Author:
Hassan Said A.,Fekry Reham A.,Fayez Yasmin M.,Kelani Khadiga M.
Abstract
AbstractThe presence of minor components represents a challenging problem in spectrophotometric analysis of pharmaceuticals. If one component has a low absorptivity or present in a low concentration compared to the other components, this will hinder its quantitation by spectrophotometric methods. Continuous Wavelet Transform (CWT) as a signal processing technique was utilized to figure out a solution to such a problem. A comparative study was established between traditional derivative spectrophotometry (Numerical Differentiation, ND) and CWT to indicate the advantages and limitations of each technique and possibility of solving the problem of minor components. A mixture of ibuprofen (IBU) and phenylephrine (PHE) with its degradation products forming a ternary mixture was used for comparing the two techniques. The two techniques were applied on raw spectral data and on ratio spectra data resulting in four methods, namely ND, CWT, Derivative Ratio-Zero Crossing (DRZC) and Continuous Wavelet Transform Ratio-Zero Crossing (CWTR-ZC) methods. By comparing the results in laboratory prepared mixtures, CWT technique showed advantages in analysis of mixtures with minor components than ND. The proposed methods were validated according to the ICH guideline Q2(R1), where their linearity was established with correlation coefficient ranging from 0.9995 to 0.9999. The linearity was in the range 3–40 μg/mL for PHE in all methods, while for IBU it was 20–180 and 30–180 μg/mL in CWT and ND methods, respectively. The CWT methods were applied for quantitative determination of the drugs in their dosage form showing the ability of the methods to quantitate minor components in pharmaceutical formulations.
Publisher
Springer Science and Business Media LLC
Reference53 articles.
1. Elghobashy M, Badran U, Salem M, Kelani K. Stability indicating spectrophotometric and chromatographic methods for the determination of azelastine hydrochloride in presence of its alkaline degradant. Anal Chem: Indian J. 2014;14:135–42.
2. Darwish HW, Hassan SA, Salem MY, El-Zeany BA. Development and validation of H-point standard addition method applied for the analysis of binary mixture of amlodipine and atorvastatin. Int J Pharma Bio Sci. 2013;4(2):230–43.
3. Ahmed MK, Michael AM, Hassan SA, Abbas SS. Different spectrophotometric methods manipulating ratio spectra for the assay of hydrocortisone acetate and clioquinol in their topical preparation. Eur J Chem. 2021;12(3):265–72.
4. Darwish HW, Hassan SA, Salem MY, El-Zeany BA. Advanced stability indicating chemometric methods for quantitation of amlodipine and atorvastatin in their quinary mixture with acidic degradation products. Spectrochim Acta A. 2016;154:58–66.
5. Basha MA, Abdelrahman MK, Bebawy L, Mostafa A, Hassan SA. A comparative Study of two analytical techniques for the simultaneous determination of Amprolium HCl and Ethopabate from combined dosage form and in presence of their alkaline degradation. Spectrochim Acta A. 2020;243: 118756.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献