RU97107020A - COMPOSITION OF STEROLES FROM SOAP AS A PULPA - Google Patents

COMPOSITION OF STEROLES FROM SOAP AS A PULPA

Info

Publication number
RU97107020A
RU97107020A RU97107020/04A RU97107020A RU97107020A RU 97107020 A RU97107020 A RU 97107020A RU 97107020/04 A RU97107020/04 A RU 97107020/04A RU 97107020 A RU97107020 A RU 97107020A RU 97107020 A RU97107020 A RU 97107020A
Authority
RU
Russia
Prior art keywords
composition
stigmastanol
campesterol
sitosterol
beta
Prior art date
Application number
RU97107020/04A
Other languages
Russian (ru)
Other versions
RU2165431C2 (en
Inventor
Новак Эгон
П.Катни Джеймс
Дж.Джонс Питер
Original Assignee
Дзе Юниверсити оф Бритиш Колумбия
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.)
Filing date
Publication date
Application filed by Дзе Юниверсити оф Бритиш Колумбия filed Critical Дзе Юниверсити оф Бритиш Колумбия
Publication of RU97107020A publication Critical patent/RU97107020A/en
Application granted granted Critical
Publication of RU2165431C2 publication Critical patent/RU2165431C2/en

Links

Claims (13)

1. Способ выделения композиции фитостеролов из мыла растительного происхождения в виде пульпы, который включает на первом этапе, смешивание мыла в виде пульпы со смесью растворителей, содержащей кетон, выбранный из группы, имеющей общую структуру RCOR1, где R и R1 являются алкильными группами, алифатический углеводород, выбранный из C5-C10 углеводородов и воды, и не содержащей спирта, при температуре, обычно, от 25 до 150oC, с образованием кремообразного осадка; и на втором этапе, очистку кремообразного осадка с получением композиции фитостерола.1. The method of isolating the composition of phytosterols from soap of plant origin in the form of pulp, which includes, at the first stage, mixing soap in the form of pulp with a solvent mixture containing a ketone selected from the group having the general structure RCOR 1 , where R and R 1 are alkyl groups an aliphatic hydrocarbon selected from C 5 -C 10 hydrocarbons and water, and not containing alcohol, at a temperature of usually from 25 to 150 o C, with the formation of a creamy precipitate; and in a second step, purifying the creamy precipitate to obtain a phytosterol composition. 2. Способ по п. 1, отличающийся тем, что кремообразный осадок очищают кристаллизацией с получением композиции фитостерола. 2. The method according to p. 1, characterized in that the creamy precipitate is purified by crystallization to obtain a phytosterol composition. 3. Способ по п.1, отличающийся тем, что мыло в виде пульпы получают из древесных стружек, включающих стружки кедра, ели, сосны, пихты, дуба, тсуги и тополя. 3. The method according to claim 1, characterized in that the soap in the form of pulp is obtained from wood chips, including shavings of cedar, spruce, pine, fir, oak, tsuga and poplar. 4. Композиция, понижающая холестерин, содержащая не более 70% по весу бета-ситостерола по крайней мере 10% по весу кампестерола и дополнительно, содержащая стигмастанол. 4. A cholesterol lowering composition containing not more than 70% by weight of beta-sitosterol at least 10% by weight of campesterol and additionally containing stigmastanol. 5. Композиция по п.4, отличающаяся тем, что общее содержание кампестерола и стигмастанола составляет по крайней мере 50% от количества бета-ситостерола. 5. The composition according to claim 4, characterized in that the total content of campesterol and stigmastanol is at least 50% of the amount of beta-sitosterol. 6. Композиция по п.4, отличающаяся тем, что соотношение бета-ситостерола, кампестерола и стигмастанола составляет 1,0 к от 0,2 до 0,4, к от 0,2 до 0,5 соответственно. 6. The composition according to claim 4, characterized in that the ratio of beta-sitosterol, campesterol and stigmastanol is 1.0 to 0.2 to 0.4, to 0.2 to 0.5, respectively. 7. Композиция по п.4, отличающаяся тем, что соотношение бета-ситостерола, кампестерола и стигмастанола составляет 1,0 : 0,354 : 0,414 соответственно. 7. The composition according to claim 4, characterized in that the ratio of beta-sitosterol, campesterol and stigmastanol is 1.0: 0.354: 0.414, respectively. 8. Композиция по п.4, отличающаяся тем, что соотношение бета-ситостерола, кампестерола и стигмастанола составляет 1,0 : 0,330 : 0,203 соответственно. 8. The composition according to claim 4, characterized in that the ratio of beta-sitosterol, campesterol and stigmastanol is 1.0: 0.330: 0.203, respectively. 9. Композиция по п.4, содержащая следующее соотношение фитостеролов: - 1,0 бета-ситостерола к 0,268 кампестерола к 0,299 стигмастанола. 9. The composition according to claim 4, containing the following ratio of phytosterols: - 1.0 beta-sitosterol to 0.268 campesterol to 0.299 stigmastanol. 10. Композиция, полученная способом, по п.1. 10. The composition obtained by the method according to claim 1. 11. Использование композиции по п.4 для производства медикаментов для снижения концентрации липопротеина-холестерина низкой плотности в плазме. 11. The use of the composition according to claim 4 for the manufacture of medicines to reduce the concentration of low density lipoprotein-cholesterol in plasma. 12. Продукт терапевтически эффективный для предотвращения или лечения первичной и вторичной дислипидимии и атеросклероза, включающий композицию по п.4 и фармацевтически эффективный носитель. 12. The product is therapeutically effective for the prevention or treatment of primary and secondary dyslipidimia and atherosclerosis, comprising the composition according to claim 4 and a pharmaceutically effective carrier. 13. Композиция по п.10, которая дополнительно включает сопутствующие соединения. 13. The composition of claim 10, which further includes concomitant compounds.
RU97107020/04A 1994-09-29 1995-09-29 Method of isolation of phytosterol composition, compositions, therapeutic product RU2165431C2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US31494594A 1994-09-29 1994-09-29
US314,945 1994-09-29
US314.945 1994-09-29

