DE2925364C2 - Verwendung eines stabilisierten Farbstoffs zum Anfärben von Arzneimittelkapseln - Google Patents
Verwendung eines stabilisierten Farbstoffs zum Anfärben von ArzneimittelkapselnInfo
- Publication number
- DE2925364C2 DE2925364C2 DE2925364A DE2925364A DE2925364C2 DE 2925364 C2 DE2925364 C2 DE 2925364C2 DE 2925364 A DE2925364 A DE 2925364A DE 2925364 A DE2925364 A DE 2925364A DE 2925364 C2 DE2925364 C2 DE 2925364C2
- Authority
- DE
- Germany
- Prior art keywords
- dye
- udf54
- udf53
- coloring
- stabilized
- 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
Links
- 239000002775 capsule Substances 0.000 title claims description 9
- 238000004040 coloring Methods 0.000 title claims description 9
- 239000003814 drug Substances 0.000 title claims description 8
- 229940079593 drug Drugs 0.000 title claims description 8
- 239000000975 dye Substances 0.000 claims description 34
- 239000003463 adsorbent Substances 0.000 claims description 15
- 239000002904 solvent Substances 0.000 claims description 7
- 229930182559 Natural dye Natural products 0.000 claims description 5
- 239000000978 natural dye Substances 0.000 claims description 5
- 230000003100 immobilizing effect Effects 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 8
- 238000001179 sorption measurement Methods 0.000 description 8
- 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 6
- VFLDPWHFBUODDF-FCXRPNKRSA-N curcumin Chemical compound C1=C(O)C(OC)=CC(\C=C\C(=O)CC(=O)\C=C\C=2C=C(OC)C(O)=CC=2)=C1 VFLDPWHFBUODDF-FCXRPNKRSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 108010010803 Gelatin Proteins 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 239000004148 curcumin Substances 0.000 description 3
- 235000012754 curcumin Nutrition 0.000 description 3
- 229940109262 curcumin Drugs 0.000 description 3
- VFLDPWHFBUODDF-UHFFFAOYSA-N diferuloylmethane Natural products C1=C(O)C(OC)=CC(C=CC(=O)CC(=O)C=CC=2C=C(OC)C(O)=CC=2)=C1 VFLDPWHFBUODDF-UHFFFAOYSA-N 0.000 description 3
- NWKFECICNXDNOQ-UHFFFAOYSA-N flavylium Chemical compound C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=[O+]1 NWKFECICNXDNOQ-UHFFFAOYSA-N 0.000 description 3
- 239000008273 gelatin Substances 0.000 description 3
- 229920000159 gelatin Polymers 0.000 description 3
- 235000019322 gelatine Nutrition 0.000 description 3
- 235000011852 gelatine desserts Nutrition 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 229960002477 riboflavin Drugs 0.000 description 3
- MIDXCONKKJTLDX-UHFFFAOYSA-N 3,5-dimethylcyclopentane-1,2-dione Chemical compound CC1CC(C)C(=O)C1=O MIDXCONKKJTLDX-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 244000017106 Bixa orellana Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000001654 beetroot red Substances 0.000 description 2
- 235000012677 beetroot red Nutrition 0.000 description 2
- 235000013736 caramel Nutrition 0.000 description 2
- 235000012730 carminic acid Nutrition 0.000 description 2
- 239000003086 colorant Substances 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
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 1
- DHHFDKNIEVKVKS-FMOSSLLZSA-N Betanin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC(C(=C1)O)=CC(C[C@H]2C([O-])=O)=C1[N+]2=C\C=C\1C=C(C(O)=O)N[C@H](C(O)=O)C/1 DHHFDKNIEVKVKS-FMOSSLLZSA-N 0.000 description 1
- DHHFDKNIEVKVKS-MVUYWVKGSA-N Betanin Natural products O=C(O)[C@@H]1NC(C(=O)O)=C/C(=C\C=[N+]/2\[C@@H](C(=O)[O-])Cc3c\2cc(O)c(O[C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O2)c3)/C1 DHHFDKNIEVKVKS-MVUYWVKGSA-N 0.000 description 1
