Paclitaxel-loaded poly(N-vinylpyrrolidone)-b-poly(ε-caprolactone) nanoparticles: Preparation and antitumor activity in vivo

被引:140
|
作者
Zhu, Zhenshu [1 ,2 ]
Li, Yuan [1 ,2 ]
Li, Xiaolin [3 ,4 ]
Li, Rutian [3 ,4 ]
Jia, Zhijun [5 ]
Liu, Baorui [3 ,4 ]
Guo, Wanhua [5 ]
Wu, Wei [1 ,2 ]
Jiang, Xiqun [1 ,2 ,6 ]
机构
[1] Nanjing Univ, Lab Mesoscop Chem, Coll Chem & Chem Engn, Nanjing 210093, Peoples R China
[2] Nanjing Univ, Dept Polymer Sci & Engn, Coll Chem & Chem Engn, Nanjing 210093, Peoples R China
[3] Nanjing Univ, Dept Oncol, Sch Med, Nanjing 210093, Peoples R China
[4] Nanjing Univ, Clin Canc Inst, Nanjing 210093, Peoples R China
[5] Nanjing Univ, Sch Med, Dept Nucl Med, Affiliated Drum Tower Hosp, Nanjing 210093, Peoples R China
[6] Nanjing Univ, Jiangsu Prov Lab Nanotechnol, Nanjing 210093, Peoples R China
关键词
Polymeric nanoparticles; Poly(N-vinylpyrrolidone); Drug delivery; Antitumor effect; BLOCK-COPOLYMER MICELLES; PEGYLATED LIPOSOMES; POLYMERIC NANOPARTICLES; RADICAL POLYMERIZATION; BLOOD CLEARANCE; BIODISTRIBUTION; INJECTION; DELIVERY; DRUGS; VITRO;
D O I
10.1016/j.jconrel.2009.11.002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Paclitaxel (PTX)-loaded poly(N-vinylpyrrolidone)-b-poly(epsilon-caprolactone) (PVP-b-PCL) nanoparticles with high drug payload were successfully prepared by a modified nano-precipitation method and characterized by transmission electron microscopy (TEM), atomic force microscopy (AFM), dynamic light scattering (DLS) and zeta potential. The satisfactory drug loading content (>25%) and high encapsulation efficiency (>85%) were achieved. The in vivo real-time biodistribution of PTX-loaded nanoparticles was investigated using near-infrared fluorescence (NIRF) imaging. The antitumor effect of PTX-loaded nanoparticles was evaluated, both, in vitro on three different cancer cell lines and in vivo on hepatic H22 tumor bearing mice model via intravenous administration (i.v.). It is found that PTX-loaded nanoparticles exhibit significant superior in vivo antitumor effect than the commercially available Taxol formulation by combining the tumor volumes and survival rates measurement, intravital positron emission tomography and computed tomography (PET/CT) imaging. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:438 / 446
页数:9
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