SENSORS AND ACTUATORS B-CHEMICAL
·
2021
·
IF 7.46
Yang Li,Jia-Jia Li,Qing Zhang,Jian-Yong Zhang,Na Zhang,Yong-Zheng Fang,Jinwu Yan,Qinfei Ke
The highly emissive BODIPY (boron-dipyrromethene) have been grafted on the Eu-based metal-organic frameworks (Eu-MOFs) via the covalent F-B bonding using a facile one-pot solvothermal reaction. The fluorescence emission ratio of [email protected] has been applied to construct the ratiometric fluorescence sensor for the F - , H 2 O 2 and glucose detection in water solution and living cells. The produced [email protected] probe provided enhanced sensitivity, higher selectivity and lower lower limits of detection (LOD) for the detection of F - (0.1737 μM), H 2 O 2 (6.22 nM) and glucose (6.92 nM), and 5.96, 6.52 and 6.95 times lower than that for single Eu-MOF, respectively. More importantly, the probe also exhibited the lower biotoxic in living cells for bioimaging and the better visualization performance with multiplex channels. The results indicated the π-conjugated BODIPY derivative not only acted as the surfactant molecule or template agent for preferred growth, but also modulated the fluorescent emissions drastically, and thus induced excellent fluorescent detecting performances.
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高影响因子
Nature Communications
·
2021
·Vol. 12
·期 1
·1-15
·
IF 14.919
Chen Junjie,Chen Longqi,Wu Yinglong,Fang Yichang,Zeng Fang,Wu Shuizhu,Zhao Yanli
Developing high-quality NIR-II fluorophores (emission in 1000–1700 nm) for in vivo imaging is of great significance. Benzothiadiazole-core fluorophores are an important class of NIR-II dyes, yet ongoing limitations such as aggregation-caused quenching in aqueous milieu and non-activatable response are still major obstacles for their biological applications. Here, we devise an activatable nanoprobe to address these limitations. A molecular probe named BTPE-NO 2 is synthesized by linking a benzothiadiazole core with two tetraphenylene groups serving as hydrophobic molecular rotors, followed by incorporating two nitrophenyloxoacetamide units at both ends of the core as recognition moieties and fluorescence quenchers. An FDA-approved amphiphilic polymer Pluronic F127 is then employed to encapsulate the molecular BTPE-NO 2 to render the nanoprobe BTPE-NO 2 @F127. The pathological levels of H 2 O 2 in the disease sites cleave the nitrophenyloxoacetamide groups and activate the probe, thereby generating strong fluorescent emission (950~1200 nm) and ultrasound signal for multi-mode imaging of inflammatory diseases. The nanoprobe can therefore function as a robust tool for detecting and imaging the disease sites with NIR-II fluorescent and multispectral optoacoustic tomography (MSOT) imaging. Moreover, the three-dimensional MSOT images can be obtained for visualizing and locating the disease foci.
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PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2025
·
IF 8.2
Huiru Zhu,Xiaoying Ni,Jiaxin Su,Yong Qin,Xiaoya He,Bo Liu,Shuang Ding,Haoru Wang,Xiangmin Zhang,Jie Huang,Qian Hu,Ruofei Ma,Jinhua Cai
To overcome the limited efficacy of chemodynamic therapy (CDT) caused by insufficient hydrogen peroxide (H2O2) in the tumor microenvironment, we engineered a glutathione (GSH)-responsive multifunctional nanosystem, HCTG-C, based on hollow mesoporous organosilica nanoparticles. This system integrates tirapazamine (TPZ), glucose oxidase (GOx), in situ-synthesized copper sulfide (CuS), and CT2A glioma cell membrane coating to enable dual tumor-targeted therapy and self-imaging capabilities. The therapeutic mechanism relies on three synergistic cascades: (1) GOx-mediated glucose oxidation to deplete oxygen and generate H2O2, establishing a self-sustaining H2O2 supply; (2) GSH-triggered CuS conversion to Cu(I), amplifying Fenton-like reactions for efficient H2O2-to-reactive oxygen species conversion and ferroptosis induction; and (3) hypoxia-activated TPZ to exert cytotoxic effects, synergizing chemotherapy with CDT. Experimental results demonstrated that HCTG-C achieves real-time MRI monitoring via GSH depletion-driven Cu valence transitions, while its self-replenishing H2O2 and oxygen-activation mechanisms significantly enhance antitumor efficacy against CT2A glioma in vitro and in vivo. By innovatively combining H2O2 self-supply cascades, hypoxia-activated chemotherapy, and ferroptosis-driven CDT, this work presents a paradigm-shifting strategy for self-imaging-guided combinatorial therapy, advancing ferroptosis-based approaches for precision glioma treatment.
