1Department of Chemistry, R.V.R. & J.C. College of Engineering, Guntur, Andhra Pradesh, India
2Department of Chemistry, S.V. University, Tirupathi, Andhra Pradesh, India
*Corresponding Author E-mail: srinunarala@gmail.com
Online published on 6 March, 2013.
Three new, simple and sensitive visible spectrophotometric methods (A, B and C) have been developed for the determination of Mosapride Citrate in bulk drug and pharmaceutical formulations. Method A is based on the condensation of Mosapride Citrate with salicylaldehyde to form schiff's base, which was a yellow colored chromogen exhibiting λmax at 410 nm. Method B is based on the formation of pink colored chromogen obtained when Mosapride Citrate was diazotized with nitrous acid followed by coupling with α-naphthyl amine, exhibiting λmax at 520 nm. Method C is based on the oxidation of Mosapride Citrate with Fe (III) and the estimation of Fe (II) produced after chelation with potassium ferricyanide, which was a bluish green colored chromogen, exhibiting λmax at 770 nm. The Beer's law was obeyed in the concentration range of 4–20, 10–40 and 4–24 μg/ml for methods A, B and C respectively. The results of the proposed methods have been validated statistically and by recovery methods.
spectrophotometry, salicylaldehyde, α-naphthyl amine, potassium ferricyanide