GB886712A - Improvements in or relating to the preparation of erythropoietic factor concentrates - Google Patents
Improvements in or relating to the preparation of erythropoietic factor concentratesInfo
- Publication number
- GB886712A GB886712A GB20096/59A GB2009659A GB886712A GB 886712 A GB886712 A GB 886712A GB 20096/59 A GB20096/59 A GB 20096/59A GB 2009659 A GB2009659 A GB 2009659A GB 886712 A GB886712 A GB 886712A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cellulose
- plasma
- exchangers
- solution
- anaemic
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/475—Growth factors; Growth regulators
- C07K14/505—Erythropoietin [EPO]
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J47/00—Ion-exchange processes in general; Apparatus therefor
- B01J47/014—Ion-exchange processes in general; Apparatus therefor in which the adsorbent properties of the ion-exchanger are involved, e.g. recovery of proteins or other high-molecular compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Gastroenterology & Hepatology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Toxicology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
An erythropoietic factor is concentrated by contacting a solution of anaemic plasma with an ion exchange material and eluting the sorbed extract therefrom. The ion exchange material may be an insoluble, substantially open-chain polymer such as a polysaccharide derivative; specified polysaccharides are starches (e.g. amylose and amylopectin), inulins, cellulose (e.g. a - and oxy-celluloses), xylans, pectine and algins, glycogens, chitins and muco polysaccharides (e.g. chondroitin sulphuric acid, heparin and hyaluronic acid), levans and dextrans. Particularly preferred ion-exchangers are the anion-exchangers cellulose-dimethylaminoethyl- or diethylaminoethyl-ethers (prepared by condensing sodium cellulose with 2-chloroethyl-dimethylamine or -diethylamine respectively); carboxyf methylcellulose, cellulose citrate (esterification oan a -cellulose with citric acid) and cellulose phosphate are mentioned as cation-exchangers. The anaemic plasma may be from ovine, bovine, porcine or other mammalian sources, but sheep plasma is preferred. The plasma solution preferably has a pH of 3.5-8.5, particularly 4.0-6.0, e.g. 4.2-4.8, and an alkali metal salt concentration of 0.01-0.06M, e.g. 0.03-0.04M NaCl (in the example NaH2PO4 is also present). Elution is preferably effected with a 0.1-0.5M NaCl solution with a pH below 7.0. Details are given of biological assay of the product.ALSO:An erythropoietic factor is concentrated by contacting a solution of anaemic plasma with an ion exchange material and eluting the sorbed extract therefrom. The ion exchange material may be an insoluble, substantially open-chain polymer such as a polysaccharide derivative; specified polysaccharides are starches (e.g. amylose and amylopectin), inulins, cellulose (e.g. a - and oxy-celluloses), xylans, pectine and algins, glycogens, chitins and muco polysaccharides (e.g. chondroitin sulphuric acid, heparin and hyaluronic acid), levans and dextrans. Particularly preferred ion-exchangers are the anion-exchangers cellulose-dimethylaminoethyl- or diethylaminoethyl-ethers (prepared by condensing sodium cellulose with 2-chloroethyl-dimethylamine or -diethylamine respectively); carboxymethylcellulose, cellulose citrate (esterification of an -cellulose with citric acid) and cellulose phosphate are mentioned as cation-exchangers. The anaemic plasma may be from ovine, p bovine, porcine or other mammalian sources, but sheep plasma is preferred. The plasma solution preferably has a pH of 3.5-8.5, particularly 4.0-6.0, e.g. 4.2-4.8, and an alkali metal salt concentration of 0.01-0.06 M, e.g. 0.03-0.04 M NaCl (in the example NaH2PO4 is also present). Elution is preferably effected with a 0.1-0.5 M NaCl solution with a pH below 7.0. Details are given of a biological assay of the product.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US886712XA | 1958-06-12 | 1958-06-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB886712A true GB886712A (en) | 1962-01-10 |
