WO2002063961B1 - Composition and methods for modulation of vascular structure and/or function - Google Patents

Composition and methods for modulation of vascular structure and/or function

Info

Publication number
WO2002063961B1
WO2002063961B1 PCT/US2002/003792 US0203792W WO02063961B1 WO 2002063961 B1 WO2002063961 B1 WO 2002063961B1 US 0203792 W US0203792 W US 0203792W WO 02063961 B1 WO02063961 B1 WO 02063961B1
Authority
WO
WIPO (PCT)
Prior art keywords
acetylglucosamine
polymers
daltons
substantially free
semi
Prior art date
Application number
PCT/US2002/003792
Other languages
French (fr)
Other versions
WO2002063961A1 (en
Inventor
John N Vournakis
Sergio Finkeilsztein
Original Assignee
Marinepolymer Tech Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority to IL15732702A priority Critical patent/IL157327A0/en
Priority to CA 2437812 priority patent/CA2437812C/en
Priority to DK02740104T priority patent/DK1365651T3/en
Priority to EP20020740104 priority patent/EP1365651B1/en
Priority to AU2002306455A priority patent/AU2002306455B2/en
Priority to JP2002563772A priority patent/JP5303088B2/en
Priority to NZ527872A priority patent/NZ527872A/en
Priority to ES02740104T priority patent/ES2456695T3/en
Application filed by Marinepolymer Tech Inc filed Critical Marinepolymer Tech Inc
Priority to MXPA03007176A priority patent/MXPA03007176A/en
Publication of WO2002063961A1 publication Critical patent/WO2002063961A1/en
Publication of WO2002063961B1 publication Critical patent/WO2002063961B1/en
Priority to IL15732703A priority patent/IL157327A/en
Priority to AU2007251899A priority patent/AU2007251899B2/en
Priority to AU2011200400A priority patent/AU2011200400B2/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/726Glycosaminoglycans, i.e. mucopolysaccharides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/716Glucans
    • A61K31/722Chitin, chitosan
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/737Sulfated polysaccharides, e.g. chondroitin sulfate, dermatan sulfate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0014Skin, i.e. galenical aspects of topical compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/70Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
    • A61K9/7007Drug-containing films, membranes or sheets
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/14Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0024Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Glucans; (beta-1,3)-D-Glucans, e.g. paramylon, coriolan, sclerotan, pachyman, callose, scleroglucan, schizophyllan, laminaran, lentinan or curdlan; (beta-1,6)-D-Glucans, e.g. pustulan; (beta-1,4)-D-Glucans; (beta-1,3)(beta-1,4)-D-Glucans, e.g. lichenan; Derivatives thereof
    • C08B37/00272-Acetamido-2-deoxy-beta-glucans; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0024Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Glucans; (beta-1,3)-D-Glucans, e.g. paramylon, coriolan, sclerotan, pachyman, callose, scleroglucan, schizophyllan, laminaran, lentinan or curdlan; (beta-1,6)-D-Glucans, e.g. pustulan; (beta-1,4)-D-Glucans; (beta-1,3)(beta-1,4)-D-Glucans, e.g. lichenan; Derivatives thereof
    • C08B37/00272-Acetamido-2-deoxy-beta-glucans; Derivatives thereof
    • C08B37/003Chitin, i.e. 2-acetamido-2-deoxy-(beta-1,4)-D-glucan or N-acetyl-beta-1,4-D-glucosamine; Chitosan, i.e. deacetylated product of chitin or (beta-1,4)-D-glucosamine; Derivatives thereof

Abstract

The present invention relates to compositions comprising semi-crystalline β-1-4-N-acetylglucosamine polymers (p-GlcNac) and methods utilizing such polymers modulation of vascular structure and/or function. The compositions and methods disclosed are useful for stimulating, in a p-GlcNac concentration-dependent manner, endothelin-1 release, vasoconstriction, and/or reduction in blood flow out of a breached vessel, as well as for contributing to or effecting cessation of bleeding. The methods of the present invention comprise topical administration of materials comprising semi-crystalline p-GlcNac polymers that are free of proteins, and substantially free of single amino acids as well as other organic and inorganic contaminants, and whose constituent monosaccharide sugars are attached in a β-1-4 conformation.

