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Targeted drug distribution in tumor extracellular fluid of GD2-expressing neuroblastoma patient-derived xenografts using SN-38-loaded nanoparticles conjugated to the monoclonal antibody 3F8

机译:使用与单克隆抗体3F8偶联的SN-38负载的纳米颗粒将表达GD2的神经母细胞瘤患者来源的异种移植物在肿瘤细胞外液中靶向药物分布

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摘要

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.
机译:神经母细胞瘤是一种小儿实体瘤,其与肿瘤相关的抗原二唾液酸神经节苷脂GD2高表达。尽管对诱导疗法产生了最初的反应,但近50%的高危神经母细胞瘤由于化学耐药而复发。在这里,我们将拓扑异构酶-I抑制剂SN-38封装在用抗GD2小鼠mAb 3F8表面修饰的聚合物纳米颗粒(NPs)中,平均密度为每个NP 7个抗体分子。通过微透析监测患者来源的表达GD2的神经母细胞瘤异种移植物中靶向3F8与对照抗体的载药NP的积累。我们显示,与非靶向系统或游离药物相比,接受靶向纳米药物递送系统的小鼠中SN-38的肿瘤渗透程度明显更高。肿瘤细胞外液的这种选择性渗透转化为强的抗肿瘤作用,从而延长了患有GD2高神经母细胞瘤的小鼠的体内存活。

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