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首页> 外文期刊>Journal of liquid chromatography and related technologies >Optimization of gradient elution in UPLC: A core study on the separation of homoserine Lactones produced by Bukholderia ubonensis and structure confirmation with ultra high resolution mass Spectrometry
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Optimization of gradient elution in UPLC: A core study on the separation of homoserine Lactones produced by Bukholderia ubonensis and structure confirmation with ultra high resolution mass Spectrometry

机译:UPLC中梯度洗脱的优化:乌氏白假单胞菌产生的高丝氨酸内酯的分离和超高分辨率质谱法结构确认的核心研究

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摘要

Speed of analysis is a key factor in liquid chromatography. One possible way is to decrease the particle size and thus increase the pressure (ultra high pressure liquid chromatography, UHPLC). For the separation of a complex mixture, the application of gradient elution techniques is expedient. From a practical point of view, it has to be questioned how the high pressure influences the separation parameters at gradient mode. In our study we investigated the following chromatographic parameters: peak width versus temperature, peak width versus gradient time, retention time versus temperature, and retention factor versus flow rate. It was shown that even in sample volume overload conditions the gradient system worked in a reproducible way; the maximum possible sample volume (20 mu L) was injected to get the lowest possible limit of detection. Increasing the flow rate, the peak width increased only moderately, and the same was found when the temperature was decreased. However, at 60 degrees C the signal to noise ratio decreased in a small compass showing the thermal disequilibrium between the column outlet and the detector cell, which might have caused extra noise. Finally, a practical separation was presented in which the UHPLC can be applied for the determination of N-acylhomoserine lantones (AHLs), which have a relatively low UV absorption at low wavelength. The detection limit was low enough for practical applications because of the low dispersion due to a small diameter stationary phase and the low dead volume in the column. The UPLC method was applied as a first screening for AHLs and the results were confirmed by fourier transformation ion cyclotron resonance mass spectrometry (FTICR-MS), which has a high selectivity.
机译:分析速度是液相色谱分析的关键因素。一种可能的方法是减小粒径,从而增加压力(超高压液相色谱,UHPLC)。为了分离复杂的混合物,梯度洗脱技术的应用是有利的。从实践的角度来看,必须质疑高压如何影响梯度模式下的分离参数。在我们的研究中,我们研究了以下色谱参数:峰宽与温度,峰宽与梯度时间,保留时间与温度以及保留因子与流速之间的关系。结果表明,即使在样品体积过载的情况下,梯度系统也可以以可重现的方式工作。进样最大可能的样品量(20μL)以获得最低的检测限。流速增加时,峰宽仅适度增加,而温度降低时也是如此。但是,在60摄氏度时,信噪比在一个小的罗盘中降低,显示出色谱柱出口和检测器池之间的热不平衡,这可能会引起额外的噪声。最后,提出了一种实用的分离方法,其中UHPLC可用于测定在低波长下具有相对较低的紫外线吸收率的N-酰基高丝氨酸lantones(AHLs)。检测限对于实际应用而言足够低,这是由于小直径固定相的分散性低和色谱柱中的死体积小。 UPLC方法首次用于AHL的筛选,并通过具有高选择性的傅里叶变换离子回旋共振质谱(FTICR-MS)证实了结果。

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