Current Drug Delivery
·
2015
·Vol. 12
·期 6
·726-735
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IF 1.478
Chenhui Wang,Changhui Yu,Kongtong Yu,Lesheng Teng,Jiaxin Liu,Xuesong Wang,Fengying Sun,Youxin Li
The use of biodegradable polymers such as PLGA to encapsulate therapeutic proteins for their controlled release has received tremendous interest. However, an acidic environment caused by PLGA degradation productions leads to protein incomplete release and chemical degradation. The aim of this study was to develop novel PCADK/PLGA microspheres to improve protein stability and release behavior. Bovine serum albumin (BSA) incubated in PCADK and PLGA degradation products was investigated using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), size exclusion chromatography (SEC-HPLC), circular dichroism (CD) and fluorescence spectroscopy. Blended microspheres of PCADK/PLGA were prepared in different ratios and the release behaviors of the microspheres and the protein stability were then measured. The degradation properties of the microspheres and the pH inside the microspheres were systematically investigated by scanning electron microscopy (SEM) and confocal laser scanning microscopy (CLSM) to examine the mechanism of autocatalytic degradation and protein stability. BSA was more stable in the presence of PCADK monomers than it was in the presence of PLGA monomers, revealing that PCADK is highly compatible with this protein. PCADK/PLGA microspheres were successfully prepared, and 2/8 was determined to be the optimal ratio. Further, 43% of the BSA formed water-insoluble aggregates in the presence of PCADK/PLGA microspheres, compared with 57% for the PLGA microspheres, demonstrating that the BSA encapsulated in PCADK/PLGA blended microspheres was more stable than in PLGA microspheres. The PCADK/PLGA blended microspheres improved protein stability and release behavior, providing a promising protein drug delivery system.
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ACS Sustainable Chemistry & Engineering
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2017
·
IF 5.951
Xinzhi Ma,Jing Wen,Shen Zhang,Haoran Yuan,Kaiyue Li,Feng Yan,Xitian Zhang,Yujin Chen
Development of noble-metal-free and active electrocatalysts is crucial for the oxygen evolution reaction (OER) in the water-splitting process. Herein, crystal CoxB catalysts (x = 1–3) of the OER are fabricated by a ball-milling method. Among these CoxB catalysts, Co2B exhibits the best OER activity, with a current density of 10 mA cm–2 at an overpotential of 287 mV in 1 M KOH solution. Such OER activity of Co2B is favorably comparable to that of the commercial IrO2 and most recently reported OER catalysts. Furthermore, the Co2B catalyst exhibits excellent stability with a stable current density of 50 mA cm–2 over 12 h of continuous electrolysis operation. X-ray photoelectron spectroscopy and cyclic voltammetry demonstrate that the B in CoxB makes oxidation easier, leading to their enhanced OER activities in comparison to metal Co. In addition, the Co2B electrocatalyst also exhibits high activity in the hydrogen evolution reaction; thus, the catalyst can be used as a bifunctional catalyst for full water splitting.
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Journal of Fungi
·
2026
·Vol. 12
·期 2
·157
·
IF 4.3
Yajing Yin,Hanxing Zhang,Zhenying Zhang,Mi Zhou,Shaojie Li,Chengcheng Hu
Fusarium verticillioides is a significant agricultural pathogen and an emerging causative agent of invasive fusariosis in clinical settings. Fusarium species frequently exhibit resistance to available antifungal agents, yet the molecular mechanisms underlying azole resistance remain poorly characterized. In this study, we identified the Zn(II) 2 Cys 6 transcription factor FvADS-1 as a positive regulator of the azole stress response in F. verticillioides . The transcription of FvADS-1 was significantly induced by ketoconazole (KTC), and its deletion increased susceptibility to multiple azole compounds. Mechanistically, FvADS-1 positively regulates the KTC-induced expression of genes encoding ABC transporters and ergosterol biosynthesis enzymes, thereby modulating intracellular KTC accumulation and sterol homeostasis under azole stress. Furthermore, FvADS-1 positively regulates the transcriptional response of peroxisomal genes and contributes to fungal tolerance to oxidative stress. Notably, deletion of FvADS-1 attenuates the virulence of F. verticillioides on maize. The function of ADS-1 is evolutionarily conserved: heterologous expression of N. crassa ads-1 restored azole resistance in FvADS-1 deletion mutant, and the deletion of the F. oxysporum homolog FoADS-1 similarly increased azole susceptibility. Collectively, our study demonstrates that the conserved transcription factor ADS-1 plays a central role in regulating azole resistance and virulence in the pathogen F. verticillioides , offering new insights into antifungal resistance mechanisms in pathogenic filamentous fungi.
