Biosynthesis and characterisation of nano‐silica as potential system for carrying streptomycin at nano‐scale drug delivery

A growing trend within nanomedicine has been the fabrication of self‐delivering supramolecular nanomedicines containing a high and fixed drug content ensuring eco‐friendly conditions. This study reports on green synthesis of silica nanoparticles (Si‐NPs) using Azadirachta indica leaves extract as an effective chelating agent. X‐ray diffraction analysis and Fourier transform‐infra‐red spectroscopic examination were studied. Scanning electron microscopy analysis revealed that the average size of particles formed via plant extract as reducing agent without any surfactant is in the range of 100–170 nm while addition of cetyltrimethyl ammonium bromide were more uniform with 200 nm in size. Streptomycin as model drug was successfully loaded to green synthesised Si‐NPs, sustain release of the drug from this conjugate unit were examined. Prolong release pattern of the adsorbed drug ensure that Si‐NPs have great potential in nano‐drug delivery keeping the environment preferably biocompatible, future cytotoxic studies in this connection is helpful in achieving safe mode for nano‐drug delivery.Inspec keywords: silicon compounds, nanofabrication, nanomedicine, drug delivery systems, nanoparticles, X‐ray diffraction, Fourier transform infrared spectra, scanning electron microscopyOther keywords: nanosilica, streptomycin, nanoscale drug delivery, nanomedicine, silica nanoparticles, Azadirachta indica leaves extract, X‐ray diffraction analysis, Fourier transform‐infrared spectroscopy, scanning electron microscopy, cetyltrimethyl ammonium bromide, SiO₂      

Potential visible WO3/GO composite photocatalyst

Graphene oxide (GO) was synthesized by Hummers method. GO and tungsten oxide (WO₃) composites were successfully prepared by deposition of WO₃ on GO surface to make efficient visible light catalyst. Scanning electron microscopy of pure GO revealed that GO films are folded with kinked and wrinkled edges. The interspaces layers are partially filled by WO₃ nanoparticles with their less wrinkled edges and smooth surface of composite. Moreover, composite sheets are thin and transparent which allow easy penetration of light. EDS showed the presence of C, O, and W in GO/WO₃ composites with no impurity. UV-Vis diffused reflectance spectra showed red shift with the increase in WO₃ contents. Raman spectra of GO and GO/WO₃ composite show G and D bands. These bands reduced in intensity in composite sample due to removal of oxygenated functional groups with some new peaks of WO₃. FT-IR confirmed successful oxidation of graphite into GO with reduction in GO because oxide-related bond groups decrease after reduction. The transmittance peaks of WO₃ in composite sample are appeared indicating W-O-C linkages. The highest visible light activity of the composite is due to easy penetration of light with deposition of WO₃, low band gap, and new linkages.     

ZnO/WO3 nanostructure as an efficient visible light catalyst

Highly photosensitive ZnO/WO₃ photocatalysts were fabricated by wet impregnation of zinc oxide (ZnO) in different contents. Tungsten trioxide (WO₃) was synthesized by hydrothermal route. The presence of ZnO inhibited the crystallization of WO₃ and caused agglomeration of WO₃ nanoparticles surface. The formation of Zn-O-W linkage was studied by X-ray photoelectron emission (XPS) and Fourier transforms Infra-red spectra (FTIR). These linkages were responsible for red shift of absorption peak of composites as compared to individual ZnO and WO₃. The band gap was decreased due to incorporation of ZnO in WO₃ which promoted the separation of photo-generated carriers. As a result, ZnO/WO₃ composite showed extremely high efficiency for MO degradation in comparison with Degussa P25, pure ZnO and WO₃. 2.0% ZnO/WO₃ composite displayed the highest activity in photocatalytic decomposition of methyl orange (MO) dye.     

Synergistic evaluation of AgO2 nanoparticles with ceftriaxone against CTXM and blaSHV genes positive ESBL producing clinical strains of Uro‐pathogenic E. coli

The silver oxide nanoparticles (AgO₂ ‐NPs) were synthesised using silver foil as a new precursor in wet chemical method. X‐ray diffraction analysis shows crystallographic structures of AgO₂ ‐NPs with crystallite size of 35.54 nm well‐matched with standard cubic structure. Scanning electron microscopy analysis clearly shows the random distribution of spherical‐shaped nanoparticles. Energy dispersive X‐ray analysis confirmed the purity of the samples as it shows no impurity element. Fourier transforms infra‐red analysis confirmed the formation of AgO₂ ‐NPs with the presence of Ag‐O‐Ag stretching bond. All the techniques also confirmed the loading of ceftriaxone drug on the surface of AgO₂ ‐NPs. This study also described the effect of AgO₂ ‐NPs having synergistic activity with β lactam antibiotic i.e. ceftriaxone against ESBL generating Escherichia coli (E. coli). Among isolated strains of E. coli, 60.0% were found to be ESBL producer. The synergistic activities of AgO₂ ‐NPs with ceftriaxone suggest that these combinations are effective against MDR‐ESBL E. coli strains as evident by increase in zone sizes. The present study observed rise in MDR‐ESBL E. coli with polymorphism of blaCTXM and blaSHV causing UTI infections in Pakistani population. The antibiotic and AgO₂ ‐NPs synergistic effect can be used as an efficient approach to combat uro‐pathogenic infections.Inspec keywords: antibacterial activity, nanofabrication, nanomedicine, drugs, nanoparticles, microorganisms, crystallites, scanning electron microscopy, silver compounds, X‐ray diffraction, X‐ray chemical analysis, Fourier transform infrared spectra, organic compounds, geneticsOther keywords: synergistic evaluation, clinical strains, silver oxide nanoparticles, silver foil, wet chemical method, X‐ray diffraction analysis, crystallographic structures, standard cubic structure, spherical‐shaped nanoparticles, energy dispersive X‐ray analysis, ceftriaxone drug, synergistic activity, ESBL producer, scanning electron microscopy, Fourier transform infrared analysis, Escherichia coli, blaSHV gene positive ESBL, crystallite size, random distribution, β lactam antibiotics, MDR‐ESBL E. coli strains, polymorphism, blaCTXM, uro‐pathogenic infections, uro‐pathogenic E. coli, AgO₂      

