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Tanshinone IIA has a potential therapeutic effect on cerebral ischemia/reperfusion injury (CIRI). In this study, tanshinone IIA was encapsulated in poly(lactic-co-glycolic acid)-block-poly (ethylene glycol)-carboxylic acid (PLGA-PEG-COOH) nanoparticles, and its therapeutic efficacy on CIRI was investigated. Morphology and dynamic light scattering analyses were performed to identify and optimize nano-formulations. A drug release test was conducted using the dialysis method. The cytotoxic effect of tanshinone IIA on human neuroblastoma cells (SH-SY5Y) and brain endothelial capillary cells (hCMEC/D3) was measured using the MTT assay. The protective effect of PLGA-PEG-COOH-encapsulated tanshinone IIA against CIRI was evaluated in oxygen and glucose deprivation/reoxygenation-induced SH-SY5Y/IR cells and middle cerebral artery occlusion (MCAO) rats. Results showed that PLGA-PEG-COOH-encapsulated tanshinone IIA promoted viability and inhibited apoptosis of SH-SY5Y/IR cells (P < 0.01). Moreover, PLGA-PEG-COOH-encapsulated tanshinone IIA facilitated the invasion of SH-SY5Y/IR cells and repressed inflammation in MCAO rats (P < 0.01). Noteworthy, PLGA-PEG-COOH-encapsulated tanshinone IIA combined with angiopep-2 peptide presented a better inhibitory effect on CIRI than tanshinone IIA alone (P < 0.01). Angiopep-2 peptide contributes to traversing blood–brain barrier by recognizing lipoprotein-related protein expressed in the brain capillary endothelial cells. In conclusion, PLGA-PEG-COOH-encapsulated tanshinone IIA plus angiopep-2 peptide holds promising therapeutic potential toward CIRI.

The electrochemical reduction of biomass-derived furfural (FF) is an advantageous route to alleviate the consumption of fossil fuels and hydrogen. However, the development of efficient catalytic systems to obtain furfuryl alcohol (FAL) with high selectivity is still challenging. Herein, a copper nitride nanowire catalyst in situ grown on copper foam (Cu3N Nw/CF) is synthesized, which achieves nearly 100% selectivity for FAL with 94.6% faradaic efficiency (FE) in the electrochemical reduction of FF. Thiol assembly and operando Raman investigations reveal an adsorptive hydrogen (Hads) dependent electrocatalytic hydrogenation (ECH) pathway for FAL production. Moreover, electrokinetic studies have demonstrated that the FF hydrogenation on Cu3N Nw/CF follows the Langmuir–Hinshelwood (L–H) mechanism. The much higher activity of Cu3N Nw/CF than that of copper foam (CF) is due to the promoted Hads spillover from water dissociation, which then reacts efficiently with FF via the ECH mechanism. Furthermore, density functional theory (DFT) calculations verify that the superior water dissociation ability and the preferable parallel FF adsorption on Cu3N synergistically enhance the thermodynamics and kinetics of FAL production. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: Solar‐driven cross‐coupling reactions by dual nickel/photocatalysis under mild conditions have received considerable attention. However, the existing photo/nickel dual catalytic cross‐coupling reactions require the addition of expensive photosensitizers and organic ligands, and the catalytic activity is inadequate. Herein, we report a nickel single‐atom heterogeneous catalyst supported on mesoporous carbon nitride for photocatalytic C—O coupling reaction between 4‐bromobenzonitrile and ethanol, affording 4‐ethoxybenzonitrile in excellent yield compared to a semi‐heterogeneous catalytic system. The catalytic system exhibits a broad substrate scope including ketones, aldehydes, esters, and amides. This work presents a simple and cost‐effective strategy for anchoring metal single atoms onto carbon nitride, providing a new platform for enabling high‐performance photocatalytic production of aryl ether compounds. [ABSTRACT FROM AUTHOR]