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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Artificial neural network assisted kinetic spectrophotometric technique for simultaneous determination of paracetamol and p-aminophenol in pharmaceutical samples using localized surface plasmon resonance band of silver nanoparticles
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Artificial neural network assisted kinetic spectrophotometric technique for simultaneous determination of paracetamol and p-aminophenol in pharmaceutical samples using localized surface plasmon resonance band of silver nanoparticles

机译:人工神经网络辅助动力学分光光度法同时测定银纳米颗粒的表面等离振子共振带同时测定药物样品中对乙酰氨基酚和对氨基苯酚

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摘要

Spectrophotometric analysis method based on the combination of the principal component analysis (PCA) with the feed-forward neural network (FFNN) and the radial basis function network (RBFN) was proposed for the simultaneous determination of paracetamol (PAC) and p-aminophenol (PAP). This technique relies on the difference between the kinetic rates of the reactions between analytes and silver nitrate as the oxidizing agent in the presence of polyvinylpyrrolidone (PVP) which is the stabilizer. The reactions are monitored at the analytical wavelength of 420 nm of the localized surface plasmon resonance (LSPR) band of the formed silver nanoparticles (Ag-NPs). Under the optimized conditions, the linear calibration graphs were obtained in the concentration range of 0.122-2.425 mu g mL(-1) for PAC and 0.021-5.245 mu g mL(-1) for PAP. The limit of detection in terms of standard approach (LODSA) and upper limit approach (LODULA,) were calculated to be 0.027 and 0.032 mu g mL(-1) for PAC and 0.006 and 0.009 mu g mL(-1) for PAP. The important parameters were optimized for the artificial neural network (ANN) models. Statistical parameters indicated that the ability of the both methods is comparable. The proposed method was successfully applied to the simultaneous determination of PAC and PAP in pharmaceutical preparations. (C) 2014 Elsevier B.V. All rights reserved.
机译:提出了一种将主成分分析(PCA)与前馈神经网络(FFNN)和径向基函数网络(RBFN)相结合的分光光度法同时测定对乙酰氨基酚(PAC)和对氨基苯酚( PAP)。该技术依赖于在作为稳定剂的聚乙烯吡咯烷酮(PVP)存在下,分析物与作为氧化剂的硝酸银之间的反应动力学速率之间的差异。在形成的银纳米颗粒(Ag-NPs)的局部表面等离振子共振(LSPR)带的分析波长420 nm处监控反应。在优化的条件下,线性校正图在PAC浓度范围为0.122-2.425μg mL(-1)和PAP浓度范围为0.021-5.245μg mL(-1)的范围内获得。根据标准方法(LODSA)和上限方法(LODULA,)计算得出的检测极限分别为PAC为0.027和0.032μg mL(-1),PAP为0.006和0.009μgmL(-1)。重要参数已针对人工神经网络(ANN)模型进行了优化。统计参数表明这两种方法的能力是可比的。该方法成功地用于药物制剂中PAC和PAP的同时测定。 (C)2014 Elsevier B.V.保留所有权利。

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