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SENSORS AND ACTUATORS B-CHEMICAL · 2025 · IF 7.7

Simultaneous profiling of cholinesterases and NAD(P)H in murine hippocampus via a dual-responsive indicator to investigate cholinergic impairment in Alzheimer's disease

Bin Jiang,Jiayun Guan,Yilin Lv,Chaojie Yang,Minfeng Yang,Xinyu Shen,Bin Xu,Qi Wang,Yuling Qin,Li Wu

The cholinergic hypothesis constitutes a pivotal theoretical framework for elucidating the pathological mechanisms underpinning Alzheimer's disease (AD). Quantitative assessment of cholinesterases (ChEs) and NAD(P)H levels in neuronal cells, particularly within the septo-hippocampal pathway, is imperative for the comprehensive study of the cholinergic system. In this study, we designed and synthesized a dual-channel, dual-enzyme-responsive fluorescent indicator that was chemically optimized for detecting levels of ChEs and NAD(P)H in neuronal cells. Biological experiments demonstrated that this indicator can sensitively and reliably visualize the dynamics of intracellular ChEs and NAD(P)H following stimulation. The corresponding ChEs activities and NAD(P)H concentrations demonstrated a linear correlation with fluorescence intensity, reaching equilibrium within a few minutes. This innovative and precise technique for visualizing ChEs and NAD(P)H dynamics with high spatial resolution during the progression of AD is expected to serve as a robust tool for investigating alterations in the cholinergic nervous system, including changes in acetylcholine neurotransmission and neuronal energy metabolism.

CAS / MDL: 50-23-7
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Acta Biomaterialia · 2022 · IF 10.633

Injectable temperature-sensitive hydrogel system incorporating deferoxamine-loaded microspheres promotes H-type blood vessel-related bone repair of a critical size femoral defect

Yuwei Zeng,Chuang Huang,Dongming Duan,Aiju Lou,Yuan Guo,Tianhua Xiao,Jianguo Wei,Song Liu,Zhao Wang,Qihao Yang,Lei Zhou,Zenghui Wu,Le Wang

Insufficient vascularization is a major challenge in the repair of critical-sized bone defects. Deferoxamine (DFO) has been reported to play a potential role in promoting the formation of H-type blood vessels, a specialized vascular subtype with coupled angiogenesis and osteogenesis. However, whether DFO promotes the expression of H-type vessels in critical femoral defects with complete periosteal damage remains unknown. Moreover, stable drug loading systems need to be designed owing to the short half-life and high-dose toxic effects of DFO. In this study, we developed an injectable DFO-gelatin microspheres (GMs) hydrogel complex as a stable drug loading system for the treatment of critical femoral defects in rats. Our results showed that sustained release of DFO in critical femoral defects stimulated the generation of functional H-type vessels. The DFO-GMs hydrogel complex effectively promoted proliferation, formation, and migration of human umbilical vein endothelial cells in vitro. In vivo , the application of the DFO-GMs hydrogel complex expanded the distribution range and prolonged the expression time of H-type vessels in the defect area and was positively correlated with the number of osterix+ cells and new bone tissue. Topical application of the HIF-1α inhibitor PX-478 partially blocked the stimulation of H-type vessels by DFO, whereas the osteogenic potential of the latter was also weakened. Our results extended the local application of DFO and provided a theoretical basis for targeting H-type vessels to treat large femoral defects. Statement of significance Abundant functional blood vessels are essential for bone repair . The H-type blood vessel is a functional subtype with angiogenesis and osteogenesis coupling potential. A drug loading system with long-term controlled release was first used to investigate the formation of H-type blood vessels in critical femoral defects and promotion of bone repair. Our results showed that the application of DFO-GMs hydrogel complex expanded the distribution range and expression time of H-type vessels, and was positively correlated with the number of osteoblasts and volume of new bone tissue. These results expanded the local application approach of DFO and provide a theoretical basis for targeting H-type vessels to treat large femoral defects.

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ACS Omega · 2020 · IF 2.87

Electrosynthesis of Quinazolines and Quinazolinones via an Anodic Direct Oxidation C(sp3)-H Amination/C-N Cleavage of Tertiary Amine in Aqueous Medium

Zhenghong Zhou,Kangfei Hu,Jiawei Wang,Zhibin Li,Yan Zhang,Zhenggen Zha,Zhiyong Wang

An electrochemical synthesis for quinazolines and quinazolinones was developed via a C(sp3)-H amination/C-N cleavage by virtue of the anodic oxidation. The reaction can be carried out in aqueous media under mild conditions to afford the desired products with high yields. The reaction mechanism was proposed after detailed investigation.

