NO317265B1 - Fremgangsmate for fremstilling av aloin ved hjelp av ekstraksjon - Google Patents
Fremgangsmate for fremstilling av aloin ved hjelp av ekstraksjon Download PDFInfo
- Publication number
- NO317265B1 NO317265B1 NO20006424A NO20006424A NO317265B1 NO 317265 B1 NO317265 B1 NO 317265B1 NO 20006424 A NO20006424 A NO 20006424A NO 20006424 A NO20006424 A NO 20006424A NO 317265 B1 NO317265 B1 NO 317265B1
- Authority
- NO
- Norway
- Prior art keywords
- extraction
- aloin
- aloe
- glycol
- triol
- Prior art date
Links
- AFHJQYHRLPMKHU-UHFFFAOYSA-N isobarbaloin Natural products OC1C(O)C(O)C(CO)OC1C1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC=C21 AFHJQYHRLPMKHU-UHFFFAOYSA-N 0.000 title claims abstract description 41
- AFHJQYHRLPMKHU-WEZNYRQKSA-N aloin B Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1[C@H]1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC=C21 AFHJQYHRLPMKHU-WEZNYRQKSA-N 0.000 title claims abstract description 40
- AFHJQYHRLPMKHU-XXWVOBANSA-N Aloin Natural products O=C1c2c(O)cc(CO)cc2[C@H]([C@H]2[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O2)c2c1c(O)ccc2 AFHJQYHRLPMKHU-XXWVOBANSA-N 0.000 title claims abstract description 39
- CPUHNROBVJNNPW-UHFFFAOYSA-N aloin A Natural products OC1C(O)C(O)C(CO)OC1OC1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC=C21 CPUHNROBVJNNPW-UHFFFAOYSA-N 0.000 title claims abstract description 39
- 238000000605 extraction Methods 0.000 title claims abstract description 30
- 238000002360 preparation method Methods 0.000 title claims abstract 3
- 238000000034 method Methods 0.000 title claims description 28
- 235000011399 aloe vera Nutrition 0.000 claims abstract description 19
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims abstract description 14
- 241001116389 Aloe Species 0.000 claims abstract description 14
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 claims abstract description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 30
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 24
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 23
- 235000011389 fruit/vegetable juice Nutrition 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- 238000000746 purification Methods 0.000 claims description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 8
- 238000001953 recrystallisation Methods 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 6
- 235000002961 Aloe barbadensis Nutrition 0.000 claims description 5
- 244000186892 Aloe vera Species 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 238000002425 crystallisation Methods 0.000 claims description 3
- 230000008025 crystallization Effects 0.000 claims description 3
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 claims description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 2
- 239000000047 product Substances 0.000 description 9
- 239000007858 starting material Substances 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 3
- 235000008504 concentrate Nutrition 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- YDQWDHRMZQUTBA-UHFFFAOYSA-N Aloe emodin Chemical compound C1=CC=C2C(=O)C3=CC(CO)=CC(O)=C3C(=O)C2=C1O YDQWDHRMZQUTBA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- AFHJQYHRLPMKHU-GIWDNFATSA-N 1,8-dihydroxy-3-(hydroxymethyl)-10-[(3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10h-anthracen-9-one Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1C1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC=C21 AFHJQYHRLPMKHU-GIWDNFATSA-N 0.000 description 1
- POJWUDADGALRAB-PVQJCKRUSA-N Allantoin Natural products NC(=O)N[C@@H]1NC(=O)NC1=O POJWUDADGALRAB-PVQJCKRUSA-N 0.000 description 1
- 229920001875 Ebonite Polymers 0.000 description 1
