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. 2020 Sep 1;10(24):10973–10992. doi: 10.7150/thno.49670

Figure 5.

Figure 5

Improved tumor accumulation of 89Zr-labelled SN38 thMBs +T compared with VEGFR2-targeted 89Zr-labelled SN38 liposomes alone. (A) Schematic depicting the strategy used for radiolabeling of SN38 liposomes and SN38 thMBs. DSPE was radiolabeled with 89Zr and incorporated into the lipid shell of liposomes encapsulating SN38 and used to generate therapeutic MBs. (B) Schematic of the experimental groups used to compare VEGFR2-targeted liposomally encapsulated SN38 (LE-SN38) with SN38 thMB +T (n = number of mice per group). (C) Schematic of the experimental protocol used (n = 5 animals per time point). The mean (± S.D.) starting tumor volume measured by mechanical calipers was 340 mm3 ± 134 mm3. (D) PET image from the thMB +T group at each imaging time point. Signal in the liver, spleen and bladder are arrowed, tumor is circled. (E) The percentage injected dose per gram of tissue (%ID/g tissue) in tumor (F) blood (G) liver and (H) spleen were calculated with mean and SEM shown. Unpaired T-test tumor, ***p = 0.0006 at 1 h, *p = 0.0432 at 24 h and *p = 0.026 at 72 h. Blood ****p < 0.0001 at 1 h, liver *p = 0.0494 at 72 h, spleen *p = 0.0326 at 72 h.