ANALYTICA CHIMICA ACTA
·
2022
·
IF 6.911
Guiyin Li,Min Chen,Bo Wang,Chaoxian Wang,Guanxiong Wu,Jintao Liang,Zhide Zhou
Golgi protein 73 (GP73) is a new type of marker that can specifically detect hepatocellular carcinoma (HCC). Herein, a dual-signal sandwich-type electrochemical aptasensor for GP73 determination was constructed on the basis of hemin-reduced graphene oxide-manganese oxide (H-rGO-Mn 3 O 4 ) nanozymes. [email protected] ( o -phenylenediamine) ( [email protected] ) nanohybrids with a large specific surface area and conductance were co-electro-deposited onto a screen-printed electrode (SPE) surface to immobilize GP73 capture aptamer 2 (Apt2). H-rGO-Mn 3 O 4 nanozymes were used not only to immobilize amino functionalised GP73 aptamer 1 (Apt1) as the detection probe, but also to serve as an in-situ redox signal indicator because of the redox reaction of Hemin (Fe(Ш)/Hemin(Fe(II)). In addition, given their excellent peroxidase-like activity, H-rGO-Mn 3 O 4 nanozymes can catalyse the decomposition of H 2 O 2 and oxidation of substrate (3,3′,5,5′-tetramethylbenzidine, TMB) to oxTMB, which is used as another redox signal. In the presence of the target GP73, the two aptamers specifically bind to the target, thereby affecting two electrochemical signals. Under optimal conditions, the dual-signal sandwich-type electrochemical aptasensor had a salient analytical performance. The two electrochemical redox signals linearly increase with the logarithm of the GP73 concentration in the range of 0.01–100.0 ng/mL with the limit of detection (LOD) of 0.0071 ng/mL and sensitivity of 2.441 μA/μM/cm 2 . Moreover, the recovery of human serum samples ranged from 98.66% to 121.11%. Furthermore, the two redox signals can simultaneously corroborate each other, thereby preventing missed diagnosis and misdiagnosis. All the results can provide new insights into the clinically effective determination of HCC.
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DOI
PubMed
高影响因子
ANALYST
·
2019
·Vol. 144
·期 13
·4086-4092
·
IF 4.019
Lili Chen,Xiangguang Li,Tongda Zou,Tiantian Wang,Xiping Cui,Yingshan Chen,Chunguo Zhang,Suqing Zhao
Given that Helicobacter pylori (H. pylori) generally infects people in early childhood and that such persons when not treated with antibiotics remain infected for the rest of their lives, it is quite important to detect H. pylori in children, and convenient to do so using non-invasive methods. Stool antigen tests constitute such an effective non-invasive method. In the current work, a novel fecal test was developed to detect H. pylori based on immunomagnetic beads (IMBs) with monoclonal antibodies sensitively recognizing and capturing the H. pylori, coupled with a polyclonal antibody-conjugating quantum dot probe, and ultrasensitive detection was achieved by using a fluorescence spectrometer. The detection method took 120 min to perform, and showed a limit of detection of 102 CFU mL−1 and a linear range of 10 to 106 CFU mL−1 (R2 = 0.9962). Most importantly, this method can be effectively applied to real samples. This study provided a novel method for the non-invasive detection of the fecal antigen H. pylori.
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高影响因子
TETRAHEDRON
·
2020
·
IF 2.233
Xianxia Tu,Haiyun Peng,Guisheng Deng
In Ph 3 PAuCl/AgOTf/TsOH system, 2-diazo-5-alkynyl-1,7-diketo carbonyl compounds were transformed into diazo furans . Rh 2 (OAc) 4 -mediated conversion of the diazo furan derivatives into 4 H -cyclopenta[ c ]furan-5(6 H )-one derivatives was accomplished via C(sp 2 )−H insertion reaction at 4-position on the furan ring.
