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学者姓名:林祖金
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Abstract :
Wound infections pose a critical global health threat, largely exacerbated by biofilm formation and escalating antimicrobial resistance (AMR). This research introduces a novel nanocomposite CCFc that integrates ultrasmall CuS nanoparticles within a copper-based ferrocene-terephthalate metal-organic framework for the promotion of infected wound healing. This elegant design leverages photothermal-enhanced chemodynamic therapy (CDT) and photothermal therapy (PTT) to effectively combat biofilm-related infections and bypass AMR. CCFc exhibits potent peroxidase (POD)-like activity, stemming from both copper and ferrous ions, enabling powerful CDT. Furthermore, copper (II) reacts with reductive glutathione (GSH), enhancing the POD-like activity by forming catalytic Cu(I) sites and intensifying oxidative stress by GSH consume, thereby amplifying CDT efficacy. Under near-infrared (NIR) irradiation, the CuS component provides robust PTT and enhances CDT via localized hyperthermia. The synergistic CDT and PTT results in exceptional in vitro antimicrobial efficacy of CCFc, with a remarkably low minimum bactericidal concentration (MBC) of 6 mu g mL- 1 against MRSA under NIR irradiation (808 nm, 1.0 W cm- 2) and H2O2 (1.0 mM) assistance. Remarkably, CCFc can effectively inhibit both immature biofilm formation and eradicate mature biofilms. In vivo assays demonstrated CCFc's superior antimicrobial and anti-inflammatory properties, thereby significantly accelerating the infected wound healing. With low cytotoxicity and excellent biocompatibility, CCFc shows promising potential for future clinical translation.
Keyword :
Bacterial disinfection Bacterial disinfection Chemodynamic Therapy Chemodynamic Therapy CuS NPs CuS NPs Photothermal therapy Photothermal therapy Wound healing Wound healing
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| GB/T 7714 | Hui, Yi-Fei , Jiang, Jilin , Lin, Yi-Han et al. A CuS-loaded copper-ferrocene framework with synergistic chemodynamic and photothermal antimicrobial therapy for accelerated infected wound healing [J]. | COLLOIDS AND SURFACES B-BIOINTERFACES , 2026 , 258 . |
| MLA | Hui, Yi-Fei et al. "A CuS-loaded copper-ferrocene framework with synergistic chemodynamic and photothermal antimicrobial therapy for accelerated infected wound healing" . | COLLOIDS AND SURFACES B-BIOINTERFACES 258 (2026) . |
| APA | Hui, Yi-Fei , Jiang, Jilin , Lin, Yi-Han , Zhou, Zijie , Hu, Duan-Ping , Li, Lin-Yi et al. A CuS-loaded copper-ferrocene framework with synergistic chemodynamic and photothermal antimicrobial therapy for accelerated infected wound healing . | COLLOIDS AND SURFACES B-BIOINTERFACES , 2026 , 258 . |
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| GB/T 7714 | Hui, Yi-Fei , Jiang, Jilin , Lin, Yi-Han et al. A CuS-loaded copper-ferrocene framework with synergistic chemodynamic and photothermal antimicrobial therapy for accelerated infected wound healing (vol 258, 115239, 2026) [J]. | COLLOIDS AND SURFACES B-BIOINTERFACES , 2026 , 258 . |
| MLA | Hui, Yi-Fei et al. "A CuS-loaded copper-ferrocene framework with synergistic chemodynamic and photothermal antimicrobial therapy for accelerated infected wound healing (vol 258, 115239, 2026)" . | COLLOIDS AND SURFACES B-BIOINTERFACES 258 (2026) . |
| APA | Hui, Yi-Fei , Jiang, Jilin , Lin, Yi-Han , Zhou, Zijie , Hu, Duan-Ping , Li, Lin-Yi et al. A CuS-loaded copper-ferrocene framework with synergistic chemodynamic and photothermal antimicrobial therapy for accelerated infected wound healing (vol 258, 115239, 2026) . | COLLOIDS AND SURFACES B-BIOINTERFACES , 2026 , 258 . |
