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Penetration of Endothelial Cell Coated Multicellular Tumor Spheroids by Iron Oxide Nanoparticles

机译:氧化铁纳米粒子穿透内皮细胞包被的多细胞肿瘤球体。

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摘要

Iron oxide nanoparticles are a useful diagnostic contrast agent and have great potential for therapeutic applications. Multiple emerging diagnostic and therapeutic applications and the numerous versatile parameters of the nanoparticle platform require a robust biological model for characterization and assessment. Here we investigate the use of iron oxide nanoparticles that target tumor vasculature, via the tumstatin peptide, in a novel three-dimensional tissue culture model. The developed tissue culture model more closely mimics the in vivo environment with a leaky endothelium coating around a glioma tumor mass. Tumstatin-iron oxide nanoparticles showed penetration and selective targeting to endothelial cell coating on the tumor in the three-dimensional model, and had approximately 2 times greater uptake in vitro and 2.7 times tumor neo-vascularization inhibition. Tumstatin provides targeting and therapeutic capabilities to the iron oxide nanoparticle diagnostic contrast agent platform. And the novel endothelial cell-coated tumor model provides an in vitro microtissue environment to evaluate nanoparticles without moving into costly and time-consuming animal models.
机译:氧化铁纳米粒子是有用的诊断造影剂,在治疗应用中具有巨大潜力。多种新兴的诊断和治疗应用以及纳米颗粒平台的众多通用参数需要用于表征和评估的强大生物学模型。在这里,我们研究了通过肿瘤抑素肽靶向新型肿瘤血管的氧化铁纳米颗粒在新型三维组织培养模型中的应用。发达的组织培养模型通过胶质瘤肿瘤块周围的内皮膜渗漏,更紧密地模拟了体内环境。 Tumstatin-氧化铁纳米颗粒在三维模型中显示出渗透性和选择性靶向肿瘤上的内皮细胞涂层,并且在体外的吸收率约高2倍,对肿瘤新血管形成的抑制作用是2.7倍。 Tumstatin为氧化铁纳米颗粒诊断造影剂平台提供靶向和治疗功能。新型的内皮细胞包被的肿瘤模型提供了一种体外微组织环境,可以评估纳米颗粒,而无需进入昂贵且耗时的动物模型。

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