Karioti Anastasia, Timoteo Patricia, Bergonzi Maria Camilla, Bilia Anna Rita
Department of Chemistry, Building of Pharmaceutical Sciences, University of Florence, Sesto Fiorentino (FI), Firenze, Italy.
Department of Pharmacognosy-Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Planta Med. 2017 Oct;83(14-15):1207-1213. doi: 10.1055/s-0043-113827. Epub 2017 Jun 26.
is a herbal drug of Asian traditional medicine largely employed for the treatment of several diseases. Recently, it has been introduced in Europe for the prophylactic and symptomatic treatment of common cold and as an ingredient of dietary supplements. The active principles are diterpenes with andrographolide as the main representative. In the present study, an analytical protocol was developed for the determination of the main constituents in the herb and preparations of . Three different extraction protocols (methanol extraction using a modified Soxhlet procedure, maceration under ultrasonication, and decoction) were tested. Ultrasonication achieved the highest content of analytes. HPLC conditions were optimized in terms of solvent mixtures, time course, and temperature. A reversed phase C18 column eluted with a gradient system consisting of acetonitrile and acidified water and including an isocratic step at 30 °C was used. The HPLC method was validated for linearity, limits of quantitation and detection, repeatability, precision, and accuracy. The overall method was validated for precision and accuracy over at least three different concentration levels. Relative standard deviation was less than 1.13%, whereas recovery was between 95.50% and 97.19%. The method also proved to be suitable for the determination of a large number of commercial samples and was proposed to the European Pharmacopoeia for the quality control of Andrographidis herba.
是一种亚洲传统草药,广泛用于治疗多种疾病。最近,它已在欧洲被引入用于普通感冒的预防和对症治疗,并作为膳食补充剂的一种成分。其活性成分是二萜类化合物,穿心莲内酯是主要代表。在本研究中,开发了一种分析方法,用于测定该草药及其制剂中的主要成分。测试了三种不同的提取方法(使用改良索氏提取法的甲醇提取、超声浸渍和煎煮)。超声处理获得了最高的分析物含量。对高效液相色谱(HPLC)条件在溶剂混合物、时间进程和温度方面进行了优化。使用反相C18柱,用由乙腈和酸化水组成的梯度系统洗脱,并在30°C下包括一个等度洗脱步骤。对HPLC方法的线性、定量限和检测限、重复性、精密度和准确度进行了验证。整个方法在至少三个不同浓度水平上对精密度和准确度进行了验证。相对标准偏差小于1.13%,而回收率在95.50%至97.19%之间。该方法还被证明适用于大量商业样品的测定,并被提交给欧洲药典用于穿心莲草的质量控制。