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Graphical abstract Highlights • NiO, a new cataluminescence sensing material, was synthesized by a simple template-free hydrothermal method. • Camellia-like NiO with high specific surface area showed excellent sensing performance towards H 2 S. • The sensing mechanism was studied which proved the main emission peak is from SO 2 *. Abstract In this work, three different microstructures of NiO nanomaterials including tremella, camellia and hexagonal nanosheets were successfully synthesized by a simple template-free hydrothermal method. Among them, camellia-like NiO was reported and applied to cataluminescence (CTL) for the first time. SEM, TEM, XRD, XPS, BET and BJH were employed to characterize the as-prepared samples. As sensing materials, these NiO with various morphologies showed different CTL capabilities to detect H 2 S, and the camellia-like NiO exhibited the best catalytic performance with high sensitivity and selectivity, which may be attributed to the synergistic effect of its high specific surface area, porous nanostructure, as well as the surface adsorption oxygen. After optimization, a good linear relationship was obtained in the range of 0.8–30.8 ppm and the detection limit (S/N = 3, LOD) was 0.3 ppm. Sixteen common volatile organic compounds (VOCs), such as carbon disulfide, ethyl mercaptan and formaldehyde, were discussed as possible interferent components, and the sensing mechanism of the CTL sensing towards H 2 S was discussed in detail. Camellia-like NiO could be used as a new sensing material for H 2 S monitoring. [ABSTRACT FROM AUTHOR]

• The SO-DLLME combined with MECC was developed for determination of fluoroquinolones. • Deep eutectic solvent (DES) was used as an extraction solvent combined with back extraction. • A detection limit less than 10 ng mL−1 for fluoroquinolones could be achieved. • The method was successfully applied to determination of fluoroquinolones in food and water samples. A simple and sensitive salting out-assisted dispersive liquid-liquid microextraction method using deep eutectic solvent combined with back extraction and micellar electrokinetic capillary chromatography (SO-DLLME-DES-BE-MECC) was developed for the determination of fluoroquinolones in milk, honey and water samples. Several parameters affecting the extraction efficiency including DES volume, vortex time, centrifugation time, salt type and amount, sample pH and volume, etc. were investigated. Good linearity were obtained for fluoroquinolones in a range of 0.020–3.200 μg mL−1 and 0.030–4.800 μg mL−1 with LODs less than 0.010 μg mL−1. The recoveries were in the ranges of 95.0–104.9%, 90.1–110.2% and 87.8–114.1% for water, honey and milk samples, respectively. The relative standard deviations for reproducibility were all below 7.6%. Under the optimized conditions, the enrichment factors for analytes were achieved in the range from 531 to 858 folds. The presented method was successfully applied for the determination of fluoroquinolones in milk, honey and water samples. [ABSTRACT FROM AUTHOR]

• The hypothesis that propofol alters gut microbes was tested in a rat model with continuous intravenous infusion of propofol. • Changes in the abundance and diversity of intestinal flora were assessed by 16s ribosomal RNA sequencing and fecal sample analysis. • The results indicate that continuous intravenous infusion of propofol had little effect on intestinal flora of rats in a short period of time. Under normal circumstances, the gut microbiota, host, and external environment establish a dynamic ecological balance and maintain human health. Once this balance is broken, the intestinal flora dysregulation will form, manifested by changes in the diversity, richness, proportion, location and biological characteristics of the gut microbiota. The hypothesis that propofol alters gut microbes was tested in a rat model with continuous intravenous infusion of propofol. Eight male wistar rats underwent tail vein puncture and catheterization respectively, and were continuously pumped with propofol for 3 h. Feces were collected from each rat before and on the 1 st, 3rd, 7th and 14th days after intervention. Finally, the effect of continuous intravenous infusion of propofol on the intestinal flora of rats was analyzed by high-throughput 16S rRNA gene amplification sequencing. Through high-throughput 16S rRNA gene amplicon sequencing analysis, we found that continuous intravenous infusion of propofol had little effect on intestinal flora in rats. Analysis of Alpha (shannon diversity index) showed that group A-7 was different from group P and group A-1 (P = 0.034), and recovered on the 14th day. Although the species diversity analysis showed a significant difference among the five groups (P = 0.049), the distribution of most fecal samples in the PCoA showed a clustered distribution, indicating similarity. In addition, no significant difference was found in the statistical KEGG difference pathway through LEfSe analysis. [ABSTRACT FROM AUTHOR]