Author(s):
                        DG Umalkar,  GV Shinde,  GS Bangale,  Rajesh KS,  RSR Murthy
                    
                    
                        Email(s):
                        duatujwalpharm@yahoo.co.in 
                    
                      
                        DOI:
                        Not Available
                    
  
                    
                        Address:
                        DG Umalkar1*, GV Shinde1, GS Bangale1, Rajesh KS2 and  RSR Murthy2 
1Parul Institute of Pharmacy, Limda, Vadodara-391760, Gujarat, India
2Indo Soviet Friendship College of Pharmacy, Ghalkalan Moga Punjab.
*Corresponding Author:
                    
                    
                        Published In:
                         
                        Volume - 2,     
                                Issue - 2,    
                                Year - 2010
                        
                    
					
					 
						
					
					
				
                 
				
                					
                    
                    
                        ABSTRACT: 
                        In the present work, Orodispersible tablet of Aceclofenac were designed with a view to Enhance patient compliance. A combination of super-disintegrants i.e.Ac-di-sol (Croscarmellose sodium), Polyplasdone XL-10, Microcrystalline Cellulose pH 102 was Used along with directly compressible dextrose to enhance mouth feel. The prepared Batches of tablet were evaluated for hardness, friability, drug content uniformity, wetting time, water absorption ratio and in vitro dispersion time. Based on in vitro dispersion time, two formulation were tested for in vitro drug release pattern (in pH7.4phosphatebuffer), short – term stability at 250C   20C/60% RH, 300C   20C/65% RH, 400C   20C/75% RH for 3 month and drug –excipient interaction (IR Spectroscopy) among the two formulation, the formulation prepared by direct Compression method using Ac-di-sol (croscarmellose sodium) 50mg, Polyplasdone XL- 10 -25mg, Microcrystalline Cellulose pH 102- 25mg was found tobe better formulation  T80% = 5 min. based on in- vitro drug release characteristics. Short term stability studies on the formulation indicated that there is no significant change in drug content and in vitro dispersion time
                    
                    
                    
                 
				
				
                    
                    
                        Cite this article:
                        
                        DG Umalkar, GV Shinde, GS Bangale, Rajesh KS, RSR Murthy. Design and Evaluation of Orodispersible Tablet of Aceclofenac Using Different Superdisintegrants by 23 Factorial Designs. Research J. Pharma. Dosage Forms and Tech. 2010; 2(2):198-203  .
						
						 Cite(Electronic):
						 
						 DG Umalkar, GV Shinde, GS Bangale, Rajesh KS, RSR Murthy. Design and Evaluation of Orodispersible Tablet of Aceclofenac Using Different Superdisintegrants by 23 Factorial Designs. Research J. Pharma. Dosage Forms and Tech. 2010; 2(2):198-203  .   Available on: https://www.rjpdft.com/AbstractView.aspx?PID=2010-2-2-15