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含弹性蛋白酶抑制剂DMP 777的胶囊制剂中一种降解产物的分离与鉴定。

Isolation and identification of a degradation product in a capsule formulation containing the elastase inhibitor, DMP 777.

作者信息

Buckley D, Haas M J, Scholz T H, Sigvardson K W

机构信息

The DuPont Pharmaceuticals Company, Wilmington, DE 19880, USA.

出版信息

J Pharm Biomed Anal. 2001 Feb;24(4):651-7. doi: 10.1016/s0731-7085(00)00461-1.

Abstract

An unexpected degradation product, greater than 0.10%, was observed in a DMP 777 capsule formulation stored at 40 degrees C/75% r.h. for 3 months and 25 degrees C/60% r.h. for 2 years. The degradant of interest was prepared in quantity by refluxing the drug substance in dilute acid. A preparative HPLC method was developed to separate the various degradants and to collect each as a separate fraction. Each fraction was analyzed by the analytical HPLC gradient test method to assure positive identification of each peak and to correlate each peak to the original capsule sample. Key isolated degradation products were used for structure elucidation with mass spectrometry and NMR. The major degradant of interest in the capsule formulation was found to be a carboxylic acid resulting from the acid hydrolysis of an amide bond.

摘要

在DMP 777胶囊制剂中,于40摄氏度/相对湿度75%下储存3个月以及在25摄氏度/相对湿度60%下储存2年后,观察到一种含量超过0.10%的意外降解产物。通过在稀酸中回流原料药来大量制备感兴趣的降解产物。开发了一种制备型高效液相色谱方法来分离各种降解产物,并将每种降解产物作为单独的馏分收集。通过分析型高效液相色谱梯度测试方法对每个馏分进行分析,以确保对每个峰进行阳性鉴定,并将每个峰与原始胶囊样品相关联。关键的分离降解产物用于通过质谱和核磁共振进行结构解析。发现该胶囊制剂中感兴趣的主要降解产物是酰胺键酸水解产生的羧酸。

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