In this study, methodological factors influencing the dissolution of metal(loid)s in simulated lung fluid (SLF) was assessed in order to develop a standardised method for the assessment of inhalation bioaccessibility in PM. To achieve this aim, the effects of solid to liquid (S/L) ratio (1:100 to 1:5000), agitation (magnetic agitation, occasional shaking, orbital and end-over-end rotation), composition of SLF (artificial lysosomal fluid: ALF; phagolysosomal simulant fluid: PSF) and extraction time (1-120 h) on metal(loid) bioaccessibility were investigated using PM from three Australian mining/smelting impacted soils and a certified reference material. The results highlighted that SLF composition significantly (p < 0.001) influenced metal(loid) bioaccessibility and that when a S/L ratio of 1:5000 and end-over-end rotation was used, metal(loid) solubility plateaued after approximately 24 h. Additionally, in order to assess the exposure of metal(loid)s via incidental ingestion of surface dust, PM was subjected to simulated gastro-intestinal tract (GIT) solutions and the results were compared to extraction using SLF. Although As bioaccessibility in SLF (24 h) was significantly lower than in simulated GIT solutions (p < 0.05), Pb bioaccessibility was equal to or significantly higher than that extracted using simulated GIT solutions (p < 0.05).
Although metal(loid) bioaccessibility of ambient particulate matter, with an aerodynamic diameter of <10μm (PM), has recently received increasing attention, limited research exists into standardising in-vitro methodologies using simulated lung fluid (SLF). Contradictions exist regarding which assay parameters should be adopted. Additionally, potential continuation of metal(loid) dissolution once PM is cleared from the lungs and passed through the gastro-intestinal tract (GIT) has rarely been addressed. The objective of this study was to assess parameters that influence inhalation bioaccessibility in order to develop a conservative assay that is relevant to a human inhalation scenario. To achieve this aim, the effect of solid to liquid (S/L) ratio, extraction time, agitation and five major SLF compositions on the bioaccessibilities of arsenic (As) and lead (Pb) was investigated using PM from three Australian mining/smelting impacted regions. Using the biologically relevant parameters that resulted in the most conservative outcomes, bioaccessibility of metal(loid)s in PM was assessed in SLF, followed by simulated GIT solutions. Results from this study revealed that fluid composition and S/L ratio significantly affected metal(loid) dissolution (p<0.05). The highest Pb bioaccessibility resulted using simulated lung-gastric solution, while that of As resulted using simulated lung-gastric-small intestinal tract solutions. Compared to SLF alone, metal(loid) dissolution using the inhalation-ingestion bioaccessibility assay (IIBA) was significantly higher (p<0.05) for all PM samples.
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Lead (Pb) exposure from household
dust is a major childhood health
concern because of its adverse impact on cognitive development. This
study investigated the absorption kinetics of Pb from indoor dust
following a single dose instillation into C57BL/6 mice. Blood Pb concentration
(PbB) was assessed over 24 h, and the dynamics of particles in the
lung and gastro-intestinal (GI) tract were visualized using X-ray
fluorescence (XRF) microscopy. The influence of mineralogy on Pb absorption
and particle retention was investigated using X-ray absorption near-edge
structure spectroscopy. A rapid rise in PbB was observed between 0.25
and 4 h after instillation, peaking at 8 h and slowly declining during
a period of 24 h. Following clearance from the lungs, Pb particles
were detected in the stomach and small intestine at 4 and 8 h, respectively.
Analysis of Pb mineralogy in the residual particles in tissues at
8 h showed that mineral-sorbed Pb and Pb-phosphates dominated the
lung, while organic-bound Pb and galena were the main phases in the
small intestines. This is the first study to visualize Pb dynamics
in the lung and GI tract using XRF microscopy and link the inhalation
and ingestion pathways for metal exposure assessment from dust.
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