In this study, an ultrasonic-assisted procedure for the extraction of mulberry leaf polysaccharides (MLPs) was investigated using response surface methodology with a 29-run Box–Behnken design. Four factors were investigated, and it was found that the factors influencing the process, in order of significance, were the extraction temperature > liquid-to-material ratio > ultrasonic power. Considering practical conditions, the parameters were adjusted to a liquid-to-material ratio of 16:1 mL/g, extraction time of 58 min, extraction temperature of 65 °C, and ultrasonic power of 500 W. Under these conditions, the yield of MLPs was 14.47%, which is close to the predicted value, indicating that the extraction process optimized by response surface methodology (RSM) is feasible. The separation and purification effects of macroporous resin and activated carbon on MLPs were investigated, with the D152 resin being considered the most suitable choice. The optimal separation conditions were found to be a sample concentration of 0.5 g/mL and an optimal flow rate of 1 mL/min. Thin-layer chromatography and infrared spectroscopy revealed that polysaccharides extracted from mulberry leaves are primarily composed of rhamnose, xylose, and arabinose. In conclusion, this study successfully optimized the ultrasonic-assisted extraction process of MLPs through response surface methodology, determined the optimal parameter combination, and verified its efficiency and stability. Under the optimal conditions obtained for ultrasonic-assisted extraction, the yield of MLPs is significantly higher than that reported in the previous literature. The decolorization process of crude mulberry leaf polysaccharide extract was also investigated, and the purified MLPs have clear monosaccharide composition and structural characteristics, providing a theoretical basis and technical support for their application in functional food or drug development.

Ionic liquid-assisted extraction can improve the recovery of monoterpene glycosides from Radix Paeoniae Alba, whereas post-extraction purification and ionic-liquid-associated marker-level quality control remain necessary before further bioactivity evaluation. In this study, a macroporous resin-based purification process was developed for monoterpene glycoside-enriched extracts obtained by conventional reflux extraction and ionic liquid-assisted microwave–ultrasound extraction. Among the five tested resins, AB-8 resin showed the best adsorption performance and was selected for further process optimization. The optimized purification conditions were a loading concentration of 13 mg/mL, loading pH of 7, elution with 70% ethanol, loading volume of 6 BV and elution volume of 9 BV. After purification, the total quantified monoterpene glycoside content increased from 6.59% to 51.68% in the conventional extract and from 15.30% to 75.30% in the ionic liquid-assisted extract. The ionic-liquid-associated elemental marker content in the ionic liquid-assisted extract decreased from 5.593% to 0.072% after purification, corresponding to an approximately 98.7% reduction at the elemental-marker level. Stability evaluation indicated that Na₂SO₃, Fe³⁺, ascorbic acid, sucrose and light exposure affected the detected monoterpene glycoside content to different extents, whereas short-term heating within 20–80 °C caused only slight fluctuations. The purified extracts showed stronger DPPH and ABTS radical scavenging activities and reducing power than the crude extracts. In LPS-stimulated RAW264.7 cells, the purified extracts reduced NO production and downregulated the mRNA expression of IL-6, IL-1β, TNF-α, iNOS and COX-2, suggesting anti-inflammatory potential at the NO and gene-expression levels. AB-8 resin purification enriched the monitored monoterpene glycosides, reduced the selected ionic-liquid-associated elemental marker, and generated purified fractions suitable for subsequent stability and bioactivity evaluation.

Radix Paeoniae Alba, the dried root of Paeonia lactiflora Pall., contains characteristic monoterpene glycosides, but efficient recovery of these polar constituents remains challenging. This study developed an ionic liquid-assisted sequential ultrasound–microwave extraction method and evaluated paeoniflorin, oxypaeoniflorin and albiflorin by HPLC as multi-marker responses. Among the ionic liquids tested, 1-propyl-3-methylimidazolium dihydrogen phosphate showed the best extraction response. Box–Behnken response surface optimization gave practical extraction conditions of a solid-to-liquid ratio of 1:26 g/mL, ionic liquid concentration of 0.12 mol/L and ultrasound time of 22 min. Under these conditions, paeoniflorin and total marker glycosides reached 29.12 and 34.98 mg/g dry material, respectively, representing increases of 32.4% and 34.5% compared with conventional reflux extraction. UPLC-QTOF-MS profiling provided complementary chemical profile information for the optimized extract and tentatively annotated Paeonia-related monoterpene glycoside derivatives, galloylated glucose derivatives and polyphenolic constituents. Electrostatic potential, SAPT and non-covalent interaction analyses, supported by ¹H NMR chemical shift perturbation, suggested possible hydrogen bonding, electrostatic and dispersion interactions between paeoniflorin and the selected ionic liquid. These results support the optimized process as an efficient extraction approach and provide molecular interaction insights into ionic liquid-assisted recovery of monoterpene glycosides.

Oil-mist coalescing filters are commonly compared using filtration efficiency and pressure drop from short tests, although retained liquid continues to redistribute during operation. This critical review examines how liquid morphology, distribution and connectivity affect the interpretation of wet performance and service-life evidence. Imaging reveals substantial local saturation differences and extensive inter-fiber liquid structures. Within one hybrid–Janus comparison, whole-filter saturation ranged from 54.47% to 61.96%, whereas source-reported wet-to-clean pressure-drop ratios ranged from 3.32 to 22.36. These observations support considering liquid arrangement alongside bulk inventory, but do not isolate connectivity from pore geometry and wettability. Long-duration experiments also show that drainage can coexist with pressure-drop creep over 1100 h. We distinguish measured endpoints, observation durations and lifetime estimates extrapolated from short degradation records. A traceable service-life claim requires defined loading and operating conditions, concurrent resistance and outlet measurements, an explicit endpoint, and separation of measured duration from predicted life. A proposed reporting framework and a conditional pressure-scaling analysis identify the evidence needed to assess transfer from laboratory media to compressed-air cartridges.