ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Qin-ying Li,Xu Yu,Xi Li,Li-na Bao,Yu Zhang,Min-Jie Xie,Ming Jiang,Ya Qian Wang,Kun Huang,Li Xu
The redox-active metal ions, especially Cu2+, are highly correlated to Alzheimer’s disease (AD) by causing metal ion-mediated oxidative stress and toxic metal-bound β-amyloid (Aβ) aggregates. Numerous pieces of evidence have revealed that the regulation of metal homeostasis could be an effective therapeutic strategy for AD. Herein, in virtue of the interaction of both amino-containing silane and ethylenediaminetetraacetic acid disodium salt for Cu2+, the silicon–carbon dots (SiCDs) are deliberately prepared using these two raw materials as the cocarbon source; meanwhile, to realize the local enrichment of SiCDs and further maximize the chelating ability to Cu2+, the SiCDs are feasibly loaded to the biocompatible mesoporous silica nanoparticles (mSiO2) with the interaction between residual silane groups on SiCDs and silanol groups of mSiO2. Thus-obtained nanocomposites (i.e., mSiO2@SiCDs) could serve as an efficient Cu2+ chelator with satisfactory metal selectivity and further modulate the enzymic activity of free Cu2+ and the Aβ42–Cu2+ complex to alleviate the pathological oxidative stress with an anti-inflammatory effect. Besides, mSiO2@SiCDs show an inspiring inhibitory effect on Cu2+-mediated Aβ aggregation and further protect the neural cells against the toxic Aβ42–Cu2+ complex. Moreover, the transgenic Caenorhabditis elegans CL2120 assay demonstrates the protective efficacy of mSiO2@SiCDs on Cu2+-mediated Aβ toxicity in vivo, indicating its potential for AD treatment.
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Analytical Methods
·
2020
·Vol. 12
·期 42
·5110-5119
·
IF 2.596
Shanshan Wei,Tinghua Li,Xinyu Zhang,Hongyuan Zhang,Chunzhu Jiang,Guoying Sun
The abnormal level of Cu2+ or GSH can cause variety of neurodegenerative diseases in humans. Thus, the selective and sensitive detection of Cu2+ and GSH has inspired intensive research efforts in biological sample analysis fields. Herein, an “on–off–on” fluorescent probe based on nitrogen and sulfur co-doped carbon dots (N,S-CDs) has been successfully prepared for the detection of Cu2+ and GSH. The “turn-off” process of fluorescence in the presence of Cu2+ ions was induced by forming a non-luminescent ground state complex due to the interaction between surface groups of the probe and Cu2+ ions. Moreover, the strong coordination between GSH and Cu2+ could destroy the structure of the complex and restore the fluorescence to “turn-on”. This fluorescent probe had excellent selectivity and high sensitivity toward Cu2+ and GSH with the limits of detection (LODs) of 38 nM and 41 nM. More importantly, the as-prepared N,S-CDs served as an efficient fluorescent probe for not only detecting Cu2+ ions in lake water and tap water, and GSH in BSA solution, but also sensing Cu2+ and GSH in living cells. Therefore, these N,S-CDs could be considered as a promising fluorescence probe candidate for environmental monitoring and biological imaging.
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FOOD CHEMISTRY
·
2020
·
IF 6.306
Yuning Yang,Wei Liu,Jie Cao,Yiwei Wu
A ratiometric sensor of MOF/ CdTe QDs was constructed by physically mixing CdTe QDs ( λ em = 605 nm) with MOF (Fe-MIL-88NH 2, λ em = 425 nm). Under an UV lamp ( λ ex = 365 nm), orange-red CdTe QDs is gradually quenched with increasing levels of Hg 2+ or Cu 2+ , while blue MOF is unchanged, accompanying with a visual change from bright pink to blue fluorescence. Hence, a new method for determining Hg 2+ and Cu 2+ by MOF/CdTe QDs sensor is established, whose detection limits are 0.22 ng mL −1 for Hg 2+ (2.1% RSD) and 0.26 ng mL −1 for Cu 2+ (1.1% RSD), respectively. In addition, on-site, rapid and visual determination of Hg 2+ /Cu 2+ in red wine without any pretreatment is realized by using a MOF/CdTe QDs paper-based sensor. For Hg 2+ and Cu 2+ , the semi-quantitative detection ranges of the paper-based sensor are both 10 ~ 5000 ng mL −1 , implying that it has great application value in analyzing Hg 2+ and Cu 2+ in liquid samples.
