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学者姓名：林立森
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Abstract ：
Real-time monitoring of hydroxyl radical (& sdot;OH) generation is crucial for both the efficacy and safety of chemodynamic therapy (CDT). Although & sdot;OH probe-integrated CDT agents can track & sdot;OH production by themselves, they often require complicated synthetic procedures and suffer from self-consumption of & sdot;OH. Here, we report the facile fabrication of a self-monitored chemodynamic agent (denoted as Fc-CD-AuNCs) by incorporating ferrocene (Fc) into beta-cyclodextrin (CD)-functionalized gold nanoclusters (AuNCs) via host-guest molecular recognition. The water-soluble CD served not only as a capping agent to protect AuNCs but also as a macrocyclic host to encapsulate and solubilize hydrophobic Fc guest with high Fenton reactivity for in vivo CDT applications. Importantly, the encapsulated Fc inside CD possessed strong electron-donating ability to effectively quench the second near-infrared (NIR-II) fluorescence of AuNCs through photoinduced electron transfer. After internalization of Fc-CD-AuNCs by cancer cells, Fenton reaction between redox-active Fc quencher and endogenous hydrogen peroxide (H2O2) caused Fc oxidation and subsequent NIR-II fluorescence recovery, which was accompanied by the formation of cytotoxic & sdot;OH and therefore allowed Fc-CD-AuNCs to in situ self-report & sdot;OH generation without undesired & sdot;OH consumption. Such a NIR-II fluorescence-monitored CDT enabled the use of renal-clearable Fc-CD-AuNCs for efficient tumor growth inhibition with minimal side effects in vivo. A NIR-II fluorescence-monitored chemodynamic therapy agent (Fc-CD-AuNCs) is prepared by integrating ferrocene (Fc) into beta-cyclodextrin-functionalized gold nanoclusters via host-guest interaction. In addition to producing & sdot;OH, Fenton reaction between redox-active Fc quencher and H2O2 causes Fc oxidation and consequent NIR-II fluorescence recovery, allowing renal-clearable Fc-CD-AuNCs to self-monitor & sdot;OH formation without undesired & sdot;OH consumption.image
Keyword ：
Antitumor Agents Antitumor Agents Chemodynamic Therapy Chemodynamic Therapy Ferrocene Ferrocene Host-Guest Systems Host-Guest Systems NIR-II Fluorescence NIR-II Fluorescence
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| GB/T 7714 | Yu, Meili , Ye, Zhuangjie , Liu, Siqin et al. Redox-Active Ferrocene Quencher-Based Supramolecular Nanomedicine for NIR-II Fluorescence-Monitored Chemodynamic Therapy [J]. | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2024 . |
| MLA | Yu, Meili et al. "Redox-Active Ferrocene Quencher-Based Supramolecular Nanomedicine for NIR-II Fluorescence-Monitored Chemodynamic Therapy" . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2024) . |
| APA | Yu, Meili , Ye, Zhuangjie , Liu, Siqin , Zhu, Yang , Niu, Xuegang , Wang, Jun et al. Redox-Active Ferrocene Quencher-Based Supramolecular Nanomedicine for NIR-II Fluorescence-Monitored Chemodynamic Therapy . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2024 . |
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Abstract ：
Ferrous iron (Fe2+) has more potent hydroxyl radical (*OH)-generating ability than other Fenton-type metal ions, making Fe-based nanomaterials attractive for chemodynamic therapy (CDT). However, because Fe2+ can be converted by ferritin heavy chain (FHC) to nontoxic ferric form and then sequestered in ferritin, therapeutic outcomes of Fe-mediated CDT agents are still far from satisfactory. Here we report the synthesis of siRNA-embedded Fe-0 nanoparticles (Fe-0-siRNA NPs) for self-reinforcing CDT via FHC downregulation. Upon internalization by cancer cells, pH-responsive Fe-0-siRNA NPs are degraded to release Fe2+ and FHC siRNA in acidic endo/lysosomes with the aid of oxygen (O-2). The accompanied O-2 depletion causes an intracellular pH decrease, which further promotes the degradation of Fe-0-siRNA NPs. In addition to initiating chemodynamic process, Fe2+-catalyzed *OH generation facilitates endo/lysosomal escape of siRNA by disrupting the membranes, enabling FHC downregulation-enhanced CDT.