研究领域:
纳米医学
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肿瘤治疗
·
影像学
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生物材料
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PubMed
高影响因子
ACS Applied Nano Materials
·
2024
·
IF 5.3
Peng Bo Niu,Yong Qiong Wang,Rong Hu,Tong Yang
With the improvement of the quality of life, the assessment of total antioxidant capacity (TAC) has attracted much attention in the field of a healthy diet, food analysis, or health guidelines. In this work, Cu nanoparticles (NPs)/CoO/carbon nanofibers (CNFs) as a promising nanozyme for peroxidase (POD) mimicking was synthesized by electrospinning and carbonation. Subsequently, a colorimetric sensing platform is constructed for TAC assessment by using 3,3′,5,5′-tetramethylbenzidine (TMB) as a chromogenic substrate based on Cu NPs/CoO/CNFs under presence of H2O2. The enhanced POD catalytic efficiency of Cu NPs/CoO/CNFs for TMB oxidation (ox-TMB) was about 3.2-fold higher than that of bare Cu NPs/CNFs or CoO/NFs, which was ascribed to the synergistic catalytic effect and the generation of heterogeneous interfaces between Cu NPs and CoO in CNFs. When some antioxidants such as AA, FA, TA, and GA were introduced in the chromogenic system, ox-TMB was reduced to colorless TMB, allowing the subsequent assessment of TAC. The results show that the limits of detection toward AA, FA, TA, and GA were 8.7, 8.3, 2.7, and 2.4 μM, respectively. Moreover, this proposed method was used for the TAC assay in real samples including fresh juices and commercial beverages, which showed good promise in practical applications such as food nutrition assessment, food analysis, personalized nutrition intervention, or staple food research.
研究领域:
材料科学
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分析化学
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食品科学
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生物技术
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高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2024
·
IF 3.8
Xuliang Deng,Yang Xu,Jincheng Liu,Dong Lin,Ze Zong,Juncong Yuan,Zhiyang Li,Guanghui Zhao,Yongjun Zhang,Yibin Liu,Xiaobo Chen,Xiang Feng,De Chen,Chaohe Yang,Honghong Shan
Regulating the Ti active sites in titanosilicates with different coordination modes is of prime scientific and industrial significance to the rational design of efficient catalysts for olefin epoxidation. In this study, the Ti species in Ti-beta zeolite catalysts (open/closed tetra-coordinated Ti sites, hexa-coordinated Ti species, and TiO2) were keenly controlled via the dealumination-metallization approach. By multiple characterizations, kinetics study, and multivariate model analysis, it is found that the open tetra-coordinated framework Ti(OH)(OSi)3 species contribute more to the catalytic performance for 1-hexene epoxidation with H2O2. Moreover, the Ti-beta with rich open tetra-coordinated Ti(OH)(OSi)3 species showed significantly improved reaction performance (TON: 401, conversion: 64%, selectivity: 98%, H2O2 efficiency: 97%) with lower apparent activation energy. This study not only opens up new prospects for the design of efficient titanosilicates by modifying Ti microenvironments but also proposes the strategy to improve the content of open tetra-coordinated Ti sites.
