Development of Phospholipids Vesicular Nanocarrier for Topical Delivery of Tea Tree Oil in Management of Atopic Dermatitis Using BALB/c Mice Model

This work aims to develop and evaluate the efficacy of tea tree oil (TTO) ethosomal cream with improved deposition in skin layers for treatment of atopic dermatitis (AD). Ethosomes of TTO are developed using phosphatidylcholine (2% and 3% w/v) and ethanol (20%, 30%, and 40% w/v). Ethosomes are evaluated for percent entrapment efficiency (%EE), vesicle size, zeta potential, and in vitro drug diffusion. Ethosomal creams with optimized ethosomal dispersion are developed and evaluated for physicochemical parameters, thermal stability, ex vivo permeation, skin retention, and in vitro cytotoxicity using HaCat skin cell lines in comparison to conventional creams of TTO. In vivo investigations of optimized creams are performed using BALB/c mice model. The %EE, vesicle size, and zeta potential for optimized ethosomes are found to be 76.19 ± 3.26%, 333.6 nm, and –35.3 mV, respectively. Ethosomal creams showed higher deposition in the epidermis and dermis. The optimized creams are non-cytotoxic to HaCat cell lines. The creams significantly reduce the inflammatory response by decreasing the clinical score and infiltration of white blood cells, eosinophils, and IgE antibodies. Overall efficacy of ethosomal cream is higher than conventional cream. In conclusion, optimized ethosomal cream of TTO shows good efficacy for treatment of AD. Practical applications : The method used for the formulation of ethosomes is simple and can be easily scaled up on the industrial level. The loading of TTO within ethosomes can increase the efficiency by enhanced drug deposition in the epidermis and might also improve its stability against oxidative degradation. Topical ethosomal cream of TTO can improve patient compliance by avoidance of adverse effects linked with corticosteroids and could be a possible complementary or alternative therapy in management of AD.     

Fabrication of ZnO-functionalized polypyrrole microcomposite as a protective coating to enhance anticorrosion performance of low carbon mild steel

In the present work, PPy, ZnO, and polypyrrole/zinc oxide (PPy/ZnO) microcomposites (1, 2, and 5 wt%) were prepared and their properties have been tuned for anticorrosion applications on low carbon mild steel. The synthesized products: ZnO, PPy, and composites were characterized by various sophisticated analytical techniques such as XRD, FTIR, Raman, FESEM, EDX, UV–VIS, TGA, and BET. The band frequencies observed at 480 and 588 cm⁻¹ in FTIR spectrum correspond to stretching vibrations of Zn-O and N-H bonds, respectively, broadening of the bands in the composites indicate strong interactions between ZnO and PPy matrix. The potentiodynamic polarization study of PPy and PPy/ZnO composite was carried out in 3.5% NaCl solution to investigate the corrosion resistance efficiency. PPy/1 wt% ZnO (I_corr = 190 nA) composite coating on low carbon mild steel was observed to exhibit best corrosion protection property compared to PPy (121 μA), 2 and 5 wt% ZnO (242, 295 nA) composites. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48319.     

Impressed Current Cathodic Protection of Low Carbon Steel in Conjunction with Conducting Polyaniline based Paint Coating

Protection of Metals and Physical Chemistry of Surfaces - Epoxy, Fusion bonded epoxy and conducting polyaniline based paints were applied on low carbon steel sample. Conducting polyaniline and...     

Multifunctional plasmonic Ag-hematite nano-dendrite electro-catalysts for methanol assisted water splitting: Synergism between silver nanoparticles and hematite dendrites

Hydrogen is the most environment friendly fuel and has the largest energy density but still much away from being a viable technology due to the cost associated with its production on-site on-demand. However, hydrogen production via water splitting could become potential commercial technology by designing new catalyst materials with low cost, desired surface structures and properties that govern hydrogen evolution reaction (HER) activity and stability. Here, we report the methanol assisted electrochemical water splitting using silver nanoparticles decorated hematite (Ag-hematite) dendrite nanostructures. Ag-hematite nano-dendrites prepared via two different methods viz. chemical co-precipitation and hydrothermal treatment are analysed and compared for their potential applications towards methanol assisted water splitting. It is found that Ag-hematite nano-dendrites prepared by chemical precipitation method shows much better activity as compared to both the parent materials (i.e. Ag NPs and hematite nano-dendrites) as well as Ag-hematite nano-dendrites synthesized by hydrothermal treatment. A baseline study showing the influence of methanol concentration, catalyst, catalyst support, and operating mode has been established. The analysis of the system was carried out as a function of onset potentials and kinetic parameters, including the Tafel slopes and exchange current densities. The effect of electrochemical promotion was investigated to see if it can increase the efficiency and performance of H₂ production through electrochemical processes. The observed electro-catalytic enhancement could be attributed to the synergistic effect of hematite dendrites, larger surface area of dendrite structure leading to higher loading of Ag NPs on the surface of HDs. Moreover, the endurance study was performed to check the stability of the presented electrocatalyst in acidic medium under both dark and light illumination conditions which shows that the presented composite catalyst is stable for minimum 100 scans even under light illumination with no signs of photo-corrosion.     