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As an antibacterial agent, H2O2 is widely used to combat pathogenic bacterial infections clinically. To mitigate potential side effects associated with a high dosage of H2O2, it is pivotal to improve its antibacterial efficacy. Herein, a nanoscale porphyrin-based mesoporous metal-organic framework (MOF) nanozyme, Nano-PCN-222(Fe), was readily prepared by a one pot. Nano-PCN-222(Fe) shows a striking peroxidase (POD)-like activity comparable to that of natural enzyme horse radish peroxidase. Such a high POD-like activity of Nano-PCN-222(Fe) nanozyme is primarily attributed to both the monodispersion and the accessibility of single-atom catalytic sites Fe within the framework. As a consequence of its ability to effectively catalyze the decomposition of H2O2 into more toxic hydroxyl radicals, Nano-PCN-222(Fe) shows excellent antibacterial activity against both Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria with the assistance of H2O2. Remarkably, only 10 mM H2O2 is sufficient to fully kill E. coli and S. aureus in the presence of Nano-PCN-222(Fe) (10 ppm), which is significantly lower than that used in actual clinical disinfection (166-1000 mM). Moreover, Nano-PCN-222(Fe) could significantly accelerate infected wound healing due to its superior antimicrobial activity. Additionally, no appreciable biotoxicity of Nano-PCN-222(Fe) was observed even though its dosage was up to 30 ppm.
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| GB/T 7714 | Feng, Han-Xiao , Zhou, Zijie , Jiang, Jilin et al. A Porphyrin-Based Metal-Organic Framework Nanozyme with Superior Peroxidase-like Activity for Combating Antibacterial Infections and Promoting Wound Healing [J]. | INORGANIC CHEMISTRY , 2025 , 64 (7) : 3541-3552 . |
| MLA | Feng, Han-Xiao et al. "A Porphyrin-Based Metal-Organic Framework Nanozyme with Superior Peroxidase-like Activity for Combating Antibacterial Infections and Promoting Wound Healing" . | INORGANIC CHEMISTRY 64 . 7 (2025) : 3541-3552 . |
| APA | Feng, Han-Xiao , Zhou, Zijie , Jiang, Jilin , Hui, Yi-Fei , Li, Bing-Xin , Li, Shulin et al. A Porphyrin-Based Metal-Organic Framework Nanozyme with Superior Peroxidase-like Activity for Combating Antibacterial Infections and Promoting Wound Healing . | INORGANIC CHEMISTRY , 2025 , 64 (7) , 3541-3552 . |
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In our study, DFT calculations were employed to study the influence of both adsorbed H2 and H2O upon the catalysis reactivity of CO2 hydrogenation to methanol over two exposed planes of In-Rh alloy. For InRh(011), CH3OH formation is not viable from both "Formate" and "RWGS+CO-Hydro" mechanisms owing to the substantial kinetic barrier encountered. For In3Rh(212), the activated H* prefers to adsorb at surface Rh atoms from the first layer and thereby generates three potentially reactive sites (Rh_I, Rh_II and Rh_III), from which methanol is produced through the "Formate" pathway. Based on the microkinetic model, methanol is selectively produced from Rh_III while CO is the favorable product from the other two. Methanol formation from both Rh_I and Rh_II is substantially limited by the rate-determining step (RDS) owing to the bridging configuration of H* being too stable. As a major side product of CO2 hydrogenation, H2O introduction could lower the RDS of the "Formate" pathway from Rh_III and thereby substantially improve its production rate of methanol. Overall, our calculation determines the reactive site of In-Rh alloy and explains the way how H2 and H2O influence the reaction mechanism and catalysis performance of the bimetallic system.
