Investigating the in vitro photothermal effect of green synthesized apigenin‐coated gold nanoparticle on colorectal carcinoma

Applying toxic chemical to the synthesis of stable gold nanoparticles is one of the limitations of gold nanoparticles for therapeutic applications such as photothermal therapy. Plant compounds such as apigenin (API) with therapeutic potential can be applied in the synthesis of gold nanoparticles. API‐coated gold nanoparticles (Api@AuNPs) with an average size of 19.1 nm and a surface charge of −4.3 mV have been synthesized by a simple and efficient technique. The stability of Api@AuNPs in the biological environment was verified through UV‐Vis spectroscopy. Based on Raman and FTIR spectroscopy analysis, chemical binding of API on the surface of Api@AuNPs through hydroxyl and carbonyl functional groups was found to be the main reason for the stability of the Api@AuNPs in comparison with citrate‐coated gold nanoparticles (Cit@AuNPs). The synthesized Api@AuNPs do not cause major toxic effects up to 128 ppm. Api@AuNP‐mediated photothermal therapy leads to the indiscriminate eradication of almost half of both mouse fibroblastic (L929) and colorectal cancer (CT26) cells. Flow‐cytometry analysis revealed that the cell death mechanism is mainly apoptosis. In the apoptosis triggered cell death in photothermal treatment, Api@AuNPs are preferred over commonly used gold nanoparticles in photothermal treatments which mostly trigger the necrosis cell death pathway.     

Design and Implementation of a Gas Generating System for Complex Gas Mixtures and Calibration Gases

A test gas generation system for complex gas mixtures designed to mimic real industrial gas matrices with traces raging from low pptv to high ppmv level and minor and main components ranging from low to high percentage levels with variable relative humidity levels (0–80 % RH) is presented. It combines different gas generation methods to study fragmentation patterns under controlled conditions by means of a proton transfer reaction time-of-flight mass spectrometer, the application of alternative feedstocks in catalytic processes as well as the performance of gas purification and conditioning processes.     

Isolation and Identification of Current Biosurfactant-Producing Microbacterium maritypicum ABR5 as a Candidate for Oily Sludge Recovery

Biosurfactants have a wide range of applications in different areas, including petroleum microbiology and environmental biotechnology. In this study, removing and recovering oil from oily sludge using microbactan-producing bacteria have been investigated. The best biosurfactant-producing isolate was obtained from a petroleum reservoir and was identified by 16S rDNA analysis as Microbacterium maritypicum ABR5. Its 16S rDNA sequence was deposited in GenBank, NCBI under the accession number MK100468. Chemical analysis using thin-layer chromatography and Fourier Transform Infrared confirmed that the produced biosurfactant was glycolipoprotein. The strain reduced surface tension from 72 to 34.6 mN m⁻¹. The addition of 5 mg L ZnO nanoparticles to the biosurfactant-producing medium showed no bacterial toxicity effect and raised the emulsification index to 25.7%. Higher concentrations of ZnO nanoparticles, such as 10 and 100 mg L, decreased the bacterial growth rate and biosurfactant production. The mixing of M. maritypicum ABR5 culture medium and oily sludge increased the oil recovery from oily sludge by up to 70% after 5 days of incubation. This is the first report of biosurfactant production by a newly identified strain, M. maritypicum ABR5, isolated from a petroleum reservoir. We proposed that the isolated biosurfactant-producing strain could be considered an economical asset for oil recovery from oily sludge in the petroleum industry and environmental biotechnology.     

Rice Bran Oil Improves Insulin Resistance by Affecting the Expression of Antioxidants and Lipid‐Regulatory Genes

