Beads of acryloylated polyaminoacidic matrices containing 5-fluorouracil for drug delivery

Abstract

Spherical polymeric microparticles have been prepared by a reverse phase suspension polymerization technique. The starting polymer was α,β-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA), partially derivatized with glycidylmethacrylate (GMA). PHEA-GMA copolymer (PHG) was crosslinked in the presence of N, N′-dimethylacrylamide (DMAA) or N,N′-ethylenebisacrylamide (EBA). 5-fluorouracil was incorporated into PHG-DMAA or PHG-EBA beads both during and after the crosslinking process. Swelling studies revealed a high affinity toward aqueous medium, influenced by the presence of 5-fluorouracil. The in vitro release study showed that the release rate depends on the chemical structure of the beads and the procedure adopted to incorporate 5-fluorouracil into the microparticles.