm/L, the pH was 3.86, the emulsion stability was "◎", and the coagulation property was "◎". The results are shown in Table 2.
(実施例5)
実施例1において、食物繊維の重量平均分子量を2,000、食物繊維の5質量%溶液の粘度を3mPa・s、食物繊維の種類をイヌリン(Fuji FF、フジ日本精糖株式会社)に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、粘度は24,500mPa・s、浸透圧は483mOsm/L、pHは3.85、乳化安定性は「◎」、凝集性は「◎」であった。結果を表2に示す。
Example 5
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the weight average molecular weight of the dietary fiber was changed to 2,000, the viscosity of a 5% by mass solution of the dietary fiber was changed to 3 mPa·s, and the type of dietary fiber was changed to inulin (Fuji FF, Fuji Nippon Seito Co., Ltd.). The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the viscosity was 24,500 mPa·s, the osmotic pressure was 483 mOsm/L, the pH was 3.85, the emulsion stability was "◎", and the coagulation property was "◎". The results are shown in Table 2.
(実施例6)
実施例1において、食物繊維の重量平均分子量を1,500、食物繊維の5質量%溶液の粘度を3mPa・s、食物繊維の種類をポリデキストロース(ライテスウルトラ、ダニスコジャパン株式会社)、食物繊維の配合量を4質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、粘度は22,500mPa・s、浸透圧は492mOsm/L、pHは3.84、乳化安定性は「◎」、凝集性は「◎」であった。結果を表3に示す。
Example 6
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the weight average molecular weight of the dietary fiber was changed to 1,500, the viscosity of a 5% by mass solution of the dietary fiber was changed to 3 mPa·s, the type of dietary fiber was changed to polydextrose (Lites Ultra, Danisco Japan Co., Ltd.), and the amount of dietary fiber was changed to 4% by mass. The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the viscosity was 22,500 mPa·s, the osmotic pressure was 492 mOsm/L, the pH was 3.84, the emulsion stability was "◎", and the coagulation property was "◎". The results are shown in Table 3.
(実施例7)
実施例1において、寒天の配合量を0.2質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、粘度は25,000mPa・s、浸透圧は451mOsm/L、pHは3.87、乳化安定性は「◎」、凝集性は「◎」であった。結果を表3に示す。
(Example 7)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the amount of agar in Example 1 was changed to 0.2% by mass. The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the viscosity was 25,000 mPa·s, the osmotic pressure was 451 mOsm/L, the pH was 3.87, the emulsion stability was "◎", and the coagulation property was "◎". The results are shown in Table 3.
(実施例8)
実施例1において、寒天の配合量を0.6質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、粘度は27,500mPa・s、浸透圧は475mOsm/L、pHは3.84、乳化安定性は「◎」、凝集性は「◎」であった。結果を表3に示す。
(Example 8)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the amount of agar in Example 1 was changed to 0.6% by mass. The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the viscosity was 27,500 mPa·s, the osmotic pressure was 475 mOsm/L, the pH was 3.84, the emulsion stability was "◎", and the coagulation property was "◎". The results are shown in Table 3.
(実施例9)
実施例1において、ペクチンのエステル化度を72(GENUペクチンYM-150-LJ、CP Kelco社)、ペクチンの配合量を0.4質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、粘度は24,500mPa・s、浸透圧は455mOsm/L、pHは3.85、乳化安定性は「◎」、凝集性は「◎」であった。結果を表3に示す。
(Example 9)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the degree of esterification of pectin was changed to 72 (GENU Pectin YM-150-LJ, CP Kelco) and the blending amount of pectin was changed to 0.4 mass%. The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the viscosity was 24,500 mPa s, the osmotic pressure was 455 mOsm/L, the pH was 3.85, the emulsion stability was "◎", and the coagulation property was "◎". The results are shown in Table 3.