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CHEMICAL ENGINEERING JOURNAL
·
2026
·
IF 13.2
Liuzi Du,Xiaodong Zhai,Jianchun Wu,Xiaowei Huang,Xiaobo Zou,Zhihua Li
To address the challenge of short shelf life and microbial contamination in food preservation, this study aims to develop an intelligent pH-responsive antibacterial fiber film with controlled release capability. The modification of alkaline lignin improved the structural stability and specific surface area of HKUST-1 (from 547 to 1483 m 2 /g), while the composite film exhibited excellent mechanical properties (tensile strength: 3.74 MPa, elongation: 96.25%) and hydrophobicity (water contact angle: 120.55°). The film exhibited strong pH-dependent controlled release, with 81% of antibacterial agents released at pH 6.0 within 120 h. In vitro antibacterial tests demonstrated broad-spectrum activity against Escherichia coli ( E. coli ), Staphylococcus aureus ( S. aureus ), and Pseudomonas aeruginosa ( P. aeruginosa ). When applied to beef preservation, the film significantly reduced total volatile basic nitrogen (15.35 mg/100 g), total viable count (6.23 log CFU/g), and pH (6.02) after 9 days of storage, extending the shelf life by 4 days compared to the control. This work provides a feasible strategy for developing intelligent pH-controlled-release antibacterial packaging materials.
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JOURNAL OF ETHNOPHARMACOLOGY
·
2025
·
IF 5.4
Xiaolin Xie,Haikang Fu,Zhixuan Ai,Ziwei Huang,Wenwen Tan,Qingfeng Xie,Yuhong Liu,Yucui Li,Jiannan Chen,Xiaobo Yang,Ziren Su,Zhengquan Lai,Jianhui Xie
Ethnopharmacological relevance Coptidis Rhizome (CR), a cornerstone medicinal herb, is routinely used to treat metabolic diseases for centuries in China. However, the potential mechanism has not been completely elucidated. Preceding investigation has reported that berberine in CR can bind to hemoglobin (Hb) and utilize erythrocyte-Hb self-assembly drug delivery system to significantly upregulate HO-1 expression. Aim of the study This study was designed in a pioneering endeavor to explore the therapeutic potential and underlying mechanism of CR in dexamethasone- and fructose-induced glycolipid metabolism disorders (GLD) rat models. Material and methods The major elements of CR were identified by high performance liquid chromatograph (HPLC). Dexamethasone- and fructose-induced rat GLD model was constructed. Glucolipid metabolism, oxidative status, and insulin sensitivity were investigated. Histopathological, transcriptomic, in silico simulations, immunofluorescence, immunohistochemistry, and Western blotting analyses were performed to gain further mechanism insight. Results HPLC analysis revealed that berberine, palmatine, coptisine, epiberberine, and jatrorrhizine were detected in CR, with berberine as the most abundant. Administration of CR favorably regulated the organ indexes, and significantly improved glucose metabolism by decreasing the FBG and GSP levels along with improved OGTT. CR promoted insulin sensitivity by suppressing the increased levels of FINS, HOMA-IR and ISI, and concomitantly improving ITT. Furthermore, CR normalized lipid metabolism by decreasing the elevated TG, TC and LDL-C levels. Additionally, CR effectively ameliorated histopathological deterioration in pancreatic and hepatic tissues and reduced serum ALT and AST activities. CR also ameliorated oxidative stress by remarkably lowering hepatic ROS fluorescence intensity and serum MDA content, whereas enhancing SOD and CAT enzymatic activity, and T-AOC level. Hepatic transcriptomics analysis revealed the oxidative stress-related gene HMOX1 encoding HO-1 and AMPK pathway critically involved in the therapeutic effect of CR. Furthermore, CR was found to significantly up-regulate the protein expression levels of HO-1, NQO1 and p-AMPK. On the other hand, in silico simulations indicated that strong van der Waals forces interaction between these alkaloids and HO-1. Notably, CR exhibited potent HO-1 agonistic activity comparable to the HO-1 inducer hemin, as manifested by enhanced HMOX1 mRNA level, HO-1 expression level, cytoplasmic HO-1 fluorescence intensity, carbon monoxide production, and reduced heme level, which were the markers of erythrocyte metabolism. Administration of CR or hemin significantly improved fasting glycemia, blood fat, insulin sensitivity, and antioxidant capacity. Nevertheless, these effects were observably reversed by the HO-1 inhibitor zinc protoporphyrin (ZnPP). Conclusion CR effectively ameliorated insulin resistance, hyperglycemia, and dyslipidemia, and its mechanism of action may be at least partially, mediated through HO-1 activation via erythrocyte metabolic regulation. This study provided further evidences for the historical use of CR in the therapy of metabolic diseases. These results highlighted the potential of CR as a novel HO-1 agonist for the development of innovative treatments for GLD.
