EP0097625A2
Expired / Lapsed
EP
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Process for producing substantially pure dermatan sulfate and heparan sulfate glycosaminoglycans, and pharmaceutical use thereof
Assignee: Italo-Britannica L Manetti - H Roberts & C Soc
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Filing: 1983-06-17
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Granted: —
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Expires: 2003-06-17
Abstract
Abstract Substantially pure dermatan sulfate and heparan sulfate are produced starting from a mixture of mucopolysaccharides on an industrial scale by means of a process of precipitation involving saline substances and enzymatic purification. Heparan sulfate shows selective fibrinolytic activity when administered orally, and dermatan sulfate shows antiedemigenic, local anti - congestive and healing activity in topical administration.
Inventors
- 👤 Giovanni Orzalesi
- 👤 Ivo Volpato
- 👤 Renzo Cappelletti
Bibliographic Details
Application Number
—
Jurisdiction
EP
Data Source
google_patents
Last Synchronized
2026-10-25 22:44
CPC Classifications
C; C08; C08B; C08B37/00; C08B37/006; C08B37/0063; C08B37/0075; C08B37/0069
Claims Analysis
Total Claims: 11
Claim 1
Independent Claim
196 words
Process for producing substantially pure dermatan sulfate and heparan sulfate, starting from a mixture of mucopolysaccharides in aqueous solution which contains them, characterized by operations of: a) introducing in said starting solution a water soluble ionizing salt'consisting of ammonium or potassium as the cation part, up to a concentration of 70 - 90% of the saturation level of said salt at 25°C, so as to produce at room temperature a first precipitate containing dermatan sulfate in a substantially pure state; b) separating said precipitate from the solution and recovering the substantially pure dermatan sulfate as first product; c) cooling the solution removed from the precipitate to approximately O°C in order to produce a second precipitate at said temperature containing chondroitin sulfate A; d) removing said second precipitate from the solution; e) separating from the residual solution the salt introduced in operation (a) so as to prepare a desalinified solution; f) removing the water from said desalinified solution so as to prepare a solid containing heparan sulfate contaminated with other glycosaminiglycanes; g) subjecting said solid to enzymatic treatment with pndroitinase ABC, so as to eliminate said impurities and recover the heparan sulfate substantially pure as second product.
Claim 2
Dependent Claim
196 words
Process for producing substantially pure dermatan sulfate and heparan sulfate, starting from a mixture of mucopolysaccharides in aqueous solution which contains them, characterized by operations of: a) introducing in said starting solution a water soluble ionizing salt'consisting of ammonium or potassium as the cation part, up to a concentration of 70 - 90% of the saturation level of said salt at 25°C, so as to produce at room temperature a first precipitate containing dermatan sulfate in a substantially pure state; b) separating said precipitate from the solution and recovering the substantially pure dermatan sulfate as first product; c) cooling the solution removed from the precipitate to approximately O°C in order to produce a second precipitate at said temperature containing chondroitin sulfate A; d) removing said second precipitate from the solution; e) separating from the residual solution the salt introduced in operation (a) so as to prepare a desalinified solution; f) removing the water from said desalinified solution so as to prepare a solid containing heparan sulfate contaminated with other glycosaminiglycanes; g) subjecting said solid to enzymatic treatment with pndroitinase ABC, so as to eliminate said impurities and recover the heparan sulfate substantially pure as second product.
Claim 3
Dependent Claim
19 words
Process according to claim 1, in which said salt is protassium acetate, ammonium chloride, ammonium acetate or potassium sulfate.
Claim 4
Dependent Claim
20 words
process according to claim 1, in which said concentration in operation (a) is 80% of the saturation concentration at 25°C.
Claim 5
Dependent Claim
23 words
Frocess according to claim 1, in which said separation operation (e) is an operation of d&alysis, precipitation with solvents, ultrafiltration and the like.
Claim 6
Dependent Claim
14 words
Substantially pure dermatan sulfate obtained by means of the process claimed in claim 1.
Claim 7
Dependent Claim
14 words
Substantially pure heparan sulfate obtained by means of the process claimed in claim 1.
Claim 8
Dependent Claim
23 words
Active fibrinolytic agent consisting of heparan sulfate as claimed in claim 6, when administered orally in a dose of 1 - 30 mg/kg/day.
Claim 9
Dependent Claim
26 words
Pharmaceutical composition for oral administration, containing a quantity effective for fibrinolytic activity of heparan sulfate as claimed in claim 6, as well as pharmacologically compatible excipients.
Claim 10
Dependent Claim
16 words
Active antiedemigenic, local anti-congestive and healing agent consisting of dermatan sulfate as claimed in claim 5.
Claim 11
Dependent Claim
34 words
Pharmaceutical composition for topical use containing a quantity effective for the anti - edemigenic, anti - congestive and healing activity of dermatan sulfate as claimed in claim 5, as well as pharmacologically compatible excipients.
References Cited (Backward Citations)
No citation records indexed.
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