Effervescence tablets based on magnetic ionic liquids as simple microdevices for the in situ dispersive liquid-liquid microextraction of urinary biomarkers

• Published in: Analytica chimica acta Vol. 1328; p. 343187
• Main Authors: González-Martín, Raúl, Trujillo-Rodríguez, María J., Freire, Mara G., Ayala, Juan H., Pino, Verónica
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.11.2024
• Subjects: Biomarkers - analysis; Biomarkers - urine; Effervescence tablets; Humans; In situ dispersive liquid-liquid microextraction; Ionic Liquids - chemistry; Limit of Detection; Liquid Phase Microextraction - methods; Magnetic ionic liquids; Magnetic Phenomena; Magnetic separation; On-site microextraction; Tablets - chemistry; Urine; Urine; On-site microextraction; Effervescence tablets; Magnetic separation; Magnetic ionic liquids; In situ dispersive liquid-liquid microextraction
• ISSN: 0003-2670; 1873-4324; 1873-4324
• DOI: 10.1016/j.aca.2024.343187

Magnetic ionic liquids (MILs) have been explored in dispersive liquid-liquid microextraction (DLLME). Their usage allows to substitute centrifugation and/or filtration steps by a quick magnetic separation. Besides, effervescence-assisted DLLME is one of the most known options to improve the dispersion of the extractant in the sample, while allowing to avoid the consumption of external energy during dispersion. Despite these interesting features, only one study incorporates MILs containing the tetrachloroferrate anion in effervescence tablets. These MILs are highly viscous and liquid at room temperature, thus compromising the stability of the tablets when used as extraction microdevices in effervescence-assisted DLLME, and only allowing their use in the conventional MIL-DLLME mode. A new class of effervescence tablets containing a Ni(II)-based MIL, that is solid at room temperature, is here proposed. This type of tablets permits their use, for first time, in the in situ DLLME mode, occurring through the transformation of a water-soluble MIL into a water-insoluble MIL microdroplet. This way, the tablet formulation included: the MIL, the metathesis reagent lithium bis[(trifluoromethyl)sulfonyl]imide, NaH2PO4 and K2CO3 as effervescence precursors salts, and Na2SO4 as salting-out and desiccating agent. The method is combined with high-performance liquid-chromatography and both fluorescence and ultraviolet detection, for the determination of monohydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) and benzophenones (BPs), as biomarkers in urine. The method simply involved the addition of the effervescence tablet to the sample, thus taken place simultaneously the effervescence process and the metathesis reaction, without requiring any external energy consumption. The method presented limits of detection down to 10 ng L−1 for OH-PAHs and to 0.60 μg L−1 for BPs, inter-day relative standard deviations lower than 17 %, and average relative recoveries of 94 % in urine. The determined OH-PAHs contents in urine were between 0.40 and 16 μg L−1, and between 17.8 and 334 μg L−1 for BPs. We have developed the first MIL-based effervescence tablets that are completely solid, thus improving the stability and robustness of these microdevices with respect to previously reported tablets involving MILs, while permitting to perform into the in situ DLLME mode (thus gaining in extraction efficiency). This approach including the MIL-based effervescence tablets constitutes an alternative on-site platform for the analysis of urine, as satisfactory precision, accuracy, and sensitivity are achieved despite not involving any external energy input within the analytical sample preparation setup. This method also constitutes the first application of MIL-based effervescence tablets for bioanalysis. [Display omitted] •A new type of effervescence tablets containing a water-soluble Ni(II)-based MIL.•The MIL is solid at room temperature, improving the stability of the tablets.•The tablet formulation ensures the in situ formation of a water-insoluble MIL.•The effervescence promotes dispersion without any external energy assistance.•The method succeeds determining urinary biomarkers with simple magnetic retrieval.