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Frontiers of Chemical Science and Engineering · 2017 ·Vol. 11 ·期 4 ·564-574 · IF 1.712

The effect of doping and steam treatment on the catalytic activities of nano-scale H-ZSM-5 in the methanol to gasoline reaction

Song Baodong,Li Yongqiang,Cao Gang,Sun Zhenhai,Han Xu

In the transformation of methanol to gasoline (MTG), the selectivity to gasoline and the aromatic content in the produced gasoline are important factors. The catalytic activities of steam-treated and non-steam-treated nano-scale H-ZSM-5 (NHZ5) catalysts impregnated with Ag(I), Zn(II) or P(V) have been investigated in a continuous flow fixed bed reactor. The NH 3 -TPD results showed that after impregnation, the Ag/NHZ5, Zn/NHZ5 and P/NHZ5 catalysts contained comparatively more strong, medium-strong and weak acid sites, respectively. Treatment with steam decreased the number of acid sites in all the catalysts, but the pore volumes in the catalysts were larger which improved carbon deposition resistance resulting in prolonged lifetimes. After 6 h of MTG reaction, the selectivity to gasoline for the steam-treated catalysts, \(Ag_{H_2 O} /NHZ5\) , \(Zn_{H_2 O} /NHZ5\) and \(P_{H_2 O} /NHZ5\) were 70.5, 68.4 and 68.7 wt-%, respectively, whereas their respective aromatic contents in the produced gasoline were 61.9, 55.4 and 39.0 wt-%. Thus \(P_{H_2 O} /NHZ5\) is the most promising catalyst for MTG applications which can meet the China IV gasoline standard that the amount of aromatics in gasoline should be less than 48 wt-%.

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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2024 ·Vol. 31 ·期 16 ·24398-24411 · IF 0

Structural/surface characterization of transition metal element–doped H-ZSM-5 adsorbent for CH3SH removal: identification of active adsorption sites and deactivation mechanism

Xie Yuxuan,Peng Xiao,Song Xin,Ning Ping,Sun Xin,Ma Yixing,Wang Chi,Li Kai

CH 3 SH is a potential hazard to both chemical production and human health, so controlling its emissions is an urgent priority. In this work, a series of transition metal-loaded H-ZSM-5 adsorbents (Si/Al = 25) (Cu, Fe, Co, Ni, Mn, and Zn) were synthesized through the wet impregnation method and tested for CH 3 SH physicochemical adsorption at 60 °C. It was shown that the Cu-modified H-ZSM-5 adsorbent was much more active for CH 3 SH removal due to its abundant strong acid sites than other transition metal-modified H-ZSM-5 adsorbents. The detailed physicochemical properties of various modified H-ZSM-5 adsorbents were characterized by SEM, XRD, N 2 physisorption, XPS, H 2 -TPR, and NH 3 -TPD. The effects of metal loading mass ratio, calcination temperature, and acid or alkali modification on the performance of the adsorbent were also investigated, and finally 20% Cu/ZSM-5 was found to have the best adsorption capacity after calcined at 350 °C. Additionally, the Cu/ZSM-5 adsorbent modified by sodium bicarbonate could expose more active components, which improved the adsorbent’s stability. However, the consumption and reduction of the active component Cu 2+ and the accumulation of sulfate during the adsorption process are the main reasons for the deactivation of the adsorbent. In addition, the simultaneous purging of N 2  + O 2 can effectively restore the adsorption capacity of the deactivated adsorbent and can be used as a potential strategy to regenerate the adsorbent. Graphical

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Surfaces and Interfaces · 2025 · IF 6.3

Magnetically aligned h-BN-modified superporous carbon foam skeletons-based form-stable phase-change materials for superior thermal conductivity and photothermal conversion efficiency

Ziqian Ding,Xiaolin Qiu,Huaxuan Liu,Lingli Gu

Functional form-stable phase change materials (FPCMs) offer great promise for thermal management in transport packaging due to their stability after phase change cycle and the extension of service life. However, challenges remain in enhancing thermal conductivity and energy storage efficiencies. In this study, a magnetically aligned h-BN-embedded superporous carbon foam-based FPCM containing paraffin (M-BN-CPCMs) was fabricated via a foam polymerization method followed by high-temperature carbonization. A super-porous hydrogel (SPH) precursor was used to construct a robust, highly porous carbon skeleton to accommodate more PCMs. To further enhance thermal conductivity, h-BN was functionalized with Fe 3 O 4 nanoparticles, and the resulting BN-Fe 3 O 4 was magnetically oriented within the carbon skeleton using a synchronous magnetization process. This novel design achieved a thermal conductivity improvement of over 90% compared to SPH. Additionally, the synergistic photothermal conversion effect achieved by the magnetic nanoparticles and carbon skeleton resulted in an outstanding photothermal conversion efficiency of approximately 90% for M-BN-CPCMs. Notably, the incorporation of BN-Fe 3 O 4 increased pore sizes, enabling higher paraffin loading capacity. The M-BN-CPCMs with large holes exhibit a remarkable phase change enthalpy of 154.9 J/g, demonstrating excellent energy storage capability, which surpasses that of superporous carbon foam skeleton-based FPCMs (CPCMs). The optimized M-BN-CPCMs demonstrated superior thermal energy storage, faster thermal charging rates, and improved thermal regulation, effectively reducing temperature fluctuations within insulated packaging. These findings underscore the potential of M-BN-CPCMs as a groundbreaking solution for energy storage and thermal management in transport packaging, addressing critical challenges in the field.

