Effects of film thickness and alkaline concentration on dissolution kinetics of poly(4-hydroxystyrene) in alkaline aqueous solution

The dissolution behavior of a simple combination of poly(4-hydroxystyrene) (PHS) films and tetramethylammonium hydroxide (TMAH) aqueous solution was analyzed to gain a fundamental understanding of the effects of film thickness and alkaline concentration on the dissolution kinetics of chemically amplified resists (CARs). Films of four different thicknesses, from thick (approximately 900 nm) to thin (approximately 50 nm), were developed in 22 different developers of different concentrations. The dissolution behavior of each combination was observed using a quartz crystal microbalance (QCM). Differences in dissolution kinetics due to film thickness were observed even between relatively thick films such as 900- and 500-nm thick films in dilute developers. These differences were considered to be caused by the diffusion of the solution into the films. Thin films also showed characteristic behavior with dilution. This behavior was due to the interaction between the substrate and the films, unlike in the case of thick films.

Study of the Electrochemical Dissolution Behavior of Nitinol Shape Memory Alloy in Different Electrolytes for Micro-ECM Process

Nickel-Titanium alloy (Nitinol) is an excellent shape memory alloy (SMA) for Micro electro-mechanical systems (MEMS) particularly in biomedical applications owing to its three excellent features like shape memory effect (SME), superelasticity, and biocompatibility. The fabrication of micro features on Nitinol SMAs through conventional machining has been challenging due to its temperature-dependent material transformation properties. Micro electrochemical machining (micro-ECM), a nonconventional machining method for conductive material irrespective of strength and hardness has the potential for microfeature fabrication on Nitinol. This study presents the investigation on electrochemical dissolution behavior of Nitinol in different electrolytes for micro-ECM. The influence of electrolytes on the nature of dissolution of Nitinol has been studied by fabricating microchannels in three levels of parameters containing applied voltage and electrolyte concentration. The first three electrolytes were all aqueous neutral electrolytes i.e. sodium chloride (NaCl), sodium nitrate (NaNO3), and sodium bromide (NaBr). For profound analysis of dissolution behavior and its influence on machining performance, potentiodynamic polarization (PDP) tests of Nitinol were performed in aqueous NaCl, aqueous NaNO3, and aqueous NaBr solutions. The PDP tests that are conducted here are cyclic voltammetry (CV) and linear sweep voltammetry (LSV). The three aqueous solutions were utilized for microchannel fabrication in Nitinol through micro ECM in three levels of parameters out of which aqueous NaNO3 was successful in fabricating microchannel. Then nonaqueous electrolyte of ethylene glycol-based NaNO3 has been used to fabricate microchannels with lower depth overcut (DOC), width overcut (WOC), and length overcut (LOC) with respect to aqueous NaNO3 electrolyte.

Effect of Ni Concentration on the Surface Morphology and Corrosion Behavior of Zn-Ni Alloy Coatings

This research work aims to develop electrodeposited Zn-Ni alloy coatings with controlled dissolution tendencies on a mild steel substrate. The varying Ni concentration in the electroplating bath, i.e., 10, 15, 20 and 25 g·L−1, affected the surface morphology and electrochemical properties of the deposited Zn-Ni alloy coatings. SEM and EDS analysis revealed the resulting variation in surface morphology and composition. The electrochemical behavior of different coatings was evaluated by measuring the open circuit potential and cyclic polarization trends in 3.5 wt.% NaCl solution. The degradation behavior of the electrodeposited Zn-Ni coatings was estimated by conducting a salt spray test for 96 h. The addition of Ni in the coating influenced the coating thickness and surface morphology of the coatings. The coating thickness decreased from 38.2 ± 0.5 μm to 20.7 ± 0.5 μm with the increase in Ni concentration. Relatively negative corrosion potential (<−1074 ± 10 mV) of the Zn-Ni alloy coatings compared to the steel substrate (−969 mV) indicated the sacrificial dissolution behavior of the Zn-rich coatings. On the other hand, compared to the pure Zn (26.12 mpy), ~4 times lower corrosion rate of the Zn-Ni coating (7.85 mpy) was observed by the addition of 25 g·L−1 Ni+2 in the bath solution. These results highlighted that the dissolution rate of the sacrificial Zn-Ni alloy coatings can effectively be tuned by the addition of Ni in the alloy coating during the electrodeposition process.

Development of a gliclazide ionic liquid and its mesoporous silica particles: an effective formulation strategy to improve oral absorption properties

An ionic liquid (IL) form of gliclazide with enhanced solubility characteristics was successfully synthesized. This IL could be loaded into mesoporous silica carrier and exhibited improved dissolution behavior in vitro.

Crystal Structure, Solubility, and Pharmacokinetic Study on a Hesperetin Cocrystal with Piperine as Coformer

Hesperetin (HES) is a key biological active ingredient in citrus peels, and is one of the natural flavonoids that attract the attention of researchers due to its numerous therapeutic bioactivities that have been identified in vitro. As a bioenhancer, piperine (PIP) can effectively improve the absorption of insoluble drugs in vivo. In the present study, a cocrystal of HES and PIP was successfully obtained through solution crystallization. The single-crystal structure was illustrated and comprehensive characterization of the cocrystal was conducted. The cocrystal was formed by two drug molecules at a molar ratio of 1:1, which contained O–H–O hydrogen bonds between the carbonyl and ether oxygen of PIP and the phenolic hydroxyl group of HES. In addition, a solubility experiment was performed on powder cocrystal in simulated gastrointestinal fluid, and the result revealed that the cocrystal improves the dissolution behavior of HES compared with that of the pure substance. Furthermore, HES’s bioavailability in the cocrystal was six times higher than that of pristine drugs. These results may provide an efficient oral formulation for HES.