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Method for provoking angiogenesis by administration of angiogenically active oligosaccharides

Assignee: ANGIO-MEDICAL Corp 1350 AVENUE OF AMERICAS NEW YORK NEW YORK 10019 A DE CORP
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Filing: 1988-03-09
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Granted: 1990-01-23
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Expires: 2008-03-09
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Abstract

Abstract A method for causing or increasing angiogenesis is described. The method involves administering to a subject, such as a human being in need of angiogenesis an angiogenically effective amount of an angiogenically effective, pharmaceutically acceptable oligosaccharide or mixture of oligosaccharides.

Inventors

  • 👤 Robert McCluer
  • 👤 Nicholas Catsimpoolas
  • 👤 Michael Klibaner
  • 👤 Ann Griffith
  • 👤 Robert Sinn

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 18:08
CPC Classifications
A; A61; A61K; A61K31/00; A61K31/70; A61K31/7004; C; C07; C07H; C07H13/00; C07H13/02; C07H13/04; C07H15/00; C07H15/02; C07H15/04; C07H3/00; C07H3/06

Claims Analysis

Total Claims: 23
Claim 1
Independent Claim 28 words
Method for causing or enhancing angiogenesis in a subject in need thereof, comprising administering to said subject an angiogenically effective amount of at least one angiogenically active oligosaccharide.
Claim 2
Dependent Claim 28 words
Method for causing or enhancing angiogenesis in a subject in need thereof, comprising administering to said subject an angiogenically effective amount of at least one angiogenically active oligosaccharide.
Claim 3
Dependent Claim 10 words
Method of claim 1, wherein said oligosaccharide is a tetrasaccharide.
Claim 4
Dependent Claim 23 words
Method of claim 2, wherein said tetrasaccharide is selected from the group consisting of O-α-D-glucopyranosyl-(1→6)-O-α-D-glucopyranosyl-(1.fwdarw.4-O-α-D-glucopyranosyl-(43 4) 1→4)-D-glucose, O-(2-Acetamido-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2 (2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1→4)-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1→4)2-acetamido-2-deoxy-D-glucose (N,N',N",N'"-Tetraacetyl chitotetraose), and 2-(2-Carbomethoxyethylthio)ethyl-O-α-D-glucopyranosyl-(1→6)-O-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranosyl-(1.fwdarw.4)-β-D-glucopyranoside.
Claim 5
Dependent Claim 10 words
Method of claim 1, wherein said oligosaccharide is a trisaccharide.
Claim 6
Dependent Claim 24 words
Method of claim 4, wherein said trisaccharide is selected from the group consisting O-(2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→4)-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1→4)-2-acetamido-2-deoxy-D-glucose (N,N',N"-Triacetyl chitotriose), O-β-D-Galactopyranosyl-(1→4)-O-β-D-galactopyranosyl-(1.fwdarw.4)-D-glucose, Ethyl O-α-D-galactopyranosyl-(1→4)-O-β-D-galactopyranosyl-(1.fwdarw.4)β-D-glucopyranoside, Ethyl O-α-D-galactopyranosyl-(1→4)-O-β-D-galactopyranosyl-(1.fwdarw.4)-2-acetamido-2-deoxy-β-D-glucopyranoside, and Methyl O-α-D-mannopyranosyl-(1→6)-[O-α-D-mannopyranosyl-(1.fwdarw.3)-α-D-mannopyranoside.
Claim 7
Dependent Claim 10 words
Method of claim 1, wherein said oligosaccharide is a disaccharide.
Claim 8
Dependent Claim 30 words
Method of claim 6, wherein said disaccharide is selected from the group consisting of Methyl O-β-D-galactopyranosyl-(1→3)-2-acetamido-2-deoxy-β-D-glucopyranoside, Ethyl O-α-D-galactopyranosyl-(1→4)-O-β-D-galactopyranoside, 2-(Octadecylthio)ethyl O-α-D-galactopyranosyl-(1→4)-β-D-galactopyranoside, Methyl O-(2-acetamide-2-deoxy-β-D-galactopyranosyl)-(1→3)-α-D-galactopyranoside, O-(2-Acetamido-2-deoxy-β-D-glucopyranosyl)-(1→4)-2-acetamido-2-deoxy-D-glucose (N,N'-Diacetyl chitobiose), Methyl O-α-D-galactopyranosyl-(1→3)-α-D-galactopyranoside, and Methyl O-α-D-mannopyranosyl-(1→6)-α-D-mannopyranoside.
Claim 9
Dependent Claim 13 words
Method of claim 1, comprising administering a mixture of oligosaccharides to said subject.
Claim 10
Dependent Claim 14 words
Method of claim 8, wherein said mixture of oligosaccharides is derived from human milk.
Claim 11
Dependent Claim 11 words
Method of claim 9, wherein said mixture of oligosaccharides contain lactose.
Claim 12
Dependent Claim 11 words
Method of claim 9, wherein said mixture of oligosaccharides contains lacto-N-neotetraose.
Claim 13
Dependent Claim 11 words
Method of claim 9, wherein said mixture of oligosaccharides contains lactodifucotetraose.
Claim 14
Dependent Claim 13 words
Method of claim 9 wherein said mixture of oligosaccharides contains lacto-N-fuco pentaose II.
Claim 15
Dependent Claim 11 words
Method of claim 1, wherein said subject is a human being.
Claim 16
Dependent Claim 23 words
Method of claim 1, wherein said oligosaccharide is administered in an amount ranging from about 100 μg to about 20 mg per day.
Claim 17
Dependent Claim 11 words
Method of claim 1, wherein said oligosaccharide contains only glucose residues.
Claim 18
Dependent Claim 11 words
Method of claim 1, wherein said oligosaccharide contains only galactose residues.
Claim 19
Dependent Claim 11 words
Method of claim 1, wherein said oligosaccharide contains only mannose residues.
Claim 20
Dependent Claim 20 words
Method of claim 1, wherein said oligosaccharide contains a mixture of at least two of glucose, galactose, and mannose residues.
Claim 21
Dependent Claim 13 words
Method of claim 1, wherein said oligosaccharide is conjugated to bovine serum albumin.
Claim 22
Dependent Claim 28 words
Method of claim 20, wherein said oligosaccharide complexed to obvine serum albumin is selected from the group consisting of O-β-(2-(2-carbomethoxyethylthio)ethyl)-N-acetyl-D-galactosamine; O-β-(2-(2-carboxymethoxyethylthio)ethyl-N-acetyl-D-glucosamine; O-2-(2-carbomethoxylethylthio)ethyl-methyl; and O-β-(2-(2-carboxymethoxyethylthio)ethyl galactose 1→3 N-acetyl glucosamine.
Claim 23
Dependent Claim 23 words
Method of claim 1, wherein said oligosaccharide is a substituted monosaccharide selected from the group consisting of 2-(2-Carbomethoxyethylthio)ethyl-β-D-galactopyranoside, 2-l -(Octadecylthio)ethyl-β-D-galactopyranoside, 2-(2-Carbomethoxyethylthio)ethyl-β-D-glucopyranoside, and 2-(Octadecylthio)ethyl-β-D-glucopyranoside.

References Cited (Backward Citations)

US4057685A Cited
US4401662A Cited
US4496550A Cited
US4710490A Cited
US4710490B1 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1993-01-22 1993-07-24 1994-01-23 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1997-01-22 1997-07-24 1998-01-23 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2001-01-22 2001-07-24 2002-01-23 $7700.00 Window Closed / Lapsed

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