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商业制剂及非常规胶束体系中孕酮的测定

Determination of progesterone in commercial formulations and in non conventional micellar systems.

作者信息

Pucci Vincenzo, Bugamelli Francesca, Mandrioli Roberto, Luppi Barbara, Raggi Maria Augusta

机构信息

Department of Pharmaceutical Sciences, University of Bologna, Via Belmeloro 6, Bologna, Italy.

出版信息

J Pharm Biomed Anal. 2003 Jan 1;30(5):1549-59. doi: 10.1016/s0731-7085(02)00547-2.

Abstract

Progesterone was determined in commercial pharmaceutical formulations and experimental micellar systems by means of two analytical methods based on liquid chromatography and derivative spectrophotometry. The chromatographic analysis, with ultraviolet detection at 245 nm, was carried out on a C8 column using a mobile phase composed of 2-propanol and a pH 2.5, 30 mM phosphate buffer. Derivative spectrophotometry (DS) used the difference between the values of the first derivative at 227.2 and 253.6 nm. Both methods require only a simple extraction procedure of progesterone from the formulations before analysis. The high-performance liquid chromatography (HPLC) procedure allows for the quantitative determination of progesterone in all pharmaceutical formulations tested (oily and alcoholic injectable solutions, gel preparations and soft capsules) and also of the newly-developed polymeric micellar system. On the contrary, the derivative spectrophotometric method is not suitable for the pharmaceutical formulation containing estradiol and for the new micellar systems. The results obtained with the two methods are in good agreement and always satisfactory in terms of precision and accuracy.

摘要

采用基于液相色谱和导数分光光度法的两种分析方法,对市售药物制剂和实验性胶束体系中的孕酮进行了测定。在C8柱上进行色谱分析,以2 - 丙醇和pH值为2.5、30 mM的磷酸盐缓冲液组成的流动相,于245 nm处进行紫外检测。导数分光光度法(DS)利用227.2和253.6 nm处一阶导数的值之差。两种方法在分析前仅需对制剂中的孕酮进行简单提取。高效液相色谱(HPLC)方法可对所有测试的药物制剂(油性和酒精性注射溶液、凝胶制剂和软胶囊)以及新开发的聚合物胶束体系中的孕酮进行定量测定。相反,导数分光光度法不适用于含雌二醇的药物制剂和新的胶束体系。两种方法所得结果吻合良好,在精密度和准确度方面均令人满意。

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