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Computation of geometric representation of novel spectrophotometric methods used for the analysis of minor components in pharmaceutical preparations.

Authors
  • Lotfy, Hayam M1
  • Saleh, Sarah S2
  • Hassan, Nagiba Y3
  • Salem, Hesham4
  • 1 Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr-El Aini, 11562 Cairo, Egypt; Pharmaceutical Chemistry department, Faculty of Pharmaceutical sciences & Pharmaceutical industries, Future University in Egypt (FUE), 12311 Cairo, Egypt. , (Egypt)
  • 2 Analytical Chemistry Department, Faculty of Pharmacy, October University for Modern Sciences and Arts (MSA), 11787 6th October, Egypt. Electronic address: [email protected] , (Egypt)
  • 3 Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr-El Aini, 11562 Cairo, Egypt. , (Egypt)
  • 4 Analytical Chemistry Department, Faculty of Pharmacy, Deraya University, Minia, Egypt. , (Egypt)
Type
Published Article
Journal
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
Publication Date
Jan 01, 2015
Volume
151
Pages
628–643
Identifiers
DOI: 10.1016/j.saa.2015.06.103
PMID: 26163786
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

Novel spectrophotometric methods were applied for the determination of the minor component tetryzoline HCl (TZH) in its ternary mixture with ofloxacin (OFX) and prednisolone acetate (PA) in the ratio of (1:5:7.5), and in its binary mixture with sodium cromoglicate (SCG) in the ratio of (1:80). The novel spectrophotometric methods determined the minor component (TZH) successfully in the two selected mixtures by computing the geometrical relationship of either standard addition or subtraction. The novel spectrophotometric methods are: geometrical amplitude modulation (GAM), geometrical induced amplitude modulation (GIAM), ratio H-point standard addition method (RHPSAM) and compensated area under the curve (CAUC). The proposed methods were successfully applied for the determination of the minor component TZH below its concentration range. The methods were validated as per ICH guidelines where accuracy, repeatability, inter-day precision and robustness were found to be within the acceptable limits. The results obtained from the proposed methods were statistically compared with official ones where no significant difference was observed. No difference was observed between the obtained results when compared to the reported HPLC method, which proved that the developed methods could be alternative to HPLC techniques in quality control laboratories. Copyright © 2015 Elsevier B.V. All rights reserved.

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