哈尔滨商业大学学报(自然科学版)
哈爾濱商業大學學報(自然科學版)
합이빈상업대학학보(자연과학판)
Journal of Harbin University of Commerce (Natural Sciences Edition)
2015年
5期
536-539
,共4页
吴伦%苏阳%范海潮%刘杰%田振坤
吳倫%囌暘%範海潮%劉傑%田振坤
오륜%소양%범해조%류걸%전진곤
北五味子%木脂素%高效液相色谱法%含量测定
北五味子%木脂素%高效液相色譜法%含量測定
북오미자%목지소%고효액상색보법%함량측정
fructus schisandrae chinensis%lignans%RP-HPLC%content determination
采用RP-HPLC法同时测定北五味子中6种木脂素类成分.色谱柱为Agilent ZORBAX SB-C18(5μm,4.6×150 mm),流动相为甲醇-水溶液梯度洗脱,检测波长为254 nm,柱温为25℃.结果表明:五味子甲素在40.4~600.0μg/mL(r=0.9998)、五味子乙素在42.0~420.0μg/mL(r=0.9999)、五味子丙素在15.8~118.8μg/mL(r=0.9995)、五味子醇甲在10.0~160.0μg/mL(r=0.9999)、五味子醇乙在15.5~388.0μg/mL(r=0.9995)、五味子酯甲在16.3~408.0μg/mL(r=0.9999)范围内峰面积与对照品质量浓度呈良好的线性关系(n=6).6种成分的加样回收率均高于98%,RSD值小于3%本方法简便,准确,快速,重现性好,可用于北五味子中有效成分的定量分析.
採用RP-HPLC法同時測定北五味子中6種木脂素類成分.色譜柱為Agilent ZORBAX SB-C18(5μm,4.6×150 mm),流動相為甲醇-水溶液梯度洗脫,檢測波長為254 nm,柱溫為25℃.結果錶明:五味子甲素在40.4~600.0μg/mL(r=0.9998)、五味子乙素在42.0~420.0μg/mL(r=0.9999)、五味子丙素在15.8~118.8μg/mL(r=0.9995)、五味子醇甲在10.0~160.0μg/mL(r=0.9999)、五味子醇乙在15.5~388.0μg/mL(r=0.9995)、五味子酯甲在16.3~408.0μg/mL(r=0.9999)範圍內峰麵積與對照品質量濃度呈良好的線性關繫(n=6).6種成分的加樣迴收率均高于98%,RSD值小于3%本方法簡便,準確,快速,重現性好,可用于北五味子中有效成分的定量分析.
채용RP-HPLC법동시측정북오미자중6충목지소류성분.색보주위Agilent ZORBAX SB-C18(5μm,4.6×150 mm),류동상위갑순-수용액제도세탈,검측파장위254 nm,주온위25℃.결과표명:오미자갑소재40.4~600.0μg/mL(r=0.9998)、오미자을소재42.0~420.0μg/mL(r=0.9999)、오미자병소재15.8~118.8μg/mL(r=0.9995)、오미자순갑재10.0~160.0μg/mL(r=0.9999)、오미자순을재15.5~388.0μg/mL(r=0.9995)、오미자지갑재16.3~408.0μg/mL(r=0.9999)범위내봉면적여대조품질량농도정량호적선성관계(n=6).6충성분적가양회수솔균고우98%,RSD치소우3%본방법간편,준학,쾌속,중현성호,가용우북오미자중유효성분적정량분석.
In this paper , RP-HPLC to simultaneously determine 6 kinds of lignans in fruc-tus schisandrae chinensis was adopted .The column was Agilent ZORBAX SB -C18 (5 μm, 4.6 ×150 mm).The mobile phase was consisted of methanol -water solution(gradient elu-tion).The detect wavelength was set at 254 nm, and the column temperature was 25 ℃. Results indicated that deoxyschizandrin at the range of 40.4~600.0μg/mL (r=0.999 8),γ-Schisandrin at the range of 42.0~420.0 μg/mL (r=0.999 9), Schisandrin C at the range of 15.8~118.8μg/mL (r=0.999 5), Schisandrin at the range of 10.0~160.0μg/mL (r =0.999 9), Schisandrol at the range of 15.5 ~388.0 μg/mL ( r =0.999 5) Schisantherin A at the range of 16.3~408.0 μg/mL (r=0.999 9) have good linear rela-tionship between peak area and concentration of reference substance ( n=6 ) .The sample recovery rate of 6 kinds of ingredients was higher than 98%, and the RSD value was less than 3%.This method was simple , accurate , celerity and good reproducibility , and can be used for quantitative analysis of effective ingredients of fructus schisandrae chinensis.