- -1 H-propanol Chemical compound 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229960000458 allantoin Drugs 0.000 description 1
- RJGDLRCDCYRQOQ-UHFFFAOYSA-N anthrone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3CC2=C1 RJGDLRCDCYRQOQ-UHFFFAOYSA-N 0.000 description 1
- 230000002456 anti-arthritic effect Effects 0.000 description 1
- 230000003356 anti-rheumatic effect Effects 0.000 description 1
- 239000003435 antirheumatic agent Substances 0.000 description 1
- 206010003246 arthritis Diseases 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 210000000416 exudates and transudate Anatomy 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000008141 laxative Substances 0.000 description 1
- 230000002475 laxative effect Effects 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 201000008482 osteoarthritis Diseases 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H7/00—Compounds containing non-saccharide radicals linked to saccharide radicals by a carbon-to-carbon bond
- C07H7/04—Carbocyclic radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compounds Of Unknown Constitution (AREA)
- Medicines Containing Plant Substances (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/IB1999/000771 WO2000066601A1 (fr) | 1999-04-28 | 1999-04-28 | Procede de preparation d'aloine par extraction |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20006424D0 NO20006424D0 (no) | 2000-12-15 |
| NO20006424L NO20006424L (no) | 2001-02-26 |
| NO317265B1 true NO317265B1 (no) | 2004-09-27 |
Family
ID=11004854
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20006424A NO317265B1 (no) | 1999-04-28 | 2000-12-15 | Fremgangsmate for fremstilling av aloin ved hjelp av ekstraksjon |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US6506387B1 (zh) |
| EP (1) | EP1091970B1 (zh) |
| JP (1) | JP4698841B2 (zh) |
| KR (1) | KR100529765B1 (zh) |
| CN (1) | CN1144809C (zh) |
| AT (1) | ATE240965T1 (zh) |
| AU (1) | AU774470B2 (zh) |
| BR (1) | BR9911646A (zh) |
| CA (1) | CA2334656C (zh) |
| CZ (1) | CZ293949B6 (zh) |
| DE (1) | DE69908127T2 (zh) |
| DK (1) | DK1091970T3 (zh) |
| ES (1) | ES2197632T3 (zh) |
| HK (1) | HK1038567A1 (zh) |
| HU (1) | HUP0200346A3 (zh) |
| IL (2) | IL140469A0 (zh) |
| MX (1) | MXPA00012485A (zh) |
| NO (1) | NO317265B1 (zh) |
| NZ (1) | NZ508963A (zh) |
| PL (1) | PL192930B1 (zh) |
| PT (1) | PT1091970E (zh) |
| SI (1) | SI20820A (zh) |
| SK (1) | SK283953B6 (zh) |
| TR (1) | TR200100738T1 (zh) |
| WO (1) | WO2000066601A1 (zh) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7534770B2 (en) * | 2004-03-31 | 2009-05-19 | Morinaga Milk Industry Co., Ltd. | Glycoside having 4-methylergost-7-en-3-ol skeleton and hyperglycemia improving agent |
| EP1666446A1 (en) * | 2004-11-12 | 2006-06-07 | Laboratoire Medidom S.A. | Process for preparing rhein and diacerein |
| GB0511051D0 (en) * | 2005-05-31 | 2005-07-06 | Exxonmobil Chem Patents Inc | Molecular sieve catalyst treatment |
| JP4162703B2 (ja) * | 2005-09-22 | 2008-10-08 | 森永乳業株式会社 | 内臓脂肪蓄積抑制剤 |
| CN101804144A (zh) * | 2005-09-22 | 2010-08-18 | 森永乳业株式会社 | 内脏脂肪蓄积抑制剂 |
| CN100453548C (zh) * | 2006-10-11 | 2009-01-21 | 上海华震科技有限公司 | 一种从芦荟制品中分离高纯度芦荟苷的方法 |
| FR2908770B1 (fr) * | 2006-11-21 | 2009-02-06 | Pierre Fabre Medicament Sa | Procede d'extraction d'aloine |
| CN104844547B (zh) * | 2015-04-30 | 2017-03-01 | 云南万绿生物股份有限公司 | 一种芦荟苷的高效提取和分级纯化方法 |
| CN106421282A (zh) * | 2016-10-20 | 2017-02-22 | 王凯茜 | 一种治疗非淋球菌性细菌性关节炎的中药 |
| ES2684782B1 (es) * | 2017-03-29 | 2019-04-24 | Biovet S A | Producto alimenticio para animales que comprende aloína, apigenina y ácido cafeico y procedimiento para su obtención |
