NO328117B1 - Fremgangsmate ved fremstilling av sma perler som inneholder fettloselige substanser - Google Patents

Fremgangsmate ved fremstilling av sma perler som inneholder fettloselige substanser Download PDF

Info

Publication number: NO328117B1
Authority: NO; Norway
Prior art keywords: weight; fat; cross; gelatin; linking
Prior art date: 1999-08-05

Application number

NO20003948A

Other languages

English (en)

Norwegian (no)

Other versions

NO20003948D0 (no

NO20003948L (no

Inventor

Bruno Leuenberger

Johann Ulm

Jean-Claude Tritsch

Original Assignee

Dsm Ip Assets Bv

Priority date (The priority date 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 date listed.)

1999-08-05

Filing date

2000-08-04

Publication date

2009-12-14

2000-08-04 Application filed by Dsm Ip Assets Bv filed Critical Dsm Ip Assets Bv

2000-08-04 Publication of NO20003948D0 publication Critical patent/NO20003948D0/no

2001-02-06 Publication of NO20003948L publication Critical patent/NO20003948L/no

2009-12-14 Publication of NO328117B1 publication Critical patent/NO328117B1/no

Links

239000000126 substance Substances 0.000 title claims abstract description 23
238000004519 manufacturing process Methods 0.000 title claims abstract description 6
239000011324 bead Substances 0.000 title claims description 8
238000004132 cross linking Methods 0.000 claims abstract description 30
108010010803 Gelatin Proteins 0.000 claims abstract description 22
239000008273 gelatin Substances 0.000 claims abstract description 22
229920000159 gelatin Polymers 0.000 claims abstract description 22
235000019322 gelatine Nutrition 0.000 claims abstract description 22
235000011852 gelatine desserts Nutrition 0.000 claims abstract description 22
239000011159 matrix material Substances 0.000 claims abstract description 8
230000005855 radiation Effects 0.000 claims abstract description 5
238000000034 method Methods 0.000 claims description 23
239000002245 particle Substances 0.000 claims description 17
239000000839 emulsion Substances 0.000 claims description 16
239000000843 powder Substances 0.000 claims description 14
102000004190 Enzymes Human genes 0.000 claims description 13
108090000790 Enzymes Proteins 0.000 claims description 13
235000019155 vitamin A Nutrition 0.000 claims description 13
239000011719 vitamin A Substances 0.000 claims description 13
239000000203 mixture Substances 0.000 claims description 12
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 claims description 10
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 claims description 10
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 claims description 10
235000000346 sugar Nutrition 0.000 claims description 10
229940045997 vitamin a Drugs 0.000 claims description 10
SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 claims description 8
239000003963 antioxidant agent Substances 0.000 claims description 8
235000006708 antioxidants Nutrition 0.000 claims description 8
239000003638 chemical reducing agent Substances 0.000 claims description 8
229930091371 Fructose Natural products 0.000 claims description 7
239000005715 Fructose Substances 0.000 claims description 7
230000003078 antioxidant effect Effects 0.000 claims description 7
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims description 6
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Chemical compound 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 claims description 6
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 claims description 6
108060008539 Transglutaminase Proteins 0.000 claims description 6
PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims description 6
SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims description 6
102000003601 transglutaminase Human genes 0.000 claims description 6
239000000080 wetting agent Substances 0.000 claims 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 claims description 5
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 claims description 5
206010073306 Exposure to radiation Diseases 0.000 claims description 4
235000021466 carotenoid Nutrition 0.000 claims description 4
150000001747 carotenoids Chemical class 0.000 claims description 4
239000008103 glucose Substances 0.000 claims description 4
235000020777 polyunsaturated fatty acids Nutrition 0.000 claims description 4
229960000342 retinol acetate Drugs 0.000 claims description 4
