Pluronics P94 are block-copolymer showing prolonged circulation time and tumor-cell internalization in vitro, suggesting a potential for tumor accumulation and as a drug carrier. Here we report the results of the radiolabeled-P94 unimers (P94-111In-DTPA) on tumor uptake/retention and biodistribution after intravenous and intratumoral injection to tumor-bearing mice. Intravenous administration results in a high radioactive signal in the liver; while in tumor and other healthy tissues only low levels of radioactivity could be measured. In contrast, the intratumoral injection of P94 resulted in elevated levels of radioactivity in the tumor and low levels in other organs, including the liver. Independently from the injection route, the tumor tissue presented long retention of radioactivity. The minimal involvement of off-target tissues of P94, together with the excellent tracer retention over-time in the tumor designates Pluronic P94 copolymer as a highly promising carrier for anti-tumor drugs.

Additional Metadata
Keywords Intratumoral injection, Intravenous injection, Pluronics, Tumor retention, Unimers
Persistent URL dx.doi.org/10.1016/j.nano.2017.04.015, hdl.handle.net/1765/101118
Journal Nanomedicine: Nanotechnology, Biology, and Medicine
Grant This work was funded by the European Commission 7th Framework Programme; grant id fp7/317019 - Molecular technology for nuclear imaging and radionuclide therapy (TRACENTREAT)
Citation
Santini, C, Arranja, A.G. (Alexandra G.), Denkova, A.G, Schosseler, F. (François), Morawska, K. (Karolina), Dubruel, P. (Peter), … Bernsen, M.R. (2017). Intravenous and intratumoral injection of Pluronic P94: The effect of administration route on biodistribution and tumor retention. Nanomedicine: Nanotechnology, Biology, and Medicine, 13(7), 2179–2188. doi:10.1016/j.nano.2017.04.015