Nano-precipitation : preparation and application in the field of pharmacy

Over the last 30 years, nanoparticle-based medicine has received tremendous attention due to its advances with smart therapeutics and less toxicity. Few nanomedicine products have been approved for commercial use in the clinic (such as Doxil®, Ambraxane®…). Nanomedicine research is still at its early stage and the preparation of nanoparticles must be carefully considered. Systems involving further increased supersaturation, either via solvent evaporation, temperature reduction or anti-solvent mixture, were suggested to be capable of inducing nanoprecipitation (NPT). Since this technique is straight-forward, fast and easy to duplicate in practice, it is highly preferred and recommended. In this review, the process of NTP was described and discussed in detail. Factors that affect the encapsulation efficiency, the nanoparticle size, the morphology and the stability of nanoparticles prepared by NTP were described. This process is one of the most preferable processes for preparing solid nano-protein due to their elegant techniques that preserve the bioactivity of proteins. Although the production of nanoparticles by this process has not been applied in the pharmaceutical industry due to the organic solvent issue, the production equipment for large-scale has been marketed.

Effect of cold plasma pre-treatment on photocatalytic activity of 3D fabric loaded with nano-photocatalysts: response surface methodology

In this study, the physico-chemical effects occasioned by the cold plasma discharge (CPD) on the photo-decolorization of Reactive Orange 16 (RO16) by 3D fabrics (spacer fabrics) loaded with ZnO:TiO2 nano-photocatalysts (nphs) were optimized via response surface methodology (RSM). CPD was employed to improve the surface characteristics of the spacer fabrics for nphs loading. Surface morphology and color variation were studied utilizing scanning electron microscopy (SEM) and CIE-Lab system, respectively. The effect of CPD on the wetting ability of the spacer fabrics was examined using dynamic adsorption measurement (DAM). Also, X-ray fluorescence (XRF) was utilized to investigate the durability of the nphs on the spacer fabrics. All the experiments were implemented in a Box-Behnken design (BBD) with three independent variables (CPD treatment time, dye concentration and irradiation time) in order to optimize the decolorization of RO16. The anticipated values of the decolorization efficiency were found to be in excellent agreement with the experimental values (R2 = 0.9996, Adjusted R2 = 0.9992). The kinetic analysis demonstrated that the photocatalytic decolorization followed the Langmuir-Hinshelwood kinetic model. In conclusion, this heterogeneous photocatalytic process is capable of decolorizing and mineralizing azoic reactive dye in textile wastewater. Moreover, the results confirmed that RSM based on the BBD was a suitable method to optimize the operating conditions of RO16 degradation.

Novel feature of nano-titanium dioxide on textiles: antifelting and antibacterial wool

In this study, the antifelting and antibacterial features of wool samples treated with nanoparticles of titanium dioxide (TiO2) were evaluated. To examine the antifelting properties of the treated samples, the fabric shrinkage after washing was determined. The antimicrobial activity was assessed through the calculation of bacterial reduction against Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) bacteria. TiO 2 was stabilized on the wool fabric surface by means of carboxylic acids, including citric acid (CA) and butane tetracarboxylic acid (BTCA). Both oxidized samples with potassium permanganate and nonoxidized wool fabrics were used in this study. The relations between both the TiO2 and carboxylic acid concentrations in the impregnated bath and the antifelting and antibacterial properties are discussed. With increasing concentration in the impregnated bath, the amount of TiO2 nanoparticles on the surface of the wool increased; subsequently, lower shrinkage and higher antibacterial properties were obtained. The existence of TiO2 nanoparticles on the surface of the treated samples was proven with scanning electron microscopy images and energy-dispersive spectrometry.

