Scopus İndeksli Yayınlar Koleksiyonu
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12416/8651
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Article Citation - WoS: 8Citation - Scopus: 8Continuous Wavelet Transform Applied To the Quantitative Analysis of a Binary Mixture(Revista Chimie Srl, 2009) Dinc, Erdal; Baleanu, Dumitru; Baleanu, Dumitru; Üstündag, Ö; Aboul-Enein, HY; MatematikSignal processing methods, continuous wavelet transform (CWT) methods, were proposed for the simultaneous spectral determination of ampicillin sodium (AS) and sulbactam sodium (SS) in their synthetic binary mixtures and pharmaceutical preparations. Firstly, the ratio spectra were obtained by dividing the absorption spectra of a pure compound and its binary mixture by a standard spectrum of one of the compounds in binary mixture. Secondly, the ratio spectra of AS, SS and their samples were processed by the Mexican hat-CWT and Symtles3-CWT (MEX-CWT and SYM3-CWT, respectively). hi this application, the MEX and SYM3 among wavelet families were found to be optimal to obtain the highest spectral recoveries. Calibration graphs of AS and SS in the linear concentration range of 10-70 mu g/mL and 10-55 mu g/mL were obtained by measuring the amplitudes of the transformed ratio signals, respectively. Percent mean recoveries obtained by application of the CWT methods to the synthetic mixtures were found between 99.1 % and 103.6 %. Both SYM3-CWT and MEX-CWT methods were applied to the real samples containing two active compounds and successful results were obtained.Article Citation - WoS: 6Citation - Scopus: 7Fractional-Continuous Wavelet Transforms and Ultra-Performance Liquid Chromatography for the Multicomponent Analysis of a Ternary Mixture Containing Thiamine, Pyridoxine, and Lidocaine in Ampules(Oxford Univ Press inc, 2012) Baleanu, Dumitru; Dinc, ErdalNew chemometric approaches based on the application of partial least squares (PLS) and principal component regression (PCR) algorithms with fractional wavelet transform (FWT) and continuous wavelet transform (CWT) are proposed for the spectrophotometric multicomponent determination of thiamine hydrochloride (B-1), pyridoxine hydrochloride (B-6), and lidocaine hydrochloride (LID) in ampules without any separation step. In this study PLS and PCR techniques were applied to the raw spectral data, FWT-coefficients, and FWT-CWT-coefficients. These calibration models were labeled as Raw-PLS and Raw-PCR, FWT-PLS and FWT-PCR, and FWT-CWT-PLS and FWT-CWT-PCR, respectively. A new ultra-performance liquid chromatographic (UPLC) method was developed for the comparison of the results obtained by applying the chemometric calibration methods. Chromatographic separation and determination of B-1, B-6, and LID in ampules were performed on an Acquity UPLC (R) BEH C18 column (50 x 2.1 mm id, 1.7 mu m particle size) using gradient elution with a mobile phase consisting of methanol and 0.01 M HCl at a constant flow rate of 0.6 mL/min. These combined chemometric calibrations and UPLC were validated by analyzing various ternary mixtures, B-1, B-6, and LID. The proposed chemometric approaches (signal processing-multivariate calibrations) and UPLC method were applied to the quantitative multicomponent analysis of marketed ampules containing the vitamins B1 and B-6 with LID.Article Citation - WoS: 7Citation - Scopus: 10Simultaneous Chemometric Determination of Pyridoxine Hydrochloride and Isoniazid in Tablets by Multivariate Regression Methods(Wiley-blackwell, 2010) Ustundag, Ozgur; Baleanu, Dumitru; Dinc, ErdalThe sole use of pyridoxine hydrochloride during treatment of tuberculosis gives rise to pyridoxine deficiency. Therefore, a combination of pyridoxine hydrochloride and isoniazid is used in pharmaceutical dosage form in tuberculosis treatment to reduce this side effect. In this study, two chemometric methods, partial least squares (PLS) and principal component regression (PCR), were applied to the simultaneous determination of pyridoxine (PYR) and isoniazid (ISO) in their tablets. A concentration training set comprising binary mixtures of PYR and ISO consisting of 20 different combinations were randomly prepared in 0.1 M HCl. Both multivariate calibration models were constructed using the relationships between the concentration data set (concentration data matrix) and absorbance data matrix in the spectral region 200-330 nm. The accuracy and the precision of the proposed chemometric methods were validated by analyzing synthetic mixtures containing the investigated drugs. The recovery results obtained by applying PCR and PLS calibrations to the artificial mixtures were found between 100.0 and 100.7%. Satisfactory results obtained by applying the PLS and PCR methods to both artificial and commercial samples were obtained. The results obtained in this manuscript strongly encourage us to use them for the quality control and the routine analysis of the marketing tablets containing PYR and ISO drugs. Copyright (C) 2010 John Wiley & Sons, Ltd.Article Citation - WoS: 37Citation - Scopus: 43Multivariate Analysis of Paracetamol, Propiphenazone, Caffeine and Thiamine in Quaternary Mixtures by Pcr, Pls and Ann Calibrations Applied on Wavelet Transform Data(Elsevier, 2008) Baleanu, Dumitru; Ioele, Giuseppina; De Luca, Michele; Ragno, Gaetano; Dinc, ErdalThe quantitative resolution of a quaternary pharmaceutical mixture consisting of paracetamol, propiphenazone, caffeine and thiamine was performed by the simultaneous use of fractional wavelet transform (FWT) with principal component regression (PCR), partial least squares (PLS) and artificial neural networks (ANN) methods. A calibration set consisting of 22 mixture solutions was prepared by means of an orthogonal experimental design and their absorption spectra were recorded in the spectral range of 210.0-312.3 nm and then transferred into the fractional wavelet domain and processed