IP Library Granted Patent US 8,835,403
Granted Patent B2
US 8,835,403 · App. 10/594,100 · Granted Sep 16, 2014

Algin oligosaccharides and the derivatives thereof as well as the manufacture and the use of the same

Inventors: Meiyu Geng (Qingdao, CN); Huashi Guan (Qingdao, CN); Xianliang Xin (Qingdao, CN); Zhao Yang (Qingdao, CN); Guangqiang Sun (Qingdao, CN)
C08B37/0084C07H3/06C07H3/04C08B37/0024
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Quick Facts
Patent No.
US 8,835,403
App. No.
10/594,100
Granted
Sep 16, 2014
Kind
B2
Abstract

The present invention provides an alginate oligosaccharide and its derivatives with the degree of polymerization ranging from 2 to 22. The alginate oligosaccharide is composed of β-D-mannuronic acid linked by 1,4 glycosidic bonds. The derivatives with the reduced terminal in position 1 of carboxyl radical can be prepared by oxidative degradation. The present invention also provides a process for preparing the alginate oligosaccharide and its derivatives, which includes the procedures that an alginate solution is reacted for 2 to 6 h in an autoclave at pH 2-6 and the temperature of 100-120° C., and pH is adjusted to 7 after the reaction is stopped, after which the resultant oligosaccharide is oxidized in the presence of an oxidant to obtain an oxidative degradation product. The alginate oligosaccharide and its derivatives of the invention can be used in the manufacture of a medicament for the prophylaxis and treatment of AD and diabetes.

Claims (19)

1. A composition consisting essentially of alginate oligosaccharide derivatives or their pharmaceutically-acceptable salts, wherein the alginate oligosaccharide derivatives are composed of β-D-mannuronic acid linked by 1,4 glycosidic bonds, wherein the reduced terminal in position 1 is carboxyl radical, as shown by the following formula II:

wherein, n represents 0 or an integer of 1 to 8.

2. The composition according to claim 1 , wherein n is 2 to 8.

3. The composition according to claim 2 , wherein n is 4 to 8.

4. A process for preparing alginate oligosaccharide derivatives or their pharmaceutically-acceptable salts, wherein the alginate oligosaccharide derivatives are composed of β-D-mannuronic acid linked by 1,4 glycosidic bonds, wherein the reduced terminal in position 1 is carboxyl radical, as shown by the following formula II:

wherein, n represents 0 or an integer of 1 to 8, the process comprising the following steps in order:

acid hydrolysis step: an alginate aqueous solution is reacted for about 2 to 6 hrs in an autoclave at pH 2-6 and a temperature of about 100-120° C.;

pH-adjusting step: after the acid hydrolysis reaction is stopped, the value of pH is adjusted to about 7; and

oxidative degradation step: an oxidant is added and reacted for 15 min to 2 hrs at a temperature of 100-120° C.

5. The process according to claim 4 , wherein said alginate is sodium alginate and the acid hydrolysis reaction is carried out for 4 hrs under the condition of pH 4 and 110° C.

6. The process according to claim 4 , wherein after adjusting the pH to about 7, alcohol is added to give a precipitate; the precipitate is filtered off with suction, dehydrated, dried and desalted.

7. The process according to claim 4 , wherein the oxidant is copper hydroxide and the oxidative degradation is performed for 30 min at a temperature of 100° C.

8. A method for the treatment of Alzheimer's disease in a subject, comprising: administering, to the subject, a therapeutically effective amount of an active ingredient consisting essentially of mannuronic acid oligosaccharides represented by the following formula II,

wherein, n represents 0 or an integer of 1 to 8.

9. A pharmaceutical composition, consisting essentially of:

i) an effective amount of mannuronic acid oligosaccharide derivatives represented by the following formula (II) for the prophylaxis and treatment of Alzheimer's disease or for the prophylaxis and treatment of diabetes;

wherein, n represents 0 or an integer of 1 to 8.

and ii) a pharmaceutically-acceptable carrier.

10. The pharmaceutical composition according to claim 9 , wherein the composition is any one selected from the group consisting of an amyloid-β protein fibrils forming inhibitor, an islet amyloid protein fibrils forming inhibitor and a fibrils disaggregating promoter.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2016
From: GENG, MEIYU; GUAN, HUASHI; XIN, XIANLIANG; YANG, ZHAO; SUN, GUANGQIANG
To: OCEAN UNIVERSITY OF CHINA
Reel/Frame 038417/0415 →
Priority Claims (1)
CN 2004 1 0023827 · Mar 24, 2004 · national
Continuity (1)
Related Publication 20070254848A1 · Nov 1, 2007