研究领域:
有机化学
·
合成化学
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高影响因子
Nanomaterials
·
2022
·Vol. 12
·期 11
·1860
·
IF 5.719
Dan Li,Mengyuan Li,Shiping Zhu,Yanmei Gao,Mengyao Mu,Ning Zhang,Youmei Wang,Minghua Lu
Sample pretreatment plays important role in the analysis and detection of trace pollutants in complex matrices, such as environmental and biological samples. The adsorption materials of sample pretreatment receive considerable attention, which has a significant effect on the sensitivity and selectivity of the analytical method. In this work, the porous hexagonal boron nitride (h-BN) was utilized as a coating material of solid-phase microextraction (SPME) to extract and preconcentrate polycyclic aromatic hydrocarbons (PAHs) prior to separation and detection with GC-FID. Attributed to the multiple interactions including hydrophobicity, hydrogen bonding and strong π–π interaction, the h-BN coating showed excellent extraction performance for PAHs. Under the optimal conditions, the method showed the linear relationship in the range of 0.1–50 ng mL−1for acenaphthene, 0.05–50 ng mL−1for pyrene, and 0.02–50 ng mL−1for fluorene, phenanthrene and anthracene with a correlation coefficient (R2) not lower than 0.9910. The enrichment factors were achieved between 1526 and 4398 for PAHs with h-BN as SPME fiber coating. The detection limits were obtained in the range of 0.004–0.033 ng mL−1, which corresponds to 0.08–0.66 ng g−1for soil. The method was successfully applied to analysis of real soil samples. The recoveries were determined between 78.0 and 120.0% for two soil samples. The results showed that h-BN material provided a promising alternative in sample pretreatment and analysis.Keywords:sample pretreatment;solid-phase microextraction (SPME);hexagonal boron nitride (h-BN);nanomaterials;polycyclic aromatic hydrocarbons (PAHs);soil
研究领域:
分析化学
·
环境科学
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高影响因子
CRYSTAL GROWTH & DESIGN
·
2019
·
IF 4.153
Yu Liu,Shijie Xu,Xu Zhang,Weiwei Tang,Junbo Gong
There has been growing interest in investigating the role of solvents played in nucleation pathways; nevertheless, the nucleation mechanism is still poorly understood. In this work, flufenamic acid (FFA) was selected as model compound to investigate the relationship between solvent and nucleation kinetics. Over 1000 induction time experiments were conducted. Solution IR spectroscopy and molecular dynamic simulations were used to explore the solvent–solute interaction and conformation distribution in solutions. Given the same driving force, the order of nucleation rate of FFA was found following acetonitrile > methanol > toluene, in which dimers are significantly distributed in toluene solutions. The observation cannot support the previously proposed hypothesis that the breakage of solvent–solute hydrogen bonds and dimerization determine the nucleation rate. Through crystal growth experiment and detailed discussions, we have reached an interesting conclusion that the weak C–H···π interactions play a vital role in the nucleation pathway via probably regulating the growth of the nucleating clusters.
研究领域:
物理化学
·
晶体学
·
分子动力学
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DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2018
·
IF 11.698
Yongfeng Zhi,Si Ma,Hong Xia,Yumin Zhang,Zhan Shi,Ying Mu,Xiaoming Liu
Metal-free, visible-light driven, solid organic photocatalysts provide a more green and environmentally friendly alternative to traditional metal-based photocatalysts. Donor-Acceepor (D-A) dyads possess a feature of easy to adjust the photoelectric properties, and enhance their photocatalytic performances. Here we report a fascinating strategy for screening excellent organic porous photocatalysts through oxidative coupling of single D -A based monomer, which has still an important advantage to ensure uniformity of polymer structure except for the inherent characteristics of D -A polymers. According to this strategy, three D -A typed conjugated microporous polymer (DA-CMP) photocatalysts consisting of alternating electron-rich (carbazole) and electron-deficient (benzene, 4,7-diphenyl-2,1,3-benzothiadiazole or anthraquinone) units have been synthesized, and their porosity and photoelectric properties including adsorption, emission, lifetime, optical bandgaps, energy levels and transient photocurrent response as well as photocatalytic activity, were conveniently tuned by selecting different D -A monomers with tunable electron-deficient moiety. These DA-CMPs were exploited as metal-free photocatalysts in the oxidative C-H functionalization reactions in the presence of visible-light and molecular oxygen. They showed excellent photocatalytic activity, extensive substrate adaptability and outstanding reusability, due to combining some key features like permanent porosity, outstanding stability and optoelectronic properties. In addition, the reaction mechanism for DA-CMP photocatalyzed C-H functionalization reactions under visible-light irradiation was investigated in detail. Moreover, to prove in depth the benefits of the heterogeneous photocatalysis, a continuous flow procedure has been conducted with an excellent yield.
