[feed] Atom [feed] RSS 1.0 [feed] RSS 2.0

Depolymerized products of chitosan as potent inhibitors of tumor-induced angiogenesis.

Harish Prashanth, K. V. and Tharanathan, R. N. (2005) Depolymerized products of chitosan as potent inhibitors of tumor-induced angiogenesis. Biochimica et Biophysica Acta, 1722 (1). pp. 22-29. ISSN 0304-4165

[img] PDF
Biochimica_et_Biophysica_Acta_1722_(2005)_22-_29.pdf
Restricted to Registered users only

Download (366kB) | Request a copy
Official URL: http://www.elsevier.com/locate/bba

Abstract

Water-soluble low-molecular weight chitosan (LMWC) and chitooligosaccharides (COs) were obtained from chitosan (16% Nacetylation) by depolymerization induced by potassium persulfate under nitrogen atmosphere for 2 h. They were characterized by IR, X-ray, HPLC and 13C-NMR. Splitting of C3/C5 signals in the latter indicated a newer conformation, and also showed prominence of acetyl groups in LMWC, may be due to cleavage between two consecutive deacetylated residues. Molecular weight of LMWC, determined by HPSEC, showed a single peak of ~37 kDa. HPLC analysis of the solvent-extracted fraction revealed COs enriched with pentamer, hexamer and higher oligomers. The effect of LMWC and COs on the growth of Ehrlich ascites tumor (EAT) cells and tumor-induced neovascularization was studied. COs (50 Ag) were more effective compared to LMWC (100 Ag) and proved to be potent angioinhibitory and antitumor compounds, as shown by inhibition of angiogenesis and inducing apoptosis as a function of DNA fragmentation.

Item Type: Article
Additional Information: Copyright of this article belongs to Elsevier Ltd.
Uncontrolled Keywords: Low molecular weight chitosan; Chitooligosaccharide; Anti-angiogenesis; Apoptosis; DNA
Subjects: 600 Technology > 08 Food technology > 28 Meat, Fish & Poultry
Divisions: Dept. of Biochemistry
Depositing User: Food Sci. & Technol. Information Services
Date Deposited: 25 Jun 2007 06:45
Last Modified: 25 Sep 2018 09:06
URI: http://ir.cftri.res.in/id/eprint/1261

Actions (login required)

View Item View Item