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首页> 外文期刊>Journal of Planar Chromatography-Modern TLC: JPC >Simultaneous identification of rutin, chlorogenic acid and gallic acid in Moringa oleifera by densitometric high-performance thin-layer chromatography method
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Simultaneous identification of rutin, chlorogenic acid and gallic acid in Moringa oleifera by densitometric high-performance thin-layer chromatography method

机译:用密度计量高性能薄层色谱法同时鉴定Moringa Oleifera的芦丁,绿原酸和小酸

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摘要

An HPTLC (high-performance thin-layer chromatography) method was carried out to develop a feasible, simple and accurate method for the estimation of exact concentration of flavonoids in Moringa oleifera. The simultaneous determination of rutin, chlorogenic acid, and gallic acid extracted from different parts (leaf, stem, flower, and root) of M. oleifera was performed and analysis was carried out on glass-backed plates (10 cm x 20 cm) coated silica gel 60 F-254 (0.2 mm thickness, Merck, Germany) under CAMAG TLC Scanner III with UV densitometrically at lambda(max) = 254 nm. The mobile phase of ethyl acetate:acetone:water:formic acid with a ratio of 6:3:2:2 (v/v) was used for these flavonoids. The findings of HPTLC gave sharp, symmetrical and well-resolved peaks at Rf values of 0.51 +/- 0.02, 0.72 +/- 0.04 and 0.83 +/- 0.03 with linearity ranging 100-700 ng/spot (r(2) = 0.9989), (r(2) = 0.9992), and (r(2) = 0.9984) for rutin (0.066 +/- 0.003%), chlorogenic acid (0.033 +/- 0.005%), and gallic acid (0.031 +/- 0.005%), respectively. The developed method can also be used as a platform for estimation of complex bioactive(s) bio-synthesized in medicinal or aromatic plants.
机译:进行了HPTLC(高性能薄层色谱)方法,以制定可行,简单准确的方法,用于估计Moringa Oleifera的精确浓度的黄酮类化合物。在玻璃背板(10cm×20cm)涂覆的玻璃背衬板(10cm×20cm)上进行了从不同部件(叶,茎,花和根)中萃取的不同部件(叶,茎,花和根)中萃取的芦丁,绿原酸和无碱酸,分析在Camag TLC扫描仪III下,硅胶60 F-254(0.2毫米厚度,德国),紫外线在Lambda(Max)= 254nm处。乙酸乙酯的流动相:丙酮:水:比例为6:3:2:2(v / v)的甲酸用于这些黄酮醇。 HPTLC的发现在射频值为0.51 +/- 0.02,0.72 +/- 0.04和0.83 +/- 0.03的RF值下进行了尖锐,对称和良好的峰,线性度范围为100-700 ng /斑点(R(2)= 0.9989 ),(R(2)= 0.9992),(R(2)= 0.9984)用于芦丁(0.066 +/- 0.003%),绿原酸(0.033 +/- 0.005%)和无碱酸(0.031 +/-分别0.005%)。开发方法也可用作估计在药用或芳族植物中的复杂生物活性的复杂生物活性的平台。

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