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Probiotics and Antimicrobial Proteins · 2025 · IF 4.4

Characterization of Enterococcus faecalis JM263 from the Yak Gut on the Qinghai–Tibet Plateau: A Probiotic Candidate with Strong Fiber-Degrading Capacity

Cidan Yangji,Zhou Xinhong,Cisang Zhuoma,Kangji Lamu,Liu Guifang,Wu Dan,Basang Wangdui,Deji Quzhen,Ciwang Renzeng,Zhu Yanbin

This study aimed to isolate and evaluate a novel cellulolytic probiotic strain from the intestinal contents of yaks on the Qinghai–Tibet Plateau. A strain identified as Enterococcus faecalis JM263 exhibited strong cellulolytic activity, with CMCase, FPase, and β-glucosidase activities reaching 29.5, 23.58, and 15.62 U/mL, respectively. It exhibited strong tolerance to simulated gastric (75.3%) and intestinal (68.5%) fluids, dose-dependent bile salt resistance, and broad-spectrum antimicrobial activity—most notably, a 21.27-mm inhibition zone against Salmonella. Additionally, E. faecalis JM263 scavenged DPPH and hydroxyl radicals at rates of 41.05% and 36.54%, respectively. Additionally, E. faecalis JM263 exhibited strong degradation abilities toward cellulose, lignin, and hemicellulose in both corn straw and oatgrass. In vitro rumen fermentation experiments revealed that E. faecalis JM263 significantly increased acetate and VFAs while reducing ammonia-N levels. 16S rRNA sequencing revealed that E. faecalis JM263 altered the rumen microbial composition by increasing the abundance of beneficial taxa such as Fibrobacterota, Prevotella, and Succinivibrio. Functional prediction via PICRUSt and COG annotation suggested that E. faecalis JM263 supplementation may enhance microbial metabolism, particularly pathways involved in carbohydrate metabolism, amino acid biosynthesis, and energy production. Additionally, E. faecalis JM263 was shown to promote cooperative interactions among functional microbes, contributing to a more efficient and stable rumen microbial ecosystem. Overall, E. faecalis JM263 is a promising candidate functional probiotic for improving fiber digestibility and rumen fermentation efficiency in ruminants, offering great potential for application in sustainable animal production.

CAS / MDL: 9001-75-6 9002-07-7
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CELLULOSE · 2025 · IF 4.8

Preparation of cellulose-based fluorescent elastomers via RAFT polymerization and lanthanide coordination

Hu Rui,Zheng Anjia,Zhang Cancan,Wang Chuanxi,Zhang Jiaming,Ge Chongxiao,Li Qing,Zhang Bin,Jiang Feng

High-performance sustainable elastomers with tunable fluorescent behavior designed via robust and facile strategies are highly pursued. In this work, cellulose- graft -poly(tetrahydrofurfuryl acrylate- co -2-(methacryloyloxy)ethyl acetoacetate) (Cell- g -P(THFA- co -AAEM)) copolymers with different compositions were prepared through homogeneous reversible addition-fragmentation chain transfer (RAFT) polymerization. In this design, cellulose acts as the backbone, while the hemicellulose derivative tetrahydrofurfuryl acrylate (THFA) and the petroleum-based monomer 2-(methacryloyloxy)ethyl acetoacetate (AAEM) play the role of soft and rigid segments in the grafted side chains. By tuning the THFA/AAEM feed ratio and cellulose content, the mechanical and adhesion properties of these Cell- g -P(THFA- co -AAEM) copolymers were well manipulated. In addition, the β -diketone groups in THFA repeating units can be further used as the ligands to form dynamic networks in the copolymer matrix with terbium (Tb 3+ ) and europium (Eu 3+ ) ions via lanthanide coordination. The resulting coordinated Cell- g -P(THFA- co -AAEM) copolymers exhibit significantly improved tensile strength and tunable fluorescent colors by adjusting the Tb 3+ /Eu 3+ ratio. The combination of bio-based resources and lanthanide coordination can be further performed to achieve strong sustainable elastomers with improved macroscopic mechanical properties and unique fluorescent behavior.

