1Professor, Dept. of Quality Assurance, AISSMS College of Pharmacy, Maharashtra
2Research Student, Dept. of Quality Assurance, AISSMS College of Pharmacy, Maharashtra
3Associate Professor, Dept. of Pharmacology, AISSMS College of Pharmacy, Maharashtra
*Corresponding Author: Email: santoshvgandhi@rediffmail.com
Online published on 19 September, 2016.
The present work was done to evaluate pharmacokinetic parameters of ritonavir standard, ritonavir crystallo co agglomerates and marketed formulation of ritonavir. The aim of formulation of Ritonavir crystallo co agglomerates was immediate drug release and solubility enhancement. The analysis was carried out by HPLC. The parameters evaluated were Cmax, Tmax, area under curve (AUC 0-t, AUC 0-∞), t1/2, k elimination (ke).
Ritonavir, Pharmacokinetic study, HPLC, Crystallo co agglomerates