Abstract
Neuroblastoma is a pediatric solid tumor with high expression of the tumor associated antigen disialoganglioside GD2. Despite initial response to induction therapy, nearly 50% of high-risk neuroblastomas recur because of chemoresistance. Here we encapsulated the topoisomerase-I inhibitor SN-38 in polymeric nanoparticles (NPs) surface-decorated with the anti-GD2 mouse mAb 3F8 at a mean density of seven antibody molecules per NP. The accumulation of drug-loaded NPs targeted with 3F8 versus with control antibody was monitored by microdialysis in patient-derived GD2-expressing neuroblastoma xenografts. We showed that the extent of tumor penetration by SN-38 was significantly higher in mice receiving the targeted nano-drug delivery system when compared to non-targeted system or free drug. This selective penetration of the tumor extracellular fluid translated into a strong anti-tumor effect prolonging survival of mice bearing GD2-high neuroblastomas in vivo.
Original language | English |
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Pages (from-to) | 108-119 |
Number of pages | 12 |
Journal | Journal of Controlled Release |
Volume | 255 |
DOIs | |
State | Published - 10 Jan 2017 |
Keywords
- GD2-targeted nanoparticles
- Intratumor drug distribution
- Irinotecan/SN-38
- Microdialysis
- Neuroblastoma
- PDX models
- Tumor extracellular fluid
All Science Journal Classification (ASJC) codes
- Pharmaceutical Science