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APPLIED ORGANOMETALLIC CHEMISTRY · 2017 ·Vol. 31 ·期 12 ·e3854 · IF 2.319

Novel cyclodextrin-modified h-BN@Pd(II) nanomaterial: An efficient and recoverable catalyst for ligand-free C-C cross-coupling reactions in water

Xiaojun Ma,Guanghui Lv,Xu Cheng,Weijian Li,Rui Sang,Yong Zhang,Qiantao Wang,Li Hai,Yong Wu

An environmentally friendly palladium(II) catalyst supported on cyclodextrin-modified h-BN was successfully prepared. The catalyst was characterized by FT-IR, SEM, TG, XRD and XPS, and the loading level of Pd in h-BN@β-CD@Pd(II) was measured to be 0.088 mmol g −1 by ICP. It exhibits excellent catalytic activity for the Suzuki and Heck reactions in water, and can be easily separated and consecutively reused for at least nine times. In addition, a series of pharmacologically interesting products were successfully synthesized using this catalyst to demonstrate its potential applications in pharmaceutical industries. Above all, this work opens up an interesting and attractive avenue for the use of cyclodextrin-functionalized h-BN as an efficient support for hydrophilic heterogeneous catalysts.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2025 · IF 8.5

An innovative method for the removal of impurities and bleaching of cotton fabrics by UV/H₂O₂/pectinase: Intrinsic mechanisms and treatment effects

Ziying Guo,Yuting Zhou,Ping Wang,Qiang Wang,Bo Xu,Man Zhou,Li Cui,Ying Zhang,Yuanyuan Yu

The high energy consumption and pollution associated with traditional cotton fabric treatment have become increasingly serious concerns; thus, in this study, a synergistic cotton fabric treatment based on Novozymes pectinate lyase (NPL) scouring/ultraviolet light-mediated catalytic (UV/H 2 O 2 ) bleaching was innovatively proposed. This study investigated the degradation mechanisms of impurities in cotton fabrics, concluding that the oxidative bleaching reaction of morin follows first-order kinetics; in the UV/H 2 O 2 /NPL system, pectin degradation occurs through the β-elimination of NPL and oxidation by free radicals. Under optimized conditions—254 nm UV irradiation, 8 g⋅L −1 NPL, 30 g⋅L −1 H 2 O 2 , pH 9, and one-side irradiation for 45 min. The fabric whiteness could reach 79.04 %,but the fiber damage was severe, manifested by a 40 % decrease in polymerization and strength. After adjusting the process parameters, adjust the UV wavelength to 302 nm and add 6 g⋅L −1 of the activator (NOBS), whiteness of the fabric was about 76.7 % and strength retention rate was 96.38 %. This method overcomes the shortcomings of traditional pretreatment processes for cotton fabrics, under low temperature and alkaline conditions, low-strength damaged fabrics can be obtained, providing a new strategy for developing environmentally friendly pre-treatment processes for cotton fabrics.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

Simultaneously elevating the resistive switching level and ambient-air-stability of 3D perovskite (TAZ-H)PbBr3-based memory device by encapsulating into polyvinylpyrrolidone

Kaiyue Song,Lingling Du,Guoli Yue,Tao Li,Haohong Li,Shoutian Zheng,Zhirong Chen,Huidong Zheng

The study about simultaneously enhancing the resistive switching level and ambient-air-stability of perovskite-based memorizers will promote its commercialization. Here, a new 3D perovskite (TAZ-H)PbBr 3 (TAZ-H + = protonated thiazole) has been fabricated as FTO/(TAZ-H)PbBr 3 /Ag device, which only exhibits binary memory performance with the high tolerant temperature of 170 °C. After encapsulating by polyvinylpyrrolidone (PVP), the (TAZ-H)PbBr 3 @PVP composite-based device can demonstrate ternary resistive switching behavior with considerable ON2/ON1/OFF ratio (10 5.9 : 10 3.9 :1) and high ternary yield (68 %). Specially, this device presents good ambient-air stability at RH 80 % and thermal tolerance of 100 °C. The binary resistive switching mechanism can be ascribed to the halogen ion migration induced by bromine defects in the (PbBr 3 ) n n – framework. But the ternary resistive switching phenomenon in the (TAZ-H)PbBr 3 @PVP-based device could be depicted as the carrier transport from filled traps of PVP to (PbBr 3 ) n n – framework (ON1 state) and then carriers flowing in the re-arranged (TAZ-H) n n + chain in 3D channels (ON2 state). The PVP treatment can not only modify the grain boundary defects, but also facilitate the transport of injected carriers to the perovskite films via Pb-O coordinated bonds and inhibition of order-disorder transformation. This facial strategy for implementing ternary perovskite-based memorizers with good ambient-air-stability is quite meaningful for high-density memory in harsh environments.

