JPH04617B2 - - Google Patents
Info
- Publication number
- JPH04617B2 JPH04617B2 JP61282003A JP28200386A JPH04617B2 JP H04617 B2 JPH04617 B2 JP H04617B2 JP 61282003 A JP61282003 A JP 61282003A JP 28200386 A JP28200386 A JP 28200386A JP H04617 B2 JPH04617 B2 JP H04617B2
- Authority
- JP
- Japan
- Prior art keywords
- jelly
- maltose
- pectin
- vitamin
- sugar
- 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.)
- Expired - Lifetime
Links
- 235000015110 jellies Nutrition 0.000 claims description 54
- 239000008274 jelly Substances 0.000 claims description 54
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 claims description 40
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 claims description 40
- 239000001814 pectin Substances 0.000 claims description 24
- 235000010987 pectin Nutrition 0.000 claims description 24
- 229920001277 pectin Polymers 0.000 claims description 24
- 229940088594 vitamin Drugs 0.000 claims description 21
- 229930003231 vitamin Natural products 0.000 claims description 21
- 235000013343 vitamin Nutrition 0.000 claims description 21
- 239000011782 vitamin Substances 0.000 claims description 21
- 239000000845 maltitol Substances 0.000 claims description 9
- 235000010449 maltitol Nutrition 0.000 claims description 9
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 claims description 9
- 229940035436 maltitol Drugs 0.000 claims description 9
- 239000000839 emulsion Substances 0.000 claims description 8
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 7
- 229930195725 Mannitol Natural products 0.000 claims description 7
- 239000000594 mannitol Substances 0.000 claims description 7
- 235000010355 mannitol Nutrition 0.000 claims description 7
- 150000007524 organic acids Chemical class 0.000 claims description 7
- 235000005985 organic acids Nutrition 0.000 claims description 7
- 238000009495 sugar coating Methods 0.000 claims description 6
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 claims description 5
- 150000003722 vitamin derivatives Chemical class 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 27
- 229920002472 Starch Polymers 0.000 description 20
- 239000008107 starch Substances 0.000 description 20
- 235000019698 starch Nutrition 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 235000000346 sugar Nutrition 0.000 description 13
- 239000006188 syrup Substances 0.000 description 13
- 235000020357 syrup Nutrition 0.000 description 13
- 229930006000 Sucrose Natural products 0.000 description 12
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 229920001817 Agar Polymers 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 239000008272 agar Substances 0.000 description 6
- 235000010419 agar Nutrition 0.000 description 6
- 239000000872 buffer Substances 0.000 description 6
- 239000013078 crystal Substances 0.000 description 6
- 229940093915 gynecological organic acid Drugs 0.000 description 6
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 235000019155 vitamin A Nutrition 0.000 description 5
- 239000011719 vitamin A Substances 0.000 description 5
- 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
- PYMYPHUHKUWMLA-UHFFFAOYSA-N 2,3,4,5-tetrahydroxypentanal Chemical compound OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 4
- 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 4
- ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 150000008163 sugars Chemical class 0.000 description 4
- 229940042585 tocopherol acetate Drugs 0.000 description 4
- 235000019166 vitamin D Nutrition 0.000 description 4
- 239000011710 vitamin D 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
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- VYGQUTWHTHXGQB-FFHKNEKCSA-N Retinol Palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C VYGQUTWHTHXGQB-FFHKNEKCSA-N 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
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000001509 sodium citrate Substances 0.000 description 3
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 3
- 239000003826 tablet Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 3
- 239000011709 vitamin E Substances 0.000 description 3
- 235000019165 vitamin E Nutrition 0.000 description 3
- 229940045997 vitamin a Drugs 0.000 description 3
- 244000215068 Acacia senegal Species 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- 229930091371 Fructose Natural products 0.000 description 2
- 239000005715 Fructose Substances 0.000 description 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 2
- 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 2
- 229920000084 Gum arabic Polymers 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- VYGQUTWHTHXGQB-UHFFFAOYSA-N Retinol hexadecanoate Natural products CCCCCCCCCCCCCCCC(=O)OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C VYGQUTWHTHXGQB-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
