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A validated stability-indicating TLC-densitometric method for the determination of stanozolol in pharmaceutical formulations

机译:经验证的稳定性指示薄层色谱-光密度法测定药物制剂中的康力龙

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摘要

BackgroundStanozolol is a synthetic derivative of dihydrotestosterone (DHT), and one of the frequently detected anabolic steroids in doping analysis. The current work describes the development and validation of the stability-indicating TLC-densitometric method for sensitive and specific estimation of stanozolol even its degradation product being there. Precoated silica gel TLC aluminium plates were utilized as the stationary phase and the eluent comprised of petroleum ether: acetone (6:4, v/v). Densitometric analysis of stanozolol was achieved at λmax 750 nm in the absorbance mode after staining with phosphomolybdic acid (PMA). Stress degradation of stanozolol was carried out under various reaction conditions including acid, base and neutral hydrolysis, wet and dry heating treatment, oxidation, and photo-degradation. Resulted stress samples and pharmaceutical products were analyzed with the developed TLC method.
机译:背景司坦唑醇是二氢睾丸激素(DHT)的合成衍生物,是掺杂分析中经常检测到的合成代谢类固醇之一。当前的工作描述了稳定性指示TLC密度测定方法的开发和验证,该方法用于灵敏和特异的替诺洛尔的估计,即使其中存在降解产物。将预涂的硅胶TLC铝板用作固定相,洗脱液由石油醚:丙酮(6:4,v / v)组成。在用磷钼酸(PMA)染色后,在吸光度模式下的λmax750 nm处进行了甾醇的光密度分析。替诺洛尔的应力降解是在各种反应条件下进行的,包括酸,碱和中性水解,湿法和干法热处理,氧化和光降解。用开发的TLC方法分析所得的应力样品和药品。

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