色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2010年
2期
209-214
,共6页
胶束电动色谱%半枝莲%有效成分%中草药
膠束電動色譜%半枝蓮%有效成分%中草藥
효속전동색보%반지련%유효성분%중초약
micellar electrokinetic chromatography (MEKC)%Scutellaria barbata D.Don%active ingredients%Chinese medicinal herb
建立了毛细管胶束电动色谱同时分析检测中药半枝莲药材及其膏剂中黄芩素、柚皮素、汉黄芩素、野黄芩苷、芹菜素、木犀草素和原儿茶酸7种有效成分的方法.半枝莲样品中7种有效成分经甲醇超声提取.实验考察了运行缓冲溶液的pH值和浓度、添加剂、检测波长、分离电压和进样时间等重要参数对目标物分离的影响.得到的优化条件为:运行缓冲液50 mmol/L 硼砂-0.20 mol/L 硼酸溶液(pH 8.4),含8.5 mmol/L 十二烷基硫酸钠(SDS),分离电压25 kV,检测波长260 nm和335 nm.在此条件下,7种组分于12 min内达到基线分离.各组分在8×10~(-6)~3.2×10~(-4) mol/L 范围内呈良好的线性关系,相关系数(r~2)为 0.996 5~0.999 9;检出限为7.0×10~(-8)~2.0×10~(-6) mol/L;回收率均大于85% .该方法提取简便、准确可靠、重复性好、灵敏度高,可以用于中药半枝莲中7种有效成分的定量检测.
建立瞭毛細管膠束電動色譜同時分析檢測中藥半枝蓮藥材及其膏劑中黃芩素、柚皮素、漢黃芩素、野黃芩苷、芹菜素、木犀草素和原兒茶痠7種有效成分的方法.半枝蓮樣品中7種有效成分經甲醇超聲提取.實驗攷察瞭運行緩遲溶液的pH值和濃度、添加劑、檢測波長、分離電壓和進樣時間等重要參數對目標物分離的影響.得到的優化條件為:運行緩遲液50 mmol/L 硼砂-0.20 mol/L 硼痠溶液(pH 8.4),含8.5 mmol/L 十二烷基硫痠鈉(SDS),分離電壓25 kV,檢測波長260 nm和335 nm.在此條件下,7種組分于12 min內達到基線分離.各組分在8×10~(-6)~3.2×10~(-4) mol/L 範圍內呈良好的線性關繫,相關繫數(r~2)為 0.996 5~0.999 9;檢齣限為7.0×10~(-8)~2.0×10~(-6) mol/L;迴收率均大于85% .該方法提取簡便、準確可靠、重複性好、靈敏度高,可以用于中藥半枝蓮中7種有效成分的定量檢測.
건립료모세관효속전동색보동시분석검측중약반지련약재급기고제중황금소、유피소、한황금소、야황금감、근채소、목서초소화원인다산7충유효성분적방법.반지련양품중7충유효성분경갑순초성제취.실험고찰료운행완충용액적pH치화농도、첨가제、검측파장、분리전압화진양시간등중요삼수대목표물분리적영향.득도적우화조건위:운행완충액50 mmol/L 붕사-0.20 mol/L 붕산용액(pH 8.4),함8.5 mmol/L 십이완기류산납(SDS),분리전압25 kV,검측파장260 nm화335 nm.재차조건하,7충조분우12 min내체도기선분리.각조분재8×10~(-6)~3.2×10~(-4) mol/L 범위내정량호적선성관계,상관계수(r~2)위 0.996 5~0.999 9;검출한위7.0×10~(-8)~2.0×10~(-6) mol/L;회수솔균대우85% .해방법제취간편、준학가고、중복성호、령민도고,가이용우중약반지련중7충유효성분적정량검측.
A method of capillary micellar electrokinetic chromatography with a diode array detector was developed for the simultaneous determination of 7 active ingredients (baicalein,naringenin,wogonin,scutellarin,apigenin,luteolin,and protocatechuic acid) in Scutellaria barbata D.Don and its ointment.The 7 ingredients in samples were extracted with methanol in an ultrasonic bath.The important factors,such as pH,running buffer concentration,additive,detection wavelength,separation voltage and injection time,were optimized.Under the optimum conditions,the 7 analytes were separated within 12 min at a separation voltage of 25 kV in a 50 mmol/L borate-0.20 mol/L boric acid buffer (pH 8.4) containing 8.5 mmol/L sodium dodecyl sulfate (SDS).The detection was carried out at 260 nm and 335 nm.Notably,the linearity ranged from 8×10~(-6) to 3.2×10~(-4) mol/L with the correlation coefficients (r~2) at the range of 0.996 5-0.999 9.The detection limits (S/N=3) ranged from 7.0×10~(-8) mol/L to 2.0×10~(-6) mol/L for all the 7 analytes.The recoveries of the 7 active ingredients were all over 85% .This method is of good sensitivity,simple preparation,good reproducibility and reliability.It was successfully applied to the analysis of the 7 active ingredients in Scutellaria barbata D.Don and its ointment.