- 239000000205 acacia gum Substances 0.000 description 2
- 235000010489 acacia gum Nutrition 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- OENHQHLEOONYIE-UKMVMLAPSA-N all-trans beta-carotene Natural products CC=1CCCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C OENHQHLEOONYIE-UKMVMLAPSA-N 0.000 description 2
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- 235000013734 beta-carotene Nutrition 0.000 description 2
- TUPZEYHYWIEDIH-WAIFQNFQSA-N beta-carotene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2=CCCCC2(C)C TUPZEYHYWIEDIH-WAIFQNFQSA-N 0.000 description 2
- 239000011648 beta-carotene Substances 0.000 description 2
- 229960002747 betacarotene Drugs 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 229930182830 galactose Natural products 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
- 239000008103 glucose Substances 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000016709 nutrition Nutrition 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 235000019172 retinyl palmitate Nutrition 0.000 description 2
- 229940108325 retinyl palmitate Drugs 0.000 description 2
- 239000011769 retinyl palmitate Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- -1 vitamin A palmitate ester Chemical group 0.000 description 2
- 150000003710 vitamin D derivatives Chemical group 0.000 description 2
- 239000011653 vitamin D2 Substances 0.000 description 2
- 229940046009 vitamin E Drugs 0.000 description 2
- 229940046008 vitamin d Drugs 0.000 description 2
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 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
- LKDRXBCSQODPBY-AMVSKUEXSA-N L-(-)-Sorbose Chemical compound OCC1(O)OC[C@H](O)[C@@H](O)[C@@H]1O LKDRXBCSQODPBY-AMVSKUEXSA-N 0.000 description 1
- SHZGCJCMOBCMKK-JFNONXLTSA-N L-rhamnopyranose Chemical compound C[C@@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O SHZGCJCMOBCMKK-JFNONXLTSA-N 0.000 description 1
- PNNNRSAQSRJVSB-UHFFFAOYSA-N L-rhamnose Natural products CC(O)C(O)C(O)C(O)C=O PNNNRSAQSRJVSB-UHFFFAOYSA-N 0.000 description 1
- 235000019501 Lemon oil Nutrition 0.000 description 1
- UPYKUZBSLRQECL-UKMVMLAPSA-N Lycopene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1C(=C)CCCC1(C)C)C=CC=C(/C)C=CC2C(=C)CCCC2(C)C UPYKUZBSLRQECL-UKMVMLAPSA-N 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- 235000019502 Orange oil Nutrition 0.000 description 1
- 241001310492 Pectis angustifolia Species 0.000 description 1
- MUPFEKGTMRGPLJ-RMMQSMQOSA-N Raffinose Natural products O(C[C@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O[C@@]2(CO)[C@H](O)[C@@H](O)[C@@H](CO)O2)O1)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 MUPFEKGTMRGPLJ-RMMQSMQOSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- MUPFEKGTMRGPLJ-UHFFFAOYSA-N UNPD196149 Natural products OC1C(O)C(CO)OC1(CO)OC1C(O)C(O)C(O)C(COC2C(C(O)C(O)C(CO)O2)O)O1 MUPFEKGTMRGPLJ-UHFFFAOYSA-N 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 229940062353 acid jelly Drugs 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- PBUBJNYXWIDFMU-UHFFFAOYSA-L calcium;butanedioate Chemical compound [Ca+2].[O-]C(=O)CCC([O-])=O PBUBJNYXWIDFMU-UHFFFAOYSA-L 0.000 description 1
- 150000001746 carotenes Chemical class 0.000 description 1
- 235000005473 carotenes Nutrition 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 235000012716 cod liver oil Nutrition 0.000 description 1
- 239000003026 cod liver oil Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 235000001727 glucose Nutrition 0.000 description 1
- 239000010501 lemon oil Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- MUPFEKGTMRGPLJ-ZQSKZDJDSA-N raffinose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)O1 MUPFEKGTMRGPLJ-ZQSKZDJDSA-N 0.000 description 1
- 229960000342 retinol acetate Drugs 0.000 description 1
- 235000019173 retinyl acetate Nutrition 0.000 description 1
- 239000011770 retinyl acetate Substances 0.000 description 1
- QGNJRVVDBSJHIZ-QHLGVNSISA-N retinyl acetate Chemical compound CC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C QGNJRVVDBSJHIZ-QHLGVNSISA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000007940 sugar coated tablet Substances 0.000 description 1
- 235000019605 sweet taste sensations Nutrition 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- NCYCYZXNIZJOKI-UHFFFAOYSA-N vitamin A aldehyde Natural products O=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-UHFFFAOYSA-N 0.000 description 1
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Landscapes
- Jellies, Jams, And Syrups (AREA)
Description
【発明の詳細な説明】
本発明は、安定性に優れた脂溶性ビタミン含有
ゼリー剤の製造法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a highly stable jelly containing fat-soluble vitamins.
