Claes P J, Busson R, Vanderhaeghe H
J Chromatogr. 1984 Aug 31;298(3):445-57. doi: 10.1016/s0021-9673(01)92742-6.
Commercial samples of gentamicin from different origins were analyzed by paired-ion high-performance liquid chromatography (HPLC) on a C18 bonded phase. The procedure uses pre-column derivatization with a omicron-phthalaldehyde-mercaptoacetic acid reagent and UV detection (350 nm). The ratios of the four gentamicin components (C1, C1a, C2a and C2) were determined and compared with the compositions obtained by an independent method based on 13C NMR spectrometry. Quantitation by HPLC, based on peak heights and peak areas, was performed with the aid of an external standard, which was an artificial mixture of the four components. The latter were prepared by separation of the gentamicins C1, C2 + C2a and C1a by chromatography on silica gel, followed by chromatography of the C2 + C2a fraction on a cellulose phosphate column.
采用C18键合相的离子对高效液相色谱法(HPLC)对不同来源的庆大霉素商业样品进行分析。该方法采用邻苯二甲醛-巯基乙酸试剂进行柱前衍生化,并采用紫外检测(350nm)。测定了四种庆大霉素组分(C1、C1a、C2a和C2)的比例,并与基于13C NMR光谱法的独立方法获得的组成进行比较。借助外标(四种组分的人工混合物),基于峰高和峰面积通过HPLC进行定量。后者是通过硅胶柱色谱分离庆大霉素C1、C2 + C2a和C1a,然后在磷酸纤维素柱上对C2 + C2a馏分进行色谱分离制备而成。