In vivo antitumor activity of chitosan nanoparticles

被引:121
作者
Qi, Lifeng [1 ]
Xu, Zirong
机构
[1] Zhejiang Univ, Nanobiol Lab, Anim Sci Coll, Hangzhou 310029, Peoples R China
[2] W Virginia Univ, Sch Med, Dept Orthopaed, Orthopaed Res Lab, Morgantown, WV 26506 USA
关键词
chitosan nanoparticles; in vivo antitumor; S-180; H22;
D O I
10.1016/j.bmcl.2006.05.078
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Chitosan nanoparticles have been synthesized as potential anticancer agents, and evaluated, in vitro, against various cancer cell lines. In this study, in vivo antitumor activity of chitosan nanoparticles against Sarcoma-180 and mouse hepatoma H22 was investigated. Chitosan nanoparticles showed significant antitumor activity in vivo. The doses and particle size made a great effect on their efficacy. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4243 / 4245
页数:3
相关论文
共 20 条
[1]   Development of superparamagnetic nanoparticles for MRI: Effect of particle size, charge and surface nature on biodistribution [J].
Chouly, C ;
Pouliquen, D ;
Lucet, I ;
Jeune, JJ ;
Jallet, P .
JOURNAL OF MICROENCAPSULATION, 1996, 13 (03) :245-255
[2]   Chitosan nanoparticles:: a new vehicle for the improvement of the delivery of drugs to the ocular surface.: Application to cyclosporin A [J].
De Campos, AM ;
Sánchez, A ;
Alonso, MJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 224 (1-2) :159-168
[3]   Positively charged nanoparticles for improving the oral bioavailability of cyclosporin-A [J].
El-Shabouri, MH .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 249 (1-2) :101-108
[4]   Chemotherapeutic engineering: Application and further development of chemical engineering principles for chemotherapy of cancer and other diseases [J].
Feng, SS ;
Chien, S .
CHEMICAL ENGINEERING SCIENCE, 2003, 58 (18) :4087-4114
[5]   The oral absorption of micro- and nanoparticulates: Neither exceptional nor unusual [J].
Florence, AT .
PHARMACEUTICAL RESEARCH, 1997, 14 (03) :259-266
[6]   Chitosan nanoparticles as delivery systems for doxorubicin [J].
Janes, KA ;
Fresneau, MP ;
Marazuela, A ;
Fabra, A ;
Alonso, MJ .
JOURNAL OF CONTROLLED RELEASE, 2001, 73 (2-3) :255-267
[7]  
KONDO N, 1993, BIOL PHARM BULL, V16, P796
[8]   PERORAL ADMINISTRATION OF NANOPARTICLES [J].
KREUTER, J .
ADVANCED DRUG DELIVERY REVIEWS, 1991, 7 (01) :71-86
[9]   PARTICLE-SIZE REDUCTION FOR IMPROVEMENT OF ORAL BIOAVAILABILITY OF HYDROPHOBIC DRUGS .1. ABSOLUTE ORAL BIOAVAILABILITY OF NANOCRYSTALLINE DANAZOL IN BEAGLE DOGS [J].
LIVERSIDGE, GG ;
CUNDY, KC .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 125 (01) :91-97
[10]  
Moghimi SM, 2001, PHARMACOL REV, V53, P283