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Enhanced MRI T 2 Relaxivity in Contrast-Probed Anchor-Free PEGylated Iron Oxide Nanoparticles.
Thapa, Bibek; Diaz-Diestra, Daysi; Beltran-Huarac, Juan; Weiner, Brad R; Morell, Gerardo.
Afiliação
  • Thapa B; Department of Physics, University of Puerto Rico, San Juan, PR, 00931, USA. bibech.thapa@gmail.com.
  • Diaz-Diestra D; Molecular Sciences Research Center, University of Puerto Rico, San Juan, PR, 00926, USA. bibech.thapa@gmail.com.
  • Beltran-Huarac J; Institute for Functional Nanomaterials, University of Puerto Rico, San Juan, PR, 00936, USA. bibech.thapa@gmail.com.
  • Weiner BR; Molecular Sciences Research Center, University of Puerto Rico, San Juan, PR, 00926, USA.
  • Morell G; Institute for Functional Nanomaterials, University of Puerto Rico, San Juan, PR, 00936, USA.
Nanoscale Res Lett ; 12(1): 312, 2017 Dec.
Article em En | MEDLINE | ID: mdl-28454478
ABSTRACT
Superparamagnetic iron oxide nanoparticles (SPIONs, ~11-nm cores) were PEGylated without anchoring groups and studied as efficient MRI T 2 contrast agents (CAs). The ether group of PEG is efficiently and directly linked to the positively charged surface of SPIONs, and mediated through a dipole-cation covalent interaction. Anchor-free PEG-SPIONs exhibit a spin-spin relaxivity of 123 ± 6 mM-1s-1, which is higher than those of PEG-SPIONs anchored with intermediate biomolecules, iron oxide nanoworms, or Feridex. They do not induce a toxic response for Fe concentrations below 2.5 mM, as tested on four different cell lines with and without an external magnetic field. Magnetic resonance phantom imaging studies show that anchor-free PEG-SPIONs produce a significant contrast in the range of 0.1-0.4 [Fe] mM. Our findings reveal that the PEG molecules attached to the cores immobilize water molecules in large regions of ~85 nm, which would lead to blood half-life of a few tens of minutes. This piece of research represents a step forward in the development of next-generation CAs for nascent-stage cancer detection. Contrast-probed anchor-free PEGylated iron oxide contrast agent.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article