ビタミンA、D、Eなどの脂溶性ビタミンは、
栄養上不可欠の要素であるが、油状の物質が多
く、用量が少量であるため、服用及び取扱いが困
難である。またこれらのビタミンは空気との接
触、酸、アルカリ、金属イオンなどにより分解し
やすく不安定である。これらの点を改善するた
め、各種の剤形に製剤化することが試みられてお
り、脂溶性ビタミンをゼリー剤に配合することに
より、安定性に優れ、服用の容易な製剤が得られ
ることが知られている(特公昭38−6568号、同46
−23273号各広報参照)。 Fat-soluble vitamins such as vitamins A, D, and E are
Although it is an essential nutritional element, it is difficult to take and handle because it contains many oily substances and the dosage is small. Furthermore, these vitamins are unstable and easily decompose due to contact with air, acids, alkalis, metal ions, etc. In order to improve these points, attempts have been made to formulate formulations into various dosage forms, and by incorporating fat-soluble vitamins into jelly formulations, formulations with excellent stability and ease of administration can be obtained. known (Special Publication No. 38-6568, 46
-Refer to each bulletin number 23273).
一般にゼリーを製造するためには、ゼラチン、
寒天、ペクチンなどの高分子増粘剤と糖類を水に
溶解し、濃縮、PH調整などを行つたのち、冷却し
て凝固させる方法が用いられている。この場合、
糖類としては主に白糖、ぶどう糖又は水飴が用い
られ、特に増粘剤としてペクチンを用いたペクチ
ンゼリーは、砂糖・酸ゼリーと呼ばれるように、
ペクチン、白糖及び酸の三者のバランスによりゼ
リーを形成するもので、そのゼリー化に白糖が重
要な役割を果たし、他の糖類を配合してもゼリー
化が困難な場合が多い。しかし最近では一般に甘
味に対する嗜好が変化し、また白糖のカロリー価
の点などから、白糖よりもカロリー価及び甘味の
低い種類を用いたゼリー剤の開発が要望されてい
る。 Generally, to produce jelly, gelatin,
The method used is to dissolve polymer thickeners such as agar and pectin and sugars in water, concentrate, adjust the pH, and then cool and solidify. in this case,
The sugars mainly used are white sugar, glucose, or starch syrup, and pectin jelly, which uses pectin as a thickener, is called sugar-acid jelly.
Jelly is formed by the balance of pectin, sucrose, and acid, and sucrose plays an important role in making jelly, and it is often difficult to make jelly even if other sugars are added. However, in recent years, preferences for sweetness have generally changed, and in view of the caloric value of white sugar, there has been a demand for the development of jelly preparations using a type of sugar with a lower caloric value and sweetness than white sugar.
本発明者らは、これらの観点から研究を進めた
結果、ペクチンゼリーの糖成分としてマルトース
(麦芽糖)を用いると、白糖を用いたものと類似
したゼリーが得られることを見出した。しかしマ
ルトース含有ペクチンゼリーでは、マルトース含
量を多くすると、ゼリー中にマルトースの結晶が
折出し、ゼリーの外観が白つぽくなるという欠点
が認められた。そこでさらに研究を進めた結果、
マルチトールを併用することにより、マルトース
の結晶折出を防止できることを見出した。 As a result of conducting research from these viewpoints, the present inventors found that when maltose (maltose) is used as the sugar component of pectin jelly, a jelly similar to that using white sugar can be obtained. However, maltose-containing pectin jelly has a drawback in that when the maltose content is increased, maltose crystals are precipitated in the jelly, resulting in a whitish appearance. As a result of further research,
It has been found that crystal precipitation of maltose can be prevented by using maltitol in combination.
本発明はこの知見に基づくもので、ペクチン並
びにマルトース及びマルチトールを含むゼリー基
剤に、脂溶性ビタミン及び有機酸を加えてPH29〜
4.0の乳化液を調製し、この乳化液を成形乾燥し、
必要に応じてマンニトールで糖衣を施すことを特
徴とするビタミン含有ゼリー剤の製造法である。 The present invention is based on this knowledge, and is made by adding fat-soluble vitamins and organic acids to a jelly base containing pectin, maltose, and maltitol.
4.0 emulsion was prepared, this emulsion was molded and dried,
This is a method for producing a vitamin-containing jelly, which is characterized by sugar-coating with mannitol if necessary.