by FWT. The chemometric calibrations FWT-PCR, FWT-PLS and FWT-ANN were computed by using the relationship between the coefficients provided by FWT method and the concentration data from calibration set. An external validation was carried out by applying the developed methods to the analysis of synthetic mixtures of the related compounds, obtaining successful results. The models were finally used to assay the studied drugs in the commercial pharmaceutical formulations. (c) 2008 Elsevier B.V. All rights reserved.Article Citation - WoS: 49Citation - Scopus: 55Continuous Wavelet and Derivative Transforms for the Simultaneous Quantitative Analysis and Dissolution Test of Levodopa-Benserazide Tablets(Elsevier, 2007) Kaya, Sueha; Doganay, Tanver; Baleanu, Dumitru; Dinc, ErdalSimultaneous analyses and dissolution tests of levodopa-benserazide tablets were carried out by continuous wavelet transform (CWT) and classic derivative spectrophotometry (DS) without using any chemical separation step. The developed two spectrophotometric resolutions are based on the transformation of the original UV spectra. The original absorption spectra of levodopa and benserazide in the concentration range of 1-80 mu g/mL and 5-240 mu g/mL in USP simulated gastric juice were registered in the spectral range of 250-310 nm, respectively. Various wavelet families and different spectrophotometric derivative orders were tested to find the optimal signal processing for obtaining desirable calibration graphs and reliable determinations of the investigated drugs. Under the optimized conditions of the methods, symlets wavelet family using a = 128 with sixth order (SYM6-CWT) and the first derivative transform with Delta lambda = 10 nm were identified as optimal signal processing methods for the determinations and dissolution tests. The calibration functions for each drug were obtained by measuring the values of the CWT and derivative amplitudes. The validation of the developed methods was confirmed by analyzing various synthetic mixtures of the investigated drugs. Mean recovery values were found between 99.1% and 104.7% for DS and 100% and 102.9% for CWT, respectively for determination of BEN and LEV in synthetic mixtures. Each developed approaches were successfully applied to the simultaneous determination and dissolution test of levodopa and benserazide in their commercial tablets and a good agreement was observed. (c) 2007 Elsevier B.V. All rights reserved.Article Citation - WoS: 24Citation - Scopus: 26Comparative Spectral Analysis of Veterinary Powder Product by Continuous Wavelet and Derivative Transforms(Pergamon-elsevier Science Ltd, 2007) Kanbur, Murat; Baleanu, Dumitru; Dinc, ErdalComparative simultaneous determination of chlortetracycline and benzocaine in the commercial veterinary powder product was carried out by continuous wavelet transform (CWT) and classical derivative transform (or classical derivative spectrophotometry). In this quantitative spectral analysis, two proposed analytical methods do not require any chemical separation process. In the first step, several wavelet families were tested to find an optimal CWT for the overlapping signal processing of the analyzed compounds. Subsequently, we observed that the coiflets (COIF-CWT) method with dilation parameter, a = 400, gives suitable results for this analytical application. For a comparison, the classical derivative spectrophotometry (CDS) approach was also applied to the simultaneous quantitative resolution of the same analytical problem. Calibration functions were obtained by measuring the transform amplitudes corresponding to zero-crossing points for both CWT and CDS methods. The utility of these two analytical approaches were verified by analyzing various synthetic mixtures consisting of chlortetracycline and benzocaine and they were applied to the real samples consisting of veterinary powder formulation. The experimental results obtained from the COIF-CWT approach were statistically compared with those obtained by classical derivative spectrophotometry and successful results were reported. (C) 2006 Elsevier B.V. All rights reserved.Article Citation - WoS: 29Citation - Scopus: 30Fractional Wavelet Analysis for the Simultaneous Quantitative Analysis of Lacidipine and Its Photodegradation Product by Continuous Wavelet Transform and Multilinear Regression Calibration(Oxford Univ Press inc, 2006) Ragno, Gaetano; Ioele, Giuseppina; Baleanu, Dumitru; Dinc, ErdalFractional wavelet transform (FWT) was applied to the original absorption spectra of lacidipine (LAC) and its photodegradation product (LACD), and the resulting FWT spectra were processed by continuous wavelet transform (CWT) and multilinear regression calibration (MLRC) for the simultaneous quantitative analysis of both products in their binary mixtures. These methods do not require any chemical separation step and chemical complex reaction to obtain a detectable signal for the degradation product. By using the Mexican hat function, 2 calibration functions for LAC and LACD were obtained by measuring the CWT transformed signals at 416.1 nm for LAC and 414.6 nm for LACD, after FWT processing of the original absorption spectra. The calibration graphs were linear in the concentration range of 5.08-40.64 mu g/mL for LAC and 0.51-8.16 mu g/mL for LACD. The limit of detection and the limit of quantitation were found to be 0.289 and 0.956 mu g/mL for LAC and 0.036 and 0.118 mu g/mL for LACD, respectively. For comparison, the MLRC algorithm was applied to the linear regression functions for the individual drug and its photoproduct. In this approach, a set of linear regression functions was obtained from the relationship between concentrations and FWT signals in the wavelength range 411.0-412.4 nm. Both methods were applied to the quantitative evaluation of LAC and LACD in laboratory and pharmaceutical samples, and produced very satisfactory results.