Application of Argon Plasma Technology for the Synthesis of Anti-Infective Copper Nanoparticles.

The synthesis of copper nanoparticles (CuNPs) was accomplished by using a rapid, green, and versatile argon plasma reduction method that involves solvent extraction. With this method, a plasma-solid state interaction forms and CuNPs can be synthesized from copper(II) sulfate using a low-pressure, low-temperature argon plasma. Characterization studies of the CuNPs revealed that when a metal precursor is treated under optimal experimental conditions of 80 W of argon plasma for 300 s, brown CuNPs are synthesized. However, when those same brown CuNPs are placed in Milli-Q water for a period of 10 days, oxidation occurs and green CuNPs are formed. Confirmation of the chemical identity of the CuNPs was performed by using X-ray photoelectron spectroscopy. The results reveal that the brown CuNPs are predominantly Cu0 or what we refer to as CuNPs, while the green CuNPs are a mixture of Cu0 and Cu(OH)2 NPs. Upon further characterization of both brown and green CuNPs with scanning electron microscopy (SEM), the results depict brown CuNPs with a rod-like shape and approximate dimensions of 40 nm × 160 nm, while the green CuNPs were smaller in size, with dimensions of 40-80 nm, and more of a round shape. When testing the antibacterial activity of both brown and green CuNPs, our findings demonstrate the effectiveness of both CuNPs against Escherichia coli and Staphylococcus aureus bacteria at a concentration of 17 µg/mL. The inactivation of S. aureus and E. coli 7-day-old biofilms required CuNP concentrations of 99 µg/mL. SEM images of treated 7-day-old S. aureus and E. coli biofilms depict cell membranes that are completely damaged, suggesting a physical killing mechanism. In addition, when the same concentration of CuNPs used to inactivate biofilms were tested with human fibroblasts, both brown and green CuNPs were found to be biocompatible.

Rapid Synthesis of Metal Nanoparticles Using Low-Temperature, Low-Pressure Argon Plasma Chemistry and Self-Assembly.

The synthesis of metal nanoparticles has become a priority for the advancement of nanotechnology. In attempts to create these nanoparticles, several different methods: chemistry, physics, and biology, have all been used. In this study, we report the reduction of cations using argon plasma chemistry to produce nanoparticles of gold (AuNPs), silver (AgNPs), and copper (CuNPs). Although other groups have used plasma-reduction methods to synthesize metal nanoparticles from their cation counterparts, these approaches often require plasma|liquid state interactions, high temperature, specific combinations of gases, and extended treatment times (>10 minutes), for which only specific cations (noble or non-noble) may be reduced. As a result, we have developed a non-thermal, low-pressure argon-plasma|solid state approach for the reduction of both noble and non-noble cations. More specifically, when 50-µL droplets of 2-mM solutions of gold(III) chloride, silver nitrate, or copper(II) sulfate are exposed to vacuum, they undergo an evaporation process. As the pressure in the chamber decreases to 220 mtorr, the droplets become completely evaporated, leaving behind a metal precursor. Nucleation and growth studies reveal that when the metal precursors of gold(III) chloride, silver nitrate, and copper(II) sulfate are treated with 80 watts of argon plasma for 5, 60, and 150 seconds, respectively, nanoparticles could be synthesized with efficiency rates of upwards of 98%. The size of nanoparticles synthesized in this work was studied using Scanning Electron Microscopy, and the scattering properties of the nanoparticles was studied using UV/Vis spectroscopy. Transmission Electron Microscopy with corresponding elemental analysis was also very useful in confirming the identity of the synthesized nanoparticles. The results from this study reveal that we have synthesized metal nanoparticles with distinct chemical and physical properties. Scanning Electron Microscopy depicts AgNPs with a round-shape and diameters from 40 - 80 nm, while AuNPs were hexagonal, with sizes from 40 - 80 nm, and CuNPs were rod-shaped, with dimensions 40 by 160 nm. Our findings demonstrate that the argon plasma approach used in this study is a rapid, green, and versatile reduction method for the synthesis of both noble and non-noble metal nanoparticles.