NEW JOURNAL OF CHEMISTRY
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2025
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IF 2.5
Hongbing Mao,Huijun Wang,Yanyan Xing,Deyong Wang,Xiujun Cao,Jie Yu,Junya Yan
In this work, a boronic acid decorated mesoporous iron-based metal-organic framework (MIL-100(Fe)-B) nanozyme as an efficient immobilization matrix for glucose oxidase (GOx) was designed and prepared through a facile microwave-assisted metal-ligand-fragment co-assembly strategy. Compared with the unboric acid-modified MIL-100(Fe), boron-doped MIL-100(Fe) exhibited enhanced peroxidase-like activity, which was mainly due to the introduced B causing MIL-100(Fe) defects, accelerating mass transfer, facilitating more active sites for H2O2 decomposition. Besides, the MIL-100(Fe)-B nanozyme possessed sufficient recognition sites for immobilizing glucose oxidase with little enzyme leakage to form a cascade nanozyme with both peroxidase-like and cascade catalytic activities. A colormetric biosensor based on the integrated nanozyme reactor (GOx@MIL-100(Fe)-B) was developed for glucose detection. The proposed cascade biosensor had a linear range of 5-150 μM and a limit of detection (LOD) of 0.97 μM (3.3 δ/S). Interestingly, a portable microfluidic paper-based analytic device (μPAD) biosensor based on the cascade nanoplatform was further fabricated for visualized detection of glucose combined with a ColorPicker App on smartphone. It indicated that the integrated nanozyme GOx@MIL-100(Fe)-B was a promising candidate for glucose detection and provided a potentially analytical avenue for biosensing and other applications.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
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2024
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IF 7.7
Jingjing Wang,Xiaoyuan Wang,Yawen Ji,Qi Qi,Qingru Shi,Dacheng Zhong
Tetracycline hydrochloride (TCH) removal from wastewater has drawn much attention recently, although it still remains challenging. Herein, Fe-based metal-organic frameworks (MOFs) incorporated nanofibrous membranes were prepared by green electrospinning and applied as adsorbents to remove TCH. The presence of MOFs noticeably improved specific surface area of the nanofibrous membranes, and adsorption capability increased with the amount of MOFs within membranes. As the temperature increased, the amount of TCH that was adsorbed continuously reduced, and the maximum adsorption capacity (248.5 mg/g) was attained at 273 K. The adsorption behavior of the nanofibrous membranes followed Langmuir isotherm model and pseudo-second-order kinetic model. Thermodynamic parameters suggested that the adsorption process was spontaneous and exothermic. A series of interactions between the membrane and TCH, such as pore filling, coordination bonding, π-π interaction, hydrogen bonding interaction and electrostatic interaction, combined to enhance the adsorption performance. Good stability and adsorption capability were demonstrated by the nanofibrous membranes, suggesting that they could be used for effective and affordable water purification.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2024
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IF 7.7
Mengke Lu,Jianxia Ding,Yupeng Zhang,Xuan Gu,Jiaying Liu,Qinxin Wang,Xiaonan Qiu,Huijun Yu,Fengyi Du,Wei Zhang
Single atom nanozyme (SAzyme) based on carbon dots (CDs) has showed great potential in oncotherapy via ultrasmall size-reinforced atomically dispersed catalytic sites. However, its curative effect is still unsatisfactory due to complex tumor microenvironment and intrinsic resistance. Herein, a coordinated carbon dots (CCDs)-integrated ZIF-8 nanoassembly (Ru/CCDs-PTX@ZIF) was constructed by loading paclitaxel and coating with rutin for synergistic catalytic/chemotherapy. Benefiting from inherited metal-polyphenol coordination, the CCDs exhibited superior peroxidase-like (POD) activity and served as a SAzyme to produce large amounts of hydroxyl radical, resulting in radical-dependent cell cycle arrest. With the assistance of GLUT receptor-mediated endocytosis, the Ru/CCDs-PTX@ZIF triggered the tumor-targeted killing and migration inhibition to suppress tumor progression. This study highlights a promising avenue to broaden the design and applications of CDs-based SAzyme in tumor treatment.
