首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development of magnetic molecularly imprinted polymers with double templates for the rapid and selective determination of amphenicol antibiotics in water, blood, and egg samples
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Development of magnetic molecularly imprinted polymers with double templates for the rapid and selective determination of amphenicol antibiotics in water, blood, and egg samples

机译:具有双模板的磁性分子印迹聚合物的开发,用于快速,选择性地测定水,血液和卵样品中的苯酚类抗生素

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A magnetic mesoporous dual-template molecularly imprinted polymer (Fe3O4@mSiO(2) @DMIP) with a specific recognition capability for chloramphenicol (CAP) and florfenicol (FF) was synthesised. CAP and FF were used as dual-template molecules, alpha-methacrylic acid and Fe3O4@mSiO(2)@-CH=CH2 as dual functional monomers, and ethylene glycol dimethyl methacrylate as a crosslinking agent. For comparison, a magnetic mesoporous non-molecularly imprinted polymer (Fe3O4@mSiO(2)@NIP) was also prepared using the same synthesis procedure, but without the dual templates. The prepared polymers were characterised using scanning electron microscopy, Fourier-transform infrared spectroscopy and adsorption experiments. Results indicated that both the Fe3O4@mSiO(2)@DMIP and the Fe3O4@mSiO(2) @NIP were microspherical nanoparticles, and the surface of the Fe3O4@mSiO(2)@DMIP was rougher than that of the Fe3O4@mSiO(2)@NIP. In addition, the prepared Fe3O4@mSiO(2)@DMIP possessed a higher adsorption capacity and better selectivity for CAP and FF than the Fe3O4@mSiO(2)@NIP. The maximum static adsorption capacities of the Fe3O4@mSiO(2)@ DMIP for CAP and FF were 146.5 and 190.1 mg g(-1), respectively, whereas those of the Fe3O4@mSiO(2) @NIP were 50.0 and 44.0 mg g(-1), respectively. The obtained Fe3O4@mSiO(2)@DMIP particles were applied as a magnetic solid-phase extraction sorbent for the rapid and selective extraction of CAP, FF, and thiamphenicol (TAP) in water, chicken blood and egg samples. The method of magnetic molecularly imprinted solid -phase extraction (M-MISPE) coupled to high-performance liquid chromatography with UV detection (HPLC-UV) was conducted to detect CAP, FF, and TAP. The limits of detection for CAP, FF, and TAP were 0.16, 0.08, and 0.08 mu g kg(-1), respectively. The average recovery and precision values for the spiked water, chicken blood, and egg samples ranged from 88.3% to 99.1% and 2.7% to 7.9%, respectively. Given its rapidity, selectivity, and sensitivity, the developed method of M-MISPE coupled to HPLC-UV detection has good application prospects in environmental, biological, and food samples. (C) 2016 Elsevier B.V. All rights reserved.
机译:磁性介孔双模板分子印迹聚合物(Fe3O4 @ mSiO(2)@DMIP)具有氯霉素(CAP)和氟苯尼考(FF)的特定识别能力。 CAP和FF被用作双模板分子,α-甲基丙烯酸和Fe3O4 @ mSiO(2)@-CH = CH2被用作双功能单体,乙二醇二甲基丙烯酸甲酯被用作交联剂。为了进行比较,还使用相同的合成方法制备了磁性介孔非分子印迹聚合物(Fe3O4 @ mSiO(2)@NIP),但没有双模板。使用扫描电子显微镜,傅立叶变换红外光谱和吸附实验对制备的聚合物进行表征。结果表明,Fe3O4 @ mSiO(2)@DMIP和Fe3O4 @ mSiO(2)@NIP均为微球形纳米粒子,Fe3O4 @ mSiO(2)@DMIP的表面比Fe3O4 @ mSiO( 2)@NIP。此外,与Fe3O4 @ mSiO(2)@NIP相比,制备的Fe3O4 @ mSiO(2)@DMIP具有更高的吸附能力和对CAP和FF的更好选择性。 Fe3O4 @ mSiO(2)@ DMIP对CAP和FF的最大静态吸附容量分别为146.5和190.1 mg g(-1),而Fe3O4 @ mSiO(2)@NIP的最大静态吸附容量分别为50.0和44.0 mg g (-1)。将获得的Fe3O4 @ mSiO(2)@DMIP颗粒用作磁性固相萃取吸附剂,用于快速,选择性地萃取水,鸡血和蛋样品中的CAP,FF和甲砜霉素(TAP)。进行了磁性分子印迹固相萃取(M-MISPE)结合高效液相色谱和紫外检测(HPLC-UV)的方法,以检测CAP,FF和TAP。 CAP,FF和TAP的检出限分别为0.16、0.08和0.08μg kg(-1)。加标水,鸡血和鸡蛋样品的平均回收率和精密度值分别为88.3%至99.1%和2.7%至7.9%。鉴于其快速,选择性和灵敏性,M-MISPE结合HPLC-UV检测的开发方法在环境,生物和食品样品中具有良好的应用前景。 (C)2016 Elsevier B.V.保留所有权利。

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