Claims

78AMENDED CLAIMS[received by the International Bureau on 31 July 2002 (31.07.02); original claims 1-25 replaced by new claims 1-38 (5 pages)]
1. A method for achieving at least a transient, localized, modulation of vascular 5 structure and/or function, comprising: topically administering to a patient in need of said modulation, a sufficient amount of material comprising semi-crystalline poly-β-l- 4 N-acetylglucosamine polymers, wherein said administering induces at least a transient, localized physiological response selected from the group consisting of stimulation of endothelin-1 release, vasoconstriction, I o and reduction in blood flow out of a breached vessel, whereby the patient experiences at least a transient, localized modulation of vascular structure and/or function.
2. The method of claim 1 , wherein the physiological response comprises 15 stimulation of endothelin-1 release.
3. The method of claim 2, wherein the endothelin- 1 is released from vascular endothelial cells.
0 4. The method of claim 1, wherein the physiological response comprises vasoconstriction.
5. The method of claim 1, wherein the physiological response comprises reduction in blood flow out of a breached vessel.
25
6. The method of claim 1, wherein the poly-β-l→-4 N-acetylglucosamine polymer comprises about 50 to about 150,000 N-acetylglucosamine monosaccharides covalently attached in a β-l- conformation, and said polymer has a molecular weight of about 10,000 daltons to about 30 million daltons.
30
7. The method of claim 6, wherein the poly-β-1 →4 N-acetylglucosamine polymer comprises about 50 to about 50,000 N-acetylglucosamine monosaccharides covalently attached in a β-l→-4 conformation, and said polymer has a molecular weight of about 10,000 daltons to about 10 million daltons.
35 79
8. The method of claim 7, wherein the poly-β- 1 →4 N-acetylglucosamine polymer comprises about 50 to about 10,000 N-acetylglucosamine monosaccharides covalently attached in a β-l→-4 conformation, and said polymer has a molecular weight of about 10,000 daltons to about 2 million daltons.
9. The method of claim 8, wherein the poly-β- 1 → N-acetylglucosamine polymer comprises about 50 to about 4,000 N-acetylglucosamine monosaccharides covalently attached in a β-l→-4 conformation, and said polymer has a molecular weight of about 10,000 daltons to about 800,000 daltons.
10. The method of claim 6, wherein the semi-crystalline poly-β- 1→4 N-acetylglucosamine polymer comprises at least one N-acetylglucosamine monosaccharide that is deacetylated, and wherein at least 40% of said N-acetylglucosamine monosaccharides are acetylated.
11. The method of claim 1 , wherein the patient is a human.
12. The method of claim 1 , wherein the material is in the form of a gel, sponge, film, membrane, foam, spray, emulsion, suspension, or solution.
13. The method of claim 1 , wherein the material is applied directly to a blood vessel.
14. The method of claim 1, wherein the vascular structure is a blood vessel selected from the group consisting of capillary, vein, and artery.
15. The method of claim 14, wherein the blood vessel is a breached blood vessel.
16. The method of claim 15, whereby the patient experiences cessation of bleeding.
17. The method of claim 1, wherein the extent of the transient, localized modulation of vascular structure and/or function is substantially proportional to the amount of semi-crystalline poly-β- 1 → N-acetylglucosamine administered. 80
18. A biodegradable, non-barrier-forming material comprising semi-crystalline ρoly-β-l→-4 N-acetylglucosamine polymers comprising about 50 to about 150,000 N-acetylglucosamine monosaccharides covalently attached in a β-l-→-4 conformation, and having a molecular weight of about 10,000 daltons to about 30 million daltons.
19. The material of claim 18, wherein the semi-crystalline ρoly-β-l→-4 N-acetylglucosarnine polymer comprises about 50 to about 50,000 N-acetylglucosamine monosaccharides covalently attached in a β-l→-4 conformation and has a molecular weight of about 10,000 daltons to about 10 million daltons.
20. The material of claim 18, wherein the semi-crystalline ρoly-β-l→4 N-acetylglucosamine polymer comprises about 50 to about 10,000 N-acetylglucosamine monosaccharides covalently attached in a β-l→4 conformation and has a molecular weight of about 10,000 daltons to about 2 million daltons.
21. The material of claim 18, wherein the semi-crystalline poly-β-l→4 N-acetylglucosarnine polymer comprises about 50 to about 4,000 N-acetylglucosamine monosaccharides covalently attached in a β-l→4 conformation and has a molecular weight of about 10,000 daltons to about 800,000 daltons.
22. The material of claim .18, wherein the semi-crystalline poly-β-l→4 N-acetylglucosamine polymer comprises at least one N-acetylglucosamine monosaccharide that is deacetylated, and wherein at least 40% of said N-acetylglucosamine monosaccharides are acetylated.
23. The material of claim 18, wherein the material is a gel, sponge, film, membrane, foam, spray, emulsion, suspension, or solution.
