Verma Arvind, Hartonen Kari, Riekkola Marja-Liisa
Laboratory of Analytical Chemistry, Department of Chemistry, University of Helsinki, Finland.
Phytochem Anal. 2008 Jan-Feb;19(1):52-63. doi: 10.1002/pca.1015.
Response surface modelling, using MODDE 6 software for Design of Experiments and Optimisation, was applied to optimise supercritical fluid extraction (SFE) conditions for the extraction of indole alkaloids from the dried leaves of Catharanthus roseus. The effects of pressure (200-400 bar), temperature (40-80 degrees C), modifier concentration (2.2-6.6 vol%) and dynamic extraction time (20-60 min) on the yield of alkaloids were evaluated. The extracts were analysed by high-performance liquid chromatography and the analytes were identified using ion trap-electrospray ionisation-mass spectrometry. The method was linear for alkaloid concentration in the range 0.18-31 microg/mL. The limits of detection and quantification for catharanthine, vindoline, vinblastine and vincristine were 0.2, 0.15, 0.1 and 0.08 microg/mL and 2.7, 2.0, 1.3 and 1.1 microg/g, respectively. The dry weight content of major alkaloids in the plants were compared using different extraction methods, i.e. SFE, Soxhlet extraction, solid-liquid extraction with sonication and hot water extraction at various temperatures. The extraction techniques were also compared in terms of reproducibility, selectivity and analyte recoveries. Relative standard deviations for the major alkaloids varied from 4.1 to 17.5% in different extraction methods. The best recoveries (100%) for catharanthine were obtained by SFE at 250 bar and 80 degrees C using 6.6 vol% methanol as modifier for 40 min, for vindoline by Soxhlet extraction using dichloromethane in a reflux for 16 h, and for 3',4'-anhydrovinblastine by solid-liquid extraction using a solution of 0.5 m sulphuric acid and methanol (3:1 v/v) in an ultrasonic bath for 3 h.
使用MODDE 6软件进行实验设计和优化的响应面建模,用于优化从长春花干燥叶片中提取吲哚生物碱的超临界流体萃取(SFE)条件。评估了压力(200 - 400 bar)、温度(40 - 80℃)、改性剂浓度(2.2 - 6.6 vol%)和动态萃取时间(20 - 60分钟)对生物碱产量的影响。提取物通过高效液相色谱分析,并使用离子阱 - 电喷雾电离 - 质谱法鉴定分析物。该方法对生物碱浓度在0.18 - 31μg/mL范围内呈线性。长春质碱、文多灵、长春碱和长春新碱的检测限和定量限分别为0.2、0.15、0.1和0.08μg/mL以及2.7、2.0、1.3和1.1μg/g。使用不同的提取方法,即SFE、索氏提取、超声辅助固液提取和不同温度下的热水提取,比较了植物中主要生物碱的干重含量。还在重现性、选择性和分析物回收率方面比较了提取技术。不同提取方法中主要生物碱的相对标准偏差在4.1%至17.5%之间变化。长春质碱在250 bar和80℃下使用6.6 vol%甲醇作为改性剂进行40分钟的SFE可获得最佳回收率(100%),文多灵通过使用二氯甲烷在回流下进行16小时的索氏提取可获得最佳回收率,3',4'-脱水长春碱通过在超声浴中使用0.5 m硫酸和甲醇(3:1 v/v)溶液进行3小时的固液提取可获得最佳回收率。