目的:建立同时测定延胡索中巴马汀、脱氢紫堇碱和延胡索乙素的HPLC方法。方法:采用C18柱(4.6 mm×250nm,5μm),以乙腈(A)-0.1%磷酸(加三乙胺调节pH 6.0,B)进行梯度洗脱(0~20 min,25%A;20~30 min,25%~55%A;30~45 min,55%A;45~50 min,55%~25%A;50~55 min,25%A);检测波长为270,280 nm,柱温30℃。结果:巴马汀在2.12×10-2~1.59μg呈良好的线性关系(r=0.999 9);脱氢紫堇碱在4.10×10-2~3.07μg呈良好的线性关系(r=0.999 9);延胡索乙素在2.10×10-2~1.57μg呈良好的线性关系(r=0.999 9);加样回收率分别为100.10%,100.03%,97.47%。结论:该方法准确、稳定、分离效果好,可用于测定延胡索药材中巴马汀、脱氢紫堇碱和延胡索乙素的含量。
Objective: To develop a new method dehydrocorydaline nitrate and tetrahydropalmatine in Rhizoma adopted performing on a C18column (4.6 mm ×250 for determination of palmatine hydrochloride, Corydalis by HPLC. Method: The HPLC was nm, 5 μm) with a mobile phase of acetonitrile (A) 43.1%phosphoric acid (B). The gradient elution program was as follows: 0-20 min, 25% A; 20-30 min, 25%-55% A; 30-45 min, 55%A; 45-50 min, 55%-25%A; 50-55 min, 25%A; The detection wavelength was set at270 nm and 280 nm. The column temperature was at 30 ℃. Result: Palmatine hydrochloride was linear in the range of 2. 12 × 10^-2 -1.59 μg (r =0. 999 9) ; dehydrocorydaline nitrate was linear in the range of 4. 10 ×10^-2 -3.07 μg (r =0. 999 9) ; tetrahydropalmatine was linear in the range of 2. 10× 10^-2 -1. 57 μg (r =0. 999 9). The average recovery was 100. 10%, 100.03% and 97.47%. Conclusion: The method was accurate and had satisfactory efficacy; it can determine palmatine hydrochloride, dehydrocorydaline nitrate and tetrahydropalmatine in Rhizoma Corydalis.