Assessment of dermal absorption of beryllium and copper contained in temple tips of eyeglasses

Dermal exposure to hazardous substances such as chemicals, toxics, metallic items and other contaminants may present substantial danger for health. Beryllium (Be) is a hazardous metal, especially when inhaled and/or in direct contact with the skin, associated with chronic beryllium disease (CBD) and Be sensitization (BeS). The objective of this study was to investigate the percutaneous penetration of beryllium and copper contained in metallic items as eyeglass temple tips (specifically BrushCAST (R) Copper Beryllium Casting Alloys containing Be 0.35 < 2.85%; Cu 95.3-98.7%), using Franz diffusion cells. This work demonstrated that the total skin absorption of Cu was higher (8.86%) compared to Be (4.89%), which was expected based on the high percentage of Cu contained in the eyeglass temple tips. However, Be accumulated significantly in the epidermis and dermis (up to 0.461 mu g/cm(2)) and, to a lesser extent, in the stratum corneum (up to 0.130 mu g/cm2) with a flux of permeation of 3.52 +/- 4.5 mu g/cm(2)/hour and lag time of 2.3 +/- 1.3 h, after cutaneous exposure of temple tip into 1.0 mL artificial sweat for 24 h. Our study highlights the importance of avoiding the use of Be alloys in items following long-term skin contact

In vitro dermal penetration of nickel nanoparticles.

Nickel nanoparticles (NiNPs) represent a new type of occupational exposure because, due to the small size/high surface, they can release more Ni ions compared to bulk material. It has been reported a case of a worker who developed sensitization while handling nickel nanopowder without precautions. Therefore there is the need to assess whether the skin absorption of NiNPs is higher compared to bulk nickel. Two independent in vitro experiments were performed using Franz diffusion cells. Eight cells for each experiment were fitted using intact and needle-abraded human skin. The donor phase was a suspension of NiNPs with mean size of 77.7 \ub1 24.1 nm in synthetic sweat. Ni permeated both types of skin, reaching higher levels up to two orders of magnitude in the damaged skin compared to intact skin (5.2 \ub1 2.0 vs 0.032 \ub1 0.010 \u3bcg cm(-2), p = 0.006) at 24 h. Total Ni amount into the skin was 29.2 \ub1 11.2 \u3bcg cm(-2) in damaged skin and 9.67 \ub1 2.70 \u3bcg cm(-2) in intact skin (mean and SD, p = 0.006). Skin abrasions lead to doubling the Ni amount in the epidermis and to an increase of ten times in the dermis. This study demonstrated that NiNPs applied on skin surface cause an increase of nickel content into the skin and a significant permeation flux through the skin, higher when a damaged skin protocol was used. Preventive measures are needed when NiNPs are produced and used due to their higher potential to enter in our body compared to bulk nickel

Two-year monitoring of water hydrochemistry in a Pb-Zn Mississippi Valley-Type mine (MVT) in the Southeastern Alps (Raibl, Friuli Venezia Giulia)

