ANALYTICAL AND BIOANALYTICAL CHEMISTRY
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2018
·Vol. 410
·期 18
·4285-4291
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IF 3.307
Liu Dongkui,Lu Xing,Yang Yiwen,Zhai Yunyun,Zhang Jian,Li Lei
Acute myocardial infarction (AMI) is one of the leading risks to global health. Thus, the rapid, accurate early diagnosis of AMI is highly critical. Human cardiac troponin I (cTnI) has been regarded as a golden biomarker for AMI due to its excellent selectivity. In this work, a novel fluorescent aptasensor based on a graphene oxide (GO) platform was developed for the highly sensitive and selective detection of cTnI. GO binds to the fluorescent anti-cTnI aptamer and quenches its fluorescence. In the presence of cTnI, the fluorescent anti-cTnI aptamer leaves the surface of GO, combines with cTnI because of the powerful affinity of the fluorescent anti-cTnI aptamer and cTnI, and then restores the fluorescence of the fluorescent anti-cTnI aptamer. Fluorescence-enhanced detection is highly sensitive and selective to cTnI. The method exhibited good analytical performance with a reasonable dynamic linearity at the concentration range of 0.10–6.0 ng/mL and a low detection limit of 0.07 ng/mL ( S / N = 3). The fluorescent aptasensor also exhibited high selectivity toward cTnI compared with other interference proteins. The proposed method may be a potentially useful tool for cTnI determination in human serum.
A novel fluorescent aptasensor for the highly sensitive and selective detection of cardiac troponin I based on a graphene oxide platform.
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APPLIED CATALYSIS A-GENERAL
·
2018
·
IF 4.521
Fengjiao Wang,Yuyao Gu,Zhenya Yang,Yanyu Xie,Jiangjie Zhang,Xiaotong Shang,Huibo Zhao,Zizhong Zhang,Xuxu Wang
We developed a simple X − -assisted (X = Cl, Br, I) one-pot hydrothermal reaction to successfully synthesize a series of BiOX/Bi 2 WO 6 heterojunction. The effect of different halogens and their addition amount on the photocatalytic performance of BiOX/Bi 2 WO 6 composites was investigated using benzyl alcohol selective oxidation under visible-light irradiation. All BiOX could enhance the photocatalytic activity of Bi 2 WO 6 , but the BiOBr was the optimum for the maximum improvement of Bi 2 WO 6 . The match of energy band structure between BiOX and Bi 2 WO 6 resulted in the highly efficient separation of photogenerated charges, which was mainly attributed to their fundamental distinction of the photocatalytic activity. This work clarified the essential distinction in photocatalytic performance of the different halogen of BiOX/Bi 2 WO 6 heterojunction, and also provided guidance for the construction of efficient heterojunction photocatalysts.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2019
·
IF 4.084
Chunpeng Bai,Jingce Bi,Junbiao Wu,Yan Xu,Sebastian Wohlrab,Yide Han,Xia Zhang
In this work, a series of Ag/AgX (X = Cl, Br, I)/g-C 3 N 4 (Ag/AgX/CN) composites were successfully fabricated by an in-situ solid phase method. The morphology and structure, photoluminescence and photoelectrochemical properties of composites were investigated in detail. The as-prepared Ag/AgX/CN composites were used as H 2 evolution photocatalysts under visible-light irradiation with a sacrificial agent . The experimental results revealed that Ag/AgI/CN-4 composite possesses highest-H 2 evolution rate (up to 59.22 μmol g −1 h −1 ) which are approximately 31 times higher than that of pure g-C 3 N 4 (1.94 μmol g −1 h −1 ). In addition, Ag/AgCl/CN-4 and Ag/AgBr/CN-4 composites also present high photocatalytic activities yielding, 26.39 and 18.05 μmol H2 g −1 h −1 , respectively. The enhanced photocatalytic activities of Ag/AgI/CN-4 composite might be attributed to the synergistic effect between Ag/AgI nanoparticles and g-C 3 N 4 and the localized surface plasmon resonance effect of metallic Ag. Moreover, Ag/AgI/CN-4 composite showed excellent recyclability and stability after five cycling photocatalytic tests (about 25 h). Furthermore, the possible photocatalytic mechanism of Ag/AgI/CN composites is proposed.
