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首页> 外文期刊>Journal of Analytical Methods in Chemistry >Extraction and Bioactivity Analysis of Major Flavones Compounds fromScutellaria baicalensisUsing In Vitro Assay and Online Screening HPLC-ABTS System
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Extraction and Bioactivity Analysis of Major Flavones Compounds fromScutellaria baicalensisUsing In Vitro Assay and Online Screening HPLC-ABTS System

机译:黄ical中主要黄酮类化合物的提取及生物活性的体外测定及在线筛选HPLC-ABTS系统

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The extraction efficiency of a number of solvent compositions for the improvement of bioactive compounds yield fromS. baicalensishas been investigated. Also, free radical scavengers in the glycoside baicalin (BG), wogonoside (WG), aglycon baicalein (B), and wogonin (W) compounds ofS. baicalensiswere screened, identified, and quantified using coupled offline ABTS and online screening HPLC-ABTS assay. Increasing ethanol content fractions resulted in decreased extract yield of bioactive compounds. In this case, the best yield of 37.01 mg/g in BG, WG, B, and W compounds was obtained by a dipping method with an extraction time of 4 h. In addition, the yield (43.05%) and IC50(34.04 μg/mL) determined through ABTS assay of the 60% aqueous ethanol extract were the most satisfactory of all solvent solutions tested. This result shows that an online screening HPLC-ABTS assay can be a powerful technique for the rapid characterization of bioactivity compounds in plant extracts. Moreover, their anti-inflammatory activities were evaluated via analyzed inhibitory effect on NO and inflammatory cytokine production. Furthermore, WG and W exhibited the strong inhibitory effects on inflammatory mediator production including NO, IL-6, and IL-1βin LPS-stimulated RAW 264.7 macrophages.
机译:用于改善生物活性化合物的多种溶剂组合物的萃取效率来自S。黄ical已被调查。此外,S的糖苷黄ical苷(BG),渥脱皂苷(WG),糖苷配基黄ical苷(B)和沃戈宁(W)化合物中的自由基清除剂。使用耦合的离线ABTS和在线筛选HPLC-ABTS分析对黄ical进行筛选,鉴定和定量。乙醇含量分数的增加导致生物活性化合物的提取率降低。在这种情况下,BG,WG,B和W化合物的最佳收率为37.01 mg / g,采用浸没法,萃取时间为4 h。此外,通过ABTS分析测定的60%乙醇水溶液的收率(43.05%)和IC50(34.04μg/ mL)是所有测试的溶剂溶液中最令人满意的。该结果表明,在线筛选HPLC-ABTS分析可能是一种快速表征植物提取物中生物活性化合物的有力技术。此外,通过分析对NO和炎性细胞因子产生的抑制作用来评估它们的抗炎活性。此外,WG和W在LPS刺激的RAW 264.7巨噬细胞中对包括NO,IL-6和IL-1β在内的炎症介质产生具有较强的抑制作用。

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