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Bioinspired nanomaterials for the treatment of bacterial infections

Nano Research 2024年第2期17卷 691-714页

作者： Xiaojing Ma Wenjing Tang rong yang Robert F.Smith School of Chemical&Biomolecular Engineering Cornell UniversityIthacaNY 14853USA

Infectious diseases pose a serious threat to global health.Although immunizations can control most viral infections,bacterial infections,particularly those caused by drug-resistant strains,continue to cause high rates of illness and death.Unfortunately,the creation of new antibiotics has come to a grinding halt in the last ten years.In response to this crisis,nanotechnology has emerged as a hopeful solution to tackle drug resistance and enhance treatment results.A large variety of biomimetic nanomaterials,termed nanozymes,have demonstrated strong antimicrobial efficacy.While the inherent toxicity of nanomaterials is a concern,recent studies have harnessed the stimuli-responsiveness of nanomaterials to enable local and/or targeted delivery to reduce the treatment side effects.Indeed,the physicochemical versatility of nanomaterials affords many degrees of freedom that enable rational design of smart or autonomous therapeutics,which cannot be achieved using conventional antibiotics.The design straddles the fields of catalysis,nanoscience,microbiology,and translational medicine.To provide an overview of this interdisciplinary landscape,this review is organized based on composition into lipid,metal,metal oxide,and non-metallic nanomaterials.Liposomes as a delivery vehicle enhance bioavailability and reduce toxicity.Metal-and metal oxide-based nanomaterials inhibit bacterial growth by mimicking natural enzymatic activities such as peroxidase(POD)and oxidase.Furthermore,carbon-,polymer-,and cell membrane-based nanomaterials are combined into a discussion on non-metallic materials.At the end of this review,potentially fruitful directions for future bioinspired nanomaterials in infectious disease treatment are included.

关键词： bioinspired nanomaterial bacteria infectious disease antimicrobial liposome nanozyme

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Atomistic mechanism of high ionic conductivity in lithium ytterbium-based halide solid electrolytes:A first-principles study

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Journal of Rare Earths 2024年第1期42卷 155-162,I0006页

作者： Limin Wang Wei Xiao Lu Sun rong yang Jinqiu Yu Ligen Wang State Key Laboratory of Nonferrous Metals and Processes China GRINM Group Co.Ltd.Beijing100088China GRIMAT Engineering Institute Co. Ltd.Beijing101407China General Research Institute for Nonferrous Metals Beijing100088China China Automotive Battery Research Institute Co. Ltd.Beijing101407China Rare Earth Functional Materials(Xiong'an)Innovation Center Co. Ltd.Xiong'an071700China

As the next generation of commercial automotive power batteries begins replacing liquid lithium batteries,many look towards all-solid-state batteries to pioneer the future.All-so lid-state batteries have attracted the attention of countless researchers around the world because of their high safety and high energy density.In recent times,halide solid-state electrolytes have become a research hotspot within solid-state electrolytes because of their potentially superior properties.In this paper,in the framework of DFT,we investigated the atomic mechanisms of improving the ionic conductivity and stability of Li_(3)YbCl_(6).Our calculations show that both trigonal and orthorhombic Li_(3)YbCl_(6) exhibit wide electrochemical windows and metastable properties(100 meV/atom>Ehull>0 meV/atom).However,the orthorhombic Li_(3)YbCl_(6) can be stabilized at high temperatures by taking the vibrational entropy into account,which is supported by the experimental results.Moreover,it is expected that because of the Yb/Li synergistic interactions that,due to their strong mutual coulomb repulsion,influence the Li^(+)transport behavior,the orthorhombic Li_(3)YbCl_(6) might have superior ionic conductivities with appropriate Li+migration paths determined by the Yb^(3+) distribution.Also,higher ionic conductivities can be obtained by regulating the random distribution of Li^(+) ions.Further Li^(+)-deficiency can also largely increase the ionic conductivity by invoking vacancies.This study helps gain a deeper understanding of the laws that govern ionic conductivities and stabilities and provides a certain theoretical reference for the experimental development and design of halide solid-state electrolytes.

