The biological fate of synthetic water-soluble polymers administered t
o mice by injection at different sites is described. After intraperito
neal tip), subcutaneous (sc), and intramuscular (im) injections of (12
5)l-labeled poly(vinyl alcohol) (PVA) and poly(ethylene glycol) (PEG)
with various molecular weights, the time-course of polymer concentrati
on in the blood was measured and analyzed pharmacokinetically. The loc
ation of PVA in the body was similar to that of PEG; that is, the elim
ination from the injection sites and the translocation from the inject
ion sites into the blood circulation were similar for both polymers. T
he elimination rate of both polymers from the injection sites increase
d in the order ip > sc > im. After sc and im injections of polymers, t
he elimination rate decreased with an increase in the molecular weight
, whereas the elimination rate of polymers injected showed no molecula
r weight dependence over the range studied, regardless of the type of
polymers used. The time-course of polymer concentration in the blood d
epended largely on the injection route of the polymers, and the polyme
r elimination from the blood circulation was enhanced with the decreas
ing molecular weight of polymers injected. It was concluded that the m
olecular weight and the injection site are the important factors that
affect the concentration profile of polymers in the blood circulation.