Effect of particle size on in vitro and in vivo behavior of astilbin nanosuspensions

被引:16
作者
Wang, Xiao-han [1 ,2 ]
Liu, Yuan [1 ]
Shen, Cheng-ying [1 ,2 ]
Shen, Bao-de [1 ]
Zhong, Rui-na [1 ,2 ]
Yuan, Hai-long [1 ]
机构
[1] PLA, Air Force Med Ctr, Beijing 100142, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Pharm Coll, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Astilbin; Nanosuspensions; Particle size; In vitro; In vivo; Behavior; NANOCRYSTALS; INJURY;
D O I
10.1016/j.jddst.2019.05.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, the effect of particle size on in vitro and in vivo behavior of astilbin nanosuspensions (AT-NSs) was investigated. AT-NSs with three different particle sizes (215.17 +/- 4.83 nm, 496.51 +/- 12.94 nm, and 803.34 +/- 9.06 nm) were prepared using a simplified wet media milling technique by adjusting milling time. SEM and XRPD results showed that the three AT-NSs had similar appearance and crystalline state. The dissolution of AT-NSs was particle size dependent and in an order of 215.17 nm > 496.51 nm > 803.34 nm, however the AUC(0-infinity) of pharmacokinetics was in an order of 496.51 nm > 803.34 nm > 215.17 nm. AT-NSs with a larger particle size showed a higher accumulation in lung and liver because of reticuloendothelial system (RES). In conclusion, particle size had obvious impact on dissolution, pharmacokinetics and tissue distribution of AT-NSs, and the optimal particle size was 496.51 nm for the oral administration of AT-NSs.
引用
收藏
页码:778 / 783
页数:6
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