目的建立HPLC法同时测定乐脉胶囊(丹参、川芎、赤芍、红花、香附等)中丹参索、丹参酮ⅡA、原儿茶醛、原儿茶酸、阿魏酸、没食子酸、芍药苷、羟基红花黄色素A和d一香附酮9种有效成分的量。方法采用AgilentTC—C18色谱柱(4.6mm×250mm,5μm);以0.2%甲酸水.甲醇为流动相梯度洗脱;体积流量0.6mlfmin;柱温30℃;检测波长280nm(0—20min),403nm(20一22min),230nm(22~26rain),320nm(26~45rain)和254nm(45—60min)。结果丹参素在5.0~500.0μ∥mL,丹参酮ⅡA和d一香附酮在1.0—100.0仙g/mL,原儿茶酸和原儿茶醛在2.5—250.0Ixg/mL,阿魏酸在1.7~170.0斗∥mL,没食子酸在10.0~1000.0μ/mL,芍药苷在20.0~2000.0μg/mL,羟基红花黄色素A在4.6~460.0p∥mL范围内线性关系良好(r≥0.9990),平均加样回收率均大于95.0%。结论本方法简便、准确、重复性好,可作为乐脉胶囊的质量控制方法。
AIM To establish an HPLC method for simultaneously determining nine components in Lemai Cap- sules (Salviae miltiorrhizae Radix et Rhizome, Chuanxioag Rhizome, Paeoaiae Radix rubra, Carthami Flos, Cyperi Rhizoma), including danshensu, tanshinone II A, protocatechuic aldehyde, protocatechuic acid, ferulic acid, gal- lic acid, peoniflorin, hydroxysafflor yellow A and ot-cyperone. METHODS The analysis was carried out on Agi- lent TC-Cls column (4. 6 mmx 250 ram, 5 iμm). The mobile phase consisted of methanol-0. 2% formic acid-wa- ter with step gradient elution. The flow rate was 0.6 mL/min, the column temperature was 30 C and the detection wavelengths were 230 rim, 254 nm, 280 nm, 320 nm, and 403 nm respectively. RESULTS The samples showed a good relationship in the ranges of 5.0 500. 0 Ixg/mL for danshensu, 1.0 100.0 μg/mL for tanshinone II A and c-cyperone, 2.5 -250. 0 ixg/mL for protocatechuic acid and protocatechuic aldehyde, 1.7 - 170. 0 Ixg/mL for fer- ulic acid, 10.0 1 000.0 μg/mL for gallic acid, 20.0 - 2 000.0 μg/mL for peoniflorin and 4.6 460 g/mL for hydroxysafflor yellow A, respectively ( r I〉 0. 999 0). The average recoveries of the nine compoments were more than 95.0%. CONCLUSION This method with strong specificity is simple, accurate, reproducible and can be used for quality control of Lemai Capsules.KEY WORDS :