Abstract

Objective: Superparamagnetic Iron Oxide Nanoparticles (SPIONs) are widely researched as contrast agents in clinical magnetic resonance imaging (MRI). SPIONs are frequently coated with anti-biofouling substances such as poly(ethylene glycol) (PEG) to prevent protein deposition and improve circulation time in vivo. The aim of this study is to optimize SPION MR properties with respect to physicochemical properties of the core SPION and the polymeric coating to better understand the interaction of these parameters and the efficacy of the designed agent. Methods: We used different methods of chemical attachment of a polymer, polymer chain length, and polymer coating density and examined their effects on the MR relaxivities of SPIONs. Results: These studies indicate that the chemical composition and, in particular, the hydrophobicity/hydrophilicity of the chemical group linking PEG chains to a SPION core may play a larger role in the resulting MR relaxivities than other variable properties such as SPION core size and PEG chain length. Conclusions: The method of SPION fabrication and chemical composition of the coating play a significant role in the MR relaxivities of the resulting particles. These results should be considered in the fabrication of particles for clinical purposes, particularly when optimization of the MR relaxivities is desired.

Highlights

  • Superparamagnetic iron oxide nanoparticles (SPIONs) are used as contrast agents for clinical magnetic resonance imaging (MRI) [1]–[3]

  • In phosphine oxide (PO)-poly(ethylene glycol) (PEG) SPIONs, nanoparticle effective diameter appears to increase as PEG chain length increases, yet these differences were not statistically significant across multiple batches (p > 0.05)

  • For DSPE-PEG SPIONs, this was not the case. It can be observed for all samples that for a given core size and PEG chain length, the effective diameter observed between different PEGylation methods was such that NH2-PEG SPIONs < PO-PEG SPIONs < DSPE-PEG

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Summary

Introduction

Superparamagnetic iron oxide nanoparticles (SPIONs) are used as contrast agents for clinical magnetic resonance imaging (MRI) [1]–[3]. SPION variability in terms of iron core size, surface functionalization, and targeting moieties makes them potentially well-suited for detection of a wide array of diseases [4]–[9]. SPIONs hold specific advantages over widely-used gadolinium-based MR contrast agents: each nanoparticle contains thousands of iron atoms and approaches saturation magnetization in magnetic fields typically used. SPIONs have demonstrably lower toxicity in vivo than gadolinium-based contrast agents [11]–[15]. These two features make SPIONs wellsuited for early detection or diagnosis of diseases ranging from cancer to atherosclerosis

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