A New Application of Continuous Wavelet Transform to Overlapping Chromatograms for the Quantitative Analysis of Amiloride Hydrochloride and Hydrochlorothiazide in Tablets by Ultra-Performance Liquid Chromatography

2012 ◽  
Vol 95 (3) ◽  
pp. 751-756 ◽  
Author(s):  
Erdal Dinç ◽  
Eda Büker

Abstract A new application of continuous wavelet transform (CWT) to overlapping peaks in a chromatogram was developed for the quantitative analysis of amiloride hydrochloride (AML) and hydrochlorothiazide (HCT) in tablets. Chromatographic analysis was done by using an ACQUITY ultra-performance LC (UPLC) BEH C18 column (50 × 2.1 mm id, 1.7 μm particle size) and a mobile phase consisting of methanol–0.1 M acetic acid (21 + 79, v/v) at a constant flow rate of 0.3 mL/min with diode array detection at 274 nm. The overlapping chromatographic peaks of the calibration set consisting of AML and HCT mixtures were recorded rapidly by using an ACQUITY UPLC H-Class system. The overlapping UPLC data vectors of AML and HCT drugs and their samples were processed by CWT signal processing methods. The calibration graphs for AML and HCT were computed from the relationship between concentration and areas of chromatographic CWT peaks. The applicability and validity of the improved UPLC-CWT approaches were confirmed by recovery studies and the standard addition technique. The proposed UPLC-CWT methods were applied to the determination of AML and HCT in tablets. The experimental results indicated that the suggested UPLC-CWT signal processing provides accurate and precise results for industrial QC and quantitative evaluation of AML-HCT tablets.

2013 ◽  
Vol 44 (4) ◽  
pp. 608-621 ◽  
Author(s):  
Ahmad Esmaielzadeh Kandjani ◽  
Matthew J. Griffin ◽  
Rajesh Ramanathan ◽  
Samuel J. Ippolito ◽  
Suresh K. Bhargava ◽  
...  

2008 ◽  
Vol 59 (5) ◽  
Author(s):  
Erdal Dinc ◽  
Dumitru Baleanu

Simultaneous spectrophotometric analysis of tablets and binary mixtures containing vitamin C (VC) and aspirin (ASP) with overlapping spectra was performed by ratio spectra-continuous wavelet transform (RS-CWT) and ratio spectra-derivative spectrophotometry (RS-DS). In the application of RS-CWT and RS-DS to the simultaneous analysis of VC and ASP no separation step was considered. The basis of RS-CWT and RS-DS approaches is the transformation and the derivation of the ratio spectra of the related compounds and their samples. Calibration graphs in the linear concentration range 4-20 mg/mL for both compounds were obtained by measuring the CWT and first derivative amplitudes at 260.8 nm for VC and 234.6 nm for ASP in the BIOR-CWT spectra and at 256.0 nm for VC and 230.7 nm for ASP in the first derivative of ratio spectra, respectively. Both methods were tested by using the synthetic mixtures and standard addition technique, and were applied to the simultaneous determination of VC and ASP in commercial effervescent tablets and a good coincidence was reported for experimental results obtained by the proposed RS-CWT and RS-DS.


2008 ◽  
Vol 35 (8) ◽  
pp. 1235-1239 ◽  
Author(s):  
刘寿先 Liu Shouxian ◽  
李泽仁 Li Zeren ◽  
吴建荣 Wu Jianrong ◽  
王德田 Wang Detian ◽  
刘俊 Liu Jun ◽  
...  

2006 ◽  
Vol 89 (6) ◽  
pp. 1538-1546 ◽  
Author(s):  
Erdal Din ◽  
Gaetano Ragno ◽  
Giuseppina Ioele ◽  
Dumitru Baleanu

Abstract Fractional 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 5.0840.64 μg/mL for LAC and 0.518.16 μg/mL for LACD. The limit of detection and the limit of quantitation were found to be 0.289 and 0.956 μg/mL for LAC and 0.036 and 0.118 μg/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 411.0412.4 nm. Both methods were applied to the quantitative evaluation of LAC and LACD in laboratory and pharmaceutical samples, and produced very satisfactory results.


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