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NEW JOURNAL OF CHEMISTRY
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2024
·Vol. 48
·期 26
·11776-11782
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IF 2.7
Yuwei Yan,Hongyan Li,Songnan Li,Jiawei Zhang,Jingxiang Zhao,Qinghai Cai
Copper, iron–chloride ionic liquids (ILs) were immobilized on SBA-15 via N-methylimidazole grafting with C–Cl in chloropropylsilane pre-anchored on SBA-15, followed by FeCl3 and CuCl2 coordination to imidazolium chloride to generate a double metal IL-supported mesoporous composite (SIL-CuFe). The prepared composite exhibited an effective catalytic performance for the solvent-free oxidation of styrene to benzaldehdye (BzH) with H2O2 oxidant, offering 51% conversion, a turnover number (TON) of 330.5 mol molFe+Cu−1, and a selectivity of 71% at a reaction temperature of 70 °C. The composite catalyst can be easily recovered and effectively reused without a significant loss in activity and selectivity. The quenching experiments by adding tert-butanol (TBA), 1,4-benzoquinone (p-BQ) and L-histidine (L-HIS) in the reaction system were conducted to identify the type of reactive O species, specifically ˙OH, ˙O2−, and 1O2, produced by catalyst activation with H2O2 and played a main role in the oxidation. The reaction mechanism of the oxidation process is also proposed.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2024
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IF 9.4
Mengwei Ye,Weikang Zhang,Hongwei Xu,Peiyu Xie,Luming Song,Xiaohan Sun,Yian Li,Siling Wang,Qinfu Zhao
Combination therapies have attracted significant attention because they address the limitations of monotherapy while improving overall efficacy. In this study, we designed a novel nanoplatform, named GOx@Fe-DMSN@PDA (GFDP), by integrating Fe 2+ into dendritic mesoporous silica nanoparticles (DMSN) and selecting glucose oxidase (GOx) as the model drug loaded into the DMSN pores. Additionally, we coated the surface of the DMSN with polydopamine (PDA) to confer pH/near infrared (NIR) light-responsive controlled-release behavior and photothermal therapy (PTT). The introduction of Fe 2+ into the DMSN framework greatly improved biodegradability and enhanced the peroxidase (POD)-like activity of GFDP. In addition, GOx could consume glucose and generate hydrogen peroxide (H 2 O 2 ) within tumor cells to facilitate starvation therapy and enhance cascade catalysis. The PDA coating provided the DMSN with an intelligent response release ability, promoting efficient photothermal conversion and achieving the PTT effect. Cellular tests showed that under NIR light irradiation, GFDP exhibited a synergistic effect of PTT-enhanced starvation therapy and cascade catalysis, with a half-maximal inhibitory concentration (IC 50 ) of 2.89 μg/mL, which was significantly lower than that of GFDP without NIR light irradiation (18.29 μg/mL). The in vivo anti-tumor effect indicated that GFDP could effectively accumulate at the tumor site for thermal imaging and showed remarkable synergistic therapeutic effects. In summary, GFDP is a promising nanoplatform for multi-modal combination therapy that integrates starvation therapy, PTT, and cascade catalysis.
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JOURNAL OF HAZARDOUS MATERIALS
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2025
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IF 11.3
Ping Cheng,Botao Wang,Qianyu Ji,Pingping Yuan,Shixin Gui,Shuying Liang,Lin Li,Hongwei Xu,Shaoqi Qu
