CN1699428A - Process for preparing chondroitin sulfate - Google Patents
Process for preparing chondroitin sulfate Download PDFInfo
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- CN1699428A CN1699428A CN 200510027279 CN200510027279A CN1699428A CN 1699428 A CN1699428 A CN 1699428A CN 200510027279 CN200510027279 CN 200510027279 CN 200510027279 A CN200510027279 A CN 200510027279A CN 1699428 A CN1699428 A CN 1699428A
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Abstract
The invention relates to a process for preparing chondroitin sulfate which comprises boiling treatment, protecting or mild leaching, enzymolysis, filtering and removing protein, ultrafiltration purifying, vacuum concentrating, spraying and seasoning, the yield is between 5-35%.
Description
Technical field
The present invention relates to a kind of preparing chondroitin sulfates.
Background technology
Chondroitin sulfate mainly is the medicine of treatment rheumatism and rheumatism, and it also has effects such as anti-freezing, anti-class, anticancer, antithrombotic, reducing blood-fat.Now export to the many countries of US and European in a large number, be badly in need of occupying the 3rd in the ten big class Chinese patent medicine raw materials in the world market.Domestic have many plant produced chondroitin sulfates.The method of domestic production chondroitin sulfate mainly contains three kinds at present: salt solution, alkaline hydrolysis method and enzymolysis process.The main separating and purifying technology that adopts has: ethanol precipitation method, Mierocrystalline cellulose partition method, absorption method, quaternary amine complexometry, ion exchange chromatography, zone electrophoresis partition method etc.Salt solution and enzymolysis process are owing to the hydrolysis gentleness, though yield is higher, quality product is lower, does not reach the outgoing quality index, so generally do not adopt separately on producing.The general alkaline hydrolysis method-enzymolysis process bonded production technique that adopts in the current technology.But during alkaline purification, because more side reaction can take place, the chondroitin sulfate yield is reduced, cost is higher, loses competitive power.Simultaneously, now produce and go up the general method collection product that adopts ethanol sedimentation, have bigger potential safety hazard, the throughput and the scale of product that alcoholic acid has reclaimed speed limit, the rate of recovery of product is all undesirable in the alcoholic acid rate of recovery and the ethanol sedimentation, has influence on the cost of product.Number of patent application is to mention in 200310115383.9 " the double-enzyme method production chondroitin sulfates " adopting the MNWC6000 hollow fiber ultrafiltration membrane to carry out concentration, in fact the chondroitin sulfate of molecular weight 6000 ~ 20000 can not effectively catching in producing for chondroitin sulfate, and it produces product yield can be very not high.
Summary of the invention
The objective of the invention is to overcome above-mentioned the deficiencies in the prior art, provide that a kind of cost is low, quality good, the chondroitin sulfate production method of simple and safe operation.
For achieving the above object, the present invention adopts following technical scheme:
A kind of preparing chondroitin sulfates is characterized in that, the concrete processing step of this method is:
A. the cartilage with cleaning places jar, handles 3-6 hour through 90-120 ℃ of boiling;
B. in above-mentioned boiling treatment solution, add restitutive protection's agent, its add-on is 0.5 ~ 2wt% of raw material cartilage amount, adds highly basic again, and its add-on is the 6-8wt% of raw material cartilage amount, leaches 6-8 hour in 50 ℃ of protections; Or highly basic in above-mentioned boiling treatment solution, adding, its add-on is the 6-8wt% of raw material cartilage amount, in 50 ℃ of gentle leachings 6-8 hour;
C. get the leach liquor of gained among the step b, regulating pH is 8.5, adds pancreatin, and its add-on was raw material cartilage amount 0.5-1.5wt%, at 48-50 ℃ of following enzymolysis 6-8 hour;
D. above-mentioned material is heated to 85 ℃, heated 15 to 40 minutes, filter after the thermal treatment, remove albumen precipitation;
E. with ultra-fine filter steps d gained filtrate is carried out ultrafiltration purification;
F. to step e gained filtrate vacuum concentration to 15 to 20 degree Beaume;
G. step f gained concentrated solution is spray-dried, and finished product packing, sterilization are preserved.
Above-mentioned restitutive protection's agent is solubility sulphite, solubility nitrite or hydroborates; Used highly basic is sodium hydroxide or potassium hydroxide; Used middle highly basic is calcium hydroxide or calcium oxide.
