对映体不完全高效液相色谱的定量分析。D-苯丙氨酸和l -苯丙氨酸的偏振检测符合高斯函数。

Enantiomer Pub Date : 2002-01-01 DOI:10.1080/10242430210703
T. J. Edkins, P. C. Meier, R. Shah, D. R. Bobbitt, H. Saranadasa, Romeo D Lodevico
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引用次数: 6

摘要

本报告比较了用高效液相色谱法定量不完全分辨对映体的激光偏振和紫外数据。使用L-和D-苯丙氨酸作为工作模型,响应数据显示在整个检测区域,同时强调在0.4和1.4之间分辨率为100% L, 100% D和50:50 L:D或接近的区域。一般来说,分辨率越差,与紫外检测相比,偏振计的可检测性改进越大。这是由于极化信号固有的双极性性质,这为对映体对的整合创造了一个定义良好的交叉点。在我们之前的工作中,我们描述了将双极高斯峰模型应用于原始色谱峰数据时测量精度的提高。本研究将测量模型对提高准确性的影响。这项研究应该适用于其他对映体产生双极性信号的chiroptic检测策略,如圆二色性和圆偏振发光。
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Quantitative analysis of incomplete HPLC resolution of enantiomers. Fit of polarimetric detection for D- and L-phenylalanine to a gaussian function.
This report compares laser-based polarimetric and UV data for quantitating incompletely resolved enantiomers by HPLC. Using L- and D-phenylalanine as a working model, response data is shown across the entire detection region while emphasizing the regions at or near 100% L, 100% D and 50:50 L:D at resolutions between 0.4 and 1.4. In general, the poorer the resolution, the greater the improvement in detectability with the polarimeter when compared to UV detection. This is due to the inherent bipolar nature of the polarimetric signal, which creates a well-defined crossing point for integration of an enantiomeric pair. In our previous work, we described the improvement in measurement precision when applying a bipolar gaussian peak model to the raw chromatographic peak data. This study will measure the model's effect on improving accuracy. This study should be applicable to other chiroptical detection strategies that produce a bipolar signal for enantiomers, such as circular dichroism and circularly polarized luminescence.
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