Keyword ：
Chemodynamic Therapy Chemodynamic Therapy Fenton Reaction Fenton Reaction Ferritin Heavy Chain Ferritin Heavy Chain Iron Nanoparticles Iron Nanoparticles Small Interfering RNA Small Interfering RNA
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| GB/T 7714 | Wang, Jun , Ding, Hongye , Zhu, Yang et al. Iron-siRNA Nanohybrids for Enhanced Chemodynamic Therapy via Ferritin Heavy Chain Downregulation [J]. | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2023 , 62 (22) . |
| MLA | Wang, Jun et al. "Iron-siRNA Nanohybrids for Enhanced Chemodynamic Therapy via Ferritin Heavy Chain Downregulation" . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 62 . 22 (2023) . |
| APA | Wang, Jun , Ding, Hongye , Zhu, Yang , Liu, Yina , Yu, Meili , Cai, Huilan et al. Iron-siRNA Nanohybrids for Enhanced Chemodynamic Therapy via Ferritin Heavy Chain Downregulation . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2023 , 62 (22) . |
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Abstract ：
Ferrous iron (Fe2+) has more potent hydroxyl radical ((OH)-O-center dot)-generating ability than other Fenton-type metal ions, making Fe-based nanomaterials attractive for chemodynamic therapy (CDT). However, because Fe2+ can be converted by ferritin heavy chain (FHC) to nontoxic ferric form and then sequestered in ferritin, therapeutic outcomes of Fe-mediated CDT agents are still far from satisfactory. Here we report the synthesis of siRNA-embedded Fe-0 nanoparticles (Fe-0-siRNA NPs) for self-reinforcing CDT via FHC downregulation. Upon internalization by cancer cells, pH-responsive Fe-0-siRNA NPs are degraded to release Fe2+ and FHC siRNA in acidic endo/lysosomes with the aid of oxygen (O-2). The accompanied O-2 depletion causes an intracellular pH decrease, which further promotes the degradation of Fe-0-siRNA NPs. In addition to initiating chemodynamic process, Fe2+-catalyzed (OH)-O-center dot generation facilitates endo/lysosomal escape of siRNA by disrupting the membranes, enabling FHC downregulation-enhanced CDT.
Keyword ：
Chemodynamic Therapy Chemodynamic Therapy Fenton Reaction Fenton Reaction Ferritin Heavy Chain Ferritin Heavy Chain Iron Nanoparticles Iron Nanoparticles Small Interfering RNA Small Interfering RNA
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| GB/T 7714 | Wang, Jun , Ding, Hongye , Zhu, Yang et al. Iron-siRNA Nanohybrids for Enhanced Chemodynamic Therapy via Ferritin Heavy Chain Downregulation [J]. | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2023 , 62 (22) . |
| MLA | Wang, Jun et al. "Iron-siRNA Nanohybrids for Enhanced Chemodynamic Therapy via Ferritin Heavy Chain Downregulation" . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 62 . 22 (2023) . |
| APA | Wang, Jun , Ding, Hongye , Zhu, Yang , Liu, Yina , Yu, Meili , Cai, Huilan et al. Iron-siRNA Nanohybrids for Enhanced Chemodynamic Therapy via Ferritin Heavy Chain Downregulation . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2023 , 62 (22) . |
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Abstract ：
Lipid peroxidation (LPO) is one of the most damaging processes in chemodynamic therapy (CDT). Although it is well known that polyunsaturated fatty acids (PUFAs) are much more susceptible than saturated or monounsaturated ones to LPO, there is no study exploring the effect of cell membrane unsaturation degree on CDT. Here, we report a self-reinforcing CDT agent (denoted as OA@Fe-SAC@EM NPs), consisting of oleanolic acid (OA)-loaded iron single-atom catalyst (Fe-SAC)-embedded hollow carbon nanospheres encapsulated by an erythrocyte membrane (EM), which promotes LPO to improve chemodynamic efficacy via modulating the degree of membrane unsaturation. Upon uptake of OA@Fe-SAC@EM NPs by cancer cells, Fe-SAC-catalyzed conversion of endogenous hydrogen peroxide into hydroxyl radicals, in addition to initiating the chemodynamic therapeutic process, causes the dissociation of the EM shell and the ensuing release of OA that can enrich cellular membranes with PUFAs, enabling LPO amplification-enhanced CDT.
