Activation of Ibuprofen via Ultrasonic Complexation with Silver in N-Doped Oxidized Graphene Nanoparticles for Microwave Chemotherapy of Cervix Tumor Tissues.

An ultrasonic method (20 kHz) is introduced to activate pristine ibuprofen organic molecular crystals via complexation with silver in nitrogen-doped oxidized graphene nanoplatforms (∼50 nm). Ultrasonic complexation occurs in a single-step procedure through the binding of the carboxylic groups with Ag and H-bond formation, involving noncovalent π → π transitions in the altered phenyl ring and π → π in ibuprofen occurring between the phenyl ring and C-O bonds as a result of interaction with hydroxyl radicals. The ibuprofen-silver complex in ≪NrGO≫ exhibits a ∼42 times higher acceleration rate than free ibuprofen of the charge transfer between hexacyanoferrate and thiosulfate ions.

Ultrasonic Formation of FeO-Reduced Graphene Oxide-Salicylic Acid Nanoparticles with Switchable Antioxidant Function.

We demonstrate a single-step ultrasonic in situ complexation of salicylic acid during the growth of FeO-reduced graphene oxide nanoparticles (∼10 nm) to improve the antioxidant and antiproliferative effects of pristine drug molecules. These nanoparticles have a precisely defined electronic molecular structure with salicylic acid ligands specifically complexed to Fe(III)/Fe(II) sites, four orders of magnitude larger electric surface potential, and enzymatic activity modulated by ascorbic acid molecules. The diminishing efficiency of hydroxyl radicals by FeO-rGO-SA nanoparticles is tenfold higher than that by pristine salicylic acid in the electro-Fenton process.

Sonochemical Formation of Copper/Iron-Modified Graphene Oxide Nanocomposites for Ketorolac Delivery.

A feasible sonochemical approach is described for the preparation of copper/iron-modified graphene oxide nanocomposites through ultrasonication (20 kHz, 18 W cm ) of an aqueous solution containing copper and iron ion precursors. Unique copper-, copper/iron- and iron-modified graphene oxide nanocomposites have a submicron size that is smaller than that of pristine GO and a higher surface area enriched with Cu O, CuO, and Fe O of multiform phases (α-, β-, ϵ-, or γ), FeO(OH), and sulfur- or carbon-containing compounds. These nanocomposites are sonochemically intercalated with the nonsteroidal anti-inflammatory drug ketorolac, which results in the formation of nanoscale carriers.

Sonochemically Assembled Photoluminescent Copper-Modified Graphene Oxide Microspheres.

A new accessible sonochemical assembly method is developed for the preparation of photoluminescent oil-filled silica@CuS/CuO/CuO-graphene oxide (GO) microspheres that emit light of green, yellow, and red colors. This method is based on the ultrasonic emulsification of a biphasic mixture consisting of CuS/CuO/CuO-graphene oxide (GO) nanocomposites with poly(vinyl alcohol) (PVA) (aqueous phase) and tetraethyl orthosilicate with sunflower oil (organic phase). CuS/CuO/CuO-GO nanocomposites are composed of sonochemically formed three phases of copper: covellite CuS (p-type semiconductor), cuprite CuO (Bloch p-type semiconductor), and CuO (charge-transfer insulator).

Ultrasonic Mastering of Filter Flow and Antifouling of Renewable Resources.

Inadequate access to pure water and sanitation requires new cost-effective, ergonomic methods with less consumption of energy and chemicals, leaving the environment cleaner and sustainable. Among such methods, ultrasound is a unique means to control the physics and chemistry of complex fluids (wastewater) with excellent performance regarding mass transfer, cleaning, and disinfection. In membrane filtration processes, it overcomes diffusion limits and can accelerate the fluid flow towards the filter preventing antifouling.

Ultrasonically treated liquid interfaces for progress in cleaning and separation processes.

Ultrasound and acoustic cavitation enable ergonomic and eco-friendly treatment of complex liquids with outstanding performance in cleaning, separation and recycling of resources. A key element of ultrasonic-based technology is the high speed of mixing by streams, flows and jets (or shock waves), which is accompanied by sonochemical reactions. Mass transfer across the phase boundary with a great variety of catalytic processes is substantially enhanced through acoustic emulsification.

