Development and Validation of RP-HPLC Method for Analysis of Novel Self-emulsifying Paclitaxel Formulation

A stability indicating liquid chromatography method was developed and validated for quantitation of aliquots of the in-vitro drug release and ex-vivo permeation study for paclitaxel in a new pharmaceutical dosage form. The reverse phase high performance liquid chromatography separation was achieved on C18 LiChrospher100 (250x4.6mm, 5 μm particle size… CONTINUE READING