235000019173 retinyl acetate Nutrition 0.000 claims description 4
239000011770 retinyl acetate Substances 0.000 claims description 4
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 claims description 4
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 3
GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 claims description 3
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 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 claims description 3
238000011534 incubation Methods 0.000 claims description 3
-1 invert sugar Chemical compound 0.000 claims description 3
229940108325 retinyl palmitate Drugs 0.000 claims description 3
235000019172 retinyl palmitate Nutrition 0.000 claims description 3
239000011769 retinyl palmitate Substances 0.000 claims description 3
235000019166 vitamin D Nutrition 0.000 claims description 3
239000011710 vitamin D Substances 0.000 claims description 3
239000011709 vitamin E Substances 0.000 claims description 3
235000019165 vitamin E Nutrition 0.000 claims description 3
235000019168 vitamin K Nutrition 0.000 claims description 3
239000011712 vitamin K Substances 0.000 claims description 3
WQZGKKKJIJFFOK-WHZQZERISA-N D-aldose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-WHZQZERISA-N 0.000 claims description 2
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 claims description 2
HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 claims description 2
PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 claims description 2
HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 claims 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 claims description 2
PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 claims description 2
229930182830 galactose Natural products 0.000 claims description 2
235000019534 high fructose corn syrup Nutrition 0.000 claims description 2
229960004903 invert sugar Drugs 0.000 claims description 2
238000001694 spray drying Methods 0.000 claims description 2
229940088594 vitamin Drugs 0.000 claims description 2
229930003231 vitamin Natural products 0.000 claims description 2
235000013343 vitamin Nutrition 0.000 claims description 2
239000011782 vitamin Substances 0.000 claims description 2
150000003722 vitamin derivatives Chemical class 0.000 claims 1
238000010438 heat treatment Methods 0.000 description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
239000000047 product Substances 0.000 description 7
229920002261 Corn starch Polymers 0.000 description 6
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
239000008120 corn starch Substances 0.000 description 6
238000001035 drying Methods 0.000 description 5
239000004322 Butylated hydroxytoluene Substances 0.000 description 3
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
235000010354 butylated hydroxytoluene Nutrition 0.000 description 3
229940095259 butylated hydroxytoluene Drugs 0.000 description 3
230000002255 enzymatic effect Effects 0.000 description 3
239000007921 spray Substances 0.000 description 3
239000004809 Teflon Substances 0.000 description 2
229920006362 Teflon® Polymers 0.000 description 2
MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 description 2
YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
FDSDTBUPSURDBL-LOFNIBRQSA-N canthaxanthin Chemical compound CC=1C(=O)CCC(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)C(=O)CCC1(C)C FDSDTBUPSURDBL-LOFNIBRQSA-N 0.000 description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
239000008367 deionised water Substances 0.000 description 2
229910021641 deionized water Inorganic materials 0.000 description 2
238000004945 emulsification Methods 0.000 description 2
230000001804 emulsifying effect Effects 0.000 description 2
DECIPOUIJURFOJ-UHFFFAOYSA-N ethoxyquin Chemical compound N1C(C)(C)C=C(C)C2=CC(OCC)=CC=C21 DECIPOUIJURFOJ-UHFFFAOYSA-N 0.000 description 2
235000019197 fats Nutrition 0.000 description 2
150000002402 hexoses Chemical class 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
150000002772 monosaccharides Chemical class 0.000 description 2
229920001542 oligosaccharide Polymers 0.000 description 2
150000002482 oligosaccharides Chemical class 0.000 description 2
150000002972 pentoses Chemical class 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
238000003756 stirring Methods 0.000 description 2
