Siegel M M, Mills R, Gehrlein L, Gore W E, Morton G, Chang T, Cosulich D, Medwid J, Mirando P
J Pharm Sci. 1984 Apr;73(4):498-501. doi: 10.1002/jps.2600730417.
Piperacillin amide (IV) was successfully identified as the predominant impurity in commercial lots of piperacillin monohydrate (III). The impurity was isolated via a preparative liquid chromatographic scheme utilizing Florisil as the adsorbent and a mobile phase of water-acetonitrile (4:96, v/v). The isolated component had nearly the same reverse-phase HPLC properties as piperacillin and was chemically and thermally unstable. This labile impurity was spectroscopically identified by field desorption (FD), fast atom bombardment (FAB) with collision activation decomposition (CAD), and desorption chemical ionization (DCI) mass spectrometries , and NMR and IR spectrometries . Identity was confirmed on comparison of the chromatographic and spectrometric data of the impurity with an independently synthesized sample of piperacillin amide.
哌拉西林酰胺(IV)被成功鉴定为市售一水合哌拉西林(III)批次中的主要杂质。通过以弗罗里硅土为吸附剂、水 - 乙腈(4:96,v/v)为流动相的制备液相色谱方案分离出该杂质。分离出的组分具有与哌拉西林几乎相同的反相高效液相色谱性质,并且化学和热不稳定。通过场解吸(FD)、带有碰撞活化分解(CAD)的快原子轰击(FAB)以及解吸化学电离(DCI)质谱法,以及核磁共振和红外光谱法对这种不稳定杂质进行了光谱鉴定。通过将该杂质的色谱和光谱数据与独立合成的哌拉西林酰胺样品进行比较,确认了其身份。