(実施例10)
実施例1において、ペクチンのエステル化度を72(GENUペクチンYM-115-H-J、CP Kelco社)、ペクチンの配合量を0.8質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、粘度は28,000mPa・s、浸透圧は465mOsm/L、pHは3.84、乳化安定性は「◎」、凝集性は「◎」であった。結果を表3に示す。
(Example 10)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the degree of esterification of pectin was changed to 72 (GENU Pectin YM-115-H-J, CP Kelco) and the blending amount of pectin was changed to 0.8% by mass. The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the viscosity was 28,000 mPa s, the osmotic pressure was 465 mOsm/L, the pH was 3.84, the emulsion stability was "◎", and the coagulation property was "◎". The results are shown in Table 3.
(比較例1)
実施例1において、デキストリンのDEを11、デキストリンの種類をマルトデキストリン(パインデックス#2、松谷化学工業株式会社)に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、浸透圧は455mOsm/L、pHは3.86、乳化安定性は「◎」、凝集性は「◎」であったが、粘度は33,000mPa・sであった。結果を表4に示す。
(Comparative Example 1)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the DE of the dextrin was changed to 11 and the type of dextrin was changed to maltodextrin (Pine Index #2, Matsutani Chemical Industry Co., Ltd.). The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the osmotic pressure was 455 mOsm/L, the pH was 3.86, the emulsion stability was "◎", the coagulation property was "◎", but the viscosity was 33,000 mPa s. The results are shown in Table 4.
(比較例2)
実施例1において、デキストリンのDEを40、デキストリンの種類をマルトデキストリン(パインデックス#6、松谷化学工業株式会社)に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、粘度は23,000mPa・s、pHは3.84、乳化安定性は「◎」、凝集性は「◎」であったが、浸透圧は512mOsm/Lであった。結果を表4に示す。
(Comparative Example 2)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the DE of the dextrin was changed to 40 and the type of dextrin was changed to maltodextrin (pine index #6, Matsutani Chemical Industry Co., Ltd.). The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the viscosity was 23,000 mPa·s, the pH was 3.84, the emulsion stability was "◎", the coagulation property was "◎", and the osmotic pressure was 512 mOsm/L. The results are shown in Table 4.
(比較例3)
実施例1において、食物繊維の重量平均分子量を250,000、食物繊維の5質量%溶液の粘度を200mPa・s、食物繊維の種類をグアーガム(GR-10、伊那食品工業株式会社)に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、浸透圧は439mOsm/L、pHは3.85、乳化安定性は「◎」、凝集性は「◎」であったが、粘度は48,500mPa・sであった。結果を表4に示す。
(Comparative Example 3)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the weight average molecular weight of the dietary fiber was changed to 250,000, the viscosity of a 5% by mass solution of the dietary fiber was changed to 200 mPa·s, and the type of dietary fiber was changed to guar gum (GR-10, Ina Food Industry Co., Ltd.). The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the osmotic pressure was 439 mOsm/L, the pH was 3.85, the emulsion stability was "◎", and the coagulation property was "◎", but the viscosity was 48,500 mPa·s. The results are shown in Table 4.
(比較例4)
実施例1において、食物繊維の重量平均分子量を550,000、食物繊維の5質量%溶液の粘度を30mPa・s、食物繊維の種類を大豆ふすま(FIBRIM2000、デュポン株式会社)に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、浸透圧は439mOsm/L、pHは3.86、乳化安定性は「◎」、凝集性は「◎」であったが、粘度は45,500mPa・sであった。結果を表4に示す。
(Comparative Example 4)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the weight average molecular weight of the dietary fiber was 550,000, the viscosity of a 5% by mass solution of the dietary fiber was 30 mPa·s, and the type of dietary fiber was soybean bran (FIBRIM2000, DuPont). The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the osmotic pressure was 439 mOsm/L, the pH was 3.86, the emulsion stability was "◎", and the coagulation property was "◎", but the viscosity was 45,500 mPa·s. The results are shown in Table 4.
