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. 2019 Feb 28;9(6):1666–1682. doi: 10.7150/thno.27891

Figure 5.

Figure 5

Blood circulation, excretion and organ biodistribution profiles of membrane-labelled B16F10 exosomes in melanoma-bearing C57Bl/6 mice. The [111In]DTPA group was injected with 0.02M DTPA complexed with 0.5-1MBq of 111InCl3 while the [111In]DTPA- ExoB16 group was injected with 1x1011 [111In]DTPA-ExoB16 (0.5-1MBq). (A) Blood circulation profile of [111In]DTPA and [111In]DTPA-ExoB16. 5 µl blood were taken via tail bleeding at 2 min, 5 min, 10 min, 30 min, 1 h, 4 h and 24 h following intravenous injection of each compound. (B) Excretion profile of [111In]DTPA and [111In]DTPA-ExoB16 where urine and faeces were collected from the animals 24 h post-injection. (C) and (D) Organ biodistribution of [111In]DTPA and [111In]DTPA-ExoB16 respectively. Animals were culled at 1 h, 4 h and 24 h post-injection, perfused with saline and their organs were excised for analysis by gamma counting. Inset shows the zoomed-in tumour accumulation values for each group. (E) Comparison of organ biodistribution of [111In]DTPA and [111In]DTPA-ExoB16 24 h post-injection, where inset shows zoomed-in tumour accumulation values for each group. Values are normalised to organ weight and expressed as mean ± SD, where n=3 for each group. For (C), (D) and (E), statistical analyses were done on liver, spleen, kidneys and tumour (p*<0.05, p** < 0.01, p*** <0.001).