In vitro effects of nanoparticles on renal cells

Background  

The ability of nanoparticles to cross the lung-blood barrier suggests that they may translocate to blood and to targets distant from their portal of entry. Nevertheless, nanotoxicity in organs has received little attention. The purpose of this study was to evaluate nanotoxicity in renal cells using in vitro models. Various carbon black (CB) (FW2–13 nm, Printex60-21 nm and LB101-95 nm) and titanium dioxide (TiO₂-15 and TiO₂-50 nm) nanoparticles were characterized on size by electron microscopy. We evaluated theirs effects on glomerular mesangial (IP15) and epithelial proximal tubular (LLC-PK₁) renal cells, using light microscopy, WST-1 assay, immunofluorescence labeling and DCFH-DA for reactive oxygen species (ROS) assay.     

Visible light induced self-cleaning performance of iron-doped TiO2 nanoparticles for surface applications

This study aimed to enhance the visible light photosensitivity of TiO₂ nanoparticles for self-cleaning applications by doping with Fe³⁺. Nanocrystalline undoped and Fe-doped TiO₂ (Ti_1 − xFe_xO₂, x = .01–.04) were synthesized via sol–gel method. The results demonstrated that Fe-doped TiO₂ nanoparticles exhibited visible light sensitivity and self-cleaning properties. An increased Fe concentration resulted in a red shift in the absorption band edge. Fe_0.03-doped TiO₂ with an average particle size of ∼21 nm, a crystallite size of ∼12 nm, and a band gap of ∼2.86 eV showed the highest photocatalytic activity (60% methylene blue degradation) and super-hydrophilicity (water droplet contact angle 9°) under visible light radiation. These findings highlight the potential of Fe-doped TiO₂ nanoparticles as a promising material for self-cleaning applications.     

Plasmonic Effects of Infiltrated Silver Nanoparticles Inside TiO2 Film: Enhanced Photovoltaic Performance in DSSCs

The plasmonic effects of infiltrated silver (Ag) nanoparticles, with different contents, inside a nanostructured TiO₂ film on the photovoltaic performance of dye‐sensitized solar cells (DSSCs) are explored. The synthesized Ag nanoparticles are immobilized onto deposited TiO₂ nanoparticles by a new strategy using 3‐mercaptopropionic acid (MPA), a bifunctional linker molecule. Transmission electron microscope (TEM) images show that monodispersed Ag and polydispersed TiO₂ nanoparticles have an average diameter of 12 ± 3 nm and 5 ± 1 nm, respectively. Moreover, Fourier transform infrared spectroscopy (FTIR) analysis reveals that Ag nanoparticles were successfully functionalized and capped with MPA. Optical studies on the MPA‐capped Ag nanoparticles inside TiO₂ film show an increase in the total absorbance of the electrode. Moreover, EIS measurements confirm that MPA‐capped Ag nanoparticles inhibit the charge recombination and improve the stability of nanoparticles in I₃^?/I^? electrolyte. The DSSC assembled with optimal content of MPA‐capped Ag nanoparticles demonstrated an enhanced power conversion efficiency (8.82% ± 0.07%) compared with the pure TiO₂ (7.30% ± 0.05%). The increase in cell efficiency was attributed to the enhanced dye light absorption in strength and spectral range due to the surface plasmon resonance of MPA‐capped Ag nanoparticles in the photoanode.     

Photodegradation of Famotidine by Integrated Photocatalytic Adsorbent (IPCA) and Kinetic Study

