CN1789261A - Method for refining lipoic acid - Google Patents
Method for refining lipoic acid Download PDFInfo
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- CN1789261A CN1789261A CN 200510057458 CN200510057458A CN1789261A CN 1789261 A CN1789261 A CN 1789261A CN 200510057458 CN200510057458 CN 200510057458 CN 200510057458 A CN200510057458 A CN 200510057458A CN 1789261 A CN1789261 A CN 1789261A
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- thioctic acid
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- thioctic
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Abstract
The invention discloses a refining method for preparing lipoicin, comprising: dissolving the coarse lipoicin in the alkali solution, moderating the pH to be 9.6-11.6, filtering to remove the insoluble particle; acidifying the filtering solution to make the pH be 6-7, filtering to remove the polymer-rich lipoicin; acidifying the filtering solution further to make Ph be 2.0-6.4, crystallizing, filtering; vacuum drying and getting lipoicin of high purity. The lipocin produced in this invention does not contain organic dissolvent, and the purity is high, the single foreign matter content is less than 0.1%. The invention is characterized by the convenient process, simple operation and suitness for industrial production.
Description
Technical field
The present invention relates to the process for purification of Thioctic Acid bulk drug.
Background technology
Thioctic Acid, also claim the d-Thioctic Acid (α-Lipoic acid, d-LA), CAS:1077-28-7, chemistry (±)-5-[3 '-(1 ', 2 '-dithiolane) by name-] valeric acid, its structural formula is as follows:
Thioctic Acid is the natural product of separating from pork liver first nineteen fifty-one, and it participates in the oxidation depickling reaction of 2-ketone acid in the tricarboxylic acid cycle as coenzyme.It is a synthetic disulphide in a few cell, it is the cofactor of pyruvic oxidase, it changes acetyl-CoA at pyruvic acid, generates flavin adenine dinucleotide reduced form (FADH), and participating in the tricarboxylic acid cycle process is indispensable material.Thioctic Acid is the metabolic antioxidant, can be converted into the Thioctic acid, dihydro-(DHLA) of reduced form in vivo.In recent years, Thioctic Acid (LA) and Thioctic acid, dihydro-(DHLA) are subjected to showing great attention to of international biomedical boundary in the vital role aspect anti-oxidant, carbohydrate metabolism, diabetic complication and other the multiple disease treatments.Existing industrialization technology is to adopt 6,8-dichloro ethyl octylate and SULPHUR POWDER, sodium disulfide cyclization generate the Thioctic Acid ethyl ester, obtain the Thioctic Acid crude product through hydrolysis then, then with refining operational paths (US3223712) that obtains the pure product of Thioctic Acid such as sherwood oil, normal hexane, isopropyl ether, hexanaphthenes.The indudstrialized refining method generally is to adopt freezing crystallization under ethyl acetate and the hexanaphthene mixed solvent now, obtains the pure product of Thioctic Acid (EP0593896 or US5455264) through filtration, filter cake drying under reduced pressure.Because Thioctic Acid is an organic carboxyl acid, recrystallization solvent preferably adopts the esters solvent dissolving of middle polarity, promotes separating out of product with the less solvent of polarity again.And in the recrystallization method now, because solvent itself has a part of impurity.As: a spot of alcohols in the esters solvent, often with the newly-generated lipoate impurity of Thioctic Acid.Like this, often produced new impurity in the product that recrystallization is separated out.Our experiments show that, through recrystallization repeatedly, this impurity peaks still can not reduce or disappear (seeing accompanying drawing 1 and Fig. 2).Simultaneously, the medicine of root a tree name ICH regulation is to the regulation of Determination of Residual Organic Solvents, and recrystallization method often causes that organic solvent exceeds standard in the product, thereby causes adopting the requirement that the Thioctic Acid of solvent recrystallization can not fulfilling medicinal.After the experimental verification, recrystallization four times, measuring (method is seen 28 editions 2110 pages of American Pharmacopeias) its content with the HPLC method is 99.49% (seeing accompanying drawing 2), and maximum single impurity peaks content is 0.21%, and the original R that just exists in the raw material
f=2.692 peaks (content 0.21%), R
f=5.828 peaks (content 0.19%) and R
f=12.923 peaks three impurity such as (content 0.05%) are not removed yet.
