Kazemifard A G, Moore D E
College of Pharmacy, University of Tehran, Iran.
J Pharm Biomed Anal. 1997 Dec;16(4):689-96. doi: 10.1016/s0731-7085(97)00089-7.
A sensitive high-performance liquid chromatographic technique with amperometric detection has been developed for the determination of seven commercially used tetracyclines in bulk powders and pharmaceutical preparations. The technique is based on the oxidation of these compounds and their contaminants at the glassy carbon electrode. The extraction procedures are simple and the HPLC conditions separate the tetracyclines from their major degradation products. The chromatography was performed using a commercially available octadecylsilane column, with a mobile phase: KH2 PO4 (pH = 2.5; 0.05 M) - acetonitrile (84:16, v/v) and detection at 1.2 V. The technique permits the simultaneous determination of trace amounts of chlortetracycline, demeclocycline, doxycycline, methacycline, minocycline, oxytetracycline and tetracycline as well as the separation of their common impurities (epi, anhydro and epianhydro contaminants) with detection limits of 0.1-1.0 ng microl(-1) and recoveries of 99.1-100.4%. No interference was observed from the commonly present excipients in pharmaceutical formulations.
已开发出一种采用安培检测的灵敏高效液相色谱技术,用于测定散装粉末和药物制剂中七种商业使用的四环素。该技术基于这些化合物及其污染物在玻碳电极上的氧化。提取程序简单,HPLC条件可将四环素与其主要降解产物分离。使用市售的十八烷基硅烷柱进行色谱分析,流动相为KH2PO4(pH = 2.5;0.05 M)-乙腈(84:16,v/v),检测电压为1.2 V。该技术可同时测定痕量的金霉素、地美环素、多西环素、甲烯土霉素、米诺环素、土霉素和四环素,以及分离它们的常见杂质(表异构、脱水和表异构脱水污染物),检测限为0.1 - 1.0 ng μL-1,回收率为99.1 - 100.4%。未观察到药物制剂中常见辅料的干扰。