Cho S-K, Abd El-Aty A M, Choi J-H, Kim M R, Shim J H
Natural Products Chemistry Laboratory, Institute of Agricultural Science and Technology, College of Agriculture and Life Science, Chonnam National University, 300 Yong-Bong Dong, Buk-Ku, Gwangju 500-757, Republic of Korea.
J Pharm Biomed Anal. 2007 Sep 3;44(5):1154-8. doi: 10.1016/j.jpba.2007.03.011. Epub 2007 Mar 18.
Accelerated solvent extraction (ASE) of three common Angelica species found in Asia: Angelica sinensis (Oliv.) Diels from China, Angelica acutiloba (Sieb. et Zucc.) Kitagawa from Japan, and Angelica gigas Nakai from Korea was investigated. Preliminary experiments, including the selection of the solvent, extraction time, pressure, static cycle and time were investigated to optimize experimental parameters. Kováts indices and mass spectra were used to identify the components in the various fractions. These were then confirmed using gas chromatography-mass spectrometry (GC-MS). A total of 18 compounds were identified, with qualitative differences and similarities observed among the cultivars. From the 18 compounds found in the ASE extract of danggui cultivars, the major components were decursin, decursinol angelate (A. gigas); butylidene dihydrophthalide, 4-hydroxy-4-methyl-2-pentanone (A. sinensis); and 9,12-octadecanoic acid in Angelica acutiloba. The optimum ASE operating conditions were n-hexane as extraction solvent, extraction temperature and pressure of 80 degrees C and 1500 atm, respectively, static cycle of 2 min, and static time of 10 min. Under these conditions, the percentages of main analytes were increased.
对亚洲发现的三种常见当归属植物进行了加速溶剂萃取(ASE)研究:来自中国的当归(Angelica sinensis (Oliv.) Diels)、来自日本的东当归(Angelica acutiloba (Sieb. et Zucc.) Kitagawa)和来自韩国的紫花前胡(Angelica gigas Nakai)。进行了初步实验,包括对溶剂、萃取时间、压力、静态循环和时间的选择,以优化实验参数。使用科瓦茨指数和质谱来鉴定各馏分中的成分,然后用气相色谱 - 质谱联用仪(GC - MS)进行确认。共鉴定出18种化合物,各品种之间存在定性的差异和相似性。在当归品种的ASE提取物中发现的18种化合物中,主要成分分别为紫花前胡醇、紫花前胡醇当归酸酯(紫花前胡);丁烯基苯酞、4 - 羟基 - 4 - 甲基 - 2 - 戊酮(当归);以及东当归中的9,12 - 十八碳二烯酸。ASE的最佳操作条件为:以正己烷作为萃取溶剂,萃取温度和压力分别为80℃和1500 atm,静态循环时间为2分钟,静态时间为10分钟。在这些条件下,主要分析物的百分比有所增加。