Optimized supercritical fluid extraction and effect of ionic liquids on picroside I and picroside II recovery from Picrorhiza scrophulariiflora rhizomes

被引:4
|
作者
Patil A.A. [1 ]
Sachin B.S. [1 ]
Wakte P.S. [1 ]
Shinde D.B. [1 ]
机构
[1] Pharmaceutical Technology Division, Department of Chemical Technology, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad
关键词
Box-Behnken design; Ionic liquid; Picroside I; Picroside II; Supercritical carbon dioxide assisted extraction;
D O I
10.1007/s40005-013-0068-1
中图分类号
学科分类号
摘要
The supercritical carbon dioxide-assisted extraction (SC CO2E) process was optimized for extracting picroside I and picroside II from Picrorhiza scrophulariiflora rhizomes. The picroside I and picroside II content was determined using validated LC-MS methodology. The response surface methodology (RSM) was employed to study quantitative effects of extraction parameters viz. operating pressure, temperature, modifier concentration and extraction time using Box-Behnken design. The experimental data were fitted to second-order polynomial equation using multiple regression analysis and analyzed using the appropriate statistical method. By solving the regression equation and analyzing 3D plots, the optimum extraction conditions were found to be: extraction pressure, 25 MPa; temperature, 40 °C; modifier concentration, 15 % and extraction time, 90 min. The effect of four different ionic liquids (IL) as a modifier additive has been investigated using optimized SC CO2E conditions. None of the IL showed equivalent or enhanced recovery of analytes of interest. The conventional hot percolation of P. scrophulariiflora powder resulted in 23.69 ± 1.02 and 10.22 ± 0.71 mg g-1 picroside I and II, respectively, after an extraction period of 6 h whereas SC CO2E with methanol as modifier showed 33.14 ± 1.23 and 16.77 ± 0.82 mg g-1 recovery of picroside I and II, respectively in 90 min. The comparison of yield and extraction time demonstrated that SC CO2E using methanol as modifier is more efficient than conventional hot percolation method. © 2013 The Korean Society of Pharmaceutical Sciences and Technology.
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页码:215 / 228
页数:13
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