Synthesis and characterization of novel Pr6O11/Mn3O4 nanocomposites for electrochemical supercapacitors

This study presents the successful synthesis of praseodymium oxide, Pr₆O₁₁ and hausmannite manganese oxide, Mn₃O₄ nanoparticles, along with a novel synthesis of (Pr₆O₁₁/Mn₃O₄) nanocomposites by employing the hydrothermal route followed by post thermal annealing. X-ray Diffraction, Field Emission Scanning Electron Microscopy and Energy Dispersive X-ray characterization techniques are being adapted to analyze the physical characteristics of all the synthesized materials. XRD results reveal the crystalline nature of the synthesized materials. FE-SEM results display the irregular nanograins of Mn₃O₄ and a regular network of interconnected Pr₆O₁₁ nanoparticles. Nitrogen adsorption/desorption tests confirm the mesoporous nature of all the synthesized electrode materials. The Pr₆O₁₁/Mn₃O₄ ??2 electrode material exhibits an outstanding specific capacitance of 794.58?F/g at a current density of 0.5?A/g, as compared to the 521.24?F/g for the Pr₆O₁₁ electrode material. These investigations provide an easy and efficient method to develop nanocomposites (Pr₆O₁₁/Mn₃O₄) with better electrochemical characteristics, as electrode materials for supercapacitor applications.     

Synthesis and characterization of mesoporous-TiO2 with enhanced photocatalytic activity for the degradation of chloro-phenol

Mesoporous-titania (TiO₂) photocatalysts have been synthesized using polyethylene glycol (PEG) as a template in dilute acetic acid aqueous solution by hydrothermal process. The effect of PEG molecular weights and thermal treatment on the resultant structure and photocatalytic activity are investigated. Structural and phase compositional properties of the resultant photocatalysts are characterized by transmission electron microscopy, X-ray diffraction and nitrogen sorption analysis. When the molecular weights of PEG vary from 600 to 20,000, the particle sizes of mesoporous structure decrease from 15.1 to 13.3 nm and mean pore sizes increase from 6.9 to 10.6 nm. The chemical reactions of the formation of mesoporous-TiO₂ during its synthesis have been proposed and discussed. The activities of mesoporous-TiO₂ photocatalysts are evaluated and compared with Degussa P-25 using chloro-phenol as a testing compound. The reaction mechanism of photodegradation is also described on the basis of high performance liquid chromatography.     

Electro‐Oxidation of Ni42 Steel: A Highly Active Bifunctional Electrocatalyst

Janus type water‐splitting catalysts have attracted highest attention as a tool of choice for solar to fuel conversion. AISI Ni42 steel is upon harsh anodization converted into a bifunctional electrocatalyst. Oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are highly efficiently and steadfast catalyzed at pH 7, 13, 14, 14.6 (OER) and at pH 0, 1, 13, 14, 14.6 (HER), respectively. The current density taken from long‐term OER measurements in pH 7 buffer solution upon the electro‐activated steel at 491 mV overpotential (η) is around four times higher (4 mA cm^?2) in comparison with recently developed OER electrocatalysts. The very strong voltage–current behavior of the catalyst shown in OER polarization experiments at both pH 7 and at pH 13 are even superior to those known for IrO₂‐RuO₂. No degradation of the catalyst is detected even when conditions close to standard industrial operations are applied to the catalyst. A stable Ni‐, Fe‐oxide based passivating layer sufficiently protects the bare metal for further oxidation. Quantitative charge to oxygen (OER) and charge to hydrogen (HER) conversion are confirmed. High‐resolution XPS spectra show that most likely γ?NiO(OH) and FeO(OH) are the catalytic active OER and NiO is the catalytic active HER species.     