Preparation and characterization of carbon-encapsulated iron nanoparticles and their catalytic activity in the hydrogenation of levulinic acid

This study describes the synthesis of carbon-encapsulated iron nanoparticles using an ultrasonic method and also investigates their catalytic activity. These nanoparticles have been prepared using ultrasonic irradiation followed by annealing at various temperatures. As the annealing temperature of as-prepared α-Fe₂O₃ nanoparticles increased, the sample transformed into γ-Fe₂O₃, Fe₃O₄, and Fe nanoparticles via the reduction process without requiring any additional reducing agents such as H₂ gas, thus, creating a carbon shell surrounding the nanoparticles. By controlling the experimental conditions, Fe nanoparticles of various sizes can be formed with diameters in the range 100–800 nm; these nanoparticles are tightly encapsulated by 20-nm-thick carbon shells. Because of their high saturation magnetization 212 emu g^?1, the carbon-encapsulated Fe nanoparticles can be used for magnetic resonance imaging with a dramatically enhanced efficiency compared to commercially available T ₂ contrast agents. Moreover, the carbon-encapsulated Fe nanoparticles showed its superior catalytic activity and reusability for the hydrogenation of biomass-derived levulinic acid to GVL (99.6 %) in liquid phase.     

Development of pellets of nifedipine using HPMC K15 M and κ-carrageenan as mucoadhesive sustained delivery system and in vitro evaluation

Polymeric mucoadhesive pellets of nifedipine were designed using computer software and they were prepared by extrusion-spheronization using HPMC K15M and κ-carrageenan with microcrystalline cellulose. A randomized rotatable two factor central composite design was applied for assessment of influence of two independent variables such as concentration of κ-carrageenan and HPMC K15M on dependent variables. Pellets were characterized by FTIR, DSC, SEM, flow properties, particle size, abrasion resistance, sphericity, drug content, percent production yield, in vitro drug release, ex vivo mucoadhesion, stability studies and similarity factor. The optimized formulation was selected based on criteria of sphericity nearest to 1.0 with maximum cumulative drug release percentage. Formulation NF6 exhibited sufficient porous spheres, free flowing and smooth surface mucoadhesion of 91.34 % and drug content 98.22 ± 0.37 %. Kinetic modeling revealed that the formulation followed the Higuchi model and showed the Quassi-Fickian drug release mechanism. The similarity factor, F2 value, was found to be 74 ± 6 and there was no significant change in drug content and ex vivo mucoadhesion after 90 days at 40 ± 2 °C, and 75 ± 5 % RH clearly indicated the optimized batch NF6 was stable. Thus, it can be concluded that use of κ-carrageenan, microcrystalline cellulose and HPMC K15M at the 20:35:10 w/w ratio could provide an effective carrier for enhancement of sphericity and sustained release of matrix pellets.     

Multilayered large‐area WO3 films on sheet and mesh‐type stainless steel substrates for photoelectrochemical hydrogen generation

The objective of this study is to demonstrate the significant improvement in the photoelectrochemical (PEC) hydrogen generation by a photoanode owing to the increased surface area of the substrate. In this work, multilayered tungsten oxide (WO₃) films have been successfully synthesized onto the large‐area sheet (9 × 9cm²) and mesh (1 × 20cm²) ‐type stainless steel (SS) substrates using screen printing and brush painting methods, respectively. All the WO₃ films are porous and nanocrystalline (30–80 nm) in nature with a monoclinic crystal structure as revealed from X‐ray diffraction and scanning electron microscopy studies. The PEC water splitting study is performed under simulated 1 SUN illumination (AM1.5 G) in a typical two‐electrode cell configuration with WO₃ photoanode and Pt wire immersed in 0.5 M H₂SO₄ electrolyte. The photocurrent as well as hydrogen generation rate for WO₃ photoanodes coated on the plane SS sheet substrate is relatively low and showed minimal change with increasing film thickness. On the other hand, the photocurrent as well as the hydrogen generation is enhanced by a 3–4 fold degree for the WO₃ photoanodes coated on SS mesh. We attribute such efficient water splitting to the increment in the filling factor of the WO₃ material due to the large effective surface area of the SS mesh as compared to the SS sheet substrate. Copyright © 2011 John Wiley & Sons, Ltd.