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Correction of retention time shifts for chromatographic fingerprints of herbal medicines

机译:校正草药色谱指纹图谱的保留时间偏移

摘要

In this study, the combination of chemometric resolution and cubic spline data interpolation was investigated as a method to correct the retention time shifts for chromatographic fingerprints of herbal medicines obtained by high-performance liquid chromatography-diode array detection (HPLC-DAD). With the help of the resolution approaches in chemometrics, it was easy to identify the purity of chromatographic peak clusters and then resolve the two-dimensional response matrix into chromatograms and spectra of pure chemical components so as to select multiple mark compounds involved in chromatographic fingerprints. With these mark components determined, the retention time shifts of chromatographic fingerprints might be then corrected effectively. After this correction, the cubic spline interpolation technique was then used to reconstruct new chromatographic fingerprints. The results in this work showed that, the purity identification of the chromatographic peak clusters together with the resolution of overlapping peaks into pure chromatograms and spectra by means of chemometric approaches could provide the sufficient chromatographic and spectral information for selecting multiple mark compounds to correct the retention time shifts. The cubic spline data interpolation technique was user-friendly to the reconstruction of new chromatographic fingerprints with correction. The successful application to the simulated and real chromatographic fingerprints of two Cortex cinnamomi, fifty Rhizoma chuanxiong, ten Radix angelicae and seventeen Herba menthae samples from different sources demonstrated the reliability and applicability of the approach investigated in this work. Pattern recognition based on principal component analysis for identifying inhomogenity in chromatographic fingerprints from real herbal medicines could further interpret it.
机译:在这项研究中,化学计量学分辨率和三次样条数据插值的组合被研究作为一种方法来校正通过高效液相色谱-二极管阵列检测(HPLC-DAD)获得的草药色谱指纹图谱的保留时间偏移。借助化学计量学中的拆分方法,可以轻松地鉴定色谱峰簇的纯度,然后将二维响应矩阵解析为色谱图和纯化学成分的光谱,从而选择涉及色谱指纹图谱的多种标记化合物。确定这些标记成分后,可以有效地校正色谱指纹的保留时间偏移。进行此校正后,然后使用三次样条插值技术重建新的色谱指纹图谱。这项工作的结果表明,通过化学计量学方法对色谱峰簇的纯度鉴定以及将重叠峰拆分为纯色谱图和光谱的方法,可以为选择多种标记化合物以纠正保留问题提供足够的色谱和光谱信息。时移。三次样条数据插值技术对校正新色谱指纹图谱的用户友好。成功地将来自不同来源的两个皮层肉桂,五十个川ten,十个当归和十七个薄荷脑样品应用于模拟和真实色谱指纹图谱,证明了该方法的可靠性和适用性。基于主成分分析的模式识别可以识别真实草药的色谱指纹图谱中的不均匀性。

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