Department of Materials Science and Engineering, Molecular Imaging Program at Stanford, Stanford University, Stanford, California 94305, USA.
ACS Nano. 2012 Aug 28;6(8):6862-9. doi: 10.1021/nn301670a. Epub 2012 Aug 13.
Early detection and targeted therapy are two major challenges in the battle against cancer. Novel imaging contrast agents and targeting approaches are greatly needed to improve the sensitivity and specificity of cancer theranostic agents. Here, we implemented a novel approach using a magnetic micromesh and biocompatible fluorescent magnetic nanoparticles (FMN) to magnetically enhance cancer targeting in living subjects. This approach enables magnetic targeting of systemically administered individual FMN, containing a single 8 nm superparamagnetic iron oxide core. Using a human glioblastoma mouse model, we show that nanoparticles can be magnetically retained in both the tumor neovasculature and surrounding tumor tissues. Magnetic accumulation of nanoparticles within the neovasculature was observable by fluorescence intravital microscopy in real time. Finally, we demonstrate that such magnetically enhanced cancer targeting augments the biological functions of molecules linked to the nanoparticle surface.
早期检测和靶向治疗是癌症防治的两大挑战。需要新型的成像对比剂和靶向方法来提高癌症治疗剂的灵敏度和特异性。在这里,我们采用了一种新方法,使用磁性微网和生物相容性荧光磁性纳米颗粒(FMN)来在活体动物中实现对癌症的磁性靶向。该方法可以对系统给予的单个 FMN 进行磁性靶向,每个 FMN 包含一个 8nm 的超顺磁性氧化铁核心。我们用人胶质母细胞瘤小鼠模型证明,纳米颗粒可以在肿瘤新生血管和周围肿瘤组织中被磁性保留。荧光活体显微镜可以实时观察到纳米颗粒在新生血管中的磁性积累。最后,我们证明这种磁性增强的癌症靶向增强了与纳米颗粒表面相连的分子的生物学功能。