本発明に用いられる脂溶性ビタミンとしては、
肝油、ビタミンA油、ビタミンA酢酸エステル、
ビタミンAパルミチン酸エステル、ビタミンD2、
ビタミンD3、ビタミンE、ビタミンE酢酸エス
テル、ビタミンEこはく酸エステルカルシウムな
ど、並びにこれらの2種以上の混合物があげられ
る。これらは日本薬局方の規格に適合するものが
好ましい。 The fat-soluble vitamins used in the present invention include:
Cod liver oil, vitamin A oil, vitamin A acetate,
Vitamin A palmitate, vitamin D2 ,
Examples include vitamin D 3 , vitamin E, vitamin E acetate, vitamin E calcium succinate, and mixtures of two or more of these. These preferably meet the standards of the Japanese Pharmacopoeia.
ゼリー基剤に含まれるペクチンとしては、エス
テル化度7〜12%の高メトキシルペクチンに属
し、スローセツトペクチンと呼ばれるものが用い
られる。低メトキシルペクチン及び高メキシルペ
クチン中のラビツドセツトペクチンは好ましくな
い。ペクチンは米国薬局方の規格に適合する品質
のものが好ましい。 The pectin contained in the jelly base is a type of high methoxyl pectin with a degree of esterification of 7 to 12%, and is called slow set pectin. Low methoxyl pectin and high methoxyl pectin in rabid set pectin are not preferred. The pectin is preferably of a quality that meets USP standards.
マルトースは白糖より甘味が弱く、甘味の質も
まろやかである。またマルチトールは還元麦芽糖
水飴の主成分として知られている糖であつて、白
糖よりもカロリー価が低い。マルトースは日本薬
局方の規格に適合するものが好ましいが、糖食品
製造用のものでもよい。マルチトールとしては、
結晶品を用いてもよいが、還元麦芽水飴を用いる
と経済的に有利である。還元麦芽糖水飴はマルチ
トール濃度70〜80%の製品がよく、マルチトール
濃度がこれより高いときは水で希釈して用いるこ
とが好ましい。 Maltose is less sweet than white sugar, and its sweetness is mellow. Furthermore, maltitol is a sugar known as the main component of reduced maltose starch syrup, and has a lower caloric value than white sugar. It is preferable that maltose conforms to the standards of the Japanese Pharmacopoeia, but maltose for sugar food production may also be used. As maltitol,
Although crystalline products may be used, it is economically advantageous to use reduced malt starch syrup. Reduced maltose starch syrup is preferably a product with a maltitol concentration of 70 to 80%, and when the maltitol concentration is higher than this, it is preferable to use it after diluting it with water.
本発明のゼリー剤を製造するに際しては、まず
ペクチン、マルトース及びマルチトールを70〜90
℃の水に溶解してゼリー基剤を調製する。 When producing the jelly of the present invention, first add pectin, maltose, and maltitol to a concentration of 70 to 90%.
Prepare the jelly base by dissolving in water at °C.
ペクチンを溶解する際に10〜30倍量のマルトー
スを一緒に加えると、ペクチンを容易に溶解する
ことができる。マルトースの配合量はペクチン1
部に対し、30〜90部が好ましい。マルチトールの
配合量はペクチン1部に対し、還元麦芽糖水飴と
して10〜30部が好ましい。またマルトースに対す
る還元麦芽糖水飴の配合比率は、マルトース1に
対して0.2〜0.75が好ましい。ゼリー基剤には、
ゼリーの強度、保湿性などを向上させるため、寒
天、グリセリンなどを添加してもよい。 Pectin can be easily dissolved by adding 10 to 30 times the amount of maltose when dissolving pectin. The amount of maltose is 1 part pectin
parts, preferably 30 to 90 parts. The blending amount of maltitol is preferably 10 to 30 parts as reduced maltose starch syrup per 1 part of pectin. Further, the blending ratio of reduced maltose starch syrup to maltose is preferably 0.2 to 0.75 to 1 part maltose. For the jelly base,
Agar, glycerin, etc. may be added to improve the strength and moisturizing properties of the jelly.
次いでゼリー基剤に脂溶性ビタミン及び有機酸
を加えてPH2.9〜4.0の乳化液を調製する。 Next, fat-soluble vitamins and organic acids are added to the jelly base to prepare an emulsion with a pH of 2.9 to 4.0.
脂溶性ビタミンはそのまま用いてもよく、食用
油に溶解して用いてもよい。ゼリー基剤を70〜90
℃ゐ保持し、脂溶性ビタミンを加えたのちよく撹
拌すると、ビタミンが粒径2〜15μmの粒径に均
等に分散した乳化液が得られる。 Fat-soluble vitamins may be used as they are or dissolved in edible oil. 70-90% jelly base
When the temperature is maintained at 0.degree. C. and the fat-soluble vitamins are added and stirred well, an emulsion in which the vitamins are evenly dispersed in particles with a particle size of 2 to 15 .mu.m is obtained.