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TURKISH JOURNAL OF CHEMISTRY
·
2024
·Vol. 48
·期 4
·597-619
·
IF 1.3
YUAN HANG,CAO GUI-PING,LV HUI
The reaction solvent and catalyst play an essential role in the Prins reaction for the synthesis of 3-methyl-3-buten-1-ol (MBO) from formaldehyde and isobutene. The reactivity of the solid base catalyzed Prins condensation reaction by formaldehyde and isobutene in supercritical CO2 was investigated using CsH2PO4 modified HZSM-5. We finds that the alkaline sites of the alkali-loaded catalyst can extract the α-H on isobutene to generate olefin carbon negative ions, while the supercritical CO2 with weak Lewis acidity can activate formaldehyde to carbon positive ions, which can combine more easily with the carbon negative isobutene to react, thus improving the reactivity of the reaction system.
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BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
·
2026
·Vol. 1870
·期 11
·130988
·
IF 2.9
Jingxian Han,Lei Hua,Siqi Zhang,Bin Yang,Zhiying Li,Xiangguang Meng
Background Heart failure (HF) remains a leading cause of death worldwide. Stem cells represent a promising strategy for myocardial regeneration due to their differentiation potential and paracrine effects. This study investigated the effect of human pericardial fluid Sca-1 + /Nanog + cells Conditioned Medium (hPFCs-CM) on doxorubicin (DOX)-induced damage to AC16 cardiomyocytes using transcriptomic analysis. Methods Human AC16 cardiomyocytes were divided into Control (CON), DOX, DOXh, and hPFCs groups. Cell viability, cytotoxicity (LDH release), reactive oxygen species (ROS) levels, and apoptosis were assessed. Transcriptomic sequencing was performed on CON, DOX, and DOXh groups. MYH3 and IFI16 genes were knocked down using siRNA, followed by Western blot analysis of apoptosis. Results DOX significantly increased ROS and apoptosis compared with CON group ( P < 0.05), while hPFCs-CM attenuated these effects ( P < 0.05). RNA-seq identified 52 differentially expressed genes between DOX and DOXh groups (adj P < 0.05). Three target genes ( MYH3 , IFI16 , and KCTD14 ) were selected for RT-qPCR validation. Further functional assays revealed that MYH3 knockdown significantly potentiated the anti-apoptotic activity of hPFCs-CM ( P < 0.05), whereas IFI16 knockdown showed no significant effect. Conclusion hPFCs-CM effectively attenuated DOX-induced AC16 cardiomyocyte damage through MYH3, providing potential molecular targets for future mechanistic studies in myocardial injury treatment.
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CHINESE JOURNAL OF CHEMICAL ENGINEERING
·
2026
·
IF 3.5
Linlin Zhang,Yanfen Chen,Fangyu Wu,Aoxing Feng,Jiaqi Zhang,Tianyu Zhang,Xuenan Yang,Sisi Li,Qilin Lu,Jingjing Hou,Yuanhui Tang,Lixin Yu,Xiaolin Wang,Yakai Lin
Plasma leakage and thrombosis remain critical challenges limiting the long-term performance of poly(4-methyl-1-pentene) (PMP) hollow fiber membranes (HFMs) in extracorporeal membrane oxygenation (ECMO). In this work, a hierarchical hydrophobic modification strategy was developed to construct a stable anti-wetting interface on PMP HFMs. Surface hydroxyl groups were first generated via Fenton-induced oxidation, followed by interfacial coupling with trimesoyl chloride (TMC). Subsequently, SiO 2 nanoparticles were grafted to create a micro/nano-structured rough surface, and further modified with 1H,1H,2H,2H-perfluorodecyltrimethoxysilane (17-FAS) to reduce surface energy. Under the optimized conditions (120 min Fenton pre-treatment, 60 min TMC reaction, and 0.1% (mass) SiO 2 nanoparticles), the modified PMP–SiO 2 /17-FAS membrane exhibited a high N 2 flux of 54.1 ml·cm –2 ·min –1 ·MPa –1 , while the plasma leakage resistance time was significantly prolonged from 5910 to 8775 min. In addition, bovine serum albumin adsorption was reduced by approximately 50%, indicating enhanced antifouling performance. Coagulation tests further revealed a selective prolongation of activated partial thromboplastin time, while prothrombin time, thrombin time, and international normalized ratio remained nearly unchanged, suggesting suppressed contact-induced coagulation activation without disturbing normal coagulation pathways. The enhanced performance could be attributed to the synergistic effect of micro/nano-structured roughness and the fluorinated low-surface-energy layer, which stabilizes a non-wetting interfacial state and reduces protein-surface interactions. This work provides a feasible strategy for simultaneously improving plasma leakage resistance and hemocompatibility of PMP-based oxygenation membranes. Download: Download high-res image (297KB) Download: Download full-size image