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SENSORS AND ACTUATORS B-CHEMICAL
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2016
·
IF 4.758
Dan Yan,Yu He,Yili Ge,Gongwu Song
A novel fluorescence “turn on-off” method for sensitive and selective detection of heparin and heparinase I was developed based on near infrared Polyethyleneimine Capped Ag 2 S Quantum Dots (PEI-Ag 2 S QDs). The fluorescence “turn-on” arose from aggregation-induced emission enhancement (AIEE) characteristics of PEI-Ag 2 SQDs induced by electrostatic interaction between PEI-Ag 2 SQDs and heparin. Heparinase I, which can specifically hydrolyze heparin into short fragments would de-aggregate PEI-Ag 2 S QDs/heparin system and lead to fluorescence “turn-off”. Under optimal conditions described, the fluorescence enhancement at 685 nm was linearly related to the concentration of heparin and heparinase I in the range of 0.069–2.275 μM and 0–103 ng mL −1 with the relative correlation coefficient of R 2 = 0.997 and 0.99 and detection limit as low as 6 nM and 0.5 ng mL −1 , respectively. The activity of the heparinase I was further investigated using steady-state kinetic for the reaction. In ddition, the proposed method was successfully utilized in serum samples, which presaged more opportunities for application in related biochemical and biomedical researches.
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ACS Applied Materials & Interfaces
·
2017
·
IF 7.504
Daqin Chen,Xiao Chen,Zhongyi Wan,Gaoliang Fang
Full-color visible emissions are particularly crucial for applications in displays and lightings. In this work, we developed a facile room-temperature ligand-assisted supersaturated recrystallization synthesis of monodisperse, cubic structure Cs1–mFAmPbX3 (X = Cl, Br, and I or their mixtures Cl/Br and Br/I, 0 ≤ m ≤ 1) hybrid perovskite quantum dots (QDs). Impressively, cation substitution of Cs+ by FA+ was beneficial in finely tuning the band gap and in exciton recombination kinetics, improving the structural stability, and raising the absolute quantum yields up to 85%. With further assistance of anion replacement, full-spectral visible emissions in the wavelength range of 450–750 nm; narrow full width at half-maxima, and a wide color gamut, encompassing 130% of National Television System Committee television color standard, were achieved. Finally, Cs1–mFAmPbX3-polymer films retaining multicolor luminescence are prepared and a prototype white light-emitting diode device was constructed using green Cs0.1FA0.9PbBr3 and red Cs0.1FA0.9Br1.5I1.5 QDs as color converters, certainly suggesting their potential applications in the optoelectronics field.
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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY
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2016
·Vol. 311
·期 3
·1577-1591
·
IF 0.983
Zong Youli,Zhang Yongde,Lin Xiaoyan,Ye Dong,Luo Xuegang,Wang Jing
A novel microsphere adsorbent based upon carboxymethyl cellulose sodium/prussian blue composite loaded with Lanthanum(III) (CMC/PB-La) was successfully synthesized via electrostatic ejection device for removal of cesium from contaminated water, and characterized by FT-IR, SEM, EDX and XPS. Influencing factors to adsorption cesium were investigated, including solution pH, adsorbent dosage, contact time, initial concentration, temperature and competing ions. Linear Freundlich isotherm was fitted satisfactorily to the adsorption data, and the adsorption kinetic data was fitted well with pseudo-second-order model. Moreover, the results of γ-irradiation experiments indicate that CMC/PB-La has good radiation stability.