- 235000006010 Bixa orellana Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 244000163122 Curcuma domestica Species 0.000 description 1
- 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 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000004258 Ethoxyquin Substances 0.000 description 1
- QAQJMLQRFWZOBN-LAUBAEHRSA-N L-ascorbyl-6-palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)[C@H]1OC(=O)C(O)=C1O QAQJMLQRFWZOBN-LAUBAEHRSA-N 0.000 description 1
- 235000000072 L-ascorbyl-6-palmitate Nutrition 0.000 description 1
- 239000011786 L-ascorbyl-6-palmitate 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
- 229910019142 PO4 Inorganic materials 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229930003270 Vitamin B Natural products 0.000 description 1
- 239000002156 adsorbate Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 235000012665 annatto Nutrition 0.000 description 1
- 239000010362 annatto Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000002185 betanin Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000012978 bixa orellana Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000004106 carminic acid Substances 0.000 description 1
- DGQLVPJVXFOQEV-NGOCYOHBSA-N carminic acid Chemical compound OC1=C2C(=O)C=3C(C)=C(C(O)=O)C(O)=CC=3C(=O)C2=C(O)C(O)=C1[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O DGQLVPJVXFOQEV-NGOCYOHBSA-N 0.000 description 1
- 229940114118 carminic acid Drugs 0.000 description 1
- 150000001746 carotenes Chemical class 0.000 description 1
- 235000005473 carotenes Nutrition 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- -1 ethanol or propanol Chemical class 0.000 description 1
- 235000019285 ethoxyquin Nutrition 0.000 description 1
- 229940093500 ethoxyquin Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007903 gelatin capsule Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 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
- 235000019156 vitamin B Nutrition 0.000 description 1
- 239000011720 vitamin B Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B61/00—Dyes of natural origin prepared from natural sources, e.g. vegetable sources
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B63/00—Lakes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH797678A CH642990A5 (de) | 1978-07-24 | 1978-07-24 | Verfahren zum faerben von gelatine fuer kapseln mit hilfe eines gegen den abbau durch licht oder oxidation stabilisierten natuerlichen farbstoffes. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2925364A1 DE2925364A1 (de) | 1980-02-28 |
| DE2925364C2 true DE2925364C2 (de) | 1987-01-15 |
Family
ID=4333251
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2925364A Expired DE2925364C2 (de) | 1978-07-24 | 1979-06-22 | Verwendung eines stabilisierten Farbstoffs zum Anfärben von Arzneimittelkapseln |
Country Status (14)
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE148681T1 (de) * | 1983-12-21 | 1985-11-21 | Secta-Laboratoires De Cosmetologie Yves Rocher, Paris | Verfahren zum faerben mit pulverfoermigen farbstoffen und zusammensetzung zur durchfuehrung desselben. |
| FR2574098B1 (fr) * | 1984-12-04 | 1986-12-26 | Rocher Secta Labo Cosmetologie | Procede de teinture avec des colorants en poudre et composition pour sa realisation |
| FR2557123B1 (fr) * | 1983-12-21 | 1987-07-03 | Rocher Secta Labo Cosmetologie | Procede de realisation d'extraits colorants vegetaux et leurs utilisations |