Just because of this, H. relax to breathe out Bauer, and S. Wen Keqin and A. Ge Lubai have applied for the Chinese patent of " method for preparing solvent-free d-Thioctic Acid ", and its Granted publication number is CN1131227C.In their invention, illustrated a kind of method for preparing solvent-free Thioctic Acid.This method adopt first alkali molten, remove by filter insoluble impurities, under acidic conditions, separate out the solvent-free Thioctic Acid of the chemical purity that has been improved again.But this invention has only guaranteed the solvent residual amount in the Thioctic Acid sample, and R
f=5.556, R
f=13.234 impurity is not removed (seeing accompanying drawing 3) yet, has produced the impurity (R of polymer property simultaneously
f=41.845), can not reach the pharmaceutical grade raw material single impurity is no more than 0.1% standard, especially not be suitable for the preparation injection.
Summary of the invention
The object of the present invention is to provide a kind of process for purification of Thioctic Acid, can solve the organic solvent residual problem in the Thioctic Acid product, can obtain the higher Thioctic Acid that is applicable to injection of purity again.
Purpose of the present invention is molten by first alkali, part alkali insoluble impurities is removed in filtration, and insoluble impurity under solutions of weak acidity is removed in acidifying again, filtration, and last further acidifying is separated out Thioctic Acid and is achieved.Concrete technical scheme is come as follows.
A) Thioctic Acid crude product to be purified is dissolved in alkaline aqueous solution, regulating the pH value is 9.6-11.6, removes by filter particulate matter;
B) filtrate is acidified to the pH value for 6-7, removes by filter the Thioctic Acid that is rich in polymeric impurities;
C) filtrate further is acidified to the pH value for 2.0-6.4, and crystallization filters;
D) drying under reduced pressure promptly gets highly purified Thioctic Acid.
In the present invention, the Thioctic Acid crude product can adopt any means preparation, also can buy commercially available technical grade or food grade materials.
In the step a), the content of Thioctic Acid is 5-20% in the alkaline aqueous solution, preferred 10%.With the alkaline solution adjust pH is 9.6-11.6, preferred 10.2.The alkali that said basic solution contains is the oxyhydroxide of basic metal or alkaline-earth metal, carbonate, and supercarbonate, ammonia or the primary, the second month in a season or tertiary amine, its concentration is 5-15%.
In step a), embodiment preferred is the gac that adds before filtration based on the 0.1-0.5% of Thioctic Acid weight, plays the purpose of decolouring, removal partial impurities.
Step b) is a key of the present invention, and the filtrate of step a) gained is acidified to pH6-7, and in test, we are unexpected to find that with this understanding polymeric impurities is easily separated out, and filtration can be removed this part impurity.Preferred pH value is 6.4.
Step b) and c) in the used acid of acidifying can be mineral acid, also can use organic acid.Preferred mineral acid, for example hydrochloric acid, nitric acid, sulfuric acid, phosphoric acid etc.The concentration of acid solution is generally 5-20%.
In the step a), temperature can be selected 0-30 ℃, preferred 0-10 ℃.
Step b) and c) in, temperature can be selected 0-30 ℃, preferred 2-15 ℃.In step b), must strict controlled temperature, otherwise easily separate out the solid of a large amount of thick attached walls, thus cause separation difficulty, can not reach the purpose of separating impurity.
In the step d), temperature can be selected-50 ℃ to+45 ℃.Because the fusing point lower (61-62 ℃) of Thioctic Acid sample belongs to heat-sensitive substance, in drying process, be easy to cause the sample polymerization rotten because of overtemperature (＞50 ℃).Therefore the general method that adopts drying under reduced pressure, but conventional hypobaric drying method is consuming time longer.In process of the test, we find that the freeze-drying effect is better, so our preferably freeze drying method.