Photo induced silver on nano titanium dioxide as an enhanced antimicrobial agent for wool

In this study an effective nanocomposite antimicrobial agent for wool fabric was introduced. The silver loaded nano TiO(2) as a nanocomposite was prepared through UV irradiation in an ultrasonic bath. The nanocomposite was stabilized on the wool fabric surface by using citric acid as a friendly cross-linking agent. The treated wool fabrics indicated an antimicrobial activity against both Staphylococcus aureus and Escherichia coli bacteria. Increasing the concentration of Ag/TiO(2) nanocomposite led to an improvement in antibacterial activities of the treated fabrics. Also increasing the amount of citric acid improved the adsorption of Ag/TiO(2) on the wool fabric surface leading to enhance antibacterial activity. The EDS spectrum, SEM images, and XRD patterns was studied to confirm the presence of existence of nanocomposite on the fabric surface. The role of both cross-linking agent and nanocomposite concentrations on the results was investigated using response surface methodology (RSM).

Self-cleaning and color reduction in wool fabric by nano titanium dioxide

Wool is a textile material that is valued for its strength, warmth, water resistance, and texture. But this natural fiber of the protein keratin lacks the stain resistance of synthetic fabrics and is also generally susceptible to harsh processing conditions. In this study, raw and oxidized wool fabrics were treated with nano titanium dioxide (TiO2) powder in an ultrasonic bath. These particles were linked to the wool surface by butane tetra carboxylic acid and also sodium hypophosphite was used as a catalyst. The photo-catalytic activity of TiO2 nanoparticles deposited on the wool fabrics was followed by the degradation of Acid Blue 113 as a stain and also determined by the degradation rate of food stains such as coffee, tea, and fruit juice under the ultraviolet rays. The results showed that increasing the amount of nano TiO2 leads to improved degradation of stains on the treated fabric.

The role of nano colloid of TiO2 and butane tetra carboxylic acid on the alkali solubility and hydrophilicity of proteinous fibers

One of the main problems of wool as an important proteinous fiber is low resistance against alkali media. Finding a way to solve this problem without any influences on other fiber characteristics is still a matter of research. Using nano particles on textile materials is a new approach to produce novel properties. Here, nano titanium dioxide (NTO) particles along with butane tetra carboxylic acid (BTCA) were sonicated in the ultra sound bath and applied as a nano colloid on the wool fabric. BTCA played different roles as wool cross-linker, a polyanionic agent, and stabilizer for nano TiO2. Various concentrations of NTO and BTCA were applied through impregnation of the fabric in ultrasonic bath followed by curing. The resistance of fabrics against alkali was assessed by solubility in sodium hydroxide and the hydrophilicity monitored by the water drop absorption time and the contact angle before and after UV irradiation. Interestingly, the alkali solubility of the nano TiO2 treated wool fabrics reduced while the fabric became more hydrophilic. This fact was shown by the testing results and is thoroughly discussed in the article. The response surface methodology (RSM) was also applied to find the optimum conditions for the wool fabric treatment.

Nano titanium dioxide on wool keratin as UV absorber stabilized by butane tetra carboxylic acid (BTCA): a statistical prospect

Photo yellowing of wool is one of the most important problems which have negative impacts on various aspects of wool prompting scientists to find a solution over the past decades. In this research the protective features of nano-titanium dioxide particles against UV on wool fabric were discussed and the color variations of wool samples after UV irradiation were measured and reported. It was shown that nano TiO2 is a suitable UV absorber and its effect depends on the concentration. Also, it was assumed that butane tetracarboxylic acid plays a prominent role as a cross-linking agent to stabilize the nano-titanium dioxide as well as a polyanion to maintain negative charges on the wool surface for higher nano particles absorption. Also the variables conditions were optimized using response surface methodology (RSM).

Reducing photoyellowing of wool using nano TiO2

Wool is the most important animal fiber used in textile industries, but its photostability is very low. Scientists have searched for new ways to increase the photostability of wool. As TiO2 nano particles have features suitable for new applications, the UV-blocking power of nano TiO2 may be used for protecting fabrics against UV rays. Treatment of wool with TiO 2 can be effective for controlling photodegradation. This study focused on protecting wool fabric against UV rays using nano TiO2. To this end, oxidized and raw wool were treated with citric acid as the cross-linking agent and different concentrations of nano TiO2. The whiteness and yellowness of wool fabric samples were reported. XRD patterns proved the existence of TiO2 nano-particles on the wool surface. Finally, the results revealed that nano TiO2 is a suitable UV absorber on wool fabric and its effect depends on concentration.

