Fluoroquinolones (FQs) have emerged as one of the most important class of antibiotics. Due to their low concentration in bio-matrix samples which contain a lot of interfering substances, the efficient solid phase extraction and accurate determination of FQs remain a challenge. In this paper, a new strategy for the isolation and enrichment of FQs from egg samples was obtained by molecularly imprinted polymers on the surface of magnetic carbon nanotubes (MCNTs@MIP), which not only can be collected and separated rapidly by an external magnetic field, but also have a high specific surface area, outstanding mechanical properties and specific recognition for FQs. MCNTs@MIP were prepared using ofloxacin as a pseudo template, methacrylic acid as a functional monomer, and ethylene glycol dimethacrylate as a cross-linker. The characteristics of the MCNTs@MIP were assessed by transmission electron microscopy (TEM), multipoint Brunauer-Emmett-Teller (BET) analysis, vibrating sample magnetometry (VSM), X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) spectroscopy. The results of the adsorption experiments not only demonstrated rapid dynamic adsorption but also showed a high selectivity toward FQs. An extraction method using MCNTs@MIP coupled with high performance liquid chromatography (HPLC) was developed for the determination of four FQs in egg samples. The recovery of four FQs ranged from 95.2% ± 3.2% to 100.7% ± 3.1% and the detection limits ranged from 0.25-0.40 ng g(-1). The results demonstrate that the proposed method based on pseudo template MCNTs@MIP is a promising approach for the preconcentration, purification, and simultaneous analysis of four FQs in bio-matrix samples.
The ashy-throated parrotbill ( Paradoxornis alphonsianus) is a sexually monomorphic species with high abundance in Southwest China, which has been widely used as a fighting bird across Guizhou Province, leading it to become one of the most coveted and heavily hunted wild birds in the region at present. Information on the sexes is a fundamental requirement for a wide variety of avian studies. From a conservation perspective, knowledge necessary for quick sexing of this species should be important, as the determination of sex contributes to the understanding of which sexes are used for fighting. Our goal was to develop a quick method that can be used to identify sex of the ashy-throated parrotbill in the field. Seven body traits were measured and compared between the sexes among 124 individual ashy-throated parrotbills, with sex determined by molecular techniques. Data revealed that the male is the larger sex, with significantly greater measurements than the female in bill length, wing length, and middle claw length. The univariate discriminant function based on bill length featured the highest identification accuracy (67.7%). The larger body size of males may have evolved by sexual selection, but additional data are needed to test this hypothesis. This study found that male and female ashy-throated parrotbills are divergent in size, although further efforts are required for a discriminant function with more robust accuracy.
Jatrorrhizine was considered as one of the active constituents of Coptis chinensis Franch. Herein, jatrorrhizine derivatives with substituted amino groups linked at the 3-position were designed, synthesized, and biologically evaluated as inhibitors of acetylcholinesterase. Jatrorrhizine derivatives inhibited the activity of acetylcholinesterase (AChE) to a greater extent than the lead compound jatrorrhizine. All these jatrorrhizine derivatives were proved to be potent inhibitors of acetylcholinesterase (AChE) with submicromolar IC 50 values, but less sensitive to butyrylcholinesterase (BuChE), which suggests that these jatrorrhizine derivatives are selective for AChE/BuChE. Compound g gave the most potent inhibitor activity for AChE (IC 50 = 0.301 M), which is greater than the lead compound jatrorrhizine. All these results demonstrated that these jatrorrhizine derivatives are potential inhibitors for AChE.
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