4.7 Article

In Vivo Tumor Vasculature Targeted PET/NIRF Imaging with TRC105(Fab)-Conjugated, Dual-Labeled Mesoporous Silica Nanoparticles

期刊

MOLECULAR PHARMACEUTICS
卷 11, 期 11, 页码 4007-4014

出版社

AMER CHEMICAL SOC
DOI: 10.1021/mp500306k

关键词

vasculature targeting; positron emission tomography (PET) imaging; near-infrared fluorescence (NIRF) imaging; mesoporous silica nanoparticle (MSN)

资金

  1. University of Wisconsin-Madison
  2. National Institutes of Health [NIBIB/NCI 1R01CA169365, P30CA014520]
  3. Department of Defense [W81XWH-11-1-0644]
  4. American Cancer Society [125246-RSG-13-099-01-CCE]

向作者/读者索取更多资源

Multifunctional mesoporous silica nanoparticles (MSN) with well-integrated multimodality imaging properties have generated increasing research interest in the past decade. However, limited progress has been made in developing MSN-based multimodality imaging agents to image tumors. We describe the successful conjugation of, copper-64 (Cu-64, t(1/2) = 12.7 h), 800CW (a near-infrared fluorescence [NIRF] dye), and TRC105 (a human/murine chimeric IgG1 monoclonal antibody) to the surface of MSN via well-developed surface engineering procedures, resulting in a dual-labeled MSN for in vivo targeted positron emission tomography (PET) imaging/NIRF imaging of the tumor vasculature. Pharmacokinetics and tumor targeting efficacy/specificity in 4T1 murine breast tumor-bearing mice were thoroughly investigated through various in vitro, in vivo, and ex vivo experiments. Dual-labeled MSN is an attractive candidate for future cancer theranostics.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据