KBPHJBAIARWVSC-XQIHNALSSA-N trans-lutein Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C(=CC(O)CC2(C)C)C KBPHJBAIARWVSC-XQIHNALSSA-N 0.000 description 2
JKQXZKUSFCKOGQ-JLGXGRJMSA-N (3R,3'R)-beta,beta-carotene-3,3'-diol Chemical compound C([C@H](O)CC=1C)C(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)C[C@@H](O)CC1(C)C JKQXZKUSFCKOGQ-JLGXGRJMSA-N 0.000 description 1
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
JEBFVOLFMLUKLF-IFPLVEIFSA-N Astaxanthin Natural products CC(=C/C=C/C(=C/C=C/C1=C(C)C(=O)C(O)CC1(C)C)/C)C=CC=C(/C)C=CC=C(/C)C=CC2=C(C)C(=O)C(O)CC2(C)C JEBFVOLFMLUKLF-IFPLVEIFSA-N 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
239000004217 Citranaxanthin Substances 0.000 description 1
SLQHGWZKKZPZEK-JKEZLOPUSA-N Citranaxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C(=O)C)C=CC=C(/C)C=CC1=C(C)CCCC1(C)C SLQHGWZKKZPZEK-JKEZLOPUSA-N 0.000 description 1
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 1
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 1
239000004258 Ethoxyquin Substances 0.000 description 1
239000004606 Fillers/Extenders Substances 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
JEVVKJMRZMXFBT-XWDZUXABSA-N Lycophyll Natural products OC/C(=C/CC/C(=C\C=C\C(=C/C=C/C(=C\C=C\C=C(/C=C/C=C(\C=C\C=C(/CC/C=C(/CO)\C)\C)/C)\C)/C)\C)/C)/C JEVVKJMRZMXFBT-XWDZUXABSA-N 0.000 description 1
239000004909 Moisturizer Substances 0.000 description 1
OOUTWVMJGMVRQF-DOYZGLONSA-N Phoenicoxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)C(=O)C(O)CC1(C)C)C=CC=C(/C)C=CC2=C(C)C(=O)CCC2(C)C OOUTWVMJGMVRQF-DOYZGLONSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
241000282887 Suidae Species 0.000 description 1
102000004357 Transferases Human genes 0.000 description 1
108090000992 Transferases Proteins 0.000 description 1
JKQXZKUSFCKOGQ-LQFQNGICSA-N Z-zeaxanthin Natural products C([C@H](O)CC=1C)C(C)(C)C=1C=CC(C)=CC=CC(C)=CC=CC=C(C)C=CC=C(C)C=CC1=C(C)C[C@@H](O)CC1(C)C JKQXZKUSFCKOGQ-LQFQNGICSA-N 0.000 description 1
QOPRSMDTRDMBNK-RNUUUQFGSA-N Zeaxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCC(O)C1(C)C)C=CC=C(/C)C=CC2=C(C)CC(O)CC2(C)C QOPRSMDTRDMBNK-RNUUUQFGSA-N 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
238000013019 agitation Methods 0.000 description 1
JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 description 1
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 1
JKQXZKUSFCKOGQ-LOFNIBRQSA-N all-trans-Zeaxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2=C(C)CC(O)CC2(C)C JKQXZKUSFCKOGQ-LOFNIBRQSA-N 0.000 description 1
DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
235000020661 alpha-linolenic acid Nutrition 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
DFMMVLFMMAQXHZ-CMGSAFQJSA-N apocarotenal Chemical compound O=CC(/C)=C/C=C/C(/C)=C/C=C/C=C(\C)/C=C/C=C(\C)C=CC1=C(C)CCCC1(C)C DFMMVLFMMAQXHZ-CMGSAFQJSA-N 0.000 description 1
229940019834 apocarotenal Drugs 0.000 description 1
229940114079 arachidonic acid Drugs 0.000 description 1
235000021342 arachidonic acid Nutrition 0.000 description 1
235000013793 astaxanthin Nutrition 0.000 description 1
239000001168 astaxanthin Substances 0.000 description 1
MQZIGYBFDRPAKN-ZWAPEEGVSA-N astaxanthin Chemical compound C([C@H](O)C(=O)C=1C)C(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)C(=O)[C@@H](O)CC1(C)C MQZIGYBFDRPAKN-ZWAPEEGVSA-N 0.000 description 1
229940022405 astaxanthin Drugs 0.000 description 1
235000013734 beta-carotene Nutrition 0.000 description 1
239000011648 beta-carotene Substances 0.000 description 1
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 1
229960002747 betacarotene Drugs 0.000 description 1
235000019282 butylated hydroxyanisole Nutrition 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
239000000378 calcium silicate Substances 0.000 description 1
229910052918 calcium silicate Inorganic materials 0.000 description 1
OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
235000012682 canthaxanthin Nutrition 0.000 description 1
239000001659 canthaxanthin Substances 0.000 description 1
229940008033 canthaxanthin Drugs 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
235000010980 cellulose Nutrition 0.000 description 1
235000019247 citranaxanthin Nutrition 0.000 description 1
PRDJTOVRIHGKNU-ZWERVMMHSA-N citranaxanthin Chemical compound CC(=O)\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 PRDJTOVRIHGKNU-ZWERVMMHSA-N 0.000 description 1
