Method for preparing water-soluble free amine chitosan
View Patent ↗A method for the preparation of water-soluble chitosan with high purity and biological activity includes steps of: reacting chitosan oligo sugar acid salt, covalently bonded to an organic or inorganic acid, with trialkylamine in phosphate buffered saline followed by addition of an organic solvent to remove acid salt at C-2 position; adding the thus obtained reaction mixture to an inorganic acid to remove trialkylamine salt at C-6 position; and passing the thus obtained free amine chitosan through an activated carbon/ion exchange resin. The free amine chitosan is water-soluble and has a high bioavailability for application to the medicine and food industries.
1. A method for preparing water-soluble chitosan having free amine groups, comprising the steps of:
(a) enzymatically hydrolyzing an organic or inorganic acid salt of chitosan oligo sugar;
(b) reacting the hydrolysis product of step (a) with trialkylamine;
(c) adding an organic solvent to the product of step (b) to remove the acid salt at C-2 position of the chitosan oligo sugar;
(d) adding an inorganic acid to the product of step (c) to remove trialkylamine salt at C-6 position of the chitosan oligo sugar; and
(e) purifying a chitosan having free amine groups from the products of step (d).
2. The method according to claim 1 , wherein the molecular weight of the water-soluble chitosan ranges from 1,000 to 100,000 Da.
3. The method according to claim 1 , wherein the organic acid of said step (a) is selected from the group consisting of lactic acid, acetic acid, propionic acid, formic acid, ascorbic acid and tartaric acid.
4. The method according to claim 1 , wherein the inorganic acid of said step (a) is selected from the group consisting of hydrochloric acid, nitric acid, and sulfuric acid.
5. The method according to claim 1 , wherein the trialkylamine is selected from the group consisting of trimethylamine, triethylamine, tripropylamine, triisopropylethylamine, and tributylamine.
6. The method according to claim 1 , wherein the trialkylamine is trimethylamine.
7. The method according to claim 1 , wherein the trialkylamine is used in an amount of two to three parts relative to one part of the amine group of chitosan oligo sugar acid salt.
8. The method according to claim 1 , wherein said step (b) occurs in phosphate buffered saline solution in a range of from pH 6.8 to pH 7.4.
9. The method according to claim 1 , wherein the organic solvent is selected from the group consisting of acetone; alcohols selected from the group consisting of methanol, ethanol, and propanol; and carbon chlorides selected from the group consisting of chloroform and dichloromethane.
10. The method according to claim 1 , wherein the inorganic acid of said step (d) is selected from the group consisting of hydrochloric acid, nitric acid, and sulfuric acid.
11. The method according to claim 1 , wherein the inorganic acid of said step (d) is hydrochloric acid.
12. The method according to claim 1 , wherein the concentration of the inorganic acid of said step (d) ranges from 0.0005 to 0.600 N.
13. The method according to claim 1 , wherein the organic or inorganic acid salt of chitosan oligo sugar is prepared by dissolving chitosan oligo sugar in an organic acid or inorganic acid.
14. The method according to claim 1 , wherein the organic or inorganic acid salt of chitosan oligo sugar is treated with chitosanase.
15. The method according to claim 1 , wherein the organic or inorganic acid salt of chitosan oligo sugar is dissolved in phosphate buffered saline solution.
16. The method according to claim 1 , wherein step (e) includes passing the product of step (d) through an activated carbon/ion exchange to recover a chitosan having free amine groups.