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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Short columns with molecularly imprinted monolithic stationary phases for rapid separation of diastereomers and enantiomers
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Short columns with molecularly imprinted monolithic stationary phases for rapid separation of diastereomers and enantiomers

机译:具有分子印迹单片固定阶段的短柱,用于快速分离非对映异构体和对映体

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Three molecularly imprinted monolithic columns with different length but almost identical column volume had been prepared. It was observed that the separation factors of diastereomers and enantiomers were almost unaffected by column length. However, the short column with dimension of 38 mm×8 mm i.d. showed much lower resistance to flow rate so that it could be operated at much higher flow rates. By combining stepwise gradient elution with elevated flow rate, the diastereomers of cinchonine and cinchonidine and the enantiomers of Cbz-DL-Trp and Fmoc-DL-Trp were successfully separated within 3 min on the short column with dimension of 38 mm×8 mm i.d.. Based on the above results, a cinchonine imprinted monolithic disk with dimension of 10 mm×16 mm i.d. was further developed. The SEM image and the pore size distribution profile showed that large flow-through pores are present on the prepared monolith, which allowed mobile phase to flow through the disk with very low resistance. Chromatographic performances on the monolithic disk were almost unchanged compared with the long columns. A rapid separation of cinchonine and cinchonidine was achieved in 2.5 min at the flow rate of 9.0 ml/min. Furthermore, it was observed that there was almost no effect of the flow rate on the dynamic binding capacity at high flow rates. In addition, the effect of the loading concentration of analytes on the dynamic binding capacity, namely adsorption isotherm, was also investigated. A non-linear adsorption isotherm of cinchonine was observed on the molecularly imprinted monolith with cinchonine as template, which might be a main reason to result in the peak tailing of template molecule.
机译:已经制备了三种分子印迹的整体柱,但已经制备了不同但几乎相同的柱体积。观察到,非对映异构体和对映体的分离因子几乎不受柱长的影响。但是,短柱的尺寸为38mm×8mm i.d.显示出耐力耐力耐力较低,使其可以以更高的流速操作。通过将逐步梯度洗脱用升高的流速结合,Cinchonine和Cinchonidine的非对映异构体和CBZ-D1-TRP和FMOC-DL-TRP的对映体在短柱内在3分钟内成功分离,尺寸为38mm×8mm ID 。基于上述结果,Cinchonine压印整体圆盘,尺寸为10 mm×16mm id进一步发展。 SEM图像和孔径分布曲线显示,制备的整体上存在大的流通孔,其允许移动相流过具有非常低的电阻的圆盘。与长柱相比,整体盘上的色谱性能几乎不变。在2.5分钟的流速为9.0ml / min的2.5分钟内实现了快速分离。此外,观察到流速几乎没有对高流速的动态结合能力的影响。此外,还研究了分析物的负载浓度对动态结合能力,即吸附等温线的影响。在与Cinchonine作为模板的分子印记的整料上观察到肺炎的非线性吸附等温线,这可能是导致模板分子峰尾的主要原因。

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