| Literature DB >> 23374706 |
Sixiang Shi1, Kai Yang, Hao Hong, Hector F Valdovinos, Tapas R Nayak, Yin Zhang, Charles P Theuer, Todd E Barnhart, Zhuang Liu, Weibo Cai.
Abstract
Graphene-based nanomaterials have attracted tremendous attention in the field of biomedicine due to their intriguing properties. Herein, we report tumor vasculature targeting and imaging in living mice using reduced graphene oxide (RGO), which was conjugated to the anti-CD105 antibody TRC105. The RGO conjugate, (64)Cu-NOTA-RGO-TRC105, exhibited excellent stability in vitro and in vivo. Serial positron emission tomography (PET) imaging studies non-invasively assessed the pharmacokinetics and demonstrated specific targeting of (64)Cu-NOTA-RGO-TRC105 to 4T1 murine breast tumors in vivo, compared to non-targeted RGO conjugate ((64)Cu-NOTA-RGO). In vivo (e.g., blocking 4T1 tumor uptake with excess TRC105), in vitro (e.g., flow cytometry), and ex vivo (e.g., histology) experiments confirmed the specificity of (64)Cu-NOTA-RGO-TRC105 for tumor vascular CD105. Since RGO exhibits desirable properties for photothermal therapy, the tumor-specific RGO conjugate developed in this work may serve as a promising theranostic agent that integrates imaging and therapeutic components.Entities:
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Year: 2013 PMID: 23374706 PMCID: PMC3570619 DOI: 10.1016/j.biomaterials.2013.01.047
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479