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The nonspecific adsorption of proteins and bacteria on the surface of polydimethylsiloxane (PDMS) had been a serious concern in a wide range of applications, such as medical devices. In order to improve the anti-adhesive and antibacterial capability, bare silver nanoparticles (AgNPs, ~15 nm) were generated in-situ on their surface without extra reducing and stabilizing agents. The main reason for this was that the SiO2 microspheres that are covalent bonded to the bulked PDMS could not only generate AgNPs spontaneously but also insure that no AgNPs were released to the environment. Meanwhile, the thiol-group-functionalized SiO2 microspheres self-assembled on the surface of PDMS by thiol-vinyl click reaction without any impact on their biomedical applications. After the modification of SiO2 microspheres with AgNPs, the surface of PDMS showed a smaller water contact angle than before, and the adhesion and growth of E. coli and Bacillus subtilis were effectively inhibited. When the monolayer of SiO2 microspheres with AgNPs was assembled completely on the surface of PDMS, they present improved bacterial resistance performance (living bacteria, 0%). This approach offers an antibacterial and anti-adhesive surface bearing small and well-defined quantities of in-situ generated AgNPs, and it is a novel, green, simple, and low-cost technique to generate AgNPs on soft biomedical substrates.

A green and simple approach has been developed to synthesize un-coated Ag nanoparticles (AgNPs) in situ on the surface of thiol-group-functionalized silica dioxide microspheres (TSMs) in the aqueous solution. As soon as the Ag+ ions attach onto the surface of TSMs, nucleation and growth of AgNPs can spontaneously complete within one minute without other reducing agents or capping agents. The main reason is that the self-assembled silane-layer formed by mercaptosilane molecules could reduce the Ag0 formation energy, transport electrons efficiently, improve the nucleation density, and protect AgNPs against oxidation. Thus, the supported AgNPs show excellent chemical/photochemical stability in air and solution. Meanwhile, the size of as-prepared AgNPs could be controlled by tuning the concentration of Ag+ ions. This process provides a general route to generate bare AgNPs on the surface of silica dioxide in situ, which might be extended to other materials and is promising in developing novel methodologies for making supported noble metal NPs with desired structure and properties. [ABSTRACT FROM AUTHOR]

The nonspecific adsorption of proteins and bacteria on the surface of polydimethylsiloxane (PDMS) had been a serious concern in a wide range of applications, such as medical devices. In order to improve the anti-adhesive and antibacterial capability, bare silver nanoparticles (AgNPs, ~15 nm) were generated in-situ on their surface without extra reducing and stabilizing agents. The main reason for this was that the SiO2 microspheres that are covalent bonded to the bulked PDMS could not only generate AgNPs spontaneously but also insure that no AgNPs were released to the environment. Meanwhile, the thiol-group-functionalized SiO2 microspheres self-assembled on the surface of PDMS by thiol-vinyl click reaction without any impact on their biomedical applications. After the modification of SiO2 microspheres with AgNPs, the surface of PDMS showed a smaller water contact angle than before, and the adhesion and growth of E. coli and Bacillus subtilis were effectively inhibited. When the monolayer of SiO2 microspheres with AgNPs was assembled completely on the surface of PDMS, they present improved bacterial resistance performance (living bacteria, 0%). This approach offers an antibacterial and anti-adhesive surface bearing small and well-defined quantities of in-situ generated AgNPs, and it is a novel, green, simple, and low-cost technique to generate AgNPs on soft biomedical substrates. [ABSTRACT FROM AUTHOR]

As soon as the Ag+ ions attach onto the surface of thiol group functionalized silica dioxide microspheres in aqueous solution, nucleation and growth of Ag nanoparticles can spontaneously complete within one minute without other reducing agents or capping agents. The main reason is that the self ‐ assembled layer formed by mercaptosilane molecules could reduce the Ag0 formation energy, transport electrons efficiently, improve the nucleation density, and protect Ag nanoparticles against oxidation. More information can be found in the Communication by Q. Shen, X. Liu, et al. on page 6244 ff. [ABSTRACT FROM AUTHOR]