Novel core (polyester)-shell(polysaccharide) nanoparticles: protein loading and surface modification with lectins

被引:89
作者
Rodrigues, JS
Santos-Magalhaes, NS
Coelho, LCBB
Couvreur, P
Ponchel, G
Gref, R
机构
[1] Univ Paris Sud, Fac Pharm, CNRS, UMR 8612, F-92296 Chatenay Malabry, France
[2] Univ Fed Pernambuco, Dept Bioquim, Lab Imunopatol, Recife, PE, Brazil
关键词
dextran; caprolactone; copolymer; core-corona nanoparticle; lectin; Bauhinia monandra; lens culinaris;
D O I
10.1016/S0168-3659(03)00296-7
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study describes new lectin-decorated or protein-loaded nanoparticles with a hydrophobic poly(e-caprolactone) (PCL) core and a hydrophilic dextran (Dex) corona. In this view, a family of block Dex-PCLn copolymers was first synthesized, consisting of a Dex backbone to which n preformed PCL blocks were grafted. The ability of these new copolymers to form nanoparticles was evaluated in comparison with a series of PCL homopolymers of various molecular weights (2000, 10 000 and 40 000 g/mole). Two different nanoparticle preparation methods have been developed and tested for their efficacy to incorporate proteins. For this, three proteins were used: a model protein, bovine serum albumin (BSA), a lectin from leaves of Bauhinia monandra (BmoLL) and Lens culinaris (LC) lectin. All these proteins were successfully incorporated in nanoparticles with a mean diameter around 200 nm. Lectins could also be adsorbed onto the surface of Dex-PCLn nanoparticles. Surface-bound BmoLL conserved its hemagglutinating activity, suggesting the possible application of this type of surface-modified nanoparticles for targeted oral administration. Caco-2 cellular viability was higher than 70% when put in contact with Dex-PCLn nanoparticles, even at concentrations as high as 660 mug/ml. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 112
页数:10
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