Preparation and characterization of cationic curcumin nanoparticles for improvement of cellular uptake

被引:113
作者
Liu, Jinsong [1 ]
Xu, Lihua [2 ]
Liu, Chuantong [1 ]
Zhang, Dafeng [1 ]
Wang, Sigian [1 ]
Deng, Zhennan [1 ]
Lou, Weiwei [1 ]
Xu, Haihong [1 ]
Bai, Qing [1 ]
Ma, Jianfeng [1 ]
机构
[1] Wenzhou Med Coll, Sch & Hosp Stomatol, Dept Prosthodont, Wenzhou 325027, Peoples R China
[2] Whenzhou Med College, Affiliated Hosp 1, Dept Gen Med, Whenzhou 325000, Peoples R China
关键词
Curcumin; Chitosan/PCL; Nanoparticles; In vitro cytotoxicity; Cell uptake; PLGA NANOPARTICLES; TUMOR-GROWTH; IN-VITRO; KAPPA-B; CHITOSAN; DELIVERY; BIOAVAILABILITY; MICROPARTICLES; COMPLEXATION; ANGIOGENESIS;
D O I
10.1016/j.carbpol.2012.04.036
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In the present paper, cationic nanoparticles of curcumin, chitosan and poly(epsilon-caprolactone) were developed by a simple nano-precipitation method. The developed curcumin loaded chitosan/poly(epsilon-caprolactone) (chitosan/PCL) nanoparticle showed almost spherical shape and its diameter was varied between 220 nm and 360 nm and zeta potential was varied between +30 mV and 0 mV as a function with pH value. The encapsulation of curcumin into nanoparticles was confirmed by fluorescence spectral analysis. In vitro release study showed the sustained release behavior of curcumin from nanoparticles during the period of 5 days study. In vitro cytotoxicity test revealed the drug concentration dependent on the cell viability against Hela cells and OCM-1 cells after 48 h co-incubation. Furthermore, in vitro cell uptake study revealed that the cell uptake of curcumin was greatly enhanced by encapsulated curcumin into cationic chitosan/PCL nanoparticles. Therefore, the developed cationic chitosan/PCL nanoparticles might be a promising candidate for curcumin delivery to cancer cells. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:16 / 22
页数:7
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