M. S. Uma Shankar 1*, Ajithadas Aruna 2, N. V. Satheesh Madhav 3, M. K. Ranganath 4
- Department of Pharmaceutical Technology, Krupanidhi College of Pharmacy, #12/1, Chikkabellandur, Carmelaram Post, Bengaluru - 560 035, Karnataka, India
- Department of Pharmaceutical Chemistry, Madras Medical College, Park Town, Chennai-600 003, India
- Department of Pharmaceutics, Dehradun Institute of Technology, Faculty of Pharmacy, Mussoorie-Diverson Road, Makkawala, P.O. Bhawantpur, Dehredun (Uttarakhand), India
- Department of Pharmaceutical Analysis, Krupanidhi College of Pharmacy, #12/1, Chikkabellandur, Carmelaram Post, Bengaluru - 560 035, Karnataka, India
Abstract
Two simple, validated and sensitive spectrophotometric methods have been developed for the estimation of nicorandil in bulk and in pharmaceutical formulation (Method A&Method B). The method A involves the determination of nicorandil by standard absorbance method at 262 nm which obeys Beer's law in concentration range of 20-120 � g/mL. Method B is based on the formation of intensely yellow ammonium salts by the interaction of nicorandil with phenol-2,4-disulphonic acid which obeys Beer's law in concentration range of 10-60 ?g/ml exhibiting maximum absorption at 405 nm under the optimized experimental conditions. The results obtained by the proposed method are acceptable. The methods were extended to tablet formulation and there was no interference from excipients and diluents. These methods have been statistically validated and are found to be precise and accurate.
