The Effect of Nanobubbles on Transdermal Applications.

In the present work, a new method for dermal delivery using nanobubbles (NBs) is investigated. Oxygen NBs are generated in deionized water and used to produce cosmetic formulations with hyaluronic acid as an active ingredient. Nanobubbles result in the improvement of the effect and penetration of the active ingredient through Strat-M, a synthetic membrane that resembles human skin. Experiments conducted with the Franz Cell device confirm the greater penetration of the active ingredient into Strat-M due to NBs, compared to cosmetic formulations that do not contain NBs. The effect of NBs was further examined by measuring UV-Vis and FTIR spectra. A possible mechanism was outlined, too. It was also found that NBs do not change the pH or the FTIR spectrum of the cosmetic serum indicating non-toxicity.

Bulk nanobubbles: Production and investigation of their formation/stability mechanism.

Nanobubbles (ΝΒs) have attracted concentrated scientific attention due to their unique physicochemical properties and large number of potential applications. In this study, a novel nanobubble generator with low energy demand, operating continuously, is presented. Air and oxygen bulk nanobubbles (NBs@air and NBs@O2) with narrow size distribution and outstanding stability were prepared in water solution. The bulk NBs' behavior was evaluated taking into consideration the hydrodynamic diameter and ζ-potential as a function of processing time, gas type, pH value and NaCl concentration. According to the results the optimum processing time was 30 min, whereas the effect of water salinity was stronger in NBs@O2 than NBs@air. In order to investigate further the NBs properties, Electron Paramagnetic Resonance (EPR) spectroscopy was applied for quantitative analysis of free radicals following the spin trapping methodology. The mechanism of bulk NBs' generation and their extremely long-time stability can be attributed mainly to the hydrogen bonding interactions. The formation of a diffusion layer, by absorption of OH- due to electrostatic interaction, contributing to negative surface charge, whereas the interaction of ions with the surface hydroxylic groups provide the equilibrium between the protonation and deprotonation of water and finally the formation of a stable interface layer. A remarkable highlight of this work is the long-time stability of generated bulk NBs which is up to three months.

Small-angle X-ray scattering (SAXS) and nitrogen porosimetry (NP): two novel techniques for the evaluation of urinary stone hardness.

PURPOSE: To evaluate urinary stones using small-angle X-ray scattering (SAXS) and nitrogen porosimetry (NP). Traditionally, stones are categorized as hard or soft based on their chemical composition. We hypothesized that stone hardness is associated not only with its chemical composition but also with its internal architecture. SAXS and NP are well-known techniques in material sciences. We tested whether SAXS and NP are applicable for evaluating human urinary stones and whether they provide information at the nanoscale level that could be useful in clinical practice. METHODS: Thirty endoscopically removed urinary stones were studied. Standard techniques for stone analysis were used to determine the stone composition. SAXS was used to evaluate the solid part of the stone by measuring the crystal thickness (T) and the fractal dimension (Dm/Ds), while NP was used to evaluate the porosity of the stone, i.e., the pore radius, pore volume, and specific surface area (SSA). RESULTS: All stones were successfully analyzed with SAXS and NP. Each stone demonstrated unique characteristics regarding T, Dm/Ds, pore radius, pore volume, and SSA. Significant differences in those parameters were seen among the stones with almost identical chemical compositions. The combination of high T, high SSA, low Dm/Ds, low pore volume, and low pore radius is indicative of a hard material and vice versa. CONCLUSIONS: SAXS and NP can be used to evaluate human urinary stones. They provide information on stone hardness based on their nanostructure characteristics, which may be different even among stones with similar compositions.

A rotating sample cell for in situ measurements of adsorption with x-rays.

A sample cell which facilitates adsorption in conjunction with small angle x-ray scattering under a rotational field is presented. The device allows dynamic phenomena that take place within a pore system to be investigated in situ by x-rays. As an example, a sample of Vycor porous glass was measured at relative pressures p/po = 0 and p/po = 0.5. For the static measurements, the results were as expected. Under rotation, an increase in the scattered intensity of the loaded sample, over the corresponding static one, is observed. Fractal analysis has shown an increase in the fractal dimension even higher than that of the dry sample. It was suggested that the increase in the scattered intensity was due to the rotation, while the abnormality in the fractal dimension was due to asymmetric ripples of the adsorbed layers. The limits of the technique are given too.

Scanning of Adsorption Hysteresis In Situ with Small Angle X-Ray Scattering.

Everett's theorem-6 of the domain theory was examined by conducting adsorption in situ with small angle x-ray scattering (SAXS) supplemented by the contrast matching technique. The study focuses on the spectrum differences of a point to which the system arrives from different scanning paths. It is noted that according to this theorem at a common point the system has similar macroscopic properties. Furthermore it was examined the memory string of the system. We concluded that opposite to theorem-6: a) at a common point the system can reach in a finite (not an infinite) number of ways, b) a correction for the thickness of the adsorbed film prior to capillary condensation is necessary, and c) the scattering curves although at high-Q values coincide, at low-Q values are different indicating different microscopic states. That is, at a common point the system holds different metastable states sustained by hysteresis effects. These metastable states are the ones which highlight the way of a system back to a return point memory (RPM). Entering the hysteresis loop from different RPMs different histories are implanted to the paths toward the common point. Although in general the memory points refer to relaxation phenomena, they also constitute a characteristic feature of capillary condensation. Analogies of the no-passing rule and the adiabaticity assumption in the frame of adsorption hysteresis are discussed.