posted on 2016-11-17, 00:00authored byMathias Glassner, Luca Palmieri, Bryn D. Monnery, Thomas Verbrugghen, Steven Deleye, Sigrid Stroobants, Steven Staelens, Leonie wyffels, Richard Hoogenboom
Poly(2-alkyl-2-oxazoline)s
(PAOx) have received increasing interest
for biomedical applications. Therefore, it is of fundamental importance
to gain an in-depth understanding of the biodistribution profile of
PAOx. We report the biodistribution of poly(2-ethyl-2-oxazoline) (PEtOx)
with a molar mass of 5 kDa radiolabeled with PET isotopes 89Zr and 18F. 18F-labeled PEtOx is prepared by
the strain-promoted azide–alkyne cycloaddition (SPAAC) of [18F]fluoroethylazide to bicyclo[6.1.0]non-4-yne (BCN)-functionalized
PEtOx as many common labeling strategies were found to be unsuccessful
for PEtOx. 89Zr-labeled PEtOx is prepared using desferrioxamine
end-groups as a chelator. Five kDa PEtOx shows a significantly faster
blood clearance compared to PEtOx of higher molar mass while uptake
in the liver is lower, indicating a minor contribution of the liver
in excretion of the 5 kDa PEtOx. While [18F]-PEtOx displays
a rapid and efficient clearance from the kidneys, 5 kDa [89Zr]-Df-PEtOx is not efficiently cleared over the time course of the
study, which is most likely caused by trapping of 89Zr-labeled
metabolites in the renal tubules and not the polymer itself, demonstrating
the importance of selecting the appropriate label for biodistribution
studies.