Abstract  

Integrated photocatalytic adsorbents (IPCAs) comprised of nanocrystalline titanium dioxide (TiO₂) and activated carbon (AC) were prepared using an ultrasonic impregnation technique. The IPCAs were characterised by scanning electron microscopy (SEM) and Fourier-transform infrared (FT-IR) spectroscopy and were employed as catalysts for the photodegradation of famotidine-an active pharmaceutical ingredient-in aqueous solutions using illumination from a 125 W medium pressure mercury lamp. The degradation kinetics were found to follow a pseudo-first-order rate law and varying TiO₂ loadings induced different increases in the apparent first-order rate constant of the process. The kinetic behaviour can be described in terms of a modified Langmuir–Hinshelwood (LH) model. The IPCA prepared using a 10% TiO₂ to AC loading exhibited the highest rate constant with a K _C and k _r of 0.0172 L/mg and 0.237 mg/L/min, respectively. The LH model fits the experimental data and elucidates the effect of the TiO₂ content of the IPCA on the degradation rate. The use of calcination (heat treatment) in IPCA preparation and its effect on photocatalytic and adsorption performance were also investigated. The present work demonstrates that the combination of TiO₂ and AC results in a promising material for application in the degradation of organic pollutants.     

Lamellar silica mesostructures assembled from a new class of Gemini surfactants: alkyloxypropyl-1,3-diaminopropanes

Abstract  

Representative members of a new class of commercially available Gemini surfactants, namely, the alkyloxypropyl-1,3-diaminopropanes, are shown to template the direct assembly of mesoporous silicas with lamellar framework structures. The hydrolysis of tetraethylorthosilicate in the presence of a derivative with a straight hydrophobic chain, C _n H_2n+1O(CH₂)₃NH(CH₂)₃NH₂ with n = 8 and 10 (Tomah3 DA1214), afforded a layered mesophase with a surface area of 464 m²/g, a pore volume of 0.39 cm³/g, a pore size of 3.6 nm and a vesicular hierarchical structure. The introduction of electrostatic forces into the assembly process through the protonation of up to 33% of the amine centers improves the quality of the lamellar framework order as evidenced by increases in X-ray diffraction and textural properties. Also, the vesicular hierarchical structure formed under electrically neutral assembly conditions is replaced by well dispersed multilamellar nanoparticles upon surfactant protonation. Chain branching in the hydrophobic segment of Gemini derivative i-C₁₀H₂₁O(CH₂)₃NH(CH₂)₃NH₂ (Tomah3 DA14) compromises the quality of the lamellar framework structure, but affords higly dispersed nanoparticles with hierarchical coiled slab to vesicular motifs depending on the degree of surfactant protonation. In addition to providing unusual lamellar framework structures, these Gemini surfactants afford hierarchical nanoparticle motifs of relatively uniform size (50–200 nm) and a very high degree of dispersion for a potential use in a variety of materials applications.     

Cu/Cu2O nanoparticles modified Ti3C2 MXene with in-situ formed TiO2-X for detection of hydrogen peroxide

Hydrogen peroxide (H₂O₂) is frequently used in various chemical reactions, the food industry, environmental protection, and the medical and biological fields. Cost-effective, simple, and quick detection technologies with great sensitivity are highly desired. The emerging two-dimensional MXene is favorable in the sensing field due to its outstanding conductivity, stability, and large surface area. Moreover, the in-situ generated TiO_2-X on Ti₃C₂ MXene has been proven an excellent biosensor material due to its biocompatibility. Herein, we decorated Cu/Cu₂O nanoparticles onto Ti₃C₂ MXene with in-situ generated TiO_2-X nanoparticles, forming heterojunction through a simple one-step hydrothermal process. The Cu/Cu₂O/TiO_2-X/Ti₃C₂ (Cu/Cu₂O/TT) exhibits good electrochemical sensing capability toward H₂O₂, with a linear range up to 28.328 mM, a sensitivity of 312 μA mM^?1 cm^?2, and a detection limit (LOD) of 0.42 μΜ. The synergistic interactions between Cu/Cu₂O nanoparticles and TiO_2-X/Ti₃C₂ heterojunction not only improved electron transfer and electrocatalytic activity, but also facilitated the mobility of targeting molecules on the catalyst due to the abundance of exposed catalytic sites. Therefore, compared to TiO_2-X/Ti₃C₂, Cu/Cu₂O/TT has a lower LOD, faster reaction, and five times the sensitivity. Additionally, the outstanding photoelectrochemical (PEC) sensing performance is demonstrated of Cu/Cu₂O/TT for H₂O₂ detection, displaying a low LOD, long-term stability, repeatability, and selectivity. This report may expand the application of MXene-based materials as electrochemical sensors.     

