Two types of aliphatic poly(ester-amides) (PEAs) were subjected to mic
robial degradation in basal mineral salt broth, under the attack of a
yeast, Cryptococcus laurentii, at 20 degrees C. PEA-I copolymers were
made by the anionic ring-opening copolymerization of of epsilon-caprol
actone and epsilon-caprolactam, whereas PEA-II copolymers were synthes
ized by a two-step polycondensation reaction of hexanediol-1,6, hexane
diamine-1,6, and adipoyl chloride. These copolymers were found to be r
eadily degradable under biotic conditions, based on weight loss, GPC,
NMR spectroscopy, and tensile property measurements. Compared to abiot
ic hydrolysis, biodegradation occurred much faster under milder condit
ions. Furthermore, NMR spectroscopic analysis proved that the biodegra
dation of poly(ester-amides) involves the enzymatic hydrolysis of este
r groups on the backbones of polymers into acid and hydroxyl groups. N
o breakdown of amide bonds was observed under the given biotic conditi
ons. (C) 1993 John Wiley & Sons, Inc.