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POLYMER BULLETIN
·
2016
·Vol. 74
·期 4
·1091-1101
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IF 1.371
Li Hu,Zhou Zhen,Liu Jingcheng,Xu Wenjia,Liu Ren,Liu Xiaoya
Positive chemically amplified molecular glass with pendant t -butyloxy carbonyl ( t -BOC) groups based on β-cyclodextrin (β-CD) was prepared. The β-CD derivatives were obtained from the reaction of β-CD and di- tert -butyl dicarbonate (DBDC) in the presence of 4-dimethylaminopyridine, and the protecting ratio was controlled using various feed amounts of DBDC. Fourier-transform infrared spectroscopy and proton nuclear magnetic resonance were employed to characterize the chemical structure, indicating that the synthesis was successful. Thermal behavior was characterized by thermogravimetric analysis; the results showed that the initial thermal decomposition temperature occurred at approximately 160 °C, which could satisfy the lithography process. Ultraviolet–visible spectrophotometer indicated that the t -BOC-protected β-CD derivatives had low absorbance at 365 nm wavelength. Additionally, X-ray diffraction analysis results showed that the β-CD derivatives had amorphous form, and exhibited excellent film-forming property. The photoresists consisting of different t -BOC protecting groups showed high sensitivity when exposed to 365 nm light and post-baked at 105 °C for 90 s, followed by developing in 2.38 wt% aqueous tetramethylammonium hydroxide solution at room temperature. An enhanced line and space positive patterns with 1 μm resolution were delineated according to digital microscope.
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ACS Sustainable Chemistry & Engineering
·
2016
·
IF 5.267
Yuling Zhao,Jikuan Qiu,Li Tian,Zhiyong Li,Maohong Fan,Jianji Wang
Carbon dioxide (CO2) is an abundant and renewable feedstock for the production of high-value chemicals. Herein, CuI and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) were employed as an efficient catalyst system to synthesize 2-oxazolidinones through the coupling reaction of CO2 and propargylic amines. It was found that this cost-competitive catalyst system could efficiently catalyze the reaction within only 4 h at atmospheric pressure CO2, and a wide range of substrates were suitable for this reaction. Various target products were obtained in excellent yields. Furthermore, the catalytic mechanism of the CuI/DBU system was investigated by using density functional theory. It was shown that copper(I) and DBU played synergistic roles in activating both the C≡C triple bond and the amino group of propargylic amines in the reaction.
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GREEN CHEMISTRY
·
2016
·Vol. 19
·期 4
·1109-1116
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IF 8.506
Huan Liu,Dong-Liang Wang,Xia Chen,Yong Lu,Xiao-Li Zhao,Ye Liu
Mono-phosphines (L1 and L2) and diphosphines (L3 and L4) with typical π-acceptor character were prepared and applied in Ir(I)-catalyzed N-alkylation of amines with alcohols. It was found that the π-acceptor character of the applied phosphines is closely correlated to the catalytic efficiency of the [Ir(COD)Cl]2 complex for this green reaction. Compared to PPh3 as the typical σ-donor (i.e. with poor π-acceptor character), L1–L4 all resulted in the efficient N-alkylation of aniline to benzyl-aniline. While L1–L4 coordinated to the Ir(I)-catalyst, the consolidated Ir–P linkages due to π-backdonation could well protect the Ir-catalyst against deactivation, giving rise to the N-alkylation of aniline. On the other hand, the stabilized Ir-catalyst with the involvement of L2 could be recycled successfully for at least 4 runs in the ionic liquid of [MePh3P]Br without the detectable leaching of Ir and P elements in the organic products.