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JOURNAL OF SOLUTION CHEMISTRY · 2025 · IF 1.3

Real-Time Analysis of Salt Scale Dissolution: Enhancing the Traditional Gravimetric Method and Comparing Precision and Efficiency

Huang Rui,Zhao Renbao,Yuan Yuting,Pu Yuanpeng,Zhang Jiapeng,Bai Shixun,Huang Jingjie

Scale deposition in oil/gas/water wells is a critical factor affecting well stability, making targeted selection of descaling agents and their field application parameters crucial for enhancing and sustaining production. Currently, the petroleum industry commonly employs traditional gravimetry to evaluate dissolution rates—an intermittent testing method with discontinuous data acquisition, susceptible to human interference, and incapable of real-time monitoring. This results in insufficient data for dissolution process analysis, leading to significant testing errors and low efficiency. To address these limitations, this study considers the universal phenomenon of real-time volume reduction and buoyancy loss during solid dissolution. By introducing parameters such as “buoyancy-equivalent mass” and “tension-equivalent mass”, a real-time dissolution rate calculation method was established based on dynamic force variations. Furthermore, a real-time scale dissolution rate testing procedure was designed and refined, and a testing platform was constructed. To demonstrate the superiority of the new method, comparative experiments were conducted between this method and the traditional gravimetric method for scale dissolution rate testing, comparing their testing precision and efficiency. The comparative experimental results are as follows: (1) The new method exhibits superior testing precision : Compared to the traditional gravimetric method, its standard deviation and relative standard deviation decreased by 11.3% (3.07% vs. 3.46%) and 25.9% (5.31% vs. 7.17%), respectively; (2) The new method demonstrates higher testing efficiency : Compared to the traditional gravimetric method, it offers better time efficiency (shorter testing duration: 7.3 h vs. 8.5 h), superior resource efficiency (fewer equipment usage instances: 7 times vs. 15 times), and better output efficiency (larger volume of data collected: sampling frequency 1 Hz vs. 1 h −1 , a 3600-fold difference). This study proposes a novel real-time scale dissolution rate testing method that addresses the issue of discontinuous data acquisition. The method exhibits enhanced precision and efficiency. It holds great potential for studying the dissolution kinetics of salt scales and significant application value in the precise treatment of long-standing scale issues in oil and gas transportation pipelines.

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EMBO Molecular Medicine · 2025 · IF 8.3

Brown remodeling of white adipose tissue protects against abdominal aortic aneurysm via batokine FSTL1

HuangChunling,HuangYuna,HuangBoshui,YaoLei,ZhangZenghui,DongLuoxiao,GuanChang,LiJunping,HuangZhaoqi,ChenSixu,JiangYuan,ZhangYuling,WangJingfeng,ChenYangxin,LiuZhaoyu

Abdominal aortic aneurysm (AAA) is a life-threatening vascular disease without effective medical therapies. Emerging evidence have suggested a crosstalk between adipose tissue and vascular cells. Besides, brown adipose tissue is considered beneficial for cardiovascular health. Nevertheless, whether brown remodeling of white adipose tissue would protect against AAA remains unclear. Here, we showed that patients with AAA had a decreased browning level of adipose tissue, and induction of adipose tissue browning significantly reduced AAA incidence and attenuated AAA development in mice. Using LC-MS/MS and proteomic analysis, we further identified Follistatin-like 1 (FSTL1) as a novel vessel-protective adipokine secreted by browning adipocytes. Mechanistically, FSTL1 inhibited VSMC apoptosis through DIP2A/AKT signaling. Furthermore, we demonstrated that adipocyte-specific deficiency of FSTL1 abrogated the protective effect of browning induction. Moreover, supplementation of FSTL1 either systemically or patched into hydrogel placing around the abdominal aorta markedly limited aortic dilation and AAA progression. Our data suggest a protective role of adipose tissue browning and batokine FSTL1 in the development of AAA, which may represent a novel intervention strategy for AAA.

✓ 已验证 DOI PubMed 高影响因子
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Nature Communications · 2025 ·Vol. 16 ·期 1 ·1-14 · IF 15.7

Intrinsic metal-support interactions break the activity-stability dilemma in electrocatalysis

Zhou Lingxi,Yang Menghao,Liu Yihong,Kang Feiyu,Lv Ruitao

Electrocatalysis plays a central role in clean energy conversion and sustainable technologies. However, the trade-off between activity and stability of electrocatalysts largely hinders their practical applications, notably in the oxygen evolution reaction for producing hydrogen and solar fuels. Here we report a steam-assisted synthesis armed with machine learning screening of an integrated Ru/TiMnO x electrode, featuring intrinsic metal-support interactions. These atomic-scale interactions with self-healing capabilities radically address the activity-stability dilemma across all pH levels. Consequently, the Ru/TiMnO x electrode demonstrate enhanced mass activities—48.5×, 112.8×, and 74.6× higher than benchmark RuO 2 under acidic, neutral, and alkaline conditions, respectively. Notably, it achieves stable operation for up to 3,000 h, representing a multi-fold stability improvement comparable to other state-of-the-art catalysts. The breakthrough in activity-stability limitations highlights the potential of intrinsic metal-support interactions for enhancing electrocatalysis and heterogeneous catalysis in diverse applications.