24. A method for treating a patient having a vascular disorder, comprising: topically administering to a patient in need of such treatment, a sufficient amount of material comprising semi-crystalline poly-β-l→-4 N-acelylglucosamine polymers, wherein said administering induces at least a transient, localized physiological response selected from the group consisting of stimulation of endothelin-1 release, vasoconstriction, and reduction in blood flow out of a breached vessel, whereby the patient experiences at least a transient, localized modulation of vascular structure and/or function, 81
whereby said administering ameliorates said vascular condition.
25. The method of claim 24, wherein the vascular disorder is selected from the group consisting of menorrhagia, cerebral aneurysm, abdominal aneurysm, uterine fibroid lesion, and blood vessel puncture.
26. The method of claim 1, wherein said polymers are substantially free of protein.
27. The method of claim 1, wherein said polymers are substantially free of organic contaminants.
28. The method of claim 1, wherein said polymers are substantially free of inorganic contaminants.
29. The biodegradable, non-barrier forming material of claim 18, wherein said polymers are substantially free of protein.
30. The biodegradable, non-barrier forming material of claim 18, wherein said polymers are substantially free of organic contaminants.
31. The biodegradable, non-barrier forming material of claim 18, wherein said polymers are substantially free of inorganic contaminants.
32. The method of claim 24, wherein said polymers are substantially free of protein.
33. The method of claim 24, wherein said polymers are substantially free of organic contaminants.
34. The method of claim 24, wherein said polymers are substantially free of inorganic contaminants.
35. A pharmaceutically-acceptable composition comprising a therapeutically effective amount of a biodegradable, non-barrier-fonning material comprising 82
semi-crystalline poly-β-l→4 N-acetylglucosamine polymers comprising about 50 to about 150,000 N-acetylglucosamine monosaccharides covalently attached in a β-l→4 conformation, and having a molecular weight of about 10,000 daltons to about 30 million daltons.
36. The pharmaceutical composition of claim 34, wherein said polymers are substantially free of protein.
37. The pharmaceutical composition of claim 34, wherein said polymers are substantially free of organic contaminants.
38. The pharmaceutical composition of claim 34, wherein said polymers are substantially free of inorganic contaminants.
PCT/US2002/003792 2001-02-12 2002-02-08 Composition and methods for modulation of vascular structure and/or function WO2002063961A1 (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
NZ527872A NZ527872A (en) 2001-02-12 2002-02-08 Composition and methods for modulation of vascular structure and/or function with a material comprising semi- crystalline poly-beta-1-4 N-acetylglucosasmine (p-GlcNac) polymers
DK02740104T DK1365651T3 (en) 2001-02-12 2002-02-08 COMPOSITION AND PROCEDURES FOR MODULATING VASCULAR STRUCTURE AND / OR FUNCTION
EP20020740104 EP1365651B1 (en) 2001-02-12 2002-02-08 Composition and methods for modulation of vascular structure and/or function
AU2002306455A AU2002306455B2 (en) 2001-02-12 2002-02-08 Composition and methods for modulation of vascular structure and/or function
JP2002563772A JP5303088B2 (en) 2001-02-12 2002-02-08 Compositions and methods for modulation of vasculature and / or function
IL15732702A IL157327A0 (en) 2001-02-12 2002-02-08 Composition and methods for modulation of vascular structure and/or function
ES02740104T ES2456695T3 (en) 2001-02-12 2002-02-08 Compositions and procedures for the modulation of vascular structure and / or function
CA 2437812 CA2437812C (en) 2001-02-12 2002-02-08 Compositions and methods for modulation of vascular structure and/or function
MXPA03007176A MXPA03007176A (en) 2001-02-12 2002-02-08 Composition and methods for modulation of vascular structure and/or function.
IL15732703A IL157327A (en) 2001-02-12 2003-08-11 Use of n-acetylglucosamine polymers for the preparation of medicaments for modulation of vascular structure and/or function
AU2007251899A AU2007251899B2 (en) 2001-02-12 2007-12-20 Compositions and methods for modulation of vascular structure and/or function
AU2011200400A AU2011200400B2 (en) 2001-02-12 2011-01-31 Compositions and methods for modulation of vascular structure and/or function

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/781,182 US7041657B2 (en) 2001-02-12 2001-02-12 Compositions and methods for modulation of vascular structure and/or function
US09/781,182 2001-02-12

Publications (2)

Publication Number Publication Date
WO2002063961A1 WO2002063961A1 (en) 2002-08-22
WO2002063961B1 true WO2002063961B1 (en) 2003-03-06

Family

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PCT/US2002/003792 WO2002063961A1 (en) 2001-02-12 2002-02-08 Composition and methods for modulation of vascular structure and/or function

Country Status (12)

Country Link
US (7) US7041657B2 (en)
EP (2) EP2468094B1 (en)
JP (4) JP5303088B2 (en)
AU (3) AU2002306455B2 (en)
CA (1) CA2437812C (en)
DK (2) DK2468094T3 (en)
ES (2) ES2477316T3 (en)
HK (1) HK1172504A1 (en)
IL (2) IL157327A0 (en)
MX (1) MXPA03007176A (en)
NZ (1) NZ527872A (en)
WO (1) WO2002063961A1 (en)

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