Family
ID=22212728
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB20096/59A Expired GB886712A (en) | 1958-06-12 | 1959-06-11 | Improvements in or relating to the preparation of erythropoietic factor concentrates |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB886712A (en) |
NL (1) | NL239896A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0187670A2 (en) * | 1985-01-11 | 1986-07-16 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Process for recovering adsorbent for use in extracorporeal circulation treatment |
WO1997017366A1 (en) * | 1995-11-08 | 1997-05-15 | Hoechst Marion Roussel, Inc. | Heparin chromatography of erythropoietins |
-
0
- NL NL239896D patent/NL239896A/xx unknown
-
1959
- 1959-06-11 GB GB20096/59A patent/GB886712A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0187670A2 (en) * | 1985-01-11 | 1986-07-16 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Process for recovering adsorbent for use in extracorporeal circulation treatment |
EP0187670A3 (en) * | 1985-01-11 | 1987-04-08 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Process for recovering adsorbent for use in extracorporeal circulation treatment |
WO1997017366A1 (en) * | 1995-11-08 | 1997-05-15 | Hoechst Marion Roussel, Inc. | Heparin chromatography of erythropoietins |
AU704509B2 (en) * | 1995-11-08 | 1999-04-22 | Aventisub Ii Inc. | Heparin chromatography of erythropoietins |
Also Published As
Publication number | Publication date |
---|---|
NL239896A (en) |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE3463386D1 (en) | Process for the preparation of oligosaccharide fractions having pharmacological properties by chemical degradation of heparin | |
Peat et al. | 778. The structure of lichenin | |
DE1642661A1 (en) | Process for the production of urokinase | |
GB1471482A (en) | Heparing salts | |
ES8100763A1 (en) | Prothrombin complex concentrates,preparation and application thereof | |
Wolfrom et al. | Sulfated Nitrogenous Polysaccharides and Their Anticoagulant ACTIVITY1 | |
Kenne et al. | The structure of capsular polysaccharide of the pneumococcus type II | |
GB886712A (en) | Improvements in or relating to the preparation of erythropoietic factor concentrates | |
Wu-Yuan et al. | Architecture and chemistry of microconidial walls of Trichophyton mentagrophytes | |
DE3479503D1 (en) | Process for the preparation of an antithrombin iii-heparin, e.g. an antithrombin iii-heparinoid concentrate | |
GB908333A (en) | Method for the production of substantially protein-free callicrein | |
Connell et al. | 688. The constitution of laminarin. Part I. An investigation on laminarin isolated from Laminaria cloustoni | |
ES8404378A1 (en) | Process for preparing alkali metal salt of carboxymethyl cellulose | |
Hillestad et al. | Structural studies of water-soluble glycoproteins from Cannabis sativa L | |
Margolis et al. | Alkali-labile oligosaccharides of brain glycoproteins | |
Matulewicz et al. | Methylation analysis of carrageenans from tetrasporic and cystocarpic stages of Gigartina skottsbergii | |
GB914421A (en) | Improvements in or relating to cellulosic sponge material | |
Egami et al. | Chemical Studies on Charoninsulfuric Acid | |
Weber et al. | Sulfonated amino sugars derived from alkaline sulfite-treated glycoproteins | |
Charlson et al. | The composition of acacia cyanophylla gum | |
Ricketts | 730. The distribution of ester groups in dextran sulphate and their stability towards hydrolytic reagents | |
GB1222810A (en) | Prothrombin complex | |
BR8800713A (en) | USE OF PARTIAL ESTERS OF CITRIC ACID, AS WELL AS MIXTURES USABLE IN THE EXTRACTION OF IRON FROM ACID AQUEOUS SOLUTIONS | |
KR910015699A (en) | Method of Purifying Lipocotin | |
GB785112A (en) | Improvements in the treatment of hides, skins and tanning liquors therefor |