Nanoparticles are known to accumulate in the phagocytic cells of the m
ononuclear phagocyte system. Therefore, the use of this carrier system
for the targeting of antiviral drugs to monocytes/macrophages (MO/MAC
) is an attractive concept in the treatment of diseases involving MO/M
AC, e.g. infection with HIV. In this study, the ability of macrophages
isolated from peripheral blood of healthy blood donors to phagocytose
and metabolize human serum albumin microspheres was investigated by t
ransmission electron microscopy. Furthermore, nanoparticles manufactur
ed using human serum albumin or polyhexylcyanoacrylate were loaded wit
h nucleoside analogues (AZT and ddC) and tested for their ability to p
revent HIV infection in MO/MAC cultures. Our results demonstrate the e
ffectiveness of this drug-targeting system to one of the major target
cells for HIV.