Keyword ：
Antitumor Agents Antitumor Agents Chemodynamic Therapy Chemodynamic Therapy Lipid Peroxidation Lipid Peroxidation Polyunsaturated Fatty Acids Polyunsaturated Fatty Acids Single-Atom Catalysts Single-Atom Catalysts
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| GB/T 7714 | Zhu, Yang , Gong, Peng , Wang, Jun et al. Amplification of Lipid Peroxidation by Regulating Cell Membrane Unsaturation To Enhance Chemodynamic Therapy [J]. | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2023 . |
| MLA | Zhu, Yang et al. "Amplification of Lipid Peroxidation by Regulating Cell Membrane Unsaturation To Enhance Chemodynamic Therapy" . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2023) . |
| APA | Zhu, Yang , Gong, Peng , Wang, Jun , Cheng, Junjie , Wang, Wenyu , Cai, Huilan et al. Amplification of Lipid Peroxidation by Regulating Cell Membrane Unsaturation To Enhance Chemodynamic Therapy . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2023 . |
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Abstract ：
As a rising generation of nanozymes, single atom enzymes show significant promise for cancer therapy, due to their maximum atom utilization efficiency and well-defined electronic structures. However, it remains a tremendous challenge to precisely produce a heteroatom-doped single atom enzyme with an expected coordination environment. Herein, we develop an anion exchange strategy for precisely controlled production of an edge-rich sulfur (S)-and nitrogen (N)-decorated nickel single atom enzyme (S-N/Ni PSAE). In particular, sulfurized S-N/Ni PSAE exhibits stronger peroxidase-like and glutathione oxidase-like activities than the nitrogen-monodoped nickel single atom enzyme, which is attributed to the vacancies and defective sites of sulfurized nitrogen atoms. Moreover, both in vitro and in vivo results demonstrate that, compared with nitrogen-monodoped N/Ni PSAE, sulfurized S-N/Ni PSAE more effectively triggers ferroptosis of tumor cells via inactivating glutathione peroxidase 4 and inducing lipid peroxidation. This study highlights the enhanced catalytic efficacy of a polynary heteroatom-doped single atom enzyme for ferroptosis-based cancer therapy.
Keyword ：
ferroptosis ferroptosis heteroatom doping heteroatom doping lipid peroxidation lipid peroxidation single atom enzyme single atom enzyme tumor therapy tumor therapy
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| GB/T 7714 | Zhu, Yang , Wang, Wenyu , Gong, Peng et al. Enhancing Catalytic Activity of a Nickel Single Atom Enzyme by Polynary Heteroatom Doping for Ferroptosis-Based Tumor Therapy [J]. | ACS NANO , 2023 . |
| MLA | Zhu, Yang et al. "Enhancing Catalytic Activity of a Nickel Single Atom Enzyme by Polynary Heteroatom Doping for Ferroptosis-Based Tumor Therapy" . | ACS NANO (2023) . |
| APA | Zhu, Yang , Wang, Wenyu , Gong, Peng , Zhao, Yafei , Pan, Yuanbo , Zou, Jianhua et al. Enhancing Catalytic Activity of a Nickel Single Atom Enzyme by Polynary Heteroatom Doping for Ferroptosis-Based Tumor Therapy . | ACS NANO , 2023 . |
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Abstract ：
Nanomaterials with enzyme-mimicking properties, coined as nanozymes, are a promising alternative to natural enzymes owing to their remarkable advantages, such as high stability, easy preparation, and favorable catalytic performance. Recently, with the rapid development of nanotechnology and characterization techniques, single atom nanozymes (SAzymes) with atomically dispersed active sites, well-defined electronic and geometric structures, tunable coordination environment, and maximum metal atom utilization are developed and exploited. With superior catalytic performance and selectivity, SAzymes have made impressive progress in biomedical applications and are expected to bridge the gap between artificial nanozymes and natural enzymes. Herein, the recent advances in SAzyme preparation methods, catalytic mechanisms, and biomedical applications are systematically summarized. Their biomedical applications in cancer therapy, oxidative stress cytoprotection, antibacterial therapy, and biosensing are discussed in depth. Furthermore, to appreciate these advances, the main challenges, and prospects for the future development of SAzymes are also outlined and highlighted in this review.
