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991.
Ruoxi?Zhang Li?Deng Paijin?Zhu Shuxia?Xu Chengpeng?Huang Ying?Zeng Shijun?Ni Xinfeng?ZhangEmail author 《Mikrochimica acta》2017,184(2):541-546
The article describes a bienzyme visual system for aptamer-based assay of Hg(II) at nanomolar levels. The detection scheme is based on the finding that Hg(II) ions captured by aptamer-functionalized magnetic beads are capable of inhibiting the enzymatic activity of uricase and thus affect the formation of H2O2 and the blue product, i.e., oxidized tetramethylbenzidine. This strategy allows for a visual detection of Hg(II) at nanomolar levels without additional amplification procedure. Measuring the absorbance at 650 nm, the logarithmic calibration plot is linear in the concentration range of 0.5–50 nM and the limit of detection (LOD) is 0.15 nM. This is as low as the LOD obtained by atomic fluorescence spectrometry (AFS). The ions K+, Mg2+, Na+, Ca2+, Cu2+, Zn2+, Fe3+, Al3+, Co2+, AsO2 ?, Ni2+, Cd2+ and Pb2+ do not have a significant effect on color formation. The method was applied to the analysis of (spiked) river water, lake water, mineral water, tap water and certified reference water samples, and the results agreed well with those obtained by AFS or certified values, with recoveries ranging from 97% to 109%. The relative standard deviation for five parallel detections at a 10 nM Hg(II) level is 5.2%. 相似文献
992.
Wenyue?Gao Pan?Hui Liming?Qi Zhongyuan?Liu Wei?ZhangEmail author Guobao?XuEmail author 《Mikrochimica acta》2017,184(3):693-697
A simple method is described for the determination of copper(II) ions based on the cathodic electrochemiluminescence (ECL) of lucigenin which is quenched by Cu(II). The blue ECL is best induced at ?0.45 V (vs. Ag/AgCl) at a scan rate of 50 mV·s?1. Under optimum conditions, the calibration plot is linear in the 3.0 to 1000 nM Cu(II) concentration range. The limit of detection is 2.1 nM at a signal-to-noise ratio of 3. Compared to other analytical methods, the one presented here is simple, fast, selective and cost-effective. It has been successfully applied in the analysis of copper ions in spiked tap water samples with recoveries ranging from 93.0% (at 50 nM concentration) to 105.7% (at 150 nM). 相似文献
993.
Yushu?Shi Guoqing?Zhang Jiaojiao?Li Yong?ZhangEmail authorView authors OrcID profile Yanbao?Yu Qin?Wei 《Mikrochimica acta》2017,184(5):1379-1387
The authors describe a highly sensitive and selective photoelectrochemical (PEC) assay for mercury(II) ions. It is based on a dual signal amplification strategy. The first enhancement results from the surface plasmon resonance (SPR) of Au@Ag nanoparticles (NPs) absorbed on MoS2 nanosheets. Here, the injection of hot electrons of Au@Ag NPs into MoS2 nanosheets produces a strong photocurrent, while background signals are strongly reduced. The second enhancement results from the use of a thymine rich ct-DNA aptamer attached to the Au@Ag-MoS2 nanohybrid. The DNA specifically binds Hg(II) ions to form thymine-Hg(II)-thymine (T-Hg-T) complexes. This leads to the formation of a hairpin-shaped dsDNA structure. The use of a CdSe quantum dot label at the terminal end of the ct-DNA further facilitates electron–hole separation. The photocurrent of the detector is measured as a function of Hg(II) concentration at a bias voltage of 0.1 V and under irradiation of 430 nm light. Due to the two-fold amplification strategy presented here, the linear range extends from 10 pmol·L?1 to 100 nmol·L?1, with a detection limit of 5 pmol·L?1 (at S/N?=?3). 相似文献
994.
Xiaolong?Zhang Yongyi?Zeng Aixian?Zheng Zhixiong?Cai Aimin?Huang Jinhua?Zeng Xiaolong?LiuEmail author Jingfeng?LiuEmail author 《Mikrochimica acta》2017,184(7):1933-1940
The authors describe a fluorescence immunoassay for galectin-4, a candidate biomarker for various cancers. Glucose oxidase was encapsulated into a zeolitic imidazolate framework to give a composite (GOx/ZIF-8 composite) that acts as a signal-transduction tag via a biomimetic mineralization process. After modification of the composite with streptavidin, it binds biotinylated antibody against galectin-4. In the immunoassay, the response to galectin-4 results from the enzymatic oxidation of glucose. This reaction produces hydrogen peroxide (H2O2) that reacts with iron(II) ions to generate hydroxy radical (?OH), which leads to the quenching of the fluorescence of gold nanoclusters (AuNCs). Accordingly, the fluorescence quenching of AuNCs depends on the concentration of target galectin-4. The GOx/ZIF-8 composite has a high loading capacity for GOx at uncompromised enzymatic activity. The fluorescence of AuNCs is sensitively quenched by ?OH radicals. Galectin-4 can be detected by this method in concentrations as low as 10 pg·mL?1. It is expected that this kind of enzyme/MOF composite-based immunoassay has a wide scope in that it may be adapted to other low-abundance proteins and biomarkers. 相似文献
995.
