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This document details the development and validation of a rapid reversed phase high performance liquid chromatography (RP-HPLC) method for determining Lutein concentration in pharmaceutical dosage forms. The method demonstrated high accuracy, precision, and specificity, with recovery rates between 99.89% and 100.16%, making it suitable for routine quality control analysis. The validation included assessments of selectivity, sensitivity, linearity, and robustness according to ICH guidelines.

Author

victoria riquelme

Language

EN