Keyword ：
antibacterial therapy antibacterial therapy biosensing biosensing cancer therapy cancer therapy oxidative-stress cytoprotection oxidative-stress cytoprotection reactive oxygen species reactive oxygen species single-atom nanozymes single-atom nanozymes
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| GB/T 7714 | Zhu, Yang , Liao, Yaxin , Zou, Jianhua et al. Engineering Single-Atom Nanozymes for Catalytic Biomedical Applications [J]. | SMALL , 2023 , 19 (30) . |
| MLA | Zhu, Yang et al. "Engineering Single-Atom Nanozymes for Catalytic Biomedical Applications" . | SMALL 19 . 30 (2023) . |
| APA | Zhu, Yang , Liao, Yaxin , Zou, Jianhua , Cheng, Junjie , Pan, Yuanbo , Lin, Lisen et al. Engineering Single-Atom Nanozymes for Catalytic Biomedical Applications . | SMALL , 2023 , 19 (30) . |
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Abstract ：
Mild photothermal therapy (mPTT) has emerged as a highly promising approach for tumor ablation. However, the heat-induced overexpression of heat shock proteins (HSPs) limits its efficacy by increasing cellular temperature tolerance. Herein, a self-catalytically enhanced mild PTT strategy that directly disrupts the structure of HSPs to restore tumor cell sensitivity is proposed. In the proof-of-concept study, AgFeCu nanoparticles (AgFeCu NPs) with dual-active catalytic centers (Fe-Cu) and near-infrared photothermal properties are developed. The AgFeCu NPs can efficiently catalyze the conversion of endogenous hydrogen peroxide into hydroxyl radicals in situ, leading to the degradation of HSPs and enhancing the therapeutic effects of mild PTT mediated by their Ag-based substrates. Furthermore, AgFeCu NPs can also induce oxidative stress by depleting intracellular glutathione and promoting lipid peroxidation, thereby triggering tumor ferroptosis and resulting in significant tumor elimination in a U87MG murine tumor model. This self-catalytically enhanced strategy maximizes the efficacy of mild PTT while minimizing damage to healthy tissues, which is expected to provide valuable insights for the development of next-generation photothermal nanoagents for improved tumor therapeutics.