One-step hydrothermal synthesis of a TiO2-Ti3C2Tx nanocomposite with small sized TiO2 nanoparticles

A TiO₂-Ti₃C₂T_x nanocomposite was prepared using a simple and facile one-step hydrothermal method. The small sized TiO₂ nanoparticles were synthesized and assembled on the surface of Ti₃C₂T_x nanosheets using Ti₃C₂T_x itself as titanium source by in-situ technique. The microstructure of TiO₂-Ti₃C₂T_x nanocomposite was characterized by means of XRD、FESEM、TEM、XPS and Raman, respectively. The effects of ethanol and hydrothermal holding time on the size of TiO₂ nanoparticles were investigated. The results show that adding proper amount of ethanol into pure water results in decrease of the size of TiO₂ nanoparticles. Under ethanol-water mixed solution, increasing the time of hydrothermal treatment results in growth and even aggregation of TiO₂ nanoparticles. The TiO₂ nanoparticles with average particle size of 30 nm were obtained when the hydrothermal treatment was conducted in ethanol-water mixed solution at 200 ℃ for 12 h.     

Characterizations of TiO2/SiO2/Ni–Cu–Zn Ferrite Composite for Magnetic Photocatalysts

The TiO₂/SiO₂/Ni–Cu–Zn ferrite composite for magnetic photocatalysts with high photocatalytic activity is successfully prepared in this study. The composite are composed of spherical or elliptical Ni–Cu–Zn ferrite nanoparticles about 20–60 nm as magnetic cores, silica as barrier layers with thickness of 15 nm between the magnetic cores and titania shells with thickness approximately 1.5 nm. Photodegradation examination of TiO₂/SiO₂/ Ni–Cu–Zn ferrite composite was carried out in methylene blue (MB) solutions illuminated under a Xe arc lamp with 35 W and color temperature of 6000 K. The results indicated that about 47.1% of MB molecules adsorbed on the TiO₂/SiO₂/Ni–Cu–Zn ferrite composite within 30 min mixing due to it higher pore volume of 0.034 cm³/g, and after 6 h Xe lamp irradiation, 83.9% of MB 16.1% was photodegraded. Compared with the TiO₂ /Ni–Cu–Zn ferrite composite, the TiO₂/SiO₂/Ni–Cu–Zn ferrite composite with silica barrier layer prohibited the photodissolution and enhanced the photocatalytic ability. The magnetic photocatalyst shows high photocatalytic efficiency that the apparent first‐order rate constant k_obs is 0.18427 h^?1, and good magnetic property that the saturation magnetization (M_s) of is 37.45 emu/g, suggesting the magnetic photocatalyst can be easily recovered by the application of an external magnetic field.     

Multifunctionality of poly(vinyl alcohol) nanofiber webs containing titanium dioxide

We prepared titanium dioxide/PVA nanocomposite fiber webs for application in multifunctional textiles by electrospinning. The morphological properties of the TiO₂/PVA nanocomposite fibers were characterized using scanning electron microscopy and transmission electron microscopy. Layered fabric systems with electrospun TiO₂ nanocomposite fiber webs were developed using various concentrations of TiO₂ and a range of web area densities, and then the UV‐protective properties, antibacterial functions, formaldehyde decomposition ability, and ammonia deodorization efficiency of the fabric systems were assessed. Layered fabric systems with TiO₂ nanocomposite fiber webs containing 2 wt% TiO₂ nanoparticles at 3.0 g m^?2 web area density exhibited an ultraviolet protection factor of greater than 50, indicating excellent UV protection. The same system showed a 99.3% reduction in Staphylococcus aureus. Layered fabric systems with TiO₂ nanocomposite fiber webs containing 3 wt % TiO₂ nanoparticles at 3.0 g m^?2 web area density exhibited a 85.3% reduction in Klebsiella pneumoniae. Titanium dioxide nanocomposite fiber webs containing 3 wt % TiO₂ nanoparticles at 3.0 g m^?2 web area density exhibited a formaldehyde decomposition efficiency of 40% after 2 h, 60% after 4 h, and 80% after 15 h under UV irradiation. The same system showed an ammonia deodorization efficiency of 32.2% under UV irradiation for 2 h. These results demonstrate that TiO₂ nanocomposite fibers can be used to produce advanced textile materials with multifunctional properties. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effect of the Amount of H2O on the Crystallization of TiO2 Films Prepared from Alkoxide Solutions Containing Acetylacetone