Keyword :
CO 2 hydrogenation to methanol CO 2 hydrogenation to methanol Density functional theory Density functional theory H influence H influence In-Rh alloy In-Rh alloy Water promotion effect Water promotion effect
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| GB/T 7714 | Yu, Jie , Xiao, Ai-Ting , Li, Lin-Yi et al. Mechanistic investigation into influence of adsorbed H and H2O on In-Rh alloy during CO2 hydrogenation to methanol [J]. | COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS , 2025 , 714 . |
| MLA | Yu, Jie et al. "Mechanistic investigation into influence of adsorbed H and H2O on In-Rh alloy during CO2 hydrogenation to methanol" . | COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS 714 (2025) . |
| APA | Yu, Jie , Xiao, Ai-Ting , Li, Lin-Yi , Tan, Kai , Lin, Zu-Jin . Mechanistic investigation into influence of adsorbed H and H2O on In-Rh alloy during CO2 hydrogenation to methanol . | COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS , 2025 , 714 . |
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Bacterial infections pose an increasing threat to human health. Chemodynamic therapy (CDT), which utilizes nanozymes to catalyze H2O2 into highly toxic hydroxyl radicals (OH), offers a promising disinfection strategy because of its high efficacy, broad-spectrum antibacterial activity, and low risk of inducing drug resistance. Herein, we developed a self-powered CDT nanocomposite, CaO2@PCN-222(Fe), via a facile one-pot synthesis for wound disinfection. In infected wounds, the CaO2 component of the composite gradually hydrolyzes to H2O2, while the PCN-222(Fe) component acts as peroxidase mimics to efficiently catalyze the generated H2O2 into OH, thus achieving self-powered CDT. In vitro assays confirmed that the minimum bactericidal concentration of the composite against Staphylococcus aureus is as low as 31.25 mu g mL-1. Furthermore, in vivo assays demonstrated that the composite could effectively accelerate infected wound healing. To broaden application scenarios, the composite was further integrated into poly(vinylidene fluoride) (PVDF) to form CaO2@PCN-222(Fe)@PVDF mixed matrix membranes (MMMs), which inherit the self-powered CDT capability, exhibiting high antimicrobial activity and promoting infected wound healing. Notably, no significant toxicity was observed for CaO2@PCN-222(Fe) and its MMMs. This work presents an efficient self-powered CDT modality, combining the advantages of CaO2 and peroxidase mimics for treating bacterial infections and promoting infected wound healing.
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| GB/T 7714 | Feng, Han-Xiao , Su, Xian-Feng , Hu, Duan-Ping et al. Metal-Organic Framework-Based Self-Powered Chemodynamic Therapy Nanosystem: CaO2@PCN-222(Fe) and Its Mixed Matrix Membranes for Promoting Infected Wound Healing [J]. | INORGANIC CHEMISTRY , 2025 , 64 (26) : 13557-13568 . |
| MLA | Feng, Han-Xiao et al. "Metal-Organic Framework-Based Self-Powered Chemodynamic Therapy Nanosystem: CaO2@PCN-222(Fe) and Its Mixed Matrix Membranes for Promoting Infected Wound Healing" . | INORGANIC CHEMISTRY 64 . 26 (2025) : 13557-13568 . |
| APA | Feng, Han-Xiao , Su, Xian-Feng , Hu, Duan-Ping , Hui, Yi-Fei , Su, Hongxin , Jiang, Jilin et al. Metal-Organic Framework-Based Self-Powered Chemodynamic Therapy Nanosystem: CaO2@PCN-222(Fe) and Its Mixed Matrix Membranes for Promoting Infected Wound Healing . | INORGANIC CHEMISTRY , 2025 , 64 (26) , 13557-13568 . |
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Covalent organic frameworks (COFs) are a promising platform for heterogeneous photocatalysis due to their stability and design diversity, but their potential is often restricted by unmanageable targeted excitation and charge transfer. Herein, a bimetallic COF integrating photosensitizers and catalytic sites is designed to facilitate locally ultrafast charge transfer, aiming to improve the photocatalytic reduction of CO2. The strategy uses a "one-pot" method to synthesize the bimetallic COF (termed PBCOFRuRe) through in situ Schiff-base condensation of Pyrene with MBpy (M = Ru, Re) units. In this structure, Ru and Re are anchored within bipyridine as the photosensitive center and catalytic site, respectively. The bimetallic architecture of PBCOFRuRe significantly boosts the photocatalytic efficiency for CO2 reduction, achieving an impressive CO yield of 8306.6 mu mol g(-1) h(-1) with 99.8% selectivity, surpassing most reported COF materials. This improvement is attributed to the localized ultrafast charge transfer (0.23 ps) from Ru to Re, as demonstrated by femtosecond transient absorption spectroscopy (TAS). Further investigations demonstrate its heterogeneous feature, showcasing exceptional long-term stability and recyclability. This study represents a versatile approach for designing bimetallic COFs with ultrafast charge transfer, paving the pathway for advancements in artificial photosynthesis.