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ACS Sustainable Chemistry & Engineering · 2022 · IF 9.224

Nano-H-ZSM-5 with Short b-Axis Channels as a Highly Efficient Catalyst for the Synthesis of Ethyl Levulinate from Furfuryl Alcohol

Yafei Li,Shiqing Wang,Shunxin Fan,Babar Ali,Xiaocheng Lan,Tiefeng Wang

For the ethanolysis of biomass-derived furfuryl alcohol (FA) to value-added ethyl levulinate (EL), the development of an efficient solid acid catalyst is very important for industrial application with high FA concentration. Herein, a H-ZSM-5 catalyst with nano b-axis channels (NB-H-ZSM-5) was synthesized and used for the conversion of FA. Detailed catalyst characterization proved that the NB-H-ZSM-5 catalysts (Si/Al = 25∼125) with ∼70 nm b-axis channels were successfully prepared. The NB-H-ZSM-5 catalyst with Si/Al = 75 showed the highest activity. Its structural characteristics allowed for fast diffusion of reactants and products and full utilization of active sites, which endowed it with higher activity compared to commercial H-ZSM-5 (C-H-ZSM-5). Its moderate acidity effectively inhibited the polymerization of FA even at a high FA concentration of 20 wt %. The spent catalyst was easily regenerated by coke burn-off to give a good recyclability. Furthermore, based on the proposed reaction network, a method of physically mixing the NB-H-ZSM-5 (75) catalyst with a small amount of Amberlyst-15 was proposed to further increase the EL yield from 64.7 to 82.1% at an FA concentration of 6 wt %.

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JOURNAL OF HAZARDOUS MATERIALS · 2025 · IF 11.3

Mechanisms of cypermethrin degradation and remediation by Rhodococcus sp. H-3: Insights from comparative genomics, hydrolase CymE1 secretory expression, and bacterial community analysis

Guoqiang Zhao,Wenjing Chen,Rongrong Zhang,Rui Zhang,Bo Jiang,Ruyan Hou,Xing Huang

Cypermethrin, a common pyrethroid insecticide, raises significant ecological concerns due to its widespread use. In this study, a highly efficient cypermethrin-degrading strain, Rhodococcus sp. H-3, was isolated. The strain was capable of degrading 30 mg/L cypermethrin at the rate of 83.48 % within 7 days and it could hydrolyze cypermethrin into 3-phenoxybenzoic acid (3-PBA) and permethric acid (DCVA). A novel cypermethrin degradation gene, cymE1 , was identified in strain H-3 through genome analysis, and its highest level of amino acid sequence similarity observed was 33.50 % in the Swiss-Prot database. The functional strain, SCK6-E, which could secrete CymE1, was successfully constructed by using double-exchange strategies. Strain SCK6-E could be applied for the removal of cypermethrin residues from tea plant leaves with a removal rate of 57.83 % within 2 h. Furthermore, strain H-3 demonstrated the capability to remediate cypermethrin-contaminated soil, exhibiting a degradation rate of 65.80 % over 10 days. The results of the 16S rRNA high-throughput sequencing indicated that strain H-3 was conducive to the restoration of the diversity and richness of the bacterial community in the soil. This study provides novel strain and gene resources for researching the degradation mechanism of pyrethroids, and offers valuable insights for developing effective pesticide residue remediation strategies.

CAS / MDL: 52315-07-8
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TETRAHEDRON · 2019 ·Vol. 75 ·期 31 ·4174-4179 · IF 2.379

An internal oxidant-directing strategy enabling transition metal-free C–S bond ligation

Yingying Zuo,Feng Xiong,Jing Zhao

Organic sulfur compounds have broad applications in biology, medicine and material sciences and intensive efforts have been devoted to developing mild and general C–S bond-forming methods. However, a mild, transition-metal-free, direct C–H bond functionalization method remains elusive. Here, we report the use of an internal oxidant-directing strategy to achieve this goal. The cascade reactions described here show excellent chemoselectivity and a wide substrate scope for both oxyamines and sulfenylation reagents. This study enlarges the synthesis toolbox for preparing structurally diverse sulfilimines under mild conditions.

研究领域: 有机化学 · 合成化学 · 药物化学 · 生物医学材料 · 分子生物学
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