Targeting microbial biofilms: by Arctium lappa l. synthesised biocompatible CeO2 ‐NPs encapsulated in nano‐chitosan

This study is planned to synthesise new biocompatible, nano antimicrobial formulation against biofilm producing strains. Aqueous root extract of Arctium lappa l. was used to synthesise ceria nanoparticles (CeO₂ ‐NPs). The synthesised nanoparticles were encapsulated with nano‐chitosan by sol–gel method and characterised using standard techniques. Gas chromatography‐mass spectrometer of Arctium lappa l. revealed the presence of ethanol, acetone, 1‐ propanol, 2‐methylethane, 1,1‐di‐ethoxy, 1‐Butanol, and oleic acid acted as reducing and surface stabilising agents for tailoring morphology of CeO₂ ‐NPs. Erythrocyte integrity after treatment with synthesised nanomaterials was evaluated by spectrophotometer measurement of haemoglobin release having biocompatibility. Scanning electron microscopy revealed the formation of mono dispersed beads shaped particles with mean particle size of 26.2 nm. X‐ray diffractometry revealed cubic crystalline structure having size of 28.0 nm. After encapsulation by nano‐chitosan, the size of CeO₂ ‐NPs enhances to 48.8 nm making average coverage of about 22.6 nm. The synthesised nanomaterials were found effective to disrupt biofilm of S. aureus and P. aeruginosa. Interestingly, encapsulated CeO₂ ‐NPs revealed powerful antibacterial and biofilm disruption activity examined by fluorescent live/dead staining using confocal laser scanning microscopy. The superior antibacterial activities exposed by encapsulated CeO₂ ‐NPs lead to the conclusion that they could be useful for controlling biofilm producing multidrug resistance pathogens.Inspec keywords: particle size, microorganisms, organic compounds, nanomedicine, sol‐gel processing, cellular biophysics, scanning electron microscopy, optical microscopy, nanoparticles, antibacterial activity, fluorescence, biomedical materials, nanofabrication, X‐ray diffraction, chromatography, filled polymers, cerium compoundsOther keywords: microbial biofilms, aqueous root extract, sol–gel method, gas chromatography‐mass spectrometer, 1‐di‐ethoxy, 1‐Butanol, nanomaterial synthesis, mean particle size, antibacterial activities, ethanol, acetone, 1‐ propanol, biocompatible ceria‐nanoparticle encapsulation, nano‐chitosan, Arctium lappa l., oleic acid, erythrocyte integrity, spectrophotometer measurement, haemoglobin release, mono dispersed beads shaped particle formation, X‐ray diffractometry, cubic crystalline structure, fluorescent live/dead staining, confocal laser scanning microscopy, multidrug resistance pathogens, size 26.2 nm, size 28.0 nm, size 48.8 nm, size 22.6 nm, CeO₂      

Lipids as biomarkers of brain disorders

Abstract

Brain is a central and pivotal organ of human body containing the highest lipids content next to adipose tissue. It works as a monitor for the whole body and needs an adequate supply of energy to maintain its physiological activities. This high demand of energy in the brain is chiefly maintained by the lipids along with its reservoirs. Thus, the lipid metabolism is also an important for the proper development and function of the brain. Being a prominent part of the brain, lipids play a vast number of physiological activities within the brain starting from the structural development, impulse conduction, insulation, neurogenesis, synaptogenesis, myelin sheath formation and finally to act as the signaling molecules. Interestingly, lipids bilayer also maintains the structural integrity for the physiological functions of protein. Thus, in light to all of these activities, lipids and its metabolism can be attributed pivotal for brain health and its activities. Decisively, the impaired/altered metabolism of lipids and its intermediates puts forward a key step in the progression of different brain ailments including neurodegenerative, neurological and neuropsychiatry disorders. Depending on their associated underlying pathways, they serve as the potential biomarkers of these disorders and are considered as necessary diagnostic tools. The present review discusses the role and level of altered lipids metabolism in brain diseases including neurodegenerative diseases, neurological diseases, and neuropsychiatric diseases. Moreover, the possible mechanisms of altered level of lipids and their metabolites have also been discussed in detail.     

Uniform and Homogeneous Growth of Copper Nanoparticles on Electrophoretically Deposited Carbon Nanotubes Electrode for Nonenzymatic Glucose Sensor

The multiwalled carbon nanotubes thin-film-based electrode was fabricated by electrophoretic deposition and modified with copper(Cu) nanoparticles to fabricate Cu/CNTs nanocomposite sensor for nonenzymatic glucose detection.The expensive glassy carbon electrode was replaced by fluorine-doped tin oxide glass containing CNTs film to confine the Cu nanoparticles growth by electrodeposition through cyclic voltammetry(CV). The ultraviolet visible and X-ray diffraction analysis revealed the successful deposition of Cu nanoparticles on the CNTs-modified electrode. The atomic force microscopy images confirmed the morphology of electrodeposited Cu on CNTs film as uniformly dispersed particles.The electrocatalytic activity of electrode to the glucose oxidation was investigated in alkaline medium by CV and amperometric measurements. The fabricated sensor exhibited a fast response time of less than 5 s and the sensitivity of 314μA mM~(-1)cm~(-2)with linear concentration range(0.02–3.0 mM) having detection limit 10.0μM. Due to simple preparation of sensor, Cu/CNTs nanocomposite electrodes are a suitable candidate for reliable determination of glucose with good stability.