研究领域:
材料科学
·
有机化学
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DOI
高影响因子
Journal of Materials Chemistry B
·
2017
·Vol. 5
·期 17
·3111-3121
·
IF 4.543
Yan-Ling Luo,Xue-Yin Zhang,Yuan Wang,Fang-Jie Han,Feng Xu,Ya-Shao Chen
pH-Sensitive H-type multiblock copolymers, namely, poly(methacrylic acid)2-block-epoxidized hydroxyl-terminated polybutadiene-block-poly(methacrylic acid)2 (PMAA2-b-epoHTPB-b-PMAA2), were synthesized by atom-transfer radical polymerization and subsequent in situ epoxidation by peracetic acid and characterized by 1H NMR, FT-IR and SEC techniques. The impact of epoxidation on the physicochemical and biomedical properties of copolymer self-assembly micelle nanoparticles was investigated by fluorescence spectrometry, DLS, TEM and an MTT assay. The experimental results indicated that epoxidation resulted in the formation of more stable copolymer micelle nanoparticles with a lower critical micelle concentration, smaller micelle size, and higher loading capacity and encapsulation efficiency of drugs than those without epoxidation. In particular, epoxidized copolymer micelle nanoparticles exhibited reasonable pH sensitivity at a pH of 5.3–5.6. The hydrophobic anticancer drug paclitaxel (PTX) displayed faster release rates from epoxidized nanomicelles than from unepoxidized nanomicelles in a PBS solution of a pH of 4.8–6.6, whereas in PBS of a pH of 7.4 smaller amounts of PTX were released from epoxidized nanomicelles than from unepoxidized nanomicelles. Epoxidized copolymer nanomicelles were reasonably biodegradable after the drug was released, and their degradation rate was faster than that of their unepoxidized counterparts. An MTT assay was performed to determine the biocompatibility of epoxidized copolymer micelle nanoparticles and the anticancer activities of PTX-loaded nanomicelles, which were important for applications in the therapy of cancers as a controlled-release drug carrier.
研究领域:
材料科学
·
药物递送
·
生物医学工程
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高影响因子
Energetic Materials Frontiers
·
2022
·
IF 0
Zhi-qiang Wang,Zhen-qi Zhang,Shan-hu Sun,Mi Yan,Shi-liang Huang,Shuang-qi Hu,Jin-jiang Xu,Li-shuang Hu
Polymorphs of energetic materials generally exhibit distinct features, such as density, thermal stability, sensitivity, and detonation performance. These features are important in determining the appropriate applications of a given polymorph. To understand the thermal stability of new high explosive 4,4′,5,5′-tetranitro-1H,1′H- [2,2′-biimidazole]-1,1′-diamine (DATNBI), we systematically investigated its polymorphic transition (PT) under thermal stimulation and discovered a novel stable γ form of DATNBI. The results showed that the solid-solid PT path was β → α → γ . In this study, the three polymorphs of DATNBI were prepared through solvent recrystallization, and their PT processes in solution were explored. Crystal structure analysis of γ -DATNBI suggested that its special cross-cross grid crystal packing may be the main reason for its stable existence at room temperature and its lack of PT process before chemical decomposition, which starts at 240 °C. To further explore the PT process of DATNBI, the solid phase transition mechanism of DATNBI was analyzed using non-isothermal kinetics. The results demonstrated that the two high-temperature PT processes— β → α and α → γ —were not single-step reactions but complex multi-step reactions. The PT activation energy of the β → α process was slightly higher than that of the α → γ process. In addition, the influences of different polymorphs on the performance of DATNBI were explored. The results revealed that safety and detonation performance should decrease as a result of the incorporation of γ -DATNBI. This study contributes to understanding the PT behavior and the crystal structure evolutionary mechanism of DATNBI. This study provides practical support for formula design, process condition selection, and thermal stability evaluation of DATNBI explosives.
研究领域:
材料科学
·
化学
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DOI
Journal of Environmental Chemical Engineering
·
2023
·
IF 7.7
Jing Wang,Jia-Wei Fang,Zhi-Yong Ji,Zhi-Yuan Guo,Xin-Wei Li,Jie Liu,Ying-Ying Zhao,Zhong Liu,Feng-Feng Gao,Yuan Zhong,Jun-Sheng Yuan
Lithium extraction from the solution in low Li + concentration by an energy-saving and high-efficiency method is still a challenge. Herein, a novel hollow porous LiMn 2 O 4 (H-LMO) with highly active site was proposed to enhance the extraction performance of Li + . Based on the established hollow porous structure, the H-LMO film electrode (H-LMOE) exhibits excellent lithium electrosorption performance and stability. Under the current density of 0.5 C, the electrosorption capacity of Li + could reach 31.52 mg/g, the separation coefficient of Li + /Mg 2+ was 581.67, and the energy consumption was as low as 0.49 Wh/mol Li. This unique structural strengthening mechanism made H-LMOE maintain a good Li + extraction performance even in a solution of low Li + concentration. The Li + electrosorption capacity of H-LMOE was 2.13 times that of T-LMOE in a 60 mg/L Li + solution, while the specific energy consumption of the H-LMOE was 15.78% lower than that of the traditional-LiMn 2 O 4 film electrode (T-LMOE). Even in a 10 mg/L Li + solution, the electrosorption capacity of H-LMOE was 21.48 mg/g, which was 10.0% higher than that of T-LMOE. Moreover, after 50 recycling processes, the final electrosorption capacity of the H-LMOE was about 25.0% higher than that of the T-LMOE.
