West African e-waste-soil assessed with a battery of cell-based bioassays.

Soil samples randomly taken from major e-waste sites in West Africa (Nigeria, Benin and Ghana) were examined for an extensive range of organic contaminants. Cytotoxicity measurements and assessment of activation of xeno-sensing receptors from fish (Atlantic cod) were employed as a battery of in vitro biological assays to explore the quality and toxicity profile of West African e-waste soil. The concentrations of the measured contaminants of emerging concerns (CECs) and persistent organic pollutants (POPs) in the e-waste soil differs significantly from the reference soil with chemical profiles typically dominated by legacy polybrominated diphenyl ethers (PBDEs) (405.8 µgkg-1) and emerging organophosphate ester flame retardant tris (1-chloro-2-propyl) phosphate (TCPP) (404 µgkg-1), in addition to the short chain perfluorobutane sulfonate (PFBS) (275.3 µgkg-1) and perfluorobutanoate (PFBA) (16 µgkg-1). The study revealed that perfluorooctanoic acid (PFOA) occurred only in e-waste soil from Ghana and ranged from 2.6 to 5.0 µgkg-1. Overall, non-polar e-waste soil-derived extracts had a stronger effect on COS-7 cell viability than the polar extracts and elutriates. The highest receptor activation was observed with single polar and non-polar extracts from the Nigeria and Benin sites, indicating hotspots with Er-, PPARa- and Ahr-agonist activities. Thus, the results obtained with our battery of in vitro biological assays underscored these e-waste sites as remarkably polluted spots with complex toxicity profiles of great concern for human and environmental health.

In vitro cytotoxic assessment of e-waste-related chemical pollution in impacted soil matrix.

The environmental quality and toxicity of soil from some selected informal e-waste sites in West Africa was assessed on PLHC-1 liver cells. In addition, toxicity mechanisms such as apoptosis, necrosis and necroptosis were analysed in order to determine the effect of the actual chemical mixture present in the e-waste soil matrix. The investigation revealed that although e-waste soil extracts (polar and non-polar) and elutriates were significantly cytotoxic at the tested concentration (16 mg soil EQ/ml), PLHC-1 cell viability was not reduced below 50%. The non-polar extracts were more toxic compared to polar extracts and elutriates. The cytotoxic potency of soil from the informal e-waste-recycling sites ranged in this order: Alaba > Godome-Kouhounou > Agbogblosie. The study revealed that all e-waste soil extracts and elutriates induced significant (P < 0.01) PLHC-1 cell death by apoptosis and necrosis; however, cell death by apoptosis was higher compared to that by necrosis. The results indicated that except for non-polar extracts (N4, B4 and G4) from open burning areas that induced significant (P < 0.01) PLHC-1 cell death by necroptosis, other extracts and elutriates could not cause cell death by necroptosis. The study has demonstrated that soils from the Alaba e-waste site in Lagos could be more toxic than soils from Godome-Kouhounou (Cotonou) and Agbogblosie (Accra) e-waste sites and further highlighted open burning as an informal e-waste-handling method with greater negative impact on soil quality in the e-waste sites. The study emphasizes the urgent need for regulatory agencies to introduce regular residue-monitoring programmes in order to forestall the adverse effects of soil pollution episodes in the e-waste sites.