TY - JOUR
T1 - Simultaneous determination of active ingredients in ethnomedicine Gaultheria leucocarpa var. yunnanensis and its medicinal preparation by capillary electrophoresis with electrochemical detection
AU - Zeng, Yikun
AU - Tang, Zhuxing
AU - Wang, Qingjiang
AU - He, Pingang
AU - Fang, Yuzhi
PY - 2007/10
Y1 - 2007/10
N2 - A simple and rapid capillary electrophoresis (CE) with electrcochemical detection (ED) method has been established for the simultaneous determination of seven active ingredients in the stems and roots of Gaultheria leucocarpa var. yunnanensis and its medicinal preparation, including (+)-catechin, rutin, gentisic acid, vallinic acid, salicylic acid, quercetin, and protocatechuic acid. The effects of working potential, pH, and concentration of running buffer, separation voltage, and injection time on CE-ED are systematically investigated. Under the optimum conditions, the seven analytes could be completely separated within 23 min in a borax running buffer (pH 8.7). A good linear relationship is obtained over three orders of magnitude with detection limits (signal-to-noise ratio = 3) ranging from 5 × 10-8 g/mL to 3 × 10-7 g/mL for the analytes. The proposed method is successfully used in the analysis of real samples after a relatively simple extraction procedure, and the assay results are satisfactory.
AB - A simple and rapid capillary electrophoresis (CE) with electrcochemical detection (ED) method has been established for the simultaneous determination of seven active ingredients in the stems and roots of Gaultheria leucocarpa var. yunnanensis and its medicinal preparation, including (+)-catechin, rutin, gentisic acid, vallinic acid, salicylic acid, quercetin, and protocatechuic acid. The effects of working potential, pH, and concentration of running buffer, separation voltage, and injection time on CE-ED are systematically investigated. Under the optimum conditions, the seven analytes could be completely separated within 23 min in a borax running buffer (pH 8.7). A good linear relationship is obtained over three orders of magnitude with detection limits (signal-to-noise ratio = 3) ranging from 5 × 10-8 g/mL to 3 × 10-7 g/mL for the analytes. The proposed method is successfully used in the analysis of real samples after a relatively simple extraction procedure, and the assay results are satisfactory.
UR - https://www.scopus.com/pages/publications/35548979020
U2 - 10.1093/chromsci/45.9.610
DO - 10.1093/chromsci/45.9.610
M3 - 文章
C2 - 17988450
AN - SCOPUS:35548979020
SN - 0021-9665
VL - 45
SP - 610
EP - 615
JO - Journal of Chromatographic Science
JF - Journal of Chromatographic Science
IS - 9
ER -