研究领域:
材料科学
·
电化学
·
能源存储
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DOI
高影响因子
INORGANIC CHEMISTRY
·
2021
·
IF 5.165
Xueyu Wang,Songdong Ding,Zhipeng Wang,Lianjun Song,Xiuying Yang,Qian Xiao,Haowei Xu,Junli Wang,Zhen Shen,Hui Wang
Effective and selective separation of technetium from acidic nuclear liquid waste is highly desirable for partitioning and transmutation but is of significant challenge. Highly efficient extraction of pertechnetate can be achieved by taking H-bonding and electrostatic interaction combined strategy. Base on this strategy, an amine–amide ligand NTAamide(n-Oct) was employed to extract TcO4– in HNO3 solution. Using n-dodecane as a diluent, NTAamide(n-Oct) demonstrated excellent extractability and good selectivity toward TcO4– with a rapid extraction equilibrium that could be reached in less than 1 min. Its maximal loading capacity for TcO4– was almost 100 times as much as that of traditional amine extractant Aliquat-336 nitrate. Meanwhile, TcO4– could be efficiently stripped from the loaded organic phase by (NH4)2CO3 solution. Slope analysis indicated the formation of a 1:1 complex of NTAamide(n-Oct) with TcO4–. The extraction conformed to the anion exchange extraction model, as confirmed by analyses of single-crystal X-ray diffraction, 1H NMR titration, FTIR, and ESI-MS.
研究领域:
核化学
·
放射性废物处理
·
配位化学
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DOI
PubMed
高影响因子
ACS Catalysis
·
2026
·
IF 13.6
Wentao Hao,Zhuqian Wang,Hui Cao,Jia Qiao,Qingde Zhang,Kun Xiong,Xingchen Liu,Yong Qin,Chaoqiu Chen
The selective oxidation of CH4 to C2 oxygenates under mild conditions is a significant pathway for CH4 valorization, yet it remains extremely challenging due to the inertness of methane, the competing overoxidation, and sluggish C–C coupling kinetics. Here, we show that the N,S co-doped carbon nanotube-supported Fe5 clusters catalyst (Fe5/NSC) with adjacent Fe sites drives sequential C–H activation and C–C coupling to ethanol with a C2H5OH productivity of 1939.6 μmol·gcat–1·h–1 and a selectivity of 83.9% at 25 °C and 0.5 MPa CH4 without the assistance of CO. Comprehensive experimental investigation and density functional theory calculations reveal the critical role of adjacent Fe sites in the selective formation of C2H5OH. The adjacent Fe sites featured in Fe5/NSC synergistically facilitate the dissociation and/or partial oxidation of CH4 to distinct C1 intermediates (*OCH2 and *CH3) and subsequent OCHx–CHx coupling between them to form the key CH3CH2O* intermediate for C2H5OH production, as opposed to the conventional CHx–CO coupling pathway that primarily yields acetic acid.
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产品关联
DOI
高影响因子
LANGMUIR
·
2026
·Vol. 42
·期 31
·22950-22957
·
IF 4.4
Chen Nannan,Yuan Qingle,Liu Qin,Zhang Chao,Wu Zhengcui,Bi Wentuan
Single-atom catalysts (SACs) hold great promise for the
electrochemical
reduction of CO 2 to CO; however, the high selectivity is
typically restricted within a narrow potential window, limiting their
practical implementation. In this study, Ni–N–C catalysts
were supported on ordered and disordered carbon nanofiber membranes
(denoted as o-NiNC and d-NiNC, respectively) via electrospinning to
elucidate the effect of nanofiber alignment on CO 2 reduction
activity. The results demonstrate that o-NiNC catalysts allow for
spatially uniform H + /CO 2 delivery and consumption,
thereby mitigating the selectivity variations arising from uneven
spatial distribution of reactants. As a result, the o-NiNC catalysts
achieve a CO Faradaic efficiency (FE) of 98.5% at −1.0 V and
maintain an FE above 90% across a broad potential range (−0.6
to −1.6 V). This work provides new insights into the rational
design of high-performance CO 2 reduction electrocatalysts
through geometric engineering.
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DOI
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高影响因子
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