PRDJTOVRIHGKNU-UHFFFAOYSA-N citranaxanthine Natural products CC(=O)C=CC(C)=CC=CC(C)=CC=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C PRDJTOVRIHGKNU-UHFFFAOYSA-N 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000008121 dextrose Substances 0.000 description 1
IQDXNHZDRQHKEF-UHFFFAOYSA-N dialuminum;dicalcium;dioxido(oxo)silane Chemical compound [Al+3].[Al+3].[Ca+2].[Ca+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O IQDXNHZDRQHKEF-UHFFFAOYSA-N 0.000 description 1
239000003989 dielectric material Substances 0.000 description 1
150000002016 disaccharides Chemical class 0.000 description 1
235000020669 docosahexaenoic acid Nutrition 0.000 description 1
229940090949 docosahexaenoic acid Drugs 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
235000020673 eicosapentaenoic acid Nutrition 0.000 description 1
229960005135 eicosapentaenoic acid Drugs 0.000 description 1
JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 description 1
230000005670 electromagnetic radiation Effects 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
235000019285 ethoxyquin Nutrition 0.000 description 1
229940093500 ethoxyquin Drugs 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
239000000796 flavoring agent Substances 0.000 description 1
235000019634 flavors Nutrition 0.000 description 1
BJHIKXHVCXFQLS-UYFOZJQFSA-N fructose group Chemical group OCC(=O)[C@@H](O)[C@H](O)[C@H](O)CO BJHIKXHVCXFQLS-UYFOZJQFSA-N 0.000 description 1
239000011521 glass Substances 0.000 description 1
MNQZXJOMYWMBOU-UHFFFAOYSA-N glyceraldehyde Chemical compound OCC(O)C=O MNQZXJOMYWMBOU-UHFFFAOYSA-N 0.000 description 1
230000008642 heat stress Effects 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
229940067606 lecithin Drugs 0.000 description 1
229960004488 linolenic acid Drugs 0.000 description 1
KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
235000012680 lutein Nutrition 0.000 description 1
239000001656 lutein Substances 0.000 description 1
229960005375 lutein Drugs 0.000 description 1
KBPHJBAIARWVSC-RGZFRNHPSA-N lutein Chemical compound C([C@H](O)CC=1C)C(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\[C@H]1C(C)=C[C@H](O)CC1(C)C KBPHJBAIARWVSC-RGZFRNHPSA-N 0.000 description 1
ORAKUVXRZWMARG-WZLJTJAWSA-N lutein 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=CC2C(=CC(O)CC2(C)C)C ORAKUVXRZWMARG-WZLJTJAWSA-N 0.000 description 1
235000012661 lycopene Nutrition 0.000 description 1
239000001751 lycopene Substances 0.000 description 1
OAIJSZIZWZSQBC-GYZMGTAESA-N lycopene Chemical compound CC(C)=CCC\C(C)=C\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C=C(/C)CCC=C(C)C OAIJSZIZWZSQBC-GYZMGTAESA-N 0.000 description 1
229960004999 lycopene Drugs 0.000 description 1
230000001333 moisturizer Effects 0.000 description 1
238000013021 overheating Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
150000003538 tetroses Chemical class 0.000 description 1
229930003799 tocopherol Natural products 0.000 description 1
239000011732 tocopherol Substances 0.000 description 1
235000019149 tocopherols Nutrition 0.000 description 1
ZCIHMQAPACOQHT-ZGMPDRQDSA-N trans-isorenieratene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/c1c(C)ccc(C)c1C)C=CC=C(/C)C=Cc2c(C)ccc(C)c2C ZCIHMQAPACOQHT-ZGMPDRQDSA-N 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
229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
235000019731 tricalcium phosphate Nutrition 0.000 description 1
150000003641 trioses Chemical class 0.000 description 1
FJHBOVDFOQMZRV-XQIHNALSSA-N xanthophyll Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C=C(C)C(O)CC2(C)C FJHBOVDFOQMZRV-XQIHNALSSA-N 0.000 description 1
235000010930 zeaxanthin Nutrition 0.000 description 1
239000001775 zeaxanthin Substances 0.000 description 1
229940043269 zeaxanthin Drugs 0.000 description 1
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 1
QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09H—PREPARATION OF GLUE OR GELATINE
- C09H7/00—Preparation of water-insoluble gelatine
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1658—Proteins, e.g. albumin, gelatin
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5005—Wall or coating material
- A61K9/5021—Organic macromolecular compounds
- A61K9/5036—Polysaccharides, e.g. gums, alginate; Cyclodextrin
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/02—Nutrients, e.g. vitamins, minerals

