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Convection-enhanced delivery of targeted quantum dot-immunoliposome hybrid nanoparticles to intracranial brain tumor models

机译:对流增强靶向量子点-免疫脂质体杂化纳米粒子向颅内脑肿瘤模型的交付。

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Aim: The aim of this work is to evaluate combining targeting strategy and convection-enhanced delivery in brain tumor models by imaging quantum dot-immunoliposome hybrid nanoparticles. Materials & methods: An EGF receptor-targeted, quantum dot-immunoliposome hybrid nanoparticle (QD-IL) was synthesized. In vitro uptake was measured by flow cytometry and intracellular localization was imaged by confocal microscopy. In the in vivo study, QD-ILs were delivered to intracranial xenografts via convection-enhanced delivery and fluorescence was monitored noninvasively in real-time. Results: QD-ILs exhibited specific and efficient uptake in vitro and exhibited approximately 1.3- to 5.0-fold higher total fluorescence compared with nontargeted counterpart in intracranial brain tumor xenografts in vivo. Conclusion: QD-ILs serve as an effective imaging agent in vitro and in vivo, and the data suggest that ligand-directed liposomal nanoparticles in conjunction with convection-enhanced delivery may offer therapeutic benefits for glioblastoma treatment as a result of specific and efficient uptake by malignant cells.
机译:目的:这项工作的目的是通过对量子点-免疫脂质体杂化纳米颗粒进行成像,评估在脑肿瘤模型中结合靶向策略和对流增强的递送。材料与方法:合成了以EGF受体为靶标的量子点-免疫脂质体杂交纳米颗粒(QD-IL)。通过流式细胞术测量体外摄取,并通过共聚焦显微镜对细胞内定位进行成像。在体内研究中,通过对流增强递送将QD-ILs递送至颅内异种移植物中,并实时无创监测荧光。结果:在体外颅内脑肿瘤异种移植中,QD-ILs在体外表现出特异性和有效的摄取,与非靶向对应物相比,其总荧光约高1.3至5.0倍。结论:QD-ILs可以作为体内和体外的有效显像剂,并且数据表明配体导向的脂质体纳米颗粒与对流增强的递送相结合,可以通过特异性和有效的摄取为胶质母细胞瘤治疗提供治疗益处。恶性细胞。

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