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

被引:21
|
作者
Khodaveisi, Javad [1 ]
Dadfarnia, Shayessteh [1 ]
Shabani, Ali Mohammad Haji [1 ]
Moghadam, Masoud Rohani [2 ]
Hormozi-Nezhad, Mohammad Reza [3 ]
机构
[1] Yazd Univ, Fac Sci, Dept Chem, Yazd 89195741, Iran
[2] Vali e Asr Univ, Fac Sci, Dept Chem, Rafsanjan, Iran
[3] Sharif Univ Technol, Dept Chem, Tehran 111559516, Iran
关键词
Localized surface plasmon resonance band; Chemometric methods; Kinetic-spectrophotometry; Simultaneous determination; p-Aminophenol; Paracetamol;
D O I
10.1016/j.saa.2014.11.094
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
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.
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收藏
页码:474 / 480
页数:7
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