Synthesis and in vitro behavior of iron-crosslinked N-methyl and N-benzyl hydroxamated derivatives of alginic acid as controlled release carriers

N-methyl and N-benzyl hydroxylamines were synthetically conjugated to alginic acid to produce hydroxamated derivatives with different degrees of substitution. The new polymeric materials were used to form coordinate complexes with iron(III). The hydroxamated derivatives as well as their iron complexes were characterized using infrared spectroscopy and differential scanning calorimetry. Phenobarbitone-loaded and blank beads were prepared utilizing the new iron-crosslinked hydroxamated polymers and evaluated with respect to their ability to control drug release, as well as their iron leaching properties. The iron-crosslinked polymeric composites proved capable of encapsulating the model drug and sustaining its release in the dissolution media, the release profiles were sensitive to the type and degree of substitution.