Sol–gel‐derived TiO₂ films were prepared by dip‐coating from Ti(OC₃H₇ⁱ)₄–CH₃COCH₂COCH₃–HNO₃–H₂O–C₂H₅OH solutions, and the effect of the H₂O content in solutions on the crystallization of TiO₂ films during the heat treatment at 800°C was discussed. The crystalline phase, crystallite size, grain size, and refractive index of the TiO₂ films depended on the H₂O/Ti(OC₃H₇ⁱ)₄ mole ratios (x) in the coating solutions. Highly dense and crystalline rutile films were obtained at x = 0.5–10, where the crystallites and grains became larger with increasing x. The further increase in x from 10 to 50 reduced the crystallite size and refractive index of the films, where anatase phase appeared at x = 30–50.     

Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature

Background  

Translocation of nanoparticles (NP) from the pulmonary airways into other pulmonary compartments or the systemic circulation is controversially discussed in the literature. In a previous study it was shown that titanium dioxide (TiO₂) NP were "distributed in four lung compartments (air-filled spaces, epithelium/endothelium, connective tissue, capillary lumen) in correlation with compartment size". It was concluded that particles can move freely between these tissue compartments. To analyze whether the distribution of TiO₂ NP in the lungs is really random or shows a preferential targeting we applied a newly developed method for comparing NP distributions.     

Large Electrostrictive Strain in (Bi0.5Na0.5)TiO3–BaTiO3–(Sr0.7Bi0.2)TiO3 Solid Solutions

Relaxor ferroelectrics (0.94 ? x)(Bi_0.5Na_0.5)TiO₃–0.06BaTiO_3?x(Sr_0.7Bi_0.2□_0.1)TiO₃ (BNT–BT–xSBT) (0 ≤ x ≤ 0.5), were prepared by a solid‐state reaction process, and their structures were characterized by the transmission electron microscopy and Raman spectroscopy. The BNT–BT–0.3SBT has a very high electrostrictive strain S = 0.152% with hysteresis‐free behavior, much more than the reported S in other ferroelectrics. S–P² profiles perfectly follow the quadratic relation, which indicates a purely electrostrictive effect with a high electrostrictive coefficient (Q₁₁) of 0.0297 m⁴/C². Even, its Q₁₁ keeps at a high level in the temperature range from ambient temperature to 180°C. The field‐induced large electrostrictive strain of BNT–BT–0.3SBT was attributed to the existence of ferroelectric nanodomains.     

Crystal Structure and Electrical Properties of Lead‐Free (1 − x)BaTiO3–x(Bi1/2A1/2)TiO3 (A = Ag,Li, Na,K, Rb,Cs) Ceramics

Ceramics of solid solutions (1  ?  x)BaTiO₃–x(Bi_1/2A_1/2)TiO₃ (A = Ag, Li, Na, K, Rb, Cs, x ≤ 0.20) were prepared and their crystal structures, dielectric, ferroelectric, and piezoelectric properties were investigated. It was found that (Bi_1/2A_1/2)TiO₃‐type doping compounds broadened the temperature range of the tetragonal phase in BaTiO₃ and all the compositions examined displayed a tetragonal structure at room temperature. The Curie temperature (T_C) was observed to increase with respect to pure BaTiO₃ to the range 140°C–210°C through solid solution. Remanent polarization (P_r) tended to decrease with increased content of doping compound, whereas the coercive field (E_C) rose and piezoelectric coefficient (d₃₃) fell. The highest d₃₃ value in the solid solutions was observed in 0.97BaTiO₃–0.03(Bi_1/2Ag_1/2)TiO₃ at 90 pC/N.     

