Nanoparticles based on chitosan hydrochloride/hyaluronic acid/PEG containing curcumin: In vitro evaluation and pharmacokinetics in rats

被引:36
作者
Xu, Yurui [1 ]
Asghar, Sajid [2 ]
Yang, Liu [1 ]
Chen, Zhipeng [3 ]
Li, Hongying [4 ]
Shi, Wenwen [1 ]
Li, Yibo [1 ]
Shi, Qinqing [1 ]
Ping, Qineng [1 ]
Xiao, Yanyu [1 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Dept Pharmaceut, 24 Tong Jia Xiang, Nanjing 210009, Jiangsu, Peoples R China
[2] Govt Coll Univ Faisalabad, Fac Pharmaceut Sci, Faisalabad, Pakistan
[3] Nanjing Univ Chinese Med, Dept Pharm, Nanjing 210023, Jiangsu, Peoples R China
[4] Weifang Med Univ, Affiliated Hosp, Weifang 261031, Peoples R China
基金
中国国家自然科学基金;
关键词
Chitosan hydrochlorides-hyaluronic; acid-PEG; Curcumin; Pharmaceutics; HYALURONIC-ACID; LIPID NANOPARTICLES; DELIVERY; PENETRATION; PEGYLATION; STABILITY; GLYCOL);
D O I
10.1016/j.ijbiomac.2017.04.105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nanoparticles based on chitosan hydrochloride (CSH)-hyaluronic acid (HA)-PEG were prepared for delivering curcumin (CUR) (CUR-PNPs) to brain tumor. CUR-PNPs of 245.9 nm and spherical morphology were obtained at optimized CSH/HA/PEG20000/CUR ratios with negative charge of about 27.2 mV and EE of approximately 93.3%. Cytotoxicity studies showed that CUR-PNPs improved drug's anticancer activity in rat glioma cells (C6). The cellular uptake mechanism study showed active targeting of CUR-PNPs into C6 cells by HA mediated endocytosis. Clathrin-coated pit mediated endocytosis, clathrin-mediated endocytosis and macropincytosis were also identified as the entry pathways of PNPs into C6 cells. Pharmacokinetics of preparations in rats after i.v. administration further proved the superiority of CUR-PNPs (3.98 times greater than the area under the curve of CUR solution). In conclusion, CUR-PNPs might be a promising carrier for the therapy of brain tumors. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1083 / 1091
页数:9
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