徐晓月, 蔡宝昌, 潘扬, 王天山. 马钱子生物碱在大鼠体内的药代动力学研究马钱子生物碱在大鼠体内的药代动力学研究J. 药学学报, 2003, 38(6): 458-461.
引用本文: 徐晓月, 蔡宝昌, 潘扬, 王天山. 马钱子生物碱在大鼠体内的药代动力学研究马钱子生物碱在大鼠体内的药代动力学研究J. 药学学报, 2003, 38(6): 458-461.
XU Xiao-yue, CAI Bao-chang, PAN Yang, WANG Tian-shan. Pharmacokinetics of the alkaloids from the processed seeds of Strychnos nux-vomica in ratsJ. Acta Pharmaceutica Sinica, 2003, 38(6): 458-461.
Citation: XU Xiao-yue, CAI Bao-chang, PAN Yang, WANG Tian-shan. Pharmacokinetics of the alkaloids from the processed seeds of Strychnos nux-vomica in ratsJ. Acta Pharmaceutica Sinica, 2003, 38(6): 458-461.

马钱子生物碱在大鼠体内的药代动力学研究马钱子生物碱在大鼠体内的药代动力学研究

Pharmacokinetics of the alkaloids from the processed seeds of Strychnos nux-vomica in rats

  • 摘要: 目的用反相高效液相色谱法研究马钱子砂烫炮制品中生物碱在大鼠体内的药代动力学。方法HPLC法,色谱柱为Hypersil BDS C18,流动相为乙腈-水,流速0.8 mL·min-1,检测波长254 nm。结果大鼠iv本品后,其主要成分士的宁、马钱子碱、士的宁氮氧化物和马钱子碱氮氧化物的代谢均符合二室开放模型,主要药代动力学参数分别如下:T1/2α为(8±5), (4±3), (6.2±1.7) 和(3.0±0.8) min,T1/2β为(262±125), (416±131), (285±50)和(342±141) min,CL为(17±4), (21±12), (1.9±1.8)和(2.8±1.1) mL·min-1,Vc为(1.4±0.5), (1.7±1.1), (0.24±0.16)和(0.23±0.06) L·kg-1,Vd为(6.0±1.2), (12±7), (0.8±0.6)和(1.5±0.6) L·kg-1,AUC为(57 578±25 578),(35 240±15 616),(93 088±22 375)和(177 712±120 110) h·μg·L-1。结论此法为人体内的药代动力学研究提供参考。

     

    Abstract: AimTo study the pharmacokinetic process about the concentration in rat plasma of the alkaloids from processed seeds of Strychnos nux-vomica with RP-HPLC method. MethodsHypersil BDS C18 column was used and the mobile phase consisted of acetonitrile-water at the flow rate of 0.8 mL·min-1. The UV detection wave length was 254 nm. ResultsThe concentration-time data of strychnine, brucine, strychnine N-oxide and brucine N-oxide were all in accordance with an open two-compartment model after iv alkaloids. Their parameters were as follows: T1/2α were (8±5), (4±3), (6.2±1.7)and (3.0±0.8) min, T1/2β were (262±125), (416±131), (285±50) and (342±141) min, CL were (17±4), (21±12), (1.9±1.8) and (2.8±1.1) mL·min-1, Vc were (1.4±0.5), (1.7±1.1), (0.24±0.16) and (0.23±0.06) L·kg-1, Vd were (6.0±1.2), (12±7), (0.8±0.6) and (1.5±0.6) L·kg-1, AUC were (57 578±25 578), (35 240±15 616), (93 088±22 375) and (177 712±120 110) h·μg·L-1, respectively. ConclusionThe method is a good reference for pharmacokinetics in human bodies.

     

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