Journal
ANNALES PHARMACEUTIQUES FRANCAISES
Volume 80, Issue 6, Pages 885-896Publisher
MASSON EDITEUR
DOI: 10.1016/j.pharma.2022.06.001
Keywords
Double devisor-ratio spectra derivative; Difference spectrophotometry; Piracetam; Levetiracetam; Brivaracetam; Vincamine; Greenness
Categories
Ask authors/readers for more resources
Green spectrophotometric methods were developed and validated for the determination of CNS active drugs. The double divisor-ratio spectra derivative method was used to assay a ternary mixture of Piracetam, Levetiracetam, and Brivaracetam (method I), while the difference spectrophotometric method was applied to assay a binary co-formulated mixture of Piracetam and Vincamine (method II). The methods provided accurate results for the determination of the drugs without interference, and the use of AGREE assessment tool confirmed their environmental benignity.
Background. - Green spectrophotometric methods were developed and validated for determi-nation of some CNS active drugs as antiepileptics and brain stimulants. Objective. - Piracetam (PIR), Levetiracetam (LEV) and Brivaracetam (BRV) were assayed as a ternary mixture using double divisor-ratio spectra derivative (DDRSD) (method I). One more binary co-formulated mixture of Piracetam (PIR) and Vincamine (VIN) was assayed using differ-ence spectrophotometric procedures (method II).Method. - I was applied to determine PIR at 302 nm in the first derivative of the ratio spectra in the selected spectral region. The content of LEV was determined by measuring the spec-tra at 215 nm in the first derivative of the ratio spectra in the selected spectral region. The concentration of BRV was estimated by measuring the first derivative of the ratio spectra in the chosen spectral region and detecting the signals at 229.7 nm. The application of method (II) procedures resulted in measuring the absorbance of PIR at 220 nm which is the zero crossing point on the difference spectra of VIN in 0.1 M NaOH vs. 0.1 M HCl. Similarly, the absorbance of VIN was measured at 245.0 nm, which is the zero crossing point on the difference spectra of PIR.Results. - The suggested methods were fully validated adopting ICH guidelines. The linearity ranged from 10-100 mu g/mL for the three racetams and from 2-20 for VIN. The recovery percent-ages were ranged from 98.72% to 101.8% for method I and from 98.13% to 101.06% for method II. Moreover, the proposed methods were proved environmentally benign using the most recent assessment tool named AGREE.Conclusion. - Both procedures were successfully applied for the determination of each drug in bulk powder, checked using laboratory prepared mixtures, and directly applied on commercially available pharmaceutical products without interference. The obtained results revealed a good agreement with those obtained by the reported methods.(c) 2022 Acad acute accent emie Nationale de Pharmacie. Published by Elsevier Masson SAS. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available