Hadad Ghada M, Badr Jihan M, El-Nahriry Khaled, Hassanean Hashem A
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, University of Suez Canal, Ismailia 41522, Egypt.
J Chromatogr Sci. 2013 Mar;51(3):258-65. doi: 10.1093/chromsci/bms135. Epub 2012 Aug 21.
The present work describes validated high-performance liquid chromatography (HPLC) and high-performance thin-layer chromatography (HPTLC) methods for the simultaneous determination of colchicine and khellin. The isocratic reversed-phase HPLC separation was performed on a 5 µm C18 column (Luna, Phenomenex, Torrance, CA). Good resolution between colchicine and khellin was achieved using a mixture of acetonitrile-10 mM NaH(2)PO(4) (pH 3.0, 35:65 v/v) as a mobile phase. Quantitation was achieved with ultraviolet detection at 245 nm based on peak area. The HPTLC separation was conducted on Merck HPTLC aluminum sheets of silica gel 60 F254 as stationary phase using methylene chloride-methanol (95:5 v/v) as a mobile phase. Quantification was also achieved using densitometric measurements at 245 nm. Both methods revealed reasonable validation parameters concerning selectivity, linearity, accuracy, precision and limits of detection and quantitation.
本研究描述了用于同时测定秋水仙碱和凯林的经过验证的高效液相色谱(HPLC)和高效薄层色谱(HPTLC)方法。等度反相HPLC分离在5 µm C18柱(Luna,Phenomenex,托伦斯,加利福尼亚州)上进行。使用乙腈-10 mM NaH₂PO₄(pH 3.0,35:65 v/v)的混合物作为流动相,秋水仙碱和凯林之间实现了良好的分离度。基于峰面积,在245 nm处通过紫外检测进行定量。HPTLC分离在默克硅胶60 F254 HPTLC铝板上进行,以二氯甲烷-甲醇(95:5 v/v)作为流动相作为固定相。也使用245 nm处的光密度测量进行定量。两种方法在选择性、线性、准确性、精密度以及检测限和定量限方面均显示出合理的验证参数。