HPLC-FLU法测定血清中黄藤素的含量  

DETERMINATION OF PALMATINE IN SERUM BY HPLC-FLU

作　　者：张慧[1] 余琛[1] 洪有采[1] 蒋山好[2] 沈竞康 朱大元 

机构地区：[1]上海市徐汇区中心医院,上海200031 [2]中国科学院上海药物研究所,上海200031

出　　处：《药学学报》2000年第7期518-520,共3页Acta Pharmaceutica Sinica

摘　　要：目的　建立血清样品中黄藤素的高效液相色谱 -荧光检测法。方法　色谱柱为LiChrosorbSI 6 0 (5 μm)2 0cm× 4 0mmID ;流动相为二氯甲烷—甲醇—二乙胺—冰醋酸 (90∶9∶0 4∶0 5 ) ;流速为 1 0mL·min-1;荧光检测Ex=36 5nm ,Em=5 10nm。血清样品加 13 甲基小檗碱 (内标 ) ,用三氯乙酸 氯仿提取 ,水浴加温、氮气吹干 ,用二氯乙烷溶解进样。结果　黄藤素和内标的保留时间分别为 8 4min和 7 1min。黄藤素的最低检测浓度为 0 1ng·mL-1。在 0 1～ 10 0ng·mL-1有良好线性关系 (γ =0 9999)。血药浓度测定天内、天间精密度分别为 0 94%～1 85 %和 0 15 %～ 6 47%。结论　用高效液相色谱 荧光检测法测定黄藤素的血药浓度 ,有灵敏、专一和快速的优点 。AIM To develop a method for analysis of palmatine in serum by high performance liquid chromatography with fluorometric detector. METHODS Separation was obtained by using a LiChrosorb SI 60 column(4 0 mm×200 mm, 5 μm). The mobile phase consisted of a mixture of dichloromethane-methanol-diethyl amine-acetic acid(90∶9∶0 4∶0 5) and the flow rate was 1 mL·min -1 . Excitation and emission wavelengths were set at 365 and 510 nm respectively. To 1 0 mL of serum containing palmatine was added 13 methylberberine (internal standard, IS), then extracted with 5 0 mL chloroform containing trichloroacetic acid. The organic phase was removed with nitrogen and the residue dissolved with 100 μL dichloromethane. After centrifugation, 20 μL of the lower layer was subjected to HPLC. RESULTS The retention times of palmatine and IS were 8 4 and 7 1 min respectively. In serum the detection limit of palmatine was 0 1 ng·mL -1 . The extraction recoveries of palmatine and IS were over 85%. The relative standard deviations of within day and between day were 0 94%～1 85% and 0 10%～6 47% ( n =6) respectively. CONCLUSION This method is sensitive, simple and fast, so it can fit the need of palmatine pharmacokinetic research preferably.

关 键 词：黄藤素 高效液相色谱-荧光检测 血药浓度 

分 类 号：R931.71[医药卫生—生药学] R969.1[医药卫生—药学]