ACS Nano · 2013 · 344 citations · 35 references
PharmacyOncologyPharmaceuticsNanomaterialsNanoparticle Drug DeliveryTargeted Drug DeliveryAntibody-drug ConjugatesCancer Drug DeliveryCancer NanomedicineNanomedicineNanoparticle DesignTargeted Imaging AgentsMesoporous MaterialsMesoporous Silica NanomaterialsMesoporous Silica NanoparticlesNanoparticle ConjugationNanoparticle Imaging AgentsThiol FunctionalizationTumor Tissue TargetingTumor-targeted Drug Delivery
Since the first use of biocompatible mesoporous silica (mSiO2) nanoparticles as drug delivery vehicles, in vivo tumor targeted imaging and enhanced anticancer drug delivery has remained a major challenge. In this work, we describe the development of functionalized mSiO2 nanoparticles for actively targeted positron emission tomography (PET) imaging and drug delivery in 4T1 murine breast tumor-bearing mice. Our structural design involves the synthesis, surface functionalization with thiol groups, PEGylation, TRC105 antibody (specific for CD105/endoglin) conjugation, and (64)Cu-labeling of uniform 80 nm sized mSiO2 nanoparticles. Systematic in vivo tumor targeting studies clearly demonstrated that (64)Cu-NOTA-mSiO2-PEG-TRC105 could accumulate prominently at the 4T1 tumor site via both the enhanced permeability and retention effect and TRC105-mediated binding to tumor vasculature CD105. As a proof-of-concept, we also demonstrated successful enhanced tumor targeted delivery of doxorubicin (DOX) in 4T1 tumor-bearing mice after intravenous injection of DOX-loaded NOTA-mSiO2-PEG-TRC105, which holds great potential for future image-guided drug delivery and targeted cancer therapy.
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Jaeyun Kim, Hoe Suk Kim, Nohyun Lee et al. · Angewandte Chemie International Edition · 2008 · 1.2K citations · Full text
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