Publications (2)

Publication Number Publication Date
RU97107020A true RU97107020A (en) 1999-05-20
RU2165431C2 RU2165431C2 (en) 2001-04-20

Family

ID=23222178

Family Applications (1)

Application Number Title Priority Date Filing Date
RU97107020/04A RU2165431C2 (en) 1994-09-29 1995-09-29 Method of isolation of phytosterol composition, compositions, therapeutic product

Country Status (28)

Country Link
US (1) US5770749A (en)
EP (3) EP1707572B1 (en)
JP (1) JPH10506394A (en)
CN (1) CN1057768C (en)
AT (1) ATE216395T1 (en)
AU (1) AU3559795A (en)
BG (1) BG64054B1 (en)
BR (1) BR9509119A (en)
CA (1) CA2201328A1 (en)
CZ (1) CZ298622B6 (en)
DE (1) DE69526442T3 (en)
DK (2) DK1707572T3 (en)
EE (1) EE9700073A (en)
ES (2) ES2173966T5 (en)
GE (1) GEP20022657B (en)
HU (1) HUT77522A (en)
LT (1) LT4305B (en)
LV (1) LV11900B (en)
MD (1) MD1721C2 (en)
MX (1) MX9702308A (en)
NO (2) NO310293B1 (en)
NZ (1) NZ293210A (en)
PL (1) PL186441B1 (en)
PT (1) PT783514E (en)
RU (1) RU2165431C2 (en)
SK (1) SK284250B6 (en)
TJ (1) TJ302B (en)
WO (1) WO1996010033A1 (en)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5965449A (en) * 1996-07-03 1999-10-12 Forbes Medi-Tech, Inc. Method of assessing risk for cardiovascular disease and other disorders and phytosterol-based compositions useful in preventing and treating cardiovascular disease and other disorders
US6139872A (en) * 1996-08-14 2000-10-31 Henkel Corporation Method of producing a vitamin product
US5985936A (en) * 1997-12-18 1999-11-16 Forbes Medi-Tech, Inc. Method of preventing and delaying onset of Alzheimer's disease and composition therefor
US5952393A (en) * 1998-02-12 1999-09-14 Sorkin, Jr.; Harlan Lee Composition for reducing serum cholesterol levels
US6110502A (en) * 1998-02-19 2000-08-29 Mcneil-Ppc, Inc. Method for producing water dispersible sterol formulations
NZ508645A (en) * 1998-06-05 2003-10-31 Forbes Medi Tech Inc Compositions comprising phytosterol and/or phytostanol having enhanced solubility and dispersability and the use of these compositions to lower serum cholesterol
CA2346881A1 (en) 1998-07-20 2000-02-03 Egon Novak Compositions comprising phytosterol, phytostanol or mixtures of both and omega-3 fatty acids or derivatives thereof and use of the composition in treating or preventing cardiovascular disease and other disorders
US6242001B1 (en) 1998-11-30 2001-06-05 Mcneil-Ppc, Inc. Method for producing dispersible sterol and stanol compounds
DE19916034C1 (en) * 1999-04-09 2000-08-03 Cognis Deutschland Gmbh Isolation of phytosterols following methyl esterification of rape seed or soya fatty acids comprises crystallization from 25 - 75 wt. % methanol, useful as hypocholesterolemic agents in drugs and foods
CA2372154A1 (en) * 1999-04-27 2000-11-02 James P. Kutney Process of purifying phytosterols from wood or plant-derived sources and compositions resulting therefrom
EP1190025B1 (en) * 1999-04-27 2003-03-05 Sterol Technologies Ltd. Extraction and isolation method
US6770767B1 (en) * 1999-04-27 2004-08-03 Sterol Techologies Ltd. Method for the extraction and isolation of neutral substances from a soap
