RESUMO
A sensitive, simple, and economic spectrophotometric method was developed and validated for the determination ofgabapentin in pure form and pharmaceutical preparations. The method is based on Schiff base condensation reaction ofthe primary amino group of gabapentin with salicylaldehyde reagent in the presence of acetate solution at 45°C for 20minutes. The obtained yellow-colored derivative in methanolic medium showed absorption maxima at 403 nm. Underthe optimum conditions, Beer’s law was obeyed in the concentration range of 6 to 100 μg/ml with correlation coefficientvalue of 0.9961. Limit of detection and limit of quantification were found to be 1.16 and 3.48 μg/ml, respectively. Thevalidity of the described method was assessed according to the International Conference on Harmonization guidelines.The mean percentage recoveries ± SD were 100.57 ± 1.5 by applying the standard addition technique. The method wasrepeatable and precise (RSD ≤ 0.61% and ≤ 1.34%, respectively) and was successfully applied for the determinationof the investigated drug in its pharmaceutical dosage form without detectable interference from the additives, hence,can be suggested for routine analysis of the gabapentin.
RESUMO
A sensitive, simple, and economic spectrophotometric method was developed and validated for the determination ofgabapentin in pure form and pharmaceutical preparations. The method is based on Schiff base condensation reaction ofthe primary amino group of gabapentin with salicylaldehyde reagent in the presence of acetate solution at 45°C for 20minutes. The obtained yellow-colored derivative in methanolic medium showed absorption maxima at 403 nm. Underthe optimum conditions, Beer’s law was obeyed in the concentration range of 6 to 100 μg/ml with correlation coefficientvalue of 0.9961. Limit of detection and limit of quantification were found to be 1.16 and 3.48 μg/ml, respectively. Thevalidity of the described method was assessed according to the International Conference on Harmonization guidelines.The mean percentage recoveries ± SD were 100.57 ± 1.5 by applying the standard addition technique. The method wasrepeatable and precise (RSD ≤ 0.61% and ≤ 1.34%, respectively) and was successfully applied for the determinationof the investigated drug in its pharmaceutical dosage form without detectable interference from the additives, hence,can be suggested for routine analysis of the gabapentin.