Taha Elham A, Salama Nahla N, Wang Shudong
National Organization for Drug Control and Research (NODCAR), 6-Abu Hazem Street, Pyramids Ave. P.O. Box 29, 35521 Giza, Egypt.
Anal Chem Insights. 2009 Apr 7;4:1-9. doi: 10.4137/aci.s2274.
Two sensitive and validated methods were developed for determination of a racemic mixture citalopram and its enantiomer S-(+) escitalopram. The first method was based on direct measurement of the intrinsic fluorescence of escitalopram using sodium dodecyl sulfate as micelle enhancer. This was further applied to determine escitalopram in spiked human plasma, as well as in the presence of common and co-administrated drugs. The second method was TLC densitometric based on various chiral selectors was investigated. The optimum TLC conditions were found to be sensitive and selective for identification and quantitative determination of enantiomeric purity of escitalopram in drug substance and drug products. The method can be useful to investigate adulteration of pure isomer with the cheap racemic form.
开发了两种灵敏且经过验证的方法来测定消旋西酞普兰及其对映体S-(+)-艾司西酞普兰。第一种方法基于使用十二烷基硫酸钠作为胶束增强剂直接测量艾司西酞普兰的固有荧光。该方法进一步应用于测定加标人血浆中的艾司西酞普兰,以及在常见和共同给药药物存在的情况下的艾司西酞普兰。第二种方法是基于各种手性选择剂的薄层色谱光密度法。发现最佳薄层色谱条件对于原料药和药品中艾司西酞普兰对映体纯度的鉴定和定量测定灵敏且具有选择性。该方法可用于研究纯异构体与廉价消旋体形式的掺假情况。