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)
2014年
4期
398-401
,共4页
八珍汤%芍药苷%质量浓度测定
八珍湯%芍藥苷%質量濃度測定
팔진탕%작약감%질량농도측정
Bazhen decoction%paecniflorin%content determination
建立八珍汤中芍药苷的高效液相色谱定量方法.HPLC分析采用Symmetry C18色谱柱(4.6 mm ×250 mm,5μm);紫外检测器,检测波长为230 nm;流动相为乙腈-0.05%磷酸水溶液(15∶85);流速为1.0 mL/min;柱温为30℃;进样量为20μL.芍药苷在0.014~0.224 mg/mL范围内呈良好线性关系,线性回归方程为Y =40798281 X +2855,r =0.9998(n=5).该方法具有分析速度快,重现性好,精密度高,定量准确等特点.适用于八珍汤复方中芍药苷的定量分析.
建立八珍湯中芍藥苷的高效液相色譜定量方法.HPLC分析採用Symmetry C18色譜柱(4.6 mm ×250 mm,5μm);紫外檢測器,檢測波長為230 nm;流動相為乙腈-0.05%燐痠水溶液(15∶85);流速為1.0 mL/min;柱溫為30℃;進樣量為20μL.芍藥苷在0.014~0.224 mg/mL範圍內呈良好線性關繫,線性迴歸方程為Y =40798281 X +2855,r =0.9998(n=5).該方法具有分析速度快,重現性好,精密度高,定量準確等特點.適用于八珍湯複方中芍藥苷的定量分析.
건립팔진탕중작약감적고효액상색보정량방법.HPLC분석채용Symmetry C18색보주(4.6 mm ×250 mm,5μm);자외검측기,검측파장위230 nm;류동상위을정-0.05%린산수용액(15∶85);류속위1.0 mL/min;주온위30℃;진양량위20μL.작약감재0.014~0.224 mg/mL범위내정량호선성관계,선성회귀방정위Y =40798281 X +2855,r =0.9998(n=5).해방법구유분석속도쾌,중현성호,정밀도고,정량준학등특점.괄용우팔진탕복방중작약감적정량분석.
To establish an HPLC method for determination of paecniflorin of Bazhen decoction the assay was performed on a Symmetry C 18 column (250 mm ×4.6 mm, 5μm).UV detec-tor wavelength was at 230 nm.The mobile phase was acetonitrile -0.05%phosphoric acid solution (15∶85).The flow rate was 1.0 mL/min, and the column temperature was main-tained at 30 ℃.The sampling volume was 20μL.The calibration curve had good linear re-lationship in the range of 0.014~0.224 mg/mL, linear equation: Y =40 798 281 X +2 855(r=0.999 8).This method was simple, sensitive, accurate and reproducible .It was suitable for quality control of Bazhen decoction .