Macroporous chitosan beads used for the immobilization of an anti-inflammat
ory drug were prepared by the wet phase-inversion method. There are two sta
ges of phase-inversion observed from the cast of chitosan droplet in tripol
yphosphate (TPP) aqueous solution. The first stage of phase-inversion is do
minated by liquid-liquid demixing and the morphology of the freeze-dried ch
itosan bead shows a bundle-like porous structure. The following stage of ph
ase-inversion is attributed to the solid-liquid demixing and the morphology
of the freeze-dried chitosan bead changes to an interconnected porous stru
cture comprising particulates around the pores. The pore size and porosity
of the bead can be varied by altering synthesis conditions, such as initial
polymer concentration, and the pH value and concentration of the casting a
gent TPP aqueous solution). Quaternary ammonium, and aliphatic and aromatic
acyl groups were introduced into the porous chitosan beads to interact wit
h an anti-inflammatory drug, indomethacin, through the electrostatic intera
ction and hydrophobic interaction. The results indicated that chemical modi
fication of the porous chitosan beads have obvious effect on the adsorption
of indomethacin. (C) 2001 Published by Elsevier Science Ltd.