Hou Ting, Chen Jun, Cai Baochang, Xiao Hanlu, Chen Minglei, Zhang Ting, Fang Yun
College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210029, China.
Zhongguo Zhong Yao Za Zhi. 2011 May;36(10):1353-7.
To compare the pharmacokinetic characteristics of brucine following intravenous administration of liposomes, containing total alkaloids from seed of Strychnos nux-vomica, to rats with different phospholipids composition.
Liposomes containing the total alkaloids were prepared by the method of ammonium sulfate transmembrane gradients and stealth liposome technique. The contents of total alkaloids and brucine in liposomes were determined and compared after free drug being removed. After intravenous administration of total alkaloids solution or liposomes with different composition, plasma samples were drawn at predetermined time points and the concentrations of brucine were determined by a validated method of HPLC. Pharmacokinetic analysis was performed by 3P97 program.
The ratios of brucine to total alkaloids in liposomes hardly varied with phospholipids composition. Compared with SPC liposome, AUC of brucine was increased 13.3-fold and apparent volume of distribution was decreased to only 3.6% following intravenous administration of HSPC liposome. In addition, besides that AUC of brucine was slightly increased, most pharmacokinetic parameters were not significantly changed after administration of the novel liposome compared with those of SPC liposome.
Phospholipids composition has a significant influence on the pharmacokinetics of brucine after intravenous administration of liposomes containing total alkaloids from seed of S. nux-vomica.
比较静脉注射含马钱子种子总生物碱的脂质体后,不同磷脂组成的脂质体中士的宁在大鼠体内的药代动力学特征。
采用硫酸铵跨膜梯度法和隐形脂质体技术制备含总生物碱的脂质体。去除游离药物后,测定并比较脂质体中总生物碱和士的宁的含量。静脉注射总生物碱溶液或不同组成的脂质体后,在预定时间点采集血浆样本,采用经过验证的高效液相色谱法测定士的宁浓度。用3P97程序进行药代动力学分析。
脂质体中士的宁与总生物碱的比例几乎不随磷脂组成而变化。与大豆磷脂酰胆碱(SPC)脂质体相比,静脉注射氢化大豆磷脂酰胆碱(HSPC)脂质体后,士的宁的曲线下面积(AUC)增加了13.3倍,表观分布容积仅降至3.6%。此外,与SPC脂质体相比,新型脂质体给药后,除士的宁的AUC略有增加外,大多数药代动力学参数无显著变化。
磷脂组成对静脉注射含马钱子种子总生物碱的脂质体后士的宁的药代动力学有显著影响。