SPH fluids for viscous jet buckling

We present a novel meshfree technique for animating\ud free surface viscous liquids with jet buckling effects, such as\ud coiling and folding. Our technique is based on Smoothed Particle\ud Hydrodynamics (SPH) fluids and allows more realistic and\ud complex viscous behaviors than the preceding SPH frameworks\ud in computer animation literature. The viscous liquid is modeled\ud by a non-Newtonian fluid flow and the variable viscosity under\ud shear stress is achieved using a viscosity model known as Cross\ud model. The proposed technique is efficient and stable, and our\ud framework can animate scenarios with high resolution of SPH\ud particles in which the simulation speed is significantly accelerated\ud by using Computer Unified Device Architecture (CUDA)\ud computing platform. This work also includes several examples\ud that demonstrate the ability of our technique.FAPESP - processos nos. 2013/19760-5 e 2014/11981-5FAPES - processos no. 53600100/11CNP

Superparamagnetic Microspheres with Controlled Macroporosity Generated in Microfluidic Devices

A microfluidic approach to preparing superparamagnetic microspheres with tunable porosity is described. In this method, droplets consisting of iron oxide nanoparticles, a functional polymer and solvent are formed in a microfluidic channel. The droplets are subsequently collected in solutions of sodium dodecyl sulfate (SDS) where the solvent is left to diffuse out of the droplet phase. By adjusting the concentration of the SDS and the polarity of the solvent of the dispersed phase, the porosity of the microparticles is controlled from non porous to porous structure. The formation of the pores is shown to depend on the rate at which solvent diffuses out of the droplet phase and the availability of SDS to adsorb at the droplet interface

Manipulation and Quantification of Graphene Oxide Flake Size: Photoluminescence and Cytotoxicity

Single-layered graphene oxide (GO) has exhibited great promise in the areas of sensing, membrane filtration, supercapacitors, bioimaging, and therapeutic carriers because of its biocompatibility, large surface area, and electrochemical, photoluminescent, and optical properties. To elucidate how the physical dimensions of GO affect its intrinsic properties, we employed sonication to produce more than 130 different sizes of GO in aqueous dispersion and implemented new approaches to characterize various GO properties as a function of the average flake size. New protocols were developed to determine and compare the flake size of GO dispersions sonicated with energies up to 20 MJ/g by using dynamic light scattering and atomic force microscopy (AFM). The relationship between the average flake size and sonication energy per unit mass of GO was observed to follow a power law. AFM height measurements showed that the sonication of GO yielded monolayered flakes. Photoluminescence of GO was characterized as a function of the sonication energy (or the average flake size which is the monotonic function of the sonication energy), excitation wavelength, and pH of the dispersion. The strong dependence of the photoluminescence intensity on pH control and the variation of the photoluminescence intensity with different flake sizes were observed. An intense photoluminescence signal, likely related to the separation of the oxidative debris from the GO framework, was found at the highest sonication energies (<i>E</i> ≳ 15 MJ/g) or under extremely alkaline conditions (pH ≳ 11). The cytotoxicity of GO was studied with various flake sizes. Size- and concentration-dependent cytotoxicity was observed for cell lines NIH 3T3 and A549. The NIH 3T3 cell line also demonstrated time-dependent cytotoxicity

Ensemble and Single Particle Fluorescence Characterization of Dye-Labeled Cellulose Nanocrystals

Cellulose nanocrystals (CNCs) have been covalently labeled with both fluorescein and rhodamine and studied by a combination of UV–vis absorption spectroscopy and ensemble and single molecule fluorescence spectroscopy. For all samples, the fluorescence anisotropy and lifetimes were consistent with effects expected for covalently bound dye molecules. Low dye loading levels (∼0.1 dye/particle) were estimated for the fluorescein-labeled CNC which coupled with the strong pH dependence make this a less suitable fluorophore for most applications. Rhodamine-labeled CNCs were prepared from both sulfated and carboxylated CNCs and had loading levels that varied from 0.25 to ∼15 dye molecules/CNC. For the sulfated samples, the absorption due to (nonfluorescent) dimeric dye increased with dye loading; in contrast, the carboxylated sample, which had the highest rhodamine content, had a low dimer yield. Single particle fluorescence studies for two of the rhodamine-labeled CNCs demonstrated that individual particles are readily detected by their stepwise blinking/bleaching behavior and by polarization effects. Overall, the results indicate the importance of understanding the effects of loading on dye photophysics to select an optimal dye concentration to maximize sensitivity while minimizing the effect of the dye on the CNC behavior. The results also demonstrate that CNCs with relatively low dye loadings (e.g., ∼1 dye/particle) are readily detectable by fluorescence and should be adequate for use in fluorescence-based biological assays or to probe the distribution of CNCs in composite materials

Changes in Order Parameters Associated with Ceramide-Mediated Membrane Reorganization Measured Using pTIRFM

The enzymatic generation of ceramide has significant effects on the biophysical properties of lipid bilayers and can lead to the extensive reorganization of cell membranes. We have synthesized and characterized a headgroup-labeled fluorescent lipid probe (NBD-ceramide, NBD-Cer) and demonstrated that it can be used for polarized total internal reflection fluorescence microscopy experiments to probe changes in membrane order that result from ceramide incorporation. NBD-Cer measures significantly higher order parameters for the liquid-ordered (L_o) domains (⟨<i>P</i>₂⟩ = 0.40 ± 0.03) than for the liquid-disordered phase (L_d, fluid, ⟨<i>P</i>₂⟩ = 0.22 ± 0.02) of phase-separated bilayers prepared from egg sphingomyelin, dioleolyphosphatidylcholine, and cholesterol mixtures. The probe also responds to changes in packing induced by the direct incorporation of ceramide or the variation in the ionic strength of the aqueous medium. Order parameter maps obtained after enzyme treatment of bilayers with coexisting L_o and L_d phases show two distinct types of behavior. In regions of high enzyme activity, the initial L_o/L_d domains are replaced by large, dark features that have high membrane order corroborating previous hypotheses that these are ceramide-enriched regions of the membrane. In areas of low enzyme activity, the size and shape of the L_o domains are conserved, but there is an increase in the order parameter for the initial L_d phase (⟨<i>P</i>₂⟩ = 0.30 ± 0.01). This is attributed to the incorporation of ceramide in the L_o domains with the concomitant expulsion of cholesterol into the surrounding fluid phase, increasing its order parameter