Merck & Co., Inc., ACDS-Supply Analytical Sciences, 1011 Morris Avenue, Union, NJ 07083, USA.
J Pharm Biomed Anal. 2011 Jan 5;54(1):242-7. doi: 10.1016/j.jpba.2010.08.003. Epub 2010 Aug 13.
Currently, there are no analytical methods available in the literature that can simultaneously separate and quantitate residual levels of acetone, methylene chloride, n-butyl ether and dimethylsulfoxide in Betamethasone valerate active pharmaceutical ingredient (API). This paper describes the development and validation of a simple, efficient, accurate and robust static headspace gas chromatography method for the determination of high and low boiling residual solvents, namely acetone, methylene chloride, n-butyl ether and dimethylsulfoxide, in Betamethasone valerate API. This method has been demonstrated to be accurate, linear, precise, reproducible, specific and robust for its intended purpose. Quantitation limits (QL) for acetone, methylene chloride and n-butyl ether are 20 ppm (20 μg/g of API) and 50 ppm (50 μg/g of API) for dimethylsulfoxide. Several other APIs (Loratadine and a few other corticosteroid compounds) were analyzed using the conditions of this method to evaluate and assess the versatility of this method for the purpose of residual solvents analysis for a wide range of APIs. The results of this evaluation strongly indicates that this method can be readily used (as-is or with minor modifications) to determine both low and high boiling residual solvents present in a wide range of APIs.
目前,文献中尚无可用的分析方法可同时分离和定量测定倍他米松戊酸酯原料药(API)中残留的丙酮、二氯甲烷、正丁醚和二甲基亚砜的水平。本文描述了一种简单、高效、准确和稳健的静态顶空气相色谱法的开发和验证,用于测定高沸点和低沸点残留溶剂,即丙酮、二氯甲烷、正丁醚和二甲基亚砜,在倍他米松戊酸酯 API 中的残留水平。该方法已被证明准确、线性、精密、重现、专属性和稳健,适用于其预期用途。丙酮、二氯甲烷和正丁醚的定量限(QL)为 20 ppm(API 中的 20 μg/g),二甲基亚砜为 50 ppm(API 中的 50 μg/g)。使用该方法的条件分析了其他几种 API(氯雷他定和几种其他皮质类固醇化合物),以评估和评估该方法在广泛的 API 残留溶剂分析中的多功能性。该评估的结果强烈表明,该方法可以直接(原样或稍作修改)用于测定广泛的 API 中存在的高低沸点残留溶剂。