Abstract
The feasibility of measuring arsenic and selenium contents in a single nail clipping was investigated using a small-focus portable X-ray fluorescence (XRF) instrument with monochromatic excitation beams. Nail clipping phantoms supplemented with arsenic and selenium to produce materials with 0, 5, 10, 15, and 20 mu g/g were used for calibration purposes. In total, 10 different clippings were analyzed at two different measurement positions. Energy spectra were fit with detection peaks for arsenic K-alpha, selenium K-alpha, arsenic K-beta, selenium K-beta, and bromine K-alpha characteristic X-rays. Data analysis was performed under two distinct conditions of fitting constraint. Calibration lines were established from the amplitude of each of the arsenic and selenium peaks as a function of the elemental contents in the clippings. The slopes of the four calibration lines were consistent between the two conditions of analysis. The calculated minimum detection limit (MDL) of the method, when considering the Ka peak only, ranged from 0.210 +/- 0.002 mu g/g selenium under one condition of analysis to 0.777 +/- 0.009 mu g/g selenium under another. Compared with previous portable XRF nail clipping studies, MDLs were substantially improved for both arsenic and selenium. The new measurement technique had the additional benefits of being short in duration (similar to 3 min) and requiring only a single nail clipping. The mass of the individual clipping used did not appear to play a major role in signal strength, but positioning of the clipping is important.

Abstract
Ethionamide (ETH) is an important second-line antituberculosis drug used for the treatment of patients infected with multidrug-resistant Mycobacterium tuberculosis. Recently, we reported that the loading of ETH into thermally carbonized-porous silicon (TCPSi) nanoparticles enhanced the solubility and permeability of ETH at different pH-values and also increased its metabolization process. Based on these results, we synthesized carboxylic acid functionalized thermally hydrocarbonized porous silicon nanoparticles (UnTHCPSi NPs) conjugated with ETH and its antimicrobial effect was evaluated against Mycobacterium tuberculosis strain H37Rv. The activity of the conjugate was increased when compared to free-ETH, which suggests that the nature of the synergy between the NPs and ETH is likely due to the weakening of the bacterial cell wall that improves conjugate-penetration. These ETH-conjugated NPs have great potential in reducing dosing frequency of ETH in the treatment of multidrug-resistant tuberculosis (MDR-TB).

Abstract
A Fabry-Perot air bubble microcavity fabricated between a section of single mode fiber and a multimode fiber is proposed. The study of the microcavities growth with the number of applied arcs is performed. The sensors are tested for lateral load and strain, where sensitivities of 0.32 nm/N and 2.11 nm/N and of 4.49 pm/mu epsilon and 9.12 pm/mu epsilon are obtained for the 47 mu m and 161 mu m long cavities, respectively. The way of manufacturing using a standard fusion splicer and given that no oils or etching solutions are involved, emerges as an alternative to the previously developed air bubble based sensors.

Abstract
A Fabry-Perot air bubble microcavity fabricated between a section of single mode fiber and a multimode fiber that requires only the use of a commercial fusion splicer is proposed. The study of the microcavities growth with the number of applied arcs is performed and several sensors are tested. The sensors are tested for lateral load measurements, and it is observed that there is dependence between the sensor dimensions and its sensitivity. The maximum sensitivity of 2.11 nm/N was obtained for the 161-mu m-long cavity. Moreover, given the low temperature sensitivity (<1 pm/degrees C), the proposed cavity should be adequate to perform temperature-independent measurements. The accurate technique control leads to the fabrication of reproducible cavities with the sensitivity required for the application. The way of manufacturing using a standard fusion splicer, given that no oils or etching solutions are involved, emerges as an alternative to the previously developed air bubble-based sensors.

Abstract

Abstract