CAS / MDL: 7722-64-7
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AAPS PHARMSCITECH · 2025 ·Vol. 26 ·期 8 ·1-12 · IF 4

A Novel Felbinac Transdermal Patch with High Permeability: Design, Development and Evaluation

Qin Li,Liu Cheng,Bai Ran,Zhao Zhining,Sun Yinghua,Zhang Peng

The objective of the work was to design a novel felbinac transdermal patch to improve its transdermal delivery efficiency by adding chemical penetration enhancers. The adhesion properties and in vitro transdermal release performance were first evaluated. The transdermal stability and skin irritation were then evaluated. Moreover, in vivo tissue distribution was also examined. The novel felbinac transdermal patch with high adhesion was prepared by calendar coating method. Different types of chemical enhancers and their amount on in vitro transdermal delivery efficiency were systematically screened. In vitro transdermal release experiments showed that by adding 1% propylene glycol (PG) as penetration enhancers, the cumulative transdermal amount of the transdermal patch within 12 h was 189.03 μg/cm 2 , which was twice that of commercial product SELTOUCH® (94.44 μg/cm 2 ). In addition, the transdermal patch still maintained stable permeability after being stored at room temperature for 4 months and also had good safety. Further, in vivo experiments confirmed that the concentration of felbinac in plasma, skin, and muscle tissues was significantly increased following administration of the self-made transdermal patch compared to SELTOUCH®. In conclusion, the felbinac transdermal patch developed in this study demonstrated high adhesion, excellent transdermal delivery efficiency and good stability, representing a transdermal drug delivery system with great clinical application potential. Graphical

CAS / MDL: 110-27-0 872-50-4
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Nature Communications · 2025 ·Vol. 16 ·期 1 ·1-11 · IF 15.7

Thermal-intensified interfacial polymerization enables ultra-selective reverse osmosis membrane for toxic micropollutant removal

Zhou Shenghua,Peng Lu Elfa,Liu Wenyu,Guo Hao,Tang Chuyang Y.

Polyamide reverse osmosis (RO) membranes are widely used in seawater desalination and wastewater reuse, yet often fail to remove small toxic micropollutants. Herein, we develop a thermal-intensified interfacial polymerization (TIP) strategy to fabricate highly selective RO membranes against various micropollutants. Facile heating accelerates amine monomer diffusion, intensifying interfacial polymerization to form a highly crosslinked polyamide membrane. The resultant TIP membrane achieves rejection of 90.8%, 98.0%, and > 99% for boron, arsenite, organic micropollutants at neutral pH, respectively. Meanwhile, high temperature facilitates interfacial degassing and promotes the formation of more extensive nanovoids within the polyamide. These nanovoids increase membrane surface area and optimize water transport pathways, thereby boosting water permeance. The combination of high solute rejection and water permeance enables the membrane to achieve high water-micropollutant selectivity (e.g., water-boron). Our study demonstrates that TIP technique holds a great promise to fabricate ultra-selective polyamide membranes for desalination and wastewater reuse.

CAS / MDL: 107-21-1
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TRANSACTIONS OF TIANJIN UNIVERSITY · 2025 · IF 8.5

MOF-Derived Oxygen-Vacancy-Rich ZrO2/UiO-66-NH2 for Efficient Visible-Light-Driven Oxidation of Benzyl Alcohol