FI991533A (en) * 1999-07-05 2001-01-06 Sohkar Oy Method for treating organic matter
WO2001015552A1 (en) * 1999-08-30 2001-03-08 Ocean Nutrition Canada Ltd. A nutritional supplement for lowering serum triglyceride and cholesterol levels
US6998501B1 (en) 1999-08-30 2006-02-14 Ocean Nutrition Canada Limited Nutritional supplement for lowering serum triglyceride and cholesterol levels
US6197832B1 (en) 1999-09-14 2001-03-06 Harlan Lee Sorkin, Jr. Composition for reducing serum cholesterol levels
NZ519268A (en) * 1999-12-15 2004-12-24 Mcneil Ppc Inc Cholesterol lowering comestibles comprising policosanol (predominately octasanol) and sterol
US6355274B1 (en) 1999-12-15 2002-03-12 Mcneil-Ppc, Inc. Encapsulated long chain alcohols
US7232574B1 (en) 1999-12-15 2007-06-19 Mcneil-Ppc, Inc. Long chain alcohols provided in edible oils
BR0001794A (en) * 2000-05-15 2001-12-26 Laboratorios Biosintetica Ltda Application of phytosteroids (and their isomers), folic acid, cyanocobalamin and pyridoxine in dietary fibers (food)
US7147859B2 (en) * 2000-05-15 2006-12-12 Laboratorios Biosintetica Ltda. Application of phytosterols (and their isomers), folic acid, cyanocobalamin and pyridoxin in dietetic (alimentary) fibers
JP4707862B2 (en) * 2001-04-16 2011-06-22 花王株式会社 Production of plant sterols
WO2003009854A1 (en) * 2001-07-20 2003-02-06 Lonza Ag Lipid lowering composition comprising carnitine and phytosterol
US7368138B2 (en) * 2002-03-21 2008-05-06 Archer-Daniels-Midland Company Extraction of phytosterols from corn fiber using green solvents
CA2433246A1 (en) * 2003-06-25 2004-12-25 Telum Technologies Inc. Process for recovering value-added products from pulping soap
WO2007071036A1 (en) * 2005-12-20 2007-06-28 Forbes Medi-Tech Inc. Emulsions comprising non-esterified phytosterols in the aqueous phase
US8309156B2 (en) * 2005-12-20 2012-11-13 Pharmachem Laboratories, Inc. Compositions comprising one or more phytosterols and/or phytostanols, or derivatives thereof, and high HLB emulsifiers
WO2007124597A1 (en) * 2006-05-01 2007-11-08 Forbes Medi-Tech Inc. Composition comprising one or more esterified phytosterols and/or phytostanols into which are solubilized one or more unesterified phytosterols and/or phytostanols, in order to achieve therapeutic and formulation benefits
US20070254026A1 (en) * 2006-05-01 2007-11-01 Forbes Medi-Tech Inc. Softgel capsules
EP2036445A1 (en) * 2007-09-05 2009-03-18 Dietetics Pharma S.r.l. Nutraceutic preparation in powder form containing free plant sterols
US20110207952A1 (en) * 2010-02-22 2011-08-25 Rafael Avila Cholesterol extraction from algae and preparation of vegan vitamin d3
EA024619B1 (en) * 2014-11-21 2016-10-31 Эльвин Гаджи оглы Керимли FRAXINOSTEROL - 24β-ETHYLCHOLESTA-20-CARBOXY-6(7),8(9)-DIEN 3β-OL AND DERIVATIVE THEREOF
SE540791C2 (en) 2016-01-29 2018-11-13 Stora Enso Oyj Extraction of phytosterols
WO2017137908A1 (en) 2016-02-12 2017-08-17 Stora Enso Oyj Distillation of neutral compounds from tall oil soap