研究领域:
催化
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材料科学
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化学工程
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无机化学
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高影响因子
NANOTECHNOLOGY
·
2019
·Vol. 31
·期 1
·015101
·
IF 3.399
Keke Du,Qianqian Liu,Mei Liu,Rongmu Lv,Nongyue He,Zhifei Wang
Increasing the content of reactive oxygen species (ROS) with the assistance of nanoformulations in cancer cells via the Fenton reaction is considered an effective method to treat cancer. However, the efficiency of the Fenton reaction is affected by the level of H2O2, the selection of iron ions in different nanoformulations, etc. Herein, we use FeIII-tannic acid (FeIIITA) nanocomposites as the carrier to deliver glucose oxidase (GOD) which can solve the problem of insufficient endogenous H2O2 by catalytically converting the glucose. In comparison with traditional Fe2+/Fe3+, FeIIITA nanocomposites perform higher catalytic activity in converting H2O2 to high toxic hydroxyl radicals (·OH) due to the TA-mediated reduction of Fe3+. So, the integration of GOD and TA in the construction of nanocomposites significantly enhances the efficiency of the Fenton reaction. In vitro experiments show that ·OH produced by GOD-FeIIITA nanocomposites can not only achieve a good anticancer effect at a low concentration but also promote degradability of the nanocomposites. When it is only 1.08 μg · ml−1, the cell apoptosis rate has reached 76.91%. In vivo experiments further demonstrate that GOD-FeIIITA nanocomposites can significantly inhibit tumor growth. So this work lays a good foundation for Fenton reaction-based cancer treatment.
研究领域:
癌症治疗
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纳米技术
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生物医学工程
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化学生物学
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PubMed
高影响因子
LUMINESCENCE
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2019
·Vol. 35
·期 1
·120-128
·
IF 1.691
Jing Jie Huang,Jing Liu,Ju Xiang Liu,Jian Ping Wang
The residues of pyrethroids in foods of animal origin are dangerous to the consumers, so this study presented a chemiluminescence sensor for determination of pyrethroids in chicken samples. A dual-dummy-template molecularly imprinted polymer capable of recognizing 10 pyrethroids was synthesized. The results of computation simulation showed that the specific 3D conformations of the templates had important influences on the polymer' recognition ability. The polymer was used to prepare a sensor on conventional 96-well microplates, and the sample solution was added into the wells for direct absorption. The absorbed analytes were initiated with the bis(2,4,6-trichlorophenyl)oxalate–H 2 O 2 –imidazole system, and the chemiluminescence intensity was used for analyte quantification. Results showed that one assay was finished within 12 min, and this sensor could be reused four times. The limits of detection for the 10 analytes were in the range o0.3–6.0 pg/ml, and the recoveries from the standards of fortified blank chicken samples were in the range 70.5–99.7%.
研究领域:
分析化学
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食品安全
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环境科学
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PubMed
高影响因子
BIOSENSORS & BIOELECTRONICS
·
2021
·
IF 10.618
Yan Sun,Peipei Li,Yu Zhu,Xiaohua Zhu,Youyu Zhang,Meiling Liu,Yang Liu
A sensitive electrogenerated chemiluminescence (ECL) biosensor for glucose was developed based on in situ growth of TiO 2 nanowires on Ti 3 C 2 MXenes (TiO 2 –Ti 3 C 2 ) as the nanoplatform. Via tuning the alkaline oxidation time, different amount of TiO 2 nanowires can be found on MXenes. An ECL biosensor for glucose was constructed by covalent immobilization of glucose oxidase (GODx) on the glycine functional TiO 2 –Ti 3 C 2 surface, with the ECL signal depending on the in-situ formation of H 2 O 2 via the specifically catalysis of glucose by GODx, resulting in the apparent increase of ECL signal. The TiO 2 –Ti 3 C 2 can also act as the catalyst for the oxidation of H 2 O 2 into O 2 to enhance the ECL of luminol. Based on this strategy, a highly sensitive ECL biosensor for glucose was obtained in wide concentration range of 20 nM-12 mM with a low detection limit of 1.2 nM (S/N = 3). The synergistic effects of large surface area, excellent conductivity, and high catalytic activity of the TiO 2 –Ti 3 C 2 make the sensor highly sensitive toward glucose; the specific enzyme catalysis reaction promises excellent selectivity of the ECL sensor. The proposed biosensor has been employed to detect glucose in human serum, fruits, and sweat samples with excellent performance, providing a universal approach for glucose in various samples, which shows great prospect in clinical diagnostics and wearable sensors .