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PHOTOCHEMISTRY AND PHOTOBIOLOGY
·
2020
·Vol. 96
·期 5
·1154-1160
·
IF 2.721
Kaili He,Xin Zhan,Lian Liu,Xiaohong Ruan,Yiwei Wu
A simple and effective ratiometric fluorescence sensor of CdTe QDs/GCNNs for on-site and rapid analysis of Cu 2+ has been established by mixing physically CdTe QDs and graphite carbon nitride (GCNNs). Two emissions peaks of CdTe QDs at 572 nm and GCNNs at 436 nm are both excitated at 340 nm. Under a UV lamp, fluorescent of traffic yellow CdTe QDs is linearly quenched by Cu 2+ (as the detection signal), while blue GCNNs remains unchanged (as the reference), resulting in a distinguishable color change gradually from pink yellow to blue. The limit of detection (LOD) of this new sensor for Cu 2+ is as low as 0.47 ng mL −1 with 1.4 % RSD. The established method has been successfully applied to detection of Cu 2+ in various drinks with satisfactory results. Moreover, a paper-based sensor, which has been prepared by soaking cellulose acetate membrane in CdTe QDs/GCNNs sensor solution, has a wide semiquantitative detection range for Cu 2+ (0.01 ~ 5.0 μg mL −1 ). It has realized successfully on-site and rapid determination of Cu 2+ in red wine without any pretreatment procedure and is of great promotion and application value in determination of Cu 2+ in liquid samples.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2020
·
IF 4.65
Tong Zou,Xinxin Xing,Yue Yang,Zhezhe Wang,Zidong Wang,Rongjun Zhao,Xu Zhang,Yude Wang
Copper, as an essential element in human body, can have adverse impact on environment and healthy individuals if it is excessive. So it is necessary to establish a rapid and effective method for detecting Cu 2+ . In this work, we describe a method for determination of Cu 2+ based on water-soluble ZnO quantum dots (QDs) modified with (3-aminopropyl)triethoxysilane (APTEs). The ZnO QDs functionalized with APTEs (NH 2 –ZnO QDs) synthesized by a simple sol-gel method and displayed strong yellow-green fluorescence with a peak at 535 nm under 350 nm excitation. High-resolution transmission electron microscopy, Fourier transform infrared spectroscopy , luminescence, and UV–visible absorption spectroscopy were used to characterize the NH 2 –ZnO QDs. In addition, the emission from NH 2 –ZnO QDs was selectively quenched upon addition of Cu 2+ . Therefore, this finding was used to design a fluorescent probe based on NH 2 –ZnO QDs to detect Cu 2+ in water solution, and the linear relationships were 2–20 nM and 1–100 μM respectively, with detection limit for Cu 2+ at 1.72 nM (on the basis of 3σ/slope criterion). This fluorescent probe had also been applied in real water sample to testify its availability in drinking water. Furthermore, the quenching mechanism was studied by measurements of UV–visible absorption spectra and fluorescent lifetime of ZnO QDs, which may be attributed to the aggregation induced by Cu 2+ and the dynamic quenching existing energy transfer between QDs and Cu 2+ .