Above-mentioned solubility sulphite is S-WAT or potassium sulfite; The solubility nitrite has Sodium Nitrite or potassium nitrite; Hydroborates is sodium borohydride or POTASSIUM BOROHYDRIDE.
Above-mentioned ultra-fine filter adopts hollow fiber membrane ultrafiltration device, screw winding formula ultra-fine filter or plate-type hyperfiltration device, and used ultra-filtration membrane is the ultra-filtration membrane of molecular weight cut off 1000-3000.
Compare with prior art, the inventive method need decolouring, ethanol sedimentation and ball-milling processing, and the products obtained therefrom color and luster is pure white, loose, and yield meets the outgoing quality standard between 5-35%, and easy and simple to handle, cost is lower, with short production cycle.Because present method has adopted ultrafiltration purification technology and spraying drying, without ethanol, reduce cost, reduce potential safety hazard simultaneously; The protection or the gentle extract technology that adopt, it is few that chondroitin sulfate is destroyed in process of production, and product yield improves.
Embodiment
Embodiment one:
1, the cartilage 500Kg of cleaning is added in the retort, add appropriate amount of deionized water till the complete submergence of cartilage, handled 6 hours 100 ℃ of boilings;
2, in above-mentioned boiling treatment solution, adding the 5Kg S-WAT is protective material, and 5Kg sodium hydroxide is mixed with the solution that concentration is 1-2%, joins in the above-mentioned boiling treatment solution, leaches 8 hours in 50 ℃ of protections;
3, get leach liquor, regulating pH was 8.5, adds the 5Kg pancreatin, 50 ℃ of following enzymolysis 8 hours;
4, above-mentioned material is heated to 85 ℃, heated 40 minutes, filter the filtering albumen precipitation after the thermal treatment;
5, use hollow fiber membrane ultrafiltration device, adopt the ultra-filtration membrane of molecular weight cut off 1000-3000, process 4 gained filtrates are carried out ultrafiltration purification, earlier with the pattern of concentrating, after again with concentrating-dialysis mode, control to peritoneal effluent OD
280≤ 0.01;
6, to process 5 gained filtrate vacuum concentration to 15 to 20 degree Beaume;
7, process 6 gained concentrated solutions are spray-dried, and finished product packing, sterilization are preserved.
Finally obtaining specific rotation is-20 ~-35 °, and galn content is the chondroitin sulfate of 28 ~ 35% white powder.
Embodiment two: present embodiment and the foregoing description are basic identical, and different is that the protective material that is adopted is a potassium nitrite, and highly basic is potassium hydroxide.
Embodiment three: present embodiment and the foregoing description are basic identical, and different is that the protective material that is adopted is a sodium borohydride, and highly basic is potassium hydroxide.
Embodiment four: present embodiment and the foregoing description are basic identical, and different is in the step 2, and in the boiling treatment solution, the concentration that adding 5Kg calcium hydroxide is mixed with is 1% liquid, in 50 ℃ of gentle leachings
Adopt above its detected result of method products obtained therefrom to be:
| TESTS | RESULTS |
| The Appearance proterties | White cryst.Powder (class) white powder |
| Assay (By CPC/HPLC) (Dry basis) purity | ≥90％ |
| The Acidity potential of hydrogen | pH6.5 |
| Tpc. total count | ≤1000/g |
| Protein (By TCA) protein (TCA method) | Qualified is qualified |
| Water moisture content | 8.3％ |
| Sulfate (Dry basis) sulphur content (dry product meter) | 6.3％ |
| Nitrogen (Dry basis) nitrogen content (dry product meter) | 3.2％ |
| Heavy metals heavy metal | ≤10ppm |
By above-mentioned detected result analysis, product meets the outlet index request.