The recent and past mining activities are among the main anthropic sources of dispersion of potentially toxic trace elements (PTEs) in the environment. In this study, a two year monitoring of different water bodies in a decommissioned mining site located in the Southeastern Alps (Friuli Venezia Giulia, Raibl mine) was performed. Results have allowed to provide a characterisation of the hydrogeochemistry, the chemical signatures and the temporal-spatial variations of PTEs in a carbonate-hosted Pb-Zn Mississippi Valley-Type (MVT) mine, where no acid mine drainages (AMD) occur. Besides mineralogy and pH-Eh conditions, strong rainfalls and high-flow events are the main factors affecting the temporal variability of dissolved PTEs, promoting their dissolution and dispersion. Anomalous concentrations of trace metals (Zn, Pb, Tl) were found in near neutral pH-buffered groundwaters entrapped in tailings impoundments, whereas concentrations of metalloids (As, Sb and Ge) were more abundant in low-flow water drainage from mine adits. High concentrations of Tl were found in the saturated area of the tailings impoundments, related to relatively lower pH and sulfate ions contents, thus suggesting Tl-bearing pyrite/marcasite oxidation. At the same time, low concentrations of dissolved Ge and Cd in groundwaters entrapped in tailings are possibly associated to sphalerite-depleted post-flotation tailings. Based on chemical data, modeling and literature, attenuation processes of dissolved PTEs (mainly Pb) are mainly attributed to sorption onto Fe-oxy-hydroxides, which is pH-dependent, and precipitation of mineral phases (e.g., dissolved Zn to hydrozincite: Zn5(CO3)2(OH)6). The Tl/Zn and Tl/Pb ratios show that enrichments occur without notable attenuation inside the tailings impoundments, possibly indicating that Tl attenuation needs higher pH to effectively promote adsorption onto Fe-oxy-hydroxides, as, conversely, occurs in the Rio del Lago stream waters

Effects of hypoxia on biogeochemical cycling of nutrients and trace elements in a stratified estuarine system (Gulf of Trieste, northern Adriatic Sea)

Estuaries can be thought as a sedimentary trap leading to the accumulation of potentially toxic trace elements (PTEs) in sediments. However, biogeochemical processes at the sediment-water interface (SWI) may also be responsible for the release of dissolved PTEs and nutrients in the overlying water column affecting the water quality. The estuarine system of the Timavo River (Gulf of Trieste, northern Adriatic Sea) is a semi-closed aquatic environment where a long-lasting oxic-hypoxic interface along the water column occurred due to the scarce water circulation in the innermost sector. To prevent bloom-forming and potential production of toxins and off-flavours, artificial mixing has been provided with a bubble plume installation connected to pressurised air and built on the sediment surface aiming at reoxygenating the water column. The aim of this research was to evaluate the behaviour of PTEs (As, Cr, Hg, Fe, Mn, Ni, Pb, V) and nutrients (NO3, NO2, NH4 and SRP) along the water column and at the SWI before (June) and during (September) the activation of the forced aeration system. Water samples were collected at different depths along the water column, in situ benthic chamber experiments were performed at the SWI and short sediment cores were sampled to investigate both the sediment and porewater. Dissolved oxygen decreased along the water column, especially in June when hypoxia (2.29 mg/L) and reductive conditions (58 mV) were observed at the bottom resulting in increasing dissolved PTE and nutrient concentrations. Accordingly, a gradual oxygen depletion was observed in the benthic chamber testifying to intense organic matter remineralisation processes. Moreover, the highest concentrations of dissolved PTEs in porewater were restricted to the top of the sedimentary sequence, especially in June when hypoxic conditions may promote PTE and nutrient effluxes from the sediment to the water column

Transdermal permeation of inorganic cerium salts in intact human skin

The stratum corneum protects the body against external agents, such as metals, chemicals, and toxics. Although it is considered poorly permeable to them, comprising the major barrier to the permeation of such substances, it may become a relevant gate of entry for such molecules. Cerium (Ce) is a lanthanide that is widely used in catalytic, energy, biological and medicinal applications, owing to its intrinsic structural and unique redox properties. Cerium salts used to produce cerium oxide (CeO2) nanostructures can potentially come into contact with the skin and be absorbed following dermal exposure. The objective of this study was to investigate the percutaneous absorption of three inorganic Ce salts: cerium (III) chloride (CeCl3); cerium (III) nitrate (Ce(NO3)3) and ammonium cerium (IV) nitrate (Ce(NH4)2(NO3)6), which are commonly adopted for the synthesis of CeO2 using in vitro - ex vivo technique in Franz diffusion cells. The present work shows that Ce salts cannot permeate intact human skin, but they can penetrate significantly in the epidermis (up to 0.29 μg/cm2) and, to a lesser extent in dermis (up to 0.11 μg/cm2). Further studies are required to evaluate the potential effects of long-term exposure to Ce

