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基于净分析物信号和秩消去因子分析的两种新的多元标准加入法同时分光光度测定药物制剂中的扑热息痛和对氨基苯酚。

Simultaneous spectrophotometric determination of paracetamol and para-aminophenol in pharmaceutical dosage forms using two novel multivariate standard addition methods based on net analyte signal and rank annihilation factor analysis.

机构信息

Department of Chemistry, Shiraz University, Shiraz, Iran.

出版信息

Drug Test Anal. 2012 Jun;4(6):507-14. doi: 10.1002/dta.271. Epub 2011 Mar 9.

Abstract

Recently we proposed two multivariate standard addition methods using net analyte signal concept and rank annihilation factor analysis, which we named SANAS and SARAF, respectively. These methods could model both indirect sample matrix effects and direct interference effects of the coexisting analytes. Here, the potential of these methods for simultaneous determination of paracetamol and para-aminophenol in the synthetic mixtures and pharmaceutical products was examined. It was found that both models could predict the concentration of analytes in synthetic mixtures with relative errors of prediction lower than 7%. Moreover, the employed methods exhibited the recoveries in the range of 93.11 and 108.67 for analysis of the drugs in the real matrices. From SANAS plots, the figures of merit including sensitivity, selectivity and limit of detection were calculated as 0.143 µg/ml, 0.587 and 0.018 µg/ml for paracetamol and 0.128 µg/ml, 0.547 and 0.020 µg/ml for para-aminophenol, respectively.

摘要

最近,我们提出了两种使用净分析物信号概念和秩消去因子分析的多变量标准加入方法,分别命名为 SANAS 和 SARAF。这两种方法可以同时建模间接样品基质效应和共存分析物的直接干扰效应。在此,研究了这些方法在合成混合物和药物产品中同时测定对乙酰氨基酚和对氨基酚的潜力。结果发现,两种模型都可以用预测相对误差低于 7%的方法预测合成混合物中分析物的浓度。此外,所采用的方法在真实基质中分析药物时,回收率在 93.11%和 108.67%之间。从 SANAS 图中,计算了包括灵敏度、选择性和检测限在内的评价指标,分别为 0.143µg/ml、0.587 和 0.018µg/ml 对乙酰氨基酚和 0.128µg/ml、0.547 和 0.020µg/ml 对氨基酚。

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