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ADVANCED MATERIALS
·
2026
·
IF 29.1
Shuo Zhang,Yuyang Lu,Chong Yan,Xiangbiao Liao,Chen-Zi Zhao,Jun-Wei Zhao,Zhiyuan Dong,Zhenwei Zhu,Wenjie Meng,Xue-Fei Wen,Peng Wu,Jian Pei,Meng-Yao Wang,Xue-Kun Cao,Jiang-Kui Hu,Xiang Chen,Jingyi Qiu,Hao Zhang,Jia-Qi Huang,Qiang Zhang
The pursuit of high-energy-density lithium metal batteries requires simultaneous optimization of electrode architecture, electrolyte formulation, and interfacial stability. Here, we establish a fundamental parameter g(σ e , D e ) that quantifies the relationship between electrolyte dosage and capacity utilization in ultra-thick electrodes (>100.0 µm), enabling precise determination of the minimal electrolyte requirement (1.1 g Ah −1 ). Through systematic investigation of electrolyte compatibility with high-loading cathodes (> 10.0 mAh cm −2 ) at high voltages (4.8 V), we develop an optimized formulation that forms stable interfaces while suppressing parasitic reactions. By integrating these advances—including a lightweight lithium metal anode—we demonstrate a 54.2 Ah pouch cell achieving 769 Wh kg −1 , representing a 150% improvement over conventional lithium-ion batteries. This work provides both theoretical and practical frameworks for engineering next-generation batteries through electrolyte minimization and interface stabilization.
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COLLOIDS AND SURFACES B-BIOINTERFACES
·
2026
·
IF 5.9
Runfeng Jia,Qingliang Chen,Khan Md Sabur,Zhongyu He,Bingxue Chen,Kaidi Hu,Xiaoqing Zhao,Hanbing Rao,Zhiwei Lu,Yanying Wang,Xing Wei,Mengmeng Sun
A single oral Lut-NPs/Gel system synergistically ameliorates both colitis and associated depression-like behaviors via the gut-brain axis. • Lut-NPs/Gel combats colitis via a synergistic combination of barrier repair, anti-inflammatory action, and beneficial microbiome remodeling. • Restoration of AKK abundance plays a critical regulatory role in gut microbiota remodeling. • Multi-omics analyses identified key modulated pathways, including TRP channels and neuroactive ligand-receptor interactions, functionally connecting gut repair to brain behavioral improvement. • Recovery of AKK in normal state is coordinated with upregulation of host repair genes (such as IGF1, Reg1), delineating a collaborative host-microbe network. Inflammatory bowel disease (IBD) is a chronic immune-mediated condition affecting the intestinal tract. Though conventional therapies aim to control symptoms and induce remission, their long-term use is hindered by systemic side effects and inadequate efficacy, highlighting the need for safer and more effective treatments. In this study, we developed luteolin-loaded nanoparticles (Lut-NPs) by encapsulating luteolin within metal-phenolic networks (MPNs) formed through coordination between epigallocatechin gallate (EGCG) and Ce 3 ⁺ ions. The resulting Lut-NPs showed excellent biocompatibility, strong antioxidant and anti-inflammatory activities, and remarkable stability under gastrointestinal conditions. To improve intestinal retention, the nanoparticles were incorporated into an inulin-based hydrogel, generating a Lut-NPs/Gel composite system. In a DSS-induced colitis model, oral administration of Lut-NPs/Gel demonstrated significant therapeutic efficacy, including restoration of the intestinal barrier, suppression of pro-inflammatory pathways, and reshaping the gut microbiome. The treatment also promoted macrophage polarization from the M1 to the M2 phenotype. AKK, usually considered beneficial but elevated during inflammation, was restored to normal levels after Lut-Nps/Gel treatment, suggesting its potential as a biomarker of intestinal recovery. Additionally, the treatment alleviated depression-like behaviors via the microbiota–gut–brain axis. Overall, this work provides a safe and promising multifunctional strategy for treating IBD and associated neuropsychiatric symptoms.
