首页> 外文期刊>Journal of Planar Chromatography-Modern TLC: JPC >Densitometric high-performance thin-layer chromatography methods for the quantification of oleuropein in Olea europaea leaves and pharmaceutical preparation utilizing normal- and reversed-phase silica gel plates
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Densitometric high-performance thin-layer chromatography methods for the quantification of oleuropein in Olea europaea leaves and pharmaceutical preparation utilizing normal- and reversed-phase silica gel plates

机译:用于量化Oleuopea在OleaeFopea叶和药物制剂中使用正常和反相硅胶板的致密度高性能薄层色谱法。

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Two validated, simple and precise densitometric high-performance thin-layer chromatography (HPTLC) quantification methods were proposed for both qualitative and quantitative estimation of oleuropein in Olea europaea leaves and a pharmaceutical product utilizing normal-phase and reversed-phase silica gel TLC plates. In method I, 10 x 20 cm glass plates coated with 0.2 mm thin layers of normal-phase silica gel 60 containing F-254 (E-Merck, Germany) and a mixture of ethyl acetate-methanol-water (8:1:0.5, V/V) were used as the stationary and the mobile phase, respectively. Method II utilized 10 x 20 cm glass-backed plates supporting 0.2 mm layers of RP-18 silica gel 60 containing F-254 (E-Merck, Germany) as the stationary phase and green solvents mixture composed of ethanol-water (5.5:4.5, V/V) as the mobile phase. The two methods resulted in sharp, symmetrical, well-resolved peaks at R-F values of 0.47 +/- 0.02 and 0.78 +/- 0.03 with linearity ranges 200-1400 ng/spot (r(2) = 0.9994) and 200-1400 ng/spot (r(2) = 0.9996) for method I and method II, respectively. Spots corresponding to oleuropein were scanned at 200 nm. The two methods complied with the ICH guidelines for validation. Due to simplicity, low cost and short analysis time, the methods can be good alternatives for the quality control of different products containing olive leaves extract or pure oleuropein.
机译:提出了两种经验证的、简单且精确的密度测定高效薄层色谱(HPTLC)定量方法,用于定性和定量估计油橄榄叶中的油苷,以及使用正相和反相硅胶TLC板的医药产品中的油苷。在方法I中,10 x 20 cm的玻璃板涂有0.2 mm薄层的正相硅胶60,含有F-254(德国E-Merck)和乙酸乙酯-甲醇-水(8:1:0.5,V/V)的混合物,分别用作固定相和流动相。方法II使用10 x 20 cm的玻璃支撑板,支撑0.2 mm层的RP-18硅胶60,其中含有F-254(德国E-Merck),作为固定相,绿色溶剂混合物由乙醇-水(5.5:4.5,V/V)组成,作为流动相。这两种方法在方法I和方法II的R-F值分别为0.47+/-0.02和0.78+/-0.03时产生了尖锐、对称、分辨率良好的峰值,线性范围分别为200-1400纳克/点(R(2)=0.9994)和200-1400纳克/点(R(2)=0.9996)。在200 nm处扫描与橄榄苦苷对应的斑点。这两种方法符合ICH的验证指南。由于方法简单、成本低、分析时间短,这些方法可以很好地替代含有橄榄叶提取物或纯橄榄苦苷的不同产品的质量控制。

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