Validation, Quantification and Stress Degradation Studies of Lenvatinib Mesylate in Bulk Drug and Pharmaceutical Dosage Forms Using Ultra Performance Liquid Chromatography| Chapter 3 | Current Aspects in Pharmaceutical Research and Development Vol.9
The goal of this work was to use UPLC to establish a new method for quantifying Lenvatinib mesylate in bulk drug and pharmaceutical dose form, as well as to validate the method and conduct stress degradation experiments on the drug. UPLC HSS C18 (100 mm x 2.1mm, 1.8m) column,...
Read More