Landscapes

Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Chemical & Material Sciences (AREA)
General Health & Medical Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Medicinal Chemistry (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Epidemiology (AREA)
Organic Chemistry (AREA)
Hematology (AREA)
Diabetes (AREA)
Obesity (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Nutrition Science (AREA)
Medicinal Preparation (AREA)
General Preparation And Processing Of Foods (AREA)
Cosmetics (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Edible Oils And Fats (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Jellies, Jams, And Syrups (AREA)
Materials For Medical Uses (AREA)

NO20003948A 1999-08-05 2000-08-04 Fremgangsmate ved fremstilling av sma perler som inneholder fettloselige substanser NO328117B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP99115458		1999-08-05

Publications (3)

Publication Number	Publication Date
NO20003948D0 NO20003948D0 (no)	2000-08-04
NO20003948L NO20003948L (no)	2001-02-06
NO328117B1 true NO328117B1 (no)	2009-12-14

Family

ID=8238731

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO20003948A NO328117B1 (no)	1999-08-05	2000-08-04	Fremgangsmate ved fremstilling av sma perler som inneholder fettloselige substanser

Country Status (14)

Country	Link
US (1)	US6444227B1 (de)
EP (1)	EP1074592B1 (de)
JP (1)	JP2001131060A (de)
KR (1)	KR100794846B1 (de)
CN (1)	CN1167414C (de)
AT (1)	ATE342316T1 (de)
AU (1)	AU773280B2 (de)
BR (1)	BR0003377B1 (de)
CA (1)	CA2314848C (de)
DE (1)	DE60031208T2 (de)
ES (1)	ES2272223T3 (de)
ID (1)	ID26741A (de)
NO (1)	NO328117B1 (de)
TW (1)	TWI229678B (de)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6936279B2 (en) *	2002-06-18	2005-08-30	Zeavision Llc	Microcrystalline zeaxanthin with high bioavailability in oily carrier formulations
KR100616133B1 (ko) *	2002-11-15	2006-08-28	주식회사 그린바이오텍	유지함유 미세캡슐 제조방법
EP1605917B1 (de) *	2003-03-27	2015-04-22	DSM IP Assets B.V.	Verfahren zur herstellung von vernetzten gelatine-mikroperlen
CN102697737B (zh) *	2003-04-03	2014-03-19	杰西.L.-S.奥	负载肿瘤靶向药物的颗粒
JP5027504B2 (ja) *	2003-07-15	2012-09-19	ディーエスエムアイピーアセッツビー．ブイ．	脂溶性活性成分の粉末状製剤
EP1732405B1 (de) *	2004-03-18	2015-07-22	DSM IP Assets B.V.	Extrusionstabile zusammensetzungen von mehrfach ungesättigten fettsäuren für nahrungsmittelprodukte
JP4525529B2 (ja) *	2005-08-29	2010-08-18	味の素株式会社	加工食品の製造法
US8221809B2 (en) *	2006-06-22	2012-07-17	Martek Biosciences Corporation	Encapsulated labile compound compositions and methods of making the same
JP5275561B2 (ja) *	2006-10-30	2013-08-28	富士フイルム株式会社	水分散可能なナノ粒子
WO2008137831A1 (en) *	2007-05-07	2008-11-13	Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College	Water-soluble nanoparticles containing water-insoluble compounds
JP2008297241A (ja) *	2007-05-31	2008-12-11	Fujifilm Corp	ニキビ用皮膚外用剤
ES2607467T3 (es) *	2007-06-19	2017-03-31	Dsm Ip Assets B.V.	Composiciones de microencapsulación, métodos para hacerlas, métodos de uso y productos de las mismas
EP2153732A1 (de)	2008-08-04	2010-02-17	DSM IP Assets B.V.	Herstellung von Beadlets mit hygroskopischen Pflanzenextrakten
FR2953409B1 (fr) *	2009-12-09	2011-12-23	Adisseo France Sas	Particules de principes actifs liposolubles stables
JP5982382B2 (ja) *	2011-09-13	2016-08-31	理研ビタミン株式会社	多芯型ゼラチンマイクロカプセルの製造方法
JP6163688B2 (ja)	2012-01-19	2017-07-19	ディーエスエムアイピーアセッツビー．ブイ．	デンプンマトリックス中にホップ酸塩を含む小ビーズ
US9248106B2 (en)	2012-01-19	2016-02-02	Dsm Ip Assets B.V.	Beadlets comprising hop acid salts in a protein matrix
GB2515749B (en) *	2013-07-01	2016-08-31	Biodynamic Armor Ltd	Pressure impulse mitigation
CN103549157B (zh) *	2013-11-14	2015-09-02	厦门金达威集团股份有限公司	斥水型维生素微胶囊的制备方法
CN104587920B (zh) *	2015-01-06	2016-08-31	华中科技大学	一种微波加热制备生物大分子包裹微球的方法
CN105688269B (zh) *	2016-02-03	2021-04-16	广州迈普再生医学科技股份有限公司	一种改性明胶止血材料及其制备方法
EP3669663A1 (de)	2018-12-17	2020-06-24	DSM IP Assets B.V.	Neuartige perlenkugeln
EP3718412A1 (de)	2019-04-04	2020-10-07	DSM IP Assets B.V.	Neuartige kügelchen
EP3718411A1 (de)	2019-04-04	2020-10-07	DSM IP Assets B.V.	Neuartige kügelchen
WO2022129004A1 (en)	2020-12-15	2022-06-23	Dsm Ip Assets B.V.	Coated statin tablet comprising vitamin e acetate powder
WO2022129003A1 (en)	2020-12-15	2022-06-23	Dsm Ip Assets B.V.	Multiparticulate solid oral dosage form comprising statin and vitamin e
KR102717164B1 (ko) *	2021-08-17	2024-10-15	한스바이오메드 주식회사	지혈 조성물, 이를 포함하는 지혈 키트, 및 이의 제조 방법