有機酸としては例えばくえん酸、酒石酸、酢
酸、アスコルビン酸などが用いられる。これらの
有機酸及びそのナトリウム塩又はカリウム塩を含
有する緩衝液を用いることが好ましい。 Examples of organic acids used include citric acid, tartaric acid, acetic acid, and ascorbic acid. It is preferable to use a buffer containing these organic acids and their sodium or potassium salts.
脂溶性ビタミン及び有機酸は任意の順序で加え
ることができるが、脂溶性ビタミンを分散乳化さ
せたのち、有機酸を加えてPHを調製することが好
ましい。この乳化液には色素例えばカロチン、香
料などを添加してもよい。 Although fat-soluble vitamins and organic acids can be added in any order, it is preferable to disperse and emulsify the fat-soluble vitamins and then add the organic acids to adjust the pH. Dyes such as carotene, fragrances, etc. may be added to this emulsion.
次いで乳化液を所定量ずつ型に入れて成形、乾
燥するとゼリー剤が得られる。乾燥は35〜65℃の
温度で10〜72時間行うことが好ましい。 Next, a predetermined amount of the emulsion is placed in a mold, molded, and dried to obtain a jelly. Drying is preferably carried out at a temperature of 35-65°C for 10-72 hours.
こうして得られたゼリー剤に糖衣を施す場合
は、マルトース、還元麦芽糖水飴及びアラビアゴ
ムを含有する糊液、並びに結晶性マンニトールを
用いることが好ましい。乳糖、ガラクトース、果
糖、マルトース、ソルビトール、キシリトールな
どにより糖衣層を形成すると、吸湿性、外観、保
存性、味覚などにやや難点がある。マンニトール
は20〜48メツシユ程度の結晶が好ましい。マンニ
トールの市販品は80メツシユ以下の微細な結晶で
あるので、これらを水から再結晶したのち20〜48
メツシユに粉砕して用いることが好ましい。 When the jelly thus obtained is coated with sugar, it is preferable to use a paste containing maltose, reduced maltose starch syrup and gum arabic, and crystalline mannitol. Forming a sugar coating layer with lactose, galactose, fructose, maltose, sorbitol, xylitol, etc. has some disadvantages in terms of hygroscopicity, appearance, storage stability, taste, etc. Mannitol preferably has crystals of about 20 to 48 mesh. Commercial products of mannitol are in the form of fine crystals of less than 80 mesh, so after recrystallizing them from water,
It is preferable to use it by crushing it into a mesh.
本発明のビタミン含有ゼリー剤は、ゼリーとし
ての特製を有し、小児、老人、女性も服用が容易
であり、また白糖を用いたゼリー剤に比ベゼリー
の物性、感触などの点で優れており、甘味が弱く
まろやかで、カロリー価も低く、医療上、栄養補
給上きわめて有利である。さらに本ゼリー剤は溶
解性に優れ、主成分であるビタミンはきわめて安
定である。 The vitamin-containing jelly preparation of the present invention has special properties as a jelly, and is easy for children, the elderly, and women to take, and is superior to jelly preparations using white sugar in terms of physical properties and texture. It has a mild sweet taste and low caloric value, making it extremely advantageous for medical and nutritional purposes. Furthermore, this jelly has excellent solubility, and the main ingredient, vitamins, is extremely stable.
試験例 1
ペクチンと各種の糖を併用し、ペクチンのゼリ
ー成形について調べた。ペクチン1gに糖25gを
加えてよく混和したのち、水20mlを加えて水浴中
で80℃に加熱撹拌して溶解する。この溶液に糖30
gを追加し、加熱撹拌して溶解し、PH2.8のくえ
ん酸緩衝液を加えてPH3.0〜3.3としたのち、水を
加えて全量80gとし、この溶液をビーカーに入
れ、5℃の温度で一夜放置してゼリー形成の具合
を比較した。その結果、白糖、ぶどう糖、マンノ
ース、マルトース、果糖、ソルビトール及びキシ
ロースではゼリーの形成がみられた。なおゼリー
の硬さは糖の種類によつて著しく相違していた。
白糖含有ゼリーと最も感じの似たゼリーはマルト
ース含有ゼリーであつた。また乳糖、デキストリ
ン、ガラクトース、マンニトール、ラムノース、
ラフイノース及びソルボースではゼリーを形成し
なかつた。Test Example 1 Pectin was used in combination with various sugars to investigate the formation of pectin into jelly. Add 25 g of sugar to 1 g of pectin and mix well, then add 20 ml of water and heat to 80°C with stirring in a water bath to dissolve. Sugar 30 in this solution
g was added, heated and stirred to dissolve, and citric acid buffer with pH 2.8 was added to adjust the pH to 3.0 to 3.3. Water was added to make a total volume of 80 g. This solution was placed in a beaker and heated at 5℃. The jelly formation was compared after being left at room temperature overnight. As a result, jelly formation was observed with white sugar, glucose, mannose, maltose, fructose, sorbitol, and xylose. The hardness of the jelly differed significantly depending on the type of sugar.
