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Thiol-reactive amphiphilic block copolymer for coating gold nanoparticles with neutral and functionable surfaces.


ABSTRACT: Nanoparticles designed for biomedical applications are often coated with polymers containing reactive functional groups, such as -COOH and -NH2, to conjugate targeting ligands or drugs. However, introducing highly charged surfaces promotes binding of the nanoparticles to biomolecules in biological systems through ionic interactions, causing the nanoparticles to aggregate in biological environments and consequently undergo strong non-specific binding to off-target cells and tissues. Developing a unique polymer with neutral surfaces that can be further functionalized directly would be critical to develop suitable nanomaterials for nanomedicine. Here, we report a thiol-reactive amphiphilic block copolymer poly(ethylene oxide)-block-poly(pyridyldisulfide ethylmeth acrylate) (PEO-b-PPDSM) for coating gold nanoparticles (AuNPs). The resultant polymer-coated AuNPs have almost neutral surfaces with slightly negative zeta potentials from -10 to 0 mV over a wide pH range from 2 to 12. Although the zeta potential is close to zero we show that the PEO-b-PPDSM copolymer-coated AuNPs have both good stability in various physiological conditions and reduced non-specific adsorption of proteins/biomolecules. Because of the multiple pyridyldisulfide groups on the PPDSM block, these individually dispersed nanocomplexes with an overall hydrodynamic size around 43.8 nm can be directly functionalized via disulfide-thiol exchange chemistry.

SUBMITTER: Chen H 

PROVIDER: S-EPMC3979584 | biostudies-literature | 2014 Apr

REPOSITORIES: biostudies-literature

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Thiol-reactive amphiphilic block copolymer for coating gold nanoparticles with neutral and functionable surfaces.

Chen Hongwei H   Zou Hao H   Paholak Hayley J HJ   Ito Masayuki M   Qian Wei W   Che Yong Y   Sun Duxin D  

Polymer chemistry 20140401 8


Nanoparticles designed for biomedical applications are often coated with polymers containing reactive functional groups, such as -COOH and -NH<sub>2</sub>, to conjugate targeting ligands or drugs. However, introducing highly charged surfaces promotes binding of the nanoparticles to biomolecules in biological systems through ionic interactions, causing the nanoparticles to aggregate in biological environments and consequently undergo strong non-specific binding to off-target cells and tissues. De  ...[more]

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