The Thioctic Acid that the present invention makes does not contain organic solvent, and purity is higher, and the content of single impurity can reach the injection standard all less than 0.1%.The inventive method is easy, and easy handling is suitable for industrialized production.
Description of drawings
Fig. 1 is the HPLC collection of illustrative plates of commercially available sample
Fig. 2 adopts the solvent recrystallization method to make the HPLC collection of illustrative plates of product
Fig. 3 adopts Chinese patent CN1131227 method to make the HPLC collection of illustrative plates of product
Fig. 4 is the HPLC collection of illustrative plates of embodiment 1 products obtained therefrom
Fig. 5 is the HPLC collection of illustrative plates of embodiment 2 products obtained therefroms
Fig. 6 is the HPLC collection of illustrative plates of embodiment 3 products obtained therefroms
Embodiment
The following examples can make those skilled in the art more fully understand the present invention, but do not limit the present invention in any way.
In the 10L reaction flask, and adding Thioctic Acid crude product 300 grams (commercially available, HPLC method content 98.29%, see accompanying drawing 1, residual solvent (measuring): toluene 18ppm, hexanaphthene 480ppm according to 2005 editions two appendix VIII P of Chinese Pharmacopoeia method, ethyl acetate 200ppm, ethanol 380ppm), be suspended in the 6000ml deionized water, fully stir, be cooled to 10 ℃, slowly drip 15% NaOH solution 330ml, until the pH=10.2 of system, with the glass sand hourglass suction filtration of G4, abandon filter residue.Filtrate is poured in the 10L reaction flask, is cooled to 5 ℃, slowly drips 10%HCl solution, begins to separate out the colloidal material when pH=7.0, and when continuing to be neutralized to pH=6.4, with the glass sand hourglass suction filtration of G4, filter residue reclaims pending.Filtrate continues to be neutralized to pH=2.0 with 10%HCl solution under 10 ℃, continues to stir 30min, and suction filtration is abandoned filtrate.Filter cake divides 10 washings with the deionized water wash of a large amount of ice (about 10L), drains.
Wet sample is suspended in the 750ml deionized water, dry product weight accounts for 10-30%, pour into and carry out (40-35 ℃ of lyophilize in the stainless steel tray, 30-36h), promptly get the pure product 283.5g of Thioctic Acid, yield 96.0%, content: 99.86%, maximum single impurity peaks content is 0.07% (the HPLC method is seen accompanying drawing 4), and residual solvent (toluene, hexanaphthene, ethyl acetate and ethanol) does not all detect.
In the 10L reaction flask, add Thioctic Acid crude product 300 grams (with embodiment 1), be suspended in the 6000ml deionized water, fully stir, be cooled to 10 ℃, slowly drip 15% NaOH solution 330ml, until the pH=9.2 of system,, abandon filter residue with the glass sand hourglass suction filtration of G4.Filtrate is poured in the 10L reaction flask, is cooled to 15 ℃, slowly drips 10%HCl solution, begins to separate out the colloidal material when pH=7.0, and when continuing to be neutralized to pH=6.4, with the glass sand hourglass suction filtration of G4, filter residue reclaims pending.Filtrate continues to be neutralized to pH=2.0 with 10%HCl solution under 10 ℃, continues to stir 30min, and suction filtration is abandoned filtrate.Filter cake divides 10 washings with the deionized water wash of a large amount of ice (about 10L), drains.
Wet sample is suspended in the 750ml deionized water, dry product weight accounts for 10-30%, pour into and carry out (40-35 ℃ of lyophilize in the stainless steel tray, 30-36h), promptly get the pure product 279.5g of Thioctic Acid, yield 94.6%, content: 99.79%, maximum single impurity peaks content is 0.08% (the HPLC method is seen accompanying drawing 5), and residual solvent (toluene, hexanaphthene, ethyl acetate and ethanol) does not all detect.