The present study investigated the molecular effects of rice bran oil (RBO) on lipid‐regulatory genes (sterol regulatory element binding protein‐1 [Srebf1] and peroxisome proliferator‐activated receptors‐α [Ppara]) and the expression of catalase (CAT) and superoxide dismutase (SOD1) genes in insulin‐resistant rats. Rats were divided into five groups: animals that received standard diet (control); rats fed standard diet containing RBO as the sole source of fat (RBO); a high‐fructose diet (HFD) group, which was further divided into two subgroups: rats fed HFD either for only 1 month (HFD1) or for 2 months (HFD2) and rats fed HFD containing RBO for 1 month; while rats in the last group fed HFD for 30 days then treated with RBO for another 30 days. The HFD induced a state of insulin resistance (IR) as indicated by the hyperinsulinemia and elevated homeostasis model assessment insulin resistance index. Hepatic lipid levels and radical scavenging enzymes were altered by the HFD. Lipid‐regulatory genes, Srebf1 and Ppara, were upregulated while Sod1 and Cat were downregulated in insulin‐resistant rats. Addition of RBO to the two diet regimens alleviated the disorders of IR to some extent. RBO reduced the hepatic levels of triacylglycerol, malondialdehyde, SREBP, and PPAR‐α mRNA. Hepatic SOD and CAT were elevated at gene and protein levels. The HFD induces de novo lipogenesis by upregulating the lipid‐regulatory genes resulting in increased serum and hepatic triacylglycerol. Moreover, IR induced by the HFD caused a state of oxidative stress. Supplementation of RBO to fructose‐fed rats not only improves insulin resistance but also downregulates lipogenic genes and improves the unbalanced oxidative status.     

Effect of Medium-High Energy Emulsification Condition on Physicochemical Properties of β-Sitosterol Multiple Emulsion

Phytosterols are used to lower the blood cholesterol. β-Sitosterol is one of the most important phytosterols with very poor water solubility and bioaccessibility. The main goal of the current research was to investigate the effects of different emulsification variables (i.e. shear, time, pressure and cycle) on the physicochemical properties, release behaviour and encapsulation efficiency of β-sitosterol in water-in-oil-in water (W/O/W) emulsion. Initially, 19 β-sitosterol emulsions were prepared under different experimental conditions (shear 3000 and 6000 rpm; time 2.5 and 5 min; pressure 100, 200 and 300 bar; cycle 1–3). In this study, the β-sitosterol emulsion prepared at 6000 rpm, 5 min, 300 bar and 3 cycles had the smallest average droplet size (139 nm) among all prepared samples. The interaction between shear and time showed the most significant (P < 0.05) effect on the polydispersity index (PDI) and turbidity of the β-sitosterol emulsion. Increasing homogenization pressure and cycle led to improving emulsion stability and encapsulation efficiency. The β-sitosterol emulsion homogenised at 100 bar for 1 cycle had the highest encapsulation efficiency (81.7%) among all samples. The optimization study showed that the emulsification at 300 bar for 3 cycles resulted in the most desirable β-sitosterol emulsion.     

Production and characterization of nanocomposites based on poly(amide-imide) containing 4,4′-methylenebis(3-chloro-2,6-diethylaniline) using nano-TiO2 surface-coupled by 3-aminopropyltriethoxysilane

In this work, the poly(amide-imide) (PAI) was synthesized from the polymerization reaction of 4,4′-methylenebis(3-chloro-2,6-diethyl trimellitimidobenzene) as a diacid with 4,4′-methylenebis(3-chloro-2,6-diethylaniline) under green condition using molten tetra-n-butylammonium bromide and triphenylphosphite. Ultrasonic technique was used for preparation of PAI/TiO₂ nanocomposites (PAI/TiO₂ NCs). For the improvement of TiO₂ nanoparticles (NPs) dispersion and enhancing interactions between NPs and polymeric matrix the surface of TiO₂ was successfully modified by silane coupling agent (3-aminopropyltriethoxysilane). The resulting NCs were characterized by FT-IR, X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and thermogravimetric analysis (TGA). The TGA of the obtained NCs proves the enhancement in the thermal stability with an increase in the percentage of titania NPs. TEM and FE-SEM images showed that the NPs were uniformly dispersed in the polymer matrix. The shielding effect of nano TiO₂ under UV radiation was examined by UV–vis.     

