Abstract
The research presented in this thesis explores mPEG-b-p(HPMA-Bz)-based micelles as
nanocarriers for cancer treatment, with focus on hematological cancers. PM showed
good circulation and attractive tissue distribution in clinically relevant models of
multiple myeloma and chronic lymphocytic leukemia. However, therapeutic outcome
of the developed formulations was minimally improved. This is most likely due to
the
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