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB993138A (en)	1961-11-22	1965-05-26	Pfizer & Co C	Improvements in the preparation of vitamin-containing beadlets
JPS58149645A (ja) *	1982-03-01	1983-09-06	Ajinomoto Co Inc	ゲル化物の製造法
JPS58184587U (ja) *	1982-06-04	1983-12-08	我喜屋　良明	可撓性線材を有する編針
US4670247A (en) *	1983-07-05	1987-06-02	Hoffman-Laroche Inc.	Process for preparing fat-soluble vitamin active beadlets
EP0285682B2 (de)	1987-04-06	1997-08-06	F. Hoffmann-La Roche Ag	Verfahren zur Herstellung von Vitaminpräparaten
JP2559043B2 (ja) *	1987-08-20	1996-11-27	株式会社小森コーポレーション	印刷機における溝付き胴の紙尻保持装置
US5230969A (en) *	1990-08-09	1993-07-27	Physical Optics Corporation	Composite graft optical polymer
US5126328A (en)	1991-01-10	1992-06-30	Bower David K	Process for crosslinking gelatin
JP3048249B2 (ja) *	1991-03-01	2000-06-05	新田ゼラチン株式会社	不溶化ゼラチンの製造方法
JPH065457A (ja) *	1992-06-16	1994-01-14	Murata Mfg Co Ltd	積層電子部品
US6039901A (en) *	1997-01-31	2000-03-21	Givaudan Roure Flavors Corporation	Enzymatically protein encapsulating oil particles by complex coacervation
JP4494539B2 (ja)	1997-02-28	2010-06-30	ディーエスエムアイピーアセッツビー．ブイ．	流動自由な乾燥粒子
DE19838189A1 (de)	1998-08-24	2000-03-02	Basf Ag	Stabile pulverförmige Vitamin- und Carotinoid-Zubereitungen und Verfahren zu deren Herstellung

2000
- 2000-07-27 US US09/626,976 patent/US6444227B1/en not_active Expired - Lifetime
- 2000-07-31 ES ES00116502T patent/ES2272223T3/es not_active Expired - Lifetime
- 2000-07-31 EP EP00116502A patent/EP1074592B1/de not_active Expired - Lifetime
- 2000-07-31 DE DE60031208T patent/DE60031208T2/de not_active Expired - Lifetime
- 2000-07-31 AT AT00116502T patent/ATE342316T1/de not_active IP Right Cessation
- 2000-08-01 AU AU48963/00A patent/AU773280B2/en not_active Ceased
- 2000-08-02 KR KR1020000044740A patent/KR100794846B1/ko not_active Expired - Lifetime
- 2000-08-02 CA CA002314848A patent/CA2314848C/en not_active Expired - Fee Related
- 2000-08-02 ID IDP20000652D patent/ID26741A/id unknown
- 2000-08-02 JP JP2000233863A patent/JP2001131060A/ja active Pending
- 2000-08-02 TW TW089115504A patent/TWI229678B/zh not_active IP Right Cessation
- 2000-08-04 NO NO20003948A patent/NO328117B1/no not_active IP Right Cessation
- 2000-08-04 CN CNB001225251A patent/CN1167414C/zh not_active Expired - Lifetime
- 2000-08-07 BR BRPI0003377-4A patent/BR0003377B1/pt not_active IP Right Cessation