In the 10L reaction flask, add Thioctic Acid crude product 300 grams (with embodiment 1), be suspended in the 6000ml deionized water, fully stir, be cooled to 2 ℃, slowly drip 15% NaOH solution 330ml, until the pH=11.6 of system, use filter paper suction filtration at a slow speed, abandon filter residue.Filtrate is poured in the 10L reaction flask, is cooled to 5 ℃, slowly drips 10%HCl solution, begins to separate out the colloidal material when pH=7.0, when continuing to be neutralized to pH=6.4, uses filter paper suction filtration at a slow speed, and filter residue reclaims pending.Filtrate continues to be neutralized to pH=2.0 with 10%HCl solution under 10 ℃, continues to stir 30min, and suction filtration is abandoned filtrate.Filter cake divides 10 washings with the deionized water wash of a large amount of ice (about 10L), drains.
Wet sample is suspended in the 750ml deionized water, dry product weight accounts for 10-30%, pour into and carry out (40-35 ℃ of lyophilize in the stainless steel tray, 30-36h), promptly get the pure product 275.5g of Thioctic Acid, yield 93.3%, content: 99.81%, maximum single impurity peaks content is 0.08% (the HPLC method is seen accompanying drawing 6), and residual solvent (toluene, hexanaphthene, ethyl acetate and ethanol) does not all detect.
In the 10L reaction flask, add Thioctic Acid crude product 300 grams (with embodiment 1), be suspended in the 6000ml deionized water, fully stir, be cooled to 10 ℃, slowly drip 15% NaOH solution 330ml, until the pH=11.2 of system, the Thioctic Acid sample dissolves fully.Add 656 pharmaceutical grade gac 31.5g again, continue to stir 30 minutes,, abandon filter residue with the glass sand hourglass suction filtration of G4.Filtrate is poured in the 10L reaction flask, is cooled to 5 ℃, slowly drips 10%HCl solution, begins to separate out the colloidal material when pH=7.0, and when continuing to be neutralized to pH=6.4, with the glass sand hourglass suction filtration of G4, filter residue reclaims pending.Filtrate continues to be neutralized to pH=2.0 with 10%HCl solution under 10 ℃, continues to stir 30min, and suction filtration is abandoned filtrate.Filter cake divides 10 washings with the deionized water wash of a large amount of ice (about 10L), drains.
Wet sample is suspended in the 750ml deionized water, dry product weight accounts for 10-30%, pour into and carry out (40-35 ℃ of lyophilize in the stainless steel tray, 30-36h), promptly get the pure product of 260.3g Thioctic Acid, yield 88.2%, content: 99.89%, maximum single impurity peaks is 0.05%, and residual solvent (toluene, hexanaphthene, ethyl acetate and ethanol) does not all detect.
Claims (10)
1. the process for purification of a Thioctic Acid is characterized in that, comprises the steps:
A) Thioctic Acid crude product to be purified is dissolved in alkaline aqueous solution, regulating the pH value is 9.6-11.6, removes by filter particulate matter;
B) filtrate is acidified to the pH value for 6-7, removes by filter particulate matter;
C) filtrate further is acidified to the pH value for 2.0-6.4, and crystallization filters;
D) drying under reduced pressure promptly gets highly purified Thioctic Acid.
2. method according to claim 1, the content that it is characterized in that Thioctic Acid in the step a) neutral and alkali aqueous solution is 5-20%.
3. method according to claim 1 is characterized in that the alkali that basic solution contains is the oxyhydroxide of basic metal or alkaline-earth metal, carbonate, supercarbonate, ammonia or the primary, the second month in a season or tertiary amine.
4. method according to claim 1 before it is characterized in that filtering in the step a), adds the gac based on the 0.1-0.5% of Thioctic Acid weight.
5. method according to claim 1 is characterized in that step b) and c) in the used acid of pH regulator be mineral acids such as hydrochloric acid, nitric acid, sulfuric acid or phosphoric acid.
6. method according to claim 1 is characterized in that step d) is a freeze-drying.
7. method according to claim 1 is characterized in that step a) is to c) under 0-30 ℃ temperature, carry out.
