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. 2014 Oct 29;44(11):4884–4900. doi: 10.1039/c4dt02978j

Fig. 9. Biodistribution of 89Zr-labeled trastuzumab immunoconjugates in normal male C57Bl/6j mice at 6 h (Inline graphic), 1 day (Inline graphic), 3 days (Inline graphic), and 7 days (Inline graphic) post-injection. Top: Biodistribution for animals administered 89Zr-YM103-trastuzumab; Bottom: Biodistribution for animals administered 89Zr-DFO-trastuzumab. Error bars correspond to standard error of the mean, (n = 3 for each timepoint). Notably, animals administered 89Zr-YM103-trastuzumab demonstrated significantly higher bone uptake and lower blood pool retention compared to animals administered 89Zr-DFO-trastuzumab over the course of the experiment. This is indicative of the lower in vivo stability of the 89Zr-chelate in 89Zr-YM103-trastuzumab compared to 89Zr-DFO-trastuzumab.

Fig. 9