Also Published As

Publication number	Publication date
BR0003377A (pt)	2001-12-04
CA2314848A1 (en)	2001-02-05
ATE342316T1 (de)	2006-11-15
ES2272223T3 (es)	2007-05-01
KR100794846B1 (ko)	2008-01-15
EP1074592A1 (de)	2001-02-07
BR0003377B1 (pt)	2011-03-09
EP1074592B1 (de)	2006-10-11
AU773280B2 (en)	2004-05-20
NO20003948D0 (no)	2000-08-04
US6444227B1 (en)	2002-09-03
NO20003948L (no)	2001-02-06
CA2314848C (en)	2007-04-10
CN1283454A (zh)	2001-02-14
AU4896300A (en)	2001-02-15
TWI229678B (en)	2005-03-21
CN1167414C (zh)	2004-09-22
DE60031208T2 (de)	2007-01-18
JP2001131060A (ja)	2001-05-15
ID26741A (id)	2001-02-08
DE60031208D1 (de)	2006-11-23
KR20010049964A (ko)	2001-06-15

Legal Events

Date	Code	Title	Description
2020-09-14	MK1K	Patent expired

Publication	Publication Date	Title
CA2314848C (en)	2007-04-10	Process for preparing beadlets containing fat-soluble substances
MXPA00007576A (es)	2002-04-01	Procedimiento para la preparacion de perlitas que contienen substancias solubles en gra
EP0937412B1 (de)	2006-02-01	Herstellung eines fein verteilten, pulverförmigen Carotinoidpräparats
Muhoza et al.	2020	The protection effect of trehalose on the multinuclear microcapsules based on gelatin and high methyl pectin coacervate during freeze-drying
JP2515487B2 (ja)	1996-07-10	活性成分の小球体の製造方法
EP0684973B1 (de)	1997-05-07	Verfahren zum herstellung einer wasserdiepergierbaren pulverfoermigen carotenoidzubereitung
JP3961070B2 (ja)	2007-08-15	カロチノイド組成物の製造方法
US4844934A (en)	1989-07-04	Preparation of finely divided, water-dispersable carotenoid formulations
NO317782B1 (no)	2004-12-13	Sammensetninger som inneholder fettloselige substanser i en karbohydratmatriks
MXPA99001754A (en)	2000-04-24	Continuous procedure for the preparation of a composition in the form of powder of a carotenoid and preparation in form of dust prepared through such procedimie
EP0982038B1 (de)	2003-01-08	Stabile pulverförmige Vitamin- und Carotinoid-Zubereitungen und Vefahren zu deren Herstellung
CN1274246C (zh)	2006-09-13	新的经稳定化处理的类胡萝卜素组合物
JP2001149042A (ja)	2001-06-05	安定な粉末状のビタミンおよび／またはカロチノイド製品ならびにその製法
EP1713575A1 (de)	2006-10-25	Wässrige dispersion und ihre verwendung
EP2683745A1 (de)	2014-01-15	Pulverförmiges säurebeladenes trägermaterial
Tatar Turan et al.	2021	The effect of an ultrasonic spray nozzle on carbohydrate and protein‐based coating materials for blueberry extract microencapsulation
Ordoñez-Santos et al.	2018	Encapsulation of β-carotene extracted from peach palm residues: a stability study using two spray-dried processes
JP2002187837A (ja)	2002-07-05	微粉化カロテノイドを含有する水溶性製剤の製造方法
CN1764439B (zh)	2010-05-26	制备交联明胶珠粒的方法
EP4421064B1 (de)	2025-10-01	Verfahren zur herstellung eines carotinoidmittels
JP3363158B2 (ja)	2003-01-08	でん粉を含有する糖物質を製造する方法及び装置
WO2020184556A1 (ja)	2020-09-17	天然由来の水溶性色素の泡立ちを抑制する方法
HK1027270B (en)	2002-10-18	Water-dispersible carotenoid pigment preparation
HK1027270A1 (en)	2001-01-12	Water-dispersible carotenoid pigment preparation