Chen Ligang, Jin Haiyan, Ding Lan, Zhang Huarong, Wang Xiupin, Wang Ziming, Li Juan, Qu Chenling, Wang Yutang, Zhang Hanqi
College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, China.
J Chromatogr A. 2007 Jan 26;1140(1-2):71-7. doi: 10.1016/j.chroma.2006.11.070. Epub 2006 Dec 6.
A novel technique based on dynamic microwave-assisted extraction (DMAE) coupled on-line with high-performance liquid chromatography (HPLC) through a flow injection interface has been developed for determination of andrographolide and dehydroandrographolide in Andrographis paniculata Nees. A TM(010) microwave resonance cavity built in the laboratory was applied to concentrating the microwave energy. An extraction vessel was placed in microwave irradiation zone. The extraction was performed in a recirculating system. When a number of extraction cycles were completed, the fractional extract (20muL) was driven to the analytical column by 65% aqueous methanol and was measured by diode array detector (DAD) at 225nm. The optimized extraction conditions are follows: extraction solvent 60% aqueous methanol; microwave forward power 80W; extraction time 6min; extraction solvent flow-rate 1.0mLmin(-1). The detection and quantification limits obtained are 0.5 and 1.7microgmL(-1) for andrographolide and 0.6 and 1.9microgmL(-1) for dehydroandrographolide, respectively. The within-day and between-day precision (RSD) are 2.1% and 3.7% for andrographolide and 1.7% and 4.1% for dehydroandrographolide, respectively. Mean recoveries for andrographolide and dehydroandrographolide are 97.7% and 98.7%, respectively. Compared with ultrasonic extraction used in the Chinese pharmacopoeia, the proposed method was demonstrated to obtain higher extraction yield in a shorter time. In addition, only small quantities of solvent (5mL) and sample (10mg) were required.
建立了一种基于动态微波辅助萃取(DMAE)并通过流动注射接口与高效液相色谱(HPLC)在线联用的新技术,用于测定穿心莲中穿心莲内酯和脱水穿心莲内酯的含量。实验室自制的TM(010)微波谐振腔用于聚集微波能量。将萃取容器置于微波辐射区,萃取在循环系统中进行。完成多次萃取循环后,用65%的甲醇水溶液将20μL萃取液注入分析柱,并采用二极管阵列检测器(DAD)在225nm波长处进行测定。优化的萃取条件如下:萃取溶剂为60%的甲醇水溶液;微波正向功率80W;萃取时间6min;萃取溶剂流速1.0mLmin(-1)。穿心莲内酯的检测限和定量限分别为0.5和1.7μgmL(-1),脱水穿心莲内酯的检测限和定量限分别为0.6和1.9μgmL(-1)。穿心莲内酯日内和日间精密度(RSD)分别为2.1%和3.7%,脱水穿心莲内酯日内和日间精密度(RSD)分别为1.7%和4.1%。穿心莲内酯和脱水穿心莲内酯的平均回收率分别为97.7%和98.7%。与《中国药典》中的超声提取法相比,该方法在较短时间内具有更高的提取率。此外,该方法仅需少量溶剂(5mL)和样品(10mg)。