Poly(epsilon-caprolactone) (PCL), a biocompatible and biodegradable po
lymer hitherto thought unsuitable for protein delivery because of its
poor permeability to macromolecules, is shown to be sufficiently perme
able to proteins to function as a vaccine carrier, Using a model antig
en such as bovine serum albumin (BSA), we demonstrate that a single in
jection of BSA-loaded PCL microspheres generates an immune response co
mparable in magnitude and time kinetics to that of a conventional thre
e-injection schedule of the antigen in a rat model, Unlike polyesters
such as poly(lactic acid) (PLA) and poly(glycolic acid) (PGA), PCL deg
rades slowly and therefore does not generate an acid environment adver
sely affecting the antigenicity of vaccines and may prove to be promis
ing as a vaccine carrier.