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采用HPLC联用技术鉴定雷贝拉唑钠加速试验片的降解产物。

Identification of degradation products in stressed tablets of Rabeprazole sodium by HPLC-hyphenated techniques.

作者信息

Vasu Dev R, Sai Uday Kiran G, Venkata Subbaiah B, Suresh Babu B, Moses Babu J, Dubey P K, Vyas K

机构信息

Analytical Research, Discovery Research, Dr. Reddy's Laboratories Ltd., Miyapur, Hyderabad 500 049, India.

出版信息

Magn Reson Chem. 2009 May;47(5):443-8. doi: 10.1002/mrc.2404.

Abstract

Three unknown impurities of Rabeprazole, a proton pump inhibitor, were formed in the formulated drug under the stress conditions, [40 degrees C/75% relative humidity (RH) for 6 months] with relative retention times (RRTs) 0.17, 0.22 and 0.28. The Impurity-I (0.17 RRT) was isolated using preparative HPLC and characterized by NMR and MS. The other two impurities, Impurity-II (RRT 0.22) and Impurity-III (RRT 0.28) could not be isolated, hence they are characterized by HPLC-hyphenated techniques, LC-NMR and high-resolution LC-MS. On the basis of the spectral data, the Impurity-I, Impurity-II and Impurity-III were characterized as 1-(1H-benzo[d]imidazol-2-yl)-3-methyl-4-oxo-1,4-dihydropyridine-2-carboxylic acid, 1H-benzo [d] imidazole-2-sulfonic acid and 4-(3-methoxy propoxy)-3-methyl-2-pyridine carboxylic acid, respectively.

摘要

质子泵抑制剂雷贝拉唑在加速试验条件下(40℃/75%相对湿度,6个月)的制剂中产生了3种未知杂质,其相对保留时间(RRT)分别为0.17、0.22和0.28。杂质-I(RRT 0.17)通过制备型高效液相色谱法分离,并经核磁共振(NMR)和质谱(MS)表征。另外两种杂质,杂质-II(RRT 0.22)和杂质-III(RRT 0.28)无法分离,因此采用高效液相色谱联用技术、液相色谱-核磁共振(LC-NMR)和高分辨率液相色谱-质谱(LC-MS)对其进行表征。根据光谱数据,杂质-I、杂质-II和杂质-III分别被鉴定为1-(1H-苯并[d]咪唑-2-基)-3-甲基-4-氧代-1,4-二氢吡啶-2-羧酸、1H-苯并[d]咪唑-2-磺酸和4-(3-甲氧基丙氧基)-3-甲基-2-吡啶羧酸。

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