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Designing a structurally stable anode with a high reversible capacity for sodium ion batteries (SIBs) is particularly crucial so that batteries are able to meet the requirements for large-scale applications in grid electrical energy storage. Polyaromatic hydrocarbons (PAHs) are organic molecules with well-defined structures that demonstrate excellent performance in lithium storage. Based on our well-established correlation between battery property and molecular structure, for the first time, we applied a recently synthesized hexabenzocoronene (HBC) and corresponding derivate HBC–OMe to engage in sodium storage. The HBC molecule forms self-assemblies with a long-range ordered face-center cubed (fcc) structure due to the interaction between two HBC moieties. Such a unique 3D structure is expected to generate a strong π–π interaction between flakes and thus yield amazing durability during the long-term cycling process. In addition, the surface-dominated Na+ storage mechanism can facilitate the Na+ transport kinetics and simultaneously alleviate the structural strain during charging–discharging cycles. Benefiting from the coupling effect of the surface-driven capacitive process and the robust 3D self-assembled hierarchical nature, an oxygen-containing sample, HBC–OMe, exhibited an extraordinary sodium storage capability, attaining a high capacity of 506 mA h g−1 at 0.1 A g−1 with excellent rate capability (217 mA h g−1 at 5 A g−1) and superior long-term cycling performance (290 mA h g−1 at 2 A g−1 with negligible capacity fade after 1000 cycles). [ABSTRACT FROM AUTHOR]

Rehmannia glutinosa Libosch (RG), is officially listed in the Chinese Pharmacopoeia and is widely used in China. In this paper, a sensitive and rapid ultra-performance liquid chromatography-mass spectrometry method including multiple-reaction monitoring mode was developed and applied to study the pharmacokinetic effect of acteoside from total glycoside extracted from the leaves of Rehmannia (TLR) and Dihuangye total glycoside capsule (DTG) in normal and diabetic nephropathy rats. The diabetic nephropathy rat model was induced by intraperitoneal injection of a small dose of streptozotocin and high-fat diet and plus 5% glucose drinking water. Samples of plasma of rats were obtained at different times after rats were administered TLR (7.2 g/kg) and DTG (360 mg/kg). After deproteinization by acetonitrile, the concentrations of acteoside in rats at different time points were detected by UPLC-TQ-MS method and pharmacokinetics parameters were calculated using DAS 3.2.8 software. A good linearity of acteoside was shown in the range of 8.51-3404.8 ng/m L ( r2 = 0.9987). The mean extraction recovery of analyte was in the range of 63.55-79.49%, and the intra- and inter-day RSD values were <8.8%. Compared with the normal group, the maximum plasma concentration, AUC0- t, AUC0-∞ and apparent plasma clearance corresponding dose in model group rats decreased significantly. After rats were administered TLR and DTG, the acteoside reached the maximum plasma concentration at about 15 min. The method proved to be simple, rapid and specific, and to be suitable for the determination of acteoside in plasma of diabetic nephropathy rats and pharmacokinetic study. [ABSTRACT FROM AUTHOR]

Graphical abstract Abstract Diabetic nephropathy (DN) is a complication of diabetes that is caused by uncontrolled high blood sugar. It has been reported that Salvia miltiorrhiza (SM) possesses the ability to prevent kidney damage, although the mechanisms remain unclear. The study was to investigate whether and how SM improved DN injury via regulation of metabolome and the molecular mechanisms. In this study, SD rats were fed a high glucose / high fat diet accompanied by 0.5% glucose water. Three weeks later, the rats were given one intraperitoneal injection of 30 mg/kg STZ each day for three days for DN model. The biochemical indicators and metabolomics of plasma, urine and renal tissue were analyzed. Then the western blotting analysis of renal tissue and glomerular mesangial cells were investigated. The results showed that Salvia miltiorrhiza extracts improved the renal injury and regulation of abnormal glycolipid metabolism. The metabolites in serum, urine and renal tissues have been changed significantly. The involved metabolic pathways mainly include phospholipid, arachidonic acid, and pyrimidine metabolisms. Meanwhile, SM inhibited the relative expression levels of wnt4, β-catenin and TGF- β in renal tissue and high-glucose induced glomerular mesangial cells. [ABSTRACT FROM AUTHOR]