The widespread dissemination of antibiotic resistance genes (ARGs) via plasmid-mediated conjugation poses a serious threat to public health. Conjugation can be accelerated by selective pressures caused by antibiotics and other environmental pollutants. Fe-doped TiO 2 nanosheets (FTNs) are widely used for the photocatalytic treatment of wastewater, raising concerns about their potential presence in the environment and their role in exerting selective pressure on conjugation. In this study, FTNs at subinhibitory concentrations (25, 50, and 100 mg/L) were applied in an in vitro conjugation model to investigate their impact on ARG conjugation. The results showed that FTN exposure increased conjugative transfer frequency by more than 2.5-fold. Molecular mechanism analysis revealed that FTNs increased membrane permeability by causing physical damage and inducing oxidative stress, promoted energy supply by modulating the proton motive force (PMF) and enhancing the tricarboxylic acid (TCA) cycle, and improved intercellular contact by enhancing cell adhesion. Additionally, transcriptomic analysis indicated that FTNs upregulated the expression of genes related to energy supply, cell adhesion, cell transport and oxidative stress. Overall, the findings of this study reveal the potential risk of nanosheets accelerating the spread of ARGs via plasmid-mediated conjugation, highlighting the necessity of establishing guidelines for their appropriate use and discharge.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2024
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IF 4.9
Ying Zeng,Sitong Liu,Guopeng Zhu,Xiutao Yang,Hongwen Yu
To improve the efficiency of photocatalytic reactions, it is important to understand how to achieve fast directional migration and separation of photogenerated carriers at the interface. Here, Fe(III)-doped ZnIn 2 S 4 (ZIS)-coated graphene oxide (GO) composite (GZF) was in-situ prepared via the low-temperature water bath method. Ultrathin Fe(III)-doped ZIS nanosheets were uniformly grown upright on the GO surface. The prepared samples were studied via, such as, X-ray diffraction, scanning electron microscopy combined with energy-dispersive spectroscopy, transmission electron microscopy, ultraviolet spectroscopy, N 2 adsorption–desorption measurements, X-ray photoelectron spectroscopy, and electron spin resonance. Compared with ZnIn 2 S 4 (ZIS)-coated graphene oxide (GZ), the GZF exhibit a 2.26-fold increase in the photocatalytic degradation performance of tetracycline hydrochloride (TCH) in simulated sunlight. Through density functional theory calculations, found that Fe(III) doping introduces new energy levels into ZIS, which effectively narrow its bandgap and thus enhance its light absorption efficiency. It was found that h + , ·O 2 − , and 1 O 2 were the major reactive oxygen species involved in the photocatalysis, and the effect of pH on the catalytic degradation of TCH was examined. Electron spin resonance and density functional theory results indicate that Fe(III) acts as an electron trap in the ZIS structure to promote the separation of photogenerated electron-hole pairs, which in turn enhances the photocatalytic efficiency of GZF-25.
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SOLID STATE SCIENCES
·
2025
·
IF 3.3
Shutian Lin,Xinli Zhang,Yingzhi Chen,Yuanhong Zhong,Gao Cheng,Lin Yu
The Fe-N-C catalyst was synthesized using loofah sponge-derived carbon and applied for peroxymonosulfate (PMS) activation to degrade organic pollutants. The catalyst, featuring highly dispersed single-atom Fe on the N-C framework, showed outstanding activity for phenol degradation across a wide pH range. The incorporation of Fe significantly boosted the catalytic performance, achieving rapid degradation of phenol at 20 mg L −1 within 10 min, using 0.5 mmol L ‒ 1 of PMS and 0.2 g L −1 of catalyst. Electron paramagnetic resonance (EPR) and reactive oxygen quenching experiments identified the singlet oxygen ( 1 O 2 ) and superoxide radical (O 2 •‒ ) as the main reactive oxygen species, with the former playing a key role. It has been demonstrated that the Fe-N x structures were the active sites that facilitated the generation of 1 O 2 , thereby enhancing the catalytic activity of the Fe-N-C materials. The catalyst also effectively addressed pollutants like Rhodamine B and climbazole, indicating its potential for environmental remediation. The synthesis approach for Fe-N-C is applicable to other transition metals, such as Mn, Co, Ni, Cu, and Zn, providing valuable insights for the development of highly efficient and durable M-N-C catalysts.