8. method according to claim 1 is characterized in that step a) carries out under 0-10 ℃ temperature.
9. method according to claim 1 is characterized in that step b) and c) under 2-15 ℃ temperature, carry out.
10. method according to claim 1 is characterized in that step d) carries out under-50 to 45 ℃ temperature.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100574581A CN100375745C (en) | 2005-12-21 | 2005-12-21 | Method for refining lipoic acid |
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|---|---|---|---|
| CNB2005100574581A CN100375745C (en) | 2005-12-21 | 2005-12-21 | Method for refining lipoic acid |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101607955B (en) * | 2008-06-18 | 2012-11-28 | 上海津力化工有限公司 | Preparation method for low-residue lipoic acid |
| CN105439925A (en) * | 2015-10-29 | 2016-03-30 | 南京海融医药科技有限公司 | Preparation method for lipoic acid polymer impurities and detection method for lipoic acid polymer impurities |
| CN107652264A (en) * | 2017-09-25 | 2018-02-02 | 苏州华诺医药有限公司 | The preparation method of lipoic acid impurity A |
| CN108484570A (en) * | 2018-05-15 | 2018-09-04 | 苏州富士莱医药股份有限公司 | A kind of method and apparatus preparing lipoic acid particle |
| CN109574987A (en) * | 2017-09-29 | 2019-04-05 | 辽宁远大诺康生物制药有限公司 | Application of the preparation method and lipoic acid of lipoic acid in the drug of preparation treatment aspermia or oligospermia |
| CN113292533A (en) * | 2021-05-25 | 2021-08-24 | 四川智强医药科技开发有限公司 | Method for purifying polymer impurities in lipoic acid |
| CN114163418A (en) * | 2021-12-24 | 2022-03-11 | 山东龙辰药业有限公司 | Method for synthesizing dextro lipoic acid |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19726519A1 (en) * | 1997-06-23 | 1998-12-24 | Asta Medica Ag | Process for the production of dry thioctic acid |
| DE19938621A1 (en) * | 1999-08-14 | 2001-02-22 | Sueddeutsche Kalkstickstoff | Process for the production of solvent-free alpha-lipoic acid |
-
2005
- 2005-12-21 CN CNB2005100574581A patent/CN100375745C/en active Active
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101607955B (en) * | 2008-06-18 | 2012-11-28 | 上海津力化工有限公司 | Preparation method for low-residue lipoic acid |
| CN105439925A (en) * | 2015-10-29 | 2016-03-30 | 南京海融医药科技有限公司 | Preparation method for lipoic acid polymer impurities and detection method for lipoic acid polymer impurities |
| CN105439925B (en) * | 2015-10-29 | 2017-10-17 | 南京海融医药科技股份有限公司 | A kind of preparation of lipoic acid polymeric impurities and its detection method |
| CN107652264A (en) * | 2017-09-25 | 2018-02-02 | 苏州华诺医药有限公司 | The preparation method of lipoic acid impurity A |
| CN109574987A (en) * | 2017-09-29 | 2019-04-05 | 辽宁远大诺康生物制药有限公司 | Application of the preparation method and lipoic acid of lipoic acid in the drug of preparation treatment aspermia or oligospermia |
| CN108484570A (en) * | 2018-05-15 | 2018-09-04 | 苏州富士莱医药股份有限公司 | A kind of method and apparatus preparing lipoic acid particle |
| CN108484570B (en) * | 2018-05-15 | 2021-05-04 | 苏州富士莱医药股份有限公司 | Method and equipment for preparing lipoic acid particles |
| CN113292533A (en) * | 2021-05-25 | 2021-08-24 | 四川智强医药科技开发有限公司 | Method for purifying polymer impurities in lipoic acid |
| CN113292533B (en) * | 2021-05-25 | 2024-04-16 | 四川智强医药科技开发有限公司 | Method for purifying polymer impurities in lipoic acid |
| CN114163418A (en) * | 2021-12-24 | 2022-03-11 | 山东龙辰药业有限公司 | Method for synthesizing dextro lipoic acid |
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