Journal of the American Chemical Society · 2009 · 703 citations · 57 references
PharmacyMaterials ScienceOncologyDrug DeliveryNanomaterialsNanoparticle Drug DeliveryCancer NanomedicineInorganic NanoparticlesMagnetic NanomaterialsMagnetic Resonance ImagingNanomaterials For Drug DeliveryNanomedicineAnticancer Drug LoadingMesoporous Silica NanoparticlesNanocrystalsNanoparticle Contrast AgentsNanoparticle Imaging AgentsNanoparticlesPassive Tumor TargetingSilica-based Nanoparticles
Highly versatile nanocomposite nanoparticles were synthesized by decorating mesoporous dye‑doped silica nanoparticles with multiple magnetite nanocrystals, and they can load the anticancer drug doxorubicin into their pores for efficient cell death. The magnetite‑laden particles act as superparamagnetic MR contrast agents and fluorescent probes, exhibit synergistic MR signal enhancement, passively target tumors in vivo, and deliver doxorubicin to induce apoptotic tumor cell death.
Highly versatile nanocomposite nanoparticles were synthesized by decorating the surface of mesoporous dye-doped silica nanoparticles with multiple magnetite nanocrystals. The superparamagnetic property of the magnetite nanocrystals enabled the nanoparticles to be used as a contrast agent in magnetic resonance (MR) imaging, and the dye molecule in the silica framework imparted optical imaging modality. Integrating a multitude of magnetite nanocrystals on the silica surface resulted in remarkable enhancement of MR signal due to the synergistic magnetism. An anticancer drug, doxorubicin (DOX), could be loaded in the pores and induced efficient cell death. In vivo passive targeting and accumulation of the nanoparticles at the tumor sites was confirmed by both T2 MR and fluorescence imaging. Furthermore, apoptotic morphology was clearly detected in tumor tissues of mice treated with DOX loaded nanocomposite nanoparticles, demonstrating that DOX was successfully delivered to the tumor sites and its anticancer activity was retained.
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