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RSC Advances
·
2015
·Vol. 5
·期 17
·12517-12529
·
IF 3.84
Xiangguo Meng,Yan Liu,Minjia Meng,Zheyu Gu,Liang Ni,Guoxing Zhong,Fangfang Liu,Zhaoyong Hu,Rui Chen,Yongsheng Yan
In this work, two novel Cs(I) ion-imprinted polymers (Cs(I)-IIP1 and Cs(I)-IIP2) have been prepared by surface imprinting technique based on support matrix of SBA-15. The strategy was carried out by introducing two different reversible addition–fragmentation chain transfer (RAFT) polymerization including using the free RAFT agent in solution and surface-anchored RAFT agent with appropriate initiation method, which is expected to generate a well-defined surface ion-imprinted polymer with excellent adsorption capacity. The materials were verified by FT-IR, SEM, TEM, nitrogen adsorption–desorption and TGA. Owing to the intrinsic advantages of surface-anchored RAFT polymerization, the resultant surface ion-imprinted polymer (Cs(I)-IIP2) exhibited more homogeneous and thinner polymer layer (15 nm) with excellent macrostructure in comparison to Cs(I)-IIP1 (75 nm) prepared by using the free RAFT agent in solution. Furthermore, the adsorption capacity of both polymers are compared, indicating that Cs(I)-IIP2 displays higher adsorption property and excellent selectivity for Cs(I).
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Frontiers in Bioengineering and Biotechnology
·
2025
·
IF 4.8
Shaonian Ye,Cifu Xu,Huilin Li,Shilun Feng,Yan Wang,Fang Gao
The accurate and rapid detection of cardiac troponin I (cTnI) at the point of care is crucial for the timely diagnosis of myocardial infarction (MI). This study introduces an advanced lateral flow immunoassay (LFIA) platform for cTnI detection. We employed small-sized, large-pore dendritic mesoporous silica nanoparticles (DMSN-2) to encapsulate quantum dots (QDs), achieving an enhanced QD loading capacity of 1.427 g QD/g silica, compared to 0.881 g QD/g silica for smaller pore counterparts (DMSN-1). This nano-LFIA was further integrated with “AdaptiScan”, a smartphone-based detection system that uses adaptive detection algorithms to automatically extract and analyze fluorescence signals from LFIA strips. This integration of pore-size tailored DMSNs and “AdaptiScan” resulted in a limit of detection for cTnI of 42.6 ng/L, which meets clinical diagnostic requirements. The platform offers a sensitive, cost-effective, and portable solution for rapid detection of MI, potentially transforming point-of-care testing in resource-limited settings.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2025
·
IF 6.3
Shuang Chen,Qiule Zhao,Yangchun Mo,Xiaopeng Wei,Jilin Wang,Guoyuan Zheng,Fei Long
Organic-inorganic hybrid perovskites have attracted wide attention because of their low cost, high photoelectric conversion efficiency and simple production process. Diisopropylamine was innovatively employed, in this paper, as the A-site organic ligand for bismuth-based halide organic-inorganic hybrid crystals. [(CH 3 CH 2 CH 2 ) 2 NH 2 ] a Bi b X c (X = Cl, Br and I) crystals were synthesized by a solvent evaporation method. All three crystals belong to the P2 1 /n space group. Among them, [(CH 3 CH 2 CH 2 ) 2 NH 2 ]BiBr 4 and [(CH 3 CH 2 CH 2 ) 2 NH 2 ]BiI 4 have one-dimensional chain structures, and [(CH 3 CH 2 CH 2 ) 2 NH 2 ] 2 Bi 2 Cl 8 belongs to a zero-dimensional structure. The band gap can be adjusted between 3.04 eV and 1.61 eV by the properties of halide ligands, and the good thermal stability of the three crystals are 203°C, 258°C and 291°C. Moreover, [(CH 3 CH 2 CH 2 ) 2 NH 2 ]BiI 4 thin films were prepared by the one-step solution spin-coating as a light absorbing layer. The band gap of thin films is 1.97 eV. The maximum power conversion efficiency of the device is 0.0271 %. Therefore, this organic-inorganic hybrid compound with a suitable band gap and high stability is expected to become a potential candidate material for photoelectric devices.
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