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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Computational-aided design of magnetic ultra-thin dummy molecularly imprinted polymer for selective extraction and determination of morphine from urine by high-performance liquid chromatography
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Computational-aided design of magnetic ultra-thin dummy molecularly imprinted polymer for selective extraction and determination of morphine from urine by high-performance liquid chromatography

机译:磁性超薄虚拟分子印迹聚合物的计算辅助设计,用于高效液相色谱法从尿液中选择性提取和测定吗啡

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摘要

In this work, a novel magnetic ultra-thin dummy molecularly imprinted polymer (MMIP) for morphine (MO) was prepared. In order to obtain highly selective recognition cavities, the MMIP has been designed using semi-flexible docking to screen the optimal monomer and its ratio to morphine from six representative monomers. Furthermore, the dummy template was creatively screened by semi-flexible docking method from opioid drugs. The system of dihydrocodeine (DI) as dummy template, methacrylamide (MAC) as founctional monomer, ethyleneglycol dimethacrylate (EGDMA) as crosslinker was chosen for MO imprinting. The morphological and magnetic properties of MMIP were characterized by FT-IR, TEM and VSM. The results suggested that molecularly imprinted polymer (MIP) was synthesized evenly on Fe3O4 surface. The adsorption experiments revealed that MMIP showed better extraction capacity and selectivity toward MO and its analogues than the non-imprinted polymer (NIP). The MMIP possessed adsorption capacity of 14.71 mg/g for MO and the imprinting factor was 2.10 at separate adsorption and 1.87 at competitive adsorption. A magnetic molecularly imprinted solid phase extraction coupled with HPLC method (M-MISPE-HPLC) has been established for the analysis of MO in urine sample. The developed method was validated for its linearity (0.038-100 mg L-1 R-2 = 0.9937), precision (1.07%-3.72%) and accuracy (83.62%-100.37%). (C) 2016 Elsevier B.V. All rights reserved.
机译:在这项工作中,制备了一种新型的吗啡(MO)磁性超薄虚拟分子印迹聚合物(MMIP)。为了获得高度选择性的识别腔,已使用半柔性对接设计了MMIP,以从六个代表性单体中筛选出最佳单体及其与吗啡的比例。此外,通过半柔性对接方法从阿片类药物中创造性地筛选了假模板。 MO压印采用二氢可待因(DI)作为虚拟模板,甲基丙烯酰胺(MAC)作为功能单体,乙二醇二甲基丙烯酸酯(EGDMA)作为交联剂体系。通过FT-IR,TEM和VSM对MMIP的形貌和磁性进行了表征。结果表明,分子印迹聚合物(MIP)均匀地合成在Fe3O4表面。吸附实验表明,与非压印聚合物(NIP)相比,MMIP对MO及其类似物具有更好的提取能力和选择性。 MMIP对MO的吸附容量为14.71 mg / g,压印因子在单独吸附下为2.10,在竞争吸附下为1.87。建立了磁性分子印迹固相萃取结合HPLC方法(M-MISPE-HPLC)的方法,用于分析尿液样品中的MO。验证了所开发方法的线性(0.038-100 mg L-1 R-2 = 0.9937),精度(1.07%-3.72%)和准确性(83.62%-100.37%)。 (C)2016 Elsevier B.V.保留所有权利。

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