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2573891A (en) * 1950-05-09 1951-11-06 Pittsburgh Plate Glass Co Recovery of sterols
US2715638A (en) * 1953-07-28 1955-08-16 American Cyanamid Co Production of sterols from tall oil pitch
US2835682A (en) * 1955-08-08 1958-05-20 Swift & Co Sterol recovery process
US3840570A (en) * 1970-12-07 1974-10-08 Procter & Gamble Process for preparing sterols from tall oil pitch
SE417107B (en) * 1973-06-29 1981-02-23 Bjarne Holmbom PROCEDURE FOR PROCESSING SAPOR
US4044031A (en) * 1976-07-02 1977-08-23 Ake Allan Johansson Process for the separation of sterols
US4208286A (en) 1977-11-03 1980-06-17 Kauppi Pekka K Sulphate soap skimming apparatus
US4153622A (en) * 1978-05-18 1979-05-08 Medipolar Oy Process for the recovery of β-sitosterol
FI58333C (en) * 1978-10-27 1981-01-12 Kaukas Ab Oy PROCEDURE FOR FRAMSTATION OF UNDER 5 VIKT-% ALFA2-SITOSTEROL INNEHAOLLANDE BETA-SITOSTEROL CONCENTRATE
FI57956C (en) * 1978-12-12 1980-11-10 Farmos Oy FOER FARING ISOLERING AV BETA-SITOSTEROL MED LAOG ALFA-SITOSTEROLHALT
FI59416C (en) * 1979-11-19 1981-08-10 Farmos Oy FOERFARANDE FOER UTVINNING AV BETA-SITOSTEROL UR EN STEROLBLANDNING UTVUNNEN FRAON RAOSAOPANS NEUTRALFRAKTION
FI63423C (en) * 1981-01-27 1983-06-10 Farmos Oy FOERFARANDE FOER SEPARERING AV BETA-SITOSTEROL FRAON EN STEROLBLANDNING UTVUNNEN UR RAOSAOPANS NEUTRALFRAKTION
JPS57206336A (en) * 1981-06-12 1982-12-17 Ajinomoto Co Inc Edible oil
FI65440C (en) * 1981-07-21 1984-05-10 Kaukas Ab Oy FOERFARANDE FOER SEPARERING AV BETA-SITOSTEROL MED EN LAOG ALFA-SITOSTEROLHALT
FI812279L (en) 1981-07-21 1983-01-22 Kaukas Ab Oy FOERFARANDE FOER RENING AV -SITOSTEROL ISOLERAD FRAON NEUTRALAEMNET AV SULFATCELLULOSAPROCESSENS RAOSAOPA
JPS58116415A (en) * 1981-12-28 1983-07-11 Riyoushiyoku Kenkyukai Using method of cholesterol reducing agent
JPS6479119A (en) * 1987-09-22 1989-03-24 Daiichi Seiyaku Co Drug of blended two components
FR2653974B1 (en) * 1989-11-03 1992-12-31 Expanchimie Sarl FOOD ADDITIVE CONSISTING OF SOYBEAN AND / OR LAWYER EXTRACTS.
CA2028759A1 (en) 1989-11-22 1991-05-23 Jean-Marie Cassal Steroids
JP2708633B2 (en) * 1991-05-03 1998-02-04 ライシオン テータート オサケユイチア アクティエボラーグ Substances for lowering high cholesterol levels in serum and methods for preparing the substances
US5286845A (en) 1992-05-20 1994-02-15 Union Camp Corporation Acidification of tall oil soap using carbon dioxide

