Ashour Safwan, Al-Khalil Raghad
Department of Chemistry, Faculty of Sciences, Aleppo University, Aleppo, Syria.
Farmaco. 2005 Sep;60(9):771-5. doi: 10.1016/j.farmac.2005.06.007.
Two simple and sensitive extractive spectrophotometric methods have been described for the assay of levofloxacin (LVFX) either in pure form or in pharmaceutical formulations. The developed methods involve formation of colored chloroform extractable ion-pair complexes (1:1 and 1:2 drug/dye) of levofloxacin with bromophenol blue (BPB) and bromocresol green (BCG) in aqueous acidic medium. The extracted complexes showed absorbance maxima at 424 and 428 nm for LVFX-BPB and LVFX-BCG, respectively. Beer's law is obeyed in the concentration ranges 1.85-31.5 and 1.85-25 microg ml(-1) with BPB and BCG, respectively. The methods have been applied to the determination of drug in commercial tablets. Results of analysis were validated statistically. The excipients present in the formulations do not interfere with the assay procedure.
已描述了两种简单且灵敏的萃取分光光度法,用于测定纯形式或药物制剂中的左氧氟沙星(LVFX)。所开发的方法包括在水性酸性介质中,左氧氟沙星与溴酚蓝(BPB)和溴甲酚绿(BCG)形成可被氯仿萃取的有色离子对络合物(药物/染料比例为1:1和1:2)。对于LVFX - BPB和LVFX - BCG,萃取的络合物分别在424和428 nm处显示最大吸光度。使用BPB和BCG时,在浓度范围分别为1.85 - 31.5和1.85 - 25 μg ml(-1)内符合比尔定律。这些方法已应用于市售片剂中药物的测定。分析结果经过统计学验证。制剂中存在的辅料不干扰测定过程。