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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Preparation and evaluation of solid-phase microextraction fibers based on monolithic molecularly imprinted polymers for selective extraction of diacetylmorphine and analogous compounds
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Preparation and evaluation of solid-phase microextraction fibers based on monolithic molecularly imprinted polymers for selective extraction of diacetylmorphine and analogous compounds

机译:基于整体分子印迹聚合物选择性萃取二乙酰吗啡及类似化合物的固相微萃取纤维的制备与评价

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All of the studies on solid-phase microextraction based on molecularly imprinted polymers up to now have been carried out on the synthesis of the polymer on the surface of the fiber which is brittle and the polymer coating strips during handling. The objective of this study was to develop a method for fabrication of a monolithic and robust solid-phase microextraction fiber on the basis of molecularly imprinted polymer for selective extraction of diacetylmorphine and its structural analogues followed by their GC or GC/MS analysis. A fiber was produced by copolymerization of methacrylic acid-ethylene glycol dimethacrylate imprinted with diacetylmorphine. The effective factors influencing the polymerization have been investigated and are detailed here. Also, the influences of pH, extraction time and temperature on the extraction efficiency of analytes were investigated. The prepared fiber was thermally stable up to 300 degrees C which has vital importance in SPME coupled with GC or GC/MS. The adsorption isotherm modeling was performed by fitting the data of studied compounds to bi-Langmuir isotherm model. The evaluated equilibrium constants for diacetylmorphine were 0.011 and 1824.72 mu M-1, and the number of binding sites was 170.37 and 4.64 nmol g(-1), respectively. This fiber was successfully used for extraction of template molecule from aqueous solution and further analysis with GC or GC/MS. The high extraction efficiency was obtained for diacetylmorphine, 6-monoacetylcodeine, and 6-monoacetylmorphine, yielding the detection limits of 300, 47, and I ng mL(-1), respectively. (c) 2007 Elsevier B.V. All rights reserved.
机译:迄今为止,所有对基于分子印迹聚合物的固相微萃取的研究都是在脆性纤维表面上的聚合物合成以及在处理过程中聚合物涂层剥离的研究上进行的。这项研究的目的是在分子印迹聚合物的基础上,开发出一种整体而坚固的固相微萃取纤维的制备方法,以选择性地提取二乙酰吗啡及其结构类似物,然后对其进行GC或GC / MS分析。通过印迹有二乙酰基吗啡的甲基丙烯酸-乙二醇二甲基丙烯酸酯的共聚生产纤维。已经研究了影响聚合的有效因素,并在此进行了详细说明。此外,还研究了pH,萃取时间和温度对分析物萃取效率的影响。所制备的纤维在高达300摄氏度的温度下仍具有热稳定性,这对于结合GC或GC / MS的SPME至关重要。吸附等温线建模是通过将研究化合物的数据拟合到双朗缪尔等温线模型进行的。二乙酰吗啡的评估平衡常数分别为0.011和1824.72μM-1,结合位点数分别为170.37和4.64 nmol g(-1)。该纤维已成功用于从水溶液中提取模板分子,并通过GC或GC / MS进行进一步分析。对二乙酰吗啡,6-单乙酰基可待因和6-单乙酰吗啡有较高的提取效率,分别达到300、47和1 ng mL(-1)的检出限。 (c)2007 Elsevier B.V.保留所有权利。

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