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In addition, a supervised classification model which based on MS spectra, was used to classify seven typical hypoglycemic polysaccharides with excellent sensitivity, specificity and accuracy, indicating the good classification performance of the RF model constructed. Thus, the proposed mass spectroscopic method provides a cost effective, accurate and high throughput tool for identification and classification of polysaccharides, which is beneficial for studying the biological activity of polysaccharides.Metal-organic frameworks (MOFs) are a novel class of porous nanomaterials composed of metals and organic linkers that have been used in many fields. A novel stereoselective stationary phase for capillary electrochromatography (CEC) has been developed in this work by employing a biodegradable, easier-to-prepare and green homochiral MOFs (Cu-SD), which composed of octakis-[6-deoxy-6-(3-mercaptopropanoic sodium)]-γ-cyclodextrin (SD, sugammadex) and transition metal ion (Cu2+) supported by polydopamine as linker. The modified capillary was characterized by scanning electron microscopy (SEM), X-ray spectrometry (XRD), energy dispersive (EDS) and Fourier transform infrared spectroscopy (FT-IR). The Cu-SD modified capillary column exhibited outstanding chiral recognition separation for five Dns-DL-amino acids (the DL-forms of phenylalanine, leucine, valine, threonine, serine). In addition, the modified column showed excellent stability and reproducibility. The relative standard deviations (RSDs) of the retention time for intra-day (n = 5) and inter-day (n = 3) and between columns (n = 3) enantioseparations were less than 0.27, 1.45 and 4.88%, respectively. Conceivably, this new-type of γ-CD-MOF represents a useful chiral stationary phase in electrochromatographic separations, and it has great potential in chiral separation field.A new fluorescence aptasensor for Ochratoxin A (OTA) analysis in corn and barley flour was developed owing to the favourable quenching function of cobalt oxyhydroxide (CoOOH) nanosheets. The first combination of graphitic carbon nitride quantum dots (g-CNQDs) and CoOOH nanosheets as efficient energy donor-acceptor pair was reported, and the quenching mechanism was proved by investigating the fluorescence lifetime of g-CNQDs. The aptamer-modified g-CNQDs (g-CNQDs-apt) were adsorbed onto CoOOH nanosheets surface by van der Waals force. Consequently, the Förster resonance energy transfer (FRET) from g-CNQDs-apt to CoOOH nanosheets was initiated, leading to quenched fluorescence. With the addition of OTA, the linear aptamer specifically bound with OTA to form G-quadruplex, which had relatively weak interaction with the CoOOH nanosheets and separated from the nanosheets surface. Thus, the FRET process between g-CNQDs-apt and CoOOH nanosheets was hindered, leading to the fluorescence of g-CNQDs-apt recovered clearly. The developed aptasensor exhibited acceptable detection limit with 0.5 nM and desirable linear relationship from 1 nM to 140 nM. Meanwhile, the aptasensor possessed multiple advantages, including easy operation, rapid detection and high selectivity. Moreover, the aptamer sensing platform was favorably applied for OTA determination in cereal (barley and corn flour), in which the recoveries varied from 94.5% to 101% with the relative standard deviation under 2.24%.Due to the significant role of formamidopyrimidine DNA glycosylase (Fpg) in physiological processes and DNA oxidative damage-related diseases, it is essential to establish sensitive methods for monitoring the Fpg activity in vitro and in vivo so as to illustrate its concrete role in these events. In this work, a sensitive, simple and reliable fluorescence assay was developed by taking the advantages of DNAzyme assisted cascade signal amplification and ultra-high fluorescence quenching efficiency of reduced graphene oxide (rGO). This detection system consisted of DNAzyme, rGO and fluorescence probe allows the activity of Fpg to be detected in a linear range from 0 to 80 U/mL with a detection limit of 0.66 U/mL. With the help of this method, 11 natural compounds were screened, and 7 compounds were identified as activators of Fpg. More importantly, the developed assay was used to monitor the activity of Fpg through fluorescence imaging in living Escherichia coli for the first time. The imaging results visually demonstrated the dynamic activation effect of natural compound Ginsenoside Re on the Fpg of Escherichia coli. In summary, these results indicated that this DNAzyme and rGO based fluorescence assay provides a potent strategy for Fpg quantitative assay in vitro and real-time monitoring in living bacteria, which holds great potential for applying on biological study and Fpg-targeted drug screening.Trinitrotoluene (TNT) is a primary component in chemical explosives, making them a common focus in public safety detection. [https://www.selleckchem.com/products/harmine.html this website] However, it is very difficult to achieve selective and sensitive detection of the TNT molecule in practical application. In the present study, a simple surface enhanced Raman scattering (SERS) sensing based on monoethanolamine (MEA) - modified gold nanoparticles (Au NPs) was expanded for high selectivity and sensitive detecting of TNT in an envelope, luggage, lake water, and clothing through a quickly sampling and detection process. The monoethanolamine molecule based on Meisenheimer complex lights up ultra-high Raman scattering of a nonresonant molecule on the superficial coat of gold nanoparticles. Using this detection sensor, a molecular bridge can be established to selectively detect trinitrotoluene with a detection limit of 21.47 pM. We were able to rapidly identification trinitrotoluene molecule with a powerful selective over the familiar interfering substances nitrophenol, picric acid, 2,4-dinitrophenol, and 2,4-dinitrotoluene. The outcome in this work supply an efficient solution to the test of trinitrotoluene and to establishing a SERS sensor analytical strategy. The studies have demonstrated that the MEA-Au NPs based SERS sensing can be potentially used in field detection the trace amount of chemical explosives for public security.