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Clinical Pharmacology and Toxicology Research

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Prenatal exposure levels of Polybrominated diphenyl ethers in mother-infant pairs and their transplacental transfer characteristics in Uganda (East Africa)

2nd International Conference on TOXICOLOGY AND CLINICAL TOXICOLOGY

November 11-12, 2019 | London, UK

Patrick Ssebugere

Makerere University, Uganda

ScientificTracks Abstracts: Clin Pharmacol Toxicol Res

Abstract :

Polybrominated diphenyl ethers (PBDEs) are ubiquitous environmental pollutants with adverse effects on the fetus and infants. The aim of the present study was to assess in utero exposure levels and transplacental transfer characteristics of BDE congeners in mothers from Kampala capital city, Uganda. Paired human samples (thirty placenta and twenty nine cord blood samples) were collected from mothers at St. Francis Hospital Nsambya between April and June, 2018 and analysed for a suite of 24 tri- to deca-BDE congeners. Extraction was carried out using liquid-liquid extraction and sonication for cord blood and placenta samples, respectively. Clean-up was done on a solid phase (SPE) column and analysis was performed using gas chromatography/ mass spectrometer (GC/MS). Total (Σ) PBDEs were 0.25-30.9 ng/g lipid weight (lw), (median; 7.11 ng/g lw) in the placenta and 1.65-34.5 ng/g lw (median; 11.9 ng/g lw) in cord blood serum. Statistical analysis showed no significant difference between the levels of PBDEs in cord blood and placenta samples (Wilcoxon signed rank test: Z = -0.433, p = 0.665), possibly due to poor xenophobic metabolism by the fetus. BDE-209 was the dominant congener in both matrices (contributed 40.5% and 51.2% to ΣPBDEs in placenta and cord blood, respectively), suggesting on-going maternal exposure to deca-BDE formulation. No apparent correlation was observed between BDE congeners and meat consumption probably due to multiple sources of PBDEs. Based on absolute concentrations, the extent of transplacental transport (TPT) was high for higher congeners (BDE-209, 206 and 207) than for lower ones (such as BDE-47) suggesting alternative TPT mechanisms besides passive diffusion.

Biography :

Patrick Ssebugere completed his D.Sc in Green Chemical Technology from Lappeenranta University of Technology in 2015. He is a Lecturer of Physical Chemistry at the Department of Chemistry, School of Physical Sciences, Makerere University. He has published more than 17 papers in reputed journals and has supervised more than 8 master’s students to completion. His research group is involved in modeling and risk assessment of organic pollutants in the tropics. The group is also studying the prevalence and fate of organic chemical contaminants in the environment, their sources and climate change-energy-public health nexus and sustainability of ecosystems.

E-mail: [email protected]

Google Scholar citation report
Citations : 13

Clinical Pharmacology and Toxicology Research received 13 citations as per Google Scholar report