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首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Single-Lab Validation for Determination of Kavalactones and Flavokavains in Piper methysticum (Kava)
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Single-Lab Validation for Determination of Kavalactones and Flavokavains in Piper methysticum (Kava)

机译:用于测定哌啶萘酮和哌瓦西病的单纯实验室验证(Kava)

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摘要

Piper methysticum (Kava) is a plant whose roots are used in the preparation of traditional beverages with spiritual, medicinal, and social importance for the Pacific Islanders. Kava is also sold as a herbal supplement or recreational beverage consumed for its mild inebriating effect in Europe and North America. With an ongoing interest in the safety and quality of kava products, it is necessary to develop a validated method for determination of kava chemical composition to ensure confidence in quality assessment. Thus, an high-performance liquid chromatography with ultraviolet detection (HPLC-UV) method was developed, optimized, and validated for determining six major kavalactones and three flavokavains in kava raw materials and finished products based on AOAC single-laboratory validation guidelines. This is the first fully validated analytical method for measuring kavalactones and flavokavains in a single run. The separation of the analytes was achieved in 10min with an Agilent Poroshell C18 column using gradient separation. The sample was extracted with methanol first and then acetone. The signals were detected at 240nm and 355nm. The limit of quantification was under 1.2 mu g/mL (0.3mg/g) for kavalactones and under 0.35 mu g/mL (0.01mg/g) for flavokavains. The Horwitz ratio values described ranged from 0.3 to 1.82. The spike recovery experiments showed an accuracy between 92 and 105% for all analytes. The results of the study demonstrate that the method is fit for the purpose of determining methysticin, dihydromethysticin, kavain, dihydrokavain, yangonin, desmethoxyyangonin, flavokavain A, flavokavain B, and flavokavain C in kava raw material and finished products (dry-filled capsule, liquid phytocaps, and tincture).
机译:吹笛者甲状腺(Kava)是一种植物,其根源用于制备具有精神,药用,社会重要性的传统饮料,对太平洋岛民进行精神,药用和社会重要性。 Kava还作为其在欧洲和北美的温和醉酒效果消耗的草药补充剂或娱乐饮料。随着Kava产品的安全和质量的持续兴趣,有必要开发验证的方法,以确定Kava化学组合物,以确保对质量评估的信心。因此,开发,优化,验证了具有紫外检测(HPLC-UV)方法的高性能液相色谱法,并验证了基于AOAC单实验室验证指南的Kava原料和成品中的六个主要的kavalactones和三种血管活体。这是第一种全验证的分析方法,用于在一次运行中测量kavalactones和黄基石。使用梯度分离,10min在10m​​in中实现分析物的分离。首先用甲醇萃取样品,然后用丙酮萃取。信号在240nm和355nm处检测到。量化限制为kavalactones的1.2μmg/ ml(0.3mg / g),对于黄基石,kavalactones和0.35μmg/ ml(0.01mg / g)下。 Horlwitz比值范围为0.3至1.82。尖峰恢复实验显示所有分析物的92和105%之间的精度。研究结果表明,该方法适用于测定甲状霉素,二氢甲基菌,Kavain,Dihydrokavain,Yangonin,Desmethavain A,Flavokavain B和黄酮蛋白C中的方法(在Kava原料和成品中(干燥填充胶囊)的目的液体植物和酊剂)。

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