Multi-contaminant analysis of organophosphate and halogenated flame retardants in food matrices using ultrasonication and vacuum assisted extraction, multi-stage cleanup and gas chromatography–mass spectrometry

• Published in: Journal of Chromatography A Vol. 1401; pp. 33 - 41
• Main Authors: Xu, Fuchao, García-Bermejo, Ángel, Malarvannan, Govindan, Gómara, Belén, Neels, Hugo, Covaci, Adrian
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 03-07-2015
• Subjects: Animals; BFRs; Eggs - analysis; Environmental Pollutants - analysis; Fishes; Flame retardants; Flame Retardants - analysis; Food analysis; Food Technology - methods; Gas Chromatography-Mass Spectrometry; Halogenated Diphenyl Ethers - analysis; Halogenation; Organophosphates - analysis; PFRs; Seafood - analysis; Solid Phase Extraction; UVAE; Vacuum; Flame retardants; UVAE; PFRs; BFRs; Food analysis
• ISSN: 0021-9673; 1873-3778
• DOI: 10.1016/j.chroma.2015.05.001

•First specific method for multi-class flame retardants in food matrices.•New extraction technique based on QuEChERS with a high extraction yield.•Multi-step clean-up for removal of lipids and pigments from food samples.•Method LOQs (wet weight) were in the pg/g range for BFRs and ng/g range for PFRs.
A multi-residue analytical method was developed for the determination of a range of flame retardants (FRs), including polybrominated diphenyl ethers (PBDEs), emerging halogenated FRs (EFRs) and organophosphate FRs (PFRs), in food matrices. An ultrasonication and vacuum assisted extraction (UVAE), followed by a multi-stage clean-up procedure, enabled the removal of up to 1g of lipid from 2.5g of freeze–dried food samples and significantly reduce matrix effects. UVAE achieves a waste factor (WF) of about 10%, while the WFs of classical QuEChERS methods range usually between 50 and 90%. The low WF of UVAE leads to a dramatic improvement in the sensitivity along with saving up to 90% of spiking (internal) standards. Moreover, a two-stage clean-up on Florisil and aminopropyl silica was introduced after UVAE, for an efficient removal of pigments and residual lipids, which led to cleaner extracts than normally achieved by dispersive solid phase extraction (d-SPE). In this way, the extracts could be concentrated to low volumes, e.g. <100μL and the equivalent matrix concentrations were up to 100g ww/mL. The final analysis of PFRs was performed on GC–EI-MS, while PBDEs and EFRs were measured by GC–ECNI-MS. Validation tests were performed with three food matrices (lean beef, whole chicken egg and salmon filet), obtaining acceptable recoveries (66–135%) with good repeatability (RSD 1–24%, mean 7%). Method LOQs ranged between 0.008 and 0.04ng/g dw for PBDEs, between 0.08 and 0.20ng/g dw for EFRs, and between 1.4 and 3.6ng/g dw for PFRs. The method was further applied to eight types of food samples (including meat, eggs, fish, and seafood) with lipid contents ranging from 0.1 to 22%. Various FRs were detected above MLOQ levels, demonstrating the wide-range applicability of our method. To the best of our knowledge, this is the first method reported for simultaneous analysis of brominated and organophosphate FRs in food matrices.