Pharmacokinetics and Tissue Distribution Study of Gambogic Acid and Gambogic Acid Nanosuspension in Mice by UHPLC-MS/MS

被引:0
|
作者
Liu, Yu [1 ,3 ]
Zhao, Jinghua [1 ]
Zhang, Wenjun [1 ]
Cui, Qingguo [1 ]
Liang, Xiao [1 ]
Li, Li [1 ]
Liu, Hongsheng [2 ,4 ]
Chen, Lijiang [1 ,2 ]
机构
[1] Liaoning Univ, Sch Pharmaceut Sci, Dept Pharmaceut, Shenyang 110036, Peoples R China
[2] Res Ctr Comp Simulating & Informat Proc Biomacrom, Shenyang 110036, Peoples R China
[3] Liaoning Pharmaceut Engn Res Ctr Nat Med, Shenyang 110036, Peoples R China
[4] Liaoning Univ, Sch Life Sci, Dept Life Sci, Shenyang 110036, Peoples R China
来源
LATIN AMERICAN JOURNAL OF PHARMACY | 2017年 / 36卷 / 04期
关键词
gambogic acid; nanosuspension; pharmacokinetics; tissue distribution; UHPLC-MS/MS; IN-VIVO; RETINOIC ACID; GLIOMA-CELLS; CANCER-CELLS; DELIVERY; COMBINATION; INHIBITION; APOPTOSIS; DRUGS; VITRO;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The objectives of this study were to investigate the tissue biodistribution and pharmacokinetic properties of gambogic acid nanosuspension (GA-NS) with that of gambogic acid solution (GA-S) after intravenously administration to mice. A simple and rapid UHPLC method for determination of GA-NS presented in plasma and tissue has been developed and validated. The method was successfully applied to the pharmacokinetic and tissue distribution study of GA-NS in mice. The results of the pharmacokinetic research demonstrated that the AUC(0 similar to infinity) values of GA-NS were 4.73 times greater than GA-S. It could clearly be seen that the nanosuspension reservoir was formed in circulation, released slowly drug and prolong circulation time in vivo. The tissue distribution studies revealed that GA-NS markedly improved the concentrations of GA in liver and reduced the concentrations in heart and had more significant liver targeting characteristics compared with GA-S.
引用
收藏
页码:767 / 775
页数:9
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