BackgroundDuring the last 250 years, the level of exposure to combustion-derived particles raised dramatically in western countries, leading to increased particle loads in the ambient air. Among the environmental particles, diesel exhaust particulate matter (DEPM) plays a special role because of its omnipresence and reported effects on human health. During recent years, a possible link between air pollution and the progression of atherosclerosis is recognized. A central effect of DEPM is their impact on the endothelium, especially of the alveolar barrier. In the present study, a complex 3D tetraculture model of the alveolar barrier was used in a dose-controlled exposure scenario with realistic doses of DEPM to study the response of endothelial cells.ResultsTetracultures were exposed to different doses of DEPM (SRM2975) at the air-liquid-interface. DEPM exposure did not lead to the mRNA expression of relevant markers for endothelial inflammation such as ICAM-1 or E-selectin. In addition, we observed neither a significant change in the expression levels of the genes relevant for antioxidant defense, such as HMOX1 or SOD1, nor the release of pro-inflammatory second messengers, such as IL-6 or IL-8. However, DEPM exposure led to strong nuclear translocation of the transcription factor Nrf2 and significantly altered expression of CYP1A1 mRNA in the endothelial cells of the tetraculture.ConclusionIn the present study, we demonstrated the use of a complex 3D tetraculture system together with a state-of-the-art aerosol exposure equipment to study the effects of in vivo relevant doses of DEPM on endothelial cells in vitro. To the best of our knowledge, this study is the first that focuses on indirect effects of DEPM on endothelial cells of the alveolar barrier in vitro. Exposure to DEPM led to significant activation and nuclear translocation of the transcription factor Nrf2 in endothelial cells. The considerably low doses of DEPM had a low but measurable effect, which is in line with recent data from in vivo studies.Electronic supplementary materialThe online version of this article (doi:10.1186/s12989-017-0186-4) contains supplementary material, which is available to authorized users.

A rapid microwave solid-state synthesis method is systematically investigated to achieve a H 2 producing visible light active spinel photocatalyst. ZnFe 2 O 4 nanocrystallites were obtained by microwave irradiation of precursor compacts under optimized conditions. This investigation led to a uniform sized nanocrystalline photocatalyst that yielded a quantum-yield of H 2 evolution y3.8 times higher than that of conventionally synthesized ZnFe 2 O 4 . The synthesis parameters -microwave power, synthesis temperature, and time, were found to control the physico-chemical properties viz phase formation kinetics, phase purity, crystallinity, specific surface area and photochemical efficiency, of the synthesized photocatalyst. The study reveals that the threshold microwave power of ¢3 kW was necessary to obtain a spinel phase structure, while lower power (,3 kW) could not induce the crystallization even after prolonged low-power irradiation of 180 min. At the threshold power, a minimum of 10 min. synthesis time was enough to obtain uniform sized nanocrystallites, indicating that the synthesis method is y24 times faster than the solid state reaction method, which needs nearly 4 h. The particle morphology evolution with irradiation time from 10-150 min. exhibited de-crystallization phenomena. Longer irradiation displayed a morphological crystallization probably induced due to the simultaneous area and volumetric heating effect. The possible ''formation mechanism'' of these uniform nanocrystallites has been presented here for qualitative understanding. Thus synthesized photocatalysts generated hydrogen from a water-methanol mixture even without the co-catalyst loading. The ferrite photocatalyst was found to decolorize methylene blue dye with a maximum decay constant of 0.232 h 21 , thereby demonstrating its capability in the pollutant decomposition applications, all under visible light photons.

SummaryThis paper investigates solar radiation‐induced photocatalytic hydrogen generation using spinel ZnFe2O4 (ZFO) photocatalysts fabricated using different routes, viz., solid state reaction (SSR), polymer complex (PC), microwave sintering (μW) and self‐propagating combustion (SPC) method. The physicochemical properties of the photocatalysts like crystallinity, surface area, band gap and band energetics is studied as it influences their photochemical behavior. The study reveals a high crystallinity of the ZFO photocatalysts, those are synthesized using SSR, PC and μW methods, where SSR method yields the larger dimension crystallites of ~53 nm. The nanoparticles obtained from SPC methodology exhibit a relatively large surface area and a smaller crystallite size of around ~18 nm. Monodispersed particles with comparatively large surface area are obtained in the case of PC method. ZFO obtained from μW synthesis exhibits enhanced optical properties, thus favoring high absorption of solar photons. A relatively more negative flat band potential is displayed by the μW samples (−0.543 vs normal hydrogen electrode) as estimated from the electrochemical measurements. Consequently, these samples yield a higher quantum yield (0.19%) for hydrogen evolution even without co‐catalyst loading. On the contrary, the photocatalysts obtained by SSR and PC methods did display an enhancement in the quantum yield as compared to the μW samples but only after Pt co‐catalyst loading. Copyright © 2015 John Wiley & Sons, Ltd.