Functionality of nano and 3D-microhierarchical TiO₂ particles as coagulants for sericin extraction from the silk degumming wastewater

Amine-functionalised TiO2 particles were employed as coagulants to remove sericin from the silk degumming wastewater. Two types of TiO2 particles including 3D-microhierarchical TiO2 (Micron-size) and TiO2 nanoparticles (Degussa P-25) were used in this study. The surfaces of both types of TiO2 particles were functionalised using 3-aminopropyl trimethoxysilane (APTMS). The impacts of TiO2 type, pH, TiO2 concentration, and settling time on sericin removal efficiency were investigated. The efficiency of TiO2 particles in sericin removal was evaluated by measuring the residual turbidity and UV-vis spectra of the solutions before and after the treatment. Moreover, the COD, SDS-PAGE and protein assay tests were conducted to further analyse the treated solutions. The results demonstrated that the sericin removal efficiency of around 67% and turbidity reduction of 95% were achieved at the optimum conditions of 0.04 g TiO2, pH = 5, and 60 min settling time. Nano and micron-size TiO2 particles showed similar efficiency for sericin removal, but micron-size particles outweighed due to their higher efficiency in inducing greater turbidity reduction after 60 min. The obtained sericin/TiO2 composites were stable after several cycles of wash and could be useful in different fields including cosmetic, and textile finishing, among others.

Enhanced homogeneity and interfacial compatibility in melt-extruded cellulose nano-fibers reinforced polyethylene via surface adsorption of poly(ethylene glycol)-block-poly(ethylene) amphiphiles

In this paper, we demonstrate that an amphiphilic block copolymer such as polyethylene glycol-b-polyethylene can be used as both dispersing and interfacial compatibilizing agent for the melt compounding of LLDPE with cellulose nano-fibers. A simple and effective spray drying methodology was first used for the first time for the preparation of a powdered cellulose nano-fibers extrusion feedstock. Surface adsorption of the amphiphilic PEG-b-PE was carried out directly in solution during this process. These various dry cellulosic feedstock were subsequently combined with LLDPE via extrusion to produce a range of nano-composites. The collective outcomes of this research are several folds. Firstly we show that presence of surface adsorbed PEG-b-PE effectively hindered the aggregation of the cellulose nano-fibers during the extrusion, affording clear homogenous materials with minimum aggregation even at the highest loading of cellulose nano-fibers (∼23 vol.%). Secondly, the tailored LLDPE/cellulose interface arising from intra- and inter-molecular hydrogen and Van der Waals bonds yielded significant levels of mechanical improvements in terms of storage and tensile modulus. We believe this study provides a simple technological template to produce high quality and performant polyolefins cellulose-based nano-composites.

Decolorization and mineralization of an azo reactive dye using loaded nano-photocatalysts on spacer fabric: kinetic study and operational factors

In this study, the photocatalytic decolorization and mineralization of Remazol Black B (RBB), an azo reactive dye, in aqueous solutions was investigated using UV/H2O2/ZnO, UV/H2O2/TiO2 and UV/H2O2/ZnO:TiO2 systems. ZnO and TiO2 nanoparticles were loaded on 3-dimensional polyethylene terephthalate fabrics (spacer fabrics). Morphology of the spacer fabrics and the presence of the nanoparticles were studied by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS), respectively. Furthermore, the effects of key operational parameters on the efficiency of the decolorization were investigated. These parameters included initial pH value, initial hydrogen peroxide concentration, initial dye concentration, the loaded nanoparticle ratio and the presence of anions (sulfate, chloride and bicarbonate). Zero-, first- and second-order reaction kinetics were evaluated. Complete decolorization and high efficient mineralization with 90% total organic carbon (TOC) reduction were achieved at 120min treatment in the case of ZnO:TiO2 under optimum condition. The results proved that the novel heterogeneous photocatalytic process is capable of decolorizing and mineralizing azo reactive dyes in textile wastewater.

