Enhanced MRI T 2 Relaxivity in Contrast-Probed Anchor-Free PEGylated Iron Oxide Nanoparticles.
Bibek ThapaDaysi Diaz-DiestraJuan Beltran-HuaracBrad R WeinerGerardo MorellPublished in: Nanoscale research letters (2017)
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.
Keyphrases
- magnetic resonance
- iron oxide nanoparticles
- contrast enhanced
- iron oxide
- drug delivery
- magnetic resonance imaging
- crispr cas
- computed tomography
- genome editing
- diffusion weighted imaging
- molecular dynamics simulations
- room temperature
- genome wide
- high resolution
- ionic liquid
- gene expression
- papillary thyroid
- single molecule
- dna methylation
- fluorescence imaging
- recombinant human
- loop mediated isothermal amplification
- lymph node metastasis
- solid state