In vitro permeability of silver nanoparticles through porcine oromucosal membrane

Silver nanoparticles (AgNPs) can come in contact with human oral mucosa due to their wide use infood industry and hygiene devices. We evaluate transmucosal absorption of 19 nm AgNPs using excisedporcine buccal mucosa applied on Franz diffusion cells. Two donor solutions were used: one containingAgNPs (0.5 g/L) and one derived from the ultrafiltration of the former and containing only Ag in its solubleform. Experiments were carried out separately for 4 h. Silver flux permeation was demonstrated throughoral mucosa, showing similar values for AgNPs (6.8 \ub1 4.5 ng cm 122h 121) and Ag ions (5.2 \ub1 4.3 ng cm 122h 121).Our study demonstrates that silver can permeate the oromucosal barrier and that absorption is sub-stantially due to Ag ions, since no permeation difference was found using the two solutions. Mucosalabsorption has to be considered in further risk assessment studies

Skin contamination as pathway for nicotine intoxication in vapers

Growing warnings on health effects related to electronic cigarettes have met inconclusive findings at present. This study analyzed the in vitro percutaneous absorption of nicotine resulting by skin contamination with two e-liquids (refill 1 and 2) containing nicotine at 1.8%. Donor chambers of 6 Franz cells for each refill liquid were filled with 1 mL of nicotine e-liquid for 24 h; at selected intervals, 1.5 mL of the receptor solutions were collected for nicotine concentration analysis by mean gas chromatography\u2013mass spectrometry (LOD: 0.01 \u3bcg/mL). The experiment was repeated removing the nicotine donor solution after 10 min from the application and rinsing the skin surface three times with 3.0 mL of milliQ water. A total of 12 cells with 24 h exposure and 12 cells washed were studied. The mean concentration of nicotine in the receiving phase at the end of the experiment was 54.9 \ub1 29.5 and 30.2 \ub1 18.4 \u3bcg/cm2 for refill 1 and 2 respectively and significantly lower in washed cells (4.7 \ub1 2.4 and 3.5 \ub1 1.3 \u3bcg/cm2). The skin absorption of nicotine can lead to minor health illness in vapers, while caution must be paid to dermal contamination by e liquids in children. The skin cleaning significantly reduced the transdermal absorption kinetic and intradermal deposition of nicotine

Nanostructured Pd\u2013Pt nanoparticles: evidences of structure/performance relations in catalytic H2production reactions

A widespread approach to modulate the performances of heterogeneous catalysts is the use of bimetallic nanoparticles (NPs) as the active phase. However, studying the relationship between the NPs structure and catalytic properties requires well-defined systems, having uniform composition, size and nanostructure, which cannot be achieved by traditional methods (e.g. impregnation). Here, we developed wet-chemistry synthetic routes to prepare PdPt NPs or Pt-core@Pd-shell NPs of small size and well-controlled composition and structure, protected by mercaptoundecanoic acid (MUA) moieties. The pristine NPs were tested for H2 production by NH3BH3 hydrolysis, in order to systematically investigate the effect of composition and of synthetic route on the activity of the systems. Depending on the preparation method, two distinct trends of activity were observed, rationalized in terms of the extent of surface functionalization by MUA. The MUA protective layer was found to effectively stabilize the NPs dispersion while maintaining high activity in certain cases (Pt-rich NPs), and was demonstrated to be essential for catalyst recycling. In order to further study structure-activity relationships of PdPt NPs after ligand removal, nanostructured PdPt@CeO2-based catalysts were prepared by self-assembly route. Regardless of the starting NPs structure (alloy or core-shell), similar water gas shift reaction performances were observed, due to the structural rearrangements occurring upon oxidation and reduction thermal treatments, which led to the formation of Pt-rich core@PdPt-shell under reducing conditions