CN1141927A - Sodium alginate diester and preparation method - Google Patents

Sodium alginate diester and preparation method Download PDF

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Publication number
CN1141927A
CN1141927A CN 93111311 CN93111311A CN1141927A CN 1141927 A CN1141927 A CN 1141927A CN 93111311 CN93111311 CN 93111311 CN 93111311 A CN93111311 A CN 93111311A CN 1141927 A CN1141927 A CN 1141927A
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China
Prior art keywords
blood
propylene glycol
alginic acid
glycol alginate
alginate
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CN 93111311
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Chinese (zh)
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CN1059679C (en
Inventor
管华诗
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Ocean University of Oingdao
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Ocean University of Oingdao
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Priority to CN93111311A priority Critical patent/CN1059679C/en
Publication of CN1141927A publication Critical patent/CN1141927A/en
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Publication of CN1059679C publication Critical patent/CN1059679C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Sodium alginate is hydrolyzed in hydrochloric acid to prepare alginic acid which is then reacted with epoxy propane to obtain propane diester alginate by using NaOH or NaAC as catalyst, finally sulfonated by chlorosulfonic acid, using formylamine or pyridine as catalyst. Said medicine is low in toxicity and wide in medicinal effect, and has the functions of blood-coagulation-resisting, anti-thrombus, regulating blood-fat, reducing blood-viscosity, inhibiting the aggregation of blood cells and red blood cells, and reducing blood-pressure and blood-sugar. It can be indicated for treatment of high-coagulability high-blood-viscosity complex and infarction diseases.

Description

Sodium alginate diester and preparation method
During the preparation propylene glycol alginate sodium sulfate, allow sodium alginate hydrolysis in aqueous hydrochloric acid produce alginic acid earlier; The latter is added in the propylene oxide, the milliliter number ratio of alignic gram number and propylene oxide is 1: 2~5 again, and is catalyzer with NaOH or KOH or NaAC, and its consumption is 0.5~1.0% of an alginic acid weight, at 50~80 ℃ and 1.5~3.0kg/cm 2Pressure down or reflux under the normal pressure, 40~50 ℃ of conditions and promptly make propylene glycol alginate; Be solvent with methane amide or pyridine at last, under 60~80 ℃ condition, promptly obtain alginic acid propyl ester sulfuric ester sodium salt with the chlorsulfonic acid sulfonation.
Embodiment:
1, get 100 gram food grade sodium alginates, adding fills in the container of 500 milliliters of 0.5N hydrochloric acid solns, soaks 10 hours, stirs once every 1 hour.Soak and finish, disacidify liquid inclines.Be placed in the there-necked flask that hydrolysis uses, add 1000 milliliters of 0.5N hydrochloric acid again, in 0.6kg/cm 2Hydrolysis is 3 hours under the pressure.After hydrolysis is intact, put into the sedimentation of sedimentation container, with sediment (alginic acid after the hydrolysis) thorough washing, behind the dehydration of alcohol, drain and contain a certain amount of moisture content behind the upper strata waste acid water that inclines.
2, get the 50 gram alginic acids (water content is 40%) that said hydrolyzed obtains, put into reactor, add 100 milliliters of propylene oxide, add 0.4 gram NaOH again in 1.5kg/cm 2Under the pressure, constantly stirring reaction is 3 hours, and reaction product ethanol repetitive scrubbing three times in 60 ℃ of oven dry, promptly get propylene glycol alginate.
3, get 30 gram exsiccant propyl ester, put into 1000 milliliters there-necked flask, install whipping appts and thermometer, add 300 milliliters of formamide solvent, stir, slowly splash into 90 milliliters of chlorsulfonic acids, temperature is not higher than 5 ℃ in the dropping process, makes it be warming up to 65~70 ℃ after dripping, and reacts 3 hours.After the cooling, add 2000 milliliter of 95% alcohol and carry out post precipitation, use alcohol precipitation again, so triplicate resolution of precipitate.Dissolving again, lysate are by 717 and 732 yin, yang ion exchange column desalinations, and the solution after the desalination uses the NaOH of 4N to transfer pH to 8, uses alcohol precipitation again, promptly gets the sodium salt of alginic acid propyl ester sulfuric ester, also is propylene glycol alginate sodium sulfate.
The propylene glycol alginate sodium sulfate that makes by this technology is white amorphous powder, and tasteless, nothing is smelt, and is soluble in water, is insoluble to ether, acetone and other organic solvent.It is the identification of ester group and sodium salt.The content of this propylene glycol alginate sodium sulfate organosulfur is 9~14%, and intrinsic viscosity is 10~15, pH value 5.5~7.5, and weight loss on drying is no more than 10%, and muriate is less than 0.5%, and heavy metal is less than 15ppm, and arsenic is less than 2ppm.
Propylene glycol alginate sodium sulfate LD 50=748mg/kg, toxicity is low, and pharmacological action is extensive, as anticoagulation, antithrombotic, accent blood fat, reducing blood viscosity, inhibition red corpuscle or platelet aggregation, microcirculation improvement, and hypotensive, hypoglycemic activity is arranged.Therefore, propylene glycol alginate sodium sulfate has comparatively ideal prevention and result of treatment to hypercoagulability, high blood viscosity syndromes and infraction disease, can be used for intravascular coagulation (DIC), thrombophlebitis, vasculitis, retinal vein embolism due to thrombus, cerebral infarction, cerebral arteriosclerosis disease group, stenocardia, myocardial infarction and the various cause of disease, the prevention and the treatment of wound or operation back thrombus etc.Be used also with immunomodulator and can treat hemorrhagic fever.It is the medicine of a kind of ideal prevent and treat ischemia heart, cerebrovascular disease really.

