首页> 外文期刊>The Journal of automatic chemistry >Analytical Method for the Validation of Three Polyphenols as a Marker Compound for the Standardization of Solidago virgaurea subsp. gigantea Extracts and Antiadipogenesis of Harvesting Time and Location
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Analytical Method for the Validation of Three Polyphenols as a Marker Compound for the Standardization of Solidago virgaurea subsp. gigantea Extracts and Antiadipogenesis of Harvesting Time and Location

机译:验证三种多酚作为标记化合物的一种分析方法,用于标准化美国一枝黄花亚种。 gigantea提取物和收获时间和地点的抗脂肪生成

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Protocatechuic acid (PC), chlorogenic acid (CA), and kaempferol-3-O-rutinoside (K-O-R), isolated from the Solidago virgaurea subsp. gigantea (SV) extract, were quickly and efficiently separated using HPLC. Our chromatographic method was found to effectively separate PC, CA, and K-O-R at retention times of 5.36, 8.22, and 17.04?min, respectively. Linearity of PC, CA, and K-O-R was found to be in the range of 4.85–485.00, 47.5–1900.00, and 8.50–850.00?μg/ml. Recoveries ranged between 101.32 and 103.30%, 95.82 and 100.25%, and 96.18 and 99.37%, for PC, CA, and K-O-R, respectively. The antiadipogenesis activity of SV extracts collected from five different months and from seven different regions was evaluated using an Oil Red O staining assay in 3T3-L1 cells. Extract from SV collected in April from the Ulleung Island produced over 106.89% inhibition of adipogenesis without cytotoxicity at 50?μg/ml. This extract had a high amount of PC and K-O-R. The developed HPLC method was found to be fast, accurate, precise, and reproducible and could be applied to qualitative and quantitative analysis of three bioactive compounds in SV extracts. The SV extract collected in April from Ulleung Island can be used as a functional food ingredient preventing obesity.
机译:从儿茶固醇(Silverago virgaurea)亚种中分离得到的原儿茶酸(PC),绿原酸(CA)和山奈酚3-O-芸香苷(K-O-R)使用高效液相色谱快速有效地分离出巨大花(SV)提取物。我们的色谱方法可有效分离PC,CA和K-O-R,保留时间分别为5.36、8.22和17.04?min。 PC,CA和K-O-R的线性范围为4.85–485.00、47.5–1900.00和8.50–850.00?g / ml。 PC,CA和K-O-R的回收率分别为101.32%和103.30%,95.82和100.25%,96.18和99.37%。在3T3-L1细胞中使用油红O染色法评估了从五个不同月份和七个不同区域收集的SV提取物的抗脂肪形成活性。在4月从Ulleung岛收集的SV提取物中,以50?μg/ ml的剂量产生的脂肪生成抑制率超过106.89%,而没有细胞毒性。该提取物具有大量的PC和K-O-R。发现开发的HPLC方法快速,准确,精确且可重现,可用于SV提取物中三种生物活性化合物的定性和定量分析。 4月份从Ulleung岛收集的SV提取物可用作预防肥胖的功能性食品成分。

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