Similar Documents

Publication Publication Date Title
RU97107020A (en) COMPOSITION OF STEROLES FROM SOAP AS A PULPA
MD1721C2 (en) Process for separating a phytosterol composition from pulping soap, cholesterol reducing composition and therapeutic product
ATE42959T1 (en) TIGOGENIN CELLOBIOSIDES AND THEIR HEPTA ACETATE, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING TIGOGENIN CELLOBIOSIDES.
CA1184897A (en) Process for the separation of sterols or mixtures of sterols
KR860700354A (en) Method for preparing 1? -Hydroxy vitamin D compound
KR840007722A (en) Method for preparing 3- (5-aminopentyl) -amino-1-benzazin-2-one-1-alkanoic acid
TW330200B (en) Process for purifying acetic acid
Wildman Alkaloids of the Amaryllidaceae
Kimura et al. Cytosolic calcium increase in coronary endothelial cells after H2O2 exposure and the inhibitory effect of U78517F
Fless et al. Structural and functional changes of rhesus serum low density lipoproteins during cycles of diet-induced hypercholesterolemia.
SE9603304D0 (en) Process for purifying a compound
RU97113086A (en) METHOD FOR PRODUCING PURE HYDROCARBONS FROM A MIXTURE CONTAINING AROMATIC AND NON-AROMATIC HYDROCARBONS
SE9303446D0 (en) A novel urea fractionation process
Aoki et al. Effects of the hatomugi (Coix lachryma-jobi L. var. ma-yuen) on the blood pressure, cholesterol absorption and serum lipids level
JPH0247191A (en) Manufacture of aromatic condensate suitable for use as ingredient of caburetor fuel
SE8204273L (en) PROCEDURE FOR PURIFICATION OF BETA-SITOSTEROL ISOLATED FROM THE NEUTRAL SUBSTANCE IN THE SULPHATE CELLULOSA PROCESS
US4532327A (en) Sesbanimide and the use thereof in treating leukemic tumors
Green et al. The effect of N-bromosuccinimide on the sub-unit structure of avidin and its complexes with biotin
NO991208L (en) A method for purifying apolipoproteins and a preparation for use in the method
Arnold et al. A search for santonin in Artemisia pontica, the other wormwood of old absinthe
RU2139293C1 (en) Sitosterol production method
SU1595876A1 (en) Method of separating gas-condensate hydrocarbon mixture
JPS55141415A (en) Substance controlling the increase in serum cholosterol, which is separated from defatted rice bran
JPS5639063A (en) Beta-methylionone derivative and flavor modifier for tobacco containing the same
Conner Elucidation of the chemical structures of softwood related terpenoids