Claims (2)

1, a kind of heparitin new drug propylene glycol alginate sodium sulfate, full name are alginic acid propyl ester sulfuric ester sodium salt,
Its structural formula is R-CH in the structural formula 2CH 2CH 2(OH)
R′-SO 3Na
2, a kind of preparation method of propylene glycol alginate sodium sulfate, it is characterized in that allowing earlier sodium alginate hydrolysis in hydrochloric acid produce alginic acid, again the latter is added in the propylene oxide, the milliliter number ratio of alignic gram number and propylene oxide is 1: 2~5, and be catalyzer with NaOH or KOH or NaAC, its consumption is 0.5~1.0% of an alginic acid weight, at 50~80 ℃ and 1.5~3.0kg/cm 2Pressure down or reflux under the normal pressure, 40~50 ℃ of conditions and promptly get propylene glycol alginate; Be solvent with methane amide or pyridine at last, under 60~80 ℃ condition, use the chlorsulfonic acid sulfonation.
CN93111311A 1993-06-18 1993-06-18 Sodium alginate diester and preparation method Expired - Fee Related CN1059679C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN93111311A CN1059679C (en) 1993-06-18 1993-06-18 Sodium alginate diester and preparation method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN93111311A CN1059679C (en) 1993-06-18 1993-06-18 Sodium alginate diester and preparation method

Publications (2)

Publication Number Publication Date
CN1141927A true CN1141927A (en) 1997-02-05
CN1059679C CN1059679C (en) 2000-12-20

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CN93111311A Expired - Fee Related CN1059679C (en) 1993-06-18 1993-06-18 Sodium alginate diester and preparation method

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100425623C (en) * 2006-09-28 2008-10-15 青岛明月海藻集团有限公司 Production method of propylene glycol alginate special for beer
CN104744607A (en) * 2015-04-22 2015-07-01 青岛正大海尔制药有限公司 Method for preparing polysaccharide sulfate through nanofiltration technology
CN104774278A (en) * 2015-04-22 2015-07-15 青岛正大海尔制药有限公司 Method for preparing polysaccharide sulfate by virtue of electrochemical reaction

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60206801A (en) * 1984-03-30 1985-10-18 Kimitsu Kagaku Kenkyusho:Kk Production of organic solvent-soluble alginic acid
KR900002822B1 (en) * 1986-10-16 1990-05-01 재단법인 한국화학연구소 Process for the preparation of 2-hydronyproply alginate
FR2648463B1 (en) * 1989-06-14 1993-01-22 Inst Fs Rech Expl Mer SULPHATE POLYSACCHARIDES, ANTICOAGULATING AGENT AND ANTI-COMPLEMENTARY AGENT OBTAINED FROM BROWN ALGAE FUCANES AND PROCESS FOR OBTAINING SAME
JP2511577B2 (en) * 1991-02-05 1996-06-26 株式会社紀文食品 Sustained-release preparation consisting of propylene glycol alginate
JPH04266896A (en) * 1991-02-22 1992-09-22 Taiyo Fishery Co Ltd Purification of alginic acid oligosaccharide and sulfuric acid group-containing oligosaccharide
CN1089619A (en) * 1993-01-06 1994-07-20 山东烟台西苑制药厂 A kind of production method of propylene glycol alginate sodium sulfate
CN1089496A (en) * 1993-01-06 1994-07-20 山东烟台西苑制药厂 Compound sodium alginati diesteras

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100425623C (en) * 2006-09-28 2008-10-15 青岛明月海藻集团有限公司 Production method of propylene glycol alginate special for beer
CN104744607A (en) * 2015-04-22 2015-07-01 青岛正大海尔制药有限公司 Method for preparing polysaccharide sulfate through nanofiltration technology
CN104774278A (en) * 2015-04-22 2015-07-15 青岛正大海尔制药有限公司 Method for preparing polysaccharide sulfate by virtue of electrochemical reaction

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