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首页> 外文期刊>Acta Chromatographica >Characterization and determination of trace alkaloids in seeds extracts from Peganum harmala linn. Using LC-ESI-MS and HPLC
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Characterization and determination of trace alkaloids in seeds extracts from Peganum harmala linn. Using LC-ESI-MS and HPLC

机译:骆驼蓬种子提取物中痕量生物碱的表征和测定。使用LC-ESI-MS和HPLC

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Harmaline and harmine accounted for more than 70% in composition in extracts of P. harmala. More attention, however, should be paid to the other alkaloids which would be favorable or unfavorable to the efficacy and safety of the products. It was necessary to determine these trace alkaloids in the extracts; thereafter, most of them have been characterized. Diglycoside vasicine, vasicine, vasicinone, harmalol, harmol, tetrahydroharmine, 8-hydroxy-harmine, ruine, harmaline, and harmine were separated and identified with reference substances and characteristic MS spectra in extracts by liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) and high-performance liquid chromatography (HPLC). Three trace alkaloids, vasicine, harmalol, and harmol were determined using the developed chromatographic separation method subsequently. The average contents of vasicine, harmalol, and harmol in extracts of ten batches were 2.53 ± 0.73, 0.54 ± 0.19, and 0.077 ± 0.03%, respectively. The total content of the three alkaloids was 3.23 ± 0.90% (from 1.81 to 4.48%). For rough estimation of all the relative alkaloids except of harmaline and harmine, the average total areas of all peaks in extracts varied from 4.35 to 26.64% detected at 220, 254, 265, 280, and 380 nm, respectively. The results indicated that area normalization method was powerless for the quality evaluation for traditional herb medicine consisting of numerous compounds with highly differential features. It might be concluded that LC-MS or HPLC could be utilized as a qualitative and quantitative analytical method for quality control of the extracts from seeds of P. harmala L.
机译:危害程度和危害成分占危害程度的70%以上。但是,应该更多地关注对产品功效和安全性有利或不利的其他生物碱。有必要确定提取物中的这些痕量生物碱。此后,大多数已被表征。液相色谱-电喷雾电离质谱(LC- ESI-MS)和高效液相色谱(HPLC)。随后,使用发达的色谱分离方法测定了三种痕量生物碱,vasicine,harmalol和harmol。十批提取物中的vasicine,harmalol和harmol的平均含量分别为2.53±0.73、0.54±0.19和0.077±0.03%。三种生物碱的总含量为3.23±0.90%(从1.81至4.48%)。为了对除harmaline和harmine外的所有相对生物碱进行粗略估计,提取物中所有峰的平均总面积分别在220、254、265、265、280和380 nm处从4.35%到26.64%不等。结果表明,面积归一化方法对于传统草药的质量评估是无能为力的,而传统草药的特点是具有许多差异很大的化合物。可以得出结论,LC-MS或HPLC可以用作定性和定量分析方法,以控制harmala L.害虫的提取物的质量。

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