研究领域:
分析化学
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生物传感器
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材料科学
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生物医学工程
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临床诊断
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PubMed
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2021
·
IF 4.098
Chengna Xu,Ji Zhou,Yong Ye,Bin Tang
Peroxidase-like reaction process involving o-phenylenediamine (OPD) and silver nanoprisms in the presence of hydrogen peroxide (H 2 O 2 ) was monitored using time-resolved ultraviolet–visible (UV–Vis) absorption spectroscopy. The oxidation of OPD and etching of silver nanoprisms were investigated by analyzing the dynamic spectral data. Two-dimensional correlation spectroscopy (2D-COS) and principal component analysis (PCA) were employed to gain insights into the correlation between catalytic oxidation of OPD and etching of silver nanoprisms. It was found that OPD offered significant protection effect for silver nanoprisms so that morphologies of silver nanoprisms maintained at the beginning period after addition of H 2 O 2 . Moreover, silver nanoprisms accelerated the oxidation of OPD by H 2 O 2 , demonstrating enzymatic mimicking activity of silver nanoprisms. The combination of time-resolved UV–Vis absorption spectroscopy and spectral calculation methods could be used for exploration of complex reaction systems with spectral variations.
研究领域:
纳米技术
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催化
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光谱学
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材料科学
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PubMed
高影响因子
BIOSENSORS & BIOELECTRONICS
·
2016
·
IF 7.476
Ying Zhang,Wang Ren,Hong Qun Luo,Nian Bing Li
A new magnetic bead-based cascade amplification strategy for highly sensitive visual detection of proteins (thrombin as a model analyte) was developed by coupling target-triggered hybridization chain reaction (HCR) with the synergistic catalysis of DNA concatemer-mediated hemin/G-quadruplex DNAzymes and Pt nanozymes. Initially, the biotinylated primer DNA (P-DNA) was complementary with aptamer to form dsDNA which was further linked to streptavidin-coated magnetic bead (MB), thereby fabricating the expected MB-based aptasensor . In the presence of target TB, the aptamer was taken away from the aptasensor, and the free P-DNA immediately triggered HCR to spontaneously form DNA concatemer-directed nanochains with numerous DNAzymes and Pt nanoclusters (PtNCs) to achieve cascades signal amplification . The dual peroxidase mimetics catalyzed the H 2 O 2 -mediated oxidation of colorless 3,3′,5,5′-tetramethylbenzidine (TMB) into the colored TMB oxides (oxTMB), causing intensified color change of the chromogenic solution for the highly sensitive naked-eye detection of as low as 100.0 pM TB. In this strategy, the employment of magnetic separation and exonuclease III (Exo III)-assisted digestion of residual dsDNA minimized the background noise and avoided the false positive results, greatly improving the detection accuracy and sensitivity with a low limit of detection (LOD=15.0 pM). The proposed visual platform has promise for detecting various types of proteins with careful DNA sequence designs.