Background The present study aimed to evaluate the potential differences in the biological effects of two types of spherical silver particles of 20 and 200 nm (Ag20 and Ag200), and of PVP-coated silver nanowires (AgNWs) with a diameter of 50 nm and length up to 50 μm, using a complex 3D model representative for the alveolar barrier cultured at air-liquid interface (ALI). The alveolar model was exposed to 0.05, 0.5 and 5 μg/cm 2 of test compounds at ALI using a state-of-the-art exposure system (Vitrocell™Cloud System). Endpoints related to the oxidative stress induction, anti-oxidant defence mechanisms, pro-inflammatory responses and cellular death were selected to evaluate the biocompatibility of silver particles and nanowires (AgNMs) and to further ascribe particular biological effects to the different morphologic properties between the three types of AgNMs evaluated. Results Significant cytotoxic effect was observed for all three types of AgNMs at the highest tested doses. The increased mRNA levels of the pro-apoptotic gene CASP7 suggests that apoptosis may occur after exposure to AgNWs. All three types of AgNMs increased the mRNA level of the anti-oxidant enzyme HMOX-1 and of the metal-binding anti-oxidant metallothioneins ( MTs ), with AgNWs being the most potent inducer. Even though all types of AgNMs induced the nuclear translocation of NF-kB, only AgNWs increased the mRNA level of pro-inflammatory mediators. The pro-inflammatory response elicited by AgNWs was further confirmed by the increased secretion of the 10 evaluated interleukins. Conclusion In the current study, we demonstrated that the direct exposure of a complex tetra-culture alveolar model to different types of AgNMs at ALI induces shape- and size-specific biological responses. From the three AgNMs tested, AgNWs were the most potent in inducing biological alterations. Starting from 50 ng/cm 2 , a dose representative for an acute exposure in a high exposure occupational setting, AgNWs induced prominent changes indicative for a pro-inflammatory response. Even though the acute responses towards a dose representative for a full-lifetime exposure were also evaluated, chronic exposure scenarios at low dose are still unquestionably needed to reveal the human health impact of AgNMs during realistic conditions. Electronic supplementary material The online version of this article (10.1186/s12989-019-0297-1) contains supplementary material, which is available to authorized users.

represents the most prevalent occupational disease of the lungs in developed countries and occupational exposure to dusts, gases, fumes, vapors, and chemicals is responsible for 16% of asthma in adults (Torén and Blanc, 2009). Around a hundred chemicals were described to act as respiratory sensitizers (Bloemen et al., 2009), among which different chemical classes such as acid anhydrides, diisocyanates, and chloroplatinate salts were identified.Protein allergens (or high molecular weight; HMW compounds), which are also a potential cause of occupational asthma, are the primary cause for the development of respiratory allergy in the general population. Certain proteins from environmental sources such as pollen, animal dander and house dust mites (HDM) are common causes of asthma. Depending on the geographical location, 50 to 85% of people with asthma are allergic to certain HDM proteins (Gregory and Lloyd, 2011).An early identification of compounds with the potential to act as respiratory sensitizers is still difficult. This is due to an incomplete understanding of the systemic mechanisms involved in the development of respiratory sensitization and to the absence of fit-for-purpose, validated, or even widely accepted in vivo models or in vitro assays to identify respiratory sensitizers. Currently,

Solid polymer blend electrolyte systems have been prepared with Poly (ethylene oxide) (PEO), Poly (Vinylidene fluoride) (PVDF) and complexed with Sodium Nitrate (NaNO 3 ) salt by using solution cast technique. The complexion of salt with polymer blend has been confirmed by X-Ray diffraction, Fourier Transmission Infrared Spectroscopy and scanning electron microscopic studies. AC and DC conductivity studies of these polymer blends were carried out by changing the weight percentages of PEO and PVDF with a constant weight percentage of NaNO 3 . The electric modulus (M ' ) and the dielectric properties for all the polymer blend systems have been investigated with impedance spectroscopic analysis as a function of frequency ranging from 100-30MHz. The ionic conductivity of the blend polymer electrolyte systems followed Arrhenius behaviour and the maximum ionic conductivity was observed for PEO:PVdF:NaNO 3 (80:20:5) at room temperature which is attributed to the formation of the amorphous phase.

Respiratory sensitization as a consequence of exposure to chemical products has increased over the last decades, leading to an increase of morbidity. The increased use of synthetic compounds resulted in an exponential growth of substances to which we are potentially exposed on a daily basis. Some of them are known to induce respiratory sensitization, meaning that they can trigger the development of allergies. In the past, animal studies provided useful results for the understanding of mechanisms involved in the development of respiratory allergies. However, the mechanistic understanding of the involved cellular effects is still limited. Currently, no in vitro or in vivo models are validated to identify chemical respiratory sensitizers. Nonetheless, chemical respiratory sensitizers elicit a positive response in validated assays for skin sensitization. In this review, we will discuss how these assays could be used for respiratory sensitization and if necessary, what can be learnt from these assays to develop a model to assess the respiratory sensitizing potential of chemicals. In the last decades, much work has been done to study the respiratory toxicity of inhaled compounds especially in developing in vitro assays grown at the air-liquid interface. We will discuss how possibly the tests currently used to investigate general particle toxicity could be transformed to investigate respiratory sensitization. In the present review, we describe the most known mechanism involved in the sensitization process and the experimental in vivo and alternative in vitro models, which are currently available and how to adapt and improve existing models to study respiratory sensitization.

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