Skip to main content
. 2015 Apr 28;16(5):9573–9587. doi: 10.3390/ijms16059573

Table 1.

RSE data in LNCaP tumor bearing mice injected with polypeptide-SPIONs, non-targeted SPIONs, and PC3 tumor bearing mice injected with polypeptide-SPIONs.

Post Injection Time LNCaP + Polypeptide-SPIONs (Fe3O4 0.240 mg/mL) LNCaP + Polypeptide-SPIONs (Fe3O4 0.120 mg/mL) LNCaP + Polypeptide-SPIONs (Fe3O4 0.060 mg/mL) LNCaP + Polypeptide-SPIONs (Fe3O4 0.030 mg/mL) LNCaP + Non-Targeted SPIONs (Fe3O4 0.240 mg/mL) PC3 + Polypeptide-SPIONs (Fe3O4 0.240 mg/mL) p-Value
2 h 19.9 ± 3.4 * 15.7 ± 2.7 * 11.8 ± 1.6 11.3 ± 1.4 9.5 ± 2.0 8.7 ± 2.2 0.000
6 h 34.3 ± 3.6 * 31.1 ± 2.7 * 23.5 ± 1.4 * 19.6 ± 0.9 * 11.9 ± 3.9 11.1 ± 3.1 0.000
12 h 30.9 ± 1.4 * 30.0 ± 1.4 * 22.8 ± 1.8 * 18.5 ± 1.5 * 12.0 ± 2.0 10.4 ± 2.6 0.000
p-Value 0.000 0.000 0.000 0.000 0.304 0.179

* Compared with control groups, p < 0.05. LNCaP, human prostate adenocarcinoma cells derived from the lymph node metastasis; SPION, superparamagnetic iron oxide nanoparticles; PC3, human prostate adenocarcinoma cells derived from the bone metastasis.