Abstract

Crude chitosan was prepared from shrimp shell by HCl, NaOH and ethanol solution successively. Hydrogen peroxide was used to degrade the crude chitosan into water-soluble chitosan. A mathematical model between degradation conditions (H2O2 level, time and temperature) and the recovery of water-soluble chitosan was constructed using response surface methodology. Each factor showed a significant effect on the recovery. The model was confirmed to have a good fitness by analysis of variance. The optimal conditions to obtain the highest recovery of water-soluble chitosan were 5.5% of H2O2 level, 3.5 h of time and 42.8 °C of temperature. The predicted recovery was 93.5%. Through testing the number of colony, both crude and water-soluble chitosan showed good inhibition activities against B. subtilis. By determination of inhibition zone diameter, water-soluble chitosan showed significantly (P < 0.05) higher inhibition capabilities against E. coli, B. subtilis and S. aureus than crude chitosan. Chitin is the second abundant polymer next to cellulose over the world. Its deacetylated product, chitosan, is an important ingredient in medicine and food. However, the low solubility in water limits the application of chitosan. In this work, the chitosan was degraded by H2O2 to produce water-soluble chitosan. Response surface methodology was taken to construct a model between degradation conditions and the recovery of water-soluble chitosan. By determination of the antibacterial activity, water-soluble chitosan showed better antibacterial activity than crude chitosan without degradation treatment. The results indicated the high potential of water-soluble chitosan as an antibacterial agent. This work was helpful for applying this product in industry.

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