| CN115919960B (zh) * | 2022-12-24 | 2024-06-07 | 河北万邦复临药业有限公司 | 一种芦荟的精制方法 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4966892A (en) * | 1982-05-07 | 1990-10-30 | Carrington Laboratories, Inc. | Processes for preparation of aloe products products produced thereby and compositions thereof |
| US4670263A (en) * | 1983-12-29 | 1987-06-02 | Noorlander Daniel O | Nontoxic, germicide, and healing compositions |
| US4602004A (en) | 1984-06-14 | 1986-07-22 | Maurice Cohen | Aloin and aloe-emodin containing pesticides |
| JPS61109708A (ja) * | 1984-10-31 | 1986-05-28 | Kobayashi Kooc:Kk | 化粧料 |
| JPS63501221A (ja) * | 1985-06-28 | 1988-05-12 | カ−リントン ラボラトリ−ズ インコ−ポレ−テツド | アロエ製品の製造方法、該方法によって得られた製品およびその組成物 |
| DE3665262D1 (en) | 1985-06-28 | 1989-10-05 | Carrington Lab Inc | Processes for preparation of aloe products, products produced thereby and compositions thereof |
| US4957907A (en) * | 1985-06-28 | 1990-09-18 | Carrington Laboratories Inc. | Process for preparation of aloe products |
| GB8829782D0 (en) | 1988-12-21 | 1989-02-15 | Gamut International Inc | Isolation of aloe-emodin |
| WO1992006701A1 (en) * | 1990-10-18 | 1992-04-30 | Huffstutler, M., Conrad, Jr. | Preparation of concentrated fluid symphytum extracts, therapeutic forms and methods of use |
| JP3685833B2 (ja) * | 1995-02-06 | 2005-08-24 | 日本メナード化粧品株式会社 | 免疫抑制改善剤 |
| JPH10120576A (ja) * | 1996-10-16 | 1998-05-12 | Kureha Chem Ind Co Ltd | Ｈｓｐ６０ファミリーに属するタンパク質のアロイン誘導体含有合成抑制剤 |
| JPH1135431A (ja) * | 1997-07-24 | 1999-02-09 | Hideo Asada | アロエの薬効成分の抽出方法及び育毛剤 |
| US6290964B1 (en) * | 1998-03-06 | 2001-09-18 | Kathleen Shupe | Antimicrobial agents isolated from aloe vera |
| US6309675B1 (en) * | 1999-07-21 | 2001-10-30 | Nancy Laning Sobczak | Therapeutic composition including plantain and aloe vera for treatment of arthritis and other afflictions |
-
1999
- 1999-04-20 US US09/701,955 patent/US6506387B1/en not_active Expired - Fee Related
- 1999-04-28 AU AU33413/99A patent/AU774470B2/en not_active Ceased
- 1999-04-28 SI SI9920051A patent/SI20820A/sl not_active IP Right Cessation
- 1999-04-28 JP JP2000615630A patent/JP4698841B2/ja not_active Expired - Fee Related
- 1999-04-28 HU HU0200346A patent/HUP0200346A3/hu unknown
- 1999-04-28 SK SK1988-2000A patent/SK283953B6/sk not_active IP Right Cessation
- 1999-04-28 PL PL345150A patent/PL192930B1/pl not_active IP Right Cessation
- 1999-04-28 IL IL14046999A patent/IL140469A0/xx active IP Right Grant
- 1999-04-28 ES ES99914703T patent/ES2197632T3/es not_active Expired - Lifetime
- 1999-04-28 MX MXPA00012485A patent/MXPA00012485A/es active IP Right Grant
- 1999-04-28 DE DE69908127T patent/DE69908127T2/de not_active Expired - Lifetime
- 1999-04-28 DK DK99914703T patent/DK1091970T3/da active
- 1999-04-28 CZ CZ20004775A patent/CZ293949B6/cs not_active IP Right Cessation
- 1999-04-28 CN CNB998079634A patent/CN1144809C/zh not_active Expired - Fee Related
- 1999-04-28 WO PCT/IB1999/000771 patent/WO2000066601A1/fr active IP Right Grant
- 1999-04-28 NZ NZ508963A patent/NZ508963A/en unknown
- 1999-04-28 KR KR10-2000-7014596A patent/KR100529765B1/ko not_active IP Right Cessation
- 1999-04-28 TR TR2001/00738T patent/TR200100738T1/xx unknown
- 1999-04-28 AT AT99914703T patent/ATE240965T1/de not_active IP Right Cessation
- 1999-04-28 PT PT99914703T patent/PT1091970E/pt unknown
- 1999-04-28 EP EP99914703A patent/EP1091970B1/fr not_active Expired - Lifetime
- 1999-04-28 BR BR9911646-4A patent/BR9911646A/pt not_active IP Right Cessation
- 1999-04-28 CA CA002334656A patent/CA2334656C/en not_active Expired - Fee Related
-
2000
- 2000-12-15 NO NO20006424A patent/NO317265B1/no not_active IP Right Cessation
- 2000-12-21 IL IL140469A patent/IL140469A/en not_active IP Right Cessation
-
2001
- 2001-12-27 HK HK01109070A patent/HK1038567A1/xx not_active IP Right Cessation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |