In the presence of lincomycin, the aptamer DNA was specific binding with lincomycin, and ferrocene-DNA (Fc-DNA) was detached from the surface of aptasensor electrode, generating an obviously enhancement of ECL signal. To ensure the accuracy of the data, each electrode runs continuously for 3600 s. Under optimal experimental conditions, the detection range of the aptasensor was 0.10 ng mL-1 - 0.10 mg mL-1, and the detection limit was 0.028 ng mL-1. In addition, the aptasensor has good stability and reproducibility, and also provided a hopeful device for all kinds of other protein target.A nanocomposite of ordered mesoporous carbon/nickel oxide (OMC-NiO) was synthesized by hard-templating method. The nanocomposite remained ordered mesostructure and high surface area with the NiO nanocrystals embedded in the wall of the OMC. A sensitive sensor for electrochemical detection of epinephrine (EP) was developed with GCE modified by OMC-NiO nanocomposite. Cyclic voltammogram (CV) and differential pulse voltammetry (DPV) were used as the techniques to explore the electrochemical behavior of EP on OMC-NiO/GCE surface. The result showed that the electrode demonstrated better electrocatalytic performance to EP compared to that seen at OMC/GCE. Under the optimum condition, DPV measurements of the electrode response displayed a linear detection range for 8.0 × 10-7 to 5.0 × 10-5 M with a detection limit of 8.5 × 10-8 M (S/N = 3). It is worth noting that the electrocatalytic redox mechanism of EP on the electrode have studied through experiments and calculations (cyclic voltammetry and molecular electrostatic potential distribution). Moreover, the electrocatalytic behavior for the oxidation of EP and uric acid (UA) on OMC-NiO/GCE surface was investigated. The result showed that the sensor can be used to selectively determinate EP in the presence of an excesses of UA. Finally, the developed sensor was successfully applied to the determination of EP in spiked human blood serum and EP injection with satisfactory results.Direct molecular analysis of tissue samples is a promising approach to increase the accuracy, speed and molecular specificity of cancer diagnosis. Herein, alterations of amino acids between human lung cancer tissues and matched adjacent normal tissues were profiled by internal extraction electrospray ionization mass spectrometry (iEESI-MS). The results indicated that the levels of 11 detected amino acids (including serine, proline, valine, threonine, asparagine, aspartic acid, methionine, histidine, phenylalanine, arginine and tyrosine) in the cancerous tissues were lower than that in the adjacent normal tissues. Based on the orthogonal partial least squares discriminant analysis (OPLS-DA) model, cancerous and adjacent normal tissues were clearly discriminated, and the amino acids that played the major role in the differentiation between cancerous and adjacent normal tissues were identified. Moreover, metabolic pathway analysis revealed alterations of differential amino acids in several metabolic pathways upon lung cancer. The current study extends the power of iEESI-MS as a promising tool for quantitative characterization of amino acids in tissues, and allows the study of alterations in amino acids metabolism associated with the development of lung cancer.Lead poisoning endangers soil, plants and human health due to its toxic effect. It is urgent to develop ideal tool for the in vivo detection of Pb2+.In this study, tetrahedron-based Pb2+-sensitive DNAzyme sensor (TPS) is constructed by taking advantages of a classic Pb2+-dependent GR-5 DNAzyme and DNA tetrahedral structure, where the cleavage substrate and DNAzyme are modified with fluorophore FAM and quencher BHQ-1, respectively. DNA tetrahedron is arranged at the terminus of substrate/DNAzyme duplex to offer the protective shield against the nuclease attack. In the absence of Pb2+, FAM and BHQ-1 are kept close and FAM fluorescence is efficiently quenched. However, in the presence of Pb2+ cofactor, the DNAzyme exhibits the catalytic activity and cleaves the substrate strands, spatially separating the FAM away from BHQ-1 and releasing fluorescence. Utilizing the sensing probe, the Pb2+ can be quantitatively detected down to 1 nM without the interference from nontarget metal ions. Even if incubating in the human serum solution for 12 h, no substantial nuclease degradation is detected. In different complex biological milieu, the TPS can preserve the 85% of fluorescence signal, indicating that the developed TPS is a promising tool for the future application in the in vivo detection of Pb2+.The tailor-prepare solid phase microextraction (SPME) coatings with stable and excellent properties to effectively extract analytes from sample matrix still remains a challenge. Herein, a nitrogen doped graphitic carbon networks (NG-CNTW) coated fiber was fabricated by direct carbonization of nanosized ZIF-67 crystals (nano-ZIF-67) that grown on stainless steel wire. The NG-CNTW coated fiber coupled with gas chromatography-tandem mass spectrometry (GC-MS/MS) was applied for enrichment and determination of pyrethroids. The NG-CNTW coating exhibited high surface area and hierarchical porous structures that facilitate diffusion and accessibility of target molecules. Simultaneously, the nitrogen doped and highly graphitic structures endow the coating with high adsorption affinity for aromatic compounds. Under optimum conditions, the SPME-GC-MS/MS method presented wide range of linearity performance (0.08-200.0 ng g-1), low limits of detection (0.02-0.5 ng g-1) and good repeatability (RSD less then 9.6%) for 8 kinds of pyrethroids. Furthermore, the proposed method was successfully applied in the determination of pyrethroids in grape and cauliflower samples, as the results were in the range of 3.16-15.06 ng g-1and 2.08-9.29 ng g-1, respectively.  https://www.selleckchem.com/products/gsk8612.html  This work not only provides a new method by fabricating carbon nanomaterial coatings in situ derived from MOFs, but also shows great potential of MOFs derivative materials in environmental analysis field.The relative humidity (RH) determination is crucial in many fields. Based on the phosphorescent properties of room-temperature phosphorescent (RTP) carbon dots, the RTP carbon dots as a probe are expected to be used to rapidly detect relative humidity. In this study, matrix-free room-temperature phosphorescent N-doped carbon dots (N-CDs) were successfully prepared from urea, succinic acid, and acrylamide using a hydrothermal method. The as-synthesized N-CDs had good biocompatibility and water solubility. The N-CDs emitted blue fluorescence and green phosphorescence. Moreover, the N-CD powder exhibited stable phosphorescence with a phosphorescence lifetime of 158 ms (afterglow time to the naked eye for ~7 s). Because H2O molecules affected the afterglow time, the as-prepared N-CD test paper for the first time could be applied as a probe to monitor RH, the afterglow time of the N-CD test paper is linearly related to the RH (y = -0.0729x+7.042, R2 = 0.998) and the RH detection range is 0%-85%. And the results were consistent with those obtained using a hygrometer.