A new spectrophotometric method for the determination of gabapentin usingchromotropic acid

dc.contributor.authorAdegbolagun, O. M.
dc.contributor.authorThomas, O. E.
dc.contributor.authorAiyenale, E. O.
dc.contributor.authorAdegoke, O.A.
dc.date.accessioned2026-02-12T08:37:55Z
dc.date.issued2018
dc.description.abstractThe purpose was to develop a colorimetric method for determining gabapentin. The method was based on the diazo coupling reaction between diazotized gabapentin and chromotropic acid. The method was validated using ICH guidelines before its application to generic brands of gabapentin. Coupling reaction generated an orange azo adduct whose absorbance was linearly correlated with concentration in the range of 1-6 μg/mL at 470 nm. The method was accurate and precise with recovery range of 97.6-103.1%; intra- and inter-day precisions (%RSD) were less than 0.65% and showed no statistical difference when compared with reference method in the analysis of the dosage forms. The 3D optimization of the adduct revealed an E-type configuration around the azo linkage which would contribute to its stability. The new method can serve as a reliable alternative to the official method for the routine analysis of gabapentin in bulk and dosage forms.
dc.identifier.issn1307-2080
dc.identifier.otherui_art_adegbolagun_new_2018
dc.identifier.otherActa Pharmaceutica Sciencia 56 (3), pp. 92-110
dc.identifier.urihttps://repository.ui.edu.ng/handle/123456789/12091
dc.language.isoen
dc.publisherIstanbul Medipol University
dc.subjectGabapentin
dc.subjectcolorimetric analysis
dc.subjectchromotropic acid
dc.subjectdiazo coupling reaction.
dc.titleA new spectrophotometric method for the determination of gabapentin usingchromotropic acid
dc.typeArticle

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
(10) ui_art_adegoke_colorimetric_2015.pdf
Size:
974.76 KB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.61 KB
Format:
Item-specific license agreed upon to submission
Description:

Collections