The jelly with the most similar feel to the jelly containing white sugar was the jelly containing maltose. Also lactose, dextrin, galactose, mannitol, rhamnose,
Raffinose and sorbose did not form a jelly.
試験例 2
ペクチン3.75gにマルトース100gを加えてよ
く混合したのち、水62.25gを加えて水浴中で加
熱しながら10分間撹拌して溶解する。この溶液に
マルトース175g及び還元麦芽糖水飴100gを加え
てよく混合し、くえん酸緩衝液でPH3.2に調整し
たのち、ゼリーカツプに注ぎ、室温で3時間、次
いで5℃の温度で17時間放置する。こうして得ら
れたゼリーではマルトースの結晶析出はみられ
ず、ゼリーとして感触も満足できるものであつ
た。またカードメータによる測定の結果、ゼリー
強度480g/cm2、ゼリーの硬さ9.58×104dyne/cm2
であつた。一方、同量の白糖及び水飴を用いて調
製したデリーでは、ゼリー強度490g/cm2、ゼリ
ーの硬さ1.23×105dyne/cm2であり、両者はほぼ
同等であつた。Test Example 2 Add 100 g of maltose to 3.75 g of pectin and mix well, then add 62.25 g of water and stir for 10 minutes while heating in a water bath to dissolve. Add 175 g of maltose and 100 g of reduced maltose starch syrup to this solution, mix well, adjust the pH to 3.2 with citric acid buffer, pour into jelly cups, and leave at room temperature for 3 hours and then at 5°C for 17 hours. In the jelly thus obtained, no maltose crystal precipitation was observed, and the jelly had a satisfactory texture. Also, as a result of measurement using a card meter, the jelly strength was 480 g/cm 2 and the jelly hardness was 9.58×10 4 dyne/cm 2
It was hot. On the other hand, in the case of delhi prepared using the same amount of white sugar and starch syrup, the jelly strength was 490 g/cm 2 and the jelly hardness was 1.23×10 5 dyne/cm 2 , which were almost the same.
実施例 1
加熱装置を備えた撹拌乳化釜に水700mlを入れ、
これにペクチン(スローセツト、150ゼリーグレ
ード)50gとマルトース1000gの混合物を加え、
90℃に加温しながら撹拌して溶解する。次いでマ
ルトース700g及び還元麦芽糖水飴(水分含量25
%)500gを加え、90℃に保温しながら撹拌して
溶解する。このゼリー基剤にビタミンAD混合油
(1g中にビタミンAパルミチン酸エステル100万
国際単位、ビタミンD210万国際単位を含有する
大豆油溶液)3.75gを加え、ビタミンA及びD2を
分散乳化させたのち、β−カロチンペースト0.75
g及びレモンオイル15.5gを加えて混和する。次
いでくえん酸緩衝液30ml(くえん酸8.5g及びく
えん酸ナトリウム2.6gを含有)を加えてPH3.2に
調整する。この溶液を殿粉型に0.8gずつ摘下し、
一夜室温に放置したのち、40℃の乾燥室にさらに
一夜放置するとゼリーが得られる。このゼリーを
殿粉型から取り出し、表面の殿粉を除き製品とす
る。こうして得られた製品は、淡黄色のレモンの
香りを有し、甘味は強くなく、口当りも良好であ
る。本品は1粒中にビタミンA1000国際単位及び
ビタミンD2100国際単位を含有する。本品は、40
℃、相対温度75%の条件での分解促進試験で120
日経過後もビタミンの分解がほとんどみられず、
安定性にも優れている。また日本薬局方の崩壊試
験法により崩壊時間を測定すると10〜15分で崩壊
する。Example 1 Put 700ml of water into a stirring emulsification pot equipped with a heating device,
Add a mixture of 50g of pectin (Slowset, 150 jelly grade) and 1000g of maltose to this.
