Analysis of paracetamol, pseudoephedrine and cetirizine in Allercet Cold® capsules using spectrophotometric techniques
Date
2018
Journal Title
Journal ISSN
Volume Title
Type
Article
Publisher
Springer
Series Info
Scientific Journal Rankings
Abstract
Paracetamol (PAR), Pseudoephedrine hydrochloride (PSE) and cetirizine dihydrochloride (CET) is a ternary mixture that composes tablets which are popular for the relief of flu in Egypt. The spectra of the drugs were overlapped and no spectrophotometric methods were reported to resolve the mixture. This research proposes four spectrophotometric methods that are efficient and require water only as a solvent. The first method was ratio subtraction-ratio difference method (RSDM) where PAR was initially removed from the mixture by ratio subtraction and determined at 292.4 nm, then PSE and CET were quantified by subtracting the amplitudes of their ratio spectra between 257.0 and 230.0 nm for PSE and between 228.0 and 257.0 nm for CET. The second method was derivative ratio spectra—zero crossing (DRZC) which was based on determining both PSE and CET from the zero-crossing points of the first and third derivative of their ratio spectra at 252.0 and 237.0 nm, respectively while PAR was determined using its first derivative at 292.4 nm. Moreover, the ternary mixture was resolved using successive derivative ratio (SDR) method where PAR, PSE and CET were determined at 310.2, 257.0 and 242.4 nm, respectively. The fourth proposed method was pure component contribution algorithm (PCCA) which was applied to quantify the drugs at their λmax. Recovery percentages for RSDM were 100.7 ± 1.890, 99.69 ± 0.8400 and 99.38 ± 1.550; DRZC were 101.8 ± 0.8600, 99.04 ± 1.200 and 98.95 ± 1.300; SDR were 101.9 ± 1.060, 99.59 ± 1.010 and 100.2 ± 0.6300; PCCA were 101.6 ± 1.240, 99.10 ± 0.5400 and 100.4 ± 1.800 for PAR, PSE and BRM; respectively. The suggested methods were effectively applied to analyze laboratory prepared mixtures and their combined dosage form.
Description
Msa Google Scholar
Keywords
paracetamol
Citation
1. Moffat AC, Osselton MD, Widdop B, Watts J (2011) Clarke’s analysis of drugs and poisons. Pharmaceutical press London, London Google Scholar 2. Louis Goodman AG (1996) Goodman and Gilman’s the pharmaceutical basis of therapeutics. McGraw-Hill New York, New York Google Scholar 3. Hassaninejad-Darzi SK, Es’haghi Z, Nikou SM, Torkamanzadeh M (2017) Rapid and simultaneous determination of montelukast, fexofenadine and cetirizine using partial least squares and artificial neural networks modeling. Iran J Chem Chem Eng 36(3):81–96 CAS Google Scholar 4. Saeed AM (2017) Spectrophotometric determination of paracetamol in some manufactured tablets in Iraqi markets. Int J Pharm Sci Rev Res. 42(2):53–57 CAS Google Scholar 5. Sujana MMDK (2017) Method development and validation of simultaneous estimation of pseudoephedrine ambroxol desloratadine in tablet dosage form and degradation studies by RP-HPLC method. Int J Sci Res Manag 5(7):5959–5997 Google Scholar 6. Youssef SH, Hegazy MAM, Mohamed D, Badawey AM (2017) Analysis of paracetamol, pseudoephedrine and brompheniramine in comtrex® tablets using chemometric methods. World J Pharm Pharm Sci 6(6):1644–1659 CAS Google Scholar 7. Aly FA, Nahed E-E, Elmansi H, Nabil A (2017) Simultaneous determination of cetirizine, phenyl propanolamine and nimesulide using third derivative spectrophotometry and high performance liquid chromatography in pharmaceutical preparations. Chem Cent J 11(1):99 Article PubMed PubMed Central Google Scholar 8. Abdelwahab NS, Abdelaleem EA (2017) Stability indicating RP-HPLC method for simultaneous determination of guaifenesin and pseudoephedrine hydrochloride in the presence of syrup excepients. Arabian J Chem 10:S2896–S2901 Article CAS Google Scholar 9. Mohamed D, Hegazy MA, Elshahed MS, Toubar SS, Helmy MI (2018) Liquid chromatography-tandem MS/MS method for simultaneous quantification of paracetamol, chlorzoxazone and aceclofenac in human plasma: an application to a clinical pharmacokinetic study. Biomed Chromatogr. https://doi.org/10.1002/bmc.4232 Article PubMed Google Scholar 10. Sivasubramanian L, Lakshmi K (2009) Reverse phase-high performance liquid chromatographic method for the analysis of paracetamol, cetirizine and pseudoephedrine from tablets. Pharma Chem. 1(1):37–46 CAS Google Scholar 11. Kumudhavalli M. Determination of pseudoephedrine hydrochloride, cetirizine dihydrochloride and paracetamol uncoated tablet by RP-HPLC method. J Global Pharma Technol. 2010;2(4):97–101 CAS Google Scholar 12. Darwish IA, Hussein SA, Mahmoud AM, Hassan AI (2007) Sensitive indirect spectrophotometric method for determination of H2-receptor antagonists in pharmaceutical formulations. Int J Biomed Sci 3(2):123 CAS PubMed PubMed Central Google Scholar 13. El-Bardicy MG, Lotfy HM, El-Sayed MA, El-Tarras MF (2008) Smart stability-indicating spectrophotometric methods for determination of binary mixtures without prior separation. J AOAC Int 91(2):299–310 CAS PubMed Google Scholar 14. Lotfy HM, Hagazy MA-M (2012) Comparative study of novel spectrophotometric methods manipulating ratio spectra: an application on pharmaceutical ternary mixture of omeprazole, tinidazole and clarithromycin. Spectrochim Acta 96:259–270 Article CAS Google Scholar 15. Nevado JB, Cabanillas CG, Salinas F (1992) Spectrophotometric resolution of ternary mixtures of salicylaldehyde, 3-hydroxybenzaldehyde and 4-hydroxybenzaldehyde by the derivative ratio spectrum-zero crossing method. Talanta 39(5):547–553 Article Google Scholar 16. Afkhami A, Bahram M (2005) Successive ratio-derivative spectra as a new spectrophotometric method for the analysis of ternary mixtures. Spectrochim Acta Part A Mol Biomol Spectrosc 61(5):869–877 Article CAS Google Scholar 17. Hegazy MAM (2015) A novel pure component contribution algorithm (PCCA) for extracting components’ contribution from severely overlapped signals; an application to UV-spectrophotometric data. Spectrochim Acta Part A 151:405–414 Article CAS Google Scholar 18. Guideline IHT. Validation of analytical procedures: text and methodology. Q2 (R1). 2005;1