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首页> 外文期刊>Molecules >Simultaneous Ultra Performance Liquid Chromatography Determination and Antioxidant Activity of Linarin, Luteolin, Chlorogenic Acid and Apigenin in Different Parts of Compositae Species
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Simultaneous Ultra Performance Liquid Chromatography Determination and Antioxidant Activity of Linarin, Luteolin, Chlorogenic Acid and Apigenin in Different Parts of Compositae Species

机译:高效液相色谱法同时测定菊科植物不同部位的亚麻脂,木犀草素,绿原酸和芹菜素的抗氧化活性

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摘要

Linarin (LA), luteolin (LE), chlorogenic acid (CA) and apigenin (AP) are four major flavonoids with various promising bioactivities found in Compositae (COP) species. A reliable, reproducible and accurate method for the simultaneous and quantitative determination of these four major flavonoids by Ultra Performance Liquid Chromatography (UPLC) analysis was developed. This method should be appropriate for the quality assurance of COP. The UPLC separation was carried out using an octadecylsilane (ODS) Hypersil (2.1 mm × 250 mm, 1.9 μm) and a mobile phase composed of acetonitrile and 0.1% formic acid in water at a flow rate 0.44 mL/min and ultraviolet (UV) detection 254 nm. Gradient elution was employed. The method was precise, with relative standard deviation below 3.0% and showed excellent linearity (R 2 > 0.999). The recoveries for the four flavonoids in COP were between 95.49%–106.23%. The average contents of LA, LE, CA and AP in different parts (flower, leave and stem) of COP were between 0.64–1.47 g/100 g, 0.66–0.89 g/100 g, 0.32–0.52 g/100 g and 0.16–0.18 g/100 g, respectively. The method was accurate and reproducible and it can provide a quantitative basis for quality control of COP.
机译:亚麻脂(LA),木犀草素(LE),绿原酸(CA)和芹菜素(AP)是四种主要的黄酮类化合物,在菊科(COP)物种中具有多种有希望的生物活性。开发了一种可靠,可重现和准确的方法,可通过超高效液相色谱(UPLC)分析同时定量测定这四种主要类黄酮。此方法应适用于COP的质量保证。使用十八烷基硅烷(ODS)Hypersil(2.1 mm×250 mm,1.9μm)和流动相由乙腈和0.1%甲酸在水中的流动相以0.44 mL / min的流速和紫外线(UV)进行UPLC分离检测254nm。采用梯度洗脱。该方法非常精确,相对标准偏差低于3.0%,并且显示出极好的线性(R 2> 0.999)。 COP中四个类黄酮的回收率在95.49%–106.23%之间。 COP的不同部位(花,叶和茎)中LA,LE,CA和AP的平均含量在0.64至1.47 g / 100 g,0.66至0.89 g / 100 g,0.32至0.52 g / 100 g和0.16之间分别为–0.18 g / 100 g。该方法准确,可重复,可为COP的质量控制提供定量依据。

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