Polymer Bulletin, Vol.43, No.2-3, 191-198, 1999
Polyamides containing alpha-aminoacids and hydrophilic oxyethylene groups along the chain
Biocompatible and potentially biodegradable polyamides (PAs) containing in the chain both peptide bonds and hydrophilic triethyleneoxide segments have been prepared by interfacial polycondensation of sebacoyl dichloride with amide-diamines derived from the 4,7,10-trioxa-1,13-tridecanediamine and alpha-aminoacids such as glycine, L-valine and L-phenylalanine. These PAs exhibit moderate inherent viscosity values and show limited solubilities in CHCl3, DMF and DMSO. H-1-NMR and FTIR spectroscopy analysis confirmed the expected structures. DSC and X-rays diffraction spectra indicated crystallinity degrees from 19 to 31%. The melting temperatures range between 135-238 degrees C. Liquid water absorption measurements indicate a high equilibrium weight-uptake when a glycine residue is present in the amide-diamine moiety. In vitro tests carried out using cultures of human fibroblasts showed the biocompatibility of the prepared PAs.