Delivery of vaccine antigens by the oral route is plagued with challenges.
Much of the research has focused on the development of microparticles as an
tigen carriers to the gastrointestinal (GIT) mucosa. Polymers, either natur
al or synthetic, have been the class of compounds most often investigated f
or their ability to form microparticles containing antigen. A great deal of
research has been performed using model microparticles composed of polysty
rene. From this work it has become clear that microparticles are taken up a
nd translocated across the GIT epithelium. Antigen carrying microparticles
generated from both hydrophobic and hydrophilic polymers are able to induce
significant immune responses after oral immunization. Although very little
systematic work on the effects of the physicochemical properties of the po
lymer composing the microparticles has been done, enough is known to conclu
de that the surface of the polymeric microparticle can be decisive in deter
mining the overall uptake of the microparticles. Charge and the hydrophobic
/hydrophilic balance of the polymer are important physicochemical character
istics that determine the value of the polymer as a microparticulate carrie
r. This review examines the properties of polymeric matrices that make them
viable candidates as oral vaccine delivery vehicles. (C) 1998 Elsevier Sci
ence B.V. All rights reserved.