• Adsorption, reduction and precipitation were involved in Cr(VI) removal process. • Cr(VI) removal mechanisms were extremely dependent on solution pH.

Herein, a novel method, magnetic effervescent tablet-assisted ionic liquid-based dispersive liquid-liquid microextraction (META-IL-DLLME), was pioneered for extraction and preconcentration of polybrominated diphenyl ethers (PBDEs) in liquid matrix samples. In this proposed method, a magnetic effervescent tablet, containing CO 2 sources, ionic liquids and Fe 3 S 4 magnetic nanoparticles (MNPs), combines extractant dispersion and magnetic recovery into one-step. Fe 3 S 4 was synthesized, characterized and applied it for the first time to the newly developed method, and its extraction recoveries (ERs) for PBDEs were 20.8-32.0% higher than those of conventional Fe 3 O 4 MNPs. The increased ERs of Fe 3 S 4 resulted from its larger specific surface area and pore size. Some important parameters were rigorously optimized, such as kinds of magnetic nanoparticles, effervescent agents, extraction solvents and their volumes, elution solvents, extraction temperature and salt addition. Under the optimized conditions, the META-IL-DLLME method combined with HPLC-DAD analysis gave the linear ranges of 0.1-0.5-100 µg L −1 with correlation coefficients of > 0.9990. The ERs ranged from 80.7% to 99.3%, and the limits of detection and quantitation were 0.012-0.078 µg L −1 and 0.04-0.26 µg L −1 , respectively. The intra-and inter-day precisions, expressed as relative standard deviations (RSD, n = 6), were 1.32-4.83% and 1.99-4.25%, respectively. To evaluate its matrix effect, the relative recoveries of PBDEs from tap and river water, skim and whole milk, pregnant women and women serum samples at three fortification levels (2.0, 5.0 and 20.0 µg L −1) were in the range of 77.3-106.7%. Overall, the commercial Fe 3 O 4 MNPs can only be used for magnetic separation in microextraction procedures, while Fe 3 S 4 MNPs gave the higher adsorption and extraction efficiency for organic analytes besides the convenient magnetic separation. Therefore, the results obtained in this study provide a superior alternative for the conventional magnetic separation and adsorbent material. Also, this newly developed method has a great potential in routine monitoring of liquid matrix samples.

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Background In past few years, long non-coding RNAs (lncRNAs) have been reported to play regulatory roles during cancer progression. LncRNA SNHG10 has been explored in several sorts of cancers. However, its detailed role and mechanism are still not well understood in glioma. Methods Expression levels of genes were evaluated by RT-qPCR. EdU, TUNEL, sphere formation, wound healing and transwell assays appraised the effect of SNHG10 on glioma cellular processes. The interaction between molecules was examined by ChIP, RIP, RNA pull down and luciferase reporter assays. Results High level of SNHG10 was detected in glioma cells. Functional assay confirmed that SNHG10 promoted the proliferation, migration, invasion and stemness of glioma cells. Moreover, miR-532-3p was validated to bind with SNHG10 and expressed at a low level in glioma cells. Importantly, miR-532-3p exerted inhibitory functions in glioma. Furthermore, it was found that FBXL19 targeted by miR-532-3p facilitated cell growth and stemness in glioma, and that SNHG10 worked in glioma by increasing FBXL19 expression through sequestering miR-532-3p. More importantly, ETS1 promoted the transcription of SNHG10 and it mediated contribution to the malignant behaviors of glioma cells by SNHG10/miR-532-3p/FBXL19 signaling. Conclusion SNHG10 was transcriptionally activated by ETS1 and played an oncogenic role in glioma by sponging miR-532-3p and up-regulating FBXL19.