Fabrication of multifunctional graphene decorated with bromine and nano-Sb₂O₃ towards high-performance polymer nanocomposites

Despite great advances, it remains highly attractive but challenging to create high-performance polymeric materials combining excellent flame-retardancy and outstanding thermal, mechanical and electrical properties. We herein demonstrate a novel strategy for fabricating a multifunctional nano-additive (Br-Sb2O3@RGO) based on graphene decorated with bromine and nano-Sb2O3. Cone calorimetric tests show that incorporating 10 wt% Br-Sb2O3@RGO into thermoplastic polyurethane (TPU) strikingly prolongs the time to ignition and decreases the peak heat release rate by 72%. Besides, tensile strength and Young's modulus are enhanced by 37% and 820%, respectively. Meanwhile, the electric conductibility is increased by eleven orders of magnitude relative to the TPU matrix. This work provides a promising strategy for addressing the critical bottleneck with the existing flame retardants that only enhance flame retardancy at the expense of mechanical properties of polymeric materials. As-prepared high-performance TPU composites are expected to find many applications, especially in aerospace, tissue engineering, and cables and wires.

Molecular architecture of Aβ fibrils grown in cerebrospinal fluid solution and in a cell culture model of Aβ plaque formation

OBJECTIVES: The detailed structure of brain-derived Aβ amyloid fibrils is unknown. To approach this issue, we investigate the molecular architecture of Aβ(1-40) fibrils grown in either human cerebrospinal fluid solution, in chemically simple phosphate buffer in vitro or extracted from a cell culture model of Aβ amyloid plaque formation. METHODS: We have used hydrogen-deuterium exchange (HX) combined with nuclear magnetic resonance, transmission electron microscopy, seeding experiments both in vitro and in cell culture as well as several other spectroscopic measurements to compare the morphology and residue-specific conformation of these different Aβ fibrils. RESULTS AND CONCLUSIONS: Our data reveal that, despite considerable variations in morphology, the spectroscopic properties and the pattern of slowly exchanging backbone amides are closely similar in the fibrils investigated. This finding implies that a fundamentally conserved molecular architecture of Aβ peptide fold is common to Aβ fibrils.

Removal of Pb (II) ions using polymer based graphene oxide magnetic nano-sorbent

Graphene oxide (GO) based magnetic nano-sorbent was synthesized by assembling the Fe3O4 and GO on the surface of polystyrene (denoted as PS@Fe3O4@GO). The morphology of the nano-sorbent was studied using scanning electron microscopy (SEM), while their individual nano-components were characterized using UV-visible spectroscopy, atomic force microscopy (AFM), zeta potential, transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The assembled nano-sorbent was further investigated for Pb (II) ions removal by optimizing the parameters including pH, temperature and contact time. The obtained data was modelled for adsorption kinetics, adsorption isotherms and thermodynamics. Kinetic experiments indicated the Pb (II) adsorption followed first order kinetics. The adsorption equilibrium data fits Langmuir isotherm model well and the adsorption process was found to be spontaneous. The adsorption capacity of the prepared nano-sorbent was estimated to be 73.52mgg-1, with a maximum removal of 93.78% at pH 6. The nano-sorbent can be regenerated by nitric acid (HNO3) for reuse. FT-IR and X-ray photoelectron spectroscopy (XPS) studies confirmed the interactions between the Pb (II) ions and the nano-sorbent.

Combined nano- and macrotribology studies of titania lubrication using the oil-ionic liquid mixtures

The lubrication of titania surfaces using a series of ionic liquid (IL)-hexadecane mixtures has been probed using nanoscale atomic force microscopy (AFM) and macroscale ball-on-disk tribometer measurements. The IL investigated is trihexyl(tetradecyl)phosphonium bis(2,4,4-trimethylpentyl)phosphinate, which is miscible with hexadecane in all proportions. At both length scales, the pure IL is a much more effective lubricant than pure hexadecane. At low loads, which are comparable to common industrial applications, the pure IL reduces the friction by 80% compared to pure hexadecane; while the IL-hexadecane mixtures lubricate the titania surface as effectively as the pure IL and wear decreases with increasing IL concentration. At high test loads the adsorbed ion boundary layer is displaced leading to surface contact and high friction, and wear is pronounced for all IL concentrations. Nonetheless, the IL performs better than a traditional zinc-dialkyl-dithophosphate (ZDDP) antiwear additive at the same concentration.