The affinity of nanoparticles for hematopoietic organs could be valuab
le for the targeting of certain stimulating factors to those tissues,
but this affinity should also be taken into account in the toxicologic
al evaluation of those carriers, especially when they are loaded with
antimitotic compounds such as doxorubicin. However, the cells responsi
ble for the capture of the nanoparticles and their localization in the
se organs is an important point to know before trying to modulate the
nanoparticle's tissue distribution. Thus, we have studied, in this pap
er, the capture, the localization, and the retention in the bone marro
w and in the spleen of biodegradable poly(isohexyl cyanoacrylate) nano
particles as well as of nonbiodegradable polystyrene nanoparticles. Th
e histological localization of these nanoparticles has been completed
by cytological localization with a method used in cytochemistry for th
e evaluation of intracellular accumulation of various substances, such
as iron deposits in bone marrow sideroblasts. These data indicate tha
t, in the bone marrow, after a quick passage through the endothelium,
nanoparticles were dispersed throughout in the tissue and captured by
all types of phagocytizing cells. In the spleen, nanoparticles were ma
inly localized in large angular capturing cells in the marginal zone o
f the lymphoid follicles.