| Literature DB >> 28412222 |
Carles Monterrubio1, Sonia Paco1, Nagore G Olaciregui1, Guillem Pascual-Pasto1, Monica Vila-Ubach1, Maria Cuadrado-Vilanova1, M Mar Ferrandiz1, Helena Castillo-Ecija1, Romina Glisoni2, Nataliya Kuplennik3, Achim Jungbluth4, Carmen de Torres1, Cinzia Lavarino1, N K V Cheung4, Jaume Mora1, Alejandro Sosnik3, Angel M Carcaboso5.
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.Entities:
Keywords: GD2-targeted nanoparticles; Intratumor drug distribution; Irinotecan (PubChem CID: 60838).; Irinotecan/SN-38; Microdialysis; Neuroblastoma; PDX models; SN-38 (PubChem CID: 104842); Tumor extracellular fluid
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Year: 2017 PMID: 28412222 PMCID: PMC5564453 DOI: 10.1016/j.jconrel.2017.04.016
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776