Photodegradation kinetic study and stability-indicating assay of danazol using high-performance liquid chromatography
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A HPLC method was developed to quantify danazol and its photolytic degradation products formed under UV irradiation, determining kinetic parameters of the degradation process.
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Abstract
A selective high-performance liquid chromatographic procedure for the stability-indicating determination of danazol in the presence of its photolytic degradation products is demonstrated. The photolysis was carried out in glass vials and quartz cell under UV light at 254 nm. Satisfactory results were obtained for the assay and recovery testing with RSD values less than 2%. Kinetic parameters evaluated comprise the order of reaction and the rate constants of the degradation of the danazol irradiated in glass vials or quartz cell.
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Cited by (8)
- Development and Validation of Stability Indicating HPLC Method for Estimation of Anti-Gonadotropic Drug Danazol in Bulk and Capsule: Degradation Study Characterization of Alkali Degradation Product and ADME/Tox Evaluation 2025
- Danazol 2022
- Miniaturized ionic liquid dispersive liquid–liquid microextraction in a coupled-syringe system combined with UV for extraction and determination of danazol in danazol capsule and mice serum 2016
- Development and validation of TLC-densitometric method for the quantification of a steroidal drug, danazol in its pharmaceutical formulations 2012
- Lipid-based Formulations for Danazol Containing a Digestible Surfactant, Labrafil M2125CS: In Vivo Bioavailability and Dynamic In Vitro Lipolysis 2008
- Square-wave adsorptive stripping voltammetric determination of danazol in capsules 2006
- Voltammetric study of danazol and its determination in capsules and spiked biological fluids 2004
- Conventional and micellar liquid chromatography method development for danazol and validation in capsules 2003
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