Title Galactosylated chitosan nanoparticles for hepatocyte-targeted delivery of oridonin
Authors Zheng, Dandan
Duan, Cunxian
Zhang, Dianrui
Jia, Lejiao
Liu, Guangpu
Liu, Yue
Wang, Feihu
Li, Caiyun
Guo, Hejian
Zhang, Qiang
Affiliation Shandong Univ, Dept Pharmaceut, Coll Pharm, Jinan 250012, Shandong, Peoples R China.
Peking Univ, State Key Lab Nat & Biomimet Drugs, Sch Pharmaceut Sci, Beijing 100083, Peoples R China.
Shandong Univ, Dept Pharmaceut, Coll Pharm, 44 Wenhua Xi Rd, Jinan 250012, Shandong, Peoples R China.
Keywords Galactosylated chitosan
Nanoparticles
Oridonin
Tumor targeting
GRAFTED-PEGYLATED-CHITOSAN
TISSUE DISTRIBUTION
ASIALOGLYCOPROTEIN RECEPTOR
DRUG-DELIVERY
HEPG2 CELLS
NANOCAPSULES
PACLITAXEL
PHARMACOKINETICS
PERMEABILITY
ENHANCEMENT
Issue Date 2012
Publisher international journal of pharmaceutics
Citation INTERNATIONAL JOURNAL OF PHARMACEUTICS.2012,436,(1-2),379-386.
Abstract In this study, oridonin-loaded nanoparticles coated with galactosylated chitosan (ORI-GC-NP) were prepared for tumor targeting and their characteristics were evaluated for the morphologies, particle size and zeta potential. Oridonin-loaded nanoparticles (ORI-NP) without galactosylated chitosan were prepared as a control. The entrapment efficiency of ORI-GC-NP and ORI-NP were 72.15% and 85.31%, respectively. The in vitro drug release behavior from nanoparticles displayed biphasic drug release pattern with initial burst release and consequently sustained release. Next, the pharmacokinetics and tissue distribution of ORI-GC-NP, ORI-NP and ORI solution were carried out. Pharmacokinetic analysis showed that ORI-GC-NP and ORI-NP could prolong the drug plasma levels compared with ORI solution. Meanwhile, the distribution of ORI-GC-NP to liver was higher than that of ORI-NP and free drug. In conclusion, ORI-GC-NP, as a promising intravenous drug delivery system for ORI, could be developed as an alternative to the conventional ORI preparations. (c) 2012 Elsevier B.V. All rights reserved.
URI http://hdl.handle.net/20.500.11897/229893
ISSN 0378-5173
DOI 10.1016/j.ijpharm.2012.06.039
Indexed SCI(E)
Appears in Collections: 药学院
天然药物与仿生药物国家重点实验室

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