Surpassingly competitive electromagnetic field enhancement at the silica/silver interface for selective intracellular surface enhanced Raman scattering detection.

A thin plasmonic nanofilm is formed by preformed silver nanoparticles (30 nm) in the matrix of poly(vinyl alcohol) adsorbed on silica microparticles (1.5 μm) (SiO2@Ag-PVA). By applying finite element method (FEM) analysis the surface enhanced Raman spectroscopy (SERS) enhancement factors (EFs) can reach 10(5) with higher values from 10(9) to 10(11) in the silver layer of 5 nm thickness.

Prospects for plasmonic hot spots in single molecule SERS towards the chemical imaging of live cells.

Single molecule surface enhanced Raman scattering (SM-SERS) is a highly local effect occurring at sharp edges, interparticle junctions and crevices or other geometries with a sharp nanoroughness of plasmonic nanostructures ("hot spots"). The emission of an individual molecule at SM-SERS conditions depends on the local enhancement field of the hot spots, as well as the binding affinity and positioning at a hot spot region. In this regard, the stability of near-field nano-optics at hot spots is critical, particularly in a biological milieu.

Highly effective hot spots for SERS signatures of live fibroblasts.

Pre-formed silver-boron nanoparticles of 22 nm form pearl-like necklace nanostructures with interparticle junctions of less than 10 nm length in the matrix of polyethylene glycol (8000 Da). The silver necklace nanostructure is stable at 37 °C or 70 °C and also inside a live cell medium. A polyethylene glycol matrix with a shorter chain length (1000 Da) does not protect the nanoparticles against attraction, and random aggregates are formed.

Single bubble perturbation in cavitation proximity of solid glass: hot spot versus distance.

A systematic study of the energy loss of a cavitation bubble in a close proximity of a glass surface is introduced for the first time in a low acoustic field (1.2-2.4 bar).

Ultrasonic approach for formation of erbium oxide nanoparticles with variable geometries.

Ultrasound (20 kHz, 29 W·cm(-2)) is employed to form three types of erbium oxide nanoparticles in the presence of multiwalled carbon nanotubes as a template material in water. The nanoparticles are (i) erbium carboxioxide nanoparticles deposited on the external walls of multiwalled carbon nanotubes and Er(2)O(3) in the bulk with (ii) hexagonal and (iii) spherical geometries. Each type of ultrasonically formed nanoparticle reveals Er(3+) photoluminescence from crystal lattice.

Acoustic cavitation for engineering of gold sols in silver nitrate solutions.

Binary gold-silver nanostructures of preformed gold nanoparticles (25nm) in silver nitrate solutions are produced by a two step sonication (20kHz). Ultrasonic treatment of gold-silver mixtures is carried out in the presence of sodium dodecyl sulfate in water or 2-propanol, and poly(vinyl pyrrolidone) in ethylene glycol solutions. Gold-silver nano-worms, which consist of ripened gold particles connected by ultrasonically reduced silver, are formed after 1h of sonication in the presence of sodium dodecyl sulfate aqueous solution.

Ultrasonic alloying of preformed gold and silver nanoparticles.

Alloyed gold/silver nanoparticles with a core/shell structure are produced from preformed gold and silver nanoparticles during ultrasonic treatment at different intensities in water and in the presence of surface-active species. Preformed gold nanoparticles with an average diameter of 15 + or - 5 nm are prepared by the citrate reduction of chloroauric acid in water, and silver nanoparticles (38 + or - 7 nm) are formed after reduction of silver nitrate by sodium borohydride. Bare binary gold/silver nanoparticles with a core/shell structure are formed in aqueous solution after 1 h of sonication at high ultrasonic intensity.

Synthesis of silver nanoparticles for remote opening of polyelectrolyte microcapsules.

Silver nanoparticles of 10, 18, and 23 nm were synthesized in aqueous medium by chemical reduction of silver nitrate in excess of sodium borohydride. Modification of polyelectrolyte shells with synthesized silver nanoparticles was performed using the layer-by-layer approach. Remote opening of the polyelectrolyte/silver capsules was performed with a CW Nd:YAG FD laser with an average incident power output up to 70 mW.