Stir and dissolve while heating to 90°C. Next, 700 g of maltose and reduced maltose starch syrup (water content 25
%) and stir to dissolve while maintaining the temperature at 90°C. Add 3.75 g of vitamin AD mixed oil (soybean oil solution containing 1 million international units of vitamin A palmitate ester and 100,000 international units of vitamin D 2 in 1 g) to this jelly base to disperse and emulsify vitamins A and D 2 . After that, β-carotene paste 0.75
g and 15.5 g of lemon oil and mix. Next, add 30 ml of citric acid buffer (containing 8.5 g of citric acid and 2.6 g of sodium citrate) to adjust the pH to 3.2. Pour 0.8g of this solution into a starch mold,
After leaving it at room temperature overnight, it is left in a drying room at 40°C for another night to obtain jelly. This jelly is taken out of the starch mold and the starch on the surface is removed to form a product. The product thus obtained has a pale yellow lemon scent, is not strong in sweetness, and has a good mouthfeel. This product contains 1000 international units of vitamin A and 2 100 international units of vitamin D in one tablet. This product is 40
℃, 120 in accelerated decomposition test under conditions of relative temperature 75%
There is almost no decomposition of vitamins even after a day has passed,
It also has excellent stability. Furthermore, when the disintegration time is measured using the Japanese Pharmacopoeia's disintegration test method, it disintegrates in 10 to 15 minutes.
実施例 2
加熱装置を備えた内容積5の仕入釜に水700
mlを入れ、これにペクチン50gとマルトース750
gの混合物を加え、80℃に加温して激しく撹拌し
ながら溶解し、さらにマルトース1000g、還元麦
芽糖水飴500g、寒天水溶液250g(寒天16gを含
有)及びグリセリン60gを加え、80℃で撹拌して
溶解する。このゼリー基剤にビタミンE酢酸エス
テル150g及びフルーツミツクス香料20gを加え、
激しく撹拌してビタミンE酢酸エステルを分散乳
化させたのち、くえん酸緩衝液30ml(くえん酸
8.5g及びくえん酸ナトリウム2.6gを含有)を加
えてPH3.2に調整する。この溶液を0.6gずつ殿粉
型に流し込んで凸レンズ状に成形し、50℃で48時
間乾燥する。乾燥後、殿粉型からゼリーを取り出
し、マルトース15部、還元麦芽糖水飴30部、アラ
ビアゴム末20部及び水35部からなる糖衣液並びに
20〜48メツシユのマンニトールの結晶を用いて糖
衣を施し、50℃で5時間乾燥する。こうして得ら
れた製品は、透明感及びフルーツミツクスの香り
を有する糖衣ゼリーであり、口当りもまろやかで
ある。本品は1粒中にビタミンE酢酸エステル2
mgを含み、その安定性も良好である。また本品の
崩壊性は日本薬局方糖衣錠の規格を充分に満足す
るものであつた。Example 2 700 ml of water in a stocking pot with an internal volume of 5 equipped with a heating device
ml, add 50g of pectin and 750g of maltose.
Add 1000 g of maltose, 500 g of reduced maltose starch syrup, 250 g of agar aqueous solution (containing 16 g of agar) and 60 g of glycerin, and stir at 80°C. dissolve. Add 150g of vitamin E acetate and 20g of fruit mix flavor to this jelly base,
After stirring vigorously to disperse and emulsify the vitamin E acetate, add 30 ml of citric acid buffer (citric acid
(containing 8.5 g and 2.6 g of sodium citrate) and adjust the pH to 3.2. Pour 0.6 g of this solution into a starch mold to form a convex lens shape, and dry at 50°C for 48 hours. After drying, remove the jelly from the starch mold and add a sugar coating solution consisting of 15 parts of maltose, 30 parts of reduced maltose starch syrup, 20 parts of gum arabic powder, and 35 parts of water.
Sugar coating is applied using 20 to 48 mesh mannitol crystals and dried at 50°C for 5 hours. The product thus obtained is a sugar-coated jelly that has a transparent feel and a fruity aroma, and has a mellow texture. This product contains 2 vitamin E acetate esters in 1 tablet.
mg, and its stability is also good. In addition, the disintegration properties of this product fully met the Japanese Pharmacopoeia standards for sugar-coated tablets.
