DEVELOPMENT AND VALIDATION OF A LIQUID CHROMATOGRAPHY METHOD FOR THE DETERMINATION OF METHYL SALICYLATE IN A MEDICATED CREAM FORMULATION
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Original Article
P: 117-126
August 2011

DEVELOPMENT AND VALIDATION OF A LIQUID CHROMATOGRAPHY METHOD FOR THE DETERMINATION OF METHYL SALICYLATE IN A MEDICATED CREAM FORMULATION

Turk J Pharm Sci 2011;8(2):117-126
1. Oxford Brookes University, School Of Life Sciences, Oxford, Ox3 0Bp, Uk
No information available.
No information available
Received Date: 22.10.2009
Accepted Date: 25.02.2010
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ABSTRACT

A new reversed-phase liquid chromatographic (RPLC) method for the determination of methyl salicylate in a medicated cream formulation was developed and validated. The separation was achieved using an isocratic mobile phase, on a Lichrosorb C8 column. The eluent was monitored by photodiode array detection at 304 nm. The calibration curve showed excellent linearity (R2 = 0.9999) over the concentration range of 25-175 ug/mL. The recovery of methyl salicylate was in the range from 99.78100.0%. The percent relative standard deviation values for intra- and inter-day precision studies were <2.0%. The method is very simple, sensitive and robust with short runtime (<3.0 min) to enable the processing of numerous quality control samples.

Keywords:
Methyl salicylate, Reversed-phase LC, Method validation, Medicated cream formulation