Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
19119 | Food and Bioproducts Processing | 2013 | 9 Pages |
•Enzyme immobilization method by spray drying with in situ cross-linking was developed.•Morphology and microstructure of chitosan microparticles were investigated.•Laccase was successfully immobilized and its activity was assessed.•Particles produced by in situ cross-linking have superior properties.
The effect of processing method on the properties of cross-linked chitosan microparticles and on the enzymatic activity of laccase immobilized in the particles has been investigated. Chitosan has been cross-linked by tri-polyphosphate (TPP) using two methods – the so called ex situ cross-linking whereby the solutions of chitosan, TPP and the enzyme have been pre-mixed and spray-dried by a standard two-fluid kinetic nozzle, and a novel in situ cross-linking method, whereby the solutions have been contacted at the tip of a three-fluid nozzle and cross-linking occurred within a drying droplet. The influence of the cross-linking method on the particle size and morphology, surface charge, and swelling ratio has been determined. The enzymatic activity of laccase toward the oxidation of a chromophore substrate (ABTS) has been systematically investigated and found to be superior in particles produced by the in situ cross-linking method.
Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (138 K)Download as PowerPoint slide