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Journal of Materials Chemistry B
·
2019
·Vol. 8
·期 6
·1202-1211
·
IF 5.047
Kecan Lin,Yanbing Cao,Dongye Zheng,Qin Li,Hui Liu,Peiwen Yu,Jiong Li,Yanan Xue,Ming Wu
The development of nanotheranostic agents integrating diagnosis and therapy has gained tremendous attention in the past few decades, but many of them are inherently hydrophobic and need complicated phase-transfer and tedious surface modifications. This work proposed a facile method of transferring hydrophobic Fe3O4@Cu2−xS nanoparticles from oil to water by using red blood cell membrane to create theranostic nanobeads for T2-weighted MRI and second near-infrared photothermal ablation. The obtained nanoplatform, namely SCS@RBCM, showed a core–shell structure with the inner core densely packed with Fe3O4@Cu2−xS nanoclusters and the surface coated with a layer of RBCM. SCS@RBCM displayed a stable nanostructure, high NIR II light absorption and photothermal conversion ability, T2-weighted MR imaging and magnetic field targeting ability. Meanwhile, the RBCM cloaking endowed SCS with reduced elimination by macrophages. With the navigation of an external magnetic field (MF), the tumor accumulation of SCS@RBCM was dramatically increased, thus achieving good performance of MR imaging and antitumor efficacy through the PTT effect under NIR II irradiation. Therefore, our strategy presents a new and desirable paradigm in the phase-transfer of hydrophobic nanotheranostics for optimizing their biomedical performance.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2020
·
IF 3.232
Shengling Li,Duanlin Cao,Xianjiao Meng,Zhiyong Hu,Zhichun Li,Changchun Yuan,Tao Zhou,Xinghua Han,Wenbing Ma
In this study, a highly selective fluorescent sensor ( E )-2-((2-(benzo[ d ]thiazol-2-yl)quinolin-8-yl)oxy)- N ′ -((7-(diethylamino)-2-oxo-2 H -chromen-3-yl)methylene)acetohydrazide ( TQC ) was synthesized from 2-methylquinolin-8-ol and 4-(diethylamino)-2-hydroxybenzaldehyde and its structure was characterized by 1 H NMR, 13 C NMR, ESI-HR-MS and density functional theory (DFT) calculation. Sensor TQC showed an obvious “on-off-on” fluorescence response to Cu 2+ and PPi in a DMSO/HEPES (3:2 v/v, pH = 7.4) buffer system. The detection limits of sensor TQC were 0.06 μM to Cu 2+ and 0.01 μM to PPi. In addition, sensor TQC showed a 1:1 binding stoichiometry to Cu 2+ and TQC- Cu 2+ complex showed a 2:1 binding stoichiometry to PPi. The optimum pH range of sensor TQC and TQC- Cu 2+ was 3–8. Further studies demonstrated that sensor TQC could be made into test paper strips for the qualitative of Cu 2+ and PPi and showed sequentially “on-off-on” fluorescent bio-imaging of Cu 2+ and PPi in HeLa cells.
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ANALYTICA CHIMICA ACTA
·
2019
·
IF 5.256
Kang Zou,Yamin Fu,Ruiying Yang,Xiaohua Zhang,Cuicui Du,Jinhua Chen
By direct calcination of Cu 2+ -doped ZIF-8 in oxygen atmosphere, a new photoelectric material, CuO–ZnO heterojunction , was prepared. The morphology and structure were investigated in detail by several methods, such as scanning electron microscopy, transmission electron microscopy , nitrogen adsorption-desorption method and X-ray diffraction. Under visible light irradiation , CuO–ZnO heterojunction exhibits excellent PEC behavior in aqueous media with the presence of ascorbic acid (AA) and dissolved oxygen at −0.3 V. Taking the CA125-antibody functionalized CuO–ZnO heterojunction (CuO–ZnO-Ab 2 ) as a signal source, a novel photoelectrochemical (PEC) immunosensing platform was developed for ultrasensitive assay of CA125. Because of the target-induced introduction of photoelectric material to the sensing platform, the proposed PEC immunosensor has excellent performance for CA125 assay: near-zero background noise, wide linear response range (1 × 10 −5 U/mL to 100 U/mL) and low detection limit (3.16 × 10 −6 U/mL). The developed CuO–ZnO heterojunction and the related PEC sensing platform may have promising applications in ultrasensitive and highly accurate monitoring of various proteins in bioanalysis and disease diagnosis.
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JOURNAL OF HAZARDOUS MATERIALS
·
2018
·
IF 6.434
Xiaoqing Wang,Yan Lou,Xinyan Ye,Xuedan Chen,Lei Fang,Yinghao Zhai,Yuqiang Zheng,Chunhua Xiong
To advocate environment friendly detection idea, we adopted the green chemical method to synthesis the 1-(2 amino ethyl) piperidine functionalized polyacrylonitrile fiber (APF) and the chromogenic fiber 4-(2-pyridylazo) resorcinol (APF-PAR). The APF has high adsorption selectivity of Hg 2+ and Cu 2+ , and the change of structure, surface morphology and thermo-stability before and after adsorption have been characterized by the infrared spectra, scanning electron microscope and thermogravimetric analysis. The APF achieved the adsorption equilibrium of Hg 2+ just in 25 min and the adsorption capacity is 435.1 mg/g, while the adsorption equilibrium of Cu 2+ costs 30 min and the adsorption capacity is 141.7 mg/g. The chromogenic fiber APF-PAR can recognize the Hg 2+ and Cu 2+ in 2 s, which benefits from the rapid mass transfer and small fluid resistance of the chelating PAN fiber. The color changed from orange to purplish red due to the variation of HOMO-LOMO energy gaps during the reaction which confirmed by the UV–vis absorption spectrum. It also has high selectivity and excellent adsorption performance, which provides more convenient, accurate, reliable and faster testing methods of Hg 2+ and Cu 2+ in environmental medium.
