Physicochemical properties and blood compatibility of acylated chitosan nanoparticles

被引:138
作者
Lee, DW
Powers, K
Baney, R
机构
[1] Univ Florida, Dept Mat Sci & Engn, Gainesville, FL 32611 USA
[2] Univ Florida, NSF, Particle Engn Res Ctr, Gainesville, FL 32611 USA
基金
美国国家科学基金会;
关键词
acylation; degree of substitution; chitosan nanoparticles; hemolysis; thromboelastography;
D O I
10.1016/j.carbpol.2004.06.033
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Chitosan was N-acylated with butanoic, hexanoic and benzoic anhydride under homogeneous conditions in the presence of methanol. The degree of substitution of N-acyl chitosans was determined by H-1-NMR. The N-acyl chitosan nanoparticles were prepared by the addition of tripolyphosphate anions. Freeze-dried N-acyl chitosan nanoparticles were then analyzed for particles size, zeta potential, and blood compatibility. The N-acyl chitosan nanoparticles were in the range of 200-360 nm and positively charged (10-20 mV) in a saline solution after freeze-drying. It was found that long and bulky acyl groups hinder hydrogen bonding and prevent aggregation. Hemolysis and thromboelastography showed that the N-acyl chitosan nanoparticles were blood compatible. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:371 / 377
页数:7
相关论文
共 33 条
[1]   Preparation and characterization of chitosan microspheres as drug carrier for prednisolone sodium phosphate as model for antiinflammatory drugs [J].
Berthold, A ;
Cremer, K ;
Kreuter, J .
JOURNAL OF CONTROLLED RELEASE, 1996, 39 (01) :17-25
[2]  
Calvo P, 1997, J APPL POLYM SCI, V63, P125, DOI 10.1002/(SICI)1097-4628(19970103)63:1<125::AID-APP13>3.0.CO
[3]  
2-4
[4]  
Fernández-Urrusuno R, 1999, STP PHARMA SCI, V9, P429
[5]   Biodistribution of fluoresceinated dextran using novel nanoparticles evading reticuloendothelial system [J].
Gaur, U ;
Sahoo, SK ;
De, TK ;
Ghosh, PC ;
Maitra, A ;
Ghosh, PK .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 202 (1-2) :1-10
[6]  
HIRANO S, 1985, 130PME AM CHEM SOC, P190
[7]   Synthesis and characterization of chitosan-poly(acrylic acid) nanoparticles [J].
Hu, Y ;
Jiang, XQ ;
Ding, Y ;
Ge, HX ;
Yuan, YY ;
Yang, CZ .
BIOMATERIALS, 2002, 23 (15) :3193-3201
[8]   EFFECT OF THE NON-IONIC SURFACTANT POLOXAMER-338 ON THE FATE AND DEPOSITION OF POLYSTYRENE MICROSPHERES FOLLOWING INTRAVENOUS ADMINISTRATION [J].
ILLUM, L ;
DAVIS, SS .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1983, 72 (09) :1086-1089
[9]  
Illum L, 1998, PHARM RES-DORDR, V15, P1326
[10]   Polysaccharide colloidal particles as delivery systems for macromolecules [J].
Janes, KA ;
Calvo, P ;
Alonso, MJ .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 47 (01) :83-97