Claims (4)
1. a preparing chondroitin sulfates is characterized in that, the concrete processing step of this method is:
A. the cartilage with cleaning places jar, handles 3-6 hour through 90-120 ℃ of boiling;
B. in above-mentioned boiling treatment solution, add restitutive protection's agent, its add-on is 0.5 ~ 2wt% of raw material cartilage amount, adds highly basic again, and its add-on is the 6-8wt% of raw material cartilage amount, leaches 6-8 hour in 50 ℃ of protections; Or highly basic in above-mentioned boiling treatment solution, adding, its add-on is the 6-8wt% of raw material cartilage amount, in 50 ℃ of gentle leachings 6-8 hour;
C. get the leach liquor of gained among the step b, regulating pH is 8.5, adds pancreatin, and its add-on was raw material cartilage amount 0.5-1.5wt%, at 48-50 ℃ of following enzymolysis 6-8 hour;
D. above-mentioned material is heated to 85 ℃, heated 15 to 40 minutes, filter after the thermal treatment, remove albumen precipitation;
E. with ultra-fine filter steps d gained filtrate is carried out ultrafiltration purification;
F. to step e gained filtrate vacuum concentration to 15 to 20 degree Beaume;
G. step f gained concentrated solution is spray-dried, and finished product packing, sterilization are preserved.
2. a kind of preparing chondroitin sulfates according to claim 1 is characterized in that, used restitutive protection's agent is solubility sulphite, solubility nitrite or hydroborates among the above-mentioned steps b; Used highly basic is sodium hydroxide or potassium hydroxide; Used middle highly basic is calcium hydroxide or calcium oxide.
3. a kind of preparing chondroitin sulfates according to claim 2 is characterized in that described solubility sulphite is S-WAT or potassium sulfite; The solubility nitrite has Sodium Nitrite or potassium nitrite; Hydroborates is sodium borohydride or POTASSIUM BOROHYDRIDE.
4. a kind of preparing chondroitin sulfates according to claim 1, it is characterized in that used ultra-fine filter adopts hollow fiber membrane ultrafiltration device, screw winding formula ultra-fine filter or plate-type hyperfiltration device, used ultra-filtration membrane is the ultra-filtration membrane of molecular weight cut off 1000-3000; Earlier with the pattern of concentrating, after again with concentrating-dialysis mode, control to peritoneal effluent OD
280≤ 0.01.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200510027279 CN1273497C (en) | 2005-06-29 | 2005-06-29 | Process for preparing chondroitin sulfate |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200510027279 CN1273497C (en) | 2005-06-29 | 2005-06-29 | Process for preparing chondroitin sulfate |
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| CN1699428A true CN1699428A (en) | 2005-11-23 |
| CN1273497C CN1273497C (en) | 2006-09-06 |
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| CN 200510027279 Expired - Fee Related CN1273497C (en) | 2005-06-29 | 2005-06-29 | Process for preparing chondroitin sulfate |
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Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102190740A (en) * | 2011-04-08 | 2011-09-21 | 淮安麦德森制药有限公司 | Preparation method of chondroitin sulfate |
| CN102199229A (en) * | 2011-04-08 | 2011-09-28 | 淮安麦德森制药有限公司 | Method for preparing chondroitin sulfate |
| CN102838691A (en) * | 2012-08-29 | 2012-12-26 | 宁波绿之健药业有限公司 | Extracting and purifying method of chondroitin sulfate |
| CN102978260A (en) * | 2012-11-28 | 2013-03-20 | 康普药业股份有限公司 | Method for refining chondroitin sulfate crude product |
| CN103145874A (en) * | 2012-12-08 | 2013-06-12 | 青岛九龙生物医药有限公司 | Method for improving content of chondroitin sulfate |
| CN103601816A (en) * | 2013-10-21 | 2014-02-26 | 青岛九龙生物医药有限公司 | Sodium chondroitin sulfate reduction decoloration method |