Keyword ：
catalytic therapy catalytic therapy ferroptosis ferroptosis heat shock proteins heat shock proteins mild photothermal therapy mild photothermal therapy reactive oxygen species reactive oxygen species
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| GB/T 7714 | Niu, Xuegang , Zhu, Yang , Ding, Chenyu et al. Dual-Active Center AgFeCu Nanocatalyst for Tumor Destruction via Self-Catalytically Enhanced Mild Photothermal Therapy [J]. | ADVANCED FUNCTIONAL MATERIALS , 2023 , 33 (51) . |
| MLA | Niu, Xuegang et al. "Dual-Active Center AgFeCu Nanocatalyst for Tumor Destruction via Self-Catalytically Enhanced Mild Photothermal Therapy" . | ADVANCED FUNCTIONAL MATERIALS 33 . 51 (2023) . |
| APA | Niu, Xuegang , Zhu, Yang , Ding, Chenyu , Ma, Jing , Wei, Penghui , Lin, Yuanxiang et al. Dual-Active Center AgFeCu Nanocatalyst for Tumor Destruction via Self-Catalytically Enhanced Mild Photothermal Therapy . | ADVANCED FUNCTIONAL MATERIALS , 2023 , 33 (51) . |
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The practical applications of lithium sulfur batteries have been greatly restricted by the polysulfide shuttle effect and non-conductivity of sulfur. Here, we report a nickel-catalyzed carbonization method to synthesize three-dimensional (3D) nickel@N-doped carbon-nanotube (CNT) foams for lithium-sulfur batteries. The corresponding carbon/sulfur cathode with a high sulfur loading of 3.71 mg cm(-2) possesses a high initial capacity of 855.6 mAh g(-1) at 135 mA g(-1) and good cyclic stability with a low fading rate of 0.153% per cycle for 100 cycles at 270 mA g(-1). The growth of carbon thin layers on the nickel nanoparticles results in the encapsulation of the nanoparticles in the CNTs, which makes the carbon forms highly conductive and prevents the metal nanoparticles from being oxidized by polysulfides. The high conductivity is favorable for the electron transfer between polysulfides and carbon electrode. Moreover, the doped nitrogen atoms on the CNTs have strong chemical adsorption ability for polysulfides, accelerating redox reaction of polysulfides on the carbon electrode (i.e., suppressing the shuttle effect). These unique structural characteristics well explain the excellent electrochemical performance of the assembled batteries. It is believed that the fabricated carbon foam is a promising material for high sulfur-loading lithium-sulfur battery. (C) 2022 Published by Elsevier B.V.
Keyword ：
High sulfur loading High sulfur loading Internally grown nickel metal Internally grown nickel metal Lithium-sulfur battery Lithium-sulfur battery Stably high electrical conductivity Stably high electrical conductivity Three-dimensional carbon nanotubes foam Three-dimensional carbon nanotubes foam
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| GB/T 7714 | Hu, Haiman , Chen, Hui , Wang, Wensong et al. Synthesis of nickel@N-doped carbon nanotube foams for high sulfur-loading lithium-sulfur battery [J]. | JOURNAL OF ALLOYS AND COMPOUNDS , 2022 , 922 . |
| MLA | Hu, Haiman et al. "Synthesis of nickel@N-doped carbon nanotube foams for high sulfur-loading lithium-sulfur battery" . | JOURNAL OF ALLOYS AND COMPOUNDS 922 (2022) . |
| APA | Hu, Haiman , Chen, Hui , Wang, Wensong , Li, Senlin , Zhang, Yurong , Liu, Jingdong et al. Synthesis of nickel@N-doped carbon nanotube foams for high sulfur-loading lithium-sulfur battery . | JOURNAL OF ALLOYS AND COMPOUNDS , 2022 , 922 . |
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Abstract ：
The practical applications of lithium sulfur batteries have been greatly restricted by the polysulfide shuttle effect and non-conductivity of sulfur. Here, we report a nickel-catalyzed carbonization method to synthesize three-dimensional (3D) nickel@N-doped carbon-nanotube (CNT) foams for lithium-sulfur batteries. The corresponding carbon/sulfur cathode with a high sulfur loading of 3.71 mg cm-2 possesses a high initial capacity of 855.6 mAh g-1 at 135 mA g-1 and good cyclic stability with a low fading rate of 0.153% per cycle for 100 cycles at 270 mA g-1. The growth of carbon thin layers on the nickel nanoparticles results in the encapsulation of the nanoparticles in the CNTs, which makes the carbon forms highly conductive and prevents the metal nanoparticles from being oxidized by polysulfides. The high conductivity is favorable for the electron transfer between polysulfides and carbon electrode. Moreover, the doped nitrogen atoms on the CNTs have strong chemical adsorption ability for polysulfides, accelerating redox reaction of polysulfides on the carbon electrode (i.e., suppressing the shuttle effect). These unique structural characteristics well explain the excellent electrochemical performance of the assembled batteries. It is believed that the fabricated carbon foam is a promising material for high sulfur-loading lithium-sulfur battery. (c) 2022 Published by Elsevier B.V.
