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International audience; To date, nontargeted analysis (NTA) of halogenated organic compounds in biota has mostly been performed using GC/MS-based instruments. We intended to broaden the spectrum of physicochemical properties of amenable substances by taking advantage of liquid chromatography–high-resolution mass spectrometry coupling paired with an electrospray ionization source. Thus, a NTA strategy was applied to a set of 12 blubber samples belonging to five marine mammal sentinel species stranded on the French Atlantic coasts. It involved specific postacquisition data interpretation using open-source software HaloSeeker 1.0 for annotating chemical formulas. A total of 135 distinct unequivocal molecular formulas were assigned to 466 polyhalogenated ion clusters of interest. The most intense representative ions were identified as bioaccumulative heptachloro-1,2′-bipyrrole (Cl7-BP), α-hexabromocyclododecane, and (1R,2S,4R,5R,1′E)-2-bromo-1-bromomethyl-1,4-dichloro-5-(2′-chloroethenyl)-5-methylcyclohexane (MHC-1) in the weight range of micrograms per gram of lipids. To the best of our knowledge, this is the first time that Cl7-BP, the most intense signal observed, is reported in biota. A dozen other compound families will require further in-depth work to gain structural information.

Since the decline of the use of bisphenol A, the chemistry of the varnishes and coatings which are applied to the inner surfaces of metallic food contact materials is poorly documented. We hypothesised that can coatings are now diverse and bring forth various non-intentionally added substances (NIAS) to be described. Investigating complex components such as NIAS requires demanding non-targeted approaches. We investigated the coatings of 12 vegetable cans from the French market. More than 125 substances were pinpointed, among them 84 oligoester combinations from 8 diols and 4 diacids. Thus, oligoesters were the dominant family. Additives such as epoxidised soybean oil, bisphenol A diglycidyl ether and benzoguanamine derivatives and phenol-formaldehyde oligomers were also identified. A software for exploring databases of theoretical combinations of polyester and phenol-formaldehyde resin components (NIAS-db 1.0) was made available. The stepwise organic synthesis of native and deuterated combinations of neopentyl glycol and isophthalic acid (4 and 8 units, linear and cyclic) enabled a higher confidence level and monitoring in vegetable extracts. Migration of oligoesters averaged 330 µg/kg in the drained vegetables (43-1600 µg/kg). This study sheds light on the need to fulfil a proper risk assessment on this NIAS family (exposure and hazard characterisation).

International audience; Suspect and non-targeted screening approaches are a matter of increasing interest notably with regard to the Exposome contextual framework, but their application to human samples still remains limited at this date. The aim of the present study was to develop a non-targeted workflow from sample preparation to data processing and method assessment to characterise the human internal chemical exposure at early life stage. The method was focused on human milk to investigate mother and newborn exposure to known organic contaminants and to extend the characterisation to unknown compounds. We specifically focused on halogenated biomarkers of exposure due to persistence and potential toxicological impact reasons. The newly developed approach was based on a simple and fast sample preparation followed by a comprehensive analysis by both liquid and gas phase chromatography coupled to high resolution mass spectrometry. Critical steps of the non-targeted workflow as the method assessment have been addressed with a reference mix of 30 chlorinated and brominated contaminants encompassing various substances groups and a statistical approach. Data processing until the identification of biomarkers of exposure was possible with homemade bioinformatics tools. On the other hand, the method was validated by the identification of historical chemicals as hexachlorobenzene and p,p’-DDE and emerging chemical as 4-hydroxychlorothalonil. This approach opens the door to further extensions and consolidations to offer new capabilities for exposomics and environmental health research.

International audience; Chlorinated paraffins (CPs) are a complex family of contaminants. Lack of exposure data and an understanding of the fate of these chemicals in the environment affect our ability to reliably assess the human health risk associated with CP exposure. The present study focused on the evaluation of CP transfer from feed to eggs of laying hens exposed over 91 days. Laying hens were provided feed spiked with five technical mixtures of short-, medium- or long-chain CPs and featuring low or high chlorine contents, at concentrations of 200 ng/g each. Eggs were collected daily. All mixtures except the LCCPs with high chlorine content transferred into the eggs, with accumulation ratios increasing with the chain length and chlorine content. Concentrations at the steady-state varied between 41 and 1397 ng/g lw depending on the mixture. Additionally, the homologue-dependant transfer resulted in a change of pattern compared to that from the spiked feed.