关键词： Halide solid-state electrolytes Phase stability Ionic conductivity First-principles calculations Rare earths

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In-situ coupling construction of interface bridge to enhance electrochemical stability of all solid-state lithium metal batteries

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Journal of Energy Chemistry 2024年第2期89卷 18-26,I0003页

作者： Qianwei Zhang rong yang Chao Li Lei Mao Bohai Wang Meng Luo Yinglin Yan Yiming Zou Lisheng Zhong Yunhua Xu International Research Center for Composite and Intelligent Manufacturing Technology Institute of Chemical Power SourcesXi’an University of TechnologyXi’an 710048ShaanxiChina School of Materials Science and Engineering Xi’an University of TechnologyXi’an 710048ShaanxiChina School of Electrical Engineering Xi’an University of TechnologyXi’an 710048ShaanxiChina Yulin University Yulin 719000ShaanxiChina

Polymer-based composite electrolytes composed of three-dimensional Li_(6.4)La_(3)Zr_(2)Al_(0.2)O_(12)(3D-LLZAO)have attracted increasing attention due to their continuous ion conduction and satisfactory mechanical properties.However,the organic/inorganic interface is incompatible,resulting in slow lithium-ion transport at the interface.Therefore,the compatibility of organic/inorganic interface is an urgent problem to be solved.Inspired by the concept of“gecko eaves”,polymer-based composite solid electrolytes with dense interface structures were designed.The bridging of organic/inorganic interfaces was established by introducing silane coupling agent(3-chloropropyl)trimethoxysilane(CTMS)into the PEO-3D-LLZAO(PL)electrolyte.The in-situ coupling reaction improves the interface affinity,strengthens the organic/inorganic interaction,reduces the interface resistance,and thus achieves an efficient interface ion transport network.The prepared PEO-3D-LLZAO-CTMS(PLC)electrolyte exhibits enhanced ionic conductivity of 6.04×10^(-4)S cm^(-1)and high ion migration number(0.61)at 60℃and broadens the electrochemical window(5.1 V).At the same time,the PLC electrolyte has good thermal stability and high mechanical properties.Moreover,the Li Fe PO_(4)|PLC|Li battery has excellent rate performance and cycling stability with a capacity decay rate of 2.2%after 100 cycles at 60℃and 0.1 C.These advantages of PLC membranes indicate that this design approach is indeed practical,and the in-situ coupling method provides a new approach to address interface compatibility issues.

关键词： Organic/inorganic interphase Coupling effect Composite electrolyte Interface compatibility

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Genetic and immunologic characteristics of colorectal cancer patients with KRAS mutations and predictive significance of tumor immune microenvironment in adjuvant chemotherapy

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Genes & Diseases 2024年第3期11卷 43-46页

作者： Zhengqi Wen Wenliang Li Chengmin Shi Junrui Ma Sihui Zhao Ruize Zhou Xihong Liu rong yang Zhiping Zhang Hushan Zhang Bo Li Department of Oncology The First Affiliated Hospital of Kunming Medical UniversityKunmingYunnan 650032China The Third Affliated Hospital of Kunming Medical University(Yunnan Cancer Center) KunmingYunnan 650021China Gastrointestinal and Hernia Surgery The First Affiliated Hospital of Kunming Medical UniversityKunmingYunnan 650032China School of Nursing Yunnan University of Chinese MedicineKunmingYunnan 650022China Department of General Surgery The First People's Hospital of Yunnan ProvinceKunmingYunnan 650000China Department of General Surgery The Affiliated Hospital of Yunnan UniversityYunnan 650011China Medical Department 3D Medicines Inc.Shanghai 201114China Zhaotong Health Vocational College ZhaotongYunnan 657000China

Colorectal cancer(CRC)is one of the most common cancers around the world,and it is one of the leading causes of cancer-related death.1 Although anti-EGFR therapy and immune checkpoint inhibitor(ICl)therapy are becoming more and more important for colorectal therapy,however,clinical outcomes of current treatments for metastatic CRC,especially with ICls,have been shown to be affected by the status of KRAS.Therefore,KRAS mutation status detection has become a very important diagnostic factor for managing metastatic CRC patients.

关键词： KRAS colorectal patients

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Petrogenesis and Tectonic Significance of Shenxianshui Alkaline Granite in Gejiu,Yunnan Province,China

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Acta Geologica Sinica(English Edition) 2024年第2期98卷 368-385页

作者： yang rong CHEN Yongqing School of Earth Sciences and Resources China University of GeosciencesBeijing 100083China

The Shenxianshui granites in the western Gejiu area were formed in the Late Cretaceous.Laser ablation inductively coupled plasma mass spectrometry indicates zircon U-Pb ages ranging from 90.67±0.7 to 85.97±0.6 Ma.The intrusive rocks are peraluminous(A/CNK=1.03 to 1.33)and calc-alkaline,showing an affinity towards I-type granite.Large ion lithophilic elements are enriched in K and Rb,while high field strength elements are depleted.Moreover,light rare earth elements are significantly enriched,showing a slight negative Eu anomaly(Eu/Eu^(*)=0.39 to 0.58).Shenxianshui granite has a relatively high initial Sr isotope ratio(^(87)Sr/^(86)Sr)_(i)(0.7098-0.7105),negative ε_(Nd)(t)values(−7.99 to−7.44)and negative ε_(Hf)(t)values(−8.37 to−2.58).Combined with previous studies,these characteristics suggest that the Shenxianshui alkaline granites were formed in a post-collision extensional environment.The alkaline granitic magma possibly originated from the partial melting of the lower crust during the Mesoproterozoic era and may have contained mantle source materials.Shenxianshui alkaline granite was formed from mixed magma with a high degree of crystal differentiation.The abundance of ore-forming elements indicates that Shenxianshui granite has the potential to mineralize key metals and rare earth elements.