Fangying?Lv Ning?GanEmail author Jie?Huang Futao?Hu Yuting?CaoEmail author You?Zhou Youren?Dong Li?Zhang Shan?Jiang 《Mikrochimica acta》2017,184(8):2561-2568
The authors describe an ultrasonic-assisted headspace method for solid phase micro-extraction (UA-HS-SPME) of 7 polychlorinated biphenyls (PCBs) with codes PCB28, PCB52, PCB101, PCB118, PCB138, PCB153 and PCB180. The coating is based on a poly-dopamine metal-organic framework [PDA-MIL-53(Fe)] on a stainless steel wire. The coating can be prepared and evenly deposited on the stainless fiber by dipping the PDA fiber into a solution of MIL-53(Fe). The assay is also environmentally friendly because water is used as the solvent. The effects of extraction time, addition of salts, pH value and power of ultrasonic power were optimized. The coating is found to possess a high selectivity and adsorption capacity for PCBs compared to commercial SPME fibers such as the divinylbenzene/carboxen/polydimethylsiloxane fibers. Following desorption, the PCBs were quantified by GC-MS. The detection limits are between 50 and 90 pg?g?1 of PCBs in soil. The fibers can be easily prepared, and the batch-to-batch reproducibility (RDS) is <10% (for n = 6). The fibers are inexpensive, re-usable and can be easily manipulated, and particularly well suited for screening polychlorinated biphenyls in soil. 相似文献
996.
Su?Liu Xueqi?Leng Xu?Wang Qianqian?Pei Xuejun?Cui Yu?WangEmail author Jiadong?Huang 《Mikrochimica acta》2017,184(7):1969-1976
The authors describe a colorimetric method for the determination of Hg(II) ion. It is based on the color change from red to colorless as displayed by gold nanoparticle (AuNP) modified with thymine - rich DNA. Signal amplification is accomplished by free strand displacement recycling. In this strategy, Hg(II) unfolds the arch-trigger duplex due to the high affinity between Hg(II) and the thymines to form T-Hg(II)-T structures, thereby causing the release of trigger. The liberated trigger unfolds the hairpin structure of H1, and unfolded H1 further unfolds with H2. As a result, the H2 hairpin displaces trigger, and the released trigger unfolds another H1. This results in strong and enzyme-free strand displacement recycling amplification. The aggregation of DNA-AuNPs occurs in the presence of the duplex formed by hairpins H2 and H1. This results in a color change from red to colorless that can be visually observed. Under optimal conditions, the assay has a detection range over 4 orders of magnitude and a 3.4 nM detection limit. The assay is selective, sensitive, rapid and cost-effective. In our perception, it represents a useful platform for determination of Hg(II). 相似文献
997.
Microchimica Acta - The authors describe an aptamer based fluorometric assay for the determination of ATP. It is based on deoxyribonuclease I-aided target recycling and signal amplification. The... 相似文献
998.
Microchimica Acta - The authors describe an amperometric biosensor for the determination of organophosphate pesticides (OPs) via inhibition of the enzyme acetylcholinesterase (AChE). The enzyme was... 相似文献
999.
May Lee Low Cheang Wei Chan Pei Ying Ng Ing Hong Ooi Mohd Jamil Maah Soi Moi Chye 《Journal of Coordination Chemistry》2017,70(2):223-241
Three ternary copper(II) complexes, [Cu(phen)(L-phe)Cl]·2H2O, [Cu(phen)(L-leu)Cl]·4½H2O, and [Cu(phen)(L-tyr)Cl]·3H2O, and four binary copper(II) complexes, [Cu(phen)Cl2], Cu(L-phe)2·½H2O, Cu(L-leu)2·½H2O, and Cu(L-tyr)2·H2O (where phen = 110-phenanthroline, L-phe = L-phenylalanine, L-tyr = L-tyrosine, L-leu = L-leucine and Cl- = chloride), were synthesized and characterized by elemental analysis, spectroscopic techniques (FTIR, UV–visible, fluorescence spectroscopy), magnetic susceptibility, molar conductivity, and lipophilicity measurement. X-ray diffraction determination of a single crystal of [Cu(phen)(L-tyr)Cl] showed two independent molecules in the asymmetric unit, each with the same distorted square pyramidal geometry about copper(II). p-Nitrosodimethylaniline assay revealed that the three ternary complexes were better inducers of reactive oxygen species over time than binary complexes, CuCl2, and free ligands. All the copper(II) complexes in this series inhibited the three proteolytic activities in the order Trypsin-like > Caspase-like > Chymotrypsin-like. In terms of anticancer properties, the copper(II)-phen complexes had GI50 values of less than 4 μM against MCF-7, HepG2, CNE1 and A549 cancer cell lines, more potent than cisplatin. 相似文献
1000.
Four d10 transition-metal coordination complexes 1–4 (1: [Ag2(TPT)2(TPTH)2]; 2: [Cu6(TPT)6]·2DMF; 3: [Cd(TPT)2(TPTH)]·CH3CH2OH, 4: [Zn(TPT)2]n) have been constructed from a newly designed heterocyclic thioamide ligand, TPTH (TPTH = 4-(thiophen-2-yl)-pyrimidine-2-thiol). All complexes have been structurally elucidated by single crystal X-ray diffraction analyses. Except for 4, which shows a one-dimensional (1-D) chain structure, 1–3 are all discrete coordination complexes featuring dinuclear, hexanuclear and mononuclear entities, respectively. Their photophysical properties have been evaluated in the solid state at room temperature by UV–vis diffuse reflectance and luminescence spectra. Among them, 2 exhibits a strong red luminescence (λem = 699 nm) with a remarkable red-shift of the maximum emission compared to that of the TPTH ligand (λem = 536 nm). The red emission observed with 2 is ascribed to a LMCT (ligand-to-metal charge transfer) transition which agrees with the DFT calculations. 相似文献