(比較例5)
実施例1において、寒天のゼリー強度を100g/cm2(ウルトラ即溶性寒天UX-100、伊那食品工業株式会社)に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、浸透圧は432mOsm/L、pHは3.85、乳化安定性は「◎」、凝集性は「◎」であったが、粘度は47,500mPa・sであった。結果を表4に示す。
(Comparative Example 5)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the jelly strength of the agar was changed to 100 g / cm2 (Ultra fast-soluble agar UX-100, Ina Food Industry Co., Ltd.). The obtained semi-solid nutritional composition had a calorific value of 1.5 kcal/g, an osmotic pressure of 432 mOsm/L, a pH of 3.85, an emulsion stability of "◎", and a coagulation property of "◎", but a viscosity of 47,500 mPa·s. The results are shown in Table 4.
(比較例6)
実施例1において、寒天の配合量を0質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、浸透圧は463mOsm/L、pHは3.82、であったが、粘度は12,600mPa・s、乳化安定性は「×」、凝集性は「×」であった。結果を表5に示す。
(Comparative Example 6)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the amount of agar in Example 1 was changed to 0% by mass. The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the osmotic pressure was 463 mOsm/L, and the pH was 3.82, but the viscosity was 12,600 mPa s, the emulsion stability was "x", and the coagulation property was "x". The results are shown in Table 5.
(比較例7)
実施例1において、寒天の配合量を1.0質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、浸透圧は460mOsm/L、pHは3.81、乳化安定性は「◎」、凝集性は「◎」であったが、粘度は43,000mPa・sであった。結果を表5に示す。
(Comparative Example 7)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the amount of agar in Example 1 was changed to 1.0 mass%. The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the osmotic pressure was 460 mOsm/L, the pH was 3.81, the emulsion stability was "◎", the coagulation property was "◎", but the viscosity was 43,000 mPa s. The results are shown in Table 5.
(比較例8)
実施例1において、ペクチンのエステル化度を40(GENUペクチンLM-105AS-J、CP Kelco社)に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、浸透圧は463mOsm/L、pHは3.82、乳化安定性は「◎」、凝集性は「◎」であったが、粘度は35,500mPa・sであった。結果を表5に示す。
(Comparative Example 8)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the degree of esterification of pectin was changed to 40 (GENU Pectin LM-105AS-J, CP Kelco). The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the osmotic pressure was 463 mOsm/L, the pH was 3.82, the emulsion stability was "◎", the coagulation property was "◎", but the viscosity was 35,500 mPa s. The results are shown in Table 5.
(比較例9)
実施例1において、ペクチンの配合量を0.1質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、浸透圧は445mOsm/L、pHは3.82であったが、粘度は14,500mPa・s、乳化安定性は「×」、凝集性は「×」であった。結果を表5に示す。
(Comparative Example 9)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the amount of pectin was changed to 0.1% by mass. The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the osmotic pressure was 445 mOsm/L, and the pH was 3.82, but the viscosity was 14,500 mPa s, the emulsion stability was "x", and the coagulation property was "x". The results are shown in Table 5.
(比較例10)
実施例1において、ペクチンの配合量を1.2質量%に変えた以外は、実施例1と全く同じ調製法を繰り返して半固形栄養組成物を得た。得られた半固形栄養組成物の熱量は1.5kcal/g、浸透圧は461mOsm/L、pHは3.84、乳化安定性は「◎」、凝集性は「◎」であったが、粘度は30,200mPa・sであった。結果を表5に示す。
(Comparative Example 10)
A semi-solid nutritional composition was obtained by repeating the same preparation method as in Example 1, except that the amount of pectin was changed to 1.2% by mass. The calorific value of the obtained semi-solid nutritional composition was 1.5 kcal/g, the osmotic pressure was 461 mOsm/L, the pH was 3.84, the emulsion stability was "◎", the coagulation property was "◎", and the viscosity was 30,200 mPa s. The results are shown in Table 5.
