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用于测定头孢噻吩的光度提取法。

Photometric extraction method for determination of cefalotin.

作者信息

Papazova P, Bontchev P R, Kacarova M

出版信息

Pharmazie. 1977 Aug-Sep;32(8-9):486-8.

PMID:594112
Abstract

A selective, accurate and precise photometric method for the determination of cefalotin (1) is proposed. The method is based on a preliminary hydrolysis of the antibiotic in a strong sulphuric acid medium at 100 degrees C for 15 min. The 2-thienylacetic acid (2) formed as degradation product is determined photometrically with ninhydrin in strongly acidic solution. In these conditions 2 forms a yellow reaction product, which is extracted with chloroform and the absorbance measured at 423 nm. The reaction is practically specific as none of the initial substances used in the preparation of cefalotin or of its degradation products (except 2) reacts with ninhydrin under these conditions. The only other antibiotic which also gives a coloured product with ninhydrin in this strongly acidic medium is cefalexin. The latter however does not interfere at its coloured product absorbs at 520 nm. The method is simple, fast and with sufficient accuracy and precision (coefficient of variation 0,57--0,88% and relative error 0,41--0,64%).

摘要

提出了一种用于测定头孢噻吩(1)的选择性、准确且精密的光度法。该方法基于抗生素在100℃的浓硫酸介质中初步水解15分钟。将形成的降解产物2-噻吩乙酸(2)在强酸性溶液中用茚三酮进行光度测定。在这些条件下,2形成黄色反应产物,用氯仿萃取并在423nm处测量吸光度。该反应具有实际特异性,因为在这些条件下制备头孢噻吩所用的初始物质或其降解产物(除2外)均不与茚三酮反应。在这种强酸性介质中也能与茚三酮产生有色产物的唯一其他抗生素是头孢氨苄。然而,后者不产生干扰,因为其有色产物在520nm处有吸收。该方法简单、快速,具有足够的准确度和精密度(变异系数为0.57 - 0.88%,相对误差为0.41 - 0.64%)。

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