| DE3532129A1 (de) * | 1985-09-10 | 1987-03-12 | Bayer Ag | Ss-carotin enthaltende gelatine |
| LU86946A1 (fr) * | 1987-07-17 | 1989-03-08 | Oreal | Poudre ultrafine comportant des pigments melaniques,son procede de preparation et son utilisation en cosmetique |
| DE4200349C2 (de) * | 1992-01-09 | 1997-08-28 | Georg Dr Buech | Verfahren zur Herstellung eines natürlichen, stabilen grünen Farbstoffes auf Basis von Chlorophyll für die Lebensmittel-, Kosmetik- und Pharmaindustrie |
| US5424301A (en) * | 1993-02-01 | 1995-06-13 | Warner-Lambert Company | Starch stabilized o-substituted tetrahydropyridine oxime cholinergic agents |
| US6000928A (en) * | 1997-04-03 | 1999-12-14 | Technophar Equipment & Service Limited | Capsule making machine having improved pin bars and air flow characteristics |
| US5945136A (en) * | 1997-04-03 | 1999-08-31 | Technophar Equipment & Service Limited | Heating elevator for capsule making machine |
| US6171602B1 (en) | 1997-08-29 | 2001-01-09 | E-L Management Corp. | Natural pigment-containing flowable powder |
| ES2350822T3 (es) * | 1999-08-31 | 2011-01-27 | Chugai Seiyaku Kabushiki Kaisha | Cápsulas blandas. |
| IT1317743B1 (it) * | 2000-01-28 | 2003-07-15 | Carlo Ghisalberti | Composizioni cosmetiche decorative e lacche vegetali. |
| US8623429B2 (en) | 2007-03-15 | 2014-01-07 | Omnica Gmbh | Stabilized anthocyanin compositions |
| US7820207B2 (en) * | 2007-03-15 | 2010-10-26 | Omnica Gmbh | Stabilized anthocyanin compositions |
| US8894980B2 (en) | 2007-11-19 | 2014-11-25 | U.S. Cosmetics Corporation | Wet cake composition for cosmetic products and methods of use |
| EP2727577A1 (en) * | 2007-05-07 | 2014-05-07 | U.S. Cosmetics Corporation | Colour pigment powder, pigment dispersion and method of manufacture |
| FR2918274B1 (fr) * | 2007-07-06 | 2009-12-18 | Saint Laurent Parfums | Composition cosmetique ayant des proprietes anti-radicalaires et procede d'application correspondant |
| US20090321087A1 (en) * | 2008-06-27 | 2009-12-31 | Electrical/Electronic Mechanical Industrial Equipment Ltd. | Expandable plug |
| DE102009019411A1 (de) | 2009-04-29 | 2010-11-04 | Bayer Technology Services Gmbh | Verfahren zur UV-Stabilisierung von organischen Substanzen |
| FR2963558A1 (fr) * | 2010-08-05 | 2012-02-10 | Chanel Parfums Beaute | Materiau cosmetique comprenant un extrait de bois de sappan supporte sur une argile |
| EP3236993B1 (en) | 2014-12-23 | 2023-09-13 | Theriva Biologics, Inc. | Methods and compositions for inhibiting or preventing adverse effects of oral antibiotics |
| CN111328284A (zh) | 2017-08-07 | 2020-06-23 | 芬奇治疗公司 | 用于维持和恢复健康的肠道屏障的组合物和方法 |
| EP3737750B1 (en) | 2018-01-09 | 2024-06-05 | Theriva Biologics, Inc. | Alkaline phosphatase agents for treatment of neurodevelopmental disorders |
| AU2019224114A1 (en) | 2018-02-23 | 2020-09-10 | Finch Therapeutics Holdings Llc | Microbiome related immunotherapies |
| EP3773686B1 (en) | 2018-03-20 | 2023-06-07 | Theriva Biologics, Inc. | Alkaline phosphatase agents for treatment of radiation disorders |
| CA3146738A1 (en) | 2019-07-18 | 2021-01-21 | Synthetic Biologics, Inc. | Intestinal alkaline phosphatase-based treatments of metabolic disorders |
| AU2020316330A1 (en) | 2019-07-19 | 2022-01-06 | Finch Therapeutics Holdings Llc. | Methods and products for treatment of gastrointestinal disorders |
| JP2022547330A (ja) | 2019-09-13 | 2022-11-11 | フィンチ セラピューティクス ホールディングス エルエルシー | 自閉症スペクトラム障害を治療するための組成物および方法 |
