RP-HPLC Method Development and Validation of Stanzolol for Analysis of Tablets Dosage form

Abstract

simple, selective, linear, precise and accurate RP-HPLC method was developed and validated for rapid assay of Stanzolol in tablet dosage form. Isocratic elution at a flow rate of 1.0ml/min was employed on a symmetry C18 (250×4.6mm, 5μm in particle size) at ambient temperature. The mobile phase consisted of Methanol: water in the ratio of 90:10 v/v. The UV detection wavelength was 210 nm and 20μl sample was injected. The retention time for Stanzolol was 4.09min. The percentage RSD for precision and accuracy of the method was found to be less than 2%. The method was validated as per the ICH guidelines. The method was successfully applied for routine analysis of Stanzolol in tablet dosage form.

Issue

2011 Volume-01

Article Subject

Pharmacy

Keywords

Stanzolol, RP-HPLC, UV detection, recovery, precise, 210 nm

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