Junran Mao , Hongyan Ma , Jinsong Zhou , Lin Chen , Xinxin Chen , Jincai Wang , Zhengjin Jiang , Tingting Zhang
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引用次数: 0
Abstract
An efficient and rapid supercritical fluid chromatography (SFC) method was established for the analysis of flavonoids in Citri Reticulatae Pericarpium (CRP), the best conditions were obtained by optimizing the parameters of the SFC method. The peak area obtained by SFC analysis of CRP samples, combined with chemical pattern recognition, was used to establish a model to evaluate the quality of Guang Chenpi (GCP) and Chenpi (CP) in CRP. Partial least squares discriminant analysis (PLS-DA) proved to be an excellent method that can accurately distinguish GCP from CP. The PLS-DA model was established by selecting the training set, and the characteristic components (Didymin and Hesperidin) were screened out to further establish the model, and the testing sets were brought into the model for verification, indicating that the model established based on the peak areas is reliable, and two quality markers (Narirutin and Neohesperidin) were found to distinguish between Xinhui and Non-Xinhui in GCP based on the content determination. In conclusion, the combination of SFC and chemical pattern recognition for the quality evaluation of CRP has great potential.
期刊介绍:
This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome.
Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.