Preparation of Nanostructured ZnO Thin Films Using Magnetron Sputtering for the Gas Sensors Applications

ZnO is one of the most promising transparent conducting oxide materials, which widely used in thin film gas sensors. In this research, the dependence of the thermal oxidation time on structural, morphological and gas sensing properties of ZnO thin films is investigated. ZnO nanostructures are synthesized by using DC magnetron sputtering for deposition of pure zinc layers on glass substrates and then thermal oxidation of deposited zinc layers to produce zinc oxide (ZnO) thin films. Obtained results from X-ray diffraction revealed that the degree of crystallinity and the average grain size of the ZnO deposited thin films enhance with increasing the thermal oxidation time. Surface topography and growth behavior of ZnO thin films have important role in optimization of gas sensing properties of these films. In this study, scanning electron microscopy and atomic force microscopy have been used to investigate the effective parameters related to the surface topography of the films. Obtained results from these analyzes revealed that the surface topography of ZnO deposited samples strongly depend on thermal oxidation time. Also the effect of thermal oxidation time on the performance of ZnO gas sensors is investigated. The results indicated that the ethanol gas sensing properties of ZnO samples improve with decreasing the size of grains.     

Self-assembled micellar nanoparticles of a novel amphiphilic cholesteryl-poly(l-lactic acid)-b-poly(poly(ethylene glycol)methacrylate) block-brush copolymer

The biodegradable cholesteryl-(l-lactic acid) _n (CPLA) was synthesized via ring opening polymerization of l-lactide in the presence of cholesterol as an initiator and the catalytic amount of Sn(Oct)₂. The resulting monohydroxyl-terminated CPLA was subsequently converted to a bromine-ended macroinitiator (CPLA-Br) by esterification with 2-bromoisobutyryl bromide. Amphiphilic block-brush copolymers with different lengths of hydrophilic block (CPLA-b-P(PEGMA)₄ and CPLA-b-P(PEGMA)₁₂) were synthesized in a subsequent atom transfer radical polymerization of the poly(ethylene glycol)monomethyl ether methacrylate (PEGMA). The prepared polymers were characterized by FTIR, ¹H NMR and GPC. The self-assembly of the copolymers into the micellar aggregates in aqueous media was followed with dynamic light scattering, transmission electron microscopy and fluorescence analysis. The CMC values of the CPLA-b-P(PEGMA)₄ and CPLA-b-P(PEGMA)₁₂ samples were estimated approximately 56 × 10^?4 and 72 × 10^?4 g/L in an aqueous solution by fluorescence probe technique, respectively. The hydrophobic/hydrophilic chain ratio of the amphiphilic copolymers could have demonstrated a correlation with micelle formation ability and inter-micellar aggregation in an aqueous solution. Using the naproxen as a hydrophobic model drug, the drug-loading efficiency and drug release properties of the CPLA–PEG nanoparticles were investigated. In vitro release study of the naproxen-loaded micelles with about 54–60 % loading efficiency and 11–12 % loading capacity was performed using dialysis method in phosphate-buffered solution at 37 °C. Accordingly, these polymeric micelles may be provided as an effective drug carrier for drug controlled release by modulating the copolymer composition and molecular weight of blocks.     

A first-principles study of calcium-decorated, boron-doped graphene for high capacity hydrogen storage

Hydrogen adsorption and storage on calcium-decorated, boron-doped graphene was explored using density functional theory simulations based on local density approximation and generalized gradient approximation methods. The clustering problem for calcium-decorated graphene was investigated and it was shown that individual calcium atoms are not stable on pure graphene, and formation of aggregates is favorable. Substitutional boron doping can eliminate the clustering problem for Ca atoms on graphene. Up to four hydrogen molecules can stably bind to a Ca atom on a graphene plane with substitutional doping of a single boron atom. The average binding energy of ∼0.4 eV/H₂ is in the range that permits H₂ recycling at ambient conditions. Two binding mechanisms contribute to the adsorption of H₂ molecules: polarization of the H₂ molecule under the electric field produced by the Ca–graphene dipole, and hybridization of the 3d orbitals of Ca with the σ orbitals of H₂. Double-sided Ca-decorated graphene doped with individual boron atoms of 12 at.% can theoretically reach a gravimetric capacity of 8.38 wt.% hydrogen.     

Ensemble Boosting and Bagging Based Machine Learning Models for Groundwater Potential Prediction

Water Resources Management - Due to the rapidly increasing demand for groundwater, as one of the principal freshwater resources, there is an urge to advance novel prediction systems to more...