Claims (4)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2021056975A JP7579733B2 (en) | 2021-03-30 | 2021-03-30 | Semi-solid nutritional composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2021056975A JP7579733B2 (en) | 2021-03-30 | 2021-03-30 | Semi-solid nutritional composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2022154097A JP2022154097A (en) | 2022-10-13 |
| JP7579733B2 true JP7579733B2 (en) | 2024-11-08 |
Family
ID=83557267
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021056975A Active JP7579733B2 (en) | 2021-03-30 | 2021-03-30 | Semi-solid nutritional composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP7579733B2 (en) |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011004702A (en) | 2009-06-29 | 2011-01-13 | Asahi Kasei Pharma Kk | Dietary fiber-containing nutrient composition |
| JP2015160822A (en) | 2014-02-26 | 2015-09-07 | テルモ株式会社 | Gastric fistula semi-solid nutritive composition |
| JP2015188415A (en) | 2014-03-28 | 2015-11-02 | テルモ株式会社 | Nutritive food |
| JP2020156435A (en) | 2019-03-28 | 2020-10-01 | テルモ株式会社 | Liquid nutrient supplement composition |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2173780A1 (en) * | 1995-06-01 | 1996-12-02 | Randy Grote | Method for providing nutrition in a variety of compositional forms |
-
2021
- 2021-03-30 JP JP2021056975A patent/JP7579733B2/en active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011004702A (en) | 2009-06-29 | 2011-01-13 | Asahi Kasei Pharma Kk | Dietary fiber-containing nutrient composition |
| JP2015160822A (en) | 2014-02-26 | 2015-09-07 | テルモ株式会社 | Gastric fistula semi-solid nutritive composition |
| JP2015188415A (en) | 2014-03-28 | 2015-11-02 | テルモ株式会社 | Nutritive food |
| JP2020156435A (en) | 2019-03-28 | 2020-10-01 | テルモ株式会社 | Liquid nutrient supplement composition |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2022154097A (en) | 2022-10-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5590638B2 (en) | Emulsified food composition | |
| JP5632112B2 (en) | Semi-solidified nutrient | |
| JP6277957B2 (en) | Nutritional composition | |
| JP5925289B2 (en) | Semi-solid nutrient for gastrostoma | |
| WO2015146460A1 (en) | Liquid nutritional composition | |
| JP6084092B2 (en) | Thorough nutritional composition | |
| JP2017139974A (en) | Liquid nutritive composition | |
| JP7524490B2 (en) | Liquid nutritional composition and packaging | |
| JP6347954B2 (en) | Thorough nutritional composition | |
| JP7579733B2 (en) | Semi-solid nutritional composition | |
| JP2017171593A (en) | Liquid nutrition composition | |
| JP6575962B2 (en) | Thorough nutritional composition | |
| WO2013132670A1 (en) | Semi-solidified nutritive agent | |
| JP5652980B2 (en) | Semi-solid nutrient for gastrostoma | |
| JP2015160822A (en) | Gastric fistula semi-solid nutritive composition | |
| WO2023190293A1 (en) | Viscous nutritional composition | |
| HK40113840A (en) | Liquid nutritional composition and package | |
| HK40113840B (en) | Liquid nutritional composition and package | |
| JP6087191B2 (en) | Semisolid nutritional composition for gastrostoma | |
| JP5632113B2 (en) | Semisolid nutrient for gastrostoma | |
| JPWO2015146461A1 (en) | Soy protein-containing and nutritious nutritional composition | |
| JP2025027869A (en) | Composition for regulating protein gastric emptying, fluid nutritional composition, and composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20230125 |
|
| A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A711 Effective date: 20230125 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20230215 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20240327 |
|
| A871 | Explanation of circumstances concerning accelerated examination |
Free format text: JAPANESE INTERMEDIATE CODE: A871 Effective date: 20240327 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20240522 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20240717 |
|
| 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: 20241009 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20241028 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 7579733 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |