Development and Validation of an RP-HPLC Method for Estimation of Cefuroxime Axetil and Its Degradation Products in Tablets

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چکیده

The absorbed ester is hydrolyzed in the intestinal mucosa and in portal circulation [3]. Estimation of cefuroxime Axetil has been described by spectrophotometry [3-5], HPTLC [6-8] and HPLC [918]. HPLC methods are available in United State Pharmacopoeia [19] and in British pharmacopoeia [1]. The column in the official methods is Trimethylsilane bonded-phase. The mobile phase consisting of 0.2M ammonium dihyrogen phosphate (23 gm/ litre). In the official methods the buffer concentration is very high and that may be lead to adversely affect on the operation of HPLC system. The buffer may be precipitate in the column and LC system when it is exposed to the highest organic concentration. The backpressure is very high.

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تاریخ انتشار 2016