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PARAFAC based methods for the analysis of Diltiazem drug excitation emission matrices of fluorescence obtained by a derivatization reaction

机译:基于PARAFAC的衍生化反应获得的地尔硫卓药物激发荧光发射矩阵的分析方法

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摘要

A fluorescent derivatization reaction for Diltiazem drug quantification based on the condensation reaction of citric or malonic acid with acetic anhydride, catalyzed by the tertiary amine group of Diltiazem, was developed. Excitation emission matrices (EEMs) of fluorescence of the pure solvent (ethanol), standard and sample solutions following a standard addition methodology were analysed by PARAFAC based methods (PARAFAC, PARAFAC2 and PARALIND) to obtain robust calibration methodologies. The quantification results of the sample were compared with the official US Pharmacopeia high performance liquid chromatography-ultraviolet method (USP HPLC-UV). Although the experimental sets of EEM show linearity deviations all the PARAFAC based methods allow correct robust estimation of Diltiazem concentration in pharmaceutical formulations. The closest results were: derivatization with citric acid and PARAFAC2 six components non-negativity constraint model with a detection limit of 0.088 ppm; and, derivatization with malonic acid and PARAFAC six components non-negativity constraint model with a detection limit of 0.066 ppm for the malonic acid was observed. The simultaneous utilization of the three PARAFAC methods gives further information about the intrinsic structure of the data sets under analysis, i.e., it works as an efficient diagnostic tool for the existence of non-linearity and colinearity.
机译:开发了一种基于地尔硫卓的叔胺基催化的柠檬酸或丙二酸与乙酸酐的缩合反应的地尔硫卓定量荧光衍生反应。采用基于PARAFAC的方法(PARAFAC,PARAFAC2和PARALIND)分析遵循标准添加方法的纯溶剂(乙醇),标准溶液和样品溶液的荧光激发发射矩阵(EEM),以获得可靠的校准方法。将样品的定量结果与官方的美国药典高效液相色谱-紫外线法(USP HPLC-UV)进行比较。尽管EEM的实验组显示出线性偏差,但所有基于PARAFAC的方法都可以正确可靠地估计药物制剂中地尔硫卓的浓度。最接近的结果是:用柠檬酸和PARAFAC2衍生六种非负性约束模型,检出限为0.088 ppm;并观察到丙二酸和PARAFAC衍生化的六组分非负性约束模型,其丙二酸的检出限为0.066 ppm。同时使用这三种PARAFAC方法可提供有关正在分析的数据集的内在结构的更多信息,即,它可作为存在非线性和共线性的有效诊断工具。

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