Punukollu  Revathi
	
					    												
India						                            
                            
						
 Research Article
												Self Nanoemulsifying Drug Delivery System of Olanzapine for Enhanced
Oral Bioavailability: In vitro, In vivo Characterisation and In vitro -In vivo
Correlation 						
Author(s): Raman Suresh  Kumar, Urmila Sri  Syamala, Punukollu  Revathi, Punukollu  Revathi, Punukollu  Revathi, Sumanth  Devaki, Pathuri  Raghuveer and Kuppuswamy  GowthamarajanRaman Suresh  Kumar, Urmila Sri  Syamala, Punukollu  Revathi, Punukollu  Revathi, Punukollu  Revathi, Sumanth  Devaki, Pathuri  Raghuveer and Kuppuswamy  Gowthamarajan             
						
												
				 Lipid based self nanoemulsifying drug delivery system (SNEDDS) was explored to improve the oral bioavailability of olanzapine (OLZ), a poorly water-soluble drug candidate, using spontaneous emulsification method. Nanoemulsions have ability to enhance the oral bioavailability of poorly water soluble or lipophilic drugs through selective lymphatic pathways. Following optimization, (from pseudo ternary phase diagram) OLZ SNEDDS consisting of Capryol 90(36.2%), Brij 97(14.6%) and ethanol (42.5%) were selected. The globule size (90 nm), and polydispersity index (0.287), was found to be minimum. The pharmacokinetic study was conducted on rabbits and the parameters like peak concentration (Cmax), time of peak concentration (Tmax), etc. were evaluated by Wagner nelson method. The in vivo studies concluded that there was 1.2 fold and 1.6 fold increase in bioavailability of nanoemulsion when co.. View More»
				  
												DOI:
												 10.4172/jbb.1000159