分子印迹固相萃取-差分脉冲洗脱法测定烟草中的尼古丁

W. Mullett, E. Lai, B. Sellergren
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引用次数: 70

摘要

建立了分子印迹固相萃取-差分脉冲洗脱(MISPE-DPE)测定烟草中尼古丁的方法。以乙腈为流动相时,尼古丁和微量生物碱肌胺能够与分子印迹聚合物(MIP)结合。然而,超过95%的结合肌氨酸可以被20µl的甲醇脉冲解吸和冲走,而只有43%的结合尼古丁。用1%三氟乙酸水溶液20µl脉冲解吸剩余的结合尼古丁,在254 nm处进行直接紫外检测。MISPE-DPE方法对尼古丁具有固有的选择性,与液相色谱方法相比,分析时间更短(3 min),分析成本更低。检测限为1.8µg ml-1,线性动态范围达1000µg ml-1。预浓缩845µl 10 ng ml-1尼古丁标准溶液产生可检测的峰值信号。这些优点的分析数字优于先前报道的几种基于尼古丁- mip的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of nicotine in tobacco by molecularly imprinted solid phase extraction with differential pulsed elution
A molecularly imprinted solid phase extraction-differential pulsed elution (MISPE-DPE) method has been developed for the determination of nicotine in tobacco. Nicotine and a trace alkaloid myosmine were able to bind to the molecularly imprinted polymer (MIP) packed in a micro-column when acetonitrile was used as the mobile phase. However, over 95% of the bound myosmine could be desorbed and washed away by a 20 µl pulse of methanol, compared to only 43% of the bound nicotine. The remaining quantity of bound nicotine was desorbed by a 20 µl pulse of 1% trifluoroacetic acid in water, for direct UV detection at 254 nm. This MISPE-DPE method provided inherent selectivity for nicotine that allowed both a shorter analysis time (3 min) and a lower analysis cost than liquid chromatographic methods. A detection limit of 1.8 µg ml–1 and a linear dynamic range up to 1000 µg ml–1 were obtained. Preconcentration of 845 µl of a 10 ng ml–1 nicotine standard solution produced a detectable peak signal. These analytical figures of merit are superior to those reported previously for several nicotine–MIP-based methods.
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