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. 2018 Jun 24;8(14):3949–3963. doi: 10.7150/thno.26161

Figure 6.

Figure 6

SN38 prodrug-formulated NPs exhibited potent antitumor efficacy and survival benefits in a mouse model bearing human HCC PDX tumors. (A) Schematic illustration of the protocol for the establishment of a human HCC PDX tumor model in Balb/c nude mice. The primary HCC tissue from patient 1-150605 obtained by surgical resection was finely minced and implanted subcutaneously into nude mice at the engraftment phase (F1). Drug treatment was performed from the third generation. (B) Tumor volume (mm3) as a function of time after drug treatment (n = 7 in each group). When the tumor volumes reached ~50 mm3, NP solutions containing SN38 prodrugs (15 mg/kg, at the SN38 equivalent dose) were injected three successive times. Saline and CPT-11 (22.5 mg/kg) were also intravenously injected as controls. Arrows represent the i.v. injections; the tumor volumes are expressed as the means ± s.d.; *p < 0.05, **p < 0.01. (C) Kaplan-Meier survival plots demonstrating the survival benefit in animals with a 100% survival after treatment with PLA71-SN38-NPs.