Spectrofluorometric determination of orphenadrine, dimenhydrinate, and cinnarizine using direct and synchronous techniques with greenness assessment

• Published in: Scientific reports Vol. 13; no. 1; p. 13549
• Main Authors: Ghonim, Rana, Tolba, Manar M., Ibrahim, Fawzia, El-Awady, Mohamed I.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 20.08.2023; Nature Publishing Group; Nature Portfolio
• Subjects: 639/638/11; 639/638/224; Caustic soda; Chromatography; Correlation coefficient; Drug dosages; Ethanol; Humanities and Social Sciences; Hydrochloric acid; Mass spectrometry; Methods; multidisciplinary; Orphenadrine; Pharmaceuticals; Pharmacy; Quantitation; Science; Science (multidisciplinary); Scientific imaging; Sodium; Sodium lauryl sulfate; Wavelengths
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-40559-x

Orphenadrine (ORP), dimenhydrinate (DMN), and cinnarizine (CNN) were investigated using green-sensitive spectrofluorometric methods. Method, I used for determination of DMN in 0.1 M hydrochloric acid (HCl) and 1.0% sodium dodecyl sulphate (SDS) at 286 nm after λ ex 222 nm, while for determination of ORP in 1.0% w/v SDS involves measuring the fluorescence at 285 nm after λ ex 220 nm. For DMN and ORP, the detection and quantitation limits were 2.99 and 4.71 and 9.08 and 14.29 ng/mL, respectively. The ranges of DMN and ORP were 0.10–1.0 and 0.04–0.5 µg/mL, respectively, in micellar aqueous solution. Method II, the derivative intensities of DMN and CNN were measured at a fixed of different wavelength between the excitation and the emission wavelengths (Δλ) = 60 nm at 282 and 322 nm, at the zero crossing of each other, respectively. The detection and quantitation limits for DMN and CNN were 1.77 and 0.88 ng/mL and 5.36 and 2.65 ng/mL, correspondingly, through the entire range of 0.1–1.0 µg/mL for DMN and CNN. The linearity was perfectly determined through the higher values of the correlation coefficient ranging from 0.9997 to 0.9999 for both direct and synchronous methods. The precision of the proposed methods was also confirmed via the lower values of the standard deviation which ranged from 0.39 to 1.11. The technique was expanded to analyze this mixture in combined tablets and laboratory-prepared mixtures. The method validation was done depending on the international conference on harmonization (ICH) recommendations. An analysis of the statistical data revealed a high agreement between the proposed data and the comparison methodology. Three different assessment methods demonstrated the greenness of the technique.