ISI Document Delivery No.: IM0NO Times Cited: 1 Cited Reference Count: 25 Elsa, Omer Emmanuelle, Bichon Sebastien, Hutinet Anne-Lise, Royer Fabrice, Monteau Helene, Germon Paul, Hill Gerald, Remaud Gaud, Dervilly-Pinel Cariou, Ronan Bruno, Le Bizec ; Dervilly-Pinel, Gaud/B-5060-2016 Bichon, Emmanuelle/0000-0001-7731-8808; Dervilly-Pinel, Gaud/0000-0002-1867-0008; Cariou, Ronan/0000-0002-4669-1834 "Association Nationale de la Recherche et de la Technologie" (ANRT)French National Research Agency (ANR) The authors are grateful to Aaron Parker and Jean-Marie Casanova (Markes) as well as Benedicte Gauriat and Stephane Decouflet (Thermo) for providing access to their analytical platforms and for technical support. The authors would like to kindly thank Laura McGregor and Carmen Panayi for their proofreading of English. The "Association Nationale de la Recherche et de la Technologie" (ANRT) is acknowledged for its financial support. 1 15 24 Elsevier Amsterdam 1873-3778; International audience; Polyester-polyurethane lacquer, used to cover the inner surface of metallic food contact materials, may transfer non-intentionally added substances (NIAS) to the food. The identification of such a diversity of compounds, considered as migrating substances, requires taking advantage of complementary analytical platforms. Therefore, four types of gas chromatography-mass spectrometry (GC-MS) couplings were investigated and compared for their abilities to identify migrating substances after acetonitrile extraction of two commercialised lacquers. In parallel, various ionisation sources, i.e. electron ionisation (EI) (70 eV and soft energies) and atmospheric-pressure chemical ionisation (APCI) as well as various mass analysers, i.e. quadrupole, time-of-flight (low and high resolution) and Orbitrap, were tested. Comparison of mass spectra with a commercial library for EI ionisation source led to the identification of two NIAS compounds, isophorone diisocyanate and 4,4'-diphenylmethane diisocyanate. Additionally, many cyclic oligoesters (four monomer units) were unambiguously identified according to supplier's declaration on starting materials used, primarily based on the molecular ion observed by APCI mode and characteristic fragment ions. High resolution mass analysers also enhanced confidence level in such NIAS identification. One- and two-dimensional GC were also investigated for separation assessment. Although GC x GC did not reveal additional NIAS, its use provided a valuable mapping of oligomers according to monomers composition. These results were compared to our previously published LC-MS study, carried out on the same lacquer samples. This study shows that LC and GC, along with their related ionisation techniques and their own selectivity, are complementary approaches, revealing different classes of compounds covering a wide range of volatility and polarity.

International audience; In the present work, we address the issue of nontargeted screening of organohalogenated chemicals in complex matrixes. A global strategy aiming to seek halogenated signatures in full-scan high-resolution mass spectrometry (HRMS) fingerprints was developed. The resulting all-in-one user-friendly application, HaloSeeker 1.0, was developed to promote the accessibility of associated in-house bioinformatics tools to a large audience. The ergonomic web user interface avoids any interactions with the coding component while allowing interactions with the data, including peak detection (features), deconvolution, and comprehensive accompanying manual review for chemical formula assignment. HaloSeeker 1.0 was successfully applied to a marine sediment HRMS data set acquired on a liquid chromatography heated electrospray ionization [LC-HESI(-)] Orbitrap instrument (R = 140 000 at m/z 200). Among the 4532 detected features, 827 were paired and filtered in 165 polyhalogenated clusters. HaloSeeker was also compared to three similar tools and showed the best performances. HaloSeeker's ability to filter and investigate halogenated signals was demonstrated and illustrated by a potential homologue series with C12HxBryClzO2 as a putative general formula.

The emerging chemicals challenge clearly appears as a major current concern for the scientific community, societal actors, and public authorities. However, this issue still remains imperfectly defi...