首页> 外文期刊>Journal of separation science. >Isolation and purification of acetylshikonin and beta-acetoxyisovalerylshikonin from cell suspension cultures of Arnebia euchroma (Royle) Johnston using rapid preparative HPLC
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Isolation and purification of acetylshikonin and beta-acetoxyisovalerylshikonin from cell suspension cultures of Arnebia euchroma (Royle) Johnston using rapid preparative HPLC

机译:使用快速制备型HPLC从紫草(Royle)Johnston的细胞悬浮培养物中分离和纯化乙酰基紫草素和β-乙酰氧基异戊基紫草素

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摘要

Shikonin and its derivatives are important red colored naphthoquinone pigments found in a large number of Arnebia species, including A. euchroma, that are responsible for the various pharmacological activities exhibited by the plant. The precise separation of each naphthoquinone is essential for total quality evaluation and bioactivity analysis of herbal formulations of A. euchroma. Furthermore, the overexploitation of this useful plant has resulted in species becoming endangered. With this in mind, a simple and rapid preparative scale HPLC method with single compound recovery for the isolation and purification of two shikonin derivatives (i.e. acetylshikonin, (beta-acetoxyisovalerylshikonin) from cell suspension cultures of A. euchroma is presented. The compounds were separated on a C-18 column within 10 min using acetonitrile/methanol (95:5) as mobile phase in isocratic mode. The isolated compounds were found to be more than 98% pure. The LOD for acetylshikonin and (beta-acetoxyisovalerylshikonin was estimated at 0.063 and 0.146 mu g/mL, respectively, while the LOQ was found to be 0.209 and 0.487 mu g/mL, respectively. The recoveries accomplished for both the shikonin derivatives were in the range of 94.7-96.8%. The repeatability, expressed as %RSD, of acetylshikonin and beta-acetoxyisovalerylshikonin was found to be 1.74 and 1.27, respectively.
机译:紫草素及其衍生物是重要的红色萘醌颜料,存在于许多紫草属物种中,包括常绿拟南芥,它们负责植物表现出的各种药理活性。每个萘醌的精确分离对于常绿拟南芥草药制剂的总体质量评估和生物活性分析至关重要。此外,这种有用植物的过度开发导致物种濒临灭绝。考虑到这一点,提出了一种简单快速的制备规模的高效液相色谱方法,该方法具有单一化合物的回收率,用于从常绿假单胞菌的细胞悬浮培养物中分离和纯化两种紫草素衍生物(即乙酰紫草素,(β-乙酰氧基异戊基紫草素))。用乙腈/甲醇(95:5)作为流动相,在等速模式下于10分钟内在C-18柱上分离,发现分离出的化合物纯度超过98%,乙酰基紫草素和(β-乙酰氧基异戊基紫草素)的LOD估计为定量值分别为0.063和0.146μg / mL,而定量限分别为0.209和0.487μg/ mL,两种紫草素衍生物的回收率在94.7-96.8%之间。发现乙酰基紫草素和β-乙酰氧基异戊基紫草素的%RSD分别为1.74和1.27。

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