Preparation and characterization of mesoporous TiO<Subscript>2</Subscript> thin film

Ordered hexagonal mesoporous TiO₂ thin film was prepared by the evaporation-induced self-assembly (EISA) method using triblock copolymer (Pluronic P123) and tetrabutyl orthotitanate (Ti(OBu ⁿ )₄, TBOT) in 1-methoxy-2-propanol (C₄H₁₀O₂, PGME) solvent. The arrangement of mesopores was identified by small-angle X-ray diffraction and transmission electron microscopy (TEM). The well-ordered hexagonal mesoporous TiO₂ had a high specific surface area of 239 m²/g and an average pore size of 6.3 nm. The structure of mesoporous TiO₂ thin film was anatase with a 5.1 nm crystallite. The absorption band shift of the mesoporous TiO₂ toward longer wavelengths as calcined at 350 °C due to the residual carbon.     

Oxygen Isotope (<Superscript>18</Superscript>O<Subscript>2</Subscript>) Evidence on the Role of Oxygen in the Plasma-Driven Catalysis of VOC Oxidation

Abstract  

This paper reports isotopic evidence on nonthermal plasma-induced fixation of gas-phase oxygen on the surface of several catalysts such as TiO₂, Ag/TiO₂, Ag/γ-Al₂O₃ and Ag/MS-13X at atmospheric-pressure. On-line mass spectrometric analysis and stoichiometric comparison of reactants and products revealed that the fixed surface oxygen can be activated by nonthermal plasma. The fixed ¹⁸O by nonthermal plasma survived for a certain period of time (about 30 min), and involved in the formation of isotope-exchanged oxygen (¹⁸O¹⁶O) and isotope containing CO _x (CO and CO₂).     

Photodegradation of tetrahalobisphenol-A (X = Cl, Br) flame retardants and delineation of factors affecting the process

The photoassisted degradation (HPLC-UV absorption), dehalogenation (HPLC-IC) and mineralization (TOC decay) of the flame retardants tetrabromobisphenol-A (TBBPA) and tetrachlorobisphenol-A (TCBPA) were examined in UV-irradiated alkaline aqueous TiO₂ dispersions (pH 12), and for comparison the parent bisphenol-A (BPA, an endocrine disruptor) in pH 4–12 aqueous media to assess which factor impact most on the photodegradative process. Complete degradation (2.7–2.8 × 10⁻² min⁻¹) and dehalogenation (1.8 × 10⁻² min⁻¹) of TBBPA and TCBPA occurred within 2 h of UV irradiation, whereas only 45–60% mineralization (2.3–2.7 × 10⁻³ min⁻¹) was complete within 5 h for the flame retardants at pH 12 and ca. 80% for the parent BPA. Factors examined in the pH range 4–12 that impact the degradation of BPA were the point of zero charge of TiO₂ particles (pH_pzc; electrophoretic method), particle or aggregate sizes of TiO₂ (light scattering), and the relative number of OH radicals (as DMPO–OH adducts; ESR spectroscopy) produced in the UV-irradiated dispersion. Dynamics of BPA degradation (2.0–2.4 × 10⁻² min⁻¹) were pH-independent and independent of particle/aggregate size, but did correlate with the number of OH radicals, at least at pHs 4 to 8–9, after which the rates decreased somewhat at pH > 9 with decreasing adsorption owing to Coulombic repulsive forces between the very negative TiO₂ surface and the anionic forms of BPA (pK_as ca. 9.6–11.3), even though the number of OH radicals continued to increase at the higher pHs.     