実施例 3
加熱装置を備えた内容積5の仕入釜に水850
mlを入れ、これにペクチン60gとマルトース1000
gの混合物を加え、80℃に加温して激しく撹拌し
ながら溶解する。さらにマルトース1100g及び還
元麦芽糖水飴600gを加え、80℃に保温しながら
撹拌し、寒天水溶液300g(寒天20gを含有)及
びグリセリン70gを加えて溶解する。このゼリー
基剤にビタミンAD混合油(1g中にビタミンA
パルミチン酸エステル100万国際単位及びビタミ
ンD210万国際単位を含有する大豆油溶液)3g
及びビアミンE酢酸エステル150gを加えて撹拌
し、ビタミンを分散乳化させたのち、β−カロチ
ンペースト2g及びオレンジオイル25gを加えて
混和する。次いでくえん酸緩衝液40ml(くえん酸
12g及びくえん酸ナトリウム3.5g含有)を加え
てPH3.2に調整し、この溶液を0.7gずつ殿粉型に
流し込み、凸レンズ状に成形し、50℃で48時間乾
燥する。乾燥後、殿粉型からゼリーを取り出し、
実施例2と同様にして糖衣を施し、50℃で3時間
乾燥して製品とする。得られた製品橙黄色でオレ
ンジの香りを有し、甘味も強くなく、さつぱりと
した口当りのよいゼリーである。本品は1粒中に
ビタミンA500国際単位、ビタミンD250国際単位
及びビタミンE酢酸エステル25mgを含み、安定性
及び崩壊性も実施例1及び2の製品と同様に良好
であつた。Example 3 850 ml of water in a stocking pot with an internal volume of 5 equipped with a heating device
ml, add 60g of pectin and 1000g of maltose.
Add the mixture of g, warm to 80°C and dissolve with vigorous stirring. Furthermore, 1100 g of maltose and 600 g of reduced maltose starch syrup are added, stirred while keeping the temperature at 80°C, and 300 g of agar aqueous solution (containing 20 g of agar) and 70 g of glycerin are added and dissolved. This jelly base contains vitamin AD mixed oil (1g contains vitamin A)
3 g of soybean oil solution containing 1 million international units of palmitate ester and 100,000 international units of vitamin D2 )
After adding 150 g of Viamine E acetate and stirring to disperse and emulsify the vitamins, 2 g of β-carotene paste and 25 g of orange oil were added and mixed. Next, 40 ml of citric acid buffer (citric acid
(containing 12 g and 3.5 g of sodium citrate) to adjust the pH to 3.2, pour 0.7 g of this solution into a starch mold, form it into a convex lens shape, and dry at 50°C for 48 hours. After drying, remove the jelly from the starch mold,
Sugar coating was applied in the same manner as in Example 2, and the product was dried at 50°C for 3 hours. The resulting product is an orange-yellow jelly with an orange aroma, not a strong sweetness, and a refreshing texture. This product contained 500 international units of vitamin A, 50 international units of vitamin D, and 25 mg of vitamin E acetate in one tablet, and had good stability and disintegration properties as well as the products of Examples 1 and 2.
Claims (1)
を含むゼリー基剤に、脂溶性ビタミン及び有機酸
を加えてPH2.9〜4.0の乳化液を調製し、この乳化
液を成形、乾燥し、必要に応じてマンニトールで
糖衣を施すことを特徴とするビタミン含有ゼリー
剤の製造法。1 Add fat-soluble vitamins and organic acids to a jelly base containing pectin, maltose, and maltitol to prepare an emulsion with a pH of 2.9 to 4.0, shape and dry this emulsion, and add mannitol as necessary. A method for producing a vitamin-containing jelly characterized by sugar-coating.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61282003A JPS63137651A (en) | 1986-11-28 | 1986-11-28 | Vitanim-containing jelly agent and production thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61282003A JPS63137651A (en) | 1986-11-28 | 1986-11-28 | Vitanim-containing jelly agent and production thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63137651A JPS63137651A (en) | 1988-06-09 |
JPH04617B2 true JPH04617B2 (en) | 1992-01-08 |
Family
ID=17646870
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61282003A Granted JPS63137651A (en) | 1986-11-28 | 1986-11-28 | Vitanim-containing jelly agent and production thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63137651A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4787517B2 (en) * | 2005-03-10 | 2011-10-05 | イーエヌ大塚製薬株式会社 | Gelling agent for nutrients |
JP2017214299A (en) * | 2016-05-30 | 2017-12-07 | ライオン株式会社 | Semisolid formulation and method for producing the same |
-
1986
- 1986-11-28 JP JP61282003A patent/JPS63137651A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS63137651A (en) | 1988-06-09 |
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