关键词： I-type granite zircon U-Pb geochronology Sr-Nd-Pb isotopes Hf isotope Gejiu

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Reconstructing cell lineage trees with genomic barcoding:approaches and applications

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Journal of Genetics and Genomics 2024年第1期51卷 35-47页

作者： Zizhang Li Wenjing yang Peng Wu Yuyan Shan Xiaoyu Zhang Feng Chen Junnan yang Jian-rong yang Advanced Medical Technology Center The First Affiliated HospitalZhongshan School of MedicineSun Yat-sen UniversityGuangzhouGuangdong 510080China Department of Genetics and Biomedical Informatics Zhongshan School of MedicineSun Yat-sen UniversityGuangzhouGuangdong 510080China Key Laboratory of Tropical Disease Control Ministry of EducationSun Yat-sen UniversityGuangzhouGuangdong 510080China

In multicellular organisms,developmental history of cell divisions and functional annotation of terminal cells can be organized into a cell lineage tree(CLT).The reconstruction of the CLT has long been a major goal in developmental biology and other related fields.Recent technological advancements,especially those in editable genomic barcodes and single-cell high-throughput sequencing,have sparked a new wave of experimental methods for reconstructing CLTs.Here we review the existing experimental approaches to the reconstruction of CLT,which are broadly categorized as either image-based or DNA barcode-based methods.In addition,we present a summary of the related literature based on the biological insight pro-vided by the obtained CLTs.Moreover,we discuss the challenges that will arise as more and better CLT data become available in the near future.Genomic barcoding-based CLT reconstructions and analyses,due to their wide applicability and high scalability,offer the potential for novel biological discoveries,especially those related to general and systemic properties of the developmental process.

关键词： Cell lineage tree Developmental regulation Biotechnology Computational biology

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Emerging single-atom nanozymes for catalytic biomedical uses

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Nano Research 2023年第12期16卷 13056-13076页

作者： Shuangfei Cai Wei Zhang rong yang CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety Center of Materials Science and Optoelectronics EngineeringCAS Center for Excellence in NanoscienceNational Center for Nanoscience and TechnologyUniversity of Chinese Academy of SciencesBeijing 100190China Sino-Danish College Sino-Danish Center for Education and ResearchUniversity of Chinese Academy of SciencesBeijing 100049China Institute of Applied Physics and Computational Mathematics Beijing 100088China

The past four years have witnessed booming progress in single-atom nanozymes(SANs),one of the newest generations of nanozymes with atomically dispersed metal sites for catalytic biomedical uses.They show distinct advantages over their nanoparticle-based counterparts,such as well-defined electronic/geometric structures and complete atomic utilization efficiency,thus offering opportunities to develop advanced nanozymes for practical uses.The atomically dispersed active centers in SANs could also facilitate the precise regulation of catalytic performance,while probing structure–activity relationship for in-depth understanding of mechanism.In this review,we first introduce the synthetic approaches,surface engineering,and characterization techniques of SANs.Subsequently,we discuss the enzyme-like properties of SANs,including some strategies for boosting their catalytic activities.Furthermore,we present their biomedical applications,ranging from biosensors,antibacterial uses,antioxidants,to therapeutics.Finally,the challenges and opportunities of SANs are prospected.

关键词： single atom metal nanozyme enzyme-like catalysis biomedical

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Rb_(5)Ba_(2)(B_(10)O_(17))_(2)(BO_(2)):The formation of unusual functional [BO_(2)]^(-) in borates with deep-ultraviolet transmission window

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Science China Chemistry 2022年第4期65卷 719-725页

作者： Yanhui Zhang Fuming Li rong yang Yun yang Fangfang Zhang Zhihua yang Shilie Pan CAS Key Laboratory of Functional Materials and Devices for Special Environments Xinjiang Technical Institute of Physics&ChemistryChinese Academy of SciencesXinjiang Key Laboratory of Electronic Information Materials and DevicesUrumqi 830011China Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of SciencesBeijing 100049China

The design and synthesis of new deep-ultraviolet(DUV)optical materials are important but challenging.It is well known that the polarizability anisotropy of linear[BO_(2)]^(−)is larger than those of[BO_(3)]^(3−)and[BO_(4)]^(5−),which is the better choice for exploring excellent optical materials.Here,we search for such crystals in borate systems based on the unusual fundamental structural unit[BO_(2)]^(−).By combining the linear[BO_(2)]^(−)with the traditional triangular[BO_(3)]^(3−)and tetrahedral[BO_(4)]^(5−)units,a new mixed metal borate,Rb_(5)Ba_(2)(B_(10)O_(17))_(2)(BO_(2))was obtained via high-temperature solution method.It exhibits excellent optical properties including a DUV transmission window(188 nm)and suitable birefringence(0.06).It also has good thermal stability and its crystal plates can be prepared easily.Furthermore,the strategies of designing borates with[BO_(2)]^(−)units have been proposed from the transformation of crystal framework and the preparation method.

