One of the major drawbacks that limits the clinical application of nanoparticles is the lack of preliminary investigations related to their biocompatibility, biodegradability and biodistribution. In this work, biodegradable PEGylated polymer nanoparticles (NPs) have been synthesized by using macromonomers based on poly( ε -caprolaconte) oligomers. More in detail, NPs have been produced by adopting a surfactant-free semibatch emulsion polymerization process using PEG chains as a stabilizing agent. The NPs were also labeled with rhodamine B covalently bound to the NPs to quantitatively study their biodistribution in vivo . NPs were investigated in both in vitro and in vivo preclinical systems to study their biodistribution in mice bearing B16/F10 melanoma, as well as their biocompatibility and biodegradability. The NP concentration was evaluated in different tissues at several times after intravenous injection. The disappearance of the NPs from the plasma w...
M Lupi, C Colombo, R Frapolli, R Ferrari, L Sitia, L Dragoni, E Bello, S A Licandro, F Falcetta, P Ubezio, P Bigini, M Salmona, M D’Incalci, M Morbidelli and D Moscatelli
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M Lupi, C Colombo, R Frapolli, R Ferrari, L Sitia, L Dragoni, E Bello, S A Licandro, F Falcetta, P Ubezio, P Bigini, M Salmona, M D’Incalci, M Morbidelli and D Moscatelli
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