Author(s):
                        Mohamed Khaleel,  Nirmal T Havannavar,  Sukhen Som,  Vaseeha Banu TS
                    
                    
                        Email(s):
                        md_khaleel2009@rediffmail.com 
                    
                      
                        DOI:
                        Not Available
                    
  
                    
                        Address:
                        Mohamed Khaleel*, Nirmal T Havannavar, Sukhen Som and Vaseeha Banu TS
Department of Pharmaceutical Chemistry, M.M.U College of Pharmacy,   K, K, Doddi, Dist. Ramanagara- 571511, Karnataka (India)
*Corresponding Author
                    
                    
                        Published In:
                         
                        Volume - 2,     
                                Issue - 1,    
                                Year - 2010
                        
                    
					
					 
						
					
					
				
                 
				
                					
                    
                    
                        ABSTRACT: 
                        Atenolol is selective ß1- adrenergic receptor blocking agent with insignificant partial agonist activity and weak membrane stabilizing properties. Atenolol is official in Indian Pharmacopoeia (IP) and British Pharmacopoeia (BP) and the official method for its assay is by non-aqueous titration. Literature survey revealed non-aqueous titration used for the assay of pure drug and in formulations, High Performance Liquid Chromatography (HPLC) and Gas Liquid Chromatography (GLC) methods for the determination of this drug from serum & urine and Colorimetric and Spectrophotometric methods to estimate this drug in its formulations. But the titrimetric method suffers from various drawbacks and is not satisfactory for pharmaceutical products. This prompted us to develop a newer, simple and cost-effective method for estimation of Atenolol in formulation and bulk. This method is based upon the reaction of Atenolol with dinitrofluorobenzene in acetone in presence of borax and dioxane to develop a yellow colour which is then determined spectrophotometrically at 389 nm (? max of the complex formed). A series of dilutions containing atenolol 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34 µg /ml were prepared among which linearity showed at the range of 2-24 µg/ml. Calibration plot was obtained by using above dilutions. By using the calibration plot the amount of atenolol present in tablet formulation and bulk was found out and the results were satisfactory and encouraging.
                    
                    
                    
                 
				
				
                    
                    
                        Cite this article:
                        
                        Mohamed Khaleel, Nirmal T Havannavar, Sukhen Som, Vaseeha Banu TS. Development of a New, Simple, Sensitive and Cost-Effective Method for Estimation of Atenolol in Formulation and Bulk. Research J. Pharma. Dosage Forms and Tech. 2010; 2(1):72-76.
						
						 Cite(Electronic):
						 
						 Mohamed Khaleel, Nirmal T Havannavar, Sukhen Som, Vaseeha Banu TS. Development of a New, Simple, Sensitive and Cost-Effective Method for Estimation of Atenolol in Formulation and Bulk. Research J. Pharma. Dosage Forms and Tech. 2010; 2(1):72-76.   Available on: https://www.rjpdft.com/AbstractView.aspx?PID=2010-2-1-15