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Frontiers in Pharmacology
·
2026
·
IF 5.4
Fang Wang,Yan Qing Liu,Jun Nan Wei,Xiao Fen Wang,Feng Qin Li,Xiu Jia Tian,Dan Li,Yu Xuan Gao,Xin Zhi Guo,Xue Yan Li,Ping Luo
Introduction Metabolic dysfunction-associated steatotic liver disease (MASLD) is a highly prevalent chronic liver disorder characterized by intrahepatic lipid accumulation, oxidative stress, and inflammatory responses, underscoring the urgent need for effective therapeutic strategies. D-limonene, a cyclic monoterpenoid primarily derived from citrus fruits, possesses well-documented antioxidant, anti-fibrotic, and wound-healing properties. However, its therapeutic potential in MASLD remains largely unexplored. Methods To evaluate the therapeutic efficacy of D-limonene, a rat model of MASLD was established using a high-fat diet (HFD). An integrated approach combining metabolomics, transcriptomics, and network analysis was employed to identify key signaling pathways and molecular targets. The expression levels of candidate targets were validated by RT-qPCR and Western blotting. Molecular docking simulations were performed to predict the binding affinity between D-limonene and the target proteins. Furthermore, a cellular thermal shift assay (CETSA) was conducted to confirm direct binding and protein stabilization. In parallel, cellular experiments using BRL-3A and HepG2 cells were carried out to assess the effect of D-limonene on lipid accumulation. Results D-limonene treatment significantly ameliorated liver injury, reduced excessive lipid deposition, attenuated inflammation, and suppressed oxidative stress in HFD-induced rats. Integrated multi-omics and network analyses identified the PPAR signaling pathway as the core pathway mediating the regulatory effects of D-limonene on lipid metabolism, with PPARγ and SCD-1 pinpointed as key downstream targets. RT-qPCR and Western blot analyses confirmed that D-limonene significantly downregulated the expression of both PPARγ and SCD-1. Molecular docking simulations revealed stable binding of D-limonene to PPARγ and SCD-1. Importantly, CETSA further demonstrated that D-limonene directly binds to and stabilizes these two proteins. Consistently, cellular assays showed that D-limonene significantly reduced lipid accumulation in BRL-3A and HepG2 cells by inhibiting the PPARγ/SCD-1 axis. Conclusion Collectively, these findings suggest that D-limonene alleviates HFD-induced MASLD, and its protective effects may be mediated, at least in part, through inhibition of the PPARγ/SCD-1 axis. This study provides preliminary evidence supporting the potential development of D-limonene as a targeted therapeutic agent for MASLD. Further studies are warranted to validate these findings and elucidate additional underlying mechanisms.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2026
·
IF 9.1
Bin Wen,Fan Chen,Yi Ran,Dongyun Que,Zhihao Zhang,Youwei Zeng,Yuyuan Yao
Molybdenum disulfide (MoS₂) is a promising inorganic co-catalyst for Fenton processes due to its structural durability and avoidance of secondary organic pollution. However, the conventional 2H-phase MoS₂ suffers from intrinsically low conductivity, severely limiting Fe 3+ reduction in the Fenton reaction. Herein, L-cysteine served as a multifunctional precursor during the preparation of MoS₂, promoting a slow-release sulfur supply, carbon‑nitrogen co-doping, and the prevention of restacking. The carbon and nitrogen co-doped molybdenum disulfide (CN-MoS 2 ) architecture was fabricated via a single-step hydrothermal reaction mediated by sodium molybdate, thiourea, and L-cysteine. Remarkably, benefiting from the introduction of L-cysteine, the resulting CN-MoS 2 exhibited a high 1 T-phase content (68%), abundant sulfur vacancies, and a substantially reduced particle size. CN-MoS 2 accomplished near-complete elimination of carbamazepine (CBZ) within merely 3 min, yielding a prominent apparent rate constant of 0.7111 min −1 , which is a 19-fold kinetic acceleration over thiourea-derived MoS 2 . CN-MoS₂ also exhibited high TOC removal, broad-spectrum degradation, and robust CBZ removal under various water conditions. Additionally, electrochemical analyses further verified that CN-MoS₂ reduced charge-transfer resistance and enriched electron density, thereby facilitating rapid electron shuttling to Fe 3+ . Concurrently, quenching experiments and electron paramagnetic resonance (EPR) diagnostics unambiguously validated SO 4 •- , 1 O 2 and O 2 •- as the driving reactive forces. Moreover, a continuous-flow device incorporating a CN-MoS 2 -based membrane exhibited outstanding performance in wastewater purification. This work offers a new strategy for designing high-activity co-catalysts for advanced oxidation processes.
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危险品化学品经营许可证（带存储）