Title

Design Of A Multi-Dopamine-Modified Polymer Ligand Optimally Suited For Interfacing Magnetic Nanoparticles With Biological Systems

Abstract

We have designed a set of multifunctional and multicoordinating polymer ligands that are optimally suited for surface functionalizing iron oxide and potentially other magnetic nanoparticles (NPs) and promoting their integration into biological systems. The amphiphilic polymers are prepared by coupling (via nucleophilic addition) several amine-terminated dopamine anchoring groups, poly(ethylene glycol) moieties, and reactive groups onto a poly(isobutylene-alt- maleic anhydride) (PIMA) chain. This design greatly benefits from the highly efficient and reagent-free one-step reaction of maleic anhydride groups with amine-containing molecules. The availability of several dopamine groups in the same ligand greatly enhances the ligand affinity, via multiple coordination, to the magnetic NPs, while the hydrophilic and reactive groups promote colloidal stability in buffer media and allow subsequent conjugation with target biomolecules. Iron oxide nanoparticles ligand exchanged with these polymer ligands have a compact hydrodynamic size and exhibit enhanced long-term colloidal stability over the pH range of 4-12 and in the presence of excess electrolytes. Nanoparticles ligated with terminally reactive polymers have been easily coupled to target dyes and tested in live cell imaging with no measurable cytotoxicity. Finally, the resulting hydrophilic nanoparticles exhibit large and size-dependent r2 relaxivity values. © 2014 American Chemical Society.

Publication Date

6-3-2014

Publication Title

Langmuir

Volume

30

Issue

21

Number of Pages

6197-6208

Document Type

Article

Personal Identifier

scopus

DOI Link

https://doi.org/10.1021/la500974r

Socpus ID

84901830340 (Scopus)

Source API URL

https://api.elsevier.com/content/abstract/scopus_id/84901830340

This document is currently not available here.

Share

COinS