Keyword :
charge transfer charge transfer CO2 photoreduction CO2 photoreduction covalent organic frameworks covalent organic frameworks heterogeneous heterogeneous photocatalyst photocatalyst
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| GB/T 7714 | Liu, Jiaying , Li, Jingjun , Lin, Zujin et al. In Situ Integration of Metallic Catalytic Sites and Photosensitive Centers within Covalent Organic Frameworks for the Enhanced Photocatalytic Reduction of CO2 [J]. | SMALL , 2025 , 21 (7) . |
| MLA | Liu, Jiaying et al. "In Situ Integration of Metallic Catalytic Sites and Photosensitive Centers within Covalent Organic Frameworks for the Enhanced Photocatalytic Reduction of CO2" . | SMALL 21 . 7 (2025) . |
| APA | Liu, Jiaying , Li, Jingjun , Lin, Zujin , Ye, Shihua , Lin, Wenlie , Yang, Xue et al. In Situ Integration of Metallic Catalytic Sites and Photosensitive Centers within Covalent Organic Frameworks for the Enhanced Photocatalytic Reduction of CO2 . | SMALL , 2025 , 21 (7) . |
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Second-order nonlinear optical (NLO) materials have important applications in the realms of photoelectronics and photonics whose microstructures need to be organized into a noncentrosymmetric (NCS) structure. In this work, a mixed-ligands three-dimensional (3D) noncentrosymmetric coordination polymer Zn(OBA)(DIB)center dot 0.5H(2)O (1) was hydrothermally prepared from 4, 4'-oxydibenzoic acid (H(2)OBA), 1, 3-di(1H-imidazol-1-yl)benzene (DIB) and Zn(NO3)(2)center dot 6H(2)O via spontaneous resolution approach, which crystallizes in a noncentrosymmetric space group Fdd2. Compound 1 was characterized by powder X-ray diffraction (XRD), thermogravimetric (TGA) and IR analyses. The structural analysis shows that 1 is a two-fold self-interpenetrated three-dimensional (3D) network material. Single crystal X-ray diffraction and the topological analysis manifests that the topological structure of 1 belongs to a cds topological net. The measurement of the fluorescent properties of 1 and the free DIB ligand show that the emission peak at 460 nm of 1 can be attributed to the charge transition from the. bond electron to the. anti-bond orbital of the DIB ligand. The second-harmonic generation (SHG) measurement shows that the second-order NLO effect of compound 1 is approximately equivalent to that of potassium dihydrogen phosphate (KDP). Compound 1 is high thermal stable and insoluble in water and common organic solvents, making it to be a potential candidate as a second-order NLO material.