Keyword ：
High sulfur loading High sulfur loading Internally grown nickel metal Internally grown nickel metal Lithium -sulfur battery Lithium -sulfur battery Stably high electrical conductivity Stably high electrical conductivity Three-dimensional carbon nanotubes foam Three-dimensional carbon nanotubes foam
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| GB/T 7714 | Hu, Haiman , Chen, Hui , Wang, Wensong et al. Synthesis of nickel@N-doped carbon nanotube foams for high sulfur-loading lithium-sulfur battery [J]. | JOURNAL OF ALLOYS AND COMPOUNDS , 2022 , 922 . |
| MLA | Hu, Haiman et al. "Synthesis of nickel@N-doped carbon nanotube foams for high sulfur-loading lithium-sulfur battery" . | JOURNAL OF ALLOYS AND COMPOUNDS 922 (2022) . |
| APA | Hu, Haiman , Chen, Hui , Wang, Wensong , Li, Senlin , Zhang, Yurong , Liu, Jingdong et al. Synthesis of nickel@N-doped carbon nanotube foams for high sulfur-loading lithium-sulfur battery . | JOURNAL OF ALLOYS AND COMPOUNDS , 2022 , 922 . |
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Autophagy is an important protective mechanism in maintaining or restoring cell homeostasis under physiological and pathological conditions. Nanoparticles (NPs) with certain components and morphologies can induce autophagic responses in cancer cells, providing a new perspective for establishing cancer therapy strategies. Herein, a novel nanodrug system, cell membranes-coated zeolitic imidazolate framework-8 (ZIF-8) NPs encapsulating chloroquine (CQ) and glucose oxidase (GOx) (defined as mCG@ZIF), is designed to achieve an enhanced anticancer effect with the combination of starvation therapy and an autophagy regulation strategy. It is found that ZIF-8 as a nanocarrier can induce autophagy to promote survival of cancer cells via the upstream Zn2+-stimulated mitochondrial reactive oxygen species (ROS) so that the anticancer effect is directly achieved by inhibiting this pro-survival autophagy using CQ released from mCG@ZIF under a tumor acidic microenvironment. Moreover, a cancer cell under starvation caused by GOx harnesses autophagy to maintain intracellular ATP levels and resist starvation therapy. The released CQ further inhibits the starvation-induced pro-survival autophagy and cuts off the protective pathway of cancer cells, enhancing the anticancer efficiency of GOx-based starvation therapy. Significantly, the cell membrane coating endows mCG@ZIF with excellent in vivo homotypic targeting ability. Both in vitro and in vivo results have confirmed the enhanced anticancer effect achieved by mCG@ZIF with a negligible side effect.
Keyword ：
autophagy inhibition autophagy inhibition nanocarrier nanocarrier pro-survival autophagy pro-survival autophagy starvation therapy starvation therapy ZIF-8 ZIF-8
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| GB/T 7714 | Li, Fenglan , Chen, Tao , Wang, Fang et al. Enhanced Cancer Starvation Therapy Enabled by an Autophagy Inhibitors-Encapsulated Biomimetic ZIF-8 Nanodrug: Disrupting and Harnessing Dual Pro-Survival Autophagic Responses [J]. | ACS APPLIED MATERIALS & INTERFACES , 2022 . |
| MLA | Li, Fenglan et al. "Enhanced Cancer Starvation Therapy Enabled by an Autophagy Inhibitors-Encapsulated Biomimetic ZIF-8 Nanodrug: Disrupting and Harnessing Dual Pro-Survival Autophagic Responses" . | ACS APPLIED MATERIALS & INTERFACES (2022) . |
| APA | Li, Fenglan , Chen, Tao , Wang, Fang , Chen, Jinfa , Zhang, Yuanyuan , Song, Danting et al. Enhanced Cancer Starvation Therapy Enabled by an Autophagy Inhibitors-Encapsulated Biomimetic ZIF-8 Nanodrug: Disrupting and Harnessing Dual Pro-Survival Autophagic Responses . | ACS APPLIED MATERIALS & INTERFACES , 2022 . |
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