In vivo tumor vasculature targeted PET/NIRF imaging with TRC105(Fab)-conjugated, dual-labeled mesoporous silica nanoparticles. Academic Article uri icon

Overview

abstract

  • 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 ((64)Cu, t1/2 = 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.

authors

  • Chen, Feng
  • Nayak, Tapas R
  • Goel, Shreya
  • Valdovinos, Hector F
  • Hong, Hao
  • Theuer, Charles P
  • Barnhart, Todd E
  • Cai, Weibo

publication date

  • June 25, 2014

Research

keywords

  • Antibodies, Monoclonal
  • Mammary Neoplasms, Animal
  • Nanoparticles
  • Neovascularization, Pathologic
  • Positron-Emission Tomography
  • Radiopharmaceuticals
  • Silicon Dioxide

Identity

PubMed Central ID

  • PMC4218929

Scopus Document Identifier

  • 84965191272

Digital Object Identifier (DOI)

  • 10.1021/mp500306k

PubMed ID

  • 24937108

Additional Document Info

volume

  • 11

issue

  • 11