Keyword :
Fluorescent properties Fluorescent properties Inorganic-organic hybrids Inorganic-organic hybrids Noncentrosymmetric structure Noncentrosymmetric structure Second-order NLO materials Second-order NLO materials Spontaneous resolution Spontaneous resolution Topological analysis Topological analysis
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| GB/T 7714 | Lin, Jian-Di , Li, Zhen-Fei , Lin, Zu-Jin et al. A two-fold interpenetrated mixed-ligands acentric 3D coordination polymer Zn(OBA)(DIB)•0.5H2O: Topological analysis, fluorescent and second-order NLO properties [J]. | JOURNAL OF MOLECULAR STRUCTURE , 2024 , 1295 . |
| MLA | Lin, Jian-Di et al. "A two-fold interpenetrated mixed-ligands acentric 3D coordination polymer Zn(OBA)(DIB)•0.5H2O: Topological analysis, fluorescent and second-order NLO properties" . | JOURNAL OF MOLECULAR STRUCTURE 1295 (2024) . |
| APA | Lin, Jian-Di , Li, Zhen-Fei , Lin, Zu-Jin , Zheng, Fa-Kun . A two-fold interpenetrated mixed-ligands acentric 3D coordination polymer Zn(OBA)(DIB)•0.5H2O: Topological analysis, fluorescent and second-order NLO properties . | JOURNAL OF MOLECULAR STRUCTURE , 2024 , 1295 . |
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Although various antibacterial strategies have been developed, antibiotic chemotherapy remains the primary clinical treatment for bacterial infections. To address the limitations associated with the traditional antibiotic therapy, like burst drug release, rapid drug clearance, and the emergence of drug resistance, it is highly desirable to develop drug release systems that can realize controlled and sustained drug release to enhance the therapeutic efficacy. Herein, we present a novel drug release system, CIP@SU-102, which shows superior and long-lasting antibacterial activity. CIP@SU-102 was readily fabricated by the encapsulation of ciprofloxacin (CIP), a cationic broad-spectrum antibiotic, into an anionic Zr-based metal-organic framework SU-102 through ion-exchange. Notably, the loading capacity and efficiency of CIP were impressively high, reaching 33.3% and 66.8%, respectively. In vitro assays demonstrated that CIP@SU-102 has superior and prolonged antimicrobial activity against Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria, including the methicillin-resistant Staphylococcus aureus (MRSA). Remarkably, CIP@SU-102 could retain its antibacterial efficacy even after continuous drug release for 20 days. In vivo assays verified that CIP@SU-102 could significantly accelerate infected wound healing because of its sustained drug release properties. Due to the low cost and biocompatibility of SU-102 as well as the affordability of ciprofloxacin, CIP@SU-102 is a very promising antibacterial agent for long-lasting bacterial disinfection and boosting infected wound healing in actual clinical applications. This work highlights the potential of the metal-organic framework-based drug release systems for sustained antimicrobial therapy.
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| GB/T 7714 | Zheng, Hui-Qian , Feng, Han-Xiao , Li, Bing-Xin et al. A Zr-based metal-organic framework drug release system with long-lasting antibacterial behavior for accelerating wound healing [J]. | DALTON TRANSACTIONS , 2024 , 53 (48) : 19226-19234 . |
| MLA | Zheng, Hui-Qian et al. "A Zr-based metal-organic framework drug release system with long-lasting antibacterial behavior for accelerating wound healing" . | DALTON TRANSACTIONS 53 . 48 (2024) : 19226-19234 . |
| APA | Zheng, Hui-Qian , Feng, Han-Xiao , Li, Bing-Xin , Hui, Yi-Fei , Lin, Yi-Han , Su, Xian-Feng et al. A Zr-based metal-organic framework drug release system with long-lasting antibacterial behavior for accelerating wound healing . | DALTON TRANSACTIONS , 2024 , 53 (48) , 19226-19234 . |
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Pathogenic bacteria have consistently posed a formidable challenge to human health, creating the critical need for effective antibacterial solutions. In response, enzyme-metal-organic framework (MOF) composites have emerged as a promising class of antibacterial agents. This study focuses on the development of an enzyme-MOF composite based on HZIF-8, incorporating the advantages of simple synthesis, ZIF-8 antibacterial properties, lysozyme hydrolysis, and high biological safety. Through a one-pot method, core-shell nanoparticles (HZIF-8) were synthesized. This structure enables efficient immobilization of lysozyme and lactoferrin within the HZIF-8, resulting in the formation of the lysozyme-lactoferrin@HZIF-8 (LYZ-LF@HZIF-8) composite. Upon exposure to light irradiation, HZIF-8 itself possessed antibacterial properties. Lysozyme initiated the degradation of bacterial peptidoglycan and lactoferrin synergistically enhanced the antibacterial effect of lysozyme. All of the above ultimately contributed to comprehensive antibacterial activity. Antibacterial assessments demonstrated the efficacy of the LYZ-LF@HZIF-8 composite, effectively eradicating Staphylococcus aureus at a cell density of 1.5 x 10(6) CFU/mL with a low dosage of 200 mu g/mL and completely inactivating Escherichia coli at 400 mu g/mL with the same cell density. The enzyme-MOF composite exhibited significant and durable antibacterial efficacy, with no apparent cytotoxicity in vitro, thereby unveiling expansive prospects for applications in the medical and food industries.