| CN103665188A (en) * | 2013-11-23 | 2014-03-26 | 青岛九龙生物医药有限公司 | Alkali-enzymolysis method for extracting chondroitin sulfate sodium |
| CN105504094A (en) * | 2016-01-20 | 2016-04-20 | 定陶县地元生化制品有限公司 | Preparation method of sodium-ion-free chondroitin enzymolysis solution |
| WO2016090704A1 (en) * | 2014-12-08 | 2016-06-16 | 张木良 | Chondroitin sulfate preparation process and equipment thereof |
| CN106632731A (en) * | 2017-02-27 | 2017-05-10 | 高焕顺 | Method for producing chondroitin without using ethyl alcohol |
| CN107964055A (en) * | 2016-10-19 | 2018-04-27 | 清华大学 | Giant salamander cartilage chondroitin sulfate and its extracting method |
| CN109280095A (en) * | 2018-05-18 | 2019-01-29 | 山阳县恒桓生物科技有限公司 | A kind of extracting method of chondroitin sulfate |
| CN110760016A (en) * | 2019-05-10 | 2020-02-07 | 赤峰蒙广生物科技有限公司 | Method for purifying chondroitin sulfate from chondroitin sulfate fermentation liquor |
| CN110922503A (en) * | 2019-12-10 | 2020-03-27 | 美泰科技（青岛）股份有限公司 | Novel extraction process of chondroitin sulfate |
-
2005
- 2005-06-29 CN CN 200510027279 patent/CN1273497C/en not_active Expired - Fee Related
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102199229A (en) * | 2011-04-08 | 2011-09-28 | 淮安麦德森制药有限公司 | Method for preparing chondroitin sulfate |
| CN102190740B (en) * | 2011-04-08 | 2012-10-24 | 淮安麦德森制药有限公司 | Preparation method of chondroitin sulfate |
| CN102190740A (en) * | 2011-04-08 | 2011-09-21 | 淮安麦德森制药有限公司 | Preparation method of chondroitin sulfate |
| CN102838691A (en) * | 2012-08-29 | 2012-12-26 | 宁波绿之健药业有限公司 | Extracting and purifying method of chondroitin sulfate |
| CN102978260A (en) * | 2012-11-28 | 2013-03-20 | 康普药业股份有限公司 | Method for refining chondroitin sulfate crude product |
| CN103145874B (en) * | 2012-12-08 | 2015-11-25 | 青岛九龙生物医药有限公司 | A kind of method improving content of chondroitin sulfate |
| CN103145874A (en) * | 2012-12-08 | 2013-06-12 | 青岛九龙生物医药有限公司 | Method for improving content of chondroitin sulfate |
| CN105461826A (en) * | 2013-10-21 | 2016-04-06 | 青岛九龙生物医药有限公司 | Sodium chondroitin sulfate reduction decoloring method |
| CN103601816B (en) * | 2013-10-21 | 2016-01-27 | 青岛九龙生物医药有限公司 | A kind of Sodium chondroitin sulfate reduction decoloration method |
| CN103601816A (en) * | 2013-10-21 | 2014-02-26 | 青岛九龙生物医药有限公司 | Sodium chondroitin sulfate reduction decoloration method |
| CN103665188A (en) * | 2013-11-23 | 2014-03-26 | 青岛九龙生物医药有限公司 | Alkali-enzymolysis method for extracting chondroitin sulfate sodium |
| CN103665188B (en) * | 2013-11-23 | 2016-04-13 | 青岛九龙生物医药有限公司 | Alkali-enzymolysis process extracts Sodium chondroitin sulfate A |
| WO2016090704A1 (en) * | 2014-12-08 | 2016-06-16 | 张木良 | Chondroitin sulfate preparation process and equipment thereof |
| CN105504094A (en) * | 2016-01-20 | 2016-04-20 | 定陶县地元生化制品有限公司 | Preparation method of sodium-ion-free chondroitin enzymolysis solution |
| CN105504094B (en) * | 2016-01-20 | 2017-09-29 | 定陶县地元生化制品有限公司 | Liquid and preparation method thereof is digested without sodium ion chondroitin |
| CN107964055A (en) * | 2016-10-19 | 2018-04-27 | 清华大学 | Giant salamander cartilage chondroitin sulfate and its extracting method |
| CN106632731A (en) * | 2017-02-27 | 2017-05-10 | 高焕顺 | Method for producing chondroitin without using ethyl alcohol |
| CN109280095A (en) * | 2018-05-18 | 2019-01-29 | 山阳县恒桓生物科技有限公司 | A kind of extracting method of chondroitin sulfate |
| CN110760016A (en) * | 2019-05-10 | 2020-02-07 | 赤峰蒙广生物科技有限公司 | Method for purifying chondroitin sulfate from chondroitin sulfate fermentation liquor |
| CN110922503A (en) * | 2019-12-10 | 2020-03-27 | 美泰科技（青岛）股份有限公司 | Novel extraction process of chondroitin sulfate |
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| CN1273497C (en) | 2006-09-06 |
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