Song Yanyan,Sun Zhichao,Sun Jiamin,Liu Ying-Ya,Wang Anjie,Peng Chong

The development of efficient photocatalysts for selective organic transformations under visible light remains a major challenge in sustainable chemistry. In this study, we present a straightforward solvothermal strategy for fabricating a defect-engineered ZrO 2 /UiO-66-NH 2 hybrid material with abundant oxygen vacancies, enabling the visible-light-driven oxidation of benzyl alcohol to benzaldehyde. By optimizing the solvothermal treatment duration, the composite (UiO-66-NH 2 -2 h) achieves a 74.1% conversion of benzyl alcohol with > 99% selectivity toward benzaldehyde under mild conditions, substantially outperforming pristine UiO-66-NH 2 . Structural and mechanistic studies reveal that the solvothermal process induces the in situ formation of ultrasmall, uniformly dispersed ZrO 2 nanoparticles (~ 2.3 nm) within the MOF matrix, while simultaneously generating abundant oxygen vacancies, as confirmed by XPS, EPR, and HRTEM analyses. The defect-mediated electronic structure of the ZrO 2 /UiO-66-NH 2 hybrid enhances visible-light absorption, facilitates charge carrier separation, and promotes efficient activation of O 2 into superoxide radicals (·O 2 − ), the primary reactive species. Transient photocurrent measurements and electrochemical impedance spectroscopy further verify the improved charge separation efficiency. The synergistic interplay between oxygen vacancies and the intimate ZrO 2 /UiO-66-NH 2 interface provides a unique defect-mediated charge transfer pathway, distinguishing this system from conventional heterojunctions. This study demonstrates a facile, one-step approach to integrate defect engineering with interfacial hybridization in MOF-based photocatalysts, offering a scalable route for solar-driven organic synthesis. Graphical

CAS / MDL: 10312-55-7
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IONICS · 2025 · IF 2.6

Composition optimization and intrinsic electrochemical screening of porous Fe–Ni alloys as potential anodes for microbial fuel cells

Liu Dongni,Guo Lichi,Duan Ruochen,Zhang Shengwei,Li Mingying

Microbial fuel cells (MFCs) represent an emerging energy technology that generates electricity through microbial-organic interactions, with the anode serving as a critical component for wastewater-to-electron conversion. This study focuses on developing porous iron-nickel (Fe–Ni) alloys as potential anodes for MFCs, employing electrodeposition to fabricate these anodes with systematically varied Fe/Ni ratios. Through intrinsic electrochemical performance screening, the work aims to achieve composition optimization for high-performance microbial fuel cell anodes. Multi-dimensional analysis integrating linear sweep voltammetry (LSV), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and Tafel polarization was conducted to establish structure–activity relationships and synergistic catalytic mechanisms of the alloys. Key findings reveal that compositional optimization profoundly impacts the performance of these potential anodes: the Fe 7 Ni 3 alloy exhibited significantly superior electrochemical activity compared to pure Ni, characterized by dramatically enhanced peak current density, and improved charge storage capacity. Furthermore, Fe 7 Ni 3 demonstrated minimal charge transfer resistance and excellent reaction kinetics. These results validate that bulk composition engineering of porous Fe 7 Ni 3 offers a highly promising strategy for developing potential anode materials for high-performance MFCs, effectively addressing the stability-activity trade-off inherent in conventional surface-modified anodes. This work provides a composition-driven design paradigm for bioelectrochemical systems, paving the way for future scale-up studies focusing on long-term stability and integration into wastewater treatment modules. Graphical abstract

CAS / MDL: 7778-77-0 7758-11-4
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JOURNAL OF NANOBIOTECHNOLOGY · 2025 ·Vol. 23 ·期 1 ·1-24 · IF 12.6

Porphyromonas gingivalis extracellular vesicles exacerbated osteoporosis by disrupting osteoblast mitochondrial dynamics and inhibiting Cpt2-regulated fatty acid oxidation

Qiu Qiujing,Yan Xiaoyuan,Zhang Zeying,Zhang Xiyue,Ma Jiawei,Gao Wenqing,An Na,Qiu Lihong,Guo Jiajie

Background Recent studies have implicated periodontitis (PD) as a potential risk factor for osteoporosis; however, the precise mechanisms remain unclear. Porphyromonas gingivalis ( Pg ), a key pathogen associated with PD, can secrete extracellular vesicles (EVs). However, whether Pg EVs can be transported to the bone marrow and influence osteoporosis-related osteoblast differentiation warrants exploration. This study compares Pg EVs with EVs from  Porphyromonas endodontalis  ( Pe ), which is a less virulent congener but the evidence for its pathogenicity in PD is weak. Results Pg EVs can be translocated into the marrow of mice and be internalized by osteoblasts through clathrin- and lipid raft-mediated endocytosis, thereby exacerbating osteoporosis. Pg EVs promote mitochondrial fission and inhibit mitochondrial fusion, leading to mitochondrial fragmentation, impaired mitochondrial activity and suppressed osteogenic differentiation. Furthermore, Pg EVs downregulate the protein level of carnitine palmitoyl transferase 2 (Cpt2) and inhibit fatty acid oxidation (FAO) by disrupting mitochondrial dynamics, which impairs osteoblast ATP production and exacerbates osteoporosis. The effects of Pe EVs are similar but weaker than those of Pg EVs. Conclusions This study elucidates that Pg EVs exacerbate osteoporosis by disrupting osteoblast mitochondrial dynamics and suppressing Cpt2-regulated FAO. This study contributes to understanding of the etiological mechanisms through which Pg contributes to the progression of osteoporosis and highlights the pivotal role of EVs in the association between periodontal disease and systemic diseases. Graphical