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| GB/T 7714 | Zheng, Hao , Sun, Tong , Zeng, Yan et al. Hierarchical Micro- and Mesoporous Zeolitic Imidazolate Framework-8-Based Enzyme Hybrid for Combination Antimicrobial by Lysozyme and Lactoferrin [J]. | INORGANIC CHEMISTRY , 2024 , 63 (26) : 12377-12384 . |
| MLA | Zheng, Hao et al. "Hierarchical Micro- and Mesoporous Zeolitic Imidazolate Framework-8-Based Enzyme Hybrid for Combination Antimicrobial by Lysozyme and Lactoferrin" . | INORGANIC CHEMISTRY 63 . 26 (2024) : 12377-12384 . |
| APA | Zheng, Hao , Sun, Tong , Zeng, Yan , Zheng, Mu-Yue , Zhang, Fang-Zhong , Wang, Yu-Lin et al. Hierarchical Micro- and Mesoporous Zeolitic Imidazolate Framework-8-Based Enzyme Hybrid for Combination Antimicrobial by Lysozyme and Lactoferrin . | INORGANIC CHEMISTRY , 2024 , 63 (26) , 12377-12384 . |
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Pathogenic bacteria have consistently posed a formidable challenge to human health, emphasizing the critical need for effective antibacterial solutions. In response, metal-organic framework (MOF)-enzyme composite materials have emerged as a promising class of antibacterial agents. This study focuses on the development of a nanoenzyme hybrid based on HZIF-8, harnessing the synergistic potential of simple synthesis, ZIF-8 antibacterial properties, lysozyme hydrolysis, and high biological safety. Through a one-pot method, core-shell nanoparticles (HZIF-8) were synthesized to efficiently immobilize lysozyme and lactoferrin within the HZIF-8 structure, resulting in the formation of the lysozyme-lactoferrin@HZIF-8 (LYZ-LF@HZIF-8) nanoenzyme hybrid. Upon exposure to light irradiation, lysozyme initiated the degradation of bacterial peptidoglycan, HZIF-8 efficiently captured photogenerated reactive oxygen species (ROS), and lactoferrin synergistically enhanced the antibacterial effect of lysozyme, culminating in a comprehensive antibacterial activity. Antibacterial assessments demonstrated the efficacy of the LYZ-LF@HZIF-8 nanoenzyme hybrid, effectively eradicating S. aureus at a cell density of 1.5×106 with a low dosage of 200 μg/mL, and completely inactivating E. coli at 400 μg/mL with the same cell density. The nanoenzyme hybrid exhibited significant and durable antibacterial efficacy, with no apparent cytotoxicity in vitro, thereby unveiling expansive prospects for applications in the medical and food industries. © 2024, The Authors. All rights reserved.
Keyword :
Core shell nanoparticles Core shell nanoparticles Enzymes Enzymes Escherichia coli Escherichia coli Organometallics Organometallics Synthesis (chemical) Synthesis (chemical)
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| GB/T 7714 | Zheng, Hao , Sun, Tong , Zeng, Yan et al. Hierarchical Micro- and Mesoporous Zeolitic Imidazolate Framework-8 Based Enzyme Hybrid for Combination Antimicrobial by Lysozyme and Lactoferrin [J]. | SSRN , 2024 . |
| MLA | Zheng, Hao et al. "Hierarchical Micro- and Mesoporous Zeolitic Imidazolate Framework-8 Based Enzyme Hybrid for Combination Antimicrobial by Lysozyme and Lactoferrin" . | SSRN (2024) . |
| APA | Zheng, Hao , Sun, Tong , Zeng, Yan , Zheng, Mu-Yue , Zhang, Fang-Zhong , Wang, Yu-Lin et al. Hierarchical Micro- and Mesoporous Zeolitic Imidazolate Framework-8 Based Enzyme Hybrid for Combination Antimicrobial by Lysozyme and Lactoferrin . | SSRN , 2024 . |
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