Abstract

Synthesis of gold nanoparticles (GNP) by reacting chloroauric acid (HAuCl4) and Pluronic F127 was thoroughly investigated. The rate of reduction of HAuCl4 and the yield and morphology of GNP strongly depended on the concentration of the reactants and sodium chloride, as well as pH and temperature. Upon completion of the reaction heterogeneous mixtures of small GNP of defined shape and Pluronic aggregates were formed. GNP were separated from the excess of Pluronic by centrifugal filtration. Under optimized conditions the GNP were small (ca. 80 nm), uniform (PDI ~0.09), strongly negatively charged (ζ-potential −30 mV) and nearly spherical. They were stable in distilled water and phosphate-buffered saline. Purified GNP contained ~13% by weight of an organic component, yet presence of polypropylene oxide was not detected suggesting that Pluronic was not adsorbed on their surface. Analysis of the soluble products suggested that the copolymer undergoes partial degradation accompanied by cleavage of the C–O bonds and appearance of new primary hydroxyl groups. The reaction involves formation of free radicals and hydroperoxides depends on the oxygen concentration. GNP did not form at 4 °C when the micellization of Pluronic was abolished reinforcing the role of the copolymer self-assembly. In conclusion, this work provides insight into the mechanism of HAuCl4 reduction and GNP formation in the presence of Pluronic block copolymers. It is useful for improving the methods of manufacturing uniform and pure GNP that are needed as nanoscale building blocks in nanomedicine applications.

Highlights

  • Gold nanoparticles (GNP) have attracted considerable attention due to their potential applications in biology and medicine as drug delivery and sensory devices

  • gold nanoparticles (GNP) were synthesized in the aqueous media through a reaction of HAuCl4 ·3H2 O with Pluronic block copolymers

  • Reactions involving the reduction of Au3+ to Au0 and formation of the GNP were monitored by the changes in the UV absorption spectra (Figure S1)

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Summary

Introduction

Gold nanoparticles (GNP) have attracted considerable attention due to their potential applications in biology and medicine as drug delivery and sensory devices. Shape, and colloidal stability of the GNP is very important for these applications. A main synthetic route for GNP involves reduction of chloroauric acid (HAuCl4 ) using sodium citrate or sodium borohydrate [1]. Tuning the feed ratio of gold and sodium salts can control the size of GNP to some extent, the resulting GNP usually are not stable in aqueous solution. Their colloidal stabilization can be further achieved by surface functionalization with various SH-containing species and represents an additional synthetic task. Stable GNP can be synthesized in the presence of certain water-soluble polymers (polyethyleneimine, poly(N-isopropyl-acrylamide-N,N-dimethylaminoethyl-acrylamide [2,3,4,5], or polyethers, such as poly(ethylene oxide) (PEO) or Pluronic, a triblock copolymer of PEO and Polymers 2019, 11, 1553; doi:10.3390/polym11101553 www.mdpi.com/journal/polymers

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