Optimization of wavelength range and data interval in chemometric analysis of complex pharmaceutical mixtures

The performance of different chemometric approaches was evaluated in the spectrophotometric determination of pharmaceutical mixtures characterized by having the amount of components with a very high ratio. Principal component regression (PCR), partial least squares with one dependent variable (PLS1)...

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Main Authors: Michele De Luca (Author), Giuseppina Ioele (Author), Claudia Spatari (Author), Gaetano Ragno (Author)
Format: Book
Published: Elsevier, 2016-02-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Michele De Luca  |e author 
700 1 0 |a Giuseppina Ioele  |e author 
700 1 0 |a Claudia Spatari  |e author 
700 1 0 |a Gaetano Ragno  |e author 
245 0 0 |a Optimization of wavelength range and data interval in chemometric analysis of complex pharmaceutical mixtures 
260 |b Elsevier,   |c 2016-02-01T00:00:00Z. 
500 |a 2095-1779 
500 |a 10.1016/j.jpha.2015.10.001 
520 |a The performance of different chemometric approaches was evaluated in the spectrophotometric determination of pharmaceutical mixtures characterized by having the amount of components with a very high ratio. Principal component regression (PCR), partial least squares with one dependent variable (PLS1) or multi-dependent variables (PLS2), and multivariate curve resolution (MCR) were applied to the spectral data of a ternary mixture containing paracetamol, sodium ascorbate and chlorpheniramine (150:140:1, m/m/m), and a quaternary mixture containing paracetamol, caffeine, phenylephrine and chlorpheniramine (125:6. 25:1.25:1, m/m/m/m). The UV spectra of the calibration samples in the range of 200-320 nm were pre-treated by removing noise and useless data, and the wavelength regions having the most useful analytical information were selected using the regression coefficients calculated in the multivariate modeling. All the defined chemometric models were validated on external sample sets and then applied to commercial pharmaceutical formulations. Different data intervals, fixed at 0.5, 1.0, and 2.0 point/nm, were tested to optimize the prediction ability of the models. The best results were obtained using the PLS1calibration models and the quantification of the species of a lower amount was significantly improved by adopting 0.5 data interval, which showed accuracy between 94.24% and 107.76%. 
546 |a EN 
690 |a Chemometrics 
690 |a Spectrophotometry 
690 |a Principal component analysis 
690 |a Partial least squares 
690 |a Multivariate curve resolution 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Journal of Pharmaceutical Analysis, Vol 6, Iss 1, Pp 64-69 (2016) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S2095177915300095 
787 0 |n https://doaj.org/toc/2095-1779 
856 4 1 |u https://doaj.org/article/da75a71626ed4db096301d1590299e30  |z Connect to this object online.