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Surimi wash water treatment by chitosan-alginate complexes

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decreased for samples with lower MW. These results suggest that the effect of MW<br />

on the tensile strength of <strong>chitosan</strong> films is more dominant than the effect of DD.<br />

Finally, the elongation and the ability of film to absorb moisture decreased with<br />

increased DD.<br />

The effect of MW and DD on drug release has been recently reported.<br />

Using <strong>chitosan</strong> with 70 and 80% DD, Kofuji and others (2000) found that<br />

degradability of <strong>chitosan</strong> beads <strong>by</strong> lysozyme decreased as the DD increased but<br />

drug release was not influenced. Similar results were observed when the same<br />

authors studied the effect of DD on the biodegrability and drug release performance<br />

of <strong>chitosan</strong> beads tested on mice (Kofuji and others, 2001) using <strong>chitosan</strong> with 70,<br />

80, 90 and 100% DD. Chitosan gel beads prepared in 10% amino acid solution (pH<br />

9) were subcutaneously implanted in air pouches on the dorsal surface of mice.<br />

Degradation of the beads increased as the <strong>chitosan</strong> DD decreased. On the contrary,<br />

Chiou and others (2001) found that drug release was independent of MW or DD<br />

but the initial burst decreased as the MW increased. The difference in findings<br />

amongst these results could possibly be due to the different methods of preparation.<br />

Kofuji et al (2000, 2001) mixed the drug directly with the <strong>chitosan</strong> solutions and<br />

dropped the mixture into 10% glycine to form a hydrogel while Chiou and others<br />

(2001) applied the <strong>chitosan</strong> solution as a microcapsule coating. Drug release from<br />

the hydrogel beads will solely depend on <strong>chitosan</strong> while that for the <strong>chitosan</strong> coated<br />

microcapsules will also depend on the microcapsule used.<br />

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