For some years cyclodextrins and their hydrophilic derivatives have been de
scribed in the Literature as solubilizers capable of enhancing the loading
capacity of liposomes and microparticles. We present here two new possibili
ties of using cyclodextrins in the design of colloidal carriers. The first
possibility consists in increasing the loading capacity of poly(isobutyl cy
anoacrylate) nanospheres prepared by anionic polymerization, by employing h
ydroxypropyl cyclodextrins. The second possibility consists in the spontane
ous formation of either nanocapsules or nanospheres by the nanoprecipitatio
n of amphiphilic cyclodextrin diesters. These two new techniques are very p
romising because of the great interest presented by nanoparticles for drug
administration by the oral or parenteral routes. (C) 1999 Elsevier Science
B.V. All rights reserved.