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JOURNAL OF NANOBIOTECHNOLOGY · 2025 ·Vol. 23 ·期 1 ·1-22 · IF 12.6

Rational engineering of nanoplatforms with hierarchical targeting hepatic tumor and subcellular mitochondria for enhanced image-guided photodynamic therapy

Shang Xiaofei,Shao Wenjie,Dong Wuqi,Ren Wenxia,Du Wei,Li Chuang,Tian Yuxiang,Fang Weijun,Liu Tao,Xu Qinghua,Zhang Zhongping,Zhao Tingting

The main challenge of photosensitizer in image-guided photodynamic therapy (PDT) is the balance between the high singlet oxygen yields and strong fluorescence performance, while simultaneously targeting certain types of cancer to achieve optimal effect in both imaging and therapy. Herein, a novel donor-acceptor system, engineered with silica coated quantum dots as the donor and a typical porphyrin (T790) as the acceptor, has been further integrated with hierarchical targeting strategy, which demonstrated capability of targeting both hepatic tumors and mitochondria. The prepared nanoparticles were found to exhibit high singlet oxygen generation of 0.86, bright red fluorescence, and a large Stokes shift of 285 nm. In vitro assays revealed that they accumulated within the mitochondria of malignant hepatocytes to induce apoptosis due to their high singlet oxygen generation and disrupt the mitochondrial membrane potential, thereby leveling proteins associated with apoptosis. In vivo studies with xenograft tumor model confirmed their excelllent fluorescence imaging capability and remarkable anti-tumor effects. Transcriptomic analysis further revealed the potential molecular mechanisms of donor-acceptor system in the PDT process. This work provides insights for elucidating the transcriptional regulation of image-guided photodynamic therapy and paves the way for the development of more efficient and precise treatment methods.Graphical

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SAUDI PHARMACEUTICAL JOURNAL · 2025 ·Vol. 33 ·期 5 ·1-17 · IF 3.4

Baicalin nano-micelles for dry eye disease: LC–MS/MS method validation, pharmacokinetics and pharmacodynamics in preclinical models

Wang Ziheng,Xu Yuchen,Liu Manting,Yang Yuchang,Shi Wenjuan,Zhu Qian,Liu Juan,Yi Lisha,Wu Huimin,Yin Xingbin,Dong Xiaoxv,Ni Jian,Qu Changhai

This study aimed to establish a method for quantifying baicalin (BC) in rabbit ocular tissues and plasma, and evaluate the pharmacological efficacy and pharmacokinetic properties of BC and BC@HS15/DSPE-PEG2000-L-Val, a novel ocular formulation for dry eye treatment. BC@HS15/DSPE-PEG2000-L-Val or free BC was administered via eye drops to benzalkonium chloride (BAC)-induced dry eye mice. Corneal and conjunctival tissues were assessed for anti-dry eye efficacy. BC concentrations in cornea, conjunctiva, aqueous humor, and ocular plasma were quantified using LC–MS/MS. Noncompartmental pharmacokinetic parameters (AUC, Tmax) were calculated using DAS 2.0 software. The method demonstrated excellent linearity (0.50–500.00 ng/mL, r > 0.9905), precision (RSD < 10%), and accuracy (± 13%). Compared to free BC, BC@HS15/DSPE-PEG2000-L-Val significantly increased tear secretion, reduced MMP-3/MMP-9 expression, and preserved corneal epithelium integrity. In the micelle group, corneal and conjunctival Cmax values were 2.7- and 3.6-fold higher than the solution group, respectively. A sensitive and validated liquid chromatography-tandem mass spectrometry (LC–MS/MS) method was developed to measure baicalin concentrations in ocular plasma and tissues of rabbits. BC@HS15/DSPE-PEG2000-L-Val for treating dry eye demonstrated significantly superior outcomes. The nano-micelle notably enhanced BC concentration on the ocular surface and effectively prolonged its retention time. Graphical abstract

CAS / MDL: 21967-41-9
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