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Measure Your Gradient: A New Way to Measure Gradients in High Performance Liquid Chromatography by Mass Spectrometric or Absorbance Detection

机译:测量您的梯度:一种通过质谱或吸光度检测来测量高效液相色谱中梯度的新方法

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摘要

The gradient produced by an HPLC is never the same as the one it is programmed to produce, but non-idealities in the gradient can be taken into account if they are measured. Such measurements are routine, yet only one general approach has been described to make them: both HPLC solvents are replaced with water, solvent B is spiked with 0.1% acetone, and the gradient is measured by UV absorbance. Despite the widespread use of this procedure, we found a number of problems and complications with it, mostly stemming from the fact that it measures the gradient under abnormal conditions (e.g. both solvents are water). It is also generally not amenable to MS detection, leaving those with only an MS detector no way to accurately measure their gradients. We describe a new approach called “Measure Your Gradient” that potentially solves these problems. One runs a test mixture containing 20 standards on a standard stationary phase and enters their gradient retention times into open-source software available at . The software uses the retention times to back-calculate the gradient that was truly produced by the HPLC. Here we present a preliminary investigation of the new approach. We found that gradients measured this way are comparable to those measured by a more accurate, albeit impractical, version of the conventional approach. The new procedure worked with different gradients, flow rates, column lengths, inner diameters, on two different HPLCs, and with six different batches of the standard stationary phase.
机译:HPLC产生的梯度永远不会与编程产生的梯度相同,但是如果测量了梯度,则可以考虑梯度中的非理想性。此类测量是常规方法,但仅描述了一种通用方法:将两种HPLC溶剂都用水代替,将B溶剂掺入0.1%丙酮,并通过UV吸光度测量梯度。尽管已广泛使用此程序,但我们发现它存在许多问题和复杂性,主要是由于它在异常条件下(例如两种溶剂均为水)测量梯度的事实。通常也不适用于MS检测,仅那些MS检测器无法准确测量其梯度。我们介绍了一种称为“测量您的渐变”的新方法,该方法可以解决这些问题。一种是在标准固定相上运行包含20种标准物的测试混合物,然后将其梯度保留时间输入可在处获得的开源软件。该软件使用保留时间来反算HPLC真正产生的梯度。在这里,我们对新方法进行了初步调查。我们发现,用这种方法测得的梯度可与用常规方法的更精确(尽管不切实际)的版本测得的梯度相当。新方法在两种不同的HPLC上以六种不同批次的标准固定相在不同的梯度,流速,柱长,内径上工作。

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