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首页> 外文期刊>International journal of analytical chemistry >Rapid Screening for FlavoneC-Glycosides in the Leaves of Different Species of Bamboo and Simultaneous Quantitation of Four Marker Compounds by HPLC-UV/DAD
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Rapid Screening for FlavoneC-Glycosides in the Leaves of Different Species of Bamboo and Simultaneous Quantitation of Four Marker Compounds by HPLC-UV/DAD

机译:HPLC-UV / DAD快速筛选不同种类竹叶中的黄酮C-糖苷并同时定量四种标记化合物

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A strategy for analyzing flavoneC-glucosides in the leaves of different species of bamboo was developed. Firstly, the flavoneC-glycosides were extracted from the bamboo leaves (51 species in 17 genera) with methanol and chromatographed on silica gel 60 plates in automatic developing chamber (ADC2), and a qualitative survey using simple derivatization steps with the NP reagent was carried out. The flavoneC-glycosides were found in 40 of 51 species of bamboo examined. Secondly, an HPLC method with photodiode array and multiple wavelength detector was optimized and validated for the simultaneous determination of flavoneC-glycosides, including isoorientin, isovitexin, orientin, and vitexin in the leaves of three species of bamboo and the flavoneC-glycosides were confirmed by LC/MS. The optimized HPLC method proved to be linear in the concentration range tested (0.2–100 μg/mL,r2≥0.9997), precise (RSD≤1.56%), and accurate (88–106%). The concentration ranges of isoorientin, isovitexin, orientin, and vitexin in three bamboo leaves samples were 1.00–2.78, 0–0.31, 0–0.07, and 0.20–0.68 mg/g, respectively. The proposed method was validated to be simple and reliable and can be a tool for quality control of bamboo leaf extract or its commercial products.
机译:提出了一种分析不同种类竹叶中黄酮C-葡萄糖苷的策略。首先,用甲醇从竹叶(17属的51种)中提取黄酮C-糖苷,并在自动显影室(ADC2)中的硅胶60板上色谱分离,并使用NP试剂通过简单的衍生化步骤进行了定性研究。出来。在所检查的51种竹子中的40种中发现了黄酮C-糖苷。其次,对光电二极管阵列和多波长检测器的高效液相色谱法进行了优化和验证,以同时测定三种竹叶中的异黄酮,异维石素,Orientin和Vitexin等黄酮C-糖苷。 LC / MS。经优化的高效液相色谱方法在所测试的浓度范围内(0.2–100μg / mL,r2≥0.9997)是线性的,精确的(RSD≤1.56%),准确的(88–106%)。在三个竹叶样品中异Orientin,Isovititexin,Orientin和Vitexin的浓度范围分别为1.00–2.78、0–0.31、0–0.07和0.20–0.68μmg / g。该方法经验证简单,可靠,可作为竹叶提取物或其商品质量控制的工具。

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