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ACS Applied Materials & Interfaces
·
2015
·
IF 6.723
Tong Yang,Hong Yan Zou,Cheng Zhi Huang
A new heterogeneous catalytic composite composed of nonstoichiometric Cu2–xSe nanoparticles (NPs) with high copper deficiency and graphene oxide (GO) is prepared by coembedding in electrospun nanofibers of a poly(vinylpyrrolidone) (PVP) support, wherein GO in the nanofibers is converted into reduced GO (rGO) via heat treatment. The as-prepared composite Cu2–xSe/rGO/PVP nanofibers have demonstrated superior catalytic activity toward the reduction of a refractory organic compound by taking 4-nitrophenol (4-NP) as an example. In the presence of NaBH4, the Cu2–xSe/rGO/PVP nanofibers display a synergetic effect between Cu2–xSe and rGO in PVP nanofibers compared to their independent components or corresponding nanofibers. Furthermore, the Cu2–xSe/rGO/PVP nanofibers exhibit a favorable water-stable property via heat treatment to solidify the hydrophilic PVP matrix, which makes the composite display good reusability, stability in aqueous solution, and separability from a water medium. This work not only presents a direct, convenient, and effective approach to doping semiconductor nanomaterials into polymer nanofibers but also provides fundamental routes for further investigations about the synergetic effect between different materials based on the platform of electrospun nanofibers.
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COLLOIDS AND SURFACES B-BIOINTERFACES
·
2013
·
IF 3.554
Wen-Bo Wang,Da-Jian Huang,Yu-Ru Kang,Ai-Qin Wang
The novel granular semi-IPN hydrogels were in situ prepared in an aqueous solution by the free-radical grafting and crosslinking reactions among chitosan (CTS), acrylic acid (AA), gelatin (GE) and N , N ′-methylene- bis -acrylamide. The FTIR spectra and elemental analysis confirmed that the AA monomers were grafted onto CTS backbone, and the GE macromolecular chains interpenetrated through the CTS- g -PAA network. The hydrogels are granular, which are composed of numerous micro-spheres according to the scanning electron microscope observations. The gel strength, adsorption, reuse and recovery properties of the hydrogels for Cu 2+ ion were systematically investigated. The results indicate the hydrogel with 2 wt% GE has the highest adsorption capacity of 261.08 mg/g with the recovery ratio of 95.2%. And the incorporation of 10 wt% GE enhanced the storage modulus by 103.4% ( ω = 100 rad/s) and 115.1% ( ω = 0.1 rad/s), and the adsorption rate by 5.67%. Moreover, the adsorption capacity of the hydrogel is still as high as 153.9 mg/g, after five cycles of adsorption–desorption. It was found that the ion-exchange and complexation interactions between the functional groups ( COO − and NH 2 ) of the hydrogels and Cu 2+ ion are the predominant adsorption mechanisms.
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CARBOHYDRATE POLYMERS
·
2024
·
IF 10.7
Xiuqin Fang,Chang Wang,Hong-Hui Shu,Sheng-Li Han,Cheng-Mei Liu
Bisphenol A (BPA), a prominent endocrine-disrupting compound, has garnered considerable attention due to its urgent need for rapid removal from water. Herein, we first used a novel reactive phosphine oxide containing tertiary amines as crosslinker to prepare water-insoluble crosslinked β-cyclodextrin (β-CD) adsorbent via radical-mediated thiol–ene polymerization. Owing to the synergistic hydrogen-bond (H-bond) interactions of functional groups (tertiary amine and P O groups) toward BPA, the resulted adsorbents showed fast adsorption kinetics to BPA with an adsorption equilibrium time of 5 min. After six adsorption–desorption cycles, the removal efficiency of BPA was 92.5 %, indicating its excellent reusability. Due to the presence of the C S bonds, the β-CD -derived bio-adsorbents offered binding sites for Cu 2+ ions, resulting in a maximum adsorption capacity of 113.89 mg g −1 .
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