Author(s):
                        L. Satyanarayana,  S.V. Naidu,  M. Narasimha Rao,  C. Ayyanna,  Alok Kumar
                    
                    
                        Email(s):
                        satyadna_l@yahoo.co.in 
                    
                      
                        DOI:
                        Not Available
                    
  
                    
                        Address:
                        L. Satyanarayana1*, Prof. S.V. Naidu2, Prof. M. Narasimha Rao2, Prof. C. Ayyanna2 and Alok Kumar1. 
1Department of Pharmaceutical Chemistry, Omega College of Pharmacy, Edulabad, Ghatkesar, Ranga Reddy Dist., Hyderabad-500 034.
2Centre for Biotechnology, Department of Chemical Engineering, College of Engineering (A), Andhra University, Vishakapatnam - 530003
*Corresponding Author:
                    
                    
                        Published In:
                         
                        Volume - 3,     
                                Issue - 5,    
                                Year - 2011
                        
                    
					
					 
						
					
					
				
                 
				
                					
                    
                    
                        ABSTRACT: 
                        A simple, precise, rapid and accurate reverse phase HPLC method was developed for the estimation of Maraviroc in tablet dosage form. A RP Inertsil ODS-3V C-18, 250x4.6 mm, 5µm partical size, with mobile phase consisting of 0.02M Dipotasium hydrogen orthophosphate in water pH 2.5 with orthophosphoric acid and Acetonitrile in the ratio of 60:40 v/v was used. The flow rate was 0.8 ml/min and the effluents were monitored at 210 nm. The retention time was 4.330 min. The detector response was linear in the concentration of 80-240µg/ml. The respective linear regression equation being Y= 31018.059X + 44222.4. The limit of detection and limit of quantification was 0.2µg and 0.6µg/ml respectively. The percentage assay of Maraviroc was 99.42%. The method was validated by determining its accuracy, precision and system suitability.
The results of the study showed that the proposed RP-HPLC method is simple, rapid, precise and accurate, which is useful for the routine determination of Maraviroc in bulk drug and in its pharmaceutical dosage form.
                    
                    
                    
                 
				
				
                    
                    
                        Cite this article:
                        
                        L. Satyanarayana, S.V. Naidu,  M. Narasimha Rao,  C. Ayyanna, Alok Kumar. The Estimation of Maraviroc in Tablet dosage form by RP-HPLC. Research J. Pharma.  Dosage Forms and Tech.  2011; 3(5): 230-232 .
						
						 Cite(Electronic):
						 
						 L. Satyanarayana, S.V. Naidu,  M. Narasimha Rao,  C. Ayyanna, Alok Kumar. The Estimation of Maraviroc in Tablet dosage form by RP-HPLC. Research J. Pharma.  Dosage Forms and Tech.  2011; 3(5): 230-232 .   Available on: https://www.rjpdft.com/AbstractView.aspx?PID=2011-3-5-12