关键词： isolate BO_(2) borate crystal deep-ultraviolet transmission birefringence

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Strengthening and control of second-phase particle precipitation in ferritic/austenitic/martensitic heat-resistant alloys:a review

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Journal of Iron and Steel Research(International) 2024年第1期31卷 3-23页

作者： Xue-cheng Peng Han-jie Guo Xin-fang Zhang Yi-wa Luo Ye Sun Jing Guo rong-guang yang Xiao-dan Zheng School of Metallurgical and Ecological Engineering University of Science and Technology Beijing(USTB)Beijing100083China Beijing Key Laboratory of Special Melting and Preparation of High-End Metal Materials University of Science and Technology Beijing(USTB)Beijing100083China Beijing Shougang Gitane New MATERIALS Co. Ltd.Beijing102206China

Heat-resistant alloys with excellent mechanical properties are widely used in various fields,and further improvement in their properties is essential to meet the requirements in new-generation advanced supercritical boilers,nuclear reactors,superheaters,and other new materials applications.To effectively enhance the comprehensive performance of heat-resistant alloys,second-phase particle strengthening has been widely studied,and in the face of different service envi-ronments of advanced heat-resistant steels,the selection of suitable second-phase particles is essential to maximize the performance of these alloys.To this end,three major types of reinforcing phases in heat-resistant alloys such as carbides,rare earth oxides,and intermetallic compounds are summarized.A comparative analysis of the precipitation behavior of the reinforcing phases with different types as well as the risks and means of controlling their use in service,is presented.Key parameters for the application of various types of second-phase particles in heat-resistant alloys are provided to support the design and preparation of new ultrahigh-performance heat-resistant alloys.

关键词： Heat-resistant alloy Second-phase particle Carbide Rare earth oxide Intermetallic compound Strengthening

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Transition Metal/Lanthanide-Nitrogen Double Bonds Co-stabilized in a Carbon Cage

Precision Chemistry

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Precision Chemistry 2024年第5期2卷 193-199页

作者： Zhanxin Jiang Ziqi Hu yang-rong Yao Wenhao Xiang Xinyi Han Jinpeng Xin Huaimin Jin Shangfeng yang Key Laboratory of Precision and Intelligent Chemistry Collaborative Innovation Center of Chemistry for Energy Materials(iChEM)Department of Materials Science and EngineeringUniversity of Science and Technology of ChinaHefei 230026China

Metal-nitrogen double bonds have been commonly reported for conventional metal complexes,but the coexistence of both transition metal-nitrogen and lanthanide-nitrogen double bonds bridged by nitrogen within one compound has never been reported.Herein,by encapsulating a ternary transition metal-lanthanide heteronuclear dimetallic nitride into a C_(84) fullrene cage,transition metal-nitrogen and lanthanide-nitrogen double bonds are costabilized simultaneously within the as-formed clusterfullerene TiCeN@C_(1)(12)-C_(84))which is a representative heteronuclear dimetallic nitride clusterfullerene.Its molecular structure was unambiguously determined by single-crystal X-ray diffraction,revealing a slightly bent pu-bridged nitride cluster with short Ti-N(1.761 A)and Ce-N(2.109 A)bond lengths,which are comparable to the corresponding Ti=N and Ce=N double bonds of reported metal complexes and consistent with the theoretically predicted values,confirming their coexistence within TiCeN@C(12)-C34+Density functional theory(DFT)calculations unveil three-center two-electron(3c-2e)bonds delocalized over the entire TiCeN dluster,which are responsible for costabilization of Ti=N and Ce=N double bonds.An electronic configuration of TitCe+N3-@Cg4-is proposed featuring an intramolecular four-electron transfer,drastically diferent from the analogous actinide dimtallic nitride clusterfullerene(U2)^(9)+N^(3)-@Cgo-and trimetllic nitride clusterfullerene(Sc)'+Ti+N3-@C_(80)^(6-),indicating the peculiarity of 4-fold negatively charged fullerene cage in stabilizing the heteronuclear dimetallic nitride cluster.

关键词： Fullerene metallofullerene transitionmetal lanthanide metal−nitrogen multiplebond

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