研究领域:
生物化学
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纳米技术
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分析化学
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生物传感器
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PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2025
·
IF 8.2
Xia Li,Yuchen Yao,Zhiyuan Sang,Shengji Zhu,Jingjing Jia,Ting Lv,Weibing Ma,Min Peng,Ji Liang
The electrosynthesis of hydrogen peroxide (H2O2) via two-electron oxygen reduction reaction (2e– ORR) is a promising method with the advantages of safety, efficiency, and sustainability. However, the process is constrained by the low selectivity and catalytic activity of the catalysts. In this study, the amino-functionalized iron-based metal–organic frameworks anchored on aminated carbon nanotubes (Fe-BDC@CNT-NH2) are prepared as 2e– ORR catalysts to enhance H2O2 production. In this catalyst system: (1) carbon nanotubes (CNTs) were designed to improve the overall electron conductivity of the catalyst; (2) −NH2 groups in benzene-1,4-dicarboxylic acid (BDC) could modulate the intrinsic electron conductivity of metal–organic frameworks (MOFs); and (3) −NH2 groups on the CNT surface facilitated the anchoring and confinement of MOF growth by forming axial coordination structures (Fe–NO4). Smaller particles expose more active sites, while axial coordination structure enhances the adsorption capacity of Fe centers, effectively passivating Fe centers and optimizing the 2e– ORR performance at adjacent C sites. Thus, Fe-BDC@CNT-NH2 possesses high 2e– ORR selectivity and activity, under both alkaline and neutral conditions. For example, Fe-BDC@CNT-NH2 demonstrates a H2O2 average yield of 24 mol gcat–1 h–1 and maintains a Faraday efficiency (FE) > 80% over 12 h in alkaline. Against neutral conditions, it also exhibits approximately 84% selectivity and stability lasting up to 12 h. Especially, a large current of 1.0 A can be achieved under a 5 × 5 cm2 flow cell, thus endowing the electro-synthesized H2O2 with excellent dye degradation performance and broad application prospects.
研究领域:
电化学
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材料科学
·
催化
·
可持续能源
·
纳米材料
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DOI
PubMed
高影响因子
RESEARCH ON CHEMICAL INTERMEDIATES
·
2022
·Vol. 49
·期 1
·23-42
·
IF 3.134
Lin Yingzi,Hou Ao,Li Hao,Shi Chunyan,Chen Lei,Yuan Baoling,Liu Yi,Wang Yu,Liu Xiaochen
Dye wastewater with high concentration, large molecular weight, complex structure, and certain toxicity has brought a serious burden to the environment. In this study, acid red 73 dye (AR73) was used as the model pollutant to compare the degradation effects of different systems on AR73. The influence factors of a UV/hydrogen peroxide/peroxydisulfate (UV/H 2 O 2 /PDS) composite system, such as H 2 O 2 dosage, initial concentration of AR73, initial pH value, anion concentration, and actual water, on the degradation of AR73 were investigated. Compared with other systems, the UV/H 2 O 2 /PDS composite system had the best degradation effect of AR73, with a degradation efficiency of 98.98%, which conforms to the pseudo-first-order reaction kinetic model, the pseudo-first-order reaction kinetic constant ( k obs ) is 0.1339 min −1 . And the synergy coefficients in this complex system were all greater than 2. Specifically, the degradation efficiency of the UV/H 2 O 2 /PDS composite system for AR73 was the highest when the initial pH was neutral. The presence of anions inhibited the degradation of AR73, and the real water reduced the degradation efficiency for AR73. Electron spin resonance (ESR) detection and free radicals capture test demonstrated that hydroxyl radical ( · OH) was the main reactive species in AR73 degradation, and its 80.66–84.93% contribution. With the destruction of the structure of AR73 by free radicals, anilines, phenols, and oxalic acid were found to be the main intermediate products during the degradation of AR73 by gas-phase mass spectrometry and UV–vis spectrograms. The changes in toxicity during the degradation of AR73 by the UV/H 2 O 2 /PDS complex system were also assessed.
研究领域:
环境科学
·
化学工程
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高影响因子
危险品化学品经营许可证（带存储）