کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6376886 1624859 2013 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Comparison of matrix-solid phase dispersion and liquid-solid extraction connected with solid-phase extraction in the quantification of selected furanocoumarins from fruits of Heracleum leskowii by high performance liquid chromatography
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم کشاورزی و بیولوژیک علوم زراعت و اصلاح نباتات
پیش نمایش صفحه اول مقاله
Comparison of matrix-solid phase dispersion and liquid-solid extraction connected with solid-phase extraction in the quantification of selected furanocoumarins from fruits of Heracleum leskowii by high performance liquid chromatography
چکیده انگلیسی


- A method based on matrix solid-phase dispersion (MSPD) has been for the first time developed for the determination of furanocoumarins from fruits of Heracleum leskowii.
- MSPD technique was compared with a more conventional analytical method that combined liquid-solid extraction (LSE) with solid-phase extraction (SPE).
- MSPD proved efficient, fast, simple and easy to perform method for quantitative and qualitative determination of furanocoumarins from Heracleum leskowii.

In this study, we compared a novel application of matrix solid-phase dispersion (MSPD) methodology and classical liquid-solid extraction (LSE) connected with solid-phase extraction (SPE) for the determination of furanocoumarins from Heracleum leskowii fruits. Fruits of H. leskowii contain the following furanocoumarins: umbelliferon, xanthotoxin, angelicin, isopimpinellin, bergapten, imperatorin, isoimperatorin. Several dispersants, eluents and sample to sorbent mass ratio were examined during the optimization of the process in order to obtain the best selectivity and yield. Quantitative analysis was carried out by high performance liquid chromatography with diode array detector (HPLC-DAD). The method was validated. The calibration curves for all standards were linear over the concentration range 10-100 μg/mL. The correlation coefficients of all calibration curves were R2 > 0.9990. LOD and LOQ values ranged from 2.97 μg/mL to 10.82 μg/mL, and from 9.03 μg/mL to 38.32 μg/mL respectively. The recoveries of the LSE-SPE and MSPD method were in the range of 94.04-102.31% and 92.43-96.27%, respectively. The relative standard deviation (RSD%), as a measure of repeatability, was lower than 5.88% for MSPD and 5.09% for LSE-SPE. MSPD extraction method was compared to the classic analytical method combining liquid-solid extraction with solid-phase extraction.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Industrial Crops and Products - Volume 50, October 2013, Pages 131-136
نویسندگان
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