A mixture of anatase and rutile TiO2 nanoparticles induces histamine secretion in mast cells

Background  

Histamine released from mast cells, through complex interactions involving the binding of IgE to FcεRI receptors and the subsequent intracellular Ca²⁺ signaling, can mediate many allergic/inflammatory responses. The possibility of titanium dioxide nanoparticles (TiO₂ NPs), a nanomaterial pervasively used in nanotechnology and pharmaceutical industries, to directly induce histamine secretion without prior allergen sensitization has remained uncertain.     

Ultrahigh Active Pd Nanocatalyst Supported on Core-Sheath Conducting Polymer/Metal Oxide Composite Nanorods

Abstract  

A facile and aqueous-phase method based on the electron transfer reduction process for fabricating core-sheath structured polyaniline (PANI)/SnO₂ composite nanorods supported Pd nanocatalyst has been demonstrated. The Pd nanoparticles synthesized by this strategy have a small size of smaller than 3.0 nm. The well dispersed Pd nanoparticles with small sizes supported on core-sheath PANI/SnO₂ composite nanorods exhibited an ultrahigh catalytic activity during the catalytic reduction of p-nitrophenol into p-aminophenol by NaBH₄ in aqueous solution. The kinetic apparent rate constant (k_app) reach to be about 26.9 × 10⁻³ s⁻¹. It is believed that this method could be extended to cover many kinds of other functional composite nanomaterials where the active component is expected to bring in new features and applications.     

Optimized dispersion of nanoparticles for biological in vitro and in vivo studies

Background

The aim of this study was to establish and validate a practical method to disperse nanoparticles in physiological solutions for biological in vitro and in vivo studies.

Results

TiO₂ (rutile) dispersions were prepared in distilled water, PBS, or RPMI 1640 cell culture medium. Different ultrasound energies, various dispersion stabilizers (human, bovine, and mouse serum albumin, Tween 80, and mouse serum), various concentrations of stabilizers, and different sequences of preparation steps were applied. The size distribution of dispersed nanoparticles was analyzed by dynamic light scattering and zeta potential was measured using phase analysis light scattering. Nanoparticle size was also verified by transmission electron microscopy. A specific ultrasound energy of 4.2 × 10⁵ kJ/m³ was sufficient to disaggregate TiO₂ (rutile) nanoparticles, whereas higher energy input did not further improve size reduction. The optimal sequence was first to sonicate the nanoparticles in water, then to add dispersion stabilizers, and finally to add buffered salt solution to the dispersion. The formation of coarse TiO₂ (rutile) agglomerates in PBS or RPMI was prevented by addition of 1.5 mg/ml of human, bovine or mouse serum albumin, or mouse serum. The required concentration of albumin to stabilize the nanoparticle dispersion depended on the concentration of the nanoparticles in the dispersion. TiO₂ (rutile) particle dispersions at a concentration lower than 0.2 mg/ml could be stabilized by the addition of 1.5 mg/ml albumin. TiO₂ (rutile) particle dispersions prepared by this method were stable for up to at least 1 week. This method was suitable for preparing dispersions without coarse agglomerates (average diameter < 290 nm) from nanosized TiO₂ (rutile), ZnO, Ag, SiO_x, SWNT, MWNT, and diesel SRM2975 particulate matter.

Conclusion

The optimized dispersion method presented here appears to be effective and practicable for preparing dispersions of nanoparticles in physiological solutions without creating coarse agglomerates.     

Pulmonary response to intratracheal instillation of ultrafine versus fine titanium dioxide: role of particle surface area

Background  

The production and use of nanoparticles is growing rapidly due to the unique physical and chemical properties associated with their nano size and large surface area. Since nanoparticles have unique physicochemical properties, their bioactivity upon exposure to workers or consumers is of interest. In this study, the issue of what dose metric (mass dose versus surface area dose) is appropriate for toxicological studies has been addressed. Rats were exposed by intratracheal instillation to various doses of ultrafine or fine TiO₂. At 1, 7, or 42 days post-exposure, inflammatory and cytotoxic potential of each particle type was compared on both a mass dosage (mg/rat) as well as an equal surface area dosage (cm² of particles per cm² of alveolar epithelium) basis.