Micro and nanogram determination of lamotrigine in pharmaceuticals by visible spectrophotometry using bromophenol blue

Rajendraprasad, N. and Basavaiah, K. and Vinay, K. B. (2010) Micro and nanogram determination of lamotrigine in pharmaceuticals by visible spectrophotometry using bromophenol blue. indian journal of chemical technology, 17 (3). pp. 220-228. ISSN 0971-457X

[img] Text (Full Text)
Micro and nanogram determination.pdf - Published Version
Restricted to Registered users only

Download (166kB) | Request a copy
Official URL: http://nopr.niscair.res.in/handle/123456789/9059

Abstract

Three reliable, rapid, highly sensitive and selective methods have been developed and validated for the determination of lamotrigine (LMT) in pure drug and in tablets. The first method (method A) is based on the formation of chloroform extractable ion-pair complex between LMT and bromophenol blue (BPB) at pH 1.44 +/- 0.01 with a wavelength of maximum absorption at 420 nm. In the second (method B) and third (method C) methods, the drug-dye ion pair is dissolved in either ethanolic H2SO4 and resulting acid form of the dye is measured at 420 nm or ethanolic KOH and the resulting base form of the dye is measured at 600 nm. All variables affecting the drug-dye complex formation and its extraction into CHCl3 have been investigated and conditions optimized. Beer's law was obeyed over 2.5-25 mu g mL(-1), 50-400 ng mL(-1) and 10-80 ng mL(-1), for method A, method B and method C, respectively. The calculated molar absorptivity values are 7.26 x 10(3), 5.4 x 10(5) and 2.6 x 10(6) 1 mol(-1) cm(-1), respectively, for methods A, B and C; and the corresponding Sandell sensitivities are 0.0353, 0.0005 and 0.0001 mu g cm(-2). The limits of detection (LOD) and quantification (LOQ) have also been reported. The stoichiometry of the formed ion-pair complex was found to be 1:1.for method A, and the stability constant is also calculated. The accuracy and precision of the methods were evaluated on intra-day and inter-day basis; and the relative error (RE) and the relative standard deviation (RSD) were <= 2.0% and <= 1.4%, respectively. The proposed methods were successfully applied for the determination of LMT in bulk powder and in tablets.

Item Type: Article
Subjects: C Chemical Science > Chemistry
Divisions: Department of > Chemistry
Depositing User: LA manjunath user
Date Deposited: 12 Jul 2019 10:04
Last Modified: 12 Jul 2019 10:04
URI: http://eprints.uni-mysore.ac.in/id/eprint/5148

Actions (login required)

View Item View Item