| US20240226187A9 (en) | 2019-10-18 | 2024-07-11 | Finch Therapeutics Holdings Llc | Compositions and Methods for Delivering a Bacterial Metabolite to a Subject |
| WO2021097288A1 (en) | 2019-11-15 | 2021-05-20 | Finch Therapeutics Holdings Llc | Compositions and methods for treating neurodegenerative diseases |
| WO2021142347A1 (en) | 2020-01-10 | 2021-07-15 | Finch Therapeutics Holdings Llc | Compositions and methods for non-alcoholic steatohepatitis (nash) |
| WO2021142358A1 (en) | 2020-01-10 | 2021-07-15 | Finch Therapeutics Holdings Llc | Compositions and methods for treating hepatic encephalopathy (he) |
| TW202140049A (zh) | 2020-01-10 | 2021-11-01 | 美商芬奇治療控股有限責任公司 | 用於治療ｂ型肝炎（ｈｂｖ）及ｄ型肝炎（ｈｄｖ）之組合物及方法 |
| US20230201265A1 (en) | 2020-03-31 | 2023-06-29 | Finch Therapeutics Holdings Llc | Compositions comprising non-viable fecal microbiota and methods of use thereof |
| US20240263251A1 (en) | 2021-02-19 | 2024-08-08 | Finch Therapeutics Holdings Llc | Compositions and methods for providing secondary bile acids to a subject |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1303426A (en) * | 1919-05-13 | Edward j | ||
| US1337673A (en) * | 1917-05-18 | 1920-04-20 | Kalmus Comstock & Wescott Inc | Dye recovery |
| FR1291155A (fr) | 1961-05-13 | 1962-04-20 | Benckiser Gmbh Joh A | Procédé de préparation de colorants naturels à partir de fruits ou autres parties de plantes |
| FR6760M (US07488766-20090210-C00029.png) | 1967-05-30 | 1969-03-03 | ||
| US4082660A (en) * | 1972-11-03 | 1978-04-04 | Agence Nationale De Valorisation De La Recherche | Method of purification |
| FR2299385A1 (fr) | 1975-02-03 | 1976-08-27 | Finedoc Sica Sa | Procede d'extraction des anthocyanes des fruits |
| FR2378040B1 (US07488766-20090210-C00029.png) | 1977-01-24 | 1981-01-02 | Rhone Poulenc Ind |
-
1978
- 1978-07-24 CH CH797678A patent/CH642990A5/de not_active IP Right Cessation
-
1979
- 1979-06-22 DE DE2925364A patent/DE2925364C2/de not_active Expired
- 1979-06-29 AU AU48543/79A patent/AU536287B2/en not_active Ceased
- 1979-06-29 FR FR7917070A patent/FR2432035B1/fr not_active Expired
- 1979-07-13 US US06/057,485 patent/US4268265A/en not_active Expired - Lifetime
- 1979-07-16 JP JP9024979A patent/JPS5518480A/ja active Pending
- 1979-07-17 CA CA000331991A patent/CA1147103A/en not_active Expired
- 1979-07-18 IT IT24457/79A patent/IT1122212B/it active
- 1979-07-19 ES ES482634A patent/ES482634A1/es not_active Expired
- 1979-07-20 KR KR7902438A patent/KR820001872B1/ko not_active IP Right Cessation
- 1979-07-20 PT PT69951A patent/PT69951A/pt unknown
- 1979-07-20 GB GB7925440A patent/GB2030161B/en not_active Expired
- 1979-07-23 IN IN752/CAL/79A patent/IN151640B/en unknown
- 1979-07-23 BE BE0/196414A patent/BE877842A/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| AU4854379A (en) | 1980-01-31 |
| AU536287B2 (en) | 1984-05-03 |
| CA1147103A (en) | 1983-05-31 |
| CH642990A5 (de) | 1984-05-15 |
| US4268265A (en) | 1981-05-19 |
| BE877842A (fr) | 1980-01-23 |
| IT1122212B (it) | 1986-04-23 |
| FR2432035A1 (fr) | 1980-02-22 |
| FR2432035B1 (fr) | 1986-04-04 |
| IT7924457A0 (it) | 1979-07-18 |
| GB2030161B (en) | 1982-12-22 |
| IN151640B (US07488766-20090210-C00029.png) | 1983-06-18 |
| DE2925364A1 (de) | 1980-02-28 |
| ES482634A1 (es) | 1980-04-16 |
| KR820001872B1 (ko) | 1982-10-16 |
| PT69951A (en) | 1979-08-01 |
| GB2030161A (en) | 1980-04-02 |
| JPS5518480A (en) | 1980-02-08 |
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