首页> 外文期刊>Journal of Planar Chromatography-Modern TLC: JPC >A validated, rapid and cost-efficient HPTLC method for the quantification of plumbagin and its antioxidant activity from the different extracts of Plumbago zeylanica L.
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A validated, rapid and cost-efficient HPTLC method for the quantification of plumbagin and its antioxidant activity from the different extracts of Plumbago zeylanica L.

机译:一种验证,快速且经济高效的HPTLC方法,用于量化朱米氧甘糖蛋白L的不同提取物的肠球素及其抗氧化活性。

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摘要

In the present work, a simple, rapid, reliable and accessible high-performance thin-layer chromatography (HPTLC) technique has been established for the concurrent quantification of plumbagin. The well-known medicinal plant, Plumbago zeylanica L., has been traditionally used to treat a variety of ailments in India and other countries. Chromatographic separation was conceded on pre-coated silica gel plates F-254. The apposite mobile phase toluene-acetic acid (9.0:0.5, V/V) was developed to expand the plates which separated components according to the marker compounds. Densitometric scanning was performed by CAMAG Scanner V and measured at wavelength 272 nm. The marker compounds were practically resolved with R-F 0.44 +/- 0.02 for plumbagin. Further, the antioxidant potential of the methanolic extract of P. zeylanica was also assessed with 1,1-diphenyl-2-picrylhydrazyl (DPPH) by using an ultraviolet (UV) spectrophotometer. The percentage inhibition of free radical was found to be 76.5%. The developed HPTLC method was validated for accuracy, linearity, precision and specificity. The extract has revealed considerable antioxidant activity. The reported existing phenolic and flavonoids compounds are responsible for the antioxidant activity of the plant extract as reported in the literature.
机译:本研究建立了一种简便、快速、可靠、易获得的高效薄层色谱法(HPTLC)同时定量白花丹素。著名的药用植物白花丹在印度和其他国家传统上用于治疗各种疾病。在预涂硅胶板F-254上进行色谱分离。建立了合适的流动相甲苯-乙酸(9.0:0.5,V/V)扩展板,根据标记化合物分离组分。密度扫描由CAMAG扫描仪V进行,并在272nm波长下测量。标记化合物的R-F值为0.44+/-0.02,对铅巴金几乎是解析的。此外,还使用紫外(UV)分光光度计,用1,1-二苯基-2-吡啶酰肼(DPPH)评估了泽兰草甲醇提取物的抗氧化潜力。自由基抑制率为76.5%。对所建立的HPTLC方法的准确性、线性、精密度和特异性进行了验证。提取物显示出相当强的抗氧化活性。据文献报道,现有的酚类和黄酮类化合物对植物提取物的抗氧化活性起作用。

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