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INORGANIC CHEMISTRY
·
2025
·
IF 4.7
Jinchang Zhang,Xuefeng Cheng,Jicai Jiang,Apiladda Pattanateeradetch,Shuai Shi,Chanat Chokejaroenrat,Qingfeng Xu,Jianmei Lu
Selective enrichment of cesium ions (Cs+) at ultralow concentrations is essential for resource recovery and radioactive waste disposal, yet efficient adsorbents are lacking. Herein, we reported a Prussian blue analogue (K2Cu3(Fe(CN)6)2, Cu-PBA) decorated on MXene nanosheets by in situ fabrication, forming a composite material termed PMX, for enhanced adsorption of Cs+ in acidic solutions and seawater. The stable, negatively charged MXene effectively anchors Cu2+ precursors and promotes Cs+ adsorption. The synergistic interaction between MXene and the in situ-synthesized Cu-PBA significantly enhances the adsorption performance and water stability of PMX in both acidic solutions and seawater. PMX achieves rapid adsorption equilibrium within 5 min, with a high adsorption capacity of 408.2 mg/g at pH 1, surpassing conventional adsorbents. Moreover, PMX shows excellent Cs+ selectivity (Kd = 68,361.7 mL/g), cycle stability, and notable anti-irradiation ability, demonstrating superior efficiency in Cs+ enrichment from complex matrices. The adsorption mechanism involves electrostatic attraction and K+/Cs+ ion exchange, facilitated by MXene’s functional groups and the Cu-PBA structure. These findings underscore the excellent potential of PMX as an efficient adsorbent for resource enrichment and the removal of radioactive elements such as Cs+.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Huaimin Wang,Shuang Meng,Zixuan Zhang,Chenying Zhou,Heng Zhang,Yang Liu,Chuan-shu He,Peng Zhou,Bo Lai
It has been reported that the ultrasonic agitation coupled system (US/A) has higher oxidation efficiency than the pure ultrasonic system (US), and the atomic hydrogen ( H) and hydroxyl radicals ( OH) produced by H 2 O cracking and in situ hydrogen peroxide (H 2 O 2 ) can be significantly detected. In order to utilize the residual H 2 O 2 and explore the role and fate of H, US/A/Fe(III) as an in situ Fenton oxidation system, was constructed in this study. The experimental results proved that the system can generate H 2 O 2 in situ , and adding Fe(III) could significantly promote the oxidation of refractory organic pollutants. Quenching tests, probes experiments and EPR test were performed to successfully monitor the existence of OH. The contribution of H to Fe(III) reduction was speculated and confirmed. In addition, the kinetic model showed the decomposition rate of water molecule and the reduction rate of Fe(III) by H under different ultrasonic power. The effects of the factors (pH, coexisting substance, and actual water environment) on degrading organic pollutants were evaluated. Therefore, this work provides new strategy and mechanistic insight into in situ Fenton technique by coupling ultrasonic agitation and Fe(III) without external oxidants.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Bingxin Zhao,Wenyue Jiang,Ziting Li,Peng Zhou,Xiaoshuang Chen,Jinping Wang,Rui Yang,Chunling Zuo
The bifunctional electrocatalysts for hydrogen and oxygen evolution reactions (HER and OER) are crucial pivot in water electrolysis territory. In this study, vertically Fe incorporated CoMoP (Fe-CoMoP) nanosheet honeycomb product with super-hydrophilic and aerophobic features was projected and generated through the straightforward hydrothermal technique and phosphatized process. The Fe-CoMoP catalyst exhibits more distinguished intrinsic activity, accessible active sites, effective charge transfer and weak adhesion of gas bubbles. The overpotentials of dual-function Fe-CoMoP are 87.1 mV for HER and 244.4 mV for OER to drive the current density of 10 mA cm −2 . At room temperature, the overall water splitting reaction of Fe-CoMoP as cathode and anode is carried out at 1.54 V to reach 10 mA cm −2 with good stability. Simultaneously, the Fe-CoMoP couple electrolyzer also presents remarkable water splitting activity and durability in simulated industry circumstances of 6 M KOH, 60 °C at 500 mA cm −2 , which are close to practical conditions.
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POLYMER DEGRADATION AND STABILITY
·
2024
·
IF 6.3
Zhishuo Liu,Yifang Hua,Suqin Liu,Hongfei Li,Xiaoyu Gu,Jun Sun,Sheng Zhang
In this study, a novel approach was employed to enhance the flame retardant efficiency of an intumescent flame retardant (IFR) by growing a layered double hydroxides (LDHs) of Zn/Fe on the surface of melamine polyphosphate (MPP), denoted as Zn/Fe-LDH@MPP (LDHMPP). This modification was carried out via in-situ co-precipitation, and the resulting composite was subsequently applied to polypropylene (PP) in conjunction with piperazine pyrophosphate (PAPP). Under the same proportion and concentration, the PP/16 %LDHIFR formulation achieved a preferred V-0 rating in the UL-94 test. Furthermore, this formulation exhibited an enhanced ability to form a protective char layer, as evidenced by both cone calorimetry tests (CCT) and thermogravimetric analysis (TGA) tests. Additionally, the synergistic effect of Zn/Fe-LDH on flame retardancy was also studied.
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