目的:研究丹参与丹皮配伍的化学成分。方法:建立HPLC—MS分析方法,分析条件为:ZorbaxSB—C18柱(4.6mm×250mm,5μm),0.5%(v/v)醋酸水溶液-0.5%(v/v)醋酸乙腈溶液为流动相,线性梯度洗脱:0min,流动相比例为95:5;25min,77:23;35min,75:25;45min,75:25;50min,70:30;75rain,10:90。流速0.5mL·min^-1,柱温35℃,检测波长254nm;负离子模式扫描,扫描范围100—1000U,氮气流速10L·min^-1,雾化温度350℃,毛细管电压3500V,裂解电压100V。依据色谱保留时间、紫外光谱及质谱信息,对丹参与丹皮配伍煎液中主要化学成分进行鉴定和归属,并比较配伍前后含量的变化。结果:鉴定并归属丹参与丹皮配伍煎液中19个成分,其中11个来自丹参,8个来自丹皮;配伍后丹酚酸类、芍药苷类成分含量高于单煎,而鞣质类成分含量降低。结论:丹参与丹皮配伍后有效成分含量得到提高。
Objective:To study the chemical constituents of compatibility of Radix Salviae Mihiorrhizae and Cortex Moutan. Methods :An HPLC- MS analytical method was developed on a Zorbax SB -ClS column (4. 6 mm × 250 mm,5 μm)with 0. 5% HAc- H20 and 0. 5%HAc- CH3CN as mobile phase. A gradient programmer was adopted according to the following profile:0 min,95:5 ;25 min,77:23 ;35 min,75:25 ;45 min,75:25 ;50 min,70:30;75 min,10: 90. The flow rate was 0. 5 mL·min^-1 with UV detected at 254 nm. The column temperature was maintained at 35℃. And the conditions for the ESI interface were as follows:negative ionization mode;drying gas flow rate, 10 L·min^-1 ;the temperature of drying gas,350℃ ;capillary voltage,3500 V;fragment voltage, 100 V. Full scan data acquisition was performed from m/z 100 to 1000 in MS scan mode. According to the information of retention time, ultraviolet spectra and mass spectra, the main constituents in combined -decoction were identified and attributed, and the content of chemical constituents in combined - decoction was compared with that in decoction individually. Results:Nineteen constituents were identified and attributed, among them eleven from Radix Salviae Miltiorrhizae and eight from Cortex Moutan. The content of phenolic acids and monoterpenoids in combined - decoction was higher than those in individual decoction ,but the content of tannins was lower. Conclusion:The results indicated that the content of some effective constituents increased after compatibility.