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A molecularly imprinted polymer for microdisc solid-phase extraction of parabens from human milk samples

机译:用于从人乳样品中微盘固相萃取对羟基苯甲酸酯的分子印迹聚合物

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摘要

A new molecularly imprinted sol-gel polymer (MIP) was developed for microdisc solid phase extraction of parabens from human milk samples, followed by liquid chromatography analysis with a photometric detector (MISPE/LC-UV). The molecularly imprinted ormosil was synthesized by the sol-gel method using benzylparaben as a template. After template removal, selective cavities (benzylparaben) were revealed for parabens' extraction. The process of molecular recognition was based on the intermolecular interactions (hydrogen bonds) between the parabens and functional groups present in the MIP selective cavities. Fourier Transform-Infrared Spectroscopy (FTIR) spectra of the MIP and non-imprinted polymer (NIP) displayed feature bands of the 3-aminopropyltrimethoxysilane (APTMS) bonds. The use of Magic Angle Spinning-Nuclear Magnetic Resonance (MAS-NMR) attested to the presence of covalent Si-O-Si-R bonds in the structure of MIPs and NIPs. The effects of the microdisc SPE variables (pH of the sample, washing step, nature and volume of the elution solvent) on MISPE performance were evaluated. The linear range of the MISPE/LC-UV method ranges from the LOQ values (10-20 ng mL~(-1)) to 150 ng mL~(-1) with a correlation coefficient higher than 0.992. The interday precision of the MISPE/LC-UV method presented a coefficient of variation lower than 13%; the accuracy ranged from 86 to 117%. According to the evaluated analytical validation parameters, the MISPE/LC-UV method is suitable for the analysis of parabens in human milk samples. Analysis of the milk samples from lactating women demonstrated the effectiveness of the proposed method.
机译:开发了一种新的分子印迹溶胶-凝胶聚合物(MIP),用于从人乳样品中微盘固相萃取对羟基苯甲酸酯,然后使用光度检测器(MISPE / LC-UV)进行液相色谱分析。以对羟基苯甲酸苄酯为模板,通过溶胶-凝胶法合成了分子印迹的ormosil。去除模板后,发现选择性腔(对羟基苯甲酸苄酯)用于对羟基苯甲酸酯的提取。分子识别的过程基于对羟基苯甲酸酯与MIP选择性腔体中存在的官能团之间的分子间相互作用(氢键)。 MIP和非压印聚合物(NIP)的傅立叶变换红外光谱(FTIR)光谱显示了3-氨丙基三甲氧基硅烷(APTMS)键的特征带。魔角自旋核磁共振(MAS-NMR)的使用证明了在MIP和NIP的结构中存在共价Si-O-Si-R键。评估了微盘SPE变量(样品的pH,洗涤步骤,洗脱溶剂的性质和体积)对MISPE性能的影响。 MISPE / LC-UV方法的线性范围从LOQ值(10-20 ng mL〜(-1))到150 ng mL〜(-1),相关系数高于0.992。 MISPE / LC-UV方法的日间精确度显示变异系数低于13%;准确性从86到117%不等。根据评估的分析验证参数,MISPE / LC-UV方法适用于分析母乳样品中的对羟基苯甲酸酯。对来自哺乳期妇女的牛奶样品的分析证明了该方法的有效性。

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