Optimization of selective pressurized liquid extraction of organic pollutants in placenta to evaluate prenatal exposure

Journal of Chromatography A

https://doi.org/10.1016/j.chroma.2017.03.010

The early exposure to organic pollutants (OPs) related to dietary habit or environmental exposure is a concern of growing interest in environmental health. When OPs enter the body, they can accumulate in fatty tissue and even travel through the bloodstream being able to cross the placenta and reach the fetus through the substance exchange between the mother and the child. Epidemiologic and clinical data affirm that these chemicals increase the risk of adverse effects during childhood. This article reviews and addresses one of the most relevant analytical methods for determining OPs in placenta. We discuss and critically evaluate procedures, such as solid-liquid and selective pressurized liquid extraction (SPLE). Clean-up of extracts was performed by solid-phase extraction (SPE) using EZ-POP cartridges. Detection of OPs was carried out by gas chromatography (GC) coupled to tandem mass spectrometry (MS/MS). Recoveries ranged from 52% to 94% by SPLE with estimated quantification limits between 0.15 and 2.2 ng/g for organochlorine pesticides (OCPs), between 0.083 and 0.50 for organophosphate pesticides (OPPs), between 0.025 and 0.15 ng/g for polychlorinated biphenyl (PCBs), between 0.015 and 0.10 ng/g for polybromodiphenyl ethers (PBDEs), between 0.33 and 0.66 ng/g for pyrethroids and between 0.022 and 0.87 ng/g for polycyclic aromatic hydrocarbons (PAHs). Most of the target OPs were detected in twenty real placenta samples studied, with pyrethroids, PAHs and OPPs representing most of the 90% of OPs with means of 13–18 ng/g versus PCBs, OCPs, and PBDEs with means <4.0 ng/g. The rsults of this work indicate a prenatal exposure to OPs in Galicia.

A critical review about human exposure to Polychlorinated Dibenzo-p-Dioxins (PCDDs), Polychlorinated Dibenzofurans (PCDFs) and Polychlorinated Biphenyls (PCBs) through foods

Critical Reviews in Food Science and Nutrition, 55 (11), 2015, 1590-1617

DOI:10.1080/10408398.2012.710279

Dioxins include polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and part of polychlorinated biphenyls (PCBs). Only the compounds that are chlorinated at the 2,3,7, and 8 positions have characteristic dioxin toxicity. PCDDs, PCDFs and PCBs accumulate in the food chain due to their high lipophilicity, high stability, and low vapor pressure. They are not metabolized easily; however their hydroxylated metabolites are detected in feces. They cause a wide range of endocrine disrupting effects in experimental animals, wildlife, and humans. Endocrine related effects of PCDDs, PCDFs and PCBs on thyroid hormones, neurodevelopment and reproductive development were referenced. In addition, some studies of contamination of foods, bioaccumulation, dietary exposure assessment, as well as challenges of scientific research in these compounds were reviewed.

Atmospheric pollutants in fog and rain events at the northwestern mountains of the Iberian Peninsula

Science of The Total Environment

Volumes 497–498, 1 November 2014, Pages 188–199

http://dx.doi.org/10.1016/j.scitotenv.2014.07.093

Atmospheric polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) are persistent organic pollutants (POPs) and exist in gas and particle phases, as well as dissolved or suspended in precipitation (fog or rain). While the hydrosphere is the main reservoir for PAHs, the atmosphere serves as the primary route for global transport of PCBs. In this study, fog and rain samples were collected during fourteen events from September 2011 to April 2012 in the Xistral Mountains, a remote range in the NW Iberian Peninsula. PAH compounds [especially of low molecular weight (LMW)] were universally found, but mainly in the fog-water samples. The total PAH concentration in fog-water ranged from non-detected to 216 ng · L− 1 (mean of 45 ng · L− 1), and was much higher in fall than in winter. Total PAH levels in the rain and fog events varied from non-detected to 1272 and 33 ng · L− 1 for, respectively, LMW and high molecular weight (HMW) PAHs. Diagnostic ratio analysis (LMW PAHs/HMW PAHs) suggested that petroleum combustion was the dominant contributor to PAHs in the area. Total PCB levels in the rain and fog events varied from non-detected to 305 and 91 ng · L− 1 for, respectively, PCBs with 2–3 Cl atoms and 5–10 Cl atoms. PCBs, especially those with 5–10 Cl atoms, were found linked to rain events. The occurrence of the most volatile PCBs, PCBs with 2–3 Cl atoms, is related to wind transport from far away sources, whereas the occurrence of PCBs with 5–10 Cl atoms seems to be related with the increase of its deposition during rainfall at the end of summer and fall. The movement of this fraction of PCBs is facilitated by its binding to air-suspended particles, whose concentrations usually show an increase as the result of a prolonged period of drought in summer.

Decontamination solutions for polychlorinated biphenyls (PCBs) in raw fish oils from environmentally contaminated sea fishes

Science of The Total Environment

Volumes 468–469, 15 January 2014, Pages 1007–1013

http://dx.doi.org/10.1016/j.scitotenv.2013.09.036

Fish oil has been identified as one of the most important contributors to the levels of polychlorinated biphenyls (PCBs) in food and feed products. In this study, PCB adsorption from fish oil onto activated carbon (AC), other sustainable adsorbents (mussel shell and wood waste ashes) and organic solvent such as ethanol were compared and optimized. Regarding to adsorbents, PCBs were extracted from fish oil by a 2.0% adsorbent material dose, during 6.0 h at 25 °C. Solvent extraction was carried out using 2 × 5.0 mL ethanol by manually stirring for 3.0 min, and then by Ultrasound-Assisted Solvent Extraction (UASE) for 5.0 min. The results showed that removal rates obtained by using adsorbent materials ranged from 0.0 to 10% for marker PCBs, from 0.0 to 37% for mono-ortho-PCBs, from 0.0 to 74% for PCB11 and from 0.0 to 95% for non-ortho-PCBs. Regarding to solvent extraction, ethanol was used by manually stirring and then by Ultrasound-Assisted Solvent Extraction (UASE). The samples were then centrifuged (2000 rpm/10 min) and the alcoholic phase was removed. With this method, removal efficiencies were much better (85–116%); nevertheless, high eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) removal rates (70–78 and 71–79%, respectively) were detected. We can conclude that adsorption with adsorbents depends on the geometry of PCB congeners, as well as both type of adsorption material and their origin, and